SNP - dbSNP |
dbSNP | Type | Alleles | Het | Se(het) | Fxn-class | Gene Name | Assembly | Chr-pos | Sequence | Entrez Gene |
rs6435801 | snp | A/G | 0.478437 | 0.10157 | intron-variant | SPAG16 | GRCh38.p7 | 2:213863578 | TAGATGTTTGACCCT[A/G]CTTTATGAACATGCA | 79582 |
rs6435802 | snp | C/T | 0.3752 | 0.216391 | intron-variant | SPAG16 | GRCh38.p7 | 2:213910633 | AGCTGGGACTACAGG[C/T]GCCCGCTACCACGCC | 79582 |
rs6435803 | snp | G/T | 0.216349 | 0.247725 | intron-variant | SPAG16 | GRCh38.p7 | 2:213910665 | GGCTAATTTTTTGTA[G/T]TTTTAGTAGAGACAG | 79582 |
rs6435804 | snp | A/G | 0.192088 | 0.2432 | intron-variant | SPAG16 | GRCh38.p7 | 2:213910778 | CAGGCGTGAGCCACC[A/G]CGCCCGGCCAAGAAT | 79582 |
rs6435805 | snp | A/C | 0.240765 | 0.249829 | intron-variant | SPAG16 | GRCh38.p7 | 2:213926388 | tttacccctcgcccc[A/C]cttccattccaccct | 79582 |
rs6435806 | snp | A/C | 0.385168 | 0.210309 | intron-variant | SPAG16 | GRCh38.p7 | 2:213939247 | AACTATGTACCAAGT[A/C]ATATAGCTGGAGCTG | 79582 |
rs6435807 | snp | C/T | 0.270351 | 0.24917 | intron-variant | SPAG16 | GRCh38.p7 | 2:213977574 | CTAGGCAAATATTGG[C/T]AGTTCTTAATTGTTG | 79582 |
rs6435808 | snp | A/G | 0.49823 | 0.0296997 | intron-variant | SPAG16 | GRCh38.p7 | 2:213982686 | ATGACATACTACGGT[A/G]TATTTGAGATTATAA | 79582 |
rs6435810 | snp | A/C | 0.49928 | 0.018956 | intron-variant | SPAG16 | GRCh38.p7 | 2:214016491 | TTTGGGTGGGGAACA[A/C]AAAGCCAAGCCATAT | 79582 |
rs6435811 | snp | C/T | 0.143284 | 0.226079 | intron-variant | SPAG16 | GRCh38.p7 | 2:214038876 | aggacatgaaatcat[C/T]attttttatggctgc | 79582 |
rs6435812 | snp | A/C | 0.144632 | 0.226711 | intron-variant | SPAG16 | GRCh38.p7 | 2:214039041 | agcatgatttataat[A/C]ctttgggtatatacc | 79582 |
rs6435814 | snp | C/T | 0.0788843 | 0.182262 | intron-variant | SPAG16 | GRCh38.p7 | 2:214124715 | TTGAAGAAGTGACTG[C/T]TAGTTAACATGCAAA | 79582 |
rs6435815 | snp | A/G | 0.0422008 | 0.138995 | intron-variant | SPAG16 | GRCh38.p7 | 2:214144408 | GGCATAAATTTTTCC[A/G]TGTTTTACATTGGTT | 79582 |
rs6435816 | snp | A/G | 0.0460142 | 0.144533 | intron-variant | SPAG16 | GRCh38.p7 | 2:214149488 | AATAATATAGGTGAT[A/G]ATGTGTACTAATCTA | 79582 |
rs6435817 | snp | C/T | 0.0460142 | 0.144533 | intron-variant | SPAG16 | GRCh38.p7 | 2:214149646 | TTAGCAAAAATGAAC[C/T]TGAAATATTTTTAGT | 79582 |
rs6435818 | snp | A/C | 0.236434 | 0.249632 | intron-variant | SPAG16 | GRCh38.p7 | 2:214203029 | AGTGTAGAATACCAA[A/C]ACAGGTTTTAAATTC | 79582 |
rs6435820 | snp | G/T | 0.426354 | 0.177198 | intron-variant | SPAG16 | GRCh38.p7 | 2:214250757 | ATATATATATATATA[G/T]AGAGAGAGAGAGAGA | 79582 |
rs6435821 | snp | C/T | 0.4628 | 0.13121 | intron-variant | SPAG16 | GRCh38.p7 | 2:214285566 | gtaatcctagcacat[C/T]gggaggccgaggtgg | 79582 |
rs6435822 | snp | A/T | 0.326035 | 0.238157 | intron-variant | SPAG16 | GRCh38.p7 | 2:214378771 | TGTGCCAAGAATGTG[A/T]AGGGATAAATAAAAG | 79582 |
rs6435824 | snp | A/G | 0.284209 | 0.247648 | intron-variant | SPAG16 | GRCh38.p7 | 2:214396253 | gtggcttggcttttt[A/G]ttGTTTATTTTAATA | 79582 |
rs6650781 | snp | A/T | 0.372995 | 0.217652 | intron-variant | SPAG16 | GRCh38.p7 | 2:213496748 | AGTACTTAATTATAT[A/T]TATCCATATATAAAC | 79582 |
rs6704708 | snp | C/T | 0.479984 | 0.0980171 | intron-variant | SPAG16 | GRCh38.p7 | 2:213873103 | agtgttccctcctgt[C/T]ctattttttggaaga | 79582 |
rs6704752 | snp | A/T | 0.317451 | 0.240729 | intron-variant | SPAG16 | GRCh38.p7 | 2:214399105 | CTTACTCAGGTAATA[A/T]ATAGTGACATATATA | 79582 |
rs6704895 | snp | C/T | 0.0402882 | 0.136092 | intron-variant | SPAG16 | GRCh38.p7 | 2:214107472 | AGAGTCAAGAATGCC[C/T]GTTGAACACTGGTGT | 79582 |
rs6705291 | snp | C/G | 0.476401 | 0.106032 | intron-variant | SPAG16 | GRCh38.p7 | 2:213813220 | AAACACCTTCAAAGA[C/G]AGGCAGGGCACACCT | 79582 |
rs6705414 | snp | A/G | 0.345704 | 0.230956 | intron-variant | SPAG16 | GRCh38.p7 | 2:213836434 | ACTCAACTATCAAAA[A/G]CATTGCTGTTATTAT | 79582 |
rs6705506 | snp | A/G | 0.479744 | 0.0985793 | intron-variant | SPAG16 | GRCh38.p7 | 2:213873574 | ttgcttaagatagaa[A/G]gtttggttatgattt | 79582 |
rs6705513 | snp | G/T | 0.479744 | 0.0985793 | intron-variant | SPAG16 | GRCh38.p7 | 2:213873585 | agaaggtttggttat[G/T]atttgagatatttgt | 79582 |
rs6705518 | snp | A/G | 0.480064 | 0.0978296 | intron-variant | SPAG16 | GRCh38.p7 | 2:213873599 | tgatttgagatattt[A/G]ttctttttaaatgta | 79582 |
rs6705674 | snp | C/T | 0.3742 | 0.216966 | intron-variant | SPAG16 | GRCh38.p7 | 2:214378874 | CAATGTTTCCCCTTG[C/T]TCTATAAGGACAGTT | 79582 |
rs6705720 | snp | C/T | 0.315516 | 0.241263 | intron-variant | SPAG16 | GRCh38.p7 | 2:214399908 | CCAGATATATGGGGT[C/T]CCTGAATAAATATTA | 79582 |
rs6705746 | snp | A/G | 0.47726 | 0.104176 | intron-variant | SPAG16 | GRCh38.p7 | 2:213813616 | GTAGAAGCAAAAATT[A/G]TCTGCCAATGAAAGA | 79582 |
rs6705936 | snp | A/T | 0.0178098 | 0.0926698 | intron-variant | SPAG16 | GRCh38.p7 | 2:213709712 | CATGGAGAATATAGT[A/T]CTTTTTATATACCTG | 79582 |
rs6706069 | snp | G/T | 0.279195 | 0.248289 | intron-variant | SPAG16 | GRCh38.p7 | 2:214394239 | CTAAGTCAAGTAAGA[G/T]CTATACAGTGATGAT | 79582 |
rs6706236 | snp | C/T | 0 | 0 | intron-variant | SPAG16 | GRCh38.p7 | 2:214028514 | GTTTGCATGCTTTAG[C/T]CTCTGGTTGTATCTT | 79582 |
rs6706865 | snp | A/G | 0 | 0 | intron-variant | SPAG16 | GRCh38.p7 | 2:213472776 | ccccctactttaact[A/G]gaggaccacagtgac | 79582 |
rs6707234 | snp | A/T | 0.234401 | 0.249513 | intron-variant | SPAG16 | GRCh38.p7 | 2:214185436 | AAACAGAATAAAATA[A/T]ATTCGCATAAATAGA | 79582 |
rs6707313 | snp | C/T | 0.479663 | 0.0987666 | intron-variant | SPAG16 | GRCh38.p7 | 2:213889648 | ACATATACACACACA[C/T]ATATATACATATACA | 79582 |
rs6707387 | snp | A/G | 0.319856 | 0.240042 | intron-variant | SPAG16 | GRCh38.p7 | 2:213683813 | GGAAAAACTAGGCCA[A/G]TGTACTATAATCAGC | 79582 |
rs6707455 | snp | A/G | 0.301932 | 0.244547 | intron-variant | SPAG16 | GRCh38.p7 | 2:214185592 | ATTAAACAGTTACAT[A/G]AATGTATTTTTTAAA | 79582 |
rs6707759 | snp | C/T | 0.0482946 | 0.147699 | intron-variant | SPAG16 | GRCh38.p7 | 2:213673497 | CAATCATGGCACCTC[C/T]ATACAGTAGGCTGTT | 79582 |
rs6707923 | snp | G/T | 0 | 0 | intron-variant | SPAG16 | GRCh38.p7 | 2:213479120 | ttttttttttttttg[G/T]aaaatgccacattta | 79582 |
rs6708127 | snp | A/G | 0.499121 | 0.020948 | intron-variant | SPAG16 | GRCh38.p7 | 2:214296778 | gaaatgccatcccca[A/G]tgttggaaatggggc | 79582 |
rs6708414 | snp | C/T | 0.0475351 | 0.146656 | intron-variant | SPAG16 | GRCh38.p7 | 2:213613834 | TTCCTATTCCTCTCC[C/T]TATAGGAATAAAAAA | 79582 |
rs6708472 | snp | C/T | 0.02016 | 0.0983543 | intron-variant | SPAG16 | GRCh38.p7 | 2:213780371 | CTTCCCATTTTTCTC[C/T]GACTTGTGTGAAATA | 79582 |
rs6709277 | snp | C/T | 0.046775 | 0.145601 | intron-variant | SPAG16 | GRCh38.p7 | 2:213379095 | tcattgttgtgtctc[C/T]tgatggcagcgttcc | 79582 |
rs6709713 | snp | A/G | 0.174288 | 0.23826 | intron-variant | SPAG16 | GRCh38.p7 | 2:213513561 | TTTTGTAATACTGGT[A/G]TCTTCGACACATGAC | 79582 |
rs6710533 | snp | C/T | 0.23031 | 0.249223 | intron-variant | SPAG16 | GRCh38.p7 | 2:213339141 | TCAACATATGCTTCA[C/T]TGAGAGCCTTACTTT | 79582 |
rs6710549 | snp | A/T | 0.472803 | 0.113397 | intron-variant | SPAG16 | GRCh38.p7 | 2:213862253 | CTACTTTGTCTTGCA[A/T]ATGAGGAATCCGAGA | 79582 |
rs6710559 | snp | A/G | 0.472803 | 0.113397 | intron-variant | SPAG16 | GRCh38.p7 | 2:213862297 | ACTAGATTGATGGAG[A/G]TCAGAAAGCTACTAG | 79582 |
rs6712394 | snp | A/T | 0.429688 | 0.173817 | intron-variant | SPAG16 | GRCh38.p7 | 2:213605498 | tttacaaaaaTATAt[A/T]ttttttttgagacag | 79582 |
rs6713303 | snp | A/G | 0.49306 | 0.0584955 | intron-variant | SPAG16 | GRCh38.p7 | 2:213963297 | cttacttgatacatt[A/G]ttcaggagtatattg | 79582 |
rs6713588 | snp | G/T | 0.254944 | 0.249951 | intron-variant | SPAG16, LOC101928084 | GRCh38.p7 | 2:214100731 | tgatctcattctttt[G/T]tacgcctgaatagta | 79582 |
rs6713816 | snp | C/T | 0.0509478 | 0.151255 | intron-variant | SPAG16 | GRCh38.p7 | 2:214380747 | AATAGAAATGATAAG[C/T]ACCACAGCATGTCGG | 79582 |
rs6714039 | snp | A/G | 0.481396 | 0.0946345 | intron-variant | SPAG16 | GRCh38.p7 | 2:213896149 | cagacctgaatagac[A/G]tttatcaaaagaaga | 79582 |
rs6714095 | snp | C/T | 0.481396 | 0.0946345 | intron-variant | SPAG16 | GRCh38.p7 | 2:213896362 | gggaatgtaaatttg[C/T]atagctactatggag | 79582 |
rs6714219 | snp | A/T | 0.45866 | 0.137698 | intron-variant | SPAG16 | GRCh38.p7 | 2:214331046 | ATTCTCTTCTTAACT[A/T]TCATTCTGTATTTCC | 79582 |
rs6714235 | snp | C/T | 0.481473 | 0.0944461 | intron-variant | SPAG16 | GRCh38.p7 | 2:213896491 | gagacattacactct[C/T]atgtttactgcaaca | 79582 |
rs6714437 | snp | C/T | 0.4862 | 0.0819127 | intron-variant | SPAG16 | GRCh38.p7 | 2:214060487 | GAAAACATAGCAAAA[C/T]AAAAATCGAAAGAAA | 79582 |
rs6714461 | snp | A/G | 0.481396 | 0.0946345 | intron-variant | SPAG16 | GRCh38.p7 | 2:213896516 | gcaacactattcaca[A/G]tagccaaaatgtgga | 79582 |
rs6714666 | snp | A/G | 0.149665 | 0.228982 | intron-variant | SPAG16 | GRCh38.p7 | 2:214280215 | CGaactaaaaaacat[A/G]cagaaaaaaataaag | 79582 |
rs6714784 | snp | A/C | 0.342134 | 0.232404 | intron-variant | SPAG16 | GRCh38.p7 | 2:214398441 | TCCTGTATATAGCTA[A/C]ATCATGCGTGCCTCA | 79582 |
rs6714962 | snp | A/G | 0.0414363 | 0.137845 | intron-variant, upstream-variant-2KB | SPAG16, LOC101928084 | GRCh38.p7 | 2:214104741 | CTTATTATGTCTGAC[A/G]TGCtgcatcagacag | 79582 |
rs6715127 | snp | A/G | 0.155325 | 0.23138 | intron-variant | SPAG16 | GRCh38.p7 | 2:214280599 | TTTTTTAAATTTATC[A/G]TCTTTCTGAAAAATC | 79582 |
rs6715355 | snp | G/T | 0.46865 | 0.121211 | intron-variant | SPAG16 | GRCh38.p7 | 2:213685481 | ctgctaacaccttga[G/T]tttggccttctggcc | 79582 |
rs6715771 | snp | C/T | 0.199873 | 0.244923 | intron-variant | SPAG16 | GRCh38.p7 | 2:214076010 | AAGCATATGTCTATA[C/T]TTGAATGCATTTTTA | 79582 |
rs6715997 | snp | C/T | 0.453453 | 0.145282 | intron-variant | SPAG16 | GRCh38.p7 | 2:214076185 | TTTGAATTTGGAATG[C/T]CTTGCATGATTTTTG | 79582 |
rs6716159 | snp | C/T | 0.19334 | 0.243495 | intron-variant | SPAG16 | GRCh38.p7 | 2:213314444 | AGCAAACCACAAAAA[C/T]ATTATGTATGAGAAT | 79582 |
rs6716184 | snp | A/G | 0.0170251 | 0.090679 | intron-variant | SPAG16 | GRCh38.p7 | 2:213520128 | ctaagtgatgacaga[A/G]gcagagattggagtt | 79582 |
rs6716478 | snp | A/C | 0.483923 | 0.0882034 | intron-variant | SPAG16 | GRCh38.p7 | 2:213615622 | AACAATTAAAAAAAA[A/C]CCAAAAAACTTTATT | 79582 |
rs6716508 | snp | C/T | 0.351418 | 0.228505 | intron-variant | SPAG16 | GRCh38.p7 | 2:213851494 | GCCTGGGTGACAGAG[C/T]GAGACTCCCTCTTAA | 79582 |
rs6716909 | snp | A/G | 0.412082 | 0.190341 | intron-variant | SPAG16 | GRCh38.p7 | 2:213608767 | ctcggctcactgcca[A/G]ctccgcctcctgcgt | 79582 |
rs6717098 | snp | G/T | 0.479904 | 0.0982045 | intron-variant | SPAG16 | GRCh38.p7 | 2:213872914 | tgaaccaaccttgca[G/T]tcctgaaataaatgc | 79582 |
rs6717536 | snp | C/G | 0.0792508 | 0.182605 | intron-variant | SPAG16 | GRCh38.p7 | 2:214110534 | cttaatccagtctat[C/G]attgatggacatttg | 79582 |
rs6717618 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | SPAG16 | GRCh38.p7 | 2:214316536 | CTTTTTATAAGGACC[A/C]GCGATGAAAGTTGTA | 79582 |
rs6717752 | snp | A/T | 0.362848 | 0.228703 | intron-variant | SPAG16 | GRCh38.p7 | 2:213362809 | atttataaggaaaag[A/T]ggtttatttggcgca | 79582 |
rs6717969 | snp | G/T | 0.326741 | 0.23793 | intron-variant | SPAG16 | GRCh38.p7 | 2:213897026 | tacagtgactatatt[G/T]tacaacaatctattg | 79582 |
rs6717986 | snp | C/T | 0.151334 | 0.229706 | intron-variant | SPAG16 | GRCh38.p7 | 2:214286725 | gcactccagcctggg[C/T]gacagagtgagactg | 79582 |
rs6718201 | snp | A/G | 0.484841 | 0.0857308 | intron-variant | SPAG16 | GRCh38.p7 | 2:213904666 | ATGAGACTGGAATTT[A/G]GATAGGCCTCTCTTC | 79582 |
rs6718488 | snp | A/G | 0.484841 | 0.0857308 | intron-variant | SPAG16 | GRCh38.p7 | 2:213904929 | gtcttactgtgagaa[A/G]tgagaaaccattgga | 79582 |
rs6718695 | snp | A/G | 0.046775 | 0.145601 | intron-variant | SPAG16 | GRCh38.p7 | 2:213408080 | ggcaggagagagaga[A/G]agagaaaaatagaag | 79582 |
rs6718751 | snp | A/C/G | 0.000399281 | 0.0141238 | intron-variant | SPAG16 | GRCh38.p7 | 2:214311263 | tcccacagctcccca[A/C/G]ggacctgatggacct | 79582 |
rs6719232 | snp | C/T | 0.437824 | 0.164991 | intron-variant | SPAG16 | GRCh38.p7 | 2:214004960 | tcgaccgTATTTTCA[C/T]ATTGTTGTTATTTAA | 79582 |
rs6719752 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | SPAG16 | GRCh38.p7 | 2:214394198 | GTGCCTCTTTTTTCT[A/G]TGTGGCTTTTTTTCT | 79582 |
rs6719800 | snp | A/G | 0.494855 | 0.0504572 | intron-variant | SPAG16 | GRCh38.p7 | 2:213952712 | GAACCCATTCTAACC[A/G]TGGATGGAGGGCTAA | 79582 |
rs6720110 | snp | C/T | 0.354235 | 0.227234 | intron-variant | SPAG16 | GRCh38.p7 | 2:213797851 | ctaggagtagagctg[C/T]tgtcttatagggtta | 79582 |
rs6720429 | snp | G/T | 0.192401 | 0.243274 | intron-variant | SPAG16 | GRCh38.p7 | 2:213482196 | AGGCTGGATGGGAGT[G/T]CCTGCCCCATACTTT | 79582 |
rs6721367 | snp | A/G | 0.0456336 | 0.143994 | intron-variant | SPAG16 | GRCh38.p7 | 2:214016295 | aggaagcaaagtcac[A/G]tcatacatggcagca | 79582 |
rs6721572 | snp | A/G | | | intron-variant | SPAG16 | GRCh38.p7 | 2:213421165 | tcggggtcccaggaa[A/G]ccaccctgcccccac | 79582 |
rs6721889 | snp | A/G | 0.02016 | 0.0983543 | intron-variant | SPAG16 | GRCh38.p7 | 2:213780242 | AAAGGTAAAAGAGAT[A/G]CCTTTACTATCACAT | 79582 |
rs6722119 | snp | G/T | 0.495596 | 0.0467178 | intron-variant | SPAG16 | GRCh38.p7 | 2:214016920 | ATACAAAACATGATT[G/T]ATATAAATAAAGGAA | 79582 |
rs6722554 | snp | A/G/T | 0 | 0 | intron-variant | SPAG16 | GRCh38.p7 | 2:214178013 | TATATATATATATAT[A/G/T]CATACTTTATTTGTA | 79582 |
rs6722672 | snp | A/G | 0.328616 | 0.237317 | intron-variant | SPAG16 | GRCh38.p7 | 2:213898616 | TGTCAGAAAATTCAC[A/G]GACTTGGTTATGCAT | 79582 |
rs6722817 | snp | C/G | 0.498982 | 0.0225409 | intron-variant | SPAG16 | GRCh38.p7 | 2:213958903 | atcttgtcattttac[C/G]ctgcaggactttctc | 79582 |
rs6723049 | snp | C/T | 0 | 0 | intron-variant | SPAG16 | GRCh38.p7 | 2:214208488 | gaGTGCTGAATCTTT[C/T]TCAAACTATTTCAGT | 79582 |
rs6723346 | snp | A/C | 0.133093 | 0.220981 | intron-variant | SPAG16 | GRCh38.p7 | 2:214217911 | CTTCTGTCTCCAACC[A/C]TTTTTATACTCTTAA | 79582 |
rs6723396 | snp | A/T | 0.0482946 | 0.147699 | intron-variant | SPAG16 | GRCh38.p7 | 2:213673699 | ATTGTCCACACTGGC[A/T]TCTACTAAGGTAATG | 79582 |
rs6723575 | snp | A/G | 0.359998 | 0.2245 | intron-variant | SPAG16 | GRCh38.p7 | 2:213291661 | TTTGGAAAAAAATAG[A/G]TGAGTTCATTACCTA | 79582 |
rs6723977 | snp | A/T | 0.0399052 | 0.1355 | intron-variant | SPAG16 | GRCh38.p7 | 2:214154812 | gtagggacttctact[A/T]ccagacaagatgttg | 79582 |
rs6724980 | snp | G/T | 0.472709 | 0.11358 | intron-variant | SPAG16 | GRCh38.p7 | 2:213853673 | AGAGCCTTTATTTTT[G/T]AATCTTGTAATTATA | 79582 |
rs6725058 | snp | C/G | 0.0221141 | 0.102801 | intron-variant | SPAG16 | GRCh38.p7 | 2:214142346 | CTCACACTTTAAAAT[C/G]TTTTTCAGTCTTTCA | 79582 |
rs6725238 | snp | A/G | 0.135484 | 0.22223 | intron-variant | SPAG16 | GRCh38.p7 | 2:213728738 | aaaaattagccgggc[A/G]tggtggtgggtgcct | 79582 |
rs6725524 | snp | C/G | 0.499 | 0.0223418 | intron-variant | SPAG16 | GRCh38.p7 | 2:213959035 | atatataagaaagtt[C/G]gttgacggtttttgt | 79582 |
rs6725721 | snp | A/T | | | intron-variant | SPAG16 | GRCh38.p7 | 2:213383207 | ATATTGGATAATATA[A/T]GTATAAACACTTTAT | 79582 |
rs6725725 | snp | A/T | 0.119978 | 0.213528 | intron-variant | SPAG16 | GRCh38.p7 | 2:214325926 | CTGCCCTCCATGAGC[A/T]TAGGAATCATGCCTG | 79582 |
rs6725801 | snp | A/G | 0.0505692 | 0.150756 | intron-variant | SPAG16 | GRCh38.p7 | 2:214142803 | AGCTTCATTTTGTCA[A/G]GAAATCTTACCCCAG | 79582 |
rs6726034 | snp | A/T | 0 | 0 | intron-variant | SPAG16 | GRCh38.p7 | 2:213744459 | CTAAGAATAAGGAAT[A/T]CTGTCTTTACTCTTT | 79582 |
rs6726484 | snp | C/T | 0.0107246 | 0.0724382 | intron-variant | SPAG16 | GRCh38.p7 | 2:214373433 | CCTCTCAGAACAATA[C/T]CAAAGGTAGTGTATT | 79582 |
rs6726871 | snp | A/G | 0.447162 | 0.153712 | intron-variant | SPAG16 | GRCh38.p7 | 2:214012448 | TTACAGGCATATGCC[A/G]CCACGTCAGGCTAAT | 79582 |
rs6726965 | snp | A/C | 0.00279162 | 0.0372561 | intron-variant | SPAG16 | GRCh38.p7 | 2:213771317 | gtttttttccttgta[A/C]atttgtttaagttcc | 79582 |
rs6727597 | snp | A/G | 0.0023933 | 0.0345097 | intron-variant | SPAG16 | GRCh38.p7 | 2:213771783 | agtcttatttctgag[A/G]tctctattctgttcc | 79582 |
rs6728148 | snp | A/C | 0.0437281 | 0.141251 | intron-variant | SPAG16 | GRCh38.p7 | 2:213586844 | aataggatccaagta[A/C]gtccagaataataaa | 79582 |
rs6728177 | snp | A/G | 0.474992 | 0.108989 | intron-variant | SPAG16 | GRCh38.p7 | 2:214331489 | tacttaaagttacag[A/G]gacagaaaggaaaaa | 79582 |
rs6728361 | snp | A/G | 0.36955 | 0.219562 | intron-variant | SPAG16 | GRCh38.p7 | 2:213894918 | tcactgaacctagga[A/G]gcagaagttgcagtg | 79582 |
rs6728624 | snp | G/T | 0.0854556 | 0.188216 | intron-variant | SPAG16 | GRCh38.p7 | 2:214380356 | CTTCAAGAAAATGCC[G/T]AAAACAATTTTCAGA | 79582 |
rs6728974 | snp | C/T | 0.190519 | 0.242821 | intron-variant | SPAG16 | GRCh38.p7 | 2:214082996 | TCACCTTTCTCACTT[C/T]CAGTAAATAAGCTCT | 79582 |
rs6729931 | snp | G/T | 0.472803 | 0.113397 | intron-variant | SPAG16 | GRCh38.p7 | 2:213855990 | tctcaactcatttca[G/T]cattaactcaaaagt | 79582 |
rs6730907 | snp | G/T | 0.0103295 | 0.0711199 | intron-variant | SPAG16 | GRCh38.p7 | 2:213620876 | ATAAATTTAAGTGCT[G/T]AAGAAATTGAAACAC | 79582 |
rs6730909 | snp | C/T | 0.498871 | 0.0237351 | intron-variant | SPAG16 | GRCh38.p7 | 2:214305285 | tagacctttgtcaga[C/T]gcagtttgcaaaaat | 79582 |
rs6731015 | snp | C/T | 0.0154538 | 0.0865337 | intron-variant | SPAG16 | GRCh38.p7 | 2:214305349 | gttgataattttctt[C/T]tgctgtgcagaatct | 79582 |
rs6731046 | snp | G/T | 0.0154538 | 0.0865337 | intron-variant | SPAG16 | GRCh38.p7 | 2:214305395 | atcccatttgtcaac[G/T]ttttcattttgttgc | 79582 |
rs6731062 | snp | C/T | 0.239326 | 0.249772 | intron-variant | SPAG16 | GRCh38.p7 | 2:214305420 | tgttgcaattgcttt[C/T]ggtgtcttcatcatg | 79582 |
rs6731110 | snp | A/C | 0.301177 | 0.244706 | intron-variant | SPAG16 | GRCh38.p7 | 2:214314553 | CACTCACTAGAGAAA[A/C]CTTAGGAAAGTTACT | 79582 |
rs6731606 | snp | A/G | 0.289165 | 0.246913 | intron-variant | SPAG16 | GRCh38.p7 | 2:214219753 | AGTTTCTCTGTGTCT[A/G]TGTGTGTCTTTACTG | 79582 |
rs6731608 | snp | G/T | 0.431621 | 0.171796 | intron-variant | SPAG16 | GRCh38.p7 | 2:213654576 | AAAAAAATTAGCCGG[G/T]TGTGGTGGTGGGCGC | 79582 |
rs6731626 | snp | G/T | 0.264906 | 0.249555 | intron-variant | SPAG16 | GRCh38.p7 | 2:214386502 | ATATGGAAACAAAGT[G/T]TATCAAATAGATAAA | 79582 |
rs6732019 | snp | C/G | 0.0991586 | 0.199366 | intron-variant | SPAG16 | GRCh38.p7 | 2:214390015 | TAACCAACGTTTGTA[C/G]TGAAGCCCGACACTA | 79582 |
rs6732720 | snp | C/T | 0 | 0 | intron-variant | SPAG16 | GRCh38.p7 | 2:213450364 | TGACATTTGCTTCTG[C/T]TACTCAATTCTAGTT | 79582 |
rs6733141 | snp | A/T | 0.481319 | 0.0948228 | intron-variant | SPAG16 | GRCh38.p7 | 2:213897174 | gtattaaattattat[A/T]tgtaccctgaaacta | 79582 |
rs6733227 | snp | G/T | 0.489665 | 0.0711382 | intron-variant | SPAG16 | GRCh38.p7 | 2:214114135 | ctccagaccctgttt[G/T]cctgtgtatcaccag | 79582 |
rs6733286 | snp | C/T | 0.481087 | 0.0953875 | intron-variant | SPAG16 | GRCh38.p7 | 2:213897312 | GTTTATTTTGGAATA[C/T]CAATACCCCTTCAAC | 79582 |
rs6733377 | snp | A/G | 0.441977 | 0.16014 | intron-variant | SPAG16 | GRCh38.p7 | 2:214114234 | ccgcctgtatgaggt[A/G]tctgtcagcccctac | 79582 |
rs6733457 | snp | C/G | 0.0471551 | 0.14613 | intron-variant | SPAG16 | GRCh38.p7 | 2:213359071 | accctgtttgcctcg[C/G]tatcaccagcagagg | 79582 |
rs6733511 | snp | A/G | 0.479904 | 0.0982045 | intron-variant | SPAG16 | GRCh38.p7 | 2:213873058 | ggttttggtattaga[A/G]caatactggcctcac | 79582 |
rs6733518 | snp | A/G | 0.479904 | 0.0982045 | intron-variant | SPAG16 | GRCh38.p7 | 2:213873072 | aacaatactggcctc[A/G]cagaataagttaggc | 79582 |
rs6733563 | snp | C/G | 0.0444908 | 0.142359 | intron-variant | SPAG16 | GRCh38.p7 | 2:213700895 | ctcacacatataatc[C/G]cagcactttgggagg | 79582 |
rs6733681 | snp | C/T | 0.48491 | 0.0855403 | intron-variant | SPAG16 | GRCh38.p7 | 2:213906787 | atcctcttcaataaa[C/T]agtgctgggcaaata | 79582 |
rs6734329 | snp | A/G | 0.325563 | 0.238307 | intron-variant | SPAG16 | GRCh38.p7 | 2:214378828 | TGCCCTCAGTCACAG[A/G]CCTAGGAAACAAGTT | 79582 |
rs6734364 | snp | A/G | 0.0263992 | 0.111815 | intron-variant | SPAG16 | GRCh38.p7 | 2:214375049 | AAAAGTTTGAATTTG[A/G]GTCTTGAACATGTGT | 79582 |
rs6734444 | snp | A/G | 0.192401 | 0.243274 | intron-variant | SPAG16 | GRCh38.p7 | 2:213482765 | AGTGTAGAATTATGT[A/G]TCTAGGAACCAGATT | 79582 |
rs6734776 | snp | G/T | 0.452597 | 0.146474 | intron-variant | SPAG16 | GRCh38.p7 | 2:213952807 | CCAATAGCTGAAATA[G/T]GGGTGTCAAGTCTTT | 79582 |
rs6735162 | snp | A/G | 0.410399 | 0.191761 | intron-variant | SPAG16 | GRCh38.p7 | 2:213977565 | aacatccaactaggc[A/G]aatattggcagttct | 79582 |
rs6735183 | snp | A/G | 0 | 0 | intron-variant | SPAG16 | GRCh38.p7 | 2:213560176 | GAAGCCTCCATAGAA[A/G]AAAAGGAATGCTTAA | 79582 |
rs6735254 | snp | C/T | 0.0162398 | 0.0886349 | intron-variant | SPAG16 | GRCh38.p7 | 2:213625416 | aacacctcgtgtacc[C/T]cccgtaaatatatat | 79582 |
rs6735352 | snp | A/G | 0.401215 | 0.199083 | intron-variant | SPAG16 | GRCh38.p7 | 2:214308664 | agtttggccagatat[A/G]aaattctggtttgga | 79582 |
rs6735353 | snp | C/G | 0.47852 | 0.101384 | intron-variant | SPAG16 | GRCh38.p7 | 2:213736019 | GGAGATTAAGAATTT[C/G]CTCAATGTCACTGAG | 79582 |
rs6735405 | snp | C/G | | | intron-variant | SPAG16 | GRCh38.p7 | 2:213354609 | tggtatctcattgtg[C/G]tttttatttgcattt | 79582 |
rs6735479 | snp | A/G | 0.48995 | 0.0701706 | intron-variant | SPAG16 | GRCh38.p7 | 2:214285735 | ttgaacctgggaggc[A/G]gaggttgcagtgaac | 79582 |
rs6735700 | snp | A/G | 0.135825 | 0.222405 | intron-variant | SPAG16 | GRCh38.p7 | 2:213287727 | AGTTCTGTGAAGCTA[A/G]TCAGCTCTGAATGGA | 79582 |
rs6735936 | snp | A/C | 0.480539 | 0.0967035 | intron-variant | SPAG16 | GRCh38.p7 | 2:213889615 | ACACACACACACACA[A/C]AATATATATATACAT | 79582 |
rs6736288 | snp | A/G | 0.479904 | 0.0982045 | intron-variant | SPAG16 | GRCh38.p7 | 2:213889841 | GGGAAGCCTCTAATC[A/G]ACTAAATATCTCGAC | 79582 |
rs6737229 | snp | C/T | 0.130351 | 0.219509 | intron-variant | SPAG16 | GRCh38.p7 | 2:214351190 | GAAAAAATATTAATG[C/T]AGAAAGCAAATTTGA | 79582 |
rs6737326 | snp | A/G | 0.457737 | 0.139088 | intron-variant | SPAG16 | GRCh38.p7 | 2:214351132 | TATTGTAATCCTTCC[A/G]TGACTAGAAAACCTA | 79582 |
rs6737484 | snp | A/C | 0.0475351 | 0.146656 | intron-variant | SPAG16 | GRCh38.p7 | 2:213606812 | CATCATCCATACCTT[A/C]GGCAAAATGCAAAGC | 79582 |
rs6738356 | snp | A/G | 0.0803491 | 0.183626 | intron-variant | SPAG16 | GRCh38.p7 | 2:214133143 | ataaaaaaaaaaCCT[A/G]CCATTAGCATAGAGC | 79582 |
rs6738653 | snp | C/T | 0.479258 | 0.0997024 | intron-variant | SPAG16 | GRCh38.p7 | 2:214075634 | GAAAAACTTCATATC[C/T]TCAGGGGAATAATGA | 79582 |
rs6738701 | snp | A/T | 0.0329836 | 0.124112 | intron-variant | SPAG16 | GRCh38.p7 | 2:213978190 | ACCAGTCCTTAACTG[A/T]TAAGtctcctctcac | 79582 |
rs6738790 | snp | C/G | 0.473634 | 0.111748 | intron-variant | SPAG16 | GRCh38.p7 | 2:214221309 | ATGTTTTCTTTGTAA[C/G]TTATCTTATTTCTTT | 79582 |
rs6739233 | snp | A/G | 0.0854556 | 0.188216 | intron-variant, downstream-variant-500B | SPAG16 | GRCh38.p7 | 2:214062991 | tgaaattaatttaat[A/G]acattatatttaacc | 79582 |
rs6739393 | snp | C/T | 0.355096 | 0.226837 | intron-variant | SPAG16 | GRCh38.p7 | 2:213355809 | atcatgtcatctgca[C/T]gcagggacaatttga | 79582 |
rs6739420 | snp | C/G | 0.0267878 | 0.112589 | intron-variant | SPAG16 | GRCh38.p7 | 2:214221736 | CTCTATGCATCAGAG[C/G]AATGCTAAAGAAAGA | 79582 |
rs6739421 | snp | A/C | 0.349013 | 0.229557 | intron-variant | SPAG16 | GRCh38.p7 | 2:213774688 | aaaataaaataccag[A/C]tatttgtgtaaagaa | 79582 |
rs6739423 | snp | A/G | 0.472803 | 0.113397 | intron-variant | SPAG16 | GRCh38.p7 | 2:213862265 | GCAAATGAGGAATCC[A/G]AGATCCAGTGAAGCT | 79582 |
rs6739649 | snp | A/C | 0.475437 | 0.108066 | intron-variant | SPAG16 | GRCh38.p7 | 2:214334117 | aatcctgtagggctg[A/C]gggatacatgtcagt | 79582 |
rs6740147 | snp | C/T | 0.477853 | 0.102875 | intron-variant | SPAG16 | GRCh38.p7 | 2:213853877 | AGGGAGACCTATTTG[C/T]GGACAAAGCTTGAGG | 79582 |
rs6740402 | snp | A/G | 0.0425829 | 0.139564 | intron-variant | SPAG16 | GRCh38.p7 | 2:213707753 | CTAATTTTCTAAGGT[A/G]ATGGAAAAAAATCTA | 79582 |
rs6740801 | snp | C/T | 0.155656 | 0.231515 | intron-variant | SPAG16 | GRCh38.p7 | 2:213336446 | ggcttggaatccctg[C/T]cagccaacgcagcag | 79582 |
rs6741023 | snp | A/G | 0.0471551 | 0.14613 | intron-variant | SPAG16 | GRCh38.p7 | 2:213336477 | gtcagagactgccta[A/G]gaagacttaattccg | 79582 |
rs6741126 | snp | C/T | 0.201418 | 0.245234 | intron-variant | SPAG16 | GRCh38.p7 | 2:214257028 | tttgtatcttgcaat[C/T]cgtggaaatgatgaa | 79582 |
rs6742236 | snp | A/T | 0.409212 | 0.192748 | intron-variant | SPAG16 | GRCh38.p7 | 2:213799063 | tttggcatctttgta[A/T]ttatgtagacatttt | 79582 |
rs6742411 | snp | G/T | 0.235854 | 0.249599 | intron-variant | SPAG16 | GRCh38.p7 | 2:213954461 | ttatgaattatgaaa[G/T]atttatgtacaggtt | 79582 |
rs6742414 | snp | A/G | 0.105214 | 0.203807 | intron-variant | SPAG16 | GRCh38.p7 | 2:214380844 | GATGTGAAGTCAATT[A/G]TTGCTTCCACTTCTA | 79582 |
rs6742421 | snp | C/T | 0.357024 | 0.225933 | intron-variant | SPAG16 | GRCh38.p7 | 2:213602588 | gcagtgagccaagat[C/T]gtgccactgtgctcc | 79582 |
rs6742853 | snp | C/T | 0.481473 | 0.0944461 | intron-variant | SPAG16 | GRCh38.p7 | 2:213859769 | AATGGCATAAAATAA[C/T]AATACTGATAGTACC | 79582 |
rs6742966 | snp | A/G | 0.41833 | 0.184838 | intron-variant | SPAG16 | GRCh38.p7 | 2:214405469 | GCCAGTAAATGAAGC[A/G]AGACTTTTTGAGTAA | 79582 |
rs6743075 | snp | A/G | 0.126564 | 0.217402 | intron-variant | SPAG16 | GRCh38.p7 | 2:214340606 | GCTCCAGCAGGCCTG[A/G]TGTATGTTGCTTGGT | 79582 |
rs6743402 | snp | C/T | 0.350982 | 0.228698 | intron-variant | SPAG16 | GRCh38.p7 | 2:213824155 | gttttcccagcacca[C/T]ttactgaataggaga | 79582 |
rs6743751 | snp | C/G | 0.482979 | 0.0906686 | intron-variant | SPAG16, LOC101928084 | GRCh38.p7 | 2:214091956 | CCCACAAACACACTT[C/G]CAGACAAGGTCCTTT | 79582 |
rs6743939 | snp | G/T | 0.44252 | 0.159487 | intron-variant | SPAG16 | GRCh38.p7 | 2:214389813 | AGACTAAACTGCCAG[G/T]TATATTGCCTCATCT | 79582 |
rs6744046 | snp | C/T | 0.039522 | 0.134904 | intron-variant | SPAG16 | GRCh38.p7 | 2:214083043 | CCCTATTTTGTTCTT[C/T]GACTTTTAAAAAATT | 79582 |
rs6744356 | snp | A/C | 0.476574 | 0.105661 | intron-variant | SPAG16 | GRCh38.p7 | 2:214335644 | AGTTATAAGCACTAA[A/C]CTTGGATTTATGTAG | 79582 |
rs6744533 | snp | A/G | 0.484561 | 0.0864924 | intron-variant | SPAG16 | GRCh38.p7 | 2:213520274 | cttgatttcagactt[A/G]tggcctccagaactg | 79582 |
rs6744795 | snp | A/G | 0.474363 | 0.110278 | intron-variant | SPAG16 | GRCh38.p7 | 2:213615566 | ACTGCACTCCAGCAT[A/G]GGCGACAAAGCAAGA | 79582 |
rs6744816 | snp | A/G | 0.140242 | 0.224618 | intron-variant | SPAG16 | GRCh38.p7 | 2:213733260 | ttccttatagatgct[A/G]aatattagacctttg | 79582 |
rs6744864 | snp | C/T | 0.275999 | 0.248644 | intron-variant | SPAG16 | GRCh38.p7 | 2:213988675 | acattttagattttt[C/T]taaattaaaaaaaaa | 79582 |
rs6745002 | snp | A/G | 0.497586 | 0.0346604 | intron-variant | SPAG16 | GRCh38.p7 | 2:213997758 | ATAAAAAAATTGCCA[A/G]TCTCATAATGTTTTA | 79582 |
rs6745285 | snp | A/T | 0.177182 | 0.23916 | intron-variant | SPAG16 | GRCh38.p7 | 2:214205312 | gcataaataaaaaac[A/T]atcacaactcctgga | 79582 |
rs6745376 | snp | C/T | 0.00952359 | 0.0683454 | intron-variant | SPAG16 | GRCh38.p7 | 2:213659774 | TAATTACTGCACTTA[C/T]TTTATCAGTGTGTTG | 79582 |
rs6745832 | snp | C/T | 0.173965 | 0.238157 | intron-variant | SPAG16 | GRCh38.p7 | 2:213559135 | TTAATTTTATTCTTT[C/T]GACGCAATAAGAAGA | 79582 |
rs6745897 | snp | A/G | 0.498503 | 0.0273153 | intron-variant | SPAG16 | GRCh38.p7 | 2:214346616 | gctatgtgacctggg[A/G]ctaggtcataaaagg | 79582 |
rs6746290 | snp | A/G | 0.463666 | 0.129795 | intron-variant | SPAG16 | GRCh38.p7 | 2:213934277 | ACAGTTTATACTGCA[A/G]TTATTCTGTCCTTAC | 79582 |
rs6746741 | snp | C/T | 0 | 0 | synonymous-codon, nc-transcript-variant | SPAG16 | GRCh38.p7 | 2:214149169 | ATCCTGTGATGCCTG[C/T]GGGGTTACAAAGCTG | 79582 |
rs6747293 | snp | A/T | 0.382666 | 0.211895 | intron-variant | SPAG16 | GRCh38.p7 | 2:213621315 | TCATTTGAAAGAAAA[A/T]TATGTTACAACTGAG | 79582 |
rs6747335 | snp | C/G | 0.132409 | 0.220618 | intron-variant | SPAG16 | GRCh38.p7 | 2:213377942 | ggatagaactaataa[C/G]atatatatggggagt | 79582 |
rs6747847 | snp | A/T | 0.348134 | 0.229934 | intron-variant | SPAG16 | GRCh38.p7 | 2:213922631 | tgtcagagttctttc[A/T]ctggctttttctaat | 79582 |
rs6747910 | snp | C/T | 0.103438 | 0.202533 | intron-variant | SPAG16 | GRCh38.p7 | 2:214153283 | cttgtcttctggtca[C/T]ttctcactgtgtccc | 79582 |
rs6747982 | snp | A/G | 0.0189856 | 0.0955633 | intron-variant | SPAG16 | GRCh38.p7 | 2:213408599 | taaatcttaattacc[A/G]tacaaaggtccgacc | 79582 |
rs6748224 | snp | A/G | 0.155656 | 0.231515 | intron-variant | SPAG16 | GRCh38.p7 | 2:213378658 | acaattacagtcctc[A/G]tttctgcagctggtc | 79582 |
rs6748348 | snp | A/G | 0.0329836 | 0.124112 | intron-variant | SPAG16 | GRCh38.p7 | 2:214146473 | AATATTCACCTGCAA[A/G]ACTGCTTTGGAAGGA | 79582 |
rs6748512 | snp | A/G | 0.144632 | 0.226711 | intron-variant | SPAG16 | GRCh38.p7 | 2:213709843 | TTCTCAGAATACACA[A/G]GTTTGACCATTGCCT | 79582 |
rs6748633 | snp | A/G | 0.358728 | 0.225118 | intron-variant | SPAG16 | GRCh38.p7 | 2:213792063 | AAACACCAAGCCAGT[A/G]TTCATCGAGACAAAT | 79582 |
rs6748741 | snp | A/G | 0.0107246 | 0.0724382 | intron-variant | SPAG16 | GRCh38.p7 | 2:214153772 | AGTTATATGTAATGC[A/G]ATATATACATATATA | 79582 |
rs6748907 | snp | C/G/T | 0.102842 | 0.2021 | intron-variant | SPAG16 | GRCh38.p7 | 2:213931094 | catgatattttaatg[C/G/T]tcttttccctttttt | 79582 |
rs6749110 | snp | A/G | 0.0471551 | 0.14613 | intron-variant | SPAG16 | GRCh38.p7 | 2:213456711 | GGATCTGTTTCTCCA[A/G]ATTCTTCTTTGAGTG | 79582 |
rs6749115 | snp | C/T | 0.475965 | 0.106957 | intron-variant | SPAG16 | GRCh38.p7 | 2:213630419 | TTCTGTCTTCACAGA[C/T]GAACTGATATTGAGG | 79582 |
rs6749347 | snp | A/G | 0.232067 | 0.249356 | intron-variant | SPAG16 | GRCh38.p7 | 2:214016128 | ACTGGTAGGTTCAAG[A/G]GTGAATTTGATTTTA | 79582 |
rs6749380 | snp | C/T | 0.353587 | 0.22753 | intron-variant | SPAG16 | GRCh38.p7 | 2:214375219 | GAAACAGAACTTCAA[C/T]TTAAATGGTTTTCTA | 79582 |
rs6749651 | snp | A/G | 0.481087 | 0.0953875 | intron-variant | SPAG16 | GRCh38.p7 | 2:213704771 | TATCTTTTGGGCATT[A/G]AAGAGTTATTGGAGA | 79582 |
rs6750135 | snp | A/G | 0.48491 | 0.0855403 | intron-variant | SPAG16 | GRCh38.p7 | 2:213904991 | attcttcaggtttct[A/G]tattgaaaatagatt | 79582 |
rs6750785 | snp | C/G | 0.340784 | 0.232934 | intron-variant | SPAG16 | GRCh38.p7 | 2:213810616 | TGAAGATATAGAGGA[C/G]AATTCAGAAGAGTTT | 79582 |
rs6751454 | snp | A/C | 0.460252 | 0.135255 | intron-variant | SPAG16 | GRCh38.p7 | 2:213710083 | ATGGAGATGGAGACT[A/C]TCCTGGCTAACATGG | 79582 |
rs6751686 | snp | A/G | 0.194902 | 0.243853 | intron-variant | SPAG16 | GRCh38.p7 | 2:213379143 | cctctaggccagcag[A/G]atcaatgttgtggga | 79582 |
rs6751733 | snp | G/T | 0.155325 | 0.23138 | intron-variant | SPAG16 | GRCh38.p7 | 2:213439411 | aatactcatggtcag[G/T]acttagaaagaagta | 79582 |
rs6751787 | snp | G/T | 0.145305 | 0.227022 | intron-variant | SPAG16 | GRCh38.p7 | 2:213710191 | cgggaggctgaggca[G/T]gagaatcacttgaac | 79582 |
rs6752347 | snp | A/C | 0.0471551 | 0.14613 | intron-variant, utr-variant-3-prime | SPAG16 | GRCh38.p7 | 2:213369088 | TTTAAAGTGTGGAAA[A/C]AATTTTAATTCagaa | 79582 |
rs6752872 | snp | A/G | 0.0463947 | 0.145069 | intron-variant | SPAG16 | GRCh38.p7 | 2:214154797 | aaatgATAaaaatct[A/G]tagggacttctacta | 79582 |
rs6752968 | snp | G/T | 0.472896 | 0.113214 | intron-variant | SPAG16 | GRCh38.p7 | 2:214256562 | taacttttctgtatg[G/T]tataaatctgggcga | 79582 |
rs6753172 | snp | C/T | 0.196149 | 0.244131 | intron-variant | SPAG16 | GRCh38.p7 | 2:214020893 | AGGTTACTGCCCTTA[C/T]GTAGATTTGGTAGAg | 79582 |
rs6753360 | snp | A/G | 0.0448719 | 0.142907 | intron-variant | SPAG16 | GRCh38.p7 | 2:213610421 | atctattctctccga[A/G]ggctgctttctgtga | 79582 |
rs6753539 | snp | A/G | 0.472989 | 0.113031 | intron-variant | SPAG16 | GRCh38.p7 | 2:213853907 | GAGGGGTATCCTGCT[A/G]TCTTCAGCTCCGCAT | 79582 |
rs6753550 | snp | A/G | 0.473081 | 0.112848 | intron-variant | SPAG16 | GRCh38.p7 | 2:213853936 | ATGCCCAGGGTCTAA[A/G]ATGAGCTTTTCCCCC | 79582 |
rs6753825 | snp | G/T | 0.373799 | 0.217195 | intron-variant | SPAG16 | GRCh38.p7 | 2:213506692 | CAATATAAATTGGGA[G/T]GCCTTATGTTGCGAG | 79582 |
rs6754054 | snp | C/T | 0.479904 | 0.0982045 | intron-variant | SPAG16 | GRCh38.p7 | 2:213871073 | ACATACacaAACACA[C/T]ACACATACCATTCAT | 79582 |
rs6754362 | snp | A/G | 0.479904 | 0.0982045 | intron-variant | SPAG16 | GRCh38.p7 | 2:213871177 | TACAAAATCTTCTAT[A/G]AATAATATTACACCA | 79582 |
rs6754414 | snp | A/G | 0.232067 | 0.249356 | intron-variant | SPAG16 | GRCh38.p7 | 2:214017853 | ATCACTACAATTATT[A/G]TTGCTATTTTGTTAC | 79582 |
rs6754617 | snp | A/G | 0.0422008 | 0.138995 | intron-variant | SPAG16 | GRCh38.p7 | 2:213981942 | CATTTCAAAAACACT[A/G]TACCTTTTTCTAAAT | 79582 |
rs6754702 | snp | A/G | 0.472616 | 0.113763 | intron-variant | SPAG16 | GRCh38.p7 | 2:213605533 | tcactcttgttccct[A/G]ggctagtgtgcaatg | 79582 |
rs6754838 | snp | C/T | 0.17138 | 0.237316 | intron-variant | SPAG16 | GRCh38.p7 | 2:213510723 | AATCTGACAAGTGTA[C/T]TTGACCATGAAACAT | 79582 |
rs6754891 | snp | A/C | | | intron-variant | SPAG16 | GRCh38.p7 | 2:214218054 | catcccagcataaac[A/C]aatgttttatggaaa | 79582 |
rs6755172 | snp | A/G | 0.0162398 | 0.0886349 | intron-variant | SPAG16 | GRCh38.p7 | 2:213653060 | TCTATCTAGTTGTTC[A/G]TAGTCTCCTATCCTT | 79582 |
rs6755201 | snp | A/G | 0.47726 | 0.104176 | intron-variant | SPAG16 | GRCh38.p7 | 2:214335993 | CGATCTCTTGACCTC[A/G]TGATCCACCCGCCTT | 79582 |
rs6755408 | snp | A/G | 0.361474 | 0.223771 | intron-variant | SPAG16 | GRCh38.p7 | 2:213528131 | GTTCAGGACAAACCT[A/G]TGTTTTCAACGGGCG | 79582 |
rs6755585 | snp | C/G | 0.436265 | 0.166749 | intron-variant | SPAG16 | GRCh38.p7 | 2:213681025 | ggtgcagaggaatct[C/G]tcagatagctgactt | 79582 |
rs6755912 | snp | A/C | 0.40386 | 0.197046 | intron-variant | SPAG16 | GRCh38.p7 | 2:214155110 | ggcagcttgagtttg[A/C]agggcagggtacagg | 79582 |
rs6755913 | snp | G/T | 0.369754 | 0.219451 | intron-variant | SPAG16 | GRCh38.p7 | 2:213681117 | atttgattgtctcct[G/T]gacctggaaagaaag | 79582 |
rs6756137 | snp | A/G | 0.376989 | 0.215346 | intron-variant | SPAG16, LOC101928084 | GRCh38.p7 | 2:214100881 | tctttatggtagaaA[A/G]GCATTTTAAAATCTA | 79582 |
rs6756154 | snp | C/G | 0.415235 | 0.18761 | intron-variant | SPAG16, LOC101928084 | GRCh38.p7 | 2:214100920 | GGAAAAAAAATGAGT[C/G]AAGTGGACTCACTTC | 79582 |
rs6756446 | snp | A/G | | | intron-variant | SPAG16 | GRCh38.p7 | 2:213894802 | gagaccatcctggct[A/G]acatggtgaaaccac | 79582 |
rs6756467 | snp | A/G | 0.0479149 | 0.147179 | intron-variant | SPAG16 | GRCh38.p7 | 2:213440885 | AACCAAAGAGCAAAG[A/G]TAAATGAATTAGGTT | 79582 |
rs6756638 | snp | A/C | 0.473359 | 0.112298 | intron-variant | SPAG16 | GRCh38.p7 | 2:213854092 | AAATTTCCTTATATT[A/C]ACTTGTGAAAGTGTT | 79582 |
rs6756845 | snp | G/T | 0.477853 | 0.102875 | intron-variant | SPAG16 | GRCh38.p7 | 2:214030521 | TATTTTATGTATATG[G/T]TATAAAGAGGTCCTG | 79582 |
rs6756956 | snp | A/G | 0.159292 | 0.232964 | intron-variant | SPAG16 | GRCh38.p7 | 2:213553461 | TGGTCCACAGAGAAC[A/G]CAGGCATCTCTTGCC | 79582 |
rs6757130 | snp | C/T | 0.00159617 | 0.0282053 | intron-variant | SPAG16 | GRCh38.p7 | 2:213963183 | ccaacattcataaac[C/T]tctatctgagcacta | 79582 |
rs6757132 | snp | C/T | 0.390838 | 0.206555 | intron-variant | SPAG16 | GRCh38.p7 | 2:213963186 | acattcataaacttc[C/T]atctgagcactactt | 79582 |
rs6757177 | snp | G/T | 0.177824 | 0.239355 | intron-variant | SPAG16 | GRCh38.p7 | 2:213485977 | ttattatttttaatt[G/T]ttttcagggtacatg | 79582 |
rs6757252 | snp | A/G | 0.350546 | 0.22889 | intron-variant | SPAG16 | GRCh38.p7 | 2:213824486 | ttcccagcactattt[A/G]tggaagagattttcc | 79582 |
rs6757512 | snp | A/G | 0.48679 | 0.0801892 | intron-variant | SPAG16 | GRCh38.p7 | 2:213987986 | GATAATGTATTTTAA[A/G]TACATACATCTTATA | 79582 |
rs6757797 | snp | C/T | 0.0279526 | 0.114869 | intron-variant | SPAG16 | GRCh38.p7 | 2:214222097 | GTGTTGAGAAATTAG[C/T]TTCCTTGCTAttctt | 79582 |
rs6758256 | snp | C/T | 0.478685 | 0.10101 | intron-variant | SPAG16 | GRCh38.p7 | 2:213842045 | GAAACAGGTGTGCAT[C/T]ATGTAAACCTTGTTA | 79582 |
rs6758438 | snp | A/C | 0.4087 | 0.193169 | intron-variant | SPAG16 | GRCh38.p7 | 2:214113924 | gtttatagaattttc[A/C]gcttttctgctctgt | 79582 |
rs6758514 | snp | G/T | 0.145642 | 0.227177 | intron-variant | SPAG16 | GRCh38.p7 | 2:213707955 | AGAGTAATGAAAATG[G/T]TTTTATCTTTCTAGG | 79582 |
rs6758623 | snp | A/G | 0.194278 | 0.243711 | intron-variant | SPAG16 | GRCh38.p7 | 2:213335602 | ATATTCTTGATATAC[A/G]CAAATGGGTTAAAAT | 79582 |
rs6758779 | snp | A/T | 0.38934 | 0.207568 | intron-variant | SPAG16 | GRCh38.p7 | 2:214313980 | TGGTAATTATTCCAA[A/T]TAAATCTACTTAATA | 79582 |
rs6758979 | snp | A/C | 0.484421 | 0.0868729 | intron-variant | SPAG16 | GRCh38.p7 | 2:214036060 | atttttaaattccat[A/C]atttatttttattaa | 79582 |
rs6759138 | snp | A/G | 0.398174 | 0.201356 | intron-variant | SPAG16 | GRCh38.p7 | 2:214314339 | CAAATATTGAGTTAC[A/G]TTTACTTATATAGGA | 79582 |
rs6759627 | snp | A/G | 0.350764 | 0.228794 | intron-variant | SPAG16 | GRCh38.p7 | 2:213293374 | ttcatgctcttgtgt[A/G]atcctcacacactga | 79582 |
rs6759722 | snp | A/C | | | intron-variant | SPAG16 | GRCh38.p7 | 2:213654539 | gtctctactaaaaat[A/C]caaaaaaaaaaaaaa | 79582 |
rs6759776 | snp | A/C | 0.0471551 | 0.14613 | intron-variant | SPAG16 | GRCh38.p7 | 2:214337597 | ATTCTAGGGAGAGAA[A/C]AATAAAACCAACAGA | 79582 |
rs6759795 | snp | A/G | 0 | 0 | intron-variant | SPAG16 | GRCh38.p7 | 2:213983869 | CTTAGATTCCTAAGC[A/G]TAGGGCATGATAGTA | 79582 |
rs6760056 | snp | G/T | 0.140581 | 0.224783 | intron-variant | SPAG16 | GRCh38.p7 | 2:213733426 | TGGGGGAAAGTGATT[G/T]TCCTTggagaacaga | 79582 |
rs6760140 | snp | A/T | 0.431473 | 0.171952 | intron-variant | SPAG16 | GRCh38.p7 | 2:213668481 | AGCTGGGTAAAGTAA[A/T]TTTTTTACAGATAGA | 79582 |
rs6760156 | snp | C/T | 0.155656 | 0.231515 | intron-variant | SPAG16 | GRCh38.p7 | 2:213346705 | ttgcatatgttgaac[C/T]agccttgcatcccag | 79582 |
rs6760815 | snp | C/T | 0.0162398 | 0.0886349 | intron-variant | SPAG16 | GRCh38.p7 | 2:213311163 | AAGAAAAACAAAGTT[C/T]AGTGGAAGAAAAATA | 79582 |
rs6760883 | snp | A/G | 0.371987 | 0.218218 | intron-variant | SPAG16 | GRCh38.p7 | 2:214302325 | cagtttaagtccaaa[A/G]tttctttgttgattt | 79582 |
rs6760981 | snp | A/G | 0.0107246 | 0.0724382 | intron-variant | SPAG16 | GRCh38.p7 | 2:214149809 | TTATTCCACAATGAT[A/G]TAAGTATTATCAATT | 79582 |
rs6761153 | snp | G/T | 0.0460142 | 0.144533 | intron-variant | SPAG16 | GRCh38.p7 | 2:213362497 | cagtggggaaacctg[G/T]caaccttctcatcat | 79582 |
rs6761285 | snp | C/T | 0.34303 | 0.232046 | intron-variant | SPAG16 | GRCh38.p7 | 2:214177580 | ACTCTATTTTTTAGG[C/T]GAAATAAATTCTTTT | 79582 |
rs6761365 | snp | A/T | 0.48666 | 0.0805725 | intron-variant | SPAG16 | GRCh38.p7 | 2:213554816 | caaagaaaaaaagaa[A/T]aaaaattaatgaaga | 79582 |
rs6761404 | snp | C/T | 0.34303 | 0.232046 | intron-variant | SPAG16 | GRCh38.p7 | 2:214177676 | GTTATATTTGCTTTC[C/T]GTTGTACATTGATGT | 79582 |
rs7319160 | snp | A/G | 0.347032 | 0.230401 | intron-variant | SPAG16 | GRCh38.p7 | 2:213356560 | atagtattctctgat[A/G]gtagtttgtatttct | 79582 |
rs7340182 | snp | A/C | | | intron-variant, missense | SPAG16 | GRCh38.p7 | 2:213376145 | CTATCATAATTATAG[A/C]TTATCGTATGTGAGG | 79582 |
rs7349270 | snp | G/T | 0.427271 | 0.176281 | intron-variant | SPAG16 | GRCh38.p7 | 2:214371981 | ccactgcacccagcc[G/T]atatgtaatatatta | 79582 |
rs7349404 | snp | A/C | 0.00159617 | 0.0282053 | intron-variant | SPAG16 | GRCh38.p7 | 2:214372184 | GAGATTTGATGTTCA[A/C]GAATCATATACAAAG | 79582 |
rs7355311 | snp | A/G | 0.444444 | 0.157135 | intron-variant | SPAG16 | GRCh38.p7 | 2:214352576 | TGTGTGTGTGTGTGT[A/G]TGTGTGACTATCTCC | 79582 |
rs7355430 | snp | A/G | 0.217551 | 0.247885 | intron-variant | SPAG16 | GRCh38.p7 | 2:213357201 | aattttagaataagc[A/G]cgatatggtgccaag | 79582 |
rs7355432 | snp | C/T | 0.212425 | 0.24716 | intron-variant | SPAG16 | GRCh38.p7 | 2:213357443 | atatgggttctcttg[C/T]tttgggtgcatatat | 79582 |
rs7355567 | snp | C/G | 0.213333 | 0.247296 | intron-variant | SPAG16 | GRCh38.p7 | 2:213355670 | gccctctgtttgtct[C/G]ttattggtgtatagg | 79582 |
rs7355712 | snp | C/G | 0.481473 | 0.0944461 | intron-variant | SPAG16 | GRCh38.p7 | 2:214260738 | AACACATAGTGCCTG[C/G]GTATCTATCTTTGAC | 79582 |
rs7419851 | snp | A/G | | | intron-variant | SPAG16 | GRCh38.p7 | 2:213902067 | CATATTTAGGCCCAG[A/G]GATCTGGTAATTTAA | 79582 |
rs7419885 | snp | A/T | 0.447162 | 0.153712 | intron-variant | SPAG16 | GRCh38.p7 | 2:214129803 | CTAACATTTTCCTTT[A/T]GAAATTGAGAAAAAC | 79582 |
rs7420024 | snp | C/T | | | intron-variant | SPAG16 | GRCh38.p7 | 2:213383277 | TTGCTGATATTATTC[C/T]TATTATTATAGAAAT | 79582 |
rs7420175 | snp | A/T | | | intron-variant | SPAG16 | GRCh38.p7 | 2:213540214 | taatttttatttttt[A/T]attttttttgtattt | 79582 |
rs7420226 | snp | A/T | 0 | 0 | intron-variant | SPAG16 | GRCh38.p7 | 2:214224990 | AAGAGATTGGATTGC[A/T]AACAGAGGGAGGAAT | 79582 |
rs7420408 | snp | A/G | 0.445987 | 0.155207 | intron-variant | SPAG16 | GRCh38.p7 | 2:214370025 | TGGTCATTGGCAAAT[A/G]CTGACCCTTCATTTG | 79582 |
rs7420481 | snp | G/T | 0.0189856 | 0.0955633 | intron-variant | SPAG16 | GRCh38.p7 | 2:213383980 | tcaatgactacacac[G/T]atgtgcctgagtaca | 79582 |
rs7420670 | snp | C/T | 0.352504 | 0.228019 | intron-variant | SPAG16 | GRCh38.p7 | 2:214377183 | gagcagttcatctct[C/T]cggtaagttgcagat | 79582 |
rs7420676 | snp | A/T | 0.484421 | 0.0868729 | intron-variant | SPAG16 | GRCh38.p7 | 2:213909081 | attcttatacaccaa[A/T]aacagacaaacagag | 79582 |
rs7420738 | snp | G/T | 0.260504 | 0.249779 | intron-variant | SPAG16 | GRCh38.p7 | 2:214377564 | gtacaactacagtat[G/T]taggacatataacat | 79582 |
rs7421588 | snp | C/T | 0.371987 | 0.218218 | intron-variant | SPAG16 | GRCh38.p7 | 2:213583750 | TCCCATATTTGATCT[C/T]CATTATGATATCTTG | 79582 |
rs7421802 | snp | A/T | | | intron-variant | SPAG16 | GRCh38.p7 | 2:213540207 | gcccagctaattttt[A/T]tttttttattttttt | 79582 |
rs7421803 | snp | A/T | | | intron-variant | SPAG16 | GRCh38.p7 | 2:213540215 | aatttttattttttt[A/T]ttttttttgtatttt | 79582 |
rs7422050 | snp | A/G | 0.328616 | 0.237317 | intron-variant | SPAG16 | GRCh38.p7 | 2:213887185 | taacactggcatcat[A/G]cttttaactaaacta | 79582 |
rs7422338 | snp | G/T | 0 | 0 | intron-variant | SPAG16 | GRCh38.p7 | 2:214009369 | agaaagtcatggagg[G/T]tacagagctcatttt | 79582 |
rs7422976 | snp | A/G | 0 | 0 | intron-variant | SPAG16 | GRCh38.p7 | 2:213695511 | tcctgttctcagaaa[A/G]acgttccactgaaag | 79582 |
rs7423502 | snp | A/G | 0.479984 | 0.0980171 | intron-variant | SPAG16 | GRCh38.p7 | 2:213867377 | TGCCAAAAAGTGGGA[A/G]CATAAACATACCCTT | 79582 |
rs7423982 | snp | A/C | 0.274124 | 0.248833 | intron-variant | SPAG16 | GRCh38.p7 | 2:214369969 | CCCCTCACCTCAGTA[A/C]TGAATGTTGAAAACT | 79582 |
rs7424131 | snp | A/G | 0 | 0 | intron-variant | SPAG16 | GRCh38.p7 | 2:213768285 | CTAAGCTATATTATA[A/G]GAAAAATTTGTCACT | 79582 |
rs7424311 | snp | C/T | 0.48435 | 0.0870631 | intron-variant | SPAG16 | GRCh38.p7 | 2:213909282 | aggaagaatcaatat[C/T]gtgaaaatggccata | 79582 |
rs7424714 | snp | A/G | 0.472803 | 0.113397 | intron-variant | SPAG16 | GRCh38.p7 | 2:213857874 | ttaacagaagtttga[A/G]agaagttgatgcaaa | 79582 |
rs7425126 | snp | A/G | 0.453209 | 0.145623 | intron-variant | SPAG16 | GRCh38.p7 | 2:213953332 | ACAAAAAATATTTTA[A/G]CATCCAAAGGAAAAT | 79582 |
rs7425324 | snp | A/G | 0.361894 | 0.223562 | intron-variant | SPAG16 | GRCh38.p7 | 2:213640402 | agatctggagcacag[A/G]agctgctgttcagat | 79582 |
rs7425349 | snp | C/T | 0.354019 | 0.227333 | intron-variant | SPAG16 | GRCh38.p7 | 2:213309795 | CCAAGGTACTTAGTA[C/T]CATCTGTCATAGTAT | 79582 |
rs7425408 | snp | A/G | 0.0883596 | 0.190715 | intron-variant | SPAG16 | GRCh38.p7 | 2:214054602 | GAGTTGAGGCatata[A/G]tataatatttctata | 79582 |
rs7425431 | snp | C/T | 0.347253 | 0.230308 | intron-variant | SPAG16 | GRCh38.p7 | 2:214376174 | AAACAAAATAGAAGC[C/T]GATAGTGGAACAATT | 79582 |
rs7426086 | snp | A/T | | | intron-variant | SPAG16 | GRCh38.p7 | 2:213377905 | tatatatatatatat[A/T]tttttttttttttct | 79582 |
rs7426118 | snp | C/G | 0.484841 | 0.0857308 | intron-variant | SPAG16 | GRCh38.p7 | 2:213918039 | aatcatctggttttt[C/G]tttttagttctgttt | 79582 |
rs7426198 | snp | G/T | 0.477684 | 0.103247 | intron-variant | SPAG16 | GRCh38.p7 | 2:213879330 | tttctttcatcggtg[G/T]tttgtagttttcttt | 79582 |
rs7426381 | snp | A/T | 0.25045 | 0.25 | intron-variant | SPAG16 | GRCh38.p7 | 2:214253305 | agaagttctttagtt[A/T]aattagatcccattt | 79582 |
rs7557148 | snp | C/T | 0.0240643 | 0.107019 | intron-variant | SPAG16 | GRCh38.p7 | 2:213783042 | cccaatgctatccct[C/T]ccccctcccccgacc | 79582 |
rs7557238 | snp | G/T | | | intron-variant | SPAG16 | GRCh38.p7 | 2:213783002 | gctgcacccactaac[G/T]tgtcatctagcatta | 79582 |
rs7557589 | snp | A/C | 0.167809 | 0.236103 | intron-variant | SPAG16 | GRCh38.p7 | 2:214408881 | GCCTCTATTTCTTCA[A/C]CTACATAGAGGAGGC | 79582 |
rs7557848 | snp | C/T | 0.483923 | 0.0882034 | intron-variant | SPAG16 | GRCh38.p7 | 2:213482929 | CTGTGTTAAAAGTAA[C/T]ATTAATTCCTTATAG | 79582 |
rs7557919 | snp | A/G | 0.474903 | 0.109173 | intron-variant | SPAG16 | GRCh38.p7 | 2:214338135 | TATCCACTACAAATA[A/G]GGAGGAAACAAAATC | 79582 |
rs7557981 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | SPAG16 | GRCh38.p7 | 2:214338153 | AGGAAACAAAATCAA[A/G]TTTATGCAGAAAATC | 79582 |
rs7558420 | snp | G/T | 0.0501905 | 0.150254 | intron-variant | SPAG16 | GRCh38.p7 | 2:214028756 | AAAAATCATTTTTGT[G/T]AAAAatgtatgtatg | 79582 |
rs7559339 | snp | G/T | 0.413083 | 0.189483 | intron-variant | SPAG16 | GRCh38.p7 | 2:213965093 | ctggacttgtttgtt[G/T]atttgtttagtggct | 79582 |
rs7559483 | snp | A/C | 0.38555 | 0.210062 | intron-variant | SPAG16 | GRCh38.p7 | 2:214303671 | taacaacactcctag[A/C]aagatccgataaatt | 79582 |
rs7559518 | snp | A/G | 0.0482946 | 0.147699 | intron-variant | SPAG16 | GRCh38.p7 | 2:213666350 | ATTCCCCCCTTTTCA[A/G]TAAACTTACTGTGTA | 79582 |
rs7559594 | snp | C/T | 0.45843 | 0.138046 | intron-variant | SPAG16 | GRCh38.p7 | 2:214268887 | TTTCCCTATGCTATT[C/T]GGCAGTAATTTTTTG | 79582 |
rs7559872 | snp | C/T | 0 | 0 | intron-variant | SPAG16 | GRCh38.p7 | 2:213914500 | CATATATATAGTATA[C/T]GCTTTCTAACCTCAA | 79582 |
rs7559878 | snp | C/T | 0.484841 | 0.0857308 | intron-variant | SPAG16 | GRCh38.p7 | 2:213914526 | CTCAAAATATATGCA[C/T]AGCACAATGATTTTA | 79582 |
rs7560229 | snp | C/T | 0.372794 | 0.217765 | intron-variant | SPAG16 | GRCh38.p7 | 2:213583919 | GGTAGCAATAAATTA[C/T]GAACAACGTGAGTGC | 79582 |
rs7560270 | snp | A/G | 0.167158 | 0.235875 | intron-variant | SPAG16 | GRCh38.p7 | 2:213914732 | atttgtatactgatc[A/G]atgagtgatattgat | 79582 |
rs7560498 | snp | A/G | 0.132066 | 0.220435 | intron-variant | SPAG16 | GRCh38.p7 | 2:213448001 | ctaattacagtcacg[A/G]cactggccaccactg | 79582 |
rs7560544 | snp | C/T | 0.195526 | 0.243993 | intron-variant | SPAG16 | GRCh38.p7 | 2:213448172 | atttggcttggagat[C/T]ggctaatgagtctcg | 79582 |
rs7560655 | snp | G/T | 0.02016 | 0.0983543 | intron-variant | SPAG16 | GRCh38.p7 | 2:213865155 | CAGTATATATTTACC[G/T]CTGTACAAGGAGAGA | 79582 |
rs7560793 | snp | C/T | 0.48155 | 0.0942576 | intron-variant | SPAG16 | GRCh38.p7 | 2:213543477 | TTTTTGAATTTTATT[C/T]AGATCTTTCCCCATT | 79582 |
rs7560814 | snp | C/T | 0.0482946 | 0.147699 | intron-variant | SPAG16 | GRCh38.p7 | 2:213543533 | ATCGTAATTTATTTT[C/T]TTTATTGTTTTTCTA | 79582 |
rs7560957 | snp | A/G | 0.0248432 | 0.108648 | intron-variant | SPAG16 | GRCh38.p7 | 2:214045226 | aggatagggcaccgt[A/G]agagttgtgagacct | 79582 |
rs7561066 | snp | A/G | 0.443732 | 0.158012 | intron-variant | SPAG16 | GRCh38.p7 | 2:213985136 | CTTAGAATTGAGTGT[A/G]GAAAATAGAAGTTCC | 79582 |
rs7561092 | snp | A/G | 0.154993 | 0.231244 | intron-variant | SPAG16 | GRCh38.p7 | 2:213448524 | tgtttttagtgtgcc[A/G]taccagttaaagaat | 79582 |
rs7561615 | snp | A/G | 0.487432 | 0.0782705 | intron-variant | SPAG16 | GRCh38.p7 | 2:213506925 | GAAGCAATTTTAGAC[A/G]TCATATGCTTTCACA | 79582 |
rs7561617 | snp | A/G | 0.478354 | 0.101757 | intron-variant | SPAG16 | GRCh38.p7 | 2:214339078 | GCTAGTAAATCAATA[A/G]ATACCCAATCAAATG | 79582 |
rs7561816 | snp | A/G | 0.487621 | 0.0776941 | intron-variant, upstream-variant-2KB | SPAG16, LOC101928084 | GRCh38.p7 | 2:214103394 | cagtcacatggccac[A/G]cctgacctctagtct | 79582 |
rs7561909 | snp | C/T | | | intron-variant | SPAG16 | GRCh38.p7 | 2:213288105 | tgtttttggtagaga[C/T]gggggtctcactctg | 79582 |
rs7562291 | snp | A/T | 0.077417 | 0.180873 | intron-variant | SPAG16 | GRCh38.p7 | 2:214054008 | CACTCCCTTTTTTTT[A/T]AAAAACGGAGTCTCC | 79582 |
rs7562444 | snp | A/T | 0.398354 | 0.201224 | intron-variant | SPAG16 | GRCh38.p7 | 2:213705460 | TTTTGTTTTTTCCAA[A/T]TGGCATCTCTTAAGA | 79582 |
rs7562825 | snp | A/T | | | intron-variant | SPAG16 | GRCh38.p7 | 2:213333983 | ggcatcacatcaagt[A/T]aaaaagcttctgcat | 79582 |
rs7562951 | snp | A/G | 0.140242 | 0.224618 | intron-variant | SPAG16 | GRCh38.p7 | 2:213732036 | tttcttctagggttt[A/G]tatagtttttggttt | 79582 |
rs7563061 | snp | A/G | 0.150667 | 0.229419 | intron-variant | SPAG16 | GRCh38.p7 | 2:213589815 | TAATCCCACCTATTC[A/G]GGTGGCTGAGGCTGG | 79582 |
rs7563147 | snp | C/T | 0.130694 | 0.219696 | intron-variant | SPAG16 | GRCh38.p7 | 2:213488989 | ctgaggcacgggaat[C/T]gcctgaatccggaag | 79582 |
rs7563169 | snp | A/G | 0.138546 | 0.223781 | intron-variant | SPAG16 | GRCh38.p7 | 2:213732227 | atcagatggttgtag[A/G]tgagtggtcttattt | 79582 |
rs7563175 | snp | A/T | 0.138546 | 0.223781 | intron-variant | SPAG16 | GRCh38.p7 | 2:213732230 | agatggttgtagatg[A/T]gtggtcttatttctg | 79582 |
rs7563520 | snp | A/G | 0.338523 | 0.233803 | intron-variant | SPAG16 | GRCh38.p7 | 2:213885053 | ctttggaggtaagga[A/G]accctctgtctttat | 79582 |
rs7563592 | snp | A/C | 0.484138 | 0.0876334 | intron-variant | SPAG16 | GRCh38.p7 | 2:213489376 | GTTTGCTTGGTGGAG[A/C]GGGCGGTGACCAAGA | 79582 |
rs7563688 | snp | A/T | 0.0126979 | 0.078662 | intron-variant | SPAG16 | GRCh38.p7 | 2:213686135 | ttatttatttattta[A/T]tgagatggagtcttg | 79582 |
rs7563739 | snp | A/G | 0.305934 | 0.243663 | intron-variant | SPAG16 | GRCh38.p7 | 2:213945455 | tcaaaactgaagaac[A/G]tggagtcagttgttt | 79582 |
rs7563757 | snp | A/C | 0.390464 | 0.206809 | intron-variant | SPAG16 | GRCh38.p7 | 2:213968612 | GCAATGATTAACTAG[A/C]CTTTTTTATTTCAGT | 79582 |
rs7564920 | snp | C/T | 0 | 0 | intron-variant | SPAG16 | GRCh38.p7 | 2:213484616 | AAATCTCTTTTAATA[C/T]GGTGtttattttaaa | 79582 |
rs7565006 | snp | C/T | 0.277334 | 0.248501 | intron-variant | SPAG16 | GRCh38.p7 | 2:214039119 | tgaggaatcgccaca[C/T]tgacttccacaatgg | 79582 |
rs7565069 | snp | C/T | 0.191775 | 0.243125 | intron-variant | SPAG16 | GRCh38.p7 | 2:213440731 | aatcatttggttata[C/T]gtaaaaaatgaaact | 79582 |
rs7566391 | snp | C/T | 0.156319 | 0.231784 | intron-variant | SPAG16 | GRCh38.p7 | 2:213310715 | TTAAACAAAATATTT[C/T]CTTGTTATAATTGAA | 79582 |
rs7566804 | snp | C/T | | | intron-variant | SPAG16 | GRCh38.p7 | 2:213335201 | AAATAACAAGACAAT[C/T]CAAAAAGGTTGTCAC | 79582 |
rs7566812 | snp | C/T | 0.046775 | 0.145601 | intron-variant | SPAG16 | GRCh38.p7 | 2:213365318 | tagaaagtgctaaag[C/T]agatactttgattat | 79582 |
rs7566862 | snp | A/C/G | 0.000399281 | 0.0141238 | intron-variant | SPAG16 | GRCh38.p7 | 2:214210247 | GTAcaattgaccctc[A/C/G]aacatgtttgaacta | 79582 |
rs7567030 | snp | A/G | 0.0162398 | 0.0886349 | intron-variant | SPAG16 | GRCh38.p7 | 2:213969140 | GCTAAAGTAGATAAC[A/G]GTAAGATATAGGCAA | 79582 |
rs7567455 | snp | C/T | 0.100588 | 0.200439 | intron-variant | SPAG16 | GRCh38.p7 | 2:214235111 | ATAAGTTAATGTATA[C/T]CTAGATTTTGTGATA | 79582 |
rs7567464 | snp | C/G | 0.125528 | 0.21681 | intron-variant | SPAG16 | GRCh38.p7 | 2:213645778 | tcagtagtcacgtgg[C/G]ccccccagtcaactg | 79582 |
rs7568072 | snp | C/T | 0.498611 | 0.0263212 | intron-variant | SPAG16 | GRCh38.p7 | 2:214346337 | ttatgactaatgtgg[C/T]tgagaactttttcaa | 79582 |
rs7568792 | snp | A/T | 0.291493 | 0.246533 | intron-variant | SPAG16 | GRCh38.p7 | 2:213779391 | GAATTTAAAAATTTT[A/T]AAAAAATTGTGCTTG | 79582 |
rs7568796 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | SPAG16 | GRCh38.p7 | 2:214371066 | TAATGGAGGCATTGT[A/C]AGTTTCAGAGATTAA | 79582 |
rs7568854 | snp | G/T | | | intron-variant | SPAG16 | GRCh38.p7 | 2:213742555 | CTTAtttcttttttt[G/T]ttttttttttttttg | 79582 |
rs7568984 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | SPAG16 | GRCh38.p7 | 2:214371082 | AGTTTCAGAGATTAA[A/G]GTGGGCTATTACTGG | 79582 |
rs7569054 | snp | A/G | 0.117537 | 0.212022 | intron-variant | SPAG16 | GRCh38.p7 | 2:214070308 | ACTCTGATACCAGAT[A/G]AATATTTACTTATCT | 79582 |
rs7569105 | snp | C/T | 0 | 0 | intron-variant | SPAG16 | GRCh38.p7 | 2:214277910 | actatgccctgcccc[C/T]agaggtggagtcaac | 79582 |
rs7569202 | snp | C/T | 0.0142736 | 0.0832652 | intron-variant | SPAG16 | GRCh38.p7 | 2:214105483 | tgaagcacagtaaag[C/T]aaagcaatttgttta | 79582 |
rs7569223 | snp | C/T | 0.131723 | 0.220251 | intron-variant | SPAG16 | GRCh38.p7 | 2:213626867 | TGGCCAGGCTGGTCT[C/T]GAACTCCTGACCTCA | 79582 |
rs7569273 | snp | C/T | 0.0444908 | 0.142359 | intron-variant | SPAG16 | GRCh38.p7 | 2:214267299 | gcataaaaacagaca[C/T]attgaccagtggaat | 79582 |
rs7569487 | snp | A/C | 0.481473 | 0.0944461 | intron-variant | SPAG16 | GRCh38.p7 | 2:213468367 | gagatatatatatat[A/C]tctctctctatatat | 79582 |
rs7569570 | snp | A/G | 0 | 0 | intron-variant | SPAG16 | GRCh38.p7 | 2:214341507 | aggaaacttgtaaat[A/G]agaacattctaaaaa | 79582 |
rs7569738 | snp | C/T | 0.475613 | 0.107697 | intron-variant | SPAG16 | GRCh38.p7 | 2:213642305 | atgtgaatctccaca[C/T]gctagttctgtccat | 79582 |
rs7569899 | snp | G/T | 0.0298908 | 0.118541 | intron-variant | SPAG16 | GRCh38.p7 | 2:213857166 | acccgggaggcggag[G/T]ttgcagtgagccgag | 79582 |
rs7570054 | snp | A/G | 0.0333695 | 0.124785 | intron-variant | SPAG16 | GRCh38.p7 | 2:214270958 | ttctacctttttccc[A/G]aatatacccactgcg | 79582 |
rs7570202 | snp | C/G | 0.0178098 | 0.0926698 | intron-variant | SPAG16 | GRCh38.p7 | 2:213651722 | ATGTAATTTAGTCTA[C/G]GCAAGTCTACACATT | 79582 |
rs7570617 | snp | C/T | | | intron-variant | SPAG16 | GRCh38.p7 | 2:213848863 | TTTCTGCTTGTGGCC[C/T]ATGACGCAACTGAAA | 79582 |
rs7571177 | snp | A/T | 0.0883596 | 0.190715 | intron-variant | SPAG16 | GRCh38.p7 | 2:213910365 | attttctaggagagg[A/T]acaactcATTTCAGC | 79582 |
rs7571280 | snp | A/C | 0.48491 | 0.0855403 | intron-variant | SPAG16, LOC101928084 | GRCh38.p7 | 2:214086913 | TAACTTTGCAATGCC[A/C]AATGAACAACATGAT | 79582 |
rs7571415 | snp | C/T | 0.130351 | 0.219509 | intron-variant | SPAG16 | GRCh38.p7 | 2:213727567 | GAACTGGTACAAAGG[C/T]GCTGACGTGGAAATG | 79582 |
rs7571464 | snp | A/G | 0.101658 | 0.201233 | intron-variant | SPAG16 | GRCh38.p7 | 2:214229180 | AAGGATAATTTCACT[A/G]TAGAAGAAAGTATAT | 79582 |
rs7571692 | snp | A/T | 0.44333 | 0.158505 | intron-variant | SPAG16 | GRCh38.p7 | 2:214294389 | actttgttgcttcca[A/T]taatttctctgttga | 79582 |
rs7572369 | snp | A/G | 0.485596 | 0.0836329 | intron-variant | SPAG16 | GRCh38.p7 | 2:213627186 | GATAGGATAGAAGCG[A/G]GATCCTCACTATTGA | 79582 |
rs7572425 | snp | A/G | 0.156319 | 0.231784 | intron-variant | SPAG16 | GRCh38.p7 | 2:213333850 | atgtgcaaaaatcaa[A/G]tcaaaatgaaattcc | 79582 |
rs7572494 | snp | C/T | 0.0471551 | 0.14613 | intron-variant | SPAG16 | GRCh38.p7 | 2:213356739 | gggtgtttttgtgtc[C/T]ctgtctccttcagtt | 79582 |
rs7572550 | snp | C/T | 0.477515 | 0.103619 | intron-variant | SPAG16 | GRCh38.p7 | 2:214342023 | GTAATAAAGAAAAAA[C/T]GCTACAAGAAAAATT | 79582 |
rs7572850 | snp | A/G | 0.327445 | 0.237702 | intron-variant | SPAG16 | GRCh38.p7 | 2:213864950 | TAAACTGAGGGGATA[A/G]CTAACACTTGAGAAT | 79582 |
rs7572877 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | SPAG16 | GRCh38.p7 | 2:214032280 | AAGCAAAGGTGATTG[G/T]TAGCTCCATCTACTT | 79582 |
rs7573089 | snp | A/G | 0.19459 | 0.243782 | intron-variant | SPAG16 | GRCh38.p7 | 2:213321024 | GATTCCCTATATTGA[A/G]CTTGAGCTAATGTTT | 79582 |
rs7573228 | snp | C/T | 0.484771 | 0.0859212 | intron-variant | SPAG16 | GRCh38.p7 | 2:213922942 | tgatgtccatgtgct[C/T]cctggggaaacatgg | 79582 |
rs7573430 | snp | A/C | 0.283684 | 0.24772 | intron-variant | SPAG16 | GRCh38.p7 | 2:214400596 | GACCTGGAACCAACA[A/C]CCCCATAGATACAGA | 79582 |
rs7573564 | snp | C/T | 0.484771 | 0.0859212 | intron-variant | SPAG16 | GRCh38.p7 | 2:213923253 | ataggagtctaccca[C/T]tggttgagttcccac | 79582 |
rs7573822 | snp | A/G | 0.327211 | 0.237778 | intron-variant | SPAG16 | GRCh38.p7 | 2:213409735 | catacaagaagcatt[A/G]tcaaatataaaatgg | 79582 |
rs7573872 | snp | A/G | 0.484771 | 0.0859212 | intron-variant | SPAG16 | GRCh38.p7 | 2:213923345 | gtgtcaggcagcgtc[A/G]tgtgccctgctgtct | 79582 |
rs7574465 | snp | C/T | 0 | 0 | intron-variant | SPAG16 | GRCh38.p7 | 2:213853068 | GTCATCTAATGTTCA[C/T]GGGGCACACATTTTG | 79582 |
rs7574468 | snp | G/T | 0.472803 | 0.113397 | intron-variant | SPAG16 | GRCh38.p7 | 2:213858900 | AAAAATAAAAAGTCC[G/T]CCAGGTGCAGTGGCT | 79582 |
rs7574563 | snp | A/G | 0.493013 | 0.058691 | intron-variant | SPAG16 | GRCh38.p7 | 2:213971175 | TTTCAAAAGATATTA[A/G]TCAGAAATGTTCAAG | 79582 |
rs7574905 | snp | G/T | 0.00318978 | 0.0398085 | intron-variant | SPAG16 | GRCh38.p7 | 2:213448402 | agctgatgcattaga[G/T]caggtggaagaaagt | 79582 |
rs7575750 | snp | G/T | 0.499971 | 0.00379382 | intron-variant | SPAG16 | GRCh38.p7 | 2:214163637 | atatacatatatata[G/T]agagagagagagaga | 79582 |
rs7576252 | snp | A/C | 0.300926 | 0.244758 | intron-variant | SPAG16 | GRCh38.p7 | 2:214194954 | ATTTGGGGATGAATA[A/C]GTAAAACATAGCGTG | 79582 |
rs7576348 | snp | A/T | 0.0142736 | 0.0832652 | intron-variant | SPAG16 | GRCh38.p7 | 2:214130042 | tgagcgtgccttcca[A/T]tgaacaaagtggggg | 79582 |
rs7576499 | snp | C/T | 0.433527 | 0.169758 | intron-variant | SPAG16 | GRCh38.p7 | 2:213684519 | AAAAAAAGTTAATCC[C/T]ATTTAAAATGTGAAA | 79582 |
rs7576672 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | SPAG16 | GRCh38.p7 | 2:213811798 | AAATCAGCACTATGG[A/G]TAAGATTGCTGAGAC | 79582 |
rs7576809 | snp | A/G | 0.0486741 | 0.148216 | intron-variant | SPAG16 | GRCh38.p7 | 2:213505076 | AATATCATTTGTATC[A/G]GTGACATTTTGGTAT | 79582 |
rs7577124 | snp | G/T | 0.352721 | 0.227922 | intron-variant | SPAG16 | GRCh38.p7 | 2:214033689 | acattttactatttt[G/T]ttttatatttttctc | 79582 |
rs7577186 | snp | C/G | 0.472803 | 0.113397 | intron-variant | SPAG16 | GRCh38.p7 | 2:213858947 | GCACTTTGGGAGGCC[C/G]AGGTGGGCGGATCAT | 79582 |
rs7577317 | snp | C/T | 0.498547 | 0.0269177 | intron-variant | SPAG16 | GRCh38.p7 | 2:214304629 | cccctgattttccac[C/T]tcacacctctatatt | 79582 |
rs7577480 | snp | A/C | 0 | 0 | intron-variant | SPAG16 | GRCh38.p7 | 2:214336829 | ATGATATATCTCTAC[A/C]AGTAAGATTTAAGGT | 79582 |
rs7577685 | snp | C/G | 0.482459 | 0.0919928 | intron-variant | SPAG16 | GRCh38.p7 | 2:213593576 | GTTTCCTGAAGATTT[C/G]TGTCAATGTTGTAAG | 79582 |
rs7577800 | snp | C/T | 0.129664 | 0.219133 | intron-variant | SPAG16 | GRCh38.p7 | 2:213593727 | GTAGATTTCTCATAC[C/T]CCATCATCCCCACCA | 79582 |
rs7578018 | snp | C/T | 0.481703 | 0.0938806 | intron-variant | SPAG16 | GRCh38.p7 | 2:213915724 | atggttgaactaatt[C/T]acacacccatcaaca | 79582 |
rs7578038 | snp | A/T | 0 | 0 | intron-variant | SPAG16 | GRCh38.p7 | 2:213549858 | TATTTATAGTAAGGT[A/T]AAAAAATTTGTGCTT | 79582 |
rs7578408 | snp | C/T | 0.128632 | 0.218563 | intron-variant | SPAG16 | GRCh38.p7 | 2:213493153 | ATTTTGCCAGTAATA[C/T]ACAACTATATGACCT | 79582 |
rs7578505 | snp | A/C | 0.235273 | 0.249566 | intron-variant | SPAG16 | GRCh38.p7 | 2:214000831 | ACAGGTGGGTTAAAT[A/C]GATTTTTTTTTTCTC | 79582 |
rs7578866 | snp | A/G | 0.139903 | 0.224452 | intron-variant | SPAG16 | GRCh38.p7 | 2:213729287 | TCTGGTTTTTGACAC[A/G]TACTTCCTGTGTGAC | 79582 |
rs7578892 | snp | C/G | 0.47852 | 0.101384 | intron-variant | SPAG16, LOC101928084 | GRCh38.p7 | 2:214088924 | GAAGTAAAAATGGCA[C/G]ACCAATTTCACTTTG | 79582 |
rs7578956 | snp | A/G | 0.0162398 | 0.0886349 | intron-variant | SPAG16 | GRCh38.p7 | 2:213641759 | cattgtcacactgct[A/G]taaagatactacctg | 79582 |
rs7578987 | snp | G/T | 0.337841 | 0.23406 | intron-variant | SPAG16 | GRCh38.p7 | 2:214038981 | aagtctttgctattg[G/T]gaatagtgccgcaat | 79582 |
rs7579088 | snp | C/T | 0.484771 | 0.0859212 | intron-variant | SPAG16 | GRCh38.p7 | 2:213926290 | tggtgtttggttaca[C/T]gagtaagttctttag | 79582 |
rs7579598 | snp | A/T | 0.31503 | 0.241394 | intron-variant | SPAG16 | GRCh38.p7 | 2:214201544 | AAGGAGGATGTTAAA[A/T]GTTCCTACAAAGAAC | 79582 |
rs7579697 | snp | C/T | 0.155987 | 0.23165 | intron-variant | SPAG16 | GRCh38.p7 | 2:213328250 | CTTGTTTTGATAGCC[C/T]GCTCAGGATATTCTG | 79582 |
rs7580222 | snp | C/T | 0.47023 | 0.118317 | intron-variant | SPAG16 | GRCh38.p7 | 2:213474887 | aatctcctttggcaa[C/T]accctcacagacaca | 79582 |
rs7580474 | snp | A/C | 0.346368 | 0.23068 | intron-variant, upstream-variant-2KB | SPAG16 | GRCh38.p7 | 2:213298860 | TCATTTTAAAAAATT[A/C]TTTGGAGGAACAGTA | 79582 |
rs7580818 | snp | A/G | 0.475437 | 0.108066 | intron-variant | SPAG16 | GRCh38.p7 | 2:213654126 | GTCAATACTAAATCA[A/G]TAATGGAGTAATAAA | 79582 |
rs7581348 | snp | C/T | 0.475259 | 0.108435 | intron-variant | SPAG16 | GRCh38.p7 | 2:213645600 | tgttgccctatccta[C/T]tgtgtctgacctggt | 79582 |
rs7581545 | snp | C/T | 0.499653 | 0.0131743 | intron-variant | SPAG16 | GRCh38.p7 | 2:214180872 | CAACGTGACCTTTAA[C/T]CTTTACCTAGTTTAA | 79582 |
rs7583697 | snp | A/G | 0.262985 | 0.249663 | intron-variant | SPAG16 | GRCh38.p7 | 2:214408697 | TGCTATTTTCACAAT[A/G]TATCACTTACCTAAA | 79582 |
rs7583832 | snp | A/G | 0.353371 | 0.227628 | intron-variant | SPAG16 | GRCh38.p7 | 2:213329525 | ttaggttattatctg[A/G]tggaagaaattgcta | 79582 |
rs7583970 | snp | C/G | 0.288906 | 0.246954 | intron-variant | SPAG16 | GRCh38.p7 | 2:213961556 | ctgcctgccttttat[C/G]agattaagaaagctg | 79582 |
rs7584161 | snp | A/G | 0.130008 | 0.219321 | intron-variant | SPAG16 | GRCh38.p7 | 2:213961618 | tggattttgataaat[A/G]ttttttcagggtcaa | 79582 |
rs7584487 | snp | C/G | 0.464841 | 0.127841 | intron-variant | SPAG16 | GRCh38.p7 | 2:214285401 | cttatcagatgtatg[C/G]cttgcaaacattttt | 79582 |
rs7584542 | snp | A/G | 0.462582 | 0.131564 | intron-variant | SPAG16 | GRCh38.p7 | 2:214285249 | ccttttcatctacct[A/G]ttggccatttgtttg | 79582 |
rs7584873 | snp | A/G | 0.475437 | 0.108066 | intron-variant | SPAG16 | GRCh38.p7 | 2:213655363 | AAAATAAAACGATTT[A/G]TATGGAAACCCTGGG | 79582 |
rs7584924 | snp | A/T | 0.319136 | 0.24025 | intron-variant | SPAG16 | GRCh38.p7 | 2:214031978 | caattcaacatgaga[A/T]ctgggtgaggacaca | 79582 |
rs7585097 | snp | A/T | 0.130351 | 0.219509 | intron-variant | SPAG16 | GRCh38.p7 | 2:213727207 | CAATTGCCTTTACTG[A/T]TTCAATCAATTAATC | 79582 |
rs7585231 | snp | C/T | 0.129664 | 0.219133 | intron-variant | SPAG16 | GRCh38.p7 | 2:213727294 | ctcccttcctggaga[C/T]taattctgcagaaga | 79582 |
rs7585278 | snp | A/G | 0.234982 | 0.249549 | intron-variant | SPAG16 | GRCh38.p7 | 2:213371970 | AGGTCAAAAGTAGAA[A/G]AATTTCTGGGAGAAA | 79582 |
rs7585736 | snp | G/T | 0.498392 | 0.028309 | intron-variant | SPAG16 | GRCh38.p7 | 2:213727725 | GTGATAAGGGATACC[G/T]CTAAGGATGCTAGGC | 79582 |
rs7585808 | snp | A/T | 0.130351 | 0.219509 | intron-variant | SPAG16 | GRCh38.p7 | 2:213727753 | ggcaatggaatgaca[A/T]gaattgacttacatt | 79582 |
rs7585812 | snp | C/T | 0.130351 | 0.219509 | intron-variant | SPAG16 | GRCh38.p7 | 2:213727767 | atgaattgacttaca[C/T]tttactatgatctaa | 79582 |
rs7586466 | snp | A/G | 0.474 | 0.111014 | intron-variant | SPAG16 | GRCh38.p7 | 2:213636307 | ctgttccattggtct[A/G]tgtgcctatttttat | 79582 |
rs7586872 | snp | G/T | 0.25045 | 0.25 | intron-variant | SPAG16 | GRCh38.p7 | 2:214321088 | CAGTAAGCTGTACTT[G/T]GTCTATTTTATGCTC | 79582 |
rs7586959 | snp | C/G | 0 | 0 | intron-variant | SPAG16 | GRCh38.p7 | 2:213967845 | TATGCTACATTTAGG[C/G]CAATTTTATGGGACT | 79582 |
rs7587533 | snp | A/G | 0.0256215 | 0.110247 | intron-variant | SPAG16 | GRCh38.p7 | 2:214291601 | tgagccaccgcgccc[A/G]gcctagatcatgttt | 79582 |
rs7587811 | snp | C/T | 0.173965 | 0.238157 | intron-variant | SPAG16 | GRCh38.p7 | 2:213592533 | ACAATCCTGCCCTAC[C/T]GCCTGATATTTAATA | 79582 |
rs7587880 | snp | A/G | 0.494774 | 0.0508504 | intron-variant | SPAG16 | GRCh38.p7 | 2:213985061 | GTCTGAAAAACACAA[A/G]CACAATAATGTAAGC | 79582 |
rs7588147 | snp | A/G | 0.464629 | 0.128197 | intron-variant | SPAG16 | GRCh38.p7 | 2:214015437 | aaccccatctctact[A/G]aaaatacaaaattgg | 79582 |
rs7588307 | snp | C/T | 0.472803 | 0.113397 | intron-variant | SPAG16 | GRCh38.p7 | 2:213858906 | AAAAAGTCCGCCAGG[C/T]GCAGTGGCTCACGCC | 79582 |
rs7588433 | snp | A/G | 0.182614 | 0.240747 | intron-variant | SPAG16 | GRCh38.p7 | 2:213436000 | TCTTCATATTACTTA[A/G]ATGTCTTTTAATTCC | 79582 |
rs7588565 | snp | A/C | 0.0410537 | 0.137264 | intron-variant | SPAG16 | GRCh38.p7 | 2:214038871 | tacaaaggacatgaa[A/C]tcattattttttatg | 79582 |
rs7588604 | snp | A/T | 0.158632 | 0.232706 | intron-variant | SPAG16 | GRCh38.p7 | 2:214388286 | ttaagaaaaaaaaat[A/T]attaatagaaaattg | 79582 |
rs7588629 | snp | C/T | 0.153332 | 0.230554 | intron-variant | SPAG16 | GRCh38.p7 | 2:213531431 | GAATGTGTTAGGCTG[C/T]CTGCACTCAGCAATT | 79582 |
rs7588685 | snp | C/T | 0.130351 | 0.219509 | intron-variant | SPAG16 | GRCh38.p7 | 2:213728091 | tgacctcaggtgatc[C/T]gcctgcctcggcctc | 79582 |
rs7588845 | snp | A/G | 0.021333 | 0.101051 | intron-variant | SPAG16 | GRCh38.p7 | 2:214397450 | ggcgtgagcccccgc[A/G]cccggccATATTTTT | 79582 |
rs7589481 | snp | G/T | 0.354235 | 0.227234 | intron-variant | SPAG16, LOC101928084 | GRCh38.p7 | 2:214091214 | ATAGCTGATATTTAT[G/T]GAGTACTTATTATAT | 79582 |
rs7589549 | snp | A/G | 0.230017 | 0.2492 | intron-variant | SPAG16 | GRCh38.p7 | 2:213996162 | GGGAAATCACCAGGA[A/G]TATAAATGCAAATTA | 79582 |
rs7589753 | snp | C/T | 0.0444908 | 0.142359 | intron-variant | SPAG16 | GRCh38.p7 | 2:213702138 | gtctagcttagggat[C/T]gtaaacactccaatc | 79582 |
rs7589864 | snp | G/T | 0.353587 | 0.22753 | intron-variant | SPAG16 | GRCh38.p7 | 2:213366321 | AAACACCTAAGAAAA[G/T]AACTAATCATACACA | 79582 |
rs7589993 | snp | C/G | 0.131381 | 0.220067 | intron-variant | SPAG16 | GRCh38.p7 | 2:213637165 | gtttaaatcataaag[C/G]catgctggattttgt | 79582 |
rs7590108 | snp | C/T | 0.132409 | 0.220618 | intron-variant | SPAG16 | GRCh38.p7 | 2:213306461 | tgccctggctggtat[C/T]tcactaagtcatgtg | 79582 |
rs7590446 | snp | A/G | 0.465368 | 0.126951 | intron-variant | SPAG16 | GRCh38.p7 | 2:214079124 | TCAAGAGAAAAGATC[A/G]TCATAGCAAGATAGA | 79582 |
rs7590583 | snp | G/T | 0.125182 | 0.216612 | intron-variant | SPAG16 | GRCh38.p7 | 2:213637673 | agtttaatctaggag[G/T]gttgtatttttccag | 79582 |
rs7590768 | snp | A/G | 0.102726 | 0.202016 | intron-variant | SPAG16 | GRCh38.p7 | 2:213661975 | TACTTATGTATTATT[A/G]TGAGTTATGTTTCCA | 79582 |
rs7591006 | snp | C/T | 0.186421 | 0.24178 | intron-variant | SPAG16 | GRCh38.p7 | 2:214042737 | CAGAGTCTAAAAATC[C/T]TCTCATTCTAGTACA | 79582 |
rs7591624 | snp | C/T | 0.467744 | 0.122832 | intron-variant | SPAG16 | GRCh38.p7 | 2:213662871 | TTGACAAATACTTTG[C/T]ATTTGACAAATGTTT | 79582 |
rs7591651 | snp | G/T | 0.0166325 | 0.0896639 | intron-variant | SPAG16 | GRCh38.p7 | 2:213593564 | TTATATTTGTATGTT[G/T]CCTGAAGATTTCTGT | 79582 |
rs7592552 | snp | C/T | 0.48679 | 0.0801892 | intron-variant | SPAG16 | GRCh38.p7 | 2:213699071 | TTTCCATTGCTGTTG[C/T]TGTAGTAGTTTCTAA | 79582 |
rs7593222 | snp | C/T | 0.046775 | 0.145601 | intron-variant | SPAG16 | GRCh38.p7 | 2:213367073 | atagttggctgagaa[C/T]gatggtttccagttt | 79582 |
rs7593384 | snp | C/G | 0.0166325 | 0.0896639 | intron-variant | SPAG16 | GRCh38.p7 | 2:213637989 | gtctcgatttcctga[C/G]ctcgtgatccgcccg | 79582 |
rs7593389 | snp | C/T | 0.125182 | 0.216612 | intron-variant | SPAG16 | GRCh38.p7 | 2:213637992 | tcgatttcctgacct[C/T]gtgatccgcccgtct | 79582 |
rs7593608 | snp | A/G | 0.0356815 | 0.128715 | intron-variant | SPAG16 | GRCh38.p7 | 2:214270913 | tgtcttctaaaacaa[A/G]gtataagttccatga | 79582 |
rs7593741 | snp | G/T | 0.0166325 | 0.0896639 | intron-variant | SPAG16 | GRCh38.p7 | 2:213307188 | TCAGTGTTGaatttt[G/T]tttttttttattttt | 79582 |
rs7594164 | snp | C/T | 0.497586 | 0.0346604 | intron-variant | SPAG16 | GRCh38.p7 | 2:214043231 | TAATAAATCTAACAC[C/T]AGTATAGCCTATTTC | 79582 |
rs7594210 | snp | C/G | 0.0448719 | 0.142907 | intron-variant | SPAG16 | GRCh38.p7 | 2:213608463 | ttttctgagaatgat[C/G]gtttccagcttcatc | 79582 |
rs7594753 | snp | C/T | 0 | 0 | intron-variant | SPAG16 | GRCh38.p7 | 2:214293578 | atactccccaggtca[C/T]tagcagaatgctcag | 79582 |
rs7595160 | snp | A/G | 0.131723 | 0.220251 | intron-variant | SPAG16 | GRCh38.p7 | 2:213626494 | TAATGAAAAATATAT[A/G]TAACATTAGTTTAAC | 79582 |
rs7595592 | snp | A/G | 0.375996 | 0.215928 | intron-variant | SPAG16 | GRCh38.p7 | 2:214105484 | gaagcacagtaaagc[A/G]aagcaatttgtttaa | 79582 |
rs7596173 | snp | A/G | 0.48491 | 0.0855403 | intron-variant | SPAG16 | GRCh38.p7 | 2:213651507 | gtccatgggtagCCT[A/G]GCCACTGCACCATGG | 79582 |
rs7596582 | snp | C/T | 0.0494327 | 0.149241 | intron-variant | SPAG16, LOC101928084 | GRCh38.p7 | 2:214093058 | gtttaagcccttcat[C/T]taagtcttttaagat | 79582 |
rs7596861 | snp | A/G | 0.484771 | 0.0859212 | intron-variant | SPAG16 | GRCh38.p7 | 2:213922890 | caagggctgcggttg[A/G]cagacaagctgtatt | 79582 |
rs7597126 | snp | C/T | 0.416708 | 0.186302 | intron-variant | SPAG16 | GRCh38.p7 | 2:214144634 | TTAATTTTTCTAGTA[C/T]GCAGTATAACTCTTT | 79582 |
rs7597256 | snp | A/C | 0.499663 | 0.0129749 | intron-variant | SPAG16 | GRCh38.p7 | 2:214271853 | GGAAACCCCCCCCCC[A/C]AAAAAAAAGAAAGAA | 79582 |
rs7597489 | snp | A/G | 0.130008 | 0.219321 | intron-variant | SPAG16 | GRCh38.p7 | 2:213727267 | taactgaaatataca[A/G]tgcaaaagaacctcc | 79582 |
rs7597513 | snp | A/T | 0.404907 | 0.196224 | intron-variant | SPAG16 | GRCh38.p7 | 2:213727326 | actggcagttttttt[A/T]aaaaaaagtttaaaa | 79582 |
rs7597705 | snp | A/G | 0.130351 | 0.219509 | intron-variant | SPAG16 | GRCh38.p7 | 2:213727494 | TTGAGCAAAAACAGG[A/G]AGCCAGTGAAAGGGT | 79582 |
rs7597729 | snp | G/T | | | intron-variant | SPAG16 | GRCh38.p7 | 2:213329619 | cagagcataaaagtt[G/T]ggaaaatttgcagct | 79582 |
rs7597734 | snp | C/T | 0.443598 | 0.158176 | intron-variant | SPAG16 | GRCh38.p7 | 2:213989862 | AGAGTCCAAGCCTAG[C/T]ATTCTTTTTATGAAA | 79582 |
rs7597928 | snp | A/G | 0.239902 | 0.249796 | intron-variant | SPAG16 | GRCh38.p7 | 2:213727658 | gggagataagggaag[A/G]aaagtagcaatgggg | 79582 |
rs7597948 | snp | G/T | 0.492823 | 0.0594727 | intron-variant | SPAG16 | GRCh38.p7 | 2:213961591 | ctaaccctagttttt[G/T]tttttttttgctgga | 79582 |
rs7597983 | snp | A/C | 0.451483 | 0.148002 | intron-variant | SPAG16 | GRCh38.p7 | 2:213986131 | GACAAAGAGACTTTG[A/C]CTTTTCTAGGGTTAT | 79582 |
rs7598173 | snp | A/G | 0.49995 | 0.00499176 | intron-variant | SPAG16 | GRCh38.p7 | 2:213727904 | CCCAGGTTGGAGTGC[A/G]ATGGCGTGATCTCAG | 79582 |
rs7598392 | snp | A/C | 0.342134 | 0.232404 | intron-variant | SPAG16 | GRCh38.p7 | 2:214053784 | AAGTGACAAGGTTAG[A/C]TGAGAATCAGTCTAT | 79582 |
rs7598774 | snp | C/T | 0.046775 | 0.145601 | intron-variant | SPAG16 | GRCh38.p7 | 2:213500151 | GAATGAGGATACACC[C/T]GACAAACCCACAGAA | 79582 |
rs7599129 | snp | A/G | 0.0162398 | 0.0886349 | intron-variant | SPAG16 | GRCh38.p7 | 2:213905421 | ATTAAATGTCCAGTG[A/G]CAAATGGCACATACA | 79582 |
rs7599328 | snp | A/G | 0.0733688 | 0.176922 | intron-variant | SPAG16 | GRCh38.p7 | 2:213692827 | aaaaaaaaaaaaaag[A/G]aaaaaaaaGTTTTAT | 79582 |
rs7599344 | snp | C/G | 0.349671 | 0.229272 | intron-variant | SPAG16 | GRCh38.p7 | 2:213905563 | ATTGATTCAACAGCT[C/G]TTTATTGGGAGTCTC | 79582 |
rs7599622 | snp | A/G | 0.172028 | 0.23753 | intron-variant | SPAG16 | GRCh38.p7 | 2:214254460 | tttgagatacgttcc[A/G]ttaatacctagttta | 79582 |
rs7599738 | snp | A/T | 0.475437 | 0.108066 | intron-variant | SPAG16 | GRCh38.p7 | 2:213652326 | TTTTCTTGTTTTTTT[A/T]ATGAATATTCACCAA | 79582 |
rs7599746 | snp | G/T | 0.195837 | 0.244062 | intron-variant | SPAG16 | GRCh38.p7 | 2:214254606 | AAAGGATTGCAAGTT[G/T]ATGTGAGTTCTTTGA | 79582 |
rs7599815 | snp | C/T | 0.278399 | 0.248382 | intron-variant | SPAG16 | GRCh38.p7 | 2:213865325 | ATATGAAATTAATAA[C/T]CATGAATGAGATTAA | 79582 |
rs7600131 | snp | A/T | 0.44858 | 0.151875 | intron-variant | SPAG16 | GRCh38.p7 | 2:214272073 | CATTTCATTAAAATT[A/T]TAAGTACTTATTGGT | 79582 |
rs7600389 | snp | C/T | 0.324619 | 0.238604 | intron-variant | SPAG16 | GRCh38.p7 | 2:213937320 | TGGTACATTAATACC[C/T]GTCTTATATTGCCAA | 79582 |
rs7600945 | snp | A/C | 0.0402882 | 0.136092 | intron-variant | SPAG16 | GRCh38.p7 | 2:214124739 | ATGCAAAACCACGGG[A/C]AGAACAAGAGAGTCT | 79582 |
rs7601322 | snp | A/G | 0.0539704 | 0.155153 | intron-variant | SPAG16 | GRCh38.p7 | 2:213492525 | actgccctccagcct[A/G]ggcgacagagcgaga | 79582 |
rs7601427 | snp | A/G | 0.213937 | 0.247385 | intron-variant | SPAG16, LOC101928084 | GRCh38.p7 | 2:214094915 | TCTAGTTAGGTAGCC[A/G]GTTTCTGGACGTCAG | 79582 |
rs7601835 | snp | G/T | 0.105924 | 0.204309 | intron-variant | SPAG16 | GRCh38.p7 | 2:213661898 | TGGTTTCTATAGAAG[G/T]ATATATACCATCTTT | 79582 |
rs7601885 | snp | A/T | 0.23031 | 0.249223 | intron-variant | SPAG16 | GRCh38.p7 | 2:214015409 | ttccagaccagcctg[A/T]ccaacatggtgaaac | 79582 |
rs7602331 | snp | A/C | 0.478768 | 0.100824 | intron-variant | SPAG16 | GRCh38.p7 | 2:213665504 | AAAGATTGCAAATTT[A/C]AAATTTCTACTAATT | 79582 |
rs7602734 | snp | A/G | 0.130694 | 0.219696 | intron-variant | SPAG16 | GRCh38.p7 | 2:213723695 | AGATCACCTCAGCTA[A/G]TAGAGATTTTTAGGT | 79582 |
rs7603171 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | SPAG16 | GRCh38.p7 | 2:214366097 | gattcttctgcctca[G/T]cttcccaagtagctg | 79582 |
rs7603276 | snp | A/G | 0.472803 | 0.113397 | intron-variant | SPAG16 | GRCh38.p7 | 2:213858971 | GGATCATGAGGTCAA[A/G]AGTTTGAGACCAGCC | 79582 |
rs7604290 | snp | C/T | 0.172351 | 0.237636 | intron-variant | SPAG16 | GRCh38.p7 | 2:214205944 | ctgacacctgtagtc[C/T]cacactttgagaggc | 79582 |
rs7604356 | snp | A/G | 0.194278 | 0.243711 | intron-variant | SPAG16 | GRCh38.p7 | 2:213380655 | acattcagtttccac[A/G]aagcccagtaacagg | 79582 |
rs7604964 | snp | C/T | 0.17138 | 0.237316 | intron-variant | SPAG16 | GRCh38.p7 | 2:213972306 | atatataatataaat[C/T]tataaaaagagattt | 79582 |
rs7604980 | snp | G/T | 0.104149 | 0.203046 | intron-variant | SPAG16 | GRCh38.p7 | 2:214155916 | CCTAGCTGATTAAAT[G/T]TGGAGTTGAAATTCA | 79582 |
rs7605061 | snp | C/T | 0.194278 | 0.243711 | intron-variant, utr-variant-3-prime | SPAG16 | GRCh38.p7 | 2:213370645 | CCAATTAATCTCTAA[C/T]GATTCATTCTACTCT | 79582 |
rs7605203 | snp | A/T | 0.00874735 | 0.0655527 | intron-variant | SPAG16 | GRCh38.p7 | 2:214292738 | atgcttcctgtatcc[A/T]cacattgatatctgt | 79582 |
rs7606420 | snp | A/G/T | 0.00795532 | 0.062565 | intron-variant | SPAG16 | GRCh38.p7 | 2:214013032 | tagtctgggtaaaaa[A/G/T]ttttaaaaaccactg | 79582 |
rs7606535 | snp | A/C | 0.479824 | 0.098392 | intron-variant | SPAG16 | GRCh38.p7 | 2:213872560 | tactttttcctttct[A/C]atctagatacctttg | 79582 |
rs7606864 | snp | C/T | 0.0119091 | 0.0762411 | intron-variant | SPAG16 | GRCh38.p7 | 2:213782615 | ATATTGGTCATAACA[C/T]AGAATTTTTGAAAGC | 79582 |
rs7606949 | snp | C/T | 0.304937 | 0.243889 | intron-variant | SPAG16 | GRCh38.p7 | 2:214402057 | GGCTCACTGGGGAAA[C/T]TGTATTTGATCAATT | 79582 |
rs7606997 | snp | C/G | 0.246769 | 0.249979 | intron-variant | SPAG16 | GRCh38.p7 | 2:214066344 | AATGCTGTAGCTCTT[C/G]CTTTGTTATCAGTCA | 79582 |
rs7607479 | snp | C/T | 0.479744 | 0.0985793 | intron-variant | SPAG16 | GRCh38.p7 | 2:213678860 | TGGGTGAGGACACTC[C/T]ACTCTTACCGTTTTG | 79582 |
rs7607885 | snp | A/G | | | intron-variant | SPAG16 | GRCh38.p7 | 2:214149079 | TGTGTGTGTGTGTGT[A/G]TATATATATATATAT | 79582 |
rs7608423 | snp | A/G | 0.0715223 | 0.175059 | intron-variant | SPAG16 | GRCh38.p7 | 2:213381853 | taaataggtatagat[A/G]tatccgctgtaccat | 79582 |
rs7608735 | snp | A/G | 0.5 | 0 | intron-variant, downstream-variant-500B | SPAG16 | GRCh38.p7 | 2:213371419 | AAAAAAAAAAAAAAA[A/G]AAAAGAAAAGACGAT | 79582 |
rs7608811 | snp | A/G | 0.230017 | 0.2492 | intron-variant, downstream-variant-500B | SPAG16 | GRCh38.p7 | 2:213371441 | AAAGACGATTTATTG[A/G]TTAAGTGGTTGTTCT | 79582 |
rs7608899 | snp | A/G | 0.0232847 | 0.105357 | intron-variant | SPAG16 | GRCh38.p7 | 2:214267729 | aatgtccatactacc[A/G]aaagcattctataga | 79582 |
rs7609021 | snp | C/G | 0.34526 | 0.23114 | intron-variant, downstream-variant-500B | SPAG16 | GRCh38.p7 | 2:213371669 | AGAAAACAACAAATT[C/G]ATTGTCATTTACTCT | 79582 |
rs7609177 | snp | A/T | 0.0197687 | 0.0974348 | intron-variant | SPAG16 | GRCh38.p7 | 2:213779184 | AAGTTTTCTTTGTTT[A/T]TAGTTATACCTCCAA | 79582 |
rs8179764 | snp | C/T | 0.479177 | 0.0998894 | intron-variant | SPAG16 | GRCh38.p7 | 2:213467573 | gaggggaggcctgga[C/T]tggagaggagaacag | 79582 |
rs9283526 | snp | C/T | 0.441841 | 0.160303 | intron-variant | SPAG16 | GRCh38.p7 | 2:213730132 | ACAGTTGATTAAGCT[C/T]GTCCACTTTGCAGAT | 79582 |
rs9283527 | snp | C/T | 0.495818 | 0.0455352 | intron-variant | SPAG16 | GRCh38.p7 | 2:213983921 | AACCCGCATGCAAGT[C/T]ATTATAAATTCCTGC | 79582 |
rs9283528 | snp | A/G | 0.0433465 | 0.140692 | intron-variant | SPAG16 | GRCh38.p7 | 2:214170226 | CTTAGGTGTGTATAC[A/G]TATACACACACACTT | 79582 |
rs9283529 | snp | A/G | 0.47517 | 0.10862 | intron-variant | SPAG16 | GRCh38.p7 | 2:214397945 | ACTCTCACTTGTTCT[A/G]GTCAGCACTTAATCC | 79582 |
rs9288468 | snp | C/T | 0.0471551 | 0.14613 | intron-variant | SPAG16 | GRCh38.p7 | 2:213457024 | aggatcctaaatgtt[C/T]gcattgcattttttc | 79582 |
rs9288469 | snp | A/G | 0.101301 | 0.200969 | intron-variant | SPAG16 | GRCh38.p7 | 2:213712653 | CCTTCTTTCTCTCTA[A/G]GGAAGAAGAAAGCTT | 79582 |
rs9288470 | snp | A/G | 0.442791 | 0.15916 | intron-variant | SPAG16 | GRCh38.p7 | 2:213729677 | TTTCTACCGATTAAT[A/G]TAAAGTTGTCTAGGG | 79582 |
rs9288471 | snp | A/G | 0.472616 | 0.113763 | intron-variant | SPAG16 | GRCh38.p7 | 2:213855286 | TCATCTAAAAAAGGA[A/G]AAGTCAACAGAGGTG | 79582 |
rs9288472 | snp | C/T | 0.472616 | 0.113763 | intron-variant | SPAG16 | GRCh38.p7 | 2:213855311 | GAGGTGTTGAGCTAA[C/T]TCTACttaaagatat | 79582 |
rs9288473 | snp | C/T | 0.474544 | 0.10991 | intron-variant | SPAG16 | GRCh38.p7 | 2:213855391 | ctagctttgtgacct[C/T]gggtggatcacttaa | 79582 |
rs9288474 | snp | A/G | 0.472709 | 0.11358 | intron-variant | SPAG16 | GRCh38.p7 | 2:213855412 | gatcacttaacctct[A/G]tgtatcccagttcct | 79582 |
rs9288475 | snp | A/G | 0.472803 | 0.113397 | intron-variant | SPAG16 | GRCh38.p7 | 2:213855416 | acttaacctctatgt[A/G]tcccagttcctccac | 79582 |
rs9288476 | snp | G/T | 0.472896 | 0.113214 | intron-variant | SPAG16 | GRCh38.p7 | 2:213855618 | aaagagatttaattg[G/T]ctcacagttctgcat | 79582 |
rs9288477 | snp | A/C | 0.479824 | 0.098392 | intron-variant | SPAG16 | GRCh38.p7 | 2:213888906 | CACAGAACGTAATCA[A/C]ATCTACTTCATAGAA | 79582 |
rs9288478 | snp | A/G | 0.479744 | 0.0985793 | intron-variant | SPAG16 | GRCh38.p7 | 2:213890201 | AAAATTTCTAAGCTA[A/G]TGACTTTAGTGGCAT | 79582 |
rs9288479 | snp | C/T | 0.479824 | 0.098392 | intron-variant | SPAG16 | GRCh38.p7 | 2:213890251 | GTGTGAGGAAAACAC[C/T]CGAATATAGAACTGT | 79582 |
rs9288480 | snp | C/T | 0.472429 | 0.114129 | intron-variant | SPAG16 | GRCh38.p7 | 2:213890288 | TAAATAGAGAAACCA[C/T]TGTGTTAAATCTGAA | 79582 |
rs9288481 | snp | C/G | 0.470811 | 0.117228 | intron-variant | SPAG16 | GRCh38.p7 | 2:213900941 | TACAATTAATTCATT[C/G]TAAGGCAGAGTTTAT | 79582 |
rs9288483 | snp | A/G | 0.443732 | 0.158012 | intron-variant | SPAG16 | GRCh38.p7 | 2:213984442 | GAAGAATGGATAGCA[A/G]AGCTCACATAACTCT | 79582 |
rs9288484 | snp | C/G | 0.311123 | 0.242413 | intron-variant | SPAG16 | GRCh38.p7 | 2:214043129 | AGTCATGCAGTTCTG[C/G]CCAAGGATACTAGAT | 79582 |
rs9288485 | snp | A/G | 0.268724 | 0.249298 | intron-variant | SPAG16 | GRCh38.p7 | 2:214043568 | TACATAATTGTCAGA[A/G]AAATTGATGTAATGG | 79582 |
rs9288486 | snp | C/T | 0.459687 | 0.136129 | intron-variant | SPAG16 | GRCh38.p7 | 2:214064741 | TTTTCTAGCCTGTAA[C/T]TGCTATTAAACAGAA | 79582 |
rs9288487 | snp | A/C | 0.231775 | 0.249335 | intron-variant | SPAG16, LOC101928084 | GRCh38.p7 | 2:214090141 | GCTTTTGCAAAAGAG[A/C]TATATGGAGATATGA | 79582 |
rs9288488 | snp | G/T | 0.234109 | 0.249494 | intron-variant | SPAG16, LOC101928084 | GRCh38.p7 | 2:214091827 | CTTTATCCACTCTAA[G/T]GAACATATTAACAAC | 79582 |
rs9288489 | snp | A/G | 0.170733 | 0.237101 | intron-variant | SPAG16 | GRCh38.p7 | 2:214185151 | CTTTGAAAAGTGCTC[A/G]TTCTAGAGGCTCACT | 79582 |
rs9288490 | snp | C/T | 0.384593 | 0.210677 | intron-variant | SPAG16 | GRCh38.p7 | 2:214237071 | AGCACCAGGATATTT[C/T]TTAGTAAATATCATA | 79582 |
rs9288491 | snp | C/T | 0.295911 | 0.245748 | intron-variant, missense | SPAG16 | GRCh38.p7 | 2:214238160 | CGTATCTTTATAGAC[C/T]AGGAGCTCAGATATA | 79582 |
rs9288492 | snp | G/T | 0.493523 | 0.0565391 | intron-variant | SPAG16 | GRCh38.p7 | 2:214278730 | CTCCCATTTGATTTT[G/T]GATTATGCCACGGTG | 79582 |
rs9288493 | snp | C/T | 0.455977 | 0.141681 | intron-variant | SPAG16 | GRCh38.p7 | 2:214282201 | AATATGAATAAAGCA[C/T]GTTTTAAAACATTTA | 79582 |
rs9288494 | snp | C/T | 0 | 0 | intron-variant | SPAG16 | GRCh38.p7 | 2:214298157 | acacacacacacaca[C/T]atacacacacacaca | 79582 |
rs9631004 | snp | A/T | 0 | 0 | intron-variant | SPAG16 | GRCh38.p7 | 2:214221647 | CTTTTGACCCCCACC[A/T]GATCTCTCAAAAAAG | 79582 |
rs9636336 | snp | A/G | 0.479502 | 0.0991411 | intron-variant | SPAG16 | GRCh38.p7 | 2:213819898 | TGTAGCTGGGATTAC[A/G]GGTGCCTGCCACCAC | 79582 |
rs9636337 | snp | C/T | 0.420415 | 0.182917 | intron-variant | SPAG16 | GRCh38.p7 | 2:214395920 | ccaatttttctttaa[C/T]cagtcttcagttgat | 79582 |
rs9646759 | snp | A/G | 0.484279 | 0.0872533 | intron-variant | SPAG16 | GRCh38.p7 | 2:213728923 | AAAAAAAAAAAAAAG[A/G]TGATGGAATGATGGC | 79582 |
rs9653340 | snp | C/T | 0.209997 | 0.246779 | intron-variant | SPAG16 | GRCh38.p7 | 2:213290002 | TACCAATTGGCACCT[C/T]AAGCTCTGCGCCATT | 79582 |
rs9653342 | snp | A/C | 0.030278 | 0.119257 | intron-variant | SPAG16 | GRCh38.p7 | 2:214073201 | tttctctatgctaaa[A/C]actaaaaaatattat | 79582 |
rs9677504 | snp | A/G | 0.222333 | 0.248464 | intron-variant | SPAG16 | GRCh38.p7 | 2:214317165 | CAGGTATCAACTCCT[A/G]ATTTCACAGTTGAGA | 79582 |
rs9677640 | snp | C/G | 0.0494327 | 0.149241 | intron-variant | SPAG16 | GRCh38.p7 | 2:213367315 | acccagtaatgggat[C/G]gctgggtcaaatggt | 79582 |
rs9677726 | snp | G/T | 0.00953873 | 0.0683987 | intron-variant | SPAG16 | GRCh38.p7 | 2:213684356 | GGAAAGTGGAAGGTT[G/T]TAGTTAAAATTAGAT | 79582 |
rs9678238 | snp | C/T | 0.40157 | 0.198813 | intron-variant | SPAG16 | GRCh38.p7 | 2:214291547 | cctgacctcgtgatc[C/T]gcccgcctcggcctc | 79582 |
rs9678345 | snp | C/T | 0.359364 | 0.22481 | intron-variant | SPAG16 | GRCh38.p7 | 2:213367348 | ttctagttcaagatc[C/T]ttgaggaattgccac | 79582 |
rs9678346 | snp | C/T | 0.359364 | 0.22481 | intron-variant | SPAG16 | GRCh38.p7 | 2:213367349 | tctagttcaagatct[C/T]tgaggaattgccaca | 79582 |
rs9678777 | snp | A/C | 0.34989 | 0.229177 | intron-variant | SPAG16 | GRCh38.p7 | 2:213403373 | tttctcccattctgt[A/C]ggttgcctgttcact | 79582 |
rs9679149 | snp | G/T | 0.0217236 | 0.101931 | intron-variant | SPAG16 | GRCh38.p7 | 2:213999983 | tttacaggctcatag[G/T]tggaagggatttgcc | 79582 |
rs9679317 | snp | C/T | 0.154329 | 0.23097 | intron-variant | SPAG16 | GRCh38.p7 | 2:213377822 | AAATCAGAAAGCTTT[C/T]ATCCTGATGAGCACt | 79582 |
rs9679466 | snp | G/T | | | intron-variant | SPAG16 | GRCh38.p7 | 2:213348434 | tgtgatgttagctgg[G/T]tattttgctcattag | 79582 |
rs9679485 | snp | C/T | 0.354881 | 0.226936 | intron-variant | SPAG16 | GRCh38.p7 | 2:213403145 | tgagatggtatctca[C/T]tgtggttttgatttg | 79582 |
rs9679516 | snp | A/G | 0.128632 | 0.218563 | intron-variant | SPAG16 | GRCh38.p7 | 2:213535589 | AAATGTATTTTGTAT[A/G]TAATCTATTTTTCTG | 79582 |
rs9679714 | snp | C/T | 0.479744 | 0.0985793 | intron-variant | SPAG16 | GRCh38.p7 | 2:213684605 | AAAGTTCTATATAAA[C/T]TATATGTGTTAAATA | 79582 |
rs9711475 | snp | A/T | 0.472709 | 0.11358 | intron-variant | SPAG16 | GRCh38.p7 | 2:213860386 | gtgtgtatatctata[A/T]atagacagatattta | 79582 |
rs9711624 | snp | C/T | 0 | 0 | intron-variant | SPAG16 | GRCh38.p7 | 2:214298139 | acacacacacataca[C/T]atacacacacacaca | 79582 |
rs9711625 | snp | C/T | 0 | 0 | intron-variant | SPAG16 | GRCh38.p7 | 2:214298145 | acacatacacataca[C/T]acacacacacatata | 79582 |
rs9711627 | snp | C/T | | | intron-variant | SPAG16 | GRCh38.p7 | 2:214298175 | acacacacacacaca[C/T]atatatatatatttg | 79582 |
rs9753526 | snp | C/T | 0.00279162 | 0.0372561 | intron-variant | SPAG16 | GRCh38.p7 | 2:214170179 | GGAGAGGGatacaca[C/T]acacttaggtgtgta | 79582 |
rs9789347 | snp | G/T | 0.394904 | 0.203722 | intron-variant | SPAG16 | GRCh38.p7 | 2:213973789 | AATCTGGTGTTTTGT[G/T]GATATTGCTCTCCTT | 79582 |
rs9789685 | snp | A/G | 0.407502 | 0.194147 | intron-variant | SPAG16 | GRCh38.p7 | 2:213969940 | tagactgagtaactt[A/G]tgaaaaacaaattta | 79582 |
rs9798229 | snp | A/C | 0.372189 | 0.218105 | intron-variant | SPAG16 | GRCh38.p7 | 2:214273920 | atattgattcttcct[A/C]tccatgtgcatggaa | 79582 |
rs9798318 | snp | A/C | | | intron-variant | SPAG16 | GRCh38.p7 | 2:213761889 | aaaataaaaacaaaa[A/C]aacaaaacaaaaaaa | 79582 |
rs9807944 | snp | A/G | 0.48978 | 0.0707512 | intron-variant | SPAG16 | GRCh38.p7 | 2:214079659 | AGAAGTTTTCTACCG[A/G]CAAGATGAAAGATAA | 79582 |
rs9807973 | snp | A/C | | | intron-variant | SPAG16 | GRCh38.p7 | 2:214079868 | ATTTCAAAAACaaaa[A/C]taatttttattattt | 79582 |
rs9808122 | snp | A/G | 0.00279162 | 0.0372561 | intron-variant | SPAG16 | GRCh38.p7 | 2:214407654 | ACACTTTCTCTATAA[A/G]TGCTCCACTTTGTGG | 79582 |
rs9808551 | snp | A/G | 0.214541 | 0.247473 | intron-variant | SPAG16 | GRCh38.p7 | 2:214231372 | AGAACTATGTCAGAT[A/G]TGAAGTAGTATTTAT | 79582 |
rs9973768 | snp | C/T | 0.0755793 | 0.179102 | intron-variant | SPAG16 | GRCh38.p7 | 2:214055343 | TATCGAATAGCCCAT[C/T]TTGCATTACTAAATG | 79582 |
rs9979549 | snp | A/G | 0.277778 | 0.248452 | intron-variant | SPAG16 | GRCh38.p7 | 2:213356532 | CATAAACACCTCTAC[A/G]CAAATAAACTAGAAA | 79582 |
rs10006534 | snp | C/T | | | intron-variant | SPAG16 | GRCh38.p7 | 2:213356760 | TCCTTCAGTTCTGTT[C/T]TGATCTTAGTTATTT | 79582 |
rs10084198 | snp | C/T | 0.131038 | 0.219882 | intron-variant | SPAG16 | GRCh38.p7 | 2:213721131 | TTTGAGATGGAGTCT[C/T]TCTCTGTAACCCAGG | 79582 |
rs10084205 | snp | A/G | 0.472052 | 0.11486 | intron-variant | SPAG16 | GRCh38.p7 | 2:213721217 | CTGCCTCTTGCCTCA[A/G]CCTCCCGAGTAGCTG | 79582 |
rs10084470 | snp | C/G | 0.46703 | 0.124089 | intron-variant | SPAG16 | GRCh38.p7 | 2:213719568 | GGTGGGGCCAGATAA[C/G]AGAATAAAAGCAGGC | 79582 |
rs10153590 | snp | C/T | 0.131038 | 0.219882 | intron-variant | SPAG16 | GRCh38.p7 | 2:213718676 | gtcccccagcagtgc[C/T]ggcccacctgcgctg | 79582 |
rs10153628 | snp | G/T | 0.0471551 | 0.14613 | intron-variant | SPAG16 | GRCh38.p7 | 2:213638369 | ttcaaactttttgat[G/T]taggcatttaatgct | 79582 |
rs10153692 | snp | A/G | 0.0479149 | 0.147179 | intron-variant | SPAG16 | GRCh38.p7 | 2:213669958 | AATCATGAAAATGGA[A/G]GCTTTTTTCTTCTAC | 79582 |
rs10153700 | snp | C/G | 0.479824 | 0.098392 | intron-variant | SPAG16 | GRCh38.p7 | 2:213876412 | TATTTTGTATGAGTG[C/G]ACATCAAATTCCCTT | 79582 |
rs10153702 | snp | C/G | 0.479824 | 0.098392 | intron-variant | SPAG16 | GRCh38.p7 | 2:213876527 | GAGATTACACCAGTA[C/G]CTGAGCTTTTACTTT | 79582 |
rs10153855 | snp | G/T | 0.0329836 | 0.124112 | intron-variant | SPAG16 | GRCh38.p7 | 2:214161373 | gatctctgagaaact[G/T]ccacatcatcttcca | 79582 |
rs10153910 | snp | A/G | 0.479824 | 0.098392 | intron-variant | SPAG16 | GRCh38.p7 | 2:213876591 | TGTCAAAAGCATTAT[A/G]AGTATTCTACGACGT | 79582 |
rs10153920 | snp | G/T | 0 | 0 | intron-variant | SPAG16 | GRCh38.p7 | 2:213718652 | cagtggctgcggagg[G/T]tgtactgagtccccc | 79582 |
rs10153938 | snp | A/G | 0.0383715 | 0.133092 | intron-variant | SPAG16 | GRCh38.p7 | 2:213718862 | catcgaccacccaag[A/G]gctgaggaatgcgag | 79582 |
rs10153940 | snp | G/T | 0.140581 | 0.224783 | intron-variant | SPAG16 | GRCh38.p7 | 2:213719054 | ttgtgagtgcaccag[G/T]cgacactcggtatct | 79582 |
rs10164670 | snp | C/T | 0.175897 | 0.238765 | upstream-variant-2KB, intron-variant | SPAG16, LOC100130451 | GRCh38.p7 | 2:213283575 | tgcgacatgagctta[C/T]ctgcacttgtacccc | 79582 |
rs10164714 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | SPAG16 | GRCh38.p7 | 2:214406526 | TTCAAATATTCAAGT[C/T]TTTATAACAAATTCA | 79582 |
rs10164726 | snp | A/G | 0.472803 | 0.113397 | intron-variant | SPAG16 | GRCh38.p7 | 2:213855064 | TCTGCTTTAGACCAT[A/G]AGTGTTTCTTTAGCA | 79582 |
rs10164985 | snp | C/G | 0.155987 | 0.23165 | intron-variant | SPAG16 | GRCh38.p7 | 2:213519592 | gtaagtcaaattaaa[C/G]ctctgtcttttgtaa | 79582 |
rs10164987 | snp | C/T | 0.469642 | 0.119404 | intron-variant | SPAG16 | GRCh38.p7 | 2:213716400 | GCAAACATTTCTAAA[C/T]TGAGAGCTGTCTAAT | 79582 |
rs10165190 | snp | A/C | 0.0471551 | 0.14613 | intron-variant | SPAG16 | GRCh38.p7 | 2:213483888 | TTAAAATAATTCCTT[A/C]TATGCAAAATACTGT | 79582 |
rs10165269 | snp | C/T | 0.229429 | 0.249152 | intron-variant | SPAG16, LOC101928084 | GRCh38.p7 | 2:214100245 | aggaaaattaaacct[C/T]ttttctctataaatt | 79582 |
rs10165766 | snp | A/G | 0.484841 | 0.0857308 | intron-variant | SPAG16 | GRCh38.p7 | 2:213903294 | ttccatgggcatccc[A/G]cccctgcagcaaact | 79582 |
rs10165804 | snp | G/T | 0.40263 | 0.198 | intron-variant | SPAG16 | GRCh38.p7 | 2:213711200 | CACTCAATTTTCAAG[G/T]TTATGTACTTTCCTC | 79582 |
rs10166032 | snp | A/G | 0.468148 | 0.122112 | intron-variant | SPAG16 | GRCh38.p7 | 2:213808477 | GAGCTCAATTTCTAA[A/G]TCAAAACCAGTAAAG | 79582 |
rs10166250 | snp | C/G | 0.192401 | 0.243274 | intron-variant | SPAG16 | GRCh38.p7 | 2:213318869 | taaattttCTTCTAA[C/G]TTAAAAGAAAATTAC | 79582 |
rs10166274 | snp | A/G | 0.490175 | 0.0693959 | intron-variant | SPAG16 | GRCh38.p7 | 2:213979044 | TATCTCTTATAAGCT[A/G]TCTCAGAAATGAACA | 79582 |
rs10166399 | snp | C/T | | | intron-variant | SPAG16 | GRCh38.p7 | 2:213896613 | acacacacacacaca[C/T]acaTAGATATGTACA | 79582 |
rs10166400 | snp | A/G | 0.48435 | 0.0870631 | intron-variant | SPAG16 | GRCh38.p7 | 2:213447827 | tgcttcaggaaaagt[A/G]taatgttggttcgag | 79582 |
rs10166553 | snp | A/G | 0.444444 | 0.157135 | intron-variant | SPAG16 | GRCh38.p7 | 2:213896592 | tatacacacacacac[A/G]cacacacacacacac | 79582 |
rs10166554 | snp | A/C | 0 | 0 | intron-variant | SPAG16 | GRCh38.p7 | 2:214375380 | ACGAAGTAGGGCAAA[A/C]ATTTTTCTCTTCTAT | 79582 |
rs10166779 | snp | A/G | 0.498158 | 0.0302955 | intron-variant | SPAG16 | GRCh38.p7 | 2:214345396 | CAAACAATTCAGCCC[A/G]CTCTCATCTCTCCCT | 79582 |
rs10166816 | snp | C/T | 0.498277 | 0.0293024 | intron-variant | SPAG16 | GRCh38.p7 | 2:214345619 | TATAACATAAATATA[C/T]CCCTGAAACCACTAC | 79582 |
rs10167079 | snp | A/G | 0.278133 | 0.248412 | intron-variant | SPAG16 | GRCh38.p7 | 2:214392947 | CCATAGAAAATGTTT[A/G]AAATTGATGTATTAA | 79582 |
rs10167571 | snp | A/C | 0.472896 | 0.113214 | intron-variant | SPAG16 | GRCh38.p7 | 2:213861692 | AAAGCATTGCCATAG[A/C]TAAAATATCAGGCAT | 79582 |
rs10167662 | snp | A/G | 0.49334 | 0.057322 | intron-variant | SPAG16 | GRCh38.p7 | 2:213967437 | GAGACCAAAAGAGAG[A/G]CATGTTTAACTCACA | 79582 |
rs10167688 | snp | A/C | 0.0150286 | 0.0853723 | missense, nc-transcript-variant | SPAG16 | GRCh38.p7 | 2:213489990 | CCCATAGATATGCAA[A/C]CAAATCCAAACCTGA | 79582 |
rs10168070 | snp | C/T | 0.0463947 | 0.145069 | intron-variant | SPAG16 | GRCh38.p7 | 2:213615483 | gaaatcccagctact[C/T]gggaggctgaggcag | 79582 |
rs10168152 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | SPAG16 | GRCh38.p7 | 2:214275676 | tttgttgtgatttct[C/G]ttcttttacatttgg | 79582 |
rs10168515 | snp | A/G | 0.474182 | 0.110646 | intron-variant | SPAG16 | GRCh38.p7 | 2:213791481 | AATCATAATATTTAC[A/G]GAAGACTATTTGACA | 79582 |
rs10168637 | snp | A/G | 0.33533 | 0.234987 | intron-variant | SPAG16 | GRCh38.p7 | 2:214326742 | CGAGATCAGGAGATC[A/G]AGGCCATCCTGGCTA | 79582 |
rs10168841 | snp | C/T | 0.271702 | 0.249056 | intron-variant | SPAG16 | GRCh38.p7 | 2:214286222 | ACAAAGTTTCAGTTA[C/T]GCAAGATGAATAGGC | 79582 |
rs10169670 | snp | A/G | 0.230017 | 0.2492 | intron-variant | SPAG16, LOC101928084 | GRCh38.p7 | 2:214098182 | AGGTACAATACAATA[A/G]ATAGTATAAAATAAT | 79582 |
rs10169877 | snp | G/T | 0.046775 | 0.145601 | intron-variant | SPAG16 | GRCh38.p7 | 2:213360803 | GTAAAATAGAAGATA[G/T]GTTACTTTTGTGCTT | 79582 |
rs10169892 | snp | A/G | 0.230017 | 0.2492 | intron-variant | SPAG16, LOC101928084 | GRCh38.p7 | 2:214098445 | AAATGCAATATGACT[A/G]GTGTCCTCATAAAGA | 79582 |
rs10169990 | snp | G/T | 0 | 0 | intron-variant | SPAG16 | GRCh38.p7 | 2:213587812 | ccttccacaaaatac[G/T]gggactcaaagacaa | 79582 |
rs10170007 | snp | C/T | 0.480144 | 0.097642 | intron-variant | SPAG16 | GRCh38.p7 | 2:213867738 | CCATCCTGGCTAACA[C/T]GGTGAATCCCCGTCT | 79582 |
rs10170268 | snp | C/G | 0.479984 | 0.0980171 | intron-variant | SPAG16 | GRCh38.p7 | 2:213867785 | aaaaaatagccgggc[C/G]tggtggcgggcacct | 79582 |
rs10170275 | snp | A/G | 0.479984 | 0.0980171 | intron-variant | SPAG16 | GRCh38.p7 | 2:213867822 | CCAGCTACTCGGGAG[A/G]CTGAGGCAGGAGAAT | 79582 |
rs10170297 | snp | C/T | 0 | 0 | intron-variant | SPAG16 | GRCh38.p7 | 2:214242392 | ATCATAAAAAGACTA[C/T]GGTAATCCTACAAAT | 79582 |
rs10170343 | snp | A/G | 0.472989 | 0.113031 | intron-variant | SPAG16 | GRCh38.p7 | 2:213861889 | CTTGAATTCATTACT[A/G]TAATTTGTGTACTGT | 79582 |
rs10170921 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | SPAG16 | GRCh38.p7 | 2:214334139 | catgtcagttacatc[A/G]tctatctccttcggc | 79582 |
rs10171081 | snp | G/T | 0.327937 | 0.23877 | intron-variant | SPAG16 | GRCh38.p7 | 2:214377985 | caatatgatcacaaa[G/T]gtcctggaaagaggg | 79582 |
rs10171084 | snp | C/G | 0.00874735 | 0.0655527 | intron-variant | SPAG16 | GRCh38.p7 | 2:213832713 | atcaaactattttgt[C/G]caatcacatttttac | 79582 |
rs10171702 | snp | A/G | 0.136166 | 0.22258 | intron-variant | SPAG16 | GRCh38.p7 | 2:214357497 | ctaccccctccccca[A/G]tcttctgagtttctc | 79582 |
rs10171746 | snp | C/G | 0.0197687 | 0.0974348 | intron-variant | SPAG16 | GRCh38.p7 | 2:214026576 | ATATATAGGTTTAAT[C/G]AAATTCCAAGGAGAT | 79582 |
rs10171960 | snp | C/T | 0.130694 | 0.219696 | intron-variant | SPAG16 | GRCh38.p7 | 2:213718593 | actggaagcagccag[C/T]cagccctgctggccc | 79582 |
rs10172140 | snp | C/T | 0.212425 | 0.24716 | intron-variant | SPAG16 | GRCh38.p7 | 2:213360882 | AGAATTCATTTCCAA[C/T]CAAACTTTAGGATGT | 79582 |
rs10172164 | snp | C/T | 0.45235 | 0.146814 | intron-variant | SPAG16 | GRCh38.p7 | 2:213956202 | ctcaggtgatctgcc[C/T]gcctcggcctcccaa | 79582 |
rs10172390 | snp | C/T | 0.401747 | 0.198678 | intron-variant | SPAG16 | GRCh38.p7 | 2:214308288 | atttgggtcactgca[C/T]gtgagacggatctat | 79582 |
rs10172549 | snp | A/C | | | intron-variant | SPAG16 | GRCh38.p7 | 2:213867926 | AAGACTCTGTCTCAA[A/C]AAAAAAAAAAAAAAA | 79582 |
rs10172666 | snp | A/T | 0.00398564 | 0.0444627 | intron-variant | SPAG16 | GRCh38.p7 | 2:214223993 | AATCAATAAACTTAG[A/T]GCATTCTGCAGAAAG | 79582 |
rs10173596 | snp | C/T | 0.0452528 | 0.143452 | intron-variant | SPAG16 | GRCh38.p7 | 2:213518085 | agtatctagaatctg[C/T]aagaaacttaacaag | 79582 |
rs10173751 | snp | C/T | 0.470424 | 0.117954 | intron-variant | SPAG16 | GRCh38.p7 | 2:213923351 | ggcagcgtcgtgtgc[C/T]ctgctgtctgggtgt | 79582 |
rs10173834 | snp | C/T | 0.479824 | 0.098392 | intron-variant | SPAG16 | GRCh38.p7 | 2:213893310 | tcttacaaaaaatac[C/T]aaagagagttcttcc | 79582 |
rs10173908 | snp | C/T | 0.00874735 | 0.0655527 | intron-variant | SPAG16 | GRCh38.p7 | 2:213833184 | CCTGGCTCTGTCCTC[C/T]AGATATTATCCTTCC | 79582 |
rs10174075 | snp | A/G | 0.484841 | 0.0857308 | intron-variant | SPAG16 | GRCh38.p7 | 2:213916485 | tgtatatctgttttg[A/G]taacagtaccatgct | 79582 |
rs10174173 | snp | A/G | 0.479824 | 0.098392 | intron-variant | SPAG16 | GRCh38.p7 | 2:213886468 | TGAGGACTGCATTTT[A/G]AGGTGTCACTTTCTG | 79582 |
rs10174234 | snp | A/C | 0.484841 | 0.0857308 | intron-variant | SPAG16 | GRCh38.p7 | 2:213923846 | ggtgggatgactggg[A/C]tggaggctctagcag | 79582 |
rs10174341 | snp | C/T | 0.262159 | 0.249704 | intron-variant | SPAG16 | GRCh38.p7 | 2:214182334 | ATATACCAATGCCTC[C/T]AGTAGTACACTGGAT | 79582 |
rs10174347 | snp | G/T | 0.479744 | 0.0985793 | intron-variant | SPAG16 | GRCh38.p7 | 2:213884715 | tgtttatttttatct[G/T]actgtgttgatttga | 79582 |
rs10174362 | snp | A/T | 0.213333 | 0.247296 | intron-variant | SPAG16 | GRCh38.p7 | 2:213404216 | aaactactttaaagt[A/T]cacatggaaccaaac | 79582 |
rs10174712 | snp | A/C | 0.215747 | 0.247642 | intron-variant | SPAG16 | GRCh38.p7 | 2:213404546 | tcctcacaccttata[A/C]aaaaattaattcaag | 79582 |
rs10174722 | snp | A/G | 0.133777 | 0.221342 | intron-variant | SPAG16 | GRCh38.p7 | 2:214034716 | accagggaatgctgc[A/G]gcacctggaagcttt | 79582 |
rs10174840 | snp | A/G | 0.137867 | 0.223442 | intron-variant | SPAG16 | GRCh38.p7 | 2:213725861 | actgaaggggaagac[A/G]tagctggctgggtca | 79582 |
rs10174902 | snp | A/T | 0.484771 | 0.0859212 | intron-variant | SPAG16 | GRCh38.p7 | 2:213911344 | GAGACGAGGTTTCAC[A/T]GTGTTGCCCAGGATA | 79582 |
rs10175014 | snp | G/T | 0 | 0 | intron-variant | SPAG16 | GRCh38.p7 | 2:213483416 | attaccagcagtgta[G/T]gagagcacctgtACA | 79582 |
rs10175455 | snp | C/G | 0.286042 | 0.247388 | intron-variant | SPAG16 | GRCh38.p7 | 2:214382991 | CCACCCTACTTTCAT[C/G]CCCCTGCCTCACTCT | 79582 |
rs10175505 | snp | A/G | 0.0275645 | 0.114116 | intron-variant | SPAG16 | GRCh38.p7 | 2:213337571 | cacgagaacttcaca[A/G]tgcaataacaagcat | 79582 |
rs10175550 | snp | C/T | 0.0146672 | 0.084371 | intron-variant | SPAG16 | GRCh38.p7 | 2:214344042 | TCTACAATATAACTT[C/T]TCTTTTTTCTCAACC | 79582 |
rs10175930 | snp | A/G | 0.479744 | 0.0985793 | intron-variant | SPAG16 | GRCh38.p7 | 2:214288375 | attgtgaatagtgcc[A/G]caaagacatgcaagt | 79582 |
rs10176177 | snp | C/T | 0.479824 | 0.098392 | intron-variant | SPAG16 | GRCh38.p7 | 2:213869177 | AGAATCACTTGAACC[C/T]GGGAGGCGGAGGTTG | 79582 |
rs10176272 | snp | A/T | 0.229723 | 0.249176 | intron-variant | SPAG16, LOC101928084 | GRCh38.p7 | 2:214100103 | atagtgagtgagtta[A/T]catgagatctgatgg | 79582 |
rs10176542 | snp | C/T | | | intron-variant | SPAG16 | GRCh38.p7 | 2:213860437 | tgtatatctatatat[C/T]tatagatatatgtat | 79582 |
rs10176858 | snp | A/G | 0.484771 | 0.0859212 | intron-variant | SPAG16 | GRCh38.p7 | 2:213923896 | ccatggcaaaagtgg[A/G]tggggtcatgtgcag | 79582 |
rs10176906 | snp | A/G | 0.479177 | 0.0998894 | intron-variant | SPAG16 | GRCh38.p7 | 2:213711165 | TAGCATGGTCCAGTC[A/G]TCCAACTTATTGCCT | 79582 |
rs10176975 | snp | C/T | 0.0479149 | 0.147179 | intron-variant | SPAG16 | GRCh38.p7 | 2:213554058 | GGCCTCTCCATCAGA[C/T]ACCAGTACCACCACC | 79582 |
rs10177031 | snp | C/T | 0.453331 | 0.145452 | intron-variant | SPAG16 | GRCh38.p7 | 2:213943563 | gtattcatgttctag[C/T]attttatggaaggta | 79582 |
rs10177073 | snp | A/G | | | intron-variant | SPAG16 | GRCh38.p7 | 2:214012779 | ACTCCGTTTCATTGA[A/G]AAACAGCCTTTTCGT | 79582 |
rs10177076 | snp | A/G | 0.02016 | 0.0983543 | intron-variant | SPAG16 | GRCh38.p7 | 2:214040662 | tattccatggggtat[A/G]tggagtaccttattt | 79582 |
rs10177976 | snp | A/G | 0.472896 | 0.113214 | intron-variant | SPAG16 | GRCh38.p7 | 2:213864842 | TTTGTCCTATTTCTC[A/G]TATCATAGCAGACAT | 79582 |
rs10178106 | snp | A/G | 0.135825 | 0.222405 | intron-variant | SPAG16 | GRCh38.p7 | 2:214359170 | CTCTAAGTATTTGAC[A/G]TGTATCAAATATAAT | 79582 |
rs10178111 | snp | C/T | 0.212425 | 0.24716 | intron-variant | SPAG16 | GRCh38.p7 | 2:213358980 | agtttatgctatttc[C/T]gtttgttagttttcc | 79582 |
rs10178281 | snp | C/T | 0.486725 | 0.0803809 | intron-variant | SPAG16 | GRCh38.p7 | 2:214058677 | AATATCTGTGAAGCT[C/T]AATAAAGCAAAGTAC | 79582 |
rs10178856 | snp | C/T | 0.470715 | 0.117409 | intron-variant | SPAG16 | GRCh38.p7 | 2:213896469 | gaaaggaaatcagta[C/T]atcgaagagacatta | 79582 |
rs10178999 | snp | G/T | 0.487049 | 0.0794222 | intron-variant | SPAG16 | GRCh38.p7 | 2:213928119 | TTTTGAGATGGAGTC[G/T]CAGTCCCCCAGGCTG | 79582 |
rs10179088 | snp | A/G | 0.209388 | 0.246679 | intron-variant | SPAG16 | GRCh38.p7 | 2:213332907 | atttgtcatgccacc[A/G]tgtcatactgaatag | 79582 |
rs10179417 | snp | A/T | 0.100944 | 0.200705 | intron-variant | SPAG16 | GRCh38.p7 | 2:213715417 | AAGGATCAAATTAGA[A/T]AATTCGTGACAAGCG | 79582 |
rs10179462 | snp | A/G | 0 | 0 | intron-variant | SPAG16 | GRCh38.p7 | 2:214012889 | ctttaacatgtatca[A/G]aatcacttgaagagc | 79582 |
rs10179848 | snp | A/G | 0.0463947 | 0.145069 | intron-variant | SPAG16 | GRCh38.p7 | 2:214158884 | AACAATTTTAATCTA[A/G]CACATGCCCAAATAA | 79582 |
rs10179905 | snp | A/T | 0.472896 | 0.113214 | intron-variant | SPAG16 | GRCh38.p7 | 2:213861515 | CTTACCGCACCACAT[A/T]GGCAAGTAAATGTAT | 79582 |
rs10180128 | snp | C/T | 0.479744 | 0.0985793 | intron-variant | SPAG16 | GRCh38.p7 | 2:213891819 | TCCCCTCATTCTGCC[C/T]GCCTCCAGGTGAAGA | 79582 |
rs10180396 | snp | C/T | 0.211212 | 0.246973 | intron-variant | SPAG16 | GRCh38.p7 | 2:213314468 | TGAGAATTCAGATTT[C/T]ATTGAGAAGTATACT | 79582 |
rs10180751 | snp | A/G | 0.486464 | 0.0811471 | intron-variant | SPAG16 | GRCh38.p7 | 2:213469368 | tcacatgatagaggg[A/G]aaaggaaataaaatg | 79582 |
rs10181112 | snp | A/G | 0.484771 | 0.0859212 | intron-variant | SPAG16 | GRCh38.p7 | 2:213912881 | CTGAAATTTGAAGTC[A/G]TTTGTTCACAATAGA | 79582 |
rs10181374 | snp | A/C | 0.0150606 | 0.0854603 | intron-variant | SPAG16 | GRCh38.p7 | 2:214059486 | TGTTCTAAGTTATTT[A/C]TTCCATGTGATCTTA | 79582 |
rs10181544 | snp | A/G | 0.0452528 | 0.143452 | intron-variant | SPAG16 | GRCh38.p7 | 2:213612488 | tctaatagatatttt[A/G]aacttaacatgtgca | 79582 |
rs10181577 | snp | C/T | 0.00993419 | 0.0697739 | intron-variant | SPAG16 | GRCh38.p7 | 2:214059719 | GGATCACTCACCATT[C/T]CTCAGGTTACTTATA | 79582 |
rs10181804 | snp | A/G | 0 | 0 | intron-variant | SPAG16 | GRCh38.p7 | 2:213825510 | tccttcattctgttg[A/G]taaaatgcattgcat | 79582 |
rs10181868 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | SPAG16 | GRCh38.p7 | 2:214351661 | TGAGCCGAGATGGCA[C/T]CACTGCACTCCAGCC | 79582 |
rs10182085 | snp | A/C | 0.232359 | 0.249377 | intron-variant | SPAG16 | GRCh38.p7 | 2:214084317 | AAACAAAGCCAGGAA[A/C]TAAAAACAAAATCCT | 79582 |
rs10182104 | snp | A/G | 0 | 0 | intron-variant | SPAG16 | GRCh38.p7 | 2:214330795 | CACTTTCTCAGCTGG[A/G]AGAATGAATGTTGTG | 79582 |
rs10182262 | snp | C/T | 0.0486741 | 0.148216 | intron-variant | SPAG16 | GRCh38.p7 | 2:213599932 | acctcccgatccacc[C/T]gccttggcctctcac | 79582 |
rs10182483 | snp | C/T | 0.484841 | 0.0857308 | intron-variant | SPAG16 | GRCh38.p7 | 2:213901016 | TTAAATATTTTGTAT[C/T]ATTCATTTTCCAAAG | 79582 |
rs10182667 | snp | A/T | 0.486725 | 0.0803809 | intron-variant | SPAG16 | GRCh38.p7 | 2:214045664 | ttcttgaaacaaatg[A/T]taatgaaaacacatc | 79582 |
rs10182760 | snp | C/T | 0 | 0 | intron-variant | SPAG16 | GRCh38.p7 | 2:213950706 | CTTTTTTCTTTCTTT[C/T]TTTTTTTTTTTTTTT | 79582 |
rs10182801 | snp | C/G | 0.484841 | 0.0857308 | intron-variant | SPAG16 | GRCh38.p7 | 2:213901321 | ATTGAAAGAAATGGT[C/G]TCAGACTGTCAGCAG | 79582 |
rs10182880 | snp | A/C | 0.484841 | 0.0857308 | intron-variant | SPAG16 | GRCh38.p7 | 2:213901369 | CTAGTAAGGCCTGAA[A/C]GCATTTCACCCTGGT | 79582 |
rs10183066 | snp | C/T | 0 | 0 | intron-variant | SPAG16 | GRCh38.p7 | 2:213746319 | CTATGTTAATCcagt[C/T]ttatgccacttaacc | 79582 |
rs10183622 | snp | A/G | 0.198634 | 0.244666 | intron-variant | SPAG16 | GRCh38.p7 | 2:214285535 | AACTGCTagccgggc[A/G]tggtggctcacacct | 79582 |
rs10183630 | snp | A/T | 0.360032 | 0.224494 | utr-variant-3-prime, intron-variant | SPAG16 | GRCh38.p7 | 2:213317376 | GTTATTTTTTAAATG[A/T]CATTTTCTTCTTTTT | 79582 |
rs10183753 | snp | C/T | 0.0482946 | 0.147699 | intron-variant | SPAG16 | GRCh38.p7 | 2:213521358 | TCTCACCTGTTTTCA[C/T]TCTGACTTGCAGTGC | 79582 |
rs10183895 | snp | A/C | 0.480697 | 0.0963277 | intron-variant | SPAG16 | GRCh38.p7 | 2:213683474 | GAGAATGGCTTGAAC[A/C]CAGGATGCAGAGGTT | 79582 |
rs10184140 | snp | C/T | 0 | 0 | intron-variant | SPAG16 | GRCh38.p7 | 2:213470652 | tgaaaatccatgttg[C/T]tgagcccatgcataa | 79582 |
rs10184425 | snp | C/T | 0.266 | 0.249487 | intron-variant | SPAG16 | GRCh38.p7 | 2:214030135 | ctaactctctatttc[C/T]cccttccgcaggtcc | 79582 |
rs10184586 | snp | C/T | 0.482609 | 0.0916147 | intron-variant | SPAG16 | GRCh38.p7 | 2:214256962 | ttgtttaaaaaatta[C/T]gggaactcttttggt | 79582 |
rs10184691 | snp | A/G | 0.213937 | 0.247385 | intron-variant | SPAG16 | GRCh38.p7 | 2:214060349 | GGAGACAAAAATATT[A/G]TTTATTTTGAATAAT | 79582 |
rs10184870 | snp | C/T | 0.0146672 | 0.084371 | intron-variant | SPAG16 | GRCh38.p7 | 2:214331364 | gcttttcttctgggc[C/T]gttggcatgatgagc | 79582 |
rs10185070 | snp | A/G | 0.479824 | 0.098392 | intron-variant | SPAG16 | GRCh38.p7 | 2:213884453 | ttttcattgaccttg[A/G]tgaacctgatggcta | 79582 |
rs10185168 | snp | A/G | 0.479824 | 0.098392 | intron-variant | SPAG16 | GRCh38.p7 | 2:213884513 | tctacgctgttctcc[A/G]tatttcttgggtttg | 79582 |
rs10185770 | snp | C/T | 0.475702 | 0.107512 | intron-variant | SPAG16 | GRCh38.p7 | 2:213632808 | accatccttgcattc[C/T]agggataaatcccac | 79582 |
rs10185916 | snp | A/G | 0.484841 | 0.0857308 | intron-variant | SPAG16 | GRCh38.p7 | 2:213901883 | CATTCTGAATAGAGT[A/G]GCTTTCTTGTCCTAT | 79582 |
rs10185979 | snp | C/G | 0 | 0 | intron-variant | SPAG16 | GRCh38.p7 | 2:213601092 | ggagaacataaaatg[C/G]cctgggacaaagtct | 79582 |
rs10186170 | snp | C/T | 0.497416 | 0.0358495 | intron-variant | SPAG16 | GRCh38.p7 | 2:214127388 | TCCAACAATATCACA[C/T]GCTGTTCCTTTCAAA | 79582 |
rs10186200 | snp | C/T | 0.492037 | 0.0625946 | intron-variant | SPAG16 | GRCh38.p7 | 2:214015145 | gctggagttttcagc[C/T]gcctaacatcggaag | 79582 |
rs10186597 | snp | A/G | 0.212425 | 0.24716 | intron-variant | SPAG16 | GRCh38.p7 | 2:213358766 | tacttttgtcaactc[A/G]tcaaagtcattctcc | 79582 |
rs10186607 | snp | A/G | 0.490231 | 0.0692021 | intron-variant | SPAG16 | GRCh38.p7 | 2:214015337 | ggtgcagtggctcac[A/G]cctgtaatcccacca | 79582 |
rs10186714 | snp | C/T | 0.479904 | 0.0982045 | intron-variant | SPAG16 | GRCh38.p7 | 2:213872681 | tgattttaggtaaaa[C/T]gtgatcagtctttca | 79582 |
rs10186886 | snp | A/G | 0.470811 | 0.117228 | intron-variant | SPAG16 | GRCh38.p7 | 2:213902808 | CCCTTCTGCCTATGA[A/G]CCTGTAAAATCAAAA | 79582 |
rs10187032 | snp | A/G | 0.472803 | 0.113397 | intron-variant | SPAG16 | GRCh38.p7 | 2:213859892 | ACAGATATGAACCCC[A/G]GCTCTTTTGAGCTTT | 79582 |
rs10187292 | snp | C/G | 0.230603 | 0.249246 | intron-variant, nc-transcript-variant | SPAG16, LOC101928084 | GRCh38.p7 | 2:214096616 | GCTTTTTCTCTTTCT[C/G]AAAAACAGCTGGTTT | 79582 |
rs10187607 | snp | C/G | 0.230896 | 0.249269 | intron-variant | SPAG16, LOC101928084 | GRCh38.p7 | 2:214091097 | ACAAAATCCAAGTTT[C/G]TCCCTCTATTCCCTA | 79582 |
rs10187994 | snp | A/G | 0.453331 | 0.145452 | intron-variant | SPAG16 | GRCh38.p7 | 2:213943501 | gttattggacaatgg[A/G]gaaaaggcactcctt | 79582 |
rs10188076 | snp | C/T | 0.496483 | 0.0417852 | intron-variant | SPAG16, LOC101928084 | GRCh38.p7 | 2:214091555 | AAGCTGTTAGAACCA[C/T]GCCTGGCATATAGTA | 79582 |
rs10188153 | snp | C/G | 0.474544 | 0.10991 | intron-variant | SPAG16 | GRCh38.p7 | 2:214332142 | ctgtgagcccagcta[C/G]ttgggaggctgaagc | 79582 |
rs10188544 | snp | A/G | 0.0448719 | 0.142907 | intron-variant | SPAG16 | GRCh38.p7 | 2:214362607 | TTCCTCCTCACTGTG[A/G]CTAGTTGATAAAGCA | 79582 |
rs10188751 | snp | G/T | 0.479824 | 0.098392 | intron-variant | SPAG16 | GRCh38.p7 | 2:213869241 | CTGGGCAACAAGAGC[G/T]AAAGTCCATGTCAAA | 79582 |
rs10188781 | snp | C/T | 0.47517 | 0.10862 | intron-variant | SPAG16 | GRCh38.p7 | 2:214282868 | CAACTTGACATATTA[C/T]GTATGATAGCAGAGT | 79582 |
rs10189312 | snp | A/C | 0.484841 | 0.0857308 | intron-variant | SPAG16 | GRCh38.p7 | 2:213903047 | GGTCTTGGGCAGCTC[A/C]ACCCCTGTGGCTTTG | 79582 |
rs10189571 | snp | G/T | 0.484841 | 0.0857308 | intron-variant | SPAG16 | GRCh38.p7 | 2:213903128 | tatggtttttccagg[G/T]gcacagtgcaagctg | 79582 |
rs10190056 | snp | A/G | | | intron-variant | SPAG16 | GRCh38.p7 | 2:213979290 | ATGGAATTATACTTT[A/G]TAATTCAGGAATGTT | 79582 |
rs10190314 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | SPAG16 | GRCh38.p7 | 2:214368188 | CACTTTTTTCATCAT[C/T]GCACTAGTTATATGT | 79582 |
rs10190431 | snp | C/T | 0.484421 | 0.0868729 | intron-variant | SPAG16 | GRCh38.p7 | 2:214183488 | AAAATGTGGCTACTA[C/T]GGCTCTCAGCTTGTT | 79582 |
rs10190561 | snp | A/G | 0.067446 | 0.170804 | intron-variant | SPAG16 | GRCh38.p7 | 2:214162507 | ATAATGACTATAGAG[A/G]GAGATTCAACTTTAT | 79582 |
rs10190719 | snp | C/T | 0.498415 | 0.0281103 | intron-variant | SPAG16 | GRCh38.p7 | 2:214118798 | aaagtgatctacaaa[C/T]tcagtgcaatctcta | 79582 |
rs10191167 | snp | A/G | 0.481396 | 0.0946345 | intron-variant | SPAG16 | GRCh38.p7 | 2:213891776 | AGGAGATGGTAAGAT[A/G]ATAGGACTTCCACAT | 79582 |
rs10191191 | snp | A/G | 0.213635 | 0.247341 | intron-variant | SPAG16 | GRCh38.p7 | 2:213377709 | TTTGCTAACTGGCAA[A/G]GTTGAAGGTGCAAGG | 79582 |
rs10191219 | snp | C/T | 0.49306 | 0.0584955 | intron-variant | SPAG16 | GRCh38.p7 | 2:213967240 | TAAATTGTATTCTGT[C/T]GGACAAAATCTTCCA | 79582 |
rs10191229 | snp | A/G | 0.324855 | 0.23853 | intron-variant | SPAG16 | GRCh38.p7 | 2:214332907 | ctggaatggggatag[A/G]agttccttaattacc | 79582 |
rs10191499 | snp | A/G | | | intron-variant | SPAG16 | GRCh38.p7 | 2:213460091 | TCTTCCTGTTTCTTC[A/G]TGGTCTTCTGCCACT | 79582 |
rs10191502 | snp | A/G | 0.225301 | 0.248777 | intron-variant | SPAG16 | GRCh38.p7 | 2:213402147 | TTTTGCCCAAGTTTC[A/G]TCATAATAGGTATAA | 79582 |
rs10191619 | snp | C/T | 0.240476 | 0.25351 | intron-variant | SPAG16 | GRCh38.p7 | 2:214289376 | cagttccaggtctaa[C/T]gtttaagtttttcat | 79582 |
rs10191874 | snp | A/G | 0.466824 | 0.124448 | intron-variant | SPAG16 | GRCh38.p7 | 2:214393663 | CTATATCTCTTTTGC[A/G]TTTGATTGGAACAAA | 79582 |
rs10191898 | snp | A/G | 0.226779 | 0.248919 | intron-variant | SPAG16 | GRCh38.p7 | 2:213402474 | gtacatgtgcacaac[A/G]tgcaggtttgttaca | 79582 |
rs10192030 | snp | C/T | 0.493477 | 0.0567349 | intron-variant | SPAG16 | GRCh38.p7 | 2:213962042 | agggtttttaaatta[C/T]taATtgttatggact | 79582 |
rs10192180 | snp | A/C | 0.480539 | 0.0967035 | intron-variant | SPAG16 | GRCh38.p7 | 2:213548559 | TCTATATGATAGGTG[A/C]GTAATCAAATACTCA | 79582 |
rs10193529 | snp | G/T | 0.23031 | 0.249223 | intron-variant | SPAG16, LOC101928084 | GRCh38.p7 | 2:214098168 | TATTCATGCAATATA[G/T]GTACAATACAATAAA | 79582 |
rs10194352 | snp | C/T | 0 | 0 | intron-variant | SPAG16 | GRCh38.p7 | 2:213825705 | tttctttctttcttt[C/T]tttttTttttttttt | 79582 |
rs10194640 | snp | A/T | 0.19646 | 0.2442 | intron-variant, upstream-variant-2KB | SPAG16 | GRCh38.p7 | 2:213298935 | GGATTCATTTTATCA[A/T]AAGCATATTAGTTAT | 79582 |
rs10194844 | snp | A/G | 0.021333 | 0.101051 | intron-variant | SPAG16 | GRCh38.p7 | 2:214357302 | gaataatttctctcc[A/G]tatcctatgatctcc | 79582 |
rs10195307 | snp | A/G | 0.487809 | 0.0771174 | intron-variant | SPAG16 | GRCh38.p7 | 2:214033809 | tccaaatataccagg[A/G]tataatatctaaaaa | 79582 |
rs10195431 | snp | C/T | | | intron-variant | SPAG16 | GRCh38.p7 | 2:213725711 | aggggatggagttaa[C/T]ggagttgacttgagt | 79582 |
rs10195465 | snp | A/G | 0.470424 | 0.117954 | intron-variant | SPAG16 | GRCh38.p7 | 2:213925904 | CCTCCTTTTTTTCTT[A/G]TAATTCTTATTATTG | 79582 |
rs10195668 | snp | A/T | 0.48491 | 0.0855403 | intron-variant | SPAG16 | GRCh38.p7 | 2:213901626 | AGAAAACATGTAAAC[A/T]TGTACAGGAATGTAT | 79582 |
rs10196922 | snp | C/T | 0.212728 | 0.247206 | intron-variant | SPAG16 | GRCh38.p7 | 2:213409005 | gacatgaaggaagtt[C/T]gctttgaaaaagaat | 79582 |
rs10197091 | snp | C/G | 0.212728 | 0.247206 | intron-variant | SPAG16 | GRCh38.p7 | 2:213409006 | acatgaaggaagttc[C/G]ctttgaaaaagaatg | 79582 |
rs10197120 | snp | C/G | 0.212425 | 0.24716 | intron-variant | SPAG16 | GRCh38.p7 | 2:213409182 | gtcgaaaaaatatct[C/G]tgaaagttgtgggaa | 79582 |
rs10197261 | snp | C/G | 0.413748 | 0.188909 | intron-variant | SPAG16 | GRCh38.p7 | 2:213649988 | GACTTTAAGTGTCAT[C/G]ATTCCATACCAATCC | 79582 |
rs10197286 | snp | C/T | 0.434109 | 0.169127 | intron-variant | SPAG16 | GRCh38.p7 | 2:213650034 | AGAAAAAGAAGTTCT[C/T]GAATTTTATTTGTTC | 79582 |
rs10197682 | snp | C/T | 0.0422008 | 0.138995 | intron-variant | SPAG16 | GRCh38.p7 | 2:213710567 | GGTGTGTTAGTGTGG[C/T]GACTCTGAAAAATTA | 79582 |
rs10197830 | snp | C/G | 0.181659 | 0.240478 | intron-variant | SPAG16 | GRCh38.p7 | 2:213916501 | taacagtaccatgct[C/G]tttgggttactgtag | 79582 |
rs10197909 | snp | A/G | 0.479824 | 0.098392 | intron-variant | SPAG16 | GRCh38.p7 | 2:213893779 | gcaacaaattaaacc[A/G]tactagcagagaaaa | 79582 |
rs10197953 | snp | C/T | 0.484841 | 0.0857308 | intron-variant | SPAG16 | GRCh38.p7 | 2:213916603 | atcttgtgagacatt[C/T]actatcttgagaaca | 79582 |
rs10197985 | snp | A/G | 0.47934 | 0.0995154 | intron-variant | SPAG16 | GRCh38.p7 | 2:214365015 | ATGTGTAAATGAGAA[A/G]TAAAAAAAGAGAATG | 79582 |
rs10198101 | snp | G/T | 0.327914 | 0.237549 | intron-variant | SPAG16 | GRCh38.p7 | 2:213404046 | aaaaccactgctcaa[G/T]gaaataaaagaggat | 79582 |
rs10198311 | snp | C/G | 0.213333 | 0.247296 | intron-variant | SPAG16 | GRCh38.p7 | 2:213404250 | agcccgcattgccaa[C/G]tcaatcctaagccaa | 79582 |
rs10198318 | snp | A/G | 0.484841 | 0.0857308 | intron-variant | SPAG16 | GRCh38.p7 | 2:213916856 | tggcatttttgtcac[A/G]aaatctgtgctaaat | 79582 |
rs10198591 | snp | A/C | 0.484771 | 0.0859212 | intron-variant | SPAG16 | GRCh38.p7 | 2:213911270 | CCCACCTTGGCCTCC[A/C]AGTAGCTATGACTAC | 79582 |
rs10198811 | snp | C/T | 0.479904 | 0.0982045 | intron-variant | SPAG16 | GRCh38.p7 | 2:213872278 | acaccttgacttcaa[C/T]ccaatgaaacttatt | 79582 |
rs10198863 | snp | C/G | 0.327914 | 0.237549 | intron-variant | SPAG16 | GRCh38.p7 | 2:213404778 | AATCTTTTTACAAAT[C/G]CTTTGTATTTTTCTA | 79582 |
rs10198920 | snp | C/T | 0.232943 | 0.249417 | intron-variant | SPAG16, LOC101928084 | GRCh38.p7 | 2:214095896 | GAAACCTTGGAAAAA[C/T]GACTGTTTCTATGGG | 79582 |
rs10198923 | snp | C/T | 0.232651 | 0.249397 | intron-variant | SPAG16, LOC101928084 | GRCh38.p7 | 2:214095906 | AAAAATGACTGTTTC[C/T]ATGGGGGAAAATAAA | 79582 |
rs10199200 | snp | C/T | 0.484841 | 0.0857308 | intron-variant | SPAG16 | GRCh38.p7 | 2:213902776 | CAGTCCAAAGTCTCA[C/T]CTGAGACAAGCAAAG | 79582 |
rs10199203 | snp | C/T | 0.479904 | 0.0982045 | intron-variant | SPAG16 | GRCh38.p7 | 2:213872694 | aacgtgatcagtctt[C/T]caccgttaagtatga | 79582 |
rs10199366 | snp | A/C | 0.0399052 | 0.1355 | intron-variant | SPAG16 | GRCh38.p7 | 2:213723311 | TAGATAATCATACTA[A/C]TAATAAAGAGCTGAC | 79582 |
rs10199501 | snp | A/G | 0.485187 | 0.0847778 | intron-variant | SPAG16 | GRCh38.p7 | 2:213927648 | GACTAAATATCAGTT[A/G]CAGCACTCACAAAGA | 79582 |
rs10199633 | snp | A/G | 0.479824 | 0.098392 | intron-variant | SPAG16 | GRCh38.p7 | 2:213869165 | GGCTGAGACAGGAGA[A/G]TCACTTGAACCCGGG | 79582 |
rs10199839 | snp | A/T | | | intron-variant | SPAG16 | GRCh38.p7 | 2:214012288 | tatatatatatatat[A/T]ttttttttttttttt | 79582 |
rs10200050 | snp | C/T | 0.471388 | 0.116136 | intron-variant | SPAG16 | GRCh38.p7 | 2:213781689 | TAGGGAAGGACTGTG[C/T]ACTGGGTAAATTTTC | 79582 |
rs10200258 | snp | C/G | 0.02016 | 0.0983543 | intron-variant | SPAG16 | GRCh38.p7 | 2:214040125 | tgatgttatctgcag[C/G]agtaataggggaagt | 79582 |
rs10200422 | snp | C/T | 0.478104 | 0.102316 | intron-variant | SPAG16 | GRCh38.p7 | 2:214276355 | atgtaagctggttat[C/T]ttgcccattaattga | 79582 |
rs10200893 | snp | C/T | 0.467946 | 0.122472 | intron-variant | SPAG16 | GRCh38.p7 | 2:214276778 | tgtgtcttggggttg[C/T]tcttcttgaggagta | 79582 |
rs10201293 | snp | G/T | 0.472803 | 0.113397 | intron-variant | SPAG16 | GRCh38.p7 | 2:213857408 | atgctcattgaccat[G/T]ttgaaaatcctagga | 79582 |
rs10201885 | snp | A/G | 0.191775 | 0.243125 | intron-variant | SPAG16 | GRCh38.p7 | 2:214271650 | ACTAAAAATACAAAA[A/G]TTAGCTGGGCATGGC | 79582 |
rs10201961 | snp | C/T | 0.0535932 | 0.154675 | intron-variant | SPAG16 | GRCh38.p7 | 2:213903271 | tctgcactgccctag[C/T]agaggttttccatgg | 79582 |
rs10202506 | snp | C/T | 0.171057 | 0.237209 | intron-variant | SPAG16 | GRCh38.p7 | 2:214037019 | attaaaTTTCACTTT[C/T]AACTAAATTATTTCC | 79582 |
rs10203065 | snp | G/T | 0 | 0 | intron-variant | SPAG16 | GRCh38.p7 | 2:213687151 | ttcaagtaatattaa[G/T]ttatgtacctcttca | 79582 |
rs10203460 | snp | C/T | 0.494484 | 0.0522255 | intron-variant | SPAG16 | GRCh38.p7 | 2:213976137 | atatatatatatata[C/T]acacacacacacaca | 79582 |
rs10203517 | snp | C/T | 0.232359 | 0.249377 | intron-variant | SPAG16, LOC101928084 | GRCh38.p7 | 2:214092199 | AAAAACATACTCAGA[C/T]ATAAATTTACACATG | 79582 |
rs10203574 | snp | C/G | 0.444799 | 0.156695 | intron-variant | SPAG16 | GRCh38.p7 | 2:214306995 | tctggtagaattcag[C/G]tgtgaatccgtctag | 79582 |
rs10203639 | snp | C/T | | | intron-variant | SPAG16 | GRCh38.p7 | 2:214298113 | gcatatatatatata[C/T]acacacacacacaca | 79582 |
rs10203765 | snp | C/T | 0.438386 | 0.164349 | intron-variant | SPAG16 | GRCh38.p7 | 2:213976421 | CCTTAACTAACAGGT[C/T]TCCTCTCACACACAA | 79582 |
rs10203782 | snp | C/G | 0.434253 | 0.168969 | intron-variant | SPAG16 | GRCh38.p7 | 2:213627591 | TTATTTTAGTTGTCT[C/G]TCTCCTTTACCACAC | 79582 |
rs10203794 | snp | C/T | 0.326741 | 0.23793 | intron-variant | SPAG16 | GRCh38.p7 | 2:213307054 | ttccaaATTATTCTT[C/T]TTGAACTTTACAAAA | 79582 |
rs10203801 | snp | A/G | 0.0524604 | 0.153226 | intron-variant | SPAG16 | GRCh38.p7 | 2:213627643 | GTCAATATATTTCTT[A/G]TGTCTAAAAAGAAAA | 79582 |
rs10203848 | snp | A/G | 0 | 0 | intron-variant | SPAG16 | GRCh38.p7 | 2:213564198 | GGAGCCAAAGGCAGT[A/G]TGTGTGCCCACTCTA | 79582 |
rs10203945 | snp | A/C | 0 | 0 | intron-variant | SPAG16 | GRCh38.p7 | 2:213411410 | acagcgatttattaa[A/C]tacactaaagatgct | 79582 |
rs10204125 | snp | C/T | 0.47743 | 0.103805 | intron-variant | SPAG16 | GRCh38.p7 | 2:213827948 | gatcttctctttatc[C/T]ttgatctttggaagt | 79582 |
rs10204270 | snp | C/T | 0.213937 | 0.247385 | intron-variant | SPAG16 | GRCh38.p7 | 2:213402600 | ccccacaacagtccc[C/T]ggagtgtgatgttct | 79582 |
rs10204463 | snp | A/G | 0.00199481 | 0.0315187 | intron-variant | SPAG16 | GRCh38.p7 | 2:214342831 | TAAACATATTTATAC[A/G]TTCATAACATAGTCA | 79582 |
rs10204594 | snp | A/G | 0.498964 | 0.02274 | intron-variant | SPAG16 | GRCh38.p7 | 2:214001248 | AATTTATTTCCTTTT[A/G]TGTTTAAAGTTTTTT | 79582 |
rs10204670 | snp | A/G | 0.480064 | 0.0978296 | intron-variant | SPAG16 | GRCh38.p7 | 2:213835767 | ATTTGGAGTTTATAG[A/G]ATAACAACCCATAAC | 79582 |
rs10204925 | snp | C/T | 0.466824 | 0.124448 | intron-variant | SPAG16 | GRCh38.p7 | 2:213932376 | ACGTGCCACCACACC[C/T]GGCTAATTTTTGTAT | 79582 |
rs10204975 | snp | A/G | 0.470327 | 0.118136 | intron-variant | SPAG16 | GRCh38.p7 | 2:213971534 | TTAACCATTTTAAAC[A/G]TAGAGTTTTCAGTGG | 79582 |
rs10205070 | snp | G/T | 0.492966 | 0.0588865 | intron-variant | SPAG16 | GRCh38.p7 | 2:213971621 | TTATCACCCCAAACA[G/T]AAACTATGTTCCTTA | 79582 |
rs10205401 | snp | A/G | 0.217851 | 0.247924 | intron-variant | SPAG16 | GRCh38.p7 | 2:214272815 | tatacccagtaatgg[A/G]atggctgggtcaaat | 79582 |
rs10205601 | snp | A/G | 0.0513262 | 0.151752 | intron-variant | SPAG16 | GRCh38.p7 | 2:213582636 | AAGGGCACTCTGTGC[A/G]TAGGATGGCATGTTG | 79582 |
rs10206021 | snp | A/G | 0 | 0 | intron-variant | SPAG16 | GRCh38.p7 | 2:214355526 | agtcaggaaacaaca[A/G]gtgctggagaggatg | 79582 |
rs10206040 | snp | A/G | 0.484841 | 0.0857308 | intron-variant | SPAG16 | GRCh38.p7 | 2:213901057 | GGCTTGATAGCATGT[A/G]TGTTTTTTAAAGAAA | 79582 |
rs10206126 | snp | A/G | 0.391024 | 0.206427 | intron-variant | SPAG16 | GRCh38.p7 | 2:214378220 | gtcttttaagctact[A/G]aatttgtagcaatgt | 79582 |
rs10206470 | snp | A/G | 0.00676609 | 0.0577691 | intron-variant | SPAG16 | GRCh38.p7 | 2:213635464 | tcaaattatagattt[A/G]cttttagttttttca | 79582 |
rs10206525 | snp | A/G | 0.116838 | 0.211584 | intron-variant | SPAG16 | GRCh38.p7 | 2:213901500 | TGTTATTGTAGTGAA[A/G]AGGAATAATACCACT | 79582 |
rs10206530 | snp | C/T | 0.385168 | 0.210309 | intron-variant | SPAG16 | GRCh38.p7 | 2:214038665 | tcatttaacattagg[C/T]atatctccaaatgct | 79582 |
rs10206641 | snp | A/G | 0.484841 | 0.0857308 | intron-variant | SPAG16 | GRCh38.p7 | 2:213901622 | CCAAAGAAAACATGT[A/G]AACTTGTACAGGAAT | 79582 |
rs10206666 | snp | C/T | 0.193028 | 0.243422 | intron-variant | SPAG16 | GRCh38.p7 | 2:213327488 | ACGAGCACAAATAGG[C/T]TTCTAATGTATATTT | 79582 |
rs10206711 | snp | A/T | 0.212425 | 0.24716 | intron-variant | SPAG16 | GRCh38.p7 | 2:213408692 | aaaaagacacaatgg[A/T]tattcagtaattgat | 79582 |
rs10207007 | snp | C/T | 0.401037 | 0.199218 | intron-variant | SPAG16 | GRCh38.p7 | 2:214308283 | agcctatttgggtca[C/T]tgcatgtgagacgga | 79582 |
rs10207182 | snp | A/G | 0.493107 | 0.0583 | intron-variant | SPAG16 | GRCh38.p7 | 2:213713052 | GAGAGAATGAGTGCC[A/G]AGCGCAGTGGGGGAA | 79582 |
rs10207263 | snp | A/G | 0.492337 | 0.0614248 | intron-variant | SPAG16 | GRCh38.p7 | 2:214278273 | CCCCTGGCACTTCCC[A/G]GGTGAGGTGATGCCC | 79582 |
rs10207438 | snp | C/T | 0.232359 | 0.249377 | intron-variant | SPAG16, LOC101928084 | GRCh38.p7 | 2:214093837 | ATATAAATGGCATGC[C/T]CTGGGGTCACTCTCT | 79582 |
rs10207439 | snp | A/T | 0.232359 | 0.249377 | intron-variant | SPAG16, LOC101928084 | GRCh38.p7 | 2:214093839 | ATAAATGGCATGCTC[A/T]GGGGTCACTCTCTAT | 79582 |
rs10207486 | snp | A/G | 0.485392 | 0.0842056 | intron-variant | SPAG16 | GRCh38.p7 | 2:214278526 | GAACTGTATCATACA[A/G]TGGTATATTTGAGCT | 79582 |
rs10207496 | snp | C/T | 0.212122 | 0.247114 | intron-variant | SPAG16 | GRCh38.p7 | 2:213308432 | AGATTTTGGATTTTT[C/T]TTCAGATGTTGGAAT | 79582 |
rs10207706 | snp | G/T | 0.408871 | 0.193029 | intron-variant | SPAG16 | GRCh38.p7 | 2:213971879 | ttttcttgttttttg[G/T]tttttttttttagta | 79582 |
rs10207714 | snp | G/T | 0.49306 | 0.0584955 | intron-variant | SPAG16 | GRCh38.p7 | 2:213971930 | aagtgatatctaatt[G/T]tgTGTgtgtgtgtgt | 79582 |
rs10208956 | snp | C/G | 0.475348 | 0.108251 | intron-variant | SPAG16 | GRCh38.p7 | 2:213789588 | CTTAAAAAGACAAAC[C/G]ATTCCAGCACAACAT | 79582 |
rs10209386 | snp | A/G | 0.0209421 | 0.100162 | intron-variant | SPAG16 | GRCh38.p7 | 2:214349097 | TTCAATATTATCATG[A/G]CTATTATTGATCCTT | 79582 |
rs10209608 | snp | A/C | 0.479904 | 0.0982045 | intron-variant | SPAG16 | GRCh38.p7 | 2:213872242 | ctcccctagagagac[A/C]agagagaaccagctc | 79582 |
rs10209846 | snp | A/T | 0.476487 | 0.105846 | intron-variant | SPAG16 | GRCh38.p7 | 2:213825908 | tctttgctgggagag[A/T]ttttattatggcttt | 79582 |
rs10210123 | snp | A/G | 0.173965 | 0.238157 | intron-variant | SPAG16 | GRCh38.p7 | 2:213358629 | tttaaggtcttctct[A/G]tactgtttattatag | 79582 |
rs10210603 | snp | A/C | 0.326035 | 0.238157 | intron-variant | SPAG16 | GRCh38.p7 | 2:213318374 | gtggaactcgaggcc[A/C]tcacccttagtgaaa | 79582 |
rs10210714 | snp | A/G | 0.230603 | 0.249246 | intron-variant | SPAG16, LOC101928084 | GRCh38.p7 | 2:214096783 | CATCTTAATTACACA[A/G]GGATTCAGCAAACAT | 79582 |
rs10210945 | snp | C/T | 0.485324 | 0.0843964 | intron-variant | SPAG16 | GRCh38.p7 | 2:214273881 | aatctgtaagttacc[C/T]tgtgcagtatggcca | 79582 |
rs10210989 | snp | A/G | 0.48955 | 0.071525 | intron-variant | SPAG16 | GRCh38.p7 | 2:214003046 | CATTTGACAACTTCC[A/G]TAGTGTAAATACCCT | 79582 |
rs10211622 | snp | C/T | 0.00874735 | 0.0655527 | intron-variant | SPAG16 | GRCh38.p7 | 2:213575021 | ATTTGTCCTGAAATC[C/T]TTCTGCATTGCACCT | 79582 |
rs10221802 | snp | A/C | 0.211819 | 0.247067 | intron-variant | SPAG16 | GRCh38.p7 | 2:213307563 | tggctgcatagtatt[A/C]catggtgtatatgtg | 79582 |
rs10427259 | snp | G/T | 0.386123 | 0.209692 | intron-variant | SPAG16 | GRCh38.p7 | 2:214236685 | AATTTTGAATTCACT[G/T]CCTATATCTAATTTC | 79582 |
rs10427272 | snp | A/C | 0.492533 | 0.0606443 | intron-variant | SPAG16 | GRCh38.p7 | 2:214237119 | TTCAGGGACAGCAAT[A/C]ACATAGCAAAAGGAA | 79582 |
rs10432528 | snp | C/G | 0.48818 | 0.0759629 | intron-variant | SPAG16 | GRCh38.p7 | 2:213764692 | CTACTGAGAGAACAT[C/G]ATATTATTCCCCAAA | 79582 |
rs10439273 | snp | A/G | 0.241914 | 0.249869 | intron-variant | SPAG16 | GRCh38.p7 | 2:214283391 | TGCCAGCCCCATATT[A/G]GCACTGTATAACACT | 79582 |
rs10439348 | snp | A/G | 0.472896 | 0.113214 | intron-variant | SPAG16 | GRCh38.p7 | 2:214283249 | TATCATCATAATAAC[A/G]TGTGTGAACCAGTCT | 79582 |
rs10451582 | snp | C/T | 0.355096 | 0.226837 | intron-variant | SPAG16 | GRCh38.p7 | 2:213363354 | TAGGCATTTCATGAG[C/T]ACTCATCTATAGGtt | 79582 |
rs10451583 | snp | A/C | 0.398354 | 0.201224 | intron-variant | SPAG16 | GRCh38.p7 | 2:214382298 | GAAGCATAATTCATC[A/C]CTGCATAATGGCTTT | 79582 |
rs10451584 | snp | C/T | 0.00398564 | 0.0444627 | intron-variant | SPAG16 | GRCh38.p7 | 2:214383969 | CCATCAGCCTGTTAT[C/T]ACTGACATATTACTT | 79582 |
rs10460331 | snp | C/T | 0.0154538 | 0.0865337 | intron-variant | SPAG16 | GRCh38.p7 | 2:214178501 | CAAAGCTAGAACTTG[C/T]TAACAAGAAATAAAA | 79582 |
rs10460332 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | SPAG16 | GRCh38.p7 | 2:214178579 | AGATGATCTTTAAGT[C/T]TATATTGCTTTTGAA | 79582 |
rs10460333 | snp | C/G | | | intron-variant | SPAG16 | GRCh38.p7 | 2:214178734 | ATTAAAGTAATATTT[C/G]TAATTTCTATTACCC | 79582 |
rs10460417 | snp | G/T | 0.48498 | 0.0853497 | intron-variant | SPAG16 | GRCh38.p7 | 2:213654907 | TGTTTAAACGGTGAA[G/T]GATACTTTGAAAGGA | 79582 |
rs10460418 | snp | G/T | 0.368324 | 0.220226 | intron-variant | SPAG16 | GRCh38.p7 | 2:214176624 | TGATTCCAAAGAATG[G/T]ATAGTTGTATATTAT | 79582 |
rs10460419 | snp | C/T | 0.362941 | 0.223034 | intron-variant | SPAG16 | GRCh38.p7 | 2:214176924 | TTATTAACGTATCTC[C/T]GGAGCCAGAATTTTA | 79582 |
rs10469665 | snp | A/C | 0.451856 | 0.147493 | intron-variant | SPAG16 | GRCh38.p7 | 2:213985798 | GAGAAAAATAGAAAG[A/C]CAGACAAGGAAATAG | 79582 |
rs10469772 | snp | C/T | 0.248755 | 0.249997 | intron-variant | SPAG16 | GRCh38.p7 | 2:213720715 | TATATTCACATCATG[C/T]AGCCAAGTGCCTGGC | 79582 |
rs10469773 | snp | C/T | 0.130351 | 0.219509 | intron-variant | SPAG16 | GRCh38.p7 | 2:213727963 | aagcgattcttcttc[C/T]tcagcctcctgagta | 79582 |
rs10469774 | snp | A/G | 0.213937 | 0.247385 | intron-variant | SPAG16 | GRCh38.p7 | 2:214231663 | AGAAGAAAAGAGGTG[A/G]TAGGATAAGGAAAGA | 79582 |
rs10490486 | snp | A/G | 0.209388 | 0.246679 | intron-variant | SPAG16 | GRCh38.p7 | 2:214054387 | AATTAAAATCTCAGA[A/G]AGCGTTCATAATTCA | 79582 |
rs10490487 | snp | A/G | 0.161924 | 0.233971 | intron-variant | SPAG16 | GRCh38.p7 | 2:214056172 | AATAACTGAAATAAC[A/G]TGACAGTAAAGTCCA | 79582 |
rs10490488 | snp | G/T | 0.226484 | 0.248892 | intron-variant | SPAG16 | GRCh38.p7 | 2:214084278 | TTACAAAATAATTTC[G/T]CTGCCTAAGGGCATG | 79582 |
rs10490489 | snp | A/G | 0.270351 | 0.24917 | intron-variant | SPAG16, LOC101928084 | GRCh38.p7 | 2:214085932 | ATTTGTGTTTCTTTA[A/G]TACCTTGAACACCAT | 79582 |
rs10490490 | snp | A/C | 0.224412 | 0.248687 | intron-variant | SPAG16, LOC101928084 | GRCh38.p7 | 2:214086108 | GACTTAAAAATTTAT[A/C]TGATGCAGCCATCAC | 79582 |
rs10490491 | snp | G/T | 0.165853 | 0.235413 | intron-variant | SPAG16, LOC101928084 | GRCh38.p7 | 2:214087527 | ATTTTTCTAAAAGAT[G/T]TCACATGATAATAAA | 79582 |
rs10490492 | snp | C/T | 0.223819 | 0.248625 | intron-variant | SPAG16, LOC101928084 | GRCh38.p7 | 2:214089514 | AATACATGCTTCGGA[C/T]CTTTCTCTACAGTGT | 79582 |
rs10490493 | snp | A/G | 0.22263 | 0.248497 | intron-variant | SPAG16, LOC101928084 | GRCh38.p7 | 2:214090464 | GTATGTCATTAATAC[A/G]TCTCAATCACAGTGT | 79582 |
rs10490494 | snp | G/T | 0.230896 | 0.249269 | intron-variant | SPAG16, LOC101928084 | GRCh38.p7 | 2:214090575 | TGGGCTATTGTGACA[G/T]GGATTTAGCACCAGC | 79582 |
rs10490495 | snp | G/T | 0.226484 | 0.248892 | intron-variant | SPAG16, LOC101928084 | GRCh38.p7 | 2:214102297 | TACAATAAATAAGGA[G/T]AAAAATTCATGAAGT | 79582 |
rs10490496 | snp | G/T | 0.227664 | 0.249 | intron-variant | SPAG16, LOC101928084 | GRCh38.p7 | 2:214102392 | CATCTGTGAATATAA[G/T]TGAACCCTGAAATAT | 79582 |
rs10490497 | snp | A/G | 0.254944 | 0.249951 | intron-variant | SPAG16 | GRCh38.p7 | 2:214183631 | TACATGGCAAACCAT[A/G]ATGAAAGGGAAGCAG | 79582 |
rs10490498 | snp | A/G | 0.347032 | 0.230401 | intron-variant | SPAG16 | GRCh38.p7 | 2:214185320 | TACCACATAATATGC[A/G]CCTGATAATTTATGG | 79582 |
rs10490499 | snp | C/T | 0.345704 | 0.230956 | intron-variant | SPAG16 | GRCh38.p7 | 2:214185461 | AATAGATATACCTGT[C/T]TTAAATGTCCCTGAA | 79582 |
rs10490500 | snp | A/T | 0.347914 | 0.230028 | intron-variant | SPAG16 | GRCh38.p7 | 2:214191771 | TGCTGTGAACCAATC[A/T]TAAAAAAGAGTTCAC | 79582 |
rs10490501 | snp | C/T | 0.128632 | 0.218563 | intron-variant | SPAG16 | GRCh38.p7 | 2:214215766 | CTGCCAGTTGCAATA[C/T]ACTCCTCTGTCAACC | 79582 |
rs10490502 | snp | A/C | 0.236434 | 0.249632 | intron-variant | SPAG16 | GRCh38.p7 | 2:214244834 | ACGTATATTTTTATT[A/C]TTTGTACACTCAACA | 79582 |
rs10490503 | snp | A/G | 0.468349 | 0.121752 | intron-variant | SPAG16 | GRCh38.p7 | 2:214281041 | TCCCTCAGGGCGCCA[A/G]AAACTTTATTGCCAG | 79582 |
rs10490504 | snp | C/G | 0.340559 | 0.233022 | intron-variant | SPAG16 | GRCh38.p7 | 2:214328621 | AATGGATTTAAATCT[C/G]GTATCTCAAATTCTA | 79582 |
rs10498003 | snp | C/T | 0.330805 | 0.236581 | intron-variant | SPAG16 | GRCh38.p7 | 2:213310043 | CAGAATAAATAAATG[C/T]ACGTTTAAATTTCAG | 79582 |
rs10498004 | snp | C/T | 0.212122 | 0.247114 | intron-variant | SPAG16 | GRCh38.p7 | 2:213310546 | TATTGAGAGTATTTC[C/T]TGTATTTAGACATTA | 79582 |
rs10498005 | snp | C/G | 0.193966 | 0.243639 | intron-variant | SPAG16 | GRCh38.p7 | 2:213413994 | GGTGTCACTAATCTT[C/G]ATGTTTAACTTTGTA | 79582 |
rs10498006 | snp | A/G | 0.353154 | 0.227726 | intron-variant | SPAG16 | GRCh38.p7 | 2:213480359 | CCCTTAGCCAATAAT[A/G]CAAATAAGTTAGCCT | 79582 |
rs10498007 | snp | A/G | 0.18989 | 0.242666 | intron-variant | SPAG16 | GRCh38.p7 | 2:213480418 | GAGGAATGGAAGCAG[A/G]TTAAAGCAGGGAAGA | 79582 |
rs10498008 | snp | A/G | 0.18989 | 0.242666 | intron-variant | SPAG16 | GRCh38.p7 | 2:213480791 | TCATAGTGTTAAACA[A/G]AAGTTATAATTTACT | 79582 |
rs10498009 | snp | A/G | 0.142272 | 0.225598 | intron-variant | SPAG16 | GRCh38.p7 | 2:214342920 | ACATTCAATGCTATG[A/G]CTTCAAACAGTACAC | 79582 |
rs10498010 | snp | A/G | 0.100944 | 0.200705 | intron-variant | SPAG16 | GRCh38.p7 | 2:214341845 | CTTCATTGCCATCCT[A/G]GAATGAGTCAGTTGT | 79582 |
rs10498011 | snp | A/G | 0.208779 | 0.246578 | intron-variant | SPAG16 | GRCh38.p7 | 2:214336583 | TTCAAAAATGCCTTA[A/G]GTTGTAATACTGGCT | 79582 |
rs10498012 | snp | A/G | 0.119281 | 0.213102 | intron-variant | SPAG16 | GRCh38.p7 | 2:213996509 | TTATTTTAAGGCACT[A/G]TGATTCAATGGCCAA | 79582 |
rs10498013 | snp | A/G | 0.189576 | 0.242588 | intron-variant | SPAG16 | GRCh38.p7 | 2:213939487 | TTTTTAATTCTTTCC[A/G]TTAATAGAGAACTAG | 79582 |
rs10498014 | snp | C/T | 0.275197 | 0.248727 | intron-variant | SPAG16 | GRCh38.p7 | 2:213900422 | TCTTACAACCTTGCA[C/T]TTAGTTTTTGAACTT | 79582 |
rs10498015 | snp | G/T | 0.476052 | 0.106772 | intron-variant | SPAG16 | GRCh38.p7 | 2:213852855 | TTCCAGCAAATATGT[G/T]TTTATAGCCTATGAT | 79582 |
rs10498016 | snp | G/T | 0.0166325 | 0.0896639 | intron-variant | SPAG16 | GRCh38.p7 | 2:213794214 | ATTTTTATTTCAAAT[G/T]CAGCGAGTCTTTTTA | 79582 |
rs10514628 | snp | C/G | 0.301177 | 0.244706 | intron-variant, nc-transcript-variant | SPAG16, LOC101928084 | GRCh38.p7 | 2:214102249 | GGAGTGGATGAGTTT[C/G]TCTTGTGGAGCGTAA | 79582 |
rs10514629 | snp | C/T | 0.219049 | 0.248077 | intron-variant, upstream-variant-2KB | SPAG16, LOC101928084 | GRCh38.p7 | 2:214103488 | TGGTTGTAAGAGAGA[C/T]GTCAGGAAATTAGAT | 79582 |
rs10525863 | in-del | -/GTT | 0 | 0 | intron-variant | SPAG16 | GRCh38.p7 | 2:213705801 | GTTGTTGTTGTTGTT[-/GTT]AAGTATAAGAAGCAT | 79582 |
rs10534467 | in-del | -/TG | 0.5 | 0 | intron-variant | SPAG16 | GRCh38.p7 | 2:213325621 | GATTTTGGAAAAATA[-/TG]TGTGTGTGTGTGTGT | 79582 |
rs10538676 | in-del | -/AC | | | intron-variant | SPAG16 | GRCh38.p7 | 2:213648596 | TGTAGGCACACACAG[-/AC]ACACACACACACACA | 79582 |
rs10539063 | in-del | -/TTA | | | intron-variant | SPAG16 | GRCh38.p7 | 2:213806041 | TGGATAAAATTATTA[-/TTA]GGTTTTATGTATAAC | 79582 |
rs10547272 | in-del | -/T | | | intron-variant | SPAG16 | GRCh38.p7 | 2:213845200 | ATATATCTAGTGTTC[-/T]TTTTTTTTTTTTTTT | 79582 |
rs10548226 | in-del | -/TAAGAG | 0.49823 | 0.0296997 | intron-variant | SPAG16 | GRCh38.p7 | 2:213982733 | AAACACTTGACAACA[-/TAAGAG]TAAAAGATAACTGAA | 79582 |
rs10562719 | in-del | -/AAG | 0.475437 | 0.108066 | intron-variant | SPAG16 | GRCh38.p7 | 2:213653109 | GGCATCACTGGGTCA[-/AAG]AAGTCTTTTTTTACA | 79582 |
rs10564214 | in-del | -/ATAT | 0.00159617 | 0.0282053 | intron-variant | SPAG16 | GRCh38.p7 | 2:214323322 | TACTTGTGAGATTAA[-/ATAT]ATATATATATTTATT | 79582 |
rs10565923 | in-del | -/AATTT | | | intron-variant | SPAG16 | GRCh38.p7 | 2:213600137 | TATATTTTTTAATTT[-/AATTT]GGCTTTATATAAAAT | 79582 |
rs10569735 | in-del | -/CA | 0 | 0 | intron-variant | SPAG16 | GRCh38.p7 | 2:213648607 | ACACACACACACACA[-/CA]TTTACTAAGGCATGC | 79582 |
rs10582370 | in-del | -/TT | 0 | 0 | intron-variant | SPAG16 | GRCh38.p7 | 2:213626665 | TTTTTTTTTTTTTTT[-/TT]GAAGATGGAGTCTCT | 79582 |
rs10585217 | in-del | -/CA | | | intron-variant | SPAG16 | GRCh38.p7 | 2:213361828 | ACACACACACACACA[-/CA]GAGGCTGTGAATAAA | 79582 |
rs10592601 | in-del | -/T/TA | 0 | 0 | intron-variant | SPAG16 | GRCh38.p7 | 2:213664842 | atatatatacatata[-/T/TA]cacacacatattcat | 79582 |
rs10609015 | in-del | -/GT | | | intron-variant | SPAG16, LOC101928084 | GRCh38.p7 | 2:214093535 | ATGTGTATGTTGTGT[-/GT]CCATGTATGTGTATG | 79582 |
rs10611901 | in-del | -/GTTT | | | intron-variant | SPAG16 | GRCh38.p7 | 2:213654373 | ACATCTATTGTTTTT[-/GTTT]GTTTGTTTGTTTGTT | 79582 |
rs10622953 | in-del | -/ATAT/ATATAT | 0.5 | 0 | intron-variant | SPAG16 | GRCh38.p7 | 2:214177916 | TATATATATATATAC[-/ATAT/ATATAT]ATATATATATATATA | 79582 |
rs10625344 | in-del | -/CAG | 0.0836354 | 0.186609 | intron-variant | SPAG16 | GRCh38.p7 | 2:214050553 | TGTTATTAATGACAT[-/CAG]AGAACAGAATTGGGA | 79582 |
rs10627580 | in-del | -/TA | | | intron-variant | SPAG16 | GRCh38.p7 | 2:214175246 | ATATATAAAGAAATG[-/TA]TATATATATATAAAG | 79582 |
rs10627865 | in-del | -/T/TT | 0.612292 | 0.100964 | intron-variant | SPAG16 | GRCh38.p7 | 2:214019278 | TAAGGCTTTTTTTTT[-/T/TT]AAAGAAAAGAATGTT | 79582 |
rs10628838 | in-del | -/AT | 0.479824 | 0.098392 | intron-variant | SPAG16 | GRCh38.p7 | 2:213679543 | ATACATTTTAAAAAC[-/AT]GTGGAGAAACTTTTT | 79582 |
rs10631061 | in-del | -/AATAA | 0 | 0 | intron-variant | SPAG16 | GRCh38.p7 | 2:214186046 | CCAGGCATAAAATAA[-/AATAA]TGTTCAAAAAATAAA | 79582 |
rs10631489 | in-del | -/T/TT/TTT | 0.434253 | 0.168969 | intron-variant | SPAG16 | GRCh38.p7 | 2:213736706 | TATATTTTTAAATAA[-/T/TT/TTT]TTTTTTTTTTTTTTT | 79582 |
rs10638351 | in-del | -/GT/GTGT/TGTG | 0.5 | 0 | intron-variant | SPAG16 | GRCh38.p7 | 2:213982610 | AGGTATAGTTTCTGG[-/GT/GTGT/TGTG]TGTGTGTGTGTGTGT | 79582 |
rs10642139 | in-del | -/TCTC | 0.484841 | 0.0857308 | intron-variant | SPAG16 | GRCh38.p7 | 2:213836948 | CCTCCAACAGTGCCT[-/TCTC]TCTCTCTCTCTCTCT | 79582 |
rs10644766 | in-del | -/A | | | intron-variant | SPAG16 | GRCh38.p7 | 2:213911836 | AAAAAAAAAAAAAAA[-/A]TACACACACGCACAC | 79582 |
rs10647748 | in-del | -/ATAAA | 0.249603 | 0.25 | intron-variant | SPAG16 | GRCh38.p7 | 2:214186037 | AGCACTGTACCAGGC[-/ATAAA]ATAAAATAATGTTCA | 79582 |
rs10660514 | in-del | -/TT/TTT/TTTT | 0.443464 | 0.15834 | intron-variant | SPAG16 | GRCh38.p7 | 2:213737493 | TTTCTTTTTCTTTTC[-/TT/TTT/TTTT]TTTTTTTTTTTTGAG | 79582 |
rs10665960 | in-del | -/GTTA | 0.0577344 | 0.159793 | intron-variant | SPAG16 | GRCh38.p7 | 2:213925140 | TATCATTATTGTTTT[-/GTTA]TTTTTATTTTTACAA | 79582 |
rs10675840 | in-del | -/TCTCA | 0.432063 | 0.171327 | intron-variant | SPAG16 | GRCh38.p7 | 2:213968164 | TCTCTCCTCTTCTCT[-/TCTCA]TCTCATCTCTTTTCT | 79582 |
rs10693252 | in-del | -/ATAAT | 0.475259 | 0.108435 | intron-variant | SPAG16 | GRCh38.p7 | 2:213624241 | ATCAATGGTTGAAGA[-/ATAAT]TCAGGCTATTTATCA | 79582 |
rs10694178 | in-del | -/TT | 0 | 0 | intron-variant | SPAG16 | GRCh38.p7 | 2:214222111 | TTTTTTTTTTTTTTT[-/TT]GAAACAGAGTTTCGC | 79582 |
rs10700228 | in-del | -/AGAGAG | 0 | 0 | intron-variant | SPAG16 | GRCh38.p7 | 2:214250789 | GAGAGAGAGAGAGAG[-/AGAGAG]TCAAACTTTTAAGTT | 79582 |
rs10708109 | in-del | -/T | 0.499879 | 0.0077866 | intron-variant | SPAG16 | GRCh38.p7 | 2:213977983 | GGAATCTCTCTCTAC[-/T]TTTTTTTGTTGAGAG | 79582 |
rs10709319 | in-del | -/A | 0.496105 | 0.0439572 | intron-variant | SPAG16 | GRCh38.p7 | 2:214023408 | CCTAAGGCATTCATT[-/A]AAAAAAAAAGAAAAA | 79582 |
rs10710536 | in-del | -/A | | | intron-variant | SPAG16 | GRCh38.p7 | 2:213429092 | GTGAGACTCCATCTC[-/A]AAAAAAAAAAAAAAG | 79582 |
rs10755026 | snp | A/G | 0.00597247 | 0.0543191 | intron-variant | SPAG16 | GRCh38.p7 | 2:213541144 | ATTTACGGTGAAAAC[A/G]AAAGGCTGAGAATGG | 79582 |
rs10804214 | snp | A/G | 0.499732 | 0.0115784 | intron-variant | SPAG16 | GRCh38.p7 | 2:213352982 | TAGTTATTAGTGCTC[A/G]TTTTCTTCCTTCAAA | 79582 |
rs10804215 | snp | G/T | 0.520812 | 0.174506 | intron-variant | SPAG16 | GRCh38.p7 | 2:213652245 | AGAATAGTGCTTGTC[G/T]CATTATGTTCTGTAT | 79582 |
rs10804219 | snp | C/T | 0.476052 | 0.106772 | intron-variant | SPAG16 | GRCh38.p7 | 2:213749474 | ATCTTGTAAGGGTGA[C/T]GTGACAAGGGCAGAT | 79582 |
rs10804220 | snp | G/T | 0.334871 | 0.235153 | intron-variant | SPAG16 | GRCh38.p7 | 2:213842975 | AGGTCTCAGTATGTT[G/T]CCCAGGCTGGTTTTG | 79582 |
rs10804224 | snp | C/T | 0.48978 | 0.0707512 | intron-variant | SPAG16 | GRCh38.p7 | 2:214316716 | CGTAGTTTTCTTCAA[C/T]TTTTTATCTAGGATA | 79582 |
rs10804225 | snp | G/T | 0.480853 | 0.0959518 | intron-variant | SPAG16 | GRCh38.p7 | 2:214351027 | TTGCAGGCTAAGCTG[G/T]ACAAGCAGAGAAGCA | 79582 |
rs10804226 | snp | C/T | 0.406641 | 0.194842 | intron-variant | SPAG16 | GRCh38.p7 | 2:214379019 | CCTTGGCTCATCATA[C/T]CACCGTCTGGCTTAC | 79582 |
rs10932478 | snp | C/G | 0.0460142 | 0.144533 | intron-variant | SPAG16 | GRCh38.p7 | 2:213305276 | gaataggtttttttc[C/G]agtataacatcatag | 79582 |
rs10932479 | snp | A/C | 0.497359 | 0.0362457 | intron-variant | SPAG16 | GRCh38.p7 | 2:213337176 | aaacagaaaacaaca[A/C]caacatcaatgaaaa | 79582 |
rs10932480 | snp | A/T | 0.497473 | 0.0354532 | intron-variant, utr-variant-3-prime | SPAG16 | GRCh38.p7 | 2:213369551 | CAATAAAATGCATAA[A/T]TTTAAGTATACCTGT | 79582 |
rs10932481 | snp | A/G | 0.351418 | 0.228505 | intron-variant | SPAG16 | GRCh38.p7 | 2:213415326 | TTCCTTTGAAGCCAT[A/G]CTTAGGAATTTAGGT | 79582 |
rs10932483 | snp | C/T | 0.384401 | 0.210799 | intron-variant, downstream-variant-500B | SPAG16 | GRCh38.p7 | 2:213503687 | CACTATCCTTAAAAA[C/T]AAATCATTAAACAAG | 79582 |
rs10932485 | snp | A/C | 0.373397 | 0.217424 | intron-variant | SPAG16 | GRCh38.p7 | 2:213519833 | ttgaattgtgtctcc[A/C]aaaacaatatgttga | 79582 |
rs10932486 | snp | C/G | 0.36021 | 0.224397 | intron-variant | SPAG16 | GRCh38.p7 | 2:213520188 | actattggcaaccac[C/G]agaagttaggagaaa | 79582 |
rs10932487 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | SPAG16 | GRCh38.p7 | 2:213577215 | GAATTAAATTTAAAA[A/T]GAAAATATTCTGTGG | 79582 |
rs10932488 | snp | A/C | 0.363568 | 0.222716 | intron-variant | SPAG16 | GRCh38.p7 | 2:213626860 | ACCATGTTGGCCAGG[A/C]TGGTCTCGAACTCCT | 79582 |
rs10932489 | snp | A/G | 0.00398564 | 0.0444627 | intron-variant | SPAG16 | GRCh38.p7 | 2:213627087 | CAAACTATGTACCAT[A/G]CACCATCTGTGGATG | 79582 |
rs10932490 | snp | G/T | 0.41408 | 0.188621 | intron-variant | SPAG16 | GRCh38.p7 | 2:213629068 | GCAACAACTTTTTCA[G/T]AGGAAGAAACTCATA | 79582 |
rs10932491 | snp | C/T | 0.363776 | 0.222609 | intron-variant | SPAG16 | GRCh38.p7 | 2:213643120 | gaactctggctaata[C/T]aacaggtctgatatt | 79582 |
rs10932492 | snp | A/C | 0.363985 | 0.222503 | intron-variant | SPAG16 | GRCh38.p7 | 2:213683435 | ATGCTCCTTTAGTCC[A/C]AGCTTCTCAAGAGGC | 79582 |
rs10932493 | snp | G/T | 0.355311 | 0.226737 | intron-variant | SPAG16 | GRCh38.p7 | 2:213701118 | GGTGGCACCTGCCTG[G/T]ACTCCCAGCTACTCA | 79582 |
rs10932495 | snp | A/T | 0.49995 | 0.00499176 | intron-variant | SPAG16 | GRCh38.p7 | 2:213733615 | CCTCCAAGACTTTCT[A/T]GTATTTGGTTTCTAG | 79582 |
rs10932496 | snp | C/T | 0.140242 | 0.224618 | intron-variant | SPAG16 | GRCh38.p7 | 2:213733654 | CAAGCTAGTCCATCC[C/T]TAACCTCCAGTACTT | 79582 |
rs10932498 | snp | A/C | 0.475789 | 0.107327 | intron-variant | SPAG16 | GRCh38.p7 | 2:213800521 | TACACGTGCACACCA[A/C]CATGCTCGTTTGTTT | 79582 |
rs10932499 | snp | C/T | 0.474 | 0.111014 | intron-variant | SPAG16 | GRCh38.p7 | 2:213820057 | TGCTGGGATTACAGG[C/T]GTGAGCCACCGTTGT | 79582 |
rs10932500 | snp | A/C | 0.480853 | 0.0959518 | intron-variant | SPAG16 | GRCh38.p7 | 2:213831384 | GATATTTCTCCCTGC[A/C]AAAATGCTTTTCAAT | 79582 |
rs10932501 | snp | A/C | 0.47852 | 0.101384 | intron-variant | SPAG16 | GRCh38.p7 | 2:213836044 | GTGGAAATTGAGTTA[A/C]CCAGTGATAACATTA | 79582 |
rs10932502 | snp | C/T | 0.334871 | 0.235153 | intron-variant | SPAG16 | GRCh38.p7 | 2:213843323 | TCATGAAGCCAGTCA[C/T]ACAGAACCGTACAAT | 79582 |
rs10932503 | snp | A/G | 0.33303 | 0.235809 | intron-variant | SPAG16 | GRCh38.p7 | 2:213844401 | AAAAACAGTGATTTC[A/G]GTTATCTAGCAGACT | 79582 |
rs10932504 | snp | A/G | 0.473081 | 0.112848 | intron-variant | SPAG16 | GRCh38.p7 | 2:213856443 | tcttcttacagctcc[A/G]ttaggcaatgcccca | 79582 |
rs10932505 | snp | C/T | 0.472803 | 0.113397 | intron-variant | SPAG16 | GRCh38.p7 | 2:213856495 | tccaaacccacattt[C/T]ccttccacactgctc | 79582 |
rs10932506 | snp | A/C | 0.472803 | 0.113397 | intron-variant | SPAG16 | GRCh38.p7 | 2:213856617 | ggttcccaaacctca[A/C]ttcttgacttctgat | 79582 |
rs10932507 | snp | C/G | 0.472803 | 0.113397 | intron-variant | SPAG16 | GRCh38.p7 | 2:213856643 | ctgatcccccacagg[C/G]ccaacacatgtaagc | 79582 |
rs10932508 | snp | A/T | 0.479824 | 0.098392 | intron-variant | SPAG16 | GRCh38.p7 | 2:213886523 | AAAACAACCACAGCA[A/T]CAGTAGCAGCAGCAG | 79582 |
rs10932509 | snp | A/C | 0.479824 | 0.098392 | intron-variant | SPAG16 | GRCh38.p7 | 2:213892375 | agactgaaataaata[A/C]ctaatctttcaatgc | 79582 |
rs10932510 | snp | A/C | 0.479824 | 0.098392 | intron-variant | SPAG16 | GRCh38.p7 | 2:213895420 | atagaaaaagcaatc[A/C]taaaattcctatgga | 79582 |
rs10932513 | snp | A/T | 0.484841 | 0.0857308 | intron-variant | SPAG16 | GRCh38.p7 | 2:213903385 | ctccaattcttgatt[A/T]cccttcactcacagc | 79582 |
rs10932514 | snp | A/G | 0.470715 | 0.117409 | intron-variant | SPAG16 | GRCh38.p7 | 2:213904360 | AGGGGAACTTCTTAC[A/G]TAGTGGCAGCAAGAG | 79582 |
rs10932515 | snp | C/T | 0.484771 | 0.0859212 | intron-variant | SPAG16 | GRCh38.p7 | 2:213920065 | ttttttcgtctctat[C/T]tgtttaaagtctatt | 79582 |
rs10932516 | snp | A/C | 0.499035 | 0.0219437 | intron-variant | SPAG16 | GRCh38.p7 | 2:213939192 | TTACTAAAAATCACT[A/C]CTACTTAGAAACTGA | 79582 |
rs10932517 | snp | A/G | 0.401924 | 0.198543 | intron-variant | SPAG16 | GRCh38.p7 | 2:213953471 | ACATTTAGGTCTTGG[A/G]ACACAAATGTATCCC | 79582 |
rs10932519 | snp | A/T | 0.415235 | 0.18761 | intron-variant | SPAG16 | GRCh38.p7 | 2:213957135 | tgtgtttgttggatc[A/T]agttgctttattatg | 79582 |
rs10932520 | snp | A/G | 0.452597 | 0.146474 | intron-variant | SPAG16 | GRCh38.p7 | 2:213967164 | CCTTATATAGTTATT[A/G]TTATTTACATTCCAC | 79582 |
rs10932521 | snp | A/G | 0.417034 | 0.18601 | intron-variant | SPAG16 | GRCh38.p7 | 2:214004617 | ttttggcagccctaa[A/G]aaaggtgtccgcggc | 79582 |
rs10932522 | snp | A/G | 0.478437 | 0.10157 | intron-variant | SPAG16 | GRCh38.p7 | 2:214047575 | taaatataagacttc[A/G]aacaatgaaactact | 79582 |
rs10932524 | snp | C/T | 0.26078 | 0.249767 | intron-variant | SPAG16 | GRCh38.p7 | 2:214121324 | GGCTTCCAAATTCTG[C/T]GGATGCTTAGCTGCA | 79582 |
rs10932525 | snp | A/G | 0.232651 | 0.249397 | intron-variant | SPAG16 | GRCh38.p7 | 2:214121610 | GTGCTTAGTAACTAG[A/G]AGATGGTACTACTGC | 79582 |
rs10932526 | snp | C/T | 0.118933 | 0.212888 | intron-variant | SPAG16 | GRCh38.p7 | 2:214141293 | CCAACATGGTGAAAC[C/T]CCGTCTCTACTAAAA | 79582 |
rs10932529 | snp | A/G | 0.461592 | 0.133149 | intron-variant | SPAG16 | GRCh38.p7 | 2:214279996 | tcttaggaatttaca[A/G]cactatatgctgaca | 79582 |
rs10932530 | snp | G/T | 0.469937 | 0.118861 | intron-variant | SPAG16 | GRCh38.p7 | 2:214287534 | AGACCATAGTTGGGG[G/T]TGGGCTTTCAGAAAT | 79582 |
rs10932532 | snp | C/T | 0.387832 | 0.208572 | intron-variant | SPAG16 | GRCh38.p7 | 2:214304555 | taatgactggcttgc[C/T]gttaataaatatgtg | 79582 |
rs10932534 | snp | C/T | 0.477345 | 0.103991 | intron-variant | SPAG16 | GRCh38.p7 | 2:214335263 | GAGCCTAGTTGTAGC[C/T]GTCAGTAGCCAATAC | 79582 |
rs10932535 | snp | C/T | 0.337841 | 0.23406 | intron-variant | SPAG16 | GRCh38.p7 | 2:214407245 | ATTCATAAATTGTTA[C/T]AATTATTCTTGTTAA | 79582 |
rs11274218 | snp | C/T | 0.345925 | 0.230864 | intron-variant | SPAG16 | GRCh38.p7 | 2:214170277 | ACACACTTAGGTGTG[C/T]GTACATATACATACA | 79582 |
rs11274354 | in-del | -/AGTAGCTAGGTTGAAT/TAGTAGCTAGGTTGAA | | | intron-variant | SPAG16 | GRCh38.p7 | 2:214314754 | ATGTTTAAAAAAAGT[lengthTooLong]GGGTTCACATTATGG | 79582 |
rs11283652 | in-del | -/CACTCA | 0.111224 | 0.207945 | intron-variant | SPAG16 | GRCh38.p7 | 2:214387649 | GAAAGAGGTTTAATT[-/CACTCA]CACTCACAGTTCAGC | 79582 |
rs11291471 | in-del | -/T | 0.178144 | 0.239451 | intron-variant | SPAG16 | GRCh38.p7 | 2:213734717 | GTAGACTTGGACATG[-/T]TTTTTTTTGGTATGA | 79582 |
rs11291472 | in-del | -/T | 0 | 0 | intron-variant | SPAG16 | GRCh38.p7 | 2:213734968 | GTGCCTTTCTAGATA[-/T]TTTTTTTTCCTAATT | 79582 |
rs11292950 | in-del | -/T | 0.0995161 | 0.199636 | intron-variant | SPAG16 | GRCh38.p7 | 2:214316145 | CTTTTACTTTTTGGG[-/T]TTTTTTTTTTTTTAG | 79582 |
rs11296127 | in-del | -/A | 0.47517 | 0.10862 | intron-variant | SPAG16 | GRCh38.p7 | 2:213799961 | TGATAGACTGGATTG[-/A]AAAAAAAAAAAAAAA | 79582 |
rs11301806 | snp | C/T | 0.498967 | 0.0227038 | intron-variant | SPAG16 | GRCh38.p7 | 2:213875961 | GGAAGCTGTGACATC[C/T]CAACCTGATCCAAAA | 79582 |
rs11303162 | in-del | -/G | 0.481856 | 0.0935034 | intron-variant | SPAG16 | GRCh38.p7 | 2:214029618 | ATTAAACACACAAAA[-/G]AAAAGAATGTGGAGA | 79582 |
rs11307655 | in-del | -/A | 0.488363 | 0.0753851 | intron-variant | SPAG16 | GRCh38.p7 | 2:213761898 | ACAAAAAAACAAAAC[-/A]AAAAAAAACCCTACA | 79582 |
rs11310181 | in-del | -/T | 0 | 0 | intron-variant | SPAG16 | GRCh38.p7 | 2:213782181 | TGTAATAGTCTTTAG[-/T]TTTTTTTTTTTAAAT | 79582 |
rs11313038 | in-del | -/T | | | intron-variant | SPAG16 | GRCh38.p7 | 2:214059758 | GGTTATTTTTTTTTT[-/T]GCCATATTTTCATTA | 79582 |
rs11320402 | in-del | -/A | 0.375 | 0.216506 | intron-variant | SPAG16 | GRCh38.p7 | 2:213350970 | CTCTACTAAAAATAC[-/A]AAAAAAAAAAAACAA | 79582 |
rs11326151 | in-del | -/T | 0.46885 | 0.12085 | intron-variant, utr-variant-3-prime | SPAG16 | GRCh38.p7 | 2:213369589 | TTTAGGCAAAGAGGA[-/T]TTTTTTTTTTGGCTC | 79582 |
rs11329467 | in-del | -/A | 0.113685 | 0.209567 | intron-variant | SPAG16 | GRCh38.p7 | 2:213339025 | TGTGCCCCAGAACTT[-/A]AAAAAAAAAAAAAGA | 79582 |
rs11329697 | in-del | -/T | 0.481473 | 0.0944461 | intron-variant | SPAG16 | GRCh38.p7 | 2:213516404 | CATTTTATCTTTTTC[-/T]TAAAAAAATGAACTT | 79582 |
rs11331514 | in-del | -/A | 0.139225 | 0.224118 | intron-variant | SPAG16 | GRCh38.p7 | 2:213990326 | GCTAAGAAATTAATC[-/A]CTTTTTTGCAATACA | 79582 |
rs11336075 | in-del | -/T | 0.228547 | 0.249078 | intron-variant, upstream-variant-2KB | SPAG16 | GRCh38.p7 | 2:213299438 | ACCACACCGAGCTAA[-/T]TTTTTTTTTTTTTGT | 79582 |
rs11343232 | in-del | -/A | 0 | 0 | intron-variant | SPAG16 | GRCh38.p7 | 2:213429106 | CAAAAAAAAAAAAAA[-/A]GAGTAAGGAGAGAGG | 79582 |
rs11346646 | in-del | -/A | 0.492871 | 0.0592773 | intron-variant | SPAG16 | GRCh38.p7 | 2:214080443 | CTCTACTAAAAATAC[-/A]AAAAAAAAAAAAAAA | 79582 |
rs11357443 | in-del | -/T | 0.339195 | 0.233547 | intron-variant | SPAG16 | GRCh38.p7 | 2:214325725 | TTATTATTGATTAGC[-/T]TTTTTTTTTTACATG | 79582 |
rs11362871 | in-del | -/A | 0.173965 | 0.238157 | intron-variant, utr-variant-3-prime | SPAG16 | GRCh38.p7 | 2:213370566 | TGACTAAATAGTCTG[-/A]AAAAGAATATATGTA | 79582 |
rs11362970 | in-del | -/A | | | intron-variant | SPAG16 | GRCh38.p7 | 2:213783318 | AACTTAGAGTATAAT[-/A]AAAAAAAAAAAAAAA | 79582 |
rs11367043 | in-del | -/A | 0.444 | 0.157683 | intron-variant | SPAG16 | GRCh38.p7 | 2:214206039 | CTCTACTAAAAATAC[-/A]AAAAAAAATAGCTAG | 79582 |
rs11372174 | in-del | -/T | 0 | 0 | intron-variant | SPAG16 | GRCh38.p7 | 2:213792577 | TTTTTTTTTTTTTTT[-/T]GGAGACCGGGTCTCA | 79582 |
rs11379179 | in-del | -/C | 0.470034 | 0.11868 | intron-variant | SPAG16 | GRCh38.p7 | 2:213704670 | GGTCCTTTTAAGCTA[-/C]CCTGTTCTCCAGCGT | 79582 |
rs11381205 | in-del | -/T | 0.0770498 | 0.180522 | intron-variant | SPAG16 | GRCh38.p7 | 2:213742136 | TAGTATTTTTTTTTT[-/T]ACTCTCTTTTCTTGG | 79582 |
rs11382197 | in-del | -/T | 0.499928 | 0.00598999 | intron-variant | SPAG16 | GRCh38.p7 | 2:214013179 | TTTTTTTTTTTTTTT[-/T]GGTTTAAGTAATTAA | 79582 |
rs11382964 | in-del | -/A | 0.475437 | 0.108066 | intron-variant | SPAG16 | GRCh38.p7 | 2:213622846 | TGTCTGTGTATTTTT[-/A]AAAGTATAAGTCTAA | 79582 |
rs11388081 | in-del | -/A | | | intron-variant | SPAG16 | GRCh38.p7 | 2:214165195 | TTGCATGAAAAAAAA[-/A]GTTTGCATTTTAGGG | 79582 |
rs11403609 | in-del | -/A | 0.0807149 | 0.183963 | intron-variant, splice-acceptor-variant | SPAG16 | GRCh38.p7 | 2:214192421 | TTTCTTAGAAAAAAA[-/A]TGGAGATTTGTTTCT | 79582 |
rs11411451 | in-del | -/T | 0.352504 | 0.228019 | intron-variant | SPAG16 | GRCh38.p7 | 2:214144320 | AAAATACACAAAAGC[-/T]TTTAATAAATGACGT | 79582 |
rs11421804 | in-del | -/T | 0.422158 | 0.181278 | intron-variant | SPAG16 | GRCh38.p7 | 2:213492685 | GTTTTTTTTTTTTTT[-/T]GTGCTTGGGGACTAT | 79582 |
rs11442842 | in-del | -/G | 0.474363 | 0.110278 | intron-variant | SPAG16 | GRCh38.p7 | 2:213511166 | TGTTGGTATTCAGAT[-/G]TTTACACATTGACTG | 79582 |
rs11459677 | in-del | -/T | 0.363568 | 0.222716 | intron-variant | SPAG16 | GRCh38.p7 | 2:213288471 | AATTTTTTTTTTTTT[-/T]GTATTTTCAGTAGAG | 79582 |
rs11463113 | in-del | -/A | 0.5 | 0 | intron-variant | SPAG16 | GRCh38.p7 | 2:214131627 | GACTTAAAAAAAAAA[-/A]TGAACTATTAAGCCA | 79582 |
rs11473748 | in-del | -/AAAC | 0.487684 | 0.0775019 | intron-variant | SPAG16 | GRCh38.p7 | 2:214372470 | AGGGAAAACAGAATA[-/AAAC]AAACAAGGAATCTTC | 79582 |
rs11489044 | snp | A/C | 0.141596 | 0.225274 | intron-variant | SPAG16 | GRCh38.p7 | 2:213636736 | AAAAGGGGTTCAGTT[A/C]TTGATTTGATTCTCA | 79582 |
rs11490586 | snp | G/T | | | intron-variant | SPAG16 | GRCh38.p7 | 2:213468386 | CTCTCTATATATATA[G/T]ATATATATATATATA | 79582 |
rs11490597 | snp | A/G | | | intron-variant | SPAG16 | GRCh38.p7 | 2:213468407 | TATATATATATCTAT[A/G]TATTTATGTACAGAT | 79582 |
rs11674163 | snp | A/C | 0.467744 | 0.122832 | intron-variant | SPAG16 | GRCh38.p7 | 2:213848727 | CCTTTCTCCCATCTA[A/C]TGGAAACTGATGCAA | 79582 |
rs11674373 | snp | C/T | 0.237303 | 0.249677 | intron-variant | SPAG16 | GRCh38.p7 | 2:214049681 | GGCTCCATGGCAGAG[C/T]TGGGGACCAGCGGGG | 79582 |
rs11674546 | snp | A/G | 0.348574 | 0.229746 | intron-variant | SPAG16 | GRCh38.p7 | 2:214192163 | AAATTAGAGGGCTTC[A/G]AGAAACGAAGCATTC | 79582 |
rs11674674 | snp | G/T | 0.350546 | 0.22889 | intron-variant | SPAG16 | GRCh38.p7 | 2:213350803 | ATTCAGAAAAAGTAT[G/T]TCTCCATTTAACTAC | 79582 |
rs11675111 | snp | A/G | 0.215144 | 0.247558 | intron-variant | SPAG16 | GRCh38.p7 | 2:214122429 | CCTTTTTAAAAAACC[A/G]GTGATAAACAAAAAA | 79582 |
rs11675472 | snp | C/T | 0.347032 | 0.230401 | intron-variant | SPAG16 | GRCh38.p7 | 2:214180860 | TTGGGCTAGATGCAA[C/T]GTGACCTTTAATCTT | 79582 |
rs11675561 | snp | A/G | 0.432357 | 0.171014 | intron-variant | SPAG16 | GRCh38.p7 | 2:214022298 | CCTATATTATCTTGT[A/G]TTTACATCAGACCAT | 79582 |
rs11675655 | snp | C/T | 0.459801 | 0.135955 | intron-variant | SPAG16 | GRCh38.p7 | 2:213945927 | CAATACACCTTCTTT[C/T]TAGCCCTTTGTTTCT | 79582 |
rs11675820 | snp | C/T | 0.194278 | 0.243711 | intron-variant | SPAG16 | GRCh38.p7 | 2:214080564 | agtgagctgagatca[C/T]gcctctgcactccag | 79582 |
rs11676279 | snp | C/G | 0.45946 | 0.136478 | intron-variant | SPAG16 | GRCh38.p7 | 2:213536837 | caaaggactataaat[C/G]atgctgctataaaga | 79582 |
rs11676531 | snp | A/T | 0.349233 | 0.229462 | intron-variant | SPAG16 | GRCh38.p7 | 2:213311711 | GTATTGAATACCTTA[A/T]TTCATATGAAACATT | 79582 |
rs11676642 | snp | C/T | 0.34659 | 0.230587 | intron-variant | SPAG16 | GRCh38.p7 | 2:214202125 | TGCTGGGATTACAGG[C/T]TTAAGCTACCATGCT | 79582 |
rs11676777 | snp | C/T | 0.480223 | 0.0974544 | intron-variant | SPAG16 | GRCh38.p7 | 2:214357151 | TCATTTCTTTGGCTA[C/T]TTTATGATCTCCTTT | 79582 |
rs11677054 | snp | A/G | 0.390464 | 0.206809 | intron-variant | SPAG16, LOC101928084 | GRCh38.p7 | 2:214086712 | TTTATAGAAGCATGA[A/G]AACAGACTAATACAG | 79582 |
rs11677145 | snp | A/G | 0.347253 | 0.230308 | intron-variant | SPAG16 | GRCh38.p7 | 2:214199101 | tgcggaggctttttc[A/G]tttaattaggttcca | 79582 |
rs11677304 | snp | A/G | | | intron-variant | SPAG16 | GRCh38.p7 | 2:213509036 | gagtctcactctttc[A/G]cccaggctggagtgc | 79582 |
rs11677306 | snp | A/G | | | intron-variant | SPAG16 | GRCh38.p7 | 2:213509056 | ggctggagtgcagtg[A/G]tgcaatctcggctca | 79582 |
rs11677384 | snp | A/G | 0 | 0 | intron-variant | SPAG16 | GRCh38.p7 | 2:213993796 | GGATATGGCATATGT[A/G]AATCTACCAAGAAAT | 79582 |
rs11677418 | snp | C/G | 0 | 0 | intron-variant | SPAG16 | GRCh38.p7 | 2:213637723 | ggttttctagtttgt[C/G]catttaaatgtattc | 79582 |
rs11677521 | snp | C/G | 0.480064 | 0.0978296 | intron-variant | SPAG16 | GRCh38.p7 | 2:213537060 | AGTAAACTATCGCAA[C/G]AACAAAAAATCAAAC | 79582 |
rs11677793 | snp | A/G | 0.38286 | 0.211774 | intron-variant, utr-variant-5-prime | SPAG16 | GRCh38.p7 | 2:213296797 | CAGTACATAAGAAGC[A/G]TGTGTTAAGTCTTAA | 79582 |
rs11677794 | snp | A/G | 0.151668 | 0.229849 | intron-variant | SPAG16 | GRCh38.p7 | 2:213443898 | aagtactctcactcc[A/G]attcaggctcctgta | 79582 |
rs11677851 | snp | C/T | 0.352938 | 0.227824 | intron-variant | SPAG16 | GRCh38.p7 | 2:213321176 | AAAAAAGTCAGGTTG[C/T]AGATATGTATTATTC | 79582 |
rs11678163 | snp | A/G | 0.474363 | 0.110278 | intron-variant | SPAG16 | GRCh38.p7 | 2:213798177 | tattgacttgtaagc[A/G]ttctttatatatttt | 79582 |
rs11678221 | snp | A/T | 0.485866 | 0.0828688 | intron-variant | SPAG16 | GRCh38.p7 | 2:213938969 | AAATCCTAACACTTA[A/T]CAAAGAGAGCAGAAC | 79582 |
rs11678617 | snp | A/G | 0.212122 | 0.247114 | intron-variant | SPAG16 | GRCh38.p7 | 2:213309574 | CCTTTAGACAATCCA[A/G]TCACACTCCTGCTGC | 79582 |
rs11678758 | snp | A/G | 0.0103295 | 0.0711199 | intron-variant | SPAG16 | GRCh38.p7 | 2:213851449 | gtaggcggaggttgc[A/G]gtgagccaagattgc | 79582 |
rs11678853 | snp | A/G | 0.0970103 | 0.197722 | intron-variant | SPAG16 | GRCh38.p7 | 2:214170222 | cacacttaggtgtgt[A/G]tacgtatacacacac | 79582 |
rs11679213 | snp | A/G | 0.281049 | 0.248064 | intron-variant | SPAG16 | GRCh38.p7 | 2:214383768 | ATTATGTAAACCACA[A/G]GCAAAATGGGAAGTC | 79582 |
rs11679771 | snp | A/G | 0.0437281 | 0.141251 | intron-variant | SPAG16 | GRCh38.p7 | 2:213380738 | cttgctccataatcc[A/G]agaggcctccgctgt | 79582 |
rs11681071 | snp | C/T | 0.346811 | 0.230494 | intron-variant | SPAG16 | GRCh38.p7 | 2:213831635 | GTCTTCAATTCTGCA[C/T]GTTCGTTTTTACAAA | 79582 |
rs11681148 | snp | A/T | 0.251296 | 0.249997 | intron-variant | SPAG16 | GRCh38.p7 | 2:214277492 | atgtcctttttcttg[A/T]tgttgatgctgttcc | 79582 |
rs11681697 | snp | C/T | 0.345925 | 0.230864 | intron-variant | SPAG16 | GRCh38.p7 | 2:213765171 | GTCAGGAGACCGAGA[C/T]CATCCTGGCCAACAC | 79582 |
rs11682052 | snp | C/T | 0.216349 | 0.247725 | intron-variant | SPAG16 | GRCh38.p7 | 2:214114590 | gcaaggctccatgag[C/T]gtgggaccccctgcc | 79582 |
rs11682093 | snp | C/T | 0.328148 | 0.237472 | intron-variant | SPAG16 | GRCh38.p7 | 2:213394177 | GTACTATGTTCATAT[C/T]TTTTTTAGCATTTTT | 79582 |
rs11682310 | snp | C/T | 0.48 | 0.0979796 | intron-variant | SPAG16 | GRCh38.p7 | 2:213950723 | ttttttttttttttt[C/T]ccctcaagacggtct | 79582 |
rs11682739 | snp | A/G | 0.212425 | 0.24716 | intron-variant | SPAG16 | GRCh38.p7 | 2:213382391 | taatagagaatatgt[A/G]aaagtagttatcaac | 79582 |
rs11683006 | snp | A/C | 0.382666 | 0.211895 | intron-variant | SPAG16 | GRCh38.p7 | 2:213618804 | ACCTTAAAACACTCC[A/C]TGATTTCTTTGTCTT | 79582 |
rs11683573 | snp | A/G | 0.173965 | 0.238157 | intron-variant | SPAG16 | GRCh38.p7 | 2:213387892 | TAAAATATTATAAAG[A/G]TCTAGtaagaaaaca | 79582 |
rs11683612 | snp | A/G | 0.5 | 0 | intron-variant | SPAG16 | GRCh38.p7 | 2:213425083 | aatcccagcacttta[A/G]gaggctgaggtgggc | 79582 |
rs11683987 | snp | C/T | | | intron-variant | SPAG16 | GRCh38.p7 | 2:213571627 | tagtctgatgggctt[C/T]cctttgagggtaacc | 79582 |
rs11684113 | snp | A/C | 0.240765 | 0.249829 | intron-variant | SPAG16 | GRCh38.p7 | 2:214066092 | TCTTCCCACTATCAC[A/C]ATATTTATCTTCCTA | 79582 |
rs11684128 | snp | A/C | 0.352938 | 0.227824 | intron-variant | SPAG16 | GRCh38.p7 | 2:213476818 | tctcgctgcccacag[A/C]ttggtgagcaggagt | 79582 |
rs11684151 | snp | G/T | 0.343254 | 0.231956 | intron-variant | SPAG16 | GRCh38.p7 | 2:213842546 | GAAATGATTATATTA[G/T]ATTTAATTTATTTTT | 79582 |
rs11684376 | snp | G/T | | | intron-variant | SPAG16 | GRCh38.p7 | 2:213698114 | ATTTCCCCATTCTGG[G/T]GATATTCTCTCCCCT | 79582 |
rs11684659 | snp | A/G | 0.0410537 | 0.137264 | intron-variant | SPAG16 | GRCh38.p7 | 2:213890814 | TTGCTTTGCTCATCT[A/G]TCTTTTCATTAGTTA | 79582 |
rs11684890 | snp | C/G | 0.23031 | 0.249223 | intron-variant, utr-variant-3-prime | SPAG16 | GRCh38.p7 | 2:213371181 | TGGGAAGCCGACGCA[C/G]GCGGATCACGAGGTC | 79582 |
rs11684965 | snp | A/G | 0.363985 | 0.222503 | intron-variant | SPAG16 | GRCh38.p7 | 2:213702299 | AAGCAGGCTGCCCGA[A/G]CCAGCTGCGGCAACC | 79582 |
rs11685028 | snp | C/T | 0 | 0 | intron-variant | SPAG16 | GRCh38.p7 | 2:214258671 | acccagtagATACct[C/T]aatattgtaccacag | 79582 |
rs11685056 | snp | C/T | 0.450483 | 0.149354 | intron-variant | SPAG16 | GRCh38.p7 | 2:213672587 | AGCTCTATATTTGTA[C/T]CTCTTTGCTTTTCTA | 79582 |
rs11685260 | snp | A/G | 0.25801 | 0.249872 | intron-variant | SPAG16 | GRCh38.p7 | 2:214109628 | ATTGCTCCAATTGAA[A/G]TTGTGCTTGTGTCAT | 79582 |
rs11685322 | snp | C/G | 0.0103295 | 0.0711199 | intron-variant | SPAG16 | GRCh38.p7 | 2:213848845 | TCCTCTTGTTCACAA[C/G]AGTTTCTGCTTGTGG | 79582 |
rs11685323 | snp | A/C | 0.470034 | 0.11868 | intron-variant | SPAG16 | GRCh38.p7 | 2:213848854 | TCACAACAGTTTCTG[A/C]TTGTGGCCTATGACG | 79582 |
rs11685344 | snp | A/C | 0 | 0 | intron-variant | SPAG16 | GRCh38.p7 | 2:214262506 | ACCACCACAGACTAA[A/C]TAAAATAAACTTTGT | 79582 |
rs11685347 | snp | A/G | 0.467845 | 0.122652 | intron-variant | SPAG16 | GRCh38.p7 | 2:213848697 | ACCCCTGTTCCCTTC[A/G]TCCCATCCCTATATC | 79582 |
rs11685639 | snp | A/G | 0.193028 | 0.243422 | intron-variant | SPAG16 | GRCh38.p7 | 2:213329702 | gctgcagaaatttgc[A/G]taagtaatgaggagc | 79582 |
rs11685648 | snp | C/T | 0 | 0 | intron-variant | SPAG16 | GRCh38.p7 | 2:213778552 | TCAAATAACTCTATC[C/T]TAGGTTTTGTCATAA | 79582 |
rs11685778 | snp | C/G | 0.484771 | 0.0859212 | intron-variant | SPAG16 | GRCh38.p7 | 2:213903819 | gcacccaagtcacct[C/G]ctgaatgtttcgctg | 79582 |
rs11686107 | snp | A/G | 0.434253 | 0.168969 | intron-variant | SPAG16 | GRCh38.p7 | 2:213648178 | GCAAAGTAAAGGAAA[A/G]ATGAAACTCTAGGAA | 79582 |
rs11686643 | snp | C/T | 0.345482 | 0.231048 | intron-variant | SPAG16 | GRCh38.p7 | 2:214197934 | AAGGTAATATTTAGG[C/T]CCAATTTGCTATTGA | 79582 |
rs11687463 | snp | G/T | 0.35207 | 0.228214 | intron-variant, utr-variant-3-prime | SPAG16 | GRCh38.p7 | 2:213399111 | TCAATTCTAAAAATT[G/T]TTATTTGTATTTCTT | 79582 |
rs11687649 | snp | A/G | 0.492037 | 0.0625946 | intron-variant | SPAG16 | GRCh38.p7 | 2:214068785 | ACTTGCCTTTCTTCC[A/G]AAGCAGAATTTTAAT | 79582 |
rs11687848 | snp | A/G | 0.19459 | 0.243782 | intron-variant | SPAG16 | GRCh38.p7 | 2:213348739 | gtagagtttctgcca[A/G]gagatcagctgttag | 79582 |
rs11687976 | snp | C/T | 0.194902 | 0.243853 | intron-variant | SPAG16 | GRCh38.p7 | 2:213394203 | TTTTTCTTGTTTATT[C/T]TTTCCTTTACCAACC | 79582 |
rs11688016 | snp | C/T | 0.446118 | 0.155041 | intron-variant | SPAG16, LOC101928084 | GRCh38.p7 | 2:214093791 | AACAAATTAACTCTG[C/T]GATTGTAATACCAAA | 79582 |
rs11688212 | snp | A/C | 0.193028 | 0.243422 | intron-variant, upstream-variant-2KB | SPAG16 | GRCh38.p7 | 2:213343566 | gagaaaagaaaatta[A/C]agaattagcaggcag | 79582 |
rs11688546 | snp | A/C | | | intron-variant | SPAG16 | GRCh38.p7 | 2:213509210 | accatcttggtcagg[A/C]tggtcttgaattcct | 79582 |
rs11688633 | snp | A/G | | | intron-variant | SPAG16 | GRCh38.p7 | 2:213509232 | tgaattcctgatctc[A/G]tgatccacccgcctc | 79582 |
rs11688821 | snp | C/G | 0.202343 | 0.245416 | intron-variant | SPAG16, LOC101928084 | GRCh38.p7 | 2:214098897 | TTAGAAAAGTAGCTT[C/G]TATTGGTCAATGAGA | 79582 |
rs11688955 | snp | A/G | 0.145305 | 0.227022 | intron-variant | SPAG16, LOC101928084 | GRCh38.p7 | 2:214099196 | GATAGAGAACACTGA[A/G]TCTTTTCCTGGGAGA | 79582 |
rs11689465 | snp | A/G | 0.479824 | 0.098392 | intron-variant | SPAG16 | GRCh38.p7 | 2:213886448 | ATTGATTCTGAGGCT[A/G]TATTTGAGGACTGCA | 79582 |
rs11689583 | snp | C/T | 0.216349 | 0.247725 | intron-variant | SPAG16 | GRCh38.p7 | 2:214064589 | TTATAAACTGTTCCT[C/T]AGTTCATAGTCTTTG | 79582 |
rs11689586 | snp | A/C | 0.476314 | 0.106217 | intron-variant | SPAG16 | GRCh38.p7 | 2:213732914 | gggattgctgggttg[A/C]atagtatttctgccc | 79582 |
rs11690013 | snp | C/T | | | intron-variant | SPAG16 | GRCh38.p7 | 2:214170233 | gtgtatacgtataca[C/T]acacacttaggtgtg | 79582 |
rs11690087 | snp | A/T | 0.352938 | 0.227824 | intron-variant | SPAG16 | GRCh38.p7 | 2:213476819 | ctcgctgcccacagc[A/T]tggtgagcaggagtg | 79582 |
rs11690251 | snp | C/G | 0.232359 | 0.249377 | intron-variant | SPAG16 | GRCh38.p7 | 2:214406364 | ATTTTATTAGCATGA[C/G]AGTAAGAGTTTCCAA | 79582 |
rs11690890 | snp | A/G | 0.19334 | 0.243495 | intron-variant | SPAG16 | GRCh38.p7 | 2:214135829 | gaaaagaagcagcct[A/G]aagccctcaccagaa | 79582 |
rs11690986 | snp | C/T | 0.213635 | 0.247341 | intron-variant | SPAG16 | GRCh38.p7 | 2:213404969 | TTACTCTCCAAATTG[C/T]AGTTCTGGTTTTGGC | 79582 |
rs11691151 | snp | C/T | 0.328148 | 0.237472 | intron-variant | SPAG16 | GRCh38.p7 | 2:213405303 | TGTCCTAATTTAATC[C/T]ATGGAGGAAAATTAT | 79582 |
rs11691155 | snp | C/T | 0.49306 | 0.0584955 | intron-variant | SPAG16 | GRCh38.p7 | 2:213970518 | TGTTGCCCAGGCTGG[C/T]CTCGAGCTCCTGAAC | 79582 |
rs11691400 | snp | A/G | 0.211516 | 0.24702 | intron-variant | SPAG16 | GRCh38.p7 | 2:214035801 | ccacagccatggctg[A/G]atggtcagagctgtg | 79582 |
rs11691405 | snp | A/T | 0.462582 | 0.131564 | intron-variant | SPAG16 | GRCh38.p7 | 2:213843061 | TACTTCCCAAAAGGA[A/T]TGCAGAGGTGAGCCA | 79582 |
rs11691588 | snp | C/T | 0.469544 | 0.119585 | intron-variant | SPAG16 | GRCh38.p7 | 2:213817733 | acagaaaaccaaata[C/T]cacatgttctcactt | 79582 |
rs11691696 | snp | C/G | 0.46885 | 0.12085 | intron-variant | SPAG16 | GRCh38.p7 | 2:213817829 | tagagatgggaaaga[C/G]ggaggtgggtaagtg | 79582 |
rs11692015 | snp | A/G | 0.346368 | 0.23068 | intron-variant | SPAG16 | GRCh38.p7 | 2:213840423 | CTCAGACAAACTCTG[A/G]CATTAGTTTCCCTTG | 79582 |
rs11692125 | snp | C/T | 0.00993419 | 0.0697739 | intron-variant | SPAG16 | GRCh38.p7 | 2:213997160 | TTTGATAGCTTCACA[C/T]AACCCACACTTTCCC | 79582 |
rs11692161 | snp | C/T | 0.427423 | 0.176128 | intron-variant | SPAG16 | GRCh38.p7 | 2:214307181 | gtgcatagaggtgtt[C/T]gtaatgttctctgat | 79582 |
rs11692490 | snp | A/G | 0.212425 | 0.24716 | intron-variant | SPAG16 | GRCh38.p7 | 2:213381544 | TTAATGATTCCATAC[A/G]TAGTCTTCATCTTTA | 79582 |
rs11692961 | snp | A/G | 0.347694 | 0.230122 | intron-variant | SPAG16 | GRCh38.p7 | 2:213311557 | TTACTGTTAGTATTA[A/G]GATTTAAAGTCCTCC | 79582 |
rs11693135 | snp | A/G | 0.040671 | 0.13668 | intron-variant | SPAG16 | GRCh38.p7 | 2:213883422 | tgagacttgcttcat[A/G]accaattatgtggtt | 79582 |
rs11693179 | snp | A/C | 0.213635 | 0.247341 | intron-variant | SPAG16 | GRCh38.p7 | 2:213393963 | ATACTTGAAATGTAT[A/C]ATTGACATTAATTTT | 79582 |
rs11693246 | snp | A/G | 0.213635 | 0.247341 | intron-variant | SPAG16 | GRCh38.p7 | 2:213394063 | TTTTCAGTGAATATA[A/G]GTTCTTCATTATAAT | 79582 |
rs11693371 | snp | C/T | 0.0103295 | 0.0711199 | intron-variant | SPAG16 | GRCh38.p7 | 2:214047290 | acttcaaattatgct[C/T]cagagctttgattaa | 79582 |
rs11693601 | snp | C/T | 0.476487 | 0.105846 | intron-variant | SPAG16 | GRCh38.p7 | 2:213753345 | CTATTTATCTTACTA[C/T]TTTCTTTCTCATAAG | 79582 |
rs11694504 | snp | C/T | | | intron-variant | SPAG16 | GRCh38.p7 | 2:213509044 | ctctttcacccaggc[C/T]ggagtgcagtgatgc | 79582 |
rs11694506 | snp | C/T | 0.00358779 | 0.0422022 | intron-variant | SPAG16 | GRCh38.p7 | 2:213509057 | gctggagtgcagtga[C/T]gcaatctcggctcac | 79582 |
rs11694596 | snp | C/T | | | intron-variant | SPAG16 | GRCh38.p7 | 2:213509228 | gtcttgaattcctga[C/T]ctcgtgatccacccg | 79582 |
rs11694832 | snp | A/C | 0.224709 | 0.248717 | intron-variant | SPAG16 | GRCh38.p7 | 2:214055290 | GAGTATGTAACTTTA[A/C]AAACATGAATCCTAT | 79582 |
rs11695596 | snp | C/G | 0.289424 | 0.246872 | intron-variant, upstream-variant-2KB | SPAG16, LOC101928084 | GRCh38.p7 | 2:214103820 | GGGCTGGGTGAGAAC[C/G]GGGTGTACCTTGTGG | 79582 |
rs11695686 | snp | C/G | 0.288646 | 0.246995 | intron-variant, upstream-variant-2KB | SPAG16, LOC101928084 | GRCh38.p7 | 2:214103851 | GTACAGAAGGAAAGG[C/G]GTTATGTACCACGAG | 79582 |
rs11695933 | snp | A/T | 0.211212 | 0.246973 | intron-variant | SPAG16 | GRCh38.p7 | 2:213305901 | ttgtgatttttagaa[A/T]agtttgagtagggtt | 79582 |
rs11696036 | snp | A/G | 0.348134 | 0.229934 | intron-variant, utr-variant-3-prime | SPAG16 | GRCh38.p7 | 2:213371102 | AAAACTTGGTATCCT[A/G]CTTAGGGACTGTAAT | 79582 |
rs11884311 | snp | C/T | 0.116838 | 0.211584 | intron-variant | SPAG16 | GRCh38.p7 | 2:214065131 | TTTAAGAAGGCAGAA[C/T]AACTTATCTATGTCC | 79582 |
rs11884543 | snp | C/G | 0.4776 | 0.103433 | intron-variant | SPAG16 | GRCh38.p7 | 2:214345552 | TATTTAAAAAGACAA[C/G]TATTACTTGCATCAA | 79582 |
rs11884692 | snp | A/G | 0.104504 | 0.2033 | intron-variant | SPAG16 | GRCh38.p7 | 2:214122100 | ATATAAATTCCTTAT[A/G]GTCTATAATTTAATT | 79582 |
rs11885375 | snp | A/G | 0.0154538 | 0.0865337 | intron-variant | SPAG16 | GRCh38.p7 | 2:214326814 | cccgggcgtggtggc[A/G]ggcgcctgtggtccc | 79582 |
rs11885590 | snp | C/T | 0.224412 | 0.248687 | intron-variant, upstream-variant-2KB | SPAG16, LOC101928084 | GRCh38.p7 | 2:214104884 | aatcatcactgccca[C/T]taccactgtgtctga | 79582 |
rs11885664 | snp | A/G | 0.482683 | 0.0914256 | intron-variant | SPAG16 | GRCh38.p7 | 2:213844281 | TATCTCAGCCTAATT[A/G]ACATTCAGAGATCAG | 79582 |
rs11885827 | snp | A/G | 0.224116 | 0.248656 | intron-variant | SPAG16 | GRCh38.p7 | 2:214105192 | agaatgaatctgagg[A/G]caacagaacaaacag | 79582 |
rs11886640 | snp | C/T | 0.0193772 | 0.0965046 | intron-variant | SPAG16 | GRCh38.p7 | 2:214181675 | ATCTAAGTTTAAATT[C/T]CATAAAGCAAAGAGT | 79582 |
rs11886892 | snp | C/T | 0 | 0 | intron-variant | SPAG16 | GRCh38.p7 | 2:213461789 | ATAATAGGATAAGCC[C/T]TAGGCATGGACAAAA | 79582 |
rs11887284 | snp | A/G | 0.45866 | 0.137698 | intron-variant | SPAG16 | GRCh38.p7 | 2:213722435 | CCCTAACTACTCTAT[A/G]CTTCTTTAACTGTAA | 79582 |
rs11887348 | snp | A/G | 0.470521 | 0.117772 | intron-variant | SPAG16 | GRCh38.p7 | 2:213926757 | AACTAGTGTCCTTCA[A/G]GGTATTTGTTAATTT | 79582 |
rs11887466 | snp | C/T | 0.470521 | 0.117772 | intron-variant | SPAG16 | GRCh38.p7 | 2:213919642 | gtaattttattgtgc[C/T]gtgatgcaagagagt | 79582 |
rs11887857 | snp | A/G | 0.25912 | 0.249834 | intron-variant | SPAG16 | GRCh38.p7 | 2:214187800 | TTTTTTTTTCTGGTC[A/G]GAGGAAAGGATGAAA | 79582 |
rs11887869 | snp | A/C | 0.0611083 | 0.163768 | intron-variant | SPAG16 | GRCh38.p7 | 2:213826165 | tcacagtctggttta[A/C]agtttgttaacttcg | 79582 |
rs11888092 | snp | A/G | 0.226779 | 0.248919 | intron-variant | SPAG16, LOC101928084 | GRCh38.p7 | 2:214094744 | TTAGAACAGGAATGT[A/G]TACAGTTGTTATTCT | 79582 |
rs11888910 | snp | A/C | 0.46845 | 0.121572 | intron-variant | SPAG16 | GRCh38.p7 | 2:213839226 | GTGCTTCTATGCAGA[A/C]AGTTATAGTGGAGGA | 79582 |
rs11888991 | snp | A/G | 0.433527 | 0.169758 | intron-variant | SPAG16 | GRCh38.p7 | 2:214012178 | TTGGTTCAAGCCACA[A/G]AGGAACTAATCAAAG | 79582 |
rs11889040 | snp | C/T | 0.484771 | 0.0859212 | intron-variant | SPAG16 | GRCh38.p7 | 2:213920564 | ctgccccattggacc[C/T]ctctgccagtcaggc | 79582 |
rs11889359 | snp | A/G | 0.223522 | 0.248594 | intron-variant | SPAG16, LOC101928084 | GRCh38.p7 | 2:214095088 | AGGTGGAAGGAACTC[A/G]AAAGTTCTTAGCACA | 79582 |
rs11889393 | snp | A/G | | | intron-variant | SPAG16 | GRCh38.p7 | 2:214276828 | atttcctgaatttca[A/G]tgttggcctgcctta | 79582 |
rs11889685 | snp | A/G | 0.0640965 | 0.167152 | intron-variant | SPAG16 | GRCh38.p7 | 2:213851956 | AAAACTTAAAGTGCT[A/G]GGGAAGTATTAAGAT | 79582 |
rs11889901 | snp | A/G | 0.464096 | 0.129085 | intron-variant | SPAG16 | GRCh38.p7 | 2:214146797 | TGAGGTCAGGAGATC[A/G]AGACCATCCTGGCTA | 79582 |
rs11889980 | snp | A/G | 0.257176 | 0.249897 | intron-variant | SPAG16 | GRCh38.p7 | 2:214106158 | TTAAGACAATTTGCT[A/G]ATTTATATCTTTGTA | 79582 |
rs11890184 | snp | A/G | 0.102014 | 0.201495 | intron-variant | SPAG16 | GRCh38.p7 | 2:214076471 | TTGGCCTAAAGTGAA[A/G]ATTAGGGTATCTCAA | 79582 |
rs11890207 | snp | A/G | 0.38934 | 0.207568 | intron-variant | SPAG16 | GRCh38.p7 | 2:214289339 | tgaagtgtattttct[A/G]tgttcttttctagta | 79582 |
rs11890354 | snp | A/G | 0.0988009 | 0.199095 | intron-variant | SPAG16 | GRCh38.p7 | 2:214289634 | tgggttattatagcc[A/G]tctaacatattttga | 79582 |
rs11890459 | snp | A/G | 0.0314385 | 0.121371 | intron-variant | SPAG16 | GRCh38.p7 | 2:213539290 | TGGCAATGTGATACC[A/G]CCCCTCATGGACACC | 79582 |
rs11890624 | snp | C/T | 0 | 0 | intron-variant | SPAG16 | GRCh38.p7 | 2:213539856 | CCAAAGGACAGAAAT[C/T]TAAATACTAAGTTTG | 79582 |
rs11893486 | snp | A/C | 0.475789 | 0.107327 | intron-variant | SPAG16 | GRCh38.p7 | 2:213807567 | CAATGTTTTACCTTC[A/C]AGCAAAAGTGTCGAA | 79582 |
rs11893546 | snp | A/G | 0.339882 | 0.233284 | intron-variant | SPAG16 | GRCh38.p7 | 2:214161039 | CTCCCACTTATAAGT[A/G]AGAACATGAAGTGTT | 79582 |
rs11894175 | snp | C/T | 0.49941 | 0.0171624 | intron-variant | SPAG16 | GRCh38.p7 | 2:214362300 | CAGAATGTGGCTGTA[C/T]ACTTCTTCCACATTG | 79582 |
rs11894604 | snp | C/T | 0.0158469 | 0.0875917 | intron-variant | SPAG16 | GRCh38.p7 | 2:214313170 | TTACTTTAGTGAAAT[C/T]GAAATTATTATTTAC | 79582 |
rs11894925 | snp | A/G | 0.0984431 | 0.198823 | intron-variant | SPAG16 | GRCh38.p7 | 2:214292732 | tttttgatgcttcct[A/G]tatcctcacattgat | 79582 |
rs11895074 | snp | A/G | 0.269809 | 0.249214 | intron-variant | SPAG16 | GRCh38.p7 | 2:214167856 | CAGTAGAACAGTTAG[A/G]AACCAAGGTCTCCAG | 79582 |
rs11895383 | snp | C/T | 0.431916 | 0.171483 | intron-variant | SPAG16 | GRCh38.p7 | 2:214162693 | CTGTTTCTGATCTAG[C/T]ACAATACTGTTTTTG | 79582 |
rs11895844 | snp | A/T | 0.0166325 | 0.0896639 | intron-variant | SPAG16 | GRCh38.p7 | 2:214275741 | tttggaataagtggg[A/T]tgtggtgctaagaag | 79582 |
rs11896697 | snp | A/G | 0.436976 | 0.165952 | intron-variant | SPAG16 | GRCh38.p7 | 2:214125932 | TGATTGGGCAAAAGA[A/G]TATAATCTAATGGTA | 79582 |
rs11897203 | snp | G/T | 0.478354 | 0.101757 | intron-variant | SPAG16 | GRCh38.p7 | 2:214339840 | AAAAGGGGTTTTGTA[G/T]ATGTCATTTAGTTTA | 79582 |
rs11897357 | snp | C/T | 0.219947 | 0.248187 | intron-variant | SPAG16 | GRCh38.p7 | 2:214063612 | cctctaatactatca[C/T]atgagcaattaggtt | 79582 |
rs11898203 | snp | G/T | 0.482534 | 0.0918038 | intron-variant | SPAG16 | GRCh38.p7 | 2:213845449 | GATCCACCCTCTTCG[G/T]CCTCCCAAAGTGCTG | 79582 |
rs11898414 | snp | A/G | 0.257454 | 0.249889 | intron-variant | SPAG16 | GRCh38.p7 | 2:214127452 | AGATGGAAAGAGCAG[A/G]GTGGGAGTGAGCTGA | 79582 |
rs11898517 | snp | A/C/T | 0.000399281 | 0.0141238 | intron-variant | SPAG16 | GRCh38.p7 | 2:214114956 | CAGAACTCGCTAATA[A/C/T]GTTTTTATTTGCACA | 79582 |
rs11898702 | snp | A/G | 0.0333695 | 0.124785 | intron-variant | SPAG16 | GRCh38.p7 | 2:213467791 | acagtccaccctcca[A/G]tggttccctccagag | 79582 |
rs11899276 | snp | A/C | 0.483923 | 0.0882034 | intron-variant | SPAG16 | GRCh38.p7 | 2:213851843 | AACTGTAAGAATGCT[A/C]CACTCTAGTAAAAAA | 79582 |
rs11899471 | snp | G/T | 0.0839998 | 0.186933 | intron-variant | SPAG16 | GRCh38.p7 | 2:214224888 | CTTCTAGTGAGGGTT[G/T]TCAATATGTGGGCAG | 79582 |
rs11900000 | snp | C/T | 0.223522 | 0.248594 | intron-variant | SPAG16, LOC101928084 | GRCh38.p7 | 2:214095116 | ACATTGGAAATCTAG[C/T]TCAGCACTTTGTAAA | 79582 |
rs11900320 | snp | A/G | 0.22263 | 0.248497 | intron-variant | SPAG16 | GRCh38.p7 | 2:214125713 | AGGAAGAAAGATATG[A/G]CACCTTTCCTCACCC | 79582 |
rs11900391 | snp | C/T | 0.269267 | 0.249256 | intron-variant | SPAG16 | GRCh38.p7 | 2:214137345 | AGTTATATATTTATA[C/T]ATGTTATCTAATGAC | 79582 |
rs11900486 | snp | C/T | 0.322245 | 0.239334 | intron-variant | SPAG16 | GRCh38.p7 | 2:214137524 | TCTATGTGACAAATT[C/T]GTATCTTATTGACTA | 79582 |
rs11900858 | snp | C/T | 0.141934 | 0.225437 | intron-variant | SPAG16 | GRCh38.p7 | 2:213656918 | AGAAATAAGTGGCAG[C/T]TACAGTTTAAAATTA | 79582 |
rs11901290 | snp | C/T | 0.254664 | 0.249956 | intron-variant | SPAG16 | GRCh38.p7 | 2:214032356 | TAAAGAAACAAAGGG[C/T]CTTGAGCTGGTACAG | 79582 |
rs11901363 | snp | A/G | 0.475525 | 0.107882 | intron-variant | SPAG16 | GRCh38.p7 | 2:213895266 | taatgaaagaaatca[A/G]agaggacagaaacaa | 79582 |
rs11901413 | snp | G/T | 0.0150606 | 0.0854603 | intron-variant | SPAG16 | GRCh38.p7 | 2:214372522 | ATATCTCTGGGAATT[G/T]TTTTAAACCAAATTT | 79582 |
rs11902069 | snp | A/G | 0.231482 | 0.249313 | intron-variant | SPAG16 | GRCh38.p7 | 2:213913639 | tacatgtacatatat[A/G]tatatgtacatgtac | 79582 |
rs11902344 | snp | A/G | 0.191147 | 0.242974 | intron-variant | SPAG16 | GRCh38.p7 | 2:213959827 | cacacacctaaacct[A/G]accttcctcccattc | 79582 |
rs11903341 | snp | C/T | 0.12932 | 0.218944 | intron-variant | SPAG16 | GRCh38.p7 | 2:214234458 | aggtctttgaggaat[C/T]accacaatgtcttcc | 79582 |
rs11903543 | snp | A/G | 0.0197687 | 0.0974348 | intron-variant | SPAG16 | GRCh38.p7 | 2:214196029 | TTCAAAATAAGTGTA[A/G]AAAGTTACCAGAACC | 79582 |
rs11904339 | snp | A/G | 0.0023933 | 0.0345097 | intron-variant | SPAG16 | GRCh38.p7 | 2:214374438 | GAACATGAACCTCTC[A/G]ATATTTCATGAAAAA | 79582 |
rs11904355 | snp | G/T | 0.226779 | 0.248919 | intron-variant | SPAG16, LOC101928084 | GRCh38.p7 | 2:214094751 | AGGAATGTATACAGT[G/T]GTTATTCTGTGCCTG | 79582 |
rs11904549 | snp | C/G | 0.484771 | 0.0859212 | intron-variant | SPAG16 | GRCh38.p7 | 2:213920486 | ATATATGTGGTGGCT[C/G]TGggcctggaggaag | 79582 |
rs11904788 | snp | A/G | 0.0452528 | 0.143452 | intron-variant | SPAG16 | GRCh38.p7 | 2:213614052 | CCATCCTCCTGTTGT[A/G]TTGGGAGAACATTTT | 79582 |
rs11904795 | snp | A/G | 0.487368 | 0.0784625 | intron-variant | SPAG16 | GRCh38.p7 | 2:214304385 | aaaccacttaaaggc[A/G]ttcttaaaccacaaa | 79582 |
rs11963605 | snp | A/G | | | intron-variant | SPAG16 | GRCh38.p7 | 2:213356911 | GACACATTTAAAGCA[A/G]TGTGTAGAGGAAAAT | 79582 |
rs12052858 | snp | A/G | 0.315758 | 0.241197 | intron-variant | SPAG16 | GRCh38.p7 | 2:214166211 | CATCTAGATAGAGAG[A/G]TATATAGACAGGATG | 79582 |
rs12053561 | snp | A/G | 0.00358779 | 0.0422022 | intron-variant | SPAG16 | GRCh38.p7 | 2:213647085 | CAAACAGGCTTCAGA[A/G]GGGTTGTTCTCTTGG | 79582 |
rs12105206 | snp | C/T | 0.471673 | 0.115589 | intron-variant | SPAG16 | GRCh38.p7 | 2:214337748 | TGGTAGGTTGATTTT[C/T]AGCCATAGTGGGAAT | 79582 |
rs12151624 | snp | A/G | 0.182614 | 0.240747 | intron-variant | SPAG16, LOC101928084 | GRCh38.p7 | 2:214097027 | CAGAATATATGAAAT[A/G]TTATATAAATTGCTC | 79582 |
rs12151793 | snp | A/G/T | 0.276782 | 0.258471 | intron-variant | SPAG16 | GRCh38.p7 | 2:214407871 | CACACATTATATGCC[A/G/T]TGTAATAATCCAATA | 79582 |
rs12185594 | snp | A/G | 0.3742 | 0.216966 | intron-variant | SPAG16, LOC101928084 | GRCh38.p7 | 2:214087601 | AAGTAATGTATGTTG[A/G]GAATTATAGGTGATT | 79582 |
rs12328228 | snp | A/C | 0.472989 | 0.113031 | intron-variant | SPAG16 | GRCh38.p7 | 2:213856775 | cacaaagcagcaagt[A/C]cctgggcctggctca | 79582 |
rs12328232 | snp | C/T | | | intron-variant | SPAG16 | GRCh38.p7 | 2:213718990 | agtctttatatctag[C/T]tcagggattgtaaat | 79582 |
rs12328234 | snp | C/T | | | intron-variant | SPAG16 | GRCh38.p7 | 2:213719005 | ttcagggattgtaaa[C/T]acaccaatcagcacc | 79582 |
rs12328401 | snp | C/T | 0.482309 | 0.0923707 | intron-variant | SPAG16 | GRCh38.p7 | 2:214013491 | CTCTCCCTATTCTCC[C/T]GTCTCTTTTCCCTCC | 79582 |
rs12328993 | snp | C/T | 0.467845 | 0.122652 | intron-variant | SPAG16 | GRCh38.p7 | 2:213675102 | tgagatgatatctca[C/T]tgtggttttgatttg | 79582 |
rs12328999 | snp | C/T | 0.468047 | 0.122292 | intron-variant | SPAG16 | GRCh38.p7 | 2:213675237 | tgatgggcttgtttg[C/T]tttttccttgtaaat | 79582 |
rs12329201 | snp | C/G | 0.279726 | 0.248226 | intron-variant | SPAG16 | GRCh38.p7 | 2:214146896 | AGTCCCAGCTACTCA[C/G]GAGGCTGAGGCAGGA | 79582 |
rs12329379 | snp | G/T | 0.472989 | 0.113031 | intron-variant | SPAG16 | GRCh38.p7 | 2:213856774 | gcacaaagcagcaag[G/T]acctgggcctggctc | 79582 |
rs12463511 | snp | A/C | 0.47614 | 0.106587 | intron-variant | SPAG16 | GRCh38.p7 | 2:213760242 | gacagaaaaagattt[A/C]tcaggcaaataacca | 79582 |
rs12463525 | snp | C/T | 0.155325 | 0.23138 | intron-variant | SPAG16 | GRCh38.p7 | 2:214265822 | ATTTGTATTCTGATT[C/T]TAATGTTAAGTTCTC | 79582 |
rs12463610 | snp | C/T | 0.329317 | 0.237084 | intron-variant | SPAG16 | GRCh38.p7 | 2:213885734 | ttccatcatttacaa[C/T]gtttcacaaaacaat | 79582 |
rs12464269 | snp | C/T | 0.455263 | 0.142713 | intron-variant | SPAG16 | GRCh38.p7 | 2:214250617 | GTAAAATTAAAGCTC[C/T]TTTAGAAAAATATAT | 79582 |
rs12464278 | snp | C/T | 0.370365 | 0.219117 | intron-variant | SPAG16 | GRCh38.p7 | 2:213581233 | ATACTCTATTTCTTT[C/T]TTGAGACAGAGTCTT | 79582 |
rs12464393 | snp | A/T | 0.0995161 | 0.199636 | intron-variant | SPAG16 | GRCh38.p7 | 2:213935053 | tgaaaatacaaaaaa[A/T]tacctgggcgtggtg | 79582 |
rs12464399 | snp | A/G | | | intron-variant | SPAG16 | GRCh38.p7 | 2:213891421 | ACCTAAGTAGGCAGA[A/G]CTGTAGATACAATCA | 79582 |
rs12464580 | snp | C/T | 0.470132 | 0.118498 | intron-variant | SPAG16 | GRCh38.p7 | 2:213821079 | CAAATTTTGTTCTGC[C/T]GGCTATTTTCTTTTC | 79582 |
rs12464629 | snp | C/T | 0.00953873 | 0.0683987 | intron-variant | SPAG16 | GRCh38.p7 | 2:213520368 | gaggcgggaagatca[C/T]gaggtcaggagattg | 79582 |
rs12464836 | snp | C/G | 0.0103295 | 0.0711199 | intron-variant | SPAG16 | GRCh38.p7 | 2:213485019 | ttttttttgagacag[C/G]gtctcattctgtcca | 79582 |
rs12464916 | snp | C/T | 0.149665 | 0.228982 | intron-variant | SPAG16 | GRCh38.p7 | 2:213976273 | acacacatatacata[C/T]GCGtacacatgtgtg | 79582 |
rs12465021 | snp | A/T | | | intron-variant | SPAG16 | GRCh38.p7 | 2:213381431 | TTTTTCATGGTACGG[A/T]GCCATAACAACGGTT | 79582 |
rs12465707 | snp | C/G | 0.23846 | 0.249734 | intron-variant | SPAG16 | GRCh38.p7 | 2:213731861 | ttatccactctTGAT[C/G]gttgtcttttcactc | 79582 |
rs12465723 | snp | A/G | 0.479824 | 0.098392 | intron-variant | SPAG16 | GRCh38.p7 | 2:213880186 | tgaatggtatgaaat[A/G]gtatttaattgtagt | 79582 |
rs12465742 | snp | C/T | 0.331642 | 0.236293 | intron-variant | SPAG16 | GRCh38.p7 | 2:213822408 | atagagttgtttgag[C/T]tccttctgtattctg | 79582 |
rs12466024 | snp | A/T | 0.327445 | 0.237702 | intron-variant | SPAG16 | GRCh38.p7 | 2:213933754 | AGTGTATTGTGTCCA[A/T]TACTCTTGTAATTAC | 79582 |
rs12466029 | snp | G/T | 0 | 0 | intron-variant | SPAG16 | GRCh38.p7 | 2:213287069 | TAGACTTCAACAAGG[G/T]GAGATACAAATATAC | 79582 |
rs12466222 | snp | A/G | 0.327914 | 0.237549 | intron-variant | SPAG16 | GRCh38.p7 | 2:213905784 | GAAGATAAATTTTAA[A/G]GGGGTTATAAGCGAT | 79582 |
rs12466276 | snp | C/G | 0.479904 | 0.0982045 | intron-variant | SPAG16 | GRCh38.p7 | 2:213868548 | TTTACCTACACCAGA[C/G]GACTGCTTCATAATA | 79582 |
rs12466426 | snp | A/G | 0.148326 | 0.228391 | intron-variant | SPAG16 | GRCh38.p7 | 2:213561996 | TCATTTTGCTCTAGC[A/G]AAAGTGTCTTCCAAT | 79582 |
rs12467458 | snp | G/T | 0.286564 | 0.247312 | intron-variant | SPAG16 | GRCh38.p7 | 2:213973289 | atttaggcagtcagt[G/T]gtgtgtcttaatggt | 79582 |
rs12467712 | snp | C/T | 0.467946 | 0.122472 | intron-variant | SPAG16 | GRCh38.p7 | 2:213790310 | TTTTAACTCCTCATC[C/T]CCAACTCTCAACTCT | 79582 |
rs12467894 | snp | A/C | 0.00993419 | 0.0697739 | intron-variant | SPAG16 | GRCh38.p7 | 2:213405368 | ataatagttacacat[A/C]tatatggggtacatg | 79582 |
rs12467990 | snp | C/T | 0.0205511 | 0.0992634 | intron-variant | SPAG16 | GRCh38.p7 | 2:213690158 | GCTTGAAATGCCCTT[C/T]CTTCAGATATTTGCC | 79582 |
rs12468018 | snp | C/T | 0.104149 | 0.203046 | intron-variant | SPAG16 | GRCh38.p7 | 2:214144716 | AGAAAGGAAACAATG[C/T]CCTGGGCCTAAAATG | 79582 |
rs12468299 | snp | A/T | 0.481087 | 0.0953875 | intron-variant | SPAG16 | GRCh38.p7 | 2:213717156 | AAGCAGAAACTTTTC[A/T]TTTTTTTTTTTTTTT | 79582 |
rs12468337 | snp | A/C | 0.102014 | 0.201495 | intron-variant | SPAG16 | GRCh38.p7 | 2:214141644 | AAATGCATTCAATCC[A/C]AAGTGATATTTAACT | 79582 |
rs12468762 | snp | C/T | 0.457037 | 0.140127 | intron-variant | SPAG16 | GRCh38.p7 | 2:213821136 | TAGGTTGATTAAATC[C/T]TGTAGGTTCATTCTT | 79582 |
rs12469168 | snp | C/T | 0.32768 | 0.237625 | intron-variant | SPAG16 | GRCh38.p7 | 2:213896876 | aagtgaatctcataa[C/T]taaagggagtagatt | 79582 |
rs12469417 | snp | C/T | 0.0158111 | 0.087496 | intron-variant | SPAG16 | GRCh38.p7 | 2:213364068 | TTTCTTTGAATTTTA[C/T]TTTTTAGATTTCTGG | 79582 |
rs12469936 | snp | A/C | | | intron-variant | SPAG16 | GRCh38.p7 | 2:213859052 | gacatggtggcacgc[A/C]cctgtaatcccagct | 79582 |
rs12469976 | snp | A/C | 0 | 0 | intron-variant | SPAG16 | GRCh38.p7 | 2:213859139 | agccgagatcacacc[A/C]ctgctctccagtctg | 79582 |
rs12470022 | snp | A/C | 0.485596 | 0.0836329 | intron-variant | SPAG16 | GRCh38.p7 | 2:213941957 | tgagcaccatttctt[A/C]tctctccagcttgta | 79582 |
rs12470379 | snp | A/G | 0.286564 | 0.247312 | intron-variant | SPAG16 | GRCh38.p7 | 2:213819446 | CTTTTCAGAAGGTAG[A/G]TGGGAACTATTTTAT | 79582 |
rs12470449 | snp | G/T | 0.480064 | 0.0978296 | intron-variant | SPAG16 | GRCh38.p7 | 2:213868114 | TACCCAGTAAATGAT[G/T]AAGATAGTTATAAAC | 79582 |
rs12470452 | snp | C/T | 0.479984 | 0.0980171 | intron-variant | SPAG16 | GRCh38.p7 | 2:213868151 | CCAAATTCAATTGCT[C/T]CAAAATGTATGTTAT | 79582 |
rs12470513 | snp | G/T | 0.479984 | 0.0980171 | intron-variant | SPAG16 | GRCh38.p7 | 2:213868312 | ACTTGGCCAGAAACA[G/T]CAACAGAATTCCATT | 79582 |
rs12470525 | snp | A/T | 0.479824 | 0.098392 | intron-variant | SPAG16 | GRCh38.p7 | 2:213884819 | atgaaattcttgtag[A/T]gaatttttcagcttt | 79582 |
rs12470909 | snp | C/T | 0.266819 | 0.249434 | intron-variant | SPAG16 | GRCh38.p7 | 2:213902749 | tcatctcagcattaa[C/T]ccaaaagtccacagt | 79582 |
rs12470997 | snp | A/G | 0.464309 | 0.12873 | intron-variant | SPAG16 | GRCh38.p7 | 2:214397038 | ATAAAATCCAGTGCA[A/G]CTTGCTGTAATTGTT | 79582 |
rs12471142 | snp | A/G | 0.297128 | 0.245518 | intron-variant, missense | SPAG16 | GRCh38.p7 | 2:213376151 | TAATTATAGATTATC[A/G]TATGTGAGGTAGACT | 79582 |
rs12471401 | snp | A/G | 0.473726 | 0.111565 | intron-variant | SPAG16 | GRCh38.p7 | 2:214332036 | gtgggcagatcactc[A/G]aggtcaggagttcaa | 79582 |
rs12471409 | snp | A/G | 0.00358779 | 0.0422022 | intron-variant | SPAG16 | GRCh38.p7 | 2:213936062 | aattttaaacaggaa[A/G]gtcgagaaaattctt | 79582 |
rs12471453 | snp | A/G | 0.0973687 | 0.197999 | intron-variant | SPAG16 | GRCh38.p7 | 2:213943708 | aattgaagagaaaga[A/G]ggaatcattaagcaa | 79582 |
rs12471502 | snp | A/T | 0.479824 | 0.098392 | intron-variant | SPAG16 | GRCh38.p7 | 2:213885269 | tgggctttcatccag[A/T]agatagcatttatta | 79582 |
rs12471519 | snp | G/T | 0.158632 | 0.232706 | intron-variant | SPAG16 | GRCh38.p7 | 2:214288481 | atggtagtattattt[G/T]tgattttttgagaaa | 79582 |
rs12471539 | snp | C/G | | | intron-variant | SPAG16 | GRCh38.p7 | 2:214031734 | ctataggaagcacag[C/G]tggggaggtctcagg | 79582 |
rs12471540 | snp | A/G | 0.477004 | 0.104734 | intron-variant | SPAG16 | GRCh38.p7 | 2:213760228 | attgaaggtagaggg[A/G]cagaaaaagatttct | 79582 |
rs12471556 | snp | A/T | | | intron-variant | SPAG16 | GRCh38.p7 | 2:214204007 | cacagtgggagtgag[A/T]ccagccttttgggct | 79582 |
rs12472069 | snp | A/T | 0.473359 | 0.112298 | intron-variant | SPAG16 | GRCh38.p7 | 2:213834399 | gaaaaaagtagatag[A/T]tgtgaagaagtggat | 79582 |
rs12472276 | snp | A/G | 0.32955 | 0.237006 | intron-variant | SPAG16 | GRCh38.p7 | 2:213921261 | aactattgccattat[A/G]tagtgctcttcttta | 79582 |
rs12472290 | snp | A/G | | | intron-variant | SPAG16 | GRCh38.p7 | 2:213407259 | TGCAAAGGACCTTCA[A/G]AGGGGGAAAGGGAGA | 79582 |
rs12472371 | snp | A/G | 0.471958 | 0.115042 | intron-variant | SPAG16 | GRCh38.p7 | 2:214338559 | GGTATTCCTATGGTT[A/G]TGAAATTAGATTGCT | 79582 |
rs12472422 | snp | C/G/T | 0.00438332 | 0.0466095 | intron-variant | SPAG16 | GRCh38.p7 | 2:213377676 | TTCCTCTTACTTTTT[C/G/T]CCTTACTTTTTCCCT | 79582 |
rs12472531 | snp | G/T | 0.474634 | 0.109726 | intron-variant | SPAG16 | GRCh38.p7 | 2:214333017 | agcaattctcaaatg[G/T]tttaaatatttcttt | 79582 |
rs12472571 | snp | A/C | 0.481165 | 0.0951993 | intron-variant | SPAG16 | GRCh38.p7 | 2:213703065 | TCACTTCCTGGAAGA[A/C]GTTTTAATGGTCAGT | 79582 |
rs12472656 | snp | G/T | 0.361894 | 0.223562 | intron-variant, upstream-variant-2KB | SPAG16 | GRCh38.p7 | 2:213298283 | CCCATGGACATAGCT[G/T]CTTCTTGGTAGACAC | 79582 |
rs12473276 | snp | A/G | | | intron-variant | SPAG16 | GRCh38.p7 | 2:213874796 | AGGGAGGGATTGTGG[A/G]GACTATGAAGCTACA | 79582 |
rs12473341 | snp | A/T | 0.348794 | 0.229651 | intron-variant | SPAG16 | GRCh38.p7 | 2:213415583 | GGTACTTATGGGGCA[A/T]ATCTTCATGGTTGAT | 79582 |
rs12473521 | snp | C/T | 0.104149 | 0.203046 | intron-variant | SPAG16 | GRCh38.p7 | 2:213968034 | TTATTCACACAGCTG[C/T]CGCAATTTGTTTATT | 79582 |
rs12473593 | snp | A/T | 0.095934 | 0.196885 | intron-variant | SPAG16 | GRCh38.p7 | 2:213945442 | cccagtccgagtctc[A/T]aaactgaagaacgtg | 79582 |
rs12473856 | snp | C/T | 0.0178098 | 0.0926698 | intron-variant | SPAG16 | GRCh38.p7 | 2:214314921 | CTGCATTCAGCCTGA[C/T]GGGTAGTGGAGAAGG | 79582 |
rs12473993 | snp | C/T | 0.0952156 | 0.196321 | intron-variant | SPAG16 | GRCh38.p7 | 2:213963402 | cagagaacacgattt[C/T]tacgatttctacgat | 79582 |
rs12474173 | snp | A/G | 0.362104 | 0.223456 | intron-variant | SPAG16 | GRCh38.p7 | 2:213662326 | CCTATGCAAGAACTG[A/G]AAGAATTCATGGAAA | 79582 |
rs12474178 | snp | A/G | 0.479177 | 0.0998894 | intron-variant | SPAG16 | GRCh38.p7 | 2:213868085 | TTAGTTGGTAAAATC[A/G]TGTCTAAAATTCATA | 79582 |
rs12474183 | snp | A/G | 0.329084 | 0.237162 | intron-variant | SPAG16 | GRCh38.p7 | 2:213905198 | ACAGTTTATTTTATG[A/G]GAGCAAATTGTTTAT | 79582 |
rs12474209 | snp | A/T | 0.480064 | 0.0978296 | intron-variant | SPAG16 | GRCh38.p7 | 2:213868200 | TAAAATGTAAATGTT[A/T]CTTTAAAATTGTGCC | 79582 |
rs12474251 | snp | A/G | 0.479904 | 0.0982045 | intron-variant | SPAG16 | GRCh38.p7 | 2:213875356 | TCAAAGAGGTTCCAG[A/G]AAGCAAGAGATGAGC | 79582 |
rs12474684 | snp | C/T | 0.484771 | 0.0859212 | intron-variant | SPAG16 | GRCh38.p7 | 2:213907418 | aaggaaatttataca[C/T]gatcaatgtgaatgt | 79582 |
rs12475452 | snp | G/T | 0.499918 | 0.00638925 | intron-variant | SPAG16 | GRCh38.p7 | 2:213716338 | GATGTACAAAATGAT[G/T]TGAGAGTATCAGTGA | 79582 |
rs12475902 | snp | C/T | 0.484632 | 0.086302 | intron-variant | SPAG16 | GRCh38.p7 | 2:213908461 | TATTTTTCAGGTTTG[C/T]GTGTTTCTCTATTTC | 79582 |
rs12476185 | snp | C/G | 0.0995161 | 0.199636 | intron-variant | SPAG16 | GRCh38.p7 | 2:213935057 | aatacaaaaaattac[C/G]tgggcgtggtggcag | 79582 |
rs12476541 | snp | C/G | 0.338523 | 0.233803 | intron-variant | SPAG16 | GRCh38.p7 | 2:213782173 | CTCTAAACTGTAATA[C/G]TCTTCAGTTTTTTTT | 79582 |
rs12476948 | snp | A/G | | | intron-variant | SPAG16 | GRCh38.p7 | 2:213381484 | TAAGCTGGACATTCA[A/G]CACTGGATGGTAGCT | 79582 |
rs12477048 | snp | A/G | 0.397271 | 0.202018 | intron-variant | SPAG16 | GRCh38.p7 | 2:213971150 | TATTTCAAAACTTAT[A/G]TTTAATACATTTCAA | 79582 |
rs12477119 | snp | A/G | 0 | 0 | intron-variant, utr-variant-3-prime | SPAG16 | GRCh38.p7 | 2:213369055 | AATACTGGAGGCTAG[A/G]AACAATAAAATGGTA | 79582 |
rs12477207 | snp | A/G | 0.33303 | 0.235809 | intron-variant | SPAG16 | GRCh38.p7 | 2:213828697 | atttgaagaggcttt[A/G]gtgttttggtccaag | 79582 |
rs12477324 | snp | A/G | 0.126909 | 0.217598 | intron-variant | SPAG16 | GRCh38.p7 | 2:214084121 | ATCTTCTCTTCCTTT[A/G]CATGCCTCCCTTAAG | 79582 |
rs12477416 | snp | A/G | 0.327914 | 0.237549 | intron-variant | SPAG16 | GRCh38.p7 | 2:213906623 | caaaatatactacaa[A/G]gctatagtaacaatg | 79582 |
rs12477483 | snp | C/T | 0.00943375 | 0.0680285 | intron-variant | SPAG16 | GRCh38.p7 | 2:213451914 | cagctgcaggtgtcc[C/T]TGACTCGCCCCATAC | 79582 |
rs12477778 | snp | A/T | 0.00947846 | 0.0681864 | intron-variant | SPAG16 | GRCh38.p7 | 2:213746496 | aaataaacctactgc[A/T]ccgccagttatataa | 79582 |
rs12478028 | snp | C/T | | | intron-variant | SPAG16 | GRCh38.p7 | 2:213859152 | ccactgctctccagt[C/T]tgggcaacagagcga | 79582 |
rs12478144 | snp | A/G | 0.112983 | 0.209108 | intron-variant | SPAG16 | GRCh38.p7 | 2:214155239 | aaatctatcttaagc[A/G]ttagaaggaaaatcc | 79582 |
rs12478513 | snp | A/T | 0.484701 | 0.0861117 | intron-variant | SPAG16 | GRCh38.p7 | 2:213905625 | AAATAGCAGCAAATT[A/T]AAAAATTTCCTGCCC | 79582 |
rs12479303 | snp | C/T | 0.284471 | 0.247612 | intron-variant | SPAG16 | GRCh38.p7 | 2:213973296 | cagtcagttgtgtgt[C/T]ttaatggtaatctct | 79582 |
rs12611569 | snp | A/G | 0.472709 | 0.11358 | intron-variant | SPAG16 | GRCh38.p7 | 2:213614675 | GTCATTATAATATTT[A/G]TATCTTAAGTGTGAT | 79582 |
rs12611579 | snp | A/T | 0.135484 | 0.22223 | intron-variant | SPAG16 | GRCh38.p7 | 2:214376732 | CTTGTCTGTTTGACC[A/T]TTTTGAAAAGGGAAA | 79582 |
rs12611585 | snp | A/G | 0.370162 | 0.219229 | intron-variant | SPAG16 | GRCh38.p7 | 2:213931080 | GAAGTTGTTATCTCC[A/G]TGATATTTTAATGTT | 79582 |
rs12611598 | snp | C/T | 0.0752113 | 0.178743 | intron-variant | SPAG16 | GRCh38.p7 | 2:213751391 | TCAATATTAGAATAA[C/T]GTAAATAAGTTCTCC | 79582 |
rs12611857 | snp | G/T | 0.463451 | 0.130149 | intron-variant | SPAG16 | GRCh38.p7 | 2:214276811 | tttgtggtgttctct[G/T]tatttcctgaatttc | 79582 |
rs12611867 | snp | C/T | 0 | 0 | intron-variant | SPAG16 | GRCh38.p7 | 2:213630503 | TAAGTTATATTTCTT[C/T]TAACATTTATCAGTG | 79582 |
rs12612583 | snp | A/G | 0.162253 | 0.234095 | intron-variant | SPAG16 | GRCh38.p7 | 2:213791811 | AATGTTTTAAGTCAC[A/G]TTTTGCAAAGTTTAT | 79582 |
rs12612629 | snp | A/C | | | intron-variant | SPAG16 | GRCh38.p7 | 2:214080581 | cctctgcactccagc[A/C]tgggcgacagagcga | 79582 |
rs12612721 | snp | C/T | 0.239037 | 0.24976 | intron-variant | SPAG16 | GRCh38.p7 | 2:213918146 | gatggattagttttt[C/T]gatgtgctgctggaa | 79582 |
rs12612907 | snp | C/T | 0.34303 | 0.232046 | intron-variant | SPAG16 | GRCh38.p7 | 2:214177068 | AGATTATTTCAAGAA[C/T]TATGTTTGGAATAAA | 79582 |
rs12613120 | snp | G/T | 0 | 0 | intron-variant | SPAG16 | GRCh38.p7 | 2:213832116 | ggttctcctgcctca[G/T]cctcgtgagtagctg | 79582 |
rs12613125 | snp | A/G | 0.335101 | 0.23507 | intron-variant | SPAG16 | GRCh38.p7 | 2:213944924 | gcacctgtaatccca[A/G]ctacttgggaggctg | 79582 |
rs12613155 | snp | A/G | 0.0107246 | 0.0724382 | intron-variant | SPAG16 | GRCh38.p7 | 2:213320781 | taataacattccatt[A/G]tgtatatgtgccaca | 79582 |
rs12613493 | snp | A/G | 0.34437 | 0.231505 | intron-variant | SPAG16 | GRCh38.p7 | 2:213366669 | cccttgacacatggg[A/G]attatgggagctaca | 79582 |
rs12613522 | snp | A/G | 0.125182 | 0.216612 | intron-variant | SPAG16 | GRCh38.p7 | 2:213874949 | CATCCTTATAGAAAT[A/G]TTATTTTTTAAGAAA | 79582 |
rs12613612 | snp | C/T | 0.406986 | 0.194565 | intron-variant | SPAG16 | GRCh38.p7 | 2:213692214 | ACCTAATTATTGTCA[C/T]TCAAAAATAATAATT | 79582 |
rs12613679 | snp | A/T | 0.00995 | 0.0698283 | intron-variant | SPAG16 | GRCh38.p7 | 2:213919214 | tggttttgtatctta[A/T]taagttttttaaatt | 79582 |
rs12614799 | snp | C/G/T | 0.00358923 | 0.042236 | intron-variant | SPAG16 | GRCh38.p7 | 2:213489172 | CAAAAATTCATGATA[C/G/T]GAGCCTTCTCTCAGA | 79582 |
rs12615459 | snp | A/G | 0 | 0 | intron-variant | SPAG16 | GRCh38.p7 | 2:213333261 | atccaacttacaata[A/G]ccatggataaaatta | 79582 |
rs12615572 | snp | A/G | | | intron-variant | SPAG16 | GRCh38.p7 | 2:213599591 | tattgtaagaataca[A/G]tatataatacacgta | 79582 |
rs12616056 | snp | G/T | 0 | 0 | intron-variant | SPAG16 | GRCh38.p7 | 2:213524458 | gactgcagaatggta[G/T]gtccactgacagttt | 79582 |
rs12616176 | snp | C/T | 0.376989 | 0.215346 | intron-variant | SPAG16 | GRCh38.p7 | 2:213906433 | TATTGTTAAAATGGC[C/T]GTAATACCCAAAGTG | 79582 |
rs12616248 | snp | C/T | 0.346368 | 0.23068 | intron-variant | SPAG16 | GRCh38.p7 | 2:214185983 | TCTGTTAGGGCAGAG[C/T]CCTTGTTTGTCTTCT | 79582 |
rs12616376 | snp | A/G | 0.382666 | 0.211895 | intron-variant | SPAG16 | GRCh38.p7 | 2:213482516 | GGTTTATAAAATCAA[A/G]TGGTATAATGATTCT | 79582 |
rs12616765 | snp | A/G | 0.0803491 | 0.183626 | intron-variant | SPAG16 | GRCh38.p7 | 2:214119994 | TAATTTTTCTATGCT[A/G]TGTCTACATGTAGAT | 79582 |
rs12616916 | snp | A/T | | | intron-variant | SPAG16 | GRCh38.p7 | 2:213956279 | ttttttaaattgttt[A/T]tctattctctttttt | 79582 |
rs12617047 | snp | C/T | 0.0130921 | 0.0798413 | intron-variant | SPAG16 | GRCh38.p7 | 2:213877221 | TTAAGGATATCTTTC[C/T]CCAACCCTTAAATTA | 79582 |
rs12617276 | snp | G/T | 0.345482 | 0.231048 | intron-variant | SPAG16 | GRCh38.p7 | 2:214196369 | CCAGAGGAACTTCAT[G/T]ATGTTTAGATACCAC | 79582 |
rs12617283 | snp | C/G | 0.00934559 | 0.067716 | intron-variant | SPAG16 | GRCh38.p7 | 2:214321606 | AAAAGGGAATTTCTT[C/G]AATTGTAACATTTAA | 79582 |
rs12617636 | snp | C/T | 0.369346 | 0.219673 | intron-variant | SPAG16 | GRCh38.p7 | 2:213462282 | ACTATGCAGACAGTA[C/T]ATGGAGTTAATTTCA | 79582 |
rs12617938 | snp | A/G | 0.472709 | 0.11358 | intron-variant | SPAG16 | GRCh38.p7 | 2:213614752 | TAAGATATTAATGGG[A/G]CATTAGTATAATCTT | 79582 |
rs12618011 | snp | G/T | | | intron-variant | SPAG16 | GRCh38.p7 | 2:213633449 | tgctctaatatatag[G/T]ctatcattgagaatg | 79582 |
rs12618225 | snp | A/G | 0.391024 | 0.206427 | intron-variant | SPAG16 | GRCh38.p7 | 2:213542115 | TAATTAAAAAGAAAC[A/G]TAACAAGAACACAGT | 79582 |
rs12618720 | snp | C/T | 0.441977 | 0.16014 | intron-variant | SPAG16 | GRCh38.p7 | 2:213734813 | GAATTATTTTTAAAC[C/T]TTTGAAAAGTAGCAT | 79582 |
rs12618987 | snp | G/T | 0.348574 | 0.229746 | intron-variant | SPAG16 | GRCh38.p7 | 2:214189195 | GTTAAATTAACATCA[G/T]AAAGCAGAATTTGCA | 79582 |
rs12619224 | snp | A/C | 0 | 0 | intron-variant | SPAG16 | GRCh38.p7 | 2:213661859 | TTCCTGAATTACCCC[A/C]CCTTATAATTATCCA | 79582 |
rs12619432 | snp | C/T | 0.378174 | 0.214642 | intron-variant, utr-variant-3-prime | SPAG16 | GRCh38.p7 | 2:213369534 | agtgcataatttacC[C/T]ACAATAAAATGCATA | 79582 |
rs12619558 | snp | A/C | 0 | 0 | intron-variant | SPAG16 | GRCh38.p7 | 2:213521252 | gattgagctactgga[A/C]ccatgctgatttggg | 79582 |
rs12619750 | snp | A/T | 0.34437 | 0.231505 | intron-variant | SPAG16 | GRCh38.p7 | 2:213366670 | ccttgacacatgggg[A/T]ttatgggagctacaa | 79582 |
rs12619901 | snp | C/T | 0.348134 | 0.229934 | intron-variant | SPAG16 | GRCh38.p7 | 2:214160333 | AATATTTGATTTTTT[C/T]CTTGTATTTATACTA | 79582 |
rs12620357 | snp | C/T | 0.461037 | 0.134028 | intron-variant | SPAG16 | GRCh38.p7 | 2:213847084 | ccttcatcttcaaaa[C/T]aggctaggcagatta | 79582 |
rs12620361 | snp | C/T | 0.486067 | 0.0822953 | intron-variant | SPAG16 | GRCh38.p7 | 2:213847130 | tgagtctctctgacc[C/T]accctctgtctcatt | 79582 |
rs12620384 | snp | A/G | 0.480302 | 0.0972668 | intron-variant | SPAG16 | GRCh38.p7 | 2:213798687 | tgaaaatttactcca[A/G]tgttttctgttttat | 79582 |
rs12620411 | snp | A/G | 0.473543 | 0.111932 | intron-variant | SPAG16 | GRCh38.p7 | 2:213798784 | agggtagaaatttat[A/G]tttttacaatggatg | 79582 |
rs12620874 | snp | A/T | 0.364193 | 0.222396 | intron-variant | SPAG16 | GRCh38.p7 | 2:213633254 | ttccaatatgttggc[A/T]tatagttgctcacac | 79582 |
rs12620889 | snp | A/T | 0.45843 | 0.138046 | intron-variant | SPAG16 | GRCh38.p7 | 2:214066507 | CATATCTCCTTCCCA[A/T]ATTTATTATAGTTGT | 79582 |
rs12621291 | snp | A/G | 0.104149 | 0.203046 | intron-variant | SPAG16 | GRCh38.p7 | 2:214276552 | ttctacttcacttac[A/G]atgcttagtttggct | 79582 |
rs12622100 | snp | C/T | 0.358515 | 0.225221 | intron-variant | SPAG16 | GRCh38.p7 | 2:213442835 | aacagaaaatctaga[C/T]taccttggatttggt | 79582 |
rs12622627 | snp | A/T | 0.392881 | 0.205147 | intron-variant | SPAG16 | GRCh38.p7 | 2:213906490 | CAAAATACCAATTAC[A/T]TTATTCACAGAAATA | 79582 |
rs12622779 | snp | A/G | 0.140242 | 0.224618 | intron-variant | SPAG16 | GRCh38.p7 | 2:213728647 | TTGGGAGGCCGAAGC[A/G]GGCGGATCACCTGAG | 79582 |
rs12622832 | snp | G/T | 0.00943375 | 0.0680285 | intron-variant | SPAG16 | GRCh38.p7 | 2:214348184 | aggagtgataaccta[G/T]aaactgaacctaaag | 79582 |
rs12622833 | snp | A/G | 0.140242 | 0.224618 | intron-variant | SPAG16 | GRCh38.p7 | 2:213728771 | AGTCCCAGCTGCTCG[A/G]CAGGCTGAGGCAGGA | 79582 |
rs12623115 | snp | A/G | 0.0648419 | 0.167978 | intron-variant | SPAG16 | GRCh38.p7 | 2:213595325 | ATTTTAATATCATGC[A/G]GTTACTTTCATTAAT | 79582 |
rs12623379 | snp | A/T | 0.346368 | 0.23068 | intron-variant | SPAG16 | GRCh38.p7 | 2:214185624 | TTCGAAGAATGGACA[A/T]CTGTACATAAACTGG | 79582 |
rs12623569 | snp | A/C | 0.389018 | 0.207784 | missense, nc-transcript-variant, intron-variant | SPAG16 | GRCh38.p7 | 2:213930019 | TATGGGATCTATGTA[A/C]AGGCGATTGCATTTT | 79582 |
rs12694301 | snp | A/G | 0.5 | 0 | intron-variant | SPAG16 | GRCh38.p7 | 2:213302647 | TGTGTGTGTGTGTGT[A/G]TGTGTGTGTGTGTTG | 79582 |
rs12694302 | snp | C/T | 0.046775 | 0.145601 | intron-variant, upstream-variant-2KB | SPAG16 | GRCh38.p7 | 2:213342775 | TGACTGGACAAAATA[C/T]ATGAGGCAGTTTTTT | 79582 |
rs12694303 | snp | C/T | 0.484632 | 0.086302 | intron-variant | SPAG16 | GRCh38.p7 | 2:213447259 | gaggttcagctcatt[C/T]tttcccttaaaatgg | 79582 |
rs12694304 | snp | C/T | 0.484138 | 0.0876334 | intron-variant | SPAG16 | GRCh38.p7 | 2:213470461 | taagtgtgtattcca[C/T]tgggcacaaatctct | 79582 |
rs12694305 | snp | A/G | 0.482683 | 0.0914256 | intron-variant | SPAG16 | GRCh38.p7 | 2:213508658 | cattcacagcaaact[A/G]tcgcaaggacaaaaa | 79582 |
rs12694306 | snp | C/T | 0.482234 | 0.0925596 | intron-variant | SPAG16 | GRCh38.p7 | 2:213539085 | TTAGATTAAGATTTG[C/T]CTTCTTGTGCTTTCG | 79582 |
rs12694307 | snp | A/T | 0.432063 | 0.171327 | intron-variant | SPAG16 | GRCh38.p7 | 2:213615106 | AGTTGACAGACGGTT[A/T]ATCTGCAAATACTTA | 79582 |
rs12694309 | snp | G/T | 0.413914 | 0.188765 | intron-variant | SPAG16 | GRCh38.p7 | 2:213677642 | agtgatctacaaaga[G/T]aattagactcccaca | 79582 |
rs12694310 | snp | C/G | 0.433963 | 0.169285 | intron-variant | SPAG16 | GRCh38.p7 | 2:213681730 | TCTGAAATATGCATA[C/G]CAAAATACCCCAGAG | 79582 |
rs12694311 | snp | A/T | 0.254105 | 0.249966 | intron-variant | SPAG16 | GRCh38.p7 | 2:213727861 | attttattttatttt[A/T]ttttgagacggaatt | 79582 |
rs12694313 | snp | A/G | 0 | 0 | intron-variant | SPAG16 | GRCh38.p7 | 2:214037867 | tcccagaagcctggt[A/G]tgtgtgtgtgtgtgt | 79582 |
rs12694316 | snp | G/T | 0.239614 | 0.249784 | intron-variant | SPAG16 | GRCh38.p7 | 2:214113845 | tgtcaaagtctttct[G/T]catccagctttgttc | 79582 |
rs12694317 | snp | C/T | 0.452597 | 0.146474 | intron-variant | SPAG16 | GRCh38.p7 | 2:214132169 | TTGAAAGAGTTCTAT[C/T]GCAAATATGAGAAGT | 79582 |
rs12694318 | snp | A/G | 0.457737 | 0.139088 | intron-variant | SPAG16 | GRCh38.p7 | 2:214136191 | TCATGAGTGAGCCAC[A/G]CCTATGACTCAAAAA | 79582 |
rs12694319 | snp | C/T | 0.45762 | 0.139261 | intron-variant | SPAG16 | GRCh38.p7 | 2:214136232 | TGCCCTACTCTAACA[C/T]TGGGGATCATATTTC | 79582 |
rs12694320 | snp | A/C | 0.480853 | 0.0959518 | intron-variant | SPAG16 | GRCh38.p7 | 2:214255947 | catagtctctcatga[A/C]agtgttttcatttct | 79582 |
rs12694321 | snp | C/T | 0.499913 | 0.00658888 | intron-variant | SPAG16 | GRCh38.p7 | 2:214256048 | ttctcataataagga[C/T]ataatgttatattcc | 79582 |
rs12694322 | snp | A/G | 0 | 0 | intron-variant | SPAG16 | GRCh38.p7 | 2:214289011 | ctgacctcgtgatcc[A/G]cctgctttggcctcc | 79582 |
rs12694323 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | SPAG16 | GRCh38.p7 | 2:214306202 | tggtgtattggaatg[A/C]tagtgaattttgcac | 79582 |
rs12694325 | snp | C/T | 0.459004 | 0.137176 | intron-variant | SPAG16 | GRCh38.p7 | 2:214351531 | ACGGTGAAACCCCGT[C/T]TCTACTAAAAAAATA | 79582 |
rs12694326 | snp | A/C | 0.47023 | 0.118317 | intron-variant | SPAG16 | GRCh38.p7 | 2:214352073 | GCAGAAGGGGCAAAC[A/C]AGCTGCCTTGCACCT | 79582 |
rs12694328 | snp | C/T | 0 | 0 | intron-variant | SPAG16 | GRCh38.p7 | 2:214355564 | ataggaacacttgta[C/T]actgttggtgggact | 79582 |
rs12986556 | snp | A/G | 0.170733 | 0.237101 | intron-variant | SPAG16 | GRCh38.p7 | 2:214031570 | ctgcacattgtgcac[A/G]tgtaccctaaaactt | 79582 |
rs12986616 | snp | A/C | 0 | 0 | intron-variant | SPAG16 | GRCh38.p7 | 2:213489180 | CATGATATGAGCCTT[A/C]TCTCAGAGCAATTTT | 79582 |
rs12986619 | snp | A/C | 0 | 0 | intron-variant | SPAG16 | GRCh38.p7 | 2:213489182 | TGATATGAGCCTTCT[A/C]TCAGAGCAATTTTAA | 79582 |
rs12987615 | snp | A/G | 0.356811 | 0.226034 | intron-variant | SPAG16 | GRCh38.p7 | 2:213489497 | CCTTAGATTTAAAAA[A/G]AAAATCATAATCAAT | 79582 |
rs12987971 | snp | A/T | 0.32153 | 0.239548 | intron-variant | SPAG16 | GRCh38.p7 | 2:214136976 | TCTGCCATTTGCTTG[A/T]TGACCCCTCTTACTT | 79582 |
rs12988010 | snp | A/G | 0.342806 | 0.232136 | intron-variant | SPAG16 | GRCh38.p7 | 2:213459605 | ACCCATTTCTTGGAA[A/G]GTCTTCAGCTTCAGT | 79582 |
rs12988372 | snp | C/T | | | upstream-variant-2KB, synonymous-codon, nc-transcript-variant | VWC2L, SPAG16 | GRCh38.p7 | 2:214410273 | CGACGGGGAGATTCT[C/T]TTTTCTGGAGGCTCT | 79582 |
rs12988374 | snp | C/T | | | upstream-variant-2KB, missense, nc-transcript-variant | VWC2L, SPAG16 | GRCh38.p7 | 2:214410278 | GGGAGATTCTCTTTT[C/T]TGGAGGCTCTGACGG | 79582 |
rs12988703 | snp | A/G | 0.367091 | 0.220884 | intron-variant | SPAG16 | GRCh38.p7 | 2:213514376 | AACTTTGAAGATAAT[A/G]TAAGAATATTATCAT | 79582 |
rs12989273 | snp | C/G/T | 0.581731 | 0.123126 | intron-variant | SPAG16 | GRCh38.p7 | 2:213292446 | GAGGCGGGCGGATCA[C/G/T]GAGGTCAGGAGATCG | 79582 |
rs12989673 | snp | A/T | | | intron-variant | SPAG16 | GRCh38.p7 | 2:213720647 | catctaaaaacttaa[A/T]taaataaagaaaaaa | 79582 |
rs12990163 | snp | A/G | 0.29789 | 0.24537 | intron-variant | SPAG16 | GRCh38.p7 | 2:213720593 | cagtgagtggagatc[A/G]cgccactgcactcca | 79582 |
rs12990193 | snp | G/T | | | intron-variant | SPAG16 | GRCh38.p7 | 2:213720623 | agcctgggcgacaga[G/T]aaagactccatctaa | 79582 |
rs12990621 | snp | G/T | | | intron-variant | SPAG16 | GRCh38.p7 | 2:213477741 | acttgccttgtctca[G/T]atgagactttggact | 79582 |
rs12990693 | snp | C/T | 0.448323 | 0.15221 | intron-variant | SPAG16 | GRCh38.p7 | 2:214271104 | TTGAAGGGTAAAGTA[C/T]AATTCTGATACTTTT | 79582 |
rs12990803 | snp | A/T | 0.346147 | 0.230772 | intron-variant | SPAG16 | GRCh38.p7 | 2:214183329 | AAAGAGGAGAATTAC[A/T]GGTGAAGAGAAGCTT | 79582 |
rs12990887 | snp | C/T | | | intron-variant | SPAG16 | GRCh38.p7 | 2:213834672 | ggtctatgacatatc[C/T]tttgggagaaaatga | 79582 |
rs12990890 | snp | G/T | | | intron-variant | SPAG16 | GRCh38.p7 | 2:213896655 | TTCTATTATGTGTGT[G/T]TTTATATATACAATT | 79582 |
rs12990956 | snp | A/G | | | intron-variant | SPAG16 | GRCh38.p7 | 2:213471900 | ttatccttcacctta[A/G]aaggaatgtcttgaa | 79582 |
rs12991052 | snp | C/T | 0.343254 | 0.231956 | intron-variant | SPAG16 | GRCh38.p7 | 2:214176203 | TGACAAATAACTATG[C/T]GGTGAAATGGATCCA | 79582 |
rs12991841 | snp | C/T | 0.342806 | 0.232136 | intron-variant | SPAG16 | GRCh38.p7 | 2:213796253 | gaattgtgcaactat[C/T]ttctcaacctaattt | 79582 |
rs12991954 | snp | C/T | 0.399432 | 0.200425 | intron-variant | SPAG16 | GRCh38.p7 | 2:214153809 | GTCAAGATATAAACA[C/T]ATAGGAATCACCCCC | 79582 |
rs12991971 | snp | G/T | 0.398714 | 0.200958 | intron-variant | SPAG16 | GRCh38.p7 | 2:214153825 | ATAGGAATCACCCCC[G/T]AGAGTTTAGCTTTTC | 79582 |
rs12992361 | snp | C/G | | | intron-variant | SPAG16 | GRCh38.p7 | 2:213407625 | agagagagagagaga[C/G]agagagagagagaga | 79582 |
rs12992569 | snp | A/G | | | intron-variant | SPAG16 | GRCh38.p7 | 2:213407681 | gagagagacagagag[A/G]agagagacagaagag | 79582 |
rs12992660 | snp | A/C | | | intron-variant | SPAG16 | GRCh38.p7 | 2:214355892 | catggatgaaattgg[A/C]aatcatcattctcag | 79582 |
rs12992661 | snp | A/C | | | intron-variant | SPAG16 | GRCh38.p7 | 2:214355893 | atggatgaaattgga[A/C]atcatcattctcagt | 79582 |
rs12992679 | snp | A/C | | | intron-variant | SPAG16 | GRCh38.p7 | 2:214355911 | catcattctcagtaa[A/C]ctatcgcaaggacaa | 79582 |
rs12992686 | snp | A/T | | | intron-variant | SPAG16 | GRCh38.p7 | 2:214355923 | taaactatcgcaagg[A/T]caaaaaaccaaacac | 79582 |
rs12992687 | snp | A/T | | | intron-variant | SPAG16 | GRCh38.p7 | 2:214355925 | aactatcgcaaggac[A/T]aaaaaccaaacaccg | 79582 |
rs12992734 | snp | C/T | | | intron-variant | SPAG16 | GRCh38.p7 | 2:214298115 | atatatatatatata[C/T]acacacacacacaca | 79582 |
rs12992797 | snp | A/G | | | intron-variant | SPAG16 | GRCh38.p7 | 2:213407769 | agagacaggagagag[A/G]cagagagagacagag | 79582 |
rs12992799 | snp | C/T | 0.346368 | 0.23068 | intron-variant | SPAG16 | GRCh38.p7 | 2:213817603 | cccatcaacagtgga[C/T]tgaataaagaaaata | 79582 |
rs12992821 | snp | A/G | | | intron-variant | SPAG16 | GRCh38.p7 | 2:213407804 | agagagacaggagag[A/G]cagagagagagagag | 79582 |
rs12992873 | snp | A/C | | | intron-variant | SPAG16 | GRCh38.p7 | 2:214355967 | tcataggtgggaatt[A/C]acaatgagaacacat | 79582 |
rs12992883 | snp | A/C | | | intron-variant | SPAG16 | GRCh38.p7 | 2:214355976 | ggaattaacaatgag[A/C]acacatggacacagg | 79582 |
rs12992884 | snp | A/C | | | intron-variant | SPAG16 | GRCh38.p7 | 2:214355977 | gaattaacaatgaga[A/C]cacatggacacagga | 79582 |
rs12992934 | snp | C/T | | | intron-variant | SPAG16 | GRCh38.p7 | 2:214298173 | atacacacacacaca[C/T]acatatatatatatt | 79582 |
rs12993230 | snp | A/G | | | intron-variant | SPAG16 | GRCh38.p7 | 2:214275300 | tctctatctccttca[A/G]atctgctctgatctt | 79582 |
rs12993331 | snp | A/C | 0 | 0 | intron-variant, upstream-variant-2KB | SPAG16 | GRCh38.p7 | 2:213342153 | CTTTAAAATTCTTCA[A/C]CCATCCACAGATTAC | 79582 |
rs12993587 | snp | G/T | 0 | 0 | intron-variant | SPAG16 | GRCh38.p7 | 2:213781878 | AAATTTAAATTACTG[G/T]TTAAGATCTCCAAAA | 79582 |
rs12993729 | snp | C/T | | | intron-variant | SPAG16 | GRCh38.p7 | 2:213307355 | tgctatccctccccc[C/T]tccccccaccccaca | 79582 |
rs12993740 | snp | A/C | | | intron-variant, upstream-variant-2KB | SPAG16 | GRCh38.p7 | 2:213342275 | AAGTGtatatatatt[A/C]catacatatgtatat | 79582 |
rs12993900 | snp | C/G | 0.35809 | 0.225425 | intron-variant | SPAG16 | GRCh38.p7 | 2:213490343 | TAAAAATGCACAAAT[C/G]ATTTTTAGAGAAGTT | 79582 |
rs12993957 | snp | A/C | | | intron-variant, upstream-variant-2KB | SPAG16 | GRCh38.p7 | 2:213342363 | atgtatatatatatt[A/C]catatatatgtatta | 79582 |
rs12994113 | snp | A/G | 0.34437 | 0.231505 | intron-variant | SPAG16 | GRCh38.p7 | 2:214174878 | AGAGGCCCTCAATAA[A/G]TAACCACTTCATTCA | 79582 |
rs12994118 | snp | A/T | 0.34437 | 0.231505 | intron-variant | SPAG16 | GRCh38.p7 | 2:214174881 | GGCCCTCAATAAATA[A/T]CCACTTCATTCAGTT | 79582 |
rs12994199 | snp | A/T | | | intron-variant | SPAG16 | GRCh38.p7 | 2:213555555 | aaacctcttcccttt[A/T]taaattacccagtct | 79582 |
rs12994994 | snp | A/G | 0.479663 | 0.0987666 | intron-variant | SPAG16 | GRCh38.p7 | 2:214356665 | ACATAAACATTTACC[A/G]TAAAGATAATCCATG | 79582 |
rs12995032 | snp | A/G | | | intron-variant | SPAG16 | GRCh38.p7 | 2:214386815 | gctgcagtgagccaa[A/G]attgtgccattgcat | 79582 |
rs12995729 | snp | C/G | 0.484279 | 0.0872533 | intron-variant | SPAG16 | GRCh38.p7 | 2:213643811 | tgagacgcagtttca[C/G]tctttgttgtcaagg | 79582 |
rs12995822 | snp | A/T | 0 | 0 | intron-variant | SPAG16 | GRCh38.p7 | 2:213595985 | TGAAAGTTAATGTTC[A/T]TCCTGTGTCAGTCTG | 79582 |
rs12996058 | snp | A/C | 0.462253 | 0.132093 | intron-variant | SPAG16 | GRCh38.p7 | 2:213843948 | TAATATAATATAAAA[A/C]TTATAAAAATTTTAA | 79582 |
rs12996364 | snp | C/T | 0.343924 | 0.231686 | intron-variant | SPAG16 | GRCh38.p7 | 2:214168584 | GAAAGAGTGGATAGT[C/T]ATATTTTAGATAAGA | 79582 |
rs12996833 | snp | C/G | 0.355525 | 0.226637 | intron-variant | SPAG16 | GRCh38.p7 | 2:213566281 | AGGGAAGTGCAAAGC[C/G]TCTTAGAATCAGAAG | 79582 |
rs12996898 | snp | C/T | 0.482384 | 0.0921818 | intron-variant | SPAG16 | GRCh38.p7 | 2:213740112 | AAAATCATATTACAT[C/T]ACACATTACATATAT | 79582 |
rs12997080 | snp | A/G | 0.344815 | 0.231323 | intron-variant | SPAG16 | GRCh38.p7 | 2:213779519 | TCAAAGATGGCTGCC[A/G]TTCACAGCTAAAGCA | 79582 |
rs12997195 | snp | C/T | 0.344815 | 0.231323 | intron-variant | SPAG16 | GRCh38.p7 | 2:213837250 | AGTGATGTGCTAGGG[C/T]ACTAAATAGGAGAAA | 79582 |
rs12997208 | snp | A/G | 0.35574 | 0.226537 | intron-variant | SPAG16 | GRCh38.p7 | 2:213837312 | CCAAGTATAAAAGGA[A/G]TTCTTTTTGTTATGT | 79582 |
rs12997249 | snp | C/G | 0.467836 | 0.13033 | intron-variant | SPAG16 | GRCh38.p7 | 2:214215984 | AGGCCTGATAGATAC[C/G]CATTGCAAAAAGTTA | 79582 |
rs12997433 | snp | G/T | 0.5 | 0 | intron-variant | SPAG16 | GRCh38.p7 | 2:213469602 | ttttttttttcctgg[G/T]ggaatgacccaagcc | 79582 |
rs12997815 | snp | C/T | 0.484561 | 0.0864924 | intron-variant | SPAG16 | GRCh38.p7 | 2:213493929 | TCCTTGCCATTCTCC[C/T]CTGCCATCGGGTTCT | 79582 |
rs12997945 | snp | C/T | 0.350546 | 0.22889 | intron-variant | SPAG16 | GRCh38.p7 | 2:213824957 | ttctctggttaattc[C/T]tagatatttaatttt | 79582 |
rs12998002 | snp | G/T | 0.5 | 0 | intron-variant | SPAG16 | GRCh38.p7 | 2:214059173 | cagagcaagactctg[G/T]ctcTCTCTCTGTCta | 79582 |
rs12998008 | snp | G/T | 0.5 | 0 | intron-variant | SPAG16 | GRCh38.p7 | 2:214059185 | ctgtctcTCTCTCTG[G/T]Ctatatatatatata | 79582 |
rs12998232 | snp | A/T | 0.405429 | 0.195811 | intron-variant | SPAG16 | GRCh38.p7 | 2:214119480 | AACAAAAACTGTAAA[A/T]AATACGTGGCAGGAA | 79582 |
rs12998433 | snp | C/G | 0.222928 | 0.24853 | intron-variant | SPAG16 | GRCh38.p7 | 2:214126119 | tttcacctggcaatg[C/G]ggcaggtcccacctc | 79582 |
rs12999171 | snp | G/T | 0 | 0 | intron-variant | SPAG16 | GRCh38.p7 | 2:213552275 | TTACATTTTGAATTG[G/T]GGACTCTGCAGGTTT | 79582 |
rs12999231 | snp | C/T | | | intron-variant | SPAG16 | GRCh38.p7 | 2:214177725 | ACTTAGCACTGTAGT[C/T]TGCTGAGTATTTATA | 79582 |
rs12999442 | snp | A/T | | | intron-variant | SPAG16 | GRCh38.p7 | 2:214177811 | ataaaaaCCATAAGT[A/T]TGTTCCTATAAGTAA | 79582 |
rs12999651 | snp | A/C | 0 | 0 | intron-variant | SPAG16 | GRCh38.p7 | 2:214269018 | AGAATTATGTTAGAA[A/C]CACAATAATCAGCTA | 79582 |
rs12999652 | snp | A/C | | | intron-variant | SPAG16 | GRCh38.p7 | 2:214269020 | AATTATGTTAGAAAC[A/C]CAATAATCAGCTATT | 79582 |
rs12999791 | snp | A/C | 0 | 0 | intron-variant | SPAG16, LOC101928084 | GRCh38.p7 | 2:214093406 | CTATACATTTTATTT[A/C]ATCTCTTCTATCATT | 79582 |
rs13000000 | snp | C/T | | | intron-variant | SPAG16 | GRCh38.p7 | 2:213929001 | ATTTCTTTTCTTTTC[C/T]ttttttttttttttt | 79582 |
rs13000007 | snp | A/G | | | intron-variant | SPAG16 | GRCh38.p7 | 2:213767673 | cacacacacacacac[A/G]cacacaAAATCAGAT | 79582 |
rs13000060 | snp | C/T | 0.208474 | 0.246527 | intron-variant | SPAG16 | GRCh38.p7 | 2:214056116 | ACAGGAAGCTTTGAC[C/T]CTTAATACCCCCTTT | 79582 |
rs13000730 | snp | A/T | 0.364193 | 0.222396 | intron-variant | SPAG16 | GRCh38.p7 | 2:213636908 | tggcaaaaagtgaca[A/T]tttgacttccttttt | 79582 |
rs13001040 | snp | A/T | | | intron-variant | SPAG16 | GRCh38.p7 | 2:213540030 | CATTATATTTCTTAA[A/T]ttttttttttttttt | 79582 |
rs13001102 | snp | C/T | 0.431916 | 0.171483 | intron-variant | SPAG16 | GRCh38.p7 | 2:213665229 | CACATGTTATGTTTA[C/T]ATTAGCTTTCCAACT | 79582 |
rs13001335 | snp | A/G | 0 | 0 | intron-variant, upstream-variant-2KB | SPAG16 | GRCh38.p7 | 2:213343584 | aattagcaggcaggg[A/G]ctttacaacagttat | 79582 |
rs13001691 | snp | A/G | 0 | 0 | intron-variant | SPAG16 | GRCh38.p7 | 2:213431589 | tgcaccaaacaccag[A/G]ggacacagattcata | 79582 |
rs13001807 | snp | A/T | 0.358728 | 0.225118 | intron-variant | SPAG16 | GRCh38.p7 | 2:213792719 | CTCCCGAGTAGCTGG[A/T]ATTACAGGCATGAGC | 79582 |
rs13002044 | snp | C/G | 0.363985 | 0.222503 | intron-variant | SPAG16 | GRCh38.p7 | 2:213697492 | ttatatgacaaaaga[C/G]actttgcagatgtga | 79582 |
rs13002516 | snp | G/T | 0.454182 | 0.144256 | intron-variant | SPAG16 | GRCh38.p7 | 2:214234071 | gccccagtatgtgtt[G/T]tttccccccccatgt | 79582 |
rs13002799 | snp | C/T | 0.20511 | 0.245937 | intron-variant | SPAG16 | GRCh38.p7 | 2:214023844 | TAGATTTTTGTATAT[C/T]GGTATCAGCCTTTGA | 79582 |
rs13002822 | snp | G/T | 0.204803 | 0.245881 | intron-variant | SPAG16 | GRCh38.p7 | 2:214051324 | ATTAAACTAAGGGTA[G/T]AAATAAGAAGACCAA | 79582 |
rs13002854 | snp | G/T | | | intron-variant | SPAG16 | GRCh38.p7 | 2:213469928 | tgttgtgtctcctgg[G/T]ggaagcattcccctc | 79582 |
rs13003532 | snp | A/C/G | 0.00159617 | 0.0282053 | intron-variant | SPAG16 | GRCh38.p7 | 2:213449079 | ctgggaaacgaatgt[A/C/G]ttcctggggggaggt | 79582 |
rs13003599 | snp | A/T | 0.00199481 | 0.0315187 | intron-variant | SPAG16 | GRCh38.p7 | 2:213977698 | atgaatggtagtgca[A/T]gttcacactgagtaa | 79582 |
rs13003824 | snp | C/T | 0.480302 | 0.0972668 | intron-variant | SPAG16 | GRCh38.p7 | 2:214255817 | TCCCTTATTTCTGAG[C/T]AGTATTCTATTATAT | 79582 |
rs13004031 | snp | C/G | 0.00119737 | 0.0244387 | intron-variant | SPAG16 | GRCh38.p7 | 2:213722700 | AAGTAAGATACAAGA[C/G]AGATATGACAATATT | 79582 |
rs13004150 | snp | G/T | 0.00975586 | 0.0691575 | intron-variant | SPAG16 | GRCh38.p7 | 2:214154926 | tcagacatgtaatat[G/T]tggcaataaaaaact | 79582 |
rs13004439 | snp | A/C | 0.484138 | 0.0876334 | intron-variant | SPAG16 | GRCh38.p7 | 2:213621938 | GATCTCTTATTATTT[A/C]TCACTTCACAATAAG | 79582 |
rs13004604 | snp | A/G | 0.344147 | 0.231595 | intron-variant | SPAG16 | GRCh38.p7 | 2:213845558 | CAATATGTACACGAA[A/G]AATTTCTTCTTTCAA | 79582 |
rs13004882 | snp | C/T | 0.347253 | 0.230308 | intron-variant | SPAG16 | GRCh38.p7 | 2:214187233 | ACACACACAAAGTTC[C/T]GGTATATTCCTGTTT | 79582 |
rs13005015 | snp | C/T | 0.00716266 | 0.059414 | intron-variant, utr-variant-3-prime | SPAG16 | GRCh38.p7 | 2:213399957 | ttttttattatcttt[C/T]aaatctcaaatggat | 79582 |
rs13005075 | snp | C/G | 0 | 0 | intron-variant | SPAG16 | GRCh38.p7 | 2:213567721 | tctttatagcagcat[C/G]atttatagtcctttg | 79582 |
rs13005544 | snp | A/G | 0.34303 | 0.232046 | intron-variant | SPAG16 | GRCh38.p7 | 2:213805298 | AGTCTTGGGGTCTAT[A/G]TTTTCAAACTGGGAG | 79582 |
rs13005828 | snp | G/T | 0.360842 | 0.224085 | intron-variant | SPAG16 | GRCh38.p7 | 2:213488139 | TATTTTGTTTAGTGA[G/T]ATATTAAAAGAACTG | 79582 |
rs13005851 | snp | A/G | 0.478271 | 0.101943 | intron-variant | SPAG16 | GRCh38.p7 | 2:214340268 | ATTCACAGCATATGG[A/G]AAGGGTACACACGTA | 79582 |
rs13005887 | snp | A/G | 0.127254 | 0.217792 | intron-variant | SPAG16 | GRCh38.p7 | 2:214340329 | CTTTCACCTGCCCCA[A/G]CGTTATCCATTTTTG | 79582 |
rs13005916 | snp | A/T | 0.34526 | 0.23114 | intron-variant | SPAG16 | GRCh38.p7 | 2:213819110 | GAAGGAGTGGAACAT[A/T]TCTTTATAAAATAGA | 79582 |
rs13006105 | snp | G/T | 0.474634 | 0.109726 | intron-variant | SPAG16 | GRCh38.p7 | 2:214340448 | AATATAACAAAATAG[G/T]GCAGTTTCCAAGTAT | 79582 |
rs13006187 | snp | A/C | 0.338976 | 0.23363 | intron-variant | SPAG16 | GRCh38.p7 | 2:213916213 | tcctggatggtattg[A/C]ctaggttttcttcta | 79582 |
rs13006572 | snp | A/G | 0.31503 | 0.241394 | intron-variant | SPAG16 | GRCh38.p7 | 2:213437510 | AAATCTTTTGCCTCT[A/G]AATTTTGTAAGCTTT | 79582 |
rs13006669 | snp | A/C | 0 | 0 | intron-variant | SPAG16 | GRCh38.p7 | 2:213349713 | aagggaatactactc[A/C]cagtaaaaaggagtg | 79582 |
rs13006749 | snp | A/T | | | intron-variant | SPAG16 | GRCh38.p7 | 2:213833533 | tataatatatatatt[A/T]tatataatatatata | 79582 |
rs13006927 | snp | A/T | | | intron-variant | SPAG16 | GRCh38.p7 | 2:213833578 | tataatatatatata[A/T]tatatatattatata | 79582 |
rs13007000 | snp | A/C | 0.47934 | 0.0995154 | intron-variant | SPAG16 | GRCh38.p7 | 2:213745728 | TGCTTTATTCAAATG[A/C]CATAATTATAAAAAT | 79582 |
rs13007116 | snp | A/C | 0 | 0 | intron-variant | SPAG16 | GRCh38.p7 | 2:214124608 | AATTTACTCATAAGC[A/C]CAATTACAAGAAAAC | 79582 |
rs13007561 | snp | C/T | 0.34526 | 0.23114 | intron-variant | SPAG16 | GRCh38.p7 | 2:213833825 | ATAGTAATTCAGACC[C/T]ATTAGTTATATGGGG | 79582 |
rs13007666 | snp | A/C | 0.366885 | 0.220993 | intron-variant | SPAG16 | GRCh38.p7 | 2:214212656 | CCACCAAGCAAGGAA[A/C]AAGAACTGGAAGAGC | 79582 |
rs13008301 | snp | A/G | 0.413416 | 0.189196 | intron-variant | SPAG16 | GRCh38.p7 | 2:213645106 | ccctttccaaaggca[A/G]aggagcctcactcct | 79582 |
rs13008383 | snp | C/G | 0.00358779 | 0.0422022 | intron-variant | SPAG16 | GRCh38.p7 | 2:214324935 | TTGCACACAGAATGT[C/G]AAATGCATGTCATAA | 79582 |
rs13008455 | snp | A/C | | | intron-variant | SPAG16 | GRCh38.p7 | 2:213492597 | GATACCACCCCCTCT[A/C]CAGACATACACATAC | 79582 |
rs13008575 | snp | A/G | | | intron-variant | SPAG16 | GRCh38.p7 | 2:214395830 | agataatggcctcca[A/G]ctccatccatgttgc | 79582 |
rs13008593 | snp | A/G | 0 | 0 | intron-variant | SPAG16 | GRCh38.p7 | 2:214395852 | ccatgttgctgcaaa[A/G]acataatctcattct | 79582 |
rs13008598 | snp | A/T | 0.32153 | 0.239548 | intron-variant | SPAG16 | GRCh38.p7 | 2:214136476 | ATTGTAATGATGTAG[A/T]GCTGTGTTGTGTACT | 79582 |
rs13008610 | snp | C/T | 0 | 0 | intron-variant | SPAG16 | GRCh38.p7 | 2:213492618 | ATACACATACAGAAT[C/T]TTAGTAAGTCTACAA | 79582 |
rs13008787 | snp | C/T | 0.298398 | 0.245271 | intron-variant | SPAG16 | GRCh38.p7 | 2:213726118 | CTGAGGACTTCCTCT[C/T]CCTGCTGAAGTTCAC | 79582 |
rs13008788 | snp | C/T | 0.333491 | 0.235646 | intron-variant | SPAG16 | GRCh38.p7 | 2:213726119 | TGAGGACTTCCTCTC[C/T]CTGCTGAAGTTCACT | 79582 |
rs13009206 | snp | A/T | | | intron-variant | SPAG16 | GRCh38.p7 | 2:214373915 | tgagcgcacactatg[A/T]gcacaaaactgaacc | 79582 |
rs13009344 | snp | A/C | 0 | 0 | intron-variant | SPAG16 | GRCh38.p7 | 2:213911799 | ATTAGAAAGCAGAGA[A/C]CAATTGAGTAGGTTT | 79582 |
rs13009563 | snp | C/T | 0.5 | 0 | intron-variant | SPAG16 | GRCh38.p7 | 2:214073245 | ttctttttttttttt[C/T]ctttttttttgagac | 79582 |
rs13010455 | snp | A/G | 0.175254 | 0.238565 | intron-variant | SPAG16 | GRCh38.p7 | 2:214235429 | GATATTTAATAGAAG[A/G]TAAAGAATTTAATGT | 79582 |
rs13010563 | snp | A/G | 0.389152 | 0.207694 | intron-variant | SPAG16 | GRCh38.p7 | 2:213927637 | TATTTATTGTTGACT[A/G]AATATCAGTTACAGC | 79582 |
rs13011112 | snp | A/G | 0.270621 | 0.249148 | intron-variant | SPAG16 | GRCh38.p7 | 2:214228713 | CTGATGAAAAGGTAA[A/G]GTTGCACAACTACTC | 79582 |
rs13011158 | snp | A/G | | | intron-variant | SPAG16 | GRCh38.p7 | 2:213869285 | TATATATATATGTAT[A/G]TATATATGTATATAT | 79582 |
rs13011163 | snp | A/G | | | intron-variant | SPAG16 | GRCh38.p7 | 2:213869297 | TATATATATATGTAT[A/G]TATATATATAATATG | 79582 |
rs13011568 | snp | C/T | 0.403334 | 0.197456 | intron-variant | SPAG16 | GRCh38.p7 | 2:214060912 | TTACAGAAGCAATGA[C/T]TTTCAAGACATCAGA | 79582 |
rs13011664 | snp | A/G | | | intron-variant | SPAG16 | GRCh38.p7 | 2:213869281 | tatatatatatatat[A/G]tatatatatatgtat | 79582 |
rs13011666 | snp | A/G | 0.488846 | 0.0738428 | intron-variant | SPAG16 | GRCh38.p7 | 2:213869293 | TATGTATATATATAT[A/G]TATATATATATATAA | 79582 |
rs13011683 | snp | G/T | | | intron-variant | SPAG16 | GRCh38.p7 | 2:213383804 | taatacaataaatag[G/T]gatgttctataatat | 79582 |
rs13012341 | snp | G/T | 0.372189 | 0.218105 | intron-variant | SPAG16 | GRCh38.p7 | 2:213583894 | TTAAAAATAATTTTA[G/T]GTTTCAAAAGGTAGC | 79582 |
rs13013057 | snp | A/G | 0 | 0 | intron-variant | SPAG16 | GRCh38.p7 | 2:213437886 | GTCGCTCTTAAACTA[A/G]GTtcttttggttgca | 79582 |
rs13013058 | snp | C/T | | | intron-variant | SPAG16 | GRCh38.p7 | 2:213584174 | TTTATTTTGCATTTC[C/T]TCATTGGATTTTTTT | 79582 |
rs13013336 | snp | C/T | 0.452473 | 0.146644 | intron-variant | SPAG16 | GRCh38.p7 | 2:213292658 | GACAGAGCGAGACTC[C/T]GTCTCAAAAAAAAAA | 79582 |
rs13013585 | snp | A/C | 0 | 0 | intron-variant | SPAG16 | GRCh38.p7 | 2:214300947 | aaatcaggcaaggac[A/C]caacaacaacaaaag | 79582 |
rs13013586 | snp | A/C | 0 | 0 | intron-variant | SPAG16 | GRCh38.p7 | 2:214300950 | tcaggcaaggacaca[A/C]caacaacaaaagcta | 79582 |
rs13013701 | snp | C/G | 0.320096 | 0.239972 | intron-variant | SPAG16 | GRCh38.p7 | 2:213681331 | AAATCCATCTAATGC[C/G]AATTTATGGTTGTCA | 79582 |
rs13013902 | snp | A/G | | | intron-variant | SPAG16 | GRCh38.p7 | 2:214035093 | tagggtgtcacaaca[A/G]gtattcagctctctg | 79582 |
rs13014055 | snp | C/T | 0.498652 | 0.0259235 | intron-variant | SPAG16 | GRCh38.p7 | 2:214237689 | ACATAATTCCAGTTA[C/T]GAGTTTACTCTTGGG | 79582 |
rs13014099 | snp | A/C | 0.223225 | 0.248562 | intron-variant | SPAG16, LOC101928084 | GRCh38.p7 | 2:214095320 | AAACCCCCCCAGAAA[A/C]CTTTTCTCCAGTTCA | 79582 |
rs13014300 | snp | A/C | 0.251859 | 0.249993 | intron-variant | SPAG16, LOC101928084 | GRCh38.p7 | 2:214095390 | TTCAAATTAATCACA[A/C]GTGTCTATCATACAC | 79582 |
rs13014517 | snp | A/C | | | intron-variant | SPAG16 | GRCh38.p7 | 2:213834671 | gggtctatgacatat[A/C]ttttgggagaaaatg | 79582 |
rs13015722 | snp | C/G | 0.449091 | 0.151204 | intron-variant | SPAG16 | GRCh38.p7 | 2:214271588 | GGTGGATCACCTGAG[C/G]TCAGGAGTTTGAGAC | 79582 |
rs13015797 | snp | A/G | 0.225893 | 0.248835 | intron-variant | SPAG16 | GRCh38.p7 | 2:214118802 | tgatctacaaattca[A/G]tgcaatctctatcaa | 79582 |
rs13015825 | snp | G/T | | | intron-variant | SPAG16 | GRCh38.p7 | 2:213345407 | ccatttgtcaatttt[G/T]gcttttgttgccatt | 79582 |
rs13016014 | snp | A/C | 0.239614 | 0.249784 | intron-variant | SPAG16 | GRCh38.p7 | 2:214113116 | tgaaattctggtttg[A/C]aaattcttaaaggat | 79582 |
rs13016163 | snp | C/G | 0.345482 | 0.231048 | intron-variant | SPAG16 | GRCh38.p7 | 2:213787200 | AAATCTGCACATCCT[C/G]CACACGTACCCTGGA | 79582 |
rs13016366 | snp | A/G | 0.234982 | 0.249549 | intron-variant | SPAG16 | GRCh38.p7 | 2:214113129 | tgcaaattcttaaag[A/G]atgttgaatattgtc | 79582 |
rs13017149 | snp | A/T | | | intron-variant | SPAG16 | GRCh38.p7 | 2:213896657 | CTATTATGTGTgtgt[A/T]tatatatacaattca | 79582 |
rs13017200 | snp | C/G/T | | | intron-variant | SPAG16 | GRCh38.p7 | 2:213471862 | cctctttcttggttg[C/G/T]aggtggggtcaaatt | 79582 |
rs13017202 | snp | G/T | | | intron-variant | SPAG16 | GRCh38.p7 | 2:213471866 | tttcttggttgtagg[G/T]ggggtcaaattcagc | 79582 |
rs13017229 | snp | A/C | 0.349452 | 0.229367 | intron-variant | SPAG16 | GRCh38.p7 | 2:213363187 | TGATGTTAATGGGGG[A/C]AAAAGGGTATGGGAT | 79582 |
rs13017349 | snp | A/G | 0.466204 | 0.125522 | intron-variant | SPAG16 | GRCh38.p7 | 2:214354463 | gttcttttggcttag[A/G]attgacttggcaatg | 79582 |
rs13017566 | snp | G/T | | | intron-variant | SPAG16 | GRCh38.p7 | 2:213715223 | AGGTAGatctatctg[G/T]ctatctatctatcta | 79582 |
rs13017677 | snp | A/T | 0 | 0 | intron-variant | SPAG16 | GRCh38.p7 | 2:214338202 | TTGATAGTATATCTA[A/T]TTCCTGTAACTTTTA | 79582 |
rs13019167 | snp | C/T | | | intron-variant | SPAG16 | GRCh38.p7 | 2:214298159 | acacacacacacata[C/T]acacacacacacaca | 79582 |
rs13019248 | snp | A/C | | | intron-variant | SPAG16 | GRCh38.p7 | 2:213895019 | aaaaaaaaaaaaaaa[A/C]ctgaaagactctacc | 79582 |
rs13019516 | snp | A/G | 0.236434 | 0.249632 | intron-variant | SPAG16 | GRCh38.p7 | 2:214071375 | AGCCTTCAGGCAGTC[A/G]GACTTCTCCCTGGTA | 79582 |
rs13020325 | snp | A/G | 0.485255 | 0.0845871 | intron-variant | SPAG16 | GRCh38.p7 | 2:213624484 | AGAAAAGTTTTAACA[A/G]AGTTTATAGCCCTGG | 79582 |
rs13020625 | snp | A/T | 0.5 | 0 | intron-variant | SPAG16 | GRCh38.p7 | 2:213643348 | tattggatcttaatt[A/T]tatatatatatatat | 79582 |
rs13020757 | snp | C/T | 0.364609 | 0.222182 | intron-variant | SPAG16 | GRCh38.p7 | 2:213696344 | attgacaattggata[C/T]gtgagtttggagttc | 79582 |
rs13020812 | snp | A/T | 0.434543 | 0.168653 | intron-variant | SPAG16 | GRCh38.p7 | 2:214119225 | TTAAATTGAATTTTA[A/T]TTCTCTTATGGTATT | 79582 |
rs13020928 | snp | C/T | 0.364609 | 0.222182 | intron-variant | SPAG16 | GRCh38.p7 | 2:213555635 | gctgtcttttacata[C/T]gagacaagatacata | 79582 |
rs13021887 | snp | A/G | 0.359364 | 0.22481 | intron-variant | SPAG16 | GRCh38.p7 | 2:213426896 | ACAGGGCTACACTCT[A/G]TAGGATCCTTTATTT | 79582 |
rs13022282 | snp | C/T | | | intron-variant | SPAG16 | GRCh38.p7 | 2:213595986 | GAAAGTTAATGTTCA[C/T]CCTGTGTCAGTCTGC | 79582 |
rs13022440 | snp | A/G | 0.108048 | 0.20579 | intron-variant | SPAG16 | GRCh38.p7 | 2:214147368 | ATTTTAATATTCAAT[A/G]GGATAAAGTATACTT | 79582 |
rs13022592 | snp | A/C | | | intron-variant | SPAG16 | GRCh38.p7 | 2:214177802 | TAATAATTAATAAAA[A/C]CCATAAGTTTGTTCC | 79582 |
rs13022876 | snp | A/G | 0.269267 | 0.249256 | intron-variant | SPAG16 | GRCh38.p7 | 2:213765318 | AGGTTGCAGTGAGCC[A/G]AGATCACACCACTGC | 79582 |
rs13023095 | snp | G/T | | | intron-variant | SPAG16 | GRCh38.p7 | 2:214177778 | AACCTAACAAACAAT[G/T]AAGttttataataat | 79582 |
rs13023113 | snp | G/T | | | intron-variant | SPAG16 | GRCh38.p7 | 2:214177809 | taataaaaaCCATAA[G/T]TTTGTTCCTATAAGT | 79582 |
rs13023245 | snp | A/C | 0.339203 | 0.233544 | intron-variant | SPAG16 | GRCh38.p7 | 2:213913670 | atatatgtatatgta[A/C]atatggatatatatg | 79582 |
rs13023752 | snp | C/T | 0.345925 | 0.230864 | intron-variant | SPAG16 | GRCh38.p7 | 2:213846464 | TGACTACAGTTTTTC[C/T]GACTCAATTACAGTG | 79582 |
rs13023832 | snp | A/G | 0.193653 | 0.243567 | intron-variant | SPAG16 | GRCh38.p7 | 2:214355084 | tagaagaaaacctac[A/G]cattaccattcagga | 79582 |
rs13024256 | snp | A/G | 0.472429 | 0.114129 | intron-variant | SPAG16 | GRCh38.p7 | 2:214355302 | atatcaagaatctac[A/G]atgaactcaaacaaa | 79582 |
rs13024295 | snp | A/T | | | intron-variant | SPAG16 | GRCh38.p7 | 2:214126063 | ttccttccttccttt[A/T]ttttttttttttttt | 79582 |
rs13024335 | snp | A/C | 0.431769 | 0.17164 | intron-variant | SPAG16 | GRCh38.p7 | 2:213665252 | TTCCAACTGAAGCTA[A/C]ATTGTGGCTGCATAT | 79582 |
rs13024368 | snp | A/T | | | intron-variant | SPAG16 | GRCh38.p7 | 2:214107695 | GTATTTAAAAATGCC[A/T]CTGtatatattttat | 79582 |
rs13024791 | snp | A/C | | | intron-variant | SPAG16 | GRCh38.p7 | 2:214355804 | atagactggattaag[A/C]aaatgtggcacatat | 79582 |
rs13024805 | snp | A/C | | | intron-variant | SPAG16 | GRCh38.p7 | 2:214355822 | atgtggcacatatac[A/C]ccatggaatactatg | 79582 |
rs13024814 | snp | A/C | | | intron-variant | SPAG16 | GRCh38.p7 | 2:214355832 | tatacaccatggaat[A/C]ctatgcagccataaa | 79582 |
rs13024824 | snp | A/C | 0.339882 | 0.233284 | intron-variant | SPAG16 | GRCh38.p7 | 2:213871251 | AATGGCAGAATAAGG[A/C]CGTTCAAAAATATAT | 79582 |
rs13024923 | snp | C/T | 0.350109 | 0.229081 | intron-variant | SPAG16 | GRCh38.p7 | 2:213387431 | AATGAAATGCATGCT[C/T]TTTTTTTTTTTTTTT | 79582 |
rs13024929 | snp | A/G | | | intron-variant | SPAG16 | GRCh38.p7 | 2:214230671 | TGAAATGCAAAACCA[A/G]GATCTCTCCAGAGGA | 79582 |
rs13025224 | snp | A/G | 0.327211 | 0.237778 | intron-variant | SPAG16 | GRCh38.p7 | 2:213813456 | GATGGAGGGCAGGCG[A/G]GAGACCACAGAGGAC | 79582 |
rs13026541 | snp | A/G | 0.37138 | 0.218556 | intron-variant | SPAG16 | GRCh38.p7 | 2:213682867 | GAACTTAAAATTGCT[A/G]TGTTTGTCCTAGATG | 79582 |
rs13026978 | snp | C/G | 0.477853 | 0.102875 | intron-variant | SPAG16 | GRCh38.p7 | 2:213741046 | CATTAAGTTATTCAA[C/G]TATTAATTTAACGCC | 79582 |
rs13027030 | snp | A/G | 0.345037 | 0.231231 | intron-variant | SPAG16 | GRCh38.p7 | 2:213675862 | taggattgacttggt[A/G]atgcgggctcttttt | 79582 |
rs13027190 | snp | A/C | 0 | 0 | intron-variant | SPAG16 | GRCh38.p7 | 2:213352547 | TCAAGTTGCTCCTTG[A/C]TGGTTTAGTGGAAAG | 79582 |
rs13027499 | snp | C/T | | | intron-variant | SPAG16 | GRCh38.p7 | 2:213859176 | agagcgacactccgt[C/T]tcaaaaaaaaaaaaa | 79582 |
rs13027773 | snp | A/G | 0.00481925 | 0.0488508 | intron-variant | SPAG16 | GRCh38.p7 | 2:214360909 | tgtagtcaattttag[A/G]ggaagagaaaatgat | 79582 |
rs13028423 | snp | A/G | 0.00517822 | 0.0506191 | intron-variant | SPAG16 | GRCh38.p7 | 2:213588671 | gccgggcgcggtggc[A/G]ggcgcctgtagtccc | 79582 |
rs13028530 | snp | G/T | 0.363776 | 0.222609 | intron-variant | SPAG16 | GRCh38.p7 | 2:213603931 | GACTTCCTGGTTTTT[G/T]TTTTTTTTTTGAGAT | 79582 |
rs13028538 | snp | C/T | 0.355311 | 0.226737 | intron-variant | SPAG16 | GRCh38.p7 | 2:213700872 | ATGATCTAGGCCAGG[C/T]GTGGTGGCTCACACA | 79582 |
rs13028775 | snp | C/T | 0.467337 | 0.123551 | intron-variant | SPAG16 | GRCh38.p7 | 2:214215678 | TTTGTAACTCTTTCC[C/T]GTACTGTTGCAATGA | 79582 |
rs13029290 | snp | C/G | 0.364193 | 0.222396 | intron-variant | SPAG16 | GRCh38.p7 | 2:213613393 | tctctgaccttatct[C/G]ctaatgctctgcctc | 79582 |
rs13029303 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | SPAG16 | GRCh38.p7 | 2:214391692 | tcaaatgcctaaaga[A/C]gacgacttccacata | 79582 |
rs13029462 | snp | A/C | 0 | 0 | intron-variant | SPAG16 | GRCh38.p7 | 2:214266629 | ataaaaggtatccaa[A/C]cagaaaagaataaag | 79582 |
rs13029533 | snp | C/T | 0.339882 | 0.233284 | intron-variant | SPAG16 | GRCh38.p7 | 2:213435412 | AGCAGGGGTGAGGGA[C/T]AAGAAATTACTTAAT | 79582 |
rs13029881 | snp | G/T | 0.298144 | 0.245321 | intron-variant | SPAG16 | GRCh38.p7 | 2:213759104 | tgagggcgaaattaa[G/T]acatccccaggaaaa | 79582 |
rs13030061 | snp | C/T | 0.403158 | 0.197592 | intron-variant | SPAG16 | GRCh38.p7 | 2:214236714 | TCCCAGCATTTATTA[C/T]GATTCACCAAATAAG | 79582 |
rs13030280 | snp | A/G | 0.339203 | 0.233544 | intron-variant | SPAG16 | GRCh38.p7 | 2:213914778 | TTGTTGGCCACATGT[A/G]TGTCTTCTTTTGGAA | 79582 |
rs13030419 | snp | A/G | 0.236724 | 0.249647 | intron-variant, nc-transcript-variant | SPAG16, LOC101928084 | GRCh38.p7 | 2:214085374 | ACAGAGGGAGATTCC[A/G]CCTCAAAAAAAAAAA | 79582 |
rs13030454 | snp | A/G | 0.302936 | 0.244331 | intron-variant | SPAG16 | GRCh38.p7 | 2:213458527 | cagtgagctgagatc[A/G]cgccgctgcactcca | 79582 |
rs13030561 | snp | A/G | 0.0091503 | 0.067098 | intron-variant | SPAG16 | GRCh38.p7 | 2:213458805 | ctccctttgaataca[A/G]tatatctatatttcc | 79582 |
rs13030754 | snp | A/G | 0.241627 | 0.24986 | intron-variant | SPAG16 | GRCh38.p7 | 2:214115367 | AAATTTTAGTTATTT[A/G]GTATTAGCCTTGCTC | 79582 |
rs13030947 | snp | C/T | 0.347253 | 0.230308 | intron-variant | SPAG16 | GRCh38.p7 | 2:214187125 | CACTTGAGGAACCAC[C/T]ATGGTAGGACACTAT | 79582 |
rs13031073 | snp | A/C | 0.029116 | 0.117091 | intron-variant | SPAG16 | GRCh38.p7 | 2:214409406 | TGGACTTCCTTAATA[A/C]AAATATTAATTAAAA | 79582 |
rs13031099 | snp | G/T | 0.239326 | 0.249772 | intron-variant | SPAG16 | GRCh38.p7 | 2:214143206 | ATTCATAAAATGGAG[G/T]TGATCACCTATTCCA | 79582 |
rs13031136 | snp | G/T | 0.308908 | 0.242961 | intron-variant | SPAG16 | GRCh38.p7 | 2:213847529 | GTGAACTAAGAGGGA[G/T]AGCTCACTTAGCACC | 79582 |
rs13031278 | snp | C/T | 0.34526 | 0.23114 | intron-variant | SPAG16 | GRCh38.p7 | 2:214196412 | AAAACAGAAAAACTA[C/T]CCTAAGATAGTAGAC | 79582 |
rs13031614 | snp | C/G | 0.343924 | 0.231686 | intron-variant | SPAG16 | GRCh38.p7 | 2:214203790 | agctgaacttcgtaa[C/G]aatttcaaccaaagt | 79582 |
rs13031904 | snp | A/C | 0 | 0 | intron-variant | SPAG16 | GRCh38.p7 | 2:213784430 | TCTTGTTCTCCCTCC[A/C]CCTTGTGTAGTTTAT | 79582 |
rs13032241 | snp | G/T | | | intron-variant | SPAG16 | GRCh38.p7 | 2:214217839 | GAGTGGCTCATGGTG[G/T]TTTGTTAGACATTCT | 79582 |
rs13032246 | snp | A/G | 0.323197 | 0.239044 | intron-variant | SPAG16 | GRCh38.p7 | 2:214136502 | GTACTTTAGCTGCTC[A/G]GTAATTATTTTTGAG | 79582 |
rs13032345 | snp | A/C | | | intron-variant | SPAG16 | GRCh38.p7 | 2:213784612 | CTGGAAAATAAATGC[A/C]CAGCAATTATTTCTa | 79582 |
rs13032348 | snp | C/G | 0.16028 | 0.233346 | intron-variant | SPAG16 | GRCh38.p7 | 2:214136718 | CTTTCCGTTCTAATT[C/G]CATAATTTATTTGCT | 79582 |
rs13032381 | snp | A/C | | | intron-variant | SPAG16 | GRCh38.p7 | 2:213784655 | aaaaaaaaaaaaaaG[A/C]ACTGTGAGAGCTCCG | 79582 |
rs13032382 | snp | A/C | 0 | 0 | intron-variant | SPAG16 | GRCh38.p7 | 2:213784656 | aaaaaaaaaaaaaGA[A/C]CTGTGAGAGCTCCGT | 79582 |
rs13032485 | snp | C/G | | | intron-variant | SPAG16 | GRCh38.p7 | 2:214373917 | agcgcacactatgtg[C/G]acaaaactgaaccat | 79582 |
rs13032543 | snp | C/T | 0.00961516 | 0.0686668 | intron-variant | SPAG16 | GRCh38.p7 | 2:213784625 | GCACAGCAATTATTT[C/T]Taaaaaaaaaaaaaa | 79582 |
rs13032712 | snp | A/T | 0.466927 | 0.124269 | intron-variant | SPAG16 | GRCh38.p7 | 2:213842521 | GAAGTGAATTTTTTT[A/T]AAAAAATAGGAAATG | 79582 |
rs13032855 | snp | C/T | | | intron-variant | SPAG16 | GRCh38.p7 | 2:214073246 | TCTTTTTTTTTTTTT[C/T]TTTTTTTTTGAGACA | 79582 |
rs13033227 | snp | A/T | | | intron-variant | SPAG16 | GRCh38.p7 | 2:213833532 | atataatatatatat[A/T]atatataatatatat | 79582 |
rs13033256 | snp | A/T | | | intron-variant | SPAG16 | GRCh38.p7 | 2:213833559 | atataatatatataa[A/T]atatataatatatat | 79582 |
rs13033427 | snp | A/T | | | intron-variant | SPAG16 | GRCh38.p7 | 2:213833579 | ataatatatatataa[A/T]atatatattatatat | 79582 |
rs13033435 | snp | A/T | | | intron-variant | SPAG16 | GRCh38.p7 | 2:213833587 | tatataatatatata[A/T]tatatatatataAAA | 79582 |
rs13033690 | snp | C/T | 0.231775 | 0.249335 | intron-variant | SPAG16 | GRCh38.p7 | 2:214117364 | aggatcCTACAACAG[C/T]TGCCTGtcaaagaaa | 79582 |
rs13033890 | snp | A/G | 0.375 | 0.216506 | intron-variant, upstream-variant-2KB | SPAG16, LOC101928084 | GRCh38.p7 | 2:214103608 | taaaggaaacagaaa[A/G]cacaaaggcgggagc | 79582 |
rs13033980 | snp | A/C | 0.426507 | 0.177046 | intron-variant | SPAG16 | GRCh38.p7 | 2:213619264 | CTACTAGAGGAAAGC[A/C]TAGGGGAAATGGTTC | 79582 |
rs13034035 | snp | C/T | 0.323197 | 0.239044 | intron-variant | SPAG16 | GRCh38.p7 | 2:213714359 | AAATTGCTGAGCCAT[C/T]TTACAATAATTCCAG | 79582 |
rs13034420 | snp | A/C | 0 | 0 | intron-variant | SPAG16 | GRCh38.p7 | 2:214397751 | AATAGAAGGTAAAGC[A/C]CAGTTTTCAAGGCCT | 79582 |
rs13034567 | snp | G/T | | | intron-variant | SPAG16 | GRCh38.p7 | 2:214395801 | ggttttctgttcctg[G/T]gttagtttgcttaag | 79582 |
rs13034808 | snp | A/G | 0.354665 | 0.227036 | intron-variant | SPAG16 | GRCh38.p7 | 2:213802572 | TTGAGAAAAGTTAAA[A/G]AAAGCACCTACCCTA | 79582 |
rs13035537 | snp | A/G | 0.448708 | 0.151707 | intron-variant | SPAG16 | GRCh38.p7 | 2:214274284 | aattgaatacccttt[A/G]tttctttctcctgcc | 79582 |
rs13035658 | snp | C/T | 0.226484 | 0.248892 | intron-variant | SPAG16 | GRCh38.p7 | 2:214112348 | ggtgcagagctgagt[C/T]caagtcctggatatc | 79582 |
rs13035979 | snp | C/T | 0.286825 | 0.247273 | intron-variant | SPAG16 | GRCh38.p7 | 2:214121619 | AACTAGAAGATGGTA[C/T]TACTGCTACTACTGC | 79582 |
rs13036015 | snp | C/T | | | intron-variant | SPAG16 | GRCh38.p7 | 2:214265315 | atcagtgtacagtag[C/T]atctcattgttgttt | 79582 |
rs13036023 | snp | G/T | | | intron-variant | SPAG16 | GRCh38.p7 | 2:214265325 | agtagtatctcattg[G/T]tgttttaatttgcaa | 79582 |
rs13036025 | snp | C/T | | | intron-variant | SPAG16 | GRCh38.p7 | 2:214265329 | gtatctcattgttgt[C/T]ttaatttgcaatttc | 79582 |
rs13036191 | snp | A/T | | | intron-variant | SPAG16 | GRCh38.p7 | 2:214265386 | tttcatatgcttatt[A/T]gccatctgtgtatct | 79582 |
rs13036201 | snp | A/T | 0.483491 | 0.0893421 | intron-variant | SPAG16 | GRCh38.p7 | 2:214235322 | TCCAAACTCAATGAT[A/T]TAAACATATTTTCTC | 79582 |
rs13382294 | snp | A/G/T | 0.00159617 | 0.0282053 | intron-variant | SPAG16 | GRCh38.p7 | 2:214304619 | ggctgtgagacccct[A/G/T]attttccacttcaca | 79582 |
rs13382401 | snp | A/G | 0.00636936 | 0.0560724 | intron-variant | SPAG16 | GRCh38.p7 | 2:213878070 | TAGAATGGATTCAGA[A/G]TACTTCTTCCTGTTC | 79582 |
rs13383491 | snp | A/G | 0.00835141 | 0.0640778 | intron-variant, utr-variant-5-prime | SPAG16 | GRCh38.p7 | 2:213301511 | CTTCTTTGCAATTCA[A/G]CATTTAATTAGTTCT | 79582 |
rs13383548 | snp | A/G | 0.00716266 | 0.059414 | intron-variant | SPAG16 | GRCh38.p7 | 2:214137544 | CTTATTGACTATTTA[A/G]TGTATCCTGATGGGG | 79582 |
rs13384166 | snp | A/G | 0.211516 | 0.24702 | intron-variant | SPAG16 | GRCh38.p7 | 2:213359565 | caaggctctgtgggc[A/G]tcggacctgctgagc | 79582 |
rs13384391 | snp | A/G | 0.230017 | 0.2492 | intron-variant | SPAG16, LOC101928084 | GRCh38.p7 | 2:214097417 | TGGCAGGTGCACTTG[A/G]AGTGGCTAAGTACAG | 79582 |
rs13384459 | snp | A/G | 0.211212 | 0.246973 | intron-variant | SPAG16 | GRCh38.p7 | 2:213319045 | ATTCTGACAAGGAAT[A/G]TGTGAATGCATTAAC | 79582 |
rs13384488 | snp | A/G | 0.230017 | 0.2492 | intron-variant | SPAG16, LOC101928084 | GRCh38.p7 | 2:214097507 | TGGTTGTGACATTCC[A/G]TTATTAGGGCTCCAT | 79582 |
rs13384542 | snp | G/T | 0.452965 | 0.145963 | intron-variant | SPAG16 | GRCh38.p7 | 2:213949274 | CTCCCAGGTTCAAGC[G/T]ATTCTCGTGCCTCAG | 79582 |
rs13384688 | snp | C/T | 0 | 0 | intron-variant | SPAG16 | GRCh38.p7 | 2:213526811 | ttttccttcagaatg[C/T]tgaagTATTGCTACA | 79582 |
rs13384724 | snp | A/G | 0.142947 | 0.22592 | intron-variant | SPAG16 | GRCh38.p7 | 2:213708231 | GTTGAAAAGATTTCA[A/G]TGAATTTTAAATGCT | 79582 |
rs13384816 | snp | G/T | 0 | 0 | intron-variant | SPAG16 | GRCh38.p7 | 2:213912132 | ATTATCAATAATTTG[G/T]TTTCCTTGCTTATTT | 79582 |
rs13384916 | snp | A/G | 0.046775 | 0.145601 | intron-variant | SPAG16 | GRCh38.p7 | 2:213620349 | ccaggctggagtgca[A/G]tggcacgatctccgc | 79582 |
rs13385229 | snp | A/G/T | 0.0444908 | 0.142359 | intron-variant | SPAG16 | GRCh38.p7 | 2:213442744 | ctagacacaaggctt[A/G/T]tatctttataaaaat | 79582 |
rs13385313 | snp | A/G | 0.0479149 | 0.147179 | intron-variant | SPAG16 | GRCh38.p7 | 2:213442807 | ttactaaactatgaa[A/G]ctcctagaatataac | 79582 |
rs13385359 | snp | C/T | 0 | 0 | intron-variant | SPAG16 | GRCh38.p7 | 2:214245068 | TTGAATTACTATTGT[C/T]TGAATCTGCATTCTA | 79582 |
rs13386209 | snp | G/T | 0.0444908 | 0.142359 | intron-variant | SPAG16 | GRCh38.p7 | 2:213696097 | agggtaaagccaaaa[G/T]atttgctgatctatg | 79582 |
rs13386568 | snp | A/T | | | intron-variant | SPAG16 | GRCh38.p7 | 2:213932190 | TATATATATATATAT[A/T]TATATATATTTGTTG | 79582 |
rs13387245 | snp | C/T | 0.409212 | 0.192748 | intron-variant | SPAG16, LOC101928084 | GRCh38.p7 | 2:214101683 | AGGGCTAGGGGACTT[C/T]GGAATCAGGCAAAAC | 79582 |
rs13387383 | snp | C/T | 0.409212 | 0.192748 | intron-variant | SPAG16, LOC101928084 | GRCh38.p7 | 2:214101854 | GCATAATGCTTTAGG[C/T]ATGTAATAAACACTT | 79582 |
rs13387479 | snp | A/G | 0.229136 | 0.249128 | intron-variant | SPAG16, LOC101928084 | GRCh38.p7 | 2:214097920 | CAAAATGGCACTATC[A/G]TGTAGATACTATATT | 79582 |
rs13387481 | snp | A/G | 0.209084 | 0.246629 | intron-variant | SPAG16 | GRCh38.p7 | 2:213330244 | aatgatggatccacc[A/G]acagcttgcactgtg | 79582 |
rs13387606 | snp | A/G | 0.186737 | 0.241863 | intron-variant | SPAG16, LOC101928084 | GRCh38.p7 | 2:214098017 | CCAAATTCAGACCCA[A/G]GTAGTTTCGCTCCAG | 79582 |
rs13387629 | snp | C/T | 0.167809 | 0.236103 | intron-variant | SPAG16 | GRCh38.p7 | 2:214105174 | cggggcagagccatg[C/T]ggagaatgaatctga | 79582 |
rs13387831 | snp | A/C | 0.49645 | 0.0419827 | intron-variant | SPAG16 | GRCh38.p7 | 2:213980236 | GTGTATATATATTCT[A/C]TATATATATAGAATA | 79582 |
rs13387941 | snp | A/C | 0.485187 | 0.0847778 | intron-variant | SPAG16 | GRCh38.p7 | 2:214010439 | TAATAAAAGTCTAGG[A/C]ATAATAGGTGGACCT | 79582 |
rs13387946 | snp | C/T | 0.0130921 | 0.0798413 | intron-variant | SPAG16 | GRCh38.p7 | 2:214125907 | aagaatggacaatca[C/T]gtagaaatgtgattg | 79582 |
rs13387951 | snp | C/T | 0.0279526 | 0.114869 | intron-variant | SPAG16 | GRCh38.p7 | 2:213682758 | gagctggaatgtttc[C/T]ggtcggaggtgtcac | 79582 |
rs13388035 | snp | C/T | | | intron-variant | SPAG16 | GRCh38.p7 | 2:213867638 | AACTTAAAAAGATAG[C/T]TCggccgtgttcagt | 79582 |
rs13388292 | snp | A/G | | | intron-variant | SPAG16 | GRCh38.p7 | 2:213980473 | atatagaatatatgt[A/G]tgtatatatataata | 79582 |
rs13388507 | snp | C/T | 0 | 0 | intron-variant | SPAG16 | GRCh38.p7 | 2:213974899 | GTCACATAGCACTTT[C/T]TCCCTTTTTAACAGT | 79582 |
rs13388769 | snp | C/T | 0.472616 | 0.113763 | intron-variant | SPAG16 | GRCh38.p7 | 2:213853172 | GAAACATTTACAATG[C/T]TGAATAACCTAAAGG | 79582 |
rs13389781 | snp | A/G | 0.212122 | 0.247114 | intron-variant | SPAG16 | GRCh38.p7 | 2:213308623 | gttaacagggttgca[A/G]cattttccatacaag | 79582 |
rs13389980 | snp | A/G | 0.212122 | 0.247114 | intron-variant | SPAG16 | GRCh38.p7 | 2:213308839 | ttgcagcttcatgct[A/G]tgtggctcaggccac | 79582 |
rs13390322 | snp | C/G | 0.332106 | 0.236133 | intron-variant | SPAG16 | GRCh38.p7 | 2:214351868 | CTTTTTCAATGGACT[C/G]TGAGTCtcttagtct | 79582 |
rs13390411 | snp | C/G | 0.00874735 | 0.0655527 | intron-variant | SPAG16 | GRCh38.p7 | 2:213986304 | AGTATGTAAGATTGG[C/G]TGGACTATATTTTTC | 79582 |
rs13390634 | snp | A/G | 0.00993419 | 0.0697739 | intron-variant | SPAG16 | GRCh38.p7 | 2:213810093 | TAAGAAGTTCCATGG[A/G]TCAGAAGAGTAAGAG | 79582 |
rs13390905 | snp | C/T | 0.0479149 | 0.147179 | intron-variant | SPAG16 | GRCh38.p7 | 2:213527927 | GCAACATATAAGCTC[C/T]GCTGAAAGGTAGTTA | 79582 |
rs13391569 | snp | A/C | 0.211212 | 0.246973 | intron-variant | SPAG16 | GRCh38.p7 | 2:213321128 | AAATAAAATAGATAT[A/C]AAATACTTTTCTAAT | 79582 |
rs13391621 | snp | C/T | 0.158632 | 0.232706 | intron-variant | SPAG16 | GRCh38.p7 | 2:214157113 | AAGGAACTGGAGAAA[C/T]TGAAGGATGTCAGAC | 79582 |
rs13392718 | snp | A/G | 0.479824 | 0.098392 | intron-variant | SPAG16 | GRCh38.p7 | 2:213886580 | CCCAAACAAATGATG[A/G]ATTGAGATGCAGTGA | 79582 |
rs13392729 | snp | A/G | 0.479824 | 0.098392 | intron-variant | SPAG16 | GRCh38.p7 | 2:213886634 | ATGCCAAAAAATATG[A/G]GAGGAGTGCCAACAA | 79582 |
rs13393031 | snp | C/T | 0.0023933 | 0.0345097 | intron-variant | SPAG16 | GRCh38.p7 | 2:214358246 | TGAGCATCTCTGATC[C/T]GACCCTTGCATCTAC | 79582 |
rs13393685 | snp | A/G | 0.02016 | 0.0983543 | intron-variant | SPAG16 | GRCh38.p7 | 2:214024460 | TCTGTAGTGAACACA[A/G]AATAGTTTAAATGAT | 79582 |
rs13393815 | snp | C/T | 0.0479149 | 0.147179 | intron-variant | SPAG16 | GRCh38.p7 | 2:213421950 | acccactttgggtct[C/T]ctgagagctgttctc | 79582 |
rs13394093 | snp | G/T | 0.0452528 | 0.143452 | intron-variant | SPAG16 | GRCh38.p7 | 2:213337668 | acaggcagacaagag[G/T]agagaaaaaaagaat | 79582 |
rs13394429 | snp | C/T | 0.311123 | 0.242413 | intron-variant | SPAG16 | GRCh38.p7 | 2:214288543 | aactttcattcccac[C/T]gacagtgtatgagtt | 79582 |
rs13394492 | snp | C/T | 0.046775 | 0.145601 | intron-variant | SPAG16 | GRCh38.p7 | 2:213633087 | aattcagcagtgaag[C/T]catcaggtcctggac | 79582 |
rs13394548 | snp | A/G | 0.0111196 | 0.0737302 | intron-variant | SPAG16 | GRCh38.p7 | 2:214052607 | TTTTCTCTTTATATC[A/G]TATATTATAAGAATA | 79582 |
rs13394975 | snp | C/T | 0.375 | 0.216506 | intron-variant | SPAG16 | GRCh38.p7 | 2:214012310 | TTTTTTTTTTTTTTT[C/T]CTCGAGAGGGCATCT | 79582 |
rs13395062 | snp | A/G | 0.448708 | 0.151707 | intron-variant | SPAG16, LOC101928084 | GRCh38.p7 | 2:214100317 | ctaatacaATCACTA[A/G]TATAAAAATTGATTT | 79582 |
rs13395064 | snp | A/G | 0.18989 | 0.242666 | intron-variant | SPAG16 | GRCh38.p7 | 2:213332642 | aaaataccagccagc[A/G]gaattcaacaatata | 79582 |
rs13395079 | snp | C/G | 0.209388 | 0.246679 | intron-variant | SPAG16 | GRCh38.p7 | 2:213332764 | catcaaaagaatgaa[C/G]aacaaaaaccatatg | 79582 |
rs13395330 | snp | G/T | | | intron-variant | SPAG16 | GRCh38.p7 | 2:213518874 | tatacatatacactg[G/T]ggaatactatgcagc | 79582 |
rs13395392 | snp | A/T | 0 | 0 | intron-variant | SPAG16 | GRCh38.p7 | 2:213529733 | atagaaaatgtacat[A/T]aaaaacatggtataa | 79582 |
rs13395398 | snp | A/G | 0.334412 | 0.235318 | intron-variant | SPAG16 | GRCh38.p7 | 2:214195680 | GAGGTCATTACTGAG[A/G]TGAAGAAGACTGGGC | 79582 |
rs13395869 | snp | C/G | 0.174288 | 0.23826 | intron-variant | SPAG16 | GRCh38.p7 | 2:213292533 | gccgggcgtagtggc[C/G]ggcgcctgtagtccc | 79582 |
rs13395940 | snp | A/G | 0.445196 | 0.1562 | intron-variant | SPAG16 | GRCh38.p7 | 2:214341813 | AACTTCCTCTTAATT[A/G]AACAGGAAACTAGAA | 79582 |
rs13396612 | snp | A/G | 0.0182019 | 0.0936463 | intron-variant | SPAG16 | GRCh38.p7 | 2:214028080 | ACATTTTTATGATGT[A/G]TGAGATTGTGGGGAG | 79582 |
rs13396813 | snp | A/G | 0.493107 | 0.0583 | intron-variant | SPAG16 | GRCh38.p7 | 2:213970810 | GCAAAATAAAAATGT[A/G]TGGAGTGAATATTTG | 79582 |
rs13397646 | snp | C/T | 0.212425 | 0.24716 | intron-variant | SPAG16 | GRCh38.p7 | 2:213359840 | GGAAATGCAGAAATC[C/T]GTCTTCTGTGTTGAT | 79582 |
rs13397843 | snp | C/T | 0.499502 | 0.0157669 | intron-variant | SPAG16 | GRCh38.p7 | 2:213949315 | ATCTGGGACTACAGG[C/T]GTGCCACCACGCCCA | 79582 |
rs13398072 | snp | C/T | 0.0283406 | 0.115616 | intron-variant | SPAG16 | GRCh38.p7 | 2:213655080 | atttgtccaaaccca[C/T]agaatgcataacacc | 79582 |
rs13398806 | snp | C/T | | | intron-variant | SPAG16 | GRCh38.p7 | 2:213736359 | agtgcagtggtgtga[C/T]ctcggctcactgtaa | 79582 |
rs13399247 | snp | A/G | 0.479824 | 0.098392 | intron-variant | SPAG16 | GRCh38.p7 | 2:213888019 | TTTTGAGCATATATT[A/G]TTTATTTTGCATTTT | 79582 |
rs13399313 | snp | C/G | 0.046775 | 0.145601 | intron-variant | SPAG16 | GRCh38.p7 | 2:213469168 | tcaaccccttgtcaa[C/G]ttgaacccatacaca | 79582 |
rs13400851 | snp | G/T | 0.174288 | 0.23826 | intron-variant | SPAG16 | GRCh38.p7 | 2:213339360 | AATGGAAATGTGACA[G/T]TGTCAATGCTGTAGC | 79582 |
rs13401177 | snp | C/G/T | | | intron-variant | SPAG16 | GRCh38.p7 | 2:214355083 | ctagaagaaaaccta[C/G/T]gcattaccattcagg | 79582 |
rs13401210 | snp | A/C | | | intron-variant | SPAG16 | GRCh38.p7 | 2:214355156 | caatggcaacaaaag[A/C]caaaattgacaaatg | 79582 |
rs13401312 | snp | A/C | 0.408023 | 0.198927 | intron-variant | SPAG16 | GRCh38.p7 | 2:214047182 | agaaatagaaaaaac[A/C]gtcctaatattcata | 79582 |
rs13401350 | snp | C/T | 0.180702 | 0.240204 | intron-variant | SPAG16 | GRCh38.p7 | 2:213289910 | AGTGTGTAAGGTACT[C/T]TGCTGCTCACATCTG | 79582 |
rs13402035 | snp | G/T | 0 | 0 | intron-variant | SPAG16 | GRCh38.p7 | 2:213621471 | AACTTCATGATGGAG[G/T]GGGAATTTTTAATGG | 79582 |
rs13402894 | snp | C/T | 0.490398 | 0.0686206 | intron-variant | SPAG16 | GRCh38.p7 | 2:213761920 | aaccctacagaccaa[C/T]atctcttacgaatat | 79582 |
rs13403206 | snp | A/C | 0.0482946 | 0.147699 | intron-variant | SPAG16 | GRCh38.p7 | 2:213528287 | TATTATAATACCTAG[A/C]AAAAGTAGTCTTTGG | 79582 |
rs13403869 | snp | C/T | | | intron-variant | SPAG16 | GRCh38.p7 | 2:214155526 | ttttttttttaaaga[C/T]ggggtcctatgatgt | 79582 |
rs13404035 | snp | C/T | 0.482159 | 0.0927485 | intron-variant | SPAG16 | GRCh38.p7 | 2:214257242 | acttagctcataccc[C/T]gtgactttggtcgtt | 79582 |
rs13404045 | snp | A/C | 0 | 0 | intron-variant | SPAG16 | GRCh38.p7 | 2:213553260 | CCCCAGAAGCAGCCC[A/C]CAGTCACATTAAAGA | 79582 |
rs13404127 | snp | A/G | 0 | 0 | intron-variant | SPAG16 | GRCh38.p7 | 2:213670987 | AGGAACCATCACATG[A/G]ATACATAAAAGTGTC | 79582 |
rs13404340 | snp | G/T | 0.0452528 | 0.143452 | intron-variant | SPAG16 | GRCh38.p7 | 2:213692271 | ACAATGTTCAATACT[G/T]GGATTTGTTACAGTA | 79582 |
rs13404448 | snp | C/G | 0.49823 | 0.0296997 | intron-variant | SPAG16 | GRCh38.p7 | 2:214115016 | TATAGCTCCAAATCA[C/G]TATCCCACAGCCTCA | 79582 |
rs13404522 | snp | C/T | 0.174932 | 0.238463 | intron-variant | SPAG16 | GRCh38.p7 | 2:213331450 | tatataaagcaaata[C/T]tattagagctaaaga | 79582 |
rs13404642 | snp | G/T | 0.490007 | 0.0699769 | intron-variant | SPAG16 | GRCh38.p7 | 2:214020081 | ACTGGAATCTGATTG[G/T]GTGGGTACCATTATT | 79582 |
rs13404720 | snp | G/T | 0.209997 | 0.246779 | intron-variant | SPAG16 | GRCh38.p7 | 2:213331567 | aaacatcagacttaa[G/T]ctgcaccatagaaca | 79582 |
rs13404755 | snp | C/T | 0.213635 | 0.247341 | intron-variant | SPAG16 | GRCh38.p7 | 2:213361742 | ggcacctgcagaggt[C/T]ggtggatccccaact | 79582 |
rs13405251 | snp | A/G | 0.089084 | 0.191327 | intron-variant | SPAG16 | GRCh38.p7 | 2:214203801 | gtaacaatttcaacc[A/G]aagtttcctggacgg | 79582 |
rs13406069 | snp | A/G | 0.211516 | 0.24702 | intron-variant | SPAG16 | GRCh38.p7 | 2:213328834 | TTTGGCTGTGTCCCC[A/G]CCCAAATCTCATCTT | 79582 |
rs13406436 | snp | C/G | | | intron-variant | SPAG16 | GRCh38.p7 | 2:214191645 | attgaacttgggagg[C/G]gaaggttgcagtgat | 79582 |
rs13406586 | snp | A/G | 0.103082 | 0.202275 | intron-variant | SPAG16 | GRCh38.p7 | 2:214191624 | gaggctgagagagga[A/G]aattgattgaacttg | 79582 |
rs13406869 | snp | A/G | 0.155325 | 0.23138 | intron-variant | SPAG16 | GRCh38.p7 | 2:213619661 | aaaagacaaaaaata[A/G]taaatactagaaaag | 79582 |
rs13407029 | snp | A/T | 0.0429648 | 0.14013 | intron-variant | SPAG16 | GRCh38.p7 | 2:213684830 | aatggtaagcaaaac[A/T]gacacattatgtatc | 79582 |
rs13407282 | snp | A/G | 0.479502 | 0.0991411 | intron-variant | SPAG16 | GRCh38.p7 | 2:213890837 | ATTAGTTAAATTTTG[A/G]TGTGTTAAAGTTTGG | 79582 |
rs13407284 | snp | A/G | 0.479502 | 0.0991411 | intron-variant | SPAG16 | GRCh38.p7 | 2:213890844 | AAATTTTGATGTGTT[A/G]AAGTTTGGCATTTGA | 79582 |
rs13407602 | snp | C/G | 0.484701 | 0.0861117 | intron-variant | SPAG16 | GRCh38.p7 | 2:213907862 | GAATTATGGTTATTA[C/G]AGGCTGAGAAGGGGA | 79582 |
rs13407964 | snp | A/G | | | intron-variant | SPAG16 | GRCh38.p7 | 2:213996704 | ctcccaagtagctga[A/G]attacaggcatgtgc | 79582 |
rs13409968 | snp | A/G | 0.00478085 | 0.0486577 | intron-variant | SPAG16 | GRCh38.p7 | 2:213715226 | TAGatctatctgtct[A/G]tctatctatctatct | 79582 |
rs13410509 | snp | A/G | 0.0185938 | 0.0946107 | intron-variant | SPAG16 | GRCh38.p7 | 2:214338407 | tagtcccagctactc[A/G]ggaggctgaggcaaa | 79582 |
rs13410710 | snp | A/G | 0.48498 | 0.0853497 | intron-variant | SPAG16 | GRCh38.p7 | 2:213921665 | tttttgtagtggctg[A/G]taatgatctttcttt | 79582 |
rs13410750 | snp | C/G | 0.40263 | 0.198 | intron-variant | SPAG16 | GRCh38.p7 | 2:213407637 | agagagagagagaga[C/G]agacagacagacagg | 79582 |
rs13410835 | snp | A/G | 0 | 0 | intron-variant | SPAG16 | GRCh38.p7 | 2:213997040 | AGTTGAACTAATTGA[A/G]AAAAATATTCTGTGT | 79582 |
rs13411861 | snp | A/T | 0.498945 | 0.022939 | intron-variant | SPAG16 | GRCh38.p7 | 2:213983053 | TATATTCAATACTTT[A/T]GGGAGCAATGCTGTG | 79582 |
rs13411979 | snp | A/G | 0.17654 | 0.238964 | intron-variant | SPAG16 | GRCh38.p7 | 2:213372680 | CATTTTAGTTTACAT[A/G]TGTCCTAATCTCTTA | 79582 |
rs13411988 | snp | G/T | 0.17654 | 0.238964 | intron-variant | SPAG16 | GRCh38.p7 | 2:213372696 | TGTCCTAATCTCTTA[G/T]ACATTTTCTGTTTCT | 79582 |
rs13412082 | snp | A/G | | | intron-variant | SPAG16 | GRCh38.p7 | 2:213791809 | AAAATGTTTTAAGTC[A/G]CGTTTTGCAAAGTTT | 79582 |
rs13412855 | snp | C/G | 0.0901694 | 0.192235 | intron-variant | SPAG16 | GRCh38.p7 | 2:213749101 | gcagtgagccgagat[C/G]gcgccactgtactac | 79582 |
rs13413013 | snp | A/G | 0.0482946 | 0.147699 | intron-variant | SPAG16 | GRCh38.p7 | 2:213508445 | ggcgcggtggcgggc[A/G]cctgtagtcccagct | 79582 |
rs13413330 | snp | C/G | 0.25214 | 0.249991 | intron-variant | SPAG16 | GRCh38.p7 | 2:214132922 | ACATGGAGAAACCCC[C/G]TCTCTACTAAAAATA | 79582 |
rs13414104 | snp | C/T | 0.17654 | 0.238964 | intron-variant, utr-variant-3-prime | SPAG16 | GRCh38.p7 | 2:213369326 | AAATGAGAAATATGT[C/T]TTCCTTTTCTAATTT | 79582 |
rs13414880 | snp | C/T | 0.255224 | 0.249945 | intron-variant | SPAG16 | GRCh38.p7 | 2:214033557 | AAAGATTATATTCAA[C/T]CATTTATTCATGCCT | 79582 |
rs13415340 | snp | A/G | 0.465578 | 0.126594 | intron-variant | SPAG16 | GRCh38.p7 | 2:214080999 | aaccacactttgaga[A/G]ccactgAATAAGAAA | 79582 |
rs13416158 | snp | A/G | 0.349452 | 0.229367 | intron-variant | SPAG16 | GRCh38.p7 | 2:214139255 | GCTGAAGAATTAACA[A/G]TGAACATTAAGTCCT | 79582 |
rs13416173 | snp | A/G | 0.0170251 | 0.090679 | intron-variant | SPAG16 | GRCh38.p7 | 2:214317614 | ACAAAACAATAGGCC[A/G]GAGGTGGTGAAAGTC | 79582 |
rs13416220 | snp | G/T | 0.441021 | 0.161279 | intron-variant | SPAG16 | GRCh38.p7 | 2:213993702 | CATATTGAATCCAAA[G/T]ATAAAGTATAGTATA | 79582 |
rs13416237 | snp | A/G | 0.499879 | 0.0077866 | intron-variant | SPAG16 | GRCh38.p7 | 2:213993743 | ATGTGCTTCTGTATT[A/G]AAATACTGGTAGTTT | 79582 |
rs13416393 | snp | A/T | 0.453087 | 0.145793 | intron-variant | SPAG16 | GRCh38.p7 | 2:213954793 | agaaattcccaattc[A/T]ccacattgttgctaa | 79582 |
rs13416548 | snp | C/T | 0.470521 | 0.117772 | intron-variant | SPAG16 | GRCh38.p7 | 2:213875396 | ATGGGTCTGAAGAAG[C/T]GAAAAGGGATACATG | 79582 |
rs13416682 | snp | A/C | 0.230017 | 0.2492 | intron-variant | SPAG16, LOC101928084 | GRCh38.p7 | 2:214098992 | TAGTGAATCCTGAAC[A/C]AGTTGGCTGACTTTC | 79582 |
rs13416693 | snp | C/T | | | intron-variant | SPAG16, LOC101928084 | GRCh38.p7 | 2:214099017 | ACTTTCAAGTCGTGT[C/T]TGTTGTTATTTGACT | 79582 |
rs13416807 | snp | C/T | 0 | 0 | intron-variant | SPAG16, LOC101928084 | GRCh38.p7 | 2:214099119 | TACTTGTAAGCAGGG[C/T]TGTAGAACTGTTGCT | 79582 |
rs13416902 | snp | G/T | 0.171704 | 0.237423 | intron-variant | SPAG16 | GRCh38.p7 | 2:214194158 | TCAAATAGTTGGCGA[G/T]TTGTCATGGGGCTTT | 79582 |
rs13416921 | snp | C/T | 0.252702 | 0.249985 | intron-variant | SPAG16 | GRCh38.p7 | 2:214134116 | GTCTGGACTTAATGA[C/T]GACTCATAGTTTCTG | 79582 |
rs13417867 | snp | A/G | 0.00914312 | 0.0669923 | intron-variant | SPAG16 | GRCh38.p7 | 2:213833443 | tgtatgtgtgtgtgt[A/G]tatatatatattata | 79582 |
rs13418276 | snp | A/G | 0.212425 | 0.24716 | intron-variant | SPAG16 | GRCh38.p7 | 2:213308863 | aggccacatagtccc[A/G]ttcctctcaagcctt | 79582 |
rs13418359 | snp | A/T | 0.0479149 | 0.147179 | intron-variant | SPAG16 | GRCh38.p7 | 2:213641707 | ggtaaattattctct[A/T]gtgatccttattttc | 79582 |
rs13418493 | snp | A/G | 0.479824 | 0.098392 | intron-variant | SPAG16 | GRCh38.p7 | 2:213886661 | ACAAACTTCTGAGGG[A/G]AAACAAGcaactatc | 79582 |
rs13419169 | snp | C/T | 0.453087 | 0.145793 | intron-variant | SPAG16 | GRCh38.p7 | 2:213955048 | tttacatatttcttt[C/T]atttctttttttatt | 79582 |
rs13419185 | snp | C/T | 0.0486741 | 0.148216 | intron-variant | SPAG16 | GRCh38.p7 | 2:214325256 | atcttgttaaatgga[C/T]gtgctggtttggtag | 79582 |
rs13419939 | snp | A/T | 0.0532157 | 0.154195 | intron-variant | SPAG16 | GRCh38.p7 | 2:214337194 | TCTTTCGTAGTAAAG[A/T]TCTCTCACTGGAAAT | 79582 |
rs13420690 | snp | A/C | 0.498852 | 0.0239341 | intron-variant | SPAG16 | GRCh38.p7 | 2:214371143 | CAGAATGTAGACTAA[A/C]GTTGAGGACATTCTT | 79582 |
rs13420908 | snp | A/T | 0.00755907 | 0.0610114 | intron-variant | SPAG16 | GRCh38.p7 | 2:214128351 | GGCATGTTTTAGTTA[A/T]ATCTTATATTTCTCA | 79582 |
rs13422043 | snp | C/T | 0.439502 | 0.163061 | intron-variant | SPAG16 | GRCh38.p7 | 2:214000599 | TGTGACATATAAGGC[C/T]AGAGTCCTCATGGAG | 79582 |
rs13422754 | snp | C/T | 0.314301 | 0.241589 | intron-variant | SPAG16 | GRCh38.p7 | 2:213304918 | gaagaatgtcattgg[C/T]attttattttgttgg | 79582 |
rs13423281 | snp | G/T | 0.230017 | 0.2492 | intron-variant | SPAG16, LOC101928084 | GRCh38.p7 | 2:214097343 | AGTGTTTTATTTAGA[G/T]AAATTATTTTGTAAA | 79582 |
rs13423319 | snp | A/G | 0.00358779 | 0.0422022 | intron-variant | SPAG16 | GRCh38.p7 | 2:214141238 | ctttgggaggccaag[A/G]taggtggatcacaag | 79582 |
rs13423671 | snp | A/G | 0.487368 | 0.0784625 | intron-variant | SPAG16 | GRCh38.p7 | 2:213983015 | CACTCTTGAATGTTT[A/G]CTTTAAATCACATTG | 79582 |
rs13423895 | snp | A/G | 0.479904 | 0.0982045 | intron-variant | SPAG16 | GRCh38.p7 | 2:213870436 | TATAGATAAATAAAT[A/G]AATTTCAAGGCACTG | 79582 |
rs13424177 | snp | C/G | 0.411074 | 0.191194 | intron-variant | SPAG16, LOC101928084 | GRCh38.p7 | 2:214101356 | AAGATGGGTGTGGGG[C/G]ATTCCTGCTGGTCTT | 79582 |
rs13424226 | snp | A/C | 0 | 0 | intron-variant | SPAG16 | GRCh38.p7 | 2:214013625 | GATGAATTAGTGCAA[A/C]ATTTTTTAAACATAT | 79582 |
rs13424310 | snp | A/C | 0.0475351 | 0.146656 | intron-variant | SPAG16 | GRCh38.p7 | 2:213657699 | AAGGAAGATAATCAT[A/C]AAAAATTTGTGATTT | 79582 |
rs13424490 | snp | C/T | 0.408871 | 0.193029 | intron-variant | SPAG16, LOC101928084 | GRCh38.p7 | 2:214101593 | GAGGGTTAGGAGGTG[C/T]GTATCTACCCAGAAA | 79582 |
rs13424627 | snp | A/G | 0.326035 | 0.238157 | intron-variant, upstream-variant-2KB | SPAG16 | GRCh38.p7 | 2:213316107 | gtatactcaacgttt[A/G]tcttcacttaaatgt | 79582 |
rs13424760 | snp | G/T | 0.211212 | 0.246973 | intron-variant, upstream-variant-2KB | SPAG16 | GRCh38.p7 | 2:213316236 | gctatctgttgctca[G/T]ccaaaaaccctggag | 79582 |
rs13424980 | snp | A/G | 0 | 0 | intron-variant | SPAG16 | GRCh38.p7 | 2:213411472 | tagccagatggctta[A/G]gaaaatagaatagcc | 79582 |
rs13425079 | snp | G/T | 0.484841 | 0.0857308 | intron-variant | SPAG16 | GRCh38.p7 | 2:213918201 | gttttttgtatcagt[G/T]ttcatcaaagatatt | 79582 |
rs13425529 | snp | A/G | 0.484841 | 0.0857308 | intron-variant | SPAG16 | GRCh38.p7 | 2:213918635 | cttgtctcctgccat[A/G]taagacatgcctttt | 79582 |
rs13425584 | snp | A/T | 0.475525 | 0.107882 | intron-variant | SPAG16 | GRCh38.p7 | 2:213879586 | tcattgtaactaggt[A/T]gtgagtgtagtacag | 79582 |
rs13426013 | snp | G/T | 0.474272 | 0.110462 | intron-variant | SPAG16 | GRCh38.p7 | 2:213852890 | AAAAAAATTCCATGT[G/T]AAAGTACTTTATATA | 79582 |
rs13426014 | snp | C/T | 0.0486741 | 0.148216 | intron-variant | SPAG16 | GRCh38.p7 | 2:213552228 | TATACAGACACTCTG[C/T]GCCCCATAAATCATG | 79582 |
rs13426574 | snp | C/T | 0.0107246 | 0.0724382 | intron-variant | SPAG16 | GRCh38.p7 | 2:214067934 | AACTATAAAAAATAA[C/T]GTGTTACTTTGTAAA | 79582 |
rs13426925 | snp | C/T | 0.167158 | 0.235875 | intron-variant | SPAG16 | GRCh38.p7 | 2:214107462 | TTTCCCTACAAGAGT[C/T]AAGAATGCCCGTTGA | 79582 |
rs13427242 | snp | A/C | 0.0441095 | 0.141807 | intron-variant | SPAG16 | GRCh38.p7 | 2:213841082 | CTATTCCTGCAATAC[A/C]CACAAAGGACATTTG | 79582 |
rs13427653 | snp | G/T | 0.0452528 | 0.143452 | intron-variant | SPAG16 | GRCh38.p7 | 2:213649334 | AACTGGAAAGATAGG[G/T]CTGTGTTTCTGGAGA | 79582 |
rs13428110 | snp | A/G | 0.0197687 | 0.0974348 | intron-variant | SPAG16 | GRCh38.p7 | 2:214042251 | gacgtgcatcaccat[A/G]cccagctaatttCAG | 79582 |
rs13428211 | snp | A/C | 0.469049 | 0.120489 | intron-variant | SPAG16 | GRCh38.p7 | 2:213918940 | tattcgtaatagtct[A/C]tgatggttatttgta | 79582 |
rs13428264 | snp | A/G | 0.210301 | 0.246828 | intron-variant | SPAG16 | GRCh38.p7 | 2:213286996 | TGTAATCTCCTAGCT[A/G]TAACAGTGCCACCTA | 79582 |
rs13428777 | snp | C/G | | | intron-variant | SPAG16 | GRCh38.p7 | 2:213588528 | CTATCCATggccggg[C/G]gcggtggctcacgcc | 79582 |
rs13428969 | snp | C/T | 0.029116 | 0.117091 | intron-variant | SPAG16 | GRCh38.p7 | 2:213674656 | tttttgtccttgcga[C/T]agtttactgagaatg | 79582 |
rs13429372 | snp | G/T | 0.15665 | 0.231917 | intron-variant | SPAG16 | GRCh38.p7 | 2:214148122 | ATAAACATAATTGAT[G/T]ATTTTAATGTGGCCA | 79582 |
rs13429597 | snp | A/T | 0.479904 | 0.0982045 | intron-variant | SPAG16 | GRCh38.p7 | 2:213874986 | CTTGCTCTGTTGCCC[A/T]GGTTGGAGTGCAGTG | 79582 |
rs13430302 | snp | A/C | 0.343477 | 0.231866 | intron-variant | SPAG16 | GRCh38.p7 | 2:213990402 | ACAGTCAGAAATCTG[A/C]GTATAACTTTTGACA | 79582 |
rs13430303 | snp | A/G | 0.00874735 | 0.0655527 | intron-variant | SPAG16 | GRCh38.p7 | 2:213930232 | TTTTTTTTTTCCTTG[A/G]TGCTACCCCAGGGAA | 79582 |
rs13430858 | snp | A/C | 0.25214 | 0.249991 | intron-variant | SPAG16 | GRCh38.p7 | 2:214136529 | TGAGATTTCCAGCTC[A/C]TATCCATGGAGCATG | 79582 |
rs13431580 | snp | C/T | 0.175897 | 0.238765 | intron-variant | SPAG16 | GRCh38.p7 | 2:213328833 | gtttggctgtgtccc[C/T]acccaaatctcatct | 79582 |
rs13432207 | snp | A/C | 0.0185938 | 0.0946107 | intron-variant | SPAG16 | GRCh38.p7 | 2:214036673 | gctcccattatttat[A/C]atatattcacttaca | 79582 |
rs13432717 | snp | C/T | 0.479744 | 0.0985793 | intron-variant | SPAG16 | GRCh38.p7 | 2:213890665 | TCTTTAACTCTTATT[C/T]TATATATAGGCCAGT | 79582 |
rs13432923 | snp | C/G | 0.479744 | 0.0985793 | intron-variant | SPAG16 | GRCh38.p7 | 2:213890743 | AATTATATTCAGTTT[C/G]TATGAACTAGTTATA | 79582 |
rs13433020 | snp | A/G | 0.479744 | 0.0985793 | intron-variant | SPAG16 | GRCh38.p7 | 2:213890796 | TTATAAAATAGCAGG[A/G]TGTTGCTTTGCTCAT | 79582 |
rs13433055 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | SPAG16 | GRCh38.p7 | 2:213830791 | AGTCCTTTTCCATCA[C/T]AAATTTCCCAAATCT | 79582 |
rs16825083 | snp | A/G | 0.193966 | 0.243639 | intron-variant, utr-variant-3-prime | SPAG16 | GRCh38.p7 | 2:213401463 | TTTGGTATAAAACTC[A/G]AGAACTGGTGATCTT | 79582 |
rs16825100 | snp | A/G | 0.15665 | 0.231917 | intron-variant | SPAG16 | GRCh38.p7 | 2:213521761 | CAATAGTCATGTTTG[A/G]AAATGTGTCATTTTA | 79582 |
rs16825126 | snp | A/G | 0.499502 | 0.0157669 | intron-variant | SPAG16 | GRCh38.p7 | 2:214243674 | TATATTTAAATGTCA[A/G]TAATTATCTTCACTA | 79582 |
rs16850142 | snp | C/G | 0.00227369 | 0.0336404 | upstream-variant-2KB, missense | SPAG16, LOC100130451 | GRCh38.p7 | 2:213284072 | ACACTTGGGGATCTA[C/G]AAACATCTGAAATTG | 79582 |
rs16850173 | snp | A/G | 0.039522 | 0.134904 | intron-variant | SPAG16 | GRCh38.p7 | 2:213308204 | GAATTAGTATTCCCT[A/G]TTCCTTGGTATTTTT | 79582 |
rs16850176 | snp | A/G | 0.0119091 | 0.0762411 | intron-variant | SPAG16 | GRCh38.p7 | 2:213311606 | CATAAGATAAAATTG[A/G]TATAACGCATTTCTT | 79582 |
rs16850226 | snp | A/G | 0.0463947 | 0.145069 | intron-variant | SPAG16 | GRCh38.p7 | 2:213353577 | CCTGGAGTATCCCTA[A/G]AGTATCTGGCTTTAT | 79582 |
rs16850254 | snp | A/G | 0.0119091 | 0.0762411 | intron-variant | SPAG16 | GRCh38.p7 | 2:213383122 | TCTTGAGCAATGTTT[A/G]GACAGTAAGATTCTA | 79582 |
rs16850256 | snp | A/G | 0.131723 | 0.220251 | intron-variant | SPAG16 | GRCh38.p7 | 2:213386814 | CAGTGGATTACTAAA[A/G]TAGTCAGTGGATTAG | 79582 |
rs16850260 | snp | A/G | 0.0463947 | 0.145069 | intron-variant | SPAG16 | GRCh38.p7 | 2:213393473 | ATTTTTGTTTCTAAG[A/G]GTCTTTAGTGTTGCT | 79582 |
rs16850264 | snp | C/T | 0.0463947 | 0.145069 | intron-variant | SPAG16 | GRCh38.p7 | 2:213396294 | AGATTCTAGCATCTT[C/T]TCGATATTGAATCTT | 79582 |
rs16850268 | snp | A/G | 0.197082 | 0.244335 | intron-variant, missense, synonymous-codon | SPAG16 | GRCh38.p7 | 2:213396532 | ACAGAAATCAAGAGA[A/G]AGCTTATGAGCTCAG | 79582 |
rs16850273 | snp | A/G | 0.132409 | 0.220618 | intron-variant | SPAG16 | GRCh38.p7 | 2:213404993 | TTTTGGCATTTGGCA[A/G]CATACCCCAACAGTA | 79582 |
rs16850275 | snp | A/G | 0.155656 | 0.231515 | intron-variant | SPAG16 | GRCh38.p7 | 2:213406130 | TTCTCACCCTTTTCA[A/G]TAGTTTCCTGTTTTC | 79582 |
rs16850283 | snp | C/T | 0.00676609 | 0.0577691 | intron-variant | SPAG16 | GRCh38.p7 | 2:213412534 | TTTATCCTATGTTGG[C/T]CCTCAATAAATCCTA | 79582 |
rs16850287 | snp | A/G | 0.0463947 | 0.145069 | intron-variant | SPAG16 | GRCh38.p7 | 2:213412835 | TAGGAGTAGAGGCAA[A/G]TAATAGTGTCATAAA | 79582 |
rs16850291 | snp | A/T | 0.0399052 | 0.1355 | intron-variant | SPAG16 | GRCh38.p7 | 2:213414028 | GAAAATATAAAATAA[A/T]AGCTAATTGTGCTTT | 79582 |
rs16850294 | snp | A/G | 0.0228947 | 0.104514 | intron-variant | SPAG16 | GRCh38.p7 | 2:213414621 | GATTAATGTAACATA[A/G]AAGTGATTTTATATC | 79582 |
rs16850304 | snp | A/G | 0.32768 | 0.237625 | intron-variant | SPAG16 | GRCh38.p7 | 2:213415801 | AACTGTCGTACACAG[A/G]ACACTGGAGTTTAGG | 79582 |
rs16850307 | snp | C/T | 0.155656 | 0.231515 | intron-variant | SPAG16 | GRCh38.p7 | 2:213418628 | ATGGTCTTTTGATCC[C/T]GGCACTACTCTTTTA | 79582 |
rs16850325 | snp | C/T | 0.0452528 | 0.143452 | intron-variant | SPAG16 | GRCh38.p7 | 2:213426502 | ATGGCTAATAAATGG[C/T]TCATTTTTCAACAAT | 79582 |
rs16850326 | snp | C/T | 0.155325 | 0.23138 | intron-variant | SPAG16 | GRCh38.p7 | 2:213427446 | AATTAGTAACTGGGA[C/T]TTTTTTGACTGGCTT | 79582 |
rs16850329 | snp | A/C | 0.132409 | 0.220618 | intron-variant | SPAG16 | GRCh38.p7 | 2:213428001 | CTTATGTAGTTAAAC[A/C]CATCATCAACAGCTA | 79582 |
rs16850334 | snp | C/T | 0.0452528 | 0.143452 | intron-variant | SPAG16 | GRCh38.p7 | 2:213429206 | GCAATAATTGCTCTG[C/T]CTCAGGAATAATTGC | 79582 |
rs16850338 | snp | A/C | 0.131381 | 0.220067 | intron-variant | SPAG16 | GRCh38.p7 | 2:213451160 | TCATGAGTATTATCT[A/C]ATTATGTATATAAAT | 79582 |
rs16850348 | snp | G/T | 0.00835141 | 0.0640778 | intron-variant | SPAG16 | GRCh38.p7 | 2:213452695 | GACTGGGATGTTCTG[G/T]CCCCTGCCATTGCTT | 79582 |
rs16850351 | snp | C/T | 0.0858192 | 0.188533 | intron-variant | SPAG16 | GRCh38.p7 | 2:213454060 | TCTTCAGTATGAAAG[C/T]AGTGTACATGGACAG | 79582 |
rs16850366 | snp | C/T | 0.154993 | 0.231244 | intron-variant | SPAG16 | GRCh38.p7 | 2:213458094 | TTTTTTGCTATTCTA[C/T]TATTGCCACATTTTC | 79582 |
rs16850382 | snp | A/G | 0.0912534 | 0.193131 | intron-variant | SPAG16 | GRCh38.p7 | 2:213481672 | AGGGATAAGTAACCC[A/G]GGTGTGTCCTCTTTG | 79582 |
rs16850385 | snp | C/T | 0.0399052 | 0.1355 | intron-variant | SPAG16 | GRCh38.p7 | 2:213481954 | AAATACATACTATAA[C/T]TGGGAATTACAGACA | 79582 |
rs16850397 | snp | A/C | 0.0912534 | 0.193131 | intron-variant | SPAG16 | GRCh38.p7 | 2:213482663 | AAACCATCAGTGGAA[A/C]ATGCAATTTGAAATA | 79582 |
rs16850416 | snp | A/G | 0.191461 | 0.24305 | intron-variant | SPAG16 | GRCh38.p7 | 2:213489416 | TGTGGATTCTAATAT[A/G]TGTGATTTGACAGGA | 79582 |
rs16850420 | snp | A/T | 0.131038 | 0.219882 | intron-variant | SPAG16 | GRCh38.p7 | 2:213490966 | AGTATTTTTTTTTCA[A/T]TTGCAAAGCTTCCTC | 79582 |
rs16850422 | snp | A/C | 0.173643 | 0.238054 | intron-variant | SPAG16 | GRCh38.p7 | 2:213497663 | AGAAGGCATTGTTGG[A/C]CATACTATAATTATA | 79582 |
rs16850424 | snp | C/T | 0.0228947 | 0.104514 | intron-variant | SPAG16 | GRCh38.p7 | 2:213499036 | GCTTTAAAATCTTTA[C/T]TTTTCAAGCCCTTAA | 79582 |
rs16850428 | snp | C/T | 0.128976 | 0.218754 | intron-variant | SPAG16 | GRCh38.p7 | 2:213500680 | GAAAAGGACAGAGAA[C/T]GACCAATGTTATTTT | 79582 |
rs16850429 | snp | C/T | 0.497297 | 0.0366652 | intron-variant | SPAG16 | GRCh38.p7 | 2:213516405 | ATTTTATCTTTTTCT[C/T]AAAAAAATGAACTTA | 79582 |
rs16850445 | snp | A/T | 0.170408 | 0.236992 | intron-variant | SPAG16 | GRCh38.p7 | 2:213533140 | ATATGTGATATTAAA[A/T]GAAAATTAGCACATA | 79582 |
rs16850447 | snp | A/G | 0.17332 | 0.23795 | intron-variant | SPAG16 | GRCh38.p7 | 2:213533639 | ATGTGGGATTATTTC[A/G]CCTGTATTTTTTAGG | 79582 |
rs16850449 | snp | C/T | 0.110872 | 0.20771 | intron-variant | SPAG16 | GRCh38.p7 | 2:213537982 | ATTCTTTCAATCATT[C/T]GTGTATTAGTTCAGT | 79582 |
rs16850450 | snp | C/G | 0.197393 | 0.244402 | intron-variant | SPAG16 | GRCh38.p7 | 2:213546242 | GGCTTGCTCTCTTCT[C/G]TTTTGCTAAGTCATT | 79582 |
rs16850452 | snp | C/T | 0.181022 | 0.240296 | intron-variant | SPAG16 | GRCh38.p7 | 2:213546865 | TTTGTCTGCCTTTGG[C/T]GAATTGGAAATATAA | 79582 |
rs16850456 | snp | A/G | 0.15698 | 0.23205 | intron-variant | SPAG16 | GRCh38.p7 | 2:213549614 | TCCAACATTCTCCAT[A/G]TGGAAGCTAAACAGA | 79582 |
rs16850461 | snp | C/T | 0.111224 | 0.207945 | intron-variant | SPAG16 | GRCh38.p7 | 2:213551730 | TTTTGCTGACCACTT[C/T]CTTTTCTGTGGTTGT | 79582 |
rs16850465 | snp | C/T | 0.171057 | 0.237209 | intron-variant | SPAG16 | GRCh38.p7 | 2:213565927 | GAGGAAAATACCAGT[C/T]CTGCTAAGGGTTGAA | 79582 |
rs16850468 | snp | C/T | 0.0433465 | 0.140692 | intron-variant | SPAG16 | GRCh38.p7 | 2:213574334 | TCATGGCTATTTATG[C/T]TGACTGGTTATAGGA | 79582 |
rs16850469 | snp | C/T | 0.0482946 | 0.147699 | intron-variant | SPAG16 | GRCh38.p7 | 2:213574460 | TTGACATTTAAGGAG[C/T]TAAACATGGTGTTGG | 79582 |
rs16850471 | snp | A/G | 0.17138 | 0.237316 | intron-variant | SPAG16 | GRCh38.p7 | 2:213575308 | AAACAACCCACAGCA[A/G]TACTTTATCCTTTTA | 79582 |
rs16850472 | snp | A/G | 0.17461 | 0.238362 | intron-variant | SPAG16 | GRCh38.p7 | 2:213586026 | ACTGACGTATACCAT[A/G]CATTCAGATTCCTAT | 79582 |
rs16850475 | snp | A/G | 0.130008 | 0.219321 | intron-variant | SPAG16 | GRCh38.p7 | 2:213590198 | TAACTGTTTTTACAC[A/G]TAATTGCACTTGTTT | 79582 |
rs16850485 | snp | A/G | 0.130008 | 0.219321 | intron-variant | SPAG16 | GRCh38.p7 | 2:213594404 | AGTTGGGCTAACATA[A/G]TAGCTCCTCTTTATA | 79582 |
rs16850489 | snp | A/G | 0.132066 | 0.220435 | intron-variant | SPAG16 | GRCh38.p7 | 2:213594502 | ATTTGTGATTTTTGC[A/G]GGGAGAATGGGGGTG | 79582 |
rs16850494 | snp | C/T | 0.0263992 | 0.111815 | intron-variant | SPAG16 | GRCh38.p7 | 2:213594637 | CTAAGTGATTACTCC[C/T]GTGGGTTCCCAGTAA | 79582 |
rs16850496 | snp | C/T | 0.0271762 | 0.113356 | intron-variant | SPAG16 | GRCh38.p7 | 2:213595277 | GTAACTCTCATGCAA[C/T]TAATTAAAACTCAGT | 79582 |
rs16850500 | snp | A/G | 0.00795532 | 0.062565 | intron-variant | SPAG16 | GRCh38.p7 | 2:213595497 | ATTCTGCATTTTCTA[A/G]GATTCCTTTAAACTG | 79582 |
rs16850503 | snp | A/G | 0.127944 | 0.218179 | intron-variant | SPAG16 | GRCh38.p7 | 2:213598726 | TTTCTCCTTTTGTGG[A/G]GAAAGAGGTACTGAG | 79582 |
rs16850507 | snp | A/T | 0.125528 | 0.21681 | intron-variant | SPAG16 | GRCh38.p7 | 2:213600488 | CACTGAGCTCTTCTA[A/T]GTTCCTAGTATTGTG | 79582 |
rs16850512 | snp | A/G | 0.131723 | 0.220251 | intron-variant | SPAG16 | GRCh38.p7 | 2:213603370 | TTATACGCATTTTCC[A/G]TATCTTGCCAACTGT | 79582 |
rs16850518 | snp | G/T | 0.0520825 | 0.152737 | intron-variant | SPAG16 | GRCh38.p7 | 2:213603417 | TTGATTATGCCATGT[G/T]TTGATGAAAAGTTGT | 79582 |
rs16850527 | snp | C/G | 0.131723 | 0.220251 | intron-variant | SPAG16 | GRCh38.p7 | 2:213607551 | ACTTTTTATAAAGGA[C/G]AGTGCTAGTAGGTAT | 79582 |
rs16850537 | snp | G/T | 0.127254 | 0.217792 | intron-variant, downstream-variant-500B | SPAG16 | GRCh38.p7 | 2:213611626 | GCTCTATTTTTAGGA[G/T]ATTTGCTATTTAGAC | 79582 |
rs16850551 | snp | C/T | 0.0383715 | 0.133092 | intron-variant, downstream-variant-500B | SPAG16 | GRCh38.p7 | 2:213611930 | CTTTCAGAATGTTCT[C/T]CACAATCAATATTTT | 79582 |
rs16850557 | snp | G/T | 0.0551013 | 0.156571 | intron-variant | SPAG16 | GRCh38.p7 | 2:213612124 | TACCTATAGCAAAAA[G/T]AGAATGAGGGCTTGA | 79582 |
rs16850563 | snp | A/C | 0.127254 | 0.217792 | intron-variant | SPAG16 | GRCh38.p7 | 2:213614443 | GAAAGAGTGGATGCA[A/C]TTTACTTTAAATTCT | 79582 |
rs16850566 | snp | A/T | 0.084364 | 0.187256 | intron-variant | SPAG16 | GRCh38.p7 | 2:213614835 | AAAGATGGCTTGTGA[A/T]GTAAATATTGCTTAA | 79582 |
rs16850573 | snp | C/T | 0.127254 | 0.217792 | intron-variant | SPAG16 | GRCh38.p7 | 2:213616957 | AAAATCTGTTCAGGC[C/T]ATTGTAGCTCAGTCT | 79582 |
rs16850595 | snp | C/T | 0.127599 | 0.217986 | intron-variant | SPAG16 | GRCh38.p7 | 2:213647430 | GAGCTTCATTAGGAG[C/T]ATGCTATTATTTTAT | 79582 |
rs16850605 | snp | A/C/T | 0.131734 | 0.221373 | intron-variant | SPAG16 | GRCh38.p7 | 2:213649213 | ATGAATTTTGTGACA[A/C/T]CTGACCTACTAACAG | 79582 |
rs16850642 | snp | G/T | 0.10237 | 0.201756 | intron-variant | SPAG16 | GRCh38.p7 | 2:213666456 | TTATCCCACCTATAT[G/T]CTTAGTCTTATAAAA | 79582 |
rs16850652 | snp | A/C | 0.105924 | 0.204309 | intron-variant | SPAG16 | GRCh38.p7 | 2:213667106 | CTTTTTGAGCATCTA[A/C]TTTAGATTTCTTATA | 79582 |
rs16850663 | snp | A/G | 0.105569 | 0.204058 | intron-variant | SPAG16 | GRCh38.p7 | 2:213668499 | TTTTACAGATAGATT[A/G]AATTTTATTAAATAT | 79582 |
rs16850665 | snp | A/G | 0.105924 | 0.204309 | intron-variant | SPAG16 | GRCh38.p7 | 2:213669065 | ATACTTATGATTTTC[A/G]TATTTGCTTAGTTAC | 79582 |
rs16850667 | snp | C/T | 0.105924 | 0.204309 | intron-variant | SPAG16 | GRCh38.p7 | 2:213669168 | AACTAAAGTTGAGAA[C/T]CTTTTCCAGTGGCAT | 79582 |
rs16850669 | snp | A/T | 0.105924 | 0.204309 | intron-variant | SPAG16 | GRCh38.p7 | 2:213669620 | TCTTTATATCCTTTA[A/T]TGGTAAAATAGGACA | 79582 |
rs16850672 | snp | G/T | 0.105569 | 0.204058 | intron-variant | SPAG16 | GRCh38.p7 | 2:213670642 | AATTTTTTCATGTAC[G/T]GATAGTATATACATT | 79582 |
rs16850675 | snp | A/G | 0.105569 | 0.204058 | intron-variant | SPAG16 | GRCh38.p7 | 2:213670826 | AATTTCTCAAATGCC[A/G]CATATATCAGTAAGC | 79582 |
rs16850740 | snp | G/T | 0.125528 | 0.21681 | intron-variant | SPAG16 | GRCh38.p7 | 2:213716392 | TAAACAAAGCAAACA[G/T]TTCTAAATTGAGAGC | 79582 |
rs16850765 | snp | A/G | 0.0614824 | 0.164198 | intron-variant | SPAG16 | GRCh38.p7 | 2:213722654 | TCAGGATTATGATGC[A/G]GTTTAGGACAAGCAA | 79582 |
rs16850783 | snp | C/T | 0.406814 | 0.194704 | intron-variant | SPAG16 | GRCh38.p7 | 2:213729347 | TTACTTCCCTCAATT[C/T]TAGAATGGACACACT | 79582 |
rs16850835 | snp | G/T | 0.0581099 | 0.160244 | intron-variant | SPAG16 | GRCh38.p7 | 2:213740010 | AGGGCAACAATACTA[G/T]GAATTCTTTTGGAAA | 79582 |
rs16850841 | snp | A/T | 0.307176 | 0.243374 | intron-variant | SPAG16 | GRCh38.p7 | 2:213743990 | GCCTCTTGCATGCTT[A/T]GTTATATTTTAGTGT | 79582 |
rs16850844 | snp | C/T | 0.0581099 | 0.160244 | intron-variant | SPAG16 | GRCh38.p7 | 2:213744783 | CAACTGGATACATAG[C/T]TTGGCATATGGTGGT | 79582 |
rs16850846 | snp | A/G | 0.0611083 | 0.163768 | intron-variant | SPAG16 | GRCh38.p7 | 2:213745142 | CCAGTTATACAATGC[A/G]ATTAATTAAATGCAG | 79582 |
rs16850849 | snp | C/T | 0.0614824 | 0.164198 | intron-variant | SPAG16 | GRCh38.p7 | 2:213748649 | AAGTAAGCGTAAGGA[C/T]TATTATACATAATCT | 79582 |
rs16850853 | snp | C/T | 0.0618563 | 0.164627 | intron-variant | SPAG16 | GRCh38.p7 | 2:213749352 | CCAGTTAACATATCC[C/T]GGCAGCATAAATGAA | 79582 |
rs16850855 | snp | A/G | 0.0611083 | 0.163768 | intron-variant | SPAG16 | GRCh38.p7 | 2:213755030 | AAGGTACTGAGATGT[A/G]ATATACAAAAAGGCA | 79582 |
rs16850888 | snp | C/T | 0.344815 | 0.231323 | intron-variant | SPAG16 | GRCh38.p7 | 2:213786328 | TAGAATTTTGGAGTT[C/T]AAGTGGTGACTTTGA | 79582 |
rs16850897 | snp | A/C | 0.342134 | 0.232404 | intron-variant | SPAG16 | GRCh38.p7 | 2:213787355 | ATATAAATAAATAGA[A/C]CAAGAGCTACTAAGC | 79582 |
rs16850995 | snp | A/C | 0.0275645 | 0.114116 | intron-variant | SPAG16 | GRCh38.p7 | 2:213844201 | AACTTAGCAGCATGA[A/C]CAATGAAACCTGAAG | 79582 |
rs16851002 | snp | G/T | 0.0799831 | 0.183287 | intron-variant | SPAG16 | GRCh38.p7 | 2:213847959 | GTAATTTTGAGAGGG[G/T]TATGTGCTGCAGACA | 79582 |
rs16851059 | snp | G/T | 0.332337 | 0.236052 | intron-variant | SPAG16 | GRCh38.p7 | 2:213876292 | AAAATCTGACTAGTA[G/T]TAACTTTGAACCAAA | 79582 |
rs16851073 | snp | C/T | 0.0422008 | 0.138995 | intron-variant | SPAG16 | GRCh38.p7 | 2:213900254 | GGGGATTTTTCACTG[C/T]AAGAATGGCGTGTCT | 79582 |
rs16851076 | snp | A/G | 0.330016 | 0.236849 | intron-variant | SPAG16 | GRCh38.p7 | 2:213901253 | TTGGGCCTAAGTATC[A/G]TAGCAGCCTACAAAA | 79582 |
rs16851079 | snp | A/G | 0.32768 | 0.237625 | intron-variant | SPAG16 | GRCh38.p7 | 2:213911516 | ATGCACATGAAGAGC[A/G]TGTAATACGTGTAAT | 79582 |
rs16851119 | snp | A/T | 0.0926964 | 0.194308 | intron-variant | SPAG16 | GRCh38.p7 | 2:213923983 | TTTACACAGAAGTGG[A/T]ACAACTGGGCTGGAA | 79582 |
rs16851125 | snp | C/T | 0.32955 | 0.237006 | intron-variant | SPAG16 | GRCh38.p7 | 2:213925264 | TCCCTTTCAGATCTT[C/T]TGTCCCTAAAATATA | 79582 |
rs16851129 | snp | C/T | 0.311614 | 0.242289 | intron-variant | SPAG16 | GRCh38.p7 | 2:213928718 | AGTCATGAGGCTTGG[C/T]GCCGTAGAAACAGAG | 79582 |
rs16851148 | snp | G/T | 0.333952 | 0.235483 | intron-variant | SPAG16 | GRCh38.p7 | 2:213938345 | TCTGAGGTAAAAAAT[G/T]AAAATCACGTTTGTT | 79582 |
rs16851153 | snp | A/T | 0.108048 | 0.20579 | intron-variant | SPAG16 | GRCh38.p7 | 2:213938791 | AATTTTGGCAGCATT[A/T]AACTAAATATTTTCT | 79582 |
rs16851170 | snp | C/T | 0.0955749 | 0.196603 | intron-variant | SPAG16 | GRCh38.p7 | 2:213968842 | TTGTAAATGGCAGAG[C/T]ATTATTCTAACTTTT | 79582 |
rs16851180 | snp | A/C | 0.0356815 | 0.128715 | intron-variant | SPAG16 | GRCh38.p7 | 2:213974557 | AAGTTACTTATTAAA[A/C]TACCATTTAGAATCC | 79582 |
rs16851229 | snp | C/T | 0.0295035 | 0.117819 | intron-variant | SPAG16 | GRCh38.p7 | 2:213988117 | ACTGCCTAAACTGTT[C/T]CAAGAGAGTGTTTTT | 79582 |
rs16851244 | snp | A/G | 0.031825 | 0.122064 | intron-variant | SPAG16 | GRCh38.p7 | 2:213993897 | TCATATCCTAAGCTG[A/G]CCACTTTGTTGTATT | 79582 |
rs16851251 | snp | C/T | 0.0329836 | 0.124112 | intron-variant | SPAG16 | GRCh38.p7 | 2:213996490 | GAATAAAAGCAGATA[C/T]ATCTTGGCCATTGAA | 79582 |
rs16851267 | snp | C/T | 0.0252325 | 0.109451 | intron-variant | SPAG16 | GRCh38.p7 | 2:214000593 | ATGGATTGTGACATA[C/T]AAGGCCAGAGTCCTC | 79582 |
rs16851301 | snp | A/C | 0.495891 | 0.0451408 | intron-variant | SPAG16 | GRCh38.p7 | 2:214018843 | TCTCAAACATATACT[A/C]GTTTTAAATCATTAA | 79582 |
rs16851312 | snp | A/G | 0.484209 | 0.0874434 | intron-variant | SPAG16 | GRCh38.p7 | 2:214021709 | CAAAATTTAAAATAA[A/G]CCTCACTGCATTGAT | 79582 |
rs16851351 | snp | C/T | 0.457271 | 0.139781 | intron-variant | SPAG16 | GRCh38.p7 | 2:214062134 | ATCAAAAACCAACCT[C/T]CTGGGCCAGGCAGAG | 79582 |
rs16851360 | snp | C/G | 0.251859 | 0.249993 | intron-variant | SPAG16 | GRCh38.p7 | 2:214064819 | ACTGATTTGTGTTTT[C/G]TACAAGTTAATAACT | 79582 |
rs16851361 | snp | C/G | 0.114738 | 0.210248 | intron-variant | SPAG16 | GRCh38.p7 | 2:214065701 | GGGGAATATTTATTT[C/G]CTCTGTTAATTTTAT | 79582 |
rs16851377 | snp | C/T | 0.245346 | 0.249957 | intron-variant | SPAG16 | GRCh38.p7 | 2:214067130 | ATTAACTTTTCAGCT[C/T]TCTATGTGAAGAAAG | 79582 |
rs16851380 | snp | C/T | 0.00597247 | 0.0543191 | intron-variant | SPAG16 | GRCh38.p7 | 2:214068458 | TCAGTAACCATGGTT[C/T]CCACATAGTACTCAT | 79582 |
rs16851401 | snp | A/G | 0.030665 | 0.119967 | intron-variant | SPAG16 | GRCh38.p7 | 2:214076392 | ACATACTGATAAATG[A/G]AAATTAACTGTAAAT | 79582 |
rs16851402 | snp | A/G | 0.093777 | 0.195178 | intron-variant | SPAG16 | GRCh38.p7 | 2:214076777 | GCTTTTGGTTGGGCA[A/G]AGTTAATAAGTAAGC | 79582 |
rs16851405 | snp | C/T | 0.234109 | 0.249494 | intron-variant | SPAG16 | GRCh38.p7 | 2:214079032 | GATCTGTGGAATACA[C/T]GTTTAGGTCTTTCAT | 79582 |
rs16851418 | snp | A/C | 0.0883596 | 0.190715 | intron-variant | SPAG16 | GRCh38.p7 | 2:214080820 | GTTTTTGTAATTGCA[A/C]GTTTCTTTAACCAGA | 79582 |
rs16851420 | snp | A/G | 0.309401 | 0.24284 | intron-variant | SPAG16 | GRCh38.p7 | 2:214082315 | AATTTCTCCTCATCA[A/G]TCTTCTTTCATTAAA | 79582 |
rs16851422 | snp | C/T | 0.307919 | 0.243198 | intron-variant | SPAG16 | GRCh38.p7 | 2:214082393 | CCACTTCTTACTGTC[C/T]CATGACTTTTGGGAA | 79582 |
rs16851426 | snp | A/G | 0.23031 | 0.249223 | intron-variant | SPAG16 | GRCh38.p7 | 2:214083955 | GTCCTTCCTCATAGC[A/G]ATTCCTACCTTTTCT | 79582 |
rs16851432 | snp | A/T | 0.0209421 | 0.100162 | intron-variant | SPAG16, LOC101928084 | GRCh38.p7 | 2:214087414 | ATTATGATATGGATT[A/T]TGTTAATTCAGTCAT | 79582 |
rs16851437 | snp | A/T | 0.225301 | 0.248777 | intron-variant | SPAG16, LOC101928084 | GRCh38.p7 | 2:214089750 | GTTTGCCATTCTCTG[A/T]GGTTCTCTAAGAAAT | 79582 |
rs16851445 | snp | C/G | 0.093417 | 0.194889 | intron-variant | SPAG16, LOC101928084 | GRCh38.p7 | 2:214090711 | GCATGAGTTCCAAAC[C/G]CCATGTAACATTGTT | 79582 |
rs16851450 | snp | A/G | 0.231775 | 0.249335 | intron-variant | SPAG16, LOC101928084 | GRCh38.p7 | 2:214092575 | ATTTTTAACAAATCA[A/G]ATTTTTTCCTGTTAC | 79582 |
rs16851461 | snp | A/G | 0.224116 | 0.248656 | intron-variant | SPAG16, LOC101928084 | GRCh38.p7 | 2:214099447 | GTAAAGTGTTTATAC[A/G]AATAAGAGATAGTAT | 79582 |
rs16851464 | snp | A/G | 0.223819 | 0.248625 | intron-variant | SPAG16, LOC101928084 | GRCh38.p7 | 2:214099709 | GACTAACTTTTCATT[A/G]GAGAGTGTTTTGTAA | 79582 |
rs16851487 | snp | G/T | 0.229136 | 0.249128 | intron-variant, upstream-variant-2KB | SPAG16, LOC101928084 | GRCh38.p7 | 2:214103720 | GACAGTACAAAGGAG[G/T]TGTCTGGATCAGATA | 79582 |
rs16851489 | snp | A/G | 0.0209421 | 0.100162 | intron-variant, upstream-variant-2KB | SPAG16, LOC101928084 | GRCh38.p7 | 2:214104688 | GTGAAGATCAAAATA[A/G]ACAGTTGGGAAGTAG | 79582 |
rs16851490 | snp | A/T | 0.234692 | 0.249531 | intron-variant | SPAG16 | GRCh38.p7 | 2:214105598 | CACACAGCTTCTCTG[A/T]CTGAATCAAATGCTG | 79582 |
rs16851493 | snp | A/T | 0.224116 | 0.248656 | intron-variant | SPAG16 | GRCh38.p7 | 2:214106582 | GAGGACCAAGTAGAG[A/T]TTAGTTTAGTTATAA | 79582 |
rs16851494 | snp | A/C | 0.224116 | 0.248656 | intron-variant | SPAG16 | GRCh38.p7 | 2:214107217 | TTTATGCCTTTATCA[A/C]AAAATGCCCATCTCC | 79582 |
rs16851495 | snp | A/G | 0.161219 | 0.233705 | intron-variant | SPAG16 | GRCh38.p7 | 2:214108287 | TTCTCCCAGTAAACT[A/G]TTTTTAATGCTTCAT | 79582 |
rs16851496 | snp | A/C | 0.257176 | 0.249897 | intron-variant | SPAG16 | GRCh38.p7 | 2:214109735 | TATCTAATTTTCTGT[A/C]GTGAGCCAATTAGTT | 79582 |
rs16851506 | snp | A/G | 0.0821764 | 0.185298 | intron-variant | SPAG16 | GRCh38.p7 | 2:214124350 | AAATCTCATTTAAAC[A/G]GGTTTCACAGTACGA | 79582 |
rs16851532 | snp | A/C | 0.26818 | 0.249338 | intron-variant | SPAG16 | GRCh38.p7 | 2:214154000 | ATTTGTGAAGGGATA[A/C]GTGCTCCTTTCTCAT | 79582 |
rs16851537 | snp | A/G | 0.347253 | 0.230308 | intron-variant | SPAG16 | GRCh38.p7 | 2:214154209 | AGAATTTATATACAT[A/G]CTTTTCCACGTCTCT | 79582 |
rs16851541 | snp | A/C | 0.0349115 | 0.127424 | intron-variant | SPAG16 | GRCh38.p7 | 2:214154589 | TTCTAGAAAAATCTA[A/C]AGTTCATCATTTTTT | 79582 |
rs16851545 | snp | C/T | 0.0271762 | 0.113356 | intron-variant | SPAG16 | GRCh38.p7 | 2:214154592 | TAGAAAAATCTACAG[C/T]TCATCATTTTTTATT | 79582 |
rs16851548 | snp | A/C | 0.26818 | 0.249338 | intron-variant | SPAG16 | GRCh38.p7 | 2:214156105 | GTGATAGTTGACTCA[A/C]AGCTAAGACATGGAA | 79582 |
rs16851554 | snp | G/T | 0.254385 | 0.249962 | intron-variant | SPAG16 | GRCh38.p7 | 2:214159668 | ACTCAGAAGTATATT[G/T]TCTCACTTGTTCTAT | 79582 |
rs16851568 | snp | C/T | 0.378962 | 0.21417 | intron-variant | SPAG16 | GRCh38.p7 | 2:214182472 | CAGCCAGTCTCACAA[C/T]TGTTTCTTCTGTCCA | 79582 |
rs16851595 | snp | C/G | 0.113685 | 0.209567 | intron-variant | SPAG16 | GRCh38.p7 | 2:214209312 | GTAGAGAAACCCATT[C/G]CAGCCTATCTGAGAA | 79582 |
rs16851611 | snp | C/T | 0.386694 | 0.20932 | intron-variant | SPAG16 | GRCh38.p7 | 2:214217186 | GAGCAAGGCACAAAT[C/T]GATTTAATGGGAGAT | 79582 |
rs16851621 | snp | A/G | 0.0295035 | 0.117819 | intron-variant | SPAG16 | GRCh38.p7 | 2:214222058 | TTTCATGGTACATCT[A/G]TCTCACAGCTAAGAC | 79582 |
rs16851640 | snp | A/G | 0.0839998 | 0.186933 | intron-variant | SPAG16 | GRCh38.p7 | 2:214238724 | AAAATCTACATCCTT[A/G]TCTGTTTTACTCATA | 79582 |
rs16851644 | snp | A/G | 0.252702 | 0.249985 | intron-variant | SPAG16 | GRCh38.p7 | 2:214239716 | TCAGAGCTGCACTGG[A/G]GCTGGAGACAGGGAT | 79582 |
rs16851649 | snp | A/G | 0.0988009 | 0.199095 | intron-variant | SPAG16 | GRCh38.p7 | 2:214245700 | TCTGACCATCTGCTG[A/G]TAAAATTTAAGGGCA | 79582 |
rs16851651 | snp | C/T | 0.111576 | 0.20818 | intron-variant | SPAG16 | GRCh38.p7 | 2:214246013 | CCCATTGTATGGGTA[C/T]TGCAGATTTTCCATA | 79582 |
rs16851652 | snp | A/G | 0.107341 | 0.205301 | intron-variant | SPAG16 | GRCh38.p7 | 2:214247716 | TGAATCCAAGGTGAA[A/G]TAAGAACAGCTGATG | 79582 |
rs16851682 | snp | C/G | 0.0966517 | 0.197444 | intron-variant | SPAG16 | GRCh38.p7 | 2:214268581 | TAGGACCAACCATGT[C/G]ATCCAAAAACTCAAT | 79582 |
rs16851684 | snp | G/T | 0.0970103 | 0.197722 | intron-variant | SPAG16 | GRCh38.p7 | 2:214268869 | AGAGCTGTATAAAAC[G/T]CTTTTCCCTATGCTA | 79582 |
rs16851687 | snp | C/T | 0.0744748 | 0.178019 | intron-variant | SPAG16 | GRCh38.p7 | 2:214269803 | TGAGAAGAATCTATC[C/T]TGAGCACTTAAGCTG | 79582 |
rs16851709 | snp | C/T | 0.149999 | 0.229128 | intron-variant | SPAG16 | GRCh38.p7 | 2:214284178 | ATCCTCTGAAAGAGA[C/T]TGCGTTATGAGAAAA | 79582 |
rs16851712 | snp | C/G | 0.106987 | 0.205054 | intron-variant | SPAG16 | GRCh38.p7 | 2:214284626 | GCAGTACTCTGTTGA[C/G]ATCTACAGATGCAGA | 79582 |
rs16851715 | snp | G/T | 0.0973687 | 0.197999 | intron-variant | SPAG16 | GRCh38.p7 | 2:214284681 | ATGTAAGTTGAAAAT[G/T]ATTGGTGCATTCATT | 79582 |
rs16851742 | snp | A/G | 0.0984431 | 0.198823 | intron-variant | SPAG16 | GRCh38.p7 | 2:214315381 | TATTTAAAAGGTTCT[A/G]TGTTGGCATTCAGAT | 79582 |
rs16851747 | snp | C/T | 0.273318 | 0.24891 | intron-variant | SPAG16 | GRCh38.p7 | 2:214316379 | TGTTGAACAAGAGAC[C/T]TTCTTAGCCTCATCA | 79582 |
rs16851749 | snp | A/G | 0.108048 | 0.20579 | intron-variant | SPAG16 | GRCh38.p7 | 2:214316698 | CAATCTTAAATAAAT[A/G]AGCGTAGTTTTCTTC | 79582 |
rs16851756 | snp | A/G | 0.111224 | 0.207945 | intron-variant | SPAG16 | GRCh38.p7 | 2:214318881 | CCGAGCTGAAGTAGA[A/G]GCAAGCCTGGAGTGA | 79582 |
rs16851771 | snp | A/G | 0.157642 | 0.232314 | intron-variant | SPAG16 | GRCh38.p7 | 2:214323895 | AAACATTATATGTAA[A/G]GAAAGCTGCATAAGA | 79582 |
rs16851773 | snp | A/G | 0.477684 | 0.103247 | intron-variant | SPAG16 | GRCh38.p7 | 2:214324085 | TTTACATCAGAAACA[A/G]TGGGCTTGATAGAAA | 79582 |
rs16851777 | snp | A/G | 0.115088 | 0.210473 | intron-variant | SPAG16 | GRCh38.p7 | 2:214324784 | GGCTCATCTATGCAG[A/G]CGACTTTTGGATTTT | 79582 |
rs16851779 | snp | C/T | 0.21725 | 0.247846 | intron-variant | SPAG16 | GRCh38.p7 | 2:214325226 | AAAGCATAATATGCC[C/T]ACTACTTACCAGGGA | 79582 |
rs16851786 | snp | G/T | 0.119978 | 0.213528 | intron-variant | SPAG16 | GRCh38.p7 | 2:214326531 | ACTGAACAGCTGAAG[G/T]AGGACAGATATGAGA | 79582 |
rs16851838 | snp | G/T | 0.0115144 | 0.0749975 | intron-variant | SPAG16 | GRCh38.p7 | 2:214345041 | CACACAATATGATGG[G/T]AAACAATCGTTCTTA | 79582 |
rs16851844 | snp | A/G | 0.472803 | 0.113397 | intron-variant | SPAG16 | GRCh38.p7 | 2:214347658 | GACGATATTATCACA[A/G]TGGTGTTATGAGTTG | 79582 |
rs16851847 | snp | C/T | 0.473359 | 0.112298 | intron-variant | SPAG16 | GRCh38.p7 | 2:214347990 | GTCCTAAGCAAAGAA[C/T]TGGCAACACACACTT | 79582 |
rs16851849 | snp | A/T | 0.0614824 | 0.164198 | intron-variant | SPAG16 | GRCh38.p7 | 2:214350953 | AAAAGGCAACTTGGA[A/T]TAAGAAAAGAAAATA | 79582 |
rs16851877 | snp | A/G | 0.181022 | 0.240296 | intron-variant | SPAG16 | GRCh38.p7 | 2:214365429 | TGCTATCCTAATGTG[A/G]TCTAACAGTTGAAGC | 79582 |
rs16851881 | snp | A/G | 0.00318978 | 0.0398085 | intron-variant | SPAG16 | GRCh38.p7 | 2:214367531 | TAAACACCTAAAAGC[A/G]GAAAAGGCTTCTATG | 79582 |
rs17207263 | snp | C/T | 0.284995 | 0.247539 | intron-variant | SPAG16 | GRCh38.p7 | 2:214044212 | CATATGCATTATTTT[C/T]AATTTATAAAGGACT | 79582 |
rs17207375 | snp | C/T | 0.121717 | 0.214577 | intron-variant | SPAG16 | GRCh38.p7 | 2:214049997 | TTGGTATATTTCATT[C/T]CTTTCAGTGAGAGCT | 79582 |
rs17207529 | snp | C/T | 0.334871 | 0.235153 | intron-variant | SPAG16 | GRCh38.p7 | 2:214052375 | TTACACAGCTTTCAA[C/T]GTTTTCTGGTTTAAC | 79582 |
rs17227489 | snp | C/T | 0.354665 | 0.227036 | intron-variant | SPAG16 | GRCh38.p7 | 2:214071669 | AGCTGTCAGTCAGCC[C/T]TTCCTATCCTCCTTC | 79582 |
rs17228000 | snp | C/T | 0.191775 | 0.243125 | intron-variant | SPAG16, LOC101928084 | GRCh38.p7 | 2:214085557 | CCTCAAATTCCCAAA[C/T]ATAAAATCATCTGTT | 79582 |
rs17229840 | snp | C/T | 0.138886 | 0.22395 | intron-variant | SPAG16 | GRCh38.p7 | 2:214109906 | CATGCCCTACAAAAA[C/T]TAAATGGGAGCTGAA | 79582 |
rs17281873 | snp | A/G | 0.00874735 | 0.0655527 | intron-variant | SPAG16 | GRCh38.p7 | 2:214122003 | ACCTGTACTATTGTT[A/G]ATGGAGATAATGTTC | 79582 |
rs17298252 | snp | G/T | 0.209997 | 0.246779 | intron-variant | SPAG16 | GRCh38.p7 | 2:213289078 | CATATGACTCACCTG[G/T]GGAGCTTTAAATAAA | 79582 |
rs17364024 | snp | A/C | 0.0244538 | 0.107838 | intron-variant, upstream-variant-2KB, utr-variant-5-prime | SPAG16, LOC100130451 | GRCh38.p7 | 2:213285452 | CTCCTTTATTCAGGG[A/C]GGTAAGAAAGAGATG | 79582 |
rs17364234 | snp | A/G | 0.0498117 | 0.149749 | intron-variant | SPAG16 | GRCh38.p7 | 2:213290603 | GAGGGCTCAAAGGCA[A/G]CTTGACATTAAGAAA | 79582 |
rs17693815 | snp | C/T | 0.0248432 | 0.108648 | intron-variant | SPAG16 | GRCh38.p7 | 2:213387151 | AAAAGGATCAAATGG[C/T]ATCCACTGTAGTCCA | 79582 |
rs17694142 | snp | A/G | 0.214239 | 0.247429 | intron-variant | SPAG16 | GRCh38.p7 | 2:213405218 | TTGCTGGAATTAAAC[A/G]TCCTACAGTTAATTT | 79582 |
rs17694263 | snp | G/T | 0.0240643 | 0.107019 | intron-variant | SPAG16 | GRCh38.p7 | 2:213413655 | GTGCATAATTAAGGT[G/T]TCTGATAGATTTGGT | 79582 |
rs17694850 | snp | A/G | 0.0452528 | 0.143452 | intron-variant | SPAG16 | GRCh38.p7 | 2:213435649 | TCTCTTTAGTTATTG[A/G]ACATTTTTCATCCAT | 79582 |
rs17695086 | snp | A/C | 0.0248432 | 0.108648 | intron-variant | SPAG16 | GRCh38.p7 | 2:213452977 | TTTTTGAATTAACAG[A/C]TTTTAAGGCTATTAG | 79582 |
rs17700988 | snp | A/T | 0.0185938 | 0.0946107 | intron-variant | SPAG16 | GRCh38.p7 | 2:213487746 | GCTTATAAAAATTGC[A/T]GTGTTTATGGTTTCA | 79582 |
rs17701161 | snp | A/G | 0.0275645 | 0.114116 | intron-variant | SPAG16 | GRCh38.p7 | 2:213495072 | TACTTTATTTCATTC[A/G]TGGTTCTCAGTAGGC | 79582 |
rs17701461 | snp | A/G | 0.0240643 | 0.107019 | intron-variant | SPAG16 | GRCh38.p7 | 2:213521957 | TTTGGGAGTATCATT[A/G]GAAACCAATATTCAT | 79582 |
rs17701917 | snp | C/T | 0.0539704 | 0.155153 | intron-variant | SPAG16 | GRCh38.p7 | 2:213575082 | CACAGACTAAAACTC[C/T]ATGAAACATTATTCA | 79582 |
rs17702023 | snp | A/G | 0.093417 | 0.194889 | intron-variant | SPAG16 | GRCh38.p7 | 2:213588022 | ATAAGATAAACTCAT[A/G]CTATTTCACTAATTA | 79582 |
rs17703620 | snp | A/C | 0.0240643 | 0.107019 | intron-variant | SPAG16 | GRCh38.p7 | 2:213741613 | TGATTTCAGATTTTA[A/C]AAAATAATTCATAGC | 79582 |
rs17708794 | snp | G/T | 0.260504 | 0.249779 | intron-variant | SPAG16 | GRCh38.p7 | 2:213923990 | AGAAGTGGAACAACT[G/T]GGCTGGAAGCTCTAG | 79582 |
rs17708896 | snp | A/T | 0.484841 | 0.0857308 | intron-variant | SPAG16 | GRCh38.p7 | 2:213925287 | AAAATATATCCTTAG[A/T]AATTTCTGTAGGAGA | 79582 |
rs17748471 | snp | A/G | 0.347694 | 0.230122 | intron-variant | SPAG16 | GRCh38.p7 | 2:214181504 | CTGGCCACCAATTCT[A/G]TATATGAACACCATG | 79582 |
rs17748509 | snp | A/T | 0.347473 | 0.230215 | intron-variant | SPAG16 | GRCh38.p7 | 2:214182099 | AATGAACTGACAGTT[A/T]ATCTCTTTCTTCTCT | 79582 |
rs17748800 | snp | C/T | 0.346368 | 0.23068 | intron-variant | SPAG16 | GRCh38.p7 | 2:214186210 | TCCACCACAGAACTG[C/T]GTTGAATAAGCTCCC | 79582 |
rs17749215 | snp | A/G | 0.34659 | 0.230587 | intron-variant | SPAG16 | GRCh38.p7 | 2:214201534 | GTAGCCATATAAGGA[A/G]GATGTTAAAAGTTCC | 79582 |
rs17749383 | snp | A/G | 0.34659 | 0.230587 | intron-variant | SPAG16 | GRCh38.p7 | 2:214211182 | AAAAAAAAATTCCCT[A/G]CATTTGAATGTATTA | 79582 |
rs17749501 | snp | A/G | 0.00636936 | 0.0560724 | intron-variant | SPAG16 | GRCh38.p7 | 2:214220630 | GTTATAGCTGAATAT[A/G]CTAAAACTGGATGGC | 79582 |
rs17750216 | snp | A/T | 0.0221141 | 0.102801 | intron-variant | SPAG16 | GRCh38.p7 | 2:213390470 | GGAACAGAAGGCATG[A/T]TAGGAAGGATACATA | 79582 |
rs17750222 | snp | G/T | 0.213635 | 0.247341 | intron-variant | SPAG16 | GRCh38.p7 | 2:213391894 | ATAGAAACATGGAGA[G/T]TAGAGAATTACGGTG | 79582 |
rs17750805 | snp | G/T | 0.21303 | 0.247251 | intron-variant | SPAG16 | GRCh38.p7 | 2:213415910 | GGCAGGAAGCTGCAG[G/T]TAGTTCTTTGTGAAG | 79582 |
rs17750829 | snp | G/T | 0.0221141 | 0.102801 | intron-variant | SPAG16 | GRCh38.p7 | 2:213416338 | GTATCAGGGACCAGA[G/T]CTTTGTATGATGAGA | 79582 |
rs17750895 | snp | A/G | 0.209693 | 0.246729 | intron-variant | SPAG16 | GRCh38.p7 | 2:213419372 | CGTTGCCCTTTCCAC[A/G]CTCCTCATTATGCTG | 79582 |
rs17751271 | snp | A/G | 0.0452528 | 0.143452 | intron-variant | SPAG16 | GRCh38.p7 | 2:213435890 | CCGGTACTACTTGCT[A/G]TCTATATAATTTTGG | 79582 |
rs17751591 | snp | G/T | 0.0448719 | 0.142907 | intron-variant | SPAG16 | GRCh38.p7 | 2:213459459 | TCACCTTAATCCAAT[G/T]GGTGATTGAGATGAT | 79582 |
rs17752241 | snp | A/G | 0.0240643 | 0.107019 | intron-variant | SPAG16 | GRCh38.p7 | 2:213499893 | CATACGGACTTTCTT[A/G]TCCCTGTTTCCAGAC | 79582 |
rs17752490 | snp | A/T | 0.0189856 | 0.0955633 | intron-variant | SPAG16 | GRCh38.p7 | 2:213531188 | CACACTAGGACATTT[A/T]AACAGGTCTTTGAGC | 79582 |
rs17752934 | snp | A/G | 0.0240643 | 0.107019 | intron-variant | SPAG16 | GRCh38.p7 | 2:213586083 | AGTACATTCAACTTA[A/G]ATTCTTCTTAGCCAT | 79582 |
rs17753327 | snp | A/C | 0.0217236 | 0.101931 | intron-variant | SPAG16 | GRCh38.p7 | 2:213609310 | CTTACTTTTGGCTAA[A/C]TTGTCTTTGCTTTAG | 79582 |
rs17753664 | snp | A/T | 0.0141837 | 0.08301 | intron-variant | SPAG16 | GRCh38.p7 | 2:213648978 | TAGTCTGAAAAAAAA[A/T]AATCTAAATGAATAA | 79582 |
rs17753697 | snp | C/T | 0.0182019 | 0.0936463 | intron-variant | SPAG16 | GRCh38.p7 | 2:213649084 | TTCATTGCTCACTTA[C/T]GAATTATGGAACAGC | 79582 |
rs17753994 | snp | A/G | 0.0228947 | 0.104514 | intron-variant | SPAG16 | GRCh38.p7 | 2:213667755 | ATAACTAAAAAAATC[A/G]GCAAGTCATATCTCA | 79582 |
rs17754969 | snp | A/G | 0.283421 | 0.247756 | intron-variant | SPAG16 | GRCh38.p7 | 2:213763758 | GTGGAAAGACCGTTC[A/G]TTGCACTCATGATGC | 79582 |
rs17755390 | snp | G/T | 0.0333695 | 0.124785 | intron-variant | SPAG16 | GRCh38.p7 | 2:213787894 | TACTATCACAAAAAT[G/T]TATCGTGAAAACTAT | 79582 |
rs17756040 | snp | C/T | 0.00358779 | 0.0422022 | intron-variant | SPAG16 | GRCh38.p7 | 2:213816134 | CCCATATCAAAGGTT[C/T]CTGCTGTTTTTGAAA | 79582 |
rs17759409 | snp | C/T | 0.255224 | 0.249945 | intron-variant | SPAG16 | GRCh38.p7 | 2:213910992 | TACACTTTCCACTTC[C/T]TACTTAGTGATGTAA | 79582 |
rs17761193 | snp | A/G | 0.164873 | 0.23506 | intron-variant | SPAG16 | GRCh38.p7 | 2:213993975 | CACACATGAGAGGTA[A/G]AAAGCACATGGTAGA | 79582 |
rs17766267 | snp | A/C | 0.0858723 | 0.188781 | intron-variant | SPAG16 | GRCh38.p7 | 2:214240827 | CATCCACAGTACATA[A/C]ATAATTAAATGTAAA | 79582 |
rs17766309 | snp | G/T | 0.0682165 | 0.171742 | intron-variant | SPAG16 | GRCh38.p7 | 2:214241519 | TCATAACCCTTACAT[G/T]CAGTATCAGTAAATA | 79582 |
rs17766460 | snp | C/T | 0.215446 | 0.2476 | intron-variant | SPAG16 | GRCh38.p7 | 2:214244083 | AAACTCCTACTGTAA[C/T]AGCTTTCTTGGGAAT | 79582 |
rs17766671 | snp | A/G | 0.0123036 | 0.0774623 | intron-variant | SPAG16 | GRCh38.p7 | 2:214249531 | ATGAATAACATGTCA[A/G]CAAATTCATTTAACT | 79582 |
rs17766701 | snp | A/G | 0.0700422 | 0.173537 | intron-variant | SPAG16 | GRCh38.p7 | 2:214250512 | TATTTTAGTATGTAC[A/G]GAAGGAAGAAAACAA | 79582 |
rs17767313 | snp | A/G | 0.0955749 | 0.196603 | intron-variant | SPAG16 | GRCh38.p7 | 2:214283279 | TTCTTAAAAGTGTAA[A/G]GACTTTGGTCTCTTC | 79582 |
rs17767498 | snp | G/T | 0.226779 | 0.248919 | intron-variant | SPAG16 | GRCh38.p7 | 2:214312171 | ATATGAATCATATCT[G/T]TTAACAGTTATGATA | 79582 |
rs17767540 | snp | A/T | 0.097727 | 0.198275 | intron-variant | SPAG16 | GRCh38.p7 | 2:214313415 | TTCGATTACTTTTCA[A/T]TTTATTCTAGAATGT | 79582 |
rs17767617 | snp | A/G | 0.100231 | 0.200173 | intron-variant | SPAG16 | GRCh38.p7 | 2:214313810 | GCACTGAATGGCAGC[A/G]TAACATTTAATGTTT | 79582 |
rs17812817 | snp | A/G | 0.199254 | 0.244796 | intron-variant | SPAG16 | GRCh38.p7 | 2:214050781 | CCCTCTCTGTCACCA[A/G]ACTATTTCTTCTCCT | 79582 |
rs17813412 | snp | C/G | 0.224709 | 0.248717 | intron-variant | SPAG16 | GRCh38.p7 | 2:214069016 | AAGAAATCATAAAGC[C/G]TGTGTTTCTAAATAC | 79582 |
rs17813988 | snp | A/G | 0.203267 | 0.245593 | intron-variant, downstream-variant-500B | SPAG16, LOC101928084 | GRCh38.p7 | 2:214084852 | TTTTATGTCCTGGGG[A/G]TTACAAAGCAGAATA | 79582 |
rs17815546 | snp | A/G | 0.349233 | 0.229462 | intron-variant | SPAG16 | GRCh38.p7 | 2:214157146 | TGTGGCTCTTTGGAT[A/G]CACAAGTCTATGACT | 79582 |
rs17815611 | snp | A/G | 0.38934 | 0.207568 | intron-variant | SPAG16 | GRCh38.p7 | 2:214159653 | CTCAAATCTGATTGA[A/G]CTCAGAAGTATATTT | 79582 |
rs17815917 | snp | A/C | 0.350327 | 0.228986 | intron-variant | SPAG16 | GRCh38.p7 | 2:214181298 | CAGAAATAAGAACTG[A/C]ACATGATGTAATGAA | 79582 |
rs17816476 | snp | A/G | 0.347473 | 0.230215 | intron-variant | SPAG16 | GRCh38.p7 | 2:214193884 | TCATCTCTGTGTAAA[A/G]AAGTAGATCATTTAG | 79582 |
rs17816554 | snp | A/G | 0.0134861 | 0.0810011 | intron-variant | SPAG16 | GRCh38.p7 | 2:214196120 | TGTTTTCTTAATCCC[A/G]TGTTGAATGTCATAA | 79582 |
rs17816620 | snp | A/T | 0.110872 | 0.20771 | intron-variant | SPAG16 | GRCh38.p7 | 2:214197123 | AGGGCAATTAACCTG[A/T]CTATATTCCACTCAG | 79582 |
rs17816650 | snp | C/T | 0.345704 | 0.230956 | intron-variant | SPAG16 | GRCh38.p7 | 2:214197811 | ATATGTGTTTTTCCA[C/T]TGAATTAACCTATTA | 79582 |
rs17816758 | snp | C/T | 0.0501905 | 0.150254 | intron-variant | SPAG16 | GRCh38.p7 | 2:214208961 | TTGTTTTTATGGTTA[C/T]GGGATGAAGTTTTCT | 79582 |
rs17817541 | snp | A/G | 0.0123036 | 0.0774623 | intron-variant | SPAG16 | GRCh38.p7 | 2:214243235 | ATTCTAAGTGGTATC[A/G]GTAATCAAGGAAGAA | 79582 |
rs17817960 | snp | A/C | 0.0704125 | 0.17392 | intron-variant | SPAG16 | GRCh38.p7 | 2:214255156 | CATAAAATCAATCAT[A/C]AGTGAATCCATTATC | 79582 |
rs17818571 | snp | A/G | 0.450985 | 0.148678 | intron-variant | SPAG16 | GRCh38.p7 | 2:214284576 | CCTTTTGTCCACTGA[A/G]AAGAAAAAGTGTATA | 79582 |
rs17818709 | snp | C/G | 0.100944 | 0.200705 | intron-variant | SPAG16 | GRCh38.p7 | 2:214313517 | CAAACATTATACCTC[C/G]TTGTAAGGCTTAAAT | 79582 |
rs17818944 | snp | G/T | 0.0178098 | 0.0926698 | intron-variant | SPAG16 | GRCh38.p7 | 2:214316236 | CTATTGTGCAGAGTT[G/T]CAATAAAGGAAAACA | 79582 |
rs28368837 | snp | G/T | | | intron-variant | SPAG16 | GRCh38.p7 | 2:214128765 | ATCAAGTTTACCTTG[G/T]TGGATGCTAGATATT | 79582 |
rs28385494 | snp | A/T | 0.231775 | 0.249335 | intron-variant | SPAG16, LOC101928084 | GRCh38.p7 | 2:214092596 | TTCCTGTTACCTTAT[A/T]TATTGTATCTTTTGC | 79582 |
rs28391076 | snp | A/T | | | intron-variant | SPAG16 | GRCh38.p7 | 2:214328485 | CAGTCTTTGAGAAAA[A/T]TTTGGTTGAAGGACA | 79582 |
rs28392179 | snp | A/G | | | intron-variant | SPAG16 | GRCh38.p7 | 2:213407663 | ACAGGAGAGAGAGAG[A/G]GGGAGAGAGACAGAG | 79582 |
rs28417140 | snp | A/G | 0.0279526 | 0.114869 | intron-variant | SPAG16 | GRCh38.p7 | 2:213574623 | ACTCACTGTAGTTGT[A/G]ACTCCTTACGATCAC | 79582 |
rs28433726 | snp | C/T | 0.175576 | 0.238665 | intron-variant | SPAG16 | GRCh38.p7 | 2:213321517 | AATAACTCTAAATGC[C/T]GTCATCTCTAAGTTT | 79582 |
rs28436870 | snp | C/T | 0.0256215 | 0.110247 | intron-variant | SPAG16 | GRCh38.p7 | 2:213412079 | TCATCTGATTACCTA[C/T]TCCACCCTGACTCAT | 79582 |
rs28441286 | snp | A/G | 0.196149 | 0.244131 | intron-variant, utr-variant-5-prime | SPAG16 | GRCh38.p7 | 2:213300762 | AAAATTTAATATCCA[A/G]TATATAATTCTTGAT | 79582 |
rs28459279 | snp | A/G | 0.196149 | 0.244131 | intron-variant, utr-variant-5-prime | SPAG16 | GRCh38.p7 | 2:213300764 | AATTTAATATCCAAT[A/G]TATAATTCTTGATAG | 79582 |
rs28466574 | snp | C/T | 0.356169 | 0.226336 | intron-variant | SPAG16 | GRCh38.p7 | 2:213407498 | TTTCAAGGGTTGAAC[C/T]TGACACAACCCCCCC | 79582 |
rs28473575 | snp | A/G | 0.0279526 | 0.114869 | intron-variant | SPAG16 | GRCh38.p7 | 2:213485262 | GCCTACCAAAATGTT[A/G]GGATTACAGGCATAA | 79582 |
rs28475376 | snp | A/G/T | | | intron-variant | SPAG16 | GRCh38.p7 | 2:213407667 | GAGAGAGAGAGGGGG[A/G/T]GAGAGACAGAGAGGA | 79582 |
rs28480439 | snp | C/T | 0.209693 | 0.246729 | intron-variant | SPAG16 | GRCh38.p7 | 2:213292390 | CTATCAGAGGCCGGG[C/T]GCGGTGGCTCACGCC | 79582 |
rs28498304 | snp | C/T | | | intron-variant | SPAG16 | GRCh38.p7 | 2:214294912 | ACATTAATGACTGTT[C/T]TAATACACACTTGAT | 79582 |
rs28502212 | snp | C/G | | | intron-variant | SPAG16 | GRCh38.p7 | 2:213407674 | AGAGGGGGAGAGAGA[C/G]AGAGAGGAGAGAGAC | 79582 |
rs28526736 | snp | A/G | | | intron-variant | SPAG16 | GRCh38.p7 | 2:213407682 | AGAGAGACAGAGAGG[A/G]GAGAGACAGAAGAGA | 79582 |
rs28531720 | snp | C/T | 0.00438332 | 0.0466095 | intron-variant | SPAG16 | GRCh38.p7 | 2:214177900 | CAGAATATATATATA[C/T]ATATATATATATATA | 79582 |
rs28541574 | snp | G/T | 0.378372 | 0.214524 | intron-variant | SPAG16 | GRCh38.p7 | 2:214139156 | TTTATTTCTTGTATT[G/T]CTTTTTGTTATATTT | 79582 |
rs28545663 | snp | A/G | 0.17461 | 0.238362 | intron-variant | SPAG16 | GRCh38.p7 | 2:213292440 | GAGGCCGAGGCGGGC[A/G]GATCATGAGGTCAGG | 79582 |
rs28569212 | snp | A/G | 0.257176 | 0.249897 | intron-variant | SPAG16 | GRCh38.p7 | 2:214109697 | ATTACATTTTAATAG[A/G]TTGGTCTTTGTAAGA | 79582 |
rs28583878 | snp | C/T | | | intron-variant | SPAG16 | GRCh38.p7 | 2:214177906 | ATATATATACATATA[C/T]ATATATATACATATA | 79582 |
rs28606463 | snp | C/T | 0.000101297 | 0.00711604 | intron-variant | SPAG16 | GRCh38.p7 | 2:213929934 | TACTTTTTAAACAAG[C/T]TGTCTTTTTATGTTT | 79582 |
rs28609323 | snp | G/T | 0.030278 | 0.119257 | intron-variant | SPAG16 | GRCh38.p7 | 2:214072772 | TTTAATTAGGAGGGG[G/T]AGGACTTTTTAAAAA | 79582 |
rs28610955 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | SPAG16 | GRCh38.p7 | 2:214260692 | GAGATCTGTTATCAT[A/G]TTTCTAATTTCTTGA | 79582 |
rs28616191 | snp | G/T | 0.232651 | 0.249397 | intron-variant | SPAG16 | GRCh38.p7 | 2:214141833 | CATAATATCCCACAT[G/T]TTTCATTACACTCTG | 79582 |
rs28632788 | snp | G/T | | | intron-variant | SPAG16 | GRCh38.p7 | 2:213581682 | AAATTGAGATGAAGG[G/T]AGCTAAAAAGGAGCC | 79582 |
rs28645434 | snp | C/T | 0.499368 | 0.0177603 | intron-variant | SPAG16 | GRCh38.p7 | 2:214357696 | TCTTTGTGGGTCTGA[C/T]TTGCAGTCCATTATT | 79582 |
rs28650098 | snp | A/T | | | intron-variant | SPAG16 | GRCh38.p7 | 2:213833558 | tatataatatatata[A/T]tatatataatatata | 79582 |
rs28663384 | snp | A/G | | | intron-variant | SPAG16 | GRCh38.p7 | 2:213949380 | CACCATTGTTGGCCA[A/G]ATGGTCTTGATGTCT | 79582 |
rs28666700 | snp | A/C | 0.00716266 | 0.059414 | intron-variant | SPAG16 | GRCh38.p7 | 2:213419789 | TATGATTTAAAAGGA[A/C]ATGTTAAAAATAAAT | 79582 |
rs28667204 | snp | C/T | 0.0513262 | 0.151752 | intron-variant | SPAG16 | GRCh38.p7 | 2:213686161 | TCTTGCTTTGTTGCC[C/T]AGCCTAGAGTGCAGT | 79582 |
rs28671085 | snp | C/T | | | intron-variant | SPAG16 | GRCh38.p7 | 2:214177916 | ATATATATATATATA[C/T]ATATATATATATATA | 79582 |
rs28718439 | snp | C/T | 0.211212 | 0.246973 | intron-variant | SPAG16 | GRCh38.p7 | 2:213321579 | TCAGCAACGATGAAG[C/T]ATGAAGAAGGAAATG | 79582 |
rs28723594 | snp | A/G | 0.439918 | 0.162576 | intron-variant | SPAG16 | GRCh38.p7 | 2:213986937 | AAGAAACTATCATAT[A/G]TGTTTTTAAAATAAA | 79582 |
rs28769073 | snp | A/C | 0.0452528 | 0.143452 | intron-variant | SPAG16 | GRCh38.p7 | 2:213644551 | AGCTGTATCTACTTT[A/C]GGGGGCTCCCCAAAC | 79582 |
rs28806208 | snp | A/G | 0.480618 | 0.0965156 | intron-variant | SPAG16 | GRCh38.p7 | 2:213572512 | GTGTGAGGTGTCAGT[A/G]TGCCCCTGCTGGGGG | 79582 |
rs28807766 | snp | A/G | | | intron-variant | SPAG16 | GRCh38.p7 | 2:213468445 | TATCTATGTATTTAT[A/G]TATAGATATATATAT | 79582 |
rs28834766 | snp | A/G | 0.213635 | 0.247341 | intron-variant | SPAG16 | GRCh38.p7 | 2:213403114 | GACTTTTTAATGATC[A/G]CCATTCTAACTGGTG | 79582 |
rs28848567 | snp | C/T | | | intron-variant | SPAG16 | GRCh38.p7 | 2:213468448 | CTATGTATTTATATA[C/T]AGATATATATATCTC | 79582 |
rs28864393 | snp | A/C | | | intron-variant | SPAG16 | GRCh38.p7 | 2:213468461 | TATAGATATATATAT[A/C]TCTATGTATTTATAT | 79582 |
rs28876412 | snp | C/T | 0.5 | 0 | intron-variant | SPAG16 | GRCh38.p7 | 2:213354942 | AAGTCTTTGCCCATG[C/T]CTATGTCCTAAATGG | 79582 |
rs28888397 | snp | C/G | 0.209997 | 0.246779 | intron-variant | SPAG16 | GRCh38.p7 | 2:213293665 | GATGACTCTAATTCT[C/G]CTGTTATTTTGACTA | 79582 |
rs28897188 | snp | C/T | 0.19646 | 0.2442 | intron-variant, utr-variant-5-prime | SPAG16 | GRCh38.p7 | 2:213300864 | ACATAAAGTTTGAGA[C/T]ATTTTATAGAATTCT | 79582 |
rs33961996 | in-del | -/T | | | intron-variant | SPAG16 | GRCh38.p7 | 2:214299244 | ACAAGTGTAGTATAC[-/T]TTTTTTTTTTTTTTT | 79582 |
rs33977889 | in-del | -/C | | | intron-variant | SPAG16 | GRCh38.p7 | 2:213866978 | AAGGCATTTAAAAAT[-/C]TGCAAGTCTTCAAAA | 79582 |
rs33981125 | in-del | -/TCAGATACA | | | intron-variant, downstream-variant-500B | SPAG16, LOC101928084 | GRCh38.p7 | 2:214088352 | GTTTGAAAGAGCTCA[-/TCAGATACA]GGTGAAAAAAACCAC | 79582 |
rs33985980 | snp | C/T | | | intron-variant | SPAG16 | GRCh38.p7 | 2:214246255 | GAGGACATTGTTTTT[C/T]TCTTAGTGGCTATGG | 79582 |
rs33989475 | in-del | -/TTT | 0 | 0 | intron-variant | SPAG16 | GRCh38.p7 | 2:213433935 | TTTTTTTTTTTTTTT[-/TTT]GAGACATTGTCTCGT | 79582 |
rs33999062 | in-del | -/G | | | intron-variant | SPAG16, LOC101928084 | GRCh38.p7 | 2:214087391 | TATTAGCAAACATGG[-/G]AAAATTGATTATGAT | 79582 |
rs34000450 | in-del | -/C | | | intron-variant | SPAG16 | GRCh38.p7 | 2:213362244 | AGTGTTTGATTATAA[-/C]CCCAAAATATAAAAT | 79582 |
rs34005287 | in-del | -/T/TT | | | intron-variant | SPAG16 | GRCh38.p7 | 2:213469570 | AAGCACCTCAGCAGG[-/T/TT]TTTTTTTTTTTTTTT | 79582 |
rs34005904 | in-del | -/G | | | intron-variant | SPAG16 | GRCh38.p7 | 2:213970473 | ACCTGGCTAATTTTT[-/G]GTATGTTTTTGTAGA | 79582 |
rs34009535 | in-del | -/G | | | intron-variant | SPAG16 | GRCh38.p7 | 2:213381698 | AATAAGTATACCCAT[-/G]GGGACACCAATATTT | 79582 |
rs34015131 | in-del | -/ATA | 0.347914 | 0.230028 | intron-variant | SPAG16 | GRCh38.p7 | 2:214160196 | AAGATGGGCATTCCT[-/ATA]ATATTAGCTATATAA | 79582 |
rs34027430 | in-del | -/T | 0.376394 | 0.215696 | intron-variant | SPAG16, LOC101928084 | GRCh38.p7 | 2:214101108 | TAAGAGTTTTAAAGG[-/T]TTTTTTGTCTGAAAT | 79582 |
rs34028155 | in-del | -/T | 0.232359 | 0.249377 | intron-variant | SPAG16, LOC101928084 | GRCh38.p7 | 2:214095787 | TTGTACAACATTGTA[-/T]TTATGGTAAACAATA | 79582 |
rs34036099 | in-del | -/C | | | intron-variant | SPAG16 | GRCh38.p7 | 2:214294271 | GGCAGGAATGTGGAG[-/C]CCTGGGGATCACACA | 79582 |
rs34037668 | in-del | -/T | | | intron-variant | SPAG16 | GRCh38.p7 | 2:214402487 | GAACTGTTTTTTTTT[-/T]CAGGAACAATTAGTG | 79582 |
rs34040211 | snp | A/G | 0.00478085 | 0.0486577 | intron-variant | SPAG16 | GRCh38.p7 | 2:214289986 | TTTGAATACTTTCAG[A/G]AGAATTGGTATTAGT | 79582 |
rs34040883 | in-del | -/A | 0.4711 | 0.116682 | intron-variant | SPAG16 | GRCh38.p7 | 2:214254786 | AAGATATATTTAGTT[-/A]GGGGGAAAACTCATT | 79582 |
rs34044655 | in-del | -/T | 0.193028 | 0.243422 | intron-variant | SPAG16 | GRCh38.p7 | 2:214034056 | TTCATGATATTGACA[-/T]TTTTGGAAAAGTACA | 79582 |
rs34044762 | in-del | -/G | | | intron-variant | SPAG16 | GRCh38.p7 | 2:213935058 | TACAAAAAATTACCT[-/G]GGGCGTGGTGGCAGG | 79582 |
rs34045259 | in-del | -/G | | | intron-variant | SPAG16 | GRCh38.p7 | 2:214242105 | AAGCCCATTAGAACA[-/G]GGGGCTTCATGAAAT | 79582 |
rs34066079 | snp | C/T | 0.350327 | 0.228986 | intron-variant | SPAG16 | GRCh38.p7 | 2:214161116 | CTCCATCCATGTTTC[C/T]GCAAATAACATGATC | 79582 |
rs34066705 | in-del | -/G | | | intron-variant | SPAG16 | GRCh38.p7 | 2:213684932 | TACATGTGCTATGAA[-/G]GGAGTGGTTTCCAGG | 79582 |
rs34068237 | in-del | -/A | | | intron-variant | SPAG16 | GRCh38.p7 | 2:214382905 | GCTGAAGCGTTTCAT[-/A]AAGGAGCTCTGAATG | 79582 |
rs34070679 | in-del | -/T | 0.498794 | 0.0245311 | intron-variant | SPAG16 | GRCh38.p7 | 2:213833456 | TATATATATATATTA[-/T]TATATATATTATATA | 79582 |
rs34080486 | in-del | -/T | 0.48178 | 0.0936921 | intron-variant | SPAG16 | GRCh38.p7 | 2:213897614 | TCCTCATCTGCCTAT[-/T]ATTGGTCTCAGGGCA | 79582 |
rs34081586 | in-del | -/G | | | intron-variant | SPAG16 | GRCh38.p7 | 2:214060842 | AAAATTCCTTCCCAA[-/G]AATAAAATATATTAT | 79582 |
rs34084248 | snp | A/T | 0.394354 | 0.204112 | intron-variant | SPAG16 | GRCh38.p7 | 2:214308029 | GGGAGTCTATGTCTC[A/T]TTGAAGGTCCCTAAG | 79582 |
rs34087467 | snp | G/T | | | intron-variant | SPAG16 | GRCh38.p7 | 2:213307189 | CAGTGTTGAATTTTG[G/T]TTTTTTTTATTTTTT | 79582 |
rs34090812 | in-del | -/G | | | intron-variant | SPAG16 | GRCh38.p7 | 2:213592390 | TAAATAAAGGGTTTG[-/G]TAAGTCTACATACTA | 79582 |
rs34098152 | in-del | -/A | | | intron-variant | SPAG16 | GRCh38.p7 | 2:213524744 | TGGGTGTATTTACCT[-/A]AATGCCTGTACTCCC | 79582 |
rs34101106 | snp | C/T | 0.411242 | 0.191052 | intron-variant | SPAG16, LOC101928084 | GRCh38.p7 | 2:214101308 | CTCACAACATGTGTG[C/T]CCTGCTTCAGTTCTA | 79582 |
rs34104063 | snp | G/T | | | intron-variant | SPAG16 | GRCh38.p7 | 2:214135306 | GCTTTATATACATTG[G/T]CTTTATTTCTAGTTA | 79582 |
rs34105875 | in-del | -/ACAC | | | intron-variant | SPAG16 | GRCh38.p7 | 2:213767663 | CATACTTCACACACA[-/ACAC]CACACACACACACAC | 79582 |
rs34111831 | in-del | -/A | 0.5 | 0 | intron-variant | SPAG16 | GRCh38.p7 | 2:214115876 | GTGAGACTCCATCTC[-/A]AAAAAAAAAAAAAAA | 79582 |
rs34113895 | in-del | -/G | | | intron-variant | SPAG16 | GRCh38.p7 | 2:213866472 | ATACTTATAGATATT[-/G]GGAAGTTACTTTAAA | 79582 |
rs34119801 | snp | A/T | 0.00119737 | 0.0244387 | intron-variant | SPAG16 | GRCh38.p7 | 2:214315172 | GTGGAGCAGTCAGGG[A/T]ACAGGAAGACTGCAG | 79582 |
rs34126775 | snp | A/G | 0.251859 | 0.249993 | intron-variant | SPAG16 | GRCh38.p7 | 2:214132143 | ATCAGTGGGTATATC[A/G]GGTATAATTCTTGAA | 79582 |
rs34129838 | in-del | -/G | | | intron-variant | SPAG16 | GRCh38.p7 | 2:213622320 | ACTGAAACTCATCAG[-/G]ATCACCATGTCCAGA | 79582 |
rs34142163 | in-del | -/T | | | intron-variant | SPAG16 | GRCh38.p7 | 2:213623253 | CATTTACTTTTTTTT[-/T]AAGTGAAGGAGCTAC | 79582 |
rs34149397 | snp | C/T | | | intron-variant | SPAG16 | GRCh38.p7 | 2:213643765 | CTTCAAGCCCCCTAC[C/T]TCTTTTTTTTTTTTT | 79582 |
rs34149728 | in-del | -/AA | 0.221439 | 0.248363 | intron-variant | SPAG16, LOC101928084 | GRCh38.p7 | 2:214087199 | ATAATGGTGAGAAAT[-/AA]AGAGTTAAATGCAGA | 79582 |
rs34158333 | in-del | -/T | | | intron-variant | SPAG16 | GRCh38.p7 | 2:214306858 | TTGTTTTTGTTATTG[-/T]ATCCCTGACAGGCTT | 79582 |
rs34163209 | in-del | -/A | | | intron-variant | SPAG16 | GRCh38.p7 | 2:214212700 | TCACCCCAGCTAGCT[-/A]CTACTCTTTCTATTT | 79582 |
rs34179061 | in-del | -/T | | | intron-variant | SPAG16 | GRCh38.p7 | 2:213831413 | TTCATAATTCAGGTG[-/T]TTTTTTTTTTTTTAA | 79582 |
rs34179878 | in-del | -/C | 0.495782 | 0.0457324 | intron-variant | SPAG16 | GRCh38.p7 | 2:213836177 | AATTTTCATTATTCG[-/C]CCCCCCCCCCATTTC | 79582 |
rs34184516 | snp | G/T | 0.00119737 | 0.0244387 | intron-variant | SPAG16 | GRCh38.p7 | 2:213951820 | GCCAAGCAAAAGACA[G/T]AGTTATTTTCATTTG | 79582 |
rs34185382 | in-del | -/G | | | intron-variant | SPAG16 | GRCh38.p7 | 2:214012159 | TATATTATTGTACAT[-/G]GGCTTGGTTCAAGCC | 79582 |
rs34185957 | in-del | -/G | | | intron-variant | SPAG16 | GRCh38.p7 | 2:213711787 | GCCTCCCAAAGTGCT[-/G]GGGATTATAGGTGTG | 79582 |
rs34192658 | in-del | -/G | | | intron-variant | SPAG16 | GRCh38.p7 | 2:213327067 | TAAGACAAAGCATGT[-/G]GCAAATTGTTTTCTT | 79582 |
rs34196971 | in-del | -/A | | | intron-variant | SPAG16 | GRCh38.p7 | 2:213673896 | ATAATTGTGAAAGTG[-/A]AAAAAGTCTCATGTT | 79582 |
rs34198942 | in-del | -/C | | | intron-variant, utr-variant-3-prime | SPAG16 | GRCh38.p7 | 2:213369836 | CCCCAGACATAGCTT[-/C]CCCCTATTATCAGCA | 79582 |
rs34199387 | snp | G/T | 0.345925 | 0.230864 | intron-variant | SPAG16 | GRCh38.p7 | 2:214180300 | TATTTAGGGAATTTG[G/T]CCAGAGCAGAGTGGA | 79582 |
rs34199730 | in-del | -/GA | | | intron-variant | SPAG16 | GRCh38.p7 | 2:213922251 | TCTTTATTTTTGTCT[-/GA]CTGAGTTATTTCAGA | 79582 |
rs34202630 | in-del | -/T | 0.270351 | 0.24917 | intron-variant | SPAG16 | GRCh38.p7 | 2:213920157 | TTCTCCATCCTTTTA[-/T]TTTTGAGCCTCTGAG | 79582 |
rs34207799 | in-del | -/G | | | intron-variant | SPAG16 | GRCh38.p7 | 2:213776107 | AACATCCCAAAATAT[-/G]CTACATCCCAATCAT | 79582 |
rs34214580 | in-del | -/A | | | intron-variant | SPAG16 | GRCh38.p7 | 2:213976458 | CCTATTGGACCTTTC[-/A]AGTATATTAACTTAT | 79582 |
rs34221048 | in-del | -/TG | | | intron-variant | SPAG16 | GRCh38.p7 | 2:214284797 | AATAATATTTTACTC[-/TG]TGTGTGTGTGTGTGT | 79582 |
rs34222437 | in-del | -/G | | | intron-variant | SPAG16 | GRCh38.p7 | 2:213412976 | TAGATTTATAGCACT[-/G]GGATCTACATACTAT | 79582 |
rs34224035 | in-del | -/A | | | intron-variant | SPAG16 | GRCh38.p7 | 2:214341410 | TCAAAGAGCTCACTG[-/A]AAAACTCAGCATATT | 79582 |
rs34226361 | in-del | -/T | | | intron-variant | SPAG16 | GRCh38.p7 | 2:214245660 | TATACTAAACATACA[-/T]TTCTAGTGTGTACCC | 79582 |
rs34228424 | in-del | -/T | | | intron-variant | SPAG16 | GRCh38.p7 | 2:213587770 | TAAATCATATTTTTT[-/T]CAAATGTAGTTCACT | 79582 |
rs34228764 | in-del | -/T | | | intron-variant, upstream-variant-2KB | SPAG16, LOC100130451 | GRCh38.p7 | 2:213286171 | GACTTTTTCAAATAA[-/T]TCACACTTATTTGAA | 79582 |
rs34233398 | in-del | -/T/TT | 0 | 0 | intron-variant | SPAG16 | GRCh38.p7 | 2:213736721 | TTTTTTTTTTTTTTT[-/T/TT]GAGACAGAGTTTCAC | 79582 |
rs34239165 | in-del | -/A | 0.329084 | 0.237162 | intron-variant | SPAG16 | GRCh38.p7 | 2:214141473 | TCAAAAAAAAAAAAA[-/A]CCAAAAAAATTACTG | 79582 |
rs34241413 | snp | A/G | 0.00159617 | 0.0282053 | intron-variant | SPAG16 | GRCh38.p7 | 2:213509868 | CCTTCAAAAATTAAT[A/G]AATCCAGCAGCTGGT | 79582 |
rs34242304 | in-del | -/C | | | intron-variant | SPAG16 | GRCh38.p7 | 2:213886485 | GTGTCACTTTCTGAT[-/C]CCCCAACACTGGCCT | 79582 |
rs34243782 | in-del | -/A | | | intron-variant | SPAG16 | GRCh38.p7 | 2:213974337 | TAAAATTATATATAC[-/A]AATAAATGTGATTAT | 79582 |
rs34244139 | snp | A/G | 0.632812 | 0.151288 | intron-variant | SPAG16 | GRCh38.p7 | 2:213356446 | TATTGGTCTATTCAG[A/G]GATTCAACTTCTTCC | 79582 |
rs34244219 | in-del | -/TA | | | intron-variant | SPAG16 | GRCh38.p7 | 2:214059222 | ATATATATGTATGTG[-/TA]TATATATATATATAT | 79582 |
rs34246211 | snp | G/T | 0.5 | 0 | intron-variant | SPAG16 | GRCh38.p7 | 2:214145592 | TTCATGTGTATATGG[G/T]TTTCTCATTATAGGA | 79582 |
rs34251248 | in-del | -/CCAA | 0.135825 | 0.222405 | intron-variant | SPAG16 | GRCh38.p7 | 2:214377624 | TTATTGGTAACGCTT[-/CCAA]CCAACAGTAGGCTAT | 79582 |
rs34254283 | in-del | -/T | | | intron-variant | SPAG16 | GRCh38.p7 | 2:213558472 | GAGAATTTTTTTTTT[-/T]GTGTTAGTCATGTAC | 79582 |
rs34254709 | in-del | -/A | | | intron-variant | SPAG16 | GRCh38.p7 | 2:213684070 | TTGGATTGGCAGCTG[-/A]AAAAAGTTGTCAGCA | 79582 |
rs34255933 | in-del | -/T | | | intron-variant, upstream-variant-2KB | SPAG16 | GRCh38.p7 | 2:213316967 | TTGTCAATTTTAATA[-/T]TGTCTAGACCAGTGC | 79582 |
rs34266823 | in-del | -/A/AA | | | intron-variant | SPAG16 | GRCh38.p7 | 2:213907475 | TCAAAAAAAAAAAAA[-/A/AA]TCTAAAAATAGAACT | 79582 |
rs34269015 | in-del | -/AT/TA | | | intron-variant | SPAG16 | GRCh38.p7 | 2:213814873 | CATAACAGCCTTAAA[-/AT/TA]TATATATATATATAT | 79582 |
rs34274070 | in-del | -/G | | | intron-variant | SPAG16 | GRCh38.p7 | 2:214196155 | AGTATTGTATGCCTC[-/G]GGGAAGGTGGAGATA | 79582 |
rs34285959 | snp | A/G | 0.282632 | 0.247861 | intron-variant | SPAG16 | GRCh38.p7 | 2:214121827 | AATTACCTTCAGTCT[A/G]TATGTATAAGGTATA | 79582 |
rs34293677 | in-del | -/G | | | intron-variant | SPAG16 | GRCh38.p7 | 2:213907119 | TATTCATTCAACAAT[-/G]GGACTGATATCTGGA | 79582 |
rs34294633 | in-del | -/C | | | intron-variant | SPAG16 | GRCh38.p7 | 2:214324079 | ACACATTTACATCAG[-/C]AAACAATGGGCTTGA | 79582 |
rs34299318 | in-del | -/A | 0.493613 | 0.0561475 | intron-variant | SPAG16 | GRCh38.p7 | 2:214392698 | GGAAAAAAAAAAAAA[-/A]GATCATGGAGTGGTC | 79582 |
rs34300459 | snp | A/T | 0.249038 | 0.249998 | intron-variant | SPAG16 | GRCh38.p7 | 2:214138612 | GCAACTGGCATTTAG[A/T]TTTAGCAGGAACCAA | 79582 |
rs34304052 | in-del | -/T | | | intron-variant | SPAG16 | GRCh38.p7 | 2:213831414 | TTCATAATTCAGGTG[-/T]TTTTTTTTTTTTAAC | 79582 |
rs34304699 | in-del | -/C | | | intron-variant | SPAG16 | GRCh38.p7 | 2:214303014 | AAGACTGTGTCATTA[-/C]CCCATTATGTGAGTG | 79582 |
rs34306659 | multinucleotide-polymorphism | AG/TC | 0.5 | 0 | intron-variant | SPAG16 | GRCh38.p7 | 2:214307698 | TTCCATGTAATTGTA[AG/TC]TTTTTGAGCAAATTT | 79582 |
rs34306751 | in-del | -/G | | | intron-variant, downstream-variant-500B | SPAG16, LOC101928084 | GRCh38.p7 | 2:214088065 | AATTAAAAATAAATT[-/G]GAAAGGTTATTAACT | 79582 |
rs34307305 | in-del | -/A | | | intron-variant | SPAG16 | GRCh38.p7 | 2:214285845 | AATGAAAAAACTGCT[-/A]AAAAGCAGACGCTTT | 79582 |
rs34308255 | in-del | -/G | | | intron-variant, utr-variant-3-prime | SPAG16 | GRCh38.p7 | 2:213397394 | ATTGCTGCTTTCAGT[-/G]TTGTTCTCCCTCCTT | 79582 |
rs34317767 | in-del | -/T | | | intron-variant | SPAG16 | GRCh38.p7 | 2:213611238 | TTGTAACTTGATTTT[-/T]CAGTGACCCTTCAGA | 79582 |
rs34325675 | in-del | -/T | | | intron-variant | SPAG16 | GRCh38.p7 | 2:213612399 | TCTTTAAATTATTGA[-/T]TTTCCAAATATTTCT | 79582 |
rs34330588 | snp | A/G | 0.347253 | 0.230308 | intron-variant | SPAG16 | GRCh38.p7 | 2:214166353 | ATTGACGAATGGGAG[A/G]CACTTACAGGAGAGT | 79582 |
rs34333499 | in-del | -/C | 0.046775 | 0.145601 | intron-variant | SPAG16 | GRCh38.p7 | 2:213378534 | GTGAAGTCAGTAAAT[-/C]CTTATATCACATGAT | 79582 |
rs34334049 | snp | A/T | 0.259951 | 0.249802 | intron-variant | SPAG16 | GRCh38.p7 | 2:213878129 | CTTACTCATTTTGAA[A/T]TCTCTCTACCTTCTT | 79582 |
rs34335036 | in-del | -/T | | | intron-variant | SPAG16 | GRCh38.p7 | 2:214398733 | AATATAAATTTATTT[-/T]AGCAGTTCATGTAGC | 79582 |
rs34335974 | in-del | -/G | | | intron-variant | SPAG16 | GRCh38.p7 | 2:213286370 | TATATTCCATGCTGA[-/G]GGGAAGAGGTTTAGT | 79582 |
rs34336161 | in-del | -/T | | | intron-variant | SPAG16 | GRCh38.p7 | 2:214110141 | TATCAAAGTAGCTAA[-/T]TTTTTTTTATTATTA | 79582 |
rs34340947 | snp | A/G | 0.352287 | 0.228117 | intron-variant | SPAG16 | GRCh38.p7 | 2:214169310 | TTAAAAAAGAACACA[A/G]TCATAATTTGACTCC | 79582 |
rs34342364 | snp | A/G | 0.257176 | 0.249897 | intron-variant | SPAG16 | GRCh38.p7 | 2:214121221 | AGGAGATGAATAAAT[A/G]AATGAATGCTGAATT | 79582 |
rs34344102 | in-del | -/C | | | intron-variant | SPAG16 | GRCh38.p7 | 2:214300558 | TCAAAGTAAAAGCTA[-/C]ACAATTGTCTATAGA | 79582 |
rs34367751 | in-del | -/T/TT | | | intron-variant | SPAG16 | GRCh38.p7 | 2:213961585 | GTCTTCTAACCCTAG[-/T/TT]TTTTTTTTTTTTTTT | 79582 |
rs34369213 | in-del | -/C | | | intron-variant | SPAG16 | GRCh38.p7 | 2:213807851 | TTTGCAGTGAAGATT[-/C]CTTGGTTTACACTGG | 79582 |
rs34371300 | in-del | -/T | | | intron-variant | SPAG16 | GRCh38.p7 | 2:214180613 | AAAAACAAGGTAGCA[-/T]TCAGGAAAGCAATAT | 79582 |
rs34373389 | in-del | -/T | | | intron-variant | SPAG16 | GRCh38.p7 | 2:213943741 | GGAACCAAAACTTAG[-/T]AGATTTGGAAAATTC | 79582 |
rs34374076 | in-del | -/T | 0.444267 | 0.157354 | intron-variant | SPAG16 | GRCh38.p7 | 2:213711496 | TTTTGCCTATAATAA[-/T]TTTTTATTTATTTTT | 79582 |
rs34381468 | snp | A/T | 0 | 0 | intron-variant | SPAG16 | GRCh38.p7 | 2:214303676 | ACACTCCTAGCAAGA[A/T]CCGATAAATTTTCCT | 79582 |
rs34387558 | in-del | -/C | | | intron-variant | SPAG16 | GRCh38.p7 | 2:214161159 | TGGCTGCATAGTATT[-/C]CCATGGTGGAGATGT | 79582 |
rs34394465 | in-del | -/C | | | intron-variant | SPAG16 | GRCh38.p7 | 2:213829057 | CTACATTCAGCAAGG[-/C]CCTGGGCTCTAACAA | 79582 |
rs34406744 | in-del | -/G | 0.476487 | 0.105846 | intron-variant | SPAG16 | GRCh38.p7 | 2:214078128 | GCAAAGTATTCCCAA[-/G]AAAAAGACCCTTCCA | 79582 |
rs34415358 | snp | C/G | 0.45866 | 0.137698 | intron-variant | SPAG16 | GRCh38.p7 | 2:214277833 | GGAAGAACCACTGCT[C/G]TCTTCAGAGCTGTCA | 79582 |
rs34423954 | snp | C/T | 0.393987 | 0.204372 | intron-variant | SPAG16 | GRCh38.p7 | 2:214307633 | ACTTCTTGACTTCTA[C/T]CTTAATTTCATTATT | 79582 |
rs34425413 | in-del | -/C | | | intron-variant | SPAG16 | GRCh38.p7 | 2:213573529 | ACAGTAGCTACTTTT[-/C]CAATGCTAAAAGCTC | 79582 |
rs34425703 | in-del | -/C | | | intron-variant | SPAG16 | GRCh38.p7 | 2:214040650 | TGGCTGCATAGTATT[-/C]CCATGGGGTATATGG | 79582 |
rs34431466 | in-del | -/C | | | intron-variant | SPAG16, LOC101928084 | GRCh38.p7 | 2:214089007 | TTGAAATAACATCAG[-/C]AATCAAGCATATTAA | 79582 |
rs34434134 | in-del | -/A | | | intron-variant, utr-variant-3-prime | SPAG16 | GRCh38.p7 | 2:213399280 | TTCTTTATCAAGTTG[-/A]AAAAATTTGTTTTCC | 79582 |
rs34440269 | in-del | -/T/TA | 0.229136 | 0.249128 | intron-variant | SPAG16 | GRCh38.p7 | 2:213302647 | GTGTGTGTGTGTGTG[-/T/TA]ATGTGTGTGTGTGTT | 79582 |
rs34448340 | multinucleotide-polymorphism | AG/CC | | | intron-variant | SPAG16 | GRCh38.p7 | 2:213455714 | AATAGGGTTTGCGCT[AG/CC]TGTGATAATATAATG | 79582 |
rs34455201 | in-del | -/C | | | intron-variant | SPAG16 | GRCh38.p7 | 2:214307232 | GGTCAATGGTAATAT[-/C]CCCCTTTTTTGTTTC | 79582 |
rs34455605 | snp | C/G | 0.449726 | 0.150364 | intron-variant | SPAG16 | GRCh38.p7 | 2:214245894 | TCAAAGGGCCTAAAA[C/G]GTACGTTTTGAATGA | 79582 |
rs34460783 | in-del | -/TATA | 0 | 0 | intron-variant | SPAG16 | GRCh38.p7 | 2:214177972 | TTCACAAAGTGTATG[-/TATA]TATATATATATATAT | 79582 |
rs34461740 | in-del | -/A | | | intron-variant | SPAG16 | GRCh38.p7 | 2:213744721 | AAGACTTTGAGAAGG[-/A]AAAAGGCTGATAACT | 79582 |
rs34462560 | in-del | -/TA/TATA | 0.47726 | 0.104176 | intron-variant | SPAG16 | GRCh38.p7 | 2:214298074 | GGTTAGATGTATGCC[-/TA/TATA]TATATATATATATAT | 79582 |
rs34463701 | in-del | -/C | | | intron-variant | SPAG16 | GRCh38.p7 | 2:213881908 | CATACTTGTCATATT[-/C]CCAGTTCTCAAGGGC | 79582 |
rs34464590 | in-del | -/C | 0.345704 | 0.230956 | intron-variant | SPAG16 | GRCh38.p7 | 2:214180354 | GTTCATATGTTGCCA[-/C]AGTGATCTATGAGTT | 79582 |
rs34464604 | in-del | -/A | | | intron-variant | SPAG16 | GRCh38.p7 | 2:213856531 | AGGTTCTCCATGAGG[-/A]AAGCCACCCTACAGC | 79582 |
rs34465797 | in-del | -/A | | | intron-variant | SPAG16 | GRCh38.p7 | 2:214326556 | ATGAGAAATCATAAT[-/A]AGAAGAGAGAAATTC | 79582 |
rs34471175 | snp | C/T | 0.251859 | 0.249993 | intron-variant | SPAG16 | GRCh38.p7 | 2:214287997 | AATCACCCTACTGTG[C/T]TTTTGAATATTGGGG | 79582 |
rs34476651 | in-del | -/AT | 0.484279 | 0.0872533 | intron-variant | SPAG16 | GRCh38.p7 | 2:213545608 | CTTTTACATTGAAAC[-/AT]GTGATCAATTATGGA | 79582 |
rs34477932 | in-del | -/T | 0.499971 | 0.00379382 | intron-variant | SPAG16 | GRCh38.p7 | 2:213390845 | TTATATACAAATGGC[-/T]TTTCAAAGCTTGGTT | 79582 |
rs34479042 | in-del | -/A | | | intron-variant | SPAG16 | GRCh38.p7 | 2:213955538 | TTCTGTCAGATTGAT[-/A]CTACATGTCTATCCT | 79582 |
rs34481835 | snp | C/T | 0.225301 | 0.248777 | intron-variant | SPAG16 | GRCh38.p7 | 2:214056707 | GCCACATAGACTGAC[C/T]CTTTGATAAATGATT | 79582 |
rs34483462 | in-del | -/T | | | intron-variant | SPAG16 | GRCh38.p7 | 2:213486954 | TAACGTGATGAATGC[-/T]TTGCAGAGATTATCT | 79582 |
rs34487275 | in-del | -/G | | | intron-variant | SPAG16 | GRCh38.p7 | 2:213984659 | TGAGAAGATGCTTTA[-/G]TTATAGCTTTAATGA | 79582 |
rs34487639 | snp | A/G | 0.5 | 0 | intron-variant | SPAG16 | GRCh38.p7 | 2:213950197 | TGTAGTGTCTGCTTC[A/G]TACATATCAATGCTT | 79582 |
rs34491313 | in-del | -/A | | | intron-variant, downstream-variant-500B | SPAG16 | GRCh38.p7 | 2:213376357 | GACTTTTTATGGGAC[-/A]AAAAGATACTAAAAT | 79582 |
rs34496294 | in-del | -/TACA | | | intron-variant | SPAG16 | GRCh38.p7 | 2:213962330 | GTAGCTGGGACTACA[-/TACA]GGCGCCCGCCACCAA | 79582 |
rs34496823 | in-del | -/C | | | intron-variant | SPAG16 | GRCh38.p7 | 2:213952746 | TGTAAGGAATACTGT[-/C]CCATCGTAGATCCCC | 79582 |
rs34498718 | in-del | -/TCTCA | | | intron-variant | SPAG16 | GRCh38.p7 | 2:213968165 | CTCTCCTCTTCTCTT[-/TCTCA]CTCATCTCTTTTCTT | 79582 |
rs34509973 | in-del | -/C | | | intron-variant | SPAG16, LOC101928084 | GRCh38.p7 | 2:214086712 | TTATAGAAGCATGAG[-/C]AACAGACTAATACAG | 79582 |
rs34510138 | in-del | -/T | | | intron-variant | SPAG16 | GRCh38.p7 | 2:214219381 | TATCAAATAGAATTA[-/T]TTTGATAACTTATCA | 79582 |
rs34511017 | in-del | -/G | | | intron-variant | SPAG16 | GRCh38.p7 | 2:213466892 | CTGGGTGGTCTGGTT[-/G]GGAGGGATCCTCAAA | 79582 |
rs34515750 | in-del | -/T | 0.344592 | 0.231414 | intron-variant | SPAG16 | GRCh38.p7 | 2:213372128 | ATATTATGAGATAAA[-/T]TTTTTTTTCAAATTA | 79582 |
rs34521951 | in-del | -/A | | | intron-variant | SPAG16 | GRCh38.p7 | 2:214153875 | GCCTCTCATACATTT[-/A]AAAAGTTGTATGTGG | 79582 |
rs34522209 | in-del | -/T | 0.0138799 | 0.0821421 | intron-variant | SPAG16 | GRCh38.p7 | 2:214234079 | TGTGTTGTTTCCCCC[-/T]CCCATGTGTCCATGT | 79582 |
rs34523016 | in-del | -/T | 0.5 | 0 | intron-variant | SPAG16 | GRCh38.p7 | 2:213831046 | AAGTGAAACATGACT[-/T]TTTTTTTTTTTTTTT | 79582 |
rs34525160 | in-del | -/T | 0.468349 | 0.121752 | intron-variant | SPAG16 | GRCh38.p7 | 2:214347349 | TAGGGTTTTTTTTTT[-/T]AGTAGAATTTGGAAA | 79582 |
rs34528589 | in-del | -/G | | | intron-variant | SPAG16 | GRCh38.p7 | 2:213759504 | AGGGTGGGGGAATGG[-/G]AGCTTTTGAAGGAGC | 79582 |
rs34530714 | snp | A/G | | | intron-variant, downstream-variant-500B | SPAG16 | GRCh38.p7 | 2:213371423 | AAAAAAAAAAAAAAA[A/G]GAAAAGACGATTTAT | 79582 |
rs34532846 | in-del | -/T | | | intron-variant | SPAG16 | GRCh38.p7 | 2:214019903 | GGACAATGTATAAAG[-/T]ATAAATTATCTTAAA | 79582 |
rs34534630 | in-del | -/T | | | intron-variant | SPAG16 | GRCh38.p7 | 2:213626963 | TGAATTTTTTCTTTT[-/T]AGACCAAAGTACTAT | 79582 |
rs34535606 | snp | G/T | | | intron-variant | SPAG16 | GRCh38.p7 | 2:213639041 | ACTTTAAAGTCTGTT[G/T]TGTCTAAGAATAGTT | 79582 |
rs34548631 | in-del | -/G | | | intron-variant | SPAG16 | GRCh38.p7 | 2:214167346 | CAGCACCAGCAGTGG[-/G]AGGCCTGAGTTACCA | 79582 |
rs34553543 | in-del | -/T | 0.355954 | 0.226437 | intron-variant | SPAG16 | GRCh38.p7 | 2:213705609 | ACATTATTAAGAAAA[-/T]TTTTTTAGGCAAAAA | 79582 |
rs34554760 | in-del | -/T | 0.222928 | 0.24853 | intron-variant | SPAG16 | GRCh38.p7 | 2:214065579 | CACTTGACTGGATCA[-/T]TTAGAAAAACTACAA | 79582 |
rs34557739 | snp | C/T | 0.411242 | 0.191052 | intron-variant | SPAG16, LOC101928084 | GRCh38.p7 | 2:214101271 | GGCTAGCTTGTGTTA[C/T]GGTAAAAAACAACCT | 79582 |
rs34561770 | snp | A/C | 0.5 | 0 | intron-variant | SPAG16 | GRCh38.p7 | 2:213495709 | GTTTTAAAGAGAGTG[A/C]CCGGGACTTTTCTTG | 79582 |
rs34563002 | in-del | -/G | | | intron-variant | SPAG16 | GRCh38.p7 | 2:214075637 | AACTTCATATCCTCA[-/G]GGGGAATAATGAACC | 79582 |
rs34565459 | in-del | -/C | | | intron-variant | SPAG16 | GRCh38.p7 | 2:213923935 | ACCTGAGTGTTTCCC[-/C]GGGACATCAGGAGGC | 79582 |
rs34577767 | in-del | -/T | | | intron-variant | SPAG16 | GRCh38.p7 | 2:214392528 | CATGACAGCAAGCCC[-/T]TTGTTTGGGAGGTAG | 79582 |
rs34582059 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | SPAG16 | GRCh38.p7 | 2:214049826 | GGGAAGTTATATTTA[C/T]GTCACAAATTAAAAG | 79582 |
rs34584281 | snp | C/T | 0.187369 | 0.242028 | intron-variant | SPAG16 | GRCh38.p7 | 2:214054735 | TTATATAGTTACATA[C/T]ATCATCTCAGCCCAA | 79582 |
rs34585691 | in-del | -/C | | | intron-variant | SPAG16 | GRCh38.p7 | 2:213825623 | TGTTGAATTTGGTTT[-/C]GCTAGTATTTTATTG | 79582 |
rs34585781 | snp | G/T | | | intron-variant | SPAG16 | GRCh38.p7 | 2:213734719 | TAGACTTGGACATGT[G/T]TTTTTTGGTATGAAC | 79582 |
rs34598875 | snp | C/T | 0.0486741 | 0.148216 | intron-variant | SPAG16 | GRCh38.p7 | 2:214253266 | GTTGCCTGTTCACTC[C/T]TATGATAGTTTCTTT | 79582 |
rs34600511 | in-del | -/T | 0.00318978 | 0.0398085 | intron-variant | SPAG16 | GRCh38.p7 | 2:213679266 | AACCTGAGAAAAACA[-/T]TTTTTACTTACAATT | 79582 |
rs34601560 | in-del | -/T | | | intron-variant | SPAG16 | GRCh38.p7 | 2:214351129 | TTTATTGTAATCCTT[-/T]CCGTGACTAGAAAAC | 79582 |
rs34602955 | snp | A/T | | | intron-variant | SPAG16 | GRCh38.p7 | 2:213407972 | GAGGCAGAGAGAGAG[A/T]CAGGAGAGAGAGAGG | 79582 |
rs34604325 | snp | C/T | 0.345704 | 0.230956 | intron-variant | SPAG16 | GRCh38.p7 | 2:214180187 | TAATTCAGAGGGAAA[C/T]TGGGAACTTACCCAG | 79582 |
rs34606568 | in-del | -/G | | | intron-variant | SPAG16 | GRCh38.p7 | 2:213510759 | TACTGAACTGTGAGT[-/G]GGATTAAGTGAGAAA | 79582 |
rs34614899 | in-del | -/G | | | intron-variant, frameshift-variant, utr-variant-3-prime | SPAG16 | GRCh38.p7 | 2:213396599 | CAGCAGCAGTGGACA[-/G]GGGAACTCTCAAACT | 79582 |
rs34615727 | in-del | -/A | | | intron-variant | SPAG16 | GRCh38.p7 | 2:213664843 | TATATATACATATAT[-/A]CACACACATATTCAT | 79582 |
rs34616486 | in-del | -/A/AA/AAA | 0.494651 | 0.0514399 | intron-variant | SPAG16 | GRCh38.p7 | 2:214322509 | GGCAAAAAAAAAAAA[-/A/AA/AAA]GGCATCAGAAAAATT | 79582 |
rs34620001 | snp | C/T | | | intron-variant | SPAG16 | GRCh38.p7 | 2:214392641 | AGAAGTTTTATAGTT[C/T]TGAAGAAGAGTTTAG | 79582 |
rs34626747 | in-del | -/AC/AT/TA | | | intron-variant | SPAG16 | GRCh38.p7 | 2:214298131 | CACACACACACACAT[-/AC/AT/TA]ACATACACATACACA | 79582 |
rs34632426 | snp | A/C | 0.250168 | 0.25 | intron-variant | SPAG16 | GRCh38.p7 | 2:214145659 | TCAGGAGTGGTGACT[A/C]TTCATTTTCATCTCA | 79582 |
rs34641241 | in-del | -/G | | | intron-variant | SPAG16 | GRCh38.p7 | 2:213423000 | GTCTTCCTTTCCTTA[-/G]GCTGTTACTTCAAAC | 79582 |
rs34641505 | in-del | -/C | | | intron-variant | SPAG16 | GRCh38.p7 | 2:213595569 | TATGGAGTTAATAGT[-/C]TTTAGAATATTTCTG | 79582 |
rs34643841 | in-del | -/G | | | intron-variant | SPAG16 | GRCh38.p7 | 2:213816530 | AAATATGTCATTTGT[-/G]AATAAAGTGCTAAAT | 79582 |
rs34645008 | in-del | -/T | 0.479824 | 0.098392 | intron-variant | SPAG16 | GRCh38.p7 | 2:213879136 | TGTCTATTTGAGCTC[-/T]TTTTTTGATTCCATA | 79582 |
rs34647268 | in-del | -/C | | | intron-variant | SPAG16 | GRCh38.p7 | 2:213825790 | GGGTTCGGAAAAATT[-/C]CCCTCCTCCCCTATT | 79582 |
rs34650209 | in-del | -/C | | | intron-variant, utr-variant-3-prime | SPAG16 | GRCh38.p7 | 2:213397152 | TTTGTATAGTGTTTT[-/C]CCAGTTTCTGTGCTG | 79582 |
rs34652685 | in-del | -/G | | | intron-variant | SPAG16 | GRCh38.p7 | 2:213372004 | GAAATAATTATTATT[-/G]GAGTAGATATTTAAA | 79582 |
rs34655448 | in-del | -/T | | | intron-variant | SPAG16 | GRCh38.p7 | 2:214174419 | CAAAAATCACAAGCA[-/T]TTCTTATACACCAGT | 79582 |
rs34664637 | in-del | -/A/AA | 0.225893 | 0.248835 | intron-variant | SPAG16 | GRCh38.p7 | 2:214031628 | AATAAAATAAACATG[-/A/AA]AAAAAAAAAAGAAAA | 79582 |
rs34668843 | in-del | -/A | | | intron-variant | SPAG16 | GRCh38.p7 | 2:213427648 | TTTTAGGTGGAACAG[-/A]AAAAATCAGAGAAAA | 79582 |
rs34672490 | in-del | -/C | | | intron-variant, downstream-variant-500B | SPAG16, LOC101928084 | GRCh38.p7 | 2:214084533 | TGCTTTTCTCACATT[-/C]CAGTCTCTCTCCTTT | 79582 |
rs34674082 | multinucleotide-polymorphism | GC/TA | | | intron-variant | SPAG16 | GRCh38.p7 | 2:213856774 | GCACAAAGCAGCAAG[GC/TA]CCTGGGCCTGGCTCA | 79582 |
rs34675325 | in-del | -/A | | | intron-variant | SPAG16 | GRCh38.p7 | 2:213666097 | GAGTGGGCAATTCAT[-/A]AAATGTAAAATCACA | 79582 |
rs34679393 | in-del | -/A | | | intron-variant | SPAG16 | GRCh38.p7 | 2:213519947 | ATTAGCATGAGCCCT[-/A]ATGCAGTATGACTGA | 79582 |
rs34681208 | in-del | -/G | | | intron-variant | SPAG16 | GRCh38.p7 | 2:214145861 | ATTCATTCATTCATT[-/G]CAATTGTTTATTCAA | 79582 |
rs34681807 | in-del | -/G | | | intron-variant | SPAG16 | GRCh38.p7 | 2:214124523 | TTGTTTTACATAACA[-/G]GGGATAATGTCTAAT | 79582 |
rs34699753 | in-del | -/G | | | intron-variant | SPAG16 | GRCh38.p7 | 2:214154784 | TTTTTGTATTTAAAA[-/G]TGATAAAAATCTATA | 79582 |
rs34707976 | snp | C/T | 0.447809 | 0.152878 | intron-variant | SPAG16 | GRCh38.p7 | 2:214272680 | CCACATTTTCTTAAT[C/T]CAGTGTATCACTGAT | 79582 |
rs34711921 | in-del | -/G | | | intron-variant | SPAG16 | GRCh38.p7 | 2:213381442 | CGGTGCCATAACAAC[-/G]GGTTCCATGTTGGTT | 79582 |
rs34712920 | in-del | -/TA/TATA | | | intron-variant | SPAG16 | GRCh38.p7 | 2:214059260 | GTATATATATGTATG[-/TA/TATA]TATATATATATATAT | 79582 |
rs34712970 | in-del | -/G | | | intron-variant | SPAG16 | GRCh38.p7 | 2:213734777 | TATTATAAGCCAGAC[-/G]AATATGCTATTTATT | 79582 |
rs34713586 | in-del | -/C | | | intron-variant | SPAG16 | GRCh38.p7 | 2:214017201 | AAAAATAAAATCAGG[-/C]ATGATTTTTTGTTAG | 79582 |
rs34717856 | in-del | -/C | | | intron-variant | SPAG16 | GRCh38.p7 | 2:213685276 | GGTCACTGGGGTAGA[-/C]CCCCAATCCAATATG | 79582 |
rs34727166 | in-del | -/C | | | intron-variant | SPAG16 | GRCh38.p7 | 2:213955075 | ATTAGGCAAATAATT[-/C]TTCAAATTTTTTCCT | 79582 |
rs34730703 | snp | A/G | | | intron-variant | SPAG16 | GRCh38.p7 | 2:213415390 | CTCTGAAGCGGCTTA[A/G]AAACTTTGTGCCTGG | 79582 |
rs34739969 | in-del | -/T | | | intron-variant | SPAG16 | GRCh38.p7 | 2:214278365 | AACCAGGTACCTGAC[-/T]TTGGAAATGGAGAAA | 79582 |
rs34741797 | in-del | -/A | | | intron-variant | SPAG16 | GRCh38.p7 | 2:213941393 | ATCACTGAGGTACAT[-/A]AAATATAATTTATTT | 79582 |
rs34745239 | snp | A/C | 0.343477 | 0.231866 | intron-variant | SPAG16 | GRCh38.p7 | 2:214176290 | TTTTTTAAAAAAAAA[A/C]CAATATTATTGCTAG | 79582 |
rs34756709 | snp | C/T | | | intron-variant | SPAG16 | GRCh38.p7 | 2:213822184 | GTGTATGAGGGGTCC[C/T]CCTTCTTCATATCCT | 79582 |
rs34758902 | snp | C/T | 0 | 0 | intron-variant | SPAG16 | GRCh38.p7 | 2:213376106 | TAATCTTGTGCTTTT[C/T]CAGATTAGTGTTTTG | 79582 |
rs34761592 | in-del | -/T | | | intron-variant | SPAG16 | GRCh38.p7 | 2:214235673 | CTGTGGTCGCCAAGG[-/T]TTTTTTTTAACAATT | 79582 |
rs34775123 | in-del | -/A | | | intron-variant | SPAG16 | GRCh38.p7 | 2:214312796 | TTAGATATTCTAAGC[-/A]AAAAGTCTCATACAG | 79582 |
rs34776958 | in-del | -/G | | | intron-variant | SPAG16 | GRCh38.p7 | 2:213706635 | TCAAAATTGGATCAC[-/G]GGCACTCCCTATTTA | 79582 |
rs34787452 | in-del | -/A/AA | 0.496681 | 0.0405994 | intron-variant | SPAG16 | GRCh38.p7 | 2:214056528 | GGTAAAAAAAAAAAA[-/A/AA]TTCTCACAATCAACT | 79582 |
rs34788311 | in-del | -/GT | 0.427727 | 0.175821 | intron-variant | SPAG16 | GRCh38.p7 | 2:213765594 | TGTGTGTGTGTGTGT[-/GT]TATTTACTTGTTTCT | 79582 |
rs34789172 | in-del | -/TA | | | intron-variant | SPAG16 | GRCh38.p7 | 2:214059240 | ATATATATATATATA[-/TA]TGTATGTATATATAT | 79582 |
rs34792958 | in-del | -/A | 0.5 | 0 | intron-variant | SPAG16 | GRCh38.p7 | 2:214080607 | GCGAGACTCTGTCTC[-/A]AAAAAAAAAAAAAAA | 79582 |
rs34804587 | snp | A/G | 0.35144 | 0.228495 | intron-variant | SPAG16 | GRCh38.p7 | 2:214210839 | CACACATGCGCGCGC[A/G]CACACACACACACAC | 79582 |
rs34807287 | snp | A/G | 0.00159617 | 0.0282053 | intron-variant | SPAG16 | GRCh38.p7 | 2:214200769 | GTTTTTGAGAAAACA[A/G]TTAATTTTAATGTTT | 79582 |
rs34808886 | in-del | -/A | 0.386123 | 0.209692 | intron-variant | SPAG16 | GRCh38.p7 | 2:213923203 | CAGGGGTTGGTGGGG[-/A]TGCTTGTCCTGCTTT | 79582 |
rs34813393 | in-del | -/C | | | intron-variant | SPAG16 | GRCh38.p7 | 2:213494807 | ATGCTCTCCCACTCT[-/C]CCCTTGCCCTATCTC | 79582 |
rs34821468 | in-del | -/C | | | intron-variant | SPAG16 | GRCh38.p7 | 2:213762399 | ATAAAAAATGGAGAA[-/C]AACAACAAAAAACAA | 79582 |
rs34823564 | snp | C/T | 0.0023933 | 0.0345097 | intron-variant | SPAG16 | GRCh38.p7 | 2:214041420 | TGCACTTCTACATTT[C/T]AATGGTCTAGGTTGG | 79582 |
rs34832125 | snp | A/G | 0.418007 | 0.185132 | intron-variant | SPAG16, LOC101928084 | GRCh38.p7 | 2:214101323 | TCCTGCTTCAGTTCT[A/G]TGTCCTTCATGGGTT | 79582 |
rs34834613 | in-del | -/G | | | intron-variant | SPAG16 | GRCh38.p7 | 2:213462374 | CAATCTCTAGAAATT[-/G]GGATGGCTTCCCATT | 79582 |
rs34836461 | snp | C/G | 0.472709 | 0.11358 | intron-variant | SPAG16 | GRCh38.p7 | 2:213762121 | TGATTATCTCAATTG[C/G]AGAAGAAAAAGTATT | 79582 |
rs34837953 | in-del | -/G | | | intron-variant | SPAG16 | GRCh38.p7 | 2:214277757 | CAGTTAGGCTACACA[-/G]GGGGTCAGGGACCCA | 79582 |
rs34838000 | in-del | -/A | | | intron-variant | SPAG16 | GRCh38.p7 | 2:213887544 | AAAATATTAACTACT[-/A]AAATGTTTTCATAAT | 79582 |
rs34838185 | snp | C/T | 0.00953873 | 0.0683987 | intron-variant | SPAG16 | GRCh38.p7 | 2:213501315 | TCCTTGCTTTAGTAA[C/T]AATATTGAACATTTA | 79582 |
rs34840824 | in-del | -/T | | | intron-variant | SPAG16 | GRCh38.p7 | 2:213552166 | TTAGGTCAAAGCTAG[-/T]TTTAGCCATTCTTAT | 79582 |
rs34843702 | in-del | -/A/AA | | | intron-variant | SPAG16 | GRCh38.p7 | 2:213425651 | GCAAGACTCCATCTC[-/A/AA]AAAAAAAAAAAAAAA | 79582 |
rs34843980 | in-del | -/C | | | intron-variant | SPAG16 | GRCh38.p7 | 2:213636354 | TTCATGACTATAGCC[-/C]TTGTAGTATAGTTTG | 79582 |
rs34844271 | in-del | -/C | | | intron-variant | SPAG16, LOC101928084 | GRCh38.p7 | 2:214094766 | GTTATTCTGTGCCTG[-/C]CCCAACAATGTATAT | 79582 |
rs34846102 | in-del | -/A | 0.5 | 0 | intron-variant | SPAG16 | GRCh38.p7 | 2:214241376 | CAAGACTCCGTTGCC[-/A]AAAAAAAAAAAAAAA | 79582 |
rs34850189 | in-del | -/AC | | | intron-variant | SPAG16 | GRCh38.p7 | 2:214298113 | CATATATATATATAT[-/AC]ACACACACACACACA | 79582 |
rs34850431 | in-del | -/CTAA | 0.498182 | 0.0300969 | intron-variant | SPAG16 | GRCh38.p7 | 2:214311575 | CCTTTTGTCAGGACT[-/CTAA]CTAACTTCCTCTGGG | 79582 |
rs34855120 | in-del | -/A | | | intron-variant | SPAG16 | GRCh38.p7 | 2:214370280 | TAGAGTTGTTTTTAG[-/A]AAAAGAAGTCATGAC | 79582 |
rs34856658 | in-del | -/T | 0.479984 | 0.0980171 | intron-variant | SPAG16 | GRCh38.p7 | 2:213605269 | ATACTTTGGAATGCA[-/T]TTTTTTTTTTTTTTT | 79582 |
rs34865278 | in-del | -/C | | | intron-variant | SPAG16 | GRCh38.p7 | 2:213442094 | GGATGTTGCAGTGAG[-/C]CCGAGATCGCCCCAC | 79582 |
rs34869910 | snp | A/G | 0.221439 | 0.248363 | intron-variant | SPAG16 | GRCh38.p7 | 2:214140326 | GTTTCTAATTTAATT[A/G]CATCATCGTCATAAA | 79582 |
rs34871813 | in-del | -/C | | | intron-variant | SPAG16 | GRCh38.p7 | 2:213573920 | AATGTGCATACTTGT[-/C]CCCCTGGGGATCTTG | 79582 |
rs34872091 | in-del | -/G | | | intron-variant | SPAG16 | GRCh38.p7 | 2:214383294 | TACTTAGACTACACT[-/G]GGGCACAGTGGCTCA | 79582 |
rs34878088 | in-del | -/G | | | intron-variant | SPAG16, LOC101928084 | GRCh38.p7 | 2:214097368 | GTAAAAATATACGCA[-/G]GGAATGCTGTCTCTG | 79582 |
rs34879537 | in-del | -/T | 0.45889 | 0.13735 | intron-variant | SPAG16 | GRCh38.p7 | 2:214351775 | GGAAAATTGTATCAA[-/T]TTTTTTTTTAGTTTT | 79582 |
rs34885602 | in-del | -/C | | | intron-variant | SPAG16 | GRCh38.p7 | 2:213443333 | TGTCACTAGTAACCA[-/C]CCATTGTATTCTCTG | 79582 |
rs34889683 | in-del | -/T | | | intron-variant | SPAG16 | GRCh38.p7 | 2:213427680 | ATCTTTATCTACATA[-/T]TTCTCATCCTGAAAG | 79582 |
rs34891230 | in-del | -/T | 0.483852 | 0.0883933 | intron-variant | SPAG16 | GRCh38.p7 | 2:214133106 | TCAAATAAAATAAAA[-/T]AAAATAAATAAATAA | 79582 |
rs34892063 | snp | C/T | 0.0023933 | 0.0345097 | intron-variant | SPAG16 | GRCh38.p7 | 2:213737644 | AGGCGCCCGCCACCA[C/T]GCCCGGCTAATTTTT | 79582 |
rs34893069 | in-del | -/T | 0.261056 | 0.249755 | intron-variant | SPAG16 | GRCh38.p7 | 2:214123290 | ACCTCCAATCACTCC[-/T]TATAGTCAAATGGAG | 79582 |
rs34900197 | in-del | -/T | 0.208474 | 0.246527 | intron-variant | SPAG16 | GRCh38.p7 | 2:214055929 | CAATAAATTGGAAAA[-/T]TTTTACCATGAAGTG | 79582 |
rs34906305 | in-del | -/C | | | intron-variant | SPAG16 | GRCh38.p7 | 2:214010406 | AAAAAGTCACAGGGG[-/C]AAGAAACTTTCCTGG | 79582 |
rs34908676 | in-del | -/AG | | | intron-variant | SPAG16 | GRCh38.p7 | 2:214163637 | TATACATATATATAT[-/AG]AGAGAGAGAGAGAGA | 79582 |
rs34910668 | in-del | -/T | | | intron-variant | SPAG16 | GRCh38.p7 | 2:213774026 | CCTCTGTCTGTTCAC[-/T]TCCTATTTTCTATTC | 79582 |
rs34910737 | in-del | -/AT | | | intron-variant | SPAG16 | GRCh38.p7 | 2:213522799 | AAACTTACATGCCAA[-/AT]ATATATATATATATA | 79582 |
rs34912425 | snp | C/T | | | intron-variant | SPAG16 | GRCh38.p7 | 2:213643758 | AGCCTGTCTTCAAGC[C/T]CCCTACCTCTTTTTT | 79582 |
rs34913196 | snp | C/T | 0.347032 | 0.230401 | intron-variant | SPAG16 | GRCh38.p7 | 2:213832082 | GCTCACTGCAACCTC[C/T]TTCCCCCCGGGTTCA | 79582 |
rs34917660 | in-del | -/A | | | intron-variant | SPAG16 | GRCh38.p7 | 2:213896714 | TCATTTAGCTATACC[-/A]AAAATGAAATTCTGT | 79582 |
rs34920760 | in-del | -/G | | | intron-variant | SPAG16 | GRCh38.p7 | 2:213883888 | CTGTCCATTTACTTT[-/G]GAGCCTGAGTCCTTA | 79582 |
rs34923875 | in-del | -/T | | | intron-variant | SPAG16 | GRCh38.p7 | 2:214318374 | GTGAGAGTGAATTCT[-/T]TTTTTTTTTTTTTTT | 79582 |
rs34929055 | in-del | -/T | 0.304937 | 0.243889 | intron-variant | SPAG16 | GRCh38.p7 | 2:213908760 | TTTGTCTTTTTTTTT[-/T]CCTTTTTTTAATTAT | 79582 |
rs34930585 | in-del | -/T | | | intron-variant | SPAG16 | GRCh38.p7 | 2:214390332 | ATGAATGGGTATGCT[-/T]TTTTTTTTTAAAAAA | 79582 |
rs34931057 | in-del | -/C | | | intron-variant | SPAG16 | GRCh38.p7 | 2:213391314 | TTTGTTAAGGGAAAA[-/C]AAATATTTTAGCTTA | 79582 |
rs34931921 | in-del | -/AG | 0.327914 | 0.237549 | intron-variant | SPAG16 | GRCh38.p7 | 2:213906954 | CATTATTCTAGACAA[-/AG]ATTTTGTGGGTAAGA | 79582 |
rs34934423 | in-del | -/C | | | intron-variant | SPAG16 | GRCh38.p7 | 2:214041679 | CTTATTTCTTGCTTT[-/C]TGATTCTCTTCTTGA | 79582 |
rs34935044 | snp | A/G | 0.00398564 | 0.0444627 | intron-variant | SPAG16 | GRCh38.p7 | 2:214351193 | AAAATATTAATGCAG[A/G]AAGCAAATTTGAAAT | 79582 |
rs34935815 | in-del | -/C | | | intron-variant | SPAG16 | GRCh38.p7 | 2:214250464 | TAATAATTATTCAGT[-/C]TTCTCAAACCTAATC | 79582 |
rs34942799 | snp | C/G | 0.0019968 | 0.0315343 | intron-variant | SPAG16 | GRCh38.p7 | 2:214409268 | ACAATAATATGCCTT[C/G]TAAGTATGATTAAAT | 79582 |
rs34950865 | multinucleotide-polymorphism | AA/TG | | | intron-variant | SPAG16 | GRCh38.p7 | 2:213886861 | ATTTAAAATTAGAAC[AA/TG]TGGACACTATGCTGG | 79582 |
rs34952255 | in-del | -/A | | | intron-variant | SPAG16 | GRCh38.p7 | 2:213904601 | AAGGATAAATTTTGC[-/A]AAAAAAAAAAAAAAA | 79582 |
rs34952338 | in-del | -/T | 0.342806 | 0.232136 | intron-variant | SPAG16 | GRCh38.p7 | 2:214176865 | TCTTTGGCAAAAAAA[-/T]ATGTGCTATCAATTT | 79582 |
rs34956068 | in-del | -/G | | | intron-variant | SPAG16 | GRCh38.p7 | 2:213514226 | CACATTATGGTTTAT[-/G]GGAGAAGTGCATGAA | 79582 |
rs34964441 | in-del | -/TG | 0.131038 | 0.219882 | intron-variant | SPAG16 | GRCh38.p7 | 2:213462481 | TTGATATGACTAGAC[-/TG]TGTCCCTACCCAAAT | 79582 |
rs34966585 | in-del | -/CTAA | 0.0460142 | 0.144533 | intron-variant | SPAG16 | GRCh38.p7 | 2:214148672 | TATAAATTATCAATG[-/CTAA]CTAACTGTGAGCATA | 79582 |
rs34967158 | snp | A/C | | | intron-variant | SPAG16 | GRCh38.p7 | 2:214398180 | AATCAGAATATAGAG[A/C]CAATGAAAGAAGGCA | 79582 |
rs34970936 | snp | C/G | 0.414576 | 0.188188 | intron-variant | SPAG16 | GRCh38.p7 | 2:214377731 | CCTGAGTATTGAAGG[C/G]TCAACCATACTTGAT | 79582 |
rs34971645 | in-del | -/ATA | | | intron-variant | SPAG16 | GRCh38.p7 | 2:213788874 | CGTCTTTATGAGTGA[-/ATA]TTCTCAAATTATTGT | 79582 |
rs34974160 | in-del | -/G | | | intron-variant | SPAG16 | GRCh38.p7 | 2:214387919 | TTCAAGATGAGATTT[-/G]GGGTGGGGACACAGC | 79582 |
rs34983374 | in-del | -/C | | | intron-variant | SPAG16 | GRCh38.p7 | 2:213687630 | AATTGGCTGTCATTT[-/C]TGATCTTTGTCTTTT | 79582 |
rs34992362 | in-del | -/A | 0.474182 | 0.110646 | intron-variant | SPAG16 | GRCh38.p7 | 2:214351537 | TTTCTACTAAAAAAA[-/A]TACAAAAAATTAGCC | 79582 |
rs34993587 | in-del | -/A | | | intron-variant | SPAG16 | GRCh38.p7 | 2:214390509 | CTCAGGCTCACTTTG[-/A]AGCACAAACTGGTTA | 79582 |
rs34993614 | in-del | -/TAGT | 0.40157 | 0.198813 | intron-variant | SPAG16 | GRCh38.p7 | 2:214308097 | CATATATATTTAGGA[-/TAGT]TAGTTAGCTCTTCTT | 79582 |
rs34996952 | in-del | -/G | | | intron-variant | SPAG16 | GRCh38.p7 | 2:214306911 | TCATAGAATGAATTA[-/G]GGGGGAGTCCCTCCC | 79582 |
rs35001612 | in-del | -/A | | | intron-variant | SPAG16 | GRCh38.p7 | 2:213877435 | CCACCTCAGCTCCCC[-/A]AAAAGCTGGGACCAC | 79582 |
rs35003594 | in-del | -/A | | | intron-variant | SPAG16 | GRCh38.p7 | 2:213312603 | TCACCTTTTTACTTC[-/A]GTATTCAACACTTAG | 79582 |
rs35009507 | in-del | -/T | 0.472896 | 0.113214 | intron-variant | SPAG16 | GRCh38.p7 | 2:214256580 | AAATCTGGGCGAGAG[-/T]TTTTTGTTGTTGCTG | 79582 |
rs35010847 | in-del | -/A/AA | 0.117188 | 0.211804 | intron-variant | SPAG16 | GRCh38.p7 | 2:213556312 | AAAAAAAAAAAAACC[-/A/AA]AAAAAAAAAAAAAAA | 79582 |
rs35013602 | snp | C/G | | | intron-variant | SPAG16 | GRCh38.p7 | 2:213856729 | CCCTGTTAGTCATTG[C/G]TGGGATGCAGGGCAC | 79582 |
rs35013692 | in-del | -/A | 0.472989 | 0.113031 | intron-variant | SPAG16 | GRCh38.p7 | 2:213857555 | AGACCTACTGTTCAG[-/A]AAAAAAAATGATTCT | 79582 |
rs35016109 | in-del | -/A | 0 | 0 | intron-variant | SPAG16 | GRCh38.p7 | 2:214133114 | AATAAAATAAAAAAA[-/A]TAAATAAATAATAAT | 79582 |
rs35019214 | in-del | -/T | 0.480081 | 0.109421 | intron-variant | SPAG16 | GRCh38.p7 | 2:214041452 | TTCTTTTTTTTTTTT[-/T]AAATCATGGCTAAAA | 79582 |
rs35022515 | in-del | -/A | | | intron-variant | SPAG16 | GRCh38.p7 | 2:213652904 | TTCTGTGTCATGTCT[-/A]AAAATTCTTTGCCTA | 79582 |
rs35025898 | snp | A/G | 0.00358779 | 0.0422022 | intron-variant | SPAG16 | GRCh38.p7 | 2:213935338 | ATATGTTTTTCCCTC[A/G]TGACATATTATTAAG | 79582 |
rs35025961 | snp | G/T | | | intron-variant | SPAG16 | GRCh38.p7 | 2:213293857 | TTTACATATACATTG[G/T]GAAATGATTACCACA | 79582 |
rs35026128 | in-del | -/A | | | intron-variant | SPAG16 | GRCh38.p7 | 2:213752301 | TTATGTTTTTAATTT[-/A]AAATAATATGTACTT | 79582 |
rs35027044 | in-del | -/A/AA | 0.533429 | 0.21487 | intron-variant | SPAG16 | GRCh38.p7 | 2:213680434 | CCTTCTCTAGTAGTT[-/A/AA]AAAAAAAAAAAAAAG | 79582 |
rs35030080 | in-del | -/A | | | intron-variant | SPAG16 | GRCh38.p7 | 2:213552638 | AGGATTGTGATGTTT[-/A]AATATTGAGTGTCAA | 79582 |
rs35031602 | in-del | -/T | | | intron-variant | SPAG16 | GRCh38.p7 | 2:214047769 | TCACAGAATGGGAGA[-/T]AAATACTTGCAAACT | 79582 |
rs35035036 | in-del | -/A | 0.499326 | 0.0183414 | intron-variant | SPAG16 | GRCh38.p7 | 2:214046907 | AAAGTAAACAATCTG[-/A]AAAAAAAAAACAATT | 79582 |
rs35037228 | snp | C/G | 0.259674 | 0.249813 | intron-variant | SPAG16 | GRCh38.p7 | 2:214040359 | TACATAGGTATACTT[C/G]TGTCATAGGGGTTTG | 79582 |
rs35039048 | in-del | -/G | | | intron-variant | SPAG16 | GRCh38.p7 | 2:213334043 | ACAAACCCATAGAAT[-/G]GGGAGAAAATATTTG | 79582 |
rs35041693 | in-del | -/A | | | intron-variant | SPAG16 | GRCh38.p7 | 2:214012898 | TATCAGAATCACTTG[-/A]AAGAGCTTGCTAAAA | 79582 |
rs35041810 | snp | A/G | 0.342358 | 0.232314 | intron-variant | SPAG16 | GRCh38.p7 | 2:213336710 | TTTCAGCATCCCTAG[A/G]CAGGAGTTTATGAAC | 79582 |
rs35051527 | in-del | -/T | | | intron-variant | SPAG16 | GRCh38.p7 | 2:213927250 | ATTGGAATTAGGGCA[-/T]TCAATGTACGGATCT | 79582 |
rs35055268 | snp | A/C | | | intron-variant | SPAG16 | GRCh38.p7 | 2:214149610 | AAGGCAAAATAGCTA[A/C]CAGTAGAGAAGAACA | 79582 |
rs35057623 | snp | A/T | 0.484561 | 0.0864924 | intron-variant | SPAG16 | GRCh38.p7 | 2:214350243 | AAATGTCAAACATGA[A/T]CTCTTCAAGTACTTT | 79582 |
rs35058987 | snp | C/T | 0.298144 | 0.245321 | intron-variant | SPAG16 | GRCh38.p7 | 2:214287925 | TATGTGTTAGTAACA[C/T]GTCAAGTCCTCTCTC | 79582 |
rs35060290 | in-del | -/C | | | intron-variant | SPAG16 | GRCh38.p7 | 2:214034772 | TAGAGGATGTCACGG[-/C]CCCTGGCTTAAGGAG | 79582 |
rs35062212 | snp | A/G | 0.25045 | 0.25 | intron-variant | SPAG16 | GRCh38.p7 | 2:214137998 | GTGTTCATTGGCTCT[A/G]TAGAGGAGGGAAAGA | 79582 |
rs35062218 | snp | C/T | | | intron-variant | SPAG16 | GRCh38.p7 | 2:213566028 | GGAATAGCTTTTAAA[C/T]TAGAGGTCATGGTGA | 79582 |
rs35063151 | snp | A/G | 0.346368 | 0.23068 | intron-variant | SPAG16 | GRCh38.p7 | 2:214200438 | CCTGATATGAGACCC[A/G]CTTGATCATAATGGA | 79582 |
rs35069430 | in-del | -/C | 0.455502 | 0.142369 | intron-variant | SPAG16 | GRCh38.p7 | 2:214272862 | CCCTGAGGAATCACC[-/C]ACACTGTCTTCCACA | 79582 |
rs35072219 | snp | C/T | 0 | 0 | intron-variant | SPAG16 | GRCh38.p7 | 2:214042007 | ATATATATATATATA[C/T]ACACACACACACAAA | 79582 |
rs35082796 | in-del | -/C | | | intron-variant, downstream-variant-500B | SPAG16 | GRCh38.p7 | 2:214192651 | TTTTTTTGTACTTTT[-/C]CCAAAGAGACAGTTC | 79582 |
rs35084540 | snp | C/T | 0.00159617 | 0.0282053 | intron-variant | SPAG16 | GRCh38.p7 | 2:213410700 | ATGGATCAAATATTC[C/T]GTCCACACATTAAAC | 79582 |
rs35094396 | in-del | -/A | | | intron-variant | SPAG16 | GRCh38.p7 | 2:213983323 | CTCAAGTTTATTAAG[-/A]AAAAGTTTGAGGCAG | 79582 |
rs35096661 | in-del | -/C | | | intron-variant | SPAG16 | GRCh38.p7 | 2:214149732 | ACTAATTTGAGATAA[-/C]ACATTTATCTTATTG | 79582 |
rs35100066 | in-del | -/TCTG | 0.317451 | 0.240729 | intron-variant | SPAG16 | GRCh38.p7 | 2:214022727 | GAGGAAAAAAAAGAA[-/TCTG]TCTTACCATGGTGTT | 79582 |
rs35101370 | in-del | -/A | | | intron-variant | SPAG16 | GRCh38.p7 | 2:214078534 | GTAAGAGCCTGTCTC[-/A]AAAAAAAAAAAAAAA | 79582 |
rs35115619 | snp | A/G | 0.00993419 | 0.0697739 | intron-variant | SPAG16 | GRCh38.p7 | 2:213410076 | CCGAGACTGCTGTTC[A/G]TACAGCAAAAAGGGG | 79582 |
rs35126197 | snp | A/T | | | intron-variant | SPAG16 | GRCh38.p7 | 2:213782250 | GAAGGGAAGGAAGAA[A/T]CTGTTTTTTAGTGTT | 79582 |
rs35135100 | in-del | -/C | | | intron-variant | SPAG16 | GRCh38.p7 | 2:213336928 | GACTAGGTGAGACCT[-/C]CCCAACAGGAGTCCA | 79582 |
rs35135844 | in-del | -/A | | | intron-variant | SPAG16 | GRCh38.p7 | 2:214162037 | TTTTAGGTCTTTAAT[-/A]CCGAGGTGCAAGGGA | 79582 |
rs35139889 | in-del | -/G/GG | | | intron-variant | SPAG16 | GRCh38.p7 | 2:213409115 | TGAAATAAATTAACT[-/G/GG]GTTTTTTTTTTTTAA | 79582 |
rs35141566 | in-del | -/T | 0 | 0 | intron-variant | SPAG16 | GRCh38.p7 | 2:214081838 | TGTATTTTTTTTTTT[-/T]CATCCTTAGGAGGGT | 79582 |
rs35142663 | in-del | -/A | 0.0622301 | 0.165053 | intron-variant | SPAG16 | GRCh38.p7 | 2:213731039 | CATCTCTCTGCTTAC[-/A]ATTATCCTTCTATTT | 79582 |
rs35142955 | in-del | -/C | | | intron-variant | SPAG16 | GRCh38.p7 | 2:213857586 | TACAAAATATTACTT[-/C]CCCATTTAAAATTCA | 79582 |
rs35144945 | in-del | -/A | | | intron-variant | SPAG16 | GRCh38.p7 | 2:214330112 | CTCTACCAAAAATAG[-/A]AAAAAAAAAAAAAAA | 79582 |
rs35146057 | in-del | -/C | | | intron-variant | SPAG16 | GRCh38.p7 | 2:214406998 | AATCAATCTTCTCCC[-/C]TAGACTGTTTATTTT | 79582 |
rs35146206 | in-del | -/T | | | intron-variant | SPAG16 | GRCh38.p7 | 2:214328962 | ACTAGCCTAAATTTT[-/T]CATTATATACATAAG | 79582 |
rs35146619 | in-del | -/C | | | intron-variant | SPAG16 | GRCh38.p7 | 2:213759518 | GAGCTTTTGAAGGAG[-/C]CCGAGTTTTTATATA | 79582 |
rs35148800 | in-del | -/A | | | intron-variant | SPAG16 | GRCh38.p7 | 2:213542010 | TTAGTTTAATCCAGC[-/A]AAAAAAGTCTATTTT | 79582 |
rs35150155 | in-del | -/G | | | intron-variant | SPAG16 | GRCh38.p7 | 2:213341045 | TCACATAAAATTCAT[-/G]CATTTTAGATTACAT | 79582 |
rs35151127 | in-del | -/G | | | intron-variant | SPAG16 | GRCh38.p7 | 2:213814836 | ATTACATGAAGATAA[-/G]GGGGGTTAACTTTTC | 79582 |
rs35158427 | in-del | -/T | | | intron-variant | SPAG16 | GRCh38.p7 | 2:213670805 | TAGAAAGTTGCTTAG[-/T]TTTTGAATTTCTCAA | 79582 |
rs35159799 | in-del | -/C | | | intron-variant | SPAG16 | GRCh38.p7 | 2:214269329 | AGCCTAATGTGACCT[-/C]CCCAAATATAGAAAT | 79582 |
rs35160302 | in-del | -/C | | | intron-variant | SPAG16 | GRCh38.p7 | 2:213934538 | AAGAAAGGATGACAG[-/C]ATATTTGGTGAGAAA | 79582 |
rs35168911 | in-del | -/G | | | intron-variant | SPAG16 | GRCh38.p7 | 2:214373034 | TAGCTCCAAGTCTCT[-/G]GGGAAAATCAGAGAG | 79582 |
rs35173979 | in-del | -/A | 0.47614 | 0.106587 | intron-variant | SPAG16 | GRCh38.p7 | 2:214356577 | TGAAAGCCCCACCCC[-/A]ACCATATTTCTCTCT | 79582 |
rs35174487 | in-del | -/A | | | intron-variant | SPAG16 | GRCh38.p7 | 2:214117422 | TTCTACCAAACATGT[-/A]AAAAAAGAGCTAATA | 79582 |
rs35183893 | in-del | -/A | | | intron-variant | SPAG16 | GRCh38.p7 | 2:214321619 | TGAATTGTAACATTT[-/A]AATTATTTTAGACCC | 79582 |
rs35187948 | in-del | -/G | | | intron-variant | SPAG16 | GRCh38.p7 | 2:213334004 | CTTCTGCATAGAAAA[-/G]GGGAATAATCAACAA | 79582 |
rs35201837 | in-del | -/A | | | intron-variant | SPAG16 | GRCh38.p7 | 2:213415236 | CTAGAGGTCAGCCCC[-/A]AGCTTTTCAGAGGGG | 79582 |
rs35205215 | in-del | -/G | | | intron-variant | SPAG16 | GRCh38.p7 | 2:214302903 | TCTTTTATTACTACT[-/G]GTTGGTTTAATCTCT | 79582 |
rs35206510 | in-del | -/G | | | intron-variant | SPAG16 | GRCh38.p7 | 2:214174522 | GAATCCAACTTACAA[-/G]GGGACGTGAAGAGAA | 79582 |
rs35217259 | snp | A/C/G | | | intron-variant | SPAG16 | GRCh38.p7 | 2:213760582 | ACCTAACTCTGTGCA[A/C/G]CAACAGCGTACACAT | 79582 |
rs35219412 | in-del | -/T | 0.410399 | 0.191761 | intron-variant | SPAG16 | GRCh38.p7 | 2:214384696 | CAGGCAGCAAAACTC[-/T]TTTTCATTTCCCTAA | 79582 |
rs35223577 | in-del | -/C | | | intron-variant | SPAG16 | GRCh38.p7 | 2:213944060 | CAGGGCTGCCACTCT[-/C]CACCAAAGGTCCAGA | 79582 |
rs35224942 | in-del | -/C | | | intron-variant | SPAG16 | GRCh38.p7 | 2:213595575 | GTTAATAGTTTTAGA[-/C]ATATTTCTGTTACAA | 79582 |
rs35231219 | snp | A/C | | | intron-variant | SPAG16 | GRCh38.p7 | 2:213714077 | AATCTTCCACTGATG[A/C]CAGTAAAGAGAGAGT | 79582 |
rs35236344 | in-del | -/G | | | intron-variant | SPAG16 | GRCh38.p7 | 2:213451915 | GCTGCAGGTGTCCCT[-/G]GACTCGCCCCATACC | 79582 |
rs35237695 | in-del | -/T | | | intron-variant | SPAG16 | GRCh38.p7 | 2:213692320 | GGGTTAACATAATTT[-/T]GAGTTGTGCATATTT | 79582 |
rs35239333 | snp | A/C | 0.444444 | 0.157135 | intron-variant | SPAG16 | GRCh38.p7 | 2:214279547 | AATGAAAATGAGAGC[A/C]CAGGGACAGCAAGGC | 79582 |
rs35242124 | snp | A/G | 0.33533 | 0.234987 | intron-variant, downstream-variant-500B | SPAG16, MIR4438 | GRCh38.p7 | 2:213758524 | AAGAAGTTAAAAAAA[A/G]TTGGGAGCTGAAAAG | 79582 |
rs35243603 | in-del | -/C | | | intron-variant | SPAG16 | GRCh38.p7 | 2:214021692 | GTGCAATAATACAAT[-/C]ACAAAATTTAAAATA | 79582 |
rs35244594 | in-del | -/C | | | intron-variant | SPAG16 | GRCh38.p7 | 2:214076398 | GATAAATGGAAATTA[-/C]ACTGTAAATTAAATT | 79582 |
rs35247517 | in-del | -/G | | | intron-variant | SPAG16 | GRCh38.p7 | 2:214139419 | TCTACACTTTTCAAA[-/G]GAGCGGCTTTTGATT | 79582 |
rs35253771 | in-del | -/A | 0.34526 | 0.23114 | intron-variant | SPAG16 | GRCh38.p7 | 2:214210279 | GAGGTCCACTTATAC[-/A]TGGATTTTTTCAATA | 79582 |
rs35270878 | in-del | -/C | | | intron-variant | SPAG16 | GRCh38.p7 | 2:213291217 | TCCAATTTCCACATT[-/C]CATTAATTGTTACAT | 79582 |
rs35292427 | in-del | -/T | | | intron-variant | SPAG16 | GRCh38.p7 | 2:213586905 | CCCTCTGGGCCCTCT[-/T]GGGGTCATAGCCCTG | 79582 |
rs35298178 | in-del | -/A | 0.472709 | 0.11358 | intron-variant | SPAG16 | GRCh38.p7 | 2:213855946 | CTCAAATTTCAAAAC[-/A]CAATCATGTCCTTCC | 79582 |
rs35301802 | in-del | -/A | 0.377385 | 0.215112 | intron-variant | SPAG16 | GRCh38.p7 | 2:213763229 | GTTTGGAGGTTCCTC[-/A]AAAAAATCAAAAACA | 79582 |
rs35304295 | snp | C/T | | | intron-variant | SPAG16 | GRCh38.p7 | 2:213864561 | TACTAACATTTACTG[C/T]CCTCCTATGCTCTTC | 79582 |
rs35308900 | snp | C/G | 0.00755907 | 0.0610114 | intron-variant | SPAG16 | GRCh38.p7 | 2:213524232 | CAGCTTCCATGTAGT[C/G]TTGAGCCTGCAGATG | 79582 |
rs35309095 | in-del | -/T | 0 | 0 | intron-variant | SPAG16 | GRCh38.p7 | 2:213925355 | CTTTTTTTTTTTTTT[-/T]GAGGTGGAGTCTTGC | 79582 |
rs35309895 | in-del | -/A | | | intron-variant | SPAG16 | GRCh38.p7 | 2:214357987 | ATTTTCCTGGATTTT[-/A]AAAAACAAAATCCTG | 79582 |
rs35310085 | snp | C/T | 0.284995 | 0.247539 | intron-variant | SPAG16 | GRCh38.p7 | 2:214055388 | ACTAACTTGGCACTT[C/T]TAAGTATATAAAGAA | 79582 |
rs35311469 | in-del | -/C | | | intron-variant | SPAG16 | GRCh38.p7 | 2:214162579 | ACTATTGAAACTTGT[-/C]CTCGTTGATTTGTGA | 79582 |
rs35315473 | in-del | -/G | | | intron-variant | SPAG16 | GRCh38.p7 | 2:214379056 | AGGTCACTGAACTCT[-/G]GGAGTAGATTGACAT | 79582 |
rs35316956 | in-del | -/A | | | intron-variant | SPAG16 | GRCh38.p7 | 2:213556297 | GGGGCTGAATGGGTC[-/A]AAAAAAAAAAAAACC | 79582 |
rs35323974 | in-del | -/C | | | intron-variant | SPAG16 | GRCh38.p7 | 2:213668989 | GTCTCTGGAAAATAG[-/C]ACCATAATTTTTTTT | 79582 |
rs35328442 | in-del | -/A | | | intron-variant | SPAG16 | GRCh38.p7 | 2:214326557 | TGAGAAATCATAATA[-/A]GAAGAGAGAAATTCA | 79582 |
rs35338872 | in-del | -/A | | | intron-variant | SPAG16 | GRCh38.p7 | 2:213822917 | ATACTATGTAGCCAT[-/A]AAAAATGATGAGTTC | 79582 |
rs35338900 | snp | A/G | | | intron-variant | SPAG16 | GRCh38.p7 | 2:214261309 | GAGAGCTAGGCTTCA[A/G]AAGCCCCCTGGAATT | 79582 |
rs35340440 | in-del | -/G | | | intron-variant | SPAG16 | GRCh38.p7 | 2:213954772 | ATTCCTACCAGCAGT[-/G]CTATGAGAAATTCCC | 79582 |
rs35341781 | in-del | -/A | 0.493107 | 0.0583 | intron-variant | SPAG16 | GRCh38.p7 | 2:213589922 | ACGAAACTCCATCTC[-/A]AAAAAAAAAAAAAAA | 79582 |
rs35345360 | snp | A/C | | | intron-variant | SPAG16 | GRCh38.p7 | 2:214337884 | CAATAAACCAGGTGA[A/C]TAAAGAATTACTCTT | 79582 |
rs35350705 | in-del | -/GTCT | | | intron-variant | SPAG16 | GRCh38.p7 | 2:213451133 | ACAATTATCCACATT[-/GTCT]GTGAAGCACTTTCAT | 79582 |
rs35351598 | snp | C/T | | | intron-variant | SPAG16 | GRCh38.p7 | 2:214298161 | ACACACACACATATA[C/T]ACACACACACACACA | 79582 |
rs35357164 | in-del | -/T | | | intron-variant | SPAG16 | GRCh38.p7 | 2:213902595 | AACATGTGGGAATTA[-/T]TGGGAGTACAATTCA | 79582 |
rs35360758 | in-del | -/G | | | intron-variant | SPAG16 | GRCh38.p7 | 2:214211700 | TCCCTAGTGGTCCAA[-/G]GGAGTGGTCCAGGCT | 79582 |
rs35366236 | snp | C/T | 0.410737 | 0.191478 | intron-variant | SPAG16, LOC101928084 | GRCh38.p7 | 2:214101310 | CACAACATGTGTGTC[C/T]TGCTTCAGTTCTATG | 79582 |
rs35368252 | in-del | -/G | | | intron-variant | SPAG16 | GRCh38.p7 | 2:213466879 | CCATCCAGGTTAGCT[-/G]GGGTGGTCTGGTTGG | 79582 |
rs35372593 | snp | C/T | | | intron-variant | SPAG16 | GRCh38.p7 | 2:213639072 | GACTCCTTCTTGCTT[C/T]TGGTGTCCATTGCAT | 79582 |
rs35377871 | in-del | -/G | | | intron-variant | SPAG16 | GRCh38.p7 | 2:213450072 | ACTTTGGTAGGCCAA[-/G]GGCAGGTGGATCACC | 79582 |
rs35379088 | in-del | -/C | | | intron-variant | SPAG16 | GRCh38.p7 | 2:213576638 | CATGGGATACTATGG[-/C]AGCCATAAAAAAGAA | 79582 |
rs35393972 | in-del | -/G | | | intron-variant | SPAG16 | GRCh38.p7 | 2:213788004 | AGAATCATAAGAGCT[-/G]GGTGTTGTTGATAGG | 79582 |
rs35396406 | in-del | -/G | | | intron-variant | SPAG16 | GRCh38.p7 | 2:213803887 | CAAACAAATCAGCCA[-/G]GACTTCATGGCACAG | 79582 |
rs35398177 | in-del | -/ACT/GCT | 0.00119737 | 0.0244387 | intron-variant | SPAG16 | GRCh38.p7 | 2:213962328 | TCCTGAGTAGCTGGG[-/ACT/GCT]ACTACAGGCGCCCGC | 79582 |
rs35399771 | in-del | -/C | | | intron-variant | SPAG16 | GRCh38.p7 | 2:213796368 | CTATATTTGTCTCTT[-/C]CTGGACATTTAATGT | 79582 |
rs35402153 | in-del | -/GAGA | 0.289424 | 0.246872 | intron-variant, upstream-variant-2KB | SPAG16, LOC101928084 | GRCh38.p7 | 2:214103965 | AGAGAGAGAGACAGT[-/GAGA]GAGGGAGGGAGAGAG | 79582 |
rs35403780 | in-del | -/G | | | intron-variant | SPAG16 | GRCh38.p7 | 2:213534792 | AAACGCTACTATTAT[-/G]GGGGCTGAATTTTGT | 79582 |
rs35410623 | snp | A/G | 0.148326 | 0.228391 | intron-variant | SPAG16 | GRCh38.p7 | 2:214131972 | AATGTAGGTTCACCA[A/G]TTGTAACAAGTGTAC | 79582 |
rs35417015 | in-del | -/TG/TGTGTG | | | intron-variant | SPAG16 | GRCh38.p7 | 2:214227702 | CTTGTGGAAGGTGTA[-/TG/TGTGTG]TGTGTGTGTGTGTGT | 79582 |
rs35417207 | in-del | -/C | | | intron-variant | SPAG16 | GRCh38.p7 | 2:214010410 | AGTCACAGGGGAAGA[-/C]AACTTTCCTGGAATA | 79582 |
rs35418877 | in-del | -/AT | | | intron-variant | SPAG16 | GRCh38.p7 | 2:213833522 | TATATAATATATATA[-/AT]ATATATATTATATAT | 79582 |
rs35434401 | snp | A/G | 0.5 | 0 | intron-variant | SPAG16 | GRCh38.p7 | 2:213976882 | AAAACCCAGCTGGCT[A/G]ACACCTTCATTTCAG | 79582 |
rs35437741 | snp | A/T | 0.215144 | 0.247558 | intron-variant | SPAG16 | GRCh38.p7 | 2:214055113 | GCATAAAATAAGATA[A/T]GTAAAATCACCTCAT | 79582 |
rs35440495 | snp | A/C | 0.496105 | 0.0439572 | intron-variant | SPAG16 | GRCh38.p7 | 2:214366116 | CCCAAGTAGCTGGGA[A/C]TACAGGTATGCATCA | 79582 |
rs35442419 | in-del | -/T | 0.259674 | 0.249813 | intron-variant | SPAG16 | GRCh38.p7 | 2:213933026 | CTTGGCACATGGTGG[-/T]TTACTTACATAAATG | 79582 |
rs35445604 | in-del | -/A | | | intron-variant | SPAG16 | GRCh38.p7 | 2:214021330 | ACTGGGCAATGTATG[-/A]AAAGAATGAAGTTTA | 79582 |
rs35448067 | in-del | -/TA | | | intron-variant | SPAG16 | GRCh38.p7 | 2:214037865 | TTCCCAGAAGCCTGG[-/TA]TGTGTGTGTGTGTGT | 79582 |
rs35449458 | snp | G/T | | | intron-variant | SPAG16 | GRCh38.p7 | 2:213995007 | TGGTATTTATTATTG[G/T]ATTTTGAAGGTAAAT | 79582 |
rs35453731 | snp | C/T | 0.232651 | 0.249397 | intron-variant | SPAG16, LOC101928084 | GRCh38.p7 | 2:214099335 | AGGCATTATGTTAAT[C/T]GCTTTACATAAATTT | 79582 |
rs35458359 | in-del | -/T | | | intron-variant, upstream-variant-2KB | SPAG16 | GRCh38.p7 | 2:213294516 | GCAAGTATGCAACTA[-/T]TTTTTTTGTTTAATC | 79582 |
rs35459039 | in-del | -/T | | | intron-variant | SPAG16 | GRCh38.p7 | 2:213789277 | GTAAGATGAACACCA[-/T]TTTTGACAGTTAGTG | 79582 |
rs35460171 | in-del | -/G | | | intron-variant | SPAG16 | GRCh38.p7 | 2:213868804 | GAACTTCTACCCTTA[-/G]GAGCTGATTCATGAA | 79582 |
rs35460403 | in-del | -/G | | | intron-variant | SPAG16 | GRCh38.p7 | 2:214342001 | TTCTCTTTTTTAGTT[-/G]GGGGATGTAATAAAG | 79582 |
rs35468522 | in-del | -/T | | | intron-variant | SPAG16 | GRCh38.p7 | 2:213820301 | AATAGATATCAATGC[-/T]CTGTAAATAGATGTA | 79582 |
rs35475768 | in-del | -/A | | | intron-variant | SPAG16 | GRCh38.p7 | 2:213807379 | ATAGTGCCATTCATT[-/A]CTGTCACCTCCCAAT | 79582 |
rs35476156 | in-del | -/A | | | intron-variant, utr-variant-3-prime | SPAG16 | GRCh38.p7 | 2:213369254 | ATATTTGCCAGAAGG[-/A]AAATTAATATCTACC | 79582 |
rs35483460 | in-del | -/G | | | intron-variant | SPAG16 | GRCh38.p7 | 2:213549111 | TATGGAACTCAAAAT[-/G]GGAACTCAATTTTAA | 79582 |
rs35488902 | in-del | -/T | | | intron-variant | SPAG16 | GRCh38.p7 | 2:213773785 | CCTGAACTCCTGACC[-/T]TTGTGATCCACCCGC | 79582 |
rs35494598 | in-del | -/C | | | intron-variant | SPAG16 | GRCh38.p7 | 2:213598196 | TCTGTGGTTCTCCCC[-/C]TGTACACATTAATAA | 79582 |
rs35495166 | in-del | -/AT/TA | | | intron-variant | SPAG16 | GRCh38.p7 | 2:214175247 | ATATAAAGAAATGTA[-/AT/TA]TATATATATATAAAG | 79582 |
rs35499878 | in-del | -/CTCT | 0.233527 | 0.249457 | intron-variant | SPAG16 | GRCh38.p7 | 2:214181849 | GTTGTGGTTGAAAGG[-/CTCT]CTATCTACCATGCCT | 79582 |
rs35501630 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | SPAG16 | GRCh38.p7 | 2:213356390 | CTTGGACTTTATTTG[G/T]TTGGTAGGTTATTAA | 79582 |
rs35502279 | in-del | -/A | | | intron-variant | SPAG16 | GRCh38.p7 | 2:213393199 | AACTGAGACTGCAGT[-/A]AAAAAAAAATGCTGA | 79582 |
rs35508590 | in-del | -/T | 0 | 0 | intron-variant, upstream-variant-2KB | SPAG16 | GRCh38.p7 | 2:213315695 | GACTCTATTGAAAAC[-/T]TTTTTTTTTTTAATA | 79582 |
rs35511213 | in-del | -/G | | | intron-variant | SPAG16 | GRCh38.p7 | 2:213616902 | AATAGGAAGGAATGG[-/G]AGTTACCTTGGGGTC | 79582 |
rs35519694 | snp | A/C | | | intron-variant | SPAG16 | GRCh38.p7 | 2:213363491 | TTGGTATAATCATAT[A/C]CAATGCAAGATGAAA | 79582 |
rs35523556 | in-del | -/G | 0.47023 | 0.118317 | intron-variant | SPAG16 | GRCh38.p7 | 2:214352082 | CAAACAAGCTGCCTT[-/G]GCACCTGTGTTCTAA | 79582 |
rs35525350 | snp | G/T | 0.5 | 0 | intron-variant | SPAG16 | GRCh38.p7 | 2:214265948 | TCTAAAATTATATTG[G/T]TCTTTATTTATTTTC | 79582 |
rs35528975 | in-del | -/TTTC | 0.478186 | 0.102134 | intron-variant | SPAG16 | GRCh38.p7 | 2:214290398 | ATCTGATATTTACTA[-/TTTC]TTTCCTTCTGATAAT | 79582 |
rs35536127 | in-del | -/T | | | intron-variant | SPAG16 | GRCh38.p7 | 2:213704819 | CATTTAGATTCACAG[-/T]ATTAAAAAGGTGACT | 79582 |
rs35540273 | in-del | -/A | | | intron-variant | SPAG16 | GRCh38.p7 | 2:213748817 | GTTTTTTTCTGTGTG[-/A]AAAAATACTTTCATT | 79582 |
rs35547318 | in-del | -/TTCC | 0.443464 | 0.15834 | intron-variant | SPAG16 | GRCh38.p7 | 2:213694777 | TTCTCTTTTCCTTCT[-/TTCC]TTCCTTCCTTCCTTC | 79582 |
rs35549155 | in-del | -/T | 0.492386 | 0.0612297 | intron-variant | SPAG16 | GRCh38.p7 | 2:213961526 | AGCTATTTTTTTTTT[-/T]GTAGCTGCCTGCCTT | 79582 |
rs35553091 | in-del | -/A | | | intron-variant | SPAG16 | GRCh38.p7 | 2:213835541 | AACACATTATGGTCT[-/A]CCCTGGTTGGATGTC | 79582 |
rs35554346 | snp | A/G | | | intron-variant | SPAG16 | GRCh38.p7 | 2:213718889 | CGAGCACACGGCGCA[A/G]GACTGGCAGGCAGCT | 79582 |
rs35554459 | in-del | -/T | 0.495016 | 0.0496707 | intron-variant | SPAG16 | GRCh38.p7 | 2:214279104 | ATATATGAAACAAGC[-/T]TTTTTTTTTTTTTTT | 79582 |
rs35561423 | snp | G/T | | | intron-variant | SPAG16 | GRCh38.p7 | 2:213485508 | TATTGCTTCTTTATT[G/T]GCTTATTATCTTTTG | 79582 |
rs35564156 | in-del | -/GT | | | intron-variant | SPAG16 | GRCh38.p7 | 2:214037914 | TGTGTGTGTGTGTGT[-/GT]ATCCAAGTCTTTCTA | 79582 |
rs35565941 | in-del | -/G | | | intron-variant | SPAG16 | GRCh38.p7 | 2:214293452 | GTCTGGTAATCCCTA[-/G]GCCTTTGGAATGTGT | 79582 |
rs35567755 | in-del | -/C | | | intron-variant | SPAG16 | GRCh38.p7 | 2:213320579 | GTTCCCCACATACTT[-/C]CCCAGCCTCTGGTAA | 79582 |
rs35575934 | multinucleotide-polymorphism | CA/TG | | | intron-variant | SPAG16 | GRCh38.p7 | 2:213881390 | TCAGATTTTCCTATA[CA/TG]TAGGATCATATAGTC | 79582 |
rs35578332 | in-del | -/A | | | intron-variant | SPAG16 | GRCh38.p7 | 2:214169183 | TTCATAATTAAATTG[-/A]AAAAGTCATTATTTC | 79582 |
rs35579680 | in-del | -/G | 0.237014 | 0.249662 | intron-variant | SPAG16 | GRCh38.p7 | 2:214223157 | TATTTGGATCTTCCT[-/G]GGGAGACTTTATCTC | 79582 |
rs35579878 | snp | G/T | | | intron-variant | SPAG16 | GRCh38.p7 | 2:214081836 | CTCTCCTACTCATTG[G/T]ATTTTTTTTTTTCAT | 79582 |
rs35580523 | in-del | -/G | | | intron-variant | SPAG16 | GRCh38.p7 | 2:214020325 | TAAGCAATTACTACT[-/G]GTGCTGGTATTTTAT | 79582 |
rs35581234 | in-del | -/G | | | intron-variant | SPAG16 | GRCh38.p7 | 2:213902596 | ACATGTGGGAATTAT[-/G]GGGAGTACAATTCAA | 79582 |
rs35588542 | in-del | -/T | | | intron-variant | SPAG16 | GRCh38.p7 | 2:213959418 | GTTAAAACTTCCTTT[-/T]CCCTGAATGGTTGTT | 79582 |
rs35594452 | in-del | -/C | | | intron-variant | SPAG16 | GRCh38.p7 | 2:213521449 | ATTTCAGGAAGACTT[-/C]CCAGGATGTTAGAGC | 79582 |
rs35594739 | in-del | -/T | | | intron-variant | SPAG16 | GRCh38.p7 | 2:214382017 | TCCATAAATTTATTT[-/T]CCCTGTAGATTTGGA | 79582 |
rs35596036 | in-del | -/G | | | intron-variant, utr-variant-3-prime | SPAG16 | GRCh38.p7 | 2:213400384 | TAAGGTTTCCATTAT[-/G]GGTTTGTTCTTTGTC | 79582 |
rs35596487 | in-del | -/C | | | intron-variant | SPAG16 | GRCh38.p7 | 2:214001620 | TTTAGCTCTTACTGT[-/C]CCTTTATAATATTCA | 79582 |
rs35598286 | in-del | -/TTTA/TTTATTTA | 0.270892 | 0.249126 | intron-variant | SPAG16 | GRCh38.p7 | 2:213991859 | TTTGACAATTGAGAG[-/TTTA/TTTATTTA]TTTATTTATTTATTT | 79582 |
rs35599893 | in-del | -/T | | | intron-variant | SPAG16 | GRCh38.p7 | 2:214237550 | ATATAGTCCTCCCAG[-/T]AAAAAAGGAAAAGGC | 79582 |
rs35604281 | in-del | -/AT | | | intron-variant | SPAG16 | GRCh38.p7 | 2:213679544 | TACATTTTAAAAACG[-/AT]TGGAGAAACTTTTTT | 79582 |
rs35606696 | in-del | -/A | 0.470424 | 0.117954 | intron-variant | SPAG16 | GRCh38.p7 | 2:214050292 | TCCTGGGCCCCAGCT[-/A]AAAAAAAAAAAAAAA | 79582 |
rs35615203 | in-del | -/A | | | intron-variant | SPAG16 | GRCh38.p7 | 2:214168069 | ATCTGAGCTCACTGC[-/A]AACTCCGTCTCCCGA | 79582 |
rs35617863 | in-del | -/G | | | intron-variant | SPAG16 | GRCh38.p7 | 2:213393729 | TTATAAACCCACACA[-/G]GAGAGCTCCTACTAC | 79582 |
rs35618061 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | SPAG16 | GRCh38.p7 | 2:213891401 | TACCAACCATAATAC[C/G]TAATACCTAAGTAGG | 79582 |
rs35620715 | in-del | -/C | | | intron-variant | SPAG16 | GRCh38.p7 | 2:213546700 | TTAAAGCGGCCTCCT[-/C]CCTTGTTTCTTGATA | 79582 |
rs35638284 | in-del | -/C | | | intron-variant | SPAG16 | GRCh38.p7 | 2:214349131 | TTTGCATGGCACCTA[-/C]CCTGCAGGGAGCAGA | 79582 |
rs35638596 | snp | A/T | 0.00755907 | 0.0610114 | intron-variant | SPAG16 | GRCh38.p7 | 2:213599823 | TCTCCTGCCTCAGCA[A/T]CCCGAGTAGCTGGGT | 79582 |
rs35645581 | snp | C/G | 0.133093 | 0.220981 | intron-variant | SPAG16 | GRCh38.p7 | 2:214010457 | AATAGGTGGACCTTT[C/G]CATTAGGGTATGCTG | 79582 |
rs35646400 | snp | G/T | | | intron-variant | SPAG16 | GRCh38.p7 | 2:213961646 | CAATTAAAATTATTG[G/T]GTGGTATTATTCTTC | 79582 |
rs35647469 | in-del | -/TTCT | | | intron-variant | SPAG16 | GRCh38.p7 | 2:214260553 | AAGTCTATTATTTCT[-/TTCT]TTGGTTATTTGTCAT | 79582 |
rs35653546 | in-del | -/A | | | intron-variant | SPAG16 | GRCh38.p7 | 2:214004114 | TGTCTACAAATGAGC[-/A]AAAAGGGCTGTGAGT | 79582 |
rs35653633 | in-del | -/G | | | intron-variant | SPAG16 | GRCh38.p7 | 2:214286183 | TGGTGAACGGAGTAA[-/G]GGGGGAGATGTTGGT | 79582 |
rs35657382 | in-del | -/C | | | intron-variant | SPAG16 | GRCh38.p7 | 2:213618718 | TTCTGTTTTTTTTTT[-/C]TTCTTTGCATGCACA | 79582 |
rs35659073 | snp | A/C | 0.00953873 | 0.0683987 | intron-variant | SPAG16 | GRCh38.p7 | 2:213353495 | GTAAAATATGAAGGA[A/C]TCTTTAAGGGGTTGT | 79582 |
rs35673156 | in-del | -/A | | | intron-variant | SPAG16 | GRCh38.p7 | 2:214228292 | ATATGCATATAATTG[-/A]AAAAGTTTTCTCAAA | 79582 |
rs35674864 | in-del | -/A | | | intron-variant | SPAG16 | GRCh38.p7 | 2:214246328 | CTCATCCAACATTCT[-/A]CTTCCACAATGTCAC | 79582 |
rs35678406 | in-del | -/A | | | intron-variant | SPAG16 | GRCh38.p7 | 2:213969869 | AATTATTTAACAGTT[-/A]AAAAAAAGGCACAGT | 79582 |
rs35678411 | in-del | -/T | | | intron-variant, downstream-variant-500B | SPAG16 | GRCh38.p7 | 2:213376219 | TTGTCATCAGAAACA[-/T]TTTTCATCTTCTAAC | 79582 |
rs35680123 | in-del | -/G | | | intron-variant | SPAG16 | GRCh38.p7 | 2:213871222 | CAAAACCCAATAATA[-/G]GAAGCACTTCCAGAA | 79582 |
rs35680863 | in-del | -/A | | | intron-variant, utr-variant-5-prime | SPAG16 | GRCh38.p7 | 2:213299830 | ATCAGTAGTTTCTTG[-/A]AATTTAAGTATTTTA | 79582 |
rs35684058 | in-del | -/G | | | intron-variant | SPAG16 | GRCh38.p7 | 2:213580590 | AACCCCAACAACAAT[-/G]GGATACAGTGCTATC | 79582 |
rs35689066 | in-del | -/G | 0.144632 | 0.226711 | intron-variant | SPAG16 | GRCh38.p7 | 2:213974798 | GACTTCTATAAATTA[-/G]GGAACTTGGCTTGCC | 79582 |
rs35691403 | in-del | -/G | | | intron-variant | SPAG16 | GRCh38.p7 | 2:213958190 | GTTTGGTTTCCTGCA[-/G]GGGAATTCTAACTGA | 79582 |
rs35691540 | in-del | -/T | | | intron-variant | SPAG16 | GRCh38.p7 | 2:213413365 | AAAATCCAGTAATAG[-/T]TTTTTCTTCCTACAA | 79582 |
rs35705901 | in-del | -/G | | | intron-variant | SPAG16 | GRCh38.p7 | 2:214182688 | TTAATGTTATAAATT[-/G]GGGATAAAGACCAAA | 79582 |
rs35711030 | in-del | -/G | | | intron-variant | SPAG16 | GRCh38.p7 | 2:213630986 | ACTGAATAATCAGGG[-/G]AAGGTTACTCTTAGG | 79582 |
rs35717491 | in-del | -/C | | | intron-variant | SPAG16 | GRCh38.p7 | 2:213980534 | ATAGAATATATGTGT[-/C]ATATATAATATATAT | 79582 |
rs35721062 | snp | A/G | 0.00398564 | 0.0444627 | intron-variant | SPAG16 | GRCh38.p7 | 2:214224021 | AAGGTAAGCTGTTCA[A/G]TAGGGACAGAAATGA | 79582 |
rs35737344 | in-del | -/CAG | | | intron-variant | SPAG16 | GRCh38.p7 | 2:214050554 | GTTATTAATGACATA[-/CAG]GAACAGAATTGGGAC | 79582 |
rs35737499 | in-del | -/A | | | intron-variant | SPAG16 | GRCh38.p7 | 2:214004888 | AATATTTGTGATTAC[-/A]AAATATATTTTATTA | 79582 |
rs35741532 | in-del | -/T | | | intron-variant | SPAG16 | GRCh38.p7 | 2:214261675 | ATTTTAACAGAGTAA[-/T]TTTTTATTTGTGCTT | 79582 |
rs35742442 | in-del | -/G | | | intron-variant | SPAG16 | GRCh38.p7 | 2:213430554 | TTCCAATGTGGCCCA[-/G]GGGAAGCCAAAAGAT | 79582 |
rs35744538 | in-del | -/A | | | intron-variant | SPAG16 | GRCh38.p7 | 2:213683799 | CAATGTTACATTTGG[-/A]AAAAACTAGGCCAAT | 79582 |
rs35744697 | snp | A/C | | | intron-variant | SPAG16 | GRCh38.p7 | 2:213643760 | CCTGTCTTCAAGCCC[A/C]CTACCTCTTTTTTTT | 79582 |
rs35747291 | snp | C/T | 0.351635 | 0.228408 | intron-variant | SPAG16 | GRCh38.p7 | 2:214351127 | GATTTTATTGTAATC[C/T]TTCCGTGACTAGAAA | 79582 |
rs35760455 | in-del | -/G | | | intron-variant | SPAG16 | GRCh38.p7 | 2:213410266 | TAGTTATTAACATAA[-/G]GCAAGTCAATTTTGC | 79582 |
rs35766718 | in-del | -/C | | | intron-variant | SPAG16 | GRCh38.p7 | 2:213825595 | GTCATGATGAGTCAT[-/C]CTTTGTAATGTATTG | 79582 |
rs35768541 | in-del | -/G | | | intron-variant | SPAG16 | GRCh38.p7 | 2:213800564 | ATTTTTATATGGACA[-/G]GGGACTCACTAAGTT | 79582 |
rs35773073 | snp | C/T | 0.479824 | 0.098392 | intron-variant | SPAG16 | GRCh38.p7 | 2:213880348 | TGCTTGTTGATTTGT[C/T]TAAGTTCCTTGTAGA | 79582 |
rs35779841 | in-del | -/A | 0.479744 | 0.0985793 | intron-variant | SPAG16 | GRCh38.p7 | 2:214342062 | ATGAGAAACTCCAAG[-/A]AAAAAAACAAAATTG | 79582 |
rs35781804 | in-del | -/C | | | intron-variant | SPAG16 | GRCh38.p7 | 2:214391598 | GAAACACAGAGGATA[-/C]CAACAGAGGGAAAGA | 79582 |
rs35782265 | in-del | -/C | | | intron-variant | SPAG16 | GRCh38.p7 | 2:214342687 | ATGTGCTTGAATCAT[-/C]CCCAAAACCACCCCC | 79582 |
rs35790335 | in-del | -/G | | | intron-variant | SPAG16 | GRCh38.p7 | 2:214144600 | TCATGTATACATAGT[-/G]TGATGTAAAATCATT | 79582 |
rs35795865 | in-del | -/A | | | intron-variant | SPAG16 | GRCh38.p7 | 2:213867926 | AGACTCTGTCTCAAC[-/A]AAAAAAAAAAAAAAA | 79582 |
rs35798649 | in-del | -/AG | 0.300926 | 0.244758 | intron-variant | SPAG16 | GRCh38.p7 | 2:213520086 | GAGAGAGCAAGAGCA[-/AG]AGAGAGAGAGAGAGA | 79582 |
rs35799597 | in-del | -/C | | | intron-variant | SPAG16 | GRCh38.p7 | 2:214018241 | ACTTCATTTCAGATA[-/C]TAGCTAATTTATTAA | 79582 |
rs35802074 | snp | C/T | 0.472896 | 0.113214 | intron-variant | SPAG16 | GRCh38.p7 | 2:213859500 | AATTGGTTCTTTACC[C/T]CAGGGCTTAATAATG | 79582 |
rs35802462 | in-del | -/T | 0 | 0 | intron-variant | SPAG16 | GRCh38.p7 | 2:214318399 | TTTTTTTTTTTTTTT[-/T]GAGACAGGGTCTCGC | 79582 |
rs35808382 | in-del | -/A | | | intron-variant | SPAG16 | GRCh38.p7 | 2:213899915 | CTTCACAAGTTTGTG[-/A]AAAAACAATTCTCTT | 79582 |
rs35813611 | in-del | -/C | | | intron-variant | SPAG16 | GRCh38.p7 | 2:213779939 | GCATAAAAATGACTT[-/C]CTCAGAAAAGTACAG | 79582 |
rs35818932 | in-del | -/C | | | intron-variant | SPAG16 | GRCh38.p7 | 2:213616856 | TTACTAAGAGCACCC[-/C]AAAAGTTACTGAGAC | 79582 |
rs35821000 | in-del | -/TT/TTT | 0.228547 | 0.249078 | intron-variant | SPAG16, LOC101928084 | GRCh38.p7 | 2:214098913 | TGAGACTTTTTTTTT[-/TT/TTT]GCCAGTTACAGAAGT | 79582 |
rs35824328 | snp | C/G | 0.238171 | 0.24972 | intron-variant | SPAG16 | GRCh38.p7 | 2:214229542 | TGTATATATGTATTT[C/G]AAATCCAAAATGTTT | 79582 |
rs35826219 | in-del | -/T | | | intron-variant | SPAG16 | GRCh38.p7 | 2:213417587 | TAATTTTGGTAAACC[-/T]TTAACAGTTTCTCTT | 79582 |
rs35829494 | in-del | -/T | | | intron-variant | SPAG16 | GRCh38.p7 | 2:213623297 | GTAGGAAACTTTTTT[-/T]CACTATGTCATCACT | 79582 |
rs35832751 | in-del | -/ATT | 0.339656 | 0.233371 | intron-variant | SPAG16 | GRCh38.p7 | 2:213806034 | GCATATATGGATAAA[-/ATT]ATTATTAGGTTTTAT | 79582 |
rs35833232 | snp | G/T | | | intron-variant | SPAG16 | GRCh38.p7 | 2:213897489 | TCTATGACTTTATTG[G/T]TTTCTTGGATATATT | 79582 |
rs35833973 | in-del | -/G | | | intron-variant | SPAG16 | GRCh38.p7 | 2:213855441 | TCCACCTGGAAAAAT[-/G]GGGGATAGTGGTAAA | 79582 |
rs35837849 | in-del | -/TA | 0 | 0 | intron-variant | SPAG16 | GRCh38.p7 | 2:214335481 | ATTAACATGGAGGAA[-/TA]TATATATATATAGAT | 79582 |
rs35844452 | in-del | -/T | | | intron-variant | SPAG16 | GRCh38.p7 | 2:214283405 | AGCACTGTATAACAC[-/T]TTCACATATTCCCAC | 79582 |
rs35845932 | in-del | -/T | | | intron-variant | SPAG16 | GRCh38.p7 | 2:213914983 | ACCCGAGACTAGGTA[-/T]TTTTATAAAGGAAAG | 79582 |
rs35850810 | in-del | -/T/TT/TTT | | | intron-variant | SPAG16 | GRCh38.p7 | 2:213742547 | TATTTTGCTTATTTC[-/T/TT/TTT]TTTTTTGTTTTTTTT | 79582 |
rs35852133 | in-del | -/T | | | intron-variant | SPAG16 | GRCh38.p7 | 2:213851123 | AATTTAAGAATAAAA[-/T]TACAAGTTTTTAGAA | 79582 |
rs35853335 | in-del | -/A | | | intron-variant | SPAG16 | GRCh38.p7 | 2:214285406 | AGATGTATGCCTTGC[-/A]AAACATTTTTTCCCA | 79582 |
rs35860142 | snp | A/C | | | intron-variant | SPAG16 | GRCh38.p7 | 2:213867925 | CAAGACTCTGTCTCA[A/C]CAAAAAAAAAAAAAA | 79582 |
rs35863253 | in-del | -/T | 0.485392 | 0.0842056 | intron-variant | SPAG16 | GRCh38.p7 | 2:213668316 | TACTCATATGGGTGC[-/T]TTTTTTTTTTTGAAA | 79582 |
rs35867919 | in-del | -/C | | | intron-variant | SPAG16 | GRCh38.p7 | 2:214163187 | TAATCATTATACATT[-/C]CTTGATCTTTTTTCC | 79582 |
rs35870972 | in-del | -/C | | | intron-variant | SPAG16 | GRCh38.p7 | 2:213789920 | TCATCCAATGTATTT[-/C]TGAGTCAAAACTGTG | 79582 |
rs35877599 | in-del | -/T | 0.406814 | 0.194704 | intron-variant | SPAG16 | GRCh38.p7 | 2:214140258 | ATTTTGTGTTTTTTT[-/T]CTTTTAGCTTCCAAA | 79582 |
rs35878518 | snp | G/T | 0 | 0 | intron-variant | SPAG16 | GRCh38.p7 | 2:213634347 | TTTAACTTTTTATTG[G/T]TTCTATTTATATCTT | 79582 |
rs35892821 | snp | A/G | | | intron-variant | SPAG16 | GRCh38.p7 | 2:213293823 | ATTACATATATTCTA[A/G]GTGTACAACATATTT | 79582 |
rs35910856 | in-del | -/T | | | intron-variant | SPAG16 | GRCh38.p7 | 2:213621917 | CAGGACTACATTTTT[-/T]AGCAAGATCTCTTAT | 79582 |
rs35918628 | in-del | -/C | | | intron-variant | SPAG16 | GRCh38.p7 | 2:213451912 | TGCAGCTGCAGGTGT[-/C]CCTGACTCGCCCCAT | 79582 |
rs35926780 | in-del | -/C | | | intron-variant | SPAG16 | GRCh38.p7 | 2:213995656 | TCCTGGAGCCTTATT[-/C]CTACATTAGTCATCA | 79582 |
rs35930357 | in-del | -/C | | | intron-variant | SPAG16 | GRCh38.p7 | 2:213738747 | GTTCACCAATTATTT[-/C]CCAACTCTCCGTTCT | 79582 |
rs35935229 | in-del | -/G | | | intron-variant | SPAG16 | GRCh38.p7 | 2:213430025 | CAGATAAAGAGTTCA[-/G]AAATATTGATTTTTA | 79582 |
rs35937038 | in-del | -/C | | | intron-variant | SPAG16 | GRCh38.p7 | 2:214333264 | ATATATGCTTGATTT[-/C]CCTTGGATTACATAG | 79582 |
rs35938019 | in-del | -/G | | | intron-variant | SPAG16 | GRCh38.p7 | 2:214144432 | ATTGGTTCTATAATT[-/G]TGTTTTAATGGCTTT | 79582 |
rs35945601 | snp | C/T | 0.49925 | 0.0193545 | intron-variant | SPAG16 | GRCh38.p7 | 2:214246447 | TGACAGAATTAACAT[C/T]GAGTGACTTCTGAAG | 79582 |
rs35947469 | in-del | -/G | | | intron-variant | SPAG16 | GRCh38.p7 | 2:213290434 | CAATCTAGAAAACAA[-/G]GGCACAGTATTAAGT | 79582 |
rs35950921 | in-del | -/T | 0.319616 | 0.240112 | intron-variant | SPAG16 | GRCh38.p7 | 2:213938864 | ATAATAAAGATGAGG[-/T]TTTTTTTTTCTCTTA | 79582 |
rs35962279 | in-del | -/G | | | intron-variant | SPAG16 | GRCh38.p7 | 2:214394424 | TATTTTGCTGATTCT[-/G]GATTATGTAATTGAG | 79582 |
rs35963701 | snp | C/G | | | intron-variant | SPAG16 | GRCh38.p7 | 2:213523877 | TGTTCAAAGGAAGCA[C/G]AGCATAAAAATTTGG | 79582 |
rs35966000 | snp | A/C | | | intron-variant | SPAG16 | GRCh38.p7 | 2:213384917 | GCCCTTACCACCTTG[A/C]TGTTCTTTTCCATAA | 79582 |
rs35966160 | snp | C/T | 0.262435 | 0.249691 | intron-variant | SPAG16 | GRCh38.p7 | 2:214216504 | TTTTTTGTATTTTAG[C/T]AGAGATGGGGTTCCA | 79582 |
rs35966545 | in-del | -/A | | | intron-variant | SPAG16 | GRCh38.p7 | 2:213501442 | TAACAGCACTTGGTG[-/A]AAAAAATATACGTCT | 79582 |
rs35966581 | in-del | -/C | | | intron-variant | SPAG16 | GRCh38.p7 | 2:214006570 | TGCTTGTGAACTTCT[-/C]TCCTAAAAAATGATA | 79582 |
rs35966826 | in-del | -/C | | | intron-variant | SPAG16 | GRCh38.p7 | 2:214162333 | AGTCTGTTTAACATT[-/C]CCATTGACCATAAGA | 79582 |
rs35976332 | snp | A/T | 0.211819 | 0.247067 | intron-variant | SPAG16 | GRCh38.p7 | 2:214043436 | TTTTTCCCCAGGAGC[A/T]CTCAACCCCCCAAAA | 79582 |
rs35981578 | in-del | -/G | | | intron-variant | SPAG16 | GRCh38.p7 | 2:214029062 | AGAAATCAGGAATCA[-/G]GGGAAATAATGTAAG | 79582 |
rs35985159 | in-del | -/C | | | intron-variant | SPAG16, LOC101928084 | GRCh38.p7 | 2:214092860 | CCTTTTCTATGTACT[-/C]CCTTGTCTACTTCCT | 79582 |
rs35992664 | in-del | -/A | | | intron-variant | SPAG16 | GRCh38.p7 | 2:213898360 | AAGGAATTCACACAG[-/A]AAAACTAAATGCTTA | 79582 |
rs35994037 | in-del | -/A | | | intron-variant | SPAG16 | GRCh38.p7 | 2:214037366 | TACCTTTTTTATTTT[-/A]AAAATAATCTGTTTT | 79582 |
rs35995845 | in-del | -/C | | | intron-variant | SPAG16 | GRCh38.p7 | 2:213350126 | AGACTATCCTTTAGT[-/C]TTATTTTGATGTGAA | 79582 |
rs36006046 | in-del | -/TA | | | intron-variant | SPAG16 | GRCh38.p7 | 2:214059186 | GTCTCTCTCTCTGTC[-/TA]TATATATATATATAT | 79582 |
rs36007824 | in-del | -/T | 0.232067 | 0.249356 | intron-variant, upstream-variant-2KB | SPAG16, MIR4438 | GRCh38.p7 | 2:213756769 | AAGACACTCAAATAG[-/T]TTTTTTTTTATATGA | 79582 |
rs36009811 | in-del | -/A | | | intron-variant | SPAG16 | GRCh38.p7 | 2:213654541 | CTCTACTAAAAATAC[-/A]AAAAAAAAAAAAAAA | 79582 |
rs36011812 | in-del | -/C | | | intron-variant | SPAG16 | GRCh38.p7 | 2:213990652 | CCTAAAGGTCTTCAT[-/C]CCTTGTTATCTTCAC | 79582 |
rs36013816 | in-del | -/T | | | intron-variant, upstream-variant-2KB | SPAG16, LOC100130451 | GRCh38.p7 | 2:213285937 | CCAGGCATCTTGTAA[-/T]TTTTGTTTGCATTAA | 79582 |
rs36017056 | in-del | -/A | | | intron-variant | SPAG16 | GRCh38.p7 | 2:214389802 | CAAGGATAGAAGACT[-/A]AAACTGCCAGGTATA | 79582 |
rs36024096 | in-del | -/T | | | intron-variant | SPAG16 | GRCh38.p7 | 2:213944856 | GACATGAGATGGCGA[-/T]AACCCCGTGTCTACT | 79582 |
rs36028568 | in-del | -/TT | 0.046119 | 0.144681 | intron-variant | SPAG16 | GRCh38.p7 | 2:214163204 | TTGATCTTTTTTCCC[-/TT]TGTCAAATATAACAT | 79582 |
rs36029532 | in-del | -/C | | | intron-variant | SPAG16 | GRCh38.p7 | 2:214262629 | ATAATTTATGTCAAA[-/C]ACAATATTTTTTCTG | 79582 |
rs36033418 | in-del | -/T | 0.397813 | 0.201621 | intron-variant | SPAG16 | GRCh38.p7 | 2:213763659 | AAAGGGTGGATCTCA[-/T]TTTTTTTTTACCACG | 79582 |
rs36034989 | in-del | -/C | | | intron-variant | SPAG16 | GRCh38.p7 | 2:213507983 | CAGGTAAAATAAATG[-/C]ATTGATACTTTAAGC | 79582 |
rs36035610 | in-del | -/T | | | intron-variant | SPAG16 | GRCh38.p7 | 2:214368149 | CTCTCTATCAGTCCC[-/T]TGTCATTAGCATATT | 79582 |
rs36040110 | in-del | -/G | | | intron-variant | SPAG16 | GRCh38.p7 | 2:213665453 | CCTATTAAGGGACAA[-/G]GGATATGTTGAATTG | 79582 |
rs36040723 | in-del | -/G | | | intron-variant | SPAG16 | GRCh38.p7 | 2:214237251 | ACTTAAGAGAATTTT[-/G]GGGATGTGTTCCACA | 79582 |
rs36045589 | snp | C/T | 0.104149 | 0.203046 | intron-variant | SPAG16 | GRCh38.p7 | 2:214209257 | GAATATAACTAAAAC[C/T]CTAGATAGGAAGAAG | 79582 |
rs36047694 | in-del | -/A | | | intron-variant | SPAG16 | GRCh38.p7 | 2:214319503 | AGAAAGATCCACTGG[-/A]AAAAAAAAAAAAAAA | 79582 |
rs36052396 | in-del | -/TTTC | | | intron-variant | SPAG16 | GRCh38.p7 | 2:214260549 | TTAAAAGTCTATTAT[-/TTTC]TTCTTTGGTTATTTG | 79582 |
rs36055082 | snp | A/G | 0.030665 | 0.119967 | intron-variant | SPAG16 | GRCh38.p7 | 2:213462453 | TGGAGGAGATCACAT[A/G]TTAGTTGGGGGTTTG | 79582 |
rs36055287 | in-del | -/C | | | intron-variant | SPAG16 | GRCh38.p7 | 2:213944745 | ATTGAAGCTTAAATT[-/C]CCCAATGTGATAGTA | 79582 |
rs36055706 | in-del | -/TATC | 0.410399 | 0.191761 | intron-variant | SPAG16 | GRCh38.p7 | 2:213860426 | AAATATATGTGTGTA[-/TATC]TATATATTTATAGAT | 79582 |
rs36059669 | in-del | -/TTT | | | intron-variant | SPAG16 | GRCh38.p7 | 2:213620308 | CAATAATTTATTGAG[-/TTT]TTTTTTTTTTTTTTT | 79582 |
rs36064138 | snp | A/C | 0.470521 | 0.117772 | intron-variant | SPAG16 | GRCh38.p7 | 2:213905970 | GTTGAGTTGTCTAGC[A/C]CATTGTAATCAACTT | 79582 |
rs36065594 | in-del | -/ATA | 0.251296 | 0.249997 | intron-variant | SPAG16 | GRCh38.p7 | 2:214256824 | CCTTAATGTAGCATT[-/ATA]ATAAGTCTTAAAGTC | 79582 |
rs36065885 | in-del | -/G | | | intron-variant | SPAG16 | GRCh38.p7 | 2:213610747 | ACGCGTCTACCCTAG[-/G]TACAATGCTTGTATA | 79582 |
rs36069141 | in-del | -/T/TT/TTT | 0.5 | 0 | intron-variant | SPAG16 | GRCh38.p7 | 2:214062667 | TGTAATAGCCTCCTC[-/T/TT/TTT]TTTTTTTTTTTTTTT | 79582 |
rs36070442 | in-del | -/C | | | intron-variant | SPAG16 | GRCh38.p7 | 2:213857671 | TGCCTGCTGACAGAA[-/C]CATCAATTCTGCTTC | 79582 |
rs36082474 | in-del | -/G | | | intron-variant | SPAG16 | GRCh38.p7 | 2:214341924 | CTAAGGGCTCTGGCA[-/G]GGGAGGTCTCCAAGG | 79582 |
rs36084411 | snp | A/G | 0.39325 | 0.204889 | intron-variant | SPAG16 | GRCh38.p7 | 2:214307748 | TTTGATTGTGCTATG[A/G]TCTGAGAGAGTGGTT | 79582 |
rs36084438 | in-del | -/T | | | intron-variant | SPAG16 | GRCh38.p7 | 2:214105882 | AGCTTTTTAAACTTA[-/T]TTTTAATTCATGAAA | 79582 |
rs36084744 | in-del | -/T | 0.5 | 0 | intron-variant | SPAG16 | GRCh38.p7 | 2:214038537 | TTCTCAATTCATTTC[-/T]TTTTTTTTAGATTTT | 79582 |
rs36093574 | in-del | -/T | | | intron-variant | SPAG16 | GRCh38.p7 | 2:213759507 | GTGGGGGAATGGAGC[-/T]TTTTGAAGGAGCCGA | 79582 |
rs36096525 | in-del | -/G | | | intron-variant, upstream-variant-2KB, utr-variant-5-prime | SPAG16, LOC100130451 | GRCh38.p7 | 2:213285406 | TCCTACTAGGGAGAC[-/G]GGGGAGGGTTCATGA | 79582 |
rs36096579 | in-del | -/C | | | intron-variant | SPAG16 | GRCh38.p7 | 2:213973431 | AGAACATTATGTCAG[-/C]CCTCAGGTAGCACCC | 79582 |
rs36102881 | in-del | -/G | | | intron-variant | SPAG16 | GRCh38.p7 | 2:213939068 | TCTCCACACAATCTA[-/G]GAATGAGCCATGAGG | 79582 |
rs36103656 | in-del | -/G | | | intron-variant | SPAG16 | GRCh38.p7 | 2:213542136 | GAACACAGTTTACAT[-/G]GGGAAACTGTCTCAT | 79582 |
rs36106715 | in-del | -/A | | | intron-variant | SPAG16 | GRCh38.p7 | 2:213364860 | ATTGCAAATCTGGCC[-/A]TGCCTGGGTGGAAAG | 79582 |
rs36118137 | snp | A/G | 0.00159617 | 0.0282053 | intron-variant | SPAG16 | GRCh38.p7 | 2:213337868 | ATTCAGGAAACCCAG[A/G]CAACCCTAGTAAGAT | 79582 |
rs36122523 | in-del | -/A | | | intron-variant, utr-variant-5-prime | SPAG16 | GRCh38.p7 | 2:213300554 | ACAGGTCAAATGCAG[-/A]AAAAAATATGGGGAT | 79582 |
rs36137307 | snp | G/T | 0.168785 | 0.236441 | intron-variant | SPAG16 | GRCh38.p7 | 2:214039124 | AATCGCCACACTGAC[G/T]TCCACAATGGTTGAA | 79582 |
rs36141778 | snp | G/T | 0.5 | 0 | intron-variant | SPAG16 | GRCh38.p7 | 2:213356725 | TTTGATTTTTTGAAG[G/T]GTGTTTTTGTGTCCC | 79582 |
rs36155260 | snp | A/G | 0.346811 | 0.230494 | intron-variant | SPAG16 | GRCh38.p7 | 2:214195246 | TTAAAAATGTAGGAA[A/G]AGGCAGAGTGACCAG | 79582 |
rs36167543 | snp | C/T | 0.00636936 | 0.0560724 | intron-variant | SPAG16 | GRCh38.p7 | 2:213356453 | TAAACTAGGAAGAAG[C/T]TGAATCTCTGAATTG | 79582 |
rs36169193 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | SPAG16 | GRCh38.p7 | 2:213356463 | CTCACAAGAATAAAC[A/T]AGGAAGAAGTTGAAT | 79582 |
rs36169399 | snp | A/G | 0.111576 | 0.20818 | intron-variant | SPAG16 | GRCh38.p7 | 2:213345207 | CTGTTCATATCCTTC[A/G]CCCACTTGTTGATGG | 79582 |
rs36171946 | in-del | -/A | 0.346811 | 0.230494 | intron-variant | SPAG16 | GRCh38.p7 | 2:214195244 | AGTTAAAAATGTAGG[-/A]AAAGGCAGAGTGACC | 79582 |
rs36181178 | in-del | -/T | | | intron-variant | SPAG16 | GRCh38.p7 | 2:214057179 | AGGTTTTCAGTTTAC[-/T]TTTTTTTTTTTTTTA | 79582 |
rs36192495 | snp | C/T | | | intron-variant | SPAG16 | GRCh38.p7 | 2:213822921 | TGGAATACTATGCAG[C/T]CATAAAAAATGATGA | 79582 |
rs36229390 | in-del | -/TGTGTGTGTG | 0.5 | 0 | intron-variant | SPAG16 | GRCh38.p7 | 2:214284798 | AATAATATTTTACTC[-/TGTGTGTGTG]TGTGTGTGTGTGTGT | 79582 |
rs41435446 | snp | A/C | 0.362523 | 0.223246 | intron-variant | SPAG16 | GRCh38.p7 | 2:214179511 | AGAATTGCTCCATGA[A/C]GTCAAAAACACTTTT | 79582 |
rs41484647 | snp | C/T | 0.178465 | 0.239547 | intron-variant | SPAG16 | GRCh38.p7 | 2:213386549 | CTAAGGAAGATTAGA[C/T]GAGCTTATAGAGGCA | 79582 |
rs41519048 | snp | C/T | 0.0107246 | 0.0724382 | intron-variant | SPAG16 | GRCh38.p7 | 2:214069761 | TTAGGTTCTTCAGTA[C/T]ATATGAGTAGATATA | 79582 |
rs41520348 | snp | C/T | 0.0588605 | 0.161139 | intron-variant | SPAG16 | GRCh38.p7 | 2:214230215 | ATTGTTACGTGATTC[C/T]AGATAATATTTCTAT | 79582 |
rs55637823 | snp | A/C | 0.029116 | 0.117091 | intron-variant | SPAG16 | GRCh38.p7 | 2:213648204 | AGGAATAGCAAGCAA[A/C]GTTTTAACATTTACA | 79582 |
rs55638542 | snp | A/G | | | intron-variant | SPAG16 | GRCh38.p7 | 2:213980225 | AGAATATATGTGTGT[A/G]TATATATTCTCTATA | 79582 |
rs55639832 | snp | A/C | 0.00318978 | 0.0398085 | intron-variant | SPAG16 | GRCh38.p7 | 2:214336958 | GAGGCTTCTAGACTA[A/C]CTCACTTCTTCCAAT | 79582 |
rs55658550 | snp | G/T | 0.424037 | 0.179474 | intron-variant | SPAG16 | GRCh38.p7 | 2:213826259 | ATTTATTTCTTCTAT[G/T]ATCTTTATTATTTAT | 79582 |
rs55664424 | snp | A/C | 0.41023 | 0.191902 | intron-variant | SPAG16 | GRCh38.p7 | 2:213843696 | TCTCTACTAAAAATA[A/C]AAAAATTAGCTAGGT | 79582 |
rs55676249 | snp | A/C | 0.228842 | 0.249103 | intron-variant | SPAG16 | GRCh38.p7 | 2:213976520 | GTTAATAATCAGTGA[A/C]TATAAAATAGGGATA | 79582 |
rs55683310 | in-del | -/CA | 0.488118 | 0.0761554 | intron-variant | SPAG16 | GRCh38.p7 | 2:213929633 | TGAAGCCCGATCATC[-/CA]CAGAGCCTAATATAT | 79582 |
rs55684824 | in-del | -/A | | | intron-variant | SPAG16 | GRCh38.p7 | 2:213932296 | GCTCACTGCTCTGCA[-/A]CCTCTGCTTTCTGGG | 79582 |
rs55690277 | snp | A/T | 0.0383715 | 0.133092 | intron-variant | SPAG16 | GRCh38.p7 | 2:214322602 | ATATAAAGTTGGGGT[A/T]TATTTTAGATGGAAA | 79582 |
rs55703454 | in-del | -/TT | 0.137867 | 0.223442 | intron-variant | SPAG16 | GRCh38.p7 | 2:213845214 | ATATATCTAGTGTTC[-/TT]TTTTTTTTTTTTTTG | 79582 |
rs55710221 | in-del | -/TG/TT | | | intron-variant | SPAG16 | GRCh38.p7 | 2:213908757 | TCATTCTTTTTTTTT[-/TG/TT]GTCTTTTTTTTTCCT | 79582 |
rs55714143 | snp | A/G | 0.0154538 | 0.0865337 | intron-variant | SPAG16 | GRCh38.p7 | 2:214260433 | TTTGGTATCTTCTCC[A/G]TTTTCTTCCCAGGGA | 79582 |
rs55720212 | snp | C/T | 0.345037 | 0.231231 | intron-variant | SPAG16 | GRCh38.p7 | 2:213675861 | ttaggattgacttgg[C/T]gatgcgggctctttt | 79582 |
rs55721834 | snp | A/T | 0.0244538 | 0.107838 | intron-variant | SPAG16 | GRCh38.p7 | 2:213575110 | TCATCAACACAATGC[A/T]ACTAGTATCTCTAAA | 79582 |
rs55730342 | snp | A/T | 0.479824 | 0.098392 | intron-variant | SPAG16 | GRCh38.p7 | 2:213883230 | TTAATTAATTTCAAT[A/T]CTTTTTTATTTTTGC | 79582 |
rs55755300 | snp | C/T | | | intron-variant | SPAG16 | GRCh38.p7 | 2:214177910 | ATATACATATATATA[C/T]ATATACATATATATA | 79582 |
rs55756728 | snp | C/T | 0.0988009 | 0.199095 | intron-variant | SPAG16 | GRCh38.p7 | 2:214300410 | AGCAATCCTCATGAA[C/T]ACATAAGCTTTTTAA | 79582 |
rs55762327 | snp | C/T | 0.0103295 | 0.0711199 | intron-variant | SPAG16 | GRCh38.p7 | 2:213971224 | CCAATTGTTGACATT[C/T]TAAATCCAAGTACAT | 79582 |
rs55764407 | in-del | -/TGATCTACCTTT | 0.029116 | 0.117091 | intron-variant | SPAG16 | GRCh38.p7 | 2:214106666 | TGAGGGGCATCATGA[-/TGATCTACCTTT]GGTAGCTCATTTTGC | 79582 |
rs55768746 | snp | G/T | 0.109814 | 0.206997 | intron-variant | SPAG16 | GRCh38.p7 | 2:214265646 | TTATGGATCAAACTT[G/T]TGGTACTGTATCTAA | 79582 |
rs55774604 | in-del | -/GA/TGTGTGTGTGT | | | intron-variant | SPAG16 | GRCh38.p7 | 2:214193427 | GTGTGTGTGTGTATG[-/GA/TGTGTGTGTGT]AGAGAGAGAGAGAGA | 79582 |
rs55786740 | in-del | -/A | 0.0785177 | 0.181917 | intron-variant | SPAG16 | GRCh38.p7 | 2:214137810 | AGCATATGTCATGGC[-/A]AAAAACTGTTAATTT | 79582 |
rs55792553 | snp | A/G | 0.346147 | 0.230772 | intron-variant | SPAG16 | GRCh38.p7 | 2:214202369 | TTGAGCAACATGGGA[A/G]GGTTGCTGATGGACT | 79582 |
rs55799425 | snp | A/C | 0.0023933 | 0.0345097 | intron-variant | SPAG16 | GRCh38.p7 | 2:214322191 | TCACCTCACCCCTGG[A/C]TGCAAGTTAGAATCA | 79582 |
rs55804157 | in-del | -/AAGAAATATATATATA | | | intron-variant | SPAG16 | GRCh38.p7 | 2:214175330 | AGAAATATATATATA[-/AAGAAATATATATATA]TGAATCAGAGAAATT | 79582 |
rs55815930 | in-del | -/CTTT | | | intron-variant | SPAG16 | GRCh38.p7 | 2:214260555 | GTCTATTATTTCTTT[-/CTTT]GGTTATTTGTCATCT | 79582 |
rs55828216 | snp | A/T | 0.345704 | 0.230956 | intron-variant | SPAG16 | GRCh38.p7 | 2:214186586 | CCCTCCTTCCACTGA[A/T]ATAACATGACATAAG | 79582 |
rs55848552 | snp | G/T | 0.0228947 | 0.104514 | intron-variant | SPAG16 | GRCh38.p7 | 2:213578481 | ATTTTCCACATTATT[G/T]TAAAAGTTGAATATT | 79582 |
rs55859105 | in-del | -/A | 0 | 0 | intron-variant | SPAG16 | GRCh38.p7 | 2:213760511 | CTCAATAATGGCTAG[-/A]AAAAAAAAACAAAGA | 79582 |
rs55863252 | snp | A/T | 0.0433465 | 0.140692 | intron-variant | SPAG16 | GRCh38.p7 | 2:214061102 | GAGTACTAAGAGAGG[A/T]AAGTCCTTCATAGAG | 79582 |
rs55886363 | snp | G/T | 0.473359 | 0.112298 | intron-variant | SPAG16 | GRCh38.p7 | 2:213863919 | TTAGCACTTTCTTAC[G/T]GCAGAATTGTAGTAA | 79582 |
rs55890854 | snp | C/T | 0.0988009 | 0.199095 | intron-variant | SPAG16 | GRCh38.p7 | 2:214302772 | ACAGGTGTGAGCCAC[C/T]GCGCCTGGCCAAATA | 79582 |
rs55892981 | in-del | -/CTCT | | | intron-variant | SPAG16 | GRCh38.p7 | 2:214152178 | GTATAACAAAATTTT[-/CTCT]ATTTATTAACCTCAT | 79582 |
rs55899353 | in-del | -/AC/ACACAC | 0 | 0 | intron-variant | SPAG16 | GRCh38.p7 | 2:213385817 | CACACACACACACAC[-/AC/ACACAC]GTATGACTTCTTGTA | 79582 |
rs55909135 | snp | A/T | 0.0554779 | 0.157039 | intron-variant | SPAG16 | GRCh38.p7 | 2:214331748 | ATCATCTTGAGCACA[A/T]TTCTACATCTGCTTT | 79582 |
rs55915116 | in-del | -/GT | | | intron-variant | SPAG16 | GRCh38.p7 | 2:214175223 | TATAAAGAAATGTGT[-/GT]ATATATATATATAAA | 79582 |
rs55932005 | snp | A/T | | | intron-variant | SPAG16 | GRCh38.p7 | 2:213980233 | TGTGTGTATATATAT[A/T]CTCTATATATATAGA | 79582 |
rs55935607 | in-del | -/AA | | | intron-variant | SPAG16 | GRCh38.p7 | 2:213322358 | AAAAAAAAAAAAAAC[-/AA]AAAACTCGTTTGGGT | 79582 |
rs55949811 | in-del | -/ATAT/ATATAT | 0 | 0 | intron-variant | SPAG16 | GRCh38.p7 | 2:214177934 | TATATATATATATAT[-/ATAT/ATATAT]GGCCAGAATTGTTAT | 79582 |
rs55949963 | snp | C/T | 0.0189856 | 0.0955633 | intron-variant | SPAG16 | GRCh38.p7 | 2:213286655 | TGATGTCCTCTGCTT[C/T]GCACATATACTCAAT | 79582 |
rs55950408 | snp | A/T | 0.226188 | 0.248863 | intron-variant | SPAG16 | GRCh38.p7 | 2:213991999 | AATGAAGACTTGTTT[A/T]GTGTCACATCGGACT | 79582 |
rs55953297 | snp | C/T | 0.47666 | 0.105476 | intron-variant | SPAG16 | GRCh38.p7 | 2:214332777 | AAAATCACCCCCTCC[C/T]CACATTTGATTTTTC | 79582 |
rs55963106 | snp | A/C | | | intron-variant | SPAG16 | GRCh38.p7 | 2:213497729 | AATCCCACCCTTTAA[A/C]TACGGTTGGTAAGAA | 79582 |
rs55972413 | in-del | -/TT | | | intron-variant | SPAG16 | GRCh38.p7 | 2:213970300 | TTGCTTTTTTTTTTT[-/TT]GTTTATTTTTAAAAA | 79582 |
rs55973567 | snp | C/T | 0.495999 | 0.0445491 | intron-variant | SPAG16 | GRCh38.p7 | 2:214018894 | ATCAAAGATAATTAA[C/T]GTGGAGGCCTAAGTC | 79582 |
rs55974276 | snp | A/G | 0.0509478 | 0.151255 | intron-variant | SPAG16 | GRCh38.p7 | 2:213488990 | TGAGGCACGGGAATC[A/G]CCTGAATCCGGAAGG | 79582 |
rs55987430 | snp | A/G | 0.0178098 | 0.0926698 | intron-variant | SPAG16 | GRCh38.p7 | 2:213419515 | AGATTTGTAGTACTC[A/G]TGTAGCACTTAACAC | 79582 |
rs55994306 | snp | A/T | 0.314301 | 0.241589 | intron-variant | SPAG16 | GRCh38.p7 | 2:214122374 | TAATTGCTTTTCCTA[A/T]GTTGCCGGTAAGTAG | 79582 |
rs56003260 | snp | C/T | 0.0185938 | 0.0946107 | intron-variant, downstream-variant-500B | SPAG16 | GRCh38.p7 | 2:214062987 | TAAGTGAAATTAATT[C/T]AATAACATTATATTT | 79582 |
rs56011234 | in-del | -/GA/GT/GTGA/GTGT | 0.5 | 0 | intron-variant | SPAG16 | GRCh38.p7 | 2:213531359 | TGTGTGTGTGTGTGT[-/GA/GT/GTGA/GTGT]TTATGATTCTCTTTG | 79582 |
rs56023061 | snp | C/T | 0.215446 | 0.2476 | intron-variant | SPAG16, LOC101928084 | GRCh38.p7 | 2:214095435 | ACTTTGGAGTGTGGA[C/T]TCTGTTGTTGTCAGG | 79582 |
rs56032998 | snp | A/C | 0.182933 | 0.240836 | intron-variant | SPAG16 | GRCh38.p7 | 2:213588046 | CTAATTATACTGTAA[A/C]ATGTATTTTTCATAA | 79582 |
rs56037152 | in-del | -/A | 0.212728 | 0.247206 | intron-variant | SPAG16 | GRCh38.p7 | 2:213323441 | GCAAGACTCCGTCTC[-/A]AAAAAAAAATAGAAA | 79582 |
rs56050211 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | SPAG16 | GRCh38.p7 | 2:213962280 | CTCACTGCAAGCTCG[C/T]CTCCTGGGTTCACGC | 79582 |
rs56060918 | snp | A/G | 0.497502 | 0.035255 | intron-variant | SPAG16 | GRCh38.p7 | 2:213303115 | ATAATTTCCTGTGCT[A/G]GTAACCAGCACACTG | 79582 |
rs56068983 | snp | A/G | 0.00993419 | 0.0697739 | intron-variant | SPAG16 | GRCh38.p7 | 2:213885164 | TTTTAGACAGCCAAT[A/G]TGCTCTCTGTAGGGT | 79582 |
rs56069759 | snp | A/T | | | intron-variant | SPAG16 | GRCh38.p7 | 2:213670542 | GATGATTTAAAAATT[A/T]TCTTTTGACTTTTCA | 79582 |
rs56071870 | snp | A/T | 0.00478085 | 0.0486577 | intron-variant | SPAG16 | GRCh38.p7 | 2:213533165 | CACATATATGCATGA[A/T]TGGATGTCAAATGTC | 79582 |
rs56104652 | in-del | -/C | 0.470521 | 0.117772 | intron-variant | SPAG16 | GRCh38.p7 | 2:213883692 | ATGAATCTGGATGCT[-/C]CAGTGTTGGGTGCAT | 79582 |
rs56106328 | snp | C/G | 0.140242 | 0.224618 | intron-variant | SPAG16 | GRCh38.p7 | 2:213731655 | CCCTGCCCTCCAACA[C/G]GTCCCAGTGTGTGTG | 79582 |
rs56113142 | in-del | -/A | 0 | 0 | intron-variant | SPAG16 | GRCh38.p7 | 2:214351719 | AACAAAAAAAAAAAA[-/A]CAACAAAACTTAAAT | 79582 |
rs56138456 | snp | A/C | | | intron-variant | SPAG16 | GRCh38.p7 | 2:214225612 | ACAAAGGCTTCTTCA[A/C]CTCTAAAACAGTTAA | 79582 |
rs56147430 | snp | A/G | 0.0162398 | 0.0886349 | intron-variant | SPAG16 | GRCh38.p7 | 2:214178174 | ATCTAAATATACCTA[A/G]CTAGGGTATTTTGAG | 79582 |
rs56147676 | snp | G/T | | | intron-variant | SPAG16 | GRCh38.p7 | 2:213643645 | GGCCAATAACTCTTA[G/T]ATTTGCCCTTTGGAG | 79582 |
rs56164657 | snp | A/G | 0.105569 | 0.204058 | intron-variant | SPAG16 | GRCh38.p7 | 2:214162219 | ATTTCAGATCCCAGG[A/G]CCTTTTGGTGGGACA | 79582 |
rs56166027 | snp | C/T | 0.447938 | 0.152711 | intron-variant | SPAG16 | GRCh38.p7 | 2:214265322 | TACAGTAGTATCTCA[C/T]TGTTGTTTTAATTTG | 79582 |
rs56169433 | snp | C/T | 0.182614 | 0.240747 | intron-variant | SPAG16 | GRCh38.p7 | 2:213427152 | AGCATTGTCTGGCAC[C/T]TGTATGAGAAAAAGT | 79582 |
rs56176911 | snp | G/T | 0.0142736 | 0.0832652 | intron-variant | SPAG16 | GRCh38.p7 | 2:213344988 | TTGAACTAGTTTACA[G/T]TCCCATCAACAGTGT | 79582 |
rs56177202 | snp | C/T | 0.328148 | 0.237472 | intron-variant | SPAG16 | GRCh38.p7 | 2:213391905 | GAGATTAGAGAATTA[C/T]GGTGGCTAATTCTGA | 79582 |
rs56183094 | snp | A/G | 0.029116 | 0.117091 | intron-variant | SPAG16 | GRCh38.p7 | 2:213349150 | TACAGAATATTTTGC[A/G]CTGAATGATTAAAAA | 79582 |
rs56188460 | snp | A/G | 0.0298908 | 0.118541 | intron-variant | SPAG16 | GRCh38.p7 | 2:213671288 | TGTAGGAGCTTGACT[A/G]TGGCAGCCATTCTAA | 79582 |
rs56189766 | snp | G/T | | | intron-variant | SPAG16 | GRCh38.p7 | 2:213346850 | AATTCTCTTTTTTTT[G/T]TTGTTGTGTCTCTGC | 79582 |
rs56198465 | snp | C/T | 0.00279162 | 0.0372561 | intron-variant | SPAG16 | GRCh38.p7 | 2:214403328 | TAAAATTGATATATT[C/T]ATTTATATATTTATA | 79582 |
rs56257081 | snp | A/T | 0.000798403 | 0.0199641 | intron-variant | SPAG16 | GRCh38.p7 | 2:214231778 | TTGGGGACCATTGTC[A/T]GTTTTCTTTAAGAGA | 79582 |
rs56257811 | in-del | -/T | | | intron-variant | SPAG16 | GRCh38.p7 | 2:213709809 | AAGAATATTTGATTT[-/T]CATAATGTTTAAGGT | 79582 |
rs56258151 | in-del | -/ATAAA | | | intron-variant | SPAG16 | GRCh38.p7 | 2:214031620 | ATAAAATAAAATAAA[-/ATAAA]CATGAAAAAAAAAAG | 79582 |
rs56258457 | snp | A/T | 0.345704 | 0.230956 | intron-variant | SPAG16 | GRCh38.p7 | 2:214186578 | CAGCTTCCCCCTCCT[A/T]CCACTGAAATAACAT | 79582 |
rs56259213 | snp | C/T | 0.0228947 | 0.104514 | intron-variant | SPAG16 | GRCh38.p7 | 2:213563391 | TGTCATAACAATATA[C/T]TATAGACTAGGTGGC | 79582 |
rs56260410 | in-del | -/T | 0 | 0 | intron-variant | SPAG16 | GRCh38.p7 | 2:213345107 | ATCTCATTGTGGTTT[-/T]GATTTGCATTTCTCT | 79582 |
rs56269906 | snp | A/C | 0.0217236 | 0.101931 | intron-variant | SPAG16 | GRCh38.p7 | 2:213938420 | CTCACACATTTATGT[A/C]TATATACTTATTTGT | 79582 |
rs56274520 | snp | A/G | 0.174288 | 0.23826 | intron-variant | SPAG16 | GRCh38.p7 | 2:214019129 | TTGTCAGAAAGTGAT[A/G]TATCACATAGCAAAC | 79582 |
rs56276886 | in-del | -/C | 0.458315 | 0.13822 | intron-variant | SPAG16 | GRCh38.p7 | 2:214351836 | ATTCTATTTGACACA[-/C]AAAAAAAATATACTG | 79582 |
rs56310582 | snp | A/G | 0.474813 | 0.109357 | intron-variant | SPAG16 | GRCh38.p7 | 2:213764184 | ACGAGATTTTAAAAT[A/G]ATGACTAAGTTTTTT | 79582 |
rs56312142 | in-del | -/T | | | intron-variant | SPAG16 | GRCh38.p7 | 2:214193428 | TGTGTGTGTGTATGA[-/T]GAGAGAGAGAGAGAG | 79582 |
rs56318609 | snp | A/C | 0.482609 | 0.0916147 | intron-variant | SPAG16 | GRCh38.p7 | 2:214351719 | AAACAAACAAACAAA[A/C]AAAAAAAACAACAAA | 79582 |
rs56324885 | snp | G/T | | | intron-variant | SPAG16 | GRCh38.p7 | 2:214368325 | CTTATCAAACTTTTC[G/T]ACTATAATATCTCCT | 79582 |
rs56325677 | snp | A/G | 0.00557542 | 0.0525036 | intron-variant | SPAG16 | GRCh38.p7 | 2:213515342 | CACATTGTTAGATGC[A/G]AGGAAGTCACATTGA | 79582 |
rs56325852 | snp | A/T | 0.0209421 | 0.100162 | intron-variant | SPAG16 | GRCh38.p7 | 2:214081341 | ACCCCCAATTACTTA[A/T]CTCTGTTTTCAGTGG | 79582 |
rs56333652 | snp | A/G | 0.0166325 | 0.0896639 | intron-variant | SPAG16 | GRCh38.p7 | 2:213314681 | ACTATTTTATTTATA[A/G]TATTTAATTTAGAGG | 79582 |
rs56334842 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | SPAG16 | GRCh38.p7 | 2:213323821 | GGAAATTCTGTAATA[C/T]GTGAGGACATGCATG | 79582 |
rs56336545 | snp | A/G | 0.0279526 | 0.114869 | intron-variant | SPAG16 | GRCh38.p7 | 2:213320488 | CTACTGTGATATTGA[A/G]CACTAGAAGTTAACC | 79582 |
rs56361042 | in-del | -/A | 0.499137 | 0.0207489 | intron-variant | SPAG16 | GRCh38.p7 | 2:213336397 | GGGCCAAGTGGCCTC[-/A]ACTTCCACAGAACCC | 79582 |
rs56362536 | snp | A/C | 0.0185938 | 0.0946107 | intron-variant | SPAG16 | GRCh38.p7 | 2:213558235 | CCACAGAGCATCATA[A/C]TAACAGGTTCTAAAA | 79582 |
rs56365941 | in-del | -/GT/TG | | | intron-variant | SPAG16 | GRCh38.p7 | 2:214268745 | GTGTGTGTGTGTGTG[-/GT/TG]GGTGTGTATGTATGT | 79582 |
rs56370619 | snp | A/T | | | intron-variant | SPAG16 | GRCh38.p7 | 2:213497727 | AAAATCCCACCCTTT[A/T]ACTACGGTTGGTAAG | 79582 |
rs56373102 | snp | A/G | 0.153 | 0.230415 | intron-variant | SPAG16 | GRCh38.p7 | 2:213421556 | TGGCCTAAAGCCTGG[A/G]GGCCAGGCTCCCAAT | 79582 |
rs56382949 | snp | A/G | 0.116838 | 0.211584 | intron-variant | SPAG16 | GRCh38.p7 | 2:213302917 | CCATAAGTGTCTTTA[A/G]AAATGAGAATAGATA | 79582 |
rs56385748 | snp | C/T | 0.19646 | 0.2442 | intron-variant, utr-variant-5-prime | SPAG16 | GRCh38.p7 | 2:213299601 | ATGATTTCCTTTAAA[C/T]GTGGGTAGTATAGAT | 79582 |
rs56393190 | snp | C/T | 0.345037 | 0.231231 | intron-variant | SPAG16 | GRCh38.p7 | 2:214204352 | CTTGAAAGCACCACC[C/T]TCTGGCTGAAAGCCA | 79582 |
rs56402449 | in-del | -/AG/GA | 0 | 0 | intron-variant | SPAG16 | GRCh38.p7 | 2:213520087 | AGAGAGAGAGAGAGA[-/AG/GA]ATGCTAAGTGATGAC | 79582 |
rs56414504 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | SPAG16 | GRCh38.p7 | 2:213310445 | AGTTTAAGTAATTTT[C/T]AAAAAATCAAGACAC | 79582 |
rs56693089 | in-del | -/AA | | | intron-variant | SPAG16 | GRCh38.p7 | 2:214062443 | AAAAAAAAAAAAAAA[-/AA]GAAACCAAAACCAAC | 79582 |
rs56693992 | snp | A/T | 0.0460142 | 0.144533 | intron-variant, upstream-variant-2KB | SPAG16 | GRCh38.p7 | 2:213295118 | TAATCAGCAGCAAAA[A/T]GAAAACTAGGCTAAT | 79582 |
rs56695682 | in-del | -/AAT | 0 | 0 | intron-variant | SPAG16 | GRCh38.p7 | 2:213788875 | GTCTTTATGAGTGAT[-/AAT]TCTCAAATTATTGTG | 79582 |
rs56704459 | in-del | -/CTT | 0.28052 | 0.24813 | intron-variant | SPAG16 | GRCh38.p7 | 2:214383922 | ATGGACATGGCAAAC[-/CTT]CTTTAAATCTCTGTT | 79582 |
rs56714449 | in-del | -/GTGTGTGTGT | | | intron-variant | SPAG16 | GRCh38.p7 | 2:214227730 | TGTGTGTGTGTGTGT[-/GTGTGTGTGT]AAATGTGTATATCTA | 79582 |
rs56736513 | snp | C/T | 0.111224 | 0.207945 | intron-variant | SPAG16 | GRCh38.p7 | 2:214256937 | ATATAAATTTTAACA[C/T]CTTGTCAATTTGTTT | 79582 |
rs56760104 | in-del | -/T | | | intron-variant | SPAG16 | GRCh38.p7 | 2:213961600 | TTTTTTTTTTTTTTT[-/T]GCTGGATTTTGATAA | 79582 |
rs56771172 | in-del | -/TT | 0 | 0 | intron-variant | SPAG16 | GRCh38.p7 | 2:214291323 | TTTTTTTTTTTTTTT[-/TT]GAGACGGAGTCTTGC | 79582 |
rs56776022 | in-del | -/T/TTT | 0 | 0 | intron-variant | SPAG16 | GRCh38.p7 | 2:214112656 | TTTTTTTTTTTTTTT[-/T/TTT]GGCTTTCCATTTTCT | 79582 |
rs56781283 | in-del | -/A/ACA/CCAC | | | intron-variant | SPAG16 | GRCh38.p7 | 2:214108480 | CACACACACACACAC[-/A/ACA/CCAC]CCCCACACACACCCC | 79582 |
rs56835961 | snp | C/G | 0.0205511 | 0.0992634 | intron-variant | SPAG16 | GRCh38.p7 | 2:214225941 | TACAGTCTAGAAGTG[C/G]TATCTTTTCTTCCTG | 79582 |
rs56836715 | in-del | -/AA | | | intron-variant | SPAG16 | GRCh38.p7 | 2:214181794 | AATTTTTACATTAAA[-/AA]GTGTAAACAATAGGA | 79582 |
rs56840095 | snp | C/T | 0.00438332 | 0.0466095 | intron-variant | SPAG16 | GRCh38.p7 | 2:214277083 | CTTGATCGAATCGGC[C/T]ACTGAAGCTTGTGCA | 79582 |
rs56846656 | in-del | -/T | | | intron-variant | SPAG16 | GRCh38.p7 | 2:213652498 | ATTGTGTCTTTTTTT[-/T]ATATTTCCAGCAGCA | 79582 |
rs56859716 | snp | C/T | | | intron-variant | SPAG16 | GRCh38.p7 | 2:213780571 | ATTTTTCTTTTCTTT[C/T]TTTTTTTTTTTTTTT | 79582 |
rs56892491 | snp | A/T | 0.0577344 | 0.159793 | intron-variant | SPAG16 | GRCh38.p7 | 2:214340712 | CCATTATGGCATATA[A/T]GGATTCTTTGCTTAG | 79582 |
rs56893647 | in-del | -/GGGG | | | intron-variant | SPAG16 | GRCh38.p7 | 2:214140943 | ATTGGTGGGGGGGGG[-/GGGG]TGGGGGGTGGGGGGA | 79582 |
rs56896079 | snp | A/T | 0.0345262 | 0.126772 | intron-variant | SPAG16 | GRCh38.p7 | 2:214339599 | AACAAAGCTTTCTGC[A/T]CAGCTTGTAGTATTA | 79582 |
rs56921175 | snp | C/T | 0.0629771 | 0.165899 | intron-variant | SPAG16 | GRCh38.p7 | 2:213929793 | AATTCAAGTTAGCAA[C/T]TGTGTAGACCCAAAT | 79582 |
rs56944461 | in-del | -/T | | | intron-variant | SPAG16 | GRCh38.p7 | 2:213588465 | ATTTTTTTTTTTTTT[-/T]GTAAGGGAATCCAAA | 79582 |
rs56973442 | in-del | -/AAAGACCT | 0 | 0 | intron-variant | SPAG16 | GRCh38.p7 | 2:213796932 | CATGTTATTTCTCCT[-/AAAGACCT]TTTAGTGAGAGAAGA | 79582 |
rs56978658 | in-del | -/A | | | intron-variant | SPAG16 | GRCh38.p7 | 2:214069791 | ATTTTCTAAAAAAAA[-/A]TCATAGATTTTATTA | 79582 |
rs56995755 | snp | G/T | 0.021333 | 0.101051 | intron-variant | SPAG16 | GRCh38.p7 | 2:214020278 | CGAGTTTCTACCACA[G/T]TAGTCTCCAAACTAT | 79582 |
rs57008274 | snp | C/T | 0.0209421 | 0.100162 | intron-variant | SPAG16 | GRCh38.p7 | 2:214009475 | ATGTGTGTAATTTTA[C/T]AGTTGCTTATTATAA | 79582 |
rs57025359 | in-del | -/GCACACACAC | | | intron-variant | SPAG16 | GRCh38.p7 | 2:213896593 | TACACACACACACGC[-/GCACACACAC]ACACACACACACACA | 79582 |
rs57030129 | snp | A/C/G | 0.0115144 | 0.0749975 | intron-variant | SPAG16 | GRCh38.p7 | 2:214065920 | CAACCACAAAATATC[A/C/G]TATGACACATTATAT | 79582 |
rs57047043 | snp | A/G | | | intron-variant | SPAG16 | GRCh38.p7 | 2:213848184 | CTCTACGTCTTGTCT[A/G]GATTGTAGCAAGTTG | 79582 |
rs57050231 | in-del | -/T | | | intron-variant | SPAG16 | GRCh38.p7 | 2:214137465 | TATTGATGATTTTTT[-/T]AGGTTTCTACAGTTT | 79582 |
rs57056536 | in-del | -/ATATATGT | | | intron-variant | SPAG16 | GRCh38.p7 | 2:213860359 | TATATATATATATAT[-/ATATATGT]GTGTGTGTGTATATC | 79582 |
rs57058757 | in-del | -/AATGATGATGAT | | | intron-variant | SPAG16 | GRCh38.p7 | 2:214233344 | GTAAAAATAGATAAT[-/AATGATGATGAT]GATGATGATGATGAT | 79582 |
rs57074369 | in-del | -/TT | 0 | 0 | intron-variant | SPAG16 | GRCh38.p7 | 2:213731172 | TTTTTTTTTTTTTTT[-/TT]GAGTTGGAGTTTTGC | 79582 |
rs57090419 | in-del | -/GTCTATCT | | | intron-variant | SPAG16 | GRCh38.p7 | 2:213715225 | TAGATCTATCTGTCT[-/GTCTATCT]ATCTATCTATCTATC | 79582 |
rs57100155 | in-del | -/T | | | intron-variant | SPAG16 | GRCh38.p7 | 2:213996586 | TTTTTTTTTTTTTTT[-/T]GAGATGGAGTCTCTC | 79582 |
rs57102028 | in-del | -/GAGT/TGAG | 0 | 0 | intron-variant | SPAG16 | GRCh38.p7 | 2:214352585 | TGTGTATGTGTGACT[-/GAGT/TGAG]ATCTCCTAACATTTT | 79582 |
rs57118142 | in-del | -/T | 0.5 | 0 | intron-variant | SPAG16 | GRCh38.p7 | 2:213672186 | TTGATTTTTTTTTTT[-/T]CATTTCCTTTTCTGT | 79582 |
rs57148252 | snp | A/G | 0 | 0 | intron-variant | SPAG16 | GRCh38.p7 | 2:213899347 | ATCCCTTATATAGAA[A/G]AAAAACATATCAATA | 79582 |
rs57166260 | snp | C/G/T | 0.000798403 | 0.0199641 | intron-variant | SPAG16 | GRCh38.p7 | 2:213669903 | TTTACTCAGCAACAT[C/G/T]TAGTATTTTGCTGCT | 79582 |
rs57174578 | in-del | -/ATAT | 0 | 0 | intron-variant | SPAG16 | GRCh38.p7 | 2:213860361 | TATATATATATATAT[-/ATAT]GTGTGTGTGTGTATA | 79582 |
rs57176592 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | SPAG16 | GRCh38.p7 | 2:213899640 | TCTATAATATGACCA[C/T]TGATGGAAAACAACC | 79582 |
rs57188434 | snp | A/G | 0.0490535 | 0.14873 | intron-variant | SPAG16 | GRCh38.p7 | 2:213702426 | TGTAACACTCACCGC[A/G]AAGGTCTGCACCTTC | 79582 |
rs57239275 | snp | C/T | 0.0023933 | 0.0345097 | intron-variant | SPAG16 | GRCh38.p7 | 2:214298814 | ATGGTCCAAATTTGG[C/T]AAAGACTGCTCTAGA | 79582 |
rs57259138 | in-del | -/A | | | intron-variant | SPAG16 | GRCh38.p7 | 2:213389403 | GCAACAATAGAAAAA[-/A]CTGGACTTTATAAAC | 79582 |
rs57270824 | snp | A/T | | | intron-variant | SPAG16 | GRCh38.p7 | 2:213672969 | GTTCACCCATTGTCC[A/T]GCCTCAGCCAATGAT | 79582 |
rs57290289 | snp | A/G | 0.192715 | 0.243348 | intron-variant | SPAG16 | GRCh38.p7 | 2:213444076 | TGGAAGTACACGTGC[A/G]TCCATTTAAAATCAC | 79582 |
rs57315930 | snp | C/T | 0.483053 | 0.0904792 | intron-variant | SPAG16 | GRCh38.p7 | 2:213573092 | TGCCTCGCCCTGCTT[C/T]GGCTCACGCACGGTG | 79582 |
rs57320263 | in-del | -/TCAATA | | | intron-variant | SPAG16 | GRCh38.p7 | 2:214301225 | AATCATATGATAATA[-/TCAATA]GATGTAGAAAAAGCA | 79582 |
rs57344108 | snp | A/G | 0.37955 | 0.213815 | intron-variant | SPAG16 | GRCh38.p7 | 2:214047228 | CCTAGAATATCCAAA[A/G]CTATCCTAAGCAAAA | 79582 |
rs57358797 | in-del | -/AA | 0 | 0 | intron-variant | SPAG16 | GRCh38.p7 | 2:213720487 | AAAAAAAAAAAAAAA[-/AA]TTAGCTGGGCATGGT | 79582 |
rs57377846 | in-del | -/AT | 0 | 0 | intron-variant, upstream-variant-2KB | SPAG16 | GRCh38.p7 | 2:213342343 | ATATATTACATATAT[-/AT]GTATATATATATTAC | 79582 |
rs57419838 | in-del | -/CAGA | | | intron-variant | SPAG16 | GRCh38.p7 | 2:213860392 | ATATCTATAAATAGA[-/CAGA]TATTTATACATATAT | 79582 |
rs57433486 | in-del | -/T | 0.495855 | 0.045338 | intron-variant | SPAG16 | GRCh38.p7 | 2:214019074 | TTTTCTTCAAAGTTG[-/T]AAGACTATTTTATTA | 79582 |
rs57433786 | in-del | -/A/ATTTATTTATTT | | | intron-variant | SPAG16 | GRCh38.p7 | 2:213667962 | TTTATTTATTTATTT[-/A/ATTTATTTATTT]TTGAGACAAAGTCTC | 79582 |
rs57482112 | in-del | -/CCT | | | intron-variant | SPAG16 | GRCh38.p7 | 2:213863400 | TGTTTTCACTAAACT[-/CCT]TTTTTAAATCAGTTT | 79582 |
rs57482935 | snp | A/G | 0.5 | 0 | intron-variant | SPAG16 | GRCh38.p7 | 2:214210155 | GGGGGGAAGGGTCTT[A/G]TCTCCCTATCAATAT | 79582 |
rs57494025 | in-del | -/ATAAAACC/ATAAAACCG | 0.495855 | 0.045338 | intron-variant | SPAG16 | GRCh38.p7 | 2:214019073 | TTTTTCTTCAAAGTT[-/ATAAAACC/ATAAAACCG]GAAGACTATTTTATT | 79582 |
rs57529616 | in-del | -/TG/TGTGTG | 0 | 0 | intron-variant | SPAG16 | GRCh38.p7 | 2:213982649 | GTGTGTGTGTGTGTG[-/TG/TGTGTG]AAAGACAGAGTGGTG | 79582 |
rs57534934 | in-del | -/GA | | | intron-variant, upstream-variant-2KB | SPAG16, LOC101928084 | GRCh38.p7 | 2:214103959 | AGAGAGAGAGAGAGA[-/GA]CAGTGAGAGAGGGAG | 79582 |
rs57541370 | in-del | -/GTGT | | | intron-variant | SPAG16 | GRCh38.p7 | 2:214227736 | TGTGTGTGTGTGTGT[-/GTGT]AAATGTGTATATCTA | 79582 |
rs57542028 | snp | C/T | 0.0185938 | 0.0946107 | intron-variant | SPAG16 | GRCh38.p7 | 2:213810239 | AGACTGAGAATAGCA[C/T]GGACATTAAGAAGGT | 79582 |
rs57560803 | snp | C/T | 0.0298908 | 0.118541 | intron-variant | SPAG16 | GRCh38.p7 | 2:213907619 | TTCACAATAAATCAA[C/T]CTAAATGTCCATCAA | 79582 |
rs57597754 | snp | C/T | 0.0228947 | 0.104514 | intron-variant | SPAG16 | GRCh38.p7 | 2:213961651 | AAAATTATTGTGTGG[C/T]ATTATTCTTCATTTT | 79582 |
rs57603901 | snp | C/T | 0.0444908 | 0.142359 | intron-variant | SPAG16 | GRCh38.p7 | 2:214342680 | TAAATGTAATGTGCT[C/T]GAATCATCCCAAAAC | 79582 |
rs57605351 | in-del | -/T/TT | 0 | 0 | intron-variant | SPAG16 | GRCh38.p7 | 2:213733230 | GGTTGTTTTTTTTTT[-/T/TT]CTTGTAAATTTAAGT | 79582 |
rs57605719 | snp | A/C | 0.00676609 | 0.0577691 | intron-variant | SPAG16 | GRCh38.p7 | 2:213833015 | AATACTTTTTGATTC[A/C]AATTTCCTTTGAATT | 79582 |
rs57610812 | in-del | -/GGAGTGTTACAGCTCTTTCA | | | intron-variant | SPAG16 | GRCh38.p7 | 2:213476829 | ACAGCTTGGTGAGCA[-/GGAGTGTTACAGCTCTTTCA]TTCAAGCAGTTCAGA | 79582 |
rs57614898 | in-del | -/AA | 0 | 0 | intron-variant | SPAG16 | GRCh38.p7 | 2:213654566 | AAAAAAAAAAAAAAA[-/AA]TTAGCCGGGTGTGGT | 79582 |
rs57639856 | in-del | -/G | 0.174288 | 0.23826 | intron-variant | SPAG16 | GRCh38.p7 | 2:213731463 | CATGTCCAGCTGTTT[-/G]TTTTTTTTTTTTTTC | 79582 |
rs57668640 | snp | A/C | 0.174288 | 0.23826 | intron-variant | SPAG16 | GRCh38.p7 | 2:213388523 | AAGTCCTGAGAAAAC[A/C]GTAAGGTTACTGATC | 79582 |
rs57712962 | snp | A/G | 0.341235 | 0.232758 | intron-variant | SPAG16 | GRCh38.p7 | 2:214026230 | CATACATGCATATAT[A/G]TACATACACATATTA | 79582 |
rs57716656 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | SPAG16 | GRCh38.p7 | 2:213805624 | AACCACTTATAATAA[C/T]AGTGTAGAAAATATT | 79582 |
rs57749786 | in-del | -/AT/TA | 0 | 0 | intron-variant | SPAG16 | GRCh38.p7 | 2:213302648 | TGTGTGTGTGTGTGT[-/AT/TA]GTGTGTGTGTGTTGT | 79582 |
rs57811186 | snp | C/T | | | intron-variant | SPAG16 | GRCh38.p7 | 2:213500239 | GATTGAATCCATGGG[C/T]TTAGGACTTTTCAAT | 79582 |
rs57824653 | snp | A/G | 0.0209421 | 0.100162 | intron-variant | SPAG16 | GRCh38.p7 | 2:213814362 | TTAAATGTTAATTAC[A/G]TCTAAAAATATACCT | 79582 |
rs57829323 | snp | A/T | 0 | 0 | intron-variant | SPAG16 | GRCh38.p7 | 2:214133110 | ATAAAATAAAATAAA[A/T]AAAATAAATAAATAA | 79582 |
rs57831612 | snp | A/C | | | intron-variant | SPAG16 | GRCh38.p7 | 2:214154511 | AGACCCCCCCCCCCC[A/C]TTTTTTCATAACCTA | 79582 |
rs57849800 | in-del | -/T | 0 | 0 | intron-variant | SPAG16 | GRCh38.p7 | 2:213869661 | GTTTTTTTTTTTTTT[-/T]GTCTAATTCTAAAAG | 79582 |
rs57878279 | in-del | -/A | 0.497668 | 0.0340657 | intron-variant | SPAG16 | GRCh38.p7 | 2:214251278 | ACTTGTTGCAGAAAG[-/A]AAAAAAAAAAGTCAC | 79582 |
rs57904445 | in-del | -/ATCTC | | | intron-variant | SPAG16 | GRCh38.p7 | 2:213968173 | TTCTCTTCTCATCTC[-/ATCTC]TTTTCTTTTCTTTTC | 79582 |
rs57907847 | snp | A/G | 0.0325976 | 0.123435 | intron-variant | SPAG16 | GRCh38.p7 | 2:213656217 | TTTTTTGTTTTTGGG[A/G]CGGAGTCTCGCTCTG | 79582 |
rs57936781 | snp | A/T | 0.385359 | 0.210185 | intron-variant | SPAG16 | GRCh38.p7 | 2:213638973 | TTTCCTGTTGCATTT[A/T]TCTCTTTATCATTTT | 79582 |
rs57948016 | in-del | -/ACACAC | | | intron-variant | SPAG16 | GRCh38.p7 | 2:213932986 | CACACACACACACAC[-/ACACAC]CAGTGTAACCCAGAG | 79582 |
rs57950097 | snp | A/G | 0.104149 | 0.203046 | intron-variant | SPAG16 | GRCh38.p7 | 2:214190191 | TCTGTGTCTGCCTCA[A/G]TACTGGTAATCTCTC | 79582 |
rs57954043 | in-del | -/T | 0 | 0 | intron-variant, upstream-variant-2KB | SPAG16 | GRCh38.p7 | 2:213299451 | AATTTTTTTTTTTTT[-/T]GTATTTTTAGTAGAG | 79582 |
rs57957773 | snp | A/G | 0.030665 | 0.119967 | intron-variant | SPAG16 | GRCh38.p7 | 2:213887578 | AAACTGGAGGGGAAG[A/G]AAAATGCACTTGTTC | 79582 |
rs57997386 | in-del | -/A/AA | 0 | 0 | intron-variant | SPAG16 | GRCh38.p7 | 2:214322521 | GGCAAAAAAAAAAAA[-/A/AA]GGCATCAGAAAAATT | 79582 |
rs57998726 | in-del | -/A/AA | 0.360462 | 0.230271 | intron-variant | SPAG16 | GRCh38.p7 | 2:213411892 | ATGTTAAAAAAAAAA[-/A/AA]GAAAAAAAGGTTTGA | 79582 |
rs58001128 | snp | C/T | 0.0279526 | 0.114869 | intron-variant | SPAG16 | GRCh38.p7 | 2:213631997 | ATATAAATATTAGGA[C/T]TTTTTTTCTATTTCT | 79582 |
rs58012287 | snp | C/T | 0.173643 | 0.238054 | intron-variant | SPAG16 | GRCh38.p7 | 2:213561493 | TTACCTTGATATAAT[C/T]ACTCATTGTATGCCT | 79582 |
rs58019498 | snp | C/T | 0.155656 | 0.231515 | intron-variant | SPAG16 | GRCh38.p7 | 2:213394494 | ACTATAATATAGTAT[C/T]AAGATTAGGATGTTG | 79582 |
rs58022107 | snp | A/G | 0.174932 | 0.238463 | intron-variant | SPAG16 | GRCh38.p7 | 2:213503917 | GCAAACTGAGAACAT[A/G]GTGAACTAGTACTCT | 79582 |
rs58045755 | snp | C/G | | | intron-variant | SPAG16 | GRCh38.p7 | 2:213457474 | TGAGATGCCATTATA[C/G]GCATACTTGTTCTTT | 79582 |
rs58046783 | snp | C/T | 0.195526 | 0.243993 | intron-variant | SPAG16 | GRCh38.p7 | 2:213980234 | GTGTGTATATATATT[C/T]TCTATATATATAGAA | 79582 |
rs58049912 | snp | A/G | 0.155656 | 0.231515 | intron-variant | SPAG16 | GRCh38.p7 | 2:213434551 | TGCAGAATAGGAGAA[A/G]GTATTTGCAAACTAT | 79582 |
rs58052314 | snp | A/G | 0.0471551 | 0.14613 | intron-variant | SPAG16 | GRCh38.p7 | 2:214335062 | AAACCGATGAGGAAG[A/G]ACAGTAATGAACTTG | 79582 |
rs58054043 | snp | A/T | 0.47666 | 0.105476 | intron-variant | SPAG16 | GRCh38.p7 | 2:213887432 | ATCGTATTCGTCTGA[A/T]GTTTTCTCCTGATTA | 79582 |
rs58056064 | in-del | -/ATTT/ATTTATTTATTT/ATTTATTTATTTATTT | 0 | 0 | intron-variant | SPAG16 | GRCh38.p7 | 2:214288786 | TTTATTTATTTATTT[lengthTooLong]GAGACGTTGTCTCGC | 79582 |
rs58069845 | in-del | -/TT | 0 | 0 | intron-variant | SPAG16 | GRCh38.p7 | 2:214327708 | AAATTTTTTTTTTTT[-/TT]GCATCCTCTCTTGGG | 79582 |
rs58070679 | in-del | -/AAAAAAAAAA | | | intron-variant | SPAG16 | GRCh38.p7 | 2:213728912 | AAAAAAAAAAAAAAA[-/AAAAAAAAAA]GATGATGGAATGATG | 79582 |
rs58071177 | snp | C/T | 0.154993 | 0.231244 | intron-variant | SPAG16 | GRCh38.p7 | 2:213475425 | GGAGTCCCAGTGATT[C/T]AGGATACACTTGAGG | 79582 |
rs58075048 | snp | C/T | 0.0387552 | 0.1337 | intron-variant, upstream-variant-2KB | SPAG16 | GRCh38.p7 | 2:213342370 | TATATATTACATATA[C/T]ATGTATTATATATAT | 79582 |
rs58087200 | snp | A/G | 0.174288 | 0.23826 | intron-variant | SPAG16 | GRCh38.p7 | 2:213576875 | AGGAGAGGATCAGGA[A/G]AAATAACAAATGGGT | 79582 |
rs58113131 | in-del | -/A | | | intron-variant | SPAG16 | GRCh38.p7 | 2:213843701 | CTAAAAATACAAAAA[-/A]TTAGCTAGGTGTGGT | 79582 |
rs58117443 | in-del | -/T | | | intron-variant | SPAG16 | GRCh38.p7 | 2:213540052 | TTTTTTTTTTTTTTT[-/T]GAGACGGAGTCTCGC | 79582 |
rs58144064 | snp | A/G | 0.0471551 | 0.14613 | intron-variant | SPAG16 | GRCh38.p7 | 2:213495084 | TTCATGGTTCTCAGT[A/G]GGCATGCAGTGTTTT | 79582 |
rs58146727 | snp | A/T | | | intron-variant | SPAG16 | GRCh38.p7 | 2:213948189 | CGTTTCCTAAGAAAT[A/T]TTCCTGTCTAACCTC | 79582 |
rs58151001 | snp | A/G | 0.0414363 | 0.137845 | intron-variant | SPAG16 | GRCh38.p7 | 2:214026731 | ACCGGTTATTAATCT[A/G]TAAATTTACTATACA | 79582 |
rs58151966 | in-del | -/A | | | intron-variant | SPAG16 | GRCh38.p7 | 2:213489097 | AAAAAAAAAAAAAAA[-/A]GATTTTTCATGCCTA | 79582 |
rs58156064 | snp | C/T | 0.0402882 | 0.136092 | intron-variant | SPAG16 | GRCh38.p7 | 2:214044614 | GCTTTTAACTTCATA[C/T]TGAAAGAGGCACTGA | 79582 |
rs58158058 | snp | G/T | 0.00318978 | 0.0398085 | intron-variant | SPAG16 | GRCh38.p7 | 2:213927109 | TGTCCTCACAATGCA[G/T]GGAGCGAGTTAACTC | 79582 |
rs58161125 | in-del | -/T/TT | 0 | 0 | intron-variant | SPAG16 | GRCh38.p7 | 2:214013195 | TTTTTTTTTTTTTTT[-/T/TT]GGTTTAAGTAATTAA | 79582 |
rs58172382 | snp | C/G | 0.0126979 | 0.078662 | intron-variant | SPAG16 | GRCh38.p7 | 2:214116395 | CTAACCTCCATTTCA[C/G]AGCAGATTTTGAGGT | 79582 |
rs58185195 | snp | A/G | 0.399968 | 0.200024 | intron-variant | SPAG16 | GRCh38.p7 | 2:214227648 | AAATTCTAACTTCCA[A/G]TTGAGTAGCCAGGAA | 79582 |
rs58187547 | in-del | -/A | | | intron-variant | SPAG16 | GRCh38.p7 | 2:213704625 | ACAAATAAAAAAAAA[-/A]CCCTGAATAATTCAA | 79582 |
rs58203527 | snp | C/T | | | intron-variant | SPAG16 | GRCh38.p7 | 2:214326829 | GGGCGCCTGTGGTCC[C/T]AGCTACTTGGGAGGC | 79582 |
rs58206498 | snp | C/T | 0.0189856 | 0.0955633 | intron-variant | SPAG16 | GRCh38.p7 | 2:213942347 | AATGTGAGATGAGTA[C/T]TTCACACCTTCCTCC | 79582 |
rs58213648 | snp | A/C | 0.132066 | 0.220435 | intron-variant | SPAG16 | GRCh38.p7 | 2:213598402 | AGGTATCAAATTAAT[A/C]TTTATTATTAATGTG | 79582 |
rs58228952 | snp | A/G | 0.0614824 | 0.164198 | intron-variant | SPAG16 | GRCh38.p7 | 2:214118493 | TCACAGTTCCACATC[A/G]TTGGGGAGGCCTCAG | 79582 |
rs58245100 | snp | C/T | 0.155325 | 0.23138 | intron-variant | SPAG16 | GRCh38.p7 | 2:213473358 | TGTAGATGAGAACTG[C/T]GGTTCCTACTATTAG | 79582 |
rs58261582 | snp | A/G | | | intron-variant, utr-variant-3-prime | SPAG16 | GRCh38.p7 | 2:213399746 | CTTAAATGTATGGTA[A/G]AAGTCTTCTGTAAAA | 79582 |
rs58261587 | snp | G/T | 0.480144 | 0.097642 | intron-variant | SPAG16 | GRCh38.p7 | 2:213873172 | GGGAAAATTCATCAG[G/T]GAAGCCATCTGGTCT | 79582 |
rs58271674 | in-del | -/AACA | 0.460589 | 0.13473 | intron-variant | SPAG16 | GRCh38.p7 | 2:214379829 | CACTTGCAGAGGACT[-/AACA]AACACCAAAGAGAAT | 79582 |
rs58301419 | snp | C/T | 0.149665 | 0.228982 | intron-variant | SPAG16 | GRCh38.p7 | 2:214295337 | ATGATTTTAACAAAA[C/T]CCTAAACTTACTCCA | 79582 |
rs58314068 | snp | A/G | 0.0023933 | 0.0345097 | intron-variant | SPAG16 | GRCh38.p7 | 2:214260379 | TTTTTTCTTTTCATT[A/G]TAAGCCTCTACCACC | 79582 |
rs58314513 | snp | C/G | | | intron-variant | SPAG16 | GRCh38.p7 | 2:214076545 | TGTGTGTGTGTGTCT[C/G]TGTGTGTGTGTGTGT | 79582 |
rs58328649 | snp | C/T | 0.0275645 | 0.114116 | intron-variant | SPAG16 | GRCh38.p7 | 2:213359363 | CTGCCTTTTGTTCAG[C/T]TATGCCCTGCCCACA | 79582 |
rs58334762 | snp | C/G | 0.00755907 | 0.0610114 | intron-variant | SPAG16 | GRCh38.p7 | 2:214123683 | CAATCAGGTAGAAAA[C/G]AGCAATAAGGTGAGA | 79582 |
rs58340658 | snp | A/C | 0.33875 | 0.233717 | intron-variant | SPAG16 | GRCh38.p7 | 2:213832832 | TGTAAATCTTCGATT[A/C]AATAAATTTGCCATG | 79582 |
rs58408162 | snp | A/C | 0.000799041 | 0.019972 | intron-variant | SPAG16 | GRCh38.p7 | 2:213468487 | TATATATAGATATAT[A/C]TATGTATTTATATAT | 79582 |
rs58420627 | snp | C/T | | | intron-variant | SPAG16 | GRCh38.p7 | 2:213800327 | TTCCCTCCCTCCCTC[C/T]CTCCCTCTCTCCCTC | 79582 |
rs58426025 | in-del | -/T | 0.0433465 | 0.140692 | intron-variant | SPAG16 | GRCh38.p7 | 2:214147018 | AAAAAAAAAAAAAAA[-/T]TTTCATATTCATTTT | 79582 |
rs58446753 | snp | C/T | 0.039522 | 0.134904 | intron-variant | SPAG16, LOC101928084 | GRCh38.p7 | 2:214100290 | ATTGCTTTATAGCAG[C/T]GTGAAAATGGACTAA | 79582 |
rs58454395 | snp | A/G | 0.0444908 | 0.142359 | intron-variant | SPAG16 | GRCh38.p7 | 2:213619453 | ATATAAGGAATTCAA[A/G]CAAGTCAACAGCAAA | 79582 |
rs58463135 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | SPAG16 | GRCh38.p7 | 2:213963788 | TCCCTGTTTAACTTC[C/G]TTTTACATTTTTGGT | 79582 |
rs58517900 | in-del | -/TTTT | | | intron-variant | SPAG16 | GRCh38.p7 | 2:213469593 | TTTTTTTTTTTTTTT[-/TTTT]CCTGGTGGAATGACC | 79582 |
rs58519182 | snp | G/T | 0.282632 | 0.247861 | intron-variant | SPAG16 | GRCh38.p7 | 2:213997699 | AAAGAAGAAGAATTG[G/T]CTTGGGCCACACATA | 79582 |
rs58522972 | snp | C/T | 0.00755907 | 0.0610114 | intron-variant | SPAG16 | GRCh38.p7 | 2:214334038 | CCCATATAGGTAATC[C/T]CTCCCATATCCAATA | 79582 |
rs58525787 | snp | A/G | 0.0551013 | 0.156571 | intron-variant | SPAG16 | GRCh38.p7 | 2:214330281 | AAACTCTGTCTCAAA[A/G]AAAAAAAAAGGAAAA | 79582 |
rs58529682 | snp | A/C | 0.00517822 | 0.0506191 | intron-variant | SPAG16 | GRCh38.p7 | 2:213701863 | AGCTCAGGGATTGTA[A/C]ACACACCAAGCAGCA | 79582 |
rs58541568 | snp | A/C | 0.140242 | 0.224618 | intron-variant | SPAG16 | GRCh38.p7 | 2:213731628 | CTTCCTGATCCTGCC[A/C]CTCTTCCCACCCCCT | 79582 |
rs58554134 | snp | C/T | 0.155656 | 0.231515 | intron-variant | SPAG16 | GRCh38.p7 | 2:213403296 | TTTTTCTTGTAAATT[C/T]GTTTGAGTTCATTGT | 79582 |
rs58560991 | in-del | -/AAAAAAAAAAAAAAAAAAA | | | intron-variant | SPAG16 | GRCh38.p7 | 2:213728903 | AAAAAAAAAAAAAAA[-/AAAAAAAAAAAAAAAAAAA]GATGATGGAATGATG | 79582 |
rs58561514 | snp | A/G | 0.0209421 | 0.100162 | intron-variant | SPAG16 | GRCh38.p7 | 2:214009732 | AGATACACGTCAGGG[A/G]TTGGGTCAACAGCAC | 79582 |
rs58575813 | in-del | -/A | 0.170733 | 0.237101 | intron-variant | SPAG16 | GRCh38.p7 | 2:213563147 | TGGGGAGATAGCTTC[-/A]TTTTTTTACTTTCAA | 79582 |
rs58582439 | in-del | -/ACAC/ACACACACAT/ACAT/AT | 0 | 0 | intron-variant | SPAG16 | GRCh38.p7 | 2:214062020 | CACACACACACACAC[-/ACAC/ACACACACAT/ACAT/AT]GCAGTGTGTAGTATT | 79582 |
rs58597939 | in-del | -/AT | | | intron-variant | SPAG16 | GRCh38.p7 | 2:213860363 | TATATATATATATAT[-/AT]GTGTGTGTGTGTATA | 79582 |
rs58670800 | snp | G/T | 0.0221141 | 0.102801 | intron-variant | SPAG16 | GRCh38.p7 | 2:213961604 | TTTTTTTTTTTTGCT[G/T]GATTTTGATAAATGT | 79582 |
rs58677283 | snp | C/T | | | intron-variant | SPAG16 | GRCh38.p7 | 2:214380784 | GCAGTATGCTGAACA[C/T]GGACACCACTGTTTG | 79582 |
rs58694237 | snp | C/T | 0.155325 | 0.23138 | intron-variant | SPAG16 | GRCh38.p7 | 2:213539348 | TGAAGTCATAGCTTG[C/T]GGTGACAATGTTTAA | 79582 |
rs58696884 | in-del | -/AA | | | intron-variant | SPAG16 | GRCh38.p7 | 2:214191742 | AAAAAAAAAAAAAAA[-/AA]GGAAAAACCAGGATG | 79582 |
rs58745929 | in-del | -/TT | | | intron-variant | SPAG16 | GRCh38.p7 | 2:213831056 | TTTTTTTTTTTTTTT[-/TT]GAGATGGAGTCTTGC | 79582 |
rs58758480 | snp | A/G | 0.0256215 | 0.110247 | intron-variant | SPAG16 | GRCh38.p7 | 2:213514311 | GACTTTACTTCCTAA[A/G]TAAATGTTGCATTCT | 79582 |
rs58767621 | snp | C/T | 0.192715 | 0.243348 | intron-variant | SPAG16 | GRCh38.p7 | 2:213434388 | AAGACCTAGGAAAAA[C/T]ACTTCTGGACATTGA | 79582 |
rs58785566 | in-del | -/ATAAA | | | intron-variant | SPAG16 | GRCh38.p7 | 2:214031624 | ATAAAATAAAATAAA[-/ATAAA]CATGAAAAAAAAAAG | 79582 |
rs58828682 | snp | A/G | 0.192715 | 0.243348 | intron-variant | SPAG16 | GRCh38.p7 | 2:213444420 | ATTGACCTATAAATA[A/G]CTGTTTACTTAGTAC | 79582 |
rs58853937 | snp | A/T | 0.155656 | 0.231515 | intron-variant | SPAG16 | GRCh38.p7 | 2:213359364 | TGCCTTTTGTTCAGC[A/T]ATGCCCTGCCCACAG | 79582 |
rs58879510 | in-del | -/TCTA | | | intron-variant | SPAG16 | GRCh38.p7 | 2:213802444 | CTATCTATCTATCTA[-/TCTA]CACATACCTGGAGTT | 79582 |
rs58882072 | in-del | -/T | | | intron-variant | SPAG16 | GRCh38.p7 | 2:213739543 | TTCAGCATATCATTT[-/T]ATGGAAAAAATTGTT | 79582 |
rs58902400 | snp | A/C | 0.0387552 | 0.1337 | intron-variant | SPAG16 | GRCh38.p7 | 2:214051883 | GTTTTTATCCTACAT[A/C]ATTAGACGTACTTCA | 79582 |
rs58934784 | snp | A/G | 0.0287284 | 0.116357 | intron-variant | SPAG16 | GRCh38.p7 | 2:213674442 | ACAATGTGCAGGTTA[A/G]GTACATATGTATACC | 79582 |
rs58940778 | in-del | -/TATT/TATTTATT/TATTTATTTATT | 0 | 0 | intron-variant | SPAG16 | GRCh38.p7 | 2:213991893 | ATTTATTTATTTATT[-/TATT/TATTTATT/TATTTATTTATT]CTTGTTTCAGTGATT | 79582 |
rs58952646 | snp | A/G | 0.324855 | 0.23853 | intron-variant | SPAG16 | GRCh38.p7 | 2:213330543 | AATGCCTGTAGCCCC[A/G]TTGTATCTAGGAAGT | 79582 |
rs58953893 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | SPAG16 | GRCh38.p7 | 2:213468543 | TATATAGATATATAT[A/C]TATGTATTTATATAT | 79582 |
rs58963688 | in-del | -/TGTGTG | | | intron-variant | SPAG16 | GRCh38.p7 | 2:214284828 | GTGTGTGTGTGTGTG[-/TGTGTG]CATATGTATTTGTGT | 79582 |
rs58965394 | snp | A/G | 0.0275645 | 0.114116 | intron-variant | SPAG16 | GRCh38.p7 | 2:213321207 | TTGATTATACTAATA[A/G]CATTTAGTGATGTAT | 79582 |
rs58977269 | in-del | -/C | 0.211212 | 0.246973 | intron-variant | SPAG16 | GRCh38.p7 | 2:213658091 | CAACACAATTCTGCT[-/C]ATGAGGAGGTGTTTC | 79582 |
rs58982473 | snp | C/G | 0.00517822 | 0.0506191 | intron-variant | SPAG16 | GRCh38.p7 | 2:213364525 | TGAGCTCTGCCATCA[C/G]CATGGCTTTGGGTCT | 79582 |
rs58988529 | in-del | -/TT | | | intron-variant, upstream-variant-2KB | SPAG16 | GRCh38.p7 | 2:213299450 | TAATTTTTTTTTTTT[-/TT]GTATTTTTAGTAGAG | 79582 |
rs59004035 | snp | C/T | 0.140242 | 0.224618 | intron-variant | SPAG16 | GRCh38.p7 | 2:213731626 | TTCTTCCTGATCCTG[C/T]CCCTCTTCCCACCCC | 79582 |
rs59028917 | snp | A/G | 0.0252325 | 0.109451 | intron-variant | SPAG16 | GRCh38.p7 | 2:214251960 | GAATTGCATCAGACT[A/G]ATAATCTTAAATGAA | 79582 |
rs59035635 | snp | A/G | 0.0433465 | 0.140692 | intron-variant | SPAG16 | GRCh38.p7 | 2:213751156 | TTTTTTTTACTAAAG[A/G]AAATGTACTTATATG | 79582 |
rs59040837 | snp | A/G | 0.0513262 | 0.151752 | intron-variant | SPAG16 | GRCh38.p7 | 2:214283399 | CCATATTAGCACTGT[A/G]TAACACTTCACATAT | 79582 |
rs59050563 | snp | A/G | 0.00517822 | 0.0506191 | intron-variant | SPAG16 | GRCh38.p7 | 2:213711821 | CACCACGCCCGACCC[A/G]TTCTTACAATTTTCT | 79582 |
rs59063344 | snp | C/T | 0.5 | 0 | intron-variant | SPAG16 | GRCh38.p7 | 2:213567388 | CCCTCCCCCCTCCCC[C/T]GACCCCACCACAGTC | 79582 |
rs59065833 | snp | C/T | 0.265453 | 0.249522 | intron-variant | SPAG16 | GRCh38.p7 | 2:214054106 | CCTCCGCCTCCCGGG[C/T]TCAAGCAATTCTCCT | 79582 |
rs59078087 | snp | A/G | 0.029116 | 0.117091 | intron-variant | SPAG16 | GRCh38.p7 | 2:213314037 | ATCCTTATTCTTCTG[A/G]CACCATTTCTGTTTT | 79582 |
rs59081641 | snp | A/G | 0.00557542 | 0.0525036 | intron-variant | SPAG16 | GRCh38.p7 | 2:213565459 | TATCATTTGTTATAA[A/G]GCATGCGAGAGCTAC | 79582 |
rs59087440 | in-del | -/A | | | intron-variant | SPAG16 | GRCh38.p7 | 2:214260347 | GAGCTCCCAGAAAAA[-/A]GAATATCTAATTTTT | 79582 |
rs59092974 | snp | A/G | 0.254944 | 0.249951 | intron-variant | SPAG16 | GRCh38.p7 | 2:214267023 | TACCCAAAGCATTCT[A/G]TAGATTCAATGTAAT | 79582 |
rs59130850 | snp | C/T | 0.00597247 | 0.0543191 | intron-variant | SPAG16 | GRCh38.p7 | 2:213599977 | AGGCATGAGCCGCTG[C/T]GCCTGGCCTATTAGT | 79582 |
rs59138793 | snp | C/T | 0.154329 | 0.23097 | intron-variant | SPAG16 | GRCh38.p7 | 2:213327474 | CTTTGTTTCCTGGGA[C/T]GAGCACAAATAGGCT | 79582 |
rs59163769 | snp | C/G | 0.0252325 | 0.109451 | intron-variant | SPAG16 | GRCh38.p7 | 2:213446164 | TAAGAAACAGTGCAA[C/G]AACTCTGGCAACTCT | 79582 |
rs59212531 | snp | C/T | | | intron-variant | SPAG16 | GRCh38.p7 | 2:214167979 | TTTCTGTTTTCTTTT[C/T]TTTTTTCTTTTTCTC | 79582 |
rs59212620 | snp | A/G | 0.0197687 | 0.0974348 | intron-variant | SPAG16 | GRCh38.p7 | 2:214021392 | CCTCACAATCATGGC[A/G]GAAGGCAAAAAGTAC | 79582 |
rs59238394 | snp | C/T | 0.0486741 | 0.148216 | intron-variant | SPAG16 | GRCh38.p7 | 2:214337811 | CTCAGGGCTTCCTTT[C/T]TGTCTTTTATCTTCT | 79582 |
rs59239191 | snp | C/T | 0.479583 | 0.0989539 | intron-variant | SPAG16 | GRCh38.p7 | 2:214161611 | GTCTTTTTTGGGAAG[C/T]GTCTGTTGGACAGTG | 79582 |
rs59253430 | snp | C/T | 0.155656 | 0.231515 | intron-variant, utr-variant-3-prime | SPAG16 | GRCh38.p7 | 2:213398245 | TGCTTTTGTCTTTAC[C/T]TTTCTTCAGTCTCTT | 79582 |
rs59264716 | snp | A/G | | | intron-variant | SPAG16 | GRCh38.p7 | 2:213654735 | AAAAAAAATAAAGAA[A/G]AAGTTTCAATGTAAA | 79582 |
rs59323884 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | SPAG16 | GRCh38.p7 | 2:213751664 | TTGTGTCTCCCCTGA[C/T]GCACACGCACGCCTG | 79582 |
rs59353089 | in-del | -/T | | | intron-variant | SPAG16 | GRCh38.p7 | 2:213950722 | TTTTTTTTTTTTTTT[-/T]TCCCTCAAGACGGTC | 79582 |
rs59354451 | snp | C/T | 0.245916 | 0.249967 | intron-variant | SPAG16 | GRCh38.p7 | 2:214035817 | ATGGTCAGAGCTGTG[C/T]CCAGGGAGCACGAAG | 79582 |
rs59383398 | snp | A/G | 0.0256215 | 0.110247 | intron-variant | SPAG16 | GRCh38.p7 | 2:213509340 | GATGACCTCATAAGC[A/G]TGTTTCATAAATGTC | 79582 |
rs59407158 | in-del | -/CACACA | | | intron-variant | SPAG16 | GRCh38.p7 | 2:213310369 | ACACACACACACACA[-/CACACA]AATCAGAATAGCAGT | 79582 |
rs59445663 | snp | A/T | | | intron-variant | SPAG16 | GRCh38.p7 | 2:214023864 | TCAGCCTTTGAAAAA[A/T]TATCATATTCAATAA | 79582 |
rs59458890 | snp | A/G | 0.0189856 | 0.0955633 | intron-variant | SPAG16 | GRCh38.p7 | 2:214216110 | TATTTTAAATTGGTA[A/G]AATAATGACAGAAGG | 79582 |
rs59465924 | snp | C/G | | | intron-variant | SPAG16 | GRCh38.p7 | 2:214036683 | TTTATAATATATTCA[C/G]TTACATGTTTAATCT | 79582 |
rs59467918 | snp | A/C | | | intron-variant | SPAG16 | GRCh38.p7 | 2:213860429 | TATATGTGTGTATAT[A/C]TATATATTTATAGAT | 79582 |
rs59504197 | in-del | -/AA | | | intron-variant | SPAG16 | GRCh38.p7 | 2:214197301 | AATAAATAAGAAAAA[-/AA]TGCTTACTGAGTTTA | 79582 |
rs59507502 | in-del | -/A | | | intron-variant | SPAG16 | GRCh38.p7 | 2:213648321 | CTATTCAAAAAAAAA[-/A]TGTAGCACAGATGTA | 79582 |
rs59514054 | snp | C/T | 0.107341 | 0.205301 | intron-variant | SPAG16 | GRCh38.p7 | 2:214173568 | TAACAGGCTCTGAAA[C/T]TGTGGCAATAATCAA | 79582 |
rs59516920 | in-del | -/TA/TACCACAGTATAAG | | | intron-variant | SPAG16 | GRCh38.p7 | 2:213381084 | AATCCACTGGGCTTA[-/TA/TACCACAGTATAAG]CCGTAAAATAGACTT | 79582 |
rs59519539 | in-del | -/A/AA | 0 | 0 | intron-variant | SPAG16 | GRCh38.p7 | 2:213867950 | AAAAAAAAAAAAAAA[-/A/AA]GATAGCTCAAACGTT | 79582 |
rs59544374 | snp | G/T | 0.251014 | 0.249998 | intron-variant | SPAG16 | GRCh38.p7 | 2:214397974 | CCTGGCCTGGTGAAT[G/T]AGTAAATCACACCCT | 79582 |
rs59548846 | snp | G/T | 0.0444908 | 0.142359 | intron-variant | SPAG16 | GRCh38.p7 | 2:213576017 | AGATTGTCCTGAATG[G/T]TATTGCCTAGGTTGT | 79582 |
rs59548915 | in-del | -/T | | | intron-variant | SPAG16 | GRCh38.p7 | 2:213777256 | TTTTTTTTTTTTTTT[-/T]GAGACGTAGTCTCAT | 79582 |
rs59571736 | snp | C/T | 0.288646 | 0.246995 | intron-variant | SPAG16 | GRCh38.p7 | 2:214033064 | TCAGAAAATGTTTAT[C/T]GTTTTCCTGCAATTA | 79582 |
rs59575951 | snp | A/G | | | intron-variant, utr-variant-3-prime | SPAG16 | GRCh38.p7 | 2:213399079 | CTGTGAAAAATAATA[A/G]TTGTGACTTTCATTT | 79582 |
rs59581905 | in-del | -/TTATATATATATATATATATATATATATATAT | | | intron-variant | SPAG16 | GRCh38.p7 | 2:213643348 | TATTGGATCTTAATT[lengthTooLong]ATATATATATATATA | 79582 |
rs59588246 | snp | A/G | 0.0360663 | 0.129354 | intron-variant | SPAG16 | GRCh38.p7 | 2:214210291 | TACATGGATTTTTTC[A/G]ATAAGTTTACTGAAA | 79582 |
rs59590839 | snp | C/T | 0.192715 | 0.243348 | intron-variant | SPAG16 | GRCh38.p7 | 2:213474354 | GGTCTCTCAGGGAAA[C/T]CTTGGCAGATTTGAG | 79582 |
rs59608529 | snp | A/G | 0.376195 | 0.215812 | intron-variant | SPAG16, LOC101928084 | GRCh38.p7 | 2:214095538 | AAATATTTGTTGAGC[A/G]AAGGAAAGCCACCTA | 79582 |
rs59642738 | snp | C/T | | | intron-variant | SPAG16 | GRCh38.p7 | 2:214167994 | CTTTTTTCTTTTTCT[C/T]TTTTTTTTTTTTTTG | 79582 |
rs59644776 | in-del | -/TATA | | | intron-variant | SPAG16 | GRCh38.p7 | 2:214250753 | ATATATATATATATA[-/TATA]TAGAGAGAGAGAGAG | 79582 |
rs59646839 | snp | A/G | 0.494896 | 0.0502606 | intron-variant | SPAG16 | GRCh38.p7 | 2:214067920 | ATTAGAGACATAAAA[A/G]CTATAAAAAATAATG | 79582 |
rs59655277 | snp | A/G | 0.0209421 | 0.100162 | intron-variant | SPAG16 | GRCh38.p7 | 2:213830866 | ATGCATTTGTCTTTC[A/G]GGACATTTGTATTAT | 79582 |
rs59673804 | in-del | -/T | 0.354881 | 0.226936 | intron-variant | SPAG16 | GRCh38.p7 | 2:213363053 | ATATTCTGGATGCGA[-/T]TTTGAAACATAAAAA | 79582 |
rs59704390 | snp | C/G | 0.030665 | 0.119967 | intron-variant | SPAG16 | GRCh38.p7 | 2:213873590 | GTTTGGTTATGATTT[C/G]AGATATTTGTTCTTT | 79582 |
rs59711456 | snp | G/T | 0.16846 | 0.236329 | intron-variant | SPAG16 | GRCh38.p7 | 2:213468562 | GTATTTATATATAGA[G/T]ATATATATATCTATG | 79582 |
rs59713406 | snp | G/T | 0.182933 | 0.240836 | intron-variant | SPAG16 | GRCh38.p7 | 2:213428697 | AGTTATACAGCTCAG[G/T]GTGACTTTGCAGACT | 79582 |
rs59725146 | snp | C/G | 0.145305 | 0.227022 | intron-variant | SPAG16 | GRCh38.p7 | 2:214366035 | CCAGGCCAGAGTGCA[C/G]TGGTATGATCTCGGC | 79582 |
rs59742033 | snp | A/G | 0.0115144 | 0.0749975 | intron-variant | SPAG16 | GRCh38.p7 | 2:214129242 | TGGACCCTCAGCTTC[A/G]TTTCTTTAATTAGGG | 79582 |
rs59750241 | snp | C/T | 0.179425 | 0.239831 | intron-variant | SPAG16 | GRCh38.p7 | 2:213539169 | AAATGCTCTTAAATA[C/T]TATAAATTCCGTAGA | 79582 |
rs59768181 | snp | A/G | 0.0217236 | 0.101931 | intron-variant | SPAG16 | GRCh38.p7 | 2:213992453 | AAAACACATTTTTTG[A/G]TATATATTACTGACT | 79582 |
rs59798233 | snp | A/G | 0.233818 | 0.249476 | intron-variant | SPAG16 | GRCh38.p7 | 2:213654674 | TTGAGCCGAGATTGC[A/G]CCACTGCACTCCACC | 79582 |
rs59805227 | in-del | -/A | 0.39214 | 0.205661 | intron-variant | SPAG16 | GRCh38.p7 | 2:214061704 | GGCCTATGTTTGACC[-/A]AAAACTGGATACTAT | 79582 |
rs59810311 | in-del | -/GT | | | intron-variant | SPAG16 | GRCh38.p7 | 2:214076565 | TGTGTGTGTGTGTGT[-/GT]TTGTGTTGAGAGAGT | 79582 |
rs59813410 | in-del | -/AAAAAA | | | intron-variant | SPAG16 | GRCh38.p7 | 2:213588838 | AAAAAAAAAAAAAAA[-/AAAAAA]GACTCCCTATCCATT | 79582 |
rs59816395 | snp | A/G | | | intron-variant | SPAG16 | GRCh38.p7 | 2:213914495 | TCTATCATATATATA[A/G]TATACGCTTTCTAAC | 79582 |
rs59820424 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | SPAG16 | GRCh38.p7 | 2:213767248 | TATCCAAGTATTAAT[C/T]TTCTATCATATAATT | 79582 |
rs59832932 | in-del | -/ATAT | | | intron-variant | SPAG16, LOC101928084 | GRCh38.p7 | 2:214092506 | TATATATATATATAT[-/ATAT]GGCCCTTTATCTGTT | 79582 |
rs59837523 | in-del | -/TGTG | | | intron-variant | SPAG16 | GRCh38.p7 | 2:214284798 | AATAATATTTTACTC[-/TGTG]TGTGTGTGTGTGTGT | 79582 |
rs59845389 | in-del | -/GT | | | intron-variant | SPAG16 | GRCh38.p7 | 2:213302660 | TGTGTGTGTGTGTGT[-/GT]TGTGTATAAATGCAG | 79582 |
rs59846941 | in-del | -/GTGTGTGTGTGTGTGTGT | 0 | 0 | intron-variant | SPAG16 | GRCh38.p7 | 2:214352575 | TGTGTGTGTGTGTGT[-/GTGTGTGTGTGTGTGTGT]ATGTGTGACTGAGTA | 79582 |
rs59852734 | snp | G/T | 0.00755907 | 0.0610114 | intron-variant | SPAG16 | GRCh38.p7 | 2:214136577 | TGTTAATGCCTAACA[G/T]ACTGATGATGGCATA | 79582 |
rs59862062 | snp | A/G | 0.155325 | 0.23138 | intron-variant | SPAG16 | GRCh38.p7 | 2:213457820 | CATTCAATGTAATTA[A/G]ATGACATATTGGGAT | 79582 |
rs59906563 | snp | A/G | 0.266819 | 0.249434 | intron-variant | SPAG16 | GRCh38.p7 | 2:213897375 | GAGATACTAGTCTTT[A/G]TGCTGCTTATTGTGC | 79582 |
rs59910884 | in-del | -/T | | | intron-variant | SPAG16 | GRCh38.p7 | 2:214143255 | TTTTTTTTTTTTTTT[-/T]GGTTTCCTGATATAT | 79582 |
rs59918252 | snp | G/T | | | intron-variant | SPAG16 | GRCh38.p7 | 2:214394999 | TTCTTTCACTTAGTA[G/T]TATGCATTTATGTTT | 79582 |
rs59920491 | in-del | -/A | 0.373799 | 0.217195 | intron-variant | SPAG16 | GRCh38.p7 | 2:213732340 | GATTGCCCCCCCCGC[-/A]AAAAAAAATGCCCAG | 79582 |
rs59926735 | snp | C/G | 0.0444908 | 0.142359 | intron-variant | SPAG16 | GRCh38.p7 | 2:213667088 | TCTCCAAGTCATATT[C/G]TTCTTTTTGAGCATC | 79582 |
rs59951859 | snp | A/G | 0.121369 | 0.214369 | intron-variant | SPAG16 | GRCh38.p7 | 2:213350999 | AAAAAACAAATAGCC[A/G]GGTGTGGTGGCACAG | 79582 |
rs59978989 | snp | C/G | 0.00119737 | 0.0244387 | intron-variant | SPAG16 | GRCh38.p7 | 2:214224856 | AGTAGAACTGTCCCT[C/G]ACCTCATAGGGCTTA | 79582 |
rs59985368 | snp | C/T | 0.0418186 | 0.138422 | intron-variant | SPAG16, LOC101928084 | GRCh38.p7 | 2:214091304 | ATAAAACTACTAATA[C/T]TACTCCATTTTGCAG | 79582 |
rs59993057 | in-del | -/TTTTT | | | intron-variant | SPAG16 | GRCh38.p7 | 2:213929027 | TTTTTTTTTTTTTTT[-/TTTTT]AAGACTGAGTCTTAC | 79582 |
rs60003843 | in-del | -/G | | | intron-variant | SPAG16 | GRCh38.p7 | 2:214144435 | GGTTCTATAATTGTT[-/G]TTTTAATGGCTTTAT | 79582 |
rs60010934 | snp | A/T | 0.0023933 | 0.0345097 | intron-variant | SPAG16 | GRCh38.p7 | 2:213831039 | TGAAACATGACTTTT[A/T]TTTTTTTTTTTTTTT | 79582 |
rs60013080 | snp | A/T | 0.00755907 | 0.0610114 | intron-variant | SPAG16, LOC101928084 | GRCh38.p7 | 2:214102431 | TGACACAGTGGAAGC[A/T]CAGTTCTCATTCATG | 79582 |
rs60021439 | snp | G/T | | | intron-variant | SPAG16 | GRCh38.p7 | 2:213468480 | ATGTATTTATATATA[G/T]ATATATATATGTATT | 79582 |
rs60024655 | in-del | -/TGATGATGATGATGATGA | | | intron-variant | SPAG16 | GRCh38.p7 | 2:213860020 | TGATGATGATGATGA[-/TGATGATGATGATGATGA]CAGTTATGTCTCATT | 79582 |
rs60032489 | in-del | -/A | | | intron-variant | SPAG16 | GRCh38.p7 | 2:213287702 | CTGAGAGTTCAGTAA[-/A]GTTTAAGCCAGTTCT | 79582 |
rs60038353 | snp | A/C | 0.0652144 | 0.168387 | intron-variant | SPAG16 | GRCh38.p7 | 2:213597025 | GTGAAAAAGACATTA[A/C]AAGACACCAAAGACT | 79582 |
rs60054966 | snp | C/T | | | intron-variant | SPAG16 | GRCh38.p7 | 2:213292520 | ATACAAAAAATTAGC[C/T]GGGCGTAGTGGCGGG | 79582 |
rs60060007 | snp | C/T | 0.128976 | 0.218754 | intron-variant | SPAG16 | GRCh38.p7 | 2:213515341 | TCACATTGTTAGATG[C/T]GAGGAAGTCACATTG | 79582 |
rs60117167 | snp | A/G | 0.155656 | 0.231515 | intron-variant | SPAG16 | GRCh38.p7 | 2:213406836 | GGTCTCTCCTCTCTC[A/G]TGAGGAGGCGCACCC | 79582 |
rs60128650 | in-del | -/T | 0.164546 | 0.234942 | intron-variant | SPAG16 | GRCh38.p7 | 2:213544108 | GTACTGGCTTTCTGA[-/T]TTTTTTTTTATCACT | 79582 |
rs60144296 | snp | A/G | 0.155656 | 0.231515 | intron-variant | SPAG16 | GRCh38.p7 | 2:213327799 | CACTCCTTATTGTAG[A/G]AAGATAAATTTAGCG | 79582 |
rs60156223 | snp | A/G | 0.0505692 | 0.150756 | intron-variant | SPAG16 | GRCh38.p7 | 2:213655913 | TATTAAAAAATACAC[A/G]AACAATTGTTTGGAG | 79582 |
rs60171215 | in-del | -/TTTTC | 0.493154 | 0.0581045 | intron-variant | SPAG16 | GRCh38.p7 | 2:213968097 | TTTTCTTTTCTTTTC[-/TTTTC]CTCCCTCCCTCTCTC | 79582 |
rs60188291 | snp | G/T | | | intron-variant | SPAG16 | GRCh38.p7 | 2:213468534 | ATGTATTTATATATA[G/T]ATATATATATATGTA | 79582 |
rs60190376 | snp | A/G | 0.118933 | 0.212888 | intron-variant | SPAG16 | GRCh38.p7 | 2:214362882 | ATAATAACACAAGAT[A/G]GGAACCATTCACTCA | 79582 |
rs60197199 | snp | A/T | 0.00597247 | 0.0543191 | intron-variant | SPAG16 | GRCh38.p7 | 2:213648261 | CTAACTTTGGGAATG[A/T]CTACAAAGGGTGTTA | 79582 |
rs60198877 | in-del | -/T | | | intron-variant, utr-variant-5-prime | SPAG16 | GRCh38.p7 | 2:213296327 | GATTCTTTTGATTTT[-/T]CCTGTTAATCGTCCT | 79582 |
rs60205580 | snp | C/T | 0.287085 | 0.247234 | intron-variant | SPAG16 | GRCh38.p7 | 2:214029712 | TAACTCTATGCCTTT[C/T]CCTACTAATTCAGCC | 79582 |
rs60219499 | snp | C/G | | | intron-variant | SPAG16 | GRCh38.p7 | 2:213468517 | TAGATATATATATAT[C/G]TATGTATTTATATAT | 79582 |
rs60221504 | in-del | -/A | 0.185155 | 0.241444 | intron-variant | SPAG16 | GRCh38.p7 | 2:213431498 | TAAATCAGAAACTGT[-/A]AAAAAAAAGAAAAAG | 79582 |
rs60247479 | in-del | -/ACACAC | | | intron-variant | SPAG16 | GRCh38.p7 | 2:214056309 | CACACACACACACAC[-/ACACAC]GCATAGAGAGAGAGA | 79582 |
rs60254790 | snp | A/G | 0.040671 | 0.13668 | intron-variant | SPAG16, LOC101928084 | GRCh38.p7 | 2:214095393 | AAATTAATCACACGT[A/G]TCTATCATACACGGT | 79582 |
rs60271146 | snp | A/G | | | intron-variant | SPAG16 | GRCh38.p7 | 2:213420997 | GGCCAGGGCTGCAGG[A/G]GAGTCACAGCTGGGG | 79582 |
rs60275602 | in-del | -/T | 0 | 0 | intron-variant | SPAG16 | GRCh38.p7 | 2:213469596 | TTTTTTTTTTTTTTT[-/T]CCTGGTGGAATGACC | 79582 |
rs60281335 | snp | C/T | 0.170733 | 0.237101 | intron-variant | SPAG16 | GRCh38.p7 | 2:213514756 | AAATTATAATTTTAA[C/T]ACTGAAATTATTTGC | 79582 |
rs60283448 | snp | C/T | 0.37138 | 0.218556 | intron-variant | SPAG16 | GRCh38.p7 | 2:214298131 | ACACACACACACACA[C/T]ACATACACATACACA | 79582 |
rs60295641 | in-del | -/AT | 0 | 0 | intron-variant | SPAG16 | GRCh38.p7 | 2:213643081 | TATATATATATATAT[-/AT]CCATTAGTTTTGTCC | 79582 |
rs60317879 | snp | C/T | 0.0437281 | 0.141251 | intron-variant | SPAG16 | GRCh38.p7 | 2:213748718 | ATAATTACTAATACC[C/T]AGATGATCAATTTAA | 79582 |
rs60318469 | snp | C/T | 0.00279162 | 0.0372561 | intron-variant | SPAG16 | GRCh38.p7 | 2:213831419 | AATTCAGGTGTTTTT[C/T]TTTTTTTAACCTCAT | 79582 |
rs60352388 | snp | C/T | 0.0205511 | 0.0992634 | intron-variant | SPAG16 | GRCh38.p7 | 2:214272714 | TAGTTGGGTTGGTTC[C/T]AAGTCTTTGCTATCG | 79582 |
rs60357532 | in-del | -/TT | | | intron-variant | SPAG16 | GRCh38.p7 | 2:214309572 | GGATAGGTTTTTTTT[-/TT]CTTTTATCCTATTTG | 79582 |
rs60358609 | snp | C/G | 0.0429648 | 0.14013 | intron-variant | SPAG16 | GRCh38.p7 | 2:214363011 | TTTAATACCAGGACT[C/G]TTAATACCATTTTCT | 79582 |
rs60365919 | in-del | -/TTATATATATATAT | | | intron-variant | SPAG16 | GRCh38.p7 | 2:213643348 | TATTGGATCTTAATT[-/TTATATATATATAT]ATATATATATATATA | 79582 |
rs60380038 | snp | A/T | 0.17138 | 0.237316 | intron-variant | SPAG16 | GRCh38.p7 | 2:213576144 | TCTTCTGCATATGGC[A/T]AGCCAGATATTCCAG | 79582 |
rs60381472 | in-del | -/TATATA | | | intron-variant | SPAG16 | GRCh38.p7 | 2:214250751 | ATATATATATATATA[-/TATATA]TAGAGAGAGAGAGAG | 79582 |
rs60401743 | snp | C/T | 0.0414363 | 0.137845 | intron-variant | SPAG16 | GRCh38.p7 | 2:213735500 | GCTTCTTCCACCATG[C/T]GATTCATCAACTGAA | 79582 |
rs60405512 | in-del | -/TATACACA | | | intron-variant | SPAG16 | GRCh38.p7 | 2:213976136 | ATATATATATATATA[-/TATACACA]CACACACACACACAC | 79582 |
rs60427789 | snp | C/G | 0.029116 | 0.117091 | intron-variant | SPAG16 | GRCh38.p7 | 2:213656293 | CTCCTGCCTCAGCCT[C/G]CGGAGTAGCTGGGAC | 79582 |
rs60435896 | snp | A/G | 0.155987 | 0.23165 | intron-variant | SPAG16 | GRCh38.p7 | 2:213406660 | AGCGGTGTGCTCACC[A/G]TTGTTCCATCTGTAT | 79582 |
rs60445909 | snp | C/T | 0.0622301 | 0.165053 | intron-variant | SPAG16 | GRCh38.p7 | 2:214112373 | GATATCCTTGTTAAC[C/T]TTCTGTCTCATTGAT | 79582 |
rs60465888 | snp | A/G | 0.0513262 | 0.151752 | intron-variant | SPAG16 | GRCh38.p7 | 2:213707280 | TTCATCCTGCCCCTC[A/G]TGAATCATGTTCAAG | 79582 |
rs60494365 | snp | A/G | | | intron-variant | SPAG16 | GRCh38.p7 | 2:213997123 | TGACTTAGGAAGTTC[A/G]AGCTAGGTTTAATTT | 79582 |
rs60506175 | in-del | -/CTCT | | | intron-variant | SPAG16 | GRCh38.p7 | 2:213949203 | TGAGGTAGAGTCTCT[-/CTCT]GTCACCAGGCTGGAG | 79582 |
rs60552203 | in-del | -/TTATATATATATATATATATATATATATATATATAT | | | intron-variant | SPAG16 | GRCh38.p7 | 2:213643348 | TATTGGATCTTAATT[lengthTooLong]ATATATATATATATA | 79582 |
rs60566840 | snp | A/G | 0.313082 | 0.241911 | intron-variant | SPAG16 | GRCh38.p7 | 2:213390137 | AAACCAATAACAGAA[A/G]GACAAATACTATATG | 79582 |
rs60590594 | snp | C/T | 0.5 | 0 | intron-variant | SPAG16 | GRCh38.p7 | 2:214326609 | AAGTTTGCTCAGCCC[C/T]AGCATGATAGAGGTA | 79582 |
rs60591047 | in-del | -/A | 0.046775 | 0.145601 | intron-variant | SPAG16 | GRCh38.p7 | 2:213423737 | TCTCATTTTTTAGGT[-/A]AAAAATACTAAAGCC | 79582 |
rs60652223 | snp | C/T | 0.0189856 | 0.0955633 | intron-variant | SPAG16 | GRCh38.p7 | 2:214222208 | TGCAACCCCCGCCTC[C/T]TGGGTTCAAGCGAGT | 79582 |
rs60663474 | in-del | -/GAGA | | | intron-variant | SPAG16 | GRCh38.p7 | 2:214269962 | AATTAATGCCAGAGA[-/GAGA]CAGAACTTGGATTAA | 79582 |
rs60672157 | in-del | -/AGAA | | | intron-variant | SPAG16 | GRCh38.p7 | 2:214329298 | CCAAACCTTAAAGAA[-/AGAA]TTCTTATTATGTTTT | 79582 |
rs60707204 | in-del | -/A | 0 | 0 | intron-variant | SPAG16 | GRCh38.p7 | 2:213406957 | AAAAAAAAAAAAAAA[-/A]GGGAAAAGAAACTGG | 79582 |
rs60735161 | snp | C/T | 0.0225045 | 0.103662 | intron-variant | SPAG16 | GRCh38.p7 | 2:213937656 | ATTTTTTTATTTTCC[C/T]TTCCCCCCCAAAAGT | 79582 |
rs60749528 | snp | A/G | 0.00557542 | 0.0525036 | intron-variant | SPAG16 | GRCh38.p7 | 2:213589410 | TTCAAATCAATTAGA[A/G]TATTTCAATAAACAA | 79582 |
rs60768952 | in-del | -/T | | | intron-variant | SPAG16 | GRCh38.p7 | 2:213733500 | AGAGTTATGAAGGGA[-/T]TTTTTTTTTTTTTTT | 79582 |
rs60774375 | snp | C/T | | | intron-variant | SPAG16 | GRCh38.p7 | 2:213896617 | ACACACACACACACA[C/T]AGATATGTACATATA | 79582 |
rs60777017 | snp | C/T | | | intron-variant | SPAG16 | GRCh38.p7 | 2:213886654 | AGTGCCAACAAACTT[C/T]TGAGGGGAAACAAGC | 79582 |
rs60839638 | in-del | -/GT | | | intron-variant | SPAG16 | GRCh38.p7 | 2:214193423 | TGTGTGTGTGTGTGT[-/GT]ATGAGAGAGAGAGAG | 79582 |
rs60852712 | in-del | -/A | | | intron-variant | SPAG16 | GRCh38.p7 | 2:213654727 | ATCTCAAAAAAAAAA[-/A]TAAAGAAGAAGTTTC | 79582 |
rs60878472 | in-del | -/G | 0.02016 | 0.0983543 | intron-variant | SPAG16 | GRCh38.p7 | 2:213705792 | GGTGGAGGGTTTGTT[-/G]TTGTTGTTGTTGTTG | 79582 |
rs60882756 | snp | G/T | | | intron-variant | SPAG16 | GRCh38.p7 | 2:214268236 | TTGCAAATTAATACA[G/T]CCATTTTGGAAAACA | 79582 |
rs60901776 | snp | A/G | 0.0498117 | 0.149749 | intron-variant | SPAG16 | GRCh38.p7 | 2:213385760 | AGATTTAAGATTTTT[A/G]AGTACGTTGTCTCAG | 79582 |
rs60931346 | snp | C/G | 0.0279526 | 0.114869 | intron-variant | SPAG16 | GRCh38.p7 | 2:213368426 | ATCTCAAAATAATAA[C/G]AGCTATTTATGACAA | 79582 |
rs60939945 | snp | C/T | 0.00557542 | 0.0525036 | intron-variant | SPAG16 | GRCh38.p7 | 2:213608771 | GCTCACTGCCAACTC[C/T]GCCTCCTGCGTTCAC | 79582 |
rs60944676 | snp | C/T | 0.0218376 | 0.102186 | intron-variant | SPAG16 | GRCh38.p7 | 2:214163203 | CTTGATCTTTTTTCC[C/T]TTTGTCAAATATAAC | 79582 |
rs60963174 | in-del | -/AT | 0 | 0 | intron-variant | SPAG16 | GRCh38.p7 | 2:213976347 | CACATATATATATAT[-/AT]CAGATGATATATATA | 79582 |
rs60966185 | in-del | -/A | 0 | 0 | intron-variant | SPAG16 | GRCh38.p7 | 2:213556304 | TCAAAAAAAAAAAAA[-/A]CCAAAAAAAAAAAAA | 79582 |
rs60972251 | snp | A/G | | | intron-variant | SPAG16 | GRCh38.p7 | 2:213565582 | TTTTAATTCCAAAGC[A/G]TCTATTGAAAGGCTG | 79582 |
rs60978774 | snp | A/G | 0.046775 | 0.145601 | intron-variant | SPAG16 | GRCh38.p7 | 2:213322367 | AAAAACAAAAAACTC[A/G]TTTGGGTGATTGATT | 79582 |
rs60981785 | in-del | -/C | | | intron-variant | SPAG16 | GRCh38.p7 | 2:213322357 | AAAAAAAAAAAAAAA[-/C]AAAAAACTCGTTTGG | 79582 |
rs60986001 | in-del | -/G | | | intron-variant | SPAG16 | GRCh38.p7 | 2:213724802 | AAAAAAAAAAAAAAA[-/G]AAAAAAGGATAAACT | 79582 |
rs60989008 | in-del | -/AAAGGAT | | | intron-variant | SPAG16 | GRCh38.p7 | 2:214229196 | TAGAAGAAAGTATAT[-/AAAGGAT]GTAAAGGTCACTACG | 79582 |
rs61009839 | snp | A/G | | | intron-variant | SPAG16 | GRCh38.p7 | 2:213475324 | TCTATAGGGGCATGA[A/G]CAAGGCTTGGACCTG | 79582 |
rs61032382 | snp | C/G | 0.427423 | 0.176128 | intron-variant | SPAG16 | GRCh38.p7 | 2:213975096 | TAAATATAATTAATA[C/G]TAGCAAGATATTCAT | 79582 |
rs61037020 | snp | A/C | | | intron-variant | SPAG16 | GRCh38.p7 | 2:214280116 | GGAAAGTATAAATAG[A/C]AGGACAGAAATGATC | 79582 |
rs61040316 | in-del | -/A | | | intron-variant | SPAG16 | GRCh38.p7 | 2:213508594 | AAAAGAAAAAAAAAA[-/A]TGATGAGTTCATGTC | 79582 |
rs61051829 | in-del | -/AT | | | intron-variant | SPAG16 | GRCh38.p7 | 2:213468545 | TATAGATATATATAT[-/AT]GTATTTATATATAGA | 79582 |
rs61054165 | snp | A/G/T | 0.0189856 | 0.0955633 | intron-variant | SPAG16 | GRCh38.p7 | 2:214109880 | AGTCCATTAAGTGGC[A/G/T]TATAGCTTCACATGC | 79582 |
rs61056930 | in-del | -/T | 0 | 0 | intron-variant, utr-variant-3-prime | SPAG16 | GRCh38.p7 | 2:213398181 | CTGTTTTTTTTTTTT[-/T]GCCACCGTCTGTAGT | 79582 |
rs61063237 | snp | A/G | 0.194902 | 0.243853 | intron-variant | SPAG16 | GRCh38.p7 | 2:213573013 | TTTCCAGGTGCGTCC[A/G]TCACCCCTTTCTTTG | 79582 |
rs61071600 | in-del | -/AACT | | | intron-variant | SPAG16 | GRCh38.p7 | 2:214311581 | GTCAGGACTCTAACT[-/AACT]TCCTCTGGGGTCAAT | 79582 |
rs61092508 | snp | C/T | 0.00279162 | 0.0372561 | intron-variant | SPAG16 | GRCh38.p7 | 2:213816783 | TTCATGGATTAAAAA[C/T]ATGCATAATTTCATA | 79582 |
rs61098635 | in-del | -/A | 0.480144 | 0.097642 | intron-variant | SPAG16 | GRCh38.p7 | 2:213873170 | TTGGGAAAATTCATC[-/A]GTGAAGCCATCTGGT | 79582 |
rs61122230 | snp | G/T | 0.247905 | 0.249991 | intron-variant | SPAG16 | GRCh38.p7 | 2:214405811 | TCAAAAATAAATAAA[G/T]AAAGAAAATCCCAAT | 79582 |
rs61132261 | snp | G/T | 0.0329836 | 0.124112 | intron-variant | SPAG16 | GRCh38.p7 | 2:213686711 | TTTTTTTTTGAGACA[G/T]AGTCTCGCTCTGTCA | 79582 |
rs61153369 | snp | G/T | 0.0988009 | 0.199095 | intron-variant | SPAG16 | GRCh38.p7 | 2:214195909 | ACTGCTATCTTCCAG[G/T]ATCACAGAGAGAGTG | 79582 |
rs61158521 | in-del | -/T | | | intron-variant | SPAG16 | GRCh38.p7 | 2:213975354 | CACATTCTCAATTTT[-/T]CACTAACACAAAACT | 79582 |
rs61162445 | snp | A/T | 0.394171 | 0.204242 | intron-variant | SPAG16 | GRCh38.p7 | 2:214307698 | TTCCATGTAATTGTA[A/T]CTTTTTGAGCAAATT | 79582 |
rs61178108 | snp | C/T | 0.00557542 | 0.0525036 | intron-variant | SPAG16 | GRCh38.p7 | 2:213514111 | AGAGTTTTGAAAAGA[C/T]GGAGTGCCCAAACAG | 79582 |
rs61181248 | snp | A/G | 0.0988009 | 0.199095 | intron-variant | SPAG16 | GRCh38.p7 | 2:214195908 | AACTGCTATCTTCCA[A/G]GATCACAGAGAGAGT | 79582 |
rs61193296 | in-del | -/T | | | intron-variant | SPAG16 | GRCh38.p7 | 2:213963108 | CTTTTTTTTTTTTTT[-/T]AATGTCTAAAGATAG | 79582 |
rs61199650 | snp | G/T | 0.00159617 | 0.0282053 | intron-variant | SPAG16 | GRCh38.p7 | 2:214153972 | TATAGTAGTATATAT[G/T]TATATCCCAAGTATT | 79582 |
rs61213830 | snp | A/T | 0.0119091 | 0.0762411 | intron-variant | SPAG16 | GRCh38.p7 | 2:214356827 | TTTTAATAATGATTT[A/T]GTATTACCTACATGA | 79582 |
rs61233318 | in-del | -/G | | | intron-variant | SPAG16 | GRCh38.p7 | 2:213705789 | CATGGTGGAGGGTTT[-/G]TTGTTGTTGTTGTTG | 79582 |
rs61263090 | in-del | -/GT | | | intron-variant | SPAG16 | GRCh38.p7 | 2:213440124 | TGTGTGTGTGTGTGT[-/GT]TGTTAGCAAGCTTGC | 79582 |
rs61263594 | snp | C/T | 0.121022 | 0.21416 | intron-variant | SPAG16 | GRCh38.p7 | 2:213384960 | TGCTTTTGACATTTA[C/T]GTGCTTCTGGCTGGC | 79582 |
rs61264162 | in-del | -/ATATATATATATAT | | | intron-variant | SPAG16 | GRCh38.p7 | 2:213932186 | TATATATATATATAT[-/ATATATATATATAT]TTGTTGTTGTTGTTG | 79582 |
rs61276205 | snp | A/C | 0.0023933 | 0.0345097 | intron-variant | SPAG16 | GRCh38.p7 | 2:214372832 | CTGTTCACTTCCCCC[A/C]ACCCCAAATAAATGC | 79582 |
rs61276240 | snp | C/T | 0.04875 | 0.148319 | intron-variant | SPAG16 | GRCh38.p7 | 2:213963886 | AATGGTGTTTCCTTT[C/T]CCTATTCTTTTCAAT | 79582 |
rs61277094 | snp | C/T | | | intron-variant | SPAG16 | GRCh38.p7 | 2:213365281 | CCTACCCTTAAGTAG[C/T]TAAACTGTTGCATTT | 79582 |
rs61283019 | snp | C/T | 0.0700422 | 0.173537 | intron-variant | SPAG16 | GRCh38.p7 | 2:214021467 | CTCCCGTTTTTAAAA[C/T]CATCAGATCTCATGA | 79582 |
rs61312464 | in-del | -/ATG | | | intron-variant | SPAG16 | GRCh38.p7 | 2:214136472 | GTTATTGTAATGATG[-/ATG]TAGTGCTGTGTTGTG | 79582 |
rs61322411 | snp | C/T | 0.0475351 | 0.146656 | intron-variant | SPAG16 | GRCh38.p7 | 2:213367250 | CCGCAATAAACATAA[C/T]GTGTGCATGTGTCTT | 79582 |
rs61322948 | in-del | -/GAGAGA | | | intron-variant | SPAG16 | GRCh38.p7 | 2:214193457 | AGAGAGAGAGAGAGA[-/GAGAGA]AGGGGGTAGAGCTCA | 79582 |
rs61325223 | in-del | -/TA | | | intron-variant | SPAG16 | GRCh38.p7 | 2:214298159 | ACACACACACACATA[-/TA]CACACACACACACAC | 79582 |
rs61341736 | in-del | -/A/AA/AAA | | | intron-variant | SPAG16 | GRCh38.p7 | 2:214015600 | AGAAAAAAAAAAAAA[-/A/AA/AAA]TCAAAGAAAGAAAGG | 79582 |
rs61354468 | snp | A/G | 0.405429 | 0.195811 | intron-variant | SPAG16, LOC101928084 | GRCh38.p7 | 2:214099420 | AAAGAATTGCTATAC[A/G]CAAAGTACTTAGTAA | 79582 |
rs61361592 | snp | A/T | 0.0228947 | 0.104514 | intron-variant | SPAG16 | GRCh38.p7 | 2:213588058 | TAACATGTATTTTTC[A/T]TAATGGTTTGTTATT | 79582 |
rs61383927 | in-del | -/AG | 0.194278 | 0.243711 | intron-variant | SPAG16 | GRCh38.p7 | 2:213408576 | AGCAGGTTTCCTAAC[-/AG]GGGATTTAAATCTTA | 79582 |
rs61398752 | snp | C/T | | | intron-variant | SPAG16 | GRCh38.p7 | 2:213352959 | TAACTGAATGTTTAG[C/T]TAAAACATAGTTATT | 79582 |
rs61400369 | in-del | -/GCT | 0.153332 | 0.230554 | intron-variant | SPAG16 | GRCh38.p7 | 2:213552783 | GGCACCATTTAATCA[-/GCT]GCTGCTAGCGTGGCT | 79582 |
rs61407265 | snp | A/T | | | intron-variant | SPAG16 | GRCh38.p7 | 2:214060412 | AATGAAATGCTTTTT[A/T]AACATAAGATAATTC | 79582 |
rs61428891 | in-del | -/TA | | | intron-variant | SPAG16 | GRCh38.p7 | 2:213515179 | GTATATATATATATA[-/TA]AACCCATTCTATCTG | 79582 |
rs61447331 | snp | C/G/T | 0.00755907 | 0.0610114 | intron-variant | SPAG16, LOC101928084 | GRCh38.p7 | 2:214096101 | TATTTGCTCTGAGAT[C/G/T]TCATTCTTATTCCCT | 79582 |
rs61449420 | in-del | -/TT | 0.46348 | 0.130102 | intron-variant | SPAG16 | GRCh38.p7 | 2:213831425 | GGTGTTTTTTTTTTT[-/TT]AACCTCATATTTTCA | 79582 |
rs61476874 | snp | A/C | 0.0505692 | 0.150756 | intron-variant | SPAG16 | GRCh38.p7 | 2:213645643 | AGGCAAAGTCCTCTC[A/C]CTTCTTCTCTCTCCT | 79582 |
rs61480308 | in-del | -/C | | | intron-variant | SPAG16 | GRCh38.p7 | 2:213859217 | AAAAAAAAAAAAAAA[-/C]TCAATGTCCTCTGAC | 79582 |
rs61522336 | snp | G/T | 0.000798403 | 0.0199641 | intron-variant | SPAG16 | GRCh38.p7 | 2:214339149 | GTAAGGTGCTATTTA[G/T]AGGTTGATTGCATTA | 79582 |
rs61528899 | snp | G/T | 0.0225045 | 0.103662 | intron-variant | SPAG16 | GRCh38.p7 | 2:213967334 | TAGGTATCCATTAGA[G/T]AATTGGTTTTCTATC | 79582 |
rs61529213 | snp | C/T | 0.0376037 | 0.131863 | intron-variant | SPAG16 | GRCh38.p7 | 2:213897245 | GTATAATTTGATGTA[C/T]TGAACAGAAAATCAA | 79582 |
rs61544755 | snp | C/T | | | intron-variant | SPAG16 | GRCh38.p7 | 2:213674745 | CTGCATAGTATTCCA[C/T]GGTGTATATGTGCCA | 79582 |
rs61548174 | in-del | -/G/GT/TG | 0 | 0 | intron-variant | SPAG16 | GRCh38.p7 | 2:213742554 | CTTATTTCTTTTTTT[-/G/GT/TG]TTTTTTTTTTTTTTT | 79582 |
rs61548703 | in-del | -/A | 0.212425 | 0.24716 | intron-variant | SPAG16 | GRCh38.p7 | 2:213359401 | GTCTATAGAGGCAGT[-/A]AGGCCTTGCTGAGCT | 79582 |
rs61557867 | snp | C/T | 0.00517822 | 0.0506191 | intron-variant | SPAG16 | GRCh38.p7 | 2:214284840 | GTGTGTGTGCATATG[C/T]ATTTGTGTGTAACCA | 79582 |
rs61567019 | snp | A/T | 0.21725 | 0.247846 | intron-variant | SPAG16 | GRCh38.p7 | 2:214328738 | TTTATCTTTTGATGA[A/T]GTTATTAAAACTATC | 79582 |
rs61577965 | snp | C/T | 0.029116 | 0.117091 | intron-variant | SPAG16 | GRCh38.p7 | 2:213965834 | TCTGCACTACTTCTC[C/T]GAAGAACAGCTTCCA | 79582 |
rs61586440 | in-del | -/AAAA | | | intron-variant | SPAG16 | GRCh38.p7 | 2:213904618 | AAAAAAAAAAAAAAA[-/AAAA]CAAAGTAGGTAAAGG | 79582 |
rs61608932 | in-del | -/ATAT | | | intron-variant | SPAG16 | GRCh38.p7 | 2:213643408 | TATATATATATATAT[-/ATAT]TTTATCTCTTGCTGC | 79582 |
rs61614177 | snp | C/T | 0.173643 | 0.238054 | intron-variant | SPAG16 | GRCh38.p7 | 2:213564909 | ATTCTGTAGTCTGGC[C/T]CCTGAGCCTGCACAT | 79582 |
rs61618578 | snp | A/G | 0.0287284 | 0.116357 | intron-variant | SPAG16 | GRCh38.p7 | 2:213674510 | TCTAGCATTAGGTAT[A/G]TCTCCCAATGCTATC | 79582 |
rs61632904 | snp | A/G | 0.0577344 | 0.159793 | intron-variant | SPAG16 | GRCh38.p7 | 2:214348053 | TGCTGTGCACCTTTT[A/G]TCTCCCACTTTTTTG | 79582 |
rs61644666 | snp | A/G | | | intron-variant | SPAG16 | GRCh38.p7 | 2:213302649 | TGTGTGTGTGTGTGT[A/G]TGTGTGTGTGTTGTG | 79582 |
rs61648543 | snp | A/G | 0.00557542 | 0.0525036 | intron-variant | SPAG16 | GRCh38.p7 | 2:213618566 | GCTATCATAATGCCA[A/G]TCTCTTTAACAGGGG | 79582 |
rs61661660 | snp | A/G | 0.00517822 | 0.0506191 | intron-variant | SPAG16 | GRCh38.p7 | 2:213460563 | TAATTTTGACCATAA[A/G]AAAAATGTTTGCAAT | 79582 |
rs61687683 | snp | C/T | 0.155325 | 0.23138 | intron-variant | SPAG16 | GRCh38.p7 | 2:213436894 | TATGACATGTAATAC[C/T]ACGCAAAAATGATAA | 79582 |
rs61711759 | in-del | -/CACACACA/CACACACACACACA | 0 | 0 | intron-variant | SPAG16 | GRCh38.p7 | 2:214319224 | ACACACACACACACA[-/CACACACA/CACACACACACACA]AGAAGTGTAGAAAAG | 79582 |
rs61752198 | snp | A/G | 0.0362817 | 0.129709 | missense, nc-transcript-variant, intron-variant, upstream-variant-2KB, utr-variant-5-prime | SPAG16 | GRCh38.p7 | 2:213296093 | GAAGCATCTGAAGAT[A/G]ACTATGAATATGAAG | 79582 |
rs61752199 | snp | A/G | 0.0374032 | 0.131539 | missense, nc-transcript-variant | SPAG16 | GRCh38.p7 | 2:213490087 | ATGAACTTCCAGTGA[A/G]CTGGTAGGATTTTTG | 79582 |
rs61815717 | snp | A/T | 0.375 | 0.216506 | intron-variant | SPAG16 | GRCh38.p7 | 2:213733095 | GAGATGCTATCTCAT[A/T]GTGGTTTTGATTTGC | 79582 |
rs61816041 | snp | C/G | 0.5 | 0 | intron-variant | SPAG16 | GRCh38.p7 | 2:213733048 | CACCTGTTGTTTCCT[C/G]ACTTTTTAATGATTG | 79582 |
rs61956776 | snp | C/T | 0.530697 | 0.238155 | intron-variant | SPAG16 | GRCh38.p7 | 2:213356454 | TATTCAGAGATTCAA[C/T]TTCTTCCTTGTTTAG | 79582 |
rs61969728 | snp | A/C/G/T | 0.00755907 | 0.0610114 | intron-variant | SPAG16 | GRCh38.p7 | 2:213733076 | AGATACCATCTCACA[A/C/G/T]CAGTTAGAATGGCAA | 79582 |
rs62001971 | snp | A/G | 0.53125 | 0.20492 | intron-variant | SPAG16 | GRCh38.p7 | 2:213356458 | AAGAATAAACTAGGA[A/G]GAAGTTGAATCTCTG | 79582 |
rs62186594 | snp | A/G | | | intron-variant | SPAG16 | GRCh38.p7 | 2:213292543 | GTGGCGGGCGCCTGT[A/G]GTCCCAGCTACTTGG | 79582 |
rs62191877 | snp | C/T | 0.499809 | 0.00978247 | intron-variant | SPAG16 | GRCh38.p7 | 2:213896581 | AAAATGTGATATATA[C/T]ACACACACACGCACA | 79582 |
rs62191878 | snp | C/T | 0.499816 | 0.0095829 | intron-variant | SPAG16 | GRCh38.p7 | 2:213896583 | AATGTGATATATACA[C/T]ACACACACGCACACA | 79582 |
rs62191879 | snp | C/T | 0.499809 | 0.00978247 | intron-variant | SPAG16 | GRCh38.p7 | 2:213896585 | TGTGATATATACACA[C/T]ACACACGCACACACA | 79582 |
rs62191880 | snp | C/T | 0.499816 | 0.0095829 | intron-variant | SPAG16 | GRCh38.p7 | 2:213896587 | TGATATATACACACA[C/T]ACACGCACACACACA | 79582 |
rs62191881 | snp | C/T | 0.446771 | 0.154211 | intron-variant | SPAG16 | GRCh38.p7 | 2:213896589 | ATATATACACACACA[C/T]ACGCACACACACACA | 79582 |
rs62191882 | snp | A/G | | | intron-variant | SPAG16 | GRCh38.p7 | 2:213896594 | TACACACACACACGC[A/G]CACACACACACACAC | 79582 |
rs62191891 | snp | C/T | 0.470521 | 0.117772 | intron-variant | SPAG16 | GRCh38.p7 | 2:213909571 | CCTCAGAAATAACGC[C/T]GCATATCTACAACTA | 79582 |
rs62191892 | snp | A/G | 0.339803 | 0.233314 | intron-variant | SPAG16 | GRCh38.p7 | 2:213916112 | TGCAGAAGCTCTTTA[A/G]TTTAATTAGATCCTA | 79582 |
rs62191893 | snp | G/T | | | intron-variant | SPAG16 | GRCh38.p7 | 2:213918401 | AATCTATCTGGTCCT[G/T]GGTTTTTTTCTGGTT | 79582 |
rs62191903 | snp | A/T | 0.5 | 0 | intron-variant | SPAG16 | GRCh38.p7 | 2:213958849 | CTTACCAGTAATGAA[A/T]TCTTTATTTCTTAAT | 79582 |
rs62191922 | snp | A/T | | | intron-variant | SPAG16 | GRCh38.p7 | 2:214008438 | TGTACATATGTAGCA[A/T]TTAAAAAAAAAAATT | 79582 |
rs62191923 | snp | A/T | | | intron-variant | SPAG16 | GRCh38.p7 | 2:214008453 | TTTAAAAAAAAAAAT[A/T]ACATGCTGGGGCTGG | 79582 |
rs62191924 | snp | C/T | | | intron-variant | SPAG16 | GRCh38.p7 | 2:214011028 | GTAAGAAAGTATCTA[C/T]GTGACTTTCAGCAAT | 79582 |
rs62191925 | snp | C/T | 0.205417 | 0.245993 | intron-variant | SPAG16 | GRCh38.p7 | 2:214023371 | CCTAGAGGAGTAGTA[C/T]TTGAGTGGCTATCAA | 79582 |
rs62191926 | snp | A/T | 0.00318978 | 0.0398085 | intron-variant | SPAG16 | GRCh38.p7 | 2:214023408 | CCTAAGGCATTCATT[A/T]AAAAAAAAAGAAAAA | 79582 |
rs62191927 | snp | A/G | 0.230017 | 0.2492 | intron-variant | SPAG16 | GRCh38.p7 | 2:214024311 | ACCCAACTGATTTTT[A/G]TTCATTACTGAAATG | 79582 |
rs62191931 | snp | G/T | 0.228842 | 0.249103 | intron-variant | SPAG16 | GRCh38.p7 | 2:214036886 | ATTATTTATTTAAAG[G/T]ATACTGGGTCATTTG | 79582 |
rs62191932 | snp | C/T | 0.290977 | 0.246619 | intron-variant | SPAG16 | GRCh38.p7 | 2:214037132 | TTTTTATTGATGAAA[C/T]GTTTGAGGTTATAGG | 79582 |
rs62191934 | snp | A/G | 0.346811 | 0.230494 | intron-variant | SPAG16 | GRCh38.p7 | 2:214040970 | TTGGAGACTCCAGTT[A/G]TAGTAAATTGGATCT | 79582 |
rs62191935 | snp | A/G | 0.302184 | 0.244493 | intron-variant | SPAG16 | GRCh38.p7 | 2:214041116 | AATATATTCTTTCTT[A/G]GGTATCTCGTAATTT | 79582 |
rs62191954 | snp | A/G | 0.180702 | 0.240204 | intron-variant | SPAG16 | GRCh38.p7 | 2:214045349 | CAGGATCCATCACCT[A/G]TTGATTAAAAAGCTC | 79582 |
rs62191955 | snp | A/G | 0.00517822 | 0.0506191 | intron-variant | SPAG16 | GRCh38.p7 | 2:214045517 | AAAGCAGAGGGAAAC[A/G]TAAAGGGGACTTTGT | 79582 |
rs62191957 | snp | A/C | 0.2768 | 0.248559 | intron-variant | SPAG16 | GRCh38.p7 | 2:214048082 | GGAACCCTCCTCATA[A/C]ACTGTTGGTGGTAAT | 79582 |
rs62191958 | snp | G/T | 0.220843 | 0.248294 | intron-variant | SPAG16 | GRCh38.p7 | 2:214048694 | TTGTACACTGTAAAA[G/T]AACTGAAGGAGTATA | 79582 |
rs62192300 | snp | A/T | 0.5 | 0 | intron-variant, upstream-variant-2KB | SPAG16 | GRCh38.p7 | 2:213299436 | CCACCACACCGAGCT[A/T]ATTTTTTTTTTTTTT | 79582 |
rs62192301 | snp | A/C | 0.5 | 0 | intron-variant | SPAG16 | GRCh38.p7 | 2:213306866 | TCAAGACTGTCTTTT[A/C]TGCCTTCTTCAGTGC | 79582 |
rs62192302 | snp | A/G | 0.5 | 0 | intron-variant | SPAG16 | GRCh38.p7 | 2:213314093 | TCATTTATGGCAGTG[A/G]GTCTTAAATGCTTTT | 79582 |
rs62192306 | snp | A/C | | | intron-variant | SPAG16 | GRCh38.p7 | 2:213329839 | GTTCTATGGGCTGGG[A/C]CTAGGGTCCCTCTGC | 79582 |
rs62192307 | snp | A/C | | | intron-variant | SPAG16 | GRCh38.p7 | 2:213334223 | TGTTCAACATCATTG[A/C]TCATCAGGCAAATAT | 79582 |
rs62192309 | snp | A/G | | | intron-variant | SPAG16 | GRCh38.p7 | 2:213344700 | CATGTCCCTACAAAG[A/G]ACATGAACTCATCAT | 79582 |
rs62192310 | snp | A/T | | | intron-variant | SPAG16 | GRCh38.p7 | 2:213344934 | TGGTATTTCTAGTTC[A/T]AGATCCCTGAGGAAT | 79582 |
rs62192313 | snp | C/G | 0.0333695 | 0.124785 | intron-variant | SPAG16 | GRCh38.p7 | 2:213353212 | ACCCAACACACCTTG[C/G]TAAATCCATGGCCTC | 79582 |
rs62192325 | snp | A/T | 0.5 | 0 | intron-variant | SPAG16 | GRCh38.p7 | 2:213406934 | TCTCAGCGACGCGGA[A/T]TTAAAAAAAAAAAAA | 79582 |
rs62192326 | snp | A/G | | | intron-variant | SPAG16 | GRCh38.p7 | 2:213406960 | AAAAAAAAAAAAAGG[A/G]AAAAGAAACTGGCCA | 79582 |
rs62192327 | snp | C/G | | | intron-variant | SPAG16 | GRCh38.p7 | 2:213407950 | AGAGGCAGAGAGAGA[C/G]AGGAGAGAGGCAGAG | 79582 |
rs62192328 | snp | A/C | 0.5 | 0 | intron-variant | SPAG16 | GRCh38.p7 | 2:213410451 | AGATTTCGATAAAGA[A/C]CTAAATGTCAACCAG | 79582 |
rs62192329 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | SPAG16 | GRCh38.p7 | 2:213449572 | TTTATACTGTCTCTC[C/T]TTATTTCTCAGCTGG | 79582 |
rs62192330 | snp | G/T | | | intron-variant | SPAG16 | GRCh38.p7 | 2:213452798 | TGGGCCTTTGCATAT[G/T]CCCTAACACAACTTA | 79582 |
rs62192331 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | SPAG16 | GRCh38.p7 | 2:213457495 | CTTGTTCTTTTAAAC[A/G]TTTGAGGTTTATAGT | 79582 |
rs62192332 | snp | C/T | 0.5 | 0 | intron-variant | SPAG16 | GRCh38.p7 | 2:213466396 | GGTGAAAGGCCCTTT[C/T]AATATTTGGTTCCCC | 79582 |
rs62192345 | snp | A/G | 0.5 | 0 | intron-variant | SPAG16 | GRCh38.p7 | 2:213482412 | TTTGTCTCAGTTTAA[A/G]GAAATGTCAGCAGCA | 79582 |
rs62192346 | snp | A/G | 0.0126979 | 0.078662 | intron-variant | SPAG16 | GRCh38.p7 | 2:213486754 | CAATCAATATCCCAG[A/G]AGAATATTAAACTTA | 79582 |
rs62192347 | snp | C/T | 0.5 | 0 | intron-variant | SPAG16 | GRCh38.p7 | 2:213499713 | TATAAACACTACTCT[C/T]GTAATAATTAGAGTT | 79582 |
rs62192348 | snp | A/T | 0.5 | 0 | intron-variant | SPAG16 | GRCh38.p7 | 2:213521284 | TGACTTCTCATTCAC[A/T]TTGGACATATGACAA | 79582 |
rs62192349 | snp | C/G | 0.00438332 | 0.0466095 | intron-variant | SPAG16 | GRCh38.p7 | 2:213527293 | TTCTTGTGAGTGTTA[C/G]CCCTACAAGCTGCTT | 79582 |
rs62192350 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | SPAG16 | GRCh38.p7 | 2:213535405 | AATATAAAAAAGACA[C/G]AAATTCAACTTCTAG | 79582 |
rs62192351 | snp | A/G | 0.5 | 0 | intron-variant | SPAG16 | GRCh38.p7 | 2:213540850 | ATGCCAGACAGAACA[A/G]GAACATTATGGTACC | 79582 |
rs62192352 | snp | C/T | 0.00517822 | 0.0506191 | intron-variant | SPAG16 | GRCh38.p7 | 2:213541452 | GGTGAAATCTCTTCT[C/T]TACTAAAAATAACAA | 79582 |
rs62192353 | snp | C/T | 0.0766824 | 0.180169 | intron-variant | SPAG16 | GRCh38.p7 | 2:213551048 | CAGAATTTTCCTAAC[C/T]GTAATAGTCAGAGAT | 79582 |
rs62192354 | snp | C/T | 0.5 | 0 | intron-variant | SPAG16 | GRCh38.p7 | 2:213560833 | CTACTATCTTTCAAC[C/T]ACACACAATGAATGA | 79582 |
rs62192356 | snp | G/T | | | intron-variant | SPAG16 | GRCh38.p7 | 2:213569986 | TATGTGTCGAGGAAT[G/T]TATCCATTTCTTCTA | 79582 |
rs62192358 | snp | A/G | 0.356811 | 0.226034 | intron-variant | SPAG16 | GRCh38.p7 | 2:213572840 | CCCTCCCCCAGCCTC[A/G]CTGCTGCCTTGCAGT | 79582 |
rs62192576 | snp | C/T | 0.479744 | 0.0985793 | intron-variant | SPAG16 | GRCh38.p7 | 2:213869408 | ACAGATATTGATATA[C/T]TGTCTCTCTAAAAAT | 79582 |
rs62192577 | snp | A/G | 0.479744 | 0.0985793 | intron-variant | SPAG16 | GRCh38.p7 | 2:213869410 | AGATATTGATATACT[A/G]TCTCTCTAAAAATTA | 79582 |
rs62192578 | snp | A/G | 0.479904 | 0.0982045 | intron-variant | SPAG16 | GRCh38.p7 | 2:213871790 | GAAGAAACTTCTGTG[A/G]CCACACCAAACATGG | 79582 |
rs62192579 | snp | A/G | | | intron-variant | SPAG16 | GRCh38.p7 | 2:213871848 | GAAATTCACACACAC[A/G]CACACACACACACAC | 79582 |
rs62192580 | snp | C/G | | | intron-variant | SPAG16 | GRCh38.p7 | 2:213871883 | ACACACACACACAGA[C/G]AGAGAGAGAGAGAGA | 79582 |
rs62192581 | snp | C/G | | | intron-variant | SPAG16 | GRCh38.p7 | 2:213871885 | ACACACACACAGAGA[C/G]AGAGAGAGAGAGAGC | 79582 |
rs62192582 | snp | C/G | | | intron-variant | SPAG16 | GRCh38.p7 | 2:213871887 | ACACACACAGAGAGA[C/G]AGAGAGAGAGAGCAA | 79582 |
rs62192583 | snp | C/G | 0.5 | 0 | intron-variant | SPAG16 | GRCh38.p7 | 2:213871889 | ACACACAGAGAGAGA[C/G]AGAGAGAGAGCAAAC | 79582 |
rs62192584 | snp | C/G | 0.5 | 0 | intron-variant | SPAG16 | GRCh38.p7 | 2:213871891 | ACACAGAGAGAGAGA[C/G]AGAGAGAGCAAACAG | 79582 |
rs62192585 | snp | A/G | 0.479904 | 0.0982045 | intron-variant | SPAG16 | GRCh38.p7 | 2:213871932 | AAACCTTAGAAGGAA[A/G]CCTGATTTTCAGAAA | 79582 |
rs62192604 | snp | C/G | 0.453087 | 0.145793 | intron-variant | SPAG16 | GRCh38.p7 | 2:213878687 | TCTAGTTTGGTTTTT[C/G]TTGCTTGTGCTTCTG | 79582 |
rs62192605 | snp | C/T | 0.479744 | 0.0985793 | intron-variant | SPAG16 | GRCh38.p7 | 2:213879404 | GTGTGTGTGTATATA[C/T]ATATACACACACACA | 79582 |
rs62192660 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | SPAG16 | GRCh38.p7 | 2:213673704 | CCACACTGGCTTCTA[C/T]TAAGGTAATGTAATA | 79582 |
rs62192661 | snp | A/C | 0.5 | 0 | intron-variant | SPAG16 | GRCh38.p7 | 2:213683550 | AGTGAGACTCCATCT[A/C]CAAAAAAAAAAAAGA | 79582 |
rs62192662 | snp | G/T | 0.141934 | 0.225437 | intron-variant | SPAG16 | GRCh38.p7 | 2:213710534 | GATGGGAATCACATT[G/T]TATGGCTGTGTTGTA | 79582 |
rs62192706 | snp | C/G | 0.5 | 0 | intron-variant | SPAG16 | GRCh38.p7 | 2:213759411 | ACATAATTTAAGAGA[C/G]TAATGAATTTAAAAT | 79582 |
rs62192728 | snp | A/G | | | intron-variant | SPAG16 | GRCh38.p7 | 2:213763548 | CTGTTCAATTGGTGT[A/G]GAGTTTCAGTTATGC | 79582 |
rs62192729 | snp | C/T | 0.347914 | 0.230028 | intron-variant | SPAG16 | GRCh38.p7 | 2:213774793 | GGCAGGCTGACTCAA[C/T]CTATATTTTATCTGG | 79582 |
rs62192730 | snp | A/G | | | intron-variant | SPAG16 | GRCh38.p7 | 2:213775413 | TATTTTATAAACACA[A/G]CTATCACCTCCAAAA | 79582 |
rs62192731 | snp | C/T | 0.5 | 0 | intron-variant | SPAG16 | GRCh38.p7 | 2:213807349 | TCTTTTTTTTTTCCC[C/T]TCAACATTTCCCTAC | 79582 |
rs62194367 | snp | G/T | | | intron-variant | SPAG16 | GRCh38.p7 | 2:213820392 | CTTTTTATTTTGTCG[G/T]AGCTTACAGATTCTT | 79582 |
rs62194368 | snp | G/T | 0.0383715 | 0.133092 | intron-variant | SPAG16 | GRCh38.p7 | 2:213831567 | TTCATTTGTTTGCTT[G/T]TTTGTATTCAGCTCA | 79582 |
rs62194370 | snp | A/T | | | intron-variant | SPAG16 | GRCh38.p7 | 2:213833495 | TATATATTATATATA[A/T]TATATATATTATATA | 79582 |
rs62194390 | snp | C/G | | | intron-variant | SPAG16 | GRCh38.p7 | 2:213847864 | AATATAAACAAATGA[C/G]ACACACACACACACA | 79582 |
rs62194391 | snp | G/T | 0.472989 | 0.113031 | intron-variant | SPAG16 | GRCh38.p7 | 2:213860771 | TATCTTTCAAAGTTC[G/T]TAAAAACATCAATGA | 79582 |
rs62195174 | snp | A/G | 0.370568 | 0.219005 | intron-variant | SPAG16 | GRCh38.p7 | 2:213590917 | CTACTCATCAGTGAT[A/G]GATTGGTTAAAGAAA | 79582 |
rs62195175 | snp | C/T | 0.367091 | 0.220884 | intron-variant | SPAG16 | GRCh38.p7 | 2:213591038 | CTAAGCAAATTAACA[C/T]AGTAACAGAAAACCA | 79582 |
rs62195176 | snp | C/T | 0.155325 | 0.23138 | intron-variant | SPAG16 | GRCh38.p7 | 2:213594107 | TTAAACTTCAACTCT[C/T]TAGCTTTGAGTCACA | 79582 |
rs62195177 | snp | C/T | 0.5 | 0 | intron-variant | SPAG16 | GRCh38.p7 | 2:213595585 | TTTAGAATATTTCTG[C/T]TACAAAACATAAATA | 79582 |
rs62196163 | snp | A/T | | | intron-variant | SPAG16 | GRCh38.p7 | 2:214193428 | GTGTGTGTGTGTATG[A/T]GAGAGAGAGAGAGAG | 79582 |
rs62196165 | snp | A/G/T | 0.5 | 0 | intron-variant | SPAG16 | GRCh38.p7 | 2:214195336 | ATAGATAGATAGATA[A/G/T]TTGAGAGATATATAG | 79582 |
rs62196166 | snp | A/T | 0.5 | 0 | intron-variant | SPAG16 | GRCh38.p7 | 2:214195338 | AGATAGATAGATATT[A/T]GAGAGATATATAGAC | 79582 |
rs62196167 | snp | G/T | 0.5 | 0 | intron-variant | SPAG16 | GRCh38.p7 | 2:214195341 | TAGATAGATATTTGA[G/T]AGATATATAGACTTG | 79582 |
rs62196168 | snp | G/T | 0.5 | 0 | intron-variant | SPAG16 | GRCh38.p7 | 2:214195347 | GATATTTGAGAGATA[G/T]ATAGACTTGACATAT | 79582 |
rs62196169 | snp | C/T | 0.289165 | 0.246913 | intron-variant | SPAG16 | GRCh38.p7 | 2:214196395 | ACCACTTAACAAATA[C/T]GAAAACAGAAAAACT | 79582 |
rs62196170 | snp | A/C | 0.00597247 | 0.0543191 | intron-variant | SPAG16 | GRCh38.p7 | 2:214197034 | TAAAGGCTTAAATGG[A/C]CCTGGGATATTCAGT | 79582 |
rs62196171 | snp | C/T | | | intron-variant | SPAG16 | GRCh38.p7 | 2:214203567 | GGGGAACCTCAAGTT[C/T]CAGATCAGGGGATAA | 79582 |
rs62196173 | snp | A/G | 0.0379877 | 0.132479 | intron-variant | SPAG16 | GRCh38.p7 | 2:214205004 | GAGGCTGAGGCAGGT[A/G]GATCACTTGAGACCA | 79582 |
rs62196174 | snp | C/T | 0.286825 | 0.247273 | intron-variant | SPAG16 | GRCh38.p7 | 2:214208154 | GTCCTTCTGGAGAAC[C/T]CTGAAAAATACAGAT | 79582 |
rs62196176 | snp | A/G | 0.5 | 0 | intron-variant | SPAG16 | GRCh38.p7 | 2:214227702 | TCTTGTGGAAGGTGT[A/G]TGTGTGTGTGTGTGT | 79582 |
rs62196177 | snp | A/G | 0 | 0 | intron-variant | SPAG16 | GRCh38.p7 | 2:214246191 | TGCCTCTAACAGAGG[A/G]ACTTTAGACAAATCC | 79582 |
rs62196789 | snp | A/G | 0.450357 | 0.149522 | intron-variant | SPAG16 | GRCh38.p7 | 2:214254315 | TGGCCAGAACTTCCA[A/G]TACTGTGTTGAATAG | 79582 |
rs62196790 | snp | A/T | 0.5 | 0 | intron-variant | SPAG16 | GRCh38.p7 | 2:214260356 | AGAAAAAGAATATCT[A/T]ATTTTTTTTTTTTCT | 79582 |
rs62196791 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | SPAG16 | GRCh38.p7 | 2:214262775 | ACTAAGTATAGACAA[C/T]GAGTATCAAAGGAAT | 79582 |
rs62196796 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | SPAG16 | GRCh38.p7 | 2:214280758 | ACTTATTTCCTGGGC[A/G]TCTTCTCATAGACTA | 79582 |
rs62196825 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | SPAG16 | GRCh38.p7 | 2:214301535 | ATCATTTCCTGGAAT[G/T]TATCCATTTCCTCTA | 79582 |
rs62196826 | snp | A/C | | | intron-variant | SPAG16 | GRCh38.p7 | 2:214305019 | GTGTTCCTTTCTCTC[A/C]ACAACCTCACCAGAA | 79582 |
rs62196827 | snp | A/C | | | intron-variant | SPAG16 | GRCh38.p7 | 2:214311261 | GATCCCACAGCTCCC[A/C]AGGGACCTGATGGAC | 79582 |
rs62196828 | snp | C/G/T | | | intron-variant | SPAG16 | GRCh38.p7 | 2:214311497 | TTGATAGGGGAACCC[C/G/T]GACAGTTTGGCTGTT | 79582 |
rs62196829 | snp | C/T | | | intron-variant | SPAG16 | GRCh38.p7 | 2:214326695 | TCACGCCTGTAATCC[C/T]AGCACTTTGGGAGGC | 79582 |
rs62196830 | snp | A/G | | | intron-variant | SPAG16 | GRCh38.p7 | 2:214326717 | TTGGGAGGCCGAGGC[A/G]GGCGGATCACGAGAT | 79582 |
rs62196831 | snp | C/T | | | intron-variant | SPAG16 | GRCh38.p7 | 2:214326727 | GAGGCAGGCGGATCA[C/T]GAGATCAGGAGATCG | 79582 |
rs62196832 | snp | A/G | | | intron-variant | SPAG16 | GRCh38.p7 | 2:214326731 | CAGGCGGATCACGAG[A/G]TCAGGAGATCGAGGC | 79582 |
rs62196833 | snp | A/G | | | intron-variant | SPAG16 | GRCh38.p7 | 2:214326745 | GATCAGGAGATCGAG[A/G]CCATCCTGGCTAACA | 79582 |
rs62196834 | snp | A/C/T | 0.000399281 | 0.0141238 | intron-variant | SPAG16 | GRCh38.p7 | 2:214326761 | CCATCCTGGCTAACA[A/C/T]GGTGAAACCCTGTCT | 79582 |
rs62196835 | snp | C/T | | | intron-variant | SPAG16 | GRCh38.p7 | 2:214326772 | AACACGGTGAAACCC[C/T]GTCTCTACTAAAAAT | 79582 |
rs62196836 | snp | A/G | | | intron-variant | SPAG16 | GRCh38.p7 | 2:214326786 | CTGTCTCTACTAAAA[A/G]TACAAAAAATTACCC | 79582 |
rs62196837 | snp | C/G | | | intron-variant | SPAG16 | GRCh38.p7 | 2:214326799 | AAATACAAAAAATTA[C/G]CCGGGCGTGGTGGCG | 79582 |
rs62196838 | snp | C/T | | | intron-variant | SPAG16 | GRCh38.p7 | 2:214326807 | AAAATTACCCGGGCG[C/T]GGTGGCGGGCGCCTG | 79582 |
rs62196839 | snp | A/G | | | intron-variant | SPAG16 | GRCh38.p7 | 2:214326824 | GTGGCGGGCGCCTGT[A/G]GTCCCAGCTACTTGG | 79582 |
rs62196840 | snp | C/T | | | intron-variant | SPAG16 | GRCh38.p7 | 2:214326837 | GTGGTCCCAGCTACT[C/T]GGGAGGCTGAGGCAG | 79582 |
rs62196841 | snp | C/T | | | intron-variant | SPAG16 | GRCh38.p7 | 2:214326861 | GAGGCAGGAGAATGG[C/T]GTGAACCCAGGAGGC | 79582 |
rs62196842 | snp | A/G | | | intron-variant | SPAG16 | GRCh38.p7 | 2:214326870 | GAATGGTGTGAACCC[A/G]GGAGGCAGAGCTTGC | 79582 |
rs62196843 | snp | A/G | 0.120674 | 0.21395 | intron-variant | SPAG16 | GRCh38.p7 | 2:214326877 | GTGAACCCAGGAGGC[A/G]GAGCTTGCAGTGAGC | 79582 |
rs62196844 | snp | A/G | 0.0433465 | 0.140692 | intron-variant | SPAG16 | GRCh38.p7 | 2:214340133 | AACAAGAACGCAAGA[A/G]AGTAAGAGACATGTG | 79582 |
rs62197893 | snp | A/G | 0.430434 | 0.173042 | intron-variant, nc-transcript-variant | SPAG16, LOC101928084 | GRCh38.p7 | 2:214085280 | GAGAGGCTGAGGCGG[A/G]AGAATCACTTGAACC | 79582 |
rs62197894 | snp | A/C | 0.5 | 0 | intron-variant | SPAG16, LOC101928084 | GRCh38.p7 | 2:214085379 | GGGAGATTCCACCTC[A/C]AAAAAAAAAAAAAAG | 79582 |
rs62197895 | snp | G/T | 0.494896 | 0.0502606 | intron-variant | SPAG16, LOC101928084 | GRCh38.p7 | 2:214085458 | TCCATATGTTGGTAT[G/T]GAGTTAGTGATCAAA | 79582 |
rs62197896 | snp | G/T | 0.225597 | 0.248806 | intron-variant | SPAG16 | GRCh38.p7 | 2:214113645 | GCATGCATCATGTAG[G/T]TCTTGTGCCATGGTT | 79582 |
rs62197897 | snp | C/T | 0.223819 | 0.248625 | intron-variant | SPAG16 | GRCh38.p7 | 2:214113739 | AATCTTTTTTCAAGG[C/T]TTTTAGCTTCCTTGT | 79582 |
rs62197898 | snp | G/T | | | intron-variant | SPAG16 | GRCh38.p7 | 2:214116071 | TGATCTGCTGATTAT[G/T]CTCCCAGGTTCAAGC | 79582 |
rs62197899 | snp | C/T | 0.262435 | 0.249691 | intron-variant | SPAG16 | GRCh38.p7 | 2:214117950 | CTGGACTAAGACAAA[C/T]ATGCCTATCTTTACT | 79582 |
rs62197900 | snp | A/G | 0.262985 | 0.249663 | intron-variant | SPAG16 | GRCh38.p7 | 2:214117966 | ATGCCTATCTTTACT[A/G]TTTCTGTTCAACATA | 79582 |
rs62197901 | snp | A/C | 0.252983 | 0.249982 | intron-variant | SPAG16 | GRCh38.p7 | 2:214118492 | CTCACAGTTCCACAT[A/C]GTTGGGGAGGCCTCA | 79582 |
rs62197902 | snp | C/T | 0.253264 | 0.249979 | intron-variant | SPAG16 | GRCh38.p7 | 2:214119485 | AAACTGTAAATAATA[C/T]GTGGCAGGAAAATGA | 79582 |
rs62197903 | snp | A/G | 0 | 0 | intron-variant | SPAG16 | GRCh38.p7 | 2:214144495 | ATTCTACAATTATCT[A/G]TTGAACATGAACTAT | 79582 |
rs62197904 | snp | A/G | 0.328382 | 0.237395 | intron-variant | SPAG16 | GRCh38.p7 | 2:214144590 | TTACAACATTCTCAT[A/G]TATACATAGTTGATG | 79582 |
rs62197905 | snp | A/T | 0.32153 | 0.239548 | intron-variant | SPAG16 | GRCh38.p7 | 2:214145782 | CAGTTAATATTTCTA[A/T]ATTTTTGAAACAAAT | 79582 |
rs62197906 | snp | C/G | 0.321053 | 0.23969 | intron-variant | SPAG16 | GRCh38.p7 | 2:214145818 | TAAATCACATAGAGT[C/G]AACGTTGATTACTCT | 79582 |
rs62197907 | snp | A/T | | | intron-variant | SPAG16 | GRCh38.p7 | 2:214147021 | AAAAAAAAAAAATTT[A/T]CATATTCATTTTACC | 79582 |
rs62197908 | snp | C/G | 0.302936 | 0.244331 | intron-variant | SPAG16 | GRCh38.p7 | 2:214149800 | ATTTAGTTTTTATTC[C/G]ACAATGATATAAGTA | 79582 |
rs62197909 | snp | A/T | 0.348574 | 0.229746 | intron-variant | SPAG16 | GRCh38.p7 | 2:214159309 | TTTAGATCTAATAGC[A/T]TATACTAGTCATTAG | 79582 |
rs62197910 | snp | G/T | 0.5 | 0 | intron-variant | SPAG16 | GRCh38.p7 | 2:214159508 | AGCTGTAGTTCAACA[G/T]ATGTGCAAATCAACC | 79582 |
rs62197912 | snp | C/T | 0.343701 | 0.231776 | intron-variant | SPAG16 | GRCh38.p7 | 2:214168736 | TGTTGCAGAGGTCCA[C/T]GTGATTAGAGTGGAA | 79582 |
rs62197913 | snp | A/G | 0.0879971 | 0.190408 | intron-variant | SPAG16 | GRCh38.p7 | 2:214170250 | CACACTTAGGTGTGT[A/G]TACATATACACACAC | 79582 |
rs62197915 | snp | A/T | | | intron-variant | SPAG16 | GRCh38.p7 | 2:214173921 | CAAGGCTGGTTCAAT[A/T]TATGCAAATCAATAA | 79582 |
rs62198192 | snp | C/G | 0.483418 | 0.0895317 | intron-variant | SPAG16 | GRCh38.p7 | 2:214352558 | CTTGACTTTTTTTCT[C/G]TGTGTGTGTGTGTGT | 79582 |
rs62198193 | snp | A/C | | | intron-variant | SPAG16 | GRCh38.p7 | 2:214357192 | TTCTCTGCAGTTTCA[A/C]TATGATGTGCCCAAT | 79582 |
rs62198194 | snp | A/G | 0.0433465 | 0.140692 | intron-variant | SPAG16 | GRCh38.p7 | 2:214360876 | TACCCTCTTTCTGGG[A/G]AAGAAAAAAGCGAGG | 79582 |
rs62198195 | snp | C/T | 0.00557542 | 0.0525036 | intron-variant | SPAG16 | GRCh38.p7 | 2:214365261 | GAATCTGAACGTGAA[C/T]ATCAGCACCTACTTA | 79582 |
rs62198196 | snp | C/T | 0.130694 | 0.219696 | intron-variant | SPAG16 | GRCh38.p7 | 2:214375545 | TACAACACACAAATA[C/T]ACACACACAAACTTA | 79582 |
rs62198249 | snp | A/C | 0.5 | 0 | intron-variant | SPAG16 | GRCh38.p7 | 2:214395040 | TTTTCATGGCTTGTT[A/C]GCTCATTTCTTTTTA | 79582 |
rs62198250 | snp | A/G | 0.176219 | 0.238865 | intron-variant | SPAG16 | GRCh38.p7 | 2:214406777 | AATTCATCCAACAGA[A/G]TGAAATGGACAGCAA | 79582 |
rs62241774 | snp | A/C | 0.56 | 0.195959 | intron-variant | SPAG16 | GRCh38.p7 | 2:213733082 | TTCTAACTGGTGTGA[A/C]ATGATATCTCATTGT | 79582 |
rs62354462 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | SPAG16 | GRCh38.p7 | 2:213733086 | AACTGGTGTGAGATG[A/G]TATCTCATTGTGGTT | 79582 |
rs62534096 | snp | C/T | 0.5 | 0 | intron-variant | SPAG16 | GRCh38.p7 | 2:213733067 | TTTTAATGATTGCCA[C/T]TCTAACGGGTGTGAG | 79582 |
rs62567289 | snp | G/T | 0.5 | 0 | intron-variant | SPAG16 | GRCh38.p7 | 2:213733079 | CCATTCTAACTGGTG[G/T]GAGATGGTATCTCAT | 79582 |
rs62587391 | snp | G/T | 0.5 | 0 | intron-variant | SPAG16 | GRCh38.p7 | 2:213733109 | TTGTGGTTTTGATTT[G/T]CATTTCTCTGATGGC | 79582 |
rs63415960 | snp | G/T | 0.5 | 0 | intron-variant | SPAG16 | GRCh38.p7 | 2:214326558 | GAGAAATCATAATAA[G/T]AAGAGAGAAATTCAG | 79582 |
rs66466028 | in-del | -/TCTC | 0.424348 | 0.179172 | intron-variant | SPAG16 | GRCh38.p7 | 2:214152177 | TGTATAACAAAATTT[-/TCTC]TATTTATTAACCTCA | 79582 |
rs66474271 | in-del | -/CTT | | | intron-variant | SPAG16 | GRCh38.p7 | 2:214383923 | TGGACATGGCAAACC[-/CTT]TTTAAATCTCTGTTG | 79582 |
rs66479012 | in-del | -/TT | | | intron-variant | SPAG16 | GRCh38.p7 | 2:213754691 | AGTCAAAATGAAATA[-/TT]AAATTAATGTATCAC | 79582 |
rs66504434 | snp | A/G | 0 | 0 | intron-variant | SPAG16 | GRCh38.p7 | 2:213724802 | AAAAAAAAAAAAAAA[A/G]AAAAAAGGATAAACT | 79582 |
rs66518306 | in-del | -/ATAAT | | | intron-variant | SPAG16 | GRCh38.p7 | 2:213624242 | TCAATGGTTGAAGAT[-/ATAAT]CAGGCTATTTATCAT | 79582 |
rs66523241 | in-del | -/TATG | | | intron-variant | SPAG16 | GRCh38.p7 | 2:213860362 | ATATATATATATATA[-/TATG]TGTGTGTGTGTATAT | 79582 |
rs66524283 | in-del | -/T | 0.479904 | 0.0982045 | intron-variant | SPAG16 | GRCh38.p7 | 2:213870361 | CTTGTCTATTGTGGC[-/T]TGCTAGTGTTAACTA | 79582 |
rs66552769 | in-del | -/CTA | 0.475437 | 0.108066 | intron-variant | SPAG16 | GRCh38.p7 | 2:214354116 | CATAAATATATATAC[-/CTA]CTATGTACCCCAAAA | 79582 |
rs66580402 | in-del | -/T/TT | 0 | 0 | intron-variant | SPAG16 | GRCh38.p7 | 2:214397158 | TTTTTTTTTTTTTTT[-/T/TT]GAGATGGAGTCTCGC | 79582 |
rs66638113 | in-del | -/ATAA | 0 | 0 | intron-variant | SPAG16 | GRCh38.p7 | 2:213701257 | TAAATAAATAAATAA[-/ATAA]GATGATCTTATAGGA | 79582 |
rs66674310 | in-del | -/GAGAGAGAGAGA | 0 | 0 | intron-variant | SPAG16 | GRCh38.p7 | 2:213407625 | AGAGAGAGAGAGAGA[-/GAGAGAGAGAGA]CAGACAGACAGACAG | 79582 |
rs66685116 | in-del | -/ACACACACACAGAGAGAGAGAG | | | intron-variant | SPAG16 | GRCh38.p7 | 2:213871870 | CACACACACACACAC[-/ACACACACACAGAGAGAGAGAG]AGAGAGAGCAAACAG | 79582 |
rs66735884 | in-del | CCT/G | 0.5 | 0 | intron-variant | SPAG16, LOC101928084 | GRCh38.p7 | 2:214085458 | TCCATATGTTGGTAT[CCT/G]GAGTTAGTGATCAAA | 79582 |
rs66763977 | in-del | -/T | 0.450985 | 0.148678 | intron-variant | SPAG16 | GRCh38.p7 | 2:213878257 | TGAGAAATCATCATA[-/T]TGTTTTCCAAAGAGG | 79582 |
rs66796332 | snp | A/C | 0.499816 | 0.0095829 | intron-variant | SPAG16 | GRCh38.p7 | 2:213349639 | GCCCAAACTAAAATC[A/C]ACTCAAGTTTTCATC | 79582 |
rs66803661 | in-del | -/A | | | intron-variant, downstream-variant-500B | SPAG16 | GRCh38.p7 | 2:214192637 | GTATATTCCTTTATT[-/A]TTTTTTGTACTTTTC | 79582 |
rs66881080 | in-del | -/T | 0 | 0 | intron-variant | SPAG16 | GRCh38.p7 | 2:213833457 | ATATATATATATTAT[-/T]ATATATATTATATAT | 79582 |
rs66883735 | in-del | -/T | | | intron-variant | SPAG16 | GRCh38.p7 | 2:213791399 | TTTAGTATAACTTCT[-/T]TTTTTTATACAAAGA | 79582 |
rs66892769 | snp | C/T | 0.352938 | 0.227824 | intron-variant | SPAG16 | GRCh38.p7 | 2:214034465 | TTTGCTTGGGCCTGC[C/T]GGGCCAACTCAGCAG | 79582 |
rs66894850 | in-del | -/AGAC | | | intron-variant | SPAG16 | GRCh38.p7 | 2:213860389 | TGTATATCTATAAAT[-/AGAC]AGATATTTATACATA | 79582 |
rs66900646 | in-del | -/TAAG | 0.297636 | 0.24542 | intron-variant | SPAG16 | GRCh38.p7 | 2:213737992 | ATTCATTGAATTTCT[-/TAAG]TGTTTCTCTTCATTG | 79582 |
rs66904718 | in-del | -/AT | 0.478768 | 0.100824 | intron-variant | SPAG16 | GRCh38.p7 | 2:213664837 | CATGCATATATATAC[-/AT]ATATACACACACATA | 79582 |
rs66986750 | in-del | -/CTAT | 0 | 0 | intron-variant | SPAG16 | GRCh38.p7 | 2:213860429 | TATATGTGTGTATAT[-/CTAT]ATATTTATAGATATA | 79582 |
rs66999154 | snp | A/G | 0.472989 | 0.113031 | intron-variant | SPAG16 | GRCh38.p7 | 2:214247737 | ACAGCTGATGTGACA[A/G]AAAATCAACGAGATC | 79582 |
rs67039793 | in-del | -/TTAT | 0.175254 | 0.238565 | intron-variant | SPAG16 | GRCh38.p7 | 2:213335573 | TGTTGTCAGCTTATG[-/TTAT]TTGTCAAATTATATT | 79582 |
rs67057975 | in-del | -/AAGTGTT | 0.255503 | 0.249939 | intron-variant | SPAG16 | GRCh38.p7 | 2:214033666 | TCACCCAGATTTCCC[-/AAGTGTT]AACATTTTACTATTT | 79582 |
rs67083613 | snp | A/T | 0 | 0 | intron-variant | SPAG16 | GRCh38.p7 | 2:214147018 | AAAAAAAAAAAAAAA[A/T]TTTCATATTCATTTT | 79582 |
rs67086240 | snp | A/G | 0.499631 | 0.0135733 | intron-variant | SPAG16 | GRCh38.p7 | 2:213386573 | TCCTTAGACAATTGT[A/G]TATCTTTACTTCTCA | 79582 |
rs67115144 | snp | A/G | 0.19459 | 0.243782 | intron-variant | SPAG16 | GRCh38.p7 | 2:213951861 | GATGTTTTGAGATTC[A/G]CTAAAACCAAATATT | 79582 |
rs67211471 | snp | C/T | 0.492727 | 0.0598633 | intron-variant | SPAG16 | GRCh38.p7 | 2:214062020 | ACACACACACACACA[C/T]GCAGTGTGTAGTATT | 79582 |
rs67243428 | in-del | -/A | | | intron-variant | SPAG16 | GRCh38.p7 | 2:214326969 | AAAAAAAAAAAAAAA[-/A]GTCACTAGTATTCTG | 79582 |
rs67316414 | in-del | -/G | | | intron-variant, downstream-variant-500B | SPAG16 | GRCh38.p7 | 2:213371419 | AAAAAAAAAAAAAAA[-/G]AAAAGAAAAGACGAT | 79582 |
rs67346409 | multinucleotide-polymorphism | CCA/TCT | 0.5 | 0 | intron-variant | SPAG16, LOC101928084 | GRCh38.p7 | 2:214093839 | ATATAAATGGCATGC[CCA/TCT]GGGGTCACTCTCTAT | 79582 |
rs67405710 | in-del | -/TT | | | intron-variant | SPAG16 | GRCh38.p7 | 2:213968174 | TTCTCTTCTCATCTC[-/TT]TTCTTTTCTTTTCCT | 79582 |
rs67407044 | snp | A/C | 0.433963 | 0.169285 | intron-variant | SPAG16 | GRCh38.p7 | 2:214212743 | ATAGATGAACCAAAA[A/C]AGTCTTTCTTTTCTC | 79582 |
rs67415849 | in-del | -/GTAT | 0.0425829 | 0.139564 | intron-variant | SPAG16 | GRCh38.p7 | 2:214160695 | ATTCTGTGTATGTAC[-/GTAT]GTAAGTTTCTAAAAA | 79582 |
rs67524501 | in-del | -/GTTA | | | intron-variant | SPAG16 | GRCh38.p7 | 2:213925141 | ATCATTATTGTTTTT[-/GTTA]TTTTATTTTTACAAG | 79582 |
rs67537759 | in-del | -/C | 0 | 0 | intron-variant | SPAG16 | GRCh38.p7 | 2:214154510 | CAGACCCCCCCCCCC[-/C]ATTTTTTCATAACCT | 79582 |
rs67576718 | snp | A/G | 0.371582 | 0.218444 | intron-variant | SPAG16 | GRCh38.p7 | 2:214255863 | TTTACGAATTACGCT[A/G]TTAATGTGGGCATGA | 79582 |
rs67580788 | in-del | -/GT | | | intron-variant | SPAG16 | GRCh38.p7 | 2:213705789 | CATGGTGGAGGGTTT[-/GT]TGTTGTTGTTGTTGT | 79582 |
rs67591422 | snp | A/G | 0.499631 | 0.0135733 | intron-variant | SPAG16 | GRCh38.p7 | 2:213340864 | AAATTTACAATCCTT[A/G]AATAAAATTATATTT | 79582 |
rs67604431 | snp | A/G | 0.343254 | 0.231956 | intron-variant | SPAG16 | GRCh38.p7 | 2:214178064 | TATTTGTGTTTATAT[A/G]TATTTTCAAATACAT | 79582 |
rs67683060 | in-del | -/AA | 0.0103295 | 0.0711199 | intron-variant | SPAG16 | GRCh38.p7 | 2:214055410 | TATAAAGAAGCAAAC[-/AA]TAATGATTTTTAAAA | 79582 |
rs67689337 | in-del | -/CAGA | 0 | 0 | intron-variant | SPAG16 | GRCh38.p7 | 2:213871879 | ACACACACACACACA[-/CAGA]GAGAGAGAGAGAGAG | 79582 |
rs67689423 | in-del | -/T | | | intron-variant | SPAG16 | GRCh38.p7 | 2:214143235 | CATCATAGTTTTGGG[-/T]TTTTTTTTTTTTTTT | 79582 |
rs67701768 | in-del | -/T | | | intron-variant | SPAG16 | GRCh38.p7 | 2:213954140 | AAGAGTCACTCCTAT[-/T]TTTTTTTTTTTTTTT | 79582 |
rs67705468 | in-del | -/G | 0 | 0 | intron-variant | SPAG16, LOC101928084 | GRCh38.p7 | 2:214102116 | TGAGGGTGGTTTTTT[-/G]TTTTTTTTTTTTTGC | 79582 |
rs67714838 | in-del | -/A | | | intron-variant | SPAG16 | GRCh38.p7 | 2:214351716 | AAACAAACAAACAAA[-/A]CAAAAAAAACAACAA | 79582 |
rs67726428 | in-del | -/TTTTTTTTTTT | 0 | 0 | intron-variant | SPAG16 | GRCh38.p7 | 2:214165496 | TTTTTTTTTTTTTTT[-/TTTTTTTTTTT]GCCAAAATTGACATC | 79582 |
rs67742153 | snp | C/T | 0.283684 | 0.24772 | intron-variant | SPAG16 | GRCh38.p7 | 2:214044783 | AGTGCTGCCCTGTCA[C/T]AGCACAAAGCAAAAC | 79582 |
rs67787854 | in-del | -/ATTGGTTAAAGAAAATATGTTATCT | | | intron-variant | SPAG16 | GRCh38.p7 | 2:213590919 | ACTCATCAGTGATGG[-/ATTGGTTAAAGAAAATATGTTATCT]ATACACCATAGAATA | 79582 |
rs67801275 | snp | C/T | 0.366885 | 0.220993 | intron-variant | SPAG16 | GRCh38.p7 | 2:214323720 | ATTACACTAAACTAA[C/T]AAACAAAATTCTCCC | 79582 |
rs67830923 | snp | A/C | 0 | 0 | intron-variant | SPAG16 | GRCh38.p7 | 2:213322357 | AAAAAAAAAAAAAAA[A/C]AAAAAACTCGTTTGG | 79582 |
rs67870564 | in-del | -/AT | 0.425277 | 0.178263 | intron-variant | SPAG16 | GRCh38.p7 | 2:214335470 | AATTAACATGGAGGA[-/AT]ATATATATATATAGA | 79582 |
rs67910834 | in-del | -/TATA | | | intron-variant | SPAG16 | GRCh38.p7 | 2:213860354 | ATTTACAGATATATA[-/TATA]TATATATATATGTGT | 79582 |
rs67988930 | in-del | -/T | 0.485049 | 0.0851591 | intron-variant | SPAG16 | GRCh38.p7 | 2:214073233 | GGTGGAAATTTTTTC[-/T]TTTTTTTTTTTTCTT | 79582 |
rs67989120 | in-del | CTCTTTAGT/GTCTTTAG | 0.5 | 0 | intron-variant | SPAG16 | GRCh38.p7 | 2:213782173 | CTCTAAACTGTAATA[CTCTTTAGT/GTCTTTAG]TTTTTTTTTTTAAAT | 79582 |
rs68023665 | in-del | -/CAGGAGTGTTACAGCTCTTT | 0.352938 | 0.227824 | intron-variant | SPAG16 | GRCh38.p7 | 2:213476827 | CCACAGCTTGGTGAG[-/CAGGAGTGTTACAGCTCTTT]CATTCAAGCAGTTCA | 79582 |
rs68045407 | multinucleotide-polymorphism | ATA/TTC | 0.5 | 0 | intron-variant | SPAG16 | GRCh38.p7 | 2:213819112 | GAAGGAGTGGAACAT[ATA/TTC]TTTATAAAATAGAGC | 79582 |
rs68049944 | in-del | -/T | 0 | 0 | intron-variant | SPAG16 | GRCh38.p7 | 2:213516405 | ATTTTATCTTTTTCT[-/T]CAAAAAATGAACTTA | 79582 |
rs68152101 | in-del | -/A/AA/AAAAA | 0.410061 | 0.192043 | intron-variant | SPAG16 | GRCh38.p7 | 2:213694042 | GACAAAAAAAAAAAA[-/A/AA/AAAAA]GAAAAAAGAGAGGGA | 79582 |
rs68156608 | in-del | -/TGAAATCTTAAATATAACGT | | | intron-variant | SPAG16 | GRCh38.p7 | 2:213754685 | TACATTAGTCAAAAT[-/TGAAATCTTAAATATAACGT]GAAATAAAATTAATG | 79582 |
rs68157142 | snp | A/T | 0.5 | 0 | intron-variant | SPAG16 | GRCh38.p7 | 2:214390343 | ATGCTTTTTTTTTTA[A/T]AAAAAAAAAAAAAAA | 79582 |
rs71001501 | in-del | -/TGT | 0 | 0 | intron-variant | SPAG16 | GRCh38.p7 | 2:213733040 | CTCTCCAGCACCTGT[-/TGT]TTCCTGACTTTTTAA | 79582 |
rs71034604 | in-del | -/ATATATATATATATATA | 0 | 0 | intron-variant | SPAG16 | GRCh38.p7 | 2:214012289 | TATATATATATATAT[-/ATATATATATATATATA]TTTTTTTTTTTTTTT | 79582 |
rs71034608 | in-del | -/A | | | intron-variant | SPAG16 | GRCh38.p7 | 2:214046913 | ACAATCTGAAAAAAA[-/A]AAAACAATTTAGCAA | 79582 |
rs71034609 | in-del | -/ACAC | 0 | 0 | intron-variant | SPAG16 | GRCh38.p7 | 2:214056311 | CACACACACACACAC[-/ACAC]GCATAGAGAGAGAGA | 79582 |
rs71034612 | in-del | -/ATAT | 0 | 0 | intron-variant | SPAG16 | GRCh38.p7 | 2:214059241 | TATATATATATATAT[-/ATAT]GTATGTATATATATG | 79582 |
rs71034613 | in-del | -/TATA | 0 | 0 | intron-variant | SPAG16 | GRCh38.p7 | 2:214059276 | ATATATATATATATA[-/TATA]ATCAAGAATTTTTGT | 79582 |
rs71034614 | in-del | -/T | 0.375 | 0.216506 | intron-variant | SPAG16 | GRCh38.p7 | 2:214070081 | AATTTTTTTTTTTTT[-/T]CTGATTGGTTTGAAA | 79582 |
rs71034615 | in-del | -/TG | 0 | 0 | intron-variant | SPAG16 | GRCh38.p7 | 2:214076563 | GTGTGTGTGTGTGTG[-/TG]TGTTTGTGTTGAGAG | 79582 |
rs71034616 | in-del | -/AAA | 0 | 0 | intron-variant | SPAG16 | GRCh38.p7 | 2:214078552 | AAAAAAAAAAAAAAA[-/AAA]TCTGTTATTTATTGC | 79582 |
rs71037336 | in-del | -/A | | | intron-variant | SPAG16 | GRCh38.p7 | 2:214080608 | CGAGACTCTGTCTCA[-/A]AAAAAAAAAAAAAAT | 79582 |
rs71037337 | in-del | -/TGAGA | 0 | 0 | intron-variant | SPAG16 | GRCh38.p7 | 2:214083567 | TTGTTTCCCAACTTA[-/TGAGA]GGAAGAACCTCAAGA | 79582 |
rs71037338 | in-del | -/AT/TA | | | intron-variant | SPAG16, LOC101928084 | GRCh38.p7 | 2:214093428 | TGTATATATATATAT[-/AT/TA]TTCACTTGATTAAAA | 79582 |
rs71037341 | in-del | -/T | 0.37778 | 0.214877 | intron-variant | SPAG16, LOC101928084 | GRCh38.p7 | 2:214101149 | ATGAGTATTACTTAA[-/T]TTTTTTTTCAAATTT | 79582 |
rs71037342 | in-del | -/ACACACACACAC | 0 | 0 | intron-variant | SPAG16 | GRCh38.p7 | 2:214108469 | CACACACACACACAC[-/ACACACACACAC]CCCCACACACACCCC | 79582 |
rs71037343 | in-del | -/A | 0 | 0 | intron-variant | SPAG16 | GRCh38.p7 | 2:214115897 | AAAAAAAAAAAAAAA[-/A]GTAACCCTCCTATCT | 79582 |
rs71037345 | in-del | -/A/TA | 0.478437 | 0.10157 | intron-variant | SPAG16 | GRCh38.p7 | 2:214133129 | ATAATAAAAAAAAAA[-/A/TA]CCTACCATTAGCATA | 79582 |
rs71037347 | in-del | -/GG | 0 | 0 | intron-variant | SPAG16 | GRCh38.p7 | 2:214140945 | TGGTGGGGGGGGGGG[-/GG]TGGGGGGTGGGGGGA | 79582 |
rs71037350 | in-del | -/A | 0.49423 | 0.0534032 | intron-variant | SPAG16 | GRCh38.p7 | 2:214191714 | CTCAAAAAAAAAAAA[-/A]GAAAAAAAAAAAAAA | 79582 |
rs71037352 | in-del | -/G | 0 | 0 | intron-variant | SPAG16 | GRCh38.p7 | 2:214232588 | GACTGTGAAGGAGTC[-/G]GGGGGGGCTCAGATT | 79582 |
rs71037353 | in-del | -/A | 0.483418 | 0.0895317 | intron-variant | SPAG16 | GRCh38.p7 | 2:214241890 | AAATGTAAGTTGTAT[-/A]AAAAAAAAAAAATTC | 79582 |
rs71037358 | in-del | -/TG | 0 | 0 | intron-variant | SPAG16 | GRCh38.p7 | 2:214284833 | GTGTGTGTGTGTGTG[-/TG]CATATGTATTTGTGT | 79582 |
rs71037359 | in-del | -/C | 0 | 0 | intron-variant | SPAG16 | GRCh38.p7 | 2:214290406 | TTTACTATTTCTTTC[-/C]TTCTGATAATTTTGG | 79582 |
rs71037360 | in-del | -/AT | 0 | 0 | intron-variant | SPAG16 | GRCh38.p7 | 2:214298093 | TATATATATATATAT[-/AT]GTATGCATATATATA | 79582 |
rs71037361 | in-del | -/AT/TA | 0 | 0 | intron-variant | SPAG16 | GRCh38.p7 | 2:214298132 | ACACACACACACACA[-/AT/TA]CATACACATACACAC | 79582 |
rs71037363 | in-del | -/TAA/TAATAA | 0 | 0 | intron-variant | SPAG16 | GRCh38.p7 | 2:214301068 | TAATAATAATAATAA[-/TAA/TAATAA]AAGTTAGCAAGCTAA | 79582 |
rs71037364 | in-del | -/T | 0.383824 | 0.211166 | intron-variant | SPAG16 | GRCh38.p7 | 2:214305888 | AATAGTTTTTTTTTT[-/T]CTAGTTCTTTGAAGA | 79582 |
rs71037365 | in-del | -/A | | | intron-variant | SPAG16 | GRCh38.p7 | 2:214314960 | ATTAAAAAAAAAAAA[-/A]GAAGGAATTGGAAAA | 79582 |
rs71037367 | in-del | -/A | | | intron-variant | SPAG16 | GRCh38.p7 | 2:214330113 | TCTACCAAAAATAGA[-/A]AAAAAAAAAAAAAAG | 79582 |
rs71037369 | in-del | -/TTTT | 0 | 0 | intron-variant | SPAG16 | GRCh38.p7 | 2:214335774 | TTTTTTTTTTTTTTT[-/TTTT]GAGATGGAGTCTCAC | 79582 |
rs71037371 | in-del | -/A | 0 | 0 | intron-variant | SPAG16 | GRCh38.p7 | 2:214355337 | CAAGAAAAAAAAAAA[-/A]CAACCCCATCAAAAA | 79582 |
rs71060421 | in-del | -/CACACACA | 0 | 0 | intron-variant | SPAG16 | GRCh38.p7 | 2:213310367 | ACACACACACACACA[-/CACACACA]AATCAGAATAGCAGT | 79582 |
rs71060423 | in-del | -/CACACA | 0 | 0 | intron-variant | SPAG16 | GRCh38.p7 | 2:213361829 | ACACACACACACACA[-/CACACA]GAGGCTGTGAATAAA | 79582 |
rs71060424 | in-del | -/TTTA | 0 | 0 | intron-variant, downstream-variant-500B | SPAG16 | GRCh38.p7 | 2:213371716 | ACACATTAATTGTTA[-/TTTA]ATCTAAATTTAGGGA | 79582 |
rs71060428 | in-del | -/TTT | 0 | 0 | intron-variant | SPAG16 | GRCh38.p7 | 2:213387460 | TTTTTTTTTTTTTTT[-/TTT]GAGACAGAGTCTCGC | 79582 |
rs71060431 | in-del | -/GT/T | 0.61521 | 0.13444 | intron-variant | SPAG16 | GRCh38.p7 | 2:213409116 | GAAATAAATTAACTG[-/GT/T]TTTTTTTTTTTTAAA | 79582 |
rs71060433 | in-del | -/GATATATA | 0 | 0 | intron-variant | SPAG16 | GRCh38.p7 | 2:213468504 | ATGTATTTATATATA[-/GATATATA]TATATCTATGTATTT | 79582 |
rs71060434 | in-del | -/CTTTT | 0 | 0 | intron-variant | SPAG16 | GRCh38.p7 | 2:213509008 | CTTTTCTTTTCTTTT[-/CTTTT]TTTTTTGAGATGGAG | 79582 |
rs71060436 | in-del | -/T | 0 | 0 | intron-variant | SPAG16 | GRCh38.p7 | 2:213525306 | TTTTTTTTTTTTTTT[-/T]GAGACAGAGTCTCGC | 79582 |
rs71060438 | in-del | -/T | 0.438946 | 0.163706 | intron-variant | SPAG16 | GRCh38.p7 | 2:213540215 | TTTTTTATTTTTTTT[-/T]GTATTTTTAGTAGAG | 79582 |
rs71063761 | in-del | -/T/TT | 0.298144 | 0.245321 | intron-variant | SPAG16 | GRCh38.p7 | 2:213585281 | GATTTTTTTTTTTTT[-/T/TT]GAAATGGAGTCTCAC | 79582 |
rs71063763 | in-del | -/TTATATATATATATATAT | 0 | 0 | intron-variant | SPAG16 | GRCh38.p7 | 2:213643348 | TATTGGATCTTAATT[-/TTATATATATATATATAT]ATATATATATATATA | 79582 |
rs71063764 | in-del | -/T | 0.375 | 0.216506 | intron-variant | SPAG16 | GRCh38.p7 | 2:213643768 | TTTTTTTTTTTTTTT[-/T]GAGACGCAGTTTCAC | 79582 |
rs71063766 | in-del | -/A | | | intron-variant | SPAG16 | GRCh38.p7 | 2:213680435 | TAAAAAAAAAAAAAA[-/A]GATGTTTTATTACAA | 79582 |
rs71063769 | in-del | -/A | | | intron-variant | SPAG16 | GRCh38.p7 | 2:213718149 | TTAAACAAGTTTACA[-/A]AAAAAAAAAAAAAAA | 79582 |
rs71063770 | in-del | -/AAGT | 0 | 0 | intron-variant | SPAG16 | GRCh38.p7 | 2:213737993 | TTCATTGAATTTCTT[-/AAGT]GTTTCTCTTCATTGT | 79582 |
rs71063776 | in-del | -/T | | | intron-variant | SPAG16 | GRCh38.p7 | 2:213780572 | TTTTCTTTTCTTTCT[-/T]TTTTTTTTTTTTTTT | 79582 |
rs71063777 | in-del | -/A | 0 | 0 | intron-variant | SPAG16 | GRCh38.p7 | 2:213784653 | AAAAAAAAAAAAAAA[-/A]GAACTGTGAGAGCTC | 79582 |
rs71063780 | in-del | -/A | 0.474723 | 0.109542 | intron-variant | SPAG16 | GRCh38.p7 | 2:213797052 | AAAAAAATTAAAATT[-/A]AAAAAAAAAACATTA | 79582 |
rs71063781 | in-del | -/TCTATCTATCTATCTA | 0 | 0 | intron-variant | SPAG16 | GRCh38.p7 | 2:213802432 | CTATCTATCTATCTA[-/TCTATCTATCTATCTA]CACATACCTGGAGTT | 79582 |
rs71063783 | in-del | -/AT | 0 | 0 | intron-variant | SPAG16 | GRCh38.p7 | 2:213814890 | TATATATATATATAT[-/AT]CCATAGCTTCTAAAT | 79582 |
rs71063784 | in-del | -/AT | 0.402806 | 0.197864 | intron-variant | SPAG16 | GRCh38.p7 | 2:213817214 | TTGTACAAAGCATGC[-/AT]ATATATATATATATG | 79582 |
rs71063785 | in-del | -/TT | 0 | 0 | intron-variant | SPAG16 | GRCh38.p7 | 2:213819958 | TTTTTTTTTTTTTTT[-/TT]AGTAGAGACGGGTTT | 79582 |
rs71063786 | in-del | -/T | | | intron-variant | SPAG16 | GRCh38.p7 | 2:213825702 | TTCTTTCTTTCTTTC[-/T]TTTTTTTTTTTTTTT | 79582 |
rs71063788 | in-del | -/TTATATATATAATAATATATATATTATATATATATTATTATATATA | 0 | 0 | intron-variant | SPAG16 | GRCh38.p7 | 2:213833464 | ATATTATTATATATA[lengthTooLong]TTATATATAATAATA | 79582 |
rs71063790 | in-del | -/CA | 0 | 0 | intron-variant | SPAG16 | GRCh38.p7 | 2:213847874 | ACACACACACACACA[-/CA]GACATATAATACAAA | 79582 |
rs71063792 | in-del | -/A | 0 | 0 | intron-variant | SPAG16 | GRCh38.p7 | 2:213876305 | AAAAAAAAAAAAAAA[-/A]GAAGAAGAAAAGAAA | 79582 |
rs71063793 | in-del | -/AAAA | 0 | 0 | intron-variant | SPAG16 | GRCh38.p7 | 2:213895016 | AAAAAAAAAAAAAAA[-/AAAA]CTGAAAGACTCTACC | 79582 |
rs71063796 | in-del | -/CTGA | 0.377187 | 0.215229 | intron-variant | SPAG16 | GRCh38.p7 | 2:213922249 | TTTCTTTATTTTTGT[-/CTGA]CTGAGTTATTTCAGA | 79582 |
rs71063798 | in-del | -/CACACA | 0 | 0 | intron-variant | SPAG16 | GRCh38.p7 | 2:213928938 | ACACACACACACACA[-/CACACA]AAACCAACTAGATGT | 79582 |
rs71063800 | in-del | -/ATATAT | 0 | 0 | intron-variant | SPAG16 | GRCh38.p7 | 2:213932194 | TATATATATATATAT[-/ATATAT]TTGTTGTTGTTGTTG | 79582 |
rs71063801 | in-del | -/ACACAC | 0.405255 | 0.195948 | intron-variant | SPAG16 | GRCh38.p7 | 2:213932950 | AATGGTTGTTTGAAA[-/ACACAC]ACACACACACACACA | 79582 |
rs71189164 | multinucleotide-polymorphism | CA/TG | 0 | 0 | intron-variant | SPAG16 | GRCh38.p7 | 2:213733062 | CACCAGTTAGAATGG[CA/TG]ATCATTAAAAAGTCA | 79582 |
rs71219508 | snp | A/G | 0.5 | 0 | intron-variant | SPAG16 | GRCh38.p7 | 2:213733047 | AATCATTAAAAAGTC[A/G]GGAAACAACAGGTGC | 79582 |
rs71221383 | snp | C/T | 0.68431 | 0.133912 | intron-variant | SPAG16 | GRCh38.p7 | 2:213356341 | CAGCTCCTCCTTGTA[C/T]CTCTGGTAGAATTCG | 79582 |
rs71301556 | in-del | -/T | 0.356811 | 0.226034 | intron-variant | SPAG16 | GRCh38.p7 | 2:213798426 | CCTGGCTAATTTTTG[-/T]TTTTTTTTTATAGAG | 79582 |
rs71350755 | snp | A/G | 0 | 0 | intron-variant | SPAG16 | GRCh38.p7 | 2:213572818 | GGGGGAGGGGCGCCC[A/G]CCATTGCCCAGGCTT | 79582 |
rs71350773 | snp | A/G | 0.358303 | 0.225323 | intron-variant | SPAG16 | GRCh38.p7 | 2:213593796 | TTTTTTTTTTTTGGG[A/G]CGGAGTCTGGCTCTG | 79582 |
rs71350776 | snp | G/T | 0.471483 | 0.115954 | intron-variant | SPAG16, LOC101928084 | GRCh38.p7 | 2:214101119 | AAGGTTTTTTTGTCT[G/T]AAATATGACTTTTGA | 79582 |
rs71394385 | in-del | ATGTATGTG/GTATGTGTATATA | 0.5 | 0 | intron-variant | SPAG16 | GRCh38.p7 | 2:214059214 | TATATATATATATAT[ATGTATGTG/GTATGTGTATATA]TATATATATATATAT | 79582 |
rs71397185 | in-del | -/ATTTGATCT | 0.5 | 0 | intron-variant | SPAG16 | GRCh38.p7 | 2:213352734 | TAAAAAGTTAAAATC[-/ATTTGATCT]ATGAGTTAGAGTTGA | 79582 |
rs71397187 | in-del | -/TG/TGTG | 0.1652 | 0.235179 | intron-variant | SPAG16 | GRCh38.p7 | 2:213361364 | CAGAATATGTATGTA[-/TG/TGTG]TGTGTGTGTGTGTGT | 79582 |
rs71397192 | in-del | -/CCTAAAGA | 0.474182 | 0.110646 | intron-variant | SPAG16 | GRCh38.p7 | 2:213796929 | ATGCATGTTATTTCT[-/CCTAAAGA]CCTTTTAGTGAGAGA | 79582 |
rs71397194 | in-del | -/TCCC | 0.5 | 0 | intron-variant | SPAG16 | GRCh38.p7 | 2:213800313 | CCCTCCCTTTCTCCT[-/TCCC]TCCCTCCCTCCCTCC | 79582 |
rs71397195 | in-del | -/CTCT | 0.5 | 0 | intron-variant | SPAG16 | GRCh38.p7 | 2:213800332 | TCCCTCCCTCCCTCC[-/CTCT]CTCCCTCTCTCCCTC | 79582 |
rs71397197 | in-del | -/AT | 0.5 | 0 | intron-variant | SPAG16 | GRCh38.p7 | 2:213814872 | ACATAACAGCCTTAA[-/AT]ATATATATATATATA | 79582 |
rs71397199 | in-del | -/A | | | intron-variant | SPAG16 | GRCh38.p7 | 2:213894988 | ACAAGGCTCCATCTC[-/A]AAAAAAAAAAAAAAA | 79582 |
rs71399103 | in-del | -/T | 0.5 | 0 | intron-variant | SPAG16 | GRCh38.p7 | 2:214043524 | TGATTTTCTCTTTTG[-/T]ATTTTTTTCTAAAAC | 79582 |
rs71399105 | in-del | -/TGTGTGTGTGTGTGTGTGTGTG | 0.5 | 0 | intron-variant | SPAG16 | GRCh38.p7 | 2:214076513 | CTTCTTATTTTATTC[-/TGTGTGTGTGTGTGTGTGTGTG]TGTGTGTGTGTGTGT | 79582 |
rs71399106 | in-del | -/TC | 0.5 | 0 | intron-variant | SPAG16 | GRCh38.p7 | 2:214076545 | GTGTGTGTGTGTGTG[-/TC]TGTGTGTGTGTGTGT | 79582 |
rs71399107 | in-del | -/ATGAG | 0.225301 | 0.248777 | intron-variant | SPAG16 | GRCh38.p7 | 2:214083566 | ATTGTTTCCCAACTT[-/ATGAG]AGGAAGAACCTCAAG | 79582 |
rs71399109 | in-del | -/A | 0.222333 | 0.248464 | intron-variant | SPAG16, LOC101928084 | GRCh38.p7 | 2:214092917 | TTGATTCTTCATCCC[-/A]GCAGCTCTTTTTATG | 79582 |
rs71399110 | in-del | -/TA | 0.227959 | 0.249026 | intron-variant | SPAG16, LOC101928084 | GRCh38.p7 | 2:214093427 | TCTATCATTCTAATG[-/TA]TATATATATATATTT | 79582 |
rs71399111 | in-del | -/A | 0.5 | 0 | intron-variant | SPAG16, LOC101928084 | GRCh38.p7 | 2:214096279 | TGGTTTTTTTAATGC[-/A]AAAAAAAAAATGTAG | 79582 |
rs71399112 | multinucleotide-polymorphism | CA/TG | 0.5 | 0 | intron-variant | SPAG16, LOC101928084 | GRCh38.p7 | 2:214099419 | AAAAGAATTGCTATA[CA/TG]CAAAGTACTTAGTAA | 79582 |
rs71399117 | in-del | -/TTG | 0.375 | 0.216506 | intron-variant | SPAG16 | GRCh38.p7 | 2:214144430 | ACATTGGTTCTATAA[-/TTG]TTGTTTTAATGGCTT | 79582 |
rs71399119 | in-del | -/ATACATATACACACACACTTAGGTGTGC | 0.5 | 0 | intron-variant | SPAG16 | GRCh38.p7 | 2:214170250 | CACACTTAGGTGTGT[-/ATACATATACACACACACTTAGGTGTGC]GTACATATACATACA | 79582 |
rs71399120 | in-del | -/T | 0.5 | 0 | intron-variant | SPAG16 | GRCh38.p7 | 2:214176273 | AAGGAAAGAAACTTC[-/T]TTTTTTTAAAAAAAA | 79582 |
rs71399122 | in-del | -/T | 0.5 | 0 | intron-variant | SPAG16 | GRCh38.p7 | 2:214180680 | AAAGGATGTATACTT[-/T]GGAGTTAAGACACCT | 79582 |
rs71399124 | in-del | -/TTT/TTTT/TTTTTTTT | 0.5 | 0 | intron-variant | SPAG16 | GRCh38.p7 | 2:214214185 | AACCTTCCTTTTTAC[-/TTT/TTTT/TTTTTTTT]TTTTTTTTTTTTTGA | 79582 |
rs71399125 | in-del | -/C | 0.5 | 0 | intron-variant | SPAG16 | GRCh38.p7 | 2:214248609 | GTGTGAGCCACCATG[-/C]CCCGGCCGTGCTAGG | 79582 |
rs71399128 | in-del | -/TTAT/TTATTTAT/TTATTTATTTAT | 0.0182019 | 0.0936463 | intron-variant | SPAG16 | GRCh38.p7 | 2:214288752 | TTGTCCTTTGCCCAC[-/TTAT/TTATTTAT/TTATTTATTTAT]TTATTTATTTATTTA | 79582 |
rs71399130 | in-del | -/AA | | | intron-variant | SPAG16 | GRCh38.p7 | 2:214326968 | AAAAAAAAAAAAAAA[-/AA]GTCACTAGTATTCTG | 79582 |
rs71399131 | in-del | -/ACAA/CAAA | 0.5 | 0 | intron-variant | SPAG16 | GRCh38.p7 | 2:214372473 | GAAAACAGAATAAAA[-/ACAA/CAAA]CAAGGAATCTTCCTG | 79582 |
rs71409872 | in-del | -/G | 0.5 | 0 | intron-variant | SPAG16 | GRCh38.p7 | 2:213660387 | AATTCTCCTGCCTCA[-/G]GTGTATACATATGTA | 79582 |
rs71409873 | multinucleotide-polymorphism | CCT/TCC | 0.5 | 0 | intron-variant | SPAG16, LOC101928084 | GRCh38.p7 | 2:214101308 | CTCACAACATGTGTG[CCT/TCC]TGCTTCAGTTCTGTG | 79582 |
rs71409878 | in-del | -/TCTG/TGTGTGTGTGTGTGTG | 0.5 | 0 | intron-variant | SPAG16 | GRCh38.p7 | 2:214352556 | CCTTGACTTTTTTTC[-/TCTG/TGTGTGTGTGTGTGTG]TGTGTGTGTGTGTGT | 79582 |
rs71426333 | snp | A/C | 0.5 | 0 | intron-variant, upstream-variant-2KB | SPAG16 | GRCh38.p7 | 2:213298786 | ACCTTACATGAGTTA[A/C]CATTCTTGATTTCTG | 79582 |
rs71426334 | snp | A/T | 0.00716266 | 0.059414 | intron-variant | SPAG16 | GRCh38.p7 | 2:213373663 | GGAATTATCTGTTGG[A/T]TTCTTGAGTTTCTCT | 79582 |
rs71426335 | snp | C/G | 0.5 | 0 | intron-variant | SPAG16 | GRCh38.p7 | 2:213387618 | CGCCACCACGCCCGG[C/G]TAATTTTTTGTATTT | 79582 |
rs71426336 | snp | A/G | 0.5 | 0 | intron-variant | SPAG16 | GRCh38.p7 | 2:213387772 | CATGCTCTTTTAAAA[A/G]AAAATTCTTCCCTAG | 79582 |
rs71426337 | snp | A/C/T | 0.00953873 | 0.0683987 | intron-variant | SPAG16 | GRCh38.p7 | 2:213429138 | GGGTCCTATATTCGT[A/C/T]TGCCTAGATTAAGGA | 79582 |
rs71426338 | snp | C/G/T | 0.000399281 | 0.0141238 | intron-variant | SPAG16 | GRCh38.p7 | 2:213461287 | ATATGGCATGGCTTA[C/G/T]TATAGGGTGTTATAT | 79582 |
rs71426339 | snp | A/G | 0.00478085 | 0.0486577 | intron-variant | SPAG16 | GRCh38.p7 | 2:213532981 | AGTAAATTATCAAAG[A/G]AATACAGCCATTCAA | 79582 |
rs71426340 | snp | A/T | 0.5 | 0 | intron-variant | SPAG16 | GRCh38.p7 | 2:213547832 | CTTATGTACCTAAAA[A/T]TTAGCTTATTTTAAG | 79582 |
rs71426341 | snp | C/T | 0.00914312 | 0.0669923 | intron-variant | SPAG16 | GRCh38.p7 | 2:213548029 | GCAATCAATGACCTA[C/T]ATTTAAATTGTTTTG | 79582 |
rs71426342 | snp | A/G | 0.5 | 0 | intron-variant | SPAG16 | GRCh38.p7 | 2:213645953 | CCAGGATTCTCCTCA[A/G]GCTGGGGCTGGTTTA | 79582 |
rs71426343 | snp | C/T | 0.00318978 | 0.0398085 | intron-variant | SPAG16 | GRCh38.p7 | 2:213676696 | ACATTTATTGATTTG[C/T]GTATATTGAACCAGC | 79582 |
rs71426344 | snp | A/C | 0.000798403 | 0.0199641 | intron-variant | SPAG16 | GRCh38.p7 | 2:213715010 | TCAGCTGGCCGTTAG[A/C]AGCTACTGAAGAGTT | 79582 |
rs71426345 | snp | A/G | 0.5 | 0 | intron-variant | SPAG16 | GRCh38.p7 | 2:213728310 | GAGTCTCAGCCCCCA[A/G]AGTGTCTACTGCCTC | 79582 |
rs71426346 | snp | G/T | 0.5 | 0 | intron-variant | SPAG16 | GRCh38.p7 | 2:213738011 | TGTTTCTCTTCATTG[G/T]AGTTTTAAATTTTTC | 79582 |
rs71426347 | snp | C/T | 0.00318978 | 0.0398085 | intron-variant | SPAG16 | GRCh38.p7 | 2:213833612 | ATAAAATCTCCTTGA[C/T]CTAACTTGTTCAGAT | 79582 |
rs71426348 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | SPAG16 | GRCh38.p7 | 2:213873261 | TCTATCCAGGTTATC[C/T]AATTTGCTGCCATTT | 79582 |
rs71426349 | snp | A/C/G | 0.000798403 | 0.0199641 | intron-variant | SPAG16 | GRCh38.p7 | 2:213906259 | AAAGCAATCGCATAT[A/C/G]CAATAGAAACAAAAT | 79582 |
rs71426350 | snp | A/T | 0.5 | 0 | intron-variant | SPAG16 | GRCh38.p7 | 2:213955972 | TATTATTTATTTATT[A/T]ATTTATTTATTTTTT | 79582 |
rs71426351 | snp | A/G | 0.5 | 0 | intron-variant | SPAG16 | GRCh38.p7 | 2:213958238 | GGCACAAGTTCCGTG[A/G]AGTCTGTGACTGAGA | 79582 |
rs71426352 | snp | G/T | 0.5 | 0 | intron-variant | SPAG16 | GRCh38.p7 | 2:213961736 | GTGAAAATCTCACTG[G/T]TCATTGTGTATAATC | 79582 |
rs71426353 | snp | A/G | 0.00199481 | 0.0315187 | intron-variant | SPAG16 | GRCh38.p7 | 2:214036465 | TTCTAGGCATTGTTA[A/G]TATTAATAAACAAAG | 79582 |
rs71426354 | snp | A/G | 0.5 | 0 | intron-variant | SPAG16 | GRCh38.p7 | 2:214039947 | GCAGCTGATTGGCTA[A/G]GGGTACAGTCATAGG | 79582 |
rs71426865 | snp | A/G | 0.5 | 0 | intron-variant | SPAG16 | GRCh38.p7 | 2:213387469 | TTTTTTTGAGACAGA[A/G]TCTCGCTCTGTCGCC | 79582 |
rs71426866 | snp | A/G/T | 0.0130921 | 0.0798413 | intron-variant | SPAG16 | GRCh38.p7 | 2:213387640 | TTTGTATTTTTAGTA[A/G/T]AGACGGGGTTTCACC | 79582 |
rs71428314 | snp | G/T | 0.151668 | 0.229849 | intron-variant | SPAG16 | GRCh38.p7 | 2:214040233 | CCTCCTAGCCTGGTG[G/T]TCTCTCATTTGCTTT | 79582 |
rs71428315 | snp | C/T | 0.186421 | 0.24178 | intron-variant | SPAG16 | GRCh38.p7 | 2:214053293 | CTATATTAAATCTTC[C/T]TAACTAGAACAAAGA | 79582 |
rs71428316 | snp | C/G | 0.301681 | 0.2446 | intron-variant | SPAG16 | GRCh38.p7 | 2:214059121 | GGCAGAGGTTGCAGT[C/G]AGCCAAGATCATGCC | 79582 |
rs71428317 | snp | C/T | 0.5 | 0 | intron-variant | SPAG16 | GRCh38.p7 | 2:214062410 | GGCGGCAGAGCACGA[C/T]TCTGACTCAAAAAAA | 79582 |
rs71428318 | snp | A/G | 0.5 | 0 | intron-variant | SPAG16 | GRCh38.p7 | 2:214080381 | AGGCAGGCGGATCAC[A/G]AGGTCAGGAGATCAA | 79582 |
rs71428319 | snp | A/G | 0.225597 | 0.248806 | intron-variant | SPAG16, LOC101928084 | GRCh38.p7 | 2:214092736 | GCTCTGTGATCCTGG[A/G]GCTGAAATTGCAATT | 79582 |
rs71428320 | snp | A/G | 0.226779 | 0.248919 | intron-variant | SPAG16, LOC101928084 | GRCh38.p7 | 2:214093209 | TTTTATATATATAAT[A/G]GTTGTATCTTAAATT | 79582 |
rs71428321 | snp | C/T | 0.226484 | 0.248892 | intron-variant | SPAG16, LOC101928084 | GRCh38.p7 | 2:214093228 | GTATCTTAAATTATA[C/T]GTTTTGGAATAAATG | 79582 |
rs71428322 | snp | A/G | 0.224116 | 0.248656 | intron-variant | SPAG16, LOC101928084 | GRCh38.p7 | 2:214095362 | TTTCATATGCTCCAC[A/G]TGGAAAAAGAGCTTC | 79582 |
rs71428323 | snp | A/G | 0.223819 | 0.248625 | intron-variant | SPAG16, LOC101928084 | GRCh38.p7 | 2:214095439 | TGGAGTGTGGACTCT[A/G]TTGTTGTCAGGCTTA | 79582 |
rs71428324 | snp | A/G | 0.223819 | 0.248625 | intron-variant | SPAG16, LOC101928084 | GRCh38.p7 | 2:214095546 | GTTGAGCGAAGGAAA[A/G]CCACCTATTATAAAA | 79582 |
rs71428325 | snp | C/T | 0.233249 | 0.257729 | intron-variant | SPAG16, LOC101928084 | GRCh38.p7 | 2:214095552 | CGAAGGAAAGCCACC[C/T]ATTATAAAACTGAGA | 79582 |
rs71428326 | snp | A/T | 0.227074 | 0.248947 | intron-variant | SPAG16, LOC101928084 | GRCh38.p7 | 2:214099134 | CTGTAGAACTGTTGC[A/T]AATTGATTAGATGAG | 79582 |
rs71428328 | snp | A/G | 0.250732 | 0.249999 | intron-variant | SPAG16 | GRCh38.p7 | 2:214112204 | TTTCTGTTCTTTTAC[A/G]TTTGCTGAGGAGTGC | 79582 |
rs71428329 | snp | A/T | 0.223225 | 0.248562 | intron-variant | SPAG16 | GRCh38.p7 | 2:214112599 | TGATCTTTGTTGGTT[A/T]AAAGTCTGTTTTATC | 79582 |
rs71428330 | snp | C/T | 0.0146672 | 0.084371 | intron-variant | SPAG16 | GRCh38.p7 | 2:214116349 | CCCATATTCTCTCAA[C/T]CTGGGAGTCTAAGCC | 79582 |
rs71428331 | snp | C/G | 0.154329 | 0.23097 | intron-variant | SPAG16 | GRCh38.p7 | 2:214119839 | TGTATATCTGGAAAT[C/G]TCATTATTTTATTTT | 79582 |
rs71428332 | snp | A/T | 0.5 | 0 | intron-variant | SPAG16 | GRCh38.p7 | 2:214133106 | TCAAATAAAATAAAA[A/T]AAATAAATAAATAAA | 79582 |
rs71428333 | snp | C/G | 0.5 | 0 | intron-variant | SPAG16 | GRCh38.p7 | 2:214146927 | GAATGGCGTTAACCC[C/G]GGAGACGGACATTGC | 79582 |
rs71428334 | snp | C/T | 0.00358779 | 0.0422022 | intron-variant | SPAG16 | GRCh38.p7 | 2:214302205 | TAGGCAAATATGTAA[C/T]TATTTTTGAAGAATG | 79582 |
rs71428335 | snp | A/C | 0.00358779 | 0.0422022 | intron-variant | SPAG16 | GRCh38.p7 | 2:214336335 | AGCATAATCCAGTTA[A/C]ATTTTAAAAGTATTT | 79582 |
rs71428336 | snp | G/T | 0.5 | 0 | intron-variant | SPAG16 | GRCh38.p7 | 2:214361569 | ACTTCATCCAGGTTG[G/T]TTTGTTTAAGCATAT | 79582 |
rs71461376 | snp | A/G | 0.5 | 0 | intron-variant | SPAG16 | GRCh38.p7 | 2:213733085 | TAACTGGTGTGAGAT[A/G]GTATCTCATTGTGGT | 79582 |
rs71490651 | snp | C/G | 0.5 | 0 | intron-variant | SPAG16 | GRCh38.p7 | 2:213733038 | AAAGTCAGGAAACAA[C/G]AGGTGCTGGAGAGGA | 79582 |
rs71498373 | snp | C/T | 0 | 0 | intron-variant | SPAG16 | GRCh38.p7 | 2:213823020 | ATGTTTATTGCGGCA[C/T]TATTCACAATAGCAA | 79582 |
rs71498374 | snp | A/G | 0 | 0 | intron-variant | SPAG16 | GRCh38.p7 | 2:213823006 | ATTATTCACAATAGC[A/G]AAGACTTGGAACCAA | 79582 |
rs71498375 | snp | C/G | 0 | 0 | intron-variant | SPAG16 | GRCh38.p7 | 2:213822990 | AAGACTTGGAACCAA[C/G]CCAAATGTCCAACAA | 79582 |
rs71502877 | snp | A/G | 0 | 0 | intron-variant | SPAG16 | GRCh38.p7 | 2:213733074 | ATACCATCTCACACC[A/G]GTTAGAATGGCAATC | 79582 |
rs71525218 | snp | C/T | 0.5 | 0 | intron-variant | SPAG16 | GRCh38.p7 | 2:213733020 | GTGCTGGAGAGGATG[C/T]GGAGAAATAGGAACA | 79582 |
rs71575403 | snp | C/G | 0.5 | 0 | intron-variant | SPAG16 | GRCh38.p7 | 2:213733075 | ATTGCCATTCTAACT[C/G]GTGTGAGATGGTATC | 79582 |
rs71599079 | snp | G/T | 0.5 | 0 | intron-variant | SPAG16 | GRCh38.p7 | 2:213733055 | TGTTTCCTGACTTTT[G/T]AATGATTGCCATTCT | 79582 |
rs71620352 | snp | G/T | 0 | 0 | intron-variant | SPAG16 | GRCh38.p7 | 2:213733057 | TTAGAATGGCAATCA[G/T]TAAAAAGTCAGGAAA | 79582 |
rs71635656 | snp | G/T | 0.5 | 0 | intron-variant | SPAG16 | GRCh38.p7 | 2:213733064 | ACATCAGTTAGAATG[G/T]CAATCATTAAAAAGT | 79582 |
rs71640843 | snp | A/C | 0.5 | 0 | intron-variant | SPAG16 | GRCh38.p7 | 2:213733077 | GAGATACCATCTCAC[A/C]CCAGTTAGAATGGCA | 79582 |
rs71798133 | in-del | -/ATAT/TA/TATA | | | intron-variant | SPAG16, LOC101928084 | GRCh38.p7 | 2:214092512 | TATATATAAATATAT[-/ATAT/TA/TATA]ATATATATATGGCCC | 79582 |
rs71849901 | in-del | -/TATCTGTC | | | intron-variant | SPAG16 | GRCh38.p7 | 2:213715261 | TCTATCTATCTATCT[-/TATCTGTC]ATCTATCCATTCATC | 79582 |
rs71859265 | in-del | -/ACACAC | | | intron-variant | SPAG16 | GRCh38.p7 | 2:213928905 | CTTGCAGCTGATGTT[-/ACACAC]ACACACACACACACA | 79582 |
rs71865943 | in-del | -/ATAT | | | intron-variant | SPAG16 | GRCh38.p7 | 2:213522805 | CATGCCAAATATATA[-/ATAT]TATATATATAACAAA | 79582 |
rs71893851 | in-del | -/AG | 0.230603 | 0.249246 | intron-variant, upstream-variant-2KB | SPAG16, LOC101928084 | GRCh38.p7 | 2:214103944 | GGGAGAGAGGGAAAC[-/AG]AGAGAGAGAGAGAGA | 79582 |
rs71899530 | in-del | -/ATATATATATATATATATATAT | | | intron-variant | SPAG16 | GRCh38.p7 | 2:213932148 | TTGGCTTGATACTGC[-/ATATATATATATATATATATAT]ATATATATATATATA | 79582 |
rs71916808 | in-del | -/ACAC | | | intron-variant | SPAG16 | GRCh38.p7 | 2:214056281 | AGATGTAGTAGAAAT[-/ACAC]ACACACACACACACA | 79582 |
rs71932829 | in-del | -/A | | | intron-variant | SPAG16 | GRCh38.p7 | 2:213489082 | TCCATCTCAAAAACG[-/A]AAAAAAAAAAAAAAA | 79582 |
rs71937382 | in-del | -/ACACACACAC | | | intron-variant | SPAG16 | GRCh38.p7 | 2:213310320 | AGCCCTGAAACCACA[-/ACACACACAC]ACACACACACACACA | 79582 |
rs71945400 | in-del | -/T | 0.479984 | 0.0980171 | intron-variant | SPAG16 | GRCh38.p7 | 2:213868350 | CATCTTTTTGATTTG[-/T]TTTTTTGCACAATAT | 79582 |
rs71955587 | in-del | -/TG | 0.479744 | 0.0985793 | intron-variant | SPAG16 | GRCh38.p7 | 2:213890590 | ATAATTAAAGATGAC[-/TG]TTATTTATTATTTTG | 79582 |
rs71975870 | in-del | -/TAT | | | intron-variant | SPAG16 | GRCh38.p7 | 2:214248288 | TGGGTACTATTCTTA[-/TAT]TATTATTATTATTAT | 79582 |
rs72042440 | in-del | -/CACA | | | intron-variant | SPAG16 | GRCh38.p7 | 2:214062010 | CACACACACACACAC[-/CACA]ACACACACACGCAGT | 79582 |
rs72062288 | in-del | -/TGTATATATA | | | intron-variant | SPAG16 | GRCh38.p7 | 2:213377880 | AGAACTAATAGGATG[-/TGTATATATA]TATATATATATATAT | 79582 |
rs72076607 | in-del | -/TCATTTGTACCTAAAAGACCAAGGGCACAGAAGGGAGA | 0.0189856 | 0.0955633 | intron-variant | SPAG16 | GRCh38.p7 | 2:213863134 | TCACTGAACCTAAAT[lengthTooLong]TCATTCTTAAAGACA | 79582 |
rs72078589 | in-del | -/CTTAT | 0.171704 | 0.237423 | intron-variant | SPAG16 | GRCh38.p7 | 2:213484096 | TTTTATGGCTTCAGC[-/CTTAT]CTTATATGAGTCAAA | 79582 |
rs72079812 | in-del | -/T | 0.0766824 | 0.180169 | intron-variant | SPAG16 | GRCh38.p7 | 2:213706740 | AATGAAAACTTTTTG[-/T]TTTTTTTCCTCACAG | 79582 |
rs72094401 | in-del | -/TG | 0.0482946 | 0.147699 | intron-variant | SPAG16 | GRCh38.p7 | 2:213377878 | ATAGAACTAATAGGA[-/TG]TGTATATATATATAT | 79582 |
rs72094644 | in-del | -/ATAT | 0.289683 | 0.24683 | intron-variant | SPAG16 | GRCh38.p7 | 2:213860343 | AAAAGTCATTTACAG[-/ATAT]ATATATATATATATA | 79582 |
rs72103102 | in-del | -/CA | | | intron-variant | SPAG16 | GRCh38.p7 | 2:213385793 | TTCTTCATCTCTGTC[-/CA]CACACACACACACAC | 79582 |
rs72116571 | in-del | -/CTTC | | | intron-variant | SPAG16 | GRCh38.p7 | 2:213694792 | TTCCTTCCTTCCTTC[-/CTTC]TACTCTCCCTTGCCT | 79582 |
rs72116627 | in-del | -/ATA | | | intron-variant | SPAG16 | GRCh38.p7 | 2:213860437 | GTATATCTATATATT[-/ATA]TATAGATATATGTAT | 79582 |
rs72119233 | in-del | -/AT | | | intron-variant | SPAG16 | GRCh38.p7 | 2:213545609 | TTTTACATTGAAACG[-/AT]TGATCAATTATGGAA | 79582 |
rs72125279 | in-del | -/AC | 0.499323 | 0.0183822 | intron-variant | SPAG16 | GRCh38.p7 | 2:213847863 | TAATATAAACAAATG[-/AC]ACACACACACACACA | 79582 |
rs72150625 | in-del | -/TG | 0.154993 | 0.231244 | intron-variant | SPAG16 | GRCh38.p7 | 2:213440109 | AAATTCCTGCAGTTT[-/TG]TGTGTGTGTGTGTGT | 79582 |
rs72157076 | in-del | -/CTC | 0.0189856 | 0.0955633 | intron-variant | SPAG16 | GRCh38.p7 | 2:213863398 | CATGTTTTCACTAAA[-/CTC]CTTTTTTAAATCAGT | 79582 |
rs72164089 | in-del | -/TG | | | intron-variant | SPAG16 | GRCh38.p7 | 2:214268754 | GAAGGGTGTGTGTGT[-/TG]GTGTGTGGGTGTGTA | 79582 |
rs72175579 | in-del | -/A | | | intron-variant | SPAG16 | GRCh38.p7 | 2:213843696 | CTCTACTAAAAATAC[-/A]AAAAATTAGCTAGGT | 79582 |
rs72198417 | in-del | -/TA | | | intron-variant | SPAG16, LOC101928084 | GRCh38.p7 | 2:214092518 | ATAAATATATATATA[-/TA]TATGGCCCTTTATCT | 79582 |
rs72200284 | in-del | -/A | 0 | 0 | intron-variant | SPAG16 | GRCh38.p7 | 2:213867775 | CTCCACTAAAAATAC[-/A]AAAAAAAATAGCCGG | 79582 |
rs72209225 | in-del | -/AGAG | 0.00557542 | 0.0525036 | intron-variant | SPAG16 | GRCh38.p7 | 2:213705263 | AAAAATAAGAAAGAA[-/AGAG]AGAGAGAGGGAGGGA | 79582 |
rs72225471 | in-del | -/CTCT | | | intron-variant | SPAG16 | GRCh38.p7 | 2:214181851 | TGTGGTTGAAAGGCT[-/CTCT]ATCTACCATGCCTCT | 79582 |
rs72265888 | in-del | -/TATATATG | | | intron-variant | SPAG16 | GRCh38.p7 | 2:213860358 | ATATATATATATATA[-/TATATATG]TGTGTGTGTGTATAT | 79582 |
rs72309764 | in-del | -/TT | 0.468463 | 0.121548 | intron-variant | SPAG16 | GRCh38.p7 | 2:213868250 | TTATAAAAATGAGAA[-/TT]TTTTTTTTATTTTAG | 79582 |
rs72315187 | in-del | -/G | 0.127599 | 0.217986 | intron-variant | SPAG16 | GRCh38.p7 | 2:213412634 | TGTTTATTTTTTTTT[-/G]TTTGTTTGGCTTTTC | 79582 |
rs72346596 | in-del | -/TA | | | intron-variant | SPAG16 | GRCh38.p7 | 2:214059223 | ATATATATGTATGTG[-/TA]TATATATATATATAT | 79582 |
rs72404991 | in-del | -/GT | | | intron-variant | SPAG16 | GRCh38.p7 | 2:213325632 | AATATGTGTGTGTGT[-/GT]GTGTGTGTGTGCATA | 79582 |
rs72411246 | in-del | -/T/TT | | | intron-variant | SPAG16 | GRCh38.p7 | 2:213733229 | GGGTTGTTTTTTTTT[-/T/TT]TCTTGTAAATTTAAG | 79582 |
rs72441932 | in-del | -/TCTA | | | intron-variant | SPAG16 | GRCh38.p7 | 2:213802396 | CAAATGATTCATGTC[-/TCTA]TCTATCTATCTATCT | 79582 |
rs72448292 | in-del | -/ACTTAA | 0.153 | 0.230415 | intron-variant | SPAG16 | GRCh38.p7 | 2:214168869 | ATGTGGTACTATTTT[-/ACTTAA]TGGTGGGAAACTGTG | 79582 |
rs72450217 | in-del | -/AGAA | 0.479984 | 0.0980171 | intron-variant | SPAG16 | GRCh38.p7 | 2:213867479 | TCTCTTCTGCAAAAT[-/AGAA]AGAATAATGATGCCT | 79582 |
rs72492763 | snp | C/T | 0.00835141 | 0.0640778 | intron-variant | SPAG16 | GRCh38.p7 | 2:213584183 | CATTTCTTCATTGGA[C/T]TTTTTTTTATACTAG | 79582 |
rs72492766 | snp | A/C | | | intron-variant | SPAG16 | GRCh38.p7 | 2:213904615 | CAAAAAAAAAAAAAA[A/C]AAAAAACAAAGTAGG | 79582 |
rs72531304 | in-del | -/A | | | intron-variant | SPAG16 | GRCh38.p7 | 2:214254785 | AAAGATATATTTAGT[-/A]TGGGGGAAAACTCAT | 79582 |
rs72546139 | in-del | -/G | | | intron-variant | SPAG16 | GRCh38.p7 | 2:213511165 | CTGTTGGTATTCAGA[-/G]TTTTACACATTGACT | 79582 |
rs72546140 | in-del | -/AT | | | intron-variant | SPAG16 | GRCh38.p7 | 2:213545607 | ACTTTTACATTGAAA[-/AT]CGTGATCAATTATGG | 79582 |
rs72584991 | in-del | -/A | | | intron-variant | SPAG16 | GRCh38.p7 | 2:213826226 | AATTGAAATAAAAAA[-/A]ACACAAAAGATCAAT | 79582 |
rs72613744 | snp | A/G | 0.113334 | 0.209338 | intron-variant | SPAG16 | GRCh38.p7 | 2:213926024 | TCTTTCCAAACATGT[A/G]GTTCTAGGTCTTAAA | 79582 |
rs72638286 | snp | C/T | 0.0197687 | 0.0974348 | intron-variant | SPAG16 | GRCh38.p7 | 2:213356513 | ATAAACTAGAAAATT[C/T]AGAATAAATGGATAA | 79582 |
rs72934009 | snp | C/T | 0.174288 | 0.23826 | intron-variant | SPAG16 | GRCh38.p7 | 2:213964221 | TACATGTAGTATATG[C/T]ATACTATTTTATATA | 79582 |
rs72934017 | snp | A/C | 0.192715 | 0.243348 | intron-variant | SPAG16 | GRCh38.p7 | 2:213968069 | TACAAATTCAAAATT[A/C]CTTTCCTTTCCTTTC | 79582 |
rs72934026 | snp | C/T | 0.322245 | 0.239334 | intron-variant | SPAG16 | GRCh38.p7 | 2:213973033 | TGACGATTAATTCTG[C/T]GCTGGGTCACTCTTT | 79582 |
rs72934028 | snp | C/T | 0.166832 | 0.235761 | intron-variant | SPAG16 | GRCh38.p7 | 2:213973777 | TTGGAGCTGCCTAAT[C/T]TGGTGTTTTGTGGAT | 79582 |
rs72934031 | snp | A/C | 0.0232847 | 0.105357 | intron-variant | SPAG16 | GRCh38.p7 | 2:213975574 | TTTATAATTAAGTAA[A/C]ATAGAAAAGAAATAA | 79582 |
rs72934033 | snp | G/T | 0.162581 | 0.234218 | intron-variant | SPAG16 | GRCh38.p7 | 2:213975627 | GTAGCGGGGAAAACA[G/T]AAAATTCACCTGTTA | 79582 |
rs72934041 | snp | A/G | 0.130351 | 0.219509 | intron-variant | SPAG16 | GRCh38.p7 | 2:213983646 | ACAATATGAGTTTTT[A/G]TATCAATAATTTCAC | 79582 |
rs72934086 | snp | A/G | 0.450609 | 0.149185 | intron-variant | SPAG16 | GRCh38.p7 | 2:214014920 | GACAAGCTGGAAAGC[A/G]TAGCCTCCAGCCAGA | 79582 |
rs72934089 | snp | G/T | 0.157311 | 0.232183 | intron-variant | SPAG16 | GRCh38.p7 | 2:214015244 | AGTGGTCTCTTATCA[G/T]GCTAAAAGAGGAAGG | 79582 |
rs72935111 | snp | A/G | 0.0162398 | 0.0886349 | intron-variant | SPAG16 | GRCh38.p7 | 2:213287805 | CCCTGAAATATGAGG[A/G]TCACACTAGACTGAT | 79582 |
rs72935115 | snp | C/T | 0.0115144 | 0.0749975 | intron-variant | SPAG16 | GRCh38.p7 | 2:213290000 | CATACCAATTGGCAC[C/T]TCAAGCTCTGCGCCA | 79582 |
rs72935120 | snp | A/G | 0.209997 | 0.246779 | intron-variant | SPAG16 | GRCh38.p7 | 2:213291641 | TAATATAACACTTGA[A/G]AGTTTTTGGAAAAAA | 79582 |
rs72935122 | snp | A/G | 0.209997 | 0.246779 | intron-variant | SPAG16 | GRCh38.p7 | 2:213291790 | TTGTCATTCACAGCT[A/G]TGTGATCTTGGGCAA | 79582 |
rs72935124 | snp | A/G | 0.325563 | 0.238307 | intron-variant | SPAG16 | GRCh38.p7 | 2:213291855 | AATTTAGAGATGGGT[A/G]TATCTGTGCTGTTTG | 79582 |
rs72935129 | snp | A/C | 0.209997 | 0.246779 | intron-variant | SPAG16 | GRCh38.p7 | 2:213291955 | TGGTAGTTATGTACT[A/C]TCTTAATCTTTTTTG | 79582 |
rs72935143 | snp | A/C | 0.200182 | 0.244986 | intron-variant | SPAG16 | GRCh38.p7 | 2:213293869 | TTGTGAAATGATTAC[A/C]ACACCCAAGCTAATT | 79582 |
rs72935145 | snp | C/G | 0.191147 | 0.242974 | intron-variant | SPAG16 | GRCh38.p7 | 2:213293933 | TTTATATTACTTGTG[C/G]TGAGAATATTTAAGA | 79582 |
rs72935148 | snp | C/T | 0.19646 | 0.2442 | intron-variant | SPAG16 | GRCh38.p7 | 2:213294060 | TGAATGTTTGTGCAA[C/T]GTTGATGAACATCCC | 79582 |
rs72935154 | snp | C/T | 0.19646 | 0.2442 | intron-variant, upstream-variant-2KB | SPAG16 | GRCh38.p7 | 2:213297644 | TAAACCAATAATTTT[C/T]AACATTTATGTTTAG | 79582 |
rs72935161 | snp | C/T | 0.0162398 | 0.0886349 | intron-variant, utr-variant-5-prime | SPAG16 | GRCh38.p7 | 2:213299681 | TGTATTTGATACTAT[C/T]CGTTTTCTTAGTGGG | 79582 |
rs72935164 | snp | C/T | 0.19646 | 0.2442 | intron-variant, utr-variant-5-prime | SPAG16 | GRCh38.p7 | 2:213299873 | CAAGTAAAGGTAGGA[C/T]TATATATATGTTCGT | 79582 |
rs72935166 | snp | C/G | 0.19646 | 0.2442 | intron-variant, utr-variant-5-prime | SPAG16 | GRCh38.p7 | 2:213299887 | ATTATATATATGTTC[C/G]TTAGATTGTGTCTGT | 79582 |
rs72935168 | snp | A/G | 0.0166325 | 0.0896639 | intron-variant, utr-variant-5-prime | SPAG16 | GRCh38.p7 | 2:213300377 | GACTGACCCAAGCGA[A/G]AATGTTCTTTACCAT | 79582 |
rs72935174 | snp | A/G | 0.19646 | 0.2442 | intron-variant, utr-variant-5-prime | SPAG16 | GRCh38.p7 | 2:213301811 | TTTGGCCCTTTCTCC[A/G]TAAGACCCTGAGCCT | 79582 |
rs72935177 | snp | A/G | 0.196149 | 0.244131 | intron-variant, utr-variant-5-prime | SPAG16 | GRCh38.p7 | 2:213301921 | TTGTATTTCCTCATC[A/G]TCTGTAACGTTCAAC | 79582 |
rs72935187 | snp | A/T | 0.212122 | 0.247114 | intron-variant | SPAG16 | GRCh38.p7 | 2:213307160 | ATGTCATAGCAGCTA[A/T]CAGTAATAAACATCA | 79582 |
rs72935193 | snp | A/G | 0.212122 | 0.247114 | intron-variant | SPAG16 | GRCh38.p7 | 2:213309935 | AATGGTTCCTGGCAT[A/G]TAACAGTCAACAAAC | 79582 |
rs72935209 | snp | G/T | 0.375 | 0.216506 | intron-variant | SPAG16 | GRCh38.p7 | 2:213731464 | CATGTCCAGCTGTTT[G/T]TTTTTTTTTTTTTCT | 79582 |
rs72935907 | snp | C/T | 0.00716266 | 0.059414 | intron-variant | SPAG16 | GRCh38.p7 | 2:214024593 | AATACATTCTAAACT[C/T]AAAGATATTTGTTTA | 79582 |
rs72935939 | snp | C/T | 0.477515 | 0.103619 | intron-variant | SPAG16 | GRCh38.p7 | 2:214033805 | CACCTCCAAATATAC[C/T]AGGGTATAATATCTA | 79582 |
rs72935955 | snp | A/G | 0.48155 | 0.0942576 | intron-variant | SPAG16 | GRCh38.p7 | 2:214037970 | TATGTTTTGGATGCA[A/G]AACATATTGGGTTTT | 79582 |
rs72935964 | snp | A/C | 0.124491 | 0.216211 | intron-variant | SPAG16 | GRCh38.p7 | 2:214039690 | ACTTAACTGGCTATA[A/C]AATTTTTCATTCATA | 79582 |
rs72935985 | snp | A/G | 0.175897 | 0.238765 | intron-variant | SPAG16 | GRCh38.p7 | 2:214048083 | GAACCCTCCTCATAC[A/G]CTGTTGGTGGTAATG | 79582 |
rs72935988 | snp | A/G | 0.158302 | 0.232576 | intron-variant | SPAG16 | GRCh38.p7 | 2:214048532 | CTATGGAGATAGAGA[A/G]TAGGATGATTACCAG | 79582 |
rs72936000 | snp | A/C | 0.322483 | 0.239262 | intron-variant | SPAG16 | GRCh38.p7 | 2:214052761 | ATTTTTCTTCTCATA[A/C]TTCCCCTCTGTTTGC | 79582 |
rs72937005 | snp | C/T | 0.212122 | 0.247114 | intron-variant | SPAG16 | GRCh38.p7 | 2:213312667 | CTGAAGGTAGGGTGG[C/T]AATGAAAATGCCATC | 79582 |
rs72937008 | snp | A/G | 0.212122 | 0.247114 | intron-variant | SPAG16 | GRCh38.p7 | 2:213312715 | TATTTATAACATTTA[A/G]TTACTAATTTAATTT | 79582 |
rs72937011 | snp | A/T | 0.212122 | 0.247114 | intron-variant | SPAG16 | GRCh38.p7 | 2:213312735 | TAATTTAATTTTTTT[A/T]AATAATGGAAGAGAT | 79582 |
rs72937040 | snp | C/T | 0.232943 | 0.249417 | intron-variant | SPAG16 | GRCh38.p7 | 2:213322962 | CCAGTGGGTTAGTGG[C/T]AGAGGCCTTTGCTAG | 79582 |
rs72937041 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | SPAG16 | GRCh38.p7 | 2:213324132 | CATGTTACCTTCTTA[A/C]CATATACTCAAAGAA | 79582 |
rs72937048 | snp | A/T | 0.211516 | 0.24702 | intron-variant | SPAG16 | GRCh38.p7 | 2:213325800 | TGAATTATCTAATGT[A/T]TATATTTTGTTGTTG | 79582 |
rs72937049 | snp | A/T | 0.211212 | 0.246973 | intron-variant | SPAG16 | GRCh38.p7 | 2:213325895 | GTGCCTGGTACATAG[A/T]AGGAGCTTAAGTGAT | 79582 |
rs72937056 | snp | A/T | 0.210909 | 0.246925 | intron-variant | SPAG16 | GRCh38.p7 | 2:213327202 | TGCTCTACTAATGTG[A/T]TGAGGAAATATTATA | 79582 |
rs72937070 | snp | A/G | 0.174288 | 0.23826 | intron-variant | SPAG16 | GRCh38.p7 | 2:213338923 | GCGAACGTATGCTGC[A/G]CTTAATAGCTAGGTG | 79582 |
rs72937075 | snp | A/G | 0.0162398 | 0.0886349 | intron-variant, upstream-variant-2KB | SPAG16 | GRCh38.p7 | 2:213343344 | TCCAAAAAGCTTAAA[A/G]GTAAGCTTTGAAAAA | 79582 |
rs72937077 | snp | A/G | 0.377582 | 0.214995 | intron-variant | SPAG16 | GRCh38.p7 | 2:213343961 | TGCTAGCTTATTCCA[A/G]TTGTTAAGTATACAA | 79582 |
rs72937079 | snp | A/C | 0.377385 | 0.215112 | intron-variant | SPAG16 | GRCh38.p7 | 2:213344180 | TCCCCAGTACATAGT[A/C]ACTCAATTAAATAGC | 79582 |
rs72937090 | snp | C/T | 0.00318978 | 0.0398085 | intron-variant | SPAG16 | GRCh38.p7 | 2:213352515 | ATCTCCCATATACCA[C/T]GTACAATATTTGTGT | 79582 |
rs72937097 | snp | G/T | 0.212425 | 0.24716 | intron-variant | SPAG16 | GRCh38.p7 | 2:213358152 | GATGAGCTTCCCCTT[G/T]TATGTAACCTGCCCT | 79582 |
rs72937101 | snp | C/T | 0.193653 | 0.243567 | intron-variant | SPAG16 | GRCh38.p7 | 2:213359934 | AAAATTCTAAAGAGC[C/T]AATTTCTTGATATCT | 79582 |
rs72937224 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | SPAG16 | GRCh38.p7 | 2:213800158 | TGCAATCTTAGCTTC[C/T]ATGCAGCAATATTAC | 79582 |
rs72937226 | snp | A/G | 0.00914312 | 0.0669923 | intron-variant | SPAG16 | GRCh38.p7 | 2:213802185 | AGAGATGATAAGGGG[A/G]GGAATGTTTTAGTTC | 79582 |
rs72937229 | snp | C/T | 0.00159617 | 0.0282053 | intron-variant | SPAG16 | GRCh38.p7 | 2:213802381 | TGTTTACTTAAAACC[C/T]AAATGATTCATGTCT | 79582 |
rs72937235 | snp | A/T | 0.0558544 | 0.157504 | intron-variant | SPAG16 | GRCh38.p7 | 2:213803727 | CTCTTTAACTTTTTT[A/T]AAAAATGTATTATGT | 79582 |
rs72937911 | snp | A/T | | | intron-variant | SPAG16 | GRCh38.p7 | 2:214061140 | AATATCTTCAAACGG[A/T]TCTCCTGAAGCATTT | 79582 |
rs72937917 | snp | C/T | 0.0023933 | 0.0345097 | intron-variant | SPAG16 | GRCh38.p7 | 2:214066872 | ATTCTTTGATTTCAA[C/T]TTTCCAAGGAAAAAT | 79582 |
rs72937941 | snp | A/G | 0.217851 | 0.247924 | intron-variant | SPAG16, LOC101928084 | GRCh38.p7 | 2:214090135 | ATAAAAGCTTTTGCA[A/G]AAGAGATATATGGAG | 79582 |
rs72937950 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | SPAG16, LOC101928084 | GRCh38.p7 | 2:214094959 | GGATGAAACTTTTGA[A/G]AGGACTTGGGGAGGG | 79582 |
rs72937953 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | SPAG16, LOC101928084 | GRCh38.p7 | 2:214095391 | TCAAATTAATCACAC[A/G]TGTCTATCATACACG | 79582 |
rs72937967 | snp | A/G | 0.202343 | 0.245416 | intron-variant, upstream-variant-2KB | SPAG16, LOC101928084 | GRCh38.p7 | 2:214103211 | TTAATGTTCACAAGC[A/G]TGGACCATCAGGAGA | 79582 |
rs72937973 | snp | A/G/T | 0 | 0 | intron-variant, upstream-variant-2KB | SPAG16, LOC101928084 | GRCh38.p7 | 2:214103968 | GAGAGAGACAGTGAG[A/G/T]GAGGGAGGGAGAGAG | 79582 |
rs72937975 | snp | C/T | 0.5 | 0 | intron-variant, upstream-variant-2KB | SPAG16, LOC101928084 | GRCh38.p7 | 2:214103976 | TGTTCTCTCTCTCTC[C/T]CTCCCTCTCTCACTG | 79582 |
rs72937980 | snp | C/T | 0.25214 | 0.249991 | intron-variant, upstream-variant-2KB | SPAG16, LOC101928084 | GRCh38.p7 | 2:214104372 | TGACATGGTCTGATT[C/T]AGCTTTTGTTGGTTG | 79582 |
rs72937985 | snp | A/G | | | intron-variant | SPAG16 | GRCh38.p7 | 2:214109541 | CAAAATTCTGTTACC[A/G]TCCTGCTAGTATCAT | 79582 |
rs72937990 | snp | A/T | 0.214239 | 0.247429 | intron-variant | SPAG16 | GRCh38.p7 | 2:214115974 | CAGGAGTTTCAGGAT[A/T]CAGGTAGGAGGCTGC | 79582 |
rs72937993 | snp | C/G | 0.16028 | 0.233346 | intron-variant | SPAG16 | GRCh38.p7 | 2:214116916 | AGACTGTGAAGACTG[C/G]AACAAATACCCAGTC | 79582 |
rs72938000 | snp | C/T | 0.256619 | 0.249912 | intron-variant | SPAG16 | GRCh38.p7 | 2:214120223 | TCCTGTGCTTTACTA[C/T]TTTGTGTGGCATCCC | 79582 |
rs72939003 | snp | A/C | 0.212425 | 0.24716 | intron-variant | SPAG16 | GRCh38.p7 | 2:213360029 | AGGATTTATAAATAG[A/C]TTTTCTCTCTCAACC | 79582 |
rs72939007 | snp | G/T | 0.396727 | 0.202413 | intron-variant | SPAG16 | GRCh38.p7 | 2:213361547 | AGGAAAGGAAACAGG[G/T]TTCTTTGGAGAAGTG | 79582 |
rs72939041 | snp | A/G | 0.0166325 | 0.0896639 | intron-variant | SPAG16 | GRCh38.p7 | 2:213374164 | TCTAGAACTGGTATC[A/G]AATAGAAAAAATTAG | 79582 |
rs72939043 | snp | A/T | 0.213333 | 0.247296 | intron-variant | SPAG16 | GRCh38.p7 | 2:213374559 | ACTATTTTGAATATT[A/T]CCCTGTGTTTTTCCT | 79582 |
rs72939045 | snp | C/T | 0.17654 | 0.238964 | intron-variant | SPAG16 | GRCh38.p7 | 2:213376927 | AAGATTTCTCTTTTA[C/T]AAACAGTCGCTCTCT | 79582 |
rs72939053 | snp | C/T | 0.213937 | 0.247385 | intron-variant | SPAG16 | GRCh38.p7 | 2:213380775 | CCTATGGAGGCAGCA[C/T]TGGATCTGCTGGGTT | 79582 |
rs72939055 | snp | A/G | 0.213635 | 0.247341 | intron-variant | SPAG16 | GRCh38.p7 | 2:213381032 | TATTTCAAGAATACA[A/G]TCAGAAGCCAGGGAA | 79582 |
rs72939056 | snp | A/G | 0.213635 | 0.247341 | intron-variant | SPAG16 | GRCh38.p7 | 2:213381313 | TTCTGTAGTGAACCC[A/G]ACATGATACAATGAA | 79582 |
rs72939057 | snp | A/G | 0.00755907 | 0.0610114 | intron-variant | SPAG16 | GRCh38.p7 | 2:213383077 | TACATGATTCTCTCA[A/G]TCTTGTACCCCATTA | 79582 |
rs72939063 | snp | A/T | 0.0166325 | 0.0896639 | intron-variant | SPAG16 | GRCh38.p7 | 2:213388574 | AACAATAAATTTTTT[A/T]AAAAAATAAATAAAC | 79582 |
rs72939065 | snp | C/G | 0.0174175 | 0.0916809 | intron-variant | SPAG16 | GRCh38.p7 | 2:213389151 | TGACAATAGTACCAA[C/G]ACCAATCAATGGGGA | 79582 |
rs72939072 | snp | A/G | 0.213635 | 0.247341 | intron-variant | SPAG16 | GRCh38.p7 | 2:213394485 | TCTTGGAAAACTATA[A/G]TATAGTATCAAGATT | 79582 |
rs72939075 | snp | A/G | 0.214239 | 0.247429 | intron-variant | SPAG16 | GRCh38.p7 | 2:213405486 | TGTTGGGAACATTCC[A/G]AATATTCTTTTCTGG | 79582 |
rs72939086 | snp | G/T | 0.212425 | 0.24716 | intron-variant | SPAG16 | GRCh38.p7 | 2:213410021 | AAAGAAAGAAAACTT[G/T]AGCGATCCTGGGAAG | 79582 |
rs72939090 | snp | C/T | 0.212728 | 0.247206 | intron-variant | SPAG16 | GRCh38.p7 | 2:213416914 | TTACTGAGGTTTCCA[C/T]AGGAAGGGCAAGGCA | 79582 |
rs72939091 | snp | A/G | 0.193966 | 0.243639 | intron-variant | SPAG16 | GRCh38.p7 | 2:213417673 | AAAGTATATTAAGGC[A/G]TAACGAAGAAACTAA | 79582 |
rs72939092 | snp | C/T | 0.00110635 | 0.0234936 | intron-variant | SPAG16 | GRCh38.p7 | 2:213422259 | TTCCAAGCATCCAGA[C/T]GCCACTGAATTCTCA | 79582 |
rs72939095 | snp | A/G | 0.0193772 | 0.0965046 | intron-variant | SPAG16 | GRCh38.p7 | 2:213430157 | CTTAAAAACAAACAC[A/G]CAGAACTTCTGGAAA | 79582 |
rs72939099 | snp | A/C | 0.0158469 | 0.0875917 | intron-variant | SPAG16 | GRCh38.p7 | 2:213439673 | AGGAATGAAGTCTGC[A/C]TGGTTTTGAAAATCC | 79582 |
rs72939102 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | SPAG16 | GRCh38.p7 | 2:213442715 | AACAATTGGACACTC[A/G]TAAAAAAATAAATCT | 79582 |
rs72939297 | snp | C/G | 0.337841 | 0.23406 | intron-variant | SPAG16 | GRCh38.p7 | 2:213836855 | CTGACCTCAGGTGAT[C/G]CCCCGGTCTCAGCCT | 79582 |
rs72939299 | snp | A/G | 0.33533 | 0.234987 | intron-variant | SPAG16 | GRCh38.p7 | 2:213837554 | TTTTGCAACTAAGAC[A/G]TCGGGCTATTTTCAT | 79582 |
rs72939301 | snp | A/T | 0.0023933 | 0.0345097 | intron-variant | SPAG16 | GRCh38.p7 | 2:213841008 | GTGTCTGAAATAGAC[A/T]TCATGGCTCTGGAGA | 79582 |
rs72939547 | snp | A/G | 0.00835141 | 0.0640778 | intron-variant | SPAG16 | GRCh38.p7 | 2:214408333 | ATTTGGGAAAGTCAC[A/G]AACAGCAATTGCCTA | 79582 |
rs72939904 | snp | A/G | 0.210605 | 0.246877 | intron-variant | SPAG16 | GRCh38.p7 | 2:214120955 | GAAACTTGCTTTCCC[A/G]TAATCCACACTGATT | 79582 |
rs72939915 | snp | A/G | 0.46974 | 0.119223 | intron-variant | SPAG16 | GRCh38.p7 | 2:214139533 | TCTGTAGAAAAGAGC[A/G]TCTTCAATTTAATTC | 79582 |
rs72939923 | snp | A/G | 0.165527 | 0.235296 | intron-variant | SPAG16 | GRCh38.p7 | 2:214145196 | ACCATATATAAATAC[A/G]TTTGGAACCTCTGTG | 79582 |
rs72939951 | snp | G/T | 0.140919 | 0.224948 | intron-variant | SPAG16 | GRCh38.p7 | 2:214163750 | GCAAACAGTCTAGAG[G/T]CTCAGAAAAACTTGA | 79582 |
rs72939953 | snp | A/C | 0.0930568 | 0.194599 | intron-variant | SPAG16 | GRCh38.p7 | 2:214164597 | CCAACGCTGGTCTTT[A/C]TTCTAAAAAGAAGAA | 79582 |
rs72940908 | snp | G/T | 0.00755907 | 0.0610114 | intron-variant | SPAG16 | GRCh38.p7 | 2:213460423 | TACCCCTTTCTAGTT[G/T]TTTCCCTCTGCTGAA | 79582 |
rs72940924 | snp | C/T | 0.0126979 | 0.078662 | intron-variant | SPAG16 | GRCh38.p7 | 2:213494816 | CCACTCTCCCTTGCC[C/T]TATCTCCTCAATGAC | 79582 |
rs72940945 | snp | A/G | 0.150333 | 0.229274 | intron-variant | SPAG16 | GRCh38.p7 | 2:213554241 | GTGTTGGTTGCTGAG[A/G]ATCCCCTGAAATCTT | 79582 |
rs72940946 | snp | A/G | 0.0174175 | 0.0916809 | intron-variant | SPAG16 | GRCh38.p7 | 2:213554538 | TAAAAATGGAGATAC[A/G]AGAACAGCATGACAA | 79582 |
rs72940951 | snp | G/T | 0.0244538 | 0.107838 | intron-variant | SPAG16 | GRCh38.p7 | 2:213579621 | TAAAGAAGGAGTAAT[G/T]CTCATTTGTGTTTCA | 79582 |
rs72940992 | snp | A/G | 0.5 | 0 | intron-variant | SPAG16 | GRCh38.p7 | 2:213643067 | TATGTGTGTGTGTGT[A/G]TATATATATATATAT | 79582 |
rs72940995 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | SPAG16 | GRCh38.p7 | 2:213646470 | ATCATGATTAGCACT[C/T]TACAGAACAGGAATT | 79582 |
rs72941123 | snp | G/T | 0.335101 | 0.23507 | intron-variant | SPAG16 | GRCh38.p7 | 2:213856551 | CACCCTACAGCAGAC[G/T]TCTGCCTGGACATCC | 79582 |
rs72941139 | snp | A/T | 0.472803 | 0.113397 | intron-variant | SPAG16 | GRCh38.p7 | 2:213859097 | GGCAGGATAATTGCT[A/T]GAACTTGGGAGGGGG | 79582 |
rs72941141 | snp | C/G | 0.472896 | 0.113214 | intron-variant | SPAG16 | GRCh38.p7 | 2:213859128 | AGGTTGTAGTGAGCC[C/G]AGATCACACCACTGC | 79582 |
rs72941142 | snp | C/T | 0.472803 | 0.113397 | intron-variant | SPAG16 | GRCh38.p7 | 2:213859148 | CACACCACTGCTCTC[C/T]AGTCTGGGCAACAGA | 79582 |
rs72941151 | snp | C/G | 0.472803 | 0.113397 | intron-variant | SPAG16 | GRCh38.p7 | 2:213860666 | AGAAAAAAGTACTTC[C/G]AAATCTGATTAGCTA | 79582 |
rs72941157 | snp | G/T | 0.472989 | 0.113031 | intron-variant | SPAG16 | GRCh38.p7 | 2:213862188 | CTTAAAGAAAAACCA[G/T]AATTACTCTTTTCAA | 79582 |
rs72941159 | snp | A/C | 0.472709 | 0.11358 | intron-variant | SPAG16 | GRCh38.p7 | 2:213862202 | ATAATTACTCTTTTC[A/C]AACCAGAATTAGATA | 79582 |
rs72941175 | snp | C/T | 0.478768 | 0.100824 | intron-variant | SPAG16 | GRCh38.p7 | 2:213869327 | GTATACACACACACA[C/T]GCAAAACTTTTTATT | 79582 |
rs72941183 | snp | G/T | 0.0134861 | 0.0810011 | intron-variant | SPAG16 | GRCh38.p7 | 2:213870534 | CTTATTTTCCAGTAT[G/T]GGTGTGGAAGAGTAT | 79582 |
rs72941194 | snp | A/G | 0.479904 | 0.0982045 | intron-variant | SPAG16 | GRCh38.p7 | 2:213871909 | AGAGAGCAAACAGCA[A/G]TAAAAACAAACCTTA | 79582 |
rs72941195 | snp | A/C | 0.479904 | 0.0982045 | intron-variant | SPAG16 | GRCh38.p7 | 2:213871986 | GTTTTAAACAATGTC[A/C]AAAAATAGAAAACAT | 79582 |
rs72941962 | snp | A/T | 0.0923359 | 0.194016 | intron-variant | SPAG16 | GRCh38.p7 | 2:214167470 | TGGCCTTATCACATT[A/T]TAGCTGCATTCTGTT | 79582 |
rs72941963 | snp | C/T | 0.0193772 | 0.0965046 | intron-variant | SPAG16 | GRCh38.p7 | 2:214167641 | TGTGTATTTTTGTTA[C/T]TCTAAATGTCTTATA | 79582 |
rs72941980 | snp | C/T | 0.203267 | 0.245593 | intron-variant | SPAG16 | GRCh38.p7 | 2:214174670 | CTCACATCAATCCAA[C/T]GTGAGAAGGATTCTG | 79582 |
rs72941992 | snp | G/T | 0.342806 | 0.232136 | intron-variant | SPAG16 | GRCh38.p7 | 2:214179752 | ATTTACATGTATTTG[G/T]GAGTCTAGGTTTATT | 79582 |
rs72943116 | snp | A/G | 0.375 | 0.216506 | intron-variant | SPAG16 | GRCh38.p7 | 2:213876321 | AAAAAAAAAAAAAAA[A/G]AAGAAGAAAAGAAAA | 79582 |
rs72944017 | snp | A/G | 0.204189 | 0.245767 | intron-variant | SPAG16 | GRCh38.p7 | 2:214185959 | TATCTCCCCCACTAT[A/G]ATGTAAGTTCTGTTA | 79582 |
rs72944040 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | SPAG16 | GRCh38.p7 | 2:214196151 | CCATCAGTATTGTAT[A/G]CCTCGGGAAGGTGGA | 79582 |
rs72944042 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | SPAG16 | GRCh38.p7 | 2:214196152 | CATCAGTATTGTATG[C/T]CTCGGGAAGGTGGAG | 79582 |
rs72944051 | snp | C/T | 0.0689305 | 0.172377 | intron-variant | SPAG16 | GRCh38.p7 | 2:214199710 | TGGTCATTTTCACAA[C/T]ATTGTATCTTCCCAT | 79582 |
rs72944054 | snp | C/G | 0.0693013 | 0.172766 | intron-variant | SPAG16 | GRCh38.p7 | 2:214201902 | TCAGGCCAAAGTGCA[C/G]TGGCACAATCACAAC | 79582 |
rs72944057 | snp | A/G | 0.290201 | 0.246747 | intron-variant | SPAG16 | GRCh38.p7 | 2:214203522 | GAAAGGGGGATCATC[A/G]GCCTGAACACACATC | 79582 |
rs72944060 | snp | A/G | 0.0221141 | 0.102801 | intron-variant | SPAG16 | GRCh38.p7 | 2:214205963 | ACTTTGAGAGGCCGA[A/G]GTGGGCAGATTACGA | 79582 |
rs72944061 | snp | C/T | 0.067446 | 0.170804 | intron-variant | SPAG16 | GRCh38.p7 | 2:214206732 | TACTAAGTTACATTC[C/T]TACCAAAGGTGTATG | 79582 |
rs72944062 | snp | A/T | 0.089084 | 0.191327 | intron-variant | SPAG16 | GRCh38.p7 | 2:214208991 | TATTTCTTGAACCCA[A/T]TTGCTCTGTTTTTTG | 79582 |
rs72944072 | snp | A/G | 0.0298908 | 0.118541 | intron-variant | SPAG16 | GRCh38.p7 | 2:214221453 | GAAAGACATAGACAC[A/G]TCCATTTTATATTTC | 79582 |
rs72944097 | snp | C/T | 0.0182019 | 0.0936463 | intron-variant | SPAG16 | GRCh38.p7 | 2:214266701 | AAATATTAAATAATC[C/T]AACAAAAAATGTTAG | 79582 |
rs72944099 | snp | A/T | 0.00358779 | 0.0422022 | intron-variant | SPAG16 | GRCh38.p7 | 2:214268324 | AAAGGAACTGAAATC[A/T]GTATGTTGAAGAGTT | 79582 |
rs72944954 | snp | G/T | 0.479824 | 0.098392 | intron-variant | SPAG16 | GRCh38.p7 | 2:213879386 | AAATATATCCATGGG[G/T]GTGTGTGTGTGTATA | 79582 |
rs72944979 | snp | G/T | 0.0162398 | 0.0886349 | intron-variant | SPAG16 | GRCh38.p7 | 2:213885626 | CTTAAGGCAATGTGA[G/T]AGCCATGAGGTCTTT | 79582 |
rs72944993 | snp | A/C | 0.263809 | 0.249618 | intron-variant | SPAG16 | GRCh38.p7 | 2:213887656 | ATAGTAATTTTTAGC[A/C]AAATATTGTAAAATA | 79582 |
rs72944998 | snp | C/G | 0.0460142 | 0.144533 | intron-variant | SPAG16 | GRCh38.p7 | 2:213888657 | AGCTGGAAAACAGAT[C/G]TTTTTCTAAGGCAAA | 79582 |
rs72946119 | snp | C/T | 0.218151 | 0.247963 | intron-variant | SPAG16 | GRCh38.p7 | 2:214293542 | TATGTTCAGGCACTA[C/T]GTATGATAGGCAGAG | 79582 |
rs72946817 | snp | A/G | 0.331642 | 0.236293 | intron-variant | SPAG16 | GRCh38.p7 | 2:213893306 | TATGTCTTACAAAAA[A/G]TACCAAAGAGAGTTC | 79582 |
rs72946857 | snp | C/T | 0.259397 | 0.249823 | intron-variant | SPAG16 | GRCh38.p7 | 2:213900619 | ACTGCCTTTCCTAAG[C/T]CCTTTTATTATTTGA | 79582 |
rs72946876 | snp | C/T | 0.32885 | 0.23724 | intron-variant | SPAG16 | GRCh38.p7 | 2:213903735 | AAATGGATTTTTCTT[C/T]TCTATCACATTGTCA | 79582 |
rs72946879 | snp | A/G | 0.259674 | 0.249813 | intron-variant | SPAG16 | GRCh38.p7 | 2:213904100 | TAAATTTTCCCACAT[A/G]TTCCTGTCTTCATCT | 79582 |
rs72946968 | snp | C/G | 0.0189856 | 0.0955633 | intron-variant | SPAG16 | GRCh38.p7 | 2:213704352 | GGCACTACAGTATTT[C/G]ATTTTATTCAATAGG | 79582 |
rs72948711 | snp | A/T | 0.327445 | 0.237702 | intron-variant | SPAG16 | GRCh38.p7 | 2:213910323 | ACTTCTCTTCAGATC[A/T]TATAAATCTATTACT | 79582 |
rs72948790 | snp | G/T | | | intron-variant | SPAG16 | GRCh38.p7 | 2:213935508 | CGCAATGCTGTTGGA[G/T]TCCATGAAATCCTGC | 79582 |
rs72948801 | snp | A/G | 0.190833 | 0.242898 | intron-variant | SPAG16 | GRCh38.p7 | 2:213941237 | TTCAATCCCTTCAAG[A/G]TACAATTTATCTTCT | 79582 |
rs72950711 | snp | A/T | 0.176861 | 0.239062 | intron-variant | SPAG16 | GRCh38.p7 | 2:213947619 | TTAGGTCAAGGACAT[A/T]TTTTTTGGCTTACAA | 79582 |
rs72950717 | snp | A/T | 0.189576 | 0.242588 | intron-variant | SPAG16 | GRCh38.p7 | 2:213951032 | TAGTTTTTTTTTTTT[A/T]AATAATACATTTAGC | 79582 |
rs72950719 | snp | A/G | | | intron-variant | SPAG16 | GRCh38.p7 | 2:213951277 | ATAAAAGCTTGTAGC[A/G]TTTAAAATTTGGTTG | 79582 |
rs72950722 | snp | A/G | 0.189576 | 0.242588 | intron-variant | SPAG16 | GRCh38.p7 | 2:213951292 | ATTTAAAATTTGGTT[A/G]TCATAATGATACAAA | 79582 |
rs72950724 | snp | G/T | 0.189576 | 0.242588 | intron-variant | SPAG16 | GRCh38.p7 | 2:213951487 | TGATTTCTCCTGTTC[G/T]CAATTTAAATAGTTA | 79582 |
rs72950726 | snp | A/G | 0.189576 | 0.242588 | intron-variant | SPAG16 | GRCh38.p7 | 2:213951520 | CAATATGCAAAAGAC[A/G]AAAGCACATAAAAGA | 79582 |
rs72950729 | snp | A/G | 0.189576 | 0.242588 | intron-variant | SPAG16 | GRCh38.p7 | 2:213951933 | TTTAACTGATGGAGC[A/G]CATCAAAGAACATAG | 79582 |
rs72950730 | snp | A/G | 0.18989 | 0.242666 | intron-variant | SPAG16 | GRCh38.p7 | 2:213951964 | GCAGGTGCATTAAAT[A/G]ATGTTATAAAGAATA | 79582 |
rs72950732 | snp | A/G | 0.189576 | 0.242588 | intron-variant | SPAG16 | GRCh38.p7 | 2:213952134 | TTGAATCATCTTTAG[A/G]CTATAGATAATTTAA | 79582 |
rs72950735 | snp | A/T | 0.189576 | 0.242588 | intron-variant | SPAG16 | GRCh38.p7 | 2:213952165 | GGAAACCTAAATATG[A/T]GAAGAATACAAAAAT | 79582 |
rs72950738 | snp | A/C | 0.189261 | 0.242509 | intron-variant | SPAG16 | GRCh38.p7 | 2:213952341 | CAGAAAACAAGGAGA[A/C]GTTTATAGAGATTTT | 79582 |
rs72950740 | snp | G/T | 0.187053 | 0.241946 | intron-variant | SPAG16 | GRCh38.p7 | 2:213952721 | CTAACCGTGGATGGA[G/T]GGCTAAGAAATGTAA | 79582 |
rs72950746 | snp | A/G | 0.176219 | 0.238865 | intron-variant | SPAG16 | GRCh38.p7 | 2:213953173 | AAAGCAATGTTTAAA[A/G]CTATATTTTTAATCC | 79582 |
rs72950750 | snp | A/T | 0.18989 | 0.242666 | intron-variant | SPAG16 | GRCh38.p7 | 2:213954279 | ATATAAATGGAATCA[A/T]ATAATATGCAACCTT | 79582 |
rs72950751 | snp | A/G | 0.207864 | 0.246424 | intron-variant | SPAG16 | GRCh38.p7 | 2:213954692 | GAGCTGAATTGCTGG[A/G]TCCCACAGTGACTGT | 79582 |
rs72950755 | snp | C/T | 0.18989 | 0.242666 | intron-variant | SPAG16 | GRCh38.p7 | 2:213954885 | AGTCATAAAACATTG[C/T]GATTTTAATTTGCAT | 79582 |
rs72950760 | snp | A/G | 0.192715 | 0.243348 | intron-variant | SPAG16 | GRCh38.p7 | 2:213956835 | GTTTTGGTATGTTGC[A/G]TTTCTGTTTTCATTC | 79582 |
rs72950764 | snp | C/T | 0.192715 | 0.243348 | intron-variant | SPAG16 | GRCh38.p7 | 2:213957543 | ATCATGGTTTTTAAT[C/T]CATTCTGCTAATCTG | 79582 |
rs72950766 | snp | A/C | 0.190519 | 0.242821 | intron-variant | SPAG16 | GRCh38.p7 | 2:213958634 | TACATATAATGTGCC[A/C]AAAACATAAACTAAC | 79582 |
rs72950769 | snp | A/C | 0.187369 | 0.242028 | intron-variant | SPAG16 | GRCh38.p7 | 2:213958989 | TCTGGGAATGTCATA[A/C]TTTTTCCTCATTTTG | 79582 |
rs72950772 | snp | A/T | 0.173643 | 0.238054 | intron-variant | SPAG16 | GRCh38.p7 | 2:213959033 | GGATATATAAGAAAG[A/T]TCGTTGACGGTTTTT | 79582 |
rs72950773 | snp | C/T | 0.187369 | 0.242028 | intron-variant | SPAG16 | GRCh38.p7 | 2:213959088 | ATTTTGCATCACTGC[C/T]TTCTGGCTTCCATAG | 79582 |
rs72950775 | snp | C/T | 0.187053 | 0.241946 | intron-variant | SPAG16 | GRCh38.p7 | 2:213959598 | ACCTTCACAGGAAAC[C/T]CTAAGGAATAATACC | 79582 |
rs72952020 | snp | C/T | 0.103082 | 0.202275 | intron-variant | SPAG16 | GRCh38.p7 | 2:214310095 | GGAGGTGTCAAAGCA[C/T]TCTTTTTACACTGCT | 79582 |
rs72952021 | snp | C/T | 0.103082 | 0.202275 | intron-variant | SPAG16 | GRCh38.p7 | 2:214310290 | GTGCTTTTAGACAAC[C/T]GAGGCTCTGTATGAA | 79582 |
rs72952023 | snp | C/T | 0.111224 | 0.207945 | intron-variant | SPAG16 | GRCh38.p7 | 2:214313266 | ACTAATTATTCCAAC[C/T]AATACTACTACTATC | 79582 |
rs72952024 | snp | A/G | 0.113334 | 0.209338 | intron-variant | SPAG16 | GRCh38.p7 | 2:214313362 | GACTTTCTTTTCCCT[A/G]GATCTTTAATTTACA | 79582 |
rs72952025 | snp | C/T | 0.243633 | 0.249919 | intron-variant | SPAG16 | GRCh38.p7 | 2:214313545 | AATAGGTCAGTGTAC[C/T]GCCCTGGCACATAGT | 79582 |
rs72952034 | snp | A/G | 0.0178098 | 0.0926698 | intron-variant | SPAG16 | GRCh38.p7 | 2:214316094 | TTCAATATTACAGGA[A/G]CCTTGGGTCACTGTG | 79582 |
rs72952036 | snp | C/T | 0.102014 | 0.201495 | intron-variant | SPAG16 | GRCh38.p7 | 2:214316538 | TTTTATAAGGACCCG[C/T]GATGAAAGTTGTAGA | 79582 |
rs72952044 | snp | A/G | 0.0298908 | 0.118541 | intron-variant | SPAG16 | GRCh38.p7 | 2:214326175 | TCCTGGATTACCCAG[A/G]TGGGCTCTAAGTCTA | 79582 |
rs72952050 | snp | C/T | 0.00398564 | 0.0444627 | intron-variant | SPAG16 | GRCh38.p7 | 2:214329179 | TGAAGCTGGGGATGG[C/T]TCCATCTCAAATCAG | 79582 |
rs72952054 | snp | C/T | 0.10237 | 0.201756 | intron-variant | SPAG16 | GRCh38.p7 | 2:214329308 | AAGAAAGAATTCTTA[C/T]TATGTTTTATGTATG | 79582 |
rs73072714 | snp | C/T | 0.317451 | 0.240729 | intron-variant | SPAG16 | GRCh38.p7 | 2:214396619 | CCTTCTTCTTACATG[C/T]TCATGTGTTTTGTTC | 79582 |
rs73072726 | snp | C/T | 0.251014 | 0.249998 | intron-variant | SPAG16 | GRCh38.p7 | 2:214401442 | GGCACACAATGATTT[C/T]TGTCTCTATTCTTGT | 79582 |
rs73072727 | snp | A/G | 0.156319 | 0.231784 | intron-variant | SPAG16 | GRCh38.p7 | 2:214402253 | ACACCACCACAGTAA[A/G]TGTGCCTCAACCAGT | 79582 |
rs73072927 | snp | A/G | 0.00993419 | 0.0697739 | intron-variant | SPAG16 | GRCh38.p7 | 2:213912637 | TTGCTATGTGCATTC[A/G]GTGTAGAGCTTGCTG | 79582 |
rs73072936 | snp | C/T | 0.00597247 | 0.0543191 | intron-variant | SPAG16 | GRCh38.p7 | 2:213941026 | AAATGATTGTTCACC[C/T]TCTCTTGAGGCCATT | 79582 |
rs73072940 | snp | A/G | 0.00597247 | 0.0543191 | intron-variant | SPAG16 | GRCh38.p7 | 2:213957285 | TTTGCTGGTCAGACC[A/G]TTGATGGTCTGTTAT | 79582 |
rs73072942 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | SPAG16 | GRCh38.p7 | 2:213975889 | GGTGGCAGCTCGGCT[A/G]GGTGGTTCTGGTTAA | 79582 |
rs73072944 | snp | A/G | 0.00795532 | 0.062565 | intron-variant | SPAG16 | GRCh38.p7 | 2:213986830 | TGTAAGTATTTGTCT[A/G]ATTTAATAATGCCAA | 79582 |
rs73072953 | snp | A/G | 0.00914312 | 0.0669923 | intron-variant | SPAG16 | GRCh38.p7 | 2:214023208 | AACTTCTCTCACTTC[A/G]TTAAAAATGTAGTAG | 79582 |
rs73072957 | snp | G/T | 0.00993419 | 0.0697739 | intron-variant | SPAG16 | GRCh38.p7 | 2:214030799 | GGGTCCCTTATCTAC[G/T]TCCCACCTCAAGGGT | 79582 |
rs73074926 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | SPAG16 | GRCh38.p7 | 2:213287465 | TTCCTTGTCTAAAGA[G/T]ACTTTGTTCAAGGAA | 79582 |
rs73074944 | snp | G/T | 0.113334 | 0.209338 | intron-variant, upstream-variant-2KB | SPAG16 | GRCh38.p7 | 2:213316011 | TGGTCTTTTTCAGTC[G/T]CATGACTTTAAATAG | 79582 |
rs73074947 | snp | A/G | 0.0162398 | 0.0886349 | intron-variant | SPAG16 | GRCh38.p7 | 2:213319733 | TATGCCATAAGTTTA[A/G]CTCCAGTGACATTGA | 79582 |
rs73074953 | snp | A/G | 0.5 | 0 | intron-variant | SPAG16 | GRCh38.p7 | 2:213324505 | AATTTCATAAATGGA[A/G]TCACAGTATATTATT | 79582 |
rs73075036 | snp | A/T | 0.00835141 | 0.0640778 | intron-variant | SPAG16 | GRCh38.p7 | 2:214042172 | ATTACTGCAACCTCT[A/T]TCTCCTGGGTTCGTG | 79582 |
rs73075039 | snp | A/C | 0.0134861 | 0.0810011 | intron-variant | SPAG16 | GRCh38.p7 | 2:214044646 | AAGGATAGAAAAGAC[A/C]GTCTTGAATTGCCAT | 79582 |
rs73075041 | snp | A/G | 0.0107246 | 0.0724382 | intron-variant | SPAG16 | GRCh38.p7 | 2:214047444 | ACACACACCTGGGGG[A/G]AAAATATCTTTTCAA | 79582 |
rs73075052 | snp | C/T | 0.0103295 | 0.0711199 | intron-variant | SPAG16 | GRCh38.p7 | 2:214056676 | GGCAATTTTTAAAAA[C/T]AAGACAATAAAGTTT | 79582 |
rs73075055 | snp | C/G | 0.00953873 | 0.0683987 | intron-variant | SPAG16 | GRCh38.p7 | 2:214061317 | AACTCATAATCCACA[C/G]GGCACTAGGTTAGTA | 79582 |
rs73075056 | snp | A/T | 0.00835141 | 0.0640778 | intron-variant | SPAG16 | GRCh38.p7 | 2:214061341 | GTTAGTACTCAGGAA[A/T]GTCTCATAATTTCAT | 79582 |
rs73075074 | snp | A/T | 0.00755907 | 0.0610114 | intron-variant | SPAG16, LOC101928084 | GRCh38.p7 | 2:214089779 | ATTCCATCCAGTTCT[A/T]CAAATTTAGAAGTCA | 79582 |
rs73076840 | snp | A/G | 0.00755907 | 0.0610114 | intron-variant | SPAG16, LOC101928084 | GRCh38.p7 | 2:214095716 | ATCATATAAAATATA[A/G]ATCCTTAATGTGCAT | 79582 |
rs73076849 | snp | C/T | 0.00795532 | 0.062565 | intron-variant, upstream-variant-2KB | SPAG16, LOC101928084 | GRCh38.p7 | 2:214103908 | AATTTTCTTTCTTCC[C/T]TCTGGGGAGTGGGGG | 79582 |
rs73076851 | snp | A/G | 0.00755907 | 0.0610114 | intron-variant | SPAG16 | GRCh38.p7 | 2:214107256 | AATATAAGGTCCGTG[A/G]GAATAAGGTTCTTTG | 79582 |
rs73076854 | snp | A/G | 0.00755907 | 0.0610114 | intron-variant | SPAG16 | GRCh38.p7 | 2:214107836 | AGCAGTAGATATGCT[A/G]TGCTGAAAATAACAG | 79582 |
rs73076856 | snp | A/G/T | 0.00755907 | 0.0610114 | intron-variant | SPAG16 | GRCh38.p7 | 2:214108014 | TATGGTATGCTCCCC[A/G/T]CTCTAGGTCTGTACT | 79582 |
rs73076863 | snp | A/G | 0.00716266 | 0.059414 | intron-variant | SPAG16 | GRCh38.p7 | 2:214116004 | CAGAGCCCCAGTGGA[A/G]CCCAAGACTTAGGAG | 79582 |
rs73076866 | snp | A/G | 0.0023933 | 0.0345097 | intron-variant | SPAG16 | GRCh38.p7 | 2:214118714 | AGACATATGGCGATT[A/G]TGGGAACTACAATTC | 79582 |
rs73076869 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | SPAG16 | GRCh38.p7 | 2:214119947 | AGGTTGGATCTTTCT[C/T]ATACATTTTAATATC | 79582 |
rs73076877 | snp | A/T | 0.00755907 | 0.0610114 | intron-variant | SPAG16 | GRCh38.p7 | 2:214125008 | CTAAATTCATTGAAT[A/T]TTTTTCTGAAACCAT | 79582 |
rs73076883 | snp | A/G | 0.00755907 | 0.0610114 | intron-variant | SPAG16 | GRCh38.p7 | 2:214132252 | AAATATTTACTAAGT[A/G]TATAATATAAACCCA | 79582 |
rs73076885 | snp | A/G | 0.00755907 | 0.0610114 | intron-variant | SPAG16 | GRCh38.p7 | 2:214134572 | CATAAATATTTGTTT[A/G]ATGAATGAAGAGATA | 79582 |
rs73077046 | snp | A/G | 0.116488 | 0.211364 | intron-variant, utr-variant-3-prime | SPAG16 | GRCh38.p7 | 2:213370699 | ATCCTTGACATATCA[A/G]TTAAAATAAACTGAT | 79582 |
rs73077065 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | SPAG16 | GRCh38.p7 | 2:213385192 | TATGGTGTATCCACT[C/T]TCACAGGCTCACTTC | 79582 |
rs73081029 | snp | A/G | 0.0248432 | 0.108648 | intron-variant | SPAG16 | GRCh38.p7 | 2:214158556 | TCTTCTTACAGGACT[A/G]TATAAGAACCTGACT | 79582 |
rs73081032 | snp | C/G | 0.00438332 | 0.0466095 | intron-variant | SPAG16 | GRCh38.p7 | 2:214174792 | CTAGCCAGTGGACAG[C/G]AAAAGATAGGGAAAG | 79582 |
rs73081037 | snp | A/G | 0.00199481 | 0.0315187 | intron-variant | SPAG16 | GRCh38.p7 | 2:214191987 | GGACATTACTTTGGG[A/G]AAAAAAAAACAGGAC | 79582 |
rs73081038 | snp | A/G | | | intron-variant | SPAG16 | GRCh38.p7 | 2:214193395 | TCAAAGAGATCTTTT[A/G]TGTGTGTGTGTGTGT | 79582 |
rs73081039 | snp | C/G | 0.000798403 | 0.0199641 | intron-variant | SPAG16 | GRCh38.p7 | 2:214195084 | AGCAGAAGCTACAGG[C/G]ATGGCCTCTTGAGAA | 79582 |
rs73081040 | snp | A/G | 0.00279162 | 0.0372561 | intron-variant | SPAG16 | GRCh38.p7 | 2:214195553 | GAACAAACTTTGCGC[A/G]TAAAACTGAAAGGGC | 79582 |
rs73081043 | snp | A/T | 0.00119737 | 0.0244387 | intron-variant | SPAG16 | GRCh38.p7 | 2:214206977 | TAAGTCAGAAAAACC[A/T]TTGCCAGAGGTTTGA | 79582 |
rs73081045 | snp | C/G | 0.111224 | 0.207945 | intron-variant | SPAG16 | GRCh38.p7 | 2:214208034 | CTACTGGCTTCCTAC[C/G]TCCTCAGTTTGCAGA | 79582 |
rs73081053 | snp | A/G | 0.00755907 | 0.0610114 | intron-variant | SPAG16 | GRCh38.p7 | 2:214218459 | ATGTTTTGCCTCCAC[A/G]CTGCCTTTAATCTGA | 79582 |
rs73081059 | snp | A/G | 0.0205511 | 0.0992634 | intron-variant | SPAG16 | GRCh38.p7 | 2:214226727 | ATTTTGGACACTTAA[A/G]TGAAAAATAAGAGAT | 79582 |
rs73081074 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | SPAG16 | GRCh38.p7 | 2:214240901 | ATGGACTACTTTTAT[A/T]TGGCAACCTTTACCT | 79582 |
rs73081075 | snp | C/T | 0.0471551 | 0.14613 | intron-variant | SPAG16 | GRCh38.p7 | 2:214241414 | TTCTAACCTTTACCT[C/T]TGCAGACTTTAATGT | 79582 |
rs73081082 | snp | C/T | 0.211819 | 0.247067 | intron-variant | SPAG16 | GRCh38.p7 | 2:214248009 | CTCCAGCAGGGACAA[C/T]AGCAAGTCCGTGTCT | 79582 |
rs73081097 | snp | G/T | 0.0146672 | 0.084371 | intron-variant | SPAG16 | GRCh38.p7 | 2:214256847 | TCTTAAAGTCAAACG[G/T]TTAGAAGTCCTCCAA | 79582 |
rs73081099 | snp | A/G | 0.0209421 | 0.100162 | intron-variant | SPAG16 | GRCh38.p7 | 2:214257733 | TATATTACTGGATTA[A/G]TTTAACAATAATATT | 79582 |
rs73081101 | snp | G/T | 0.226779 | 0.248919 | intron-variant | SPAG16 | GRCh38.p7 | 2:214258607 | CTGCTGTAAACATGC[G/T]GGGGCAAGTGTCTTT | 79582 |
rs73083004 | snp | A/G | 0.0166325 | 0.0896639 | intron-variant | SPAG16 | GRCh38.p7 | 2:214261401 | CTGGCGGCTAAGAAA[A/G]CTCTGCCTTTATAAC | 79582 |
rs73083005 | snp | C/T | 0.0376037 | 0.131863 | intron-variant | SPAG16 | GRCh38.p7 | 2:214262658 | TGTATCCTTCATCTC[C/T]GTATCTATAAAATGG | 79582 |
rs73083010 | snp | C/T | 0.244205 | 0.249933 | intron-variant | SPAG16 | GRCh38.p7 | 2:214268607 | TCAATATTTTATCTT[C/T]CGGGGCTGAAAGAAG | 79582 |
rs73083011 | snp | C/T | 0.0209421 | 0.100162 | intron-variant | SPAG16 | GRCh38.p7 | 2:214270227 | GAAATGGTAACATTA[C/T]TGAACATTGGCTGCA | 79582 |
rs73083216 | snp | C/G/T | 0.0170251 | 0.090679 | intron-variant | SPAG16 | GRCh38.p7 | 2:213475839 | CTGAGAACTGGGGAC[C/G/T]TGGCCTAATAAGATG | 79582 |
rs73083223 | snp | A/G | 0.0486741 | 0.148216 | intron-variant | SPAG16 | GRCh38.p7 | 2:213501506 | TTTCTTATGCAAAAC[A/G]CTATCAGGGAACTGA | 79582 |
rs73083226 | snp | C/T | 0.046775 | 0.145601 | intron-variant | SPAG16 | GRCh38.p7 | 2:213504212 | TTTCTTAAGCAAGAA[C/T]ATAATTAGATTAGCA | 79582 |
rs73083245 | snp | C/T | 0.0479149 | 0.147179 | intron-variant | SPAG16 | GRCh38.p7 | 2:213584016 | AAAATCATGGACTAA[C/T]CTTTGTAGAAATGTA | 79582 |
rs73084641 | snp | C/T | 0.0475351 | 0.146656 | intron-variant | SPAG16 | GRCh38.p7 | 2:213616539 | ATAGAAGGGGGGTGT[C/T]AGGATGGGGAAGCCA | 79582 |
rs73084647 | snp | C/T | 0.0543475 | 0.155628 | intron-variant | SPAG16 | GRCh38.p7 | 2:213623558 | TATTATCTTTCTACC[C/T]GGCATTTAAACTGGT | 79582 |
rs73084673 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | SPAG16 | GRCh38.p7 | 2:213638716 | ATAGAATGTATATTC[C/T]ACAGTTGCTAGGTAG | 79582 |
rs73084942 | snp | A/G | 0.20111 | 0.245173 | intron-variant | SPAG16 | GRCh38.p7 | 2:214284019 | ATCAAAACGTATCCT[A/G]TTGATTTGAGAGCTT | 79582 |
rs73084945 | snp | A/G/T | 0.0279526 | 0.114869 | intron-variant | SPAG16 | GRCh38.p7 | 2:214284611 | TTTGGAGGTCTTTGC[A/G/T]CAGTACTCTGTTGAG | 79582 |
rs73084949 | snp | C/G | 0.021333 | 0.101051 | intron-variant | SPAG16 | GRCh38.p7 | 2:214286044 | AACTTTTGTACATCA[C/G]TTGACATTATGCAAA | 79582 |
rs73084981 | snp | A/G | 0.372189 | 0.218105 | intron-variant | SPAG16 | GRCh38.p7 | 2:214308457 | TTATTTTGCAGATTT[A/G]TTTATGTGGTTGCTT | 79582 |
rs73084984 | snp | A/G | 0.0287284 | 0.116357 | intron-variant | SPAG16 | GRCh38.p7 | 2:214315859 | TTTACCAAATTATGC[A/G]TAAGTATTTCCCTGA | 79582 |
rs73084986 | snp | A/G | 0.0368353 | 0.130617 | intron-variant | SPAG16 | GRCh38.p7 | 2:214317358 | TTGAGCACATACTCC[A/G]TTGAAAACAGACTAC | 79582 |
rs73084988 | snp | A/G | 0.0387552 | 0.1337 | intron-variant | SPAG16 | GRCh38.p7 | 2:214319767 | TGCCTGGAACACAAT[A/G]TATGCTCATTAATAT | 79582 |
rs73084990 | snp | C/T | 0.0360663 | 0.129354 | intron-variant | SPAG16 | GRCh38.p7 | 2:214321847 | TTAATAGGTATATTG[C/T]CCAAATAACTCCACT | 79582 |
rs73086636 | snp | A/G | 0.147321 | 0.227941 | intron-variant | SPAG16 | GRCh38.p7 | 2:213686110 | TTTCCTAGTTCCTCT[A/G]TGTGTTACTTTATTT | 79582 |
rs73086642 | snp | A/G | 0.0452528 | 0.143452 | intron-variant | SPAG16 | GRCh38.p7 | 2:213690794 | GTTCTTCAGCCTTTG[A/G]TCTGTGAGGCTTGTA | 79582 |
rs73086651 | snp | C/G | 0.0520825 | 0.152737 | intron-variant | SPAG16 | GRCh38.p7 | 2:213702811 | AGAGTTGATATATAT[C/G]AAGAAGATTTAAGAT | 79582 |
rs73086669 | snp | A/G | 0.00199481 | 0.0315187 | intron-variant | SPAG16 | GRCh38.p7 | 2:213719613 | TTGGCAACCAGCTCC[A/G]GTCACCCACCAATTC | 79582 |
rs73086672 | snp | C/T | 0.00199481 | 0.0315187 | intron-variant | SPAG16 | GRCh38.p7 | 2:213719655 | CCATCTCATGCTAGT[C/T]AGATCGGCAATCATT | 79582 |
rs73087050 | snp | A/G | 0.0260105 | 0.111035 | intron-variant | SPAG16 | GRCh38.p7 | 2:214325268 | GGACGTGCTGGTTTG[A/G]TAGGTCTAGGAGTTG | 79582 |
rs73087055 | snp | A/G | 0.0260105 | 0.111035 | intron-variant | SPAG16 | GRCh38.p7 | 2:214330569 | GCAGTGGCAACAGAA[A/G]CTCAGTTGATCCTAC | 79582 |
rs73087060 | snp | A/G | 0.474992 | 0.108989 | intron-variant | SPAG16 | GRCh38.p7 | 2:214332081 | ACATGGTGAAATCCC[A/G]CCTCTGCTAAAAATA | 79582 |
rs73087063 | snp | A/G | 0.0126979 | 0.078662 | intron-variant | SPAG16 | GRCh38.p7 | 2:214333985 | CATTCTTCCAGGGCT[A/G]TTGCCAGGTTGTTAA | 79582 |
rs73087070 | snp | A/G | 0.183886 | 0.241099 | intron-variant | SPAG16 | GRCh38.p7 | 2:214340427 | ATGAAATTTTAAATG[A/G]ATCTGAATATAACAA | 79582 |
rs73087075 | snp | C/T | 0.0263992 | 0.111815 | intron-variant | SPAG16 | GRCh38.p7 | 2:214343657 | TAAGACAAACTTAGA[C/T]ACAATGGGGAAATAG | 79582 |
rs73087078 | snp | A/G/T | 0.0498882 | 0.150224 | intron-variant | SPAG16 | GRCh38.p7 | 2:214346642 | AAAGGCCATGCATTA[A/G/T]CCACATTGCTCACTG | 79582 |
rs73087083 | snp | A/G | 0.0429648 | 0.14013 | intron-variant | SPAG16 | GRCh38.p7 | 2:214350288 | CTTTCCTCTCTTCTC[A/G]GACTCCAGTTGCAAA | 79582 |
rs73087089 | snp | G/T | 0.0577344 | 0.159793 | intron-variant | SPAG16 | GRCh38.p7 | 2:214350921 | GCATAACCTAAAGTT[G/T]CCCCAAAACATCAGC | 79582 |
rs73087099 | snp | G/T | 0.0607341 | 0.163335 | intron-variant | SPAG16 | GRCh38.p7 | 2:214352321 | TTTCAAAGTTTTGAT[G/T]TTAATGGTTTGACAC | 79582 |
rs73087101 | snp | A/G | 0.030278 | 0.119257 | intron-variant | SPAG16 | GRCh38.p7 | 2:214353043 | TTGAATGTGTAACTT[A/G]CTGCCCTTTCTACTT | 79582 |
rs73088747 | snp | A/G | 0.00597247 | 0.0543191 | intron-variant | SPAG16 | GRCh38.p7 | 2:213826339 | ATACATCATGAGGTT[A/G]TTTATGTGTAGTTTT | 79582 |
rs73089203 | snp | C/T | 0.0607341 | 0.163335 | intron-variant | SPAG16 | GRCh38.p7 | 2:214353753 | ACAAGAAAATCACCA[C/T]GTTATTTATACGGTC | 79582 |
rs73089208 | snp | A/G | 0.0345262 | 0.126772 | intron-variant | SPAG16 | GRCh38.p7 | 2:214360136 | ATATAACGAATAATT[A/G]TTGTAATATGAGATG | 79582 |
rs73089210 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | SPAG16 | GRCh38.p7 | 2:214361973 | CATCTTTAGAACTGA[A/G]GATATCTCTGATAAC | 79582 |
rs73089214 | snp | G/T | 0.0341408 | 0.126114 | intron-variant | SPAG16 | GRCh38.p7 | 2:214363091 | ACTTTAATCTCTACC[G/T]TTTTGTTATTATGTT | 79582 |
rs73089216 | snp | C/T | 0.029116 | 0.117091 | intron-variant | SPAG16 | GRCh38.p7 | 2:214363953 | TTCTTTCTCATGGCC[C/T]CTCTCAACTCTATTT | 79582 |
rs73089222 | snp | C/G | 0.0422008 | 0.138995 | intron-variant | SPAG16 | GRCh38.p7 | 2:214369849 | TGATATTCTATCAAT[C/G]ATTTCTTCTCTGGCA | 79582 |
rs73089226 | snp | A/C | 0.0126979 | 0.078662 | intron-variant | SPAG16 | GRCh38.p7 | 2:214373506 | AAATAGAAATATATT[A/C]AATTGTTAAATAGGC | 79582 |
rs73089228 | snp | C/T | 0.0352966 | 0.128072 | intron-variant | SPAG16 | GRCh38.p7 | 2:214375060 | TTTGGGTCTTGAACA[C/T]GTGTCAGAACAGGGT | 79582 |
rs73089243 | snp | G/T | 0.077417 | 0.180873 | intron-variant | SPAG16 | GRCh38.p7 | 2:214378289 | CGTTGGAGATAATTT[G/T]GGGCTTCAAATGGCA | 79582 |
rs73089262 | snp | C/T | 0.312837 | 0.241974 | intron-variant | SPAG16 | GRCh38.p7 | 2:214391787 | AATTTAAGAATGAAG[C/T]TTGGATCTGACACAT | 79582 |
rs73986834 | snp | C/T | 0.289424 | 0.246872 | intron-variant | SPAG16 | GRCh38.p7 | 2:213416553 | CTTGACTTGTTTTTT[C/T]TTTTTTTGTTACACC | 79582 |
rs73986835 | snp | A/G | 0.0263992 | 0.111815 | intron-variant | SPAG16 | GRCh38.p7 | 2:213421309 | GCGTGTGCTTGGGGT[A/G]GTGCCGACTCACCAG | 79582 |
rs73986836 | snp | A/G | 0.20511 | 0.245937 | intron-variant | SPAG16 | GRCh38.p7 | 2:213421606 | TGGGAGTGAGGACTT[A/G]TGGTGATTTTTCTGG | 79582 |
rs73986838 | snp | C/T | 0.0248432 | 0.108648 | intron-variant | SPAG16 | GRCh38.p7 | 2:213426338 | ATTTTTATAAGAAAA[C/T]GATTCTCATTTGAGA | 79582 |
rs73986841 | snp | G/T | 0.00119737 | 0.0244387 | intron-variant | SPAG16 | GRCh38.p7 | 2:213431060 | CTCTACTAGAAATGC[G/T]CAAATGAGTTCTAAA | 79582 |
rs73986842 | snp | G/T | 0.0182019 | 0.0936463 | intron-variant | SPAG16 | GRCh38.p7 | 2:213431237 | GGAGGGGAAAAAAAA[G/T]AATCTACAAAACAAC | 79582 |
rs73986845 | snp | C/T | 0.155325 | 0.23138 | intron-variant | SPAG16 | GRCh38.p7 | 2:213438109 | TCTGTCTTTGCCTTT[C/T]AATCTACCTTAACGT | 79582 |
rs73986846 | snp | A/G | 0.147321 | 0.227941 | intron-variant | SPAG16 | GRCh38.p7 | 2:213445998 | GCTGAGGCTTGGACC[A/G]CTGAAACCATCCAGA | 79582 |
rs73986847 | snp | C/T | 0.0267878 | 0.112589 | intron-variant | SPAG16 | GRCh38.p7 | 2:213446407 | AGCCAAACTGAACTT[C/T]AGGAAATGAAAAAGT | 79582 |
rs73986849 | snp | C/T | 0.0271762 | 0.113356 | intron-variant | SPAG16 | GRCh38.p7 | 2:213447608 | TATGGTGGAGAACAT[C/T]GGGCGTTCCCACCGC | 79582 |
rs73986851 | snp | G/T | 0.155325 | 0.23138 | intron-variant | SPAG16 | GRCh38.p7 | 2:213451466 | TCAGATTCAACATAT[G/T]CATACATGAACTCAT | 79582 |
rs73986872 | snp | A/G | 0.154993 | 0.231244 | intron-variant | SPAG16 | GRCh38.p7 | 2:213451976 | TCCCTCCACTCCCGC[A/G]CTTCCAGCTCAGCTT | 79582 |
rs73986873 | snp | A/G | 0.0267878 | 0.112589 | intron-variant | SPAG16 | GRCh38.p7 | 2:213453885 | GTGTCCAAAAACATT[A/G]CAGAGGAAAGATTCA | 79582 |
rs73986874 | snp | C/T | 0.155325 | 0.23138 | intron-variant | SPAG16 | GRCh38.p7 | 2:213453970 | CTCTTTCCATCTATT[C/T]CTCTTTTCTTCCCTT | 79582 |
rs73986875 | snp | A/C | 0.155325 | 0.23138 | intron-variant | SPAG16 | GRCh38.p7 | 2:213454219 | TATTTAATAGAAAAC[A/C]AAAAAATTATGTATT | 79582 |
rs73986876 | snp | C/G | 0.154993 | 0.231244 | intron-variant | SPAG16 | GRCh38.p7 | 2:213461334 | AGATAATGTTAGAGA[C/G]ATAGGCTTGAGTTAT | 79582 |
rs73986877 | snp | C/T | 0.154993 | 0.231244 | intron-variant | SPAG16 | GRCh38.p7 | 2:213461907 | GTGTATGTGTATGTG[C/T]GTGTGTATGTGTATG | 79582 |
rs73986878 | snp | C/G | 0.0279526 | 0.114869 | intron-variant | SPAG16 | GRCh38.p7 | 2:213465529 | TTTCTCTGGGAGGGA[C/G]GTGGCTGGGTTTAGG | 79582 |
rs73986879 | snp | A/G | 0.130351 | 0.219509 | intron-variant | SPAG16 | GRCh38.p7 | 2:213465623 | AATTGTTTGTTAGCC[A/G]GAGACTCCCCTTAGA | 79582 |
rs73986880 | snp | A/T | 0.154993 | 0.231244 | intron-variant | SPAG16 | GRCh38.p7 | 2:213467752 | TGAGTCTGGCTCTGG[A/T]CTCAGTGACCTGCAT | 79582 |
rs73986882 | snp | A/G | 0.0267878 | 0.112589 | intron-variant | SPAG16 | GRCh38.p7 | 2:213468191 | CTCTCCAGAAAGGAA[A/G]TGGGTCATCTGATCC | 79582 |
rs73986886 | snp | A/T | 0.0267878 | 0.112589 | intron-variant | SPAG16 | GRCh38.p7 | 2:213478750 | CTGGAAGATTCTGCC[A/T]TATTCCTACTCTGTG | 79582 |
rs73986887 | snp | A/G | 0.18989 | 0.242666 | intron-variant | SPAG16 | GRCh38.p7 | 2:213478795 | GAAGCTAAAATCAAG[A/G]AGGCTTCACTTAATT | 79582 |
rs73986888 | snp | C/T | 0.159622 | 0.233092 | intron-variant | SPAG16 | GRCh38.p7 | 2:213479094 | AGGCACACTGGCTTC[C/T]TTTTTTTTTTTTTTT | 79582 |
rs73986893 | snp | C/G | 0.166506 | 0.235645 | intron-variant | SPAG16 | GRCh38.p7 | 2:213487128 | TTATTTTAACCCTGA[C/G]TTTTATTTCACATAG | 79582 |
rs73986903 | snp | C/T | 0.00478085 | 0.0486577 | intron-variant | SPAG16 | GRCh38.p7 | 2:213725642 | AAGAAGAGGGTGCGG[C/T]GTGTCTTAGCAACAG | 79582 |
rs73986905 | snp | C/T | 0.128976 | 0.218754 | intron-variant | SPAG16 | GRCh38.p7 | 2:213725804 | TTTAGTGTTTTCCAA[C/T]AGCAACCTAAATAGC | 79582 |
rs73986909 | snp | A/G | 0.0126979 | 0.078662 | intron-variant | SPAG16 | GRCh38.p7 | 2:213740420 | GTGGACCAGAAAGGA[A/G]CAGCTGCTCACTACC | 79582 |
rs73986910 | snp | C/T | 0.00199481 | 0.0315187 | intron-variant | SPAG16 | GRCh38.p7 | 2:213744566 | CTTTTTAGCTAGAGA[C/T]TCCATCTGACAATGG | 79582 |
rs73986911 | snp | A/G | 0.0130921 | 0.0798413 | intron-variant | SPAG16 | GRCh38.p7 | 2:213745819 | ACCTTAAATACTAGA[A/G]TGTAATAATAAAAGA | 79582 |
rs73986934 | snp | C/T | 0.0463947 | 0.145069 | intron-variant, upstream-variant-2KB | SPAG16, MIR4438 | GRCh38.p7 | 2:213757591 | TATAACTATTTTGGA[C/T]TTTTGACATCTACTA | 79582 |
rs73986935 | snp | A/C | 0.0142736 | 0.0832652 | intron-variant, upstream-variant-2KB | SPAG16, MIR4438 | GRCh38.p7 | 2:213757672 | TCAGTCAATTTCAGC[A/C]CTTAACCACAGTAGT | 79582 |
rs73986938 | snp | C/T | 0.02016 | 0.0983543 | intron-variant | SPAG16 | GRCh38.p7 | 2:213762663 | AAATTTTAACAAAGA[C/T]CTGAAACTATAAATC | 79582 |
rs73986964 | snp | A/G | 0.00755907 | 0.0610114 | intron-variant | SPAG16 | GRCh38.p7 | 2:213793736 | GAATCTCAGAGACAA[A/G]GTAATGTTAATGTTG | 79582 |
rs73986966 | snp | C/T | 0.00199481 | 0.0315187 | intron-variant | SPAG16 | GRCh38.p7 | 2:213805884 | AGGCATGGTAAAAAG[C/T]CAAGTTGTAGGCAGT | 79582 |
rs73986968 | snp | A/G | 0.00676609 | 0.0577691 | intron-variant | SPAG16 | GRCh38.p7 | 2:213820959 | TGCTCCAAAAATATA[A/G]ACAACTATAAGAAAT | 79582 |
rs73986973 | snp | G/T | 0.5 | 0 | intron-variant | SPAG16 | GRCh38.p7 | 2:213869662 | TTTTTTTTTTTTTTT[G/T]TCTAATTCCAAAAGT | 79582 |
rs73986974 | snp | A/C | 0.030665 | 0.119967 | intron-variant | SPAG16 | GRCh38.p7 | 2:213871811 | CCAAACATGGAATAC[A/C]GACTTTACTGAATTA | 79582 |
rs73986982 | snp | A/G | 0.00676609 | 0.0577691 | intron-variant | SPAG16 | GRCh38.p7 | 2:213890632 | AGGATGGTTTCATTT[A/G]TATTTGTTCAATTAT | 79582 |
rs73986985 | snp | C/T | 0.00716266 | 0.059414 | intron-variant | SPAG16 | GRCh38.p7 | 2:213899934 | AACAATTCTCTTCAC[C/T]ATCCTTGTCTTGATG | 79582 |
rs73986992 | snp | A/G | 0.00199481 | 0.0315187 | intron-variant | SPAG16 | GRCh38.p7 | 2:213908164 | ACTAAAGATAAAAGA[A/G]AAAATAATTCAGTTG | 79582 |
rs73986999 | snp | C/T | 0.328148 | 0.237472 | intron-variant | SPAG16 | GRCh38.p7 | 2:213920549 | GTGTGGCCATGGGGG[C/T]TGCCCCATTGGACCT | 79582 |
rs73987001 | snp | C/T | 0.030665 | 0.119967 | intron-variant | SPAG16 | GRCh38.p7 | 2:213927906 | TTTTAAATTTTTTTA[C/T]ATGCATGTTTTTGGA | 79582 |
rs73987103 | snp | G/T | 0.5 | 0 | intron-variant | SPAG16 | GRCh38.p7 | 2:213976109 | TAAGACAGTGAGGGA[G/T]ATATATATATATATA | 79582 |
rs73987104 | snp | C/T | 0.137527 | 0.223271 | intron-variant | SPAG16 | GRCh38.p7 | 2:213978012 | AGGATTTATGATGCG[C/T]ACCCTTAAATTCTTT | 79582 |
rs73987108 | snp | C/G | 0.0217236 | 0.101931 | intron-variant | SPAG16 | GRCh38.p7 | 2:213987151 | TCACATACTCATCAG[C/G]TATTTATTAATTCAT | 79582 |
rs73987109 | snp | A/G | 0.282632 | 0.247861 | intron-variant | SPAG16 | GRCh38.p7 | 2:213990704 | GAGGAACAGGAGGAG[A/G]TGGTCTTGTTGTCTT | 79582 |
rs73987111 | snp | A/G | 0.132751 | 0.2208 | intron-variant | SPAG16 | GRCh38.p7 | 2:213994439 | AATCTGCCATGTTAT[A/G]TCATTCTGGTCAACA | 79582 |
rs73987112 | snp | G/T | 0.0221141 | 0.102801 | intron-variant | SPAG16 | GRCh38.p7 | 2:213995599 | GCTAGAAATTCTACC[G/T]TAGTCATTCTTAGGG | 79582 |
rs73987126 | snp | A/G | 0.0685596 | 0.171987 | intron-variant | SPAG16 | GRCh38.p7 | 2:213997837 | TGCATGCAGCCCATG[A/G]GCCATGGGTTGGACA | 79582 |
rs73987129 | snp | A/T | 0.11963 | 0.213316 | intron-variant | SPAG16 | GRCh38.p7 | 2:214009031 | TCCACTTCACCCAGG[A/T]TTAAACTCCAGAGTA | 79582 |
rs73987130 | snp | A/T | 0.146314 | 0.227484 | intron-variant | SPAG16 | GRCh38.p7 | 2:214009332 | CTATTTCCGTATTTG[A/T]TAGTAAAAAGTGCAT | 79582 |
rs73987131 | snp | C/T | 0.182296 | 0.240658 | intron-variant | SPAG16 | GRCh38.p7 | 2:214010577 | GGGAGATTGGAGAGA[C/T]TAGACTGACCTCAGA | 79582 |
rs73987132 | snp | A/G | 0.13446 | 0.221699 | intron-variant | SPAG16 | GRCh38.p7 | 2:214016914 | TCCCATATACAAAAC[A/G]TGATTGATATAAATA | 79582 |
rs73987134 | snp | A/G | 0.0414363 | 0.137845 | intron-variant | SPAG16 | GRCh38.p7 | 2:214027273 | ATTCTTCTTTACTGA[A/G]CAGCATAACTTGAAA | 79582 |
rs73987137 | snp | C/T | 0.0402882 | 0.136092 | intron-variant | SPAG16 | GRCh38.p7 | 2:214034393 | GTGTTACAGGATCTT[C/T]GGGGCATTGCTTTGC | 79582 |
rs73987138 | snp | C/T | 0.0402882 | 0.136092 | intron-variant | SPAG16 | GRCh38.p7 | 2:214035759 | CTTGCCTGCTTCCAG[C/T]CTCCAAAAGCACAAG | 79582 |
rs73987140 | snp | C/G/T | 0.0402882 | 0.136092 | intron-variant | SPAG16 | GRCh38.p7 | 2:214045101 | CCTCCCCCAGCCCCA[C/G/T]GCTGCACAGCTTGTG | 79582 |
rs73987143 | snp | A/G | 0.0399052 | 0.1355 | intron-variant | SPAG16 | GRCh38.p7 | 2:214052476 | ATAATTCATACCTGC[A/G]AAACTCTGACTTGCC | 79582 |
rs73987144 | snp | A/C | 0.0182019 | 0.0936463 | intron-variant | SPAG16 | GRCh38.p7 | 2:214061754 | ATAAAATTAATCACC[A/C]TACTCAGTATTTTAC | 79582 |
rs73987148 | snp | A/G | 0.0379877 | 0.132479 | intron-variant | SPAG16 | GRCh38.p7 | 2:214069220 | TAATCATTCCGATAC[A/G]TGTATATTGTTAAGC | 79582 |
rs73987149 | snp | A/G | 0.0185938 | 0.0946107 | intron-variant | SPAG16 | GRCh38.p7 | 2:214072439 | CCACTCCTACACCCC[A/G]AACAATCCCACCCAC | 79582 |
rs73987150 | snp | C/T | 0.0185938 | 0.0946107 | intron-variant | SPAG16 | GRCh38.p7 | 2:214076692 | TGACCTCTTGTAGTT[C/T]TTATTATAGAATGTG | 79582 |
rs73987151 | snp | C/T | 0.0119091 | 0.0762411 | intron-variant | SPAG16 | GRCh38.p7 | 2:214082055 | GGCTTTGATATCCTC[C/T]TCTTATGTCTTTTTG | 79582 |
rs73987153 | snp | G/T | 0.040671 | 0.13668 | intron-variant | SPAG16, LOC101928084 | GRCh38.p7 | 2:214087524 | GACATTTTTCTAAAA[G/T]ATGTCACATGATAAT | 79582 |
rs73987154 | snp | A/G | 0.040671 | 0.13668 | intron-variant | SPAG16, LOC101928084 | GRCh38.p7 | 2:214088900 | TAAAATATGGGAAAG[A/G]AAATGAAAGAAGTAA | 79582 |
rs73987174 | snp | G/T | 0.040671 | 0.13668 | intron-variant | SPAG16, LOC101928084 | GRCh38.p7 | 2:214102862 | AAAGGAAAATTCGTT[G/T]GGAAGAGACCTAAGC | 79582 |
rs73987179 | snp | C/T | 0.0402882 | 0.136092 | intron-variant | SPAG16 | GRCh38.p7 | 2:214108737 | CAGAACAGCTTTGAT[C/T]TGACAGCTTTTTAAT | 79582 |
rs73987180 | snp | C/T | 0.0726307 | 0.176182 | intron-variant | SPAG16 | GRCh38.p7 | 2:214116870 | TAGATCTCTGGAAGA[C/T]GCTCTGAAAAATGAT | 79582 |
rs73987183 | snp | A/G | 0.0185938 | 0.0946107 | intron-variant | SPAG16 | GRCh38.p7 | 2:214126978 | GTAAGTTCTCTGTAA[A/G]TGTTTGTGAAACTGA | 79582 |
rs73987184 | snp | A/G | 0.0185938 | 0.0946107 | intron-variant | SPAG16 | GRCh38.p7 | 2:214127968 | GGGTTAGAGCAGCTT[A/G]ATTAAATGTATTAAA | 79582 |
rs73987185 | snp | A/G | 0.0185938 | 0.0946107 | intron-variant | SPAG16 | GRCh38.p7 | 2:214131272 | TGCTTCGGGAAGTTG[A/G]AGTGGGAGGATGGCT | 79582 |
rs73987186 | snp | A/G | 0.0185938 | 0.0946107 | intron-variant | SPAG16 | GRCh38.p7 | 2:214132731 | AGAGTAACATATGGG[A/G]AAATTTAAGGAAGAT | 79582 |
rs73987187 | snp | C/T | 0.0984431 | 0.198823 | intron-variant | SPAG16 | GRCh38.p7 | 2:214134532 | TCCGTGAGGCTTGTC[C/T]ACCACCTAAAATCGG | 79582 |
rs73987194 | snp | A/G | 0.104859 | 0.203554 | intron-variant | SPAG16 | GRCh38.p7 | 2:214176423 | TCCAAACAGATCTTA[A/G]TATGCCCCTCTTATC | 79582 |
rs73987195 | snp | A/G | 0.104504 | 0.2033 | intron-variant | SPAG16 | GRCh38.p7 | 2:214176486 | AGTAGGCTACTAAGC[A/G]GTCTTTCAAAGATTT | 79582 |
rs73987198 | snp | C/T | 0.0279526 | 0.114869 | intron-variant | SPAG16 | GRCh38.p7 | 2:214207961 | GCCTTCGGCCACACA[C/T]GGAAGTCTGCACTGT | 79582 |
rs73987200 | snp | A/G | 0.0988009 | 0.199095 | intron-variant | SPAG16 | GRCh38.p7 | 2:214228397 | TAAAATGCATTCATA[A/G]GAAATATTTTACCTC | 79582 |
rs73987201 | snp | A/G | 0.0126979 | 0.078662 | intron-variant | SPAG16 | GRCh38.p7 | 2:214229367 | AAAGATGTGAGAGAG[A/G]AGAATGGGCATGCAT | 79582 |
rs73987202 | snp | A/T | 0.109108 | 0.206518 | intron-variant | SPAG16 | GRCh38.p7 | 2:214233352 | AGATAATAATGATGA[A/T]GATGATGATGATGAT | 79582 |
rs73987316 | snp | C/G | 0.0460142 | 0.144533 | intron-variant | SPAG16 | GRCh38.p7 | 2:214408856 | TGAGCAAGTTACTTC[C/G]CCTTTCCAAGCCTCT | 79582 |
rs73987909 | snp | G/T | 0.00199481 | 0.0315187 | intron-variant, upstream-variant-2KB, nc-transcript-variant, utr-variant-5-prime | SPAG16, LOC100130451 | GRCh38.p7 | 2:213285902 | TTATCTATATCCAGT[G/T]CCCTTGCTACTGAAT | 79582 |
rs73987911 | snp | G/T | 0.0267878 | 0.112589 | intron-variant | SPAG16 | GRCh38.p7 | 2:213290104 | TCCCTGGCAGTTTCA[G/T]TGTGGGTGTTACATT | 79582 |
rs73987914 | snp | C/G | 0.5 | 0 | intron-variant | SPAG16 | GRCh38.p7 | 2:213297499 | TTATTTGTGATCAAG[C/G]CTTCACTTTAAGGTA | 79582 |
rs73987915 | snp | A/C | 0.0252325 | 0.109451 | intron-variant, utr-variant-5-prime | SPAG16 | GRCh38.p7 | 2:213301217 | TCATTATTGAATTCC[A/C]ATTCTCTCCATGTAC | 79582 |
rs73987971 | snp | A/T | 0.00398564 | 0.0444627 | intron-variant | SPAG16 | GRCh38.p7 | 2:213309986 | GGATGAATGAATGAG[A/T]CGAAGGCTTATCTAT | 79582 |
rs73987972 | snp | C/G | 0.0252325 | 0.109451 | intron-variant | SPAG16 | GRCh38.p7 | 2:213312532 | CACTTCTTTTTAAAC[C/G]ATTTTTCCCTTTCCA | 79582 |
rs73987973 | snp | C/T | 0.0267878 | 0.112589 | intron-variant | SPAG16 | GRCh38.p7 | 2:213313807 | CTGTCTGGTTCTAAG[C/T]GATAGTCGCGATAGT | 79582 |
rs73987974 | snp | A/G | 0.00557542 | 0.0525036 | intron-variant | SPAG16 | GRCh38.p7 | 2:213319776 | AAGTACTGGTTGTTT[A/G]TTGAATATTATGTTT | 79582 |
rs73987976 | snp | A/G | 0.0263992 | 0.111815 | intron-variant | SPAG16 | GRCh38.p7 | 2:213327219 | GAGGAAATATTATAT[A/G]GTTTAAAATATTAGC | 79582 |
rs73987977 | snp | C/T | 0.0387552 | 0.1337 | intron-variant | SPAG16 | GRCh38.p7 | 2:213327970 | ATATTTAATTGAATA[C/T]GCTTTGAAGCTCATT | 79582 |
rs73987979 | snp | A/C | 0.156319 | 0.231784 | intron-variant | SPAG16 | GRCh38.p7 | 2:213335502 | ATACAATAACAAATT[A/C]GAAAAGATAAAAAGC | 79582 |
rs73987980 | snp | C/T | 0.155656 | 0.231515 | intron-variant | SPAG16 | GRCh38.p7 | 2:213336069 | GAAGAGCATCGAGGG[C/T]CCACCCAAGAGCTGT | 79582 |
rs73987993 | snp | A/G | 0.19459 | 0.243782 | intron-variant | SPAG16 | GRCh38.p7 | 2:213339189 | GGTAGCATCCCATAC[A/G]CTGATCCTCAGTGAT | 79582 |
rs73987994 | snp | A/C | 0.156319 | 0.231784 | intron-variant | SPAG16 | GRCh38.p7 | 2:213339934 | TTAGATGAAATGTAG[A/C]TGAATCATATTTTTG | 79582 |
rs73987995 | snp | A/G | 0.00199481 | 0.0315187 | intron-variant | SPAG16 | GRCh38.p7 | 2:213341070 | TTACATGTTTTTTTC[A/G]TATTTCATTATTTCA | 79582 |
rs73987996 | snp | A/G | 0.19459 | 0.243782 | intron-variant, upstream-variant-2KB | SPAG16 | GRCh38.p7 | 2:213343578 | TTACAGAATTAGCAG[A/G]CAGGGACTTTACAAC | 79582 |
rs73987997 | snp | G/T | 0.0189856 | 0.0955633 | intron-variant, utr-variant-5-prime | SPAG16 | GRCh38.p7 | 2:213343822 | AAGCTGAAAAGAAAT[G/T]AGCAGGGACTCAAAG | 79582 |
rs73987998 | snp | A/G | 0.029116 | 0.117091 | intron-variant | SPAG16 | GRCh38.p7 | 2:213343915 | GTGTATTTGAAATCC[A/G]AGAAGAGGCTGGGCA | 79582 |
rs73987999 | snp | C/T | 0.00398564 | 0.0444627 | intron-variant | SPAG16 | GRCh38.p7 | 2:213350378 | TGTATGCTTTTTGTG[C/T]TTCTTGGCTGTAGTG | 79582 |
rs73988000 | snp | C/T | 0.0271762 | 0.113356 | intron-variant | SPAG16 | GRCh38.p7 | 2:213351519 | GTGAGATACCTTTGG[C/T]ATAAAAATTTAAGAA | 79582 |
rs73988001 | snp | A/G | 0.0275645 | 0.114116 | intron-variant | SPAG16 | GRCh38.p7 | 2:213352616 | TGTTGTAAAACACCC[A/G]AGTGAGGATTCAGGT | 79582 |
rs73988002 | snp | A/G | 0.00199481 | 0.0315187 | intron-variant | SPAG16 | GRCh38.p7 | 2:213352804 | AAATATATCTTTATT[A/G]TCTGCAACTGGTTTT | 79582 |
rs73988511 | snp | C/T | 0.00557542 | 0.0525036 | intron-variant | SPAG16 | GRCh38.p7 | 2:213490301 | AGACTAAGTGCACTA[C/T]TGTGTATTTTATTGT | 79582 |
rs73988512 | snp | G/T | 0.0275645 | 0.114116 | intron-variant | SPAG16 | GRCh38.p7 | 2:213490472 | TTCTTTTTACTTGTT[G/T]GTTATGAGGACTGTA | 79582 |
rs73988514 | snp | A/G | 0.0260105 | 0.111035 | intron-variant | SPAG16 | GRCh38.p7 | 2:213490854 | ATACAAAAATATATG[A/G]CATTTGTTTTGTAAT | 79582 |
rs73988515 | snp | G/T | 0.0260105 | 0.111035 | intron-variant | SPAG16 | GRCh38.p7 | 2:213490956 | ACCTATAGTGAGTAT[G/T]TTTTTTTCATTTGCA | 79582 |
rs73988517 | snp | A/G | 0.0252325 | 0.109451 | intron-variant | SPAG16 | GRCh38.p7 | 2:213493016 | CACCTTGCGAATCAC[A/G]AAGAAAGAATTTGTG | 79582 |
rs73988518 | snp | A/G | 0.150667 | 0.229419 | intron-variant | SPAG16 | GRCh38.p7 | 2:213494791 | CCTACCTCCTTGGCT[A/G]CATGCTCTCCCACTC | 79582 |
rs73988519 | snp | C/T | 0.00517822 | 0.0506191 | intron-variant | SPAG16 | GRCh38.p7 | 2:213494908 | TACCTTCTCCACAGA[C/T]TCCCAGTATTACTTC | 79582 |
rs73988520 | snp | G/T | 0.17332 | 0.23795 | intron-variant | SPAG16 | GRCh38.p7 | 2:213495461 | TTTTAAAAATAAAAA[G/T]ATTGAAGAGATTTTC | 79582 |
rs73988521 | snp | C/T | 0.00517822 | 0.0506191 | intron-variant | SPAG16 | GRCh38.p7 | 2:213495619 | AATAGTGAACACATG[C/T]TGTATTTGATGGCCA | 79582 |
rs73988522 | snp | G/T | 0.174288 | 0.23826 | intron-variant | SPAG16 | GRCh38.p7 | 2:213496165 | AGTAATCCAAGAAAA[G/T]TATAAGGTTTCCTGG | 79582 |
rs73988523 | snp | C/G | 0.0185938 | 0.0946107 | intron-variant | SPAG16 | GRCh38.p7 | 2:213504808 | GTGAGGTTGAATTCT[C/G]GCTAAATGTCCCTGT | 79582 |
rs73988524 | snp | A/G | 0.0244538 | 0.107838 | intron-variant | SPAG16 | GRCh38.p7 | 2:213507297 | CTGAGTTTTGGCACC[A/G]TTGTTTTAAAGACCC | 79582 |
rs73988525 | snp | A/G | 0.0498117 | 0.149749 | intron-variant | SPAG16 | GRCh38.p7 | 2:213510701 | CTTAGTACAGGCATA[A/G]TTTTTTAATCTGACA | 79582 |
rs73988526 | snp | C/T | 0.0252325 | 0.109451 | intron-variant | SPAG16 | GRCh38.p7 | 2:213510874 | TTTCCAATCCTGGAA[C/T]CAATTTATAGTTCAT | 79582 |
rs73988527 | snp | C/T | 0.176219 | 0.238865 | intron-variant | SPAG16 | GRCh38.p7 | 2:213511373 | AAAATACCATCGTTT[C/T]GAGATTTGGAAAAAA | 79582 |
rs73988529 | snp | A/G | 0.170733 | 0.237101 | intron-variant | SPAG16 | GRCh38.p7 | 2:213511516 | ATGTTAGATTTTTCT[A/G]TAGCATAATTATTAT | 79582 |
rs73988530 | snp | A/C | 0.00557542 | 0.0525036 | intron-variant | SPAG16 | GRCh38.p7 | 2:213512234 | AAGAAGATAAACAAA[A/C]TAGACTTTTGAACAA | 79582 |
rs73988531 | snp | A/G | 0.173965 | 0.238157 | intron-variant | SPAG16 | GRCh38.p7 | 2:213512797 | GCATTTCCTGCGTTT[A/G]TTGGGAACTGGAAGT | 79582 |
rs73988534 | snp | C/T | 0.17138 | 0.237316 | intron-variant | SPAG16 | GRCh38.p7 | 2:213515823 | GCAAGAGATCTGTTC[C/T]TCATTTCCTGACAAG | 79582 |
rs73988535 | snp | A/G | 0.174288 | 0.23826 | intron-variant | SPAG16 | GRCh38.p7 | 2:213527080 | GCCTGGTATCCTTAA[A/G]GCTATCTCTGCCATG | 79582 |
rs73988536 | snp | C/G | 0.0252325 | 0.109451 | intron-variant | SPAG16 | GRCh38.p7 | 2:213534304 | ATGTCCACTTTAGTA[C/G]AGCCTCTATGGAAAA | 79582 |
rs73988538 | snp | A/G | 0.171704 | 0.237423 | intron-variant | SPAG16 | GRCh38.p7 | 2:213542637 | CAACAAATACTAAGT[A/G]TAAGAATATTGCGAA | 79582 |
rs73988540 | snp | A/G | 0.0236746 | 0.106192 | intron-variant | SPAG16 | GRCh38.p7 | 2:213544384 | TAAGAGCAGTTTTAG[A/G]TTCATGGCAAAACTG | 79582 |
rs73988541 | snp | A/G | 0.0252325 | 0.109451 | intron-variant | SPAG16 | GRCh38.p7 | 2:213545929 | TAAGCCTGGTTTCTG[A/G]TGACCCAAAGCTGAT | 79582 |
rs73988542 | snp | A/G | 0.0252325 | 0.109451 | intron-variant | SPAG16 | GRCh38.p7 | 2:213547005 | GGAAAAGAACCTGAG[A/G]CTAATAGAAATAGAT | 79582 |
rs73988543 | snp | C/G | 0.00557542 | 0.0525036 | intron-variant | SPAG16 | GRCh38.p7 | 2:213551350 | GGGGGCATTTCCCAA[C/G]AAAAGTACTGGCAGG | 79582 |
rs73988544 | snp | C/T | 0.154661 | 0.231107 | intron-variant | SPAG16 | GRCh38.p7 | 2:213555854 | GTATCTTTAGTATAA[C/T]GGTTGAAAGACAAAA | 79582 |
rs73988545 | snp | A/C | 0.0494327 | 0.149241 | intron-variant | SPAG16 | GRCh38.p7 | 2:213559998 | TCAAAGATAAAAATG[A/C]AACCTGTTCCCTACC | 79582 |
rs73988546 | snp | C/T | 0.173643 | 0.238054 | intron-variant | SPAG16 | GRCh38.p7 | 2:213561961 | ATGCTCAGCCAATTA[C/T]TCTGTCTTGAAACTG | 79582 |
rs73988547 | snp | C/T | 0.197082 | 0.244335 | intron-variant | SPAG16 | GRCh38.p7 | 2:213562341 | TAATTCTGAAGACTC[C/T]GATCTTTAGTAGCCA | 79582 |
rs73988548 | snp | A/T | 0.197703 | 0.244469 | intron-variant | SPAG16 | GRCh38.p7 | 2:213563600 | CACCAATCCTATTGG[A/T]TCAGGACCCCATCCT | 79582 |
rs73988550 | snp | A/G | 0.0228947 | 0.104514 | intron-variant | SPAG16 | GRCh38.p7 | 2:213565869 | ATGATTCAAAGCAAT[A/G]ATAACGATTGTTGAA | 79582 |
rs73988551 | snp | A/G | 0.240765 | 0.249829 | intron-variant | SPAG16 | GRCh38.p7 | 2:213573356 | CATTTTTATTTCTCT[A/G]TGATAATTTTTGACA | 79582 |
rs73988552 | snp | C/T | 0.171704 | 0.237423 | intron-variant | SPAG16 | GRCh38.p7 | 2:213575393 | AAAGCAATAATAAAA[C/T]TAAAGGGTATTTATT | 79582 |
rs73988553 | snp | C/T | 0.0185938 | 0.0946107 | intron-variant | SPAG16 | GRCh38.p7 | 2:213577159 | AAGGGTACATTTTAA[C/T]AGAGGAATCAACATT | 79582 |
rs73988554 | snp | A/G | 0.17332 | 0.23795 | intron-variant | SPAG16 | GRCh38.p7 | 2:213577222 | ATTTAAAAAGAAAAT[A/G]TTCTGTGGCAACATA | 79582 |
rs73988556 | snp | G/T | 0.0228947 | 0.104514 | intron-variant | SPAG16 | GRCh38.p7 | 2:213583005 | ATGCTATGTCATTTT[G/T]TATTTAAAGGTAAGT | 79582 |
rs73988557 | snp | A/G | 0.149665 | 0.228982 | intron-variant | SPAG16 | GRCh38.p7 | 2:213584602 | AAAGGAAAGGAAAAA[A/G]GAAGGAAAGAAGGAA | 79582 |
rs73988558 | snp | A/G | 0.0228947 | 0.104514 | intron-variant | SPAG16 | GRCh38.p7 | 2:213589070 | GGTTTTACAAAAAAC[A/G]TAAGCAAAAAGTATA | 79582 |
rs73988560 | snp | C/T | 0.0232847 | 0.105357 | intron-variant | SPAG16 | GRCh38.p7 | 2:213592744 | GTGCTAATGAAGTTC[C/T]TTGCTGTGCAACACA | 79582 |
rs73988561 | snp | C/T | 0.174932 | 0.238463 | intron-variant | SPAG16 | GRCh38.p7 | 2:213598278 | AGAACCTTCAGAGGG[C/T]GAAGGGGAAGTTCTC | 79582 |
rs73988562 | snp | C/G | 0.00557542 | 0.0525036 | intron-variant | SPAG16 | GRCh38.p7 | 2:213601329 | TGGAGGGGAGAGAGA[C/G]CTTGAGGCTTCTTTT | 79582 |
rs73988563 | snp | A/G | 0.0185938 | 0.0946107 | intron-variant | SPAG16 | GRCh38.p7 | 2:213606322 | ATGTTCAGGCATATT[A/G]TATATTACAAAACCA | 79582 |
rs73988575 | snp | A/T | 0.0182019 | 0.0936463 | intron-variant | SPAG16 | GRCh38.p7 | 2:213630868 | GGACATAAATAAACA[A/T]ATGTTAATATAGTTT | 79582 |
rs73988576 | snp | A/G | 0.0505692 | 0.150756 | intron-variant | SPAG16 | GRCh38.p7 | 2:213646975 | AAACATAAATACTTA[A/G]CAATTTAAACATAAA | 79582 |
rs73988578 | snp | C/G | 0.029116 | 0.117091 | intron-variant | SPAG16 | GRCh38.p7 | 2:213647388 | CAGAGCCAGTTCTGA[C/G]TCTTCTGCTTCTTTC | 79582 |
rs73988580 | snp | A/G | 0.0505692 | 0.150756 | intron-variant | SPAG16 | GRCh38.p7 | 2:213657218 | TGTAAAGTGATAAGT[A/G]CATCAATGAATATAT | 79582 |
rs73988582 | snp | C/T | 0.0505692 | 0.150756 | intron-variant | SPAG16 | GRCh38.p7 | 2:213662413 | CAATAGGGAAAGTTA[C/T]GAGAGATGAAGCTAG | 79582 |
rs73988583 | snp | G/T | 0.00597247 | 0.0543191 | intron-variant | SPAG16 | GRCh38.p7 | 2:213669392 | TAAGGCAGCCTCTAA[G/T]AAAAGCATCATTTAT | 79582 |
rs73988584 | snp | A/C | 0.0182019 | 0.0936463 | intron-variant | SPAG16 | GRCh38.p7 | 2:213669695 | AAGCGCTTGGATTTA[A/C]TGAGAAGTGTTCTGT | 79582 |
rs73988586 | snp | A/G | 0.0182019 | 0.0936463 | intron-variant | SPAG16 | GRCh38.p7 | 2:213672616 | TATTTTATTGAGTCT[A/G]TTGTCATGTCATATA | 79582 |
rs73988587 | snp | G/T | 0.0287284 | 0.116357 | intron-variant | SPAG16 | GRCh38.p7 | 2:213685452 | TCCCTAGCACCTTCA[G/T]TGGGAGCATGACTCT | 79582 |
rs73988588 | snp | C/T | 0.0279526 | 0.114869 | intron-variant | SPAG16 | GRCh38.p7 | 2:213691107 | CTGGCAACATCTGAA[C/T]TTTGGAGAGGGCACA | 79582 |
rs73988589 | snp | G/T | 0.00597247 | 0.0543191 | intron-variant | SPAG16 | GRCh38.p7 | 2:213691234 | CCTTGTGTAACCCTT[G/T]CCTCTTGAATCTGGG | 79582 |
rs73988590 | snp | A/G | 0.0490535 | 0.14873 | intron-variant | SPAG16 | GRCh38.p7 | 2:213694470 | TCAAGTTCCATATGC[A/G]TTGCTTTCTAGTATA | 79582 |
rs73988591 | snp | A/G | 0.00597247 | 0.0543191 | intron-variant | SPAG16 | GRCh38.p7 | 2:213695375 | TATGCTTATTATACT[A/G]TCCGCTAAACTGTCC | 79582 |
rs73988592 | snp | C/T | 0.0182019 | 0.0936463 | intron-variant | SPAG16 | GRCh38.p7 | 2:213700552 | GAATGTTACTTACAT[C/T]TTAATGAAGGGATAA | 79582 |
rs73988593 | snp | C/G | 0.0490535 | 0.14873 | intron-variant | SPAG16 | GRCh38.p7 | 2:213702802 | CCTATTTCTAGAGTT[C/G]ATATATATCAAGAAG | 79582 |
rs73989404 | snp | A/G | 0.00795532 | 0.062565 | intron-variant | SPAG16 | GRCh38.p7 | 2:214237374 | GTTAGCATTTTATTC[A/G]TAAGATAATTACCAT | 79582 |
rs73989405 | snp | A/G | 0.0119091 | 0.0762411 | intron-variant | SPAG16 | GRCh38.p7 | 2:214244047 | TAAGTAATTTTAATC[A/G]TAATGCATTGCGAAT | 79582 |
rs73989406 | snp | A/G | 0.0023933 | 0.0345097 | intron-variant | SPAG16 | GRCh38.p7 | 2:214245411 | TAAGTCCTGTATCTT[A/G]ATGGTACATTTTTAT | 79582 |
rs73989407 | snp | A/T | 0.0023933 | 0.0345097 | intron-variant | SPAG16 | GRCh38.p7 | 2:214255170 | TCAGTGAATCCATTA[A/T]CAATCTAATCAGTGT | 79582 |
rs73989410 | snp | A/T | 0.106633 | 0.204807 | intron-variant | SPAG16 | GRCh38.p7 | 2:214268430 | CATGAATGGATTTTT[A/T]AAATGTAATATATTT | 79582 |
rs73989412 | snp | G/T | 0.0023933 | 0.0345097 | intron-variant | SPAG16 | GRCh38.p7 | 2:214269910 | TATCCTGAAATGTTT[G/T]CTTAAAGGCAAATGT | 79582 |
rs73989414 | snp | A/T | 0.00517822 | 0.0506191 | intron-variant | SPAG16 | GRCh38.p7 | 2:214280238 | AAATAAAGAAGACAT[A/T]GAGAGCTATACTTGT | 79582 |
rs73989420 | snp | A/C | 0.119978 | 0.213528 | intron-variant | SPAG16 | GRCh38.p7 | 2:214324975 | TGCTACCATTTTATG[A/C]AGGAAATGACATTTT | 79582 |
rs73989421 | snp | A/G | 0.119978 | 0.213528 | intron-variant | SPAG16 | GRCh38.p7 | 2:214326420 | AGAACTGGGAGAGAA[A/G]CAATTTGTGTTGTTT | 79582 |
rs73989422 | snp | G/T | 0.120326 | 0.21374 | intron-variant | SPAG16 | GRCh38.p7 | 2:214328002 | AATTCTGTTTCATCT[G/T]TGTGTATGTTCCTAG | 79582 |
rs73989424 | snp | A/T | 0.119978 | 0.213528 | intron-variant | SPAG16 | GRCh38.p7 | 2:214328631 | AATCTCGTATCTCAA[A/T]TTCTATCTATCTTTA | 79582 |
rs73989426 | snp | A/G | 0.120326 | 0.21374 | intron-variant | SPAG16 | GRCh38.p7 | 2:214330468 | GAGATGAAGATCTGC[A/G]TCCAGGAGTCTTATT | 79582 |
rs73989428 | snp | A/G | 0.00279162 | 0.0372561 | intron-variant | SPAG16 | GRCh38.p7 | 2:214334563 | ACTGCCCTCCAGTTG[A/G]TGGAGTTGAAAATAT | 79582 |
rs73989431 | snp | A/G | 0.0475351 | 0.146656 | intron-variant | SPAG16 | GRCh38.p7 | 2:214337875 | AAAACAAGACAATAA[A/G]CCAGGTGACTAAAGA | 79582 |
rs73989432 | snp | A/G | 0.00676609 | 0.0577691 | intron-variant | SPAG16 | GRCh38.p7 | 2:214338681 | AGAATGAAAAGGTGA[A/G]CCACAATTCTATCAG | 79582 |
rs73989433 | snp | C/T | 0.00676609 | 0.0577691 | intron-variant | SPAG16 | GRCh38.p7 | 2:214338682 | GAATGAAAAGGTGAG[C/T]CACAATTCTATCAGC | 79582 |
rs73989434 | snp | A/T | 0.118584 | 0.212673 | intron-variant | SPAG16 | GRCh38.p7 | 2:214339879 | TTGACACTGAGTTAA[A/T]CTAAAAGGAGATTAT | 79582 |
rs73989435 | snp | A/G | 0.00676609 | 0.0577691 | intron-variant | SPAG16 | GRCh38.p7 | 2:214341485 | ATTTTCAAGGAGTCT[A/G]CAGAGAAGGAAACTT | 79582 |
rs73989438 | snp | C/T | 0.00676609 | 0.0577691 | intron-variant | SPAG16 | GRCh38.p7 | 2:214341694 | GCCAACTTATCAACC[C/T]TGAAGCAATATCAGG | 79582 |
rs73989440 | snp | A/C | 0.118933 | 0.212888 | intron-variant | SPAG16 | GRCh38.p7 | 2:214342947 | ATGTAACTCTCCACA[A/C]CCCTGACAATGAAAA | 79582 |
rs73989442 | snp | A/C | 0.0166325 | 0.0896639 | intron-variant | SPAG16 | GRCh38.p7 | 2:214347214 | AACATAAAAAGTTGT[A/C]AATGTACCTAATAAA | 79582 |
rs73989443 | snp | C/T | 0.0166325 | 0.0896639 | intron-variant | SPAG16 | GRCh38.p7 | 2:214348511 | CCAGGTCTAGGTTAC[C/T]AAAGTTATGAAGCTG | 79582 |
rs73989445 | snp | A/G | 0.118933 | 0.212888 | intron-variant | SPAG16 | GRCh38.p7 | 2:214349622 | ATAGCTGGGTCATAA[A/G]GTATGTGTAAGTTTT | 79582 |
rs73989446 | snp | A/T | 0.118933 | 0.212888 | intron-variant | SPAG16 | GRCh38.p7 | 2:214349764 | TGTCAATCTTTTTTG[A/T]TTTAGTTATTCTAAT | 79582 |
rs73989451 | snp | C/G | 0.119281 | 0.213102 | intron-variant | SPAG16 | GRCh38.p7 | 2:214353131 | TCTAAATATTTATTT[C/G]GTCTAACTATCAAAT | 79582 |
rs73989454 | snp | C/T | 0.0162398 | 0.0886349 | intron-variant | SPAG16 | GRCh38.p7 | 2:214357577 | TAAAATGTGACTAGA[C/T]ATTTGTATAGTCTCT | 79582 |
rs73989455 | snp | C/T | 0.13446 | 0.221699 | intron-variant | SPAG16 | GRCh38.p7 | 2:214358188 | GTGTGTAGTGTCTTA[C/T]GCGATGCTCTTGGTG | 79582 |
rs73989456 | snp | C/T | 0.13446 | 0.221699 | intron-variant | SPAG16 | GRCh38.p7 | 2:214358190 | GTGTAGTGTCTTATG[C/T]GATGCTCTTGGTGTC | 79582 |
rs73989457 | snp | A/G | 0.0162398 | 0.0886349 | intron-variant | SPAG16 | GRCh38.p7 | 2:214358728 | AGCCTCCAAGGACTC[A/G]AATAATAATGGGAGT | 79582 |
rs73989458 | snp | C/T | 0.0162398 | 0.0886349 | intron-variant | SPAG16 | GRCh38.p7 | 2:214359472 | TACAACTTTAGAGCA[C/T]GAGAGAGAATATTTT | 79582 |
rs73989459 | snp | A/C | 0.118584 | 0.212673 | intron-variant | SPAG16 | GRCh38.p7 | 2:214359822 | ATAAATTATTAAAAA[A/C]ACATTTAAATGAAGA | 79582 |
rs73989461 | snp | C/T | 0.0162398 | 0.0886349 | intron-variant | SPAG16 | GRCh38.p7 | 2:214362351 | GGCCAAGCCTGAATT[C/T]CATGTTTAAGGAAGA | 79582 |
rs73989463 | snp | A/G | 0.00874735 | 0.0655527 | intron-variant | SPAG16 | GRCh38.p7 | 2:214375272 | TTCCAAGAAAAATAT[A/G]TGAAATTGTTAGAAA | 79582 |
rs73989464 | snp | A/G | 0.279461 | 0.248258 | intron-variant | SPAG16 | GRCh38.p7 | 2:214376827 | TGTTGAGTAAATCAC[A/G]TGACTGAATGACACA | 79582 |
rs73989465 | snp | A/C | 0.104504 | 0.2033 | intron-variant | SPAG16 | GRCh38.p7 | 2:214379799 | CCAGGTGGGCATACT[A/C]ACCATGGCCCTAAGC | 79582 |
rs73989466 | snp | C/T | 0.0839998 | 0.186933 | intron-variant | SPAG16 | GRCh38.p7 | 2:214379853 | CAAAGAGAATTCTTC[C/T]TCTTCATTATCTTTC | 79582 |
rs73989467 | snp | A/G | 0.0729998 | 0.176553 | intron-variant | SPAG16 | GRCh38.p7 | 2:214382022 | TAAATTTATTTCCCT[A/G]TAGATTTGGAAAAAG | 79582 |
rs73990005 | snp | A/T | 0.324855 | 0.23853 | intron-variant | SPAG16 | GRCh38.p7 | 2:213947872 | CTTAAAATCAGATAG[A/T]GTGATTCCTTCAGCA | 79582 |
rs73990006 | snp | A/G | 0.181659 | 0.240478 | intron-variant | SPAG16 | GRCh38.p7 | 2:213949730 | ATTGCATAATGAGGC[A/G]TATGAAAGCACATTT | 79582 |
rs73990303 | snp | A/G | 0.194278 | 0.243711 | intron-variant | SPAG16 | GRCh38.p7 | 2:213353665 | ACTCATGTCTGACCT[A/G]TTGTTACCTCGTCCC | 79582 |
rs73990304 | snp | A/C | 0.0263992 | 0.111815 | intron-variant | SPAG16 | GRCh38.p7 | 2:213353671 | GTCTGACCTGTTGTT[A/C]CCTCGTCCCTCAGGC | 79582 |
rs73990305 | snp | A/G | 0.0189856 | 0.0955633 | intron-variant | SPAG16 | GRCh38.p7 | 2:213360323 | ATTGATGGAGCCAAT[A/G]CAAGTCCTAGTTATA | 79582 |
rs73990307 | snp | A/C | 0.155656 | 0.231515 | intron-variant | SPAG16 | GRCh38.p7 | 2:213361122 | ATCCGATAGGAAATA[A/C]ATGTTTTCAAATTTC | 79582 |
rs73990308 | snp | A/G | 0.0383715 | 0.133092 | intron-variant | SPAG16 | GRCh38.p7 | 2:213361378 | TATGTGTGTGTGTGT[A/G]TATATATATATATAT | 79582 |
rs73990310 | snp | C/T | 0.0252325 | 0.109451 | intron-variant | SPAG16 | GRCh38.p7 | 2:213361956 | TTGGGGTTTTTATTG[C/T]GGTTGGGGGTTAGGG | 79582 |
rs73990311 | snp | C/T | 0.155656 | 0.231515 | intron-variant | SPAG16 | GRCh38.p7 | 2:213362015 | GAGGCTTGAGTCATT[C/T]GAATCTCCCATCAGT | 79582 |
rs73990312 | snp | C/T | 0.0263992 | 0.111815 | intron-variant | SPAG16 | GRCh38.p7 | 2:213362310 | TGATTAGTAAGGACA[C/T]GTGAGAGAGTAGACA | 79582 |
rs73990321 | snp | A/G | 0.0283406 | 0.115616 | intron-variant | SPAG16 | GRCh38.p7 | 2:213362487 | AGTAACTTTACAGTG[A/G]GGAAACCTGTCAACC | 79582 |
rs73990322 | snp | C/T | 0.0113515 | 0.0744774 | intron-variant | SPAG16 | GRCh38.p7 | 2:213364034 | AACCTTTTTAAAAGT[C/T]ATTTAGTGTATAATT | 79582 |
rs73990323 | snp | A/G | 0.0252325 | 0.109451 | intron-variant, utr-variant-3-prime | SPAG16 | GRCh38.p7 | 2:213369954 | CTTTTGATGTTGTAC[A/G]TTCTGTGGAATTCAA | 79582 |
rs73990325 | snp | A/G | 0.19459 | 0.243782 | intron-variant, downstream-variant-500B | SPAG16 | GRCh38.p7 | 2:213371865 | TTAAAGAATCACCCC[A/G]TAATTGCTGCCATAC | 79582 |
rs73990327 | snp | A/T | 0.00557542 | 0.0525036 | intron-variant | SPAG16 | GRCh38.p7 | 2:213372602 | TTTTTCAAATATAAC[A/T]TCTTCTTATTTAACT | 79582 |
rs73990339 | snp | C/G | 0.173965 | 0.238157 | intron-variant | SPAG16 | GRCh38.p7 | 2:213386430 | CTTTAATTCTCACTC[C/G]CATCCTTCTAAATCT | 79582 |
rs73990340 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | SPAG16 | GRCh38.p7 | 2:213386541 | CTAAAACATGCCTCT[A/G]TAAGCTCGTCTAATC | 79582 |
rs73990341 | snp | G/T | 0.193966 | 0.243639 | intron-variant, utr-variant-3-prime | SPAG16 | GRCh38.p7 | 2:213398906 | ATATGTAAATTTGAA[G/T]GAATGCATAAATTAA | 79582 |
rs73990342 | snp | A/C | 0.0217361 | 0.102049 | intron-variant, downstream-variant-500B | SPAG16 | GRCh38.p7 | 2:213401679 | GTGGGCAGTCTCTTT[A/C]ATTTATCTGGTGATT | 79582 |
rs73990344 | snp | A/G | 0.155656 | 0.231515 | intron-variant | SPAG16 | GRCh38.p7 | 2:213407265 | GGACCTTCAGAGGGG[A/G]AAAGGGAGAAATAGG | 79582 |
rs73990345 | snp | A/G | 0.162537 | 0.235983 | intron-variant | SPAG16 | GRCh38.p7 | 2:213407417 | CCCCCTGGTTTACGG[A/G]GTTGAGCCTTCCGGG | 79582 |
rs73990346 | snp | A/G | 0.00557542 | 0.0525036 | intron-variant | SPAG16 | GRCh38.p7 | 2:213411514 | ATTAGCAGAAAGAGG[A/G]GTTTGCGTCATGATT | 79582 |
rs73990347 | snp | C/T | 0.0252325 | 0.109451 | intron-variant | SPAG16 | GRCh38.p7 | 2:213413071 | AGTATGTTGATACTA[C/T]AAATGGTGTTTTATA | 79582 |
rs74181304 | multinucleotide-polymorphism | AT/GA | 0 | 0 | intron-variant | SPAG16 | GRCh38.p7 | 2:213366669 | CCCTTGACACATGGG[AT/GA]TTATGGGAGCTACAA | 79582 |
rs74181305 | multinucleotide-polymorphism | AAAAC/GTTTT | 0 | 0 | intron-variant | SPAG16 | GRCh38.p7 | 2:213621059 | CTAGTACTAAAACTA[AAAAC/GTTTT]TAGTTTTAGTACTTA | 79582 |
rs74181306 | multinucleotide-polymorphism | AC/GT | 0 | 0 | intron-variant | SPAG16 | GRCh38.p7 | 2:213625661 | CTTTTTGTTGTTGTT[AC/GT]TGTTCTTTTTTTTGT | 79582 |
rs74181308 | multinucleotide-polymorphism | CA/TG | 0 | 0 | intron-variant | SPAG16 | GRCh38.p7 | 2:213719629 | GTCACCCACCAATTC[CA/TG]GACACAATACCATCT | 79582 |
rs74181309 | multinucleotide-polymorphism | CC/TT | 0 | 0 | intron-variant | SPAG16 | GRCh38.p7 | 2:213726118 | CTGAGGACTTCCTCT[CC/TT]CTGCTGAAGTTCACT | 79582 |
rs74204869 | in-del | -/TATAA/TATATATATATTATATATATAATATATATTATATATTATATATATAATATATATATTATATATATAATATATATAT | 0 | 0 | intron-variant | SPAG16 | GRCh38.p7 | 2:213833576 | ATATAATATATATAT[lengthTooLong]AATATATATATTATA | 79582 |
rs74267779 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | SPAG16 | GRCh38.p7 | 2:213700766 | GTCCCTTTCATTACC[C/T]CTTTTACAGATTTTT | 79582 |
rs74268625 | snp | A/C | 0.0930568 | 0.194599 | intron-variant | SPAG16 | GRCh38.p7 | 2:214295463 | AAGGAATTTTGAATA[A/C]CCTCCCTCCCTAAGC | 79582 |
rs74269746 | in-del | -/GAAA | | | intron-variant | SPAG16 | GRCh38.p7 | 2:213799960 | GTGATAGACTGGATT[-/GAAA]AAAAAAAAAAAAAGA | 79582 |
rs74269748 | in-del | -/ACTA | | | intron-variant | SPAG16 | GRCh38.p7 | 2:214319518 | AAAAAAAAAAAAAAA[-/ACTA]TAATAGGAATTAATG | 79582 |
rs74316770 | snp | C/T | 0.5 | 0 | intron-variant | SPAG16 | GRCh38.p7 | 2:213968088 | TCCTTTCCTTTCTTC[C/T]TTCCTTCTTTTTTCT | 79582 |
rs74319692 | snp | C/T | 0.0023933 | 0.0345097 | intron-variant | SPAG16 | GRCh38.p7 | 2:213901846 | GAGTGTAAAGAATGC[C/T]TGGAGTATATGGTTA | 79582 |
rs74321489 | snp | A/G | 0.00478085 | 0.0486577 | intron-variant, upstream-variant-2KB | SPAG16, LOC100130451 | GRCh38.p7 | 2:213286184 | TAATCACACTTATTT[A/G]AACTTTAACACATAT | 79582 |
rs74325136 | snp | G/T | 0.5 | 0 | intron-variant | SPAG16 | GRCh38.p7 | 2:213918206 | TTGTATCAGTGTTCA[G/T]CAAAGATATTGGCCT | 79582 |
rs74327137 | snp | A/T | 0.0197687 | 0.0974348 | intron-variant | SPAG16 | GRCh38.p7 | 2:214038156 | CAAAGTAGAGTATTG[A/T]CCTCTTTTATTCTAT | 79582 |
rs74332417 | snp | C/T | 0.0329836 | 0.124112 | intron-variant | SPAG16 | GRCh38.p7 | 2:214140429 | TTTGATGATACTATA[C/T]ATTTGGCAAATACTG | 79582 |
rs74337153 | snp | A/C/G | 0.0166325 | 0.0896639 | intron-variant | SPAG16 | GRCh38.p7 | 2:213451921 | AGGTGTCCCTGACTC[A/C/G]CCCCATACCCCGACC | 79582 |
rs74338931 | snp | A/G | 0.0471551 | 0.14613 | intron-variant | SPAG16 | GRCh38.p7 | 2:214002345 | GATTAAAAATAAATA[A/G]AAAACAAAACAATAA | 79582 |
rs74345516 | snp | A/C | 0.5 | 0 | intron-variant | SPAG16 | GRCh38.p7 | 2:214407728 | CTGAGAGTACCTCTT[A/C]TCTCTCAAACCAATT | 79582 |
rs74354521 | snp | A/G | 0.0410537 | 0.137264 | intron-variant | SPAG16 | GRCh38.p7 | 2:214022636 | ATTTTCACAATGGTT[A/G]GATAATAGGTGCTTA | 79582 |
rs74355617 | snp | A/G/T | 0.10589 | 0.207827 | intron-variant | SPAG16 | GRCh38.p7 | 2:213985744 | AAAAGGATGGAGTAC[A/G/T]CAAATGGTAATCATT | 79582 |
rs74359728 | in-del | -/TGTGTGTGTGTG | | | intron-variant | SPAG16 | GRCh38.p7 | 2:214284798 | AATAATATTTTACTC[-/TGTGTGTGTGTG]TGTGTGTGTGTGTGT | 79582 |
rs74360124 | snp | C/T | 0.0126979 | 0.078662 | intron-variant | SPAG16 | GRCh38.p7 | 2:213960749 | TTAATGTCTGATGCC[C/T]AAGAGGGGAAAAAGA | 79582 |
rs74360863 | snp | C/T | | | intron-variant | SPAG16 | GRCh38.p7 | 2:214001984 | ACAATTGTGGCTGAA[C/T]GTGAAAGGCACAGCT | 79582 |
rs74365153 | snp | A/G | 0.0463947 | 0.145069 | intron-variant | SPAG16 | GRCh38.p7 | 2:213336614 | CGCAGCACAGCAGCT[A/G]TGTCAGTTCATGGCT | 79582 |
rs74371214 | snp | A/G | 0.0463947 | 0.145069 | intron-variant | SPAG16 | GRCh38.p7 | 2:213353383 | AAATACAAGCCATGA[A/G]CAATTTGAAAACCAG | 79582 |
rs74373816 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | SPAG16 | GRCh38.p7 | 2:213421793 | AACCTGCCTGCAGAT[A/G]GGAGCTACCCACTCC | 79582 |
rs74378099 | snp | A/T | 0.0460142 | 0.144533 | intron-variant | SPAG16 | GRCh38.p7 | 2:213993093 | TTTGAGCTGTTTCAC[A/T]GTCTCATTGAAACAG | 79582 |
rs74383903 | snp | C/T | 0.0271762 | 0.113356 | intron-variant | SPAG16 | GRCh38.p7 | 2:213807001 | TTTTGTTGTGTTGTT[C/T]TGTTCAGTCCTTTAA | 79582 |
rs74387935 | snp | C/T | 0.0452528 | 0.143452 | intron-variant | SPAG16 | GRCh38.p7 | 2:213460510 | GCAGGGAACCTCAAT[C/T]AGGAATAAAACAGAA | 79582 |
rs74390619 | snp | A/C/G | 0.625 | 0.125 | intron-variant | SPAG16 | GRCh38.p7 | 2:213822875 | AGGGACATGGATGAA[A/C/G]CTGGAAACCGTCATT | 79582 |
rs74392856 | snp | C/T | 0.00159617 | 0.0282053 | intron-variant | SPAG16 | GRCh38.p7 | 2:213405480 | CCTTTCTGTTGGGAA[C/T]ATTCCAAATATTCTT | 79582 |
rs74399276 | snp | A/G | 0.5 | 0 | intron-variant | SPAG16 | GRCh38.p7 | 2:213432328 | GCTAGTGGTTTATCA[A/G]TTTTGTTTATCTTTT | 79582 |
rs74399470 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | SPAG16 | GRCh38.p7 | 2:213441362 | GAATGTCTTCTATAC[A/G]CATAGTATGGAATGA | 79582 |
rs74400233 | snp | C/G | 0.17138 | 0.237316 | intron-variant | SPAG16 | GRCh38.p7 | 2:213524858 | TGGACTTGGAATTTT[C/G]AGTTAATGTTGGAAT | 79582 |
rs74403093 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | SPAG16 | GRCh38.p7 | 2:213704166 | TCTTATAACAGCCAT[A/G]TAACAATATAACATA | 79582 |
rs74407465 | snp | A/G | 0.138886 | 0.22395 | intron-variant | SPAG16 | GRCh38.p7 | 2:213973243 | GTTCTCATTTCCCAA[A/G]GAAATTACCTTCCTG | 79582 |
rs74410231 | snp | C/T | 0.0150606 | 0.0854603 | intron-variant | SPAG16 | GRCh38.p7 | 2:213497732 | CCCACCCTTTAACTA[C/T]GGTTGGTAAGAAATG | 79582 |
rs74410891 | snp | G/T | 0.00636936 | 0.0560724 | intron-variant | SPAG16 | GRCh38.p7 | 2:213693566 | AATTTATGGGCTTTT[G/T]GGAAGTGTTTTGGGC | 79582 |
rs74413941 | snp | A/G | 0.0023933 | 0.0345097 | intron-variant | SPAG16 | GRCh38.p7 | 2:213454865 | ATGAAATTTTGTAAT[A/G]CAAGCACAAATGTAT | 79582 |
rs74415024 | snp | C/T | 0.132409 | 0.220618 | intron-variant | SPAG16 | GRCh38.p7 | 2:213292827 | CATAGATACTCATCT[C/T]TTTCCAGAGTGAGAA | 79582 |
rs74420064 | snp | A/G | 0.00636936 | 0.0560724 | intron-variant | SPAG16 | GRCh38.p7 | 2:213852196 | GTGGTGAAAATACCA[A/G]TATACAAAAGCGGCA | 79582 |
rs74422376 | snp | C/G | 0.375 | 0.216506 | intron-variant | SPAG16 | GRCh38.p7 | 2:213753059 | GCTCTGTCACCCAGG[C/G]TGGAGTGCAGTGGCG | 79582 |
rs74427304 | snp | A/C | 0.00159617 | 0.0282053 | intron-variant | SPAG16 | GRCh38.p7 | 2:214005427 | TTATGACCATTTGGG[A/C]ACAATGTTCAATTTA | 79582 |
rs74431158 | snp | C/T | 0.00636936 | 0.0560724 | intron-variant | SPAG16 | GRCh38.p7 | 2:213850047 | GAAGGTTCCAGGAGA[C/T]ATTTTCATAAATCTG | 79582 |
rs74437851 | snp | G/T | 0.0170251 | 0.090679 | intron-variant | SPAG16 | GRCh38.p7 | 2:213789558 | TTTATGTGTTATCTT[G/T]TATTTGAAAAGCAGC | 79582 |
rs74440697 | snp | G/T | 0.5 | 0 | intron-variant | SPAG16 | GRCh38.p7 | 2:214069711 | TGTCACCTTTTTTTT[G/T]GTTGTTTTTAAGCCC | 79582 |
rs74440909 | snp | A/G | 0.5 | 0 | intron-variant | SPAG16 | GRCh38.p7 | 2:213694055 | GACAAAAAAAAAAAA[A/G]AAAAAAGAGAGGGAG | 79582 |
rs74442522 | snp | A/G | 0.0248432 | 0.108648 | intron-variant, utr-variant-3-prime | SPAG16 | GRCh38.p7 | 2:213369768 | ATAGCAAAATTGAGT[A/G]GAAGGTACAGTGATT | 79582 |
rs74443460 | snp | A/G | 0.0441095 | 0.141807 | intron-variant | SPAG16 | GRCh38.p7 | 2:214226940 | TCAGACAACAGCTAA[A/G]TTGGATTGCCAAGTA | 79582 |
rs74446971 | snp | G/T | 0.5 | 0 | intron-variant | SPAG16 | GRCh38.p7 | 2:213792596 | TTTTTTTTTTTTTTT[G/T]TTTTGGAGACCGGGT | 79582 |
rs74447282 | snp | A/G | 0.121022 | 0.21416 | intron-variant | SPAG16 | GRCh38.p7 | 2:213325129 | TTGTATATTCTGGAT[A/G]TAAGTGCTTTGTTAG | 79582 |
rs74448169 | snp | G/T | 0.5 | 0 | intron-variant | SPAG16 | GRCh38.p7 | 2:213732752 | TCTGTGATTTTTTTT[G/T]AGCAGTGATTTATAG | 79582 |
rs74450781 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | SPAG16 | GRCh38.p7 | 2:213429810 | TACTCAGTATACATC[A/T]TAGACACATTCTCAA | 79582 |
rs74453237 | snp | C/T | 0.0205511 | 0.0992634 | intron-variant | SPAG16 | GRCh38.p7 | 2:214331832 | TTTGAATAAACACTC[C/T]GTAAGCCTTCTGATA | 79582 |
rs74454590 | snp | G/T | 0.5 | 0 | intron-variant | SPAG16 | GRCh38.p7 | 2:213604903 | CATAATTTTGTAAAC[G/T]TTTTTGTAAATATTT | 79582 |
rs74462857 | snp | C/G | 0.0429648 | 0.14013 | intron-variant | SPAG16 | GRCh38.p7 | 2:214242367 | CCCAGTACAGTTTTT[C/G]CTTGTCAAAATCATA | 79582 |
rs74467215 | snp | A/C | 0.00716266 | 0.059414 | intron-variant | SPAG16 | GRCh38.p7 | 2:213293501 | CTTGGACTGCTTATT[A/C]TGGGGGTAGTTAGCC | 79582 |
rs74467493 | snp | A/G | 0.152334 | 0.230133 | intron-variant | SPAG16 | GRCh38.p7 | 2:214006069 | ACTAAGGGTTAATAT[A/G]GTAATGAATTCTAGT | 79582 |
rs74469810 | snp | A/G | 0.0399052 | 0.1355 | intron-variant | SPAG16 | GRCh38.p7 | 2:214037314 | AACTTGTTTAATAAA[A/G]GTTATTTTTGATTAT | 79582 |
rs74473725 | snp | A/G | 0.18 | 0.24 | intron-variant | SPAG16 | GRCh38.p7 | 2:213822865 | ATGAAGCTGGAAACC[A/G]TCATTCTTAACAAAC | 79582 |
rs74474192 | snp | A/C | 0.0178098 | 0.0926698 | intron-variant | SPAG16 | GRCh38.p7 | 2:213878868 | TTCTTCTGCATATAG[A/C]AATCCAGTTTTCCCA | 79582 |
rs74485146 | snp | C/T | 0.0193772 | 0.0965046 | intron-variant | SPAG16 | GRCh38.p7 | 2:213832783 | ACAGTTTTCTTTGGG[C/T]CTTTGGATCTTCATT | 79582 |
rs74488182 | snp | A/C | 0.5 | 0 | intron-variant | SPAG16 | GRCh38.p7 | 2:213292663 | AGCGAGACTCCGTCT[A/C]AAAAAAAAAAAACAA | 79582 |
rs74494257 | snp | A/C | 0.0444908 | 0.142359 | intron-variant | SPAG16 | GRCh38.p7 | 2:214229116 | AAGCAAAACAGAGTT[A/C]TTTCTCTTATGGATC | 79582 |
rs74502509 | snp | C/G | 0.0271762 | 0.113356 | intron-variant, utr-variant-5-prime | SPAG16 | GRCh38.p7 | 2:213296173 | TTCTCATGAAATGCT[C/G]ATTTTATTTTCTGAA | 79582 |
rs74509121 | snp | A/C | 0.110519 | 0.207473 | intron-variant | SPAG16 | GRCh38.p7 | 2:213540608 | TAATGATTTTTCAAA[A/C]AGAATTAGAAGACTT | 79582 |
rs74511505 | snp | A/G | 0.0197687 | 0.0974348 | intron-variant | SPAG16 | GRCh38.p7 | 2:213830877 | TTTCGGGACATTTGT[A/G]TTATAAGTGCTGTGT | 79582 |
rs74514151 | snp | A/G | 0.232359 | 0.249377 | intron-variant | SPAG16 | GRCh38.p7 | 2:214211959 | TACCACTCTAGTTTC[A/G]GGCTACTGTGACACT | 79582 |
rs74517571 | snp | A/C | 0.0479149 | 0.147179 | intron-variant | SPAG16 | GRCh38.p7 | 2:213441585 | GTATTTATTTTTGTA[A/C]AAATGAATTGAGCTG | 79582 |
rs74532714 | snp | C/T | 0.00478085 | 0.0486577 | intron-variant | SPAG16 | GRCh38.p7 | 2:213302933 | AAATGAGAATAGATA[C/T]ACCCTCCTGCTGTCT | 79582 |
rs74537006 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | SPAG16 | GRCh38.p7 | 2:214032427 | TTTTTGTCAATAGTT[A/G]TAAGTGAACAGAGCC | 79582 |
rs74537846 | snp | C/G | 0.0456336 | 0.143994 | intron-variant | SPAG16 | GRCh38.p7 | 2:213459039 | TTTTCCAACCTGGGA[C/G]TCCAATTTACATTTT | 79582 |
rs74538156 | snp | A/G | 0.0267878 | 0.112589 | intron-variant | SPAG16 | GRCh38.p7 | 2:214226090 | AAATTACTGCATAAC[A/G]TACTACTTCAAATTT | 79582 |
rs74538847 | snp | A/G | 0.0810805 | 0.184299 | intron-variant | SPAG16 | GRCh38.p7 | 2:213859280 | AGCACAAGAAAATGA[A/G]TTAAAGATCTTAAAG | 79582 |
rs74542544 | snp | A/T | 0.127599 | 0.217986 | intron-variant | SPAG16 | GRCh38.p7 | 2:213610407 | AAGAAACACTTACCA[A/T]CTATTCTCTCCGAGG | 79582 |
rs74542728 | snp | C/T | 0.0217236 | 0.101931 | intron-variant | SPAG16 | GRCh38.p7 | 2:213890518 | AGTGTTTCCATTGTT[C/T]GCTTTCTTATTTCAA | 79582 |
rs74544202 | snp | G/T | 0.0622301 | 0.165053 | intron-variant | SPAG16 | GRCh38.p7 | 2:213957433 | TGGTATAGCCATCGT[G/T]GCTTTATTATTTGCA | 79582 |
rs74544360 | snp | A/G | 0.00517822 | 0.0506191 | intron-variant | SPAG16 | GRCh38.p7 | 2:213326388 | ATGACTTTCAGAAAC[A/G]AACACTGTGAAAATA | 79582 |
rs74560028 | snp | A/C | 0.0287284 | 0.116357 | intron-variant | SPAG16 | GRCh38.p7 | 2:213988692 | AAATTAAAAAAAAAA[A/C]CATTCAAAATAGCTC | 79582 |
rs74573364 | snp | A/G | 0.5 | 0 | intron-variant | SPAG16 | GRCh38.p7 | 2:213409472 | ATCTCTTTAACTTTA[A/G]CCAATATGTTTACAC | 79582 |
rs74578207 | snp | A/T | 0.00993419 | 0.0697739 | intron-variant | SPAG16 | GRCh38.p7 | 2:213576760 | TTCTCACTTAATGGG[A/T]GAACTAAATGATAAG | 79582 |
rs74583501 | snp | G/T | 0.00755907 | 0.0610114 | intron-variant | SPAG16 | GRCh38.p7 | 2:214266399 | TAGATAGACTTTATT[G/T]TTGGAGCAAACCTAT | 79582 |
rs74586504 | snp | C/T | 0.0360663 | 0.129354 | intron-variant | SPAG16 | GRCh38.p7 | 2:213679613 | AATTCCCTGTTGCTC[C/T]GGTGATTTATGTGTT | 79582 |
rs74590506 | snp | A/G | 0.5 | 0 | intron-variant | SPAG16 | GRCh38.p7 | 2:213539846 | AAACAACTTACCAAA[A/G]GACAGAAATCTAAAT | 79582 |
rs74591659 | snp | C/G | 0.5 | 0 | intron-variant | SPAG16 | GRCh38.p7 | 2:213651141 | TAAGAAGCAGAATCA[C/G]TATGAACATTATACA | 79582 |
rs74599497 | snp | C/T | 0.0729998 | 0.176553 | intron-variant | SPAG16 | GRCh38.p7 | 2:213428316 | TGAGAGAATACCTTG[C/T]CCTTCCCAAGCCCTG | 79582 |
rs74605217 | snp | A/C | 0.0174175 | 0.0916809 | intron-variant | SPAG16 | GRCh38.p7 | 2:213312460 | ACTGTTCCCCTATTA[A/C]CATTGTCAGAACTAC | 79582 |
rs74613397 | snp | A/C | 0.192715 | 0.243348 | intron-variant | SPAG16 | GRCh38.p7 | 2:213958127 | GAGCAAAAGAGAGAG[A/C]AAAATACCTGTGAGC | 79582 |
rs74617493 | snp | G/T | 0.00119737 | 0.0244387 | intron-variant | SPAG16 | GRCh38.p7 | 2:213954871 | CTTAGTAGCTGTGAA[G/T]TCATAAAACATTGTG | 79582 |
rs74618873 | snp | G/T | | | intron-variant | SPAG16 | GRCh38.p7 | 2:213918404 | CTATCTGGTCCTGGG[G/T]TTTTTTCTGGTTGAT | 79582 |
rs74619795 | snp | A/G | 0.0693013 | 0.172766 | intron-variant | SPAG16 | GRCh38.p7 | 2:213778064 | ATACTGTATGTATAA[A/G]CTGTCCAACCCAGGA | 79582 |
rs74624135 | snp | G/T | 0.5 | 0 | intron-variant | SPAG16 | GRCh38.p7 | 2:213327165 | GTCTGTTTGCTGTGT[G/T]TTTTTTTTTTTAACA | 79582 |
rs74639236 | snp | A/T | 0.5 | 0 | intron-variant | SPAG16 | GRCh38.p7 | 2:213440395 | TCTACTAAAAAAAAA[A/T]TACAAAAAATTTAGC | 79582 |
rs74642118 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | SPAG16, LOC101928084 | GRCh38.p7 | 2:214099678 | TAGTTGCCTCTGGAG[G/T]TGGCCTAAAATGGGA | 79582 |
rs74652560 | snp | C/T | 0.0926964 | 0.194308 | intron-variant | SPAG16 | GRCh38.p7 | 2:213762810 | ACTAAAAAGCTTCTG[C/T]ACAACAAAGGAAGCA | 79582 |
rs74654290 | snp | A/C | 0.00159617 | 0.0282053 | intron-variant | SPAG16 | GRCh38.p7 | 2:214174565 | GAAACAGTTCAGTTA[A/C]TGTTGCCTGCAGGTA | 79582 |
rs74654633 | snp | A/T | 0.0119091 | 0.0762411 | intron-variant | SPAG16 | GRCh38.p7 | 2:213389911 | AGAATTGAAAGCAGC[A/T]TGTTAAAAAGATATT | 79582 |
rs74655044 | snp | C/T | 0.0232847 | 0.105357 | intron-variant | SPAG16 | GRCh38.p7 | 2:213885852 | TTCACATTCCCTTGA[C/T]GCTCAAAATAATTCA | 79582 |
rs74661962 | in-del | -/ACAA | | | intron-variant | SPAG16 | GRCh38.p7 | 2:214372476 | AACAGAATAAAACAA[-/ACAA]GGAATCTTCCTGTTT | 79582 |
rs74670990 | snp | C/T | 0.00636936 | 0.0560724 | intron-variant | SPAG16 | GRCh38.p7 | 2:214061311 | TGGAAAAACTCATAA[C/T]CCACAGGGCACTAGG | 79582 |
rs74677682 | snp | A/C | 0.109108 | 0.206518 | intron-variant | SPAG16 | GRCh38.p7 | 2:213674259 | TCATCCAGTTCTCTA[A/C]GACAACATACTTGAT | 79582 |
rs74689219 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | SPAG16 | GRCh38.p7 | 2:214201160 | AGCCAAATTTGTCTA[C/T]AGGGCCACAATTAAG | 79582 |
rs74703106 | snp | A/G | 0.0236746 | 0.106192 | intron-variant | SPAG16 | GRCh38.p7 | 2:213642175 | TTGGGAACGCACAAT[A/G]TTTCAGCTGTTTCAT | 79582 |
rs74706923 | snp | C/T | 0.0103295 | 0.0711199 | intron-variant | SPAG16 | GRCh38.p7 | 2:213782080 | TTTACATTAGCATAA[C/T]ATATGCCAAAAATGA | 79582 |
rs74708820 | snp | A/G | 0.0298908 | 0.118541 | intron-variant | SPAG16 | GRCh38.p7 | 2:213754790 | ATCTGGTGTGTGCTC[A/G]GCTGCATTTAACTGT | 79582 |
rs74713625 | snp | A/G | 0.0182019 | 0.0936463 | intron-variant | SPAG16 | GRCh38.p7 | 2:214047696 | CATGGATAAACAGGA[A/G]CACATCATGTTAAAA | 79582 |
rs74714976 | snp | C/G | 0.127254 | 0.217792 | intron-variant | SPAG16 | GRCh38.p7 | 2:213658183 | TGAATTAAAATCTTA[C/G]AAGCCTACTCCAGTC | 79582 |
rs74717134 | snp | C/T | 0.128976 | 0.218754 | intron-variant | SPAG16 | GRCh38.p7 | 2:213721378 | TGCTGAGATTACAGG[C/T]GTAAGCCACCGCGCC | 79582 |
rs74720922 | snp | A/G | 0.0752113 | 0.178743 | intron-variant | SPAG16 | GRCh38.p7 | 2:213992818 | CAGATGATAAAACAA[A/G]GTCATATAAAAGTTG | 79582 |
rs74726337 | snp | A/G | 0.00279162 | 0.0372561 | intron-variant | SPAG16 | GRCh38.p7 | 2:213540722 | GTTGGAGAATGTTCA[A/G]TGAAATAGCATATAA | 79582 |
rs74730621 | snp | A/G | 0 | 0 | intron-variant | SPAG16 | GRCh38.p7 | 2:213733111 | GTGGTTTTGATTTGC[A/G]TTTCTCTGATGGCCA | 79582 |
rs74734245 | snp | A/T | 0.021333 | 0.101051 | intron-variant | SPAG16 | GRCh38.p7 | 2:214001771 | ACTTTACACTGAAAG[A/T]AAAGTAAAATAAGGA | 79582 |
rs74737495 | snp | A/T | 0.5 | 0 | intron-variant | SPAG16 | GRCh38.p7 | 2:213563147 | TGGGGAGATAGCTTC[A/T]TTTTTTTACTTTCAA | 79582 |
rs74756005 | snp | C/T | 0.00557542 | 0.0525036 | intron-variant | SPAG16 | GRCh38.p7 | 2:214170018 | AAAAATGTTACAGAA[C/T]GCTAAAATTCAGATG | 79582 |
rs74757657 | snp | G/T | | | intron-variant | SPAG16 | GRCh38.p7 | 2:213925141 | TATCATTATTGTTTT[G/T]TTTTATTTTTACAAG | 79582 |
rs74774632 | snp | G/T | 0.00914312 | 0.0669923 | intron-variant | SPAG16 | GRCh38.p7 | 2:213364942 | GCCTTATAAAACCAG[G/T]AACAAAGCTTACACA | 79582 |
rs74778216 | snp | A/G | 0.00478085 | 0.0486577 | intron-variant | SPAG16 | GRCh38.p7 | 2:214024923 | TTTTCTGCCTTGAGC[A/G]TAATAATGTAGAAAA | 79582 |
rs74787920 | snp | A/G | 0.0391387 | 0.134304 | intron-variant | SPAG16 | GRCh38.p7 | 2:213788303 | GTCATAATAACCTAT[A/G]AAAAGGAAATAAGCT | 79582 |
rs74789636 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | SPAG16 | GRCh38.p7 | 2:213747560 | TACTGTATTTTTTGC[A/C]CAAATTTTCTGTGTT | 79582 |
rs74794311 | snp | A/G | 0.046775 | 0.145601 | intron-variant | SPAG16 | GRCh38.p7 | 2:213429761 | CACAGATTCTTTGCC[A/G]TTGAACACACCTAGA | 79582 |
rs74795206 | snp | A/C/T | 0.625 | 0.125 | intron-variant | SPAG16 | GRCh38.p7 | 2:213822823 | CCAAAAACCAAACAC[A/C/T]GCATGTTCTCACTCA | 79582 |
rs74796742 | snp | A/G | 0.0158469 | 0.0875917 | intron-variant | SPAG16 | GRCh38.p7 | 2:213852719 | ATTCTCCCCCAAATT[A/G]TTATATCACTTTACT | 79582 |
rs74797432 | snp | A/G | 0.0107246 | 0.0724382 | intron-variant | SPAG16 | GRCh38.p7 | 2:214129919 | ATTCTTTGTGACTCA[A/G]TACTTACCGGTATTA | 79582 |
rs74800306 | snp | A/G | 0.00517822 | 0.0506191 | intron-variant | SPAG16 | GRCh38.p7 | 2:214259523 | CTCCTTTCCTGGATT[A/G]TCACCTGCCCCCCTC | 79582 |
rs74800327 | snp | A/G | 0.5 | 0 | intron-variant | SPAG16 | GRCh38.p7 | 2:214247306 | TTTTTCCAAAAAAAA[A/G]GAATCTTGAATAGAT | 79582 |
rs74801477 | snp | A/G | 0.0168055 | 0.0901129 | intron-variant | SPAG16 | GRCh38.p7 | 2:213413049 | ATATTGGGTAATGCT[A/G]TTAATTAGTATGTTG | 79582 |
rs74804771 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | SPAG16 | GRCh38.p7 | 2:213436445 | ATAGCATGTCATTAT[A/G]TCTACACAATTAACA | 79582 |
rs74805456 | snp | C/T | 0.00993419 | 0.0697739 | intron-variant | SPAG16 | GRCh38.p7 | 2:214294209 | GTTAGTTTCTAGGCT[C/T]GTGGGTGCCGAGGGG | 79582 |
rs74805627 | snp | A/C | 0.5 | 0 | intron-variant | SPAG16 | GRCh38.p7 | 2:213683553 | GAGACTCCATCTCCA[A/C]AAAAAAAAAAGATAC | 79582 |
rs74810479 | snp | C/G | 0.021333 | 0.101051 | intron-variant | SPAG16 | GRCh38.p7 | 2:213485501 | ATAGTTTTATTGCTT[C/G]TTTATTTGCTTATTA | 79582 |
rs74810552 | snp | C/G | 0.0577344 | 0.159793 | intron-variant | SPAG16 | GRCh38.p7 | 2:214351380 | CACAGATAGGATTGT[C/G]TGTGTGTCTGTGTGT | 79582 |
rs74816025 | snp | A/G | 0.0349115 | 0.127424 | intron-variant | SPAG16 | GRCh38.p7 | 2:213976994 | GTGTTGTTTTAAGTC[A/G]CTAAATTTGTGAGAA | 79582 |
rs74822432 | snp | A/T | 0.00438332 | 0.0466095 | intron-variant | SPAG16 | GRCh38.p7 | 2:213916733 | CACAGCCAAACCATA[A/T]CATATAGGTTGTCTG | 79582 |
rs74823256 | snp | A/G | 0.00914312 | 0.0669923 | intron-variant | SPAG16 | GRCh38.p7 | 2:213886392 | TAGAATGAGCAGCTA[A/G]AGAAAGAGGGGCATT | 79582 |
rs74833398 | snp | A/G | 0.00159617 | 0.0282053 | intron-variant | SPAG16 | GRCh38.p7 | 2:213510137 | CTGGAAAATTTAGAC[A/G]TCCCTCATATAGCAC | 79582 |
rs74837283 | snp | A/G | 0.0130921 | 0.0798413 | intron-variant | SPAG16 | GRCh38.p7 | 2:213801486 | TCAAATATATATTTT[A/G]CAAATCATAAGGCAC | 79582 |
rs74838816 | snp | A/G | 0.0107246 | 0.0724382 | intron-variant | SPAG16 | GRCh38.p7 | 2:214190328 | TGTTGTTTGCTTTGG[A/G]ATTTATATAGGAGAA | 79582 |
rs74840114 | in-del | -/TA | | | intron-variant | SPAG16 | GRCh38.p7 | 2:213842511 | GTTTACTAAGAAGTG[-/TA]AATTTTTTTAAAAAA | 79582 |
rs74840193 | snp | C/T | 0.5 | 0 | intron-variant | SPAG16 | GRCh38.p7 | 2:213991884 | TTATTTATTTATTTA[C/T]TTATTTATTCTTGTT | 79582 |
rs74842682 | snp | A/T | 0.00676609 | 0.0577691 | intron-variant | SPAG16 | GRCh38.p7 | 2:213586203 | TATGATGAGCCAGTA[A/T]CTTAGTTCATTCAGG | 79582 |
rs74846112 | snp | C/G | 0.5 | 0 | intron-variant | SPAG16 | GRCh38.p7 | 2:213955911 | TCTAGATAAAAGTTT[C/G]TCAATTTTGTTGAAC | 79582 |
rs74853281 | snp | A/G | 0.0463947 | 0.145069 | intron-variant | SPAG16 | GRCh38.p7 | 2:213349779 | AAGAAACATTACACT[A/G]AGTGAAATAAACTAG | 79582 |
rs74855792 | snp | A/C | | | intron-variant | SPAG16 | GRCh38.p7 | 2:213697641 | TGTACTTTTGACCTA[A/C]ATAACTGTAAGATAA | 79582 |
rs74855880 | snp | A/G | 0.0182019 | 0.0936463 | intron-variant | SPAG16 | GRCh38.p7 | 2:213380895 | CCCTTCGGGTCACTC[A/G]ATAAATGGGCCAGAG | 79582 |
rs74857060 | snp | A/G | 0.0399052 | 0.1355 | intron-variant | SPAG16 | GRCh38.p7 | 2:213762669 | TAACAAAGACCTGAA[A/G]CTATAAATCCTATTT | 79582 |
rs74857996 | snp | G/T | 0.00478085 | 0.0486577 | intron-variant | SPAG16 | GRCh38.p7 | 2:213378111 | AGAAAGATGTAGGCT[G/T]GGAGGCTAGGCCAGT | 79582 |
rs74858852 | snp | C/T | 0.192715 | 0.243348 | intron-variant | SPAG16 | GRCh38.p7 | 2:213957319 | TTGTGTAAATGTTTA[C/T]AATTATTATATCTTC | 79582 |
rs74861105 | snp | A/G | 0.5 | 0 | intron-variant | SPAG16 | GRCh38.p7 | 2:214022758 | GTTTCTTCTAACTCA[A/G]GAACTTGTGTCATGT | 79582 |
rs74861497 | snp | C/T | 0.0185938 | 0.0946107 | intron-variant | SPAG16 | GRCh38.p7 | 2:213770265 | ATTTTTTTGTTTTTA[C/T]GGATATGTCATTTTT | 79582 |
rs74865353 | snp | A/G | 0.00398564 | 0.0444627 | intron-variant | SPAG16, LOC101928084 | GRCh38.p7 | 2:214102492 | GCTTTTCTCTCTGTG[A/G]TGGTTGAGAAACCCA | 79582 |
rs74870309 | snp | G/T | 0 | 0 | intron-variant | SPAG16 | GRCh38.p7 | 2:213433935 | TTTTTTTTTTTTTTT[G/T]TTGAGACATTGTCTC | 79582 |
rs74872217 | in-del | -/G | | | intron-variant | SPAG16 | GRCh38.p7 | 2:213812754 | TATTTAGCATTTTTT[-/G]TTTTATTACATGTAA | 79582 |
rs74874130 | snp | A/T | 0.0554779 | 0.157039 | intron-variant | SPAG16 | GRCh38.p7 | 2:213988531 | CAGGAGAATTAGAAA[A/T]AATCTGACCAGAATG | 79582 |
rs74878356 | snp | C/T | 0.00597247 | 0.0543191 | intron-variant | SPAG16 | GRCh38.p7 | 2:213513707 | AGTTAAAGCACATAG[C/T]GGAATCTCTGTCACA | 79582 |
rs74881359 | snp | C/T | 0.0422008 | 0.138995 | intron-variant | SPAG16 | GRCh38.p7 | 2:213712841 | TAAGAAGATAGACAG[C/T]TTCCCTGCTTACCTG | 79582 |
rs74888889 | snp | A/G | 0.143622 | 0.226238 | intron-variant | SPAG16 | GRCh38.p7 | 2:213995078 | GGAATGAGGATGCTA[A/G]TTGAGAAGACTTCTC | 79582 |
rs74889309 | in-del | -/TT | | | intron-variant | SPAG16 | GRCh38.p7 | 2:213288657 | TAACTTTTTTTTTTT[-/TT]AAAGCTAAACATTGT | 79582 |
rs74895388 | snp | G/T | 0.00953873 | 0.0683987 | intron-variant | SPAG16 | GRCh38.p7 | 2:213725748 | GAAGTTTGGCTCAGG[G/T]CCAAAGCTAGTTTCT | 79582 |
rs74897701 | snp | C/T | 0.0279526 | 0.114869 | intron-variant | SPAG16 | GRCh38.p7 | 2:214251652 | TGGTTTTCTCATTTA[C/T]GTATTTCAAGAACAA | 79582 |
rs74906061 | in-del | -/TT | | | intron-variant | SPAG16 | GRCh38.p7 | 2:213327175 | TGTGTTTTTTTTTTT[-/TT]AACACAAAGATGCTC | 79582 |
rs74908785 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | SPAG16 | GRCh38.p7 | 2:214314348 | AGTTACATTTACTTA[C/T]ATAGGATTTCTAAAA | 79582 |
rs74912873 | snp | A/C | | | intron-variant | SPAG16 | GRCh38.p7 | 2:214164345 | GGAATATTACTTTAG[A/C]AAGGATGTTCTGAGA | 79582 |
rs74932708 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | SPAG16 | GRCh38.p7 | 2:214051338 | AGAAATAAGAAGACC[A/G]AAAGGAATTGCCAAG | 79582 |
rs74933235 | snp | C/G | 0.00676609 | 0.0577691 | intron-variant | SPAG16 | GRCh38.p7 | 2:214140690 | TATTCTTTAGTAATA[C/G]ACTCTAGTAATTTCT | 79582 |
rs74936583 | snp | C/T | 0.0182019 | 0.0936463 | intron-variant | SPAG16 | GRCh38.p7 | 2:214010521 | GAAACTGTAAGGGCT[C/T]TTGGGTGTAAACAGC | 79582 |
rs74938564 | snp | C/G | 0.00517822 | 0.0506191 | intron-variant | SPAG16 | GRCh38.p7 | 2:213456436 | GTGAATATAGCAGAA[C/G]GAAGAAGCATATGTA | 79582 |
rs74941787 | snp | C/T | 0.0225045 | 0.103662 | intron-variant | SPAG16 | GRCh38.p7 | 2:213966266 | TGTCATGGTCTCTTA[C/T]TGTTCTTACTGAGAT | 79582 |
rs74943385 | snp | A/T | 0.5 | 0 | intron-variant | SPAG16 | GRCh38.p7 | 2:213445908 | TTCCTCAAAAAACCC[A/T]GAGGGACCAGAGAAC | 79582 |
rs74947590 | snp | G/T | 0.0170251 | 0.090679 | intron-variant | SPAG16 | GRCh38.p7 | 2:214386251 | ATGGTGGCATTCGCC[G/T]GTAATCCCAGCTACT | 79582 |
rs74953023 | snp | A/T | 0.00914312 | 0.0669923 | intron-variant | SPAG16 | GRCh38.p7 | 2:213936426 | GATGACTCTGGCTAC[A/T]GTTTTGAGATTAGAT | 79582 |
rs74954637 | snp | A/G | 0.0287284 | 0.116357 | intron-variant | SPAG16 | GRCh38.p7 | 2:214074856 | CTATAAACGCAATAA[A/G]ATGCCCCAAAGTAAA | 79582 |
rs74957065 | snp | A/C | 0.0422008 | 0.138995 | intron-variant | SPAG16 | GRCh38.p7 | 2:214240299 | CAGGAAAAGAATTCC[A/C]AAGTCAAATAATTCA | 79582 |
rs74977989 | snp | A/G | | | intron-variant | SPAG16 | GRCh38.p7 | 2:213407639 | AGAGAGAGAGAGAGA[A/G]ACAGACAGACAGGAG | 79582 |
rs74980038 | snp | C/T | 0.02016 | 0.0983543 | intron-variant | SPAG16 | GRCh38.p7 | 2:213894385 | AAGCACTTGATAAAA[C/T]TTAAATCACTTTATA | 79582 |
rs74980659 | snp | A/G | 0.0107246 | 0.0724382 | intron-variant | SPAG16 | GRCh38.p7 | 2:213584658 | AACGGACAGACGGAC[A/G]GATGGACGGGAGGAA | 79582 |
rs74982916 | snp | A/G | 0.0154538 | 0.0865337 | intron-variant | SPAG16 | GRCh38.p7 | 2:214004521 | ATAAAGGAAGGATCC[A/G]CAATTGTAAGACCTT | 79582 |
rs74982984 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | SPAG16 | GRCh38.p7 | 2:213959801 | TTCCTCTTTGTCTCA[C/T]CTGACACGCACACAC | 79582 |
rs74986546 | snp | A/T | 0.5 | 0 | intron-variant | SPAG16 | GRCh38.p7 | 2:214187684 | CAATAATGTCTGCCA[A/T]AACAAACCTCAGGTT | 79582 |
rs74986993 | snp | A/T | 0.0209421 | 0.100162 | intron-variant | SPAG16 | GRCh38.p7 | 2:213876214 | CATTTGAAATGTAGG[A/T]ACATAACTTTTAGTT | 79582 |
rs74988425 | snp | G/T | 0.5 | 0 | intron-variant | SPAG16 | GRCh38.p7 | 2:213428946 | AATACAAAAAAATTA[G/T]CTGAGCATGGTGGCA | 79582 |
rs74990584 | snp | C/G/T | | | intron-variant | SPAG16, LOC101928084 | GRCh38.p7 | 2:214101564 | CTCATTACATGGTCT[C/G/T]TCATAAGCCCATGGA | 79582 |
rs74991380 | snp | A/G | 0.0260105 | 0.111035 | intron-variant | SPAG16 | GRCh38.p7 | 2:214227889 | TTCCTGAATCTAAGC[A/G]GTTAACCTTCTTTCT | 79582 |
rs74995045 | snp | C/T | 0.00318978 | 0.0398085 | intron-variant | SPAG16 | GRCh38.p7 | 2:214135258 | CCTCTTGGTCCAAGC[C/T]AGGGTCACAGTAGAG | 79582 |
rs74995919 | snp | G/T | 0.0364509 | 0.129988 | intron-variant | SPAG16 | GRCh38.p7 | 2:214302075 | TGTTTAGTTTCCATG[G/T]ACTTATACAGTTTTG | 79582 |
rs75002021 | snp | C/T | 0.00438332 | 0.0466095 | intron-variant | SPAG16 | GRCh38.p7 | 2:213692452 | CACTGATTTATTGTG[C/T]TTGGTGTCCAAGAAC | 79582 |
rs75002962 | snp | C/T | 0.0193772 | 0.0965046 | intron-variant | SPAG16 | GRCh38.p7 | 2:213923166 | CAGCCCTATCAGATG[C/T]GGCTCACCTGTCCAC | 79582 |
rs75006342 | snp | A/G | 0.5 | 0 | intron-variant | SPAG16 | GRCh38.p7 | 2:213873908 | CTACTGCTCTTCCAG[A/G]CTATATACCATAGAC | 79582 |
rs75011083 | snp | A/G | 0.110519 | 0.207473 | intron-variant | SPAG16 | GRCh38.p7 | 2:214198674 | CTTTAAGGAGGCTCT[A/G]TACTGTTTTCCATAA | 79582 |
rs75014207 | snp | A/C | 0.0715223 | 0.175059 | intron-variant | SPAG16 | GRCh38.p7 | 2:213961729 | ATTTCTAGTGAAAAT[A/C]TCACTGTTCATTGTG | 79582 |
rs75019683 | snp | G/T | 0.00676609 | 0.0577691 | intron-variant | SPAG16 | GRCh38.p7 | 2:213464360 | TCTGCCTTTCCCAAG[G/T]AATGTGGTCTCCAAG | 79582 |
rs75022987 | snp | A/C | 0.0217236 | 0.101931 | intron-variant | SPAG16 | GRCh38.p7 | 2:213453371 | GCTGACTCTAAAACT[A/C]CTATTCTGCAGTGAC | 79582 |
rs75028416 | snp | A/G | 0.447809 | 0.152878 | intron-variant | SPAG16 | GRCh38.p7 | 2:214272797 | TTTATAATCCTTTGG[A/G]TATATACCCAGTAAT | 79582 |
rs75035571 | snp | A/G | | | intron-variant | SPAG16 | GRCh38.p7 | 2:213447453 | ATTCTGAACCCCATG[A/G]TAAATCCCCTTTGAG | 79582 |
rs75036284 | snp | A/G | 0.00517822 | 0.0506191 | intron-variant | SPAG16 | GRCh38.p7 | 2:213473251 | TCTGCTATCCATTAC[A/G]GTACCTATGCTCACC | 79582 |
rs75040058 | snp | A/T | 0 | 0 | intron-variant | SPAG16 | GRCh38.p7 | 2:214319515 | TGGAAAAAAAAAAAA[A/T]AAACTATAATAGGAA | 79582 |
rs75042228 | in-del | -/TT | | | intron-variant | SPAG16 | GRCh38.p7 | 2:213392198 | GTGTTATGTCACCCT[-/TT]GGCATGATAATGGCA | 79582 |
rs75042604 | snp | C/T | 0.0150606 | 0.0854603 | intron-variant | SPAG16 | GRCh38.p7 | 2:213969799 | GTCAGTTTAATAAAC[C/T]GAGTGTGTGTAAAAT | 79582 |
rs75043219 | snp | C/T | 0.0689305 | 0.172377 | intron-variant | SPAG16 | GRCh38.p7 | 2:213897886 | AAACAATAGCAATCA[C/T]CCTCCTATAAAAAGG | 79582 |
rs75045318 | snp | C/T | 0.0146672 | 0.084371 | intron-variant | SPAG16 | GRCh38.p7 | 2:214029976 | CGTGTGTGTGTATTT[C/T]AGTGGTAAGAACAAT | 79582 |
rs75045695 | snp | A/C | 0.0622301 | 0.165053 | intron-variant | SPAG16 | GRCh38.p7 | 2:213957992 | GGAGGCAGCACAACA[A/C]AGCCCATTAGATAAC | 79582 |
rs75048300 | snp | C/T | 0.00159617 | 0.0282053 | intron-variant | SPAG16 | GRCh38.p7 | 2:214016382 | ACTTATTCACTATCA[C/T]GAGAACAGCATAGAA | 79582 |
rs75054045 | snp | A/G | 0.0562307 | 0.157967 | intron-variant | SPAG16 | GRCh38.p7 | 2:213934619 | TCCTCCTTCCATATT[A/G]GTTAGGCACTTGGCT | 79582 |
rs75054223 | snp | A/C | 0.109461 | 0.206758 | intron-variant | SPAG16 | GRCh38.p7 | 2:214041244 | TTTGCTCCATACCTC[A/C]AAGTGTTTGTTCATT | 79582 |
rs75058097 | snp | C/T | 0.100944 | 0.200705 | intron-variant | SPAG16 | GRCh38.p7 | 2:213402160 | TCGTCATAATAGGTA[C/T]AATTTTTTAAAAATT | 79582 |
rs75058174 | in-del | -/CTAA | | | intron-variant | SPAG16 | GRCh38.p7 | 2:213804729 | TAACTAACTAACTAA[-/CTAA]GATTACGAGACAGGA | 79582 |
rs75059992 | snp | C/T | | | intron-variant | SPAG16 | GRCh38.p7 | 2:214233102 | TAGAAGTACATACTA[C/T]AAAGAGCTTCACAGC | 79582 |
rs75063481 | snp | C/T | 0.00358779 | 0.0422022 | intron-variant | SPAG16 | GRCh38.p7 | 2:213340687 | TTACGTTCATCAAAT[C/T]GTGTACATAGAGAGT | 79582 |
rs75065949 | snp | C/T | 0.267908 | 0.249358 | intron-variant | SPAG16 | GRCh38.p7 | 2:213948063 | ACTCTCAGTAGTATC[C/T]AATTTATTCCTGTTA | 79582 |
rs75066207 | snp | C/T | 0.00676609 | 0.0577691 | intron-variant | SPAG16 | GRCh38.p7 | 2:214213992 | AGGTGAAACTCTATT[C/T]ATAGTGCCTTTTGTG | 79582 |
rs75066567 | snp | A/G | 0.00597247 | 0.0543191 | intron-variant | SPAG16 | GRCh38.p7 | 2:213311844 | AATATATCATTTGCT[A/G]TGAATTCACTTAATC | 79582 |
rs75068651 | snp | A/G | | | intron-variant, upstream-variant-2KB | SPAG16, LOC101928084 | GRCh38.p7 | 2:214103947 | AGAGAGGGAAACAGA[A/G]AGAGAGAGAGAGACA | 79582 |
rs75070093 | snp | C/T | 0.0418186 | 0.138422 | intron-variant | SPAG16 | GRCh38.p7 | 2:214251425 | TGACACAAAAATGAA[C/T]ATTTCTTAAAAATCT | 79582 |
rs75070597 | in-del | -/G | 0.475437 | 0.108066 | intron-variant | SPAG16 | GRCh38.p7 | 2:213872344 | TTCATGTTATGTTAT[-/G]CCACTAAGTTTGTGG | 79582 |
rs75070757 | snp | C/T | 0.5 | 0 | intron-variant | SPAG16 | GRCh38.p7 | 2:213968113 | TTTTCTTTTCTTTTC[C/T]TCCCTCCCTCTCTCT | 79582 |
rs75071717 | snp | A/G | 0.0452528 | 0.143452 | intron-variant | SPAG16 | GRCh38.p7 | 2:213444004 | GAAACTGGGAACTGG[A/G]CACTTCAGCCTATTC | 79582 |
rs75071849 | snp | A/G | 0.00478085 | 0.0486577 | intron-variant | SPAG16 | GRCh38.p7 | 2:213460680 | GCTAGAAGTCAAAAG[A/G]TAGAACTTAAATCAG | 79582 |
rs75074934 | snp | G/T | 0.0479149 | 0.147179 | intron-variant | SPAG16, LOC101928084 | GRCh38.p7 | 2:214093629 | TGTATATGTGTGGGG[G/T]TTTTTAACAGCCATA | 79582 |
rs75075592 | snp | A/G | 0.5 | 0 | intron-variant | SPAG16, LOC101928084 | GRCh38.p7 | 2:214085391 | CTCAAAAAAAAAAAA[A/G]AAGAAAGAAAGAAAG | 79582 |
rs75076803 | snp | A/G | 0.0260105 | 0.111035 | intron-variant | SPAG16 | GRCh38.p7 | 2:213979842 | GTACTGTTTTCCATA[A/G]TACATAATATTCCTA | 79582 |
rs75078482 | snp | C/T | 0.5 | 0 | intron-variant | SPAG16 | GRCh38.p7 | 2:213930226 | GTTCTTTTTTTTTTT[C/T]CCTTGATGCTACCCC | 79582 |
rs75082507 | snp | A/G | 0.02016 | 0.0983543 | intron-variant | SPAG16 | GRCh38.p7 | 2:213782538 | AAAAAGAAATTACAT[A/G]GCTGTTATTCAATAA | 79582 |
rs75082654 | snp | A/G | 0.104504 | 0.2033 | intron-variant | SPAG16 | GRCh38.p7 | 2:214206793 | CATTTGTTATTTTTT[A/G]CTTTTTTATAATATC | 79582 |
rs75093436 | snp | G/T | 0.0197687 | 0.0974348 | intron-variant | SPAG16 | GRCh38.p7 | 2:213830508 | GTTTTTTTGTGTAGT[G/T]AGTTGTTAAATTTGG | 79582 |
rs75093760 | snp | A/C | 0.0498117 | 0.149749 | intron-variant | SPAG16 | GRCh38.p7 | 2:213809807 | TGTGTTTATATGTAG[A/C]TGTGCATGTTTTCCT | 79582 |
rs75095009 | snp | A/T | | | intron-variant | SPAG16 | GRCh38.p7 | 2:214376944 | AAAATTTAGCAAAAC[A/T]TACACATGCAGGCAC | 79582 |
rs75096129 | snp | A/T | 0.0479149 | 0.147179 | intron-variant | SPAG16 | GRCh38.p7 | 2:213789090 | AAATAATTTGGAAGA[A/T]CCATTTTAATCACCA | 79582 |
rs75109320 | in-del | -/AAA | | | intron-variant | SPAG16 | GRCh38.p7 | 2:213339036 | ACTTAAAAAAAAAAA[-/AAA]GAAAAGAAGAAAGAA | 79582 |
rs75123134 | snp | A/G | 0.0722614 | 0.17581 | intron-variant | SPAG16 | GRCh38.p7 | 2:213837678 | CATGCCCCAAAACCC[A/G]GAATCCATAAATATG | 79582 |
rs75123373 | snp | A/T | 0.0479149 | 0.147179 | intron-variant | SPAG16 | GRCh38.p7 | 2:213764599 | TTTATATAGCTAAAT[A/T]GTTTCATTTTTCTGG | 79582 |
rs75124376 | snp | A/G | 0.16618 | 0.23553 | intron-variant | SPAG16 | GRCh38.p7 | 2:213330838 | GGGCAGGTCTTTCTC[A/G]TGCTGTTCTTGTGAC | 79582 |
rs75130156 | snp | A/G | 0.00835141 | 0.0640778 | intron-variant | SPAG16 | GRCh38.p7 | 2:213763149 | AATTGTAAGGATATA[A/G]AGAAATCTGAATCCT | 79582 |
rs75130947 | snp | A/C | 0.00835141 | 0.0640778 | intron-variant | SPAG16 | GRCh38.p7 | 2:213437488 | ATTTTAAAGTAGTTT[A/C]CTAAAAAAATCTTTT | 79582 |
rs75131283 | snp | A/G | 0.133435 | 0.221162 | intron-variant, utr-variant-5-prime | SPAG16 | GRCh38.p7 | 2:213299683 | TATTTGATACTATCC[A/G]TTTTCTTAGTGGGTT | 79582 |
rs75138517 | snp | A/G | 0.0267878 | 0.112589 | intron-variant | SPAG16 | GRCh38.p7 | 2:214231164 | AATGGAAACAACTAA[A/G]TGAGTCTAGGATTAG | 79582 |
rs75140210 | snp | A/C | 0.5 | 0 | intron-variant | SPAG16 | GRCh38.p7 | 2:213391291 | AAATAAATAAATGAT[A/C]CATAATATTTTGTTA | 79582 |
rs75147220 | snp | G/T | 0.00874735 | 0.0655527 | intron-variant | SPAG16 | GRCh38.p7 | 2:213919186 | TTTGTGAGTTTTGGG[G/T]TCAGTTTAATCTTGG | 79582 |
rs75148077 | snp | G/T | 0.0456336 | 0.143994 | intron-variant | SPAG16 | GRCh38.p7 | 2:213651514 | GGTAGCCTAGCCACT[G/T]CACCATGGTAATCAG | 79582 |
rs75153203 | snp | A/G | 0.0463947 | 0.145069 | intron-variant | SPAG16 | GRCh38.p7 | 2:213933006 | CCAGTGTAACCCAGA[A/G]AGTGCTTGGCACATG | 79582 |
rs75155954 | snp | C/T | 0.0611083 | 0.163768 | intron-variant | SPAG16 | GRCh38.p7 | 2:213793779 | GCTAGTTTCTTCGCT[C/T]TGTGGTCCAGTTTGG | 79582 |
rs75157562 | snp | C/T | 0.00874735 | 0.0655527 | intron-variant | SPAG16 | GRCh38.p7 | 2:213654843 | TGGAGAAAAAAGGAA[C/T]AATGCCAATACTATC | 79582 |
rs75165802 | snp | G/T | 0.5 | 0 | intron-variant | SPAG16 | GRCh38.p7 | 2:213413312 | TTATTTAAATTTTTT[G/T]GAAGTATCAGGTTGC | 79582 |
rs75175876 | snp | A/T | 0.5 | 0 | intron-variant | SPAG16 | GRCh38.p7 | 2:213617663 | ATTTTTTTTTTAAAA[A/T]TGAGCAAGGCATAGT | 79582 |
rs75176718 | snp | A/G | 0.474992 | 0.108989 | intron-variant | SPAG16 | GRCh38.p7 | 2:214355737 | acgtatgtttattgc[A/G]gcactattcacaata | 79582 |
rs75178630 | snp | A/G | 0.110167 | 0.207236 | intron-variant | SPAG16 | GRCh38.p7 | 2:213690688 | CAGAAGAAGAGGATA[A/G]GCAGCTTGTTGAGTC | 79582 |
rs75182527 | snp | C/T | 0.0166325 | 0.0896639 | intron-variant | SPAG16 | GRCh38.p7 | 2:214287920 | ATTTCTATGTGTTAG[C/T]AACACGTCAAGTCCT | 79582 |
rs75191906 | snp | C/T | 0.0452528 | 0.143452 | intron-variant | SPAG16 | GRCh38.p7 | 2:213479273 | GCCTCGCCAGATTGC[C/T]GCATGTATAATTTCA | 79582 |
rs75193285 | snp | C/T | 0.0178098 | 0.0926698 | intron-variant | SPAG16 | GRCh38.p7 | 2:213450431 | AACTTGGCTATATTG[C/T]GTATCATTTATTTTG | 79582 |
rs75196224 | snp | A/G | 0.0501905 | 0.150254 | intron-variant | SPAG16 | GRCh38.p7 | 2:214284475 | TATAATATACACCCT[A/G]CTGGTGGTGCATCTG | 79582 |
rs75198727 | snp | C/T | 0.0275645 | 0.114116 | intron-variant | SPAG16 | GRCh38.p7 | 2:214163793 | AGTCCACAGGTAGTA[C/T]AGAAGCAGAATTCCT | 79582 |
rs75201960 | snp | A/G | | | intron-variant | SPAG16 | GRCh38.p7 | 2:213385733 | AGGGCCAGAGAGTTC[A/G]GGGAAATATGAAGAT | 79582 |
rs75203629 | snp | C/T | 0 | 0 | intron-variant | SPAG16 | GRCh38.p7 | 2:213733119 | ACCATCACTGGCCAT[C/T]AGAGAAATGCAAATC | 79582 |
rs75203652 | in-del | -/AAAAA | 0.487809 | 0.0771174 | intron-variant | SPAG16 | GRCh38.p7 | 2:213761885 | CAAAAATAAAAACAA[-/AAAAA]CAAAACAAAAAAAAA | 79582 |
rs75209413 | snp | A/C | 0.0217236 | 0.101931 | intron-variant | SPAG16 | GRCh38.p7 | 2:213583676 | AACTAACTGTTTAAA[A/C]ATCTTCTCAGCTGCC | 79582 |
rs75212626 | in-del | -/T | | | intron-variant | SPAG16 | GRCh38.p7 | 2:213831426 | GTGTTTTTTTTTTTT[-/T]AACCTCATATTTTCA | 79582 |
rs75230535 | snp | C/T | 0.00398564 | 0.0444627 | intron-variant | SPAG16 | GRCh38.p7 | 2:214009324 | ACTGGGCTCTATTTC[C/T]GTATTTGATAGTAAA | 79582 |
rs75232729 | snp | A/G | 0.333722 | 0.235565 | intron-variant | SPAG16 | GRCh38.p7 | 2:213801237 | TGTGTGTGCGTGCGC[A/G]CGTGCCCACATGTGT | 79582 |
rs75234776 | snp | A/T | 0.122064 | 0.214785 | intron-variant, downstream-variant-500B | SPAG16 | GRCh38.p7 | 2:213401996 | ACATATATTTTTGTC[A/T]GGTCATATATTTTTT | 79582 |
rs75242413 | snp | A/G | 0.0154538 | 0.0865337 | intron-variant | SPAG16 | GRCh38.p7 | 2:213601658 | AACAATCAGCTGTAC[A/G]AATGTATATGACAGT | 79582 |
rs75245855 | snp | A/T | 0.0228947 | 0.104514 | intron-variant | SPAG16 | GRCh38.p7 | 2:213353421 | CCATCTACACAGATA[A/T]ACCTTTTTCAGTCCA | 79582 |
rs75246211 | snp | A/C | 0.121022 | 0.21416 | intron-variant | SPAG16 | GRCh38.p7 | 2:213334941 | ACATTTAAAAATAAC[A/C]GAAAGTAAAATTCGA | 79582 |
rs75247558 | snp | A/G | 0.0463947 | 0.145069 | intron-variant | SPAG16 | GRCh38.p7 | 2:213349480 | AATGTAGGGTACCCA[A/G]GACTGTCATATAGGG | 79582 |
rs75262475 | snp | A/C | 0.5 | 0 | intron-variant | SPAG16 | GRCh38.p7 | 2:213694043 | TGCTTTATGCAAGAC[A/C]AAAAAAAAAAAGAAA | 79582 |
rs75262777 | snp | C/T | 0.5 | 0 | intron-variant | SPAG16 | GRCh38.p7 | 2:213822808 | TTCAGATCTCACTTA[C/T]GAGTGAGACCATGCA | 79582 |
rs75265340 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | SPAG16 | GRCh38.p7 | 2:213973160 | CTTGGGTCTTTTTTG[A/G]GCATGCATCCTATCC | 79582 |
rs75273100 | snp | C/G | 0.0322114 | 0.122752 | intron-variant | SPAG16 | GRCh38.p7 | 2:213925650 | GGCCTCTATGCCCAG[C/G]CTTGTTCTTGTTTTG | 79582 |
rs75284494 | snp | A/G | 0.122064 | 0.214785 | intron-variant | SPAG16 | GRCh38.p7 | 2:213322976 | GTAGAGGCCTTTGCT[A/G]GAAACTTGCTTTTTC | 79582 |
rs75289359 | snp | A/G | 0.0205511 | 0.0992634 | intron-variant | SPAG16 | GRCh38.p7 | 2:213821159 | TCATTCTTCTGTCAT[A/G]TTGTTTTCTATTTTT | 79582 |
rs75302952 | snp | C/T | 0.00159617 | 0.0282053 | intron-variant | SPAG16 | GRCh38.p7 | 2:214233868 | ATGCAGTTTTTTGTT[C/T]GACAAACTTTTGTGG | 79582 |
rs75305889 | snp | A/T | 0.175576 | 0.238665 | intron-variant | SPAG16 | GRCh38.p7 | 2:214328795 | TCTTCTAACTTCTTC[A/T]TGAAAGCTTCAATTC | 79582 |
rs75309792 | snp | C/G | 0.0248432 | 0.108648 | intron-variant | SPAG16 | GRCh38.p7 | 2:213379329 | AGAACTTTGCCTCAG[C/G]CTAGTAAAGTATTGT | 79582 |
rs75311915 | snp | A/G | 0.0126979 | 0.078662 | intron-variant | SPAG16 | GRCh38.p7 | 2:213494362 | TTTGGTTTTCCCCCA[A/G]AAGACCTAATCTTCT | 79582 |
rs75313412 | snp | C/T | 0.0154538 | 0.0865337 | intron-variant | SPAG16 | GRCh38.p7 | 2:214364235 | ATGTCGGACATATAC[C/T]AGATTCTCAATAAAT | 79582 |
rs75316039 | snp | G/T | 0.5 | 0 | intron-variant | SPAG16 | GRCh38.p7 | 2:213868816 | TTAGGAGCTGATTCA[G/T]GAATTGTGAATAAAT | 79582 |
rs75319179 | snp | A/G | 0.00398564 | 0.0444627 | intron-variant | SPAG16 | GRCh38.p7 | 2:214333135 | AAAATCTTTCTACAA[A/G]GGAATCATGCCTTTC | 79582 |
rs75331376 | snp | A/C | 0.0185938 | 0.0946107 | intron-variant | SPAG16 | GRCh38.p7 | 2:213807633 | TTGTCAAGTGGGAAA[A/C]AGTAATTGTACAGGA | 79582 |
rs75333903 | snp | G/T | 0.5 | 0 | intron-variant | SPAG16 | GRCh38.p7 | 2:213792597 | TTTTTTTTTTTTTTT[G/T]TTTGGAGACCGGGTC | 79582 |
rs75334137 | snp | A/G | 0 | 0 | intron-variant | SPAG16 | GRCh38.p7 | 2:214308604 | CCTTTACAGACAAGC[A/G]AATGCTGAGAGATTT | 79582 |
rs75338439 | snp | G/T | 0.5 | 0 | intron-variant | SPAG16 | GRCh38.p7 | 2:213338123 | TTTCTCTTTAGCTTA[G/T]GAAGCTTAGTTTGAC | 79582 |
rs75338820 | snp | C/T | 0.00517822 | 0.0506191 | intron-variant | SPAG16 | GRCh38.p7 | 2:213638469 | TTCAGTTCAAATCAA[C/T]TTTTAATTTCCATCT | 79582 |
rs75341125 | snp | A/T | | | intron-variant | SPAG16 | GRCh38.p7 | 2:214186047 | CCAGGCATAAAATAA[A/T]GTTCAAAAAATAAAA | 79582 |
rs75343054 | snp | A/G | 0.106278 | 0.204558 | intron-variant | SPAG16 | GRCh38.p7 | 2:214285158 | ATCTTTTTGATAATA[A/G]ACAATTTAACAGGTG | 79582 |
rs75345566 | snp | A/C | 0.0520825 | 0.152737 | intron-variant | SPAG16 | GRCh38.p7 | 2:213352233 | CTCGGGTATTTCCTC[A/C]TAGTGGTGTGAGAAT | 79582 |
rs75346794 | snp | C/T | 0.0584853 | 0.160693 | intron-variant | SPAG16 | GRCh38.p7 | 2:214236120 | TGCCAGACTATATTA[C/T]TGTGTAAATAGCTCC | 79582 |
rs75350161 | snp | A/C | 0.0209421 | 0.100162 | intron-variant | SPAG16 | GRCh38.p7 | 2:214019780 | TTATCCCTCAGCCAT[A/C]TTTGATTTAGTAATG | 79582 |
rs75359596 | snp | A/T | 0.0023933 | 0.0345097 | intron-variant | SPAG16 | GRCh38.p7 | 2:214390373 | AAGTCCTTTTCACTC[A/T]TGGGCTTTAATACCC | 79582 |
rs75360464 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | SPAG16 | GRCh38.p7 | 2:213690508 | TGACTGGATTGAGGG[A/G]TGCCTAGATGGCTGA | 79582 |
rs75362034 | snp | G/T | 0.5 | 0 | intron-variant | SPAG16 | GRCh38.p7 | 2:213605281 | GCATTTTTTTTTTTT[G/T]TTTGAGATGGAGTCT | 79582 |
rs75362652 | snp | C/T | 0.084364 | 0.187256 | intron-variant | SPAG16 | GRCh38.p7 | 2:213697711 | GTGTTGCAGCAGCAA[C/T]AGGAAATTAATACAG | 79582 |
rs75363583 | snp | G/T | 0.0810805 | 0.184299 | intron-variant | SPAG16 | GRCh38.p7 | 2:213697330 | TTGCAGAGTATTAGA[G/T]AATGCCATTTTGTCA | 79582 |
rs75365682 | snp | G/T | 0.0174175 | 0.0916809 | intron-variant | SPAG16 | GRCh38.p7 | 2:214208468 | ATGCTCAAAGTAAAG[G/T]CTTTGAGTGCTGAAT | 79582 |
rs75379453 | snp | G/T | 0.5 | 0 | intron-variant | SPAG16 | GRCh38.p7 | 2:213975111 | GTAGCAAGATATTCA[G/T]ACAATAGTAGATATC | 79582 |
rs75380841 | snp | A/T | | | intron-variant | SPAG16 | GRCh38.p7 | 2:214186050 | GGCATAAAATAATGT[A/T]CAAAAAATAAAAGTT | 79582 |
rs75386216 | snp | C/T | 0.0023933 | 0.0345097 | intron-variant | SPAG16 | GRCh38.p7 | 2:213857690 | CAATTCTGCTTCCCG[C/T]GGGTCAATGAGTAAT | 79582 |
rs75386345 | snp | G/T | 0.0217236 | 0.101931 | intron-variant | SPAG16 | GRCh38.p7 | 2:213586438 | TAATGACCACCCAAA[G/T]GCACCACCTCCTAAC | 79582 |
rs75388056 | snp | A/T | | | intron-variant | SPAG16 | GRCh38.p7 | 2:214314306 | CCTAGTGTTAAAACT[A/T]ATGGATGACAATTAG | 79582 |
rs75388474 | snp | A/G | 0.0422008 | 0.138995 | intron-variant | SPAG16 | GRCh38.p7 | 2:213919021 | TTTCTAATTGTTTTT[A/G]TTTGGATCTTCTTTC | 79582 |
rs75402436 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | SPAG16 | GRCh38.p7 | 2:213547728 | AGGTACCATACTCCA[A/C]CTGCAAGTAACCATT | 79582 |
rs75409004 | snp | A/C | 0 | 0 | intron-variant | SPAG16 | GRCh38.p7 | 2:214383572 | TGAGACTTCATCTCA[A/C]AAAAAAAGAAAAAAG | 79582 |
rs75413383 | snp | G/T | 0.0185938 | 0.0946107 | intron-variant | SPAG16 | GRCh38.p7 | 2:214058426 | TTATTAATTATGTTT[G/T]CTGTCTTATATGTAT | 79582 |
rs75420745 | snp | A/G | 0.00318978 | 0.0398085 | intron-variant | SPAG16 | GRCh38.p7 | 2:213758727 | CACAGGAGGAGAGGA[A/G]AAAGAGAAGAGAAAA | 79582 |
rs75430615 | snp | C/T | 0.0821764 | 0.185298 | intron-variant | SPAG16 | GRCh38.p7 | 2:213693343 | AACATAGAGCAAAGG[C/T]GAACATTTAGCCTGA | 79582 |
rs75432170 | snp | A/G | 0.134819 | 0.221886 | intron-variant | SPAG16 | GRCh38.p7 | 2:213422340 | GCTCCAGGCTTACAC[A/G]GATCCAGTGCCTGTG | 79582 |
rs75432701 | snp | G/T | 0.0452528 | 0.143452 | intron-variant | SPAG16 | GRCh38.p7 | 2:213479432 | CTCCTCAATATATTA[G/T]AAGCTACATGAGGAT | 79582 |
rs75434656 | snp | C/T | 0.0637235 | 0.166737 | intron-variant | SPAG16 | GRCh38.p7 | 2:214006101 | TTCCCTTTGAAAACA[C/T]GGATAGATATTTTTT | 79582 |
rs75439415 | snp | A/T | 0.0287284 | 0.116357 | intron-variant | SPAG16 | GRCh38.p7 | 2:213882721 | GCTAGTGGTCTATTC[A/T]TCTAATTTTTTCAAA | 79582 |
rs75441715 | snp | A/G | 0.0197687 | 0.0974348 | intron-variant | SPAG16 | GRCh38.p7 | 2:213832462 | CCTGAAGCAAGTGAC[A/G]AAAACCTGAATTCCT | 79582 |
rs75446509 | snp | A/T | 0.0463947 | 0.145069 | intron-variant | SPAG16 | GRCh38.p7 | 2:213336947 | AACAGGAGTCCACAG[A/T]TAACTCATATGGGAG | 79582 |
rs75447442 | snp | A/G | 0.0494327 | 0.149241 | intron-variant | SPAG16 | GRCh38.p7 | 2:213543183 | ACTCAAGAAGAAATC[A/G]ATGAGCTAAAGAGCC | 79582 |
rs75450185 | snp | C/G | 0.0482946 | 0.147699 | intron-variant | SPAG16 | GRCh38.p7 | 2:213921201 | TCCACCTGGTTGTGT[C/G]AAGTTGGCCATCTTC | 79582 |
rs75450256 | snp | A/C | 0.0850919 | 0.187897 | intron-variant | SPAG16 | GRCh38.p7 | 2:214302434 | TATTGTATTGCTGCC[A/C]GTGTCTTTTTGTAGG | 79582 |
rs75453911 | snp | A/T | 0.5 | 0 | intron-variant | SPAG16 | GRCh38.p7 | 2:214187683 | ACAATAATGTCTGCC[A/T]TAACAAACCTCAGGT | 79582 |
rs75455422 | in-del | -/TCTA/TCTATCTA | | | intron-variant | SPAG16 | GRCh38.p7 | 2:213802395 | CTATCTATCTATCTA[-/TCTA/TCTATCTA]CACATACCTGGAGTT | 79582 |
rs75458867 | snp | A/G | 0.00557542 | 0.0525036 | intron-variant | SPAG16 | GRCh38.p7 | 2:213517639 | GGAACAGAATAGAAT[A/G]GAAAACTCAGAAATA | 79582 |
rs75460753 | snp | A/C | | | intron-variant | SPAG16 | GRCh38.p7 | 2:214258063 | TTGTTCATTGCACTT[A/C]TGTTGTAGAATTTCC | 79582 |
rs75463192 | snp | A/G | 0.0228947 | 0.104514 | intron-variant | SPAG16 | GRCh38.p7 | 2:213696456 | TCTAGGGAGAAATCA[A/G]AAAGAGAAAAAAATT | 79582 |
rs75470831 | snp | C/T | | | intron-variant | SPAG16 | GRCh38.p7 | 2:214155201 | GGCTAAGAGTGAATA[C/T]ATGAAAGCCTGAGGC | 79582 |
rs75473892 | snp | A/G | 0.021333 | 0.101051 | intron-variant | SPAG16 | GRCh38.p7 | 2:213908605 | TAATACCTATATATA[A/G]TGCTGTCCTCTCAGC | 79582 |
rs75475621 | snp | G/T | | | intron-variant | SPAG16 | GRCh38.p7 | 2:213525624 | ATTACCCAGTCTCAG[G/T]CATGTATTTATTAGC | 79582 |
rs75475908 | snp | A/G | 0.0741063 | 0.177655 | intron-variant | SPAG16 | GRCh38.p7 | 2:214406774 | GCAAATTCATCCAAC[A/G]GAGTGAAATGGACAG | 79582 |
rs75478665 | snp | C/T | 0.00398564 | 0.0444627 | intron-variant | SPAG16, LOC101928084 | GRCh38.p7 | 2:214101566 | CATTACATGGTCTCT[C/T]ATAAGCCCATGGAGG | 79582 |
rs75488828 | snp | A/C | 0.0228947 | 0.104514 | intron-variant | SPAG16 | GRCh38.p7 | 2:213699972 | CATTCCAGATGATTA[A/C]AGTTGTTAGGAAATT | 79582 |
rs75490695 | snp | G/T | 0.00199481 | 0.0315187 | intron-variant | SPAG16 | GRCh38.p7 | 2:214177605 | TCTTTTGTCATCTTT[G/T]TAAGAATTATGACAG | 79582 |
rs75494923 | snp | A/T | 0.125182 | 0.216612 | intron-variant | SPAG16 | GRCh38.p7 | 2:213628332 | CTCCCAGGAGTCTAG[A/T]AAAGCACAAAGCAAA | 79582 |
rs75502704 | snp | C/G | 0.0236746 | 0.106192 | intron-variant | SPAG16 | GRCh38.p7 | 2:214190126 | CACACACCTGTCACT[C/G]TCTACACAGTCATAC | 79582 |
rs75503723 | snp | A/G | 0.0368353 | 0.130617 | intron-variant | SPAG16 | GRCh38.p7 | 2:214020464 | TCTGACCAAAAAATA[A/G]CAATGACACAAAAAT | 79582 |
rs75504482 | snp | A/T | | | intron-variant | SPAG16 | GRCh38.p7 | 2:214314151 | CACATGGTCAGTTGC[A/T]TCTGGAAATAATTTT | 79582 |
rs75507656 | snp | C/T | 0.132066 | 0.220435 | intron-variant | SPAG16 | GRCh38.p7 | 2:213601938 | TGGATGAAACTGTTC[C/T]ACCTGAAGTCATCAG | 79582 |
rs75508809 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | SPAG16 | GRCh38.p7 | 2:213652548 | TCTCTGCATCCCTTG[C/T]GAGCATTTCATATTG | 79582 |
rs75509135 | snp | C/G | 0.0174175 | 0.0916809 | intron-variant | SPAG16, LOC101928084 | GRCh38.p7 | 2:214096202 | CCCTCTGCCATTATA[C/G]TATATTTCCTTTGCA | 79582 |
rs75511469 | snp | A/G | 0.0726307 | 0.176182 | intron-variant | SPAG16 | GRCh38.p7 | 2:213995487 | ATCCGTGACACATGA[A/G]TCTCTGCCTGCAAAT | 79582 |
rs75514505 | snp | A/G | 0.0170251 | 0.090679 | intron-variant | SPAG16 | GRCh38.p7 | 2:214033459 | AGAGACTGAGAGGGG[A/G]CTGGAAGACAATAAT | 79582 |
rs75515363 | snp | A/G | 0.0349115 | 0.127424 | intron-variant | SPAG16 | GRCh38.p7 | 2:214225099 | CAAGAACAAACCTCA[A/G]GTTTAAAAAGTGCTC | 79582 |
rs75515791 | snp | A/G | 0.00953873 | 0.0683987 | intron-variant | SPAG16 | GRCh38.p7 | 2:214115458 | GCTATTTACATAAAC[A/G]TAGTTTGGGGAAAAT | 79582 |
rs75520583 | snp | C/T | 0.0726307 | 0.176182 | intron-variant | SPAG16 | GRCh38.p7 | 2:213993560 | GTTCAGGCCAAAAAA[C/T]AAGGGATATGCAACT | 79582 |
rs75531846 | snp | A/G | 0.0509478 | 0.151255 | intron-variant | SPAG16 | GRCh38.p7 | 2:213618992 | AACATTTTATTTTAA[A/G]ACAAGTTTTATTTTG | 79582 |
rs75533607 | snp | C/T | 0.5 | 0 | intron-variant | SPAG16 | GRCh38.p7 | 2:214140207 | TCCTTTTTCTCTCTC[C/T]TTTTTTTTTGTTTTG | 79582 |
rs75537744 | snp | A/C/T | 0.5 | 0 | intron-variant | SPAG16 | GRCh38.p7 | 2:213822845 | CGTTTTTTGTTCTTG[A/C/T]GATAGTTTACTGAGA | 79582 |
rs75538042 | snp | A/C | 0.0119091 | 0.0762411 | intron-variant | SPAG16 | GRCh38.p7 | 2:213579852 | ATCTAATATTAATCA[A/C]GATGACATTGTGATC | 79582 |
rs75538079 | snp | A/T | 0.0023933 | 0.0345097 | intron-variant | SPAG16 | GRCh38.p7 | 2:213704588 | TTAACCACTATGATT[A/T]CTTATTCATTTTCAA | 79582 |
rs75539677 | snp | C/T | 0.110519 | 0.207473 | intron-variant | SPAG16 | GRCh38.p7 | 2:213554036 | TCAGGCCTAACCTCA[C/T]CTCTCTGGCCTCTCC | 79582 |
rs75541278 | snp | A/T | 0.100588 | 0.200439 | intron-variant | SPAG16 | GRCh38.p7 | 2:213671898 | TATACAGCAAATGAA[A/T]ACACATTCAAGACTA | 79582 |
rs75551875 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | SPAG16 | GRCh38.p7 | 2:213961163 | AGTGCGATTACAATT[A/G]TTGTTTAGGTGGGAA | 79582 |
rs75552299 | snp | A/C | 0.5 | 0 | intron-variant | SPAG16 | GRCh38.p7 | 2:213425651 | AGCAAGACTCCATCT[A/C]AAAAAAAAAAAAAAA | 79582 |
rs75553430 | snp | G/T | 0 | 0 | intron-variant | SPAG16 | GRCh38.p7 | 2:213540053 | TTTTTTTTTTTTTTT[G/T]AGACGGAGTCTCGCT | 79582 |
rs75560043 | snp | G/T | 0.0189856 | 0.0955633 | intron-variant | SPAG16 | GRCh38.p7 | 2:214303534 | TAATGTGATGCTTCT[G/T]TCTAGCTGCTTTTAA | 79582 |
rs75563512 | snp | A/G | 0.0452528 | 0.143452 | intron-variant | SPAG16 | GRCh38.p7 | 2:213467417 | AGGTAAAATATCCCT[A/G]TGTAGCAGAGGAGTT | 79582 |
rs75564639 | snp | A/T | 0.0626037 | 0.165477 | intron-variant, downstream-variant-500B | SPAG16, MIR4438 | GRCh38.p7 | 2:213758296 | TTACTATGTTATTAG[A/T]TCCAAAATCACAATT | 79582 |
rs75580821 | snp | C/G | 0.0535932 | 0.154675 | intron-variant | SPAG16 | GRCh38.p7 | 2:213730770 | CTCCTACTCTGTTCT[C/G]TCTTCTTCTTCAGGT | 79582 |
rs75582445 | snp | A/T | 0.5 | 0 | intron-variant | SPAG16 | GRCh38.p7 | 2:214268894 | ATGCTATTCGGCAGT[A/T]ATTTTTTGAAAGTCA | 79582 |
rs75586604 | snp | C/T | 0.0498117 | 0.149749 | intron-variant | SPAG16 | GRCh38.p7 | 2:213769773 | AACAAAATGCACAGA[C/T]GTGTACAGTTTGATC | 79582 |
rs75599344 | snp | A/C | 0.5 | 0 | intron-variant | SPAG16 | GRCh38.p7 | 2:213574693 | ATATATGATATATAT[A/C]TGATATATGATATAT | 79582 |
rs75609507 | snp | A/T | 0.5 | 0 | intron-variant | SPAG16 | GRCh38.p7 | 2:213857737 | TATTTTTTAAAAACT[A/T]TATTTTGTAAGGCTA | 79582 |
rs75620800 | snp | C/T | 0.0349115 | 0.127424 | intron-variant | SPAG16 | GRCh38.p7 | 2:214225020 | TTTGTTCATTTTTAT[C/T]GAATAGTTGGAGAAG | 79582 |
rs75622889 | snp | A/C | 0 | 0 | intron-variant | SPAG16 | GRCh38.p7 | 2:213895013 | AAAAAAAAAAAAAAA[A/C]AAAAAACTGAAAGAC | 79582 |
rs75626363 | snp | C/T | 0.0130921 | 0.0798413 | intron-variant | SPAG16 | GRCh38.p7 | 2:213829436 | GCCCAGAAAAGCCAT[C/T]TAAGAGTCAAGGCCT | 79582 |
rs75628433 | snp | C/T | 0.0441095 | 0.141807 | intron-variant | SPAG16 | GRCh38.p7 | 2:213464083 | TTTGACATTTGTTTC[C/T]GTTCCTGCAGGAAAT | 79582 |
rs75628622 | snp | A/G | 0.00517822 | 0.0506191 | intron-variant | SPAG16 | GRCh38.p7 | 2:213799948 | AAATGCCCATCAGTG[A/G]TAGACTGGATTGAAA | 79582 |
rs75630935 | snp | C/G | 0.0333695 | 0.124785 | intron-variant | SPAG16 | GRCh38.p7 | 2:214010165 | AAGCAGACTGAAAAA[C/G]ATCAGGAAACAAGTG | 79582 |
rs75631366 | snp | A/C | 0.000798403 | 0.0199641 | intron-variant | SPAG16 | GRCh38.p7 | 2:213513753 | ATACTTAAGCTGGTC[A/C]CCTTCATATTTATGA | 79582 |
rs75638371 | snp | C/T | 0.5 | 0 | intron-variant | SPAG16 | GRCh38.p7 | 2:213772998 | CTTATTCTTTTTTTT[C/T]CAATTTTTTCATTCA | 79582 |
rs75640042 | snp | A/G | 0.0341408 | 0.126114 | intron-variant | SPAG16 | GRCh38.p7 | 2:214015958 | GAGAATGCATTAAGC[A/G]TAGGAAGTTTATCCA | 79582 |
rs75650955 | snp | A/C | 0.154993 | 0.231244 | intron-variant | SPAG16 | GRCh38.p7 | 2:214339509 | TTTAAGACAGCCAAA[A/C]CATCCTAGGGAATGT | 79582 |
rs75655474 | snp | A/G | 0.00716266 | 0.059414 | intron-variant | SPAG16 | GRCh38.p7 | 2:213683250 | TTACTTGTGTAAAGT[A/G]TGCATTAAAAGATAC | 79582 |
rs75656091 | snp | C/T | 0.00874735 | 0.0655527 | intron-variant | SPAG16 | GRCh38.p7 | 2:214315368 | TCTCCATTTATAATA[C/T]TTAAAAGGTTCTGTG | 79582 |
rs75665484 | snp | C/T | 0.00795532 | 0.062565 | intron-variant | SPAG16 | GRCh38.p7 | 2:213498154 | AAAGGTGGCAAGACA[C/T]GGTGAAGTATGAGCA | 79582 |
rs75666304 | snp | A/G | 0.0581099 | 0.160244 | intron-variant | SPAG16 | GRCh38.p7 | 2:214005745 | TTTCATTATAAAAGT[A/G]TTCTTGACTTTTGAA | 79582 |
rs75667477 | snp | A/G | 0.0138799 | 0.0821421 | intron-variant | SPAG16 | GRCh38.p7 | 2:213886361 | TTGGCCTGGGCAGGA[A/G]GAGAGTGGTGGCGGG | 79582 |
rs75673698 | snp | A/C | 0.0107246 | 0.0724382 | intron-variant | SPAG16 | GRCh38.p7 | 2:213734481 | AAAACTTTTATTATA[A/C]AATATGCTGCTAAAT | 79582 |
rs75681443 | in-del | -/A | 0.236144 | 0.249616 | intron-variant, downstream-variant-500B | SPAG16 | GRCh38.p7 | 2:214192636 | TGTATATTCCTTTAT[-/A]TTTTTTTGTACTTTT | 79582 |
rs75685338 | snp | A/G | 0.5 | 0 | intron-variant | SPAG16 | GRCh38.p7 | 2:213332089 | GCAATACAAAAGTCA[A/G]GGAAACAAAAAATGT | 79582 |
rs75687061 | snp | C/T | 0.0185938 | 0.0946107 | intron-variant | SPAG16 | GRCh38.p7 | 2:213353675 | GACCTGTTGTTACCT[C/T]GTCCCTCAGGCATCT | 79582 |
rs75689127 | snp | C/T | 0.0711525 | 0.174681 | intron-variant | SPAG16 | GRCh38.p7 | 2:213836079 | TTACCTGTCACTAAC[C/T]GTATCTAGAAGCTTG | 79582 |
rs75691867 | snp | C/T | 0.00159617 | 0.0282053 | intron-variant | SPAG16 | GRCh38.p7 | 2:214107531 | TTTAGATCCCTATTA[C/T]AATGTGTTATAGGTC | 79582 |
rs75705913 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | SPAG16 | GRCh38.p7 | 2:213859935 | GAGAACTAAGCATTT[A/G]GTACCAGGTATGGGG | 79582 |
rs75709940 | snp | A/G | 0.0119091 | 0.0762411 | intron-variant | SPAG16 | GRCh38.p7 | 2:213900238 | GCAGATGCATCACAG[A/G]GGGGATTTTTCACTG | 79582 |
rs75715601 | snp | C/T | 0.0456336 | 0.143994 | intron-variant | SPAG16 | GRCh38.p7 | 2:213445181 | ACTAAAAATCTTCTG[C/T]GCAACAATGAGAACA | 79582 |
rs75716106 | snp | A/G | 0.00159617 | 0.0282053 | intron-variant | SPAG16 | GRCh38.p7 | 2:214126208 | GAGAAGGGAGAAGGG[A/G]TGGATTGAGCTTCCT | 79582 |
rs75717935 | snp | A/G | 0.0524604 | 0.153226 | intron-variant | SPAG16 | GRCh38.p7 | 2:213380405 | ATGCCATCAGTGCAA[A/G]CTGGGAGACAGAAGG | 79582 |
rs75722655 | snp | C/T | 0.480302 | 0.0972668 | intron-variant | SPAG16 | GRCh38.p7 | 2:214273214 | gtccgatgggtagat[C/T]gcaaaaattttctcc | 79582 |
rs75723584 | snp | C/T | 0.0178098 | 0.0926698 | intron-variant | SPAG16 | GRCh38.p7 | 2:213500715 | CTTAGAGTGGGGTGG[C/T]AGGTAATAGGTTGAA | 79582 |
rs75728835 | snp | A/G | 0.145642 | 0.227177 | intron-variant | SPAG16 | GRCh38.p7 | 2:213565658 | GGATTGTCAGGAAGC[A/G]AAACTTAGAAATAAG | 79582 |
rs75750835 | snp | A/T | 0.00438332 | 0.0466095 | intron-variant | SPAG16 | GRCh38.p7 | 2:213940318 | TTTTTTAGAGATGAC[A/T]TCTTGCTGTGTTGCC | 79582 |
rs75754016 | snp | A/T | 0.144632 | 0.226711 | intron-variant | SPAG16 | GRCh38.p7 | 2:213709699 | AGTTATAAAAAAACA[A/T]GGAGAATATAGTTCT | 79582 |
rs75755721 | snp | A/C | 0.131381 | 0.220067 | intron-variant | SPAG16 | GRCh38.p7 | 2:213331738 | GAGGAATTTTGGAAA[A/C]CATATGAACATGTAG | 79582 |
rs75772583 | snp | G/T | 0.0205511 | 0.0992634 | intron-variant | SPAG16 | GRCh38.p7 | 2:213897479 | TGATTTTGTATCTAT[G/T]ACTTTATTGTTTTCT | 79582 |
rs75781042 | snp | A/C | 0.00557542 | 0.0525036 | intron-variant | SPAG16 | GRCh38.p7 | 2:213761322 | TAAAGATCTCAAGTC[A/C]ACAACCTAGCTTTAC | 79582 |
rs75786518 | in-del | -/GGATTGGTTAA | 0.367503 | 0.220665 | intron-variant | SPAG16 | GRCh38.p7 | 2:213590917 | CTACTCATCAGTGAT[-/GGATTGGTTAA]AGAAAATATGTTATC | 79582 |
rs75792228 | snp | A/G | 0.0197687 | 0.0974348 | intron-variant | SPAG16 | GRCh38.p7 | 2:214128542 | CCAAAATCAATTAAT[A/G]TGCATCCAAATTGAA | 79582 |
rs75797179 | snp | C/T | 0.5 | 0 | intron-variant | SPAG16 | GRCh38.p7 | 2:214187675 | TCATGTAAACAATAA[C/T]GTCTGCCATAACAAA | 79582 |
rs75797288 | snp | A/G | 0.5 | 0 | intron-variant | SPAG16 | GRCh38.p7 | 2:214046907 | AAAGTAAACAATCTG[A/G]AAAAAAAAAACAATT | 79582 |
rs75797905 | snp | G/T | 0.5 | 0 | intron-variant | SPAG16 | GRCh38.p7 | 2:213927716 | GTGATTTGTTTTTTT[G/T]GCCTGGCACATGGTT | 79582 |
rs75804544 | snp | A/G | | | intron-variant | SPAG16 | GRCh38.p7 | 2:214229194 | TATAGAAGAAAGTAT[A/G]TAAAGGATGTAAAGG | 79582 |
rs75811081 | in-del | -/G | 0.470618 | 0.117591 | intron-variant | SPAG16 | GRCh38.p7 | 2:213882849 | GCTTTGTGGTTGGTT[-/G]TTTCTTTGTTTTTGT | 79582 |
rs75811526 | snp | C/G | 0.0228947 | 0.104514 | intron-variant | SPAG16 | GRCh38.p7 | 2:214353107 | CACCCTGTTACAAAT[C/G]GGTCATAATCTAAAT | 79582 |
rs75813718 | snp | A/G | 0.0217236 | 0.101931 | intron-variant | SPAG16 | GRCh38.p7 | 2:213454388 | TTTGTGTGTTAGTCT[A/G]TAGGATAATAACAAG | 79582 |
rs75825863 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | SPAG16 | GRCh38.p7 | 2:213535424 | TTCAACTTCTAGAGA[C/T]GGAAATCATGTCTGA | 79582 |
rs75829062 | snp | A/G | 0.0146672 | 0.084371 | intron-variant | SPAG16 | GRCh38.p7 | 2:214025141 | AAAAGGGTCAGTTAC[A/G]TTTTTCTATTTTTGG | 79582 |
rs75832725 | snp | A/G | 0.0126979 | 0.078662 | intron-variant | SPAG16 | GRCh38.p7 | 2:214332462 | TAAGTCAATCTGTCT[A/G]TTGACTTGTTGGTAC | 79582 |
rs75833877 | snp | G/T | 0.0494327 | 0.149241 | intron-variant | SPAG16 | GRCh38.p7 | 2:213556793 | CAGCAGAACAATACA[G/T]TTTCTTCTCAAGGGA | 79582 |
rs75835044 | snp | C/T | 0.0279526 | 0.114869 | intron-variant | SPAG16 | GRCh38.p7 | 2:213341188 | TTAAGAAAAACATCT[C/T]CATTTAACAATCTGG | 79582 |
rs75843480 | snp | C/T | 0.0663309 | 0.169604 | intron-variant | SPAG16 | GRCh38.p7 | 2:214140542 | CTGATGGACTTGTAT[C/T]ACAATCTTCCCCATT | 79582 |
rs75847619 | snp | A/T | 0.081446 | 0.184634 | intron-variant | SPAG16 | GRCh38.p7 | 2:213698041 | AAGGTGCTCTTATTC[A/T]TAATTCCAGTATATT | 79582 |
rs75849861 | snp | C/T | | | intron-variant | SPAG16 | GRCh38.p7 | 2:213587946 | ATGCCCCTTAGAAAT[C/T]TTTAAAGAAATATAT | 79582 |
rs75850468 | snp | C/T | 0.26868 | 0.249301 | intron-variant | SPAG16 | GRCh38.p7 | 2:213621059 | TACTAAAACTAAAAA[C/T]TAGTTTTAGTACTTA | 79582 |
rs75850618 | snp | A/C | 0.0463947 | 0.145069 | intron-variant, upstream-variant-2KB | SPAG16 | GRCh38.p7 | 2:213342158 | AAATTCTTCAACCAT[A/C]CACAGATTACAGTAT | 79582 |
rs75851879 | snp | G/T | 0.121022 | 0.21416 | intron-variant, utr-variant-3-prime | SPAG16 | GRCh38.p7 | 2:213369378 | TTAAAATAAAATTAT[G/T]GTGTCATAAGGTAAT | 79582 |
rs75853382 | snp | G/T | 0.0150606 | 0.0854603 | intron-variant | SPAG16 | GRCh38.p7 | 2:214295369 | ACTCTAATGAAACAG[G/T]TTTTGCTAGCTAGCA | 79582 |
rs75854726 | snp | A/G | 0.222333 | 0.248464 | intron-variant | SPAG16, LOC101928084 | GRCh38.p7 | 2:214090437 | AGTGCCTCAGAGAGA[A/G]GCACCTTCACTGTAT | 79582 |
rs75862235 | snp | A/C | 0.5 | 0 | intron-variant | SPAG16 | GRCh38.p7 | 2:214182439 | TATGTGCGTTACACA[A/C]CTAAGATTAAAAAGT | 79582 |
rs75863261 | snp | C/T | 0.00398564 | 0.0444627 | intron-variant | SPAG16 | GRCh38.p7 | 2:213429429 | GGCCTAGCTAATTGC[C/T]TGGGACAATGGATTA | 79582 |
rs75863577 | snp | A/C | 0.0130921 | 0.0798413 | intron-variant | SPAG16 | GRCh38.p7 | 2:213981037 | CAGAAATTTGTTTCT[A/C]ACAGTTCTAAAGGCT | 79582 |
rs75864958 | snp | A/T | 0.5 | 0 | intron-variant | SPAG16 | GRCh38.p7 | 2:214038548 | TTTCTTTTTTTTTAG[A/T]TTTTTTTTAATACTT | 79582 |
rs75869942 | snp | G/T | | | intron-variant | SPAG16 | GRCh38.p7 | 2:214027606 | TATATACTCTTTCCA[G/T]CAATCCATCTGTGTC | 79582 |
rs75871067 | snp | A/G | 0.264632 | 0.249571 | intron-variant | SPAG16 | GRCh38.p7 | 2:214052622 | GTATATTATAAGAAT[A/G]ATAATATAAACTCAA | 79582 |
rs75888894 | snp | C/T | 0.5 | 0 | intron-variant | SPAG16, LOC101928084 | GRCh38.p7 | 2:214097840 | AATTGTTAACATTTA[C/T]TGAGTACTTGCTTTG | 79582 |
rs75900300 | snp | A/C | 0.00119737 | 0.0244387 | intron-variant | SPAG16 | GRCh38.p7 | 2:213390980 | CTTTTGATCTTTAGA[A/C]ATTATATGGCCAGGC | 79582 |
rs75905324 | snp | A/T | 0.0744748 | 0.178019 | intron-variant | SPAG16 | GRCh38.p7 | 2:213739509 | TCTTAATCTAGGCAT[A/T]CTTATTTAGTGGAGC | 79582 |
rs75909787 | snp | A/G | | | intron-variant | SPAG16 | GRCh38.p7 | 2:213810421 | TGTAGTGGCAAGGAA[A/G]TAGACTCATATGACA | 79582 |
rs75910799 | snp | A/G | 0.00914312 | 0.0669923 | intron-variant | SPAG16 | GRCh38.p7 | 2:214280246 | AAGACATAGAGAGCT[A/G]TACTTGTTCATCAAC | 79582 |
rs75911272 | snp | A/G | 0.302184 | 0.244493 | intron-variant | SPAG16 | GRCh38.p7 | 2:213737303 | TTTCTTTGTGCATAC[A/G]TGTTTGCAGTTATAG | 79582 |
rs75928622 | snp | C/T | 0.0134861 | 0.0810011 | intron-variant | SPAG16 | GRCh38.p7 | 2:214108899 | GTCCTTTGAGTTTTC[C/T]GTGGTTTGAATGTAT | 79582 |
rs75930366 | snp | A/G | 0.0729998 | 0.176553 | intron-variant | SPAG16 | GRCh38.p7 | 2:214076884 | ATCAACTTGTACCCT[A/G]ATCAATAGCAAGTTG | 79582 |
rs75936545 | snp | C/T | 0.0425829 | 0.139564 | intron-variant | SPAG16 | GRCh38.p7 | 2:213524032 | AGACTTTCTTAGCAG[C/T]CCCTCTCATCTCAGG | 79582 |
rs75939683 | snp | C/T | 0.0505692 | 0.150756 | intron-variant | SPAG16 | GRCh38.p7 | 2:214218264 | GGGTTGGAAAAGGGA[C/T]GGCCTCGAGGTCCCC | 79582 |
rs75939785 | snp | A/G | 0.00953873 | 0.0683987 | intron-variant | SPAG16 | GRCh38.p7 | 2:213651580 | AAAGCTCTCTTGACT[A/G]TCTCAATCTCTTTCC | 79582 |
rs75941410 | snp | A/T | 0.0205511 | 0.0992634 | intron-variant | SPAG16 | GRCh38.p7 | 2:213830088 | ACTTTCCTAGGAGTT[A/T]CAGTCTTTGTGGCCT | 79582 |
rs75944432 | snp | A/G | 0.0165278 | 0.0893908 | intron-variant | SPAG16 | GRCh38.p7 | 2:213919955 | TTAAGAACTTGCTTT[A/G]TGACTCTGGTTGCTT | 79582 |
rs75945711 | snp | A/C | 0.02016 | 0.0983543 | intron-variant | SPAG16 | GRCh38.p7 | 2:213661591 | TATTTTGATTTGTTT[A/C]TTTTGATTTTAAAAC | 79582 |
rs75948830 | snp | C/G | 0.0376037 | 0.131863 | intron-variant | SPAG16 | GRCh38.p7 | 2:213419401 | TGCCTTTTTTACTCC[C/G]TAATATGCTCATACA | 79582 |
rs75960744 | snp | A/C | 0 | 0 | intron-variant | SPAG16 | GRCh38.p7 | 2:213724778 | TGAGACTCTGTCTCA[A/C]AAAAAAAAAAAAAAA | 79582 |
rs75965560 | snp | G/T | 0.0168055 | 0.0901129 | intron-variant | SPAG16 | GRCh38.p7 | 2:214169007 | TGTTGTTTCCAAAAC[G/T]AAGTCATTATGATTG | 79582 |
rs75977713 | snp | G/T | 0.5 | 0 | intron-variant | SPAG16 | GRCh38.p7 | 2:213668831 | TTTTTTGTATTTTTA[G/T]TAAAGACGGGGTTTC | 79582 |
rs75982070 | snp | G/T | 0.5 | 0 | intron-variant | SPAG16 | GRCh38.p7 | 2:213511167 | TGTTGGTATTCAGAT[G/T]TTACACATTGACTGA | 79582 |
rs75986282 | snp | C/T | 0.02016 | 0.0983543 | intron-variant | SPAG16 | GRCh38.p7 | 2:213846844 | AAATCTGTGCAGGCT[C/T]AATGGCTTCTGCTGC | 79582 |
rs75988759 | snp | C/G | 0.46875 | 0.121031 | intron-variant | SPAG16 | GRCh38.p7 | 2:213822844 | TGGTTTTCTGTTCCT[C/G]TGTTAGTTTGCTGAG | 79582 |
rs75989227 | snp | C/T | 0.0205511 | 0.0992634 | intron-variant | SPAG16 | GRCh38.p7 | 2:213816260 | GTAGTTTGGTCACTG[C/T]CTTGGCTGTATAAGA | 79582 |
rs75995253 | snp | A/G | 0.00318978 | 0.0398085 | intron-variant | SPAG16 | GRCh38.p7 | 2:213606546 | TACTTCTGGATTTGT[A/G]CTAATTACAAATAAT | 79582 |
rs75999479 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | SPAG16 | GRCh38.p7 | 2:213607818 | ACTTGTTTTCTTCTC[C/T]GGAGAAAGTTGATAA | 79582 |
rs76006428 | snp | G/T | 0.0271762 | 0.113356 | intron-variant | SPAG16 | GRCh38.p7 | 2:214398450 | TAGCTAAATCATGCG[G/T]GCCTCATTACTTTAA | 79582 |
rs76011056 | in-del | -/ACAGTATAAGTG | 0.355096 | 0.226837 | intron-variant | SPAG16 | GRCh38.p7 | 2:213381086 | TCCACTGGGCTTACC[-/ACAGTATAAGTG]GTAAAATAGACTTAT | 79582 |
rs76011200 | snp | A/C | 0.5 | 0 | intron-variant | SPAG16 | GRCh38.p7 | 2:213292664 | GCGAGACTCCGTCTC[A/C]AAAAAAAAAAACAAA | 79582 |
rs76013153 | snp | C/T | 0.030278 | 0.119257 | intron-variant | SPAG16 | GRCh38.p7 | 2:213961513 | TCTTTCATTATTAAA[C/T]ATGTTGTTAGCTATT | 79582 |
rs76015778 | snp | A/T | 0.5 | 0 | intron-variant | SPAG16 | GRCh38.p7 | 2:214008451 | CATTTAAAAAAAAAA[A/T]TTACATGCTGGGGCT | 79582 |
rs76022188 | snp | A/G | 0.0685596 | 0.171987 | intron-variant | SPAG16 | GRCh38.p7 | 2:214161592 | GTTTGTTGGTGGCAT[A/G]ACTGTCTTTTTTGGG | 79582 |
rs76032512 | snp | A/C/T | 0.0517044 | 0.152246 | intron-variant | SPAG16 | GRCh38.p7 | 2:214285479 | TGTTCAGATGAAAAA[A/C/T]TAACGAAACCCACTG | 79582 |
rs76032769 | snp | A/G | 0.491834 | 0.0633738 | intron-variant | SPAG16 | GRCh38.p7 | 2:214273325 | tctattttggctttt[A/G]ttgccattgcttttg | 79582 |
rs76035386 | snp | G/T | 0.5 | 0 | intron-variant | SPAG16 | GRCh38.p7 | 2:213643792 | TTTTTTTTTTTTTTT[G/T]TTTTGAGACGCAGTT | 79582 |
rs76048294 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | SPAG16 | GRCh38.p7 | 2:213551568 | ATTCTGTCAAAATCT[A/G]TGCAGGTTTCTATTC | 79582 |
rs76048899 | snp | A/G | 0.5 | 0 | intron-variant | SPAG16, LOC101928084 | GRCh38.p7 | 2:214085392 | TCAAAAAAAAAAAAA[A/G]AGAAAGAAAGAAAGA | 79582 |
rs76057136 | snp | A/G | 0.0236746 | 0.106192 | intron-variant | SPAG16 | GRCh38.p7 | 2:213850673 | CTAAGACTCACCTTC[A/G]AGAAGAGAAATTCTG | 79582 |
rs76059006 | snp | A/C | 0.131038 | 0.219882 | intron-variant | SPAG16 | GRCh38.p7 | 2:213359940 | CTAAAGAGCTAATTT[A/C]TTGATATCTAATATG | 79582 |
rs76069337 | snp | A/G | 0.154993 | 0.231244 | intron-variant | SPAG16 | GRCh38.p7 | 2:213968514 | ACTTCTTTTAAGCCT[A/G]TAGTATCAGGCTTCT | 79582 |
rs76071405 | snp | A/T | 0.0463947 | 0.145069 | intron-variant, upstream-variant-2KB | SPAG16 | GRCh38.p7 | 2:213342437 | AGAACTGTACATACT[A/T]CCTAAATTTTTATTT | 79582 |
rs76072407 | snp | G/T | 0.0869089 | 0.189476 | intron-variant | SPAG16 | GRCh38.p7 | 2:213747218 | AAAAGTCTTATAAAA[G/T]AAATCTATAAAGAAA | 79582 |
rs76076493 | snp | A/G | 0.0452528 | 0.143452 | intron-variant | SPAG16 | GRCh38.p7 | 2:213428612 | TGTGGGCATTTTAAT[A/G]GGGCTCTCTCCCTTC | 79582 |
rs76077626 | snp | A/G | 0.00358779 | 0.0422022 | intron-variant | SPAG16 | GRCh38.p7 | 2:213464133 | GTTAATCAAATCAAA[A/G]GTTACATGGTTAATC | 79582 |
rs76079378 | snp | C/G | 0.5 | 0 | intron-variant | SPAG16 | GRCh38.p7 | 2:213926319 | TGGGTGCACCAAAAT[C/G]TCAGAAATCACCATT | 79582 |
rs76080053 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | SPAG16 | GRCh38.p7 | 2:213556662 | GGACTTCAATATCCA[A/G]CTTTCAACAAAGAAT | 79582 |
rs76081591 | snp | A/G | 0.0182019 | 0.0936463 | intron-variant | SPAG16 | GRCh38.p7 | 2:214270206 | TATTGTTAGCAAATT[A/G]GACATGAAATGGTAA | 79582 |
rs76084061 | snp | A/C | 0.0275645 | 0.114116 | intron-variant | SPAG16 | GRCh38.p7 | 2:213357420 | GTCTCTAAGGACTTC[A/C]TTTATGAATATGGGT | 79582 |
rs76084576 | snp | A/T | 0.5 | 0 | intron-variant | SPAG16 | GRCh38.p7 | 2:213886012 | TTATAGACAGCCATG[A/T]AAAAATATGATTGGA | 79582 |
rs76084863 | snp | C/T | 0.0023933 | 0.0345097 | intron-variant | SPAG16 | GRCh38.p7 | 2:214298401 | AGATAAGGAGGATGA[C/T]GATGAAATTATCAGA | 79582 |
rs76086079 | snp | A/T | 0.5 | 0 | intron-variant | SPAG16 | GRCh38.p7 | 2:214367822 | TTTTTTTCCTTGAAG[A/T]AAATTCTGTTGCTGG | 79582 |
rs76086576 | in-del | -/A | 0.474992 | 0.108989 | intron-variant | SPAG16 | GRCh38.p7 | 2:213843953 | TAATATAAAACTTAT[-/A]AAAATTTTAATTATT | 79582 |
rs76094837 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | SPAG16 | GRCh38.p7 | 2:213978233 | ACAGAGTATATTCAA[C/T]ATTTTTAATGGAAAT | 79582 |
rs76101947 | snp | A/G | 0.00199481 | 0.0315187 | intron-variant | SPAG16 | GRCh38.p7 | 2:213617265 | TAAAAACAATGAGGC[A/G]TTTAAATGCTGATGA | 79582 |
rs76102347 | snp | A/G | 0.0752113 | 0.178743 | intron-variant | SPAG16 | GRCh38.p7 | 2:214145882 | GTTTATTCAAAGACC[A/G]AATGTCTAACACGTA | 79582 |
rs76110790 | snp | C/T | 0.00597247 | 0.0543191 | intron-variant | SPAG16 | GRCh38.p7 | 2:213725990 | GAGAGATCTCTTTTT[C/T]GGCATTTCTCAACAT | 79582 |
rs76115634 | snp | C/T | 0.0310518 | 0.120672 | intron-variant | SPAG16 | GRCh38.p7 | 2:214282177 | TCAATTATACTTTAA[C/T]GCTGTTAAAATATGA | 79582 |
rs76118196 | snp | C/G | 0.0197687 | 0.0974348 | intron-variant | SPAG16 | GRCh38.p7 | 2:214156333 | ATTTAGTTGTCACCA[C/G]AACTCAAAATGAGAT | 79582 |
rs76118901 | snp | A/G | 0.0475351 | 0.146656 | intron-variant | SPAG16 | GRCh38.p7 | 2:213980029 | GGCATTGCCTATAGC[A/G]TCATGAAAGAACCAG | 79582 |
rs76123719 | snp | A/G | 0.00993419 | 0.0697739 | intron-variant | SPAG16 | GRCh38.p7 | 2:214268082 | GAGAAAATGCTCAAC[A/G]TCTCTAATTATAAGA | 79582 |
rs76127681 | snp | A/G | 0.0551013 | 0.156571 | intron-variant | SPAG16 | GRCh38.p7 | 2:213960933 | GTAATCAGAGCACAA[A/G]TCTCTGGTATTTGGG | 79582 |
rs76136600 | snp | A/G | 0.0023933 | 0.0345097 | intron-variant | SPAG16 | GRCh38.p7 | 2:214300781 | TCATAATCTTCCAAG[A/G]AAAAGAAAGGCCCAG | 79582 |
rs76142066 | snp | A/C | 0.0182019 | 0.0936463 | intron-variant | SPAG16 | GRCh38.p7 | 2:213426272 | TGTTAACCATAGAAA[A/C]TTTTTATTTAGCCAA | 79582 |
rs76147171 | snp | C/T | 0.00398564 | 0.0444627 | intron-variant | SPAG16 | GRCh38.p7 | 2:214391972 | AAAATATGAACACAA[C/T]GCAGAGATTTGGACC | 79582 |
rs76150309 | snp | A/C | 0.5 | 0 | intron-variant | SPAG16 | GRCh38.p7 | 2:214171723 | GAATTGAATAATTTC[A/C]TGATACTAGTTTAAG | 79582 |
rs76150970 | snp | G/T | 0.00755907 | 0.0610114 | intron-variant | SPAG16 | GRCh38.p7 | 2:214398173 | CTGCTGGAATCAGAA[G/T]ATAGAGACAATGAAA | 79582 |
rs76154983 | snp | A/T | 0.5 | 0 | intron-variant | SPAG16 | GRCh38.p7 | 2:214057067 | AGTTTTGAACTTCTC[A/T]AAGACATCCATGAAA | 79582 |
rs76157229 | snp | A/T | 0.00159617 | 0.0282053 | intron-variant | SPAG16, LOC101928084 | GRCh38.p7 | 2:214086453 | CCCATGTGTTGGGGG[A/T]GGGACCTTATGGAGG | 79582 |
rs76164211 | snp | C/T | 0.125182 | 0.216612 | intron-variant | SPAG16 | GRCh38.p7 | 2:213639493 | ACTTTATCTCCCCTT[C/T]GTTTATGAAACTTAG | 79582 |
rs76168041 | snp | C/T | 0.0543475 | 0.155628 | intron-variant | SPAG16 | GRCh38.p7 | 2:213769769 | ATACAACAAAATGCA[C/T]AGACGTGTACAGTTT | 79582 |
rs76168408 | snp | C/T | 0.131723 | 0.220251 | intron-variant | SPAG16 | GRCh38.p7 | 2:213621995 | TAGCCTGTGGAGCTC[C/T]CTTCTCTAAGGTTGC | 79582 |
rs76172988 | snp | A/G | 0.00438332 | 0.0466095 | intron-variant | SPAG16 | GRCh38.p7 | 2:213907088 | AACCTGTTGAATGGA[A/G]GAAAATATTTTCAAA | 79582 |
rs76179411 | snp | A/G | 0.0178098 | 0.0926698 | intron-variant | SPAG16 | GRCh38.p7 | 2:214397885 | AGTGTCATTCCTCCT[A/G]AAATGACAGCATCTT | 79582 |
rs76179584 | snp | C/T | 0.0861826 | 0.188849 | intron-variant | SPAG16 | GRCh38.p7 | 2:213506704 | GGATGCCTTATGTTG[C/T]GAGTGACTGAAAATG | 79582 |
rs76187972 | snp | A/G | 0.0490535 | 0.14873 | intron-variant | SPAG16 | GRCh38.p7 | 2:213747025 | TTGTCATAAAAGGAG[A/G]TAACAGCTCCATGCA | 79582 |
rs76191561 | snp | A/G | 0.0150606 | 0.0854603 | intron-variant | SPAG16 | GRCh38.p7 | 2:214208614 | TTAATCCAAATTTCA[A/G]CTCTCCCACTGTGTA | 79582 |
rs76193158 | snp | A/T | 0.084364 | 0.187256 | intron-variant | SPAG16 | GRCh38.p7 | 2:213699325 | CCACTCTTTGCAGAC[A/T]TCTTCATTGCCAGGA | 79582 |
rs76203629 | snp | C/G | 0.0150606 | 0.0854603 | intron-variant | SPAG16 | GRCh38.p7 | 2:214298195 | ATATATATTTGCATG[C/G]CAATTTTAAATGAGA | 79582 |
rs76205820 | snp | C/G | | | intron-variant | SPAG16 | GRCh38.p7 | 2:213816077 | AAAACATTGTCATCT[C/G]CTGGAATCCTTATTT | 79582 |
rs76206873 | snp | A/T | 0.0260105 | 0.111035 | intron-variant | SPAG16 | GRCh38.p7 | 2:214269973 | TGCCAGAGACAGAAC[A/T]TGGATTAAAGGAAAG | 79582 |
rs76208175 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | SPAG16 | GRCh38.p7 | 2:213486076 | CTTTATGTTATAAAT[A/G]TTTGAATTATTCTCT | 79582 |
rs76210123 | snp | C/T | 0.081446 | 0.184634 | intron-variant | SPAG16 | GRCh38.p7 | 2:213699099 | TAATGTCTCCTACAA[C/T]GTTTGATGTTCACAG | 79582 |
rs76210443 | snp | C/G | 0.261056 | 0.249755 | intron-variant | SPAG16 | GRCh38.p7 | 2:213916760 | TCTGATTACTCTGCT[C/G]ACAGTTTCTTTTGCT | 79582 |
rs76211124 | snp | A/C | 0.0295035 | 0.117819 | intron-variant | SPAG16 | GRCh38.p7 | 2:213528601 | ACTTCCCTACTGAAG[A/C]TATTTTAAGTAAACT | 79582 |
rs76214041 | snp | A/T | 0.0463947 | 0.145069 | intron-variant, upstream-variant-2KB | SPAG16 | GRCh38.p7 | 2:213342157 | AAAATTCTTCAACCA[A/T]CCACAGATTACAGTA | 79582 |
rs76233584 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | SPAG16 | GRCh38.p7 | 2:214135451 | CCAATAACAAAGTAT[A/G]CATGTTTATGCATCT | 79582 |
rs76234439 | snp | A/T | 0.0429648 | 0.14013 | intron-variant | SPAG16 | GRCh38.p7 | 2:214230704 | CCAACATTCTTGGAC[A/T]ATTTCCAAAAGGAGG | 79582 |
rs76237464 | snp | C/T | 0.0916144 | 0.193427 | intron-variant | SPAG16 | GRCh38.p7 | 2:213540698 | TGTAGTTCTTCACAA[C/T]TTGGAGAAGTTGGAG | 79582 |
rs76237744 | snp | C/T | 0.00517822 | 0.0506191 | intron-variant | SPAG16 | GRCh38.p7 | 2:214184799 | ACTGAAAACTTAAAG[C/T]TTTCCAATTTTTGCT | 79582 |
rs76244503 | snp | A/G | | | intron-variant | SPAG16 | GRCh38.p7 | 2:213997149 | AATTTTCTTCCTTTG[A/G]TAGCTTCACATAACC | 79582 |
rs76246202 | snp | C/G | 0.000798403 | 0.0199641 | intron-variant | SPAG16 | GRCh38.p7 | 2:213485365 | TTTTATAATTTGTCA[C/G]ATGTAATCAGCCATC | 79582 |
rs76252788 | snp | C/T | 0.0154538 | 0.0865337 | intron-variant | SPAG16 | GRCh38.p7 | 2:213985763 | ATGGTAATCATTCTC[C/T]TAATCAATTCTATCA | 79582 |
rs76254801 | snp | A/G | 0.078151 | 0.181571 | intron-variant | SPAG16 | GRCh38.p7 | 2:213908711 | GGAACACTTGGATAT[A/G]GTCACTGATTACTTC | 79582 |
rs76255291 | snp | C/T | 0.00159617 | 0.0282053 | intron-variant | SPAG16 | GRCh38.p7 | 2:213773591 | GGAGTCTTTCTCTGT[C/T]GCCCAGGATGGAGTG | 79582 |
rs76255877 | snp | C/T | 0.0154538 | 0.0865337 | intron-variant | SPAG16 | GRCh38.p7 | 2:213995492 | TGACACATGAGTCTC[C/T]GCCTGCAAATCAGTT | 79582 |
rs76255954 | snp | A/G | 0.00716266 | 0.059414 | intron-variant | SPAG16 | GRCh38.p7 | 2:213813988 | AGCCTGAGACACAGA[A/G]GGAGAAAGTGGGTAG | 79582 |
rs76258882 | snp | C/T | 0.0429648 | 0.14013 | intron-variant | SPAG16 | GRCh38.p7 | 2:214229906 | CAAGTGTCAGCAAAA[C/T]GCAGCACAGTAATGT | 79582 |
rs76266632 | snp | C/G | 0.5 | 0 | intron-variant, nc-transcript-variant | SPAG16, LOC101928084 | GRCh38.p7 | 2:214102211 | ACCAGAGATGTCTTA[C/G]GCCTTGGGGATGAGA | 79582 |
rs76271161 | snp | G/T | 0.0562307 | 0.157967 | intron-variant | SPAG16 | GRCh38.p7 | 2:214007683 | GCCTCCATTATTTCT[G/T]TTAAAATGTCAGTTG | 79582 |
rs76280536 | snp | A/T | 0.0209421 | 0.100162 | intron-variant | SPAG16 | GRCh38.p7 | 2:213445736 | ATGAATGCAAATCTA[A/T]ACTACAATAAGATAC | 79582 |
rs76286512 | snp | G/T | 0.111224 | 0.207945 | intron-variant | SPAG16 | GRCh38.p7 | 2:214388086 | GTATTTGATACATTT[G/T]TCCTGTTGGAGAGAT | 79582 |
rs76286560 | snp | A/T | 0.128288 | 0.218372 | intron-variant | SPAG16 | GRCh38.p7 | 2:213501205 | TTCTTGCAGATGCCA[A/T]TGACAAGTTTTATAA | 79582 |
rs76290577 | in-del | -/TT | | | intron-variant | SPAG16 | GRCh38.p7 | 2:213668326 | GGTGCTTTTTTTTTT[-/TT]GAAATACATAGACTA | 79582 |
rs76291470 | snp | C/T | 0.224116 | 0.248656 | intron-variant | SPAG16, LOC101928084 | GRCh38.p7 | 2:214099419 | AAAAGAATTGCTATA[C/T]ACAAAGTACTTAGTA | 79582 |
rs76308924 | snp | A/G | 0.0170251 | 0.090679 | intron-variant | SPAG16 | GRCh38.p7 | 2:213978149 | CTATCCTTGTTTCCC[A/G]TCTTGGGACACTGGA | 79582 |
rs76316789 | snp | C/T | 0.00478085 | 0.0486577 | intron-variant | SPAG16 | GRCh38.p7 | 2:213702367 | TTTCACTTTTTGCAA[C/T]AAATCTTGCTGCTGC | 79582 |
rs76321821 | snp | A/G | 0.0221141 | 0.102801 | intron-variant | SPAG16 | GRCh38.p7 | 2:213820919 | GTACTAAGTTTGCCC[A/G]TTGGGCAAGGATCTG | 79582 |
rs76323069 | snp | G/T | 0.02016 | 0.0983543 | intron-variant | SPAG16 | GRCh38.p7 | 2:213778795 | TACCAAGCAAACTTC[G/T]CTTATGCAACTGGAA | 79582 |
rs76327353 | snp | C/T | | | intron-variant | SPAG16 | GRCh38.p7 | 2:213908770 | TTTGTCTTTTTTTTT[C/T]CTTTTTTTAATTATT | 79582 |
rs76331280 | snp | A/G | 0.0551013 | 0.156571 | intron-variant | SPAG16 | GRCh38.p7 | 2:214256135 | ACATTTTTAAGTTTA[A/G]CTATTCTGGAGTGTG | 79582 |
rs76336111 | snp | C/G | 0.5 | 0 | intron-variant | SPAG16 | GRCh38.p7 | 2:214187681 | AAACAATAATGTCTG[C/G]CATAACAAACCTCAG | 79582 |
rs76347614 | snp | C/G | 0.0023933 | 0.0345097 | intron-variant | SPAG16 | GRCh38.p7 | 2:214372946 | CAGCAAATGGGGCTA[C/G]CTGCATTTCCTGATG | 79582 |
rs76348376 | snp | A/G | 0.5 | 0 | intron-variant | SPAG16 | GRCh38.p7 | 2:213537490 | AATTTAAAAAAAAAA[A/G]GAATCTCCAAGGGCT | 79582 |
rs76358867 | snp | C/T | 0.16911 | 0.236552 | intron-variant | SPAG16 | GRCh38.p7 | 2:214290235 | TGATCTCTGATGATC[C/T]TTTGTATTTTGTTGG | 79582 |
rs76360458 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant, utr-variant-3-prime | SPAG16 | GRCh38.p7 | 2:213398065 | TGAGACGTCTCTCTC[C/T]CTCACATCTCACATC | 79582 |
rs76360541 | snp | A/G | 0.0611083 | 0.163768 | intron-variant | SPAG16 | GRCh38.p7 | 2:213713722 | CTTCCTGTTTTATCT[A/G]TTTCAAGACAAACTG | 79582 |
rs76362168 | snp | A/G | 0.00557542 | 0.0525036 | intron-variant | SPAG16 | GRCh38.p7 | 2:213673240 | TCATTAGGTTAAAGA[A/G]ATATTTTAAGAATAG | 79582 |
rs76365051 | snp | A/C | 0.5 | 0 | intron-variant | SPAG16 | GRCh38.p7 | 2:213510947 | TGATGTTTAAACTGC[A/C]ATATAAGTAATTCTG | 79582 |
rs76366232 | snp | A/G | 0.269809 | 0.249214 | intron-variant | SPAG16 | GRCh38.p7 | 2:213971856 | CCATGACATGCTAAC[A/G]TGTGCTATTTTCTTG | 79582 |
rs76369324 | snp | G/T | 0.0150606 | 0.0854603 | intron-variant | SPAG16 | GRCh38.p7 | 2:214292012 | ATGAAGAATAATTTT[G/T]CTGTGCATGATATCC | 79582 |
rs76369504 | snp | A/C | 0.0189856 | 0.0955633 | intron-variant | SPAG16 | GRCh38.p7 | 2:213544656 | CACTGCATTAAAATT[A/C]TTCTGTGCTCTACCT | 79582 |
rs76373286 | snp | A/G | 0.021333 | 0.101051 | intron-variant | SPAG16 | GRCh38.p7 | 2:213484880 | ATAAGACCTTGCTTT[A/G]TATCTCTGAATAAAG | 79582 |
rs76378039 | snp | A/C | | | intron-variant | SPAG16 | GRCh38.p7 | 2:213491894 | AGGAGGGAAGGCTGT[A/C]ACATTATTAGTTTAT | 79582 |
rs76381662 | snp | A/G | 0.0456336 | 0.143994 | intron-variant | SPAG16 | GRCh38.p7 | 2:213436221 | AGGATGTAAGTAGGA[A/G]TAAATTGGGCAATTA | 79582 |
rs76389359 | snp | A/C | 0.5 | 0 | intron-variant | SPAG16 | GRCh38.p7 | 2:213781496 | TGCTCATTCTCCTAA[A/C]CCCTCCCCTGCCCAT | 79582 |
rs76390655 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | SPAG16 | GRCh38.p7 | 2:213440663 | AGAAGTGTGGTACTA[C/T]TGAGTAGTGATAAAA | 79582 |
rs76391183 | snp | A/T | 0.5 | 0 | intron-variant | SPAG16 | GRCh38.p7 | 2:213438431 | AGGGCCCACTGCTTA[A/T]TTTTATATAACAAGT | 79582 |
rs76394809 | snp | A/C/G | 0.00119737 | 0.0244387 | intron-variant | SPAG16 | GRCh38.p7 | 2:213668928 | GCTGGGATTACAGGC[A/C/G]TGAGCCACTGCGCCC | 79582 |
rs76395330 | snp | A/C | 0.179105 | 0.239737 | intron-variant | SPAG16 | GRCh38.p7 | 2:213963199 | TCTATCTGAGCACTA[A/C]TTTAGCTGCATCCAG | 79582 |
rs76401622 | snp | A/G | 0.0240643 | 0.107019 | intron-variant | SPAG16 | GRCh38.p7 | 2:213339885 | GTTTATACTTTGGAC[A/G]TGTTCTGGCAGCATA | 79582 |
rs76405849 | snp | A/G | 0.0433465 | 0.140692 | intron-variant | SPAG16 | GRCh38.p7 | 2:213993642 | AGATTTGCTTAATAG[A/G]AAAACGGTGTTTTCT | 79582 |
rs76416819 | snp | A/G | 0.00159617 | 0.0282053 | intron-variant | SPAG16 | GRCh38.p7 | 2:214018372 | TGTCTGTATAATATG[A/G]AATTGTTAGTTGTTT | 79582 |
rs76416926 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | SPAG16 | GRCh38.p7 | 2:214131258 | CCTGTGGTCCTAGTT[A/G]CTTCGGGAAGTTGAA | 79582 |
rs76422052 | snp | C/G | 0.0182019 | 0.0936463 | intron-variant | SPAG16 | GRCh38.p7 | 2:213377752 | AAGACGAATGGAAGA[C/G]TTGTTACTGGACTTG | 79582 |
rs76424867 | snp | A/G | 0.00874735 | 0.0655527 | intron-variant | SPAG16 | GRCh38.p7 | 2:213877689 | GATGAGGATACCATA[A/G]TATCCACTTATGTAT | 79582 |
rs76425953 | snp | C/T | 0.0130921 | 0.0798413 | intron-variant | SPAG16 | GRCh38.p7 | 2:213747768 | CTCAGAATACATCAC[C/T]GTCTTGATACCATCT | 79582 |
rs76426681 | snp | G/T | 0.000798403 | 0.0199641 | intron-variant | SPAG16 | GRCh38.p7 | 2:213970299 | TTTGCTTTTTTTTTT[G/T]TTGTTTATTTTTAAA | 79582 |
rs76427705 | snp | A/G | 0.00279162 | 0.0372561 | intron-variant | SPAG16 | GRCh38.p7 | 2:213842398 | AACCAGGAGTAGTAA[A/G]AAATAGAATGTGTAT | 79582 |
rs76443707 | snp | A/G | 0.124837 | 0.216412 | intron-variant | SPAG16 | GRCh38.p7 | 2:214289582 | CTGATCCATTGGTCT[A/G]TGTGTCTGCTCTTAT | 79582 |
rs76445427 | snp | C/T | 0.00755907 | 0.0610114 | intron-variant | SPAG16 | GRCh38.p7 | 2:214224384 | TTTATATTATTTCTC[C/T]TAAAGATGAGCCATT | 79582 |
rs76450762 | snp | C/T | 0.143959 | 0.226396 | intron-variant | SPAG16 | GRCh38.p7 | 2:213991591 | CCCGCACTTGTCCCA[C/T]GCTGCATTTCTACCT | 79582 |
rs76450914 | snp | G/T | 0.5 | 0 | intron-variant | SPAG16 | GRCh38.p7 | 2:213463822 | GTGTTGCAGTTTTTT[G/T]GCTTCTGTAGTTCAG | 79582 |
rs76454693 | snp | A/T | 0.0174175 | 0.0916809 | intron-variant | SPAG16 | GRCh38.p7 | 2:214239922 | AATTCTCATTGAAAA[A/T]AAATGACCAAGAAAA | 79582 |
rs76455669 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | SPAG16 | GRCh38.p7 | 2:214225354 | GCTTTTCCTAAATCT[A/T]GATTGTGGAGAATGA | 79582 |
rs76455937 | snp | A/G | 0.0267878 | 0.112589 | intron-variant | SPAG16 | GRCh38.p7 | 2:214266383 | CCTTATCTATTGCCA[A/G]TAGATAGACTTTATT | 79582 |
rs76457769 | snp | C/T | 0.021333 | 0.101051 | intron-variant | SPAG16 | GRCh38.p7 | 2:214220254 | CTTATATCTAATCTG[C/T]TTATAACTTTTACCT | 79582 |
rs76457851 | snp | A/G | 0.0444908 | 0.142359 | intron-variant | SPAG16 | GRCh38.p7 | 2:213661525 | CTCGATTATACTCAA[A/G]CTTAAATAGATTGAT | 79582 |
rs76459684 | snp | A/G | 0.0248432 | 0.108648 | intron-variant | SPAG16 | GRCh38.p7 | 2:213389922 | CAGCATGTTAAAAAG[A/G]TATTTTACACCCATG | 79582 |
rs76460598 | snp | C/T | 0.127254 | 0.217792 | intron-variant | SPAG16 | GRCh38.p7 | 2:213622217 | AGAAATTGACTCTTA[C/T]GGTCTTAAAGTTTCA | 79582 |
rs76476440 | snp | A/G | 0.0197687 | 0.0974348 | intron-variant | SPAG16 | GRCh38.p7 | 2:214010134 | TATGATTTGTAAGAT[A/G]ATAGATGCAAATAAA | 79582 |
rs76484971 | snp | C/T | 0.0248432 | 0.108648 | intron-variant | SPAG16 | GRCh38.p7 | 2:214166522 | AGGCTCCTGTTAGGC[C/T]ATTTTCTCTCCTCAA | 79582 |
rs76488884 | snp | C/T | 0.0887219 | 0.191022 | intron-variant | SPAG16 | GRCh38.p7 | 2:213727180 | ATCATACAGGAATAT[C/T]GGTTTTCTAGACAAT | 79582 |
rs76489894 | snp | A/G | 0.0883596 | 0.190715 | intron-variant | SPAG16 | GRCh38.p7 | 2:213920217 | AGACAGCATACCAAT[A/G]AATCTTGGTTCTTTA | 79582 |
rs76493593 | snp | A/G | 0.200492 | 0.245049 | intron-variant | SPAG16 | GRCh38.p7 | 2:214278742 | TTTGGATTATGCCAC[A/G]GTGAATGCAAACAAA | 79582 |
rs76496304 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | SPAG16 | GRCh38.p7 | 2:213481898 | TTAAGGTTGCCATTG[C/T]AGTGATTTTTGTAAA | 79582 |
rs76499926 | snp | A/T | 0.0792508 | 0.182605 | intron-variant | SPAG16 | GRCh38.p7 | 2:214135577 | CTAGTAAGAGGTGTT[A/T]GGGTCATGGGAGCAA | 79582 |
rs76502307 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | SPAG16 | GRCh38.p7 | 2:214301788 | CTCATTTATTTCTCC[C/T]CTGATCATTATTATC | 79582 |
rs76506359 | snp | A/T | 0 | 0 | intron-variant | SPAG16 | GRCh38.p7 | 2:213731155 | ACATTATATCTGAGT[A/T]TTTTTTTTTTTTTTT | 79582 |
rs76516043 | snp | G/T | 0.00159617 | 0.0282053 | intron-variant | SPAG16 | GRCh38.p7 | 2:213526512 | CACCCCTTTGGCTCT[G/T]ATCTGGACCACATGC | 79582 |
rs76521752 | snp | C/G | 0.5 | 0 | intron-variant | SPAG16 | GRCh38.p7 | 2:214187676 | CATGTAAACAATAAT[C/G]TCTGCCATAACAAAC | 79582 |
rs76523775 | snp | C/T | 0.128976 | 0.218754 | intron-variant | SPAG16 | GRCh38.p7 | 2:214348116 | TCCCACCATTGTATA[C/T]GGGTTGTGTGGAGGG | 79582 |
rs76524714 | snp | A/G | 0.0154538 | 0.0865337 | intron-variant | SPAG16 | GRCh38.p7 | 2:214007112 | AAATTCTCTGTGTAT[A/G]TACATTTGTTAGATT | 79582 |
rs76524910 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | SPAG16 | GRCh38.p7 | 2:214024636 | AATAATATCAGTGAG[C/T]ATTTCTTCCTTTTAT | 79582 |
rs76528344 | snp | G/T | 0.0655868 | 0.168795 | intron-variant | SPAG16 | GRCh38.p7 | 2:213673399 | AGTATTAATTTTTAG[G/T]TTCATTTTAACATGC | 79582 |
rs76529697 | snp | C/T | 0.0505692 | 0.150756 | intron-variant | SPAG16 | GRCh38.p7 | 2:213888708 | CTTTTATATTGACAT[C/T]ATATTGCCATTGTAT | 79582 |
rs76531184 | snp | A/C | 0.0352966 | 0.128072 | intron-variant | SPAG16 | GRCh38.p7 | 2:214057214 | CTTTTCAAGATCCAT[A/C]AGAGGAATTATTAGC | 79582 |
rs76533099 | snp | C/T | 0.0193772 | 0.0965046 | intron-variant | SPAG16 | GRCh38.p7 | 2:213931683 | AACACTTTGACTTGA[C/T]AACTTTTCTTTATGA | 79582 |
rs76533164 | snp | A/G | 0.0554779 | 0.157039 | intron-variant | SPAG16 | GRCh38.p7 | 2:213981664 | CTTAAGTAGCTTCTT[A/G]TTAGAGGGTCAGATT | 79582 |
rs76533912 | snp | A/C | 0.0146672 | 0.084371 | intron-variant | SPAG16 | GRCh38.p7 | 2:214029780 | CAAAAATAAATAAAA[A/C]GTATGAAATTTAATA | 79582 |
rs76551714 | snp | A/G | 0.02016 | 0.0983543 | intron-variant | SPAG16 | GRCh38.p7 | 2:214160176 | GTATTTGAAGGTGGA[A/G]AAAAAAGATGGGCAT | 79582 |
rs76566558 | snp | A/G | 0.0217236 | 0.101931 | intron-variant | SPAG16 | GRCh38.p7 | 2:213454843 | CGTTATTGTCTTATT[A/G]GAATGCATGAAATTT | 79582 |
rs76567160 | snp | A/G | 0.0452528 | 0.143452 | intron-variant | SPAG16 | GRCh38.p7 | 2:213445059 | CAGAAGAATGAAACC[A/G]GACCCCTGTCTCTCA | 79582 |
rs76579691 | snp | C/T | 0.0429648 | 0.14013 | intron-variant | SPAG16 | GRCh38.p7 | 2:213490770 | AGTTTATATAAGTAA[C/T]ATTATTTTCTTGCAT | 79582 |
rs76585887 | snp | A/G | 0 | 0 | intron-variant | SPAG16 | GRCh38.p7 | 2:213799963 | ATAGACTGGATTGAA[A/G]AAAAAAAAAAAAAGA | 79582 |
rs76590509 | snp | C/T | | | intron-variant | SPAG16 | GRCh38.p7 | 2:213525620 | ATAAATTACCCAGTC[C/T]CAGGCATGTATTTAT | 79582 |
rs76594330 | in-del | -/TT | | | intron-variant | SPAG16 | GRCh38.p7 | 2:213782191 | TTCAGTTTTTTTTTT[-/TT]AAATAATAAAAAAAG | 79582 |
rs76600168 | snp | A/G/T | 0.0670745 | 0.170406 | intron-variant | SPAG16 | GRCh38.p7 | 2:213695956 | TGTTGATGGAGTTAC[A/G/T]TAAGGGTAGAAGAAG | 79582 |
rs76605858 | snp | A/C | 0.0225045 | 0.103662 | intron-variant | SPAG16 | GRCh38.p7 | 2:213947190 | TTGAACATAAGTCTT[A/C]ATTTCTCTAGGATAT | 79582 |
rs76606712 | in-del | -/AAATATGTTATCTA | | | intron-variant | SPAG16 | GRCh38.p7 | 2:213590931 | TGGATTGGTTAAAGA[-/AAATATGTTATCTA]TACACCATAGAATAT | 79582 |
rs76613090 | snp | C/T | 0.0275645 | 0.114116 | intron-variant | SPAG16 | GRCh38.p7 | 2:213306334 | CATTTGAATTTCATT[C/T]ATTTCTGCTCTGATG | 79582 |
rs76614271 | snp | C/T | 0.0182019 | 0.0936463 | intron-variant | SPAG16 | GRCh38.p7 | 2:214261280 | GATACCATCACATAC[C/T]GTTCACTCACACAGA | 79582 |
rs76616428 | snp | C/T | 0.0119091 | 0.0762411 | intron-variant | SPAG16 | GRCh38.p7 | 2:214312112 | TTACATGGGTTTTAG[C/T]GTGTGAATCATTTCC | 79582 |
rs76617905 | snp | C/T | 0.00199481 | 0.0315187 | intron-variant | SPAG16 | GRCh38.p7 | 2:214246659 | CCATTGCAGCTTCAG[C/T]TAATCTCTAACTGCA | 79582 |
rs76618577 | snp | A/T | | | intron-variant | SPAG16 | GRCh38.p7 | 2:213887523 | GGTGATGAAACATGT[A/T]ATTTAAAAAATATTA | 79582 |
rs76626030 | snp | C/T | 0.0023933 | 0.0345097 | intron-variant | SPAG16 | GRCh38.p7 | 2:214029468 | CATTACCTTTTATCA[C/T]ACTAGTGGGCGGGGA | 79582 |
rs76628489 | snp | A/G | 0.0126979 | 0.078662 | intron-variant | SPAG16 | GRCh38.p7 | 2:214222859 | TAGTAATCTTTGAAG[A/G]TGTGGCCTTGGGTTA | 79582 |
rs76632426 | snp | C/T | 0.0217236 | 0.101931 | intron-variant | SPAG16 | GRCh38.p7 | 2:214209923 | ATCTACAGTGTTTGT[C/T]ATATGACCTTTTACC | 79582 |
rs76636960 | snp | C/T | 0.0225045 | 0.103662 | intron-variant | SPAG16 | GRCh38.p7 | 2:213942079 | TCCTCTTCTTTTCTT[C/T]TTCCCCTGAGTAGAT | 79582 |
rs76641834 | snp | C/T | 0.0298908 | 0.118541 | intron-variant | SPAG16 | GRCh38.p7 | 2:213562954 | CCCTCATCTAAACAC[C/T]GCCTAAAGGCCTCAC | 79582 |
rs76657880 | snp | A/G | 0.0150606 | 0.0854603 | intron-variant | SPAG16 | GRCh38.p7 | 2:214050416 | CATCTGGCCCTTTCT[A/G]TATCAGCATCAATAT | 79582 |
rs76659448 | snp | C/G | 0.162909 | 0.23434 | intron-variant | SPAG16 | GRCh38.p7 | 2:214211934 | TTCCCACTTCTCCTG[C/G]CCTCCAATTTACCAC | 79582 |
rs76660764 | snp | C/T | 0.127254 | 0.217792 | intron-variant | SPAG16 | GRCh38.p7 | 2:213615083 | TTAAGTTGATTTACC[C/T]AAGGTCAAGTTGACA | 79582 |
rs76662687 | snp | A/G | 0.00199481 | 0.0315187 | intron-variant | SPAG16 | GRCh38.p7 | 2:214208411 | ACTCTACTTCTAGTA[A/G]TATGGAGAATACTGA | 79582 |
rs76663547 | snp | A/G | 0.195837 | 0.244062 | intron-variant | SPAG16 | GRCh38.p7 | 2:214235330 | CAATGATTTAAACAT[A/G]TTTTCTCCAATAAAT | 79582 |
rs76663822 | snp | C/T | 0.0170251 | 0.090679 | intron-variant | SPAG16 | GRCh38.p7 | 2:213881348 | AAGTTGTTTTATCTA[C/T]CAGTTCTAGCAGCCT | 79582 |
rs76663922 | snp | A/C | | | intron-variant | SPAG16 | GRCh38.p7 | 2:213322359 | AAAAAAAAAAAAACA[A/C]AAAACTCGTTTGGGT | 79582 |
rs76671747 | snp | C/T | 0.154329 | 0.23097 | upstream-variant-2KB, utr-variant-3-prime, nc-transcript-variant | VWC2L, SPAG16 | GRCh38.p7 | 2:214410496 | AAAAAAATAACTTTA[C/T]GCTCACCCATTTGTG | 79582 |
rs76684756 | snp | A/C | 0 | 0 | intron-variant | SPAG16 | GRCh38.p7 | 2:214024227 | AAGAAAATACCAGAT[A/C]CAAAAATTCATCTTT | 79582 |
rs76686521 | snp | C/T | 0.0205511 | 0.0992634 | intron-variant | SPAG16 | GRCh38.p7 | 2:214373969 | GTAACACAGACATGG[C/T]TTTTATCCCTGAGCT | 79582 |
rs76689042 | snp | A/G | 0.00318978 | 0.0398085 | intron-variant | SPAG16 | GRCh38.p7 | 2:214376897 | GGTTTGAACTGCCTC[A/G]GTGCACTTATGCAAA | 79582 |
rs76689978 | snp | C/T | 0.0825414 | 0.185628 | intron-variant, downstream-variant-500B | SPAG16 | GRCh38.p7 | 2:213703672 | GCCATCTGTGAACTT[C/T]GCAAGTCCATCTCAG | 79582 |
rs76691016 | snp | A/C | 0.00557542 | 0.0525036 | intron-variant | SPAG16 | GRCh38.p7 | 2:214332714 | GGGATATTATGGAGA[A/C]TACCACGCTCCATCT | 79582 |
rs76692681 | snp | A/G | 0 | 0 | intron-variant | SPAG16 | GRCh38.p7 | 2:214059242 | TATATATATATATAT[A/G]TATGTATATATATGT | 79582 |
rs76693129 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | SPAG16 | GRCh38.p7 | 2:213531349 | TTTTCTGTTTATTAA[A/G]AAAGATGTGAGTGTG | 79582 |
rs76694250 | snp | C/T | 0.00636936 | 0.0560724 | intron-variant | SPAG16 | GRCh38.p7 | 2:214215331 | AGGTGAGCCAGCATT[C/T]AGCTCCTCCCAAGAA | 79582 |
rs76696674 | snp | C/T | 0.0174175 | 0.0916809 | intron-variant | SPAG16 | GRCh38.p7 | 2:214184287 | GATATTAAAACTCAC[C/T]AAGGATTATTTTTGT | 79582 |
rs76697453 | snp | A/C | 0.0825414 | 0.185628 | intron-variant | SPAG16 | GRCh38.p7 | 2:214235737 | TTGGCAAAGTAATAC[A/C]AAATTGCAAGGTTTA | 79582 |
rs76702890 | snp | A/G | 0.5 | 0 | intron-variant | SPAG16 | GRCh38.p7 | 2:214078128 | GCAAAGTATTCCCAA[A/G]AAAAAGACCCTTCCA | 79582 |
rs76706178 | snp | A/C | 0.0456336 | 0.143994 | intron-variant | SPAG16 | GRCh38.p7 | 2:213459925 | TATTTATAAGTTTAC[A/C]TTTCTGTAATTGTGT | 79582 |
rs76706414 | snp | A/C | 0.0209421 | 0.100162 | intron-variant | SPAG16 | GRCh38.p7 | 2:213980035 | GCCTATAGCATCATG[A/C]AAGAACCAGACTTAC | 79582 |
rs76711225 | snp | A/T | | | intron-variant | SPAG16 | GRCh38.p7 | 2:213960266 | TTCAACATTGTTTTT[A/T]GTTTATTCTTTTTTT | 79582 |
rs76721767 | snp | C/T | 0.128632 | 0.218563 | intron-variant | SPAG16 | GRCh38.p7 | 2:213562564 | AGATTAGGGTGCTGG[C/T]AGATTTGATGCCTGG | 79582 |
rs76729917 | snp | C/T | 0.158632 | 0.232706 | intron-variant | SPAG16 | GRCh38.p7 | 2:214299297 | GCTGTGTCACCCAGG[C/T]TGGAGTGCAGTGGCG | 79582 |
rs76730767 | snp | G/T | 0.00597247 | 0.0543191 | intron-variant | SPAG16 | GRCh38.p7 | 2:214222660 | TGCTAGCAATGTAAT[G/T]ATCATGAACAGTGTC | 79582 |
rs76732414 | snp | A/T | 0.0448719 | 0.142907 | intron-variant | SPAG16 | GRCh38.p7 | 2:214262446 | TTTGTTATCATTATC[A/T]TAACAATAATGTGAT | 79582 |
rs76732518 | snp | A/G | 0.132066 | 0.220435 | upstream-variant-2KB, intron-variant | SPAG16, LOC100130451 | GRCh38.p7 | 2:213283028 | TACTGCTACCTTTTG[A/G]TAATAAATGGGAGCT | 79582 |
rs76735314 | snp | A/G | 0.00199481 | 0.0315187 | intron-variant | SPAG16 | GRCh38.p7 | 2:214190272 | AAGGGAATATGAGTG[A/G]GACCTTTACAAGCTT | 79582 |
rs76735751 | snp | A/G | 0.121022 | 0.21416 | intron-variant | SPAG16 | GRCh38.p7 | 2:213332133 | AGATAAACAAAATCA[A/G]CAAGTCCTTAGGCAG | 79582 |
rs76741367 | snp | G/T | 0.0360663 | 0.129354 | intron-variant | SPAG16 | GRCh38.p7 | 2:213393633 | GTGGAAGATTTTCTG[G/T]AGGACACAAACCTAG | 79582 |
rs76743192 | snp | C/T | 0.0146672 | 0.084371 | intron-variant | SPAG16 | GRCh38.p7 | 2:214053143 | AAGACAAGGAAGGCA[C/T]GCAATTCGAGCATGG | 79582 |
rs76745377 | snp | G/T | 0.0581099 | 0.160244 | intron-variant | SPAG16 | GRCh38.p7 | 2:214006694 | TCATGCTCCATCACT[G/T]TAGTCCATTTTCACC | 79582 |
rs76749298 | snp | C/T | 0.0123036 | 0.0774623 | intron-variant | SPAG16 | GRCh38.p7 | 2:214231099 | TGGTGTCCTATGTCG[C/T]TGGATCCAGACATCG | 79582 |
rs76750424 | snp | C/T | 0.0130921 | 0.0798413 | intron-variant | SPAG16 | GRCh38.p7 | 2:213987075 | GAAAATAGAAGGACA[C/T]CTAAAGTTCATTTCC | 79582 |
rs76751206 | snp | A/G | 0.00398564 | 0.0444627 | intron-variant | SPAG16 | GRCh38.p7 | 2:214037781 | AATAATTTTTCCCAT[A/G]TTTAATGCTTCTTAG | 79582 |
rs76752233 | snp | C/T | 0.0611083 | 0.163768 | intron-variant | SPAG16 | GRCh38.p7 | 2:213920557 | ATGGGGGCTGCCCCA[C/T]TGGACCTCTCTGCCA | 79582 |
rs76753267 | snp | C/T | 0.0356815 | 0.128715 | intron-variant | SPAG16 | GRCh38.p7 | 2:214083164 | TTATTCTGAATTTGT[C/T]AGATTTCCATAGAGG | 79582 |
rs76763725 | snp | C/G | 0.102726 | 0.202016 | intron-variant | SPAG16 | GRCh38.p7 | 2:213683149 | AGCATATAAGTAAAA[C/G]TCAAAGAATTAAAAC | 79582 |
rs76766968 | snp | C/T | | | intron-variant | SPAG16 | GRCh38.p7 | 2:214258060 | AATTTGTTCATTGCA[C/T]TTATGTTGTAGAATT | 79582 |
rs76767261 | snp | C/G | 0.265727 | 0.249505 | intron-variant | SPAG16 | GRCh38.p7 | 2:213855553 | AACTGAAGTGTATTG[C/G]TTAATATGCTGTTAT | 79582 |
rs76767712 | snp | C/T | 0.0452528 | 0.143452 | intron-variant | SPAG16 | GRCh38.p7 | 2:213476415 | AATAAAGTGAACATT[C/T]CCAACACCCGAGGGT | 79582 |
rs76768517 | snp | C/G | 0.0452528 | 0.143452 | intron-variant | SPAG16 | GRCh38.p7 | 2:213441142 | CTGGATACCTGCATA[C/G]AAGAAATATGGGCCC | 79582 |
rs76774218 | snp | A/C/G | 0.5 | 0 | intron-variant | SPAG16 | GRCh38.p7 | 2:214169139 | AACTTGTTATATCAC[A/C/G]TAACTCATAATTTGA | 79582 |
rs76774853 | snp | C/T | | | intron-variant | SPAG16 | GRCh38.p7 | 2:213971590 | CAACCATTACCAGAA[C/T]CTATTTCAGAATTTT | 79582 |
rs76775232 | snp | A/G | 0.5 | 0 | intron-variant | SPAG16, LOC101928084 | GRCh38.p7 | 2:214085419 | AAGAAAGAAAAAGAA[A/G]AAAAGAGAGTTATCA | 79582 |
rs76775486 | snp | C/T | 0.0360663 | 0.129354 | intron-variant | SPAG16 | GRCh38.p7 | 2:213895771 | ATCTTTTACCACACA[C/T]AAAAATAAAAATGGA | 79582 |
rs76778253 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | SPAG16 | GRCh38.p7 | 2:213901712 | CATAAATTAAAAAAT[A/G]CAATAATCTATAGCA | 79582 |
rs76781516 | snp | A/G | 0.0726307 | 0.176182 | intron-variant | SPAG16 | GRCh38.p7 | 2:213994168 | ACAGTAGTTTTCTTT[A/G]AAAGTATTAATTAGT | 79582 |
rs76783093 | snp | A/G | 0.0197687 | 0.0974348 | intron-variant | SPAG16 | GRCh38.p7 | 2:214046306 | AATCTTACTCAAACT[A/G]TTTCCAAAAATATGT | 79582 |
rs76790587 | in-del | -/TT | | | intron-variant | SPAG16 | GRCh38.p7 | 2:213734724 | TGGACATGTTTTTTT[-/TT]GGTATGAACATGAAT | 79582 |
rs76800628 | snp | C/T | 0.00199481 | 0.0315187 | intron-variant | SPAG16 | GRCh38.p7 | 2:214334793 | ATAACATTTTAACAA[C/T]TGCAAAGCTTCAACA | 79582 |
rs76801157 | snp | A/G | 0.5 | 0 | intron-variant | SPAG16 | GRCh38.p7 | 2:214248031 | TCCGTGTCTCAAAAG[A/G]AAAAAAAATCAACAA | 79582 |
rs76803954 | snp | A/C | 0 | 0 | intron-variant | SPAG16 | GRCh38.p7 | 2:214319514 | CTGGAAAAAAAAAAA[A/C]AAAACTATAATAGGA | 79582 |
rs76812923 | snp | C/T | 0 | 0 | intron-variant | SPAG16 | GRCh38.p7 | 2:213605576 | CTTGAACCCAGGAGG[C/T]GGAGGTTGCAGTGAG | 79582 |
rs76817163 | snp | G/T | 0.0182019 | 0.0936463 | intron-variant | SPAG16 | GRCh38.p7 | 2:213389003 | TGGAAGACTCATACT[G/T]TCTTATTTCTAAACT | 79582 |
rs76819226 | snp | A/G | 0.121369 | 0.214369 | intron-variant | SPAG16 | GRCh38.p7 | 2:213364249 | AGGTGAGTAAGTGGT[A/G]GCTATTTCACAAATT | 79582 |
rs76819677 | snp | A/G | 0.0490535 | 0.14873 | intron-variant | SPAG16 | GRCh38.p7 | 2:213708690 | GTTATGGCACACACC[A/G]CAGGAGAATCACTTG | 79582 |
rs76824469 | snp | C/T | 0.0283406 | 0.115616 | intron-variant | SPAG16 | GRCh38.p7 | 2:214146466 | TGGAATTAATATTCA[C/T]CTGCAAAACTGCTTT | 79582 |
rs76829423 | snp | A/T | 0.128632 | 0.218563 | intron-variant | SPAG16 | GRCh38.p7 | 2:213561457 | AGAAATAGTAAATGC[A/T]TGAGTGGATAGATAT | 79582 |
rs76831435 | snp | A/G | 0.0189856 | 0.0955633 | intron-variant | SPAG16 | GRCh38.p7 | 2:213806952 | GTTTTCAAAGATCAC[A/G]GATACATTAGCTGTT | 79582 |
rs76844958 | snp | A/G | 0.0205511 | 0.0992634 | intron-variant | SPAG16 | GRCh38.p7 | 2:214127265 | TGCCTCATTAAAATT[A/G]TCATCCCTGGTTTAC | 79582 |
rs76847036 | snp | A/T | 0.02016 | 0.0983543 | intron-variant | SPAG16 | GRCh38.p7 | 2:214135304 | TTGCTTTATATACAT[A/T]GTCTTTATTTCTAGT | 79582 |
rs76853595 | snp | A/G | 0.0023933 | 0.0345097 | intron-variant | SPAG16 | GRCh38.p7 | 2:214071372 | AAAAGCCTTCAGGCA[A/G]TCGGACTTCTCCCTG | 79582 |
rs76854438 | snp | A/G | 0.0912534 | 0.193131 | intron-variant | SPAG16 | GRCh38.p7 | 2:213955308 | GAGTTTTATGATTTT[A/G]ACCTTTAAATTTAGG | 79582 |
rs76858749 | snp | A/G | 0.0554779 | 0.157039 | intron-variant | SPAG16 | GRCh38.p7 | 2:213988760 | ATACAGGATCTGTAT[A/G]TTGAAAACTACAAAA | 79582 |
rs76865029 | snp | C/T | 0.120326 | 0.21374 | intron-variant | SPAG16 | GRCh38.p7 | 2:214329859 | AGCAAAGGTGTCAAC[C/T]TTGCCCCTATATCAT | 79582 |
rs76873187 | snp | A/G | 0.0240643 | 0.107019 | intron-variant | SPAG16 | GRCh38.p7 | 2:213585560 | GGGATTATGATGTAA[A/G]TAACCAGCCTGGCAG | 79582 |
rs76877243 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | SPAG16 | GRCh38.p7 | 2:214006882 | GCTATGTGAAGACCT[A/C]GCTTTTCTATTTTGT | 79582 |
rs76886312 | snp | G/T | 0.5 | 0 | intron-variant | SPAG16 | GRCh38.p7 | 2:213928264 | TAATTTTTTTTTTTT[G/T]TGTATTTTTAGTAGA | 79582 |
rs76888789 | snp | C/G | 0.0134861 | 0.0810011 | intron-variant | SPAG16 | GRCh38.p7 | 2:214149557 | CAAACCTCCATTCCT[C/G]AGAATCATCATCCAA | 79582 |
rs76891623 | snp | C/T | 0.089084 | 0.191327 | intron-variant | SPAG16 | GRCh38.p7 | 2:214060524 | AATGTATAATAACAA[C/T]ACAACCATAAATCTC | 79582 |
rs76893230 | snp | A/T | 0 | 0 | intron-variant | SPAG16 | GRCh38.p7 | 2:213520444 | ACAAAAAAAAAAAAA[A/T]TTCGCTGGGCGTGGT | 79582 |
rs76895819 | snp | A/C | 0 | 0 | intron-variant | SPAG16 | GRCh38.p7 | 2:213630385 | CAAGACTCCATCTCA[A/C]AAAAAAAAAAAAAGA | 79582 |
rs76896398 | snp | A/G | 0.0490535 | 0.14873 | intron-variant | SPAG16 | GRCh38.p7 | 2:213907144 | TCTGGAACATACAAG[A/G]GATTCAAAGGACTCA | 79582 |
rs76905035 | snp | G/T | 0.0217236 | 0.101931 | intron-variant | SPAG16 | GRCh38.p7 | 2:213884108 | TCCTAGTGCCTATGG[G/T]CTATGTGCCTAAGTG | 79582 |
rs76907454 | snp | C/G | 0.0107246 | 0.0724382 | intron-variant | SPAG16 | GRCh38.p7 | 2:214181176 | GAGAACATCTGAGAA[C/G]AAAGAGAAGCAATAA | 79582 |
rs76909027 | snp | A/G | 0.0217236 | 0.101931 | intron-variant | SPAG16 | GRCh38.p7 | 2:213817896 | TGGGTGGTGTGATCA[A/G]TTGTACCCTGATCCT | 79582 |
rs76913428 | snp | A/C | 0.136847 | 0.222927 | intron-variant | SPAG16 | GRCh38.p7 | 2:213991084 | TAGGTATACACGTGC[A/C]ATGGTGGTTTGCTCA | 79582 |
rs76914316 | snp | C/T | 0.00676609 | 0.0577691 | intron-variant | SPAG16 | GRCh38.p7 | 2:214106446 | AAGTGTTTCAATTTA[C/T]TTTTGTGAAATTTAA | 79582 |
rs76919062 | snp | A/G | 0.155656 | 0.231515 | intron-variant | SPAG16 | GRCh38.p7 | 2:213430545 | ATTATTCTTCTTCCA[A/G]TGTGGCCCAGGGAAG | 79582 |
rs76920193 | snp | A/G | 0.128632 | 0.218563 | intron-variant | SPAG16 | GRCh38.p7 | 2:213944720 | TGTTTGTGTCCCTCC[A/G]AAGTTCATATATTGA | 79582 |
rs76937336 | snp | C/G | 0.000798403 | 0.0199641 | intron-variant | SPAG16 | GRCh38.p7 | 2:213801678 | CAGATGAAGCACAAT[C/G]GTAGGAACAGAGACT | 79582 |
rs76942806 | snp | A/C/G | 0.625 | 0.125 | intron-variant | SPAG16 | GRCh38.p7 | 2:213822850 | TCTGTTCCTGTGTTA[A/C/G]TTTGCTGAGAATGAT | 79582 |
rs76945789 | snp | C/T | 0.0894459 | 0.191631 | intron-variant | SPAG16 | GRCh38.p7 | 2:213751942 | GACCACAAAACCAAA[C/T]TGGAAACAATTCATA | 79582 |
rs76947783 | snp | A/G | 0.00557542 | 0.0525036 | intron-variant | SPAG16 | GRCh38.p7 | 2:214316722 | TTTCTTCAATTTTTT[A/G]TCTAGGATATTTTGT | 79582 |
rs76949059 | snp | C/T | 0.030278 | 0.119257 | intron-variant | SPAG16 | GRCh38.p7 | 2:214402123 | TGATATATTAACTAG[C/T]GTTGTGAATTATTCC | 79582 |
rs76950540 | snp | C/T | 0.5 | 0 | intron-variant | SPAG16 | GRCh38.p7 | 2:213426348 | GAAAACGATTCTCAT[C/T]TGAGATTATTGAAAT | 79582 |
rs76953016 | snp | C/T | 0.0854556 | 0.188216 | intron-variant | SPAG16 | GRCh38.p7 | 2:213704520 | TCAAGACCTTAGCAA[C/T]GTGCCTGCATGGATT | 79582 |
rs76955274 | snp | C/T | 0.0115144 | 0.0749975 | intron-variant | SPAG16 | GRCh38.p7 | 2:213658082 | GTTACTCATGCAACA[C/T]AATTCTGCTATGAGG | 79582 |
rs76957025 | snp | C/G | 0.0248432 | 0.108648 | intron-variant | SPAG16 | GRCh38.p7 | 2:213393091 | TGAATCAGAATAAAA[C/G]TAATTAAGAGATACT | 79582 |
rs76957414 | snp | A/G | 0.030665 | 0.119967 | upstream-variant-2KB, intron-variant, downstream-variant-500B | VWC2L, SPAG16 | GRCh38.p7 | 2:214410505 | ACTTTATGCTCACCC[A/G]TTTGTGTCAGGGTCT | 79582 |
rs76957445 | snp | A/T | 0.0452528 | 0.143452 | intron-variant | SPAG16 | GRCh38.p7 | 2:213431015 | AATAGTTTTTCTCAG[A/T]CAAGCAAACACTGAG | 79582 |
rs76958000 | snp | C/T | 0.00159617 | 0.0282053 | intron-variant, downstream-variant-500B | SPAG16 | GRCh38.p7 | 2:213401633 | CATTTCTGTAATATG[C/T]TTAGTTGATGTTTCT | 79582 |
rs76960061 | snp | A/G | 0.00557542 | 0.0525036 | intron-variant | SPAG16 | GRCh38.p7 | 2:214197449 | TCTACAATATGAATG[A/G]ACTATGTATAATGGA | 79582 |
rs76961301 | snp | A/G | | | intron-variant | SPAG16 | GRCh38.p7 | 2:213411903 | ATGTTAAAAAAAAAA[A/G]AAAAAAAGGTTTGAA | 79582 |
rs76966546 | snp | C/G | 0.5 | 0 | intron-variant | SPAG16 | GRCh38.p7 | 2:214352560 | TGACTTTTTTTCTCT[C/G]TGTGTGTGTGTGTGT | 79582 |
rs76972259 | snp | C/T | 0.0225045 | 0.103662 | intron-variant | SPAG16 | GRCh38.p7 | 2:213906980 | GTAAGACTTAAAAAG[C/T]GCAGATGACAATAAC | 79582 |
rs76972363 | snp | A/C | 0.0452528 | 0.143452 | intron-variant | SPAG16 | GRCh38.p7 | 2:213617059 | GTAGGTGGGCCCCTG[A/C]AGATGAAACTGGATT | 79582 |
rs76973042 | snp | C/G | 0.121022 | 0.21416 | intron-variant | SPAG16 | GRCh38.p7 | 2:213328621 | TTTAGTCCATATTCA[C/G]TAGGGAGGTCTTGTG | 79582 |
rs76975810 | snp | C/T | 0.121022 | 0.21416 | intron-variant, utr-variant-5-prime | SPAG16 | GRCh38.p7 | 2:213343869 | ACATAAATAGAACCT[C/T]TGGAGCAATATTAAA | 79582 |
rs76988074 | snp | A/C | 0.0314385 | 0.121371 | intron-variant | SPAG16 | GRCh38.p7 | 2:214212638 | CAGAAGGGCAGACTA[A/C]AGCCACCAAGCAAGG | 79582 |
rs76991005 | snp | C/G | 0.0948562 | 0.196037 | intron-variant | SPAG16 | GRCh38.p7 | 2:214030036 | TTTAAGTGCACAATA[C/G]TATGTTGTTAACTTT | 79582 |
rs76992820 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant, downstream-variant-500B | SPAG16, LOC101928084 | GRCh38.p7 | 2:214084648 | TTATATGTACATTTA[C/T]AATTACTGACCTAGG | 79582 |
rs76997440 | snp | C/T | | | intron-variant | SPAG16 | GRCh38.p7 | 2:214320855 | ACCATATCACTTGTA[C/T]TTAGCAGTTGCTCAA | 79582 |
rs77002435 | snp | A/G | 0.00159617 | 0.0282053 | intron-variant | SPAG16, LOC101928084 | GRCh38.p7 | 2:214086131 | GCCATCACACCACTT[A/G]TTCTCATACAGCGTA | 79582 |
rs77004769 | snp | C/T | 0.0168055 | 0.0901129 | intron-variant | SPAG16 | GRCh38.p7 | 2:213521032 | TGATTGGCAGGTTAC[C/T]GTATCTCAATTTATC | 79582 |
rs77005689 | snp | C/T | 0.0185938 | 0.0946107 | intron-variant | SPAG16 | GRCh38.p7 | 2:214299799 | TCAATGATTTATCTA[C/T]GCCTGTAGATACCTG | 79582 |
rs77006316 | snp | A/T | 0.5 | 0 | intron-variant | SPAG16 | GRCh38.p7 | 2:214314958 | CAATATGATACTGTA[A/T]TAAAAAAAAAAAAGA | 79582 |
rs77008547 | snp | A/G | | | intron-variant | SPAG16 | GRCh38.p7 | 2:213605605 | CTACTCGGGAGGCTG[A/G]GGTGAGAGAATCGCT | 79582 |
rs77016774 | snp | C/T | 0.00716266 | 0.059414 | intron-variant | SPAG16 | GRCh38.p7 | 2:213728337 | CCTCCTTCTACCTTT[C/T]TGCAGTCAGGGGAAG | 79582 |
rs77019027 | snp | C/T | 0.0966517 | 0.197444 | intron-variant | SPAG16 | GRCh38.p7 | 2:213944495 | TTAACGGGTTTCACA[C/T]GTTCACAGGGAGAGA | 79582 |
rs77019667 | snp | A/G | 0.272241 | 0.249009 | intron-variant | SPAG16 | GRCh38.p7 | 2:213855848 | TGACATGTGGGGATT[A/G]TTATAATTCAAGGTG | 79582 |
rs77021488 | snp | A/T | 0.0433465 | 0.140692 | intron-variant | SPAG16 | GRCh38.p7 | 2:213886156 | GAAGATTCTGTCAGG[A/T]TTGGAATCTTATGAC | 79582 |
rs77022819 | in-del | -/AAA | | | intron-variant | SPAG16 | GRCh38.p7 | 2:213564510 | AAAAAAAAAAAAAAA[-/AAA]GAGTATGTCATTAAC | 79582 |
rs77023451 | snp | A/C | 0.00755907 | 0.0610114 | intron-variant | SPAG16 | GRCh38.p7 | 2:213534000 | ATTGTTGCATATTTA[A/C]GTTATTTTTATTTTT | 79582 |
rs77026735 | snp | A/C | 0.15665 | 0.231917 | intron-variant | SPAG16 | GRCh38.p7 | 2:213540356 | TGCCCGGCCCAAAAA[A/C]AATCATTGTATTTCT | 79582 |
rs77030502 | snp | A/G | 0.0452528 | 0.143452 | intron-variant | SPAG16 | GRCh38.p7 | 2:213431169 | CCCAAAGGAAGAAGA[A/G]AAAGAAATCAAATGG | 79582 |
rs77036932 | snp | A/T | 0.324855 | 0.23853 | intron-variant | SPAG16 | GRCh38.p7 | 2:213621057 | AGTACTAAAACTAAA[A/T]ACTAGTTTTAGTACT | 79582 |
rs77043981 | snp | A/G | 0.0539704 | 0.155153 | intron-variant | SPAG16 | GRCh38.p7 | 2:213439463 | GGAAGAAGGGGAACT[A/G]TCATTATGTTGTGGC | 79582 |
rs77047045 | snp | G/T | 0.5 | 0 | intron-variant | SPAG16 | GRCh38.p7 | 2:213533262 | TTTTTTGTATATATG[G/T]ATATATGCTTTCAAG | 79582 |
rs77047484 | snp | C/G | 0.0640965 | 0.167152 | intron-variant | SPAG16 | GRCh38.p7 | 2:214195142 | AAAAGGAATAGTCTG[C/G]CAGGAAAACAAATAA | 79582 |
rs77050406 | snp | C/G | 0.0562307 | 0.157967 | intron-variant | SPAG16 | GRCh38.p7 | 2:214007475 | AGTTTGGTATACATT[C/G]TTTTTGTATGCAAAT | 79582 |
rs77058300 | snp | A/G | 0.0509478 | 0.151255 | intron-variant | SPAG16 | GRCh38.p7 | 2:213976415 | ACCAGTCCTTAACTA[A/G]CAGGTCTCCTCTCAC | 79582 |
rs77059767 | snp | C/T | 0.0205511 | 0.0992634 | intron-variant | SPAG16 | GRCh38.p7 | 2:213778615 | AGAGCTTACCAACTC[C/T]CATACTCTTAGTACA | 79582 |
rs77061748 | snp | A/T | 0.100588 | 0.200439 | intron-variant | SPAG16 | GRCh38.p7 | 2:213685433 | GAGGCCTGGAACTGA[A/T]CCTTCCCTAGCACCT | 79582 |
rs77063096 | snp | C/T | 0.0236746 | 0.106192 | intron-variant | SPAG16 | GRCh38.p7 | 2:213962148 | AGCGGTAATTATGGT[C/T]AAATAAGGGTAAAGC | 79582 |
rs77063119 | snp | C/G/T | 0.0475818 | 0.146953 | intron-variant | SPAG16 | GRCh38.p7 | 2:213465318 | TTGAGCACTTGCACC[C/G/T]GAGAAAACAGGTGCA | 79582 |
rs77067509 | snp | A/G | 0.00159617 | 0.0282053 | intron-variant | SPAG16 | GRCh38.p7 | 2:214074276 | ATGGTATTCTGTCAC[A/G]GAAATCTCAACTAAG | 79582 |
rs77068078 | snp | A/T | 0.5 | 0 | intron-variant | SPAG16 | GRCh38.p7 | 2:213323759 | GAATGGGTAAAAAAA[A/T]TATGGTACATTCATG | 79582 |
rs77068856 | snp | A/G | 0.040671 | 0.13668 | intron-variant, utr-variant-3-prime | SPAG16 | GRCh38.p7 | 2:213398581 | CTTCAGATAATTCAG[A/G]TGGCTCATCTCTCAC | 79582 |
rs77072898 | snp | C/T | 0.0581099 | 0.160244 | intron-variant | SPAG16 | GRCh38.p7 | 2:213995984 | GTCCTTGAAAGCTTC[C/T]CTAAAGCCTTCTCTT | 79582 |
rs77082200 | snp | G/T | 0.04875 | 0.148319 | intron-variant | SPAG16 | GRCh38.p7 | 2:214187445 | TATGATTATTAAATC[G/T]AAGTACTCATTCATC | 79582 |
rs77082571 | snp | A/G | 0.00914312 | 0.0669923 | intron-variant | SPAG16 | GRCh38.p7 | 2:214267419 | TCCCTTCAAAAAATG[A/G]TATTAGGAATACTGG | 79582 |
rs77092415 | snp | C/T | 0.5 | 0 | intron-variant | SPAG16 | GRCh38.p7 | 2:213792578 | TGAAAATGAGTATCT[C/T]TTTTTTTTTTTTTTT | 79582 |
rs77095534 | snp | C/T | 0.00517822 | 0.0506191 | intron-variant | SPAG16 | GRCh38.p7 | 2:213760599 | AACAGCGTACACATT[C/T]TTCTCAAGTGTACAT | 79582 |
rs77099940 | snp | A/C | | | intron-variant | SPAG16 | GRCh38.p7 | 2:213584430 | TGGGGTTCAGTGTTG[A/C]TTAGGAAAGTATTGT | 79582 |
rs77104040 | snp | C/T | 0.0107246 | 0.0724382 | intron-variant | SPAG16 | GRCh38.p7 | 2:213581314 | CCTCAAGCTCCTGGG[C/T]TCAAGTGATTCTCCA | 79582 |
rs77111684 | snp | C/T | 0.0150606 | 0.0854603 | intron-variant | SPAG16 | GRCh38.p7 | 2:213592794 | TTGATGCAAATGACC[C/T]TAAATGGTGTGATCA | 79582 |
rs77113550 | snp | A/T | 0.131723 | 0.220251 | intron-variant | SPAG16 | GRCh38.p7 | 2:213642006 | GGGGAAACCATCCAC[A/T]TGATCCAATCACCTC | 79582 |
rs77118709 | snp | G/T | 0.00795532 | 0.062565 | intron-variant | SPAG16 | GRCh38.p7 | 2:213706941 | TCCACAGGGTTGCTT[G/T]AGTGTCCTCACAACA | 79582 |
rs77121096 | snp | A/C | 0.5 | 0 | intron-variant | SPAG16 | GRCh38.p7 | 2:214141466 | AGTGAGACTCGGCCT[A/C]AAAAAAAAAAAAACC | 79582 |
rs77121827 | snp | C/G | 0.0475351 | 0.146656 | intron-variant | SPAG16 | GRCh38.p7 | 2:213427782 | TCATATCTCAAGTCT[C/G]GTTGTCAAAACTGAG | 79582 |
rs77124485 | snp | G/T | 0.0174175 | 0.0916809 | intron-variant | SPAG16 | GRCh38.p7 | 2:214071695 | CCTTCAATTTGGTGT[G/T]GTAGATTGCTGAAAT | 79582 |
rs77127900 | snp | A/C | 0.0165278 | 0.0893908 | intron-variant | SPAG16 | GRCh38.p7 | 2:214005661 | CTGAATTTCATGGCT[A/C]CAAAGAAAGGAACTA | 79582 |
rs77131409 | snp | A/T | | | intron-variant | SPAG16 | GRCh38.p7 | 2:213920157 | TTCTCCATCCTTTTA[A/T]TTTTGAGCCTCTGAG | 79582 |
rs77132199 | snp | G/T | 0.0178098 | 0.0926698 | intron-variant | SPAG16 | GRCh38.p7 | 2:213834913 | TTTCTATTCTTGTGG[G/T]GTTGGGCAGATTAAA | 79582 |
rs77136679 | snp | C/T | 0.113334 | 0.209338 | intron-variant | SPAG16 | GRCh38.p7 | 2:213524075 | GGATGAAAAAATTGT[C/T]TTGTGGGCTGGGACC | 79582 |
rs77140293 | snp | A/G | 0.0166325 | 0.0896639 | intron-variant | SPAG16 | GRCh38.p7 | 2:214403805 | TTCCTGAGTAATCAC[A/G]AAGTTAAGAATGTAA | 79582 |
rs77142117 | in-del | -/AT | 0.290718 | 0.246662 | intron-variant | SPAG16 | GRCh38.p7 | 2:214037227 | TACTTTAATATACAC[-/AT]ATATGTGTATGTTTT | 79582 |
rs77142708 | snp | A/C/G | 0.0178098 | 0.0926698 | intron-variant | SPAG16 | GRCh38.p7 | 2:214053126 | ATTTCACCTGGAGGA[A/C/G]AAAGACAAGGAAGGC | 79582 |
rs77153902 | snp | A/G | 0.00716266 | 0.059414 | intron-variant | SPAG16 | GRCh38.p7 | 2:214228884 | CTCCTCAGCTACATT[A/G]ATGGCAGAACCAATA | 79582 |
rs77153943 | snp | A/G | 0.0821764 | 0.185298 | intron-variant | SPAG16 | GRCh38.p7 | 2:214264868 | GATGTCATATATTTG[A/G]AATTATATAGTTTGT | 79582 |
rs77158080 | snp | C/T | 0.00636936 | 0.0560724 | intron-variant | SPAG16 | GRCh38.p7 | 2:213323163 | CACAAACAATATGTC[C/T]GGCGCGGTGGCTTAC | 79582 |
rs77158336 | snp | G/T | | | intron-variant | SPAG16 | GRCh38.p7 | 2:213333492 | TTCTTCACAGAAATA[G/T]ATAAAAATCTTAAAA | 79582 |
rs77162935 | snp | A/G | 0.0217236 | 0.101931 | intron-variant | SPAG16 | GRCh38.p7 | 2:213405038 | GTTGCTAGCTCCTAT[A/G]CAGTTATTTTACTTT | 79582 |
rs77171371 | snp | A/G | 0.0023933 | 0.0345097 | intron-variant | SPAG16 | GRCh38.p7 | 2:214320103 | CCTACCAAACAGTCC[A/G]GCTTCATCTCTTGCT | 79582 |
rs77172483 | snp | C/G | 0.0240643 | 0.107019 | intron-variant | SPAG16 | GRCh38.p7 | 2:214404656 | AATATTAATAAATGG[C/G]TGGGTTGGATTATAG | 79582 |
rs77190346 | snp | A/C | 0.253453 | 0.251173 | intron-variant | SPAG16, LOC101928084 | GRCh38.p7 | 2:214094872 | GCTACACTTAAACTA[A/C]GTCCCAGGTGCATCA | 79582 |
rs77192248 | snp | G/T | 0.021333 | 0.101051 | intron-variant | SPAG16 | GRCh38.p7 | 2:213458117 | ACATTTTCATTTGTA[G/T]AGATTTTTTATTCTG | 79582 |
rs77196273 | snp | C/T | 0.0836354 | 0.186609 | intron-variant | SPAG16 | GRCh38.p7 | 2:214084006 | CTAAATCCACATCAC[C/T]GAGACTTTCAGTGAA | 79582 |
rs77198722 | snp | C/G | 0.0189856 | 0.0955633 | intron-variant | SPAG16 | GRCh38.p7 | 2:214302437 | TGTATTGCTGCCAGT[C/G]TCTTTTTGTAGGGCT | 79582 |
rs77203764 | snp | C/G | 0.0126979 | 0.078662 | intron-variant | SPAG16 | GRCh38.p7 | 2:213886656 | TGCCAACAAACTTCT[C/G]AGGGGAAACAAGCAA | 79582 |
rs77211787 | snp | C/T | 0.125528 | 0.21681 | intron-variant | SPAG16 | GRCh38.p7 | 2:213600502 | ATGTTCCTAGTATTG[C/T]GGTAGGTGCTGAATC | 79582 |
rs77212327 | snp | C/G | | | intron-variant | SPAG16 | GRCh38.p7 | 2:214164344 | TGGAATATTACTTTA[C/G]AAAGGATGTTCTGAG | 79582 |
rs77212883 | snp | C/G | 0.0197687 | 0.0974348 | intron-variant | SPAG16 | GRCh38.p7 | 2:214139966 | CCTATGACTTATAAG[C/G]CTCTACTTGAAGATG | 79582 |
rs77218439 | in-del | -/T | 0.479904 | 0.0982045 | intron-variant | SPAG16 | GRCh38.p7 | 2:213875961 | GGAAGCTGTGACATC[-/T]CAACCTGATCCAAAA | 79582 |
rs77219704 | snp | A/C | 0.0165278 | 0.0893908 | intron-variant | SPAG16 | GRCh38.p7 | 2:213425880 | ATAGAAAACAGGGCT[A/C]CATGGAGTAATAGCT | 79582 |
rs77220888 | snp | C/G | 0.5 | 0 | upstream-variant-2KB, intron-variant | SPAG16, LOC100130451 | GRCh38.p7 | 2:213283051 | TGGGAGCTTTTATAG[C/G]ATCACTGGCTTCCAG | 79582 |
rs77223428 | snp | G/T | 0.5 | 0 | intron-variant | SPAG16 | GRCh38.p7 | 2:214250737 | AGGAGCTTTGAGATA[G/T]ATATATATATATATA | 79582 |
rs77244774 | snp | C/T | 0.0596104 | 0.162024 | intron-variant | SPAG16 | GRCh38.p7 | 2:213842262 | AGTCTAATAACATAT[C/T]GTAGCAGATATATTG | 79582 |
rs77244961 | snp | C/T | 0.00597247 | 0.0543191 | intron-variant | SPAG16 | GRCh38.p7 | 2:213589379 | TATTTTATTGATAAA[C/T]GGAAAGTGCTAATTT | 79582 |
rs77247838 | snp | G/T | 0.0329836 | 0.124112 | intron-variant | SPAG16 | GRCh38.p7 | 2:214279095 | ACAAACAGAATATAT[G/T]AAACAAGCTTTTTTT | 79582 |
rs77248722 | snp | C/G | 0.0240643 | 0.107019 | intron-variant | SPAG16 | GRCh38.p7 | 2:213406739 | AGAAAATTTTATATG[C/G]GAGTGCAATTTCTTT | 79582 |
rs77249052 | snp | A/G | 0.00557542 | 0.0525036 | intron-variant | SPAG16 | GRCh38.p7 | 2:214359113 | ATAATAACAGCAACA[A/G]TAGTAATAGTAATAA | 79582 |
rs77250846 | snp | A/G | 0.0528381 | 0.153711 | intron-variant | SPAG16 | GRCh38.p7 | 2:214194043 | ATATAATACTCAACT[A/G]TTATAGTCAGAAAAT | 79582 |
rs77255489 | snp | G/T | 0.0170251 | 0.090679 | intron-variant | SPAG16 | GRCh38.p7 | 2:214143516 | ATTATTTACAGGTAT[G/T]TTATAAGTGATAAAG | 79582 |
rs77261743 | snp | A/T | 0.00755907 | 0.0610114 | intron-variant | SPAG16 | GRCh38.p7 | 2:213490954 | TTACCTATAGTGAGT[A/T]TTTTTTTTTCATTTG | 79582 |
rs77262206 | snp | G/T | 0.000798403 | 0.0199641 | intron-variant | SPAG16 | GRCh38.p7 | 2:213291016 | AGATATTCCTGGATA[G/T]CTGTTGAGAAACTCA | 79582 |
rs77265802 | snp | A/G | 0.00716266 | 0.059414 | intron-variant | SPAG16 | GRCh38.p7 | 2:213830410 | TCTACCCTCTTCAAT[A/G]GTCTTTAGTGCCTCT | 79582 |
rs77266474 | snp | C/T | 0.100588 | 0.200439 | intron-variant | SPAG16 | GRCh38.p7 | 2:213624568 | GATAAAAACTAAATG[C/T]CTTCCTTTTGCACAT | 79582 |
rs77270520 | snp | A/G | 0.127254 | 0.217792 | intron-variant | SPAG16 | GRCh38.p7 | 2:213656934 | TACAGTTTAAAATTA[A/G]ACTTAAATAAGACCT | 79582 |
rs77270745 | snp | C/T | 0.107341 | 0.205301 | intron-variant | SPAG16 | GRCh38.p7 | 2:213689636 | TTTTTAGTTTGAAAA[C/T]ACTCATTATTCTCAG | 79582 |
rs77271898 | snp | A/C | 0 | 0 | intron-variant | SPAG16 | GRCh38.p7 | 2:213911837 | GAGAAACAGTTAGCA[A/C]AAAAAAAAAAAAAAA | 79582 |
rs77285413 | snp | A/G | 0.0869089 | 0.189476 | intron-variant | SPAG16 | GRCh38.p7 | 2:213740807 | AGGTGAAGCTGGGCT[A/G]TGGACAAAGAAAGAC | 79582 |
rs77286526 | snp | C/T | 0 | 0 | intron-variant | SPAG16 | GRCh38.p7 | 2:214298141 | ACACACACATACACA[C/T]ACACACACACACACA | 79582 |
rs77289730 | snp | C/T | | | intron-variant | SPAG16 | GRCh38.p7 | 2:214336564 | ACATGTATATAAATA[C/T]AATAGCCAGTATTAC | 79582 |
rs77290047 | snp | G/T | 0.0267878 | 0.112589 | intron-variant | SPAG16 | GRCh38.p7 | 2:214223273 | GCTGATGTTGAAATA[G/T]TCACTGAAGTATCCA | 79582 |
rs77290751 | snp | G/T | 0.021333 | 0.101051 | intron-variant | SPAG16 | GRCh38.p7 | 2:213491969 | TTAGAGTAACATACC[G/T]CAGTGGAAGATTAAG | 79582 |
rs77296797 | snp | C/T | 0.0225045 | 0.103662 | intron-variant | SPAG16 | GRCh38.p7 | 2:213959704 | GATGCCTTTGGAATT[C/T]CAGTCAGCCTCCCAT | 79582 |
rs77306746 | snp | A/T | 0 | 0 | intron-variant | SPAG16 | GRCh38.p7 | 2:213986916 | AAAAAAAAAAAAAAA[A/T]AATCTAAGAAACTAT | 79582 |
rs77312193 | in-del | -/GAAAA | | | intron-variant | SPAG16 | GRCh38.p7 | 2:213718170 | AAAAAAAAAAAAAAA[-/GAAAA]CCACCAAATAGTGGG | 79582 |
rs77315141 | snp | C/T | 0.00478085 | 0.0486577 | intron-variant | SPAG16 | GRCh38.p7 | 2:213844964 | CAGTGAAGAGTGAAT[C/T]TGGAATTCAACATTT | 79582 |
rs77316421 | snp | A/T | 0.0217236 | 0.101931 | intron-variant | SPAG16 | GRCh38.p7 | 2:213453141 | ACATTGCCTCAGTTT[A/T]TGGTTCTTGTATTGT | 79582 |
rs77318595 | snp | A/G | 0.192715 | 0.243348 | intron-variant | SPAG16 | GRCh38.p7 | 2:213957089 | CTACTTAAGAAGAAT[A/G]TGTATGTAGCTGCTG | 79582 |
rs77324416 | snp | C/G | 0.00795532 | 0.062565 | intron-variant | SPAG16 | GRCh38.p7 | 2:214385925 | CACAGATCCAAATCT[C/G]AAGTTCAACAATAAA | 79582 |
rs77327935 | snp | A/G | | | intron-variant | SPAG16 | GRCh38.p7 | 2:214194624 | GCTAGTCAAATAAAT[A/G]TTCTCATTTTACATG | 79582 |
rs77332267 | snp | C/T | 0.0166556 | 0.0897239 | intron-variant | SPAG16 | GRCh38.p7 | 2:213887338 | CCTCCATTGTTTTTT[C/T]GTTTTGTTTTGTTTT | 79582 |
rs77333287 | snp | C/T | 0.0554779 | 0.157039 | intron-variant | SPAG16 | GRCh38.p7 | 2:213986219 | ATTTGAATTGCCCAG[C/T]GTCCAGGAAGGCATT | 79582 |
rs77338387 | snp | A/G | 0.0225045 | 0.103662 | intron-variant | SPAG16 | GRCh38.p7 | 2:213683917 | AGTATATGGATTAAA[A/G]TATAGCTTGTAGAAA | 79582 |
rs77343339 | snp | A/C | 0.127254 | 0.217792 | intron-variant | SPAG16 | GRCh38.p7 | 2:213655130 | AAAGTGTGAACTTTG[A/C]TGATAATGATGTGTT | 79582 |
rs77365151 | snp | A/G | | | intron-variant | SPAG16 | GRCh38.p7 | 2:213942771 | ATTAGAGTTCATGTG[A/G]GAGGGGAATACTCAA | 79582 |
rs77368722 | snp | A/G | 0 | 0 | intron-variant | SPAG16 | GRCh38.p7 | 2:213822863 | TAGTTTGCTGAGAAT[A/G]ATGGTTTGCAGCTTC | 79582 |
rs77370777 | snp | G/T | 0.0150606 | 0.0854603 | intron-variant | SPAG16 | GRCh38.p7 | 2:214313594 | ATCTAGTTTGAAAAG[G/T]TTTTATAATTCCTAC | 79582 |
rs77371845 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | SPAG16 | GRCh38.p7 | 2:214127190 | TTCATATCTTGGAGA[A/G]TATAAAAGGACTGAC | 79582 |
rs77376959 | snp | A/G | 0.00199481 | 0.0315187 | intron-variant | SPAG16 | GRCh38.p7 | 2:213474967 | TATTAACCATCACAC[A/G]TGTCATCATTGGGGT | 79582 |
rs77378022 | snp | C/G | 0.0263992 | 0.111815 | intron-variant | SPAG16 | GRCh38.p7 | 2:214379953 | CTGGTCTCCAGGAAA[C/G]AGCTCCAGACTTAAT | 79582 |
rs77380036 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | SPAG16 | GRCh38.p7 | 2:213427555 | CTCATTCTATATGCA[A/G]TACATCTCAATAAGA | 79582 |
rs77381062 | snp | A/C | 0.0858192 | 0.188533 | intron-variant | SPAG16 | GRCh38.p7 | 2:213601409 | CCTAACATTGTGTAC[A/C]TGCATGTATATGTGT | 79582 |
rs77386301 | snp | G/T | 0.5 | 0 | intron-variant | SPAG16 | GRCh38.p7 | 2:213784810 | TTATTATTTTTTTTT[G/T]GTAGCTAATGTCCCT | 79582 |
rs77386800 | snp | A/G | 0.0726307 | 0.176182 | intron-variant | SPAG16 | GRCh38.p7 | 2:213992243 | TACCAGAACCTTACC[A/G]AGAATTGTTTAGCGT | 79582 |
rs77390497 | snp | C/G | 0.0244538 | 0.107838 | intron-variant | SPAG16 | GRCh38.p7 | 2:213716955 | TCCTGCACATCCTTT[C/G]GTTCATAGTTTGTGC | 79582 |
rs77399220 | snp | A/G | 0.0854556 | 0.188216 | intron-variant | SPAG16 | GRCh38.p7 | 2:213704886 | TAAAGTGGGGTAAGG[A/G]AATGGTAGAATTTGT | 79582 |
rs77410861 | snp | A/T | 0.5 | 0 | intron-variant, upstream-variant-2KB | SPAG16 | GRCh38.p7 | 2:213315708 | ACTTTTTTTTTTTTA[A/T]TAGTGACTTTCACAG | 79582 |
rs77415919 | snp | C/T | 0.5 | 0 | intron-variant | SPAG16 | GRCh38.p7 | 2:213524917 | GGGCATGATTGTGTT[C/T]TGAAATGTGGGACCT | 79582 |
rs77417842 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | SPAG16 | GRCh38.p7 | 2:214148205 | GAATGAGTGAAGACT[A/G]TGAGTTGCTGGGGAG | 79582 |
rs77427328 | snp | C/T | 0.5 | 0 | intron-variant | SPAG16 | GRCh38.p7 | 2:213548295 | TTGGCGCACTACAAC[C/T]TCTGCCTCCCAGGTT | 79582 |
rs77428201 | snp | C/T | 0.0189856 | 0.0955633 | intron-variant | SPAG16 | GRCh38.p7 | 2:213870979 | ACAGAATTGAAGATG[C/T]GAGACCAGAAATGTA | 79582 |
rs77435311 | snp | C/T | 0.5 | 0 | intron-variant | SPAG16 | GRCh38.p7 | 2:213457891 | TTTATTTTTTTTTTC[C/T]TTCCTTGGCCTTTTT | 79582 |
rs77436613 | snp | A/C | 0.5 | 0 | intron-variant | SPAG16 | GRCh38.p7 | 2:214008744 | AGCAAGACTCCATCT[A/C]AAAAAAAAAAAAAAA | 79582 |
rs77438451 | in-del | -/A | 0.00398564 | 0.0444627 | intron-variant | SPAG16 | GRCh38.p7 | 2:213811188 | TTTCTCTCTTTGTTT[-/A]ACAGTAAGAACATTA | 79582 |
rs77442934 | snp | C/G | 0.00597247 | 0.0543191 | intron-variant | SPAG16 | GRCh38.p7 | 2:213935892 | GTGAAAAACTTCTGC[C/G]CTTATGTCATTGGCA | 79582 |
rs77444272 | snp | A/C | 0.0803491 | 0.183626 | intron-variant | SPAG16 | GRCh38.p7 | 2:213776585 | AGAACAACAACAAAA[A/C]ATTCTGAATATCAAT | 79582 |
rs77447515 | snp | A/G | 0.0111196 | 0.0737302 | intron-variant | SPAG16 | GRCh38.p7 | 2:214372021 | TATATCTTATATGTA[A/G]TTCATTGCTAGACCT | 79582 |
rs77457398 | snp | C/T | 0.0217236 | 0.101931 | intron-variant | SPAG16 | GRCh38.p7 | 2:213444630 | ATGGACATGAGATAT[C/T]TTTCCATTTTTTGTT | 79582 |
rs77457515 | snp | C/T | 0.0197687 | 0.0974348 | intron-variant | SPAG16 | GRCh38.p7 | 2:213839969 | AAAAGAACATTTATA[C/T]TGGCATTCTCTGGAA | 79582 |
rs77460391 | snp | G/T | 0.5 | 0 | intron-variant | SPAG16 | GRCh38.p7 | 2:214313587 | AAATATTATCTAGTT[G/T]GAAAAGTTTTTATAA | 79582 |
rs77463491 | snp | A/T | 0.324855 | 0.23853 | intron-variant | SPAG16 | GRCh38.p7 | 2:213621058 | GTACTAAAACTAAAA[A/T]CTAGTTTTAGTACTT | 79582 |
rs77463759 | snp | A/T | 0.0142736 | 0.0832652 | intron-variant | SPAG16 | GRCh38.p7 | 2:213794867 | TCTGTCTTAAATTTC[A/T]TGCTCTGATTTTCCT | 79582 |
rs77464603 | snp | A/G | 0.0209421 | 0.100162 | intron-variant | SPAG16 | GRCh38.p7 | 2:213492653 | GTGTTTATTGACCCA[A/G]TTATATACTTTTTTA | 79582 |
rs77475949 | snp | G/T | 0.00676609 | 0.0577691 | intron-variant | SPAG16 | GRCh38.p7 | 2:213412699 | CATTTTTGGAGAAGC[G/T]CTAAAGGCTTAGTTC | 79582 |
rs77476088 | snp | A/G | 0.0861826 | 0.188849 | intron-variant | SPAG16 | GRCh38.p7 | 2:213833281 | CTCTGCTCATTTTCA[A/G]ATGAGTAGAGATCCA | 79582 |
rs77476407 | snp | A/T | | | intron-variant | SPAG16 | GRCh38.p7 | 2:214320854 | AACCATATCACTTGT[A/T]CTTAGCAGTTGCTCA | 79582 |
rs77477399 | snp | C/T | 0.0111196 | 0.0737302 | intron-variant | SPAG16 | GRCh38.p7 | 2:213781612 | AATTCAAACGGAAAG[C/T]GGTATTTTACATTAA | 79582 |
rs77481695 | snp | A/G | 0.0205511 | 0.0992634 | intron-variant | SPAG16 | GRCh38.p7 | 2:213976178 | TATACATATATATAC[A/G]TGTATGTGCGTATGT | 79582 |
rs77507157 | in-del | -/TTTTTTT | | | intron-variant | SPAG16 | GRCh38.p7 | 2:213963102 | TTTGCTCTTTTTTTT[-/TTTTTTT]AATGTCTAAAGATAG | 79582 |
rs77517480 | snp | G/T | 0.0158469 | 0.0875917 | intron-variant | SPAG16 | GRCh38.p7 | 2:213992056 | AGAAAGAAAAAGCCT[G/T]TTAATATATTTTACA | 79582 |
rs77518019 | snp | G/T | 0.00993419 | 0.0697739 | intron-variant | SPAG16 | GRCh38.p7 | 2:214037836 | GATACCAATATTGCC[G/T]TTGCTCTGTTATTAT | 79582 |
rs77519701 | snp | A/G | 0.0178098 | 0.0926698 | intron-variant | SPAG16 | GRCh38.p7 | 2:214052423 | GTTACAAACGAAAGA[A/G]ACACCTTGCCCCTGG | 79582 |
rs77524642 | snp | A/T | 0.5 | 0 | intron-variant | SPAG16 | GRCh38.p7 | 2:214033883 | AGTTTTAACACTGAT[A/T]CAGCTATCTAATCTA | 79582 |
rs77526382 | snp | C/T | 0.0182019 | 0.0936463 | intron-variant | SPAG16 | GRCh38.p7 | 2:214178901 | GTTTATTATATATAG[C/T]GTGTAAATAAAAGCC | 79582 |
rs77531007 | snp | A/T | 0.130008 | 0.219321 | intron-variant | SPAG16 | GRCh38.p7 | 2:213594674 | TCGCAATTCATCATT[A/T]ACGTTTCTGGCTGCC | 79582 |
rs77531428 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | SPAG16 | GRCh38.p7 | 2:213616846 | CAAACAGGAATTTAC[C/T]AAGAGCACCCAAAAG | 79582 |
rs77537682 | snp | A/T | 0.273587 | 0.248885 | intron-variant | SPAG16 | GRCh38.p7 | 2:214203936 | CTGGTTGTTGGAGCA[A/T]GTTCTCAGCTCTGCC | 79582 |
rs77539325 | snp | A/G | 0.0126979 | 0.078662 | intron-variant | SPAG16 | GRCh38.p7 | 2:213937685 | GTGCATAATTAATAA[A/G]CACTATTCAAGAAAT | 79582 |
rs77539395 | snp | C/T | 0.0726307 | 0.176182 | intron-variant | SPAG16 | GRCh38.p7 | 2:213993311 | TCAAGGTCAATATCC[C/T]AGTCACACAGTGCAA | 79582 |
rs77541643 | snp | C/T | 0.0520825 | 0.152737 | intron-variant | SPAG16 | GRCh38.p7 | 2:213882714 | TAATCTAGCTAGTGG[C/T]CTATTCATCTAATTT | 79582 |
rs77543680 | snp | C/T | 0.0193772 | 0.0965046 | intron-variant | SPAG16 | GRCh38.p7 | 2:213862242 | ACCTAAACCAACTAC[C/T]TTGTCTTGCAAATGA | 79582 |
rs77544078 | snp | A/G | 0.0279526 | 0.114869 | intron-variant | SPAG16 | GRCh38.p7 | 2:213904847 | TCAGAGTGGTAACTC[A/G]GTGGGTGGTAGGCAG | 79582 |
rs77549117 | snp | A/G | 0.0197687 | 0.0974348 | intron-variant | SPAG16 | GRCh38.p7 | 2:213840599 | TCCATAACTGTCTAC[A/G]TCAACAGTTCAAATC | 79582 |
rs77562150 | snp | A/G | 0.155656 | 0.231515 | intron-variant | SPAG16 | GRCh38.p7 | 2:213292711 | AAAACTATCAGAAAG[A/G]TATAAATCTATAACT | 79582 |
rs77564586 | snp | G/T | 0.030278 | 0.119257 | intron-variant | SPAG16 | GRCh38.p7 | 2:214007836 | TGTTTGGATTTTGCT[G/T]AGCTTTTTCAATCTT | 79582 |
rs77567507 | snp | C/T | 0.0221141 | 0.102801 | intron-variant | SPAG16 | GRCh38.p7 | 2:213474925 | TTAATACTTTGCCTC[C/T]TTCAATTCACTGAAG | 79582 |
rs77568084 | snp | A/G | 0.0452528 | 0.143452 | intron-variant | SPAG16 | GRCh38.p7 | 2:213488607 | AGAAGACAATAGAGC[A/G]TGCTTCCAATTTTGT | 79582 |
rs77568514 | snp | A/G | 0.00318978 | 0.0398085 | intron-variant | SPAG16 | GRCh38.p7 | 2:214373603 | AGAGCAAAGACCCCA[A/G]TCTATCAGAACAACG | 79582 |
rs77570679 | snp | C/G | 0.0225045 | 0.103662 | intron-variant | SPAG16 | GRCh38.p7 | 2:213885700 | ACAGTAGATAAGGAA[C/G]GAGTATTCCTTGGTA | 79582 |
rs77577203 | snp | A/G | 0.0119091 | 0.0762411 | intron-variant | SPAG16 | GRCh38.p7 | 2:213559768 | CTTATTCTAGTTAAA[A/G]ATATATAAATACATG | 79582 |
rs77590790 | snp | C/T | 0.00874735 | 0.0655527 | intron-variant | SPAG16 | GRCh38.p7 | 2:213924907 | CTAGTGCTTTTTTCC[C/T]CCTTTCCTATTTTCT | 79582 |
rs77592792 | snp | G/T | 0.00199481 | 0.0315187 | intron-variant | SPAG16 | GRCh38.p7 | 2:213937191 | ATTTTATGTTCTTTA[G/T]GTTTCATTTGCAAAG | 79582 |
rs77600372 | snp | A/T | | | intron-variant | SPAG16 | GRCh38.p7 | 2:213804706 | AACTAACTAACTAAC[A/T]AACTAACTAACTAAC | 79582 |
rs77601511 | snp | A/C | 0.00993419 | 0.0697739 | intron-variant, upstream-variant-2KB | SPAG16 | GRCh38.p7 | 2:213342886 | CCACATATCTTCCTG[A/C]AGGTACTTTTCAGCC | 79582 |
rs77601903 | snp | C/T | 0.0225045 | 0.103662 | intron-variant | SPAG16 | GRCh38.p7 | 2:213974720 | TAACTCTCTGTTACA[C/T]GTCTGCCAGCCTGTC | 79582 |
rs77607333 | snp | A/G | 0.148661 | 0.22854 | intron-variant | SPAG16 | GRCh38.p7 | 2:213705540 | GAATTGTAGGAATAA[A/G]TATAGTGAAAAACTT | 79582 |
rs77611785 | snp | G/T | 0.0182019 | 0.0936463 | intron-variant, upstream-variant-2KB, utr-variant-5-prime | SPAG16, LOC100130451 | GRCh38.p7 | 2:213284860 | GGGAGACCTTCCAAG[G/T]CCTCATACTTAGTAA | 79582 |
rs77614612 | snp | C/T | 0.046775 | 0.145601 | intron-variant | SPAG16 | GRCh38.p7 | 2:213392318 | CAGCTATTATTATTA[C/T]TTTTTGCCTAAAGTG | 79582 |
rs77615018 | snp | C/T | 0.300926 | 0.244758 | intron-variant | SPAG16 | GRCh38.p7 | 2:214111623 | ATGCAGGCTCTTTTT[C/T]GGTTCCTGAACTTTA | 79582 |
rs77618194 | snp | C/T | 0.0456336 | 0.143994 | intron-variant | SPAG16 | GRCh38.p7 | 2:213458870 | AATAATCAGTAATTA[C/T]GTTTTAATATACATA | 79582 |
rs77634190 | snp | A/G | 0.00199481 | 0.0315187 | intron-variant | SPAG16 | GRCh38.p7 | 2:213472530 | CTCCAGGGATATGGT[A/G]TTGTTTTCAATTTAC | 79582 |
rs77635072 | snp | C/T | 0.0154538 | 0.0865337 | intron-variant | SPAG16 | GRCh38.p7 | 2:214306724 | TCTCAGGGATAATGC[C/T]GACTTGATCTTGGTG | 79582 |
rs77637615 | snp | C/T | 0.00755907 | 0.0610114 | intron-variant | SPAG16 | GRCh38.p7 | 2:213419357 | ATTAAATATTTTAGC[C/T]GTTGCCCTTTCCACG | 79582 |
rs77639507 | snp | G/T | 0.00597247 | 0.0543191 | intron-variant | SPAG16 | GRCh38.p7 | 2:213582133 | CTTACCTTTTACTCT[G/T]GGAGAGTAAAAGGAG | 79582 |
rs77640577 | snp | A/G | 0.0463947 | 0.145069 | intron-variant, upstream-variant-2KB | SPAG16 | GRCh38.p7 | 2:213341793 | TGATCCTCTCAGATC[A/G]GCCTCCCAAAGTGTT | 79582 |
rs77640880 | snp | A/C | 0.00159617 | 0.0282053 | intron-variant | SPAG16 | GRCh38.p7 | 2:213555219 | AACAACCTGCCAACC[A/C]AAAATAAGTTTTATC | 79582 |
rs77642622 | snp | C/T | 0.0126979 | 0.078662 | intron-variant | SPAG16 | GRCh38.p7 | 2:213747396 | AGCCTAAGTGTACAG[C/T]GTTTATAAAGTCGAT | 79582 |
rs77643802 | snp | C/T | 0.0130921 | 0.0798413 | intron-variant | SPAG16 | GRCh38.p7 | 2:214008072 | ATGGTTTTTCAATAT[C/T]TTTTCTGTTCTTCAA | 79582 |
rs77643890 | snp | C/T | 0.02016 | 0.0983543 | intron-variant | SPAG16 | GRCh38.p7 | 2:214144210 | TGAAATAAATAGTAA[C/T]ATGTTTGGCAATGAT | 79582 |
rs77648743 | snp | C/T | 0.127599 | 0.217986 | intron-variant | SPAG16 | GRCh38.p7 | 2:213610418 | ACCATCTATTCTCTC[C/T]GAGGGCTGCTTTCTG | 79582 |
rs77652507 | snp | A/T | 0.0314385 | 0.121371 | intron-variant | SPAG16 | GRCh38.p7 | 2:213580804 | ACAATTTTTTATTTA[A/T]CATTTTAATACAAAT | 79582 |
rs77656060 | snp | C/T | 0.0275645 | 0.114116 | intron-variant | SPAG16 | GRCh38.p7 | 2:213363469 | ATTGAACAGATGGTA[C/T]TTTGTGTTGGTATAA | 79582 |
rs77658628 | snp | A/T | 0.5 | 0 | intron-variant | SPAG16 | GRCh38.p7 | 2:214351843 | TTGACACACAAAAAA[A/T]ATATACTGTCTTTTT | 79582 |
rs77663656 | snp | G/T | 0.462472 | 0.13174 | intron-variant | SPAG16 | GRCh38.p7 | 2:214276554 | CTACTTCACTTACGA[G/T]GCTTAGTTTGGCTGG | 79582 |
rs77668165 | snp | A/G | 0.0228947 | 0.104514 | intron-variant | SPAG16 | GRCh38.p7 | 2:213954798 | TTCCCAATTCTCCAC[A/G]TTGTTGCTAACACTT | 79582 |
rs77669679 | snp | G/T | 0.0995161 | 0.199636 | intron-variant | SPAG16 | GRCh38.p7 | 2:214285271 | ATTTGTTTGCCTTCC[G/T]TGGAAAAGTATCTAC | 79582 |
rs77686959 | snp | A/G | 0.00597247 | 0.0543191 | intron-variant | SPAG16 | GRCh38.p7 | 2:214239770 | CCCACCCAGAATCCT[A/G]GAGAGGAAAGTTGCT | 79582 |
rs77693136 | snp | C/G | | | intron-variant | SPAG16 | GRCh38.p7 | 2:214314309 | AGTGTTAAAACTTAT[C/G]GATGACAATTAGCAC | 79582 |
rs77698547 | snp | G/T | 0.02016 | 0.0983543 | intron-variant | SPAG16 | GRCh38.p7 | 2:214156837 | ATTTAAAAAGAAGAA[G/T]AAAGCAGGCCAACTT | 79582 |
rs77703296 | snp | C/T | 0.00993419 | 0.0697739 | intron-variant | SPAG16 | GRCh38.p7 | 2:214043540 | ATTTTTTTCTAAAAC[C/T]GTGGGTATTAAATAC | 79582 |
rs77708750 | snp | A/C | 0.132409 | 0.220618 | intron-variant | SPAG16 | GRCh38.p7 | 2:213425890 | GGGCTCCATGGAGTA[A/C]TAGCTGATACTAAGC | 79582 |
rs77709406 | snp | C/G | 0.0569829 | 0.158885 | intron-variant | SPAG16 | GRCh38.p7 | 2:213997199 | TTCCTCATCTTTCAC[C/G]TTTGCTTATAGTTGT | 79582 |
rs77711354 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | SPAG16 | GRCh38.p7 | 2:213997588 | CACTTTCTTTTTAAC[A/G]GTGAATTATATCCTC | 79582 |
rs77715371 | snp | A/G | 0 | 0 | intron-variant | SPAG16 | GRCh38.p7 | 2:213822855 | AAACCGTCATTCTTA[A/G]CAAACTAACACAGGA | 79582 |
rs77729825 | snp | C/T | 0.119978 | 0.213528 | intron-variant | SPAG16 | GRCh38.p7 | 2:214326983 | AAGTCACTAGTATTC[C/T]GTATACTAGTGTTGG | 79582 |
rs77742377 | snp | G/T | 0.0228947 | 0.104514 | intron-variant | SPAG16 | GRCh38.p7 | 2:213938400 | TGTATGTGTGTGTGT[G/T]TATTCTCACACATTT | 79582 |
rs77747385 | snp | A/T | 0.00159617 | 0.0282053 | intron-variant | SPAG16 | GRCh38.p7 | 2:213480743 | CACTTTCCCTTTGAA[A/T]ATTTTTAGGTTTGCA | 79582 |
rs77749426 | snp | A/G | 0.0205511 | 0.0992634 | intron-variant | SPAG16 | GRCh38.p7 | 2:213808786 | GTTAAAGAAGCAGAG[A/G]TAGAAGAGTAAAGAT | 79582 |
rs77750627 | snp | A/G | 0.0232847 | 0.105357 | intron-variant | SPAG16 | GRCh38.p7 | 2:214229896 | ATTTTCATAACAAGT[A/G]TCAGCAAAATGCAGC | 79582 |
rs77754343 | snp | A/T | 0.00358779 | 0.0422022 | intron-variant | SPAG16 | GRCh38.p7 | 2:213955327 | TTTAAATTTAGGTCT[A/T]TGATCCATTTTGAGT | 79582 |
rs77760076 | snp | A/T | | | intron-variant | SPAG16 | GRCh38.p7 | 2:214314307 | CTAGTGTTAAAACTT[A/T]TGGATGACAATTAGC | 79582 |
rs77762451 | snp | G/T | | | intron-variant | SPAG16 | GRCh38.p7 | 2:213680105 | AACAAGTAGAGGCTG[G/T]GGGAGAGAGGCTTCA | 79582 |
rs77763697 | snp | C/G | 0.0178098 | 0.0926698 | intron-variant | SPAG16 | GRCh38.p7 | 2:214052181 | CAGCCAATTTAAAAA[C/G]CTTCTTACGATAGAA | 79582 |
rs77780727 | snp | A/G | 0.0528381 | 0.153711 | intron-variant | SPAG16 | GRCh38.p7 | 2:214349870 | GTTGAGCATTTGTGT[A/G]TCTATCTTTATGAAG | 79582 |
rs77781737 | snp | A/G | 0.0130921 | 0.0798413 | intron-variant | SPAG16 | GRCh38.p7 | 2:213791742 | AAATATAAGTCAAGC[A/G]TGGTTAAGACAGGCC | 79582 |
rs77783517 | snp | C/T | 0.0271762 | 0.113356 | intron-variant | SPAG16 | GRCh38.p7 | 2:214393452 | ATAAAAGGCAAGATA[C/T]TTATTTAAGTATGTA | 79582 |
rs77791724 | snp | A/T | 0.0441095 | 0.141807 | intron-variant | SPAG16 | GRCh38.p7 | 2:213725980 | ACCATGTCAAGAGAG[A/T]TCTCTTTTTCGGCAT | 79582 |
rs77792685 | snp | A/G | 0.113334 | 0.209338 | intron-variant | SPAG16 | GRCh38.p7 | 2:213690212 | TAGACTTAACTCTTC[A/G]TCTTAGTCTTAGTCC | 79582 |
rs77796698 | snp | A/G | 0 | 0 | intron-variant | SPAG16 | GRCh38.p7 | 2:213605599 | AGGAGGCTGAAACAG[A/G]AGAATCACTTGAACC | 79582 |
rs77798279 | snp | C/T | 0.0158469 | 0.0875917 | intron-variant | SPAG16 | GRCh38.p7 | 2:213933575 | GGGGTCGGAAACAGC[C/T]AAAATGTTACTGAAT | 79582 |
rs77799215 | snp | A/C | 0.00318978 | 0.0398085 | intron-variant | SPAG16 | GRCh38.p7 | 2:213712707 | AAGCTGTCTCAAAAA[A/C]GACCATACTGAGAAC | 79582 |
rs77803019 | snp | C/G | 0.0858192 | 0.188533 | intron-variant | SPAG16 | GRCh38.p7 | 2:213746071 | TTTAAGATGCTTTGA[C/G]TTGTGGACGTCAGAT | 79582 |
rs77803365 | snp | G/T | | | intron-variant | SPAG16 | GRCh38.p7 | 2:213290607 | GCTCAAAGGCAGCTT[G/T]ACATTAAGAAACTGG | 79582 |
rs77803664 | snp | A/G | 0.12932 | 0.218944 | intron-variant | SPAG16 | GRCh38.p7 | 2:214313448 | ATAAGATATATTTGG[A/G]AACATTTATCTAAGC | 79582 |
rs77805828 | snp | C/T | 0.0452528 | 0.143452 | intron-variant | SPAG16 | GRCh38.p7 | 2:213433157 | CAACATCGTACTGAT[C/T]TGGGAAGAGTTTGAA | 79582 |
rs77810836 | snp | A/C | 0.121022 | 0.21416 | intron-variant, downstream-variant-500B | SPAG16 | GRCh38.p7 | 2:213401804 | ATTTATCTTTTTATG[A/C]TTGCATTTATCTTTC | 79582 |
rs77818747 | snp | A/G | 0.00636936 | 0.0560724 | intron-variant | SPAG16 | GRCh38.p7 | 2:214245895 | CAAAGGGCCTAAAAC[A/G]TACGTTTTGAATGAA | 79582 |
rs77819355 | snp | A/T | 0.0146672 | 0.084371 | intron-variant | SPAG16 | GRCh38.p7 | 2:214319693 | TTTTCTTGAAGAAAA[A/T]GATGGCATTCTTCTC | 79582 |
rs77823049 | snp | C/T | 0.0138799 | 0.0821421 | intron-variant | SPAG16 | GRCh38.p7 | 2:213721924 | AAGCGTGTGATTAAC[C/T]GACAATCATATTACA | 79582 |
rs77824646 | snp | A/G | 0.0670745 | 0.170406 | intron-variant | SPAG16 | GRCh38.p7 | 2:214162583 | ATTGAAACTTGTCTC[A/G]TTGATTTGTGATGCC | 79582 |
rs77825319 | snp | A/G | 0.0205511 | 0.0992634 | intron-variant | SPAG16 | GRCh38.p7 | 2:214001401 | TGATTTAACTGCAGA[A/G]CATTAAAAAACAGCA | 79582 |
rs77829080 | snp | A/C | 0.5 | 0 | intron-variant | SPAG16 | GRCh38.p7 | 2:213356366 | AATTTGGCTGTGAAT[A/C]TGTCTGATCTTGGAC | 79582 |
rs77834147 | snp | A/G | | | intron-variant | SPAG16 | GRCh38.p7 | 2:213979000 | GGAGGGAGAGAGAGA[A/G]AGAGAGGAGAAATAA | 79582 |
rs77834982 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | SPAG16 | GRCh38.p7 | 2:213326488 | TATTTTTTTCTGGAC[A/G]TGAATATACCCCTTT | 79582 |
rs77839444 | snp | C/T | 0.0433465 | 0.140692 | intron-variant | SPAG16 | GRCh38.p7 | 2:214229426 | AGAACAGTGCAAACA[C/T]TTTTAATTTTCATTA | 79582 |
rs77842633 | snp | C/T | 0.029116 | 0.117091 | intron-variant | SPAG16 | GRCh38.p7 | 2:213644076 | ATGAGACACCACGCC[C/T]GGCCCAAGCTCACGA | 79582 |
rs77844269 | snp | C/G | 0.0103295 | 0.0711199 | intron-variant | SPAG16 | GRCh38.p7 | 2:214280311 | CCAGACTTATCTATA[C/G]ATTAAATACAATGCC | 79582 |
rs77845142 | snp | A/G | 0.0279526 | 0.114869 | intron-variant | SPAG16 | GRCh38.p7 | 2:214206777 | TCTGCATTCTCATCA[A/G]CATTTGTTATTTTTT | 79582 |
rs77847496 | snp | A/G | 0.0471551 | 0.14613 | intron-variant | SPAG16 | GRCh38.p7 | 2:213976212 | TATATACACATACAT[A/G]TGTACGCATATACAT | 79582 |
rs77848868 | snp | A/T | 0.5 | 0 | intron-variant | SPAG16 | GRCh38.p7 | 2:213510388 | TTTAACTATTTAACA[A/T]TTTTTTTATTATTTT | 79582 |
rs77856258 | in-del | -/AA/AG | | | intron-variant | SPAG16 | GRCh38.p7 | 2:213876319 | CAAAAAAAAAAAAAA[-/AA/AG]GAAGAAGAAAAGAAA | 79582 |
rs77863326 | snp | C/T | 0.105214 | 0.203807 | intron-variant | SPAG16 | GRCh38.p7 | 2:213679068 | CTTAGACTTCCTTAA[C/T]GAAGGACACCTTCTC | 79582 |
rs77864278 | snp | C/T | 0.00398564 | 0.0444627 | intron-variant | SPAG16 | GRCh38.p7 | 2:213414755 | AAAATAAGTAATAAC[C/T]GCTGATAAACTATTT | 79582 |
rs77893936 | snp | A/G | 0.0263992 | 0.111815 | intron-variant | SPAG16 | GRCh38.p7 | 2:214105273 | GGAACTCAGGGAGAA[A/G]TAAGGGTGGATATGT | 79582 |
rs77897955 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | SPAG16 | GRCh38.p7 | 2:214122500 | TAGCAAAGGAAGTTG[A/G]ATTTCTGATTTCTCA | 79582 |
rs77905429 | snp | A/C | | | intron-variant | SPAG16 | GRCh38.p7 | 2:214164347 | AATATTACTTTAGAA[A/C]GGATGTTCTGAGATT | 79582 |
rs77908492 | snp | C/T | 0 | 0 | intron-variant | SPAG16 | GRCh38.p7 | 2:213822857 | GGAAACCGTCATTCT[C/T]AACAAACTAACACAG | 79582 |
rs77909184 | snp | A/T | 0.5 | 0 | intron-variant | SPAG16 | GRCh38.p7 | 2:214314960 | ATATGATACTGTATT[A/T]AAAAAAAAAAAGAAG | 79582 |
rs77911936 | snp | G/T | 0.296109 | 0.245711 | intron-variant | SPAG16 | GRCh38.p7 | 2:213729242 | AATATTCTTTAAGAA[G/T]ACAAGTGAATTATTG | 79582 |
rs77912086 | snp | A/G | 0.131723 | 0.220251 | intron-variant | SPAG16 | GRCh38.p7 | 2:213610829 | TGTGGTGAAGAATTA[A/G]TTTTCTTAATTACTA | 79582 |
rs77912239 | snp | C/T | | | intron-variant | SPAG16 | GRCh38.p7 | 2:213977630 | GCTCTCTGTATCTTT[C/T]TGTTTAAGATTCTGG | 79582 |
rs77915014 | snp | C/T | 0.10237 | 0.201756 | intron-variant | SPAG16 | GRCh38.p7 | 2:213678919 | TTGTGGTTCCTTTAC[C/T]TATAACTTCCTCCTG | 79582 |
rs77915857 | snp | A/G | 0.00755907 | 0.0610114 | intron-variant | SPAG16 | GRCh38.p7 | 2:214249561 | TAGTAACTGTAAAAA[A/G]CAAATTATTTTTATA | 79582 |
rs77916724 | snp | A/C | 0.152334 | 0.230133 | intron-variant | SPAG16 | GRCh38.p7 | 2:213468377 | TATATATCTCTCTCT[A/C]TATATATAGATATAT | 79582 |
rs77916844 | snp | C/G | 0.133178 | 0.221295 | intron-variant | SPAG16 | GRCh38.p7 | 2:213652633 | ATAATTTGCATTTTC[C/G]TAAAGCTAATTATAT | 79582 |
rs77917565 | snp | C/T | 0.132751 | 0.2208 | intron-variant | SPAG16 | GRCh38.p7 | 2:214114521 | GGTGGATGCCCCTCC[C/T]CCTGCCAGGCTGAAG | 79582 |
rs77922950 | snp | C/T | 0.5 | 0 | intron-variant | SPAG16 | GRCh38.p7 | 2:214038537 | TTCTCAATTCATTTC[C/T]TTTTTTTTAGATTTT | 79582 |
rs77933478 | snp | A/T | | | intron-variant | SPAG16 | GRCh38.p7 | 2:213622846 | GTGTCTGTGTATTTT[A/T]AAAGTATAAGTCTAA | 79582 |
rs77934536 | snp | C/T | 0.030665 | 0.119967 | intron-variant | SPAG16 | GRCh38.p7 | 2:213496645 | TTTAATTATTATATA[C/T]GGATATGTATAATAT | 79582 |
rs77942248 | snp | A/G | 0.0711525 | 0.174681 | intron-variant | SPAG16 | GRCh38.p7 | 2:213580502 | GTATTACATAATTCT[A/G]TGGGAAAGTATATCT | 79582 |
rs77942389 | snp | A/G | 0.15665 | 0.231917 | intron-variant | SPAG16 | GRCh38.p7 | 2:213554710 | GAGCTGAAAAAATAC[A/G]ATGCAATGGAAAGTG | 79582 |
rs77947401 | snp | A/G | 0.0150606 | 0.0854603 | intron-variant | SPAG16 | GRCh38.p7 | 2:214315986 | ATGAGATTTGAGAAT[A/G]TGCTGTCATTGATCT | 79582 |
rs77948417 | snp | C/T | 0.12932 | 0.218944 | intron-variant | SPAG16 | GRCh38.p7 | 2:214290305 | GGGTTTTTTCTCTTC[C/T]TCACAGCAATATTGG | 79582 |
rs77948490 | snp | A/C | 0 | 0 | intron-variant | SPAG16 | GRCh38.p7 | 2:213849980 | TTAGTAACATGAAGC[A/C]CAGTATATATAAAAC | 79582 |
rs77948716 | snp | C/T | 0 | 0 | intron-variant | SPAG16 | GRCh38.p7 | 2:214042087 | TTTCTTTTTCTTTTT[C/T]TTTTTCTTTTTTTTT | 79582 |
rs77952304 | snp | G/T | 0.0185938 | 0.0946107 | intron-variant | SPAG16 | GRCh38.p7 | 2:213445954 | GTTCCAGCCCCTTAG[G/T]GTTAGAACACACAGC | 79582 |
rs77954345 | snp | C/T | 0.0119091 | 0.0762411 | intron-variant | SPAG16 | GRCh38.p7 | 2:214016609 | AATAAAGGATCCTCC[C/T]TTGTTCAGATAGGAG | 79582 |
rs77958325 | snp | A/G/T | 3.3617e-05 | 0.0040997 | missense, nc-transcript-variant, utr-variant-5-prime, upstream-variant-2KB | SPAG16 | GRCh38.p7 | 2:213317221 | GATTTTATCCTAGGT[A/G/T]TGAGTTAATACAGAA | 79582 |
rs77960400 | snp | A/G | 0.0205511 | 0.0992634 | intron-variant | SPAG16 | GRCh38.p7 | 2:213821895 | ATCTCATTTTTTTGT[A/G]GCTAAATAGTACTCC | 79582 |
rs77966888 | snp | C/G | 0.0168055 | 0.0901129 | intron-variant | SPAG16 | GRCh38.p7 | 2:214382673 | CTATGCTCACTGAAA[C/G]TTTCCATATTGAATC | 79582 |
rs77969423 | snp | A/G | 0.0505692 | 0.150756 | intron-variant | SPAG16 | GRCh38.p7 | 2:213764488 | GACTTACATTTTGCA[A/G]CGTAGTAGATGATAT | 79582 |
rs77970160 | in-del | -/A | | | intron-variant | SPAG16 | GRCh38.p7 | 2:213804722 | ACTAACTAACTAACT[-/A]AACTAACTAAGATTA | 79582 |
rs77970574 | snp | A/G | 0.0217236 | 0.101931 | intron-variant | SPAG16 | GRCh38.p7 | 2:213563583 | TCCTCTTCTTAAAAG[A/G]CCACCAATCCTATTG | 79582 |
rs77970635 | snp | A/G | 0.0505692 | 0.150756 | intron-variant | SPAG16 | GRCh38.p7 | 2:213476003 | TCTTGCACTATGCTA[A/G]TGGGTTTCTTCAACA | 79582 |
rs77974854 | snp | A/T | 0.5 | 0 | intron-variant | SPAG16 | GRCh38.p7 | 2:213763658 | TAAAGGGTGGATCTC[A/T]TTTTTTTTTTACCAC | 79582 |
rs77982526 | snp | A/G | 0.0539704 | 0.155153 | intron-variant | SPAG16 | GRCh38.p7 | 2:213543521 | ATACTCTAGTACATC[A/G]TAATTTATTTTCTTT | 79582 |
rs77983254 | snp | A/G | 0.189576 | 0.242588 | intron-variant | SPAG16 | GRCh38.p7 | 2:213951511 | ATAGTTATACAATAT[A/G]CAAAAGACAAAAGCA | 79582 |
rs77983884 | snp | C/T | 0.181022 | 0.240296 | intron-variant | SPAG16 | GRCh38.p7 | 2:213545389 | CAGTTGTGTGTTTTG[C/T]AAATATTTTCTCCCA | 79582 |
rs77983919 | snp | C/G | 0.00438332 | 0.0466095 | intron-variant | SPAG16 | GRCh38.p7 | 2:213958444 | TGGAAACTATGCAAA[C/G]TGTGACTAAGCCCCG | 79582 |
rs77985617 | snp | A/G | 0.0228947 | 0.104514 | intron-variant | SPAG16 | GRCh38.p7 | 2:213344248 | CAGTATATAATTGCT[A/G]TGGTGTTACGGAGTG | 79582 |
rs77988078 | snp | A/G | 0.0463947 | 0.145069 | intron-variant, utr-variant-5-prime | SPAG16 | GRCh38.p7 | 2:213343798 | TCCAACTGGTGCACA[A/G]AGAGAAAAAAGCTGA | 79582 |
rs77988764 | snp | A/G | 0.0023933 | 0.0345097 | intron-variant | SPAG16 | GRCh38.p7 | 2:213457782 | CAGCATACTTATTTT[A/G]ATTAGAACATTTAGT | 79582 |
rs77992680 | snp | A/C | 0.0189856 | 0.0955633 | intron-variant | SPAG16 | GRCh38.p7 | 2:213377816 | TTGGCAAAATCAGAA[A/C]GCTTTTATCCTGATG | 79582 |
rs77995688 | snp | A/G | 0.0991586 | 0.199366 | intron-variant | SPAG16 | GRCh38.p7 | 2:214389995 | CCAAGCTCAGGAATG[A/G]TTATTAACCAACGTT | 79582 |
rs77996664 | snp | C/T | 0.0883596 | 0.190715 | intron-variant | SPAG16 | GRCh38.p7 | 2:213351435 | GTACTGACTCAAGTT[C/T]TTGGTTATTTTTGCT | 79582 |
rs77996671 | snp | A/G | 0.179425 | 0.239831 | intron-variant | SPAG16 | GRCh38.p7 | 2:213955256 | CAAACACAAGATAAT[A/G]AGCATTTACTCTTAT | 79582 |
rs77999946 | snp | A/G | 0.0505692 | 0.150756 | intron-variant, utr-variant-3-prime | SPAG16 | GRCh38.p7 | 2:213398963 | TATAGATATGCATTG[A/G]TTACTACAAGTTGAT | 79582 |
rs78028021 | snp | A/G | 0.170733 | 0.237101 | intron-variant | SPAG16 | GRCh38.p7 | 2:214328862 | ATTGACTACTTATTA[A/G]GTTCTAGGCACGGGG | 79582 |
rs78033158 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | SPAG16 | GRCh38.p7 | 2:214081523 | ATAAAGACAGAGGCC[A/G]AGATTGTAATGCTGC | 79582 |
rs78036959 | snp | A/G | 0.046775 | 0.145601 | intron-variant | SPAG16 | GRCh38.p7 | 2:213985937 | ATATTCTATGTCATG[A/G]ATACTGATAAATCCA | 79582 |
rs78040575 | snp | A/C | 0.131381 | 0.220067 | intron-variant | SPAG16 | GRCh38.p7 | 2:213494100 | ATTCTAGTTTTCCTG[A/C]TGACTCCCAGGCTCA | 79582 |
rs78040844 | snp | A/G | | | intron-variant | SPAG16 | GRCh38.p7 | 2:214020827 | ATTTTAATACTATGT[A/G]GAAAATTCTTTTTCT | 79582 |
rs78060628 | snp | A/G | 0.0858192 | 0.188533 | intron-variant | SPAG16 | GRCh38.p7 | 2:213522728 | ACAAATATAATTTCA[A/G]GACTTAGTTTGAGAG | 79582 |
rs78061154 | snp | A/G | 0.144969 | 0.226867 | intron-variant | SPAG16 | GRCh38.p7 | 2:213711161 | AAATTAGCATGGTCC[A/G]GTCATCCAACTTATT | 79582 |
rs78068667 | snp | C/T | 0.483563 | 0.0891524 | intron-variant | SPAG16 | GRCh38.p7 | 2:214273707 | actgtacccttgtaa[C/T]atagtttgaagtcag | 79582 |
rs78069612 | snp | A/T | | | intron-variant | SPAG16 | GRCh38.p7 | 2:213551184 | GGTCGTTTGAGAGAC[A/T]CCTCTGAAGCTCCTT | 79582 |
rs78081328 | snp | A/G | 0.029116 | 0.117091 | intron-variant | SPAG16 | GRCh38.p7 | 2:213617682 | GCAAGGCATAGTGGC[A/G]TGTGCCTGTAGTCCT | 79582 |
rs78094480 | snp | A/C | 0.0178098 | 0.0926698 | intron-variant | SPAG16 | GRCh38.p7 | 2:214054414 | TTCAAGCTTTTATTT[A/C]TCCAATTGTTCTTAT | 79582 |
rs78098912 | snp | A/G | 0.0244538 | 0.107838 | intron-variant | SPAG16 | GRCh38.p7 | 2:214128391 | AGAAAGCAACAAGAG[A/G]GATTTTAAAACTCTA | 79582 |
rs78101381 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | SPAG16 | GRCh38.p7 | 2:213448382 | CATTTATCCATTGTG[C/T]CTGGAGCTGATGCAT | 79582 |
rs78108730 | snp | C/T | 0.00557542 | 0.0525036 | intron-variant | SPAG16, LOC101928084 | GRCh38.p7 | 2:214089080 | TCTGTATCTATTCCA[C/T]TCCCACCTTCTCAAA | 79582 |
rs78119635 | snp | A/G | 0.166506 | 0.235645 | intron-variant | SPAG16 | GRCh38.p7 | 2:213488211 | TTATTCAAAGGAAAT[A/G]ACTATTGAAAGAATG | 79582 |
rs78119775 | snp | G/T | 0.0391387 | 0.134304 | intron-variant | SPAG16 | GRCh38.p7 | 2:213311123 | TAAATTCTATGAGGA[G/T]AATTATTTTTCATTA | 79582 |
rs78121358 | snp | A/G | 0.0236746 | 0.106192 | intron-variant | SPAG16 | GRCh38.p7 | 2:214030275 | GCACAATGTCTTCCA[A/G]GTTCACCCATGTTGT | 79582 |
rs78122551 | snp | C/G | 0.00398564 | 0.0444627 | intron-variant | SPAG16 | GRCh38.p7 | 2:214005280 | GCTGAGTGAGGACTT[C/G]AAGGCACTCTGAGTT | 79582 |
rs78125250 | in-del | -/T | 0.479904 | 0.0982045 | intron-variant | SPAG16 | GRCh38.p7 | 2:213872977 | TTGCTGGATTTGGTG[-/T]TATTAGTATTTTCTT | 79582 |
rs78125546 | snp | A/G | 0.174932 | 0.238463 | intron-variant | SPAG16 | GRCh38.p7 | 2:214326384 | CCCTGCTGACACCTT[A/G]ATTTTGGACTTCTAA | 79582 |
rs78129182 | snp | A/T | 0.0562307 | 0.157967 | intron-variant | SPAG16 | GRCh38.p7 | 2:214008190 | ATTTTAATTTCACAT[A/T]TACTTATCCATTCTT | 79582 |
rs78129327 | snp | A/C | 0.499683 | 0.0125759 | intron-variant | SPAG16 | GRCh38.p7 | 2:214351836 | ATTCTATTTGACACA[A/C]AAAAAAAATATACTG | 79582 |
rs78133679 | snp | A/G | 0.00636936 | 0.0560724 | intron-variant | SPAG16 | GRCh38.p7 | 2:214409276 | ATGCCTTCTAAGTAT[A/G]ATTAAATAATCCCAT | 79582 |
rs78139656 | snp | C/G | 0.125182 | 0.216612 | intron-variant | SPAG16 | GRCh38.p7 | 2:213655544 | GGGTGGTATGGTATG[C/G]TATGCTGTTGGAAGT | 79582 |
rs78140361 | snp | C/G | 0.105569 | 0.204058 | intron-variant | SPAG16 | GRCh38.p7 | 2:214297601 | ATTGTTTCTTTCTTT[C/G]CCCATTGTTTATTTT | 79582 |
rs78142462 | snp | C/T | | | intron-variant | SPAG16 | GRCh38.p7 | 2:213704673 | TCCTTTTAAGCTACC[C/T]GTTCTCCAGCGTTGT | 79582 |
rs78150037 | snp | C/T | 0.0170251 | 0.090679 | intron-variant | SPAG16 | GRCh38.p7 | 2:213415736 | TTAATTGGTTTATGA[C/T]GTGAGGGAATTTGGA | 79582 |
rs78153551 | snp | C/T | 0.0341408 | 0.126114 | intron-variant | SPAG16 | GRCh38.p7 | 2:213978382 | CCAATAAAATTTTCC[C/T]TTCTTTCCCTTAACT | 79582 |
rs78159700 | snp | C/T | 0.0217236 | 0.101931 | intron-variant | SPAG16 | GRCh38.p7 | 2:213887193 | GCATCATACTTTTAA[C/T]TAAACTATAGACTTC | 79582 |
rs78160100 | snp | A/G | 0.0501905 | 0.150254 | intron-variant | SPAG16 | GRCh38.p7 | 2:213659601 | AGATCAAAGTGGGCT[A/G]AGCAACATTTCTAGG | 79582 |
rs78169858 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | SPAG16 | GRCh38.p7 | 2:213918929 | GTGCATAGAAGTATT[C/T]GTAATAGTCTCTGAT | 79582 |
rs78170065 | in-del | -/CAA | | | intron-variant | SPAG16 | GRCh38.p7 | 2:214016288 | GCGAAGAAGGAACAA[-/CAA]AGTCACATCTTACAT | 79582 |
rs78180986 | snp | A/G | 0.0217236 | 0.101931 | intron-variant | SPAG16 | GRCh38.p7 | 2:213918095 | TGTGTATGTTCAACC[A/G]AGCTTACATCCCAGG | 79582 |
rs78182065 | snp | A/C | 0.5 | 0 | intron-variant | SPAG16 | GRCh38.p7 | 2:214042439 | ACAAAAACAAAACAA[A/C]AACAACAACAACAAC | 79582 |
rs78183217 | snp | G/T | 0.0726307 | 0.176182 | intron-variant | SPAG16 | GRCh38.p7 | 2:213993102 | TTTCACTGTCTCATT[G/T]AAACAGAAGAGTATG | 79582 |
rs78184247 | snp | A/G | 0.0162398 | 0.0886349 | intron-variant | SPAG16 | GRCh38.p7 | 2:214006424 | CAAATCTGCTTTACA[A/G]CAAGTTGAAAGTTTA | 79582 |
rs78187557 | snp | A/G | 0.0861826 | 0.188849 | intron-variant | SPAG16 | GRCh38.p7 | 2:214116207 | CTGCCTCAGTGAAGA[A/G]ACTTGTCTGCTCAAT | 79582 |
rs78191477 | snp | A/T | 0.0240643 | 0.107019 | intron-variant | SPAG16 | GRCh38.p7 | 2:213444365 | AGTTTCCCAGTTTTT[A/T]GGGGTTTATCAACTA | 79582 |
rs78193750 | snp | A/T | 0.5 | 0 | intron-variant | SPAG16 | GRCh38.p7 | 2:214187679 | GTAAACAATAATGTC[A/T]GCCATAACAAACCTC | 79582 |
rs78194306 | snp | A/C | 0.132751 | 0.2208 | intron-variant | SPAG16 | GRCh38.p7 | 2:213437367 | ATATCCCATTTTTGA[A/C]AATAACTTTTAACGG | 79582 |
rs78194690 | snp | C/T | 0.0520825 | 0.152737 | intron-variant | SPAG16 | GRCh38.p7 | 2:214389325 | AAAATTTGTGCAATC[C/T]AACGTGTGTGACAGA | 79582 |
rs78205250 | snp | C/T | 0.0287284 | 0.116357 | intron-variant | SPAG16 | GRCh38.p7 | 2:213579175 | CACTTTGAGTTTGTT[C/T]ATTGTATAAATTCAT | 79582 |
rs78205910 | snp | G/T | 0 | 0 | intron-variant | SPAG16 | GRCh38.p7 | 2:214126079 | TTTTTTTTTTTTTTT[G/T]TTTGGCGTTTCTGTA | 79582 |
rs78210619 | snp | A/T | 0.0228947 | 0.104514 | intron-variant | SPAG16 | GRCh38.p7 | 2:213957778 | TTCTTTGTGGTTACC[A/T]TAGAGATTACATTTA | 79582 |
rs78219247 | snp | A/C/G | 0.0182344 | 0.0939844 | intron-variant | SPAG16 | GRCh38.p7 | 2:213584740 | GGAACTTAACCATTT[A/C/G]TAAAACTCATTCATC | 79582 |
rs78222505 | snp | C/T | 0.127254 | 0.217792 | intron-variant | SPAG16 | GRCh38.p7 | 2:213657222 | AAGTGATAAGTGCAT[C/T]AATGAATATATAACT | 79582 |
rs78224259 | snp | A/G | 0.0360663 | 0.129354 | intron-variant | SPAG16 | GRCh38.p7 | 2:214188974 | AACATTTTATACATA[A/G]CAACATCTCTTGTCC | 79582 |
rs78225597 | snp | C/G | 0.189576 | 0.242588 | intron-variant | SPAG16 | GRCh38.p7 | 2:213950621 | TTTGTTTGCTTGCTT[C/G]CTTCCTTCCTTGCTT | 79582 |
rs78227016 | snp | A/G | 0.0217236 | 0.101931 | intron-variant | SPAG16 | GRCh38.p7 | 2:213891600 | CATAGGAGGCTTCCA[A/G]TTCCAAAATTGTGAT | 79582 |
rs78229857 | snp | C/T | 0.0456336 | 0.143994 | intron-variant | SPAG16 | GRCh38.p7 | 2:213465261 | ATGTTAACTGCTTTC[C/T]CTTTGCTTAAATGCC | 79582 |
rs78237134 | snp | A/T | 0.5 | 0 | intron-variant | SPAG16 | GRCh38.p7 | 2:213406937 | CAGCGACGCGGATTT[A/T]AAAAAAAAAAAAAAA | 79582 |
rs78239423 | snp | A/C | 0.5 | 0 | intron-variant | SPAG16 | GRCh38.p7 | 2:213323441 | GCAAGACTCCGTCTC[A/C]AAAAAAATAAAAATA | 79582 |
rs78239739 | snp | C/T | 0.0696718 | 0.173152 | intron-variant | SPAG16 | GRCh38.p7 | 2:213887901 | TTGCAAAGGTAATTG[C/T]GACAGTTACTTTTGC | 79582 |
rs78250558 | snp | C/T | 0.0614824 | 0.164198 | intron-variant | SPAG16 | GRCh38.p7 | 2:213725914 | TTCTGGGTCAGGACA[C/T]TGAAAGAAGGCAGGG | 79582 |
rs78253321 | snp | A/C | 0.5 | 0 | intron-variant | SPAG16 | GRCh38.p7 | 2:214141467 | GTGAGACTCGGCCTC[A/C]AAAAAAAAAAAACCA | 79582 |
rs78257532 | snp | C/G | 0.0422008 | 0.138995 | intron-variant | SPAG16 | GRCh38.p7 | 2:213989752 | TGTTCAAATCGATGT[C/G]AGACATTTTCATTTT | 79582 |
rs78257964 | snp | A/T | 0.131723 | 0.220251 | intron-variant | SPAG16 | GRCh38.p7 | 2:213634257 | TTTAACCTGATAAAA[A/T]CACTGTTTGCATAAA | 79582 |
rs78259522 | snp | A/C | 0 | 0 | intron-variant | SPAG16 | GRCh38.p7 | 2:213311109 | ACATGTAATGTTAAT[A/C]AATTCTATGAGGAGA | 79582 |
rs78263384 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | SPAG16 | GRCh38.p7 | 2:213383961 | AGAAGACACATTTGC[C/T]GGATCAATGACTACA | 79582 |
rs78263732 | snp | G/T | 0.0547245 | 0.156101 | intron-variant | SPAG16 | GRCh38.p7 | 2:214013007 | CGTTTCCAAGTGACA[G/T]TGATACTGCTAGTCT | 79582 |
rs78264437 | snp | A/C | 0.375 | 0.216506 | intron-variant | SPAG16 | GRCh38.p7 | 2:213822874 | GGGACATGGATGAAG[A/C]TGGAAACTATCATTC | 79582 |
rs78266666 | snp | C/T | 0.0535932 | 0.154675 | intron-variant | SPAG16 | GRCh38.p7 | 2:214270676 | GTTTTCACTTGCTTT[C/T]CCATATGCCTGAAAT | 79582 |
rs78266769 | snp | A/G | 0.00953873 | 0.0683987 | intron-variant | SPAG16 | GRCh38.p7 | 2:214014813 | CAGGGTGACATAATC[A/G]GATTTACCTTGTCAA | 79582 |
rs78268757 | snp | C/T | 0.5 | 0 | intron-variant | SPAG16 | GRCh38.p7 | 2:213968095 | CTTTCTTCTTTCCTT[C/T]TTTTTTCTTTTCTTT | 79582 |
rs78273273 | snp | C/T | 0.00676609 | 0.0577691 | intron-variant | SPAG16 | GRCh38.p7 | 2:213565649 | AACACACCAGGATTG[C/T]CAGGAAGCGAAACTT | 79582 |
rs78273709 | snp | C/T | 0 | 0 | intron-variant | SPAG16 | GRCh38.p7 | 2:213436925 | ACTCTTTTTTTTTTT[C/T]CTTTGAGATGGAGTC | 79582 |
rs78276942 | in-del | -/TTT | | | intron-variant | SPAG16 | GRCh38.p7 | 2:213929034 | TTTTTTTTTTTTAAG[-/TTT]ACTGAGTCTTACTCT | 79582 |
rs78280452 | snp | A/T | 0.078151 | 0.181571 | intron-variant | SPAG16 | GRCh38.p7 | 2:213900029 | GTCAGAGACTACAGA[A/T]GATGACAAATATATT | 79582 |
rs78285182 | snp | G/T | 0.0178098 | 0.0926698 | intron-variant | SPAG16 | GRCh38.p7 | 2:213395752 | ATCATTTCCAGGGTT[G/T]ATAGTTTAGTTACCA | 79582 |
rs78289663 | snp | A/T | 0.0142736 | 0.0832652 | intron-variant | SPAG16 | GRCh38.p7 | 2:214045548 | CTTTCACCTTAGATA[A/T]CACCTCATCCCTGGG | 79582 |
rs78292578 | snp | A/C | 0.0463947 | 0.145069 | intron-variant | SPAG16 | GRCh38.p7 | 2:213336652 | TTCCTTAAGTAGAAC[A/C]CTGATCCATTTTTTC | 79582 |
rs78293793 | snp | C/G | 0.0603597 | 0.1629 | intron-variant, downstream-variant-500B | SPAG16, MIR4438 | GRCh38.p7 | 2:213758494 | GAAAAAAATTCAATG[C/G]ATAGGAAACCTCACA | 79582 |
rs78298037 | snp | C/T | 0.00398564 | 0.0444627 | intron-variant | SPAG16 | GRCh38.p7 | 2:213421902 | GTGGAGGGCTGGAAA[C/T]GCATTGGGCTGACGT | 79582 |
rs78300042 | snp | G/T | 0.0452528 | 0.143452 | intron-variant | SPAG16 | GRCh38.p7 | 2:213443912 | CAATTCAGGCTCCTG[G/T]AGGTCGATTGTTTAT | 79582 |
rs78316489 | snp | A/T | 0.00636936 | 0.0560724 | intron-variant | SPAG16 | GRCh38.p7 | 2:213602229 | GTACACTCTATGATG[A/T]CTGCACAATGACAAA | 79582 |
rs78317959 | snp | A/G | 0.0581099 | 0.160244 | intron-variant | SPAG16 | GRCh38.p7 | 2:214005636 | TCTCACGTCTCCACT[A/G]AATAACCAACTGAAT | 79582 |
rs78325357 | snp | C/T | 0.0154538 | 0.0865337 | intron-variant | SPAG16 | GRCh38.p7 | 2:214079154 | AAAGACATGACATAC[C/T]TCAAAATTAGCTCTC | 79582 |
rs78338309 | snp | A/C | 0.0185938 | 0.0946107 | intron-variant | SPAG16 | GRCh38.p7 | 2:214024331 | TTACTGAAATGGCTT[A/C]TTTGTAATAATTTTA | 79582 |
rs78349079 | snp | A/G | 0.0182019 | 0.0936463 | intron-variant | SPAG16 | GRCh38.p7 | 2:213327312 | AGATGGGCAGCAGGA[A/G]GGTCATAATAGGAGA | 79582 |
rs78351450 | in-del | -/GATAGATAGATAGATAGATA/GATAGATAGATC/GATT | | | intron-variant | SPAG16 | GRCh38.p7 | 2:214195335 | ATAGATAGATAGATA[lengthTooLong]TTTGAGAGATATATA | 79582 |
rs78367939 | snp | C/T | 0.00676609 | 0.0577691 | intron-variant | SPAG16 | GRCh38.p7 | 2:213497699 | CAATTATGTGTAGTG[C/T]CAACAATACATAAAA | 79582 |
rs78369763 | snp | C/T | 0.0174175 | 0.0916809 | intron-variant | SPAG16 | GRCh38.p7 | 2:213544951 | GTTGCTTCCAAGTGT[C/T]GAAAATTGTGAAGAA | 79582 |
rs78370262 | snp | A/G | 0.0310518 | 0.120672 | intron-variant | SPAG16 | GRCh38.p7 | 2:213579384 | GCTTGGTAGCAAGAA[A/G]CTTTCTCTCCTGTTT | 79582 |
rs78370968 | snp | A/G | 0.030278 | 0.119257 | intron-variant | SPAG16 | GRCh38.p7 | 2:214402730 | GGCACTGGGTACATT[A/G]GATGGTCTCCAGAAG | 79582 |
rs78373865 | snp | C/T | 0.0178098 | 0.0926698 | intron-variant | SPAG16 | GRCh38.p7 | 2:213543493 | AGATCTTTCCCCATT[C/T]CTAGGTAAAGAGATA | 79582 |
rs78380391 | snp | C/T | 0.0614824 | 0.164198 | intron-variant | SPAG16 | GRCh38.p7 | 2:213827600 | GTGTTTTCCTGATTC[C/T]TTACTATTACCAGTG | 79582 |
rs78383625 | in-del | -/TT | | | intron-variant, upstream-variant-2KB | SPAG16 | GRCh38.p7 | 2:213315705 | AAAACTTTTTTTTTT[-/TT]AATAGTGACTTTCAC | 79582 |
rs78385207 | snp | A/G | 0.0471551 | 0.14613 | intron-variant | SPAG16 | GRCh38.p7 | 2:214004890 | ATATTTGTGATTACA[A/G]ATATATTTTATTAAA | 79582 |
rs78390075 | snp | C/T | 0.0744748 | 0.178019 | intron-variant | SPAG16 | GRCh38.p7 | 2:213879823 | ATGATTTCATTCCTT[C/T]ATATGGCTGTGTAGT | 79582 |
rs78394301 | snp | G/T | 0.0205511 | 0.0992634 | intron-variant | SPAG16 | GRCh38.p7 | 2:213791000 | CACATAAGTATCCAC[G/T]GAGAAATCCCTGGTG | 79582 |
rs78396570 | snp | A/G | 0.0185938 | 0.0946107 | intron-variant | SPAG16 | GRCh38.p7 | 2:213328188 | TAAAACAAATATAGT[A/G]TTATTTTTTAGATAA | 79582 |
rs78402236 | snp | A/T | 0.021333 | 0.101051 | intron-variant | SPAG16 | GRCh38.p7 | 2:214004638 | TGTCCGCGGCTTATC[A/T]TCAGGTGTGGGCTGG | 79582 |
rs78405112 | snp | A/G | 0.5 | 0 | intron-variant | SPAG16 | GRCh38.p7 | 2:213815909 | ACCTTATTTTCATCA[A/G]AAATATACTTAGTTG | 79582 |
rs78414564 | snp | A/G | 0.021333 | 0.101051 | intron-variant | SPAG16 | GRCh38.p7 | 2:213909945 | AACTGTACATTAAAG[A/G]TATCTCAAATATGCC | 79582 |
rs78420814 | in-del | -/AC | | | intron-variant | SPAG16 | GRCh38.p7 | 2:214042008 | TATATATATATATAT[-/AC]ACACACACACAAATA | 79582 |
rs78421979 | snp | C/G | | | intron-variant | SPAG16 | GRCh38.p7 | 2:213955551 | GATCTACATGTCTAT[C/G]CTTATAATAGTACCA | 79582 |
rs78428335 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | SPAG16 | GRCh38.p7 | 2:213666810 | GAAGGAAGGCCAGTA[C/T]AAAGGAAAGTGCAGG | 79582 |
rs78432580 | snp | C/T | 0.0185938 | 0.0946107 | intron-variant | SPAG16 | GRCh38.p7 | 2:213810707 | GCTCTGGGGAAAGAC[C/T]GGTCTTTAGTTTCGT | 79582 |
rs78436861 | snp | A/G | 0.0256215 | 0.110247 | intron-variant | SPAG16 | GRCh38.p7 | 2:214375164 | TAGCTCACTTCCTTT[A/G]GCTCACACTAACTGA | 79582 |
rs78438652 | snp | C/T | 0.0267878 | 0.112589 | intron-variant | SPAG16 | GRCh38.p7 | 2:213303576 | TCTAGACTCTGCCTT[C/T]GTGAGTTCAATTGTT | 79582 |
rs78441573 | snp | A/G | 0.0178098 | 0.0926698 | intron-variant | SPAG16 | GRCh38.p7 | 2:214257255 | CCTGTGACTTTGGTC[A/G]TTTCACTTATTAATC | 79582 |
rs78443112 | snp | A/G | 0.192715 | 0.243348 | intron-variant | SPAG16 | GRCh38.p7 | 2:213948065 | TCTCAGTAGTATCTA[A/G]TTTATTCCTGTTATT | 79582 |
rs78446211 | snp | A/G | 0.0248432 | 0.108648 | intron-variant | SPAG16 | GRCh38.p7 | 2:214267853 | AGATTGAAAGCTTCT[A/G]CACAGTAGGGTAAAC | 79582 |
rs78450221 | snp | G/T | 0.5 | 0 | intron-variant | SPAG16 | GRCh38.p7 | 2:213821893 | GGATCTCATTTTTTT[G/T]TAGCTAAATAGTACT | 79582 |
rs78450272 | snp | A/G | 0.0182019 | 0.0936463 | intron-variant, utr-variant-5-prime | SPAG16 | GRCh38.p7 | 2:213302459 | TTTTGTTTTTGCTAA[A/G]TGAACCGTTCAGTTC | 79582 |
rs78455598 | snp | C/T | 0.5 | 0 | intron-variant | SPAG16 | GRCh38.p7 | 2:213593928 | TACAGGCGCCCACCA[C/T]CACGCCCGGCTAATT | 79582 |
rs78455741 | snp | C/T | 0.0329836 | 0.124112 | intron-variant | SPAG16 | GRCh38.p7 | 2:214166134 | AAAGATAGATTTTCA[C/T]AGTACATAGTGAAAA | 79582 |
rs78456588 | snp | C/T | 0.0150606 | 0.0854603 | intron-variant | SPAG16 | GRCh38.p7 | 2:213979972 | TAAATTTTCTCTCCA[C/T]CCTTCCAGATTACTA | 79582 |
rs78457435 | snp | C/G | 0.021333 | 0.101051 | intron-variant | SPAG16 | GRCh38.p7 | 2:213490459 | CCCTGTTAATAAGTT[C/G]TTTTTACTTGTTTGT | 79582 |
rs78457954 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | SPAG16 | GRCh38.p7 | 2:214379916 | AAATCACCCCAACTC[A/G]TGTATATAGCTCAGG | 79582 |
rs78458465 | snp | C/T | | | intron-variant | SPAG16 | GRCh38.p7 | 2:213447433 | TACTGCCCCTCACAT[C/T]CATGATTCTGAACCC | 79582 |
rs78462510 | snp | C/T | 0.0170251 | 0.090679 | intron-variant | SPAG16 | GRCh38.p7 | 2:213861505 | CATCATATGTCTTAC[C/T]GCACCACATTGGCAA | 79582 |
rs78463090 | snp | C/G | 0.0205511 | 0.0992634 | intron-variant | SPAG16 | GRCh38.p7 | 2:213813848 | ACAACACACACACAT[C/G]AAAAAATACAAAACA | 79582 |
rs78464779 | snp | C/T | 0.0126979 | 0.078662 | intron-variant | SPAG16 | GRCh38.p7 | 2:213766566 | CTGCTATGCTGTAAG[C/T]ATGATTCAAACCAGA | 79582 |
rs78465592 | snp | C/T | 0.0599851 | 0.162463 | intron-variant | SPAG16 | GRCh38.p7 | 2:213795940 | TATAAATTACCCAGC[C/T]TCAAGTGTTTCTTTA | 79582 |
rs78477164 | snp | A/T | 0.5 | 0 | intron-variant | SPAG16 | GRCh38.p7 | 2:213767632 | GATCTTGTCTTTTTG[A/T]AAAAAAAAGAGAACA | 79582 |
rs78478183 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | SPAG16 | GRCh38.p7 | 2:213759119 | GACATCCCCAGGAAA[A/G]CAACAGTTGGGAGAG | 79582 |
rs78482530 | snp | A/G | 0.0150606 | 0.0854603 | intron-variant | SPAG16 | GRCh38.p7 | 2:214254834 | AGAGGTATTTTTAAA[A/G]CTAAGATTGGTTTTT | 79582 |
rs78484582 | snp | A/G | 0.0700422 | 0.173537 | intron-variant | SPAG16 | GRCh38.p7 | 2:213766315 | TTCTGGAGTTAGATA[A/G]TGGTCATGGTTGTAC | 79582 |
rs78484696 | snp | A/G | 0.0524604 | 0.153226 | intron-variant | SPAG16 | GRCh38.p7 | 2:213882705 | TTTTTTTGTTAATCT[A/G]GCTAGTGGTCTATTC | 79582 |
rs78490342 | snp | A/G | 0.228842 | 0.249103 | intron-variant | SPAG16 | GRCh38.p7 | 2:213976324 | TGCGCATATGTGTAC[A/G]CATGTGTGCACATAT | 79582 |
rs78490422 | in-del | -/T | 0.355096 | 0.226837 | intron-variant | SPAG16 | GRCh38.p7 | 2:213355381 | TGAACTTTAAAGTAG[-/T]TTTCTCTAACTCTGT | 79582 |
rs78492015 | snp | A/G | 0.0162398 | 0.0886349 | intron-variant | SPAG16 | GRCh38.p7 | 2:214406796 | AATGGACAGCAACAT[A/G]TGCTCCTCATTGAGT | 79582 |
rs78500063 | snp | A/G | 0.00557542 | 0.0525036 | intron-variant | SPAG16 | GRCh38.p7 | 2:214292343 | AATAGGATCTTAACT[A/G]AACTCTTGTTTTCTC | 79582 |
rs78506781 | snp | G/T | 0.0314385 | 0.121371 | intron-variant | SPAG16 | GRCh38.p7 | 2:213581676 | CTAGGGAAATTGAGA[G/T]GAAGGTAGCTAAAAA | 79582 |
rs78507674 | snp | A/G | 0.5 | 0 | intron-variant | SPAG16 | GRCh38.p7 | 2:213561023 | CCTCTGCCTCTACAT[A/G]TAGTTAATTTTTGTA | 79582 |
rs78509239 | snp | C/G | 0.00557542 | 0.0525036 | intron-variant | SPAG16 | GRCh38.p7 | 2:213603993 | CAATGGCACGATCTT[C/G]GCTCACTGTATCCTC | 79582 |
rs78509707 | snp | A/C | 0.0460142 | 0.144533 | intron-variant | SPAG16 | GRCh38.p7 | 2:214011119 | ATATAATAGGAATAA[A/C]ATTCTTAATTTTTAT | 79582 |
rs78512990 | snp | A/G | 0.186421 | 0.24178 | intron-variant | SPAG16 | GRCh38.p7 | 2:213952388 | TTGTAACCATTCATA[A/G]AATGCTATGCCTTCC | 79582 |
rs78513530 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | SPAG16 | GRCh38.p7 | 2:213707315 | TAAAAACGTATTTCT[A/T]CAGTTCTTCTAATGC | 79582 |
rs78514493 | snp | C/T | 0.5 | 0 | intron-variant | SPAG16 | GRCh38.p7 | 2:213605592 | CCTCCCAGGTTCAAG[C/T]GATTCCCTTGCCTCA | 79582 |
rs78521149 | snp | C/T | 0.00597247 | 0.0543191 | intron-variant | SPAG16 | GRCh38.p7 | 2:213324371 | TTAAACATCCACATT[C/T]ATCTCAAGGTAGAAC | 79582 |
rs78521732 | snp | A/G | 0.00755907 | 0.0610114 | intron-variant | SPAG16 | GRCh38.p7 | 2:213641544 | GATTCCACTGGCTGC[A/G]TTCCCCAAAGGCCCC | 79582 |
rs78523198 | snp | A/C | 0.0130921 | 0.0798413 | intron-variant | SPAG16 | GRCh38.p7 | 2:213992984 | TACCAAAAGGATGAA[A/C]AAAATACTTCAAGCA | 79582 |
rs78523984 | snp | C/T | 0.00636936 | 0.0560724 | intron-variant | SPAG16 | GRCh38.p7 | 2:213480612 | CTTTGGTGTAAAGCA[C/T]TGTCTAGCACTATTT | 79582 |
rs78533048 | in-del | -/AAA | | | intron-variant | SPAG16 | GRCh38.p7 | 2:213799974 | TGAAAAAAAAAAAAA[-/AAA]GAAAAAACTGTTTTC | 79582 |
rs78534102 | snp | G/T | 0.5 | 0 | intron-variant | SPAG16 | GRCh38.p7 | 2:214397175 | TTTTTTTTTTTTTTT[G/T]AGATGGAGTCTCGCT | 79582 |
rs78540075 | snp | C/T | 0.021333 | 0.101051 | intron-variant | SPAG16 | GRCh38.p7 | 2:213997307 | ATTACATACTGTTGG[C/T]CTTTAGTTTTTGAAC | 79582 |
rs78545872 | snp | C/T | 0.128632 | 0.218563 | intron-variant | SPAG16 | GRCh38.p7 | 2:213963414 | TTTCTACGATTTCTA[C/T]GATTTAATTTCTTTA | 79582 |
rs78560295 | snp | C/T | 0.00517822 | 0.0506191 | intron-variant | SPAG16 | GRCh38.p7 | 2:213288403 | TCTGCCTCCCGGATT[C/T]GTGCCATTCTGCTGC | 79582 |
rs78562212 | snp | G/T | 0.0107246 | 0.0724382 | intron-variant | SPAG16 | GRCh38.p7 | 2:214393076 | AGTTATTTTTCACTA[G/T]AGTTCTATAGAACTT | 79582 |
rs78565581 | snp | C/T | 0.110872 | 0.20771 | intron-variant | SPAG16 | GRCh38.p7 | 2:214272223 | CTAATTATTTTATTA[C/T]ATTTTGCTATCATCT | 79582 |
rs78566248 | snp | A/T | 0.5 | 0 | intron-variant | SPAG16 | GRCh38.p7 | 2:213822856 | GAAGCCATTATCCTC[A/T]GTAAACTAAAACAGA | 79582 |
rs78567680 | snp | C/T | 0.021333 | 0.101051 | intron-variant | SPAG16 | GRCh38.p7 | 2:213928027 | TGTTGGTGAAGGGAC[C/T]AGCTGCCATTTGGTG | 79582 |
rs78568213 | snp | G/T | | | intron-variant | SPAG16 | GRCh38.p7 | 2:214001980 | CTTCACAATTGTGGC[G/T]GAATGTGAAAGGCAC | 79582 |
rs78568283 | snp | C/T | 0.0225045 | 0.103662 | intron-variant | SPAG16 | GRCh38.p7 | 2:213892192 | CTGCCAGGACATCCC[C/T]TTTAGGACCTTCTCC | 79582 |
rs78577738 | snp | G/T | 0.00557542 | 0.0525036 | intron-variant | SPAG16, LOC101928084 | GRCh38.p7 | 2:214090140 | AGCTTTTGCAAAAGA[G/T]ATATATGGAGATATG | 79582 |
rs78587285 | snp | C/T | 0.00597247 | 0.0543191 | intron-variant | SPAG16 | GRCh38.p7 | 2:213732755 | GTGATTTTTTTTGAG[C/T]AGTGATTTATAGTTC | 79582 |
rs78595874 | snp | A/T | 0.0452528 | 0.143452 | intron-variant | SPAG16 | GRCh38.p7 | 2:213462321 | CTATTATATTCAGTC[A/T]TTACAAATTGATGCC | 79582 |
rs78596803 | snp | A/G | 0.0217236 | 0.101931 | intron-variant | SPAG16 | GRCh38.p7 | 2:213810721 | CTGGTCTTTAGTTTC[A/G]TGGTGCGGAAGTACT | 79582 |
rs78600119 | snp | A/G | 0.0479149 | 0.147179 | intron-variant | SPAG16 | GRCh38.p7 | 2:213800164 | CTTAGCTTCTATGCA[A/G]CAATATTACAGTCTC | 79582 |
rs78608973 | snp | C/G | 0 | 0 | intron-variant | SPAG16 | GRCh38.p7 | 2:213733117 | TTGATTTGCATTTCT[C/G]TGATGGCCAGTGATG | 79582 |
rs78625644 | snp | C/T | 0.0689305 | 0.172377 | intron-variant | SPAG16 | GRCh38.p7 | 2:214062632 | TTCATCACAATATCT[C/T]GTTGGCACCACCGCA | 79582 |
rs78626913 | snp | A/G | 0.0158469 | 0.0875917 | intron-variant | SPAG16 | GRCh38.p7 | 2:214009103 | AATCAACCATAGAGC[A/G]GGAAATCTCTGCTAG | 79582 |
rs78636480 | snp | C/T | 0.0130921 | 0.0798413 | intron-variant | SPAG16 | GRCh38.p7 | 2:213877921 | ACTGTCACTATCTGT[C/T]ATTTATGGAAAGACA | 79582 |
rs78638358 | in-del | -/AA | | | intron-variant | SPAG16 | GRCh38.p7 | 2:213797061 | AAAATTAAAAAAAAA[-/AA]CATTAAAATAGAATC | 79582 |
rs78645056 | snp | A/G | 0.0150606 | 0.0854603 | intron-variant | SPAG16 | GRCh38.p7 | 2:214297645 | AAATATAAGTTGGTC[A/G]TACATATGTGGCTTT | 79582 |
rs78645410 | snp | C/T | 0.0244538 | 0.107838 | intron-variant | SPAG16 | GRCh38.p7 | 2:213436879 | TTTTAATTCTCAGTA[C/T]ATGACATGTAATACT | 79582 |
rs78649698 | snp | A/T | | | intron-variant | SPAG16 | GRCh38.p7 | 2:213893502 | TATCAAAAACAATAA[A/T]AGTTACAGGAACCTG | 79582 |
rs78650117 | snp | G/T | 0 | 0 | intron-variant | SPAG16 | GRCh38.p7 | 2:213869661 | GTTTTTTTTTTTTTT[G/T]GTCTAATTCCAAAAG | 79582 |
rs78657029 | snp | A/C | 0.0185938 | 0.0946107 | intron-variant | SPAG16 | GRCh38.p7 | 2:213850274 | AGAAAGATGTGATAC[A/C]TTTCTTTATAAGGGT | 79582 |
rs78657709 | snp | C/T | 0.0260105 | 0.111035 | intron-variant | SPAG16 | GRCh38.p7 | 2:213828046 | GTTCTTGAATATTGG[C/T]ATTTCTCTCTAGATT | 79582 |
rs78673645 | snp | A/G | 0.5 | 0 | intron-variant | SPAG16 | GRCh38.p7 | 2:213733134 | CATGAAAAAATGCTC[A/G]TCATCAGTGGCCATC | 79582 |
rs78674037 | snp | A/G | 0.0193772 | 0.0965046 | intron-variant | SPAG16 | GRCh38.p7 | 2:213421766 | ATTTGGGTCTCCTCA[A/G]CTCATTCAGACAACC | 79582 |
rs78674645 | snp | C/T | 0.0452528 | 0.143452 | intron-variant | SPAG16 | GRCh38.p7 | 2:213462265 | TAAACAGAGCCCACA[C/T]AACTATGCAGACAGT | 79582 |
rs78677936 | snp | A/G | 0.0260105 | 0.111035 | intron-variant | SPAG16 | GRCh38.p7 | 2:213288242 | TTAAGTAACAGTTCT[A/G]TCTAGTCTTTCATTG | 79582 |
rs78684566 | snp | C/G | 0.0267878 | 0.112589 | intron-variant | SPAG16 | GRCh38.p7 | 2:213665243 | ATATTAGCTTTCCAA[C/G]TGAAGCTAAATTGTG | 79582 |
rs78684991 | snp | C/T | 0.399432 | 0.200425 | intron-variant | SPAG16 | GRCh38.p7 | 2:213975192 | TATATTTATAGAATA[C/T]ATATCCCAAACTTTC | 79582 |
rs78690967 | snp | C/T | 0.00199481 | 0.0315187 | intron-variant | SPAG16 | GRCh38.p7 | 2:213428027 | AGCTAATATAGAAGA[C/T]GGCAGAGTAGAGGGT | 79582 |
rs78691188 | snp | C/T | 0.144969 | 0.226867 | intron-variant | SPAG16 | GRCh38.p7 | 2:213710873 | TTTAATGAGTTCTAA[C/T]TCATTTACTAATGAG | 79582 |
rs78691470 | snp | C/G | 0.0244538 | 0.107838 | intron-variant | SPAG16 | GRCh38.p7 | 2:214367077 | CTGTGGGGAATTAGT[C/G]GGGGACAGGATTGGA | 79582 |
rs78692194 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | SPAG16 | GRCh38.p7 | 2:213707314 | TTAAAAACGTATTTC[A/T]TCAGTTCTTCTAATG | 79582 |
rs78692372 | snp | C/G | 0.0452528 | 0.143452 | intron-variant | SPAG16 | GRCh38.p7 | 2:213436785 | TTCTAAATTTCTTCT[C/G]TTTTATGGGAACATT | 79582 |
rs78692382 | snp | G/T | 0.0810805 | 0.184299 | intron-variant | SPAG16 | GRCh38.p7 | 2:213695168 | CTTTTAACCATATCT[G/T]TTTCTTACTCTTCAC | 79582 |
rs78696471 | snp | C/T | 0.0248432 | 0.108648 | intron-variant | SPAG16 | GRCh38.p7 | 2:214251198 | ATTTTCACACACACA[C/T]CTGCACACACACTTA | 79582 |
rs78697702 | snp | C/T | 0.0162398 | 0.0886349 | intron-variant | SPAG16 | GRCh38.p7 | 2:214134198 | TCTTTCCTGATTTCA[C/T]ATATGAAAAGACTTT | 79582 |
rs78701851 | snp | C/T | 0.130694 | 0.219696 | intron-variant | SPAG16 | GRCh38.p7 | 2:213654903 | GGGATGTTTAAACGG[C/T]GAATGATACTTTGAA | 79582 |
rs78715614 | snp | A/G | 0.0763149 | 0.179815 | intron-variant | SPAG16 | GRCh38.p7 | 2:213824335 | GCAATGACCTGGAGA[A/G]CTTCCCCAATGTTTT | 79582 |
rs78715903 | snp | C/T | 0.00716266 | 0.059414 | intron-variant | SPAG16 | GRCh38.p7 | 2:213762187 | CAAAAGGTAGACCAG[C/T]GGCTTCCAGGGACTG | 79582 |
rs78721293 | snp | A/T | 0.00199481 | 0.0315187 | intron-variant | SPAG16 | GRCh38.p7 | 2:213872623 | GAACCTCCAGTGCAA[A/T]GTTGAAAAGAAGTGA | 79582 |
rs78722911 | snp | G/T | 0 | 0 | intron-variant | SPAG16 | GRCh38.p7 | 2:213451915 | AGCTGCAGGTGTCCC[G/T]GACTCGCCCCATACC | 79582 |
rs78733024 | snp | A/G | 0.0475351 | 0.146656 | intron-variant | SPAG16 | GRCh38.p7 | 2:213989940 | TCATATTGCAAAAAA[A/G]TAAAAATTGCCTTGA | 79582 |
rs78733093 | snp | C/T | 0.0240643 | 0.107019 | intron-variant | SPAG16 | GRCh38.p7 | 2:213327263 | ATTTTAAACTTTATT[C/T]TTTAGTACAACTTTT | 79582 |
rs78737085 | snp | C/G | 0.375 | 0.216506 | intron-variant | SPAG16 | GRCh38.p7 | 2:213717401 | TCCTGACCTCGTGAT[C/G]CGCCCGCCTCGGCCT | 79582 |
rs78741641 | snp | G/T | 0.00557542 | 0.0525036 | intron-variant | SPAG16 | GRCh38.p7 | 2:213893223 | TCAACAAAGCTGTCC[G/T]TCAGCTATGAAACAG | 79582 |
rs78742068 | snp | A/G | | | intron-variant | SPAG16 | GRCh38.p7 | 2:213363057 | TCTGGATGCGATTTT[A/G]AAACATAAAAAGGAT | 79582 |
rs78742286 | snp | A/G | 0.5 | 0 | intron-variant | SPAG16 | GRCh38.p7 | 2:213310455 | ATTTTTAAAAAATCA[A/G]GACACTTGAATATCT | 79582 |
rs78747874 | snp | A/T | 0.5 | 0 | intron-variant | SPAG16 | GRCh38.p7 | 2:213520446 | AAAAAAAAAAAAAAT[A/T]CGCTGGGCGTGGTGG | 79582 |
rs78756357 | snp | A/T | 0.0236746 | 0.106192 | intron-variant | SPAG16 | GRCh38.p7 | 2:213634539 | CATTCATGTGATTAT[A/T]TATTGCTTGTTGGTG | 79582 |
rs78756660 | snp | A/G | 0.084728 | 0.187577 | intron-variant | SPAG16 | GRCh38.p7 | 2:213698181 | ATTTGCTCTCTGACC[A/G]TTCTTCTTTATTCTC | 79582 |
rs78757257 | snp | A/G | 0.0444908 | 0.142359 | intron-variant | SPAG16 | GRCh38.p7 | 2:213679671 | TGTAAAGTTACCTTC[A/G]GTAAAAAGACTATAT | 79582 |
rs78757523 | snp | A/T | 0.132066 | 0.220435 | intron-variant | SPAG16 | GRCh38.p7 | 2:213600494 | GCTCTTCTATGTTCC[A/T]AGTATTGTGGTAGGT | 79582 |
rs78759087 | snp | G/T | 0.128632 | 0.218563 | intron-variant | SPAG16 | GRCh38.p7 | 2:213512190 | TCAGTTAAAATTCAA[G/T]GATGAGGGAAAGAAG | 79582 |
rs78759518 | snp | G/T | 0.000798403 | 0.0199641 | intron-variant | SPAG16 | GRCh38.p7 | 2:213774492 | CTTATTGATTTAGGG[G/T]TCTACCCTATTTCCT | 79582 |
rs78762194 | snp | A/T | | | intron-variant | SPAG16 | GRCh38.p7 | 2:213525622 | AAATTACCCAGTCTC[A/T]GGCATGTATTTATTA | 79582 |
rs78763835 | snp | A/G | 0.110519 | 0.207473 | intron-variant | SPAG16 | GRCh38.p7 | 2:213554855 | GGGCTTTATTGGATA[A/G]CATCAAATACAAATA | 79582 |
rs78766172 | snp | C/T | 0.26271 | 0.249677 | intron-variant, upstream-variant-2KB | SPAG16, LOC101928084 | GRCh38.p7 | 2:214103084 | CCCATCTGAGGTTTT[C/T]TCCTTTCTCCAGTGG | 79582 |
rs78767391 | snp | A/C | 0.0448719 | 0.142907 | intron-variant | SPAG16 | GRCh38.p7 | 2:213984081 | TGAAGTTCCCAATGG[A/C]AAATTGAATGCTGCT | 79582 |
rs78778415 | snp | G/T | 0.0891319 | 0.191367 | intron-variant | SPAG16 | GRCh38.p7 | 2:214162473 | CCCTATTACAGGGAA[G/T]AAGTAAGTACTGGGA | 79582 |
rs78779908 | snp | C/T | 0.110872 | 0.20771 | intron-variant | SPAG16 | GRCh38.p7 | 2:214388001 | TGAAAAAAATACCTA[C/T]TATTGCTATATTTTT | 79582 |
rs78781689 | snp | A/G | | | intron-variant | SPAG16 | GRCh38.p7 | 2:213523274 | GCCGCCATGTGAAGA[A/G]GGATGTGTTTGCTTC | 79582 |
rs78783587 | snp | C/G | 0.0185938 | 0.0946107 | intron-variant | SPAG16 | GRCh38.p7 | 2:213859774 | CATAAAATAATAATA[C/G]TGATAGTACCAACAT | 79582 |
rs78786053 | snp | C/T | 0.0248432 | 0.108648 | intron-variant | SPAG16 | GRCh38.p7 | 2:213384156 | TGATGAGAACATCCA[C/T]ATCTACATCCTTTGT | 79582 |
rs78786056 | snp | C/T | 0.021333 | 0.101051 | intron-variant | SPAG16 | GRCh38.p7 | 2:214077926 | ATGCCTTATTCCCTG[C/T]CTGTCCCTGCCTCAC | 79582 |
rs78795062 | snp | A/G | 0.0165278 | 0.0893908 | intron-variant | SPAG16 | GRCh38.p7 | 2:214019091 | AGACTATTTTATTAA[A/G]ATTGAAAGATAAGAT | 79582 |
rs78800361 | snp | A/G | 0.0205511 | 0.0992634 | intron-variant | SPAG16 | GRCh38.p7 | 2:213806133 | CAGCACACACATATC[A/G]ATGTTCCAATAAATA | 79582 |
rs78800480 | snp | G/T | 0.0168055 | 0.0901129 | intron-variant | SPAG16 | GRCh38.p7 | 2:213845944 | CATGATGAAAGTGGG[G/T]TTGGGGTAGCAGTGG | 79582 |
rs78801086 | snp | C/T | 0.154329 | 0.23097 | intron-variant | SPAG16 | GRCh38.p7 | 2:213544831 | CATTGAAGTTTTCTC[C/T]GTTTCTTTTTGAGAC | 79582 |
rs78801465 | snp | C/T | 0.0581099 | 0.160244 | intron-variant | SPAG16 | GRCh38.p7 | 2:213737983 | CACTCATTCATTCAT[C/T]GAATTTCTTAAGTGT | 79582 |
rs78808562 | snp | C/T | 0 | 0 | intron-variant | SPAG16 | GRCh38.p7 | 2:213433917 | CCTTTTTCTTTGTCT[C/T]TTTTTTTTTTTTTTT | 79582 |
rs78809990 | snp | A/G | 0.0221141 | 0.102801 | intron-variant | SPAG16 | GRCh38.p7 | 2:213407214 | CTACCTTGGCGGAGC[A/G]GCCAGAGAGGACAGC | 79582 |
rs78812496 | snp | C/T | 0.0807149 | 0.183963 | intron-variant | SPAG16 | GRCh38.p7 | 2:213340520 | GCCATCATCCCAATA[C/T]GACTGGAGTGTGAGA | 79582 |
rs78816446 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | SPAG16 | GRCh38.p7 | 2:213961326 | AGTTTTCTACATACA[A/G]GATCATGGAATCTGC | 79582 |
rs78822469 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | SPAG16 | GRCh38.p7 | 2:213417187 | GAGGTCAAGCATCAT[A/T]CTATATAGAAAAGTA | 79582 |
rs78822501 | snp | A/T | 0.105569 | 0.204058 | intron-variant | SPAG16 | GRCh38.p7 | 2:213671379 | GGTATTATTTGATTG[A/T]AAGGAGTCAAGATTT | 79582 |
rs78823659 | in-del | -/T | | | intron-variant | SPAG16 | GRCh38.p7 | 2:213807344 | TGTTTTCTTTTTTTT[-/T]TCCCCTCAACATTTC | 79582 |
rs78831594 | snp | A/G | 0.00795532 | 0.062565 | intron-variant | SPAG16 | GRCh38.p7 | 2:214223581 | GTAGCAAAATTTAAA[A/G]CAATAAAATAGTTTT | 79582 |
rs78836530 | snp | C/T | 0.180702 | 0.240204 | intron-variant | SPAG16 | GRCh38.p7 | 2:213554789 | CAGGCTATTTTAAAA[C/T]ACAAAGGAGAACAAA | 79582 |
rs78836694 | snp | A/G | 0.00835141 | 0.0640778 | intron-variant | SPAG16 | GRCh38.p7 | 2:213529280 | ACCTCAGAATAAATT[A/G]TGGTCTGCTGGTCAA | 79582 |
rs78837563 | snp | C/T | | | intron-variant | SPAG16 | GRCh38.p7 | 2:213333537 | GAATAGCTTTGGCTA[C/T]TCTGGATCTTTGGTG | 79582 |
rs78838305 | snp | G/T | | | intron-variant | SPAG16 | GRCh38.p7 | 2:213728962 | CCACAGTGCTTGCAT[G/T]GGTATAAGGAGAATG | 79582 |
rs78838663 | snp | C/T | 0.00517822 | 0.0506191 | intron-variant | SPAG16 | GRCh38.p7 | 2:213834341 | TCAGAAATGAAAATA[C/T]GTAGACCCAGGGAAA | 79582 |
rs78842017 | snp | A/G | 0.0158469 | 0.0875917 | intron-variant | SPAG16 | GRCh38.p7 | 2:213775394 | TGAAATTATTACTAC[A/G]TTCTATTTTATAAAC | 79582 |
rs78842138 | snp | C/T | 0.0352966 | 0.128072 | intron-variant | SPAG16 | GRCh38.p7 | 2:214240829 | TCCACAGTACATACA[C/T]AATTAAATGTAAATG | 79582 |
rs78842981 | snp | G/T | 0.5 | 0 | intron-variant | SPAG16 | GRCh38.p7 | 2:213996148 | CTGGAAAAAATAGGG[G/T]GAAATCACCAGGAGT | 79582 |
rs78846035 | snp | A/C | 0.00557542 | 0.0525036 | intron-variant | SPAG16 | GRCh38.p7 | 2:214129834 | TATAGACTATGAATG[A/C]ATGACTTATAAGGCT | 79582 |
rs78848212 | snp | C/T | 0 | 0 | intron-variant | SPAG16 | GRCh38.p7 | 2:213426836 | GATTATTCTGATACA[C/T]ACACACACACACACA | 79582 |
rs78848768 | snp | G/T | 0.182614 | 0.240747 | intron-variant | SPAG16 | GRCh38.p7 | 2:213431672 | ATTTCAACACCCTAC[G/T]GACACACTATAAAGA | 79582 |
rs78858391 | snp | C/T | 0.0240643 | 0.107019 | intron-variant | SPAG16 | GRCh38.p7 | 2:213332494 | TTACTCAAACAATTC[C/T]GAAAAATACAGGAAG | 79582 |
rs78866165 | snp | A/G | 0.131723 | 0.220251 | intron-variant | SPAG16 | GRCh38.p7 | 2:213644805 | TACTGGGTCAGACCT[A/G]AAGACAGCACAGTGC | 79582 |
rs78867254 | snp | A/C | 0.5 | 0 | intron-variant | SPAG16 | GRCh38.p7 | 2:213529315 | GCTTCCCTTCTACTC[A/C]TCAAAAAAGCCCTGA | 79582 |
rs78868003 | snp | C/T | 0.5 | 0 | intron-variant | SPAG16 | GRCh38.p7 | 2:213731482 | TTTTTTTTTTTCTTT[C/T]CCAACTTTTAAGTTC | 79582 |
rs78877207 | snp | A/C/G/T | 0.5 | 0 | intron-variant | SPAG16 | GRCh38.p7 | 2:213457889 | CTTTTATTTTTTTTT[A/C/G/T]CCTTCCTTGGCCTTT | 79582 |
rs78880133 | snp | A/T | 0 | 0 | intron-variant, upstream-variant-2KB | SPAG16 | GRCh38.p7 | 2:213315706 | AAACTTTTTTTTTTT[A/T]AATAGTGACTTTCAC | 79582 |
rs78882769 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | SPAG16 | GRCh38.p7 | 2:214187991 | GACTTTAAATGCTGA[C/T]GGTTTATTGCAGCAG | 79582 |
rs78885000 | snp | C/T | 0.00874735 | 0.0655527 | intron-variant | SPAG16 | GRCh38.p7 | 2:213878949 | AACTTTGTCAAAGAT[C/T]AGGTGGATGTGGATG | 79582 |
rs78887503 | snp | A/G | 0.0150606 | 0.0854603 | intron-variant | SPAG16 | GRCh38.p7 | 2:214290218 | CATATAGTTGTGCAT[A/G]ATGATCTCTGATGAT | 79582 |
rs78887714 | snp | C/G | 0.00318978 | 0.0398085 | intron-variant | SPAG16 | GRCh38.p7 | 2:213495741 | GAAAGTGATATGTAA[C/G]GGAAACCTGAAGCAG | 79582 |
rs78891625 | snp | A/C | 0.25282 | 0.250286 | intron-variant | SPAG16, LOC101928084 | GRCh38.p7 | 2:214095313 | CACACAGAAACCCCC[A/C]CAGAAACCTTTTCTC | 79582 |
rs78891775 | snp | A/G | 0.00636936 | 0.0560724 | intron-variant | SPAG16 | GRCh38.p7 | 2:213349575 | GATATATGACCAAAA[A/G]TATTACATGACTTAT | 79582 |
rs78893663 | snp | A/C | 0.131381 | 0.220067 | intron-variant | SPAG16 | GRCh38.p7 | 2:213456752 | AGTTTTGAATTGTGA[A/C]TTACAGTTTTCTTCT | 79582 |
rs78899400 | snp | A/T | 0.5 | 0 | intron-variant | SPAG16 | GRCh38.p7 | 2:213963108 | CTTTTTTTTTTTTTT[A/T]AATGTCTAAAGATAG | 79582 |
rs78902512 | snp | A/C | | | intron-variant | SPAG16 | GRCh38.p7 | 2:214027966 | AGTGTGTTATTTTAG[A/C]TAACTAATTAAAATA | 79582 |
rs78908643 | snp | A/C | 0.127599 | 0.217986 | intron-variant | SPAG16 | GRCh38.p7 | 2:213621324 | AGAAAAATATGTTAC[A/C]ACTGAGAATATACTC | 79582 |
rs78912706 | snp | A/G | 0.0182019 | 0.0936463 | intron-variant | SPAG16 | GRCh38.p7 | 2:214010559 | CCCCAAAGAAGGTTG[A/G]ATGGGAGATTGGAGA | 79582 |
rs78917283 | snp | A/G | 0.0267878 | 0.112589 | intron-variant | SPAG16 | GRCh38.p7 | 2:214223507 | ACCTTTTGTTTCAGA[A/G]CAATAAAATGCAATC | 79582 |
rs78917730 | snp | G/T | 0.0275645 | 0.114116 | intron-variant | SPAG16 | GRCh38.p7 | 2:213326708 | TGTGAGAAAAATATA[G/T]GACAAAGATAGCCTA | 79582 |
rs78918877 | snp | A/C | 0.0505692 | 0.150756 | intron-variant | SPAG16 | GRCh38.p7 | 2:213630253 | GCTGGGCATGGTGGC[A/C]GATGCCTGCAATCCG | 79582 |
rs78920274 | snp | C/T | 0.0349115 | 0.127424 | intron-variant | SPAG16 | GRCh38.p7 | 2:214237002 | TCCGTATCCATAATG[C/T]ATAATTGTGATCCTT | 79582 |
rs78925565 | snp | A/G | | | intron-variant | SPAG16 | GRCh38.p7 | 2:213693737 | GTATATTTAGTCCTT[A/G]GTGGTAGAACTCTTT | 79582 |
rs78927660 | snp | G/T | 0.0189856 | 0.0955633 | intron-variant | SPAG16 | GRCh38.p7 | 2:213894508 | TGGGGGAAAATTGAA[G/T]ACCTTTCCTCTAGAT | 79582 |
rs78928103 | snp | A/T | 0.5 | 0 | intron-variant | SPAG16 | GRCh38.p7 | 2:213429833 | ATTCTCAAGAAAAAA[A/T]TAAAAGTCCTGCCCC | 79582 |
rs78932586 | snp | C/G | 0.0130921 | 0.0798413 | intron-variant | SPAG16 | GRCh38.p7 | 2:213828860 | GTAGAGACTCTTGTT[C/G]CCTTTGCTTACTTTC | 79582 |
rs78945806 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | SPAG16 | GRCh38.p7 | 2:214347123 | AAAGAAAATGAGTAC[A/G]CTGTTATTGGTGGTG | 79582 |
rs78947950 | snp | C/T | 0.211212 | 0.246973 | intron-variant | SPAG16 | GRCh38.p7 | 2:214248682 | AAAGTCCTCCTGAGA[C/T]TTTAATTTTATAAGA | 79582 |
rs78950603 | snp | A/G | 0.00398564 | 0.0444627 | intron-variant | SPAG16 | GRCh38.p7 | 2:214389638 | GGAGTGTTTAAGTAA[A/G]AGAACAAGCTTAATA | 79582 |
rs78956271 | snp | A/C | 0.0614824 | 0.164198 | intron-variant | SPAG16 | GRCh38.p7 | 2:214061769 | ATACTCAGTATTTTA[A/C]AGTACTCAGAAGTTG | 79582 |
rs78957829 | snp | A/G | 0.00914312 | 0.0669923 | intron-variant | SPAG16 | GRCh38.p7 | 2:213710404 | TTATTATAACTAAGC[A/G]TAAGGTATCTTAAGT | 79582 |
rs78971070 | snp | A/G | 0.00557542 | 0.0525036 | intron-variant | SPAG16 | GRCh38.p7 | 2:214377292 | CCGTTGGACCCATAC[A/G]AAGTGCCACTAGTGA | 79582 |
rs78972597 | snp | A/C | 0.00438332 | 0.0466095 | intron-variant | SPAG16 | GRCh38.p7 | 2:213830812 | TCCCAAATCTGAATT[A/C]TTTTATGATTCCTAT | 79582 |
rs78975985 | snp | C/T | 0.0670745 | 0.170406 | intron-variant | SPAG16 | GRCh38.p7 | 2:214221039 | TTTTGATAATTCTAA[C/T]GGAGTGTCACACACA | 79582 |
rs78978637 | snp | C/T | 0.0460142 | 0.144533 | intron-variant | SPAG16 | GRCh38.p7 | 2:213789714 | ATCTCCATTATACTT[C/T]GTCCGTAAGCTCTAT | 79582 |
rs78979020 | snp | C/T | 0.0528381 | 0.153711 | intron-variant | SPAG16 | GRCh38.p7 | 2:214146232 | CTTCCCACATCTCTC[C/T]ATCTCCACATCCCTC | 79582 |
rs78981904 | snp | C/T | 0.5 | 0 | intron-variant | SPAG16 | GRCh38.p7 | 2:214016389 | GGGTTTTTCCCATGC[C/T]GTTCTCTTGATAGTG | 79582 |
rs78990317 | snp | G/T | 0.5 | 0 | intron-variant | SPAG16 | GRCh38.p7 | 2:213970302 | GCTTTTTTTTTTTTT[G/T]TTTATTTTTAAAAAC | 79582 |
rs78990940 | snp | C/T | 0.00795532 | 0.062565 | intron-variant | SPAG16 | GRCh38.p7 | 2:214141784 | TAAATAGGTAATCTG[C/T]CATTTTTCACTTGTA | 79582 |
rs78991667 | snp | A/G | 0.00914312 | 0.0669923 | intron-variant | SPAG16 | GRCh38.p7 | 2:213583440 | AAAGCACTTTTCCAA[A/G]TTTTGTTAACTAGCT | 79582 |
rs78992559 | snp | C/G | 0.5 | 0 | intron-variant | SPAG16 | GRCh38.p7 | 2:213923727 | AGCACACATTGATCA[C/G]CTGGCAACCAGTGAT | 79582 |
rs78995510 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | SPAG16 | GRCh38.p7 | 2:214176653 | ATTTTCCCTTGGGAG[C/T]TCGGTAAGACAATCT | 79582 |
rs78999216 | snp | C/T | 0.223819 | 0.248625 | intron-variant | SPAG16 | GRCh38.p7 | 2:214397265 | GATTCAAGCGATTCT[C/T]CTGCCTCAGCCTCCC | 79582 |
rs79010581 | snp | C/T | 0.0217236 | 0.101931 | intron-variant | SPAG16 | GRCh38.p7 | 2:214209310 | TTGTAGAGAAACCCA[C/T]TGCAGCCTATCTGAG | 79582 |
rs79015376 | snp | C/T | 0.0119091 | 0.0762411 | intron-variant | SPAG16, LOC101928084 | GRCh38.p7 | 2:214100660 | TGTTCCTTGTTGCTA[C/T]GTTAGTTCACTTAAG | 79582 |
rs79018678 | snp | C/T | 0.0130921 | 0.0798413 | intron-variant | SPAG16 | GRCh38.p7 | 2:213732992 | AATTTACACTCCCAC[C/T]AACAGTGTAAGAGTT | 79582 |
rs79027980 | snp | A/C/G | 0.000153988 | 0.00877328 | missense, nc-transcript-variant, utr-variant-5-prime | SPAG16 | GRCh38.p7 | 2:213297269 | TGATCTAGATACCAG[A/C/G]TGACAATTTTAGCAT | 79582 |
rs79028107 | snp | C/T | 0.0182019 | 0.0936463 | intron-variant | SPAG16 | GRCh38.p7 | 2:213818916 | TTCTGAAGCCTCCCC[C/T]GCCATGTGAAATTGT | 79582 |
rs79036454 | snp | G/T | 0.5 | 0 | intron-variant | SPAG16 | GRCh38.p7 | 2:214172085 | ATCCTGCATACTTTG[G/T]TTTTTTTTTAAATTT | 79582 |
rs79037599 | snp | C/T | 0.0146672 | 0.084371 | intron-variant | SPAG16 | GRCh38.p7 | 2:214380237 | CACTATTGTTGTTCA[C/T]GGGGTAGAAACTAGA | 79582 |
rs79037628 | snp | C/T | 0.0039912 | 0.0444935 | intron-variant | SPAG16 | GRCh38.p7 | 2:214356369 | GCATGCAAGTGATCC[C/T]AATTGACACAATATG | 79582 |
rs79038284 | snp | G/T | 0.5 | 0 | intron-variant | SPAG16 | GRCh38.p7 | 2:214191382 | GCTCCTCTTTAGTAA[G/T]GTAGGAAAAGTGTGA | 79582 |
rs79040963 | snp | A/G | 0.00874735 | 0.0655527 | intron-variant | SPAG16 | GRCh38.p7 | 2:214352295 | AATCATGTCCTCACA[A/G]TTATCATCATTTTCA | 79582 |
rs79041993 | snp | G/T | 0 | 0 | intron-variant | SPAG16 | GRCh38.p7 | 2:214126084 | TTTTTTTTTTTTTTG[G/T]CGTTTCTGTATAGCA | 79582 |
rs79042228 | snp | C/G | 0.5 | 0 | intron-variant | SPAG16 | GRCh38.p7 | 2:214266069 | CTTGAAAATTATTTA[C/G]TGAATAAATGAATGA | 79582 |
rs79043059 | snp | C/G | 0.5 | 0 | intron-variant | SPAG16 | GRCh38.p7 | 2:214033592 | GCATCCATCCATTCA[C/G]TCATTTAGACATAGG | 79582 |
rs79049168 | snp | A/G | | | intron-variant | SPAG16 | GRCh38.p7 | 2:214109965 | TTATTTTGGCAAGCA[A/G]TATAATAACTGCAAA | 79582 |
rs79054991 | snp | A/G | 0.0566069 | 0.158427 | intron-variant | SPAG16 | GRCh38.p7 | 2:213993491 | ACAATAGCACTGCCT[A/G]TTCAATCCCTATTTT | 79582 |
rs79055393 | snp | C/T | 0.031825 | 0.122064 | intron-variant | SPAG16 | GRCh38.p7 | 2:213868692 | CTCTATAAGTGAAAG[C/T]AGTGGGATTAGTGGT | 79582 |
rs79057531 | in-del | -/CA/GC | 0.0314242 | 0.121345 | intron-variant | SPAG16 | GRCh38.p7 | 2:214210839 | CACACATGCGCGCGC[-/CA/GC]ACACACACACACACA | 79582 |
rs79065854 | snp | A/G | | | intron-variant | SPAG16 | GRCh38.p7 | 2:214186048 | CAGGCATAAAATAAT[A/G]TTCAAAAAATAAAAG | 79582 |
rs79066770 | snp | C/T | 0.0463947 | 0.145069 | intron-variant | SPAG16 | GRCh38.p7 | 2:213339171 | TATCTCATAAACATC[C/T]TTGGTAGCATCCCAT | 79582 |
rs79074442 | snp | A/C | 0.00279162 | 0.0372561 | intron-variant | SPAG16 | GRCh38.p7 | 2:213595274 | AATGTAACTCTCATG[A/C]AATTAATTAAAACTC | 79582 |
rs79077594 | snp | C/T | 0.0130921 | 0.0798413 | intron-variant | SPAG16 | GRCh38.p7 | 2:213718046 | AAAAGAAACTATCAC[C/T]GGAGTTAAAAAGGCA | 79582 |
rs79079917 | snp | C/T | 0 | 0 | intron-variant | SPAG16 | GRCh38.p7 | 2:214042088 | TTCTTTTTCTTTTTC[C/T]TTTTCTTTTTTTTTT | 79582 |
rs79082788 | snp | A/G | 0.030278 | 0.119257 | intron-variant | SPAG16 | GRCh38.p7 | 2:213732653 | ATGAATCTGTAAATT[A/G]TTTTGGGGACTATGG | 79582 |
rs79083503 | snp | A/C | | | intron-variant | SPAG16 | GRCh38.p7 | 2:214016320 | GTTCCCCTGCACATG[A/C]TCTCTTGCTTGCTGC | 79582 |
rs79085177 | snp | A/G | 0.121369 | 0.214369 | intron-variant | SPAG16 | GRCh38.p7 | 2:213363051 | TGATATTCTGGATGC[A/G]ATTTTGAAACATAAA | 79582 |
rs79085590 | snp | A/G | 0.00279162 | 0.0372561 | intron-variant | SPAG16 | GRCh38.p7 | 2:213809105 | TTTTGGTGAAAGAAT[A/G]CCTCACCTCTGTGTG | 79582 |
rs79086070 | snp | C/T | 0.0463947 | 0.145069 | intron-variant, utr-variant-3-prime | SPAG16 | GRCh38.p7 | 2:213397365 | AAAGTCAGATAAGTG[C/T]CCCCTTTGCTTCTCA | 79582 |
rs79089583 | snp | A/G | | | intron-variant | SPAG16 | GRCh38.p7 | 2:213504853 | TGCATACATTTATAG[A/G]AGCCCATTTACTTTC | 79582 |
rs79100541 | snp | C/T | 0.0441095 | 0.141807 | intron-variant | SPAG16 | GRCh38.p7 | 2:214257228 | ATAGATTTTTATATA[C/T]TTAGCTCATACCCTG | 79582 |
rs79100561 | snp | A/C | | | intron-variant | SPAG16 | GRCh38.p7 | 2:213819221 | TAGTATCTGAACGCC[A/C]AATTCCAATCAGAGA | 79582 |
rs79104428 | in-del | -/TTT | | | intron-variant | SPAG16 | GRCh38.p7 | 2:213543108 | AACAATTTTATGGTC[-/TTT]AATAAACACACTTTG | 79582 |
rs79104575 | snp | A/G | 0.0441095 | 0.141807 | intron-variant | SPAG16 | GRCh38.p7 | 2:214284134 | TAGCACCCCTCTTTT[A/G]GGGTGTAAGGAAATA | 79582 |
rs79106693 | snp | C/T | 0.0023933 | 0.0345097 | intron-variant | SPAG16 | GRCh38.p7 | 2:214307837 | TTACAGTATGTGCCA[C/T]GTTGCAATGAAAAGA | 79582 |
rs79128228 | snp | G/T | 0.00119737 | 0.0244387 | intron-variant | SPAG16 | GRCh38.p7 | 2:214157090 | TTGGGCCTCACTGAT[G/T]CTGGAGAAAGGAACT | 79582 |
rs79139206 | snp | C/T | 0.0329836 | 0.124112 | intron-variant | SPAG16 | GRCh38.p7 | 2:213442616 | CAACAAATACAGCCA[C/T]ACAAATATAGTCAAT | 79582 |
rs79139925 | snp | C/T | 0.0209421 | 0.100162 | intron-variant | SPAG16 | GRCh38.p7 | 2:214118938 | GGAGGTATCATACTA[C/T]CTGACATTAAAATAT | 79582 |
rs79140467 | snp | C/T | 0.0174175 | 0.0916809 | intron-variant | SPAG16 | GRCh38.p7 | 2:214071565 | AAGGTACTGATTTTT[C/T]TATATTAACCCAACA | 79582 |
rs79140989 | snp | A/G | 0.0182019 | 0.0936463 | intron-variant | SPAG16 | GRCh38.p7 | 2:213584670 | GACGGATGGACGGGA[A/G]GAAGTGAGGGAAACT | 79582 |
rs79141143 | in-del | -/TCT | | | intron-variant | SPAG16 | GRCh38.p7 | 2:214259499 | TTTTTTTTTTTACTT[-/TCT]GGCTCTCTCCTTTCC | 79582 |
rs79141677 | snp | A/T | 0.0566069 | 0.158427 | intron-variant | SPAG16 | GRCh38.p7 | 2:214002446 | TATTTTAAAAATTAG[A/T]GTAATTATAAAAGGT | 79582 |
rs79146868 | snp | A/C | 0.133435 | 0.221162 | intron-variant | SPAG16 | GRCh38.p7 | 2:213629537 | CCTGTTACATATAAA[A/C]AAATCAATTGCTGCG | 79582 |
rs79152364 | snp | A/G | 0.129664 | 0.219133 | intron-variant | SPAG16 | GRCh38.p7 | 2:213564763 | TTTGTTAATATGCAC[A/G]AGAATCCTGTGAGTT | 79582 |
rs79153377 | snp | A/G | 0.0023933 | 0.0345097 | intron-variant | SPAG16 | GRCh38.p7 | 2:213942775 | GAGTTCATGTGGGAG[A/G]GGAATACTCAAAAGT | 79582 |
rs79153835 | snp | A/G | 0 | 0 | intron-variant | SPAG16 | GRCh38.p7 | 2:213733149 | GTGAGCATTTTTCAT[A/G]TGTTTTTTGGCTGCA | 79582 |
rs79154933 | snp | C/T | 0.5 | 0 | intron-variant | SPAG16 | GRCh38.p7 | 2:213926305 | TGTCAGAAATCACCA[C/T]TAAAGAATTTATTTA | 79582 |
rs79156350 | snp | A/T | 0.155325 | 0.23138 | intron-variant | SPAG16 | GRCh38.p7 | 2:213590439 | AAGAACTTCAACAAA[A/T]CAACAAGAAAAAAAA | 79582 |
rs79159348 | snp | A/G | 0.00318978 | 0.0398085 | intron-variant | SPAG16 | GRCh38.p7 | 2:213683166 | CAAAGAATTAAAACA[A/G]TAAAGTTTTCCTGGG | 79582 |
rs79170173 | snp | G/T | 0.0154538 | 0.0865337 | intron-variant | SPAG16 | GRCh38.p7 | 2:213986180 | GAAAGTGAGATTTGA[G/T]GTAGACAGTGAAAGT | 79582 |
rs79171424 | snp | C/T | 0.030665 | 0.119967 | intron-variant | SPAG16 | GRCh38.p7 | 2:213874082 | AGATAAAAAGTGGTA[C/T]ACTTGTTTAGGGCAT | 79582 |
rs79171690 | snp | A/G | 0.0158469 | 0.0875917 | intron-variant | SPAG16 | GRCh38.p7 | 2:213858135 | TGAAATAACAATGAA[A/G]GATTTAAAATATTTC | 79582 |
rs79179611 | snp | C/T | 0.5 | 0 | intron-variant | SPAG16 | GRCh38.p7 | 2:214291302 | TTAGATCATGTTTCT[C/T]TTTTTTTTTTTTTTT | 79582 |
rs79182978 | snp | C/T | 0.021333 | 0.101051 | intron-variant | SPAG16 | GRCh38.p7 | 2:213479269 | TGAGGCCTCGCCAGA[C/T]TGCCGCATGTATAAT | 79582 |
rs79183237 | snp | A/T | 0.5 | 0 | intron-variant | SPAG16 | GRCh38.p7 | 2:213635706 | GTGATTATGAAAAAA[A/T]TTAGTGACTGAAGCA | 79582 |
rs79195486 | snp | A/G | 0.00438332 | 0.0466095 | intron-variant | SPAG16 | GRCh38.p7 | 2:214231485 | AATACTTATAAGTTT[A/G]TAAGTATTGTATAAC | 79582 |
rs79202405 | snp | A/G | 0.5 | 0 | intron-variant | SPAG16 | GRCh38.p7 | 2:213566474 | AAATACAATTTGAGG[A/G]AAAAGGATCTTTTAA | 79582 |
rs79206351 | snp | A/T | 0.0275645 | 0.114116 | intron-variant | SPAG16 | GRCh38.p7 | 2:213427923 | TCTAAAAATTAGTAC[A/T]TTGTATTTCCTAATT | 79582 |
rs79207160 | snp | C/T | 0.0197687 | 0.0974348 | intron-variant | SPAG16 | GRCh38.p7 | 2:213848174 | AAAATGGAAGCTCTA[C/T]GTCTTGTCTGGATTG | 79582 |
rs79207265 | snp | C/T | 0.0228947 | 0.104514 | intron-variant | SPAG16 | GRCh38.p7 | 2:213906827 | TGTGAAGAATAAAAC[C/T]AGACTTCTATCTCAC | 79582 |
rs79207716 | snp | C/G | 0.0217236 | 0.101931 | intron-variant | SPAG16 | GRCh38.p7 | 2:213883911 | AGTCCTTACATGTGT[C/G]ATATATCTCTTGAAG | 79582 |
rs79208033 | snp | C/G | 0.121022 | 0.21416 | intron-variant | SPAG16 | GRCh38.p7 | 2:213384928 | CTTGCTGTTCTTTTC[C/G]ATAATTGTGCCCATC | 79582 |
rs79209404 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | SPAG16 | GRCh38.p7 | 2:214162599 | TTGATTTGTGATGCC[A/G]CTTTTATTAGAGATC | 79582 |
rs79209898 | snp | C/G | 0.0456336 | 0.143994 | intron-variant | SPAG16 | GRCh38.p7 | 2:213440637 | ATCCATGCATACATG[C/G]TTTATTCATGAGAAG | 79582 |
rs79212703 | snp | A/C | 0 | 0 | intron-variant | SPAG16 | GRCh38.p7 | 2:214353990 | TCAATAAAGATATAC[A/C]CAAAGGATAAATACT | 79582 |
rs79212720 | snp | C/T | 0.00676609 | 0.0577691 | intron-variant | SPAG16 | GRCh38.p7 | 2:213504684 | ACCATAAAATAATGG[C/T]AAGCTGCTAGGCTAT | 79582 |
rs79215215 | snp | G/T | 0.5 | 0 | intron-variant | SPAG16 | GRCh38.p7 | 2:214033987 | GCATTCAGTTAGTTG[G/T]CTTGTCTCTTTAGTT | 79582 |
rs79216624 | snp | A/G | | | intron-variant, upstream-variant-2KB | SPAG16, LOC101928084 | GRCh38.p7 | 2:214103938 | GTTGGAGGGAGAGAG[A/G]GAAACAGAGAGAGAG | 79582 |
rs79218614 | snp | C/T | 0.0498117 | 0.149749 | intron-variant | SPAG16 | GRCh38.p7 | 2:213795942 | TAAATTACCCAGCCT[C/T]AAGTGTTTCTTTATA | 79582 |
rs79222896 | in-del | -/TT | | | intron-variant | SPAG16 | GRCh38.p7 | 2:213850698 | ATTCTGTTTTTTTTT[-/TT]ATGATTTTCTTCTGG | 79582 |
rs79226278 | snp | C/T | 0.0205511 | 0.0992634 | intron-variant | SPAG16 | GRCh38.p7 | 2:213827205 | GTTATTAATGACCTA[C/T]TCTGGCCATTTTGTT | 79582 |
rs79233131 | snp | G/T | 0.00398564 | 0.0444627 | intron-variant | SPAG16 | GRCh38.p7 | 2:213432361 | GATTAACCAAGAAAA[G/T]AAGTGAGAAGATCCA | 79582 |
rs79234054 | snp | A/C | 0.155325 | 0.23138 | intron-variant | SPAG16 | GRCh38.p7 | 2:213436906 | TACTACGCAAAAATG[A/C]TAAACTCTTTTTTTT | 79582 |
rs79246157 | snp | A/G | 0.0463947 | 0.145069 | intron-variant | SPAG16 | GRCh38.p7 | 2:213363867 | GCTTACCTAAAATAA[A/G]TAATTAATAATTAGC | 79582 |
rs79260980 | snp | A/T | 0.0178098 | 0.0926698 | intron-variant | SPAG16 | GRCh38.p7 | 2:214148149 | GCCAATACTCATTCA[A/T]TTTGTGAGTGGACAA | 79582 |
rs79261505 | snp | C/T | 0.0349115 | 0.127424 | intron-variant | SPAG16 | GRCh38.p7 | 2:214389746 | GCCAATTTTTTGAAT[C/T]CATTTTTACTAAATA | 79582 |
rs79265151 | snp | C/T | 0.0142736 | 0.0832652 | intron-variant | SPAG16 | GRCh38.p7 | 2:214393066 | TTAAGGCAGAAGTTA[C/T]TTTTCACTATAGTTC | 79582 |
rs79272136 | snp | A/C | 0.5 | 0 | intron-variant | SPAG16 | GRCh38.p7 | 2:214078535 | TAAGAGCCTGTCTCA[A/C]AAAAAAAAAAAAAAA | 79582 |
rs79277423 | snp | A/G | 0.00755907 | 0.0610114 | intron-variant | SPAG16 | GRCh38.p7 | 2:214288162 | TCCCACGTATGCATG[A/G]AAACATATAGTATCT | 79582 |
rs79279555 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | SPAG16 | GRCh38.p7 | 2:214168746 | GTCCACGTGATTAGA[A/G]TGGAATGAATAAGGA | 79582 |
rs79283419 | snp | A/T | 0.0980852 | 0.198549 | intron-variant, upstream-variant-2KB | SPAG16 | GRCh38.p7 | 2:213342686 | ATTTCTGCTTTGGGC[A/T]ATGTCATTGTAAATA | 79582 |
rs79288876 | snp | C/G | 0.131381 | 0.220067 | intron-variant | SPAG16 | GRCh38.p7 | 2:213437269 | ATCACATTGCCCATG[C/G]CTTATCTCTTACTAA | 79582 |
rs79288941 | snp | A/C | 0.5 | 0 | intron-variant | SPAG16 | GRCh38.p7 | 2:213323440 | AGCAAGACTCCGTCT[A/C]AAAAAAAAAATAGAA | 79582 |
rs79289456 | snp | C/G | 0.0189856 | 0.0955633 | intron-variant | SPAG16 | GRCh38.p7 | 2:213869988 | ACTACCATATGTCAA[C/G]TATTGCAATTGTACG | 79582 |
rs79291285 | snp | A/G | 0.0236746 | 0.106192 | intron-variant | SPAG16 | GRCh38.p7 | 2:213528681 | GTAATCCTTTCTTGT[A/G]TCTAAATCAGGGGTA | 79582 |
rs79295463 | snp | A/C | 0.00636936 | 0.0560724 | intron-variant | SPAG16 | GRCh38.p7 | 2:214315035 | ATGAATGCTTCTGAG[A/C]CCATCACATCCTAGT | 79582 |
rs79305520 | snp | C/T | 0.00993419 | 0.0697739 | intron-variant | SPAG16 | GRCh38.p7 | 2:214311200 | CTGCATTCCCCCTCT[C/T]TCCCTCTCTCTAGGG | 79582 |
rs79306244 | snp | C/G | 0.0185938 | 0.0946107 | intron-variant | SPAG16 | GRCh38.p7 | 2:213667514 | TCACAGTAATAGACA[C/G]AGAAGTAGGAAAATT | 79582 |
rs79308629 | snp | G/T | 0.00835141 | 0.0640778 | intron-variant | SPAG16 | GRCh38.p7 | 2:213919775 | TATTCTATTTGTTTT[G/T]GGAGGGGAGAGTTCT | 79582 |
rs79311344 | snp | C/T | 0.00199481 | 0.0315187 | intron-variant | SPAG16 | GRCh38.p7 | 2:214366472 | AGAACGATTACTCAA[C/T]GCAGTGTAAAGTGAT | 79582 |
rs79331115 | snp | A/G | 0.0150606 | 0.0854603 | intron-variant | SPAG16 | GRCh38.p7 | 2:214292006 | TTATTGATGAAGAAT[A/G]ATTTTGCTGTGCATG | 79582 |
rs79334270 | snp | A/G | 0.103082 | 0.202275 | intron-variant | SPAG16 | GRCh38.p7 | 2:213685294 | CCAATCCAATATGAC[A/G]CGTGTTCTTGTAAGA | 79582 |
rs79335224 | snp | C/T | 0.0111196 | 0.0737302 | intron-variant | SPAG16 | GRCh38.p7 | 2:214213966 | TATTTTCTTCATGGC[C/T]CCTTCATTTAAGGTG | 79582 |
rs79342306 | snp | A/T | 0.5 | 0 | intron-variant, upstream-variant-2KB | SPAG16 | GRCh38.p7 | 2:213299439 | CCACACCGAGCTAAT[A/T]TTTTTTTTTTTTGTA | 79582 |
rs79342512 | snp | A/C | 0.0379877 | 0.132479 | intron-variant | SPAG16 | GRCh38.p7 | 2:214346340 | TGACTAATGTGGCTG[A/C]GAACTTTTTCAAGTT | 79582 |
rs79352227 | snp | A/C | 0.0402882 | 0.136092 | intron-variant | SPAG16 | GRCh38.p7 | 2:214112968 | CTGGTACTGGTTGTT[A/C]CTTTCTATGTTTAGT | 79582 |
rs79357572 | snp | A/C | 0.104504 | 0.2033 | intron-variant | SPAG16 | GRCh38.p7 | 2:214347934 | CCTCAGAGGACAGAG[A/C]CAAGATTCATGGAGA | 79582 |
rs79357991 | snp | C/T | 0.0236746 | 0.106192 | intron-variant | SPAG16 | GRCh38.p7 | 2:213341220 | TGAATCACTAAAGCT[C/T]ATTTTATAAAGACCT | 79582 |
rs79358385 | snp | A/T | 0 | 0 | intron-variant | SPAG16 | GRCh38.p7 | 2:213864934 | TTAATAGGTAAAAAA[A/T]TAAACTGAGGGGATA | 79582 |
rs79364370 | snp | A/G | 0.00517822 | 0.0506191 | intron-variant | SPAG16 | GRCh38.p7 | 2:213702579 | GAACCCACCAGTTCC[A/G]GACACAATAATATTT | 79582 |
rs79370332 | snp | C/T | 0.0505692 | 0.150756 | intron-variant | SPAG16 | GRCh38.p7 | 2:213633098 | GAAGCCATCAGGTCC[C/T]GGACTTTTCTTCACT | 79582 |
rs79372452 | snp | A/G | 0.102726 | 0.202016 | intron-variant | SPAG16 | GRCh38.p7 | 2:214383204 | TGGCACTGGAAAGAG[A/G]TTCTGATACTATGAA | 79582 |
rs79375345 | snp | C/T | 0.11963 | 0.213316 | intron-variant | SPAG16 | GRCh38.p7 | 2:214351791 | TTTTTTTTTAGTTTT[C/T]AGATTTTTTAACTTC | 79582 |
rs79378261 | snp | A/G | 0.00835141 | 0.0640778 | intron-variant | SPAG16 | GRCh38.p7 | 2:213645680 | AAGCAAAATGGAGGG[A/G]TCTCTTGGAGCTGGA | 79582 |
rs79391756 | snp | C/T | 0 | 0 | intron-variant | SPAG16 | GRCh38.p7 | 2:214126062 | CTTCCTTCCTTCCTT[C/T]TTTTTTTTTTTTTTT | 79582 |
rs79394204 | snp | C/T | 0.5 | 0 | intron-variant | SPAG16 | GRCh38.p7 | 2:213963095 | TGCTTAGTTTGCTCT[C/T]TTTTTTTTTTTTTAA | 79582 |
rs79396085 | snp | G/T | | | intron-variant | SPAG16 | GRCh38.p7 | 2:214001985 | CAATTGTGGCTGAAT[G/T]TGAAAGGCACAGCTT | 79582 |
rs79407203 | snp | A/G | 0.100231 | 0.200173 | intron-variant | SPAG16 | GRCh38.p7 | 2:213662379 | ACTAAAAGAAGGCCA[A/G]TGTGGAAAAAACGAA | 79582 |
rs79412442 | snp | A/G | 0 | 0 | intron-variant | SPAG16 | GRCh38.p7 | 2:213917687 | GGGCTGAGATGATGG[A/G]GTTTTCAAGATATAG | 79582 |
rs79415062 | snp | C/T | 0.0263992 | 0.111815 | intron-variant | SPAG16 | GRCh38.p7 | 2:213618321 | TGCCTTCTACTCTAT[C/T]CTCACTGCCTGATCA | 79582 |
rs79422976 | snp | G/T | 0.0554779 | 0.157039 | intron-variant | SPAG16 | GRCh38.p7 | 2:214214736 | ATTAATATAAAATTA[G/T]GTATATTTATTTAGA | 79582 |
rs79424641 | in-del | -/AAG | 0.34437 | 0.231505 | intron-variant | SPAG16 | GRCh38.p7 | 2:214205233 | TGCCAAAAAAAAAGA[-/AAG]AAGAAGAAGCTATAT | 79582 |
rs79427976 | snp | A/G | 0.00517822 | 0.0506191 | intron-variant | SPAG16 | GRCh38.p7 | 2:213566736 | CCTTCTGGTGATGGT[A/G]TATAATGACACATTC | 79582 |
rs79435921 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | SPAG16 | GRCh38.p7 | 2:213929675 | CCAAACAAACACATG[A/T]TAACAAAAACACTAA | 79582 |
rs79436075 | snp | A/G | 0.0154538 | 0.0865337 | intron-variant | SPAG16 | GRCh38.p7 | 2:213993699 | AAACATATTGAATCC[A/G]AAGATAAAGTATAGT | 79582 |
rs79439862 | snp | A/G | 0.0138799 | 0.0821421 | intron-variant | SPAG16 | GRCh38.p7 | 2:213959160 | TGCATGAAACAAGTT[A/G]CTTATTTCTTAGAAT | 79582 |
rs79440653 | snp | A/T | 0.0554779 | 0.157039 | intron-variant | SPAG16 | GRCh38.p7 | 2:213983027 | TTTACTTTAAATCAC[A/T]TTGTCTTCCATATAT | 79582 |
rs79443057 | snp | C/T | 0.0452528 | 0.143452 | intron-variant | SPAG16 | GRCh38.p7 | 2:213475822 | AGGAAAGAAAAGGAA[C/T]CCTGAGAACTGGGGA | 79582 |
rs79444819 | snp | A/G | 0.0633504 | 0.166319 | intron-variant | SPAG16 | GRCh38.p7 | 2:213744082 | ATTCATTCCTTCAGA[A/G]GATTTACTTTTGCTA | 79582 |
rs79446022 | snp | A/G | 0.0119091 | 0.0762411 | intron-variant | SPAG16 | GRCh38.p7 | 2:213605909 | ATATAAACAACTTAC[A/G]TCAGGATATATAATA | 79582 |
rs79446577 | snp | C/G | 0 | 0 | intron-variant | SPAG16 | GRCh38.p7 | 2:213718523 | TGGCGCGCAAGCGCC[C/G]CACGCAGCCCCGGTT | 79582 |
rs79456468 | snp | C/T | 0.462582 | 0.131564 | intron-variant | SPAG16 | GRCh38.p7 | 2:214276551 | TTTCTACTTCACTTA[C/T]GATGCTTAGTTTGGC | 79582 |
rs79464968 | snp | C/T | 0.0209421 | 0.100162 | intron-variant | SPAG16 | GRCh38.p7 | 2:213864982 | CAGCTAATATGATGT[C/T]GAAATATATAAAACA | 79582 |
rs79465587 | snp | G/T | 0.0168055 | 0.0901129 | intron-variant | SPAG16 | GRCh38.p7 | 2:213878368 | TTTAAATAACAGACC[G/T]TCTAACTAGTTTAAG | 79582 |
rs79471308 | snp | A/G | 0.0209421 | 0.100162 | intron-variant | SPAG16 | GRCh38.p7 | 2:213834375 | GTGTGTTTTTATGCT[A/G]AGTCTGATGAAAAAA | 79582 |
rs79475365 | snp | A/G | 0.170733 | 0.237101 | intron-variant | SPAG16 | GRCh38.p7 | 2:213560850 | CACACAATGAATGAC[A/G]AAGTTAGCAACCATT | 79582 |
rs79476377 | snp | A/C | 0.0185938 | 0.0946107 | intron-variant | SPAG16 | GRCh38.p7 | 2:213805483 | TTCAGAGAACCAACC[A/C]AGGCCAATAGAGATA | 79582 |
rs79478253 | snp | A/C | 0.021333 | 0.101051 | intron-variant | SPAG16 | GRCh38.p7 | 2:213781494 | AGTGCTCATTCTCCT[A/C]ACCCCTCCCCTGCCC | 79582 |
rs79487019 | snp | A/G | 0.0142736 | 0.0832652 | intron-variant | SPAG16 | GRCh38.p7 | 2:214367572 | GGAAGTAGCAGTTCT[A/G]CAGGGAAAAGATGAA | 79582 |
rs79487220 | snp | A/G | 0.193028 | 0.243422 | intron-variant | SPAG16 | GRCh38.p7 | 2:213449315 | TATAGACCCTTATCA[A/G]TGGCTCTGCTTTTTC | 79582 |
rs79489080 | snp | C/T | 0.0569829 | 0.158885 | intron-variant | SPAG16 | GRCh38.p7 | 2:214202131 | GATTACAGGTTTAAG[C/T]TACCATGCTCAGCCA | 79582 |
rs79492713 | snp | C/G | 0.0182019 | 0.0936463 | intron-variant | SPAG16 | GRCh38.p7 | 2:213727586 | GACGTGGAAATGTTT[C/G]TACATAGCAATTGCG | 79582 |
rs79500785 | snp | C/T | 0.046775 | 0.145601 | intron-variant | SPAG16 | GRCh38.p7 | 2:213336063 | AGCAAAGAAGAGCAT[C/T]GAGGGCCCACCCAAG | 79582 |
rs79504240 | snp | A/G | 0.144632 | 0.226711 | intron-variant | SPAG16 | GRCh38.p7 | 2:213709130 | GTCAGTGCACCATTG[A/G]CATTGAACAAAATTT | 79582 |
rs79504248 | snp | C/T | 0.0244538 | 0.107838 | intron-variant | SPAG16 | GRCh38.p7 | 2:213451578 | ACTCAGACGCACACA[C/T]GCATAGTGAAATTGG | 79582 |
rs79505302 | snp | A/T | 0.5 | 0 | intron-variant | SPAG16 | GRCh38.p7 | 2:213453854 | ATAGGTAGATTTTTT[A/T]ATGTTGTTGGCTGTT | 79582 |
rs79511084 | snp | C/T | 0.0146672 | 0.084371 | intron-variant | SPAG16 | GRCh38.p7 | 2:214362799 | AATTTTATAGGAAAG[C/T]TAAAGTACAAATAGC | 79582 |
rs79513523 | snp | A/T | 0 | 0 | intron-variant | SPAG16 | GRCh38.p7 | 2:213822820 | AAAACCAAACACCAC[A/T]TGTTCTCACTCCTAG | 79582 |
rs79514642 | snp | A/G | 0.0271762 | 0.113356 | intron-variant | SPAG16 | GRCh38.p7 | 2:213329952 | TTGCTTCAGAGGATC[A/G]AAACCCAAAGCCTTG | 79582 |
rs79514917 | snp | A/G | 0.00478085 | 0.0486577 | intron-variant | SPAG16 | GRCh38.p7 | 2:213935753 | GTAGTTAAGCTGATG[A/G]AATAAAAACAGTACC | 79582 |
rs79515104 | snp | A/G | 0.00557542 | 0.0525036 | intron-variant | SPAG16 | GRCh38.p7 | 2:213982067 | TTATAGATGAACTGT[A/G]ACAAATATGTCCTTA | 79582 |
rs79520696 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | SPAG16 | GRCh38.p7 | 2:213324365 | AAACTCTTAAACATC[C/T]ACATTCATCTCAAGG | 79582 |
rs79521074 | snp | A/C | 0.267091 | 0.249415 | intron-variant | SPAG16 | GRCh38.p7 | 2:213776238 | GTCTAATCATAGGAG[A/C]CCTTAAAAGTGGATA | 79582 |
rs79522852 | snp | A/G | 0.0287284 | 0.116357 | intron-variant | SPAG16 | GRCh38.p7 | 2:213801592 | GACCTATGTGCTAAG[A/G]TTGATTTCAAAAAGA | 79582 |
rs79524255 | snp | A/G | 0.132066 | 0.220435 | intron-variant | SPAG16 | GRCh38.p7 | 2:213289486 | TAATAAGAATTCTGA[A/G]TCCTCATGAAGACTG | 79582 |
rs79533181 | snp | A/G | 0.0166325 | 0.0896639 | intron-variant | SPAG16 | GRCh38.p7 | 2:214267534 | GTAAGACCTGAAACT[A/G]TAAAACTATTAAAAG | 79582 |
rs79533533 | snp | A/G | 0.121369 | 0.214369 | intron-variant | SPAG16 | GRCh38.p7 | 2:214142123 | AATTTTCCAGATTGT[A/G]ATATTCCAATCCACT | 79582 |
rs79534326 | snp | C/G | 0.0256215 | 0.110247 | intron-variant | SPAG16 | GRCh38.p7 | 2:214301568 | CTTTCTAGTTTGTTT[C/G]CATAGAGATGTTCAT | 79582 |
rs79534503 | snp | C/G | 0.0267878 | 0.112589 | intron-variant | SPAG16 | GRCh38.p7 | 2:214225954 | TGGTATCTTTTCTTC[C/G]TGGCTAGGTAGTTAT | 79582 |
rs79539084 | snp | A/G | 0.10237 | 0.201756 | intron-variant | SPAG16 | GRCh38.p7 | 2:213682634 | TTTTATTGTGGGGTC[A/G]GCATGTCTCTGGACA | 79582 |
rs79543117 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | SPAG16 | GRCh38.p7 | 2:213793322 | AGTACCCCAAACATA[C/T]AAAGCAACAAAACAT | 79582 |
rs79545949 | snp | A/C | 0.5 | 0 | intron-variant | SPAG16 | GRCh38.p7 | 2:214080607 | AGCGAGACTCTGTCT[A/C]AAAAAAAAAAAAAAA | 79582 |
rs79547554 | snp | A/G | 0.0729998 | 0.176553 | intron-variant | SPAG16 | GRCh38.p7 | 2:213424862 | CTCTACTGAGCTGGG[A/G]ACCCAGCCACTGAGT | 79582 |
rs79556087 | snp | C/T | 0 | 0 | intron-variant | SPAG16 | GRCh38.p7 | 2:213312676 | GGGTGGCAATGAAAA[C/T]GCCATCAAAAGTAAT | 79582 |
rs79556606 | snp | A/G | 0.00755907 | 0.0610114 | intron-variant | SPAG16 | GRCh38.p7 | 2:214296252 | CTTTTTTATGGTTGC[A/G]TAGAATTCCATAGTG | 79582 |
rs79571856 | snp | G/T | 0.0130921 | 0.0798413 | intron-variant | SPAG16 | GRCh38.p7 | 2:213664065 | TCTACAGGAGAATTA[G/T]ATTTTTTGCCTTTAA | 79582 |
rs79573482 | snp | A/C | | | intron-variant | SPAG16 | GRCh38.p7 | 2:213843738 | TGTCTGTAGTTCCAG[A/C]TACTTGGGAGGCTGA | 79582 |
rs79574741 | snp | A/C | 0.0197687 | 0.0974348 | intron-variant | SPAG16 | GRCh38.p7 | 2:213816870 | ATTCCACCTGTGAAG[A/C]CCAATATTACTGTAA | 79582 |
rs79574940 | snp | A/G | 0.0506333 | 0.150841 | intron-variant | SPAG16 | GRCh38.p7 | 2:213310201 | TTATGTAGATAAATA[A/G]TTCTCTTAAAATTCT | 79582 |
rs79587545 | snp | C/T | 0.0341408 | 0.126114 | intron-variant | SPAG16 | GRCh38.p7 | 2:214170674 | GCAAGTACTGATCAA[C/T]TTCAGGTCAATTGGA | 79582 |
rs79587720 | snp | G/T | 0.0178098 | 0.0926698 | intron-variant | SPAG16 | GRCh38.p7 | 2:213621027 | ACTAGTTTTAGTACT[G/T]ACCTTTAATTTTCTA | 79582 |
rs79589120 | snp | A/G | 0.0260105 | 0.111035 | intron-variant | SPAG16 | GRCh38.p7 | 2:214138834 | CTCCTACCTGAGCCA[A/G]ATTCCTACCCCTTAA | 79582 |
rs79589269 | snp | C/T | 0.00755907 | 0.0610114 | intron-variant | SPAG16 | GRCh38.p7 | 2:213897891 | ATAGCAATCATCCTC[C/T]TATAAAAAGGATTTC | 79582 |
rs79590848 | snp | C/G | 0.5 | 0 | intron-variant | SPAG16 | GRCh38.p7 | 2:213735271 | CTCTTTACCAGATTT[C/G]TGATTGTGAATTATT | 79582 |
rs79593886 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | SPAG16 | GRCh38.p7 | 2:214025180 | AATGCTAGAGACAAG[C/T]CTTCTCATGATTTGT | 79582 |
rs79598006 | snp | A/C | 0.0154538 | 0.0865337 | intron-variant | SPAG16 | GRCh38.p7 | 2:213340044 | CGATGAGAATTATAG[A/C]AAAATATTTGTTTTC | 79582 |
rs79604755 | snp | C/G | 0.191775 | 0.243125 | intron-variant | SPAG16 | GRCh38.p7 | 2:214352202 | ATAATTTCAACATAT[C/G]AATCAGGAGAGACAC | 79582 |
rs79611657 | snp | A/G | 0.0217236 | 0.101931 | intron-variant | SPAG16 | GRCh38.p7 | 2:214208680 | TTTTTTTTAGTTTTT[A/G]CAATCAGACCTTGGT | 79582 |
rs79611940 | snp | C/G | 0.0209421 | 0.100162 | intron-variant | SPAG16 | GRCh38.p7 | 2:214228664 | AAGTCTGCAATTAGG[C/G]CCCAGCCATCAGTAT | 79582 |
rs79613844 | snp | G/T | 0 | 0 | intron-variant | SPAG16 | GRCh38.p7 | 2:213720760 | TTTTTTTTTTTTTTT[G/T]TTTGAGATGGAGTCT | 79582 |
rs79622420 | snp | A/G | 0.0448719 | 0.142907 | intron-variant | SPAG16 | GRCh38.p7 | 2:213458251 | CATCTGAGATCATTT[A/G]CCTTCTAAATGATGA | 79582 |
rs79625560 | snp | A/T | | | intron-variant | SPAG16 | GRCh38.p7 | 2:214314152 | ACATGGTCAGTTGCT[A/T]CTGGAAATAATTTTA | 79582 |
rs79630471 | snp | A/G | 0.0170251 | 0.090679 | intron-variant | SPAG16 | GRCh38.p7 | 2:213889349 | CTGAGAAAATCTTAC[A/G]AGAATTATCTAGGTA | 79582 |
rs79630954 | snp | C/T | 0.0142736 | 0.0832652 | intron-variant | SPAG16 | GRCh38.p7 | 2:213760646 | TAGACTATATGTTAC[C/T]TCATAAATTAAGTCT | 79582 |
rs79635870 | snp | A/G | 0.00993419 | 0.0697739 | intron-variant | SPAG16 | GRCh38.p7 | 2:213648907 | CCACAATGAAAGGAT[A/G]TGGCTGACAGACCCT | 79582 |
rs79637084 | snp | A/G/T | 0.0189856 | 0.0955633 | intron-variant | SPAG16 | GRCh38.p7 | 2:213663868 | TTAGTGGGAAAAAGT[A/G/T]GGAAATTAAATTGTA | 79582 |
rs79645362 | in-del | -/CAGAGAGAGAGAGA | | | intron-variant | SPAG16 | GRCh38.p7 | 2:213871879 | ACACACACACACACA[-/CAGAGAGAGAGAGA]GAGAGAGCAAACAGC | 79582 |
rs79647926 | snp | G/T | 0.0165278 | 0.0893908 | intron-variant | SPAG16 | GRCh38.p7 | 2:214025780 | ATTTAGTATACTCAG[G/T]CATTTCATTCAATAA | 79582 |
rs79648724 | snp | C/T | 0.0984431 | 0.198823 | intron-variant | SPAG16 | GRCh38.p7 | 2:214372875 | TCACCCAGGCTGCTG[C/T]TTTTAAGATTAGAAA | 79582 |
rs79649105 | snp | C/T | 0.0364509 | 0.129988 | intron-variant, downstream-variant-500B | SPAG16 | GRCh38.p7 | 2:213703909 | GTTTCTTCACAGATA[C/T]TACCTTCCAAGATAT | 79582 |
rs79669445 | in-del | -/TTGGTTAAAGAAAATATGTTATCTAT | | | intron-variant | SPAG16 | GRCh38.p7 | 2:213590920 | CTCATCAGTGATGGA[-/TTGGTTAAAGAAAATATGTTATCTAT]ACACCATAGAATATT | 79582 |
rs79671142 | snp | C/G | 0.084728 | 0.187577 | intron-variant | SPAG16 | GRCh38.p7 | 2:213698939 | GCACATCAAGTACAA[C/G]GCATAGTACCTGGCA | 79582 |
rs79671212 | snp | G/T | 0.0165278 | 0.0893908 | intron-variant | SPAG16 | GRCh38.p7 | 2:213628019 | TCAAAGAGAAAGTAA[G/T]ACATGAGCCTTAGCA | 79582 |
rs79671248 | snp | A/T | 0.5 | 0 | intron-variant | SPAG16 | GRCh38.p7 | 2:214260358 | AAAAAGAATATCTAA[A/T]TTTTTTTTTTTCTTT | 79582 |
rs79672528 | snp | C/T | 0.0221141 | 0.102801 | intron-variant | SPAG16 | GRCh38.p7 | 2:213459644 | TTGTTTCAATTTCTT[C/T]GCTTTCTCCATCAGA | 79582 |
rs79672987 | snp | A/G | 0.021333 | 0.101051 | intron-variant | SPAG16 | GRCh38.p7 | 2:213491093 | GTGAGAACATAGCAC[A/G]TATGAATACTTCTGT | 79582 |
rs79677965 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | SPAG16 | GRCh38.p7 | 2:213460168 | TTTATTTTCACTTGC[A/G]TTTACATTTTTTTTC | 79582 |
rs79684719 | snp | C/T | 0.00835141 | 0.0640778 | intron-variant | SPAG16 | GRCh38.p7 | 2:213699010 | AGCTTCTTCTTTTCC[C/T]CTCTAAGTTCTGTTT | 79582 |
rs79687974 | snp | C/T | 0.312104 | 0.242163 | intron-variant | SPAG16 | GRCh38.p7 | 2:213736298 | TGTAGGTTCAGATTT[C/T]TTTTTCTTTTTTTGA | 79582 |
rs79692760 | snp | A/T | 0.5 | 0 | intron-variant | SPAG16 | GRCh38.p7 | 2:213647043 | TAGATGAGTAAAAAG[A/T]ATATGAAAAGAAAAG | 79582 |
rs79693060 | snp | A/C | 0.0456336 | 0.143994 | intron-variant | SPAG16 | GRCh38.p7 | 2:213450961 | TGGAATTAATTAAAA[A/C]CTGAAGCAAAATTGA | 79582 |
rs79695387 | snp | A/T | 0.0471551 | 0.14613 | intron-variant | SPAG16 | GRCh38.p7 | 2:214004900 | TTACAAATATATTTT[A/T]TTAAATAGGCAAATT | 79582 |
rs79695932 | snp | C/T | 0.128632 | 0.218563 | intron-variant | SPAG16 | GRCh38.p7 | 2:213505298 | AAATTTATATGTGGA[C/T]ACAATTTTTTTTTAC | 79582 |
rs79712479 | snp | A/G | 0.00914312 | 0.0669923 | intron-variant | SPAG16 | GRCh38.p7 | 2:214183454 | CTCTGCAAGTCTCTC[A/G]GCCCTTTTACTCTCA | 79582 |
rs79714046 | snp | A/G | 0.0352966 | 0.128072 | intron-variant | SPAG16 | GRCh38.p7 | 2:213948590 | ACACTAGCTTTTATG[A/G]ATAATTTGTTCTATG | 79582 |
rs79714211 | snp | A/G | 0.0170251 | 0.090679 | intron-variant | SPAG16 | GRCh38.p7 | 2:214120687 | ATATCCACAGGCACC[A/G]CTTCTCAATCTACTG | 79582 |
rs79722459 | snp | C/T | 0.0193772 | 0.0965046 | intron-variant | SPAG16 | GRCh38.p7 | 2:213817782 | CTGGGTACTCAGGGG[C/T]ATAAAGATGGCAACA | 79582 |
rs79731702 | snp | A/C | 0.00318978 | 0.0398085 | intron-variant | SPAG16 | GRCh38.p7 | 2:214055364 | TTACTAAATGGACTA[A/C]TTTTCTTAACTAACT | 79582 |
rs79732679 | snp | C/T | 0.155656 | 0.231515 | intron-variant, utr-variant-3-prime | SPAG16 | GRCh38.p7 | 2:213400807 | GATTTTTTTAGTCTT[C/T]GTTTTTTTCTTTTTT | 79582 |
rs79733149 | snp | A/G | 0.0209421 | 0.100162 | intron-variant | SPAG16 | GRCh38.p7 | 2:213899363 | AAAAACATATCAATA[A/G]AAGGAAGACTTTCTA | 79582 |
rs79734283 | snp | G/T | 0.0279526 | 0.114869 | intron-variant | SPAG16 | GRCh38.p7 | 2:213582357 | GTAAGGAATAAAAGT[G/T]ATTTTTAACATTGAC | 79582 |
rs79734939 | snp | C/T | 0.125182 | 0.216612 | intron-variant | SPAG16 | GRCh38.p7 | 2:213655306 | GAAAATTAATGTCTA[C/T]TTTTAAAAAACTCTT | 79582 |
rs79735036 | snp | C/T | 0.0652144 | 0.168387 | intron-variant | SPAG16 | GRCh38.p7 | 2:213963889 | GGTGTTTCCTTTCCC[C/T]ATTCTTTTCAATCTA | 79582 |
rs79736503 | snp | A/G | 0.00318978 | 0.0398085 | intron-variant | SPAG16 | GRCh38.p7 | 2:213321659 | AAGCAGGGAATTGTC[A/G]TTTTCTCTGTTGTCA | 79582 |
rs79744726 | snp | A/G | 0.0225045 | 0.103662 | intron-variant | SPAG16 | GRCh38.p7 | 2:213646291 | GGTGTCCTTATGGGG[A/G]CGGGGTTGGGGGATG | 79582 |
rs79745791 | snp | C/G | 0.00159617 | 0.0282053 | intron-variant | SPAG16 | GRCh38.p7 | 2:213763011 | CAAAGACATAAAAAT[C/G]TTCAACAGGTGTATG | 79582 |
rs79746859 | snp | A/G | 0.0174175 | 0.0916809 | intron-variant | SPAG16 | GRCh38.p7 | 2:214180903 | ACTCATGCCAAACCA[A/G]CCTGGGATCATTTTG | 79582 |
rs79748029 | snp | C/G | 0.000798403 | 0.0199641 | intron-variant | SPAG16 | GRCh38.p7 | 2:213425958 | TTGTAGTGCCAGGAA[C/G]CATTTTCTCATTCCA | 79582 |
rs79749309 | snp | A/C | 0.5 | 0 | intron-variant | SPAG16 | GRCh38.p7 | 2:213911835 | ATGAGAAACAGTTAG[A/C]AAAAAAAAAAAAAAA | 79582 |
rs79754619 | snp | C/T | 0.00199481 | 0.0315187 | intron-variant | SPAG16 | GRCh38.p7 | 2:213997795 | TTTAGTAATTTATGT[C/T]GGACCACATTCAGAG | 79582 |
rs79756641 | snp | A/C | | | intron-variant | SPAG16, LOC101928084 | GRCh38.p7 | 2:214087106 | GATATATCAGAGCCT[A/C]AGGCACTGTACTAAT | 79582 |
rs79762062 | snp | A/G | 0.0182019 | 0.0936463 | intron-variant | SPAG16 | GRCh38.p7 | 2:214261939 | CTGAATTATTAGACA[A/G]ACATCTCTGTAAATA | 79582 |
rs79767514 | snp | A/G | | | intron-variant | SPAG16 | GRCh38.p7 | 2:213389040 | AAGCTACAGTAATCA[A/G]AACAGTATGGTACTG | 79582 |
rs79767721 | snp | A/G | 0.5 | 0 | intron-variant | SPAG16 | GRCh38.p7 | 2:214164388 | GAAGTGATACACATG[A/G]GCAGACACCTGGATG | 79582 |
rs79771804 | snp | A/G | 0.0228947 | 0.104514 | intron-variant | SPAG16 | GRCh38.p7 | 2:213989802 | ATAGGGAGTATATAT[A/G]ATTTGCCTGTAGTTA | 79582 |
rs79773524 | snp | C/T | 0.0134861 | 0.0810011 | intron-variant | SPAG16 | GRCh38.p7 | 2:214014214 | GTAAAAAGTTCATAA[C/T]TACAAGATCCTTTCT | 79582 |
rs79774522 | snp | A/G | 0.0197687 | 0.0974348 | intron-variant | SPAG16 | GRCh38.p7 | 2:213849690 | GACTATATGTAGTTT[A/G]TATTTCTAGATATTC | 79582 |
rs79783691 | snp | A/T | 0.00676609 | 0.0577691 | intron-variant | SPAG16 | GRCh38.p7 | 2:214287340 | TTCTGTATCCCATTA[A/T]AGAAATGGCATCATG | 79582 |
rs79785374 | snp | G/T | 0.00119737 | 0.0244387 | intron-variant | SPAG16 | GRCh38.p7 | 2:214310234 | TCCTCCCTTGAAGGT[G/T]TGACTGTAGTACATA | 79582 |
rs79787098 | snp | C/G | 0.0275645 | 0.114116 | intron-variant | SPAG16 | GRCh38.p7 | 2:213428198 | GCAGCCTGTGTGGTG[C/G]TGTCTGACTGAGAGC | 79582 |
rs79788945 | snp | C/T | 0.00874735 | 0.0655527 | intron-variant | SPAG16 | GRCh38.p7 | 2:213365700 | TGTCTTGAAGTGATC[C/T]GCCTGCCTCAGCCTC | 79582 |
rs79792015 | snp | A/G | 0.0217236 | 0.101931 | intron-variant | SPAG16 | GRCh38.p7 | 2:213693535 | AAACAAAAATACATG[A/G]TGTAGCTTGCTAAAT | 79582 |
rs79805463 | snp | C/T | 0.0154538 | 0.0865337 | intron-variant | SPAG16 | GRCh38.p7 | 2:214006942 | ATTGAAGAATTGCTC[C/T]TTCCCCCCCACCACC | 79582 |
rs79810308 | snp | A/C | 0.0792508 | 0.182605 | intron-variant | SPAG16 | GRCh38.p7 | 2:214134740 | CTTAACTTACTGAGA[A/C]TAGTGGCCTTCAACA | 79582 |
rs79815203 | snp | C/T | 0.00398564 | 0.0444627 | intron-variant | SPAG16 | GRCh38.p7 | 2:214269937 | ATGTTATTTCCTGAT[C/T]GAGATCTTATAATGA | 79582 |
rs79816343 | snp | A/C | 0.00159617 | 0.0282053 | intron-variant | SPAG16 | GRCh38.p7 | 2:214352472 | ATTTAGACTTTCTTC[A/C]GTCTTGAAATTCCAT | 79582 |
rs79818817 | snp | A/C | 0.5 | 0 | intron-variant | SPAG16 | GRCh38.p7 | 2:213733112 | CTGGCCATCAGAGAA[A/C]TGCAAATCAAAACCA | 79582 |
rs79821764 | snp | C/T | 0.00318978 | 0.0398085 | intron-variant | SPAG16 | GRCh38.p7 | 2:213724163 | ATAGTATAAGGAAAA[C/T]ATTGTCTTGGGAAAA | 79582 |
rs79827490 | snp | C/T | 0.0271762 | 0.113356 | intron-variant | SPAG16 | GRCh38.p7 | 2:213354367 | TGCATGTATCTTTAT[C/T]GTAGCATCATTTATA | 79582 |
rs79828478 | snp | C/G | 0.0807149 | 0.183963 | intron-variant | SPAG16 | GRCh38.p7 | 2:214119819 | AGTAAACTTTTTTTG[C/G]TCTTTGTATATCTGG | 79582 |
rs79828999 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | SPAG16 | GRCh38.p7 | 2:214202967 | TCTCTTTTGGTACAA[A/G]AAAAATCTAAAGTTT | 79582 |
rs79830994 | snp | A/C | | | intron-variant | SPAG16 | GRCh38.p7 | 2:213866977 | AGAAGGCATTTAAAA[A/C]TTGCAAGTCTTCAAA | 79582 |
rs79833778 | snp | A/T | 0.131723 | 0.220251 | intron-variant | SPAG16 | GRCh38.p7 | 2:213621900 | TATGTTTGGGTGGGA[A/T]CCAGGACTACATTTT | 79582 |
rs79839364 | snp | A/G | 0 | 0 | intron-variant | SPAG16 | GRCh38.p7 | 2:213718512 | GCGCGAGCGGGAACC[A/G]GGGCTGCGTGCGGCG | 79582 |
rs79841142 | snp | A/T | 0.0209421 | 0.100162 | intron-variant | SPAG16 | GRCh38.p7 | 2:214164993 | GGAGGAGATAGTTCA[A/T]GAGTTTGCTACTTTC | 79582 |
rs79843454 | snp | A/C | 0.0193772 | 0.0965046 | intron-variant | SPAG16 | GRCh38.p7 | 2:213926019 | ATTTTTCTTTCCAAA[A/C]ATGTGGTTCTAGGTC | 79582 |
rs79845752 | snp | A/G | 0.0425829 | 0.139564 | intron-variant | SPAG16 | GRCh38.p7 | 2:214193619 | CATCATCTCTGCAAC[A/G]TCTGTCATGGGTAGC | 79582 |
rs79858733 | snp | A/C | 0.00914312 | 0.0669923 | intron-variant | SPAG16 | GRCh38.p7 | 2:214375262 | GTGCTTGGGTTTCCA[A/C]GAAAAATATGTGAAA | 79582 |
rs79860304 | snp | C/T | 0.277778 | 0.248452 | intron-variant | SPAG16 | GRCh38.p7 | 2:214016383 | TTCCTGTGCTATTCT[C/T]GTGACAGTGAATAAA | 79582 |
rs79865758 | snp | C/G | | | intron-variant | SPAG16 | GRCh38.p7 | 2:213902612 | GGGAGTACAATTCAA[C/G]ATGAGATTTGGGTGG | 79582 |
rs79871850 | snp | C/T | 0.0185938 | 0.0946107 | intron-variant | SPAG16 | GRCh38.p7 | 2:213812157 | ACTGTTAGGACAAAG[C/T]AGAATCACAGAATGA | 79582 |
rs79876603 | snp | C/G | 0.00993419 | 0.0697739 | intron-variant | SPAG16 | GRCh38.p7 | 2:214212511 | TTTGACTCTTGTGAA[C/G]TGAAGGCTTCACAAG | 79582 |
rs79879874 | snp | A/C | 0.0165278 | 0.0893908 | intron-variant | SPAG16 | GRCh38.p7 | 2:214005419 | GTGGATTTTTATGAC[A/C]ATTTGGGAACAATGT | 79582 |
rs79889063 | snp | A/T | 0 | 0 | intron-variant | SPAG16 | GRCh38.p7 | 2:214315505 | AGCCCCATCTTTTTT[A/T]TTTATTTATTTATTT | 79582 |
rs79890299 | snp | C/T | 0.0178098 | 0.0926698 | intron-variant | SPAG16 | GRCh38.p7 | 2:213372237 | TTCAGTGCAGTAATG[C/T]CTATTTTTAAACCAG | 79582 |
rs79891248 | snp | C/T | 0.5 | 0 | intron-variant | SPAG16 | GRCh38.p7 | 2:213395169 | TTATGGACTTTTTTT[C/T]AAACAACCAGCTTTT | 79582 |
rs79891292 | snp | C/T | 0.19459 | 0.243782 | intron-variant | SPAG16 | GRCh38.p7 | 2:213337819 | GGATATCATCCAGAA[C/T]TTCCTCAACCTAGCA | 79582 |
rs79892193 | snp | G/T | 0.0170251 | 0.090679 | intron-variant | SPAG16 | GRCh38.p7 | 2:213700061 | ATTACAGTTCTCTTT[G/T]TGGTAATATATTATC | 79582 |
rs79893924 | snp | A/T | 0 | 0 | intron-variant | SPAG16 | GRCh38.p7 | 2:214406109 | AAGTTCCATGATCAT[A/T]AAAAAAATTGCAATA | 79582 |
rs79906648 | snp | C/T | 0.00835141 | 0.0640778 | intron-variant | SPAG16 | GRCh38.p7 | 2:213578779 | ATATTGTTGTAAAGA[C/T]TTTAAGTTTTGAAAA | 79582 |
rs79907063 | in-del | -/GTTGGCAGGTTC | 0.455383 | 0.142541 | intron-variant | SPAG16 | GRCh38.p7 | 2:214219955 | AATTTAGCAAAACCT[-/GTTGGCAGGTTC]ATCCTCTAGAGATAC | 79582 |
rs79907925 | snp | C/T | 0.00438332 | 0.0466095 | intron-variant | SPAG16 | GRCh38.p7 | 2:213801563 | GTCCAAACAAATGTC[C/T]TCCAAGCCAAGTAGA | 79582 |
rs79915090 | snp | A/G | 0.00835141 | 0.0640778 | intron-variant | SPAG16 | GRCh38.p7 | 2:214123834 | TGACAACATGGTCCC[A/G]TGGAGGAATAGCAAA | 79582 |
rs79915777 | snp | A/C/T | 0.0209421 | 0.100162 | intron-variant | SPAG16 | GRCh38.p7 | 2:213334720 | AAAGACAAATTTCAC[A/C/T]TGTTCTCATTTATCT | 79582 |
rs79916158 | snp | A/C | | | intron-variant | SPAG16 | GRCh38.p7 | 2:213563919 | GTGCCATATATGTGG[A/C]AAAACATGGAGTATG | 79582 |
rs79920728 | snp | C/T | 0.0182019 | 0.0936463 | intron-variant | SPAG16 | GRCh38.p7 | 2:213872612 | TGCTCTGGCTCGAAC[C/T]TCCAGTGCAATGTTG | 79582 |
rs79922079 | snp | G/T | 0.0023933 | 0.0345097 | intron-variant | SPAG16 | GRCh38.p7 | 2:214130763 | TGCCAATAATGACAC[G/T]GAAAATGAAGTAAAC | 79582 |
rs79923224 | snp | G/T | | | intron-variant | SPAG16 | GRCh38.p7 | 2:213846037 | CATCTCATTGGCTAG[G/T]GCAAGTCACTTATCA | 79582 |
rs79927564 | snp | C/T | 0.0023933 | 0.0345097 | intron-variant | SPAG16 | GRCh38.p7 | 2:214316407 | TCAGCAGGTTAGCTG[C/T]ATATGAATCCTCATT | 79582 |
rs79934592 | snp | C/T | 0.127254 | 0.217792 | intron-variant | SPAG16 | GRCh38.p7 | 2:213612135 | AAAATAGAATGAGGG[C/T]TTGAAGTCATTGGCG | 79582 |
rs79936163 | in-del | -/CAACTAACTAACT | | | intron-variant | SPAG16 | GRCh38.p7 | 2:213804682 | AGCGAGACTCCGTCT[-/CAACTAACTAACT]AACTAACTAACTAAC | 79582 |
rs79936842 | snp | A/G | 0.0134861 | 0.0810011 | intron-variant, utr-variant-3-prime | SPAG16 | GRCh38.p7 | 2:213399577 | GTTAATCATTTTTTC[A/G]TAGGATGCTTACTTC | 79582 |
rs79944662 | snp | A/G | 0.0637235 | 0.166737 | intron-variant | SPAG16 | GRCh38.p7 | 2:213761142 | CAGAAAAAGTTACAA[A/G]ACTTTGGAATTTAAA | 79582 |
rs79947279 | snp | A/T | 0.00119737 | 0.0244387 | intron-variant | SPAG16 | GRCh38.p7 | 2:214408096 | AATATGAGGTTCCAA[A/T]ATCATTTTCTGTATT | 79582 |
rs79948461 | snp | A/T | 0.105924 | 0.204309 | intron-variant | SPAG16 | GRCh38.p7 | 2:213673986 | CATTTATAAATAAAG[A/T]TATATTTTTAAATTA | 79582 |
rs79951501 | snp | C/T | 0.00438332 | 0.0466095 | intron-variant | SPAG16 | GRCh38.p7 | 2:214185385 | TAGAAGCAGTTTGTG[C/T]TTGGAAATGAGAATA | 79582 |
rs79951842 | snp | A/C | 0.128288 | 0.218372 | intron-variant | SPAG16 | GRCh38.p7 | 2:214377157 | CCATGTGACACTAAC[A/C]ATCTCCCCGTGAGCA | 79582 |
rs79956388 | snp | G/T | 0.0603597 | 0.1629 | intron-variant | SPAG16 | GRCh38.p7 | 2:213942201 | TTCTCTGCCTGCTTT[G/T]CCTACATCTGTTCAG | 79582 |
rs79974059 | snp | A/G | 0.0107246 | 0.0724382 | intron-variant | SPAG16 | GRCh38.p7 | 2:214200254 | TTATTACTCGAAGGT[A/G]AGTCTGTTCTATGCC | 79582 |
rs79981806 | snp | A/G | 0.129664 | 0.219133 | intron-variant | SPAG16 | GRCh38.p7 | 2:214341136 | GAAAAAGAAAGAACC[A/G]TCCTAGGTGGAAAGC | 79582 |
rs79984017 | snp | A/G | 0.0410537 | 0.137264 | intron-variant, utr-variant-5-prime | SPAG16 | GRCh38.p7 | 2:213302041 | TCTATTGTTGCAATC[A/G]TAACACAATATAGAA | 79582 |
rs79985383 | snp | C/G | 0.00636936 | 0.0560724 | intron-variant | SPAG16 | GRCh38.p7 | 2:213484373 | TTTCCTGACCCATTC[C/G]TATTTTCATACTTAG | 79582 |
rs79995661 | snp | A/G | | | intron-variant | SPAG16 | GRCh38.p7 | 2:214322670 | ATTTCAAGTATAATT[A/G]AATTATGGTTCAAAA | 79582 |
rs79996969 | snp | C/T | 0.0197687 | 0.0974348 | intron-variant | SPAG16 | GRCh38.p7 | 2:213883998 | GTGGGGTGTTTAGCC[C/T]ATTTACATTCGGGAT | 79582 |
rs80004901 | snp | A/T | 0.0271762 | 0.113356 | intron-variant | SPAG16 | GRCh38.p7 | 2:213663538 | AAACACACTTAGAGG[A/T]TTATAATCACTAAAA | 79582 |
rs80010092 | snp | G/T | 0.077417 | 0.180873 | intron-variant | SPAG16 | GRCh38.p7 | 2:214045564 | CACCTCATCCCTGGG[G/T]GTTAGAGCACCAAGC | 79582 |
rs80012031 | snp | G/T | 0.18325 | 0.240924 | intron-variant | SPAG16 | GRCh38.p7 | 2:213486442 | CTAAGTGCCCATGAA[G/T]GGGTGAGTGAAAAAA | 79582 |
rs80016542 | snp | A/G | 0.0278466 | 0.114667 | upstream-variant-2KB, missense, nc-transcript-variant | VWC2L, SPAG16 | GRCh38.p7 | 2:214410302 | CTGACGGCACAGTTC[A/G]AACGTGGTCTTGACC | 79582 |
rs80026506 | snp | A/G | 0.00517822 | 0.0506191 | intron-variant | SPAG16 | GRCh38.p7 | 2:213622561 | GTTGGCTTTCTGTGC[A/G]GTGAGCAGCAGGACC | 79582 |
rs80027678 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | SPAG16 | GRCh38.p7 | 2:213928433 | TGAGAATATCCTCAT[C/T]ATATAATCCACCTTC | 79582 |
rs80037663 | snp | C/T | 0.0260105 | 0.111035 | intron-variant | SPAG16 | GRCh38.p7 | 2:213833163 | CTAATTTCTATAATA[C/T]ATTCTCCTGGCTCTG | 79582 |
rs80038001 | snp | A/G | 0.0452528 | 0.143452 | intron-variant | SPAG16 | GRCh38.p7 | 2:213742495 | CTCACATAAAATTAT[A/G]AATACCTCTACAGGT | 79582 |
rs80038636 | snp | A/T | 0.00716266 | 0.059414 | intron-variant | SPAG16 | GRCh38.p7 | 2:213681980 | CCTTCAGCGTGAATC[A/T]GTTACAGCTGTCCTC | 79582 |
rs80039769 | snp | A/C | 0.144969 | 0.226867 | intron-variant | SPAG16 | GRCh38.p7 | 2:213433493 | TCAAGAATGTAATCT[A/C]ATTTACAATAGCTAC | 79582 |
rs80043401 | snp | A/T | 0.0154538 | 0.0865337 | intron-variant | SPAG16 | GRCh38.p7 | 2:214251025 | TGCACATAAAGCACT[A/T]TTGTTTTATTACAGC | 79582 |
rs80043482 | snp | C/T | | | intron-variant | SPAG16 | GRCh38.p7 | 2:214258062 | TTTGTTCATTGCACT[C/T]ATGTTGTAGAATTTC | 79582 |
rs80043553 | snp | A/G | 0.0460142 | 0.144533 | intron-variant | SPAG16 | GRCh38.p7 | 2:214258880 | TATTATATAATTTCA[A/G]TTTGGTATTTTATAT | 79582 |
rs80044567 | snp | C/T | 0.0107246 | 0.0724382 | intron-variant | SPAG16 | GRCh38.p7 | 2:214066847 | GCAGAAAGGAAAACA[C/T]ATCAAAATTATTCTT | 79582 |
rs80051308 | snp | C/T | 0.5 | 0 | intron-variant | SPAG16 | GRCh38.p7 | 2:213501320 | GCTTTAGTAATAATA[C/T]TGAACATTTATTAAG | 79582 |
rs80051720 | snp | G/T | 0 | 0 | intron-variant | SPAG16 | GRCh38.p7 | 2:214050553 | ATGTTATTAATGACA[G/T]AGAACAGAATTGGGA | 79582 |
rs80052682 | snp | A/C | 0.0185938 | 0.0946107 | intron-variant | SPAG16 | GRCh38.p7 | 2:213859421 | AGAACAGGTTCTTCT[A/C]ACCCCTCTAACACTA | 79582 |
rs80057261 | snp | C/G | 0.0023933 | 0.0345097 | intron-variant | SPAG16 | GRCh38.p7 | 2:214311222 | TCTCTAGGGTCAGCA[C/G]ACTCGAAGGACTATA | 79582 |
rs80057517 | snp | C/G | | | intron-variant | SPAG16 | GRCh38.p7 | 2:213491892 | TTAGGAGGGAAGGCT[C/G]TCACATTATTAGTTT | 79582 |
rs80058086 | in-del | -/G | 0.0456336 | 0.143994 | intron-variant | SPAG16 | GRCh38.p7 | 2:214311740 | TTTCTGAGGAGAAAT[-/G]GCATCCAACATCTCT | 79582 |
rs80071244 | snp | A/C | 0.0205511 | 0.0992634 | utr-variant-3-prime, intron-variant | SPAG16 | GRCh38.p7 | 2:213317609 | TTTTATATAACATTC[A/C]CTTCCTTGTGTATTT | 79582 |
rs80071303 | snp | A/G | 0.0456336 | 0.143994 | intron-variant | SPAG16 | GRCh38.p7 | 2:213393999 | CAATTCTATTAATGC[A/G]GATATCTTGCTCCAC | 79582 |
rs80073899 | snp | G/T | 0.0240643 | 0.107019 | intron-variant | SPAG16 | GRCh38.p7 | 2:213841319 | TGGGGCATGACATAA[G/T]GGTAGTTTGTACATG | 79582 |
rs80083429 | snp | A/G/T | 0.000399281 | 0.0141238 | intron-variant | SPAG16 | GRCh38.p7 | 2:213991205 | CCCCTCCCTGTGTCC[A/G/T]TGTGTTCCCATTGTT | 79582 |
rs80086793 | snp | C/T | 0.0836354 | 0.186609 | intron-variant | SPAG16 | GRCh38.p7 | 2:213986114 | ATTCCTATGGGAATA[C/T]AGACAAAGAGACTTT | 79582 |
rs80096424 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | SPAG16 | GRCh38.p7 | 2:213687174 | CCTCTTCACATATAG[C/T]ATGAGGAACTTGTAA | 79582 |
rs80099912 | in-del | -/TTT | | | intron-variant | SPAG16 | GRCh38.p7 | 2:214316156 | TGGGTTTTTTTTTTT[-/TTT]AGATTTTCTTTGCAA | 79582 |
rs80102512 | snp | A/T | 0.5 | 0 | intron-variant | SPAG16 | GRCh38.p7 | 2:213332742 | CTCTTGATGTGATAT[A/T]TCACATTGATTAATT | 79582 |
rs80104118 | snp | G/T | 0.0505692 | 0.150756 | intron-variant | SPAG16 | GRCh38.p7 | 2:213995567 | ATTTAGACATGACTC[G/T]CTTTCTTATATGTCT | 79582 |
rs80108862 | snp | C/T | 0.0248432 | 0.108648 | intron-variant | SPAG16 | GRCh38.p7 | 2:213785483 | AAATTTTAGTTTTCT[C/T]ATTATCAGACATCAC | 79582 |
rs80110362 | snp | C/T | 0.0479149 | 0.147179 | intron-variant | SPAG16 | GRCh38.p7 | 2:213467459 | ATGATTTAAAAGGCA[C/T]GAGTAAGCAAGAGGT | 79582 |
rs80111289 | snp | G/T | 0.0217236 | 0.101931 | intron-variant | SPAG16 | GRCh38.p7 | 2:213450483 | TAGCTCTTTAGGTGT[G/T]CACATATTCATCTTT | 79582 |
rs80115255 | snp | A/G | 0.224116 | 0.248656 | intron-variant | SPAG16, LOC101928084 | GRCh38.p7 | 2:214099625 | GATTGTATATGTATG[A/G]ACTAGTCCATGAAAT | 79582 |
rs80115277 | snp | C/T | 0.5 | 0 | intron-variant | SPAG16 | GRCh38.p7 | 2:213989647 | TAGTGGAAACAATTT[C/T]TGATGGAATAATCAA | 79582 |
rs80119692 | snp | C/G | 0.00358779 | 0.0422022 | intron-variant | SPAG16 | GRCh38.p7 | 2:213562946 | GGGCTCTGCCCTCAT[C/G]TAAACACCGCCTAAA | 79582 |
rs80122347 | snp | A/G | 0.0142736 | 0.0832652 | intron-variant | SPAG16 | GRCh38.p7 | 2:214003871 | GCCTTTTTGCATTTA[A/G]GATCACTAGACAGCA | 79582 |
rs80137556 | snp | A/G | 0.5 | 0 | intron-variant | SPAG16 | GRCh38.p7 | 2:214057068 | GTTTTGAACTTCTCA[A/G]AGACATCCATGAAAG | 79582 |
rs80140178 | snp | A/G | 0.0197687 | 0.0974348 | intron-variant | SPAG16 | GRCh38.p7 | 2:214046234 | AGCAAAGAAAGTCCA[A/G]GACTCAATGCCTTCA | 79582 |
rs80141553 | snp | A/T | 0.0193772 | 0.0965046 | intron-variant | SPAG16 | GRCh38.p7 | 2:214224147 | TCTTCCCAGGGGCAA[A/T]GGAAAACCATTCAAA | 79582 |
rs80148592 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | SPAG16 | GRCh38.p7 | 2:213810409 | AATTCAAATGATTGT[A/G]GTGGCAAGGAAGTAG | 79582 |
rs80149576 | snp | A/G | 0.0279526 | 0.114869 | intron-variant | SPAG16 | GRCh38.p7 | 2:213432434 | TACCACAGAAATAAA[A/G]AAGATCACCGGAGAC | 79582 |
rs80150552 | snp | A/T | | | intron-variant | SPAG16 | GRCh38.p7 | 2:213436446 | TAGCATGTCATTATA[A/T]CTACACAATTAACAC | 79582 |
rs80150938 | snp | G/T | 0.5 | 0 | intron-variant | SPAG16 | GRCh38.p7 | 2:213689543 | CTTTTTTTTTTTTTT[G/T]TTTTTTTTTTTTGGT | 79582 |
rs80153034 | snp | G/T | 0.144969 | 0.226867 | intron-variant | SPAG16 | GRCh38.p7 | 2:213710838 | CTTTTCTCCCATCCT[G/T]ATATAATGTAATGTG | 79582 |
rs80163059 | snp | C/T | 0.0766824 | 0.180169 | intron-variant | SPAG16 | GRCh38.p7 | 2:213992342 | GTTTGCATTTATGGT[C/T]GTCACAGCTATAATG | 79582 |
rs80170438 | snp | G/T | 0.0543475 | 0.155628 | intron-variant | SPAG16 | GRCh38.p7 | 2:213439586 | TTCAAGGTGTGGTCT[G/T]TTTTCTTCTTCCTGC | 79582 |
rs80170829 | snp | A/G | 0.0283406 | 0.115616 | intron-variant | SPAG16 | GRCh38.p7 | 2:213673279 | ATTTCTAGAAATAAA[A/G]CATCTAAAAAATGGT | 79582 |
rs80172261 | snp | A/T | 0.0279526 | 0.114869 | intron-variant | SPAG16 | GRCh38.p7 | 2:214246553 | GCCCTTGACTATGCT[A/T]AGTCCACTGTGCTGC | 79582 |
rs80178691 | snp | A/C | 0.0209421 | 0.100162 | intron-variant | SPAG16 | GRCh38.p7 | 2:214266819 | CTGAAAAAAAAATTA[A/C]GAAAACAGTCCCAAT | 79582 |
rs80185491 | snp | C/G | 0.0146672 | 0.084371 | intron-variant | SPAG16 | GRCh38.p7 | 2:214376298 | ATCTAAATCACCTTT[C/G]AATTGCCTCTGGGAT | 79582 |
rs80186178 | snp | A/T | 0.0832709 | 0.186283 | intron-variant | SPAG16 | GRCh38.p7 | 2:213645866 | GACTGCCTTTCAAAT[A/T]TACCTGGAGACAAGA | 79582 |
rs80186223 | snp | C/T | 0.0607341 | 0.163335 | intron-variant | SPAG16 | GRCh38.p7 | 2:213760953 | TGACAGTAGTAGTTT[C/T]AGTCCTTATGGCAGG | 79582 |
rs80188921 | snp | C/G | 0.5 | 0 | intron-variant | SPAG16 | GRCh38.p7 | 2:214399948 | TGATCAGCTGCATAG[C/G]TGAAGACCAAGTTAG | 79582 |
rs80191661 | snp | A/G | 0.00755907 | 0.0610114 | intron-variant | SPAG16 | GRCh38.p7 | 2:214132603 | GTTGTGTTGGAGCCA[A/G]GTTTTAAGAATGGTT | 79582 |
rs80199286 | snp | C/T | 0.0726307 | 0.176182 | intron-variant | SPAG16 | GRCh38.p7 | 2:213991576 | TGGTGCTCCTGGACC[C/T]CCGCACTTGTCCCAC | 79582 |
rs80201713 | snp | C/T | 0.00279162 | 0.0372561 | intron-variant | SPAG16 | GRCh38.p7 | 2:213931722 | TCTAAATACTGACTT[C/T]CAATTGGTGCCCAGT | 79582 |
rs80203510 | snp | A/G | 0.138546 | 0.223781 | intron-variant | SPAG16 | GRCh38.p7 | 2:214325997 | GCCAATAATATAATA[A/G]GTATAGTGGATTGAA | 79582 |
rs80204332 | snp | A/G | 0.5 | 0 | intron-variant | SPAG16 | GRCh38.p7 | 2:213443799 | AGCATGAAAGTTGTG[A/G]TGCTTGATGCATGCA | 79582 |
rs80214891 | snp | A/G | 0.0166325 | 0.0896639 | intron-variant | SPAG16 | GRCh38.p7 | 2:214279890 | AAATCAAAAAAACCC[A/G]TGGATCAAAGAAGAA | 79582 |
rs80219965 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | SPAG16 | GRCh38.p7 | 2:214379724 | TCTTTCCTTTAATTG[C/T]AAGGGAAATCTAAGC | 79582 |
rs80228060 | snp | C/T | 0.0209421 | 0.100162 | intron-variant | SPAG16 | GRCh38.p7 | 2:214170940 | CTTAGAACTTTTTAA[C/T]TCTAGTCCCAATATC | 79582 |
rs80229988 | snp | C/T | 0.0345262 | 0.126772 | intron-variant | SPAG16 | GRCh38.p7 | 2:214228882 | AGCTCCTCAGCTACA[C/T]TGATGGCAGAACCAA | 79582 |
rs80231715 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | SPAG16 | GRCh38.p7 | 2:213751441 | AAACCAGCTAATCCA[C/G]AACCTCTGAGGGAAA | 79582 |
rs80233723 | snp | C/T | 0.0178098 | 0.0926698 | intron-variant | SPAG16 | GRCh38.p7 | 2:213364515 | ATTTATAAGGTGAGC[C/T]CTGCCATCACCATGG | 79582 |
rs80241713 | snp | C/T | 0.0170251 | 0.090679 | intron-variant | SPAG16 | GRCh38.p7 | 2:214144212 | AAATAAATAGTAATA[C/T]GTTTGGCAATGATAT | 79582 |
rs80248572 | snp | C/T | 0.5 | 0 | intron-variant | SPAG16 | GRCh38.p7 | 2:214187682 | AACAATAATGTCTGC[C/T]ATAACAAACCTCAGG | 79582 |
rs80250841 | snp | A/T | | | intron-variant | SPAG16 | GRCh38.p7 | 2:213925144 | CATTATTGTTTTTTT[A/T]TATTTTTACAAGCAT | 79582 |
rs80252062 | snp | A/G | 0.00199481 | 0.0315187 | intron-variant | SPAG16 | GRCh38.p7 | 2:214062162 | GAGTGGCTCATGCCT[A/G]TAATCCCAGCACTTT | 79582 |
rs80253378 | snp | A/G | 0.0232847 | 0.105357 | intron-variant | SPAG16 | GRCh38.p7 | 2:214074910 | GCAAGGATGCAGAGT[A/G]GGAAAAGAATATTAA | 79582 |
rs80253446 | snp | C/T | 0.00438332 | 0.0466095 | intron-variant | SPAG16 | GRCh38.p7 | 2:213797478 | TTAGACACACAAATA[C/T]CATTGTGTTACAATG | 79582 |
rs80261873 | snp | A/C | 0.0663309 | 0.169604 | intron-variant | SPAG16 | GRCh38.p7 | 2:214162903 | CTATGCAAATATAGA[A/C]AATTTGTTCACTGCC | 79582 |
rs80268839 | snp | A/G | 0.0115144 | 0.0749975 | intron-variant | SPAG16 | GRCh38.p7 | 2:214331515 | AAAAATTCTGCAATC[A/G]GGCCCTTGGGAAGTA | 79582 |
rs80271476 | snp | A/G | 0.0023933 | 0.0345097 | intron-variant | SPAG16 | GRCh38.p7 | 2:214261601 | ACACTATCTTATCAC[A/G]CACATTTGCCCTTTA | 79582 |
rs80271690 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | SPAG16 | GRCh38.p7 | 2:213958215 | AACTGATGGGTTTAG[A/G]GCAAGCAGGCACAAG | 79582 |
rs80280791 | snp | C/T | 0.0391387 | 0.134304 | intron-variant | SPAG16 | GRCh38.p7 | 2:213803905 | CTTCATGGCACAGGC[C/T]TTGAGTCTCTAACTT | 79582 |
rs80283966 | snp | A/C | 0.0788843 | 0.182262 | intron-variant | SPAG16 | GRCh38.p7 | 2:213916758 | TGTCTGATTACTCTG[A/C]TGACAGTTTCTTTTG | 79582 |
rs80285523 | snp | A/T | | | intron-variant | SPAG16 | GRCh38.p7 | 2:214311146 | GGAGATCAGCACTGT[A/T]ACCTGCATTTCCTCT | 79582 |
rs80286890 | snp | G/T | 0.000798403 | 0.0199641 | intron-variant | SPAG16 | GRCh38.p7 | 2:214282529 | ATCTGGGAATTGCAT[G/T]ATTTCCTAGTGATTC | 79582 |
rs80291425 | snp | A/C | 0.0185938 | 0.0946107 | intron-variant | SPAG16 | GRCh38.p7 | 2:214131440 | TTTGTATAAGGTAAC[A/C]TGTTATAAGTGCCAA | 79582 |
rs80291744 | snp | A/G | 0.0554779 | 0.157039 | intron-variant | SPAG16 | GRCh38.p7 | 2:213986250 | TTAAGATGAGGAAAT[A/G]TTATGAACTCTAGAG | 79582 |
rs80298711 | snp | C/T | 0.0279526 | 0.114869 | intron-variant | SPAG16 | GRCh38.p7 | 2:214284636 | GTTGAGATCTACAGA[C/T]GCAGAAAGTTAAGAG | 79582 |
rs80301287 | snp | A/C | 0.5 | 0 | intron-variant | SPAG16 | GRCh38.p7 | 2:213429094 | GAGACTCCATCTCAA[A/C]AAAAAAAAAAAAGAG | 79582 |
rs80303397 | snp | A/T | 0.5 | 0 | intron-variant | SPAG16 | GRCh38.p7 | 2:213658878 | CTGTCTCTACTAAAA[A/T]TGCAAAAATTAGCTG | 79582 |
rs80306743 | snp | C/G | 0.0023933 | 0.0345097 | intron-variant | SPAG16 | GRCh38.p7 | 2:214154715 | ATTTTCTCTCCACTA[C/G]TTACTAGCAAAATGA | 79582 |
rs80307240 | snp | C/T | 0.0244538 | 0.107838 | intron-variant | SPAG16 | GRCh38.p7 | 2:213445775 | CTCAGCTAAAATGGC[C/T]TTTATATTATCAAAA | 79582 |
rs80308520 | snp | C/T | 0.0174175 | 0.0916809 | intron-variant | SPAG16 | GRCh38.p7 | 2:214236274 | TTTAAGCTGCTCAAG[C/T]TTAACACAGTAAAAA | 79582 |
rs80313458 | snp | A/G | 0.0107246 | 0.0724382 | intron-variant | SPAG16 | GRCh38.p7 | 2:213494882 | TTATTCCTACTCCAA[A/G]GTCTTTCCACTACCT | 79582 |
rs80314568 | snp | G/T | 0.0228947 | 0.104514 | intron-variant | SPAG16 | GRCh38.p7 | 2:213968782 | ATGTGAATCATAATA[G/T]ATATCACCTTGATAA | 79582 |
rs80315846 | in-del | -/ACAAA | | | intron-variant | SPAG16 | GRCh38.p7 | 2:213904621 | AAAAAAAAAAAAAAA[-/ACAAA]GTAGGTAAAGGGCAT | 79582 |
rs80318795 | snp | A/T | 0.111576 | 0.20818 | intron-variant | SPAG16 | GRCh38.p7 | 2:213566757 | TGACACATTCATAAC[A/T]TAAGAAAACTGCCCT | 79582 |
rs80322943 | snp | C/T | 0.210909 | 0.246925 | intron-variant | SPAG16 | GRCh38.p7 | 2:213955143 | TTGCAGCACAAATGC[C/T]TTTAATTTTGGTTAA | 79582 |
rs80329217 | snp | A/G | 0.5 | 0 | intron-variant | SPAG16 | GRCh38.p7 | 2:213838122 | CAAAGGAAAAAAAAA[A/G]GAAAGAGACAAATGA | 79582 |
rs80331035 | snp | G/T | 0 | 0 | intron-variant | SPAG16 | GRCh38.p7 | 2:213731156 | CATTATATCTGAGTT[G/T]TTTTTTTTTTTTTTT | 79582 |
rs80338248 | snp | A/G | 0.00398564 | 0.0444627 | intron-variant | SPAG16 | GRCh38.p7 | 2:213331230 | ATGCCTGGGTCCTGA[A/G]GCCCCCATTCCAGGC | 79582 |
rs80339167 | snp | A/G | 0 | 0 | intron-variant | SPAG16 | GRCh38.p7 | 2:213733127 | TTTCTCTGATGGCCA[A/G]TGATGATGAGCATTT | 79582 |
rs80346529 | snp | C/T | 0.0368353 | 0.130617 | intron-variant | SPAG16 | GRCh38.p7 | 2:213794063 | ACCTTTTACAAAGTA[C/T]AATAAAGACTGCTCA | 79582 |
rs80353721 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | SPAG16 | GRCh38.p7 | 2:213550558 | TCTCATGGAAGAATA[G/T]GTCATGGCATTCCAC | 79582 |
rs111209666 | snp | A/C | 0.5 | 0 | intron-variant | SPAG16 | GRCh38.p7 | 2:213407886 | AGAGGAGAGAGGCAG[A/C]GAGAGAGAGACAGGA | 79582 |
rs111232691 | snp | C/T | 0.0267878 | 0.112589 | intron-variant | SPAG16 | GRCh38.p7 | 2:214226212 | TTGGTAGGGGCTAGC[C/T]CGTCTAGGATAGTCT | 79582 |
rs111234642 | snp | A/G/T | 0.0452528 | 0.143452 | intron-variant | SPAG16 | GRCh38.p7 | 2:213469331 | ATACTTAAATGCTGA[A/G/T]GTGAAGTCAATAAAT | 79582 |
rs111235535 | snp | A/T | | | intron-variant | SPAG16 | GRCh38.p7 | 2:213637918 | CCTGCCACCACGCCC[A/T]GCTAATTTTTTGTAT | 79582 |
rs111236999 | snp | A/G | 0.0298908 | 0.118541 | intron-variant | SPAG16 | GRCh38.p7 | 2:213466621 | CTCTGACAAGAGTAG[A/G]CCTAGATACTTCACT | 79582 |
rs111237515 | snp | C/T | 0.0448719 | 0.142907 | intron-variant | SPAG16 | GRCh38.p7 | 2:214252763 | ATAAACATAAGTGTG[C/T]GTGTGTCTTTATAGT | 79582 |
rs111241966 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | SPAG16 | GRCh38.p7 | 2:214227941 | TGTACTGTGACTATT[C/T]GTAAATATAAAAGCA | 79582 |
rs111244838 | snp | C/T | 0.0437281 | 0.141251 | intron-variant | SPAG16 | GRCh38.p7 | 2:214275324 | TGATCTTAGTTATTT[C/T]TTGCCTTCTGCTAGC | 79582 |
rs111250364 | snp | A/G | 0.5 | 0 | intron-variant | SPAG16 | GRCh38.p7 | 2:213701479 | GGAGTCCTTCAGCCC[A/G]CTGCTGCACTGTGGG | 79582 |
rs111251128 | snp | A/T | | | intron-variant | SPAG16 | GRCh38.p7 | 2:213677248 | CATCATAATGACAGG[A/T]TCAAATTCACACATA | 79582 |
rs111255767 | snp | C/T | | | intron-variant | SPAG16 | GRCh38.p7 | 2:213854978 | AGAGCTGAAAAGTTA[C/T]AACAGATAACATATG | 79582 |
rs111256505 | snp | A/G | 0.148661 | 0.22854 | intron-variant | SPAG16 | GRCh38.p7 | 2:213509567 | AATACCAAAATGTAC[A/G]GGATATAATCTCCTG | 79582 |
rs111258122 | snp | C/T | 0.0865458 | 0.189163 | intron-variant | SPAG16 | GRCh38.p7 | 2:213811480 | GGTGTGCTGGCAGGA[C/T]GGTGAGGAGAGCCAA | 79582 |
rs111267425 | snp | A/C | 0.5 | 0 | intron-variant | SPAG16 | GRCh38.p7 | 2:213326959 | TATAGTTCGATAAGA[A/C]TATCTGTACCTTAAT | 79582 |
rs111268856 | snp | A/G | 0.0193772 | 0.0965046 | intron-variant | SPAG16 | GRCh38.p7 | 2:213726064 | CTACAGTGCATGCCA[A/G]CCTAATACCCAACTG | 79582 |
rs111270289 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | SPAG16 | GRCh38.p7 | 2:213727814 | GAACATAAAAGGGAG[A/G]TGCTTTAGTCAGATT | 79582 |
rs111273697 | snp | A/C | 0.5 | 0 | intron-variant | SPAG16 | GRCh38.p7 | 2:213747295 | TTCAAAAGAACAAAA[A/C]AGATTTTAAAAAATT | 79582 |
rs111274173 | snp | C/G | 0.5 | 0 | intron-variant, upstream-variant-2KB | SPAG16, LOC101928084 | GRCh38.p7 | 2:214103961 | AGAGAGAGAGAGAGA[C/G]AGTGAGAGAGGGAGG | 79582 |
rs111278094 | snp | A/C | 0.5 | 0 | intron-variant | SPAG16 | GRCh38.p7 | 2:213734521 | CTCTTTGAAAAAATA[A/C]CAGAAATCATATGCT | 79582 |
rs111280495 | snp | A/C | 0 | 0 | intron-variant | SPAG16 | GRCh38.p7 | 2:213882012 | TATGTTCCTTTGATG[A/C]CTTGTCTTTTGAGAG | 79582 |
rs111281017 | snp | A/G | 0.00398564 | 0.0444627 | intron-variant | SPAG16 | GRCh38.p7 | 2:213505503 | TTAATATTTTAAAAC[A/G]TAAGTTAGTATTTAT | 79582 |
rs111283337 | snp | A/G | 0.132409 | 0.220618 | intron-variant, utr-variant-5-prime | SPAG16 | GRCh38.p7 | 2:213301284 | CTCAAAGCCATGTCT[A/G]CAGATTATCCAAGCC | 79582 |
rs111285343 | snp | G/T | 0.00358779 | 0.0422022 | intron-variant | SPAG16 | GRCh38.p7 | 2:213507384 | CATTCAGCCTTTTAT[G/T]TGGCAATATTCATCA | 79582 |
rs111291564 | snp | A/C | 0.00358779 | 0.0422022 | intron-variant | SPAG16 | GRCh38.p7 | 2:213516039 | TGAGACTTGTGTGAT[A/C]TATTGATAAATTATT | 79582 |
rs111301721 | snp | A/G | 0.00279162 | 0.0372561 | intron-variant | SPAG16 | GRCh38.p7 | 2:214212479 | CACTACCTGATACAC[A/G]GGTTACATGTCCATT | 79582 |
rs111305599 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | SPAG16 | GRCh38.p7 | 2:214367829 | CCTTGAAGAAAATTC[C/T]GTTGCTGGATTGTCA | 79582 |
rs111309353 | snp | A/T | 0.0154538 | 0.0865337 | intron-variant | SPAG16 | GRCh38.p7 | 2:213989344 | TTGTCTGCCATACAG[A/T]ACATAAAACTAACTC | 79582 |
rs111310087 | snp | C/T | 0.00914312 | 0.0669923 | intron-variant | SPAG16 | GRCh38.p7 | 2:213614374 | TATCTCTCAGTGCTA[C/T]CCAGAAGACAGTCAC | 79582 |
rs111313565 | snp | A/C/T | 0.0217236 | 0.101931 | intron-variant | SPAG16 | GRCh38.p7 | 2:214278112 | TCTGTGGGCGTGGGA[A/C/T]CCACCGAGCCAGGCG | 79582 |
rs111314466 | snp | A/G | 0.00478085 | 0.0486577 | intron-variant | SPAG16 | GRCh38.p7 | 2:213630030 | TCATTTGACTTCTCA[A/G]TGTTCCCATCATCCA | 79582 |
rs111314555 | snp | A/T | 0.0252325 | 0.109451 | intron-variant | SPAG16 | GRCh38.p7 | 2:214011375 | CACTCTCCTCAAAAA[A/T]GATTAAATGTCATAA | 79582 |
rs111316039 | snp | C/T | 0.5 | 0 | intron-variant | SPAG16 | GRCh38.p7 | 2:213392596 | TCACACCTGTAATCC[C/T]AGCACTTTGGGAGGC | 79582 |
rs111317832 | snp | C/G | 0.5 | 0 | intron-variant | SPAG16 | GRCh38.p7 | 2:213624983 | TTTAGTAGAGGCGGG[C/G]TTTCACCATGTTGGC | 79582 |
rs111318894 | snp | C/T | 0.029116 | 0.117091 | intron-variant | SPAG16 | GRCh38.p7 | 2:213526420 | TTCATCCTCAAACTT[C/T]TTGAAAGATGTGTAA | 79582 |
rs111321398 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | SPAG16 | GRCh38.p7 | 2:213939239 | TATTTACCAACTATG[C/T]ACCAAGTAATATAGC | 79582 |
rs111323679 | in-del | -/T/TT/TTT | 0.573709 | 0.125932 | intron-variant | SPAG16 | GRCh38.p7 | 2:213733220 | TTTGTAATGGGGTTG[-/T/TT/TTT]TTTTTTTTTTCTTGT | 79582 |
rs111323860 | snp | C/G | 0.212425 | 0.24716 | intron-variant | SPAG16 | GRCh38.p7 | 2:213403557 | TGATGGGTCGTATCT[C/G]AAAATAATAAGAGCT | 79582 |
rs111325206 | snp | A/G | 0.00358779 | 0.0422022 | intron-variant | SPAG16 | GRCh38.p7 | 2:213659071 | ACTAATAGCCACTCT[A/G]TTGTGTAATGTTCTA | 79582 |
rs111326325 | snp | A/G | 0.5 | 0 | intron-variant | SPAG16 | GRCh38.p7 | 2:214199376 | TCCTTTCCCCAATTT[A/G]TGTTTTTGTTTGCTT | 79582 |
rs111327225 | in-del | -/T | 0.364401 | 0.222289 | intron-variant | SPAG16 | GRCh38.p7 | 2:213915130 | AACTCCCCCCACCTC[-/T]TTTTTTTTTTTAATT | 79582 |
rs111338493 | snp | A/G | 0.5 | 0 | intron-variant | SPAG16 | GRCh38.p7 | 2:213693215 | CAGTTCTCATGCTCA[A/G]TGAATTCAGTCGTAG | 79582 |
rs111341303 | snp | C/T | 0.0422008 | 0.138995 | intron-variant | SPAG16 | GRCh38.p7 | 2:214250204 | AGGAACACTCATAGA[C/T]ATTTGATAAGCATTC | 79582 |
rs111351371 | snp | A/G | 0.132066 | 0.220435 | intron-variant | SPAG16 | GRCh38.p7 | 2:213357187 | CCAATTATATGGTCA[A/G]TTTTAGAATAAGCGC | 79582 |
rs111351727 | snp | A/G | 0.0142736 | 0.0832652 | intron-variant | SPAG16 | GRCh38.p7 | 2:213940000 | TCATATTTCGTTTCA[A/G]TACATGTCCTAGTAA | 79582 |
rs111353639 | snp | A/G | 0.00716266 | 0.059414 | intron-variant | SPAG16 | GRCh38.p7 | 2:214018957 | AATTTTGTAGAGGAT[A/G]AAAAAAGGGATATAA | 79582 |
rs111355536 | in-del | -/A | 0.336474 | 0.234568 | intron-variant | SPAG16 | GRCh38.p7 | 2:214038433 | ATAACATAAAATATT[-/A]TTACTCCACTCTCAA | 79582 |
rs111363048 | in-del | -/T | 0.5 | 0 | intron-variant | SPAG16 | GRCh38.p7 | 2:213365461 | AATAACTAAAATGAA[-/T]TTTTTTTTTTTTTTG | 79582 |
rs111363205 | in-del | -/TGCATCTTGAAGCC | 0.5 | 0 | intron-variant | SPAG16 | GRCh38.p7 | 2:213697388 | AAAATAGAATTGCTG[-/TGCATCTTGAAGCC]TGCACAATGTGATAG | 79582 |
rs111370893 | snp | C/T | | | intron-variant | SPAG16 | GRCh38.p7 | 2:213691712 | TTCCCTCAGCATTTG[C/T]TATCATTTAACATAC | 79582 |
rs111371358 | snp | A/G | 0.00358779 | 0.0422022 | intron-variant | SPAG16 | GRCh38.p7 | 2:213495658 | GTAGAAAAACATAAA[A/G]TGAGACAGAGGGAAA | 79582 |
rs111371477 | snp | G/T | 0.0154538 | 0.0865337 | intron-variant | SPAG16 | GRCh38.p7 | 2:213383000 | TAACAAGTAGTAGAG[G/T]GTATTTTTATCTGCT | 79582 |
rs111375828 | snp | A/C | 0.5 | 0 | intron-variant | SPAG16 | GRCh38.p7 | 2:214405484 | AAGACTTTTTGAGTA[A/C]TAAAGTTTTCAATTC | 79582 |
rs111376274 | snp | G/T | 0 | 0 | intron-variant | SPAG16 | GRCh38.p7 | 2:213351932 | CCCCACGTGTCAAGG[G/T]CGGGACCAGGTGGAG | 79582 |
rs111378224 | snp | C/T | 0.5 | 0 | intron-variant | SPAG16 | GRCh38.p7 | 2:214059178 | CAAGACTCTGTCTCT[C/T]TCTCTGTCTATATAT | 79582 |
rs111378390 | snp | A/G | 0.5 | 0 | intron-variant | SPAG16 | GRCh38.p7 | 2:214079785 | ATGGGAGACAAGAGA[A/G]AAGACACTGACTTTT | 79582 |
rs111385058 | snp | A/C | 0.00358779 | 0.0422022 | intron-variant | SPAG16 | GRCh38.p7 | 2:213526742 | CTTCTATTTCTGAAA[A/C]TGTCTTTATTATTCT | 79582 |
rs111389195 | snp | C/T | 0.029116 | 0.117091 | intron-variant | SPAG16 | GRCh38.p7 | 2:213500828 | GAATTAAAAGGTGCC[C/T]GAGCAAGGACTTGGG | 79582 |
rs111392448 | snp | C/T | 0.0452528 | 0.143452 | intron-variant | SPAG16 | GRCh38.p7 | 2:213431675 | TCAACACCCTACGGA[C/T]ACACTATAAAGATTA | 79582 |
rs111392846 | snp | A/T | 0.0217236 | 0.101931 | intron-variant | SPAG16 | GRCh38.p7 | 2:213852085 | TTGTTTTGTGACTTT[A/T]ATTGCATTTGCATTT | 79582 |
rs111393817 | snp | A/G | 0.0260105 | 0.111035 | intron-variant | SPAG16 | GRCh38.p7 | 2:214223978 | AGAATGGGTAAAGTG[A/G]ATCAATAAACTTAGA | 79582 |
rs111396001 | snp | C/G | 0.00159617 | 0.0282053 | intron-variant | SPAG16, LOC101928084 | GRCh38.p7 | 2:214098633 | TTTCGTTTAAGCCAC[C/G]CAGTCTGTGCCACTT | 79582 |
rs111397700 | snp | A/C | 0.0217236 | 0.101931 | intron-variant | SPAG16 | GRCh38.p7 | 2:213447760 | TTTGGACGAATAATC[A/C]AACTGTCCAATGCAT | 79582 |
rs111400937 | snp | A/G | 0.0298908 | 0.118541 | intron-variant | SPAG16 | GRCh38.p7 | 2:213566807 | GAAAATATTCAGCTC[A/G]CCTTTCCTGATTTAG | 79582 |
rs111406415 | in-del | -/AA | 0.00358779 | 0.0422022 | intron-variant | SPAG16 | GRCh38.p7 | 2:213513424 | ACACAGTTATAAAAT[-/AA]AAGTTTATTTCTCAT | 79582 |
rs111408125 | snp | C/T | 0.046775 | 0.145601 | intron-variant | SPAG16 | GRCh38.p7 | 2:213412132 | ACTCATTCCGATCAC[C/T]TGCTCCACCCTAACA | 79582 |
rs111410256 | snp | A/G | 0.0248432 | 0.108648 | intron-variant | SPAG16 | GRCh38.p7 | 2:213421338 | AGTCCCCCGCCATTT[A/G]GCCCCCTCCAGACAT | 79582 |
rs111411020 | snp | C/T | 0.0726307 | 0.176182 | intron-variant | SPAG16 | GRCh38.p7 | 2:213991964 | CCAAGCATGTTGCTG[C/T]GAGTAGGGCAGTCCT | 79582 |
rs111411189 | snp | A/G | 0.0271762 | 0.113356 | intron-variant | SPAG16 | GRCh38.p7 | 2:213656369 | TGGAGACGGGGTTTC[A/G]CCGTGTTAGCCATGA | 79582 |
rs111418006 | snp | C/T | 0.0437281 | 0.141251 | intron-variant | SPAG16 | GRCh38.p7 | 2:214283237 | ATTTTGTTGAATTAT[C/T]ATCATAATAACGTGT | 79582 |
rs111421075 | in-del | -/AA | 0.5 | 0 | intron-variant | SPAG16 | GRCh38.p7 | 2:213433265 | CCAGAACAATCAGAC[-/AA]GAGAAAGAATTAAAA | 79582 |
rs111421830 | in-del | -/C | 0.5 | 0 | intron-variant | SPAG16 | GRCh38.p7 | 2:213551808 | TATTTGACCTGAATA[-/C]CATTTTGAAGAACTA | 79582 |
rs111429236 | snp | C/G | 0.0279526 | 0.114869 | intron-variant | SPAG16 | GRCh38.p7 | 2:213378940 | GCTACCTCCATTGTG[C/G]AGTAGTAGACTGATT | 79582 |
rs111429779 | snp | A/C | 0.0821764 | 0.185298 | intron-variant | SPAG16 | GRCh38.p7 | 2:213702268 | AGGATGTGGGTGGGG[A/C]CAGATAAGGGAATAA | 79582 |
rs111430223 | snp | C/G | 0.5 | 0 | intron-variant | SPAG16 | GRCh38.p7 | 2:213719425 | GGAGAACCTGTGTGT[C/G]GAATCTCTGTATCTA | 79582 |
rs111430548 | snp | A/C | 0.00358779 | 0.0422022 | intron-variant | SPAG16 | GRCh38.p7 | 2:213520673 | CCCTAGGAGACTACT[A/C]CTGTGTTCTAATTGC | 79582 |
rs111432441 | snp | A/T | 0 | 0 | intron-variant | SPAG16 | GRCh38.p7 | 2:213335111 | TAATAATTAAAAATT[A/T]TATTTTCATTTAGCA | 79582 |
rs111433431 | snp | C/T | 0 | 0 | intron-variant | SPAG16 | GRCh38.p7 | 2:213920869 | CTCTGCATCAGCTGG[C/T]ATGCTGCCCCTACCA | 79582 |
rs111435287 | snp | A/T | 0.5 | 0 | intron-variant | SPAG16 | GRCh38.p7 | 2:213925062 | GCTGACTGAATTTAG[A/T]AAAGCCTAAATTGAT | 79582 |
rs111435391 | snp | G/T | 0.00398564 | 0.0444627 | intron-variant | SPAG16 | GRCh38.p7 | 2:213502312 | TTTTTCTGTAGAGAT[G/T]GGGTCTTGCCATGTT | 79582 |
rs111435803 | snp | A/G | 0.5 | 0 | intron-variant | SPAG16 | GRCh38.p7 | 2:213518127 | TAACCCCACTGATAA[A/G]TGGGCAAAGGACCTG | 79582 |
rs111438216 | snp | A/G | 0.5 | 0 | intron-variant | SPAG16 | GRCh38.p7 | 2:214225312 | GGAATTCATTGGACA[A/G]TCTTACATTTTAGAA | 79582 |
rs111441623 | snp | A/G | 0.00398564 | 0.0444627 | intron-variant | SPAG16 | GRCh38.p7 | 2:213508381 | ATCGAGACCATCCTG[A/G]CTAACAAGGTGAAAC | 79582 |
rs111442051 | snp | A/C | 0.444444 | 0.157135 | intron-variant | SPAG16 | GRCh38.p7 | 2:213728603 | GATGGTGGCCAGGCC[A/C]GGTGGCTCACGCCTG | 79582 |
rs111442790 | in-del | -/A | 0.0962929 | 0.197165 | intron-variant | SPAG16 | GRCh38.p7 | 2:213648312 | CACCTATGTCTATTC[-/A]AAAAAAAAATGTAGC | 79582 |
rs111442820 | snp | A/G | 0.0622301 | 0.165053 | intron-variant | SPAG16 | GRCh38.p7 | 2:213749470 | CAGGATCTTGTAAGG[A/G]TGACGTGACAAGGGC | 79582 |
rs111442907 | snp | C/T | 0.00914312 | 0.0669923 | intron-variant | SPAG16 | GRCh38.p7 | 2:214193332 | GCACCAAGATACTCA[C/T]CCAATTAAAATTTTA | 79582 |
rs111444427 | snp | C/G | 0.00318978 | 0.0398085 | intron-variant | SPAG16 | GRCh38.p7 | 2:213495534 | CAGGCACTACTCTGG[C/G]CAGTTAACTAACTAG | 79582 |
rs111444434 | snp | C/T | 0.0437281 | 0.141251 | intron-variant | SPAG16 | GRCh38.p7 | 2:213894590 | AACAGTACTGGAAAC[C/T]CTGGCCAGAGCAATT | 79582 |
rs111445647 | snp | A/G | 0.021333 | 0.101051 | intron-variant | SPAG16 | GRCh38.p7 | 2:213485488 | CTCCTCTTTTCCAAT[A/G]GTTTTATTGCTTCTT | 79582 |
rs111445953 | in-del | -/T | 0.5 | 0 | intron-variant | SPAG16 | GRCh38.p7 | 2:213603926 | CCAAAGACTTCCTGG[-/T]TTTTTTTTTTTTTTT | 79582 |
rs111449056 | snp | A/C | 0.0414363 | 0.137845 | intron-variant | SPAG16 | GRCh38.p7 | 2:213739895 | GCGTGAGCCACTGTG[A/C]CTGGCCAAAATCTCT | 79582 |
rs111450625 | snp | C/T | 0.5 | 0 | intron-variant | SPAG16 | GRCh38.p7 | 2:214063636 | TTAGGTTTCAACATA[C/T]GAATTTTGGGGACAT | 79582 |
rs111464292 | snp | A/C | 0.00358779 | 0.0422022 | intron-variant | SPAG16 | GRCh38.p7 | 2:213556673 | TCCAACTTTCAACAA[A/C]GAATACATCATCCAG | 79582 |
rs111474471 | snp | C/T | 0.00517822 | 0.0506191 | intron-variant | SPAG16 | GRCh38.p7 | 2:213606618 | TACCAAATATCCACC[C/T]GATCCTAGTGATTAA | 79582 |
rs111485151 | snp | C/G | 0.00517822 | 0.0506191 | intron-variant | SPAG16 | GRCh38.p7 | 2:213621603 | GGAGACAGATATTGT[C/G]AATATGACCAGGGAG | 79582 |
rs111486388 | snp | A/G | 0.0283406 | 0.115616 | intron-variant | SPAG16 | GRCh38.p7 | 2:213480577 | AGGTCACCATTTTCA[A/G]AAGCTGTTACATTAA | 79582 |
rs111490594 | snp | C/T | 0.00517822 | 0.0506191 | intron-variant | SPAG16 | GRCh38.p7 | 2:213579026 | AGATAATACAGTAGC[C/T]GAATCAGTGTTATAT | 79582 |
rs111494388 | snp | A/T | 0.00517822 | 0.0506191 | intron-variant | SPAG16 | GRCh38.p7 | 2:213594671 | TTATCGCAATTCATC[A/T]TTTACGTTTCTGGCT | 79582 |
rs111494797 | snp | A/G | 0.0283406 | 0.115616 | intron-variant | SPAG16 | GRCh38.p7 | 2:213981389 | CTTTTTTTCCAATGG[A/G]GGTTTTGTTTCTTTA | 79582 |
rs111498043 | snp | C/T | 0.00517822 | 0.0506191 | intron-variant | SPAG16 | GRCh38.p7 | 2:213587081 | TGGGCTTGAATCTTG[C/T]GCTGGTGATGATCAG | 79582 |
rs111501438 | snp | C/T | 0.00953873 | 0.0683987 | intron-variant | SPAG16 | GRCh38.p7 | 2:213423790 | CCAGGTCATTCAGTC[C/T]GTCTGTGTCTAAACT | 79582 |
rs111504356 | snp | C/T | | | intron-variant | SPAG16 | GRCh38.p7 | 2:213404497 | TGCTGGGAAAACTGG[C/T]TAGCCATATGTAGAA | 79582 |
rs111521007 | snp | A/G | 0.0225045 | 0.103662 | intron-variant | SPAG16 | GRCh38.p7 | 2:213680795 | AGCTTGGTTTTATAT[A/G]TTTTTAGGGAGGCAT | 79582 |
rs111521032 | in-del | -/AAAA | 0.5 | 0 | intron-variant | SPAG16 | GRCh38.p7 | 2:213953083 | ATTACATATATGATG[-/AAAA]GGACTAGTAGTTCAA | 79582 |
rs111521218 | snp | C/G | 0.5 | 0 | intron-variant | SPAG16 | GRCh38.p7 | 2:213309101 | GAATTTTTTACCTGT[C/G]GTATCATGTTGGTGC | 79582 |
rs111522332 | snp | A/T | 0.0611083 | 0.163768 | intron-variant | SPAG16 | GRCh38.p7 | 2:213718017 | CTAATTAAACTAAAT[A/T]GCTTCTGCACAGCAA | 79582 |
rs111523185 | snp | C/T | 0.00557542 | 0.0525036 | intron-variant | SPAG16 | GRCh38.p7 | 2:213702395 | TGCTGTTTGGGTCCA[C/T]GCAGCATTTATGAGC | 79582 |
rs111523903 | snp | C/T | 0.0275645 | 0.114116 | intron-variant | SPAG16 | GRCh38.p7 | 2:213705212 | GTGATCGTGCCACTG[C/T]GCTCCAGCCTGGGCA | 79582 |
rs111524317 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | SPAG16 | GRCh38.p7 | 2:213322586 | CCTCCTTCTACCTTA[A/G]TGACAGGCTTCTTTT | 79582 |
rs111526430 | snp | C/T | 0.0178098 | 0.0926698 | intron-variant | SPAG16 | GRCh38.p7 | 2:214050419 | CTGGCCCTTTCTGTA[C/T]CAGCATCAATATCTG | 79582 |
rs111534762 | snp | G/T | 0 | 0 | intron-variant | SPAG16 | GRCh38.p7 | 2:214406826 | TCCTATTGGTCAACA[G/T]AAAAGGTATTGATTT | 79582 |
rs111535099 | snp | C/T | 0.0248432 | 0.108648 | intron-variant | SPAG16 | GRCh38.p7 | 2:214225019 | ATTTGTTCATTTTTA[C/T]TGAATAGTTGGAGAA | 79582 |
rs111536963 | snp | A/G | 0.171704 | 0.237423 | intron-variant | SPAG16 | GRCh38.p7 | 2:213508433 | AAAAATTAGCCGGGC[A/G]CGGTGGCGGGCGCCT | 79582 |
rs111540290 | snp | C/G | 0.0263992 | 0.111815 | intron-variant | SPAG16 | GRCh38.p7 | 2:214265491 | TCAAAGTTTGTTGTA[C/G]ATTTTGGATATAACC | 79582 |
rs111543076 | snp | A/C | 0.5 | 0 | intron-variant | SPAG16 | GRCh38.p7 | 2:214005645 | TCCACTGAATAACCA[A/C]CTGAATTTCATGGCT | 79582 |
rs111543733 | snp | C/G | 0.00557542 | 0.0525036 | intron-variant | SPAG16 | GRCh38.p7 | 2:213380502 | GGGACCTGCTTGAGC[C/G]CGATCACACATACAC | 79582 |
rs111544695 | snp | C/T | 0.5 | 0 | intron-variant | SPAG16 | GRCh38.p7 | 2:213750188 | TAAACACAGAAAGCA[C/T]TATACAAAGTATTTG | 79582 |
rs111546163 | snp | A/G | 0.0422008 | 0.138995 | intron-variant | SPAG16 | GRCh38.p7 | 2:214252538 | CTTATATGTGAGAAT[A/G]TGTGTTTTTTGGTTT | 79582 |
rs111549839 | snp | C/T | | | intron-variant | SPAG16 | GRCh38.p7 | 2:214335774 | TTTTTTTTTTTTTTT[C/T]TTTGAGATGGAGTCT | 79582 |
rs111554256 | snp | C/T | 0.00438332 | 0.0466095 | intron-variant | SPAG16 | GRCh38.p7 | 2:213816787 | TGGATTAAAAATATG[C/T]ATAATTTCATATTTT | 79582 |
rs111554557 | snp | A/C | 0.00318978 | 0.0398085 | intron-variant | SPAG16 | GRCh38.p7 | 2:214055523 | ATTACTTTTCTCCTT[A/C]TTTAACTTCTTCTTA | 79582 |
rs111557005 | snp | C/T | 0.00358779 | 0.0422022 | intron-variant | SPAG16 | GRCh38.p7 | 2:213521855 | TAAAGTTAGCATGAC[C/T]ACAAAGTAAATTATT | 79582 |
rs111557103 | snp | A/G | 0.5 | 0 | intron-variant | SPAG16 | GRCh38.p7 | 2:213788873 | GACGTCTTTATGAGT[A/G]ATTCTCAAATTATTG | 79582 |
rs111557605 | snp | G/T | | | intron-variant | SPAG16 | GRCh38.p7 | 2:213743085 | ATTTTTTGTATTTTT[G/T]GTAGAGACAGGGTTT | 79582 |
rs111559527 | snp | A/G | 0 | 0 | intron-variant | SPAG16 | GRCh38.p7 | 2:214393598 | GTTATACATATCAAG[A/G]TCATTTAAGTCAAAA | 79582 |
rs111562816 | snp | C/T | 0 | 0 | intron-variant | SPAG16 | GRCh38.p7 | 2:213796127 | TTATTACAGATCTTT[C/T]GTGGGATTCTCAAAT | 79582 |
rs111564374 | snp | A/C | 0.5 | 0 | intron-variant | SPAG16 | GRCh38.p7 | 2:214108483 | CACACACACACACCC[A/C]CACACACACCCCAAG | 79582 |
rs111566384 | snp | A/G | 0.021333 | 0.101051 | intron-variant | SPAG16 | GRCh38.p7 | 2:213469420 | TGTATACATGCACAA[A/G]CATGTTTTTAATGAA | 79582 |
rs111568039 | snp | C/G | 0.5 | 0 | intron-variant | SPAG16 | GRCh38.p7 | 2:213996613 | TCTCCCTGTCACTCA[C/G]GCTGGAGTGCAATGG | 79582 |
rs111571789 | snp | C/T | 0.0524604 | 0.153226 | intron-variant | SPAG16 | GRCh38.p7 | 2:214286238 | GCAAGATGAATAGGC[C/T]CTGGAGATCTAACGT | 79582 |
rs111574473 | snp | G/T | 0.0505692 | 0.150756 | intron-variant | SPAG16 | GRCh38.p7 | 2:213643959 | CTAATTTTTGTATTT[G/T]TAGTAGAGATGGAGT | 79582 |
rs111574810 | in-del | -/G | 0.5 | 0 | intron-variant | SPAG16 | GRCh38.p7 | 2:213459984 | AAACAGTATATTATT[-/G]TTGAAAAATCGAATA | 79582 |
rs111584458 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | SPAG16 | GRCh38.p7 | 2:213804022 | TTTCCTCTTTCCAGC[A/C]TCTCCAACTCTTAAT | 79582 |
rs111586273 | snp | A/T | 0.0287284 | 0.116357 | intron-variant | SPAG16 | GRCh38.p7 | 2:213421433 | AGGTGCCCCTTGGCA[A/T]GAACAGCCTGGGTGC | 79582 |
rs111589744 | snp | G/T | 0.0452528 | 0.143452 | intron-variant | SPAG16 | GRCh38.p7 | 2:213473673 | GCTGCAATATTAAAT[G/T]CAGAGTCCCTACTTA | 79582 |
rs111594070 | in-del | -/A | 0.5 | 0 | intron-variant | SPAG16 | GRCh38.p7 | 2:213840548 | AAATAGTTTGGGAAG[-/A]AAAAAAAAATCCTTT | 79582 |
rs111594918 | snp | A/G | 0 | 0 | intron-variant | SPAG16 | GRCh38.p7 | 2:213584182 | GCATTTCTTCATTGG[A/G]TTTTTTTTTATACTA | 79582 |
rs111600979 | snp | A/G | 0.5 | 0 | intron-variant | SPAG16 | GRCh38.p7 | 2:214154391 | CAGTATCAGATCATT[A/G]AAATGAGCAAAGTTT | 79582 |
rs111604731 | snp | A/G | 0.0023933 | 0.0345097 | intron-variant | SPAG16 | GRCh38.p7 | 2:213545008 | TTTTCAGCTCCTTTG[A/G]ATAAATACTAAGGAG | 79582 |
rs111605591 | snp | G/T | 0.125182 | 0.216612 | intron-variant | SPAG16 | GRCh38.p7 | 2:213640494 | GCTTCCTGAGAGCTG[G/T]ACTGCCGTGATTGTT | 79582 |
rs111606497 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | SPAG16 | GRCh38.p7 | 2:213608483 | CCAGCTTCATCCATG[A/T]CCCTACAAAGGACAT | 79582 |
rs111608090 | snp | A/C | 0.00358779 | 0.0422022 | intron-variant | SPAG16 | GRCh38.p7 | 2:213517460 | AGTAGAAAAAGCTAT[A/C]CTAAAATTCATATGG | 79582 |
rs111614316 | in-del | -/GTG | 0.0275645 | 0.114116 | intron-variant | SPAG16 | GRCh38.p7 | 2:213411088 | ATGTGTGGTGGTATT[-/GTG]GTGGACCTTTACTGG | 79582 |
rs111616880 | snp | A/G | 0.0829062 | 0.185956 | intron-variant | SPAG16 | GRCh38.p7 | 2:213670288 | GGCGTGAGCCACCGC[A/G]CCAGGCCAAGCATGT | 79582 |
rs111620248 | in-del | -/A | 0.5 | 0 | intron-variant | SPAG16 | GRCh38.p7 | 2:214295789 | GAACAAGACTGTCTC[-/A]AAAAAAAAGGGAAAA | 79582 |
rs111621093 | snp | A/C | 0.00398564 | 0.0444627 | intron-variant | SPAG16 | GRCh38.p7 | 2:213541295 | GAAATTAGGACGCAT[A/C]GAGTGAAAACTGCTG | 79582 |
rs111623452 | snp | A/G | 0.5 | 0 | intron-variant | SPAG16 | GRCh38.p7 | 2:214113703 | TTCTCTACACTGTTT[A/G]TTCTAGTTAGCCATT | 79582 |
rs111626476 | snp | A/G | 0.0142736 | 0.0832652 | intron-variant | SPAG16 | GRCh38.p7 | 2:213549493 | TCACTCTGCAGTCCT[A/G]TTGATTCTGACTACT | 79582 |
rs111629022 | snp | C/T | 0.5 | 0 | intron-variant | SPAG16 | GRCh38.p7 | 2:214216017 | GAAAGGCCATTCTGG[C/T]TGCAAACAATTGCAT | 79582 |
rs111632505 | snp | A/G | 0.326976 | 0.237854 | intron-variant | SPAG16 | GRCh38.p7 | 2:213408256 | AGTGTAAACAAGGGC[A/G]TAGCCAGAAAGCACT | 79582 |
rs111634503 | snp | C/T | 0.0607341 | 0.163335 | intron-variant | SPAG16 | GRCh38.p7 | 2:213761643 | GAGGCAGGTGGATCA[C/T]GAGATCAGGAGATGA | 79582 |
rs111636596 | in-del | -/T | 0 | 0 | intron-variant | SPAG16 | GRCh38.p7 | 2:214348964 | ATACGGTCATCTTTA[-/T]TTTTTTTTTACTTTT | 79582 |
rs111637294 | in-del | -/T | 0.0248432 | 0.108648 | intron-variant | SPAG16 | GRCh38.p7 | 2:214224945 | AACTGGTGCACAATA[-/T]TAACAGATAATGGTT | 79582 |
rs111638731 | in-del | -/AAT | 0.161596 | 0.233848 | intron-variant | SPAG16 | GRCh38.p7 | 2:213814794 | GCTCTGTCTCAAAAC[-/AAT]AATAATAATAATAAT | 79582 |
rs111639413 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | SPAG16 | GRCh38.p7 | 2:213749240 | TTTTCTTCTTTTGCT[A/G]TTATATTTATATTTA | 79582 |
rs111639851 | snp | C/T | | | intron-variant | SPAG16 | GRCh38.p7 | 2:214274050 | GGTATTTTATTCTCT[C/T]TGTAGCAATTGTGAA | 79582 |
rs111640014 | snp | A/G | 0.0463947 | 0.145069 | intron-variant | SPAG16 | GRCh38.p7 | 2:213337603 | AATAGCCAAAGAGAC[A/G]AAGCAGAAGAAAGGG | 79582 |
rs111640030 | snp | C/T | 0.00318978 | 0.0398085 | intron-variant | SPAG16 | GRCh38.p7 | 2:214040164 | CTGGGACCTCCAGAA[C/T]AATGGCTGGCAATTG | 79582 |
rs111640603 | snp | A/G | | | intron-variant | SPAG16 | GRCh38.p7 | 2:213539604 | ATTTTTCTGACTTAA[A/G]AAAATGCATGATTGA | 79582 |
rs111641358 | in-del | -/T | 0.00318978 | 0.0398085 | intron-variant | SPAG16 | GRCh38.p7 | 2:213521896 | TCTGCGTGCCCTGGG[-/T]AAGACTTGCATTTGT | 79582 |
rs111642466 | snp | A/G | 0.0267878 | 0.112589 | intron-variant | SPAG16 | GRCh38.p7 | 2:214227450 | CATATAACATTTCCT[A/G]TTATCCTTGATTCAA | 79582 |
rs111647167 | snp | A/G | 0.00914312 | 0.0669923 | intron-variant | SPAG16 | GRCh38.p7 | 2:214114679 | GCATAGTATTTGGGC[A/G]GGAGTGTCCCGTTTT | 79582 |
rs111647751 | snp | C/G | 0 | 0 | intron-variant | SPAG16 | GRCh38.p7 | 2:213873986 | ACTTATATAGTTACT[C/G]TACTGAATACCATAT | 79582 |
rs111648712 | snp | A/T | 0.5 | 0 | intron-variant | SPAG16 | GRCh38.p7 | 2:214213415 | CTGTGCAACAACGCA[A/T]GGCAGTGTGAACAGG | 79582 |
rs111650593 | snp | C/T | 0.00358779 | 0.0422022 | intron-variant | SPAG16 | GRCh38.p7 | 2:213492950 | CAGTTATTATTTTTC[C/T]CTCTCTCTCTCGTTT | 79582 |
rs111654680 | snp | A/C | 0.00358779 | 0.0422022 | intron-variant | SPAG16 | GRCh38.p7 | 2:213556894 | AAAATGATCAAGTAT[A/C]TTTTTTTTGAAGATG | 79582 |
rs111658504 | snp | A/G | 0.0217236 | 0.101931 | intron-variant | SPAG16 | GRCh38.p7 | 2:213833675 | GGATCTTCTACCCAC[A/G]TGGCTATTTCTCAGA | 79582 |
rs111659742 | snp | C/T | 0.5 | 0 | intron-variant | SPAG16 | GRCh38.p7 | 2:213389110 | CAGCCCAGAAATAAA[C/T]CCTCACATATATGAT | 79582 |
rs111664006 | snp | A/G | 0.00159617 | 0.0282053 | intron-variant | SPAG16 | GRCh38.p7 | 2:214338995 | ATATTTATAAATGAT[A/G]TTTCTGCCAACAGAA | 79582 |
rs111664421 | snp | A/G | 0.00318978 | 0.0398085 | intron-variant | SPAG16 | GRCh38.p7 | 2:214282165 | TTTTATTGCAGATCA[A/G]TTATACTTTAACGCT | 79582 |
rs111666433 | snp | C/T | 0.5 | 0 | intron-variant | SPAG16 | GRCh38.p7 | 2:214277351 | GAGGAGCTGCGATAA[C/T]TTGGAGAAGAGGTGC | 79582 |
rs111667622 | snp | A/G | | | intron-variant | SPAG16 | GRCh38.p7 | 2:214269423 | GGCTGGAATTGGTGA[A/G]CATAGAATTGTGTGT | 79582 |
rs111667761 | snp | C/T | 0.00199481 | 0.0315187 | intron-variant | SPAG16 | GRCh38.p7 | 2:214083939 | TATGCTTACTATTGA[C/T]GTCCTTCCTCATAGC | 79582 |
rs111673530 | snp | A/G | 0.00358779 | 0.0422022 | intron-variant | SPAG16 | GRCh38.p7 | 2:214116003 | GCAGAGCCCCAGTGG[A/G]GCCCAAGACTTAGGA | 79582 |
rs111676368 | snp | C/T | 0 | 0 | intron-variant | SPAG16 | GRCh38.p7 | 2:214218053 | ACATCCCAGCATAAA[C/T]AAATGTTTTATGGAA | 79582 |
rs111678583 | snp | G/T | 0.5 | 0 | intron-variant | SPAG16 | GRCh38.p7 | 2:213485635 | TATTCTACTTATATT[G/T]GTGACCTAGTAATTA | 79582 |
rs111679977 | snp | A/T | 0.00318978 | 0.0398085 | intron-variant | SPAG16 | GRCh38.p7 | 2:213495438 | TTAGGCCACATATGA[A/T]AAATGAATTTTAAAA | 79582 |
rs111680989 | snp | A/G | 0 | 0 | intron-variant | SPAG16 | GRCh38.p7 | 2:214233027 | AAAACCAAAGAATAC[A/G]TATCCTATGATTCTT | 79582 |
rs111681519 | snp | A/G | 0.5 | 0 | intron-variant | SPAG16 | GRCh38.p7 | 2:213902187 | AGGCATTTATTTTCT[A/G]TGGATATACCAAAGA | 79582 |
rs111683590 | snp | C/T | 0 | 0 | intron-variant | SPAG16 | GRCh38.p7 | 2:213643068 | ATGTGTGTGTGTGTA[C/T]ATATATATATATATC | 79582 |
rs111683743 | snp | A/C | 0.5 | 0 | intron-variant | SPAG16 | GRCh38.p7 | 2:214198908 | GTATATCTTCTTTTG[A/C]GAACTCTCTATTCAT | 79582 |
rs111687963 | snp | A/C | 0.00597247 | 0.0543191 | intron-variant | SPAG16 | GRCh38.p7 | 2:214384079 | CTACTAAAGTGTCCA[A/C]GACCATCTCAGAATA | 79582 |
rs111690472 | snp | C/T | 0.5 | 0 | intron-variant | SPAG16 | GRCh38.p7 | 2:214402486 | AGAACTGTTTTTTTT[C/T]TCAGGAACAATTAGT | 79582 |
rs111691810 | snp | G/T | 0.5 | 0 | intron-variant | SPAG16 | GRCh38.p7 | 2:214148527 | GAATTTTGACTAACA[G/T]ACTACAATAGGCACC | 79582 |
rs111693668 | snp | G/T | 0.5 | 0 | intron-variant | SPAG16 | GRCh38.p7 | 2:214161489 | GACATTTTAATAATT[G/T]CCATTCTAACTGGCA | 79582 |
rs111694888 | snp | C/T | 0.00517822 | 0.0506191 | intron-variant | SPAG16 | GRCh38.p7 | 2:213605927 | AGGATATATAATAGA[C/T]CATTTACACCATACT | 79582 |
rs111695642 | snp | A/C | 0.5 | 0 | intron-variant | SPAG16 | GRCh38.p7 | 2:214165226 | TTTAGGGGGAAAACT[A/C]TTATATCAGTGAGAA | 79582 |
rs111696541 | in-del | -/AT | 0 | 0 | intron-variant | SPAG16 | GRCh38.p7 | 2:213307271 | AGGTTAGTTACATAT[-/AT]GTATACATGTGCCAT | 79582 |
rs111707615 | snp | A/G | 0.0437281 | 0.141251 | intron-variant | SPAG16 | GRCh38.p7 | 2:214277288 | CTGAAGCCTAGTTCC[A/G]TCAACTCGTCAAAGT | 79582 |
rs111719010 | snp | A/T | 0.0103295 | 0.0711199 | intron-variant | SPAG16 | GRCh38.p7 | 2:213899814 | TTCTCAAATATGCAA[A/T]AAAGAGGTTTTTTTC | 79582 |
rs111719111 | in-del | -/TG | 0.0573587 | 0.15934 | intron-variant | SPAG16 | GRCh38.p7 | 2:213742553 | GCTTATTTCTTTTTT[-/TG]TTTTTTTTTTTTTTT | 79582 |
rs111720424 | snp | A/G | 0.00517822 | 0.0506191 | intron-variant | SPAG16 | GRCh38.p7 | 2:213577484 | AATCCTCTTCCCTCC[A/G]TTTCCTGATAAGCCC | 79582 |
rs111722107 | snp | A/G | 0.0433465 | 0.140692 | intron-variant | SPAG16 | GRCh38.p7 | 2:213888462 | AGGTTATTCTTTGAT[A/G]ACTGACAGTACAAGA | 79582 |
rs111727916 | snp | A/G | 0.00557542 | 0.0525036 | intron-variant | SPAG16 | GRCh38.p7 | 2:213798331 | CAATCTTGGCTCACT[A/G]CAACCTCTGCCTCCC | 79582 |
rs111728947 | snp | A/G | 0.5 | 0 | intron-variant | SPAG16 | GRCh38.p7 | 2:213515157 | ACTATTAGATAAGTA[A/G]TACGTATGTATATAT | 79582 |
rs111729705 | snp | A/T | 0.0456336 | 0.143994 | intron-variant | SPAG16 | GRCh38.p7 | 2:213449001 | AGAGCCTATAAACAG[A/T]TGTGCAAGTAGGAGA | 79582 |
rs111729961 | snp | A/G | 0.5 | 0 | intron-variant | SPAG16 | GRCh38.p7 | 2:213699613 | AGAACCTACGGATTT[A/G]TGTGTCATGGCCCCT | 79582 |
rs111733449 | snp | C/G | 0.00358779 | 0.0422022 | intron-variant | SPAG16 | GRCh38.p7 | 2:213523124 | ACATGTCATGGGAGG[C/G]ACCCAGTGGGAGGTA | 79582 |
rs111733692 | snp | A/G | 0.0197687 | 0.0974348 | intron-variant | SPAG16 | GRCh38.p7 | 2:214258218 | TACACTGTACCCAAT[A/G]TGTAGTCTTTTATTC | 79582 |
rs111735158 | snp | A/G | 0.00597247 | 0.0543191 | intron-variant | SPAG16 | GRCh38.p7 | 2:214318656 | GCTGGGATGACAGGC[A/G]TGAGCCACCGCGCCC | 79582 |
rs111736965 | snp | A/G | 0 | 0 | intron-variant | SPAG16 | GRCh38.p7 | 2:214336049 | GCTGTGAGCCACCAC[A/G]CCCAAGCCTATTATT | 79582 |
rs111738210 | snp | C/G | 0.5 | 0 | intron-variant | SPAG16 | GRCh38.p7 | 2:213732338 | CACGATTGCCCCCCC[C/G]GCAAAAAAAATGCCC | 79582 |
rs111742342 | snp | A/C | 0 | 0 | intron-variant | SPAG16 | GRCh38.p7 | 2:213822003 | TGTGAACAGTGCTGC[A/C]CAAACATGGGAGTGC | 79582 |
rs111745737 | snp | A/G | 0.00358779 | 0.0422022 | intron-variant | SPAG16 | GRCh38.p7 | 2:213556268 | TGATTACATCTTCCA[A/G]TCAAAAGATGTAAGG | 79582 |
rs111748525 | snp | A/T | 0.19334 | 0.243495 | intron-variant | SPAG16 | GRCh38.p7 | 2:214253374 | TAGTCATGAAGTGTT[A/T]GCCCATGCCTATGTC | 79582 |
rs111751853 | snp | A/G | 0.00517822 | 0.0506191 | intron-variant | SPAG16 | GRCh38.p7 | 2:213802954 | CTGGGCAGCTACCAT[A/G]ACTGAATAGGTAGTA | 79582 |
rs111759477 | snp | A/C | 0.00835141 | 0.0640778 | intron-variant | SPAG16 | GRCh38.p7 | 2:214217562 | AAAGTTTATCCCACC[A/C]CTCTTAAGAGTACTT | 79582 |
rs111763789 | snp | C/T | 0.00478085 | 0.0486577 | intron-variant | SPAG16 | GRCh38.p7 | 2:213789898 | AATTTTCGGTAACGA[C/T]ATCATTATCATCCAA | 79582 |
rs111767335 | snp | C/T | 0.5 | 0 | intron-variant | SPAG16 | GRCh38.p7 | 2:214287455 | ATGAATCCAAAGAGA[C/T]TAAATCTCTTTAAAA | 79582 |
rs111768719 | snp | A/G | 0.0260105 | 0.111035 | intron-variant, upstream-variant-2KB | SPAG16 | GRCh38.p7 | 2:213299480 | AGACGGGGTTTCACC[A/G]TGTTAGCCAGGTTGG | 79582 |
rs111771655 | snp | A/G | 0.021333 | 0.101051 | intron-variant | SPAG16 | GRCh38.p7 | 2:213468926 | AAAGATGTAGGCTGG[A/G]AGGCTAGGCCATCTG | 79582 |
rs111772841 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | SPAG16 | GRCh38.p7 | 2:213596667 | TGAAACTCTATAATC[C/T]TAGTGGGTTGTTTGG | 79582 |
rs111773912 | snp | A/C | 0.132066 | 0.220435 | intron-variant | SPAG16 | GRCh38.p7 | 2:213470691 | CCTCCCATCATGGCC[A/C]CTTTTCTCATGGGCC | 79582 |
rs111775422 | snp | A/G | | | intron-variant | SPAG16 | GRCh38.p7 | 2:214275492 | ATTCTGGTACATTGT[A/G]TCTTTGTTCTCATTG | 79582 |
rs111777361 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | SPAG16 | GRCh38.p7 | 2:214133238 | CATTATAAGACTTTT[A/G]TCAGCATCCCTGGCC | 79582 |
rs111777630 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | SPAG16 | GRCh38.p7 | 2:214123862 | AAAATCGGGACACAT[A/G]GAGTGAACTAGGAAT | 79582 |
rs111783113 | snp | A/T | 0.18989 | 0.242666 | intron-variant | SPAG16 | GRCh38.p7 | 2:213478360 | CCACCTGAGCTGTTT[A/T]GATATCTTAAGTCTA | 79582 |
rs111784310 | snp | A/G | | | intron-variant | SPAG16 | GRCh38.p7 | 2:213854265 | TCTTTAAAAGAAAAA[A/G]GTATGAATGATAGAT | 79582 |
rs111787465 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | SPAG16 | GRCh38.p7 | 2:213454646 | AAGAAAATTATAATG[C/T]TTAGCAGTGACTTTC | 79582 |
rs111789706 | snp | C/T | 0.127254 | 0.217792 | intron-variant | SPAG16 | GRCh38.p7 | 2:213617444 | CCTCCTGGGTTAAAG[C/T]GATTTTTCTGCCTCA | 79582 |
rs111790502 | snp | A/G | 0.5 | 0 | intron-variant, upstream-variant-2KB | SPAG16, LOC101928084 | GRCh38.p7 | 2:214103103 | TTTCTCCAGTGGCAT[A/G]TGCCCCCCAGAATGT | 79582 |
rs111791519 | snp | A/C | 0.5 | 0 | intron-variant | SPAG16 | GRCh38.p7 | 2:213292682 | AAAAAAAAACAAAAA[A/C]AACAAAAAAAAACAA | 79582 |
rs111795310 | snp | A/G | 0.00676609 | 0.0577691 | intron-variant | SPAG16 | GRCh38.p7 | 2:213695699 | CAGCCATGAGAAGAC[A/G]TAGAGGAGAAGCATG | 79582 |
rs111797883 | snp | C/T | 0.039522 | 0.134904 | intron-variant | SPAG16 | GRCh38.p7 | 2:214219728 | CAAATTCTTAGAAAA[C/T]GTCCCTTCTAGTTTC | 79582 |
rs111803365 | snp | A/G | 0.5 | 0 | intron-variant | SPAG16 | GRCh38.p7 | 2:214171441 | CTTGTACAGATGCTA[A/G]CATATCAATAAATAG | 79582 |
rs111805726 | in-del | -/A | 0.0498117 | 0.149749 | intron-variant | SPAG16 | GRCh38.p7 | 2:213772730 | TTTGGGCTACTTTAG[-/A]ATCAACTTGTCTATT | 79582 |
rs111807644 | in-del | -/GG | 0.170084 | 0.236883 | intron-variant | SPAG16 | GRCh38.p7 | 2:213602363 | CAGGCCGGGCACAGT[-/GG]GGCTCTCGCCTGTAA | 79582 |
rs111811034 | in-del | -/A | 0.148326 | 0.228391 | intron-variant | SPAG16 | GRCh38.p7 | 2:213707757 | TTTCTAAGGTGATGG[-/A]AAAAAAATCTAATAA | 79582 |
rs111812056 | snp | A/G | 0.17138 | 0.237316 | intron-variant | SPAG16 | GRCh38.p7 | 2:213508596 | AAGAAAAAAAAAAAT[A/G]ATGAGTTCATGTCCT | 79582 |
rs111812933 | in-del | -/T | 0.0452528 | 0.143452 | intron-variant | SPAG16 | GRCh38.p7 | 2:213431899 | TAACTTTATCAAGTG[-/T]CTTCTCTAACTATAG | 79582 |
rs111819041 | snp | C/T | 0.00478085 | 0.0486577 | intron-variant | SPAG16 | GRCh38.p7 | 2:213900517 | ATGCCCCTGGAGTTA[C/T]TCTAAAATTAATACA | 79582 |
rs111820416 | snp | A/G | 0.00358779 | 0.0422022 | intron-variant | SPAG16 | GRCh38.p7 | 2:213658704 | AGGAACTATGTCTCT[A/G]GAGAGGTGCTGGAGT | 79582 |
rs111826583 | snp | C/T | 0.0520825 | 0.152737 | intron-variant | SPAG16 | GRCh38.p7 | 2:214348561 | GTTCACTTTTGGAGT[C/T]CTGAGCTGCCACATA | 79582 |
rs111826824 | snp | G/T | 0.0221141 | 0.102801 | intron-variant | SPAG16 | GRCh38.p7 | 2:213820533 | TATAAGCACAAAAAA[G/T]GTAGAACCTTGATTT | 79582 |
rs111827546 | snp | C/T | 0 | 0 | intron-variant | SPAG16 | GRCh38.p7 | 2:214334898 | CTAGATCCACAATCT[C/T]ATTTTAATGTTTGCT | 79582 |
rs111829596 | snp | C/G | 0.029116 | 0.117091 | intron-variant | SPAG16 | GRCh38.p7 | 2:214140727 | TAATTATTTTTTTCT[C/G]ACACTGATACTATTC | 79582 |
rs111833399 | snp | G/T | 0.5 | 0 | intron-variant | SPAG16 | GRCh38.p7 | 2:213672863 | TTATTTTGTTTGTTT[G/T]TTTTTTTTTTTTTGA | 79582 |
rs111835128 | snp | C/T | 0.00478085 | 0.0486577 | intron-variant | SPAG16 | GRCh38.p7 | 2:213633518 | CTTAGATGAAATGTT[C/T]TGTAAATATCTATGA | 79582 |
rs111835628 | snp | A/G | 0 | 0 | intron-variant | SPAG16 | GRCh38.p7 | 2:213892272 | GGGCTGAAGGCTACC[A/G]CCCAGAGCTGAAAAG | 79582 |
rs111836844 | snp | C/T | 0.029116 | 0.117091 | intron-variant | SPAG16 | GRCh38.p7 | 2:213561727 | AGACTTCTTAATGTT[C/T]TATTTTTACAAGAAT | 79582 |
rs111838164 | snp | C/T | 0.00517822 | 0.0506191 | intron-variant | SPAG16 | GRCh38.p7 | 2:213610381 | AAAGTTTAACACTTT[C/T]GAAAATCTGAAAGAA | 79582 |
rs111843712 | snp | C/T | 0.0189856 | 0.0955633 | intron-variant | SPAG16 | GRCh38.p7 | 2:214192002 | AAAAAAAAAACAGGA[C/T]TAGGACAAAAGAATG | 79582 |
rs111848405 | snp | A/G | 0.00517822 | 0.0506191 | intron-variant | SPAG16 | GRCh38.p7 | 2:213731210 | TGCCCAGGCTGGAGT[A/G]TAGTGGCGCGATCTC | 79582 |
rs111850307 | snp | C/G | 0.177182 | 0.23916 | intron-variant | SPAG16 | GRCh38.p7 | 2:213407098 | GAGGGCTAAATGTGT[C/G]TGTGCGTGAATGATC | 79582 |
rs111851971 | snp | C/T | 0.0158469 | 0.0875917 | intron-variant | SPAG16 | GRCh38.p7 | 2:213378064 | GAAGAACTTGGAGTC[C/T]GATGTTAGAGGGCAG | 79582 |
rs111857190 | in-del | -/C | 0.5 | 0 | intron-variant | SPAG16 | GRCh38.p7 | 2:213392318 | CAGCTATTATTATTA[-/C]TTTTTGCCTAAAGTG | 79582 |
rs111857429 | snp | A/G | 0.5 | 0 | intron-variant | SPAG16 | GRCh38.p7 | 2:213696984 | AAACAAATTGATGAT[A/G]TAGGAGGAAGAGGAT | 79582 |
rs111860144 | snp | A/G | 0.00358779 | 0.0422022 | intron-variant, downstream-variant-500B | SPAG16 | GRCh38.p7 | 2:213503774 | ATACAGAGGTTTAAG[A/G]GTTTAAAATTAAATA | 79582 |
rs111860798 | snp | C/T | 0.00358779 | 0.0422022 | intron-variant | SPAG16 | GRCh38.p7 | 2:213505378 | AAATTCTACTATATT[C/T]TGGTAGCATCACTCT | 79582 |
rs111862599 | snp | C/T | 0.00358779 | 0.0422022 | intron-variant | SPAG16 | GRCh38.p7 | 2:213500860 | CTCCTAGTGTCCAAA[C/T]AGCTCTAGCCCCTAA | 79582 |
rs111870265 | snp | A/T | 0.00358779 | 0.0422022 | intron-variant | SPAG16 | GRCh38.p7 | 2:213507953 | TAGATTACTCATTTG[A/T]CTGGGGCAAGAGCTT | 79582 |
rs111877788 | snp | A/C | 0.00159617 | 0.0282053 | intron-variant | SPAG16 | GRCh38.p7 | 2:214317568 | TAATTACTGCTAAAA[A/C]TAATGTAAAAAATGG | 79582 |
rs111882355 | in-del | -/A | 0 | 0 | intron-variant | SPAG16 | GRCh38.p7 | 2:213841690 | CATATTTGTAAGTAC[-/A]GGGAAGTCTTTCTTG | 79582 |
rs111891160 | snp | C/T | 0.5 | 0 | intron-variant | SPAG16 | GRCh38.p7 | 2:214161142 | TGATCTTGTTCCTTT[C/T]TATGGCTGCATAGTA | 79582 |
rs111891610 | snp | A/G | 0.0482946 | 0.147699 | intron-variant, synonymous-codon | SPAG16 | GRCh38.p7 | 2:213368878 | GAAGGACGTCTTCAA[A/G]GAGAACTACAAACCA | 79582 |
rs111894796 | snp | G/T | 0 | 0 | intron-variant | SPAG16 | GRCh38.p7 | 2:213951024 | GCCTGACATAGTTTT[G/T]TTTTTTTTAATAATA | 79582 |
rs111902073 | snp | G/T | 0.127599 | 0.217986 | intron-variant | SPAG16 | GRCh38.p7 | 2:213635996 | TGTTGCATTTGCTTT[G/T]GGGTACTTGGTCATG | 79582 |
rs111902436 | snp | A/C | 0.00199481 | 0.0315187 | intron-variant | SPAG16 | GRCh38.p7 | 2:214385731 | CACCTGTAGTCCTAG[A/C]TGCTTGGGAGGCTGA | 79582 |
rs111907683 | snp | A/G | 0.212425 | 0.24716 | intron-variant | SPAG16 | GRCh38.p7 | 2:213358377 | GGTTCCATTCTCCCC[A/G]TCACTTTCAGGTACA | 79582 |
rs111913751 | snp | A/G/T | 0.000399281 | 0.0141238 | intron-variant | SPAG16 | GRCh38.p7 | 2:213805522 | GGAAGTACCTTTTAG[A/G/T]TTTTTAGAAGAGTTA | 79582 |
rs111914904 | snp | C/T | 0 | 0 | intron-variant, upstream-variant-2KB | SPAG16 | GRCh38.p7 | 2:213342809 | TAAGATGGTGGAAAA[C/T]TGGCAAAGCAGGACC | 79582 |
rs111915982 | snp | A/G | 0.5 | 0 | intron-variant | SPAG16 | GRCh38.p7 | 2:214288450 | TAAATACCCAGTAGT[A/G]GGATTGCTGAATCTT | 79582 |
rs111918793 | snp | A/G | 0.5 | 0 | intron-variant | SPAG16 | GRCh38.p7 | 2:214065308 | TGCAAAGGGATTTTG[A/G]CCTCAAATCGATTAT | 79582 |
rs111923456 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | SPAG16 | GRCh38.p7 | 2:214243305 | CTTAAGATGAACCAA[C/T]GATTTGAAGAAAACA | 79582 |
rs111926327 | snp | C/T | 0.0154538 | 0.0865337 | intron-variant | SPAG16, LOC101928084 | GRCh38.p7 | 2:214095095 | AGGAACTCAAAAGTT[C/T]TTAGCACATTGGAAA | 79582 |
rs111932675 | snp | C/T | 0.5 | 0 | intron-variant | SPAG16 | GRCh38.p7 | 2:213722572 | ATACGGCCTTCAGAA[C/T]CTAGTACTTGAGATG | 79582 |
rs111936389 | snp | A/G | 0.00517822 | 0.0506191 | intron-variant | SPAG16 | GRCh38.p7 | 2:213626045 | CTAGGATCTTCTGGA[A/G]TTTGTCCTTTTATAT | 79582 |
rs111937407 | in-del | -/TTC | 0.5 | 0 | intron-variant, upstream-variant-2KB | SPAG16 | GRCh38.p7 | 2:213297595 | GTATCAAGTGACACC[-/TTC]TCTCTGAACTCTGAT | 79582 |
rs111941205 | snp | C/G | 0.102726 | 0.202016 | intron-variant | SPAG16 | GRCh38.p7 | 2:213686346 | CTGATCCAATCTCCT[C/G]ACTTTGTGATCCACC | 79582 |
rs111941751 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | SPAG16 | GRCh38.p7 | 2:213873928 | ATACCATAGACTATA[C/T]AGACTATAGCATATT | 79582 |
rs111944436 | snp | A/T | 0.5 | 0 | intron-variant | SPAG16 | GRCh38.p7 | 2:214138187 | GGAAAATGCTTTTAT[A/T]TTTTTTAGACAAAAA | 79582 |
rs111952440 | snp | C/T | | | intron-variant | SPAG16 | GRCh38.p7 | 2:213547287 | TTGTTCCAGTAAAAA[C/T]AGTCATGGTGTATTC | 79582 |
rs111957573 | snp | A/T | 0.5 | 0 | intron-variant | SPAG16 | GRCh38.p7 | 2:213967477 | TCTAAAAAGATTTTC[A/T]AAAAACCAGATACTA | 79582 |
rs111960094 | snp | A/C | | | intron-variant | SPAG16 | GRCh38.p7 | 2:213347234 | ATCGGTGGTGATATC[A/C]CCTTTATCATTTTTT | 79582 |
rs111961935 | snp | A/C | 0.00199481 | 0.0315187 | intron-variant | SPAG16 | GRCh38.p7 | 2:214235514 | GAGATGTCTTCCACT[A/C]AACACCTACAGCTTT | 79582 |
rs111970006 | snp | A/T | 0.235854 | 0.249599 | intron-variant | SPAG16 | GRCh38.p7 | 2:213322099 | AAATAAATAAATAAA[A/T]AAAAGTAAAAAAAAA | 79582 |
rs111971324 | snp | C/T | 0.00318978 | 0.0398085 | intron-variant | SPAG16 | GRCh38.p7 | 2:214286786 | AATAAAAAATAACAG[C/T]GATAACTTGTTCTGA | 79582 |
rs111971721 | snp | A/G | 0 | 0 | intron-variant | SPAG16 | GRCh38.p7 | 2:213485449 | TATCAGTGTAATCAT[A/G]TCTGTAATTAATGAT | 79582 |
rs111975864 | snp | C/T | 0.0626037 | 0.165477 | intron-variant | SPAG16 | GRCh38.p7 | 2:213472386 | TAAGCTTTTGATAAT[C/T]GACGATCATTCTCCA | 79582 |
rs111977041 | snp | A/G | 0.0248432 | 0.108648 | intron-variant | SPAG16 | GRCh38.p7 | 2:214249450 | GAAAGATAGGGATGG[A/G]GAGGAGAAGAGGAAG | 79582 |
rs111985730 | snp | C/T | 0.0158469 | 0.0875917 | intron-variant | SPAG16 | GRCh38.p7 | 2:213780184 | GCCTCATCCTGCACT[C/T]CACCCTCCCAACCTT | 79582 |
rs111986184 | snp | G/T | 0.00358779 | 0.0422022 | intron-variant | SPAG16 | GRCh38.p7 | 2:213574497 | AGGAAAATCCCATGT[G/T]CCAAGAAGGATATTG | 79582 |
rs111988339 | snp | A/C | 0.0295035 | 0.117819 | intron-variant | SPAG16 | GRCh38.p7 | 2:213614302 | ATTTCATTTAAAGGG[A/C]TACAAATGGCATAAT | 79582 |
rs111990089 | snp | C/T | | | intron-variant | SPAG16 | GRCh38.p7 | 2:213788872 | TGACGTCTTTATGAG[C/T]GATTCTCAAATTATT | 79582 |
rs111993898 | snp | C/T | 0.0130921 | 0.0798413 | intron-variant | SPAG16 | GRCh38.p7 | 2:213911315 | TCACTAGGCTAATTT[C/T]TGTATTTTTTCTAGA | 79582 |
rs112002008 | snp | A/G | 0.00358779 | 0.0422022 | intron-variant | SPAG16 | GRCh38.p7 | 2:213543223 | TTGGTTAGGTTGAGC[A/G]TCTCATTTTATTTCT | 79582 |
rs112004321 | snp | C/T | 0.00478085 | 0.0486577 | intron-variant | SPAG16 | GRCh38.p7 | 2:213647959 | GGTTTGATAGCAAAG[C/T]GTAGCCAGGATGTTT | 79582 |
rs112004720 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | SPAG16 | GRCh38.p7 | 2:213701784 | TCAGGGATTGTAAAC[A/G]CACCAATCAGCACTC | 79582 |
rs112006644 | snp | A/T | | | intron-variant | SPAG16 | GRCh38.p7 | 2:214146729 | TATTTGGCTGGGCGC[A/T]GTGGCTCATACCTGT | 79582 |
rs112008126 | snp | C/T | 0.00517822 | 0.0506191 | intron-variant | SPAG16 | GRCh38.p7 | 2:213581530 | CTCTATTTAAAGGCC[C/T]TAAATGTTCTTCAGA | 79582 |
rs112011689 | snp | G/T | 0.0185938 | 0.0946107 | intron-variant | SPAG16 | GRCh38.p7 | 2:214141801 | ATTTTTCACTTGTAG[G/T]TAAATATCTCTTCGT | 79582 |
rs112012046 | snp | A/G/T | 0.0495086 | 0.149714 | intron-variant | SPAG16 | GRCh38.p7 | 2:213347817 | CCAACTGTGTGGTCA[A/G/T]TTTTGGAATAAGTAC | 79582 |
rs112018152 | snp | C/G | 0.00199481 | 0.0315187 | intron-variant | SPAG16 | GRCh38.p7 | 2:214238993 | AAATAGTTACTTGCA[C/G]AAATGCTATCTATTA | 79582 |
rs112018615 | in-del | -/CT | 0.213635 | 0.247341 | intron-variant | SPAG16 | GRCh38.p7 | 2:213361678 | GAAAAGAAAAAAAAA[-/CT]CAACATAATAATGGG | 79582 |
rs112020628 | snp | C/T | 0.00279162 | 0.0372561 | intron-variant | SPAG16 | GRCh38.p7 | 2:214271575 | GGAGGCCAAGGCGGG[C/T]GGATCACCTGAGGTC | 79582 |
rs112025489 | snp | A/T | 0.00478085 | 0.0486577 | intron-variant | SPAG16 | GRCh38.p7 | 2:213635159 | CCTGCCTCAGCCTCC[A/T]GAGTAGCTGGGAATA | 79582 |
rs112025805 | snp | A/T | 0.00318978 | 0.0398085 | intron-variant | SPAG16 | GRCh38.p7 | 2:214266002 | AAGTCCTACGTGAGC[A/T]GAGACTCAGTTTGTT | 79582 |
rs112029622 | snp | C/T | 0.00358779 | 0.0422022 | intron-variant | SPAG16 | GRCh38.p7 | 2:213552894 | CTTCTTGCCCTCAAA[C/T]GTCAAACATCAAATT | 79582 |
rs112030322 | snp | A/G | 0.5 | 0 | intron-variant | SPAG16 | GRCh38.p7 | 2:213607974 | ACTTTAGAAAGTACT[A/G]AATTTAACTGTGATC | 79582 |
rs112031663 | snp | A/G | 0.0295035 | 0.117819 | intron-variant | SPAG16 | GRCh38.p7 | 2:213624551 | TAGTAGTGAATTACA[A/G]TGATAAAAACTAAAT | 79582 |
rs112032912 | snp | G/T | | | intron-variant | SPAG16 | GRCh38.p7 | 2:213409117 | GAAATAAATTAACTG[G/T]TTTTTTTTTTTAAAG | 79582 |
rs112036078 | snp | A/T | 0.00159617 | 0.0282053 | intron-variant | SPAG16 | GRCh38.p7 | 2:214325899 | ATTTCCAAAGGGTTA[A/T]CCACAATTAAACTGC | 79582 |
rs112043440 | snp | A/T | 0.5 | 0 | intron-variant | SPAG16 | GRCh38.p7 | 2:213419129 | TTAGCTCCTCTTCTC[A/T]CTGCTGTGAGAAGCT | 79582 |
rs112047561 | snp | A/G | 0.00755907 | 0.0610114 | intron-variant | SPAG16 | GRCh38.p7 | 2:214336685 | TAGAAATATTGAGCC[A/G]GATAAAGGCTGAGGT | 79582 |
rs112049752 | snp | C/T | 0.00398564 | 0.0444627 | intron-variant | SPAG16 | GRCh38.p7 | 2:214348780 | AGAAAAATCCCCCAC[C/T]GCACCCTGTCCAAAT | 79582 |
rs112052547 | snp | C/T | 0.00874735 | 0.0655527 | intron-variant | SPAG16 | GRCh38.p7 | 2:213961454 | TAGAAGTGATTAGAT[C/T]GGCCATCTTTGTCTT | 79582 |
rs112052946 | snp | A/G | 0.00279162 | 0.0372561 | intron-variant | SPAG16 | GRCh38.p7 | 2:214199999 | ATCTAGGAACTTTTT[A/G]GATGAGTTTTTAGGG | 79582 |
rs112055156 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | SPAG16 | GRCh38.p7 | 2:214314850 | AACACTACAAGAGTA[A/G]CTCATGCATGAGGAA | 79582 |
rs112055307 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | SPAG16 | GRCh38.p7 | 2:213701696 | CTGGGCTCCTGAGTC[A/G]GGTAGGGACTTGGAG | 79582 |
rs112056761 | snp | C/G | 0.5 | 0 | intron-variant | SPAG16 | GRCh38.p7 | 2:213327022 | TGGTTTCCTGAAATG[C/G]AGAAGTTAAATAATC | 79582 |
rs112057716 | snp | A/G | 0.00874735 | 0.0655527 | intron-variant | SPAG16 | GRCh38.p7 | 2:214082936 | ACTCTACCATTTACC[A/G]ACATAATCACAAACT | 79582 |
rs112060281 | in-del | -/TT | 0.211819 | 0.247067 | intron-variant | SPAG16 | GRCh38.p7 | 2:213303467 | AATGTAGTCACTCTC[-/TT]GTGCTATCAAATACT | 79582 |
rs112069376 | snp | A/G | 0 | 0 | intron-variant | SPAG16 | GRCh38.p7 | 2:214254117 | CTGTTATTGGTGTCT[A/G]GTTTTGCACATTAAT | 79582 |
rs112073565 | snp | A/T | 0.0429648 | 0.14013 | intron-variant | SPAG16 | GRCh38.p7 | 2:214229847 | CTGGTCTGCTGCAGT[A/T]TGTATAGCATTATGA | 79582 |
rs112073868 | snp | G/T | | | intron-variant | SPAG16 | GRCh38.p7 | 2:213468525 | TATATATCTATGTAT[G/T]TATATATAGATATAT | 79582 |
rs112074057 | in-del | -/TCTC | 0 | 0 | intron-variant | SPAG16 | GRCh38.p7 | 2:213949202 | TTTTTTGAGGTAGAG[-/TCTC]TCTCTGTCACCAGGC | 79582 |
rs112074071 | snp | G/T | 0.00119737 | 0.0244387 | intron-variant | SPAG16 | GRCh38.p7 | 2:213940323 | TAGAGATGACATCTT[G/T]CTGTGTTGCCTGGGC | 79582 |
rs112075907 | snp | A/T | 0.00358779 | 0.0422022 | intron-variant | SPAG16 | GRCh38.p7 | 2:213508968 | TTACTGACTGTGTTG[A/T]TATTTTCTATACAAT | 79582 |
rs112078132 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | SPAG16 | GRCh38.p7 | 2:213790640 | ACACCAATTATATAC[A/T]ATGTGAGCATACCAG | 79582 |
rs112080688 | snp | A/T | 0 | 0 | intron-variant | SPAG16 | GRCh38.p7 | 2:214324700 | AAGAAAAATGTAAAG[A/T]AAAGTTTCTGATATT | 79582 |
rs112086057 | snp | A/C | 0.125528 | 0.21681 | intron-variant | SPAG16 | GRCh38.p7 | 2:213632817 | GCATTCTAGGGATAA[A/C]TCCCACTTGGTCATG | 79582 |
rs112091147 | snp | A/G | 0 | 0 | intron-variant | SPAG16 | GRCh38.p7 | 2:213838761 | CTTGTAAAGGTTAAA[A/G]CAAAGGAAATTTTCT | 79582 |
rs112095971 | snp | A/G | | | intron-variant | SPAG16 | GRCh38.p7 | 2:213869279 | AATATATATATATAT[A/G]TGTATATATATATGT | 79582 |
rs112097808 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | SPAG16 | GRCh38.p7 | 2:213824931 | TCTAGTTTTCATTGT[A/G]TATGTTTCACTTCTC | 79582 |
rs112098701 | snp | C/T | 0.0452528 | 0.143452 | intron-variant | SPAG16 | GRCh38.p7 | 2:213472963 | TCAGTAGTGTAGTGG[C/T]GTCCTTCCTCAAGAG | 79582 |
rs112101342 | snp | A/G | 0.5 | 0 | intron-variant, utr-variant-5-prime | SPAG16 | GRCh38.p7 | 2:213343856 | AAAGACTGAAAAAAC[A/G]TAAATAGAACCTCTG | 79582 |
rs112102328 | snp | C/T | | | intron-variant | SPAG16 | GRCh38.p7 | 2:213869278 | AAATATATATATATA[C/T]ATGTATATATATATG | 79582 |
rs112104800 | in-del | -/TCTATCTATCTA | 0.5 | 0 | intron-variant | SPAG16 | GRCh38.p7 | 2:213802396 | CAAATGATTCATGTC[-/TCTATCTATCTA]TCTATCTATCTATCT | 79582 |
rs112104941 | in-del | -/G | 0.120326 | 0.21374 | intron-variant | SPAG16 | GRCh38.p7 | 2:214330646 | GAAAGGGTTTGAAAC[-/G]TTTGACCCCTACATC | 79582 |
rs112108920 | in-del | -/T | 0.00358779 | 0.0422022 | intron-variant | SPAG16 | GRCh38.p7 | 2:213608170 | ATATTATACTTTCCA[-/T]TTTTTATTCTATTAT | 79582 |
rs112110113 | snp | C/T | 0.5 | 0 | intron-variant | SPAG16 | GRCh38.p7 | 2:213309829 | TTTTTTATTTAGTTA[C/T]TCATATTCTGTCTCC | 79582 |
rs112113433 | snp | C/G | 0.131062 | 0.22214 | intron-variant | SPAG16 | GRCh38.p7 | 2:213605552 | TAGTGTGCAATGGCC[C/G]GGTCTCGGCTCACTG | 79582 |
rs112114790 | snp | A/C | 0.0267878 | 0.112589 | intron-variant | SPAG16 | GRCh38.p7 | 2:214265883 | AGCAGTCCCTCCCAA[A/C]CAATCACTGTTTGAT | 79582 |
rs112118462 | snp | G/T | 0.0154538 | 0.0865337 | intron-variant | SPAG16 | GRCh38.p7 | 2:213996353 | TGTAACTATTTCAGA[G/T]ACATGGAAATTAAAT | 79582 |
rs112118723 | snp | A/G | 0.0252325 | 0.109451 | intron-variant | SPAG16 | GRCh38.p7 | 2:213492921 | CTATGTCTGACCTTT[A/G]TATTTCTATAAGGCA | 79582 |
rs112118832 | snp | G/T | | | intron-variant | SPAG16 | GRCh38.p7 | 2:214355671 | AGCCATCCCATTACT[G/T]GGTATATACCCAAAA | 79582 |
rs112119517 | snp | C/G | 0.5 | 0 | intron-variant | SPAG16 | GRCh38.p7 | 2:213507573 | CCTATTTAGAATAGG[C/G]AGCCCTCCTTTTCAG | 79582 |
rs112122536 | snp | A/G | 0.122064 | 0.214785 | intron-variant | SPAG16 | GRCh38.p7 | 2:213337876 | AACCCAGACAACCCT[A/G]GTAAGATACTACATG | 79582 |
rs112123933 | snp | A/G | 0.00358779 | 0.0422022 | intron-variant | SPAG16 | GRCh38.p7 | 2:213540995 | CGCAGGTGCACTCGT[A/G]GAGTTACAAGTAAAG | 79582 |
rs112124801 | in-del | -/TGTC | 0.192715 | 0.243348 | intron-variant | SPAG16 | GRCh38.p7 | 2:213451132 | AACAATTATCCACAT[-/TGTC]TGTGAAGCACTTTCA | 79582 |
rs112125664 | snp | A/G | 0.5 | 0 | intron-variant | SPAG16 | GRCh38.p7 | 2:213978076 | TGAGACACCCCTTTT[A/G]ACTTTTCTGGAGTCT | 79582 |
rs112126451 | snp | A/C | 0.0138799 | 0.0821421 | intron-variant | SPAG16 | GRCh38.p7 | 2:213857075 | TCTCTATCAAAAATA[A/C]AAAAACTAGCCAGGC | 79582 |
rs112128946 | snp | A/G | 0.0279526 | 0.114869 | intron-variant | SPAG16 | GRCh38.p7 | 2:214246554 | CCCTTGACTATGCTT[A/G]GTCCACTGTGCTGCA | 79582 |
rs112132203 | snp | A/C | 0.0456336 | 0.143994 | intron-variant | SPAG16 | GRCh38.p7 | 2:213448645 | ACCCAAATGGAGGGA[A/C]GGGCTGGAGCCATGG | 79582 |
rs112138199 | snp | A/G | 0.0452528 | 0.143452 | intron-variant | SPAG16 | GRCh38.p7 | 2:213428818 | AGGAGAAGGCTGGGC[A/G]TGGTGGCTCATGCCT | 79582 |
rs112139812 | snp | C/T | 0.0166325 | 0.0896639 | intron-variant | SPAG16 | GRCh38.p7 | 2:214109737 | TCTAATTTTCTGTAG[C/T]GAGCCAATTAGTTGG | 79582 |
rs112147404 | in-del | -/ACACAC | 0.427016 | 0.176537 | intron-variant | SPAG16 | GRCh38.p7 | 2:214056281 | AGATGTAGTAGAAAT[-/ACACAC]ACACACACACACACA | 79582 |
rs112151663 | snp | C/T | 0.00358779 | 0.0422022 | intron-variant | SPAG16 | GRCh38.p7 | 2:213544306 | TATATTCTGTGAGTA[C/T]AATACCTTCTTTTAT | 79582 |
rs112151738 | snp | C/T | 0.00914312 | 0.0669923 | intron-variant | SPAG16 | GRCh38.p7 | 2:214151778 | GAGGCCAGGCAATGG[C/T]CTGCTGTCTCCGCTG | 79582 |
rs112151900 | snp | A/G | 0.00517822 | 0.0506191 | intron-variant | SPAG16 | GRCh38.p7 | 2:213585370 | GAACCTCTGCCTCCT[A/G]GGTTCAAGCAATTCT | 79582 |
rs112154383 | snp | A/C | 0.5 | 0 | intron-variant | SPAG16 | GRCh38.p7 | 2:214127744 | TGTCCTCTTCCTCAC[A/C]ACACACCCTCACCCG | 79582 |
rs112155630 | snp | C/T | 0.11963 | 0.213316 | intron-variant | SPAG16 | GRCh38.p7 | 2:214328218 | TGGAATGCAGTGGTG[C/T]GATCTTGGCTCACTG | 79582 |
rs112161376 | snp | C/G | 0.00517822 | 0.0506191 | intron-variant | SPAG16 | GRCh38.p7 | 2:213585152 | TGAGATCGTGCCACT[C/G]TACTCCAGCCTGCAC | 79582 |
rs112164332 | snp | A/T | 0.5 | 0 | intron-variant | SPAG16 | GRCh38.p7 | 2:213464011 | AAAAGGAAGAGTCCT[A/T]ACTAGTACTAAGTCC | 79582 |
rs112170845 | snp | A/T | 0.046775 | 0.145601 | intron-variant | SPAG16 | GRCh38.p7 | 2:213347764 | TGTAAAAGAACAGAA[A/T]TTATAACAAACTATC | 79582 |
rs112171721 | snp | C/T | 0.5 | 0 | intron-variant | SPAG16 | GRCh38.p7 | 2:214203814 | CCAAAGTTTCCTGGA[C/T]GGAACCTGGAGAAGG | 79582 |
rs112176869 | snp | A/G | 0 | 0 | intron-variant | SPAG16 | GRCh38.p7 | 2:214069644 | GGTGGTAAAAGCATT[A/G]TCAGGAGGAACATGA | 79582 |
rs112180010 | snp | C/G | 0.029116 | 0.117091 | intron-variant | SPAG16 | GRCh38.p7 | 2:213464523 | TTCTATCACCTCAGA[C/G]ACTTTCTCTGTCAGA | 79582 |
rs112180039 | snp | G/T | 0.0490535 | 0.14873 | intron-variant | SPAG16, LOC101928084 | GRCh38.p7 | 2:214100076 | GGCAGTGTCCCCCAT[G/T]CTGTTCTCATGATAG | 79582 |
rs112181605 | snp | C/T | 0.0107246 | 0.0724382 | intron-variant | SPAG16 | GRCh38.p7 | 2:213671865 | TCACCCAGGAGGAAA[C/T]TGAGGCCTAGGAATG | 79582 |
rs112186868 | snp | C/T | 0.0422008 | 0.138995 | intron-variant | SPAG16 | GRCh38.p7 | 2:213525278 | AATTAAACCTCTTTT[C/T]CTTTTCTTTTTTTTT | 79582 |
rs112191701 | snp | C/G | 0.0501905 | 0.150254 | intron-variant | SPAG16, LOC101928084 | GRCh38.p7 | 2:214089422 | GGTAAAGATCATGTA[C/G]AAACACTTTCATCAT | 79582 |
rs112196990 | snp | A/G | 0.00478085 | 0.0486577 | intron-variant | SPAG16 | GRCh38.p7 | 2:213641218 | TTGTCAGGGAAGTGG[A/G]GGAAAGCTGGCAGTG | 79582 |
rs112200572 | snp | A/G | 0.5 | 0 | intron-variant | SPAG16 | GRCh38.p7 | 2:214248776 | TATACAAAAATTAAT[A/G]CATAATAAGAGAATA | 79582 |
rs112201437 | snp | A/C | 0.444444 | 0.157135 | intron-variant | SPAG16 | GRCh38.p7 | 2:213858918 | AGGTGCAGTGGCTCA[A/C]GCCTGTAATCCCAGC | 79582 |
rs112201584 | snp | A/G | 0.00478085 | 0.0486577 | intron-variant | SPAG16 | GRCh38.p7 | 2:213629303 | CTTCTTAGCCATTGC[A/G]ACCAAGGACTACACG | 79582 |
rs112204735 | snp | A/T | 0.00993419 | 0.0697739 | intron-variant | SPAG16 | GRCh38.p7 | 2:214046316 | AAACTATTTCCAAAA[A/T]TATGTGAAGATGGAA | 79582 |
rs112206136 | snp | A/G | 0.5 | 0 | intron-variant | SPAG16 | GRCh38.p7 | 2:213660148 | GCAAAGAAATATGGC[A/G]AAAGGAAGTTGTGCA | 79582 |
rs112212206 | snp | A/G | 0.0726307 | 0.176182 | intron-variant | SPAG16 | GRCh38.p7 | 2:214005138 | TTGTTTTATATTTTC[A/G]GTTTTCCAGTTTACT | 79582 |
rs112213548 | snp | A/G | 0.00358779 | 0.0422022 | intron-variant | SPAG16 | GRCh38.p7 | 2:213512057 | ATTATATTTTAGCTT[A/G]ATTAGCTAAAATCAC | 79582 |
rs112215767 | snp | G/T | 0.00358779 | 0.0422022 | intron-variant | SPAG16 | GRCh38.p7 | 2:213502428 | GCACCTGTCTCAAAA[G/T]TTCCTTTTTATACAA | 79582 |
rs112219257 | snp | A/G | 0.0228947 | 0.104514 | intron-variant | SPAG16 | GRCh38.p7 | 2:213352032 | GGTGGTTGTATAAGC[A/G]TCTGGCATTTCTTTT | 79582 |
rs112219754 | in-del | -/AAAAAAAAAAAAAG | 0 | 0 | intron-variant | SPAG16 | GRCh38.p7 | 2:214330278 | GTGAAACTCTGTCTC[-/AAAAAAAAAAAAAG]GAAAAGAAATAAAGA | 79582 |
rs112223441 | in-del | -/A | 0.00318978 | 0.0398085 | intron-variant | SPAG16 | GRCh38.p7 | 2:213517130 | TCAGGACCCAAAATC[-/A]ATACAAAAATTGGTA | 79582 |
rs112228635 | snp | G/T | | | intron-variant | SPAG16 | GRCh38.p7 | 2:214031440 | CTGGGGACTGTTGTG[G/T]GGTGGGGGGAGGGGG | 79582 |
rs112231349 | snp | A/G | 0.0252325 | 0.109451 | intron-variant | SPAG16 | GRCh38.p7 | 2:214248019 | GACAACAGCAAGTCC[A/G]TGTCTCAAAAGAAAA | 79582 |
rs112235443 | snp | A/C | 0.0325976 | 0.123435 | intron-variant | SPAG16 | GRCh38.p7 | 2:213974964 | AAAAAAAAAAAAAAA[A/C]ACACAAAATGTGTAA | 79582 |
rs112235750 | snp | A/G | 0.5 | 0 | intron-variant | SPAG16 | GRCh38.p7 | 2:213934696 | GCATCACTAAGTTCT[A/G]TACAATAGAATATTA | 79582 |
rs112245421 | snp | G/T | 0.5 | 0 | intron-variant, utr-variant-3-prime | SPAG16 | GRCh38.p7 | 2:213369935 | TAGTTTACATTAGGG[G/T]TCACTTTTGATGTTG | 79582 |
rs112252274 | snp | A/T | 0.00597247 | 0.0543191 | intron-variant | SPAG16 | GRCh38.p7 | 2:214320756 | ACCCATGATTCAATT[A/T]CCTCCACCTGGTCTC | 79582 |
rs112255552 | snp | C/G | 0 | 0 | intron-variant | SPAG16 | GRCh38.p7 | 2:214373841 | GTATCATAAATCATG[C/G]TTATATTTGAAAGAA | 79582 |
rs112256292 | snp | A/C | 0.0178098 | 0.0926698 | intron-variant | SPAG16 | GRCh38.p7 | 2:214055739 | CCTTCATTTAAAAAA[A/C]ATCTTTTGCTTACAA | 79582 |
rs112258766 | snp | A/G | 0.00517822 | 0.0506191 | intron-variant | SPAG16 | GRCh38.p7 | 2:213596501 | CTTCAAATCTGAGGC[A/G]TCTCTCTGACCTAAA | 79582 |
rs112261019 | snp | C/T | 0.00636936 | 0.0560724 | intron-variant | SPAG16 | GRCh38.p7 | 2:214142088 | TTTATCTTTCAATCT[C/T]TGTGTCTACAATCTA | 79582 |
rs112261761 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | SPAG16 | GRCh38.p7 | 2:213607957 | TTCAATCCATTTACA[A/G]TACTTTAGAAAGTAC | 79582 |
rs112262670 | snp | G/T | 0.5 | 0 | intron-variant | SPAG16 | GRCh38.p7 | 2:214108798 | CTTCATAAAAACTGA[G/T]GACAAAACAAAAATA | 79582 |
rs112267858 | snp | A/G | 0 | 0 | intron-variant | SPAG16 | GRCh38.p7 | 2:214114714 | GGTACAGTCTGTCAC[A/G]GCTTCCCTTGGCTAG | 79582 |
rs112268340 | snp | A/G | 0.00557542 | 0.0525036 | intron-variant | SPAG16 | GRCh38.p7 | 2:213621896 | GTAGTATGTTTGGGT[A/G]GGAACCAGGACTACA | 79582 |
rs112273649 | snp | C/T | | | intron-variant | SPAG16 | GRCh38.p7 | 2:213869276 | AAAAATATATATATA[C/T]ATATGTATATATATA | 79582 |
rs112281403 | snp | A/G | 0.00318978 | 0.0398085 | intron-variant | SPAG16 | GRCh38.p7 | 2:214283277 | TCTTCTTAAAAGTGT[A/G]AAGACTTTGGTCTCT | 79582 |
rs112284142 | snp | A/C | 0.0267878 | 0.112589 | intron-variant | SPAG16 | GRCh38.p7 | 2:214226207 | GCAGGTTGGTAGGGG[A/C]TAGCCCGTCTAGGAT | 79582 |
rs112285665 | snp | C/G | 0.029116 | 0.117091 | intron-variant | SPAG16 | GRCh38.p7 | 2:213466996 | CCTTTAGTTCCCTCA[C/G]GTATTTGAGTTAGCA | 79582 |
rs112285866 | snp | C/T | 0.00517822 | 0.0506191 | intron-variant | SPAG16 | GRCh38.p7 | 2:213585401 | TGTGCCTCAGCCTCC[C/T]GAGTATCTGGGACTA | 79582 |
rs112294777 | snp | C/T | 0.00358779 | 0.0422022 | intron-variant | SPAG16 | GRCh38.p7 | 2:213710725 | GTGACCAAGACCTTT[C/T]AAATGAAAGAAATCC | 79582 |
rs112296231 | snp | A/G | 0.0832709 | 0.186283 | intron-variant | SPAG16 | GRCh38.p7 | 2:213702316 | CAGCTGCGGCAACCC[A/G]CTTGGGTCTCTTTTC | 79582 |
rs112297458 | snp | A/C | 0.00478085 | 0.0486577 | intron-variant | SPAG16 | GRCh38.p7 | 2:213649458 | TATCATGGCAGAATG[A/C]CACTTATAATTTAAA | 79582 |
rs112298108 | snp | A/T | 0.5 | 0 | intron-variant | SPAG16 | GRCh38.p7 | 2:214226336 | ACCTCTGCTTGTGTT[A/T]AGTCTGATAATGTCC | 79582 |
rs112300425 | snp | A/C | 0.0310518 | 0.120672 | intron-variant | SPAG16 | GRCh38.p7 | 2:213978219 | ACATTTTACTCTAAA[A/C]AGAGTATATTCAACA | 79582 |
rs112301824 | snp | A/G | 0.0295035 | 0.117819 | intron-variant | SPAG16 | GRCh38.p7 | 2:213638295 | CTGGGTTTGGGTTTG[A/G]TTTGTTCTTGTTTCT | 79582 |
rs112304073 | snp | A/C | | | intron-variant | SPAG16 | GRCh38.p7 | 2:213865721 | ATTTTTTATATATTT[A/C]TATACATATAAATAA | 79582 |
rs112304710 | snp | A/C | 0.0162398 | 0.0886349 | intron-variant, upstream-variant-2KB | SPAG16 | GRCh38.p7 | 2:213316587 | CTTTCACCATTCTCT[A/C]CTTGGTCACTTAGTT | 79582 |
rs112306452 | snp | C/T | 0.0437281 | 0.141251 | intron-variant | SPAG16 | GRCh38.p7 | 2:214275441 | ATTTAGTGCTATAAA[C/T]TTCCCTCTACACACT | 79582 |
rs112307867 | snp | A/G | 0.00199481 | 0.0315187 | intron-variant | SPAG16 | GRCh38.p7 | 2:213761706 | TGTACTAAAACTACA[A/G]AAACAAAAAATTAGC | 79582 |
rs112316531 | snp | C/T | 0.108048 | 0.20579 | intron-variant | SPAG16 | GRCh38.p7 | 2:213688113 | AACTTGGGGGGAGGA[C/T]TTCCAGGCTATAGGT | 79582 |
rs112317786 | snp | A/G | 0.00358779 | 0.0422022 | intron-variant | SPAG16 | GRCh38.p7 | 2:213671719 | AGCACCGCACCTTTG[A/G]TATAATCAGTTATGG | 79582 |
rs112318479 | snp | C/T | 0.00159617 | 0.0282053 | intron-variant | SPAG16 | GRCh38.p7 | 2:214330479 | CTGCATCCAGGAGTC[C/T]TATTAGAAAGTGCTC | 79582 |
rs112318673 | snp | A/T | 0.0146672 | 0.084371 | intron-variant | SPAG16 | GRCh38.p7 | 2:213738005 | CTTAAGTGTTTCTCT[A/T]CATTGTAGTTTTAAA | 79582 |
rs112320702 | snp | C/T | 0.5 | 0 | intron-variant | SPAG16 | GRCh38.p7 | 2:214132904 | TCGAGACCAGCCTGA[C/T]CAACATGGAGAAACC | 79582 |
rs112323774 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant, upstream-variant-2KB | SPAG16 | GRCh38.p7 | 2:213295902 | ATATCTAGATTTATA[A/G]GCTATATGGGGAAGA | 79582 |
rs112326187 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | SPAG16 | GRCh38.p7 | 2:214166356 | GACGAATGGGAGGCA[C/T]TTACAGGAGAGTGAA | 79582 |
rs112326274 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | SPAG16 | GRCh38.p7 | 2:213735900 | TTATGGATGGGGCAT[A/T]AAATGTAAGTTTAGA | 79582 |
rs112331897 | snp | A/T | 0.5 | 0 | intron-variant | SPAG16 | GRCh38.p7 | 2:213479913 | TTCCATGTTGAGGTG[A/T]TCTACGTGTTAAACA | 79582 |
rs112334899 | in-del | -/AT | 0.0452528 | 0.143452 | intron-variant | SPAG16 | GRCh38.p7 | 2:213479934 | TGTTAAACATGTAGA[-/AT]ATATATCTCTTCATA | 79582 |
rs112339310 | snp | A/G | 0.0463947 | 0.145069 | intron-variant | SPAG16 | GRCh38.p7 | 2:213350168 | GTTTAATCATCTATT[A/G]TTTGTGGCCCTTGTC | 79582 |
rs112339620 | snp | C/T | 0.00517822 | 0.0506191 | intron-variant | SPAG16 | GRCh38.p7 | 2:213582123 | AATATAAACACTTAC[C/T]TTTTACTCTTGGAGA | 79582 |
rs112341492 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | SPAG16 | GRCh38.p7 | 2:213751562 | ACCTCCAGTCTTACC[A/G]TCAGCCTCCTGTTGT | 79582 |
rs112343163 | snp | G/T | | | intron-variant | SPAG16 | GRCh38.p7 | 2:213612984 | GGCCCGAATAATTTT[G/T]TAAAATGATGGAATC | 79582 |
rs112345142 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | SPAG16 | GRCh38.p7 | 2:213324305 | TTGTTATGCTTTATA[C/T]ACATTGAAGTATATG | 79582 |
rs112345247 | snp | C/T | 0.0225045 | 0.103662 | intron-variant | SPAG16 | GRCh38.p7 | 2:213819217 | AGTATAGTATCTGAA[C/T]GCCCAATTCCAATCA | 79582 |
rs112345778 | snp | A/T | 0.233527 | 0.249457 | intron-variant | SPAG16 | GRCh38.p7 | 2:214254248 | AGAGACAATTTGACT[A/T]CCTCTCTTCCTGTTT | 79582 |
rs112346450 | snp | A/G | 0.0271762 | 0.113356 | intron-variant | SPAG16 | GRCh38.p7 | 2:213632371 | TAATAGTTTTCTTGT[A/G]GAATCTTTAGGTTTT | 79582 |
rs112346501 | snp | C/G | | | intron-variant | SPAG16 | GRCh38.p7 | 2:213676039 | AATGTTCTTCCATTT[C/G]TTTGTATCCTCTTTT | 79582 |
rs112347920 | snp | A/C | 0.0322114 | 0.122752 | intron-variant | SPAG16 | GRCh38.p7 | 2:214337807 | AAAACTCAGGGCTTC[A/C]TTTCTGTCTTTTATC | 79582 |
rs112349504 | snp | G/T | 0.0463947 | 0.145069 | intron-variant | SPAG16 | GRCh38.p7 | 2:213379891 | ATTGGTGATGACAGG[G/T]GTGGCTGGGGAAAGA | 79582 |
rs112353138 | snp | C/T | 0.00517822 | 0.0506191 | intron-variant | SPAG16 | GRCh38.p7 | 2:213593264 | ATTGAACAGTGCATT[C/T]TTCTGTAAGTCCATG | 79582 |
rs112361761 | snp | A/C | 0 | 0 | intron-variant | SPAG16 | GRCh38.p7 | 2:214370253 | AAATGGAATTCTACC[A/C]ATTTTTTTCAGTAGA | 79582 |
rs112362879 | snp | A/G | 0.5 | 0 | intron-variant | SPAG16 | GRCh38.p7 | 2:214241290 | TTGAACCTGAGAGGC[A/G]GAGCTTGCAGTGAGC | 79582 |
rs112365595 | snp | C/T | | | intron-variant, utr-variant-5-prime | SPAG16 | GRCh38.p7 | 2:213300763 | AAATTTAATATCCAA[C/T]ATATAATTCTTGATA | 79582 |
rs112366746 | snp | C/T | 0.0973687 | 0.197999 | intron-variant | SPAG16 | GRCh38.p7 | 2:213980933 | GAATAAGAGTAAATA[C/T]GTTCTGAGTAAAAAT | 79582 |
rs112370621 | snp | A/G | 0.0236746 | 0.106192 | intron-variant | SPAG16 | GRCh38.p7 | 2:213619383 | ATAGACAGCCTGTAG[A/G]ATAAGAGAGAATATT | 79582 |
rs112374141 | snp | A/G | 0.00478085 | 0.0486577 | intron-variant | SPAG16 | GRCh38.p7 | 2:213647703 | ACTAATGTGACATAG[A/G]GTCTCTTTTCCAATC | 79582 |
rs112382404 | snp | A/C/T | 0.0023933 | 0.0345097 | intron-variant, downstream-variant-500B | SPAG16 | GRCh38.p7 | 2:213371716 | ACACATTAATTGTTA[A/C/T]TTAATCTAAATTTAG | 79582 |
rs112397763 | snp | C/T | 0.00358779 | 0.0422022 | intron-variant | SPAG16 | GRCh38.p7 | 2:213517663 | AGAAATAAAGCCACA[C/T]ACATCTGATCTTTGG | 79582 |
rs112397844 | snp | A/G | 0 | 0 | intron-variant | SPAG16 | GRCh38.p7 | 2:214120113 | ATTATGTTATTAAAT[A/G]TTGTGTTTTGTCAAT | 79582 |
rs112401918 | snp | A/G | 0.0854556 | 0.188216 | intron-variant | SPAG16 | GRCh38.p7 | 2:213702101 | AGCTAGAGGATTGTA[A/G]ATGCACCAATCAGCG | 79582 |
rs112403652 | snp | A/G | | | intron-variant | SPAG16 | GRCh38.p7 | 2:213367614 | CTGTTCATATCCTTC[A/G]CCCACTTGTTGATGG | 79582 |
rs112403890 | in-del | -/T | 0 | 0 | intron-variant | SPAG16 | GRCh38.p7 | 2:213889436 | GGGCAACAAAATAGA[-/T]TTTTTTTTTAAATCT | 79582 |
rs112404036 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | SPAG16 | GRCh38.p7 | 2:214216571 | TTGATCTGCCCGCCT[C/T]GGCCTCCCAAAGTGC | 79582 |
rs112404899 | snp | C/T | 0.00597247 | 0.0543191 | intron-variant | SPAG16 | GRCh38.p7 | 2:213544858 | AGACTTGATAGCTCA[C/T]TTGTTTTTAATGTTG | 79582 |
rs112408436 | snp | A/T | 0.0456336 | 0.143994 | intron-variant | SPAG16 | GRCh38.p7 | 2:213353365 | CTGATTTCTCTATAT[A/T]GGAAATACAAGCCAT | 79582 |
rs112409377 | snp | C/T | 0.0463947 | 0.145069 | intron-variant | SPAG16 | GRCh38.p7 | 2:213338052 | CAAGCCAGAAGATAG[C/T]GGGGGCCAATATTCG | 79582 |
rs112411000 | in-del | -/T | 0.5 | 0 | intron-variant | SPAG16 | GRCh38.p7 | 2:213706732 | AATGAAAACTTTTTG[-/T]TTTTTTTTCCTCACA | 79582 |
rs112411073 | snp | A/C | 0.0162398 | 0.0886349 | intron-variant | SPAG16 | GRCh38.p7 | 2:214138583 | ACAAACCTAGACTTC[A/C]GACTGAGCAGTTGGC | 79582 |
rs112413762 | snp | A/C | 0.0433465 | 0.140692 | intron-variant | SPAG16 | GRCh38.p7 | 2:213888566 | CATATTAATAGGACA[A/C]TGTAAGTACACATGA | 79582 |
rs112416320 | snp | A/T | 0.5 | 0 | intron-variant | SPAG16 | GRCh38.p7 | 2:214148528 | AATTTTGACTAACAG[A/T]CTACAATAGGCACCA | 79582 |
rs112416767 | snp | C/T | 0.00159617 | 0.0282053 | intron-variant | SPAG16 | GRCh38.p7 | 2:214317282 | ACTTCCGGCCTAATG[C/T]TCTTTCCACTTCATT | 79582 |
rs112417589 | snp | A/C | 0.00318978 | 0.0398085 | intron-variant | SPAG16 | GRCh38.p7 | 2:213761711 | TAAAACTACAAAAAC[A/C]AAAAATTAGCTGGGC | 79582 |
rs112423297 | snp | G/T | 0.5 | 0 | intron-variant | SPAG16 | GRCh38.p7 | 2:214159490 | GGATAATCCTTTAAG[G/T]GAAGCTGTAGTTCAA | 79582 |
rs112431481 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | SPAG16 | GRCh38.p7 | 2:214037341 | TTATTTATTCCAATC[A/G]TATGACCTTTTACCT | 79582 |
rs112432634 | snp | A/G | 0.0479149 | 0.147179 | intron-variant | SPAG16 | GRCh38.p7 | 2:213473954 | AGAAGAATCAACATT[A/G]TCTTTCCTGGCAACT | 79582 |
rs112434075 | snp | C/T | 0.00358779 | 0.0422022 | intron-variant | SPAG16 | GRCh38.p7 | 2:213503004 | GAGTTTTAAAGACTC[C/T]TCTTAATAAGTATGA | 79582 |
rs112434499 | snp | A/G | 0.0232847 | 0.105357 | intron-variant | SPAG16 | GRCh38.p7 | 2:214262063 | TAGACATTTACATTA[A/G]ATATATAATTAGACT | 79582 |
rs112437358 | snp | C/T | | | intron-variant | SPAG16 | GRCh38.p7 | 2:214299263 | TTTTTTTTTTTTTTT[C/T]TTTTTGAGACGGGGT | 79582 |
rs112448179 | snp | C/T | | | intron-variant | SPAG16 | GRCh38.p7 | 2:213869409 | CAGATATTGATATAC[C/T]GTCTCTCTAAAAATT | 79582 |
rs112448614 | snp | A/G | 0.5 | 0 | intron-variant | SPAG16 | GRCh38.p7 | 2:213374819 | ACCTTGTAGTAATGC[A/G]TCTCTGCATTTTTGG | 79582 |
rs112448804 | snp | C/T | 0 | 0 | intron-variant | SPAG16 | GRCh38.p7 | 2:213836552 | TAAAATTTTTCTTTG[C/T]CTTTTAGCAACCCTG | 79582 |
rs112449223 | snp | A/G | 0.00953873 | 0.0683987 | intron-variant | SPAG16 | GRCh38.p7 | 2:214288078 | TTACCGCCCCCCCCA[A/G]TCCCACCCTTCCAAG | 79582 |
rs112450476 | snp | C/T | 0.0356815 | 0.128715 | intron-variant | SPAG16 | GRCh38.p7 | 2:213975748 | TGTCTAAGAAATAAA[C/T]ACATGGAAAGAGAAA | 79582 |
rs112451532 | snp | C/T | 0.00279162 | 0.0372561 | intron-variant | SPAG16 | GRCh38.p7 | 2:214336684 | TTAGAAATATTGAGC[C/T]GGATAAAGGCTGAGG | 79582 |
rs112456690 | snp | A/G | 0.00478085 | 0.0486577 | intron-variant | SPAG16 | GRCh38.p7 | 2:213644019 | CTCCTAACCTCAGGT[A/G]ATCCACCCTCCTCAG | 79582 |
rs112457347 | snp | A/G | 0.5 | 0 | intron-variant | SPAG16 | GRCh38.p7 | 2:214321739 | GCTTATTAGACTGGT[A/G]TATTATTGAAATCAA | 79582 |
rs112458380 | snp | C/T | 0.5 | 0 | intron-variant | SPAG16 | GRCh38.p7 | 2:213687679 | TTGTCTGACCCCTTT[C/T]GAGATTTTATCACTG | 79582 |
rs112460510 | snp | C/T | 0.00914312 | 0.0669923 | intron-variant | SPAG16 | GRCh38.p7 | 2:213555511 | AGTTTCCTGAAACTT[C/T]CTCAGCTATGAAGAA | 79582 |
rs112461570 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | SPAG16 | GRCh38.p7 | 2:213489858 | TTCATGTAAATTCTG[A/G]GCAAATATAATGTTT | 79582 |
rs112461930 | snp | A/G | 0.0452528 | 0.143452 | intron-variant | SPAG16 | GRCh38.p7 | 2:213462751 | CTGCCTAGTGATGTG[A/G]AACTGTGAGTCAATT | 79582 |
rs112464898 | snp | G/T | 0.5 | 0 | intron-variant | SPAG16 | GRCh38.p7 | 2:214013246 | CATATGGGGTACAAT[G/T]TGATGTTTCAATACA | 79582 |
rs112466833 | snp | A/G | 0.5 | 0 | intron-variant | SPAG16 | GRCh38.p7 | 2:213643069 | TGTGTGTGTGTGTAT[A/G]TATATATATATATCC | 79582 |
rs112466913 | snp | C/T | 0.5 | 0 | intron-variant | SPAG16 | GRCh38.p7 | 2:214185951 | TAGCAACCTATCTCC[C/T]CCACTATAATGTAAG | 79582 |
rs112476549 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | SPAG16 | GRCh38.p7 | 2:213346993 | ACCTCTGGTAGAATT[C/T]GGCTGTGAATCCTTC | 79582 |
rs112485531 | in-del | -/A | 0 | 0 | intron-variant | SPAG16 | GRCh38.p7 | 2:214383588 | AAAAAAAGAAAAAAG[-/A]AAAAAAAAGACATAT | 79582 |
rs112490307 | snp | C/T | 0.0456336 | 0.143994 | intron-variant | SPAG16 | GRCh38.p7 | 2:213449072 | TAATACCCTGGGAAA[C/T]GAATGTGTTCCTGGG | 79582 |
rs112495383 | snp | C/T | 0.5 | 0 | intron-variant | SPAG16 | GRCh38.p7 | 2:214234678 | TGTTTGTTGGATGCA[C/T]GTATGCCTTCTGAGA | 79582 |
rs112497455 | snp | C/T | 0.00358779 | 0.0422022 | intron-variant | SPAG16 | GRCh38.p7 | 2:213513127 | TGTGTATGTATGTTT[C/T]GTTTTGTCTGTTTCT | 79582 |
rs112500730 | snp | C/T | 0.00358779 | 0.0422022 | intron-variant | SPAG16 | GRCh38.p7 | 2:213529876 | TCTATTTTTAAAATG[C/T]TTTATAATTTTTAGT | 79582 |
rs112502844 | snp | A/G | 0.00358779 | 0.0422022 | intron-variant | SPAG16 | GRCh38.p7 | 2:213528091 | GAAAATATAACAGAA[A/G]AGATGAAGCTTATAT | 79582 |
rs112504029 | snp | C/T | 0.0126979 | 0.078662 | intron-variant | SPAG16 | GRCh38.p7 | 2:214165732 | ATAAAGTGGTGAATA[C/T]GCTGTTGAGAGTAGT | 79582 |
rs112504181 | snp | A/G | | | intron-variant | SPAG16 | GRCh38.p7 | 2:214274856 | CTATTGATTGGAATA[A/G]TTTCAGAAGCAATGG | 79582 |
rs112508147 | snp | A/G | 0.0614824 | 0.164198 | intron-variant | SPAG16 | GRCh38.p7 | 2:213742181 | CTTTTTATTACAAAA[A/G]CATTTTCAATTAAAT | 79582 |
rs112511233 | snp | C/T | 0.00755907 | 0.0610114 | intron-variant | SPAG16 | GRCh38.p7 | 2:213629922 | CCAGGGACCTCTGAC[C/T]CTCTGGCTTCAGAAA | 79582 |
rs112514788 | snp | C/T | 0.00358779 | 0.0422022 | intron-variant | SPAG16 | GRCh38.p7 | 2:213495514 | AAATGTTATTGAACA[C/T]GTGTCAGGCACTACT | 79582 |
rs112517826 | snp | C/T | 0.0711525 | 0.174681 | intron-variant | SPAG16 | GRCh38.p7 | 2:213877700 | CATAATATCCACTTA[C/T]GTATTTCCAACACCT | 79582 |
rs112518594 | snp | C/T | 0.0107246 | 0.0724382 | intron-variant | SPAG16 | GRCh38.p7 | 2:214074555 | TACTGAAAGAGAAGA[C/T]AGAAACACTTTCAAT | 79582 |
rs112519099 | snp | C/T | 0.00716266 | 0.059414 | intron-variant | SPAG16 | GRCh38.p7 | 2:213509282 | ATTTCTATACAATAT[C/T]TTCTATATTTTCTAT | 79582 |
rs112519674 | snp | A/G | 0.00358779 | 0.0422022 | intron-variant | SPAG16 | GRCh38.p7 | 2:213573720 | TTTTTGGAGTTTGGA[A/G]TTATCTTAATTTTGT | 79582 |
rs112521007 | snp | C/T | 0.00517822 | 0.0506191 | intron-variant | SPAG16 | GRCh38.p7 | 2:213801348 | TTGGCAATACAAATC[C/T]GAAAGCTGTCAGTAA | 79582 |
rs112521854 | snp | C/T | 0.5 | 0 | intron-variant | SPAG16 | GRCh38.p7 | 2:214139233 | TTTGTTCTGGAAATG[C/T]CATTTTGCTGAAGAA | 79582 |
rs112522079 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | SPAG16 | GRCh38.p7 | 2:213498433 | GAGAATGATATTGTC[A/G]TATTGGTTTATATCA | 79582 |
rs112523627 | snp | A/G | 0.00874735 | 0.0655527 | intron-variant | SPAG16 | GRCh38.p7 | 2:213384398 | GGGTTCATGGATTCC[A/G]TCTTACTGTGAGCCA | 79582 |
rs112523705 | snp | A/T | | | intron-variant | SPAG16 | GRCh38.p7 | 2:213728879 | GAGACTCCGTCTCAA[A/T]AAAAAAAAAAAAAAA | 79582 |
rs112530494 | snp | A/G | 0.0263992 | 0.111815 | intron-variant | SPAG16 | GRCh38.p7 | 2:214278453 | AGCCATCTTAGAACC[A/G]GACCACATCCTCTTT | 79582 |
rs112539865 | snp | A/G | 0.00199481 | 0.0315187 | intron-variant | SPAG16 | GRCh38.p7 | 2:213755160 | CATTTTGCAGGTTCA[A/G]TGTATTTTTTTATGT | 79582 |
rs112540387 | snp | A/G | 0.5 | 0 | intron-variant | SPAG16 | GRCh38.p7 | 2:213831966 | GCTATATTGCCTCTG[A/G]AAAGGAAATTTTTGC | 79582 |
rs112543422 | snp | A/G | 0.029116 | 0.117091 | intron-variant | SPAG16 | GRCh38.p7 | 2:213981289 | AATGTATGAGTTTGT[A/G]GGGGAATCAATTCAA | 79582 |
rs112545998 | snp | C/T | 0.0618563 | 0.164627 | intron-variant | SPAG16 | GRCh38.p7 | 2:213713246 | ACAGCCAAACCATAC[C/T]ACTGCCTTTGTCATG | 79582 |
rs112546908 | snp | C/T | 0.00517822 | 0.0506191 | intron-variant | SPAG16 | GRCh38.p7 | 2:213622980 | TGAAGAGTAACGAAG[C/T]CTTCCATTTGTTCTT | 79582 |
rs112548501 | snp | A/G | 0.0283406 | 0.115616 | intron-variant | SPAG16 | GRCh38.p7 | 2:213421429 | CTGCAGGTGCCCCTT[A/G]GCATGAACAGCCTGG | 79582 |
rs112550335 | snp | A/G | 0.5 | 0 | intron-variant | SPAG16 | GRCh38.p7 | 2:213477018 | CTGTGAAGCTGAGTC[A/G]GGTTTTTATGGGCTT | 79582 |
rs112551945 | snp | A/T | 0.0463947 | 0.145069 | intron-variant | SPAG16 | GRCh38.p7 | 2:213347851 | GTGGTGCTGAAAAGA[A/T]TGTATATTCTGTTGA | 79582 |
rs112553213 | snp | A/G | 0.0252325 | 0.109451 | intron-variant | SPAG16 | GRCh38.p7 | 2:213950066 | ACATATTTCTTATTC[A/G]TGAGTTCTACAGTGT | 79582 |
rs112556161 | snp | A/G | 0.00358779 | 0.0422022 | intron-variant | SPAG16 | GRCh38.p7 | 2:213667606 | GAGATTGACGTTGGA[A/G]AGATCCTCTTCTGAT | 79582 |
rs112564051 | in-del | -/CA/CACA/CACACA | 0.4983 | 0.0291038 | intron-variant | SPAG16 | GRCh38.p7 | 2:213385792 | TTCTTCATCTCTGTC[-/CA/CACA/CACACA]CACACACACACACAC | 79582 |
rs112571334 | snp | A/C | 0.5 | 0 | intron-variant | SPAG16 | GRCh38.p7 | 2:214039624 | TCATTTCTTTGTTGG[A/C]TTCTGTGGCACTTAA | 79582 |
rs112572396 | snp | A/G | 0.0205511 | 0.0992634 | intron-variant | SPAG16 | GRCh38.p7 | 2:213470143 | CATGCATGGCCTTCT[A/G]GAGAACTTTGCCTCA | 79582 |
rs112575139 | snp | C/T | 0.00636936 | 0.0560724 | intron-variant | SPAG16 | GRCh38.p7 | 2:214167554 | AAGGAAAGGATACTT[C/T]ACTGATGTTCTCAAA | 79582 |
rs112579129 | in-del | -/C/CC | 0.446902 | 0.154045 | intron-variant | SPAG16 | GRCh38.p7 | 2:214234074 | GTTGTTTCCCCCCCC[-/C/CC]ATGTGTCCATGTGTT | 79582 |
rs112579426 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | SPAG16 | GRCh38.p7 | 2:213719460 | ATCTGATGCAGAGGC[A/G]GAGAACCTTTGTATC | 79582 |
rs112581381 | in-del | -/GT | 0.5 | 0 | intron-variant | SPAG16 | GRCh38.p7 | 2:213361379 | TGTGTGTGTGTGTGT[-/GT]ATATATATATATATG | 79582 |
rs112581579 | snp | C/G | 0.0614824 | 0.164198 | intron-variant | SPAG16 | GRCh38.p7 | 2:213719644 | TGGACACAATACCAT[C/G]TCATGCTAGTTAGAT | 79582 |
rs112582355 | in-del | -/G | 0.0452528 | 0.143452 | intron-variant | SPAG16 | GRCh38.p7 | 2:213439283 | TAAATATCTTAAAAA[-/G]GGGAGCGGCTTTGGA | 79582 |
rs112596571 | in-del | -/TAATCA | 0.0256215 | 0.110247 | intron-variant | SPAG16 | GRCh38.p7 | 2:213291168 | GTATCTGCTGCATCT[-/TAATCA]TATTTCTATAATGCT | 79582 |
rs112598034 | snp | A/G | 0.5 | 0 | intron-variant | SPAG16 | GRCh38.p7 | 2:213721379 | GCTGAGATTACAGGC[A/G]TAAGCCACCGCGCCT | 79582 |
rs112598169 | in-del | -/AGATT | 0.00358779 | 0.0422022 | intron-variant | SPAG16 | GRCh38.p7 | 2:213504181 | GCCTGGTTTGTAGCA[-/AGATT]AGATTTTGGAATTTC | 79582 |
rs112602515 | snp | A/T | 0.0614824 | 0.164198 | intron-variant | SPAG16 | GRCh38.p7 | 2:213739613 | GCTTTTTCTTTTTTT[A/T]CCTCCTGAGACGGAG | 79582 |
rs112613257 | in-del | -/GATGA/TGATGATGA/TGATGATGATGATGA/TGATGATGATGATGATGA | 0.120326 | 0.21374 | intron-variant | SPAG16 | GRCh38.p7 | 2:213859993 | ATCATTACCATTAGT[lengthTooLong]TGATGATGATGATGA | 79582 |
rs112614168 | snp | A/G | 0.00318978 | 0.0398085 | intron-variant | SPAG16 | GRCh38.p7 | 2:213522425 | AGCTATTTAAAAAGG[A/G]GGGTGGGAAGAGAGA | 79582 |
rs112614786 | in-del | -/CC | 0.49423 | 0.0534032 | intron-variant | SPAG16, LOC101928084 | GRCh38.p7 | 2:214085457 | TCCATATGTTGGTAT[-/CC]GGAGTTAGTGATCAA | 79582 |
rs112615354 | snp | A/G | 0.00478085 | 0.0486577 | intron-variant | SPAG16 | GRCh38.p7 | 2:213594096 | GCCACATCTTATTAA[A/G]CTTCAACTCTTTAGC | 79582 |
rs112617460 | snp | A/G | 0.105214 | 0.203807 | intron-variant | SPAG16 | GRCh38.p7 | 2:214315724 | TTTTGTAGAGTTGGG[A/G]TCTCACTATGTTGTC | 79582 |
rs112618438 | snp | C/G | 0.00358779 | 0.0422022 | intron-variant | SPAG16 | GRCh38.p7 | 2:213529365 | TCTGTATTAAACCCT[C/G]CATTATGGCTGATTT | 79582 |
rs112619922 | snp | A/C | 0.00159617 | 0.0282053 | intron-variant | SPAG16 | GRCh38.p7 | 2:214317761 | GGGAAAAAGTGGCTA[A/C]TGCCTGCCTGTGGCC | 79582 |
rs112620488 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | SPAG16 | GRCh38.p7 | 2:213820746 | ATCATAATTATGATT[A/G]TATCTTTCATTAATA | 79582 |
rs112623003 | snp | A/T | 0.110872 | 0.20771 | intron-variant | SPAG16 | GRCh38.p7 | 2:213545203 | TGGTTTTAATTTGCA[A/T]TTTTCTGATGACATA | 79582 |
rs112626079 | snp | A/G | | | intron-variant | SPAG16 | GRCh38.p7 | 2:214254787 | AAGATATATTTAGTT[A/G]GGGGAAAACTCATTT | 79582 |
rs112626909 | snp | G/T | 0.5 | 0 | intron-variant | SPAG16 | GRCh38.p7 | 2:213959167 | AACAAGTTGCTTATT[G/T]CTTAGAATTTTCAAG | 79582 |
rs112628397 | snp | C/T | 0.5 | 0 | intron-variant | SPAG16 | GRCh38.p7 | 2:213978587 | ATTTGTCAATTGCTG[C/T]ATAATAAATCATCCC | 79582 |
rs112633016 | snp | A/C | 0.00953873 | 0.0683987 | intron-variant | SPAG16 | GRCh38.p7 | 2:213416789 | ACAAAGTTCATTATA[A/C]TCATGATCTTAAAGA | 79582 |
rs112633184 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | SPAG16 | GRCh38.p7 | 2:213952057 | TACTTATGGACAATC[A/G]CTGAGGGATGATCTA | 79582 |
rs112636315 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | SPAG16 | GRCh38.p7 | 2:213954627 | AGGTTTTAAGCCCTG[C/T]ATACATTAGGTTGGA | 79582 |
rs112641761 | snp | C/G | 0.0134861 | 0.0810011 | intron-variant | SPAG16 | GRCh38.p7 | 2:214234080 | TGTGTTGTTTCCCCC[C/G]CCATGTGTCCATGTG | 79582 |
rs112642910 | snp | G/T | 0.0295035 | 0.117819 | intron-variant | SPAG16 | GRCh38.p7 | 2:213613748 | TTTTTCTTTTTCTTT[G/T]CATTACTGTAGCTCC | 79582 |
rs112650124 | snp | C/T | 0.5 | 0 | intron-variant | SPAG16 | GRCh38.p7 | 2:213866511 | TAAATCTAGCAACTA[C/T]ACCTGTTAACACACG | 79582 |
rs112654247 | snp | C/T | 0.00358779 | 0.0422022 | intron-variant | SPAG16 | GRCh38.p7 | 2:213495218 | AATTTGGCCATGTGC[C/T]TAAAAATGACCAAAG | 79582 |
rs112654606 | snp | C/T | 0.173965 | 0.238157 | intron-variant | SPAG16 | GRCh38.p7 | 2:213508294 | AATGATGAGTTCGGC[C/T]GGGCGCGGTGGCTCA | 79582 |
rs112654649 | snp | A/G | 0.029116 | 0.117091 | intron-variant | SPAG16 | GRCh38.p7 | 2:213639841 | CAAATAAGTTTTCCA[A/G]ACTTTTAGATTTCTC | 79582 |
rs112655180 | snp | C/T | 0 | 0 | intron-variant | SPAG16 | GRCh38.p7 | 2:213904084 | AGTCTCTGGGAAGTT[C/T]TAAATTTTCCCACAT | 79582 |
rs112659291 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | SPAG16 | GRCh38.p7 | 2:213324202 | GATAATCAACACTCT[A/G]CTTTTGTCATTCTTA | 79582 |
rs112662216 | snp | A/G | 0.00478085 | 0.0486577 | intron-variant | SPAG16 | GRCh38.p7 | 2:213634552 | ATTTATTGCTTGTTG[A/G]TGTCCCTTTCTTACT | 79582 |
rs112672679 | snp | A/G | 0.5 | 0 | intron-variant | SPAG16 | GRCh38.p7 | 2:213727172 | AATTTCATATCATAC[A/G]GGAATATTGGTTTTC | 79582 |
rs112675312 | snp | C/T | 0.0685596 | 0.171987 | intron-variant | SPAG16 | GRCh38.p7 | 2:214016778 | TTCTTCTTAGTGATA[C/T]TTTATAAAGATCACA | 79582 |
rs112676171 | snp | C/T | 0 | 0 | intron-variant | SPAG16 | GRCh38.p7 | 2:213876554 | CTTTGACTAATCCAA[C/T]AGCTTTGGCCAAATA | 79582 |
rs112676476 | snp | C/G | | | intron-variant | SPAG16 | GRCh38.p7 | 2:214352584 | TGTGTGTATGTGTGA[C/G]TATCTCCTAACATTT | 79582 |
rs112678427 | snp | C/G | 0.5 | 0 | intron-variant | SPAG16 | GRCh38.p7 | 2:214192006 | AAAAAACAGGACTAG[C/G]ACAAAAGAATGGATT | 79582 |
rs112684337 | snp | A/G | 0 | 0 | intron-variant | SPAG16 | GRCh38.p7 | 2:214140730 | TTATTTTTTTCTGAC[A/G]CTGATACTATTCTAC | 79582 |
rs112684434 | snp | A/C | 0.000798403 | 0.0199641 | intron-variant | SPAG16 | GRCh38.p7 | 2:214129845 | AATGCATGACTTATA[A/C]GGCTTTTTAGAGAAG | 79582 |
rs112685986 | snp | C/T | 0.5 | 0 | intron-variant | SPAG16 | GRCh38.p7 | 2:214286305 | GTACTTGAAATTTGC[C/T]AAGCTCTTATTAAGT | 79582 |
rs112688844 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | SPAG16 | GRCh38.p7 | 2:213732264 | TCTCTGTTCTGTTTC[A/G]TTGGTCAATGTGTCT | 79582 |
rs112691234 | snp | C/T | 0.0263992 | 0.111815 | intron-variant | SPAG16 | GRCh38.p7 | 2:214275537 | CTTTATTTCTGCCTT[C/T]ATTTCATTATTTATC | 79582 |
rs112694209 | snp | C/G | 0.5 | 0 | intron-variant | SPAG16 | GRCh38.p7 | 2:213563530 | ACTGCCTTCTTTCTG[C/G]GCTCTCACATGGCAG | 79582 |
rs112700421 | snp | C/T | 0.0248432 | 0.108648 | intron-variant | SPAG16 | GRCh38.p7 | 2:214251246 | TGAGACCTGAGTAAA[C/T]CTAAGGCTACAGATT | 79582 |
rs112700897 | snp | C/T | 0.0599851 | 0.162463 | intron-variant | SPAG16 | GRCh38.p7 | 2:213733603 | CCAAGACTATGGCCT[C/T]CAAGACTTTCTTGTA | 79582 |
rs112702065 | snp | C/T | 0.5 | 0 | intron-variant | SPAG16 | GRCh38.p7 | 2:214256318 | TTTATTGCTGAGCAG[C/T]AGAACTTAGTTATTT | 79582 |
rs112705270 | snp | A/G | 0.0217236 | 0.101931 | intron-variant | SPAG16 | GRCh38.p7 | 2:213850991 | CTTATTTAATAATTA[A/G]TTTAATCACAGTTAG | 79582 |
rs112705284 | snp | C/G | 0.5 | 0 | intron-variant | SPAG16 | GRCh38.p7 | 2:213582464 | GGCCTTGAGGTCATG[C/G]GCTGAAAGAGATAGT | 79582 |
rs112706050 | snp | A/G | 0.00358779 | 0.0422022 | intron-variant | SPAG16 | GRCh38.p7 | 2:213535765 | TTCTTTAGCAATTAA[A/G]AGTGCAGGCTAACAA | 79582 |
rs112706462 | snp | A/G | 0.029116 | 0.117091 | intron-variant | SPAG16 | GRCh38.p7 | 2:213542181 | GTAAGAATTGTAAAA[A/G]TCTTTGCTATTATGT | 79582 |
rs112710092 | snp | C/G | 0.0460142 | 0.144533 | intron-variant | SPAG16 | GRCh38.p7 | 2:213354921 | GCTTTTGGTGTTTTA[C/G]TCACAAAGTCTTTGC | 79582 |
rs112715209 | snp | A/G | 0.00358779 | 0.0422022 | intron-variant | SPAG16 | GRCh38.p7 | 2:213551088 | CCAACTCTTAATTTT[A/G]TTTTTCTTTGCTTAT | 79582 |
rs112717444 | snp | C/T | 0.00835141 | 0.0640778 | intron-variant | SPAG16 | GRCh38.p7 | 2:213809468 | CTGCTAATAACACAG[C/T]AGCTCTAAATGAAAA | 79582 |
rs112719150 | snp | C/T | 0.00517822 | 0.0506191 | intron-variant | SPAG16 | GRCh38.p7 | 2:213585061 | AGGCATGGTGGCATA[C/T]ACCTGTAATCCCAGC | 79582 |
rs112721890 | snp | C/G | 0.00557542 | 0.0525036 | intron-variant | SPAG16 | GRCh38.p7 | 2:213607078 | AGATGAAAGAAGAGA[C/G]TAGTTGGTAAAATGT | 79582 |
rs112724196 | snp | C/T | 0.00636936 | 0.0560724 | intron-variant | SPAG16 | GRCh38.p7 | 2:214169594 | CCCTTGAGTGTAAGA[C/T]GAACGGCTGTTGAAT | 79582 |
rs112724268 | snp | C/G | 0.0437281 | 0.141251 | intron-variant | SPAG16 | GRCh38.p7 | 2:214229415 | TTGTTATCTAAAGAA[C/G]AGTGCAAACATTTTT | 79582 |
rs112725012 | snp | C/T | | | intron-variant | SPAG16 | GRCh38.p7 | 2:214135492 | ATGGGTCCCGGAGTT[C/T]GGATGTCTGACCCCT | 79582 |
rs112725928 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | SPAG16 | GRCh38.p7 | 2:213944898 | AATAAATTAGCCGGG[C/T]GTGGGGGCGTGCACC | 79582 |
rs112726351 | snp | A/G | 0.5 | 0 | intron-variant | SPAG16 | GRCh38.p7 | 2:214123906 | GGAATATCTTGAATC[A/G]TATAGATAACTGATT | 79582 |
rs112727626 | snp | C/T | 0.125182 | 0.216612 | intron-variant | SPAG16 | GRCh38.p7 | 2:213601957 | TGAAGTCATCAGGCA[C/T]TGGTTAGAGTCTCAT | 79582 |
rs112727797 | snp | G/T | 0.00398564 | 0.0444627 | intron-variant | SPAG16 | GRCh38.p7 | 2:214144657 | AACTCTTTGACAACA[G/T]AATATTATATATATT | 79582 |
rs112731192 | snp | A/G | 0.0448719 | 0.142907 | intron-variant | SPAG16 | GRCh38.p7 | 2:213619967 | ACATATACACAATGG[A/G]GTACTATCCAGACAT | 79582 |
rs112734090 | snp | C/T | 0.5 | 0 | intron-variant | SPAG16 | GRCh38.p7 | 2:213632036 | TGTAATTGGTATTTT[C/T]GTAGGGATTGCATTG | 79582 |
rs112741327 | snp | A/G | 0.00358779 | 0.0422022 | intron-variant | SPAG16 | GRCh38.p7 | 2:213705003 | TGCGCCTGTAATCCC[A/G]GCACTTTGGGAGGCG | 79582 |
rs112741961 | snp | G/T | 0.5 | 0 | intron-variant | SPAG16 | GRCh38.p7 | 2:213657077 | TTCTTTCTTTTTAAG[G/T]CTTTAAAATATTTTG | 79582 |
rs112743967 | in-del | -/CACA/CACACA/CACACACACACA | 0.258565 | 0.249853 | intron-variant | SPAG16 | GRCh38.p7 | 2:213767655 | GAGAACAACATACTT[-/CACA/CACACA/CACACACACACA]CACACACACACACAC | 79582 |
rs112747049 | snp | A/G | 0.0456336 | 0.143994 | intron-variant | SPAG16 | GRCh38.p7 | 2:213436986 | GCATGATCTCGGTTC[A/G]CTGCAAGCTCCGCCT | 79582 |
rs112750165 | in-del | -/A | 0 | 0 | intron-variant | SPAG16 | GRCh38.p7 | 2:213590446 | CAACAAAACAACAAG[-/A]AAAAAAAAAAAAACA | 79582 |
rs112751351 | snp | A/G | 0.00478085 | 0.0486577 | intron-variant, utr-variant-3-prime | SPAG16 | GRCh38.p7 | 2:213401274 | ATTTCCCTTGATAAT[A/G]TATGTTCTTCAGAAA | 79582 |
rs112751959 | snp | C/T | 0.5 | 0 | intron-variant | SPAG16 | GRCh38.p7 | 2:214164273 | AACATATTTGCCAAG[C/T]GGTGATAAGTCTTAT | 79582 |
rs112755637 | snp | A/C | 0.5 | 0 | intron-variant | SPAG16 | GRCh38.p7 | 2:213308968 | GGGACCCAGTTATAA[A/C]CATGAAATTCATTTA | 79582 |
rs112767837 | in-del | -/T | 0 | 0 | intron-variant | SPAG16 | GRCh38.p7 | 2:213819942 | TTCTAATTTTTCGTG[-/T]TTTTTTTTTTTTTTT | 79582 |
rs112769349 | in-del | -/TT | 0.0463947 | 0.145069 | intron-variant | SPAG16 | GRCh38.p7 | 2:213412625 | TGTTTTGTTTGTTTA[-/TT]TTTTTTTGTTTGTTT | 79582 |
rs112774153 | snp | C/T | 0.00597247 | 0.0543191 | intron-variant | SPAG16 | GRCh38.p7 | 2:214318532 | GATTGCAGGTGTGCA[C/T]CACCATGCCTGGCTA | 79582 |
rs112793490 | snp | A/C | 0.00358779 | 0.0422022 | intron-variant | SPAG16 | GRCh38.p7 | 2:213548575 | GTAATCAAATACTCA[A/C]GACAGTTTTTAGTTT | 79582 |
rs112800572 | snp | C/T | 0.00517822 | 0.0506191 | intron-variant | SPAG16 | GRCh38.p7 | 2:213594771 | GACAATTAACAGATG[C/T]TTGCGAACTGACACA | 79582 |
rs112803203 | snp | A/C | 0.00358779 | 0.0422022 | intron-variant | SPAG16 | GRCh38.p7 | 2:213535978 | TTTAAAGGAAATTTA[A/C]AATTAAATGTTAAAG | 79582 |
rs112806999 | snp | C/T | 0.00517822 | 0.0506191 | intron-variant | SPAG16 | GRCh38.p7 | 2:213602595 | GCCAAGATCGTGCCA[C/T]TGTGCTCCAGCCTGG | 79582 |
rs112808709 | snp | G/T | 0.0252325 | 0.109451 | intron-variant | SPAG16 | GRCh38.p7 | 2:213532739 | GTGCTGGGATTACAG[G/T]CATGAGCCATCGCAC | 79582 |
rs112810461 | snp | A/G | 0.5 | 0 | intron-variant | SPAG16 | GRCh38.p7 | 2:213594764 | CACAGGAGACAATTA[A/G]CAGATGTTTGCGAAC | 79582 |
rs112810755 | snp | A/G | 0.5 | 0 | intron-variant | SPAG16 | GRCh38.p7 | 2:213948295 | CAGATAAACAGACAC[A/G]CAAATGCATTTCTGC | 79582 |
rs112816649 | snp | A/C/T | 0.0460417 | 0.144711 | intron-variant | SPAG16 | GRCh38.p7 | 2:213447317 | CCTCATATGATATTC[A/C/T]CCATTCTGAGCCCAG | 79582 |
rs112817790 | snp | A/T | 0.5 | 0 | intron-variant | SPAG16 | GRCh38.p7 | 2:214304282 | CTCTGCAGCACTGTG[A/T]CATGTTCTTGATGGC | 79582 |
rs112821536 | snp | A/T | 0.5 | 0 | intron-variant | SPAG16 | GRCh38.p7 | 2:213471018 | TTCTCTATCCATGCA[A/T]AGTGCACAACCAGGT | 79582 |
rs112823370 | snp | A/G | 0.0505692 | 0.150756 | intron-variant | SPAG16 | GRCh38.p7 | 2:213643851 | AGTGGTGCAATCTTG[A/G]CTCACTGCAACCTCC | 79582 |
rs112832801 | snp | A/G | 0.5 | 0 | intron-variant | SPAG16 | GRCh38.p7 | 2:213656811 | GACAGTTTAATTTCA[A/G]GGATTTGTACTTTAA | 79582 |
rs112836244 | snp | C/T | 0.030665 | 0.119967 | intron-variant | SPAG16 | GRCh38.p7 | 2:213464320 | AAGTTTTCTGAAGTG[C/T]CTTTTGATAATATCA | 79582 |
rs112836517 | snp | G/T | 0.0452528 | 0.143452 | intron-variant | SPAG16 | GRCh38.p7 | 2:213429340 | CTGTTGCCCTTTCCA[G/T]TTCCACCCAACTTGA | 79582 |
rs112836710 | snp | A/C | 0.5 | 0 | intron-variant | SPAG16 | GRCh38.p7 | 2:214002083 | GTCTTGAGACTTATT[A/C]ACTACCAAGAGAACA | 79582 |
rs112836918 | snp | A/G | 0.0178098 | 0.0926698 | intron-variant | SPAG16, LOC101928084 | GRCh38.p7 | 2:214100273 | ATTACCCAGTCTCAG[A/G]TATTGCTTTATAGCA | 79582 |
rs112837166 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | SPAG16 | GRCh38.p7 | 2:213419732 | TGATATATGGACTAC[A/G]TTGTGGTTTGCCATA | 79582 |
rs112838093 | snp | A/C | 0.00358779 | 0.0422022 | intron-variant | SPAG16 | GRCh38.p7 | 2:213670077 | ACCTCACCTCACTGC[A/C]AACTCTGCCTCCGGG | 79582 |
rs112838116 | snp | G/T | 0.5 | 0 | intron-variant | SPAG16 | GRCh38.p7 | 2:214070145 | CATGAGTTTTTTCCT[G/T]GCAACAAGTATTTTT | 79582 |
rs112841353 | snp | G/T | 0.0279526 | 0.114869 | intron-variant | SPAG16 | GRCh38.p7 | 2:214246735 | CTGAACTCCAGAGCT[G/T]TGGGGAATGTTAAAT | 79582 |
rs112842476 | snp | A/G/T | 0.106987 | 0.205054 | intron-variant | SPAG16 | GRCh38.p7 | 2:213686408 | GGCATGAGCCAAAGC[A/G/T]CCCGGCTGTTACTTT | 79582 |
rs112844879 | snp | C/T | 0.00358779 | 0.0422022 | intron-variant | SPAG16 | GRCh38.p7 | 2:213510793 | GTGTCATATAGTAAA[C/T]ACTTAATGGAATATA | 79582 |
rs112845992 | in-del | -/T | 0 | 0 | intron-variant | SPAG16 | GRCh38.p7 | 2:213635041 | ATTTCTTTTTCTTTC[-/T]TTTTTTTTTTTTGAG | 79582 |
rs112846289 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | SPAG16 | GRCh38.p7 | 2:213333721 | CAGTGAACACATTTT[A/T]GACATAAGTGCCAAG | 79582 |
rs112847414 | snp | A/C | 0.0452528 | 0.143452 | intron-variant | SPAG16 | GRCh38.p7 | 2:213442237 | TAATAAAATATGCAC[A/C]AGATCTGTATGAGAA | 79582 |
rs112850274 | snp | C/G | 0.5 | 0 | intron-variant | SPAG16 | GRCh38.p7 | 2:213517143 | ATCATACAAAAATTG[C/G]TAGTATTTCTATATA | 79582 |
rs112853031 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | SPAG16 | GRCh38.p7 | 2:213855138 | CAATTTTCAGAAAAT[A/G]GCAAGTGACAATAGT | 79582 |
rs112854842 | snp | G/T | 0.0659589 | 0.169201 | intron-variant | SPAG16 | GRCh38.p7 | 2:213696495 | ATCCCTGGCTCACTC[G/T]AATACTTAAATAATA | 79582 |
rs112862682 | snp | A/G | 0.0463947 | 0.145069 | intron-variant | SPAG16 | GRCh38.p7 | 2:213340611 | GAGGAAGTGGGGTCC[A/G]CACAGTGCTCTTTGC | 79582 |
rs112867868 | snp | A/G | 0.0441095 | 0.141807 | intron-variant | SPAG16 | GRCh38.p7 | 2:214280383 | CTTATTTTAAAACTC[A/G]TATGGAAATAAAAAA | 79582 |
rs112868467 | snp | C/T | 0.5 | 0 | intron-variant, utr-variant-5-prime | SPAG16 | GRCh38.p7 | 2:213301899 | TTGGTTTATCTTTCT[C/T]TATCTGTTGTATTTC | 79582 |
rs112868870 | snp | A/C | 0.5 | 0 | intron-variant | SPAG16 | GRCh38.p7 | 2:213755876 | AAATTATTCAGACAT[A/C]TATGATAAAATATTA | 79582 |
rs112869149 | snp | C/T | 0.00597247 | 0.0543191 | intron-variant, upstream-variant-2KB | SPAG16 | GRCh38.p7 | 2:213316719 | GCCCCAGCTGCTTCT[C/T]TCCCAGCTATCCACA | 79582 |
rs112871362 | snp | C/T | 0.5 | 0 | intron-variant | SPAG16 | GRCh38.p7 | 2:213973435 | CATTATGTCAGCCCT[C/T]AGGTAGCACCCAAAC | 79582 |
rs112873185 | snp | A/T | 0.5 | 0 | intron-variant | SPAG16 | GRCh38.p7 | 2:213957583 | TGGAGAGTTTAATCC[A/T]TTTAATTTAAATTAA | 79582 |
rs112880693 | snp | A/G | 0.228842 | 0.249103 | intron-variant | SPAG16 | GRCh38.p7 | 2:214012349 | CACCCAGTCTGGAGT[A/G]CAGTGGTGTGATCTC | 79582 |
rs112885051 | snp | C/T | 0.0126979 | 0.078662 | intron-variant | SPAG16 | GRCh38.p7 | 2:214140519 | CCTTTTTTGCATTAT[C/T]TATCATTCTGATGGA | 79582 |
rs112886333 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | SPAG16 | GRCh38.p7 | 2:213801110 | CAACATTTGTAAGTG[C/T]TCATATGTCTTCAGA | 79582 |
rs112889879 | snp | A/T | | | intron-variant | SPAG16 | GRCh38.p7 | 2:213781202 | CCTACCTCCCCTTTT[A/T]TAGGCGGATGCCTCT | 79582 |
rs112897563 | snp | G/T | | | intron-variant | SPAG16 | GRCh38.p7 | 2:213668142 | AACGGTTTCACCATG[G/T]TGGCCAGGCTGGTCT | 79582 |
rs112898396 | snp | C/T | 0.193966 | 0.243639 | intron-variant | SPAG16 | GRCh38.p7 | 2:213366854 | CAGGTTTGTTACATA[C/T]GTATACATGTGCCAT | 79582 |
rs112899141 | snp | A/G | 0.5 | 0 | intron-variant | SPAG16 | GRCh38.p7 | 2:213605825 | AACTTTTAGGGCATA[A/G]TTTACATATACATAG | 79582 |
rs112902576 | snp | C/G | 0.0267878 | 0.112589 | intron-variant | SPAG16 | GRCh38.p7 | 2:213466931 | AATATTGAGAGGCAG[C/G]GTATAGTGGTATGTA | 79582 |
rs112905489 | snp | G/T | 0.5 | 0 | intron-variant | SPAG16 | GRCh38.p7 | 2:213599285 | TTTCTTGATACGAAC[G/T]ACAAATTACTTACAA | 79582 |
rs112906991 | snp | C/T | 0.00517822 | 0.0506191 | intron-variant | SPAG16 | GRCh38.p7 | 2:213607082 | GAAAGAAGAGACTAG[C/T]TGGTAAAATGTCTTG | 79582 |
rs112908729 | snp | A/G | 0 | 0 | intron-variant | SPAG16 | GRCh38.p7 | 2:213887147 | TATTACATAACCACA[A/G]TACAATTAACAGAAT | 79582 |
rs112911666 | snp | G/T | 0.5 | 0 | intron-variant | SPAG16 | GRCh38.p7 | 2:213701791 | TTGTAAACGCACCAA[G/T]CAGCACTCTGTGTCT | 79582 |
rs112912069 | snp | A/C | 0.136166 | 0.22258 | intron-variant | SPAG16 | GRCh38.p7 | 2:213593835 | GCTGGAGTGCAGTGT[A/C]GAGATCTCGGCTCAC | 79582 |
rs112918148 | snp | A/G | 0.0146672 | 0.084371 | intron-variant | SPAG16 | GRCh38.p7 | 2:213826750 | TGTTAATATCTGTTA[A/G]GTCCATTTGTTCTAT | 79582 |
rs112919986 | snp | A/G | 0 | 0 | intron-variant | SPAG16 | GRCh38.p7 | 2:213467368 | GGAGACAAAGAGCCT[A/G]CCTTGGAGCCATAAG | 79582 |
rs112920591 | snp | C/T | 0 | 0 | intron-variant | SPAG16 | GRCh38.p7 | 2:214326741 | ACGAGATCAGGAGAT[C/T]GAGGCCATCCTGGCT | 79582 |
rs112923180 | snp | C/T | 0.0498117 | 0.149749 | intron-variant | SPAG16, LOC101928084 | GRCh38.p7 | 2:214086493 | CATGGAGGCAGTCCC[C/T]CTGTGCTGTTCTGGT | 79582 |
rs112927021 | snp | C/T | 0.0456336 | 0.143994 | intron-variant | SPAG16 | GRCh38.p7 | 2:213450220 | GAGGCAGGAGAATTG[C/T]TTGAAGCTGGGAGGC | 79582 |
rs112930603 | snp | C/T | 0.0854556 | 0.188216 | intron-variant | SPAG16 | GRCh38.p7 | 2:213702948 | TAGTGTTCATCCACG[C/T]GCTCTACCCTTCTAT | 79582 |
rs112933130 | snp | G/T | 0.479014 | 0.100263 | intron-variant | SPAG16 | GRCh38.p7 | 2:214039370 | CTGTTCACATCCTTC[G/T]CCCACTTTTTAATGG | 79582 |
rs112940384 | snp | C/T | 0.00279162 | 0.0372561 | intron-variant | SPAG16 | GRCh38.p7 | 2:214205981 | GGGCAGATTACGAGG[C/T]CAGGAGATCCAGAAC | 79582 |
rs112950048 | snp | A/G | 0 | 0 | intron-variant | SPAG16 | GRCh38.p7 | 2:214232959 | CAATGCAATGCATCC[A/G]ATGATGGAAATGAAT | 79582 |
rs112954537 | snp | A/G/T | 0.000399281 | 0.0141238 | intron-variant | SPAG16 | GRCh38.p7 | 2:214280824 | ATCTCCTCCATGTCT[A/G/T]GAGTTATGCCGTTCT | 79582 |
rs112958441 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | SPAG16 | GRCh38.p7 | 2:213789697 | CTCCCTGGTTTTCTT[A/G]TATCTCCATTATACT | 79582 |
rs112958940 | snp | A/G | 0.5 | 0 | intron-variant | SPAG16 | GRCh38.p7 | 2:213597922 | GCTCTCCCTTTTTCA[A/G]TTTTGGAAAGATTAA | 79582 |
rs112962568 | snp | C/T | 0.0150606 | 0.0854603 | intron-variant | SPAG16 | GRCh38.p7 | 2:213850101 | ATTGTCCTCATTTCA[C/T]TTACCTAAATAGTGG | 79582 |
rs112962805 | snp | C/G | 0.00358779 | 0.0422022 | intron-variant | SPAG16 | GRCh38.p7 | 2:213537443 | AATTCATACATTGTT[C/G]TGTTATTTTATTAAA | 79582 |
rs112964145 | snp | A/T | 0.00358779 | 0.0422022 | intron-variant | SPAG16 | GRCh38.p7 | 2:213522716 | TTTGTGTCTACCACA[A/T]ATATAATTTCAGGAC | 79582 |
rs112968589 | snp | A/G | 0.00358779 | 0.0422022 | intron-variant | SPAG16 | GRCh38.p7 | 2:213702016 | TGTGTCTAGCTGAAG[A/G]TTTGTAAACTCACTA | 79582 |
rs112968805 | snp | C/T | 0.5 | 0 | intron-variant | SPAG16 | GRCh38.p7 | 2:213539179 | AAATATTATAAATTC[C/T]GTAGATTCATAGTAC | 79582 |
rs112969832 | snp | A/G | 0.0232847 | 0.105357 | intron-variant | SPAG16 | GRCh38.p7 | 2:214260869 | CCCAGCACTTTGGGA[A/G]GCTAAGGCAGGTGGA | 79582 |
rs112974947 | snp | G/T | 0.5 | 0 | intron-variant | SPAG16 | GRCh38.p7 | 2:214033099 | AAACATGAAATATTT[G/T]TGGTCAAAGCAGAGG | 79582 |
rs112975349 | snp | A/G | 0.00517822 | 0.0506191 | intron-variant | SPAG16 | GRCh38.p7 | 2:213589887 | AGATCGCGCCATTGC[A/G]CTCCAGCCCGGGCAA | 79582 |
rs112978514 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | SPAG16 | GRCh38.p7 | 2:213600683 | AGTGTGAATTGTCTG[A/G]AGAGAAATTTGGCCG | 79582 |
rs112983349 | snp | C/T | 0.0850919 | 0.187897 | intron-variant | SPAG16 | GRCh38.p7 | 2:213448047 | ACCAATCTGTTCAAA[C/T]GGCTTATTTTGTTAA | 79582 |
rs112985705 | snp | A/G | 0.00358779 | 0.0422022 | intron-variant | SPAG16 | GRCh38.p7 | 2:213547652 | AATGGCTATAAAATT[A/G]TATCTATAAAACTAG | 79582 |
rs112992253 | in-del | -/C | 0.0209421 | 0.100162 | intron-variant | SPAG16 | GRCh38.p7 | 2:213472236 | ATTGCTTCTAGTGGG[-/C]CTTATGGACAGGAAT | 79582 |
rs112993721 | snp | A/G | 0.00716266 | 0.059414 | intron-variant | SPAG16 | GRCh38.p7 | 2:214141928 | TTATATTTTTCTTCA[A/G]TTCTGGCAAAGTTTC | 79582 |
rs112997566 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | SPAG16 | GRCh38.p7 | 2:213645040 | CCTGGTATTGTATTC[A/G]GCTGAGCTAGCTCTC | 79582 |
rs112998711 | snp | G/T | 0.5 | 0 | intron-variant | SPAG16 | GRCh38.p7 | 2:213741037 | GGTGCTGAGCATTAA[G/T]TTATTCAACTATTAA | 79582 |
rs113001489 | snp | A/T | 0.0452528 | 0.143452 | intron-variant | SPAG16 | GRCh38.p7 | 2:213477542 | GAGACAAAGGAGATG[A/T]TTTTGGAACTTTAAG | 79582 |
rs113004365 | snp | C/T | 0.5 | 0 | intron-variant | SPAG16 | GRCh38.p7 | 2:213366034 | GTAGTCCCAGCTACT[C/T]GGGAGGCTGAGGCAG | 79582 |
rs113008159 | snp | A/G | 0.5 | 0 | intron-variant | SPAG16 | GRCh38.p7 | 2:213393888 | CATATGTTAGCTTCT[A/G]TGAAATAACAGTTCA | 79582 |
rs113008167 | snp | A/G | 0.00358779 | 0.0422022 | intron-variant | SPAG16 | GRCh38.p7 | 2:213554158 | TGAGAAAAGGAGGTC[A/G]TGAGGACATTAAAAA | 79582 |
rs113010051 | snp | A/G | 0.0498117 | 0.149749 | intron-variant | SPAG16 | GRCh38.p7 | 2:213425672 | AAAAAAAAAAAAAAG[A/G]TGTGCAAATTGTTGC | 79582 |
rs113011869 | snp | C/T | | | intron-variant | SPAG16 | GRCh38.p7 | 2:213699907 | TAATTTGTGTGAGTC[C/T]GATAGGACAGCTTGA | 79582 |
rs113018759 | snp | C/G | 0.00755907 | 0.0610114 | intron-variant | SPAG16 | GRCh38.p7 | 2:213646842 | GCACATCTGTAGAAT[C/G]AAATCAAATGCTTCC | 79582 |
rs113020475 | in-del | -/A | 0.155656 | 0.231515 | intron-variant, utr-variant-3-prime | SPAG16 | GRCh38.p7 | 2:213397510 | ATCTTTTTGTCAATT[-/A]AAAAAATTAATCCCC | 79582 |
rs113023729 | snp | G/T | 0.5 | 0 | intron-variant | SPAG16 | GRCh38.p7 | 2:213672845 | TTTTTTTGTTTGTTT[G/T]TTTTATTTTGTTTGT | 79582 |
rs113026079 | snp | C/T | 0.029116 | 0.117091 | intron-variant | SPAG16 | GRCh38.p7 | 2:213545125 | GAGTTTCTGTTGATC[C/T]ACATCCTTACCAGCA | 79582 |
rs113029282 | snp | A/C | 0.0263992 | 0.111815 | intron-variant | SPAG16 | GRCh38.p7 | 2:214267804 | AATAGAAAAAAAATC[A/C]TAGAATTTGTATGGA | 79582 |
rs113030289 | snp | A/G | 0.0182019 | 0.0936463 | intron-variant | SPAG16 | GRCh38.p7 | 2:213978544 | TTATTGTGGCACCAC[A/G]CTACTTCCAATTTCT | 79582 |
rs113033009 | snp | A/G | 0.444444 | 0.157135 | intron-variant | SPAG16 | GRCh38.p7 | 2:213879934 | ATTGTGAAAAGTGCA[A/G]CAATGAACATATGAG | 79582 |
rs113035991 | snp | A/G | 0.103082 | 0.202275 | intron-variant | SPAG16 | GRCh38.p7 | 2:213660965 | CTCCATACTAGCATC[A/G]GCCCCCTGGTCCCAC | 79582 |
rs113037392 | snp | A/G | 0.046775 | 0.145601 | intron-variant | SPAG16 | GRCh38.p7 | 2:213471375 | GGAATGCTGCTGTGC[A/G]TGCCCCACTTTATGA | 79582 |
rs113043631 | snp | A/G | 0.00716266 | 0.059414 | intron-variant | SPAG16 | GRCh38.p7 | 2:214009024 | AATTATCTCCACTTC[A/G]CCCAGGATTAAACTC | 79582 |
rs113044009 | in-del | -/GA | 0.212425 | 0.24716 | intron-variant | SPAG16 | GRCh38.p7 | 2:213407975 | CAGAGAGAGAGACAG[-/GA]GAGAGAGAGAGGAGA | 79582 |
rs113048140 | snp | C/T | 0.0023933 | 0.0345097 | intron-variant | SPAG16 | GRCh38.p7 | 2:213357338 | GTCTCGTTGATCTGT[C/T]TAATATTGACAGTAG | 79582 |
rs113049564 | snp | C/T | 0.0182019 | 0.0936463 | intron-variant, upstream-variant-2KB | SPAG16 | GRCh38.p7 | 2:213342033 | TATTCCAGTGAAATT[C/T]TATGTGTTGTTAATT | 79582 |
rs113050489 | snp | C/T | 0.00597247 | 0.0543191 | intron-variant | SPAG16 | GRCh38.p7 | 2:214113514 | TTTGGAGACTTTGTT[C/T]GTTTCTTTTTAACTC | 79582 |
rs113055445 | snp | A/G | 0.00159617 | 0.0282053 | intron-variant | SPAG16 | GRCh38.p7 | 2:213731428 | GCCTCCCAAATTGCT[A/G]GGATTACAGGCGTGA | 79582 |
rs113055731 | in-del | -/A | 0.5 | 0 | intron-variant | SPAG16 | GRCh38.p7 | 2:213972697 | AATGCAGTCAAGTTT[-/A]CACTTAAAATTAACC | 79582 |
rs113060803 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | SPAG16 | GRCh38.p7 | 2:213324310 | ATGCTTTATATACAT[G/T]GAAGTATATGTCTTA | 79582 |
rs113065625 | snp | C/T | 0.5 | 0 | intron-variant | SPAG16 | GRCh38.p7 | 2:214166579 | TGCTTCTAATTTACA[C/T]ATGTATTTCCTTAAT | 79582 |
rs113067419 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | SPAG16 | GRCh38.p7 | 2:213440541 | GCTTGGGTGACAGAG[C/T]GAGACTCCATCTCAA | 79582 |
rs113070298 | snp | A/T | 0.0452528 | 0.143452 | intron-variant | SPAG16 | GRCh38.p7 | 2:213433945 | TTTTTTTTGAGACAT[A/T]GTCTCGTTCTTGTCA | 79582 |
rs113070621 | snp | A/G | 0.0138799 | 0.0821421 | intron-variant | SPAG16 | GRCh38.p7 | 2:213360204 | TTGTTATACTTGTCA[A/G]TGGAAACTGGATGTG | 79582 |
rs113073692 | snp | C/T | 0.0471551 | 0.14613 | intron-variant | SPAG16 | GRCh38.p7 | 2:213573099 | CCCTGCTTTGGCTCA[C/T]GCACGGTGCGCGCAC | 79582 |
rs113079872 | snp | A/T | 0.5 | 0 | intron-variant | SPAG16 | GRCh38.p7 | 2:213585433 | AGGTACGTGCCACCA[A/T]GCCTGGCTAATTTTT | 79582 |
rs113089330 | snp | A/C | 0.00755907 | 0.0610114 | intron-variant, upstream-variant-2KB | SPAG16, LOC101928084 | GRCh38.p7 | 2:214104887 | CATCACTGCCCACTA[A/C]CACTGTGTCTGAAAG | 79582 |
rs113090294 | snp | C/G | 0.0217236 | 0.101931 | intron-variant | SPAG16 | GRCh38.p7 | 2:213805690 | TGAGAGCCCTTCCAA[C/G]TCCTCCATTCTGTGA | 79582 |
rs113097012 | snp | A/G | 0.00358779 | 0.0422022 | intron-variant | SPAG16 | GRCh38.p7 | 2:213539274 | TGAGTAGTTGATCTC[A/G]TGGCAATGTGATACC | 79582 |
rs113097807 | snp | A/G | 0.00279162 | 0.0372561 | intron-variant | SPAG16 | GRCh38.p7 | 2:214311102 | CCACTAGGGTCACCT[A/G]TCCACTAGGGCAGAA | 79582 |
rs113098258 | snp | A/G | 0.0295035 | 0.117819 | intron-variant | SPAG16 | GRCh38.p7 | 2:213630665 | TATAGAAACATAGAT[A/G]GAAGTAAAAGTGATT | 79582 |
rs113100482 | snp | A/G | 0.00398564 | 0.0444627 | intron-variant | SPAG16 | GRCh38.p7 | 2:213500757 | GTCATATTTGAGAGC[A/G]GAGATAAACTAGTTT | 79582 |
rs113104825 | snp | A/G | 0.029116 | 0.117091 | intron-variant | SPAG16 | GRCh38.p7 | 2:213429350 | TTCCAGTTCCACCCA[A/G]CTTGACCCCCACCAC | 79582 |
rs113105728 | snp | A/G | 0.00358779 | 0.0422022 | intron-variant | SPAG16 | GRCh38.p7 | 2:213512767 | GCTGAACAGATTATA[A/G]AGTACTATCTCCAGG | 79582 |
rs113106353 | snp | C/G | 0.000798403 | 0.0199641 | intron-variant | SPAG16 | GRCh38.p7 | 2:213829765 | AAGGCAGCAGGTTCC[C/G]TTCTGGCCCAAGATG | 79582 |
rs113109579 | snp | G/T | 0.0460142 | 0.144533 | intron-variant | SPAG16 | GRCh38.p7 | 2:213445019 | TTGTCAATAAATGAT[G/T]CTGGGAAAACTGAAT | 79582 |
rs113110533 | snp | A/C | 0.039522 | 0.134904 | intron-variant | SPAG16 | GRCh38.p7 | 2:214219715 | CCATAAAAGTCTCCA[A/C]ATTCTTAGAAAATGT | 79582 |
rs113111624 | snp | C/T | 0.0263992 | 0.111815 | intron-variant | SPAG16 | GRCh38.p7 | 2:213688148 | AATTTAAACATTTTC[C/T]AGTTGACAATTGGTT | 79582 |
rs113112135 | snp | C/T | 0.00358779 | 0.0422022 | intron-variant | SPAG16 | GRCh38.p7 | 2:213531891 | TTACAATCAGTGAAC[C/T]ATCCCTGTACCTCTT | 79582 |
rs113112155 | in-del | -/T | 0.0509478 | 0.151255 | intron-variant | SPAG16 | GRCh38.p7 | 2:213764206 | AAGTTTTTTTTTCTC[-/T]TTTTCTTCATTTCTC | 79582 |
rs113116746 | snp | A/G | 0.0422008 | 0.138995 | intron-variant | SPAG16 | GRCh38.p7 | 2:214259453 | CATATAGAAATAAAT[A/G]CGTACACACACACGT | 79582 |
rs113118474 | snp | A/T | | | intron-variant | SPAG16 | GRCh38.p7 | 2:213480249 | AATTTTCAGTTAGCT[A/T]AGATGCTATAACTTT | 79582 |
rs113125266 | snp | A/G | 0.5 | 0 | intron-variant | SPAG16 | GRCh38.p7 | 2:214058496 | CAAAGGTCACTAATC[A/G]TAGACCATCATAACA | 79582 |
rs113129187 | snp | A/T | 0.5 | 0 | intron-variant | SPAG16 | GRCh38.p7 | 2:214129724 | AGACTTTACTTTTCT[A/T]TTCCATGGAATACTT | 79582 |
rs113129753 | snp | A/C | 0.5 | 0 | intron-variant | SPAG16 | GRCh38.p7 | 2:213641337 | CCAGGCCTCCGGCAC[A/C]CAGGGCTACAAGACT | 79582 |
rs113131019 | snp | A/G | 0.0792508 | 0.182605 | intron-variant | SPAG16 | GRCh38.p7 | 2:213872699 | GATCAGTCTTTCACC[A/G]TTAAGTATGATGTTA | 79582 |
rs113133207 | snp | C/T | 0.5 | 0 | intron-variant | SPAG16 | GRCh38.p7 | 2:213762885 | TTGCAAGTTGCAAAT[C/T]TTATAAGGGGTCAAT | 79582 |
rs113134775 | snp | C/G | 0.00159617 | 0.0282053 | intron-variant | SPAG16 | GRCh38.p7 | 2:214366575 | TTCCAGTAGATAACT[C/G]TGGGGATTTTGGAAT | 79582 |
rs113136426 | snp | C/T | 0 | 0 | intron-variant | SPAG16 | GRCh38.p7 | 2:213769161 | AATCCAAACATGAGT[C/T]GAATGAGGAATTGGG | 79582 |
rs113137388 | in-del | -/T | 0 | 0 | intron-variant | SPAG16 | GRCh38.p7 | 2:214327695 | ATTCTAGATATCAAA[-/T]TTTTTTTTTTTTTTG | 79582 |
rs113138603 | snp | G/T | 0.00358779 | 0.0422022 | intron-variant | SPAG16 | GRCh38.p7 | 2:213548458 | CCTCGTGATCTGCCC[G/T]CCTCGGCCTTCCAAA | 79582 |
rs113139135 | snp | C/T | 0.0263992 | 0.111815 | intron-variant | SPAG16 | GRCh38.p7 | 2:214274875 | CAGAAGCAATGGTAC[C/T]AGCTCCTCTTTGTAC | 79582 |
rs113146783 | snp | A/G | 0.125182 | 0.216612 | intron-variant | SPAG16 | GRCh38.p7 | 2:213643672 | GGAGGCTATTTTCTA[A/G]ATCCTGTAGGCGCCC | 79582 |
rs113147091 | in-del | -/GAA | 0.5 | 0 | intron-variant | SPAG16 | GRCh38.p7 | 2:213528726 | CCCTGGGCCACACTG[-/GAA]GAAGAAGAATTGTCT | 79582 |
rs113147331 | snp | A/G | 0.0279526 | 0.114869 | intron-variant | SPAG16 | GRCh38.p7 | 2:213441534 | CAAAGTATCAGTAAT[A/G]TTCTATTTTTTGACC | 79582 |
rs113150198 | snp | A/C | 0.5 | 0 | intron-variant | SPAG16 | GRCh38.p7 | 2:213805041 | CTCATTACATATTAT[A/C]ATACCAATGTTACTG | 79582 |
rs113152019 | snp | A/G | 0 | 0 | intron-variant | SPAG16 | GRCh38.p7 | 2:213825127 | TAATGGTGTTTTGGT[A/G]GAGTCTTGGATTTCT | 79582 |
rs113156762 | snp | C/T | | | intron-variant | SPAG16 | GRCh38.p7 | 2:214182244 | TAACAAGCTCTGTTG[C/T]TATCAGTTTGTTTAT | 79582 |
rs113157160 | snp | C/T | 0.0854556 | 0.188216 | intron-variant, downstream-variant-500B | SPAG16 | GRCh38.p7 | 2:213703720 | CTCTCCTCAGAGTAA[C/T]CTCAGTCAGTGACTA | 79582 |
rs113162029 | snp | C/G | 0.5 | 0 | intron-variant | SPAG16 | GRCh38.p7 | 2:213723909 | TTTACCAGGAAGTGC[C/G]TCATCAGCATGTTTA | 79582 |
rs113168516 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | SPAG16 | GRCh38.p7 | 2:213647850 | TTTTATTCTTCAGGA[C/T]TAAACGAGACTTGAA | 79582 |
rs113168579 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | SPAG16 | GRCh38.p7 | 2:214058701 | AAAGTACAATAAAAT[A/G]AGATATGCATGTATC | 79582 |
rs113170005 | snp | A/C | 0.0441095 | 0.141807 | intron-variant | SPAG16 | GRCh38.p7 | 2:214269091 | AAAAATTTAAATTAT[A/C]ATGGTGGACATTTAT | 79582 |
rs113175183 | snp | C/T | 0.029116 | 0.117091 | intron-variant | SPAG16 | GRCh38.p7 | 2:213635303 | GGCTCCCAAAGTGCT[C/T]GGATTACAGGCGTGA | 79582 |
rs113176364 | snp | G/T | 0.5 | 0 | intron-variant | SPAG16 | GRCh38.p7 | 2:214143241 | AGTTTTGGGTTTTTT[G/T]TTTTTTTTTTTTTTG | 79582 |
rs113179848 | snp | A/C | 0.000235643 | 0.010852 | synonymous-codon, nc-transcript-variant, utr-variant-5-prime | SPAG16 | GRCh38.p7 | 2:213340214 | ACGTGATTTTCATCG[A/C]ATGCATCATAAGCGA | 79582 |
rs113179866 | snp | A/C | 0.0267878 | 0.112589 | intron-variant | SPAG16 | GRCh38.p7 | 2:214223457 | ATAAACATAGAAGTG[A/C]GGGAGTAACCAAAAA | 79582 |
rs113182413 | snp | C/T | 0.00159617 | 0.0282053 | intron-variant | SPAG16 | GRCh38.p7 | 2:213686212 | CAACCTCTGCCTCCC[C/T]GGTTCAAGTGATTCT | 79582 |
rs113184187 | snp | A/C/G | 0.0221141 | 0.102801 | intron-variant | SPAG16 | GRCh38.p7 | 2:213776829 | GCGTTCTATGCCACC[A/C/G]CCCCCCCACCCCAGG | 79582 |
rs113185470 | in-del | -/A | 0.00358779 | 0.0422022 | intron-variant | SPAG16 | GRCh38.p7 | 2:213709839 | CATTTCTCAGAATAC[-/A]ACAGGTTTGACCATT | 79582 |
rs113192772 | in-del | -/TT | 0.203059 | 0.245554 | intron-variant | SPAG16 | GRCh38.p7 | 2:214059748 | TACCCTTTAAGGTTA[-/TT]TTTTTTTTTGCCATA | 79582 |
rs113195788 | snp | A/T | 0.5 | 0 | intron-variant | SPAG16 | GRCh38.p7 | 2:213352172 | TCTTTTTTTTTTTTT[A/T]ATATATTTTTACCCT | 79582 |
rs113200149 | snp | A/C | 0.0295035 | 0.117819 | intron-variant | SPAG16 | GRCh38.p7 | 2:213616452 | AAAACAAACAACAAC[A/C]AGCATAGCTACAATC | 79582 |
rs113208255 | snp | A/G | 0.5 | 0 | intron-variant, upstream-variant-2KB | SPAG16 | GRCh38.p7 | 2:213315415 | CTCACAGACTTAAGG[A/G]TACTGCTTTTGTAAT | 79582 |
rs113212981 | snp | C/T | 0.00597247 | 0.0543191 | intron-variant | SPAG16 | GRCh38.p7 | 2:213442278 | AAGAAATCAAAGAAC[C/T]AAATAAATGGAGATT | 79582 |
rs113216946 | in-del | -/T | 0 | 0 | intron-variant | SPAG16 | GRCh38.p7 | 2:214388286 | TTAAGAAAAAAAAAT[-/T]ATTAATAGAAAATTG | 79582 |
rs113217854 | snp | C/G/T | 0.000399281 | 0.0141238 | intron-variant | SPAG16 | GRCh38.p7 | 2:213734027 | GAAGTTCACATCACA[C/G/T]TGAGACTCACTGTGA | 79582 |
rs113218296 | snp | C/T | 0.127254 | 0.217792 | intron-variant | SPAG16 | GRCh38.p7 | 2:213956048 | CTGCAATCTCCGCCT[C/T]CCAGGTTCAAGCAAT | 79582 |
rs113223518 | snp | C/T | 0.5 | 0 | intron-variant | SPAG16 | GRCh38.p7 | 2:214221303 | TGAATGATGTTTTCT[C/T]TGTAACTTATCTTAT | 79582 |
rs113224050 | snp | C/T | 0 | 0 | intron-variant | SPAG16 | GRCh38.p7 | 2:213890129 | GTCCTTTAAGTGAAT[C/T]AAGCAATTTCAAGCC | 79582 |
rs113225110 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | SPAG16 | GRCh38.p7 | 2:213764295 | ATGCTTGGAATTTTT[C/T]TTCTTTTTTCATTTG | 79582 |
rs113226827 | snp | C/T | 0.00159617 | 0.0282053 | intron-variant | SPAG16 | GRCh38.p7 | 2:214320024 | GGATACAAGCTCAGG[C/T]GAAATCGTTCTGTCA | 79582 |
rs113227078 | snp | C/T | | | intron-variant | SPAG16 | GRCh38.p7 | 2:214164480 | TGCAAAAGATTTAAA[C/T]CTAAATTATGCTTTT | 79582 |
rs113229481 | snp | C/T | 0.00199481 | 0.0315187 | intron-variant | SPAG16 | GRCh38.p7 | 2:214341381 | CTCACAATTGAAATA[C/T]CCAAGCCTTTAGATT | 79582 |
rs113230117 | snp | C/G | 0.0240643 | 0.107019 | intron-variant | SPAG16 | GRCh38.p7 | 2:213638500 | TGATTTCATTGTTGA[C/G]CCAAAGACCATTCAG | 79582 |
rs113239618 | snp | C/T | 0.5 | 0 | intron-variant | SPAG16 | GRCh38.p7 | 2:214241518 | GTCATAACCCTTACA[C/T]GCAGTATCAGTAAAT | 79582 |
rs113239825 | snp | A/G | 0.5 | 0 | intron-variant | SPAG16 | GRCh38.p7 | 2:214374032 | TTAGAATATAGTAGG[A/G]TCTAAGGCTATAACA | 79582 |
rs113263743 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | SPAG16 | GRCh38.p7 | 2:213891932 | AGCCTGGCAGGAGAC[A/G]TGTTTCTGTTTTTAC | 79582 |
rs113267483 | snp | C/T | 0.00755907 | 0.0610114 | intron-variant | SPAG16 | GRCh38.p7 | 2:213538383 | ATGTCCTTAAGAAAT[C/T]AGGATTTACTTTGAT | 79582 |
rs113282157 | snp | A/T | 0.00358779 | 0.0422022 | intron-variant | SPAG16 | GRCh38.p7 | 2:213527142 | CTCCTGCCAAGGAGG[A/T]TGTGTAGTTTAGGGA | 79582 |
rs113287985 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | SPAG16 | GRCh38.p7 | 2:213485081 | CTCACTGCAACCTTC[C/G]CCTCCTGGGCTCAAG | 79582 |
rs113289542 | snp | G/T | 0.0197687 | 0.0974348 | intron-variant | SPAG16 | GRCh38.p7 | 2:213474190 | CATTCCAAGTTGCAG[G/T]GTCCCATTCTTTTCC | 79582 |
rs113290584 | in-del | -/AGAGAGAGAGAG | 0 | 0 | intron-variant | SPAG16 | GRCh38.p7 | 2:213871880 | CACACACACACACAC[-/AGAGAGAGAGAG]AGAGAGAGCAAACAG | 79582 |
rs113291891 | snp | A/C | 0.0932157 | 0.194727 | intron-variant | SPAG16 | GRCh38.p7 | 2:213761906 | ACAAAACAAAAAAAA[A/C]CCCTACAGACCAATA | 79582 |
rs113295582 | snp | C/T | 0.5 | 0 | intron-variant | SPAG16 | GRCh38.p7 | 2:213814119 | GGGAACAGTCCTAAA[C/T]TTGCAGATCAGGCTG | 79582 |
rs113300578 | snp | A/G | 0.5 | 0 | intron-variant | SPAG16 | GRCh38.p7 | 2:214116134 | CTAGATCCTTGTTTG[A/G]CCTTAAACCTGTGCC | 79582 |
rs113301936 | snp | A/G | 0.00478085 | 0.0486577 | intron-variant | SPAG16 | GRCh38.p7 | 2:213629375 | AACTAGCAACATTTA[A/G]GGAATTAAAATGTGA | 79582 |
rs113307388 | snp | A/G | 0.0310518 | 0.120672 | intron-variant | SPAG16 | GRCh38.p7 | 2:213986325 | TATATTTTTCCCACC[A/G]TTTATTTCAGTTTTT | 79582 |
rs113311112 | snp | A/G | 0.0295035 | 0.117819 | intron-variant | SPAG16 | GRCh38.p7 | 2:213437135 | CGATTTCCTGACCTC[A/G]TGATCTGCCCGTCTC | 79582 |
rs113311632 | snp | A/T | 0.5 | 0 | intron-variant | SPAG16 | GRCh38.p7 | 2:214251041 | TTGTTTTATTACAGC[A/T]AATGAATACAGTTAA | 79582 |
rs113311929 | snp | A/G | 0.132066 | 0.220435 | intron-variant | SPAG16 | GRCh38.p7 | 2:213447083 | ATTGTGTTAACTCAC[A/G]TGTAGTAGTATTAAA | 79582 |
rs113314069 | snp | C/T | 0 | 0 | intron-variant | SPAG16 | GRCh38.p7 | 2:213901249 | CAGTTTGGGCCTAAG[C/T]ATCGTAGCAGCCTAC | 79582 |
rs113315864 | snp | A/G | 0.5 | 0 | intron-variant | SPAG16 | GRCh38.p7 | 2:213528142 | ACCTATGTTTTCAAC[A/G]GGCGCCCATCAGAAC | 79582 |
rs113315902 | snp | C/G | 0.0138799 | 0.0821421 | intron-variant | SPAG16 | GRCh38.p7 | 2:213545309 | TTTTAAAATCAAGTT[C/G]TTTATTTTCTTATTG | 79582 |
rs113316152 | snp | C/T | 0.105214 | 0.203807 | intron-variant | SPAG16 | GRCh38.p7 | 2:213687907 | AAACTCTGTAAAATA[C/T]TTGAAGGGATTTATT | 79582 |
rs113316528 | snp | A/C/T | 0 | 0 | intron-variant | SPAG16 | GRCh38.p7 | 2:214372828 | ATCACTGTTCACTTC[A/C/T]CCCCACCCCAAATAA | 79582 |
rs113320897 | snp | A/G | 0.00953873 | 0.0683987 | intron-variant | SPAG16 | GRCh38.p7 | 2:214193299 | GGAGGAGCTCTGGTC[A/G]CCTCTACTAGAACTG | 79582 |
rs113323843 | snp | C/G | 0.00358779 | 0.0422022 | intron-variant | SPAG16 | GRCh38.p7 | 2:213498580 | CTCCTGACATTATCC[C/G]AAGCTGCAATGACTG | 79582 |
rs113324121 | snp | A/C | 0.00597247 | 0.0543191 | intron-variant | SPAG16 | GRCh38.p7 | 2:214141515 | TTAAATATTTGTGCT[A/C]ACCATTATATATTTT | 79582 |
rs113324508 | snp | A/G | 0.029116 | 0.117091 | intron-variant | SPAG16 | GRCh38.p7 | 2:213455700 | CATGCACAGTTCACA[A/G]TAGGGTTTGCGCTCC | 79582 |
rs113324765 | snp | C/G | 0.0103295 | 0.0711199 | intron-variant | SPAG16 | GRCh38.p7 | 2:213381113 | TTATACCACAACACT[C/G]TTGATCAGAAGGCTA | 79582 |
rs113324964 | snp | A/G | 0.0154538 | 0.0865337 | intron-variant | SPAG16 | GRCh38.p7 | 2:213773154 | CATTTTTTTAATTTA[A/G]TGTCTTATAATTTTG | 79582 |
rs113329559 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | SPAG16 | GRCh38.p7 | 2:213824615 | TATATCTTTTTATGC[C/T]AGTACCATGCTGTTT | 79582 |
rs113330223 | snp | C/T | 0.00159617 | 0.0282053 | intron-variant | SPAG16 | GRCh38.p7 | 2:214318100 | AAGATATCAGGATCC[C/T]GGATTCATCAGCATC | 79582 |
rs113330734 | snp | A/G | 0.00159617 | 0.0282053 | intron-variant | SPAG16 | GRCh38.p7 | 2:214330213 | ACCCGGGAGGTGGAG[A/G]TGGCAGTGAGCCGAG | 79582 |
rs113330801 | snp | C/T | 0.260227 | 0.249791 | intron-variant | SPAG16 | GRCh38.p7 | 2:213338302 | AATATGAGGCAACTA[C/T]GCAAACAAGTCTACA | 79582 |
rs113340823 | snp | C/G | 0 | 0 | intron-variant | SPAG16 | GRCh38.p7 | 2:213912544 | GAAATAGTGTGCTTT[C/G]CCACCCCTAGAATTT | 79582 |
rs113346093 | snp | C/T | 0.0479149 | 0.147179 | intron-variant | SPAG16, LOC101928084 | GRCh38.p7 | 2:214099337 | GCATTATGTTAATTG[C/T]TTTACATAAATTTCT | 79582 |
rs113350347 | in-del | -/A | 0.252702 | 0.249985 | intron-variant | SPAG16 | GRCh38.p7 | 2:214407994 | ATTCAGGTAAACTTG[-/A]AAAAACCGCATAATA | 79582 |
rs113352920 | snp | C/G | 0 | 0 | intron-variant | SPAG16 | GRCh38.p7 | 2:213789101 | AAGAACCATTTTAAT[C/G]ACCATAATTGTACTG | 79582 |
rs113355200 | snp | C/T | 0 | 0 | intron-variant | SPAG16 | GRCh38.p7 | 2:213769631 | TCCTGCTGATTTCCC[C/T]AGCCTGGCTTTGCAG | 79582 |
rs113357046 | snp | A/G | 0 | 0 | intron-variant | SPAG16 | GRCh38.p7 | 2:213836797 | TTTTGTATTTTCAGT[A/G]GAGATGGGGTTTTGC | 79582 |
rs113358364 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | SPAG16 | GRCh38.p7 | 2:213572995 | GGGTGGGAGTGACCC[A/G]ATTTTCCAGGTGCGT | 79582 |
rs113360080 | snp | G/T | 0.0729998 | 0.176553 | intron-variant | SPAG16 | GRCh38.p7 | 2:213425358 | CTACATTAGTGCATA[G/T]AAATGTGTAGGCTGG | 79582 |
rs113360906 | snp | A/G | 0.00557542 | 0.0525036 | intron-variant | SPAG16 | GRCh38.p7 | 2:213589205 | TGTTGGGCTAATGTA[A/G]ATTGCCCAAACTTCT | 79582 |
rs113365880 | snp | A/C/G | 0.5 | 0 | intron-variant | SPAG16 | GRCh38.p7 | 2:214304310 | GGCCATAACACCCAC[A/C/G]CTGGAAGGTTGTGGG | 79582 |
rs113372521 | snp | C/T | 0.5 | 0 | intron-variant | SPAG16 | GRCh38.p7 | 2:213697705 | GGTACTGTGTTGCAG[C/T]AGCAATAGGAAATTA | 79582 |
rs113374025 | in-del | -/A | 0.0260105 | 0.111035 | intron-variant | SPAG16 | GRCh38.p7 | 2:214241056 | TAATTACATCTTTCT[-/A]AAAAAAATGAAGCTG | 79582 |
rs113376553 | in-del | -/T | 0 | 0 | intron-variant | SPAG16 | GRCh38.p7 | 2:213783317 | AACTTAGAGTATAAT[-/T]AAAAAAAAAAAAAAA | 79582 |
rs113379892 | snp | C/G | 0.0614824 | 0.164198 | intron-variant | SPAG16 | GRCh38.p7 | 2:213743786 | TCTTGTCTTCTATCA[C/G]TTCTAGAAAATTCTC | 79582 |
rs113387097 | snp | C/T | 0.00557542 | 0.0525036 | intron-variant | SPAG16 | GRCh38.p7 | 2:213597919 | GAGGCTCTCCCTTTT[C/T]CAATTTTGGAAAGAT | 79582 |
rs113391701 | snp | A/C | 0.0267878 | 0.112589 | intron-variant | SPAG16 | GRCh38.p7 | 2:214220482 | AGATTTGTTAGGTAA[A/C]CTTAAAGTTAAGTCA | 79582 |
rs113391896 | snp | A/C | 0.0448719 | 0.142907 | intron-variant | SPAG16 | GRCh38.p7 | 2:213448061 | ATGGCTTATTTTGTT[A/C]ATGATTGCCAGGCCA | 79582 |
rs113396392 | snp | C/G | 0.0858192 | 0.188533 | intron-variant | SPAG16 | GRCh38.p7 | 2:213803902 | AGACTTCATGGCACA[C/G]GCCTTGAGTCTCTAA | 79582 |
rs113398983 | snp | A/G | 0.125182 | 0.216612 | intron-variant | SPAG16 | GRCh38.p7 | 2:213641975 | GATAAGTCACTCACT[A/G]TCATGAGAACAGCAT | 79582 |
rs113404078 | snp | C/T | 0 | 0 | intron-variant | SPAG16 | GRCh38.p7 | 2:213892936 | GAGAAAACACATGCA[C/T]GTAAGTTACATCCAA | 79582 |
rs113404292 | in-del | -/G | 0.021333 | 0.101051 | intron-variant | SPAG16 | GRCh38.p7 | 2:213483307 | ATTTTCTCAGAGTAC[-/G]TTTTTAGAAATGGAC | 79582 |
rs113406752 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | SPAG16 | GRCh38.p7 | 2:213905829 | ATAAGGTGAAGTTAG[A/G]GAAAATGTCTTCACT | 79582 |
rs113413120 | snp | C/T | 0.5 | 0 | intron-variant, upstream-variant-2KB | SPAG16, MIR4438 | GRCh38.p7 | 2:213757193 | GTTCTCTGAAAACTA[C/T]AAACATTTCTAAAGA | 79582 |
rs113416210 | snp | A/G | 0.0248432 | 0.108648 | intron-variant | SPAG16 | GRCh38.p7 | 2:214256576 | GTTATAAATCTGGGC[A/G]AGAGTTTTTGTTGTT | 79582 |
rs113416386 | snp | A/G | 0.0103295 | 0.0711199 | intron-variant | SPAG16 | GRCh38.p7 | 2:213513289 | CACTGTGGCTGAACC[A/G]TATTCTACCTTCAAT | 79582 |
rs113416551 | snp | A/G | 0.173965 | 0.238157 | intron-variant | SPAG16 | GRCh38.p7 | 2:213593977 | AGGCGGGTTTTCACC[A/G]CGTTAGCCAGGATGG | 79582 |
rs113419989 | snp | A/T | 0.000798403 | 0.0199641 | intron-variant | SPAG16 | GRCh38.p7 | 2:213842001 | TTAAATTTGTAACTA[A/T]GCATTTATGTTCATT | 79582 |
rs113426793 | snp | C/T | 0.5 | 0 | intron-variant | SPAG16 | GRCh38.p7 | 2:214224920 | GGTAGAGTCAAATAA[C/T]AGGGAAATTAACTGG | 79582 |
rs113431045 | in-del | -/GAGACC | 0.236144 | 0.249616 | intron-variant | SPAG16, LOC101928084 | GRCh38.p7 | 2:214102777 | CATAAAGCAGAAAAA[-/GAGACC]GAGACCGGGGCAAGT | 79582 |
rs113431476 | in-del | -/AATT | 0.193028 | 0.243422 | intron-variant | SPAG16 | GRCh38.p7 | 2:213387391 | TCCTTTTTTTGCCCA[-/AATT]AATTCTTAGTCTTTT | 79582 |
rs113432445 | snp | A/G | 0.00358779 | 0.0422022 | intron-variant | SPAG16 | GRCh38.p7 | 2:213509296 | TTTTCTATATTTTCT[A/G]TTTCCAGATAGAGTA | 79582 |
rs113433177 | snp | G/T | 0.0854556 | 0.188216 | intron-variant | SPAG16 | GRCh38.p7 | 2:213702072 | TAGTGGGGACTTGGA[G/T]AACTTTTATGTCTAG | 79582 |
rs113435593 | in-del | -/G | 0.131723 | 0.220251 | intron-variant | SPAG16 | GRCh38.p7 | 2:213609331 | TTGCTTTAGAGCAAT[-/G]GGTAACCTCTTTGAC | 79582 |
rs113444204 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | SPAG16 | GRCh38.p7 | 2:213946364 | GAGATCTACCTGCCT[C/T]GGCCTCCCAGAGTGC | 79582 |
rs113444614 | snp | C/T | 0.00478085 | 0.0486577 | intron-variant | SPAG16 | GRCh38.p7 | 2:213792607 | TTTTTTTTTGGAGAC[C/T]GGGTCTCACTCTCTT | 79582 |
rs113462562 | snp | C/T | 0.5 | 0 | intron-variant | SPAG16 | GRCh38.p7 | 2:214157355 | AAAATGTAATTTTAA[C/T]GTAATGTAAATTAGG | 79582 |
rs113466730 | snp | C/T | 0.00993419 | 0.0697739 | intron-variant | SPAG16 | GRCh38.p7 | 2:214040757 | TTATTGGCTAAAGTC[C/T]GCATATTTTTCTTCT | 79582 |
rs113468927 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | SPAG16 | GRCh38.p7 | 2:213760449 | TTACATAATGGAAGG[A/G]AATGATACACAGTTC | 79582 |
rs113469204 | snp | A/G | 0.0471551 | 0.14613 | intron-variant | SPAG16 | GRCh38.p7 | 2:214259598 | TTCCTTCTTCCAGGC[A/G]TTCACTCTCCTTCAC | 79582 |
rs113473627 | snp | A/G | 0.0154538 | 0.0865337 | intron-variant | SPAG16 | GRCh38.p7 | 2:214003331 | GATAATTTCTATACA[A/G]TGTATATGTTTTCTG | 79582 |
rs113473924 | snp | A/G | 0.5 | 0 | intron-variant | SPAG16 | GRCh38.p7 | 2:213806305 | ATGAATATAACTTTT[A/G]ATTCTGCCACCAGAT | 79582 |
rs113474128 | snp | A/C | 0.0314739 | 0.12165 | intron-variant | SPAG16 | GRCh38.p7 | 2:213324273 | TTATTATAATATATA[A/C]TTTTTACAGTTATTT | 79582 |
rs113476474 | snp | A/G | 0.00517822 | 0.0506191 | intron-variant | SPAG16 | GRCh38.p7 | 2:213598283 | CTTCAGAGGGTGAAG[A/G]GGAAGTTCTCCCTTG | 79582 |
rs113479285 | snp | A/G | 0.5 | 0 | intron-variant | SPAG16 | GRCh38.p7 | 2:213814177 | ATGTTACAGTCTTCA[A/G]TACAAAATCTGCAGG | 79582 |
rs113481453 | snp | C/G | | | intron-variant | SPAG16 | GRCh38.p7 | 2:214206026 | GGTGAAACCCCGTCT[C/G]TACTAAAAATACAAA | 79582 |
rs113485179 | snp | A/C | 0.5 | 0 | intron-variant | SPAG16 | GRCh38.p7 | 2:214163709 | ATGTGATTGCGGGGG[A/C]TGGCAATTGTGAATT | 79582 |
rs113490164 | snp | A/T | 0.0162398 | 0.0886349 | intron-variant, upstream-variant-2KB | SPAG16 | GRCh38.p7 | 2:213297919 | TGGCAAAAATATTTT[A/T]AAAAATGTTTTATTT | 79582 |
rs113494376 | snp | A/G | 0.110167 | 0.207236 | intron-variant | SPAG16 | GRCh38.p7 | 2:213690663 | GCCAGTGCAGGTAGA[A/G]CAAAGCAGGCAGAAG | 79582 |
rs113495065 | in-del | -/CA | 0.5 | 0 | intron-variant | SPAG16 | GRCh38.p7 | 2:214319187 | TTCCTAATAAACTTG[-/CA]CACACACACACACCA | 79582 |
rs113496074 | snp | C/T | 0.0126979 | 0.078662 | intron-variant | SPAG16 | GRCh38.p7 | 2:213869221 | TCGCGCCATTGAACT[C/T]TAGCCTGGGCAACAA | 79582 |
rs113496260 | in-del | -/A | 0 | 0 | intron-variant | SPAG16 | GRCh38.p7 | 2:214400596 | GACCTGGAACCAACA[-/A]CCCCATAGATACAGA | 79582 |
rs113499636 | snp | C/T | 0.5 | 0 | intron-variant, utr-variant-5-prime | SPAG16 | GRCh38.p7 | 2:213343895 | TTAAATAGTCCATCA[C/T]AGGTGTGTATTTGAA | 79582 |
rs113501024 | in-del | -/A | 0.0244538 | 0.107838 | intron-variant | SPAG16 | GRCh38.p7 | 2:214236593 | GGAGGCAGAGGTTAT[-/A]GTGAGCCAAGATCGC | 79582 |
rs113502841 | snp | C/G | 0.021333 | 0.101051 | intron-variant | SPAG16 | GRCh38.p7 | 2:213777441 | AGATGGAGTCTCGCT[C/G]TGTCTCCCAGGCTGG | 79582 |
rs113503659 | snp | C/G | 0.5 | 0 | intron-variant | SPAG16 | GRCh38.p7 | 2:213582381 | CATTGACCTCAGGTT[C/G]TTTCTTATACAAAAG | 79582 |
rs113506175 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | SPAG16 | GRCh38.p7 | 2:214254534 | GTATATCTTAAAACA[A/G]TCGGTCAGCTTAGTC | 79582 |
rs113507542 | snp | G/T | 0.000798403 | 0.0199641 | intron-variant | SPAG16 | GRCh38.p7 | 2:213827073 | ATTTTCTTCTTATGT[G/T]TATCTTTATAGGTAA | 79582 |
rs113508031 | snp | A/G | 0.5 | 0 | intron-variant | SPAG16 | GRCh38.p7 | 2:214358189 | TGTGTAGTGTCTTAT[A/G]CGATGCTCTTGGTGT | 79582 |
rs113514093 | snp | A/G | 0.00478085 | 0.0486577 | intron-variant | SPAG16 | GRCh38.p7 | 2:213651114 | TTTGATAACTACTAA[A/G]TACTGTATCAATAAG | 79582 |
rs113514154 | in-del | -/T | 0.5 | 0 | intron-variant | SPAG16 | GRCh38.p7 | 2:213404843 | TTTGATTCTTTAAAA[-/T]TTTTTTTTTAATTAT | 79582 |
rs113518524 | snp | A/G | 0.00478085 | 0.0486577 | intron-variant | SPAG16 | GRCh38.p7 | 2:213638529 | AGGAGCAGATTATTT[A/G]ATTTTTATGTATTTT | 79582 |
rs113521476 | snp | C/T | 0 | 0 | intron-variant | SPAG16 | GRCh38.p7 | 2:213867997 | CCACACAGTGGGCTA[C/T]GAAGGGAAGAGGCAA | 79582 |
rs113522769 | snp | A/T | 0 | 0 | intron-variant | SPAG16 | GRCh38.p7 | 2:214262589 | GAAATTTTTAAGATC[A/T]TGTTAAATTAACCAT | 79582 |
rs113522863 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | SPAG16 | GRCh38.p7 | 2:213509691 | AGGGAAATTTATAGC[A/T]CTAAATGCCCACAAG | 79582 |
rs113523376 | snp | A/G | 0.00318978 | 0.0398085 | intron-variant | SPAG16 | GRCh38.p7 | 2:214277552 | TCAGGTCCCTCAGCT[A/G]CAGGTCTGTTGGAGT | 79582 |
rs113529201 | in-del | -/A | 0 | 0 | intron-variant | SPAG16 | GRCh38.p7 | 2:214015601 | AAAACTCCATCTCAG[-/A]AAAAAAAAAAAATCA | 79582 |
rs113529535 | in-del | -/G | 0 | 0 | intron-variant | SPAG16 | GRCh38.p7 | 2:213626374 | CCCGGATTTTTAGGG[-/G]AAAAAAATAGCTGCA | 79582 |
rs113531978 | snp | A/C | 0.5 | 0 | intron-variant | SPAG16 | GRCh38.p7 | 2:213956081 | TCCTGCCTCAGCTTC[A/C]TGAGTAGTTGGGATT | 79582 |
rs113532630 | snp | C/G | 0.5 | 0 | intron-variant | SPAG16 | GRCh38.p7 | 2:214182834 | AGATCACATTGCTCA[C/G]ATTTTTTCCAAACTT | 79582 |
rs113534947 | snp | C/G | 0.193966 | 0.243639 | intron-variant | SPAG16 | GRCh38.p7 | 2:213354805 | AAATTTTCTCCCATT[C/G]TGTAGGTTACCTGTT | 79582 |
rs113535341 | snp | A/G | 0.00716266 | 0.059414 | intron-variant | SPAG16 | GRCh38.p7 | 2:213451858 | TCTGAGCATGCTAAA[A/G]GGGAGGGAGAGTTTC | 79582 |
rs113535895 | snp | A/T | 0.0425829 | 0.139564 | intron-variant | SPAG16 | GRCh38.p7 | 2:214229472 | GTCTGTATATTATAT[A/T]TATATGTATGTGTAT | 79582 |
rs113536141 | snp | C/T | 0.00358779 | 0.0422022 | intron-variant | SPAG16 | GRCh38.p7 | 2:213526557 | GCACAGATGTCAACT[C/T]GGAGCCTCCTTTTGG | 79582 |
rs113537277 | snp | A/G | 0.00517822 | 0.0506191 | intron-variant | SPAG16 | GRCh38.p7 | 2:213591212 | ATTAGATTTTGGAGT[A/G]TGTGTTTTAAAGTAA | 79582 |
rs113542735 | snp | A/G | 0.00358779 | 0.0422022 | intron-variant | SPAG16 | GRCh38.p7 | 2:213661079 | CACTCCAACATATAG[A/G]TAGCCTTGGTCCATG | 79582 |
rs113543073 | snp | C/T | 0.00478085 | 0.0486577 | intron-variant | SPAG16 | GRCh38.p7 | 2:213630845 | TAAGATAGGCAACGG[C/T]CTACCTGGGACATAA | 79582 |
rs113544946 | snp | A/G | 0.0236746 | 0.106192 | intron-variant | SPAG16 | GRCh38.p7 | 2:213619958 | AAATGTGGTACATAT[A/G]CACAATGGAGTACTA | 79582 |
rs113548024 | snp | C/G | 0.0178098 | 0.0926698 | intron-variant | SPAG16 | GRCh38.p7 | 2:214058032 | GGTTTGATCTTCTAT[C/G]CAGACCACCAAAACT | 79582 |
rs113549112 | snp | A/G | 0.5 | 0 | intron-variant | SPAG16 | GRCh38.p7 | 2:213411932 | AAAAGAAAACTATAA[A/G]GAATACAAGGGGAAG | 79582 |
rs113549458 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | SPAG16 | GRCh38.p7 | 2:213441346 | TAATATGGAGCAAAA[C/T]GAATGTCTTCTATAC | 79582 |
rs113551597 | snp | A/G | 0.00358779 | 0.0422022 | intron-variant | SPAG16 | GRCh38.p7 | 2:213534970 | AGTAGATTAGGACAT[A/G]AAGACACACAAAGCA | 79582 |
rs113553771 | snp | G/T | 0.0463947 | 0.145069 | intron-variant | SPAG16 | GRCh38.p7 | 2:213337609 | CAAAGAGACGAAGCA[G/T]AAGAAAGGGTATCAG | 79582 |
rs113555219 | snp | C/T | 0.0448719 | 0.142907 | intron-variant | SPAG16 | GRCh38.p7 | 2:214252642 | ATCCATTTTTATAGC[C/T]GCATAGTATTCCATG | 79582 |
rs113559804 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | SPAG16 | GRCh38.p7 | 2:213291666 | AAAAAAATAGGTGAG[C/T]TCATTACCTAGGATA | 79582 |
rs113559906 | snp | C/T | 0.5 | 0 | intron-variant | SPAG16 | GRCh38.p7 | 2:214204026 | GCCTTTTGGGCTGCA[C/T]AGGAGCTGATGAGGC | 79582 |
rs113560447 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | SPAG16 | GRCh38.p7 | 2:213762603 | ATGTAAAAGAATGAA[A/G]TTGAACCCTTACCTT | 79582 |
rs113561868 | snp | C/G/T | 0.00795939 | 0.0626292 | intron-variant | SPAG16 | GRCh38.p7 | 2:213765141 | GGGAAGTGCCCGAGG[C/G/T]GGGCGGATCACAAGG | 79582 |
rs113564810 | snp | C/T | 0 | 0 | intron-variant | SPAG16 | GRCh38.p7 | 2:213896184 | CATATGGCCAAAAGG[C/T]ATATGAAAAAAATAC | 79582 |
rs113568470 | snp | C/T | 0.00358779 | 0.0422022 | intron-variant | SPAG16 | GRCh38.p7 | 2:213586325 | TTGACACATTCCATG[C/T]CTAGTGAGGCCCACC | 79582 |
rs113571644 | snp | G/T | 0.5 | 0 | intron-variant | SPAG16 | GRCh38.p7 | 2:214148160 | TTCAATTTGTGAGTG[G/T]ACAAAGAAATTAAAT | 79582 |
rs113572374 | snp | C/T | 0.5 | 0 | intron-variant | SPAG16 | GRCh38.p7 | 2:213464834 | ATTTTAAGAACTTTC[C/T]ATTGGCTGGAATTTG | 79582 |
rs113573001 | snp | C/T | 0.0919752 | 0.193722 | intron-variant | SPAG16 | GRCh38.p7 | 2:214047400 | TCCACACACCTACAG[C/T]GAACTCACTTTTGAC | 79582 |
rs113578202 | snp | C/T | 0.0252325 | 0.109451 | intron-variant | SPAG16 | GRCh38.p7 | 2:213356255 | ACTCATTTTATGAGG[C/T]CAGCATCATCCTGAT | 79582 |
rs113580181 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | SPAG16 | GRCh38.p7 | 2:213704289 | AGAGTTGTGAGAATA[A/C]TTAATAGCCAAAGTT | 79582 |
rs113581311 | snp | C/T | 0.0271762 | 0.113356 | intron-variant | SPAG16 | GRCh38.p7 | 2:213449397 | TAGTTCTGCTTTTTG[C/T]TCTTTGAAGCATGTG | 79582 |
rs113581915 | in-del | -/ACCTC | 0.00358779 | 0.0422022 | intron-variant | SPAG16 | GRCh38.p7 | 2:213555273 | TCCCACTCAAATCTT[-/ACCTC]AAATTGTAATCCCTA | 79582 |
rs113583450 | snp | A/C | 0.0130921 | 0.0798413 | intron-variant | SPAG16 | GRCh38.p7 | 2:214214248 | CAATCTGGCTCACTG[A/C]AACCTCCACCTCCCA | 79582 |
rs113585122 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | SPAG16 | GRCh38.p7 | 2:213696382 | AGGTCAGCACTGGCC[A/G]TCAATATTCAGTACC | 79582 |
rs113586302 | snp | A/G | 0.0463947 | 0.145069 | intron-variant | SPAG16 | GRCh38.p7 | 2:213337540 | ATAAATTACCTGATC[A/G]AGCTGAGAAACACAA | 79582 |
rs113586466 | snp | A/G | 0.00358779 | 0.0422022 | intron-variant | SPAG16 | GRCh38.p7 | 2:213528578 | TGTAAAACCAGAAGT[A/G]ACTTGTTACTTCCCT | 79582 |
rs113589792 | snp | A/C | 0.5 | 0 | intron-variant | SPAG16 | GRCh38.p7 | 2:214245327 | CTCCACCATCTCTTT[A/C]CCCTAGTCCCCAATG | 79582 |
rs113590841 | snp | C/G | 0.5 | 0 | intron-variant | SPAG16 | GRCh38.p7 | 2:214255336 | AGAATGTCTGTCACT[C/G]TGGCCCTGGGATTTT | 79582 |
rs113592079 | in-del | -/A | 0.5 | 0 | intron-variant | SPAG16 | GRCh38.p7 | 2:214163951 | ACTAATCACGTCTTT[-/A]AAAAAAAATACCTGT | 79582 |
rs113592244 | snp | C/T | 0 | 0 | intron-variant | SPAG16 | GRCh38.p7 | 2:213898189 | TGTATGTTTCAGAAA[C/T]AAAGCTTTTAAATGG | 79582 |
rs113592934 | snp | G/T | 0.00358779 | 0.0422022 | intron-variant | SPAG16 | GRCh38.p7 | 2:213516846 | TGTTTTTCATTAAAT[G/T]GAAAAAATAGAAAAA | 79582 |
rs113592946 | snp | A/G/T | 0.00358779 | 0.0422022 | intron-variant | SPAG16 | GRCh38.p7 | 2:213906033 | TATCTTAGCACCTAC[A/G/T]CTAAATTCCAAATAT | 79582 |
rs113596631 | snp | C/G | 0.00517822 | 0.0506191 | intron-variant | SPAG16 | GRCh38.p7 | 2:213582484 | AAAGAGATAGTTGAA[C/G]TCTGTGGCATCAGAA | 79582 |
rs113600080 | snp | C/T | 0.107694 | 0.205546 | intron-variant | SPAG16 | GRCh38.p7 | 2:214149096 | ATATATATATATATA[C/T]ACATACATACACATT | 79582 |
rs113601624 | snp | C/T | 0.5 | 0 | intron-variant | SPAG16 | GRCh38.p7 | 2:213530420 | ATATACTGTTCATCA[C/T]TGACTGAAATGTCAT | 79582 |
rs113604011 | snp | G/T | 0.0271762 | 0.113356 | intron-variant | SPAG16 | GRCh38.p7 | 2:213543240 | CTCATTTTATTTCTT[G/T]TTTATGAATGGTCAT | 79582 |
rs113607835 | snp | A/G | 0.473359 | 0.112298 | intron-variant | SPAG16 | GRCh38.p7 | 2:213859050 | CAGACATGGTGGCAC[A/G]CACCTGTAATCCCAG | 79582 |
rs113608224 | snp | C/T | | | intron-variant | SPAG16 | GRCh38.p7 | 2:213348544 | CCATGTTTAGTGCTT[C/T]CTTCAGGAGCTCTTT | 79582 |
rs113610733 | snp | C/G | 0.00636936 | 0.0560724 | intron-variant | SPAG16 | GRCh38.p7 | 2:214183050 | GTTATTTTCCTAATA[C/G]AGTAAATTAGTGATA | 79582 |
rs113618034 | snp | C/G | 0.089084 | 0.191327 | intron-variant | SPAG16 | GRCh38.p7 | 2:213752663 | TGTATTTGCTGCCTT[C/G]TTACTCTTTTTCTCT | 79582 |
rs113622440 | snp | C/G | 0.5 | 0 | intron-variant | SPAG16 | GRCh38.p7 | 2:213797397 | CATTCATAGTGCCGA[C/G]AAAATGTGTATCATT | 79582 |
rs113622873 | snp | A/G | 0.00358779 | 0.0422022 | intron-variant | SPAG16 | GRCh38.p7 | 2:213576721 | AGCAAACTAACACAT[A/G]AACAGAAAACCAAAT | 79582 |
rs113627040 | snp | A/G | 0.0275645 | 0.114116 | intron-variant | SPAG16 | GRCh38.p7 | 2:213630041 | CTCAATGTTCCCATC[A/G]TCCATATAACCATTG | 79582 |
rs113633581 | snp | G/T | 0.000798403 | 0.0199641 | intron-variant | SPAG16 | GRCh38.p7 | 2:214112041 | TGAGGCGATGGGGTT[G/T]TCTAAATATACAATC | 79582 |
rs113635309 | snp | A/C | 0.117188 | 0.211804 | intron-variant | SPAG16 | GRCh38.p7 | 2:214029685 | GCCCCAAAAACAAAT[A/C]TTACTCAAACTTAAC | 79582 |
rs113637538 | snp | A/G | 0.5 | 0 | intron-variant | SPAG16 | GRCh38.p7 | 2:214318926 | TATGAGCAACTAAAA[A/G]ATGCTACCCTTTTCC | 79582 |
rs113638522 | snp | C/T | 0.0275645 | 0.114116 | intron-variant | SPAG16 | GRCh38.p7 | 2:213494494 | TCCCACCATTAAATC[C/T]ACCAGAAAGTCTGAT | 79582 |
rs113639658 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | SPAG16 | GRCh38.p7 | 2:214137581 | TTTCTATATTTTTAA[A/G]CTTTTGTGATATACT | 79582 |
rs113639910 | snp | A/C | 0.00358779 | 0.0422022 | intron-variant | SPAG16 | GRCh38.p7 | 2:213518353 | GCTTACTGCAACCGC[A/C]AAGTCCTGGGCTCAA | 79582 |
rs113640454 | snp | A/T | 0.0329836 | 0.124112 | intron-variant | SPAG16 | GRCh38.p7 | 2:214007801 | TATATACTTAGGTGC[A/T]TTCTTTCTGTTGTTA | 79582 |
rs113641677 | in-del | -/CATCAGATA | 0.3744 | 0.216852 | intron-variant, downstream-variant-500B | SPAG16, LOC101928084 | GRCh38.p7 | 2:214088350 | CAGTTTGAAAGAGCT[-/CATCAGATA]CAGGTGAAAAAAACC | 79582 |
rs113651744 | in-del | -/TGTGGTAGCAGG | 0.479744 | 0.0985793 | intron-variant | SPAG16 | GRCh38.p7 | 2:213884130 | GCCTAAGTGTGTTTT[-/TGTGGTAGCAGG]TGTCATTCTTTTGAT | 79582 |
rs113652456 | snp | A/G | 8.44816e-05 | 0.00649874 | missense, nc-transcript-variant, utr-variant-5-prime | SPAG16 | GRCh38.p7 | 2:213340201 | AAATTCAGAAAGAAC[A/G]TGATTTTCATCGAAT | 79582 |
rs113657455 | snp | A/C | 0.00358779 | 0.0422022 | intron-variant | SPAG16 | GRCh38.p7 | 2:213536452 | TCCCACCAACAGTGT[A/C]AAAGTGTTCCTATTT | 79582 |
rs113658077 | snp | C/T | 0.00398564 | 0.0444627 | intron-variant | SPAG16 | GRCh38.p7 | 2:213552470 | GATTCTTTATTTTCT[C/T]AACTCTAGTTTTATA | 79582 |
rs113658558 | snp | C/T | 0.5 | 0 | intron-variant | SPAG16 | GRCh38.p7 | 2:213539003 | CTATAAAAATGCATT[C/T]TATTTCATTCAAACT | 79582 |
rs113660885 | snp | A/C | 0.5 | 0 | intron-variant | SPAG16 | GRCh38.p7 | 2:213292679 | AAAAAAAAAAAACAA[A/C]AAAAACAAAAAAAAA | 79582 |
rs113662230 | snp | A/C | 0.00517822 | 0.0506191 | intron-variant | SPAG16 | GRCh38.p7 | 2:213599373 | TGGCATTAAACTGCG[A/C]AGGTCCACTTATACT | 79582 |
rs113664896 | in-del | -/A | 0.00517822 | 0.0506191 | intron-variant | SPAG16 | GRCh38.p7 | 2:213584681 | GGGAGGAAGTGAGGG[-/A]AACTAGACAGAGTTA | 79582 |
rs113666242 | in-del | -/CA | 0.0283406 | 0.115616 | intron-variant | SPAG16 | GRCh38.p7 | 2:213520027 | ATATGCATGTGCGTG[-/CA]CACACACACACACAC | 79582 |
rs113667201 | snp | G/T | 0.0263992 | 0.111815 | intron-variant | SPAG16 | GRCh38.p7 | 2:214275483 | GTCCCAGAGATTCTG[G/T]TACATTGTGTCTTTG | 79582 |
rs113667638 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | SPAG16 | GRCh38.p7 | 2:214308296 | CACTGCATGTGAGAC[A/G]GATCTATTGAAGACA | 79582 |
rs113669627 | snp | C/T | 0.0475351 | 0.146656 | intron-variant | SPAG16 | GRCh38.p7 | 2:214371359 | CCAACATGGAGAAAT[C/T]CCATCTCTACTAAAA | 79582 |
rs113670874 | snp | C/T | 0.5 | 0 | intron-variant | SPAG16 | GRCh38.p7 | 2:213322795 | CAGGGAGCAGGGGAG[C/T]ACATCAGAAACCTGA | 79582 |
rs113672139 | snp | G/T | 0.00358779 | 0.0422022 | intron-variant | SPAG16 | GRCh38.p7 | 2:213507142 | TACCCTAAAGGTGGG[G/T]ATAAGTTTGAACTGA | 79582 |
rs113672725 | snp | A/G | | | intron-variant | SPAG16 | GRCh38.p7 | 2:213869277 | AAAATATATATATAT[A/G]TATGTATATATATAT | 79582 |
rs113673834 | snp | G/T | 0.00358779 | 0.0422022 | intron-variant | SPAG16 | GRCh38.p7 | 2:213531784 | TCTTTTTTACTAATT[G/T]TTCTGTAATTTTATT | 79582 |
rs113677791 | snp | A/T | | | intron-variant | SPAG16 | GRCh38.p7 | 2:213783441 | GTATCTATATCTATT[A/T]TTTTTTTTAAGAACA | 79582 |
rs113678825 | snp | G/T | 0.0209421 | 0.100162 | intron-variant | SPAG16 | GRCh38.p7 | 2:214030675 | TGTGTTCAGAGATGA[G/T]GAACTTACAGCAGAT | 79582 |
rs113682973 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | SPAG16 | GRCh38.p7 | 2:213874064 | GTAAAAATACAGTAT[A/G]AAAGATAAAAAGTGG | 79582 |
rs113684404 | snp | C/T | 0.00358779 | 0.0422022 | intron-variant | SPAG16 | GRCh38.p7 | 2:213547941 | TGTAGTATTACGTTG[C/T]ATAATATACCAAGAT | 79582 |
rs113684786 | snp | C/T | 0.0023933 | 0.0345097 | intron-variant | SPAG16 | GRCh38.p7 | 2:213351933 | CCCACGTGTCAAGGG[C/T]GGGACCAGGTGGAGG | 79582 |
rs113686984 | snp | A/C | 0.00755907 | 0.0610114 | intron-variant | SPAG16 | GRCh38.p7 | 2:213804689 | CTCCGTCTCAACTAA[A/C]TAACTAACTAACTAA | 79582 |
rs113687473 | snp | C/T | 0.00159617 | 0.0282053 | intron-variant | SPAG16 | GRCh38.p7 | 2:214328414 | GTGATCCACCCGCCT[C/T]GGCCTCCCAAAGTGT | 79582 |
rs113692357 | snp | C/G | 0.0456336 | 0.143994 | intron-variant | SPAG16 | GRCh38.p7 | 2:213447616 | AGAACATCGGGCGTT[C/G]CCACCGCCACTCCTC | 79582 |
rs113692489 | snp | A/T | 0.5 | 0 | intron-variant | SPAG16 | GRCh38.p7 | 2:213640537 | GGTCTAGCCACCCAG[A/T]GGGGCTACAGGGCTC | 79582 |
rs113694894 | snp | C/T | 0.132066 | 0.220435 | intron-variant | SPAG16 | GRCh38.p7 | 2:213625200 | AGATTGGGTAATTGA[C/T]AAAGAAAAGATGTTT | 79582 |
rs113697530 | snp | C/T | 0.00874735 | 0.0655527 | intron-variant | SPAG16 | GRCh38.p7 | 2:213670502 | TAAAGAAATCACTTA[C/T]TTGTGATTTTTTTTT | 79582 |
rs113700464 | snp | G/T | 0.0520825 | 0.152737 | intron-variant | SPAG16 | GRCh38.p7 | 2:213921365 | TGTTGTTGTTGTTGT[G/T]GTGGTGGTGGTTTAC | 79582 |
rs113701503 | snp | C/T | 0.5 | 0 | intron-variant | SPAG16 | GRCh38.p7 | 2:213939732 | GTGTCAGTTTGCTTT[C/T]TGTTTTAAGTAAGGA | 79582 |
rs113702010 | snp | A/G | | | intron-variant | SPAG16 | GRCh38.p7 | 2:213676125 | TAAGTTGGATTCCTA[A/G]GTATTTTATTCTCTT | 79582 |
rs113702878 | snp | G/T | | | intron-variant | SPAG16 | GRCh38.p7 | 2:213569898 | TAAACTATTGATTAT[G/T]GTCACAATTTCAGAG | 79582 |
rs113705128 | snp | C/G | 0.5 | 0 | intron-variant | SPAG16 | GRCh38.p7 | 2:213524979 | ATGGTTTGGCTGTTT[C/G]CCCACCCAAATCTCA | 79582 |
rs113706628 | snp | C/T | 0.00358779 | 0.0422022 | intron-variant | SPAG16 | GRCh38.p7 | 2:213541982 | ATCGTCTGTAAGTAC[C/T]ACAAAGTCAGAGTTA | 79582 |
rs113707447 | snp | C/T | 0.0444908 | 0.142359 | intron-variant | SPAG16 | GRCh38.p7 | 2:213555502 | ATGATTGAAAGTTTC[C/T]TGAAACTTCCTCAGC | 79582 |
rs113709002 | snp | C/G | 0.5 | 0 | intron-variant | SPAG16 | GRCh38.p7 | 2:213474123 | AAAAAAGTTTCATCA[C/G]AGTTTACAAACTCAG | 79582 |
rs113716800 | snp | A/T | 0.00398564 | 0.0444627 | intron-variant | SPAG16 | GRCh38.p7 | 2:213557612 | TAGTTTATACTTTTT[A/T]AATAAGTTTACATTA | 79582 |
rs113719573 | snp | C/T | 0.0209421 | 0.100162 | intron-variant | SPAG16 | GRCh38.p7 | 2:213839395 | AACATTTTTTTATGA[C/T]TTTTTCCATCTCTTC | 79582 |
rs113720931 | snp | C/G | 0.029116 | 0.117091 | intron-variant | SPAG16 | GRCh38.p7 | 2:213470357 | TGCTGTGTGGAATAA[C/G]ATGATGATGGATAAG | 79582 |
rs113723649 | in-del | -/G | 0.5 | 0 | intron-variant | SPAG16 | GRCh38.p7 | 2:213668499 | TTTTACAGATAGATT[-/G]AATTTTATTAAATAT | 79582 |
rs113725368 | snp | A/C | 0.0225045 | 0.103662 | intron-variant | SPAG16 | GRCh38.p7 | 2:213684896 | TGGGTTTAAGTCATA[A/C]TACAATGCAAAATTG | 79582 |
rs113726898 | snp | C/G | 0.0341408 | 0.126114 | intron-variant | SPAG16 | GRCh38.p7 | 2:213977443 | GGTTACTGCCCCCCC[C/G]ATACCCAATATCCTG | 79582 |
rs113727736 | snp | A/G | 0.00755907 | 0.0610114 | intron-variant | SPAG16 | GRCh38.p7 | 2:214113632 | TACTGAAGCTTGTGC[A/G]TGCATCATGTAGTTC | 79582 |
rs113732982 | snp | A/G | 0.0248432 | 0.108648 | intron-variant | SPAG16 | GRCh38.p7 | 2:214225187 | ATAGGATGACCAACA[A/G]GAGATGTGGACAAAA | 79582 |
rs113735254 | snp | A/G | 0.5 | 0 | intron-variant | SPAG16 | GRCh38.p7 | 2:214306913 | ATAGAATGAATTAGG[A/G]GGGAGTCCCTCCCCT | 79582 |
rs113736596 | in-del | -/T | 0 | 0 | intron-variant | SPAG16 | GRCh38.p7 | 2:213905625 | AAATAGCAGCAAATT[-/T]AAAAATTTCCTGCCC | 79582 |
rs113738979 | snp | A/G | 0.241914 | 0.249869 | intron-variant | SPAG16 | GRCh38.p7 | 2:213525087 | TACCTCCATGCTGCT[A/G]TTCTCATGATAGTGA | 79582 |
rs113740291 | snp | A/G | 0.00358779 | 0.0422022 | intron-variant | SPAG16 | GRCh38.p7 | 2:213553397 | AAGAAGAATGGTATA[A/G]GCTATCAGCATGGTT | 79582 |
rs113744093 | snp | A/G | 0.00478085 | 0.0486577 | intron-variant | SPAG16 | GRCh38.p7 | 2:213790170 | TTAATCATGAATTTT[A/G]TTATTAAGCATCACT | 79582 |
rs113746625 | snp | A/G | 0.0452528 | 0.143452 | intron-variant | SPAG16 | GRCh38.p7 | 2:214247035 | GTTTTAATTACACCA[A/G]GACACAACACTGCAT | 79582 |
rs113753566 | snp | A/T | 0.0729998 | 0.176553 | intron-variant | SPAG16 | GRCh38.p7 | 2:213425502 | TAAAAATACAAAAAA[A/T]TTAACTGGGTGTGGT | 79582 |
rs113753876 | snp | A/G | 0.0287284 | 0.116357 | intron-variant | SPAG16 | GRCh38.p7 | 2:214276196 | TGTGTGTCTCTGCCC[A/G]TGAGATGGGTCTCCT | 79582 |
rs113760879 | snp | C/T | 0.0919752 | 0.193722 | intron-variant | SPAG16 | GRCh38.p7 | 2:213658760 | AAAACAACACTAGGC[C/T]AGGCACTGTGGCTCA | 79582 |
rs113761807 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | SPAG16 | GRCh38.p7 | 2:213832620 | ATACCTAGGAGAGAG[G/T]AATCCTACACAGAGA | 79582 |
rs113761851 | in-del | -/T | 0.5 | 0 | intron-variant | SPAG16 | GRCh38.p7 | 2:213510388 | TTTAACTATTTAACA[-/T]TTTTTTTATTATTTT | 79582 |
rs113763213 | in-del | -/C | 0.0123036 | 0.0774623 | intron-variant | SPAG16 | GRCh38.p7 | 2:213430166 | AAACACACAGAACTT[-/C]TGGAAATGAAAAGTT | 79582 |
rs113765728 | snp | A/G | 0.0452528 | 0.143452 | intron-variant | SPAG16 | GRCh38.p7 | 2:213462968 | AGAAGAAGACACAAA[A/G]ATTTGGGAAAGTTTG | 79582 |
rs113771933 | snp | A/G | | | intron-variant | SPAG16 | GRCh38.p7 | 2:213540055 | TTTTTTTTTTTTTGA[A/G]ACGGAGTCTCGCTCT | 79582 |
rs113775429 | snp | A/T | 0.00358779 | 0.0422022 | intron-variant | SPAG16 | GRCh38.p7 | 2:213532628 | CACCATGTCCAGCTA[A/T]TTTTTTTTATTTTTA | 79582 |
rs113776150 | snp | C/T | 0 | 0 | intron-variant | SPAG16 | GRCh38.p7 | 2:214328167 | CTTTTTTTTTTTTTC[C/T]TTTTTTGAGATGGAG | 79582 |
rs113777883 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | SPAG16 | GRCh38.p7 | 2:213958470 | CCCCGCTTCTGGTAT[G/T]ATAAAATTAAACCTA | 79582 |
rs113782054 | snp | A/G | 0.0991586 | 0.199366 | intron-variant | SPAG16 | GRCh38.p7 | 2:214198998 | TTGTAGATTCTGGAT[A/G]GTGGCCCTTTGTCAG | 79582 |
rs113783271 | snp | A/C | 0.0452528 | 0.143452 | intron-variant | SPAG16 | GRCh38.p7 | 2:214249580 | ATTATTTTTATATGA[A/C]AAGTAAACACGATTG | 79582 |
rs113788134 | snp | G/T | 0.5 | 0 | intron-variant | SPAG16 | GRCh38.p7 | 2:214221596 | AGAGAAACTGCTAAA[G/T]AGTAAATATTTGTTT | 79582 |
rs113788360 | snp | C/T | 0.0402882 | 0.136092 | intron-variant | SPAG16 | GRCh38.p7 | 2:213688969 | TGACTTAAAATGTTC[C/T]CTTTTTTTGAGCCAG | 79582 |
rs113790834 | snp | C/T | 0.00358779 | 0.0422022 | intron-variant | SPAG16 | GRCh38.p7 | 2:213500904 | ATATCAGGAAAGGGA[C/T]AAGAAAGTTGAAACT | 79582 |
rs113792502 | snp | A/G | 0.5 | 0 | intron-variant | SPAG16 | GRCh38.p7 | 2:213527180 | TGGAGTCTAGATGCT[A/G]CTGATGTAAAGTTTC | 79582 |
rs113800520 | snp | A/T | 0.5 | 0 | intron-variant | SPAG16 | GRCh38.p7 | 2:214269550 | TGAGTTTTTTACTAA[A/T]TGCAATAAATTTAGT | 79582 |
rs113802023 | snp | A/G | 0 | 0 | intron-variant | SPAG16 | GRCh38.p7 | 2:213851935 | ACCTATAATTTCACA[A/G]TATTTAAAACTTAAA | 79582 |
rs113802078 | snp | A/G | 0.0494327 | 0.149241 | intron-variant | SPAG16 | GRCh38.p7 | 2:213775088 | AACTATTTTCTTCTA[A/G]CCGGCATTTATGACG | 79582 |
rs113805485 | snp | A/T | 0.5 | 0 | intron-variant | SPAG16 | GRCh38.p7 | 2:213607782 | GGTTTCATTTTATTT[A/T]TCCTGCAGATTGCAG | 79582 |
rs113807684 | snp | A/G | | | intron-variant | SPAG16 | GRCh38.p7 | 2:214149087 | TGTGTGTATATATAT[A/G]TATATATATACATAC | 79582 |
rs113809036 | snp | A/T | 0.5 | 0 | intron-variant | SPAG16 | GRCh38.p7 | 2:213577824 | ATGCTGAGACTTCTG[A/T]GATATTGAAAACCAT | 79582 |
rs113810898 | snp | A/G | 0.5 | 0 | intron-variant | SPAG16 | GRCh38.p7 | 2:213925056 | TACCATGCTGACTGA[A/G]TTTAGTAAAGCCTAA | 79582 |
rs113815383 | snp | C/T | | | intron-variant | SPAG16 | GRCh38.p7 | 2:213719031 | GCACCCTGTGTTTAG[C/T]TCAAGGTTTGTGAGT | 79582 |
rs113817291 | in-del | -/AG | 0.5 | 0 | intron-variant | SPAG16 | GRCh38.p7 | 2:214163654 | GAGAGAGAGAGAGAA[-/AG]AGAGAGAGAGGAAAA | 79582 |
rs113819347 | snp | C/T | 0.0858192 | 0.188533 | intron-variant | SPAG16 | GRCh38.p7 | 2:213701436 | TTGGCGCCTCCTCGG[C/T]CTCGGTGTCCACTCT | 79582 |
rs113820041 | snp | A/G | 0.0452528 | 0.143452 | intron-variant | SPAG16 | GRCh38.p7 | 2:213446452 | TGGAATGCAGTTCAA[A/G]CATTAATAACAGAAT | 79582 |
rs113820320 | in-del | -/T | 0.196149 | 0.244131 | intron-variant, utr-variant-5-prime | SPAG16 | GRCh38.p7 | 2:213301241 | CATGTACACACTTAA[-/T]TTTAGTTAGAGACCC | 79582 |
rs113820385 | snp | A/G | 0.5 | 0 | intron-variant | SPAG16 | GRCh38.p7 | 2:214171695 | AGTAAGACAAATTTT[A/G]TCTTTTTCCATAGAA | 79582 |
rs113823736 | snp | A/G | 0.00358779 | 0.0422022 | intron-variant | SPAG16 | GRCh38.p7 | 2:213664735 | AGAGAAACACTAAGA[A/G]ATTTCTATTATTACT | 79582 |
rs113824900 | snp | A/G | 0.5 | 0 | intron-variant | SPAG16 | GRCh38.p7 | 2:213702341 | CTTTTCATGCTGTGG[A/G]AGGTTTGTTCTTTCA | 79582 |
rs113828942 | snp | A/C | 0.5 | 0 | intron-variant | SPAG16 | GRCh38.p7 | 2:214307499 | TTGTTAACTTGAGAT[A/C]TTTCTTTCTAACTTT | 79582 |
rs113830121 | in-del | -/A | 0.5 | 0 | intron-variant | SPAG16 | GRCh38.p7 | 2:213615231 | ACCTACAGGAGTACC[-/A]AAATTGTTATTATGA | 79582 |
rs113831321 | snp | C/T | 0.00557542 | 0.0525036 | intron-variant | SPAG16 | GRCh38.p7 | 2:213665672 | ATAAATACATAACCT[C/T]GTTTTATGTGTGTTT | 79582 |
rs113831444 | in-del | -/C | 0 | 0 | intron-variant | SPAG16 | GRCh38.p7 | 2:213573191 | AATGCAGAAATCACC[-/C]GTCTTCTGCGTCGGT | 79582 |
rs113832339 | snp | A/C | | | intron-variant | SPAG16 | GRCh38.p7 | 2:213367249 | GCCGCAATAAACATA[A/C]TGTGTGCATGTGTCT | 79582 |
rs113834372 | snp | A/G | 0.5 | 0 | intron-variant | SPAG16 | GRCh38.p7 | 2:213749786 | TCATTTCTTTACTTA[A/G]GCTATAAATTTATTT | 79582 |
rs113841804 | snp | C/T | 0.5 | 0 | intron-variant | SPAG16 | GRCh38.p7 | 2:213289768 | ATTACAAAATGATTT[C/T]TGTCTATAGTAGCTT | 79582 |
rs113842736 | snp | A/G | 0.147991 | 0.228242 | intron-variant | SPAG16 | GRCh38.p7 | 2:214328360 | TAGAGATGGGGTTTC[A/G]CTCTGTTGGCCAGGT | 79582 |
rs113843394 | snp | G/T | 0 | 0 | intron-variant | SPAG16 | GRCh38.p7 | 2:213464874 | GTTTGCCATCCTCCA[G/T]TTGTAGCTGAAAGGT | 79582 |
rs113843915 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | SPAG16 | GRCh38.p7 | 2:213442550 | TAATTAAGACAGTGT[C/G]GTACTGGCAAAAGAA | 79582 |
rs113844258 | snp | A/G | 0.00993419 | 0.0697739 | intron-variant | SPAG16 | GRCh38.p7 | 2:213680926 | ATTTTCTGGTTTACA[A/G]TTGGCTGAGTTTATC | 79582 |
rs113846152 | snp | C/T | 0.00716266 | 0.059414 | intron-variant | SPAG16 | GRCh38.p7 | 2:213624804 | CTCAGGTTTTTGTTT[C/T]TTTTGAGATGGAGTC | 79582 |
rs113847509 | snp | A/G | 0.0452528 | 0.143452 | intron-variant | SPAG16 | GRCh38.p7 | 2:213465723 | CTCTGGCACCAGCTA[A/G]GCTACCGCTGCAACT | 79582 |
rs113847834 | snp | C/T | 0.021333 | 0.101051 | intron-variant | SPAG16 | GRCh38.p7 | 2:213478570 | CCTCTTCTCTACTCT[C/T]GAGGATGGTGATTCA | 79582 |
rs113849160 | snp | A/G | 0.5 | 0 | intron-variant | SPAG16 | GRCh38.p7 | 2:214161154 | TTTCTATGGCTGCAT[A/G]GTATTCCATGGTGGA | 79582 |
rs113852644 | snp | A/G | 8.26904e-05 | 0.00642949 | missense, nc-transcript-variant | SPAG16 | GRCh38.p7 | 2:214108239 | ACATGCATTCTATCA[A/G]TGATGCCATTTTTGA | 79582 |
rs113854257 | snp | A/G | 0.0287284 | 0.116357 | intron-variant | SPAG16 | GRCh38.p7 | 2:214005236 | ACCCATATTCTTTGC[A/G]AAAATGTTTCAGTTG | 79582 |
rs113855299 | snp | C/T | 0.5 | 0 | intron-variant | SPAG16 | GRCh38.p7 | 2:214253658 | GTTCTGTTCTATTGA[C/T]CTATATATCTGTTTT | 79582 |
rs113855571 | snp | C/T | 0.0193772 | 0.0965046 | intron-variant | SPAG16 | GRCh38.p7 | 2:214009880 | CCCAATAGCTGTCCT[C/T]GTAAGTCATAATAAA | 79582 |
rs113856209 | snp | A/T | 0.0652144 | 0.168387 | intron-variant | SPAG16 | GRCh38.p7 | 2:213726274 | GGCTATCTCTCAGGG[A/T]TGTGTCCTGCACTGC | 79582 |
rs113859920 | snp | C/T | 0.00358779 | 0.0422022 | intron-variant | SPAG16 | GRCh38.p7 | 2:213548908 | TTTATGATTGTATAT[C/T]TTATATTTTAATATA | 79582 |
rs113860143 | snp | A/G | 0.0652144 | 0.168387 | intron-variant | SPAG16 | GRCh38.p7 | 2:213761590 | ATTCAGGCTGGGCAC[A/G]GTGGCTCACGCCTGT | 79582 |
rs113868633 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | SPAG16 | GRCh38.p7 | 2:213943375 | AGTAAAGAAGAGAGC[C/T]AGAAAGGTCTCTTTC | 79582 |
rs113870216 | snp | C/G | 0.0260105 | 0.111035 | intron-variant | SPAG16 | GRCh38.p7 | 2:213833604 | ATATATATATAAAAT[C/G]TCCTTGACCTAACTT | 79582 |
rs113877385 | in-del | -/TT | 0 | 0 | intron-variant | SPAG16 | GRCh38.p7 | 2:213865924 | ACAGAAACTTATATT[-/TT]ATATATATATACTAT | 79582 |
rs113878664 | snp | C/T | 0.00478085 | 0.0486577 | intron-variant | SPAG16 | GRCh38.p7 | 2:213777095 | ACATTATACTATTTT[C/T]CCCTTTTTCATGTAT | 79582 |
rs113881474 | snp | C/G | 0.0217236 | 0.101931 | intron-variant | SPAG16 | GRCh38.p7 | 2:213448708 | AATATGGACATTTAT[C/G]AGTTCCCAAATAATA | 79582 |
rs113886134 | snp | A/T | 0.5 | 0 | intron-variant | SPAG16 | GRCh38.p7 | 2:214242754 | TCAAAGTTACCATAA[A/T]TTGAATACATAGGTC | 79582 |
rs113888051 | snp | C/G | | | intron-variant | SPAG16 | GRCh38.p7 | 2:213587190 | GAGGCAATTTTCTTT[C/G]TGGGCCCTACATTTC | 79582 |
rs113893966 | snp | G/T | 0 | 0 | intron-variant | SPAG16 | GRCh38.p7 | 2:213917237 | TTTGCTATTTTTTCT[G/T]AAGATTGCCTTAGCT | 79582 |
rs113894222 | snp | A/T | 0 | 0 | intron-variant | SPAG16 | GRCh38.p7 | 2:213780178 | GGTCTGGCCTCATCC[A/T]GCACTCCACCCTCCC | 79582 |
rs113895813 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | SPAG16 | GRCh38.p7 | 2:213306650 | GATGGGCAAGTCCCC[A/T]CTTGCTAGGGCTGGT | 79582 |
rs113898803 | snp | G/T | 0.5 | 0 | intron-variant | SPAG16 | GRCh38.p7 | 2:213529833 | AAATATTTTCTTTCT[G/T]TATATCCTTATTCTT | 79582 |
rs113905945 | snp | A/T | 0.00478085 | 0.0486577 | intron-variant | SPAG16 | GRCh38.p7 | 2:213640111 | TTTTTATTTATGATG[A/T]CTATTCTCTGGAGAT | 79582 |
rs113908395 | snp | G/T | 0.00597247 | 0.0543191 | intron-variant | SPAG16 | GRCh38.p7 | 2:213956474 | TTTTTTTGAGGCAGG[G/T]TCTCACTCTGTCACC | 79582 |
rs113915849 | snp | A/G | 0 | 0 | intron-variant | SPAG16 | GRCh38.p7 | 2:213974960 | CGTTAAAAAAAAAAA[A/G]AAAAACACAAAATGT | 79582 |
rs113917419 | snp | A/C | 0.00358779 | 0.0422022 | intron-variant | SPAG16 | GRCh38.p7 | 2:213702588 | AGTTCCGGACACAAT[A/C]ATATTTCATCTTTGT | 79582 |
rs113918445 | snp | G/T | 0.0232847 | 0.105357 | intron-variant | SPAG16 | GRCh38.p7 | 2:214397375 | ACGTTGGCCAGGATG[G/T]TCTCAATCTCCGGAC | 79582 |
rs113921362 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | SPAG16 | GRCh38.p7 | 2:214126873 | TGGTGTATAAAACAT[A/G]CATATATATTTTTAA | 79582 |
rs113922741 | snp | A/C | 0.00517822 | 0.0506191 | intron-variant | SPAG16 | GRCh38.p7 | 2:214123751 | CTGAGAGAATAAAGA[A/C]ATCCTAAAAGTTCTG | 79582 |
rs113926842 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | SPAG16 | GRCh38.p7 | 2:214393185 | CTAATCTCTTTTCTT[G/T]AAATTAGATTAAACA | 79582 |
rs113928539 | snp | C/G/T | 0.000399281 | 0.0141238 | intron-variant | SPAG16, LOC101928084 | GRCh38.p7 | 2:214101309 | TCACAACATGTGTGT[C/G/T]CTGCTTCAGTTCTAT | 79582 |
rs113930454 | snp | A/G | 0.00358779 | 0.0422022 | intron-variant | SPAG16 | GRCh38.p7 | 2:213635239 | ATGGGGTTTCACCAT[A/G]CTAGCCAGGATGGTC | 79582 |
rs113930613 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | SPAG16 | GRCh38.p7 | 2:213892915 | ATATTTTTCCAAACT[C/T]GTGTGGAGAAAACAC | 79582 |
rs113940091 | snp | C/G | 0.00358779 | 0.0422022 | intron-variant | SPAG16 | GRCh38.p7 | 2:213507806 | CTGTCTTCTTAGGTG[C/G]TCACCTGTGTGATTC | 79582 |
rs113942572 | in-del | -/AACTC | 0.0502198 | 0.150293 | intron-variant | SPAG16 | GRCh38.p7 | 2:213627661 | TCTAAAAAGAAAAGG[-/AACTC]AACAATTGACTGTTG | 79582 |
rs113947920 | snp | A/G | 0.5 | 0 | intron-variant | SPAG16 | GRCh38.p7 | 2:214138696 | TTGTACTAGACCTGA[A/G]CATCAGAAGGAAGAT | 79582 |
rs113957061 | snp | A/G | 0.00358779 | 0.0422022 | intron-variant | SPAG16 | GRCh38.p7 | 2:213520403 | CATCCTGGCTAACAC[A/G]GTGAAACCCCGTCTC | 79582 |
rs113957813 | snp | C/T | 0.0174175 | 0.0916809 | intron-variant | SPAG16 | GRCh38.p7 | 2:213492346 | ATCACTAGGTCAGAT[C/T]GAGACCATCCTGGCT | 79582 |
rs113958567 | snp | G/T | 0.17332 | 0.23795 | intron-variant | SPAG16 | GRCh38.p7 | 2:213537014 | CATGTCCTTTGTAGG[G/T]ACATGGATGAAATTG | 79582 |
rs113958649 | snp | A/G | | | intron-variant | SPAG16 | GRCh38.p7 | 2:213681676 | AGAAATTGAGGGCAT[A/G]GGTTTCCTCATCAAG | 79582 |
rs113964278 | snp | C/T | 0.00517822 | 0.0506191 | intron-variant | SPAG16 | GRCh38.p7 | 2:213614466 | TAAATTCTTTTTAAA[C/T]CAACCCTTGATGCCT | 79582 |
rs113966851 | in-del | -/G | 0 | 0 | intron-variant | SPAG16 | GRCh38.p7 | 2:213901621 | CCAAAGAAAACATGT[-/G]AAACTTGTACAGGAA | 79582 |
rs113967984 | snp | C/G | 0.00159617 | 0.0282053 | intron-variant | SPAG16 | GRCh38.p7 | 2:214323059 | GGAATTTATTCTGCA[C/G]TTTGTTGCTTATTCT | 79582 |
rs113968486 | snp | A/T | 0.5 | 0 | intron-variant | SPAG16 | GRCh38.p7 | 2:213982618 | AGTTTCTGGTGTGTG[A/T]GTGTGTGTGTGTGTG | 79582 |
rs113968596 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | SPAG16 | GRCh38.p7 | 2:213429129 | GAGAGAGGTGGGTCC[A/T]ATATTCGTTTGCCTA | 79582 |
rs113968829 | snp | A/C | 0.5 | 0 | intron-variant | SPAG16 | GRCh38.p7 | 2:214304267 | GGCCATAAACAAAAT[A/C]TCTGCAGCACTGTGA | 79582 |
rs113971710 | in-del | -/AT | 0.00279162 | 0.0372561 | intron-variant | SPAG16 | GRCh38.p7 | 2:213496716 | CATATATACATATCC[-/AT]ATATATATAATGCTT | 79582 |
rs113973847 | snp | A/G | 0.0225045 | 0.103662 | intron-variant | SPAG16 | GRCh38.p7 | 2:213357328 | TTAACCTTCTGTCTC[A/G]TTGATCTGTCTAATA | 79582 |
rs113973895 | in-del | -/T | 0.021333 | 0.101051 | intron-variant | SPAG16 | GRCh38.p7 | 2:213429700 | CTACTACAACCAACA[-/T]TTGAGAAAGCTACCA | 79582 |
rs113976104 | snp | A/G | 0.5 | 0 | intron-variant, downstream-variant-500B | SPAG16 | GRCh38.p7 | 2:214151308 | AATGAAGAAAGAGGT[A/G]AAAGTCACAAAGTTA | 79582 |
rs113981630 | snp | A/G | 0.021333 | 0.101051 | intron-variant | SPAG16 | GRCh38.p7 | 2:213489070 | ACAAAGCGAGACTCC[A/G]TCTCAAAAACGAAAA | 79582 |
rs113988703 | snp | C/T | 0 | 0 | intron-variant | SPAG16 | GRCh38.p7 | 2:213873741 | AATTTCTTTTTTGGC[C/T]GATTGGCTATTTTAA | 79582 |
rs113990271 | snp | A/G | 0 | 0 | intron-variant | SPAG16 | GRCh38.p7 | 2:213846425 | TTCATTGTAATGGAA[A/G]TAGCTTATTTTACTC | 79582 |
rs113990585 | snp | A/G | 0.029116 | 0.117091 | intron-variant | SPAG16 | GRCh38.p7 | 2:213561913 | TTTTGTTGTATTCCT[A/G]TCTGATGTGCAATGT | 79582 |
rs113993911 | snp | C/T | 0.0298908 | 0.118541 | intron-variant | SPAG16 | GRCh38.p7 | 2:213519034 | TTGAGCACACATAGA[C/T]GTAAACTTGGGAATA | 79582 |
rs113995258 | snp | C/T | 0.240478 | 0.249819 | intron-variant | SPAG16 | GRCh38.p7 | 2:214113565 | TCTTGCTTTATTTCA[C/T]TAATTTTATCTTCAA | 79582 |
rs113997557 | snp | C/T | 0.0333695 | 0.124785 | intron-variant | SPAG16 | GRCh38.p7 | 2:214139810 | ACTGTGGCTTACTTT[C/T]CAACCTGACTCTAGC | 79582 |
rs113998629 | snp | A/G | 0.0279526 | 0.114869 | intron-variant | SPAG16 | GRCh38.p7 | 2:214178971 | TCTTTTGACGTATGA[A/G]CATTTCTTTTGCAAA | 79582 |
rs114004450 | snp | G/T | 0.0209421 | 0.100162 | intron-variant | SPAG16 | GRCh38.p7 | 2:213733544 | CTTCATGAGAACATC[G/T]TGGGGATTCTGAAAG | 79582 |
rs114005634 | snp | A/G | 0.0150606 | 0.0854603 | intron-variant | SPAG16 | GRCh38.p7 | 2:213417492 | ACTCAGTGGCACATG[A/G]ATTTATGTAAATATT | 79582 |
rs114007778 | snp | A/C | 0.0174175 | 0.0916809 | intron-variant | SPAG16 | GRCh38.p7 | 2:214078369 | ACCAGCTTGGACAAC[A/C]TAGTGAAACCCCATA | 79582 |
rs114012695 | snp | C/T | 0.00318978 | 0.0398085 | intron-variant | SPAG16 | GRCh38.p7 | 2:213413333 | ATCAGGTTGCTGAAA[C/T]ATTAGTCTGAGGATA | 79582 |
rs114014228 | snp | C/G | 0.00398564 | 0.0444627 | intron-variant | SPAG16 | GRCh38.p7 | 2:213875431 | AGGGCTAAATGAGAA[C/G]GTCAACAGCATCAAG | 79582 |
rs114019680 | snp | A/G | 0.0433465 | 0.140692 | intron-variant | SPAG16 | GRCh38.p7 | 2:213338101 | CCAACCTAGAGTTTC[A/G]TATCTGGTCAAACTC | 79582 |
rs114021450 | snp | A/C | 0.0150606 | 0.0854603 | utr-variant-3-prime, intron-variant | SPAG16 | GRCh38.p7 | 2:213317875 | TGGGGAAGGCTGTGC[A/C]TGTGTGGGAGTAGGA | 79582 |
rs114025824 | snp | A/G | 0.0228947 | 0.104514 | intron-variant | SPAG16 | GRCh38.p7 | 2:213941164 | TCACTTACCTCTGAT[A/G]TCCTTCCACTGTATG | 79582 |
rs114035333 | snp | A/G | 0.0260105 | 0.111035 | intron-variant | SPAG16 | GRCh38.p7 | 2:213382547 | GGGCCATAAGGCCCA[A/G]GGAGAATTGTCTTAT | 79582 |
rs114037883 | snp | A/G | 0.0126979 | 0.078662 | intron-variant, upstream-variant-2KB | SPAG16, MIR4438 | GRCh38.p7 | 2:213757808 | TGTCATCCAAATATC[A/G]GCAATCTTTGCTCTG | 79582 |
rs114038533 | snp | A/T | 0.00478085 | 0.0486577 | intron-variant | SPAG16 | GRCh38.p7 | 2:214373817 | AGATTTTACTTTCTC[A/T]TAGCAACAGTATCAT | 79582 |
rs114043269 | snp | C/T | 0.00398564 | 0.0444627 | intron-variant | SPAG16 | GRCh38.p7 | 2:214023820 | TACACTGGCCAGTAG[C/T]GGGAAGACTAGATTT | 79582 |
rs114044342 | snp | A/T | 0.0452528 | 0.143452 | intron-variant | SPAG16 | GRCh38.p7 | 2:213963652 | AGACTGCTTTTGTTG[A/T]ATTGTTTATTTCTTC | 79582 |
rs114046099 | snp | A/T | 0.0130921 | 0.0798413 | intron-variant | SPAG16 | GRCh38.p7 | 2:213857393 | TTTAAGTTGAAGCCA[A/T]TGCTCATTGACCATG | 79582 |
rs114048866 | snp | A/G | 0.021333 | 0.101051 | intron-variant | SPAG16 | GRCh38.p7 | 2:214145401 | CATTGGTTTTTTCAT[A/G]ATACATTTTTCTTTA | 79582 |
rs114053932 | snp | A/G | 0.0185938 | 0.0946107 | intron-variant | SPAG16 | GRCh38.p7 | 2:213596811 | GACCTCTGAAATTAA[A/G]CACGTTGCCTTCAGT | 79582 |
rs114055217 | snp | A/G | 0.0189856 | 0.0955633 | intron-variant | SPAG16 | GRCh38.p7 | 2:213713410 | ACCACAGCAAAAGGA[A/G]GCTGGAAACAGTACT | 79582 |
rs114059306 | snp | C/T | 0.0425829 | 0.139564 | intron-variant | SPAG16 | GRCh38.p7 | 2:213311030 | TTTTATTTTTTGCTT[C/T]TTTTGGTTCTCATCT | 79582 |
rs114063212 | snp | C/T | 0.0441095 | 0.141807 | upstream-variant-2KB, intron-variant | SPAG16, LOC100130451 | GRCh38.p7 | 2:213283892 | ATCACAAGAAAGGAA[C/T]TGACAAAGCTGAACA | 79582 |
rs114067654 | snp | C/T | 0.00993419 | 0.0697739 | intron-variant | SPAG16 | GRCh38.p7 | 2:213453230 | TGAGAGGTCTGATAC[C/T]CTGTCTCTTTTTGTC | 79582 |
rs114070468 | snp | A/G | 0.046775 | 0.145601 | intron-variant | SPAG16 | GRCh38.p7 | 2:214161652 | GACACAGGGAGGGGA[A/G]TAACACACACTGGGG | 79582 |
rs114070819 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | SPAG16 | GRCh38.p7 | 2:213497093 | TTTACAGAATAATTT[A/G]AAATATTTTCTATAA | 79582 |
rs114072175 | snp | A/G | 0.0581099 | 0.160244 | intron-variant | SPAG16 | GRCh38.p7 | 2:214004121 | AAATGAGCAAAAAGG[A/G]CTGTGAGTATAATTT | 79582 |
rs114074340 | snp | A/G | 0.0818113 | 0.184966 | intron-variant | SPAG16 | GRCh38.p7 | 2:214130722 | GCCTATAAGACAAAG[A/G]TCTCATACATGAATA | 79582 |
rs114081054 | snp | A/G | 0.00993419 | 0.0697739 | intron-variant | SPAG16 | GRCh38.p7 | 2:214039896 | ATAGTTTGGGTGAGC[A/G]GTGGGGGTGGTTAGG | 79582 |
rs114083821 | snp | C/T | 0.0283406 | 0.115616 | intron-variant | SPAG16 | GRCh38.p7 | 2:214010779 | GGGGAAGGAGGGACG[C/T]TGAGTTTGAGCTTTG | 79582 |
rs114084339 | snp | C/G | 0.00993419 | 0.0697739 | intron-variant | SPAG16 | GRCh38.p7 | 2:213364693 | GAGCTGCAATGAGGA[C/G]TGGCTCAGTTTGTGA | 79582 |
rs114089206 | snp | C/T | 0.00557542 | 0.0525036 | intron-variant | SPAG16 | GRCh38.p7 | 2:214169512 | AATTGCTTTGAGCTC[C/T]GAGCACTTTGAAGAG | 79582 |
rs114090244 | snp | C/T | 0.0228947 | 0.104514 | intron-variant | SPAG16 | GRCh38.p7 | 2:213962820 | TGTATCCATTTAATC[C/T]AAGTTGTCTATCATA | 79582 |
rs114090458 | snp | C/T | 0.0722614 | 0.17581 | intron-variant | SPAG16 | GRCh38.p7 | 2:213330216 | AAGAGGGCCACTATC[C/T]GTTATACCCCAGAAT | 79582 |
rs114091572 | snp | G/T | 0.0839998 | 0.186933 | intron-variant | SPAG16 | GRCh38.p7 | 2:214106469 | AAATTTAAATTTATG[G/T]GGGGAAATTTTGCAC | 79582 |
rs114094212 | snp | A/G | 0.0256215 | 0.110247 | intron-variant | SPAG16 | GRCh38.p7 | 2:213334625 | GAGAACTGTTCAACC[A/G]TAAAAATGAATGAGA | 79582 |
rs114097671 | snp | A/C | 0.0240643 | 0.107019 | intron-variant | SPAG16 | GRCh38.p7 | 2:214401652 | TTATTATTTATAATA[A/C]GCTTAAAAGGTTTGA | 79582 |
rs114098392 | snp | A/C | 0.0126979 | 0.078662 | intron-variant, upstream-variant-2KB | SPAG16 | GRCh38.p7 | 2:213294624 | AATACTGACCTTTTG[A/C]CAGATACCTGGTATC | 79582 |
rs114100852 | snp | C/T | 0.0209421 | 0.100162 | intron-variant | SPAG16 | GRCh38.p7 | 2:213984505 | AGTAAAACAATTCCA[C/T]GCATGGTCCTTGTCT | 79582 |
rs114105345 | snp | A/G | 0.128632 | 0.218563 | intron-variant | SPAG16 | GRCh38.p7 | 2:213518902 | AGCCATAAAAAGAAC[A/G]AAATCATGTCCTTTG | 79582 |
rs114116085 | snp | C/T | 0.0178098 | 0.0926698 | intron-variant | SPAG16 | GRCh38.p7 | 2:214248921 | TGGGAGAAGACTGTT[C/T]TAAAAACTGGAACCA | 79582 |
rs114119107 | snp | A/G | 0.0414363 | 0.137845 | intron-variant | SPAG16 | GRCh38.p7 | 2:214269070 | GGGAAAAATTTGCAG[A/G]GTTTTAAAAATTTAA | 79582 |
rs114122278 | snp | C/T | 0.00953873 | 0.0683987 | intron-variant | SPAG16 | GRCh38.p7 | 2:213381558 | CGTAGTCTTCATCTT[C/T]AACACAAGGCTACAT | 79582 |
rs114123811 | snp | C/T | 0.0252325 | 0.109451 | intron-variant | SPAG16 | GRCh38.p7 | 2:214283006 | CACCTAACTCTGATA[C/T]TGACTCAGCATGAGA | 79582 |
rs114124903 | snp | A/G | 0.0154538 | 0.0865337 | intron-variant | SPAG16 | GRCh38.p7 | 2:213698771 | GGCACACTCATGTCC[A/G]ACTGCAGTGATTAAC | 79582 |
rs114125474 | snp | A/G | 0.0248432 | 0.108648 | intron-variant | SPAG16 | GRCh38.p7 | 2:214226011 | CGGTAGAAAGCCAAC[A/G]GTGGGACTTCAACCA | 79582 |
rs114126262 | snp | C/T | 0.0463947 | 0.145069 | intron-variant, upstream-variant-2KB | SPAG16 | GRCh38.p7 | 2:213342280 | TATATATATTACATA[C/T]ATATGTATATATATA | 79582 |
rs114134115 | snp | A/G | 0.0162398 | 0.0886349 | intron-variant | SPAG16 | GRCh38.p7 | 2:213982240 | AATGGAGGCTCCCAT[A/G]TGCCCATGTATTTGG | 79582 |
rs114135639 | snp | C/T | 0.00993419 | 0.0697739 | intron-variant | SPAG16 | GRCh38.p7 | 2:213634624 | TTATTATTTCGATAG[C/T]TTTAGGGGAACAGGT | 79582 |
rs114135655 | snp | A/C/G | 0.00587814 | 0.0538943 | intron-variant | SPAG16 | GRCh38.p7 | 2:213929933 | TTACTTTTTAAACAA[A/C/G]CTGTCTTTTTATGTT | 79582 |
rs114146954 | snp | A/G | 0.00597247 | 0.0543191 | intron-variant | SPAG16 | GRCh38.p7 | 2:213510787 | AAACATGTGTCATAT[A/G]GTAAATACTTAATGG | 79582 |
rs114147759 | snp | C/T | 0.0260105 | 0.111035 | intron-variant | SPAG16 | GRCh38.p7 | 2:213688930 | CTTTCCTCTCATTTT[C/T]TGAACATATGAAATT | 79582 |
rs114149249 | snp | A/G | 0.0023933 | 0.0345097 | intron-variant | SPAG16 | GRCh38.p7 | 2:213535864 | TGTAATAAATGTCAT[A/G]TGGATAGTTGAACAT | 79582 |
rs114155536 | snp | A/C | 0.00358779 | 0.0422022 | intron-variant | SPAG16 | GRCh38.p7 | 2:213791166 | AAATTTCTTTTAGAG[A/C]AAAACTAATATAGAA | 79582 |
rs114157603 | snp | A/G | 0.0991586 | 0.199366 | intron-variant | SPAG16 | GRCh38.p7 | 2:213947304 | GTGGTATTTTACACA[A/G]TGATTGGCAATAATG | 79582 |
rs114158834 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | SPAG16 | GRCh38.p7 | 2:213724968 | AGGCCAGTATGCACA[C/T]TCTCAATTTAAGGCA | 79582 |
rs114159122 | snp | C/G | 0.00636936 | 0.0560724 | intron-variant | SPAG16 | GRCh38.p7 | 2:213767574 | TGGAGGCTGCAGGGA[C/G]CTCTGATTACATTAC | 79582 |
rs114162277 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | SPAG16 | GRCh38.p7 | 2:213693404 | CCCTACCTCAGCACA[C/T]TGACGCTTCAGTTTT | 79582 |
rs114163050 | snp | C/G | 0.00478085 | 0.0486577 | intron-variant | SPAG16 | GRCh38.p7 | 2:213649209 | AATAATGAATTTTGT[C/G]ACACCTGACCTACTA | 79582 |
rs114165042 | snp | C/T | 0.0248432 | 0.108648 | intron-variant, downstream-variant-500B | SPAG16 | GRCh38.p7 | 2:213371728 | TTATTTAATCTAAAT[C/T]TAGGGAATAAGATGC | 79582 |
rs114165339 | snp | A/G | 0.0205511 | 0.0992634 | intron-variant | SPAG16 | GRCh38.p7 | 2:213820966 | AAAATATAAACAACT[A/G]TAAGAAATTCCTTTC | 79582 |
rs114174725 | snp | A/C | 0.00119737 | 0.0244387 | intron-variant | SPAG16 | GRCh38.p7 | 2:214050131 | CTTAGTGGGAAGAGG[A/C]GAGAAGTGAAGCCAT | 79582 |
rs114177813 | snp | C/T | 0.0154538 | 0.0865337 | intron-variant | SPAG16 | GRCh38.p7 | 2:213682833 | TTGGGGCTGGATTTA[C/T]GCGGTTTTTAATCAA | 79582 |
rs114179128 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | SPAG16 | GRCh38.p7 | 2:214235711 | ATTTACTTTTTACAT[A/C]TTCATGCCCATTGGC | 79582 |
rs114180024 | snp | A/G | 0.0399052 | 0.1355 | intron-variant | SPAG16 | GRCh38.p7 | 2:213579616 | CTAAATAAAGAAGGA[A/G]TAATTCTCATTTGTG | 79582 |
rs114185743 | snp | C/T | 0.0244538 | 0.107838 | intron-variant | SPAG16 | GRCh38.p7 | 2:213421174 | CAGGAAGCCACCCTG[C/T]CCCCACAGGCTTGGA | 79582 |
rs114187123 | snp | A/G | 0.095934 | 0.196885 | intron-variant | SPAG16 | GRCh38.p7 | 2:213944895 | AAAAATAAATTAGCC[A/G]GGCGTGGGGGCGTGC | 79582 |
rs114199830 | snp | C/T | 0.00279162 | 0.0372561 | intron-variant | SPAG16 | GRCh38.p7 | 2:213402420 | AATTTATTTATAGTT[C/T]TTTTTAAATTTTATT | 79582 |
rs114200909 | snp | C/T | 0.0111196 | 0.0737302 | intron-variant | SPAG16 | GRCh38.p7 | 2:214057821 | TTGCTGCAACTTCTA[C/T]ATCAGCACTGGCGCT | 79582 |
rs114206212 | snp | A/G | 0.0178098 | 0.0926698 | intron-variant | SPAG16 | GRCh38.p7 | 2:214279001 | TTGAACATGTACTTG[A/G]CTTCTGCTTCTATCT | 79582 |
rs114207387 | snp | A/G | 0.0119091 | 0.0762411 | intron-variant | SPAG16 | GRCh38.p7 | 2:213627212 | ATTGAAGAGTCTGCA[A/G]GTGCTATAAGATCCT | 79582 |
rs114208212 | snp | C/T | 0.00835141 | 0.0640778 | intron-variant | SPAG16 | GRCh38.p7 | 2:213593064 | GGGAAAAACTCAATC[C/T]GTATGTATATATATA | 79582 |
rs114215385 | snp | C/G | 0.0023933 | 0.0345097 | intron-variant | SPAG16 | GRCh38.p7 | 2:214303193 | GTTGCTTTGTAGTCT[C/G]AATTGTGTAACTGCT | 79582 |
rs114223940 | snp | C/T | 0.0178098 | 0.0926698 | intron-variant | SPAG16 | GRCh38.p7 | 2:214259679 | TTTTGTTTTCGTCTC[C/T]GGTTCCTTTGTGTAG | 79582 |
rs114226217 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | SPAG16 | GRCh38.p7 | 2:213544473 | TCTTATCAACATCCT[C/T]AACCAGAGAGGTATA | 79582 |
rs114228942 | snp | G/T | 0.0425829 | 0.139564 | intron-variant | SPAG16 | GRCh38.p7 | 2:213526252 | TTTTTAGTGTTCATA[G/T]AATACTCAATATTTA | 79582 |
rs114236831 | snp | C/T | 0.046775 | 0.145601 | intron-variant | SPAG16 | GRCh38.p7 | 2:213663821 | TGCATACAAAAACTT[C/T]AATGGAATAAGAAAA | 79582 |
rs114236932 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | SPAG16 | GRCh38.p7 | 2:214198188 | GAGATTTTGGTGCAC[C/T]GTCACCTGAGCAGTG | 79582 |
rs114242347 | snp | A/G | 0.00358779 | 0.0422022 | intron-variant | SPAG16 | GRCh38.p7 | 2:213811129 | ATAATTAAAATATAC[A/G]TTAATATTCAGTTTT | 79582 |
rs114250358 | snp | C/G | 0.00716266 | 0.059414 | intron-variant | SPAG16 | GRCh38.p7 | 2:213306584 | TTAGTACCCCAGAAC[C/G]CTTTAGCCCGTGGTG | 79582 |
rs114254712 | snp | A/T | 0.0267878 | 0.112589 | intron-variant | SPAG16 | GRCh38.p7 | 2:214226106 | TACTACTTCAAATTT[A/T]TTAGCTTAAAACATG | 79582 |
rs114258163 | snp | G/T | 0.0209421 | 0.100162 | intron-variant | SPAG16 | GRCh38.p7 | 2:213919389 | GTTAGGTTGATAAAT[G/T]GAGATCTTTCTAACT | 79582 |
rs114259171 | snp | A/G | 0.0023933 | 0.0345097 | intron-variant | SPAG16 | GRCh38.p7 | 2:213937412 | AAAGTAATGCTTAAA[A/G]TATAATTATGTTACA | 79582 |
rs114264817 | snp | C/T | 0.184838 | 0.241358 | intron-variant | SPAG16 | GRCh38.p7 | 2:213936031 | AAAAGGGATAGCAGG[C/T]ATTGGAAAGGGTTGC | 79582 |
rs114265484 | snp | C/T | 0.0267878 | 0.112589 | intron-variant | SPAG16 | GRCh38.p7 | 2:214227790 | TATTATTTTCTTCCC[C/T]TTAGACAAATCTCAG | 79582 |
rs114266860 | snp | C/T | 0.00438332 | 0.0466095 | intron-variant | SPAG16 | GRCh38.p7 | 2:213967879 | AGAACCATAGCACTA[C/T]TTTAAATGATAATGC | 79582 |
rs114269208 | snp | C/T | 0.0130921 | 0.0798413 | intron-variant | SPAG16 | GRCh38.p7 | 2:213976884 | AACCCAGCTGGCTGA[C/T]ACCTTCATTTCAGCC | 79582 |
rs114271475 | snp | G/T | 0.00358779 | 0.0422022 | intron-variant | SPAG16 | GRCh38.p7 | 2:213672410 | TTCCTTTCTCTTTCT[G/T]TCCAACATTGCCAAC | 79582 |
rs114272065 | snp | C/T | 0.0425829 | 0.139564 | intron-variant | SPAG16 | GRCh38.p7 | 2:213438587 | GAAGATGTTTACTAC[C/T]GTTCTAGGTAGAGTT | 79582 |
rs114272753 | snp | C/T | 0.0482946 | 0.147699 | intron-variant | SPAG16 | GRCh38.p7 | 2:213634118 | TCTTTCTTTCCTGTC[C/T]TCTTATAGTGAAGGT | 79582 |
rs114277203 | snp | C/G/T | 0.00954376 | 0.0684711 | intron-variant | SPAG16 | GRCh38.p7 | 2:213688864 | AATTCTATCACCAGA[C/G/T]ATTTTATTTGATCCT | 79582 |
rs114280709 | snp | A/G | 0.00318978 | 0.0398085 | intron-variant | SPAG16 | GRCh38.p7 | 2:213554890 | AGTTATAAGAGTTTA[A/G]GAAGGTGAGGAAAGA | 79582 |
rs114281046 | snp | C/G | 0.0115144 | 0.0749975 | intron-variant | SPAG16 | GRCh38.p7 | 2:214074589 | CAAAATCAAGAAATT[C/G]CATTCATTAACGCCA | 79582 |
rs114282538 | snp | A/G | 0.00398564 | 0.0444627 | intron-variant | SPAG16, LOC101928084 | GRCh38.p7 | 2:214089484 | GACTTTCCTTTAAAT[A/G]ATGCAGGTTTTCACA | 79582 |
rs114282726 | snp | A/G | 0.0170251 | 0.090679 | intron-variant | SPAG16 | GRCh38.p7 | 2:213767997 | AAGTGCTGCACTGGA[A/G]CAGCTCTTAACTCAG | 79582 |
rs114288318 | snp | G/T | 0.0150606 | 0.0854603 | intron-variant | SPAG16 | GRCh38.p7 | 2:214317245 | TTTGTGTCAACATAA[G/T]GCCAAGAATTTAAGT | 79582 |
rs114288717 | snp | A/G | 0.00874735 | 0.0655527 | intron-variant | SPAG16 | GRCh38.p7 | 2:214315290 | GTCAAATTTATAAAT[A/G]CTGTTATTTCTAAAT | 79582 |
rs114289278 | snp | G/T | 0.0422008 | 0.138995 | intron-variant | SPAG16 | GRCh38.p7 | 2:213660714 | TTGCTGGCTCCTTGC[G/T]TCAAGCACTCCCAGG | 79582 |
rs114293946 | snp | A/T | 0.0341408 | 0.126114 | intron-variant | SPAG16 | GRCh38.p7 | 2:214241667 | TAATTTTTCTATCAA[A/T]CTAAAACTGCTCTAA | 79582 |
rs114297568 | snp | A/G | 0.00398564 | 0.0444627 | intron-variant | SPAG16 | GRCh38.p7 | 2:214006102 | TCCCTTTGAAAACAC[A/G]GATAGATATTTTTTA | 79582 |
rs114298480 | snp | A/G | 0.0437281 | 0.141251 | intron-variant | SPAG16 | GRCh38.p7 | 2:214283139 | ATTATTAATAATTGC[A/G]GGGCCCACCAGTCTT | 79582 |
rs114299794 | snp | G/T | 0.0168055 | 0.0901129 | intron-variant | SPAG16 | GRCh38.p7 | 2:213287655 | AAGTTTACTGGCCAA[G/T]GAAAAAGGCTCCCCA | 79582 |
rs114300142 | snp | A/T | 0.0588605 | 0.161139 | intron-variant | SPAG16 | GRCh38.p7 | 2:213969296 | GATTATGGCTGGTTG[A/T]TACCTATGACTTACA | 79582 |
rs114300608 | snp | C/T | 0.0611083 | 0.163768 | intron-variant | SPAG16 | GRCh38.p7 | 2:213716321 | TGAAATGTTAAACAG[C/T]TGATGTACAAAATGA | 79582 |
rs114301210 | snp | A/T | 0.0244538 | 0.107838 | intron-variant | SPAG16 | GRCh38.p7 | 2:214237118 | TTTCAGGGACAGCAA[A/T]CACATAGCAAAAGGA | 79582 |
rs114302794 | snp | C/G | 0.0178098 | 0.0926698 | intron-variant | SPAG16 | GRCh38.p7 | 2:214286509 | CCCGGCACTTTGTGA[C/G]GCTAAGGTGGGCATA | 79582 |
rs114303758 | snp | C/T | 0.00636936 | 0.0560724 | intron-variant | SPAG16 | GRCh38.p7 | 2:214308303 | TGTGAGACGGATCTA[C/T]TGAAGACAGAATACC | 79582 |
rs114305969 | snp | A/G | 0.0566069 | 0.158427 | intron-variant | SPAG16 | GRCh38.p7 | 2:213999675 | AAGTCACAGACACTC[A/G]ATGCCAGCCCATGAA | 79582 |
rs114318936 | snp | C/T | 0.00438332 | 0.0466095 | intron-variant | SPAG16 | GRCh38.p7 | 2:214108946 | GTCGCAAACTTAATC[C/T]CCAATGCAAGAGTGT | 79582 |
rs114325145 | snp | A/G | 0.0248432 | 0.108648 | intron-variant | SPAG16 | GRCh38.p7 | 2:213386228 | TTGTGAATTTCTCCT[A/G]GGAGTGGGGCATGGG | 79582 |
rs114336066 | snp | A/G | 0.145305 | 0.227022 | intron-variant | SPAG16 | GRCh38.p7 | 2:213704981 | AAATAGGCTAGGCGC[A/G]TGGGCTTGCGCCTGT | 79582 |
rs114341277 | snp | A/G | 0.0966517 | 0.197444 | intron-variant | SPAG16 | GRCh38.p7 | 2:213966727 | TTTAGACCTTACACC[A/G]TGTTTAAACAAATTT | 79582 |
rs114341626 | snp | C/T | 0.0244538 | 0.107838 | intron-variant | SPAG16 | GRCh38.p7 | 2:214242854 | GATGCTAAATGTGAT[C/T]TATTAACTATCACTT | 79582 |
rs114342061 | snp | A/G | 0.0119091 | 0.0762411 | intron-variant | SPAG16 | GRCh38.p7 | 2:213485874 | AAAGAGGCCTAATAG[A/G]TAGCTTGGCTTCCCG | 79582 |
rs114342208 | snp | C/T | 0.02016 | 0.0983543 | intron-variant | SPAG16 | GRCh38.p7 | 2:213982221 | TTACAACAGTAATTT[C/T]AACAATGGAGGCTCC | 79582 |
rs114344148 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | SPAG16 | GRCh38.p7 | 2:214061624 | CCCACCTGCATTATG[A/G]AAGGTAATCTGCTTT | 79582 |
rs114344594 | snp | A/G | 0.0130921 | 0.0798413 | intron-variant | SPAG16 | GRCh38.p7 | 2:213489605 | GAATTGTAGACTTTC[A/G]ACTGCTGACACTACG | 79582 |
rs114345568 | snp | A/G | 0.00557542 | 0.0525036 | intron-variant | SPAG16 | GRCh38.p7 | 2:213584682 | GGAGGAAGTGAGGGA[A/G]ACTAGACAGAGTTAT | 79582 |
rs114349683 | snp | A/G | 0.0150606 | 0.0854603 | intron-variant | SPAG16 | GRCh38.p7 | 2:214292108 | ACAGGTTTCTGCTGA[A/G]CCCCAGTGTTAGTCT | 79582 |
rs114351575 | snp | A/G | 0.00318978 | 0.0398085 | intron-variant | SPAG16 | GRCh38.p7 | 2:213323167 | AACAATATGTCCGGC[A/G]CGGTGGCTTACGCCT | 79582 |
rs114354051 | snp | C/T | 0.0225045 | 0.103662 | intron-variant | SPAG16 | GRCh38.p7 | 2:213671609 | CAACTTCAACTATTG[C/T]TCTAAATAACTTAAT | 79582 |
rs114366120 | snp | C/G | 0.127599 | 0.217986 | intron-variant | SPAG16 | GRCh38.p7 | 2:213631445 | GAAGTGATATGGTTT[C/G]GCTCTGTGTCCCCAC | 79582 |
rs114370182 | snp | A/G | 0.00636936 | 0.0560724 | intron-variant | SPAG16 | GRCh38.p7 | 2:214015806 | GGGGGAGGGCCTTAG[A/G]ATTTTGCTTTTATTT | 79582 |
rs114376858 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | SPAG16 | GRCh38.p7 | 2:213313554 | TAAGTGGCAGAGTCA[A/T]CCTAGGACATACTGA | 79582 |
rs114380071 | snp | C/T | 0.0182019 | 0.0936463 | intron-variant | SPAG16 | GRCh38.p7 | 2:213881217 | AGTATTTCATTTTCT[C/T]TGTGGCTATTGTAAA | 79582 |
rs114380752 | snp | A/C | 0.0655868 | 0.168795 | intron-variant | SPAG16 | GRCh38.p7 | 2:213807972 | GCCTTGGTGCCAAAT[A/C]TTCTGCCCAAATGAA | 79582 |
rs114384939 | snp | C/G | 0.00636936 | 0.0560724 | intron-variant | SPAG16 | GRCh38.p7 | 2:213377678 | CCTCTTACTTTTTCC[C/G]TTACTTTTTCCCTAG | 79582 |
rs114385116 | snp | C/T | 0.067446 | 0.170804 | intron-variant | SPAG16 | GRCh38.p7 | 2:214198536 | GTTCCATATCTGAAA[C/T]TGTGAACTGTGCTGC | 79582 |
rs114393129 | snp | C/T | 0.0295035 | 0.117819 | intron-variant | SPAG16 | GRCh38.p7 | 2:213536286 | TATAGTGGGATTTCA[C/T]ATGGATCAACTTAAA | 79582 |
rs114393994 | snp | A/T | 0.00199481 | 0.0315187 | intron-variant | SPAG16 | GRCh38.p7 | 2:213849074 | TATTTTTCTCACAAT[A/T]CTGGATGGTTGGAAA | 79582 |
rs114395789 | snp | C/T | 0.00318978 | 0.0398085 | intron-variant | SPAG16 | GRCh38.p7 | 2:213565747 | AGAATCAACTAGTAA[C/T]AGCCCAGGCCTCAGA | 79582 |
rs114408005 | snp | A/T | 0.0228947 | 0.104514 | intron-variant | SPAG16 | GRCh38.p7 | 2:213940814 | ACAAACACACATAAA[A/T]TGTATATGCAATAAC | 79582 |
rs114408688 | snp | C/T | 0.0263992 | 0.111815 | intron-variant | SPAG16 | GRCh38.p7 | 2:213773219 | CAGTTTCTACGGAAT[C/T]CTGTTTTATAGATGA | 79582 |
rs114409830 | snp | A/G | 0.0165278 | 0.0893908 | intron-variant | SPAG16 | GRCh38.p7 | 2:213841455 | AAATTCTCTAACTTA[A/G]TAGAATGAGTAAAAG | 79582 |
rs114413768 | snp | G/T | 0.0341408 | 0.126114 | intron-variant | SPAG16 | GRCh38.p7 | 2:214216800 | TGGCATATTTAAAAT[G/T]TTCAATGTTCTGAAC | 79582 |
rs114421136 | snp | A/T | 0.0236746 | 0.106192 | intron-variant | SPAG16 | GRCh38.p7 | 2:213731081 | CTAGTTTTCCACTAG[A/T]GTCCTTAATATATTA | 79582 |
rs114425614 | snp | C/T | 0.00358779 | 0.0422022 | intron-variant | SPAG16 | GRCh38.p7 | 2:213842662 | GTGTAATATGTTCAT[C/T]TCCTTCTGCATATGA | 79582 |
rs114425798 | snp | C/T | 0.021333 | 0.101051 | intron-variant | SPAG16 | GRCh38.p7 | 2:213799943 | TACCCAAATGCCCAT[C/T]AGTGATAGACTGGAT | 79582 |
rs114431363 | snp | C/T | 0.0185938 | 0.0946107 | intron-variant | SPAG16 | GRCh38.p7 | 2:214299542 | ATGAGCCACCGTGCC[C/T]AGCCTATACTTCTGT | 79582 |
rs114431995 | snp | C/T | 0.00159617 | 0.0282053 | intron-variant, upstream-variant-2KB | SPAG16 | GRCh38.p7 | 2:213343549 | AAGCAGAACCAGACA[C/T]AGAGAAAAGAAAATT | 79582 |
rs114439159 | snp | C/T | 0.00517822 | 0.0506191 | intron-variant | SPAG16 | GRCh38.p7 | 2:214179149 | TAGCCTGTAGGAATT[C/T]GTTGCAATAGTATTT | 79582 |
rs114441153 | snp | G/T | 0.0119091 | 0.0762411 | intron-variant | SPAG16 | GRCh38.p7 | 2:213693715 | CTTTACATGAAGAGA[G/T]ACTTAAGTATATTTA | 79582 |
rs114445384 | snp | C/T | 0.0592355 | 0.161582 | intron-variant | SPAG16 | GRCh38.p7 | 2:213772319 | CCACCCTCAACATGC[C/T]AGATCTTGACTATCT | 79582 |
rs114448892 | snp | C/T | 0.0372196 | 0.131242 | intron-variant | SPAG16 | GRCh38.p7 | 2:214407901 | ATACTGTAAATGAAG[C/T]TGAACATGATTATAA | 79582 |
rs114449657 | snp | A/G | 0.00993419 | 0.0697739 | intron-variant | SPAG16 | GRCh38.p7 | 2:213681727 | CCTTCTGAAATATGC[A/G]TAGCAAAATACCCCA | 79582 |
rs114451263 | snp | A/C | 0.00438332 | 0.0466095 | intron-variant | SPAG16 | GRCh38.p7 | 2:213981199 | TGCTATAAGAATACA[A/C]ATCCTTTCAGATCAG | 79582 |
rs114451377 | snp | A/G | 0.0154538 | 0.0865337 | intron-variant | SPAG16 | GRCh38.p7 | 2:213454292 | TCATATCTTAAGAAA[A/G]CAGTGTATATTTCTT | 79582 |
rs114453300 | snp | A/C | 0.0217236 | 0.101931 | intron-variant | SPAG16 | GRCh38.p7 | 2:213994988 | TAAAGAAAAGATTTA[A/C]TTATGGTATTTATTA | 79582 |
rs114455892 | snp | A/C | 0.481473 | 0.0944461 | intron-variant | SPAG16 | GRCh38.p7 | 2:213516406 | TTTTATCTTTTTCTT[A/C]AAAAAATGAACTTAT | 79582 |
rs114458913 | snp | C/T | 0.0252325 | 0.109451 | intron-variant | SPAG16 | GRCh38.p7 | 2:213414679 | GACATACTGCTAATG[C/T]AAAACTTTAATCACT | 79582 |
rs114466334 | snp | A/G | 0.00636936 | 0.0560724 | intron-variant | SPAG16 | GRCh38.p7 | 2:213393812 | CAAATGAAATATGTC[A/G]CCTCACTAGGTCTTA | 79582 |
rs114467065 | snp | C/T | 0.00279162 | 0.0372561 | intron-variant | SPAG16 | GRCh38.p7 | 2:213856442 | CTCTTCTTACAGCTC[C/T]GTTAGGCAATGCCCC | 79582 |
rs114470107 | snp | A/G | 0.0248432 | 0.108648 | intron-variant | SPAG16 | GRCh38.p7 | 2:213393862 | CTAATTAAATTGAAC[A/G]TGTTCTTTTTCATAT | 79582 |
rs114472308 | snp | A/G | 0.0185938 | 0.0946107 | intron-variant | SPAG16 | GRCh38.p7 | 2:214183505 | GCTCTCAGCTTGTTC[A/G]AGTCAGGAAAAGGAG | 79582 |
rs114477900 | snp | A/G | 0.0221141 | 0.102801 | intron-variant | SPAG16 | GRCh38.p7 | 2:213483700 | GATGCCCTTGTCAGA[A/G]GCTTGCTTTTGGGAG | 79582 |
rs114479480 | snp | A/C | 0.00557542 | 0.0525036 | intron-variant | SPAG16 | GRCh38.p7 | 2:213380052 | TGTCCATCCACGTAC[A/C]TCTTTCCTGAATTTC | 79582 |
rs114481720 | snp | C/T | 0.0225045 | 0.103662 | intron-variant | SPAG16 | GRCh38.p7 | 2:213656815 | GTTTAATTTCAGGGA[C/T]TTGTACTTTAAATAT | 79582 |
rs114483329 | snp | C/T | 0.0418186 | 0.138422 | intron-variant | SPAG16 | GRCh38.p7 | 2:213499520 | CCTATAGTTCTATAG[C/T]CAGGTTTTTCAACAT | 79582 |
rs114485213 | snp | A/G | 0.0325976 | 0.123435 | intron-variant | SPAG16 | GRCh38.p7 | 2:213724010 | AAAGATAAACCACAG[A/G]CACATTGCTTTAACT | 79582 |
rs114489952 | snp | A/C | 0.029116 | 0.117091 | intron-variant | SPAG16 | GRCh38.p7 | 2:213926632 | AATATATATTTTTTT[A/C]AGATTTGCAGATTCA | 79582 |
rs114490530 | snp | C/T | 0.0103295 | 0.0711199 | intron-variant | SPAG16 | GRCh38.p7 | 2:213611185 | TTGTCCCTCCCACCT[C/T]AATAAATTTGTGTGC | 79582 |
rs114493105 | snp | A/T | 0.0150606 | 0.0854603 | intron-variant | SPAG16 | GRCh38.p7 | 2:214293931 | GGACATACAGTTGCC[A/T]CATATCTTAGTCCCA | 79582 |
rs114493713 | snp | C/T | 0.00358779 | 0.0422022 | intron-variant | SPAG16 | GRCh38.p7 | 2:213534447 | CAAAAATGTTAATTA[C/T]GTCTTTCTTCAAAAT | 79582 |
rs114497351 | snp | A/G | 0.0221141 | 0.102801 | intron-variant | SPAG16 | GRCh38.p7 | 2:213658343 | GCCCCTCTTTCCCCA[A/G]CTCATCCAACTAGAT | 79582 |
rs114497549 | snp | A/G | 0.0225045 | 0.103662 | intron-variant | SPAG16 | GRCh38.p7 | 2:213702658 | TACTTCCAATATACA[A/G]CTATCCGTAATCTAT | 79582 |
rs114498622 | snp | A/C | 0.00835141 | 0.0640778 | intron-variant | SPAG16 | GRCh38.p7 | 2:213698079 | CTTCTACCCTTTTCA[A/C]CCTCTTTGTTAATCA | 79582 |
rs114500475 | snp | G/T | 0.00557542 | 0.0525036 | intron-variant | SPAG16 | GRCh38.p7 | 2:214276656 | GAGTTTCTGCAGAGA[G/T]ATCTGCTGTTAGTCT | 79582 |
rs114503130 | snp | A/G | 0.00795532 | 0.062565 | intron-variant | SPAG16 | GRCh38.p7 | 2:213759656 | GAGAAAGAAATTTAA[A/G]CAAATCACTAAAGAA | 79582 |
rs114503698 | snp | G/T | 0.00478085 | 0.0486577 | intron-variant | SPAG16 | GRCh38.p7 | 2:214279667 | CAGAGTACTGATCAG[G/T]ACATGCATGTGAGGA | 79582 |
rs114505542 | snp | G/T | 0.0240643 | 0.107019 | intron-variant | SPAG16 | GRCh38.p7 | 2:213395476 | GTCTTCCTCTTTGAC[G/T]TATAGATTATTTAGA | 79582 |
rs114508061 | snp | C/T | 0.0513262 | 0.151752 | intron-variant | SPAG16 | GRCh38.p7 | 2:213679486 | ATTGTAATTTTGCCT[C/T]AACGTCCTTTTTTCA | 79582 |
rs114508474 | snp | A/G | 0.0182019 | 0.0936463 | intron-variant | SPAG16 | GRCh38.p7 | 2:213842689 | ATGAATTGTCCTTGG[A/G]TGTAAGTTTTCTGTA | 79582 |
rs114509242 | snp | C/T | 0.00835141 | 0.0640778 | intron-variant | SPAG16 | GRCh38.p7 | 2:213701308 | TACAGTCTGTAAGGA[C/T]GTAGGAGTCTCAAAA | 79582 |
rs114510500 | snp | C/T | 0.0170316 | 0.0907494 | intron-variant | SPAG16 | GRCh38.p7 | 2:213833070 | TTCTCTTTTTCATAT[C/T]GCTGTGTTCTTCCTT | 79582 |
rs114513902 | snp | A/C | 0.0566069 | 0.158427 | intron-variant | SPAG16 | GRCh38.p7 | 2:213992502 | TTAGGTTAATATATC[A/C]ATTTTTAAAATTATT | 79582 |
rs114514259 | snp | A/G | 0.0225045 | 0.103662 | intron-variant | SPAG16 | GRCh38.p7 | 2:214212031 | AGCCGTTGTCCAGAG[A/G]GCAAAATATACTTGT | 79582 |
rs114514538 | snp | A/G | 0.0228947 | 0.104514 | intron-variant | SPAG16 | GRCh38.p7 | 2:213996160 | GGGGGAAATCACCAG[A/G]AGTATAAATGCAAAT | 79582 |
rs114518548 | snp | A/G | 0.0221141 | 0.102801 | intron-variant, upstream-variant-2KB | SPAG16 | GRCh38.p7 | 2:213342131 | GAAATTTTGCCATCA[A/G]TATTTTCTTTAAAAT | 79582 |
rs114519138 | snp | C/G | 0.0452528 | 0.143452 | intron-variant | SPAG16 | GRCh38.p7 | 2:213471056 | TCAAAGTTCTGCCTA[C/G]TGGGAAGAATTCCCT | 79582 |
rs114519535 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant, upstream-variant-2KB | SPAG16 | GRCh38.p7 | 2:213316374 | CTGCTACCAACTTCT[G/T]TCAAGCCACCATGCT | 79582 |
rs114522107 | snp | A/G | 0.0174175 | 0.0916809 | intron-variant | SPAG16 | GRCh38.p7 | 2:214222486 | CAGCCACCTACACAA[A/G]CTCTTGTTAATCTTT | 79582 |
rs114527825 | snp | A/G | 0.00199481 | 0.0315187 | intron-variant | SPAG16 | GRCh38.p7 | 2:213423913 | TCCTGGGTGAAAACT[A/G]GTATTATCAGAGATA | 79582 |
rs114531629 | snp | A/G | 0.0205511 | 0.0992634 | intron-variant | SPAG16 | GRCh38.p7 | 2:213947673 | ATGATGAAAATTTGT[A/G]AGCAAAACTAAAACA | 79582 |
rs114533332 | snp | A/G | 0.0225045 | 0.103662 | intron-variant, downstream-variant-500B | SPAG16 | GRCh38.p7 | 2:213371731 | TTTAATCTAAATTTA[A/G]GGAATAAGATGCAAA | 79582 |
rs114535792 | snp | C/T | 0.00398564 | 0.0444627 | intron-variant | SPAG16 | GRCh38.p7 | 2:213357196 | TGGTCAATTTTAGAA[C/T]AAGCGCGATATGGTG | 79582 |
rs114538879 | snp | A/G | 0.0103295 | 0.0711199 | intron-variant | SPAG16 | GRCh38.p7 | 2:213431222 | ACCAGAAAGACAAAC[A/G]GAGGGGAAAAAAAAG | 79582 |
rs114539325 | snp | A/T | 0.00159617 | 0.0282053 | intron-variant | SPAG16 | GRCh38.p7 | 2:214268833 | TTCTAGATTTCTGCA[A/T]TAATACAGGCCATGC | 79582 |
rs114541411 | snp | A/C | 0.0023933 | 0.0345097 | intron-variant | SPAG16 | GRCh38.p7 | 2:214144955 | ACTTTCATAGAAAAA[A/C]TTATGTTACTATATA | 79582 |
rs114542126 | snp | A/G | 0.0429648 | 0.14013 | intron-variant | SPAG16 | GRCh38.p7 | 2:213416094 | GATGAGCAGGATGTC[A/G]CATACAGTGAGTTTG | 79582 |
rs114542779 | snp | C/T | 0.0228947 | 0.104514 | intron-variant | SPAG16 | GRCh38.p7 | 2:213701478 | AGGAGTCCTTCAGCC[C/T]GCTGCTGCACTGTGG | 79582 |
rs114545898 | snp | A/G | 0.0023933 | 0.0345097 | intron-variant | SPAG16 | GRCh38.p7 | 2:213441425 | GATCTATATATTTCA[A/G]AAATGGAAAACAAAA | 79582 |
rs114553466 | snp | A/G | 0.00874735 | 0.0655527 | intron-variant | SPAG16 | GRCh38.p7 | 2:213629202 | ACTTAGTATGTGACT[A/G]TTTTTGACTTGTCCC | 79582 |
rs114567002 | snp | A/G | 0.039522 | 0.134904 | intron-variant | SPAG16 | GRCh38.p7 | 2:213770928 | GCAGTGAACACATGC[A/G]TGCAAGTGTCTTTAT | 79582 |
rs114569365 | snp | C/T | 0.00914312 | 0.0669923 | intron-variant | SPAG16 | GRCh38.p7 | 2:213607613 | CTGAAATTAACTTAG[C/T]CATTGAGGACAAGGC | 79582 |
rs114571588 | snp | C/T | 0.0221141 | 0.102801 | intron-variant, utr-variant-3-prime | SPAG16 | GRCh38.p7 | 2:213399195 | GTGGTGGTTATACTA[C/T]TTGTGATTTTAAAGG | 79582 |
rs114574485 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | SPAG16 | GRCh38.p7 | 2:214264585 | TAACATTTTGCATTC[A/G]TATGGTACAATTGTT | 79582 |
rs114577931 | snp | A/G | 0.0298908 | 0.118541 | intron-variant | SPAG16 | GRCh38.p7 | 2:213760928 | TATAACTACCCCGCT[A/G]CTTCAATAATGACAG | 79582 |
rs114578734 | snp | G/T | 0.030665 | 0.119967 | intron-variant | SPAG16 | GRCh38.p7 | 2:213975262 | GTGCCTATAGAATAT[G/T]TACAACGTGAAAAAG | 79582 |
rs114582986 | snp | A/G | 0.0115144 | 0.0749975 | intron-variant | SPAG16 | GRCh38.p7 | 2:213496198 | TAAGTTGACAGTGAT[A/G]TAGAGGCTAATGAAT | 79582 |
rs114586252 | snp | A/G | 0.0154538 | 0.0865337 | intron-variant | SPAG16 | GRCh38.p7 | 2:213348962 | AATAGATCGTATACT[A/G]AGCCATAAAACAAGT | 79582 |
rs114587320 | snp | C/T | 0.00318978 | 0.0398085 | intron-variant | SPAG16 | GRCh38.p7 | 2:213541290 | ATGCAGAAATTAGGA[C/T]GCATAGAGTGAAAAC | 79582 |
rs114591977 | snp | A/G | 0.021333 | 0.101051 | intron-variant | SPAG16 | GRCh38.p7 | 2:213583922 | AGCAATAAATTACGA[A/G]CAACGTGAGTGCAGT | 79582 |
rs114593023 | snp | A/C | 0.0248432 | 0.108648 | intron-variant | SPAG16 | GRCh38.p7 | 2:213373062 | GCCTTAAAATGTTGA[A/C]TTTACCTAAGTAAAA | 79582 |
rs114598934 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | SPAG16 | GRCh38.p7 | 2:213945975 | GCAAATATAAATGTA[A/G]CATTGTTATATTTTT | 79582 |
rs114603739 | snp | A/G | 0.0165278 | 0.0893908 | intron-variant | SPAG16 | GRCh38.p7 | 2:213671235 | ATTTATAAATAAGTC[A/G]ATTTAAATAAAACAT | 79582 |
rs114609057 | snp | A/G | 0.0248432 | 0.108648 | intron-variant | SPAG16 | GRCh38.p7 | 2:214219191 | TATCAGGAATCTCCT[A/G]TTAAATCTGAATTTA | 79582 |
rs114613105 | snp | A/G | 0.00318978 | 0.0398085 | intron-variant | SPAG16 | GRCh38.p7 | 2:213715727 | GTATGGCTTTTTGAG[A/G]TTAATTTCTGCATGT | 79582 |
rs114619607 | snp | A/G | 0.0162398 | 0.0886349 | intron-variant | SPAG16 | GRCh38.p7 | 2:214247115 | GGCTACAGGCTGGGT[A/G]TGTATAGTCTACTCT | 79582 |
rs114619851 | snp | A/G | 0.0248432 | 0.108648 | intron-variant | SPAG16 | GRCh38.p7 | 2:214246680 | TCTAACTGCAGCCAC[A/G]GGAGAGACTTTAAGC | 79582 |
rs114624612 | snp | A/G | 0.0168055 | 0.0901129 | intron-variant, upstream-variant-2KB | SPAG16, MIR4438 | GRCh38.p7 | 2:213756647 | TTTCCAAACATGTTA[A/G]TATGGGATCTCTGGG | 79582 |
rs114634100 | snp | C/T | 0.0228947 | 0.104514 | intron-variant | SPAG16 | GRCh38.p7 | 2:213953988 | AGATAGATATAAATA[C/T]AATACACATACCACA | 79582 |
rs114634707 | snp | A/G | 0.131723 | 0.220251 | intron-variant | SPAG16 | GRCh38.p7 | 2:213617467 | CTGCCTCAGCCTCCC[A/G]ACTGGCTGGGATTAC | 79582 |
rs114636940 | snp | C/T | 0.0471551 | 0.14613 | intron-variant | SPAG16 | GRCh38.p7 | 2:213661452 | GTATTAAAGTATTTG[C/T]ATTTTTCTAATATGA | 79582 |
rs114637398 | snp | A/T | 0.0490535 | 0.14873 | intron-variant | SPAG16 | GRCh38.p7 | 2:214344677 | AATTTAAGATCACCA[A/T]TTCTATAAGGTATGT | 79582 |
rs114646790 | snp | C/T | 0.0777841 | 0.181223 | intron-variant | SPAG16 | GRCh38.p7 | 2:214124635 | AAACTTGATTATCCC[C/T]TTTAATGTAATTTTC | 79582 |
rs114651686 | snp | A/G | 0.0648419 | 0.167978 | intron-variant | SPAG16 | GRCh38.p7 | 2:214206411 | GTTTATTTCACTTAA[A/G]ATAATGTCCTCCAGG | 79582 |
rs114652710 | snp | C/T | 0.0158469 | 0.0875917 | intron-variant | SPAG16 | GRCh38.p7 | 2:214311166 | GCATTTCCTCTGTTC[C/T]GAGGAGCGCTTTGGC | 79582 |
rs114655555 | snp | A/C | 0.00398564 | 0.0444627 | intron-variant | SPAG16 | GRCh38.p7 | 2:214248934 | TTCTAAAAACTGGAA[A/C]CACAGCAGATAAAAG | 79582 |
rs114658141 | snp | C/T | 0.0209421 | 0.100162 | intron-variant | SPAG16 | GRCh38.p7 | 2:213877378 | GTGGTGGTGTGATCT[C/T]GGCTCACTACAGCCT | 79582 |
rs114661288 | snp | C/G | 0.0123036 | 0.0774623 | intron-variant | SPAG16 | GRCh38.p7 | 2:214263742 | CAGGATGACTTCTCT[C/G]AATGATTTTTAACTC | 79582 |
rs114665651 | snp | G/T | 0.0154538 | 0.0865337 | intron-variant | SPAG16 | GRCh38.p7 | 2:214307218 | TTGTATTTCTGTGGG[G/T]TCAATGGTAATATCC | 79582 |
rs114668188 | snp | C/T | 0.0217236 | 0.101931 | intron-variant | SPAG16 | GRCh38.p7 | 2:213887762 | ATTTCCAGCTGCCAA[C/T]ATGTAAAGAAACAAT | 79582 |
rs114668915 | snp | A/G | 0.0244538 | 0.107838 | intron-variant, utr-variant-3-prime | SPAG16 | GRCh38.p7 | 2:213369049 | ATAGGAAATACTGGA[A/G]GCTAGAAACAATAAA | 79582 |
rs114669917 | snp | C/T | 0.0410537 | 0.137264 | intron-variant | SPAG16 | GRCh38.p7 | 2:214244973 | ATGCTTTCTTAACTA[C/T]ATTTCCAAACCTTTT | 79582 |
rs114677168 | snp | A/G | 0.0142736 | 0.0832652 | intron-variant | SPAG16 | GRCh38.p7 | 2:214114543 | AGGCTGAAGCCTCAC[A/G]GTTGGATCTCAGACT | 79582 |
rs114677852 | snp | A/G | 0.146918 | 0.227759 | intron-variant | SPAG16 | GRCh38.p7 | 2:213361380 | TGTGTGTGTGTGTGT[A/G]TATATATATATATGT | 79582 |
rs114678446 | snp | A/T | 0.0287284 | 0.116357 | intron-variant | SPAG16 | GRCh38.p7 | 2:213338336 | TAACCAGCTAGCATC[A/T]TAGTGACAGGATCAA | 79582 |
rs114681706 | snp | A/G | 0.00279162 | 0.0372561 | intron-variant | SPAG16 | GRCh38.p7 | 2:213913689 | TGGATATATATGCAT[A/G]CACATACATGTGTGT | 79582 |
rs114681977 | snp | C/T | 0.021333 | 0.101051 | intron-variant | SPAG16 | GRCh38.p7 | 2:213931932 | TAGTGGCTATTGATA[C/T]ACCTTTCAGAGTCAC | 79582 |
rs114682635 | snp | C/T | 0.0341408 | 0.126114 | intron-variant | SPAG16 | GRCh38.p7 | 2:213976275 | ACACATATACATATG[C/T]GTACACATGTGTGCA | 79582 |
rs114690580 | snp | C/T | 0.0221141 | 0.102801 | intron-variant | SPAG16 | GRCh38.p7 | 2:213813971 | GAAAAGCAGCAGTCA[C/T]AAGCCTGAGACACAG | 79582 |
rs114692070 | snp | A/G | 0.00358779 | 0.0422022 | intron-variant | SPAG16 | GRCh38.p7 | 2:213421296 | CCCAGCCAGGTGTGC[A/G]TGTGCTTGGGGTGGT | 79582 |
rs114696560 | snp | A/G | 0.0217236 | 0.101931 | intron-variant | SPAG16 | GRCh38.p7 | 2:213505722 | TACTTCACTTTTCAA[A/G]TACCAAAACAGATAA | 79582 |
rs114702482 | snp | C/T | 0.0225045 | 0.103662 | intron-variant | SPAG16 | GRCh38.p7 | 2:213876250 | AAACTTCAAGGATAG[C/T]TAATTGGCTAATACA | 79582 |
rs114707042 | snp | C/T | 0.0178098 | 0.0926698 | intron-variant | SPAG16 | GRCh38.p7 | 2:214265457 | TAATTGAGTTATTTA[C/T]TTTCTTATGATTGAG | 79582 |
rs114717623 | snp | A/C | 0.00358779 | 0.0422022 | intron-variant | SPAG16 | GRCh38.p7 | 2:213511926 | CACTCACAATACTTT[A/C]GTTTTGAGCTTTGTT | 79582 |
rs114720107 | snp | A/G | 0.00438332 | 0.0466095 | intron-variant | SPAG16 | GRCh38.p7 | 2:213999300 | CTCCAGCCATGGCTG[A/G]AAGGGTCCAATGTAG | 79582 |
rs114724238 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | SPAG16 | GRCh38.p7 | 2:214377378 | TGAATTGCTTGATAT[G/T]TACCATAGATGGAGG | 79582 |
rs114725302 | snp | C/T | 0.00795532 | 0.062565 | intron-variant | SPAG16 | GRCh38.p7 | 2:213601264 | GGATCTGAACTTTAA[C/T]CAGAAAAGGGAATTT | 79582 |
rs114728663 | snp | C/T | 0.0221141 | 0.102801 | intron-variant | SPAG16 | GRCh38.p7 | 2:213437741 | GCTAAAAACAAAATG[C/T]AATAAACTTAATTTA | 79582 |
rs114728959 | snp | G/T | 0.00199481 | 0.0315187 | intron-variant | SPAG16 | GRCh38.p7 | 2:213559515 | TCTAACTTACCTACA[G/T]ATTTAATCAAACCAC | 79582 |
rs114733351 | snp | A/G | 0.00318978 | 0.0398085 | intron-variant | SPAG16 | GRCh38.p7 | 2:213722616 | CTGCTAAGGATGGTA[A/G]TAAGAAGGAATTTCA | 79582 |
rs114734309 | snp | C/T | 0.00398564 | 0.0444627 | intron-variant | SPAG16 | GRCh38.p7 | 2:214164001 | TGTTTGACCAAATAC[C/T]GGGTACCATATGTAC | 79582 |
rs114740041 | snp | A/G | 0.0146672 | 0.084371 | intron-variant | SPAG16 | GRCh38.p7 | 2:214111914 | GCTCATTCATGATTT[A/G]GTTTCCTGTTTGTCT | 79582 |
rs114743036 | snp | A/T | 0.00676609 | 0.0577691 | intron-variant | SPAG16 | GRCh38.p7 | 2:213446653 | ACACAAAATTATTCT[A/T]ATCGGGCTTATGTGC | 79582 |
rs114746380 | snp | A/T | 0.0142736 | 0.0832652 | intron-variant | SPAG16 | GRCh38.p7 | 2:214361959 | GGCAATAGGCCTTTC[A/T]TCTTTAGAACTGAAG | 79582 |
rs114746422 | snp | C/T | 0.0456336 | 0.143994 | intron-variant | SPAG16 | GRCh38.p7 | 2:214009423 | TATATTCCTGTGCTA[C/T]GTTTAGTTCAATGCC | 79582 |
rs114747807 | snp | C/T | 0.0178098 | 0.0926698 | intron-variant | SPAG16 | GRCh38.p7 | 2:214248612 | GTGAGCCACCATGCC[C/T]GGCCGTGCTAGGCAC | 79582 |
rs114749246 | snp | A/C | 0.00914312 | 0.0669923 | intron-variant | SPAG16 | GRCh38.p7 | 2:213955555 | TACATGTCTATCCTT[A/C]TAATAGTACCACACT | 79582 |
rs114750440 | snp | A/G | 0.0287284 | 0.116357 | intron-variant | SPAG16 | GRCh38.p7 | 2:213874941 | ATTCCTGTCATCCTT[A/G]TAGAAATATTATTTT | 79582 |
rs114752089 | snp | A/G | 0.0349115 | 0.127424 | intron-variant | SPAG16 | GRCh38.p7 | 2:213895163 | CAAGAATTCAATTCC[A/G]TTAACAATAGCTACA | 79582 |
rs114756201 | snp | C/T | 0.0244538 | 0.107838 | intron-variant | SPAG16 | GRCh38.p7 | 2:213428309 | CAGGCTGTGAGAGAA[C/T]ACCTTGCCCTTCCCA | 79582 |
rs114758855 | snp | A/T | 0.02016 | 0.0983543 | intron-variant | SPAG16 | GRCh38.p7 | 2:213452728 | TGAATCTTGCAACAA[A/T]CCCCCTTGTCTCTTT | 79582 |
rs114758908 | snp | A/G | 0.0240643 | 0.107019 | intron-variant | SPAG16 | GRCh38.p7 | 2:213561613 | AAATTTTGCTCCCTG[A/G]AGTGGTATATGCACA | 79582 |
rs114761228 | snp | A/G | 0.00557542 | 0.0525036 | intron-variant | SPAG16 | GRCh38.p7 | 2:214257679 | CTTTTGTAAAACAGC[A/G]AAGATAAACAACATT | 79582 |
rs114780020 | snp | A/G | 0.0103295 | 0.0711199 | intron-variant | SPAG16 | GRCh38.p7 | 2:213673857 | CACTTTAACGGACAT[A/G]CTCATTCCATTTCTA | 79582 |
rs114780125 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | SPAG16 | GRCh38.p7 | 2:213616532 | GTAAATCATAGAAGG[A/G]GGGTGTCAGGATGGG | 79582 |
rs114790536 | snp | C/G | 0.0225045 | 0.103662 | intron-variant | SPAG16 | GRCh38.p7 | 2:213950734 | TTTTTCCCTCAAGAC[C/G]GTCTTGCTCTGTCGC | 79582 |
rs114791133 | snp | G/T | 0.00318978 | 0.0398085 | intron-variant | SPAG16 | GRCh38.p7 | 2:213935505 | TATCGCAATGCTGTT[G/T]GAGTCCATGAAATCC | 79582 |
rs114793158 | snp | C/T | 0.0410537 | 0.137264 | intron-variant | SPAG16 | GRCh38.p7 | 2:213849292 | ACCGTGAGAATGGCA[C/T]CACGACATCCATGAA | 79582 |
rs114796743 | snp | A/C/G | 0.00795532 | 0.062565 | intron-variant | SPAG16 | GRCh38.p7 | 2:213547108 | TATCATTTACTTTTT[A/C/G]TATTTAAGTAATAAC | 79582 |
rs114805985 | snp | G/T | 0.0126979 | 0.078662 | intron-variant | SPAG16 | GRCh38.p7 | 2:213882286 | GGATACTGACCCAAA[G/T]ATCCTTTTTTTATTT | 79582 |
rs114806234 | snp | A/G | 0.021333 | 0.101051 | intron-variant | SPAG16 | GRCh38.p7 | 2:213986329 | TTTTTCCCACCGTTT[A/G]TTTCAGTTTTTTTCT | 79582 |
rs114806342 | snp | A/G | 0.0295035 | 0.117819 | intron-variant | SPAG16 | GRCh38.p7 | 2:213337331 | CTCCAAATGATTGCA[A/G]CATGTCTCCAGCAAA | 79582 |
rs114806980 | snp | A/T | 0.0425829 | 0.139564 | intron-variant | SPAG16 | GRCh38.p7 | 2:213514472 | ATTTTGTCGGCATAT[A/T]TTTTTTTATTATACT | 79582 |
rs114809702 | snp | C/T | 0.00517822 | 0.0506191 | intron-variant | SPAG16 | GRCh38.p7 | 2:213489538 | ATGTTAACTTTGTTA[C/T]CCAATGAAAGTGTTT | 79582 |
rs114810158 | snp | C/T | 0.0260105 | 0.111035 | intron-variant | SPAG16 | GRCh38.p7 | 2:213557492 | AAGAATAGAGTATTC[C/T]GAAAACGTTTTAAAT | 79582 |
rs114812490 | snp | A/G | 0.0244538 | 0.107838 | intron-variant | SPAG16 | GRCh38.p7 | 2:214239773 | ACCCAGAATCCTGGA[A/G]AGGAAAGTTGCTATT | 79582 |
rs114819533 | snp | A/G | 0.0256215 | 0.110247 | intron-variant | SPAG16 | GRCh38.p7 | 2:213375624 | GTATTAAAAATGGTT[A/G]GTCAAAGAGATCAAA | 79582 |
rs114820240 | snp | C/T | 0.00795532 | 0.062565 | intron-variant | SPAG16 | GRCh38.p7 | 2:213638811 | TGTTAACTTTCTGTC[C/T]TGATGACCTGTCTAG | 79582 |
rs114820312 | snp | A/G | 0.0244538 | 0.107838 | intron-variant | SPAG16 | GRCh38.p7 | 2:213461836 | TGAGGAATGAGAAAA[A/G]ATACAGATGGTTATG | 79582 |
rs114831704 | snp | A/G | 0.0158469 | 0.0875917 | intron-variant | SPAG16 | GRCh38.p7 | 2:213849897 | TTATTATTGAAATGG[A/G]TTTCTTTAGAACATA | 79582 |
rs114837033 | snp | C/T | 0.0146672 | 0.084371 | intron-variant | SPAG16 | GRCh38.p7 | 2:214076989 | GAAATGAACCCAGGC[C/T]GCCTGGAGGAGTGTG | 79582 |
rs114837427 | snp | C/T | 0.0314385 | 0.121371 | intron-variant | SPAG16 | GRCh38.p7 | 2:213580953 | TGTAATTAAGTAAGC[C/T]TATATTTTGTTTATG | 79582 |
rs114838247 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | SPAG16 | GRCh38.p7 | 2:213443111 | ATAGTAAAATGATTA[C/T]TACAGTAAAGAATTT | 79582 |
rs114842477 | snp | C/T | 0.0134861 | 0.0810011 | intron-variant | SPAG16 | GRCh38.p7 | 2:213491394 | AACTTCAGATGATCT[C/T]CCCACCTTTTTGTAA | 79582 |
rs114842599 | snp | G/T | 0.0185938 | 0.0946107 | intron-variant | SPAG16 | GRCh38.p7 | 2:213666027 | TAGTTAGAAACATGT[G/T]GGTTGGGCGTGAAAG | 79582 |
rs114849248 | snp | C/T | 0.0178098 | 0.0926698 | intron-variant | SPAG16 | GRCh38.p7 | 2:214256923 | TTTTTTGCATTTCCA[C/T]ATAAATTTTAACATC | 79582 |
rs114849510 | snp | A/G | 0.0217236 | 0.101931 | intron-variant | SPAG16 | GRCh38.p7 | 2:213624814 | TGTTTTTTTTGAGAT[A/G]GAGTCTTGATCTGTT | 79582 |
rs114851300 | snp | C/T | 0.0185938 | 0.0946107 | intron-variant | SPAG16 | GRCh38.p7 | 2:214301284 | CATGATAAAAACCCT[C/T]AAAATCTAGGCATCA | 79582 |
rs114861066 | snp | A/G | 0.0146672 | 0.084371 | intron-variant | SPAG16 | GRCh38.p7 | 2:214049797 | ACTAGGCCAACCTGA[A/G]ATTAATTTTTGAAGG | 79582 |
rs114861344 | snp | G/T | 0.0178098 | 0.0926698 | intron-variant | SPAG16 | GRCh38.p7 | 2:214227202 | TTTGTGGTCAAATAA[G/T]AGTGATTATGGAAAT | 79582 |
rs114863634 | snp | C/G | 0.0154538 | 0.0865337 | intron-variant | SPAG16 | GRCh38.p7 | 2:213490910 | TAATGACTCAGAAGA[C/G]ACATTAACCACTCTT | 79582 |
rs114864938 | snp | A/T | 0.0205511 | 0.0992634 | intron-variant | SPAG16 | GRCh38.p7 | 2:214178895 | TATATAGTTTATTAT[A/T]TATAGCGTGTAAATA | 79582 |
rs114864999 | snp | A/G | 0.0441095 | 0.141807 | intron-variant | SPAG16 | GRCh38.p7 | 2:213552053 | GTCTTCATATCAGTT[A/G]TTTGTAAGAAATAGG | 79582 |
rs114866085 | snp | C/T | 0.00676609 | 0.0577691 | intron-variant | SPAG16 | GRCh38.p7 | 2:214037600 | TGATTGATCTTATAT[C/T]AATTCTGATATATTA | 79582 |
rs114872032 | snp | C/T | 0.0130921 | 0.0798413 | intron-variant | SPAG16 | GRCh38.p7 | 2:213866465 | AATAAATTATACTTA[C/T]AGATATTGGAAGTTA | 79582 |
rs114875755 | snp | A/C | 0.0883596 | 0.190715 | intron-variant | SPAG16 | GRCh38.p7 | 2:214062648 | GTTGGCACCACCGCA[A/C]CTGTTGTAATAGCCT | 79582 |
rs114876582 | snp | A/G | 0.077417 | 0.180873 | intron-variant | SPAG16 | GRCh38.p7 | 2:214010889 | AAAAAGAAAGTGGGA[A/G]GAACATAAATACGTT | 79582 |
rs114883052 | snp | A/C | 0.0372196 | 0.131242 | intron-variant | SPAG16 | GRCh38.p7 | 2:213858985 | AAAGTTTGAGACCAG[A/C]CTGATAAACATGGTG | 79582 |
rs114883076 | snp | C/G | 0.00159617 | 0.0282053 | intron-variant | SPAG16 | GRCh38.p7 | 2:213309271 | TACATAATATGTAAA[C/G]AAATGGGCATGGGCA | 79582 |
rs114886211 | snp | A/G | 0.00159617 | 0.0282053 | intron-variant | SPAG16 | GRCh38.p7 | 2:213584360 | CAGTGGAAATATATG[A/G]TGACTTGAAAAGAAA | 79582 |
rs114893522 | snp | A/C | 0.0123036 | 0.0774623 | intron-variant | SPAG16 | GRCh38.p7 | 2:214226252 | TGACTCAGCTCTGCC[A/C]CTTGGATTCTTCTCA | 79582 |
rs114900338 | snp | A/G | 0.00517822 | 0.0506191 | intron-variant | SPAG16 | GRCh38.p7 | 2:214394792 | CAAACGTATAATGAC[A/G]TATATCCATCATGAT | 79582 |
rs114919781 | snp | A/G | 0.0221141 | 0.102801 | intron-variant | SPAG16 | GRCh38.p7 | 2:213482980 | ATGAATGAATACAAA[A/G]TATTATAAAGTAAAA | 79582 |
rs114920805 | snp | C/T | 0.0119091 | 0.0762411 | intron-variant | SPAG16 | GRCh38.p7 | 2:213920808 | ACAGGGATGGACATC[C/T]CTTGTCATACTCTGC | 79582 |
rs114924373 | snp | A/C | 0.0146672 | 0.084371 | intron-variant | SPAG16 | GRCh38.p7 | 2:213392041 | TTCTTTAATGAAAAA[A/C]TGGAATGTTATTTAA | 79582 |
rs114930851 | snp | C/G | 0.0240643 | 0.107019 | intron-variant | SPAG16 | GRCh38.p7 | 2:213374019 | AGATGCTGTGGGACT[C/G]TAGCTTAGCACCTTC | 79582 |
rs114933049 | snp | A/G | 0.0577344 | 0.159793 | intron-variant | SPAG16 | GRCh38.p7 | 2:213991283 | CTGTATTACTTTGTT[A/G]AAAATGATGGTTTCC | 79582 |
rs114934136 | snp | C/T | 0.0325976 | 0.123435 | intron-variant | SPAG16, LOC101928084 | GRCh38.p7 | 2:214089027 | AAGCATATTAAAGAA[C/T]AAGTAATAGATTCAA | 79582 |
rs114934691 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | SPAG16 | GRCh38.p7 | 2:214310579 | TGTGTGGAAGCACCT[C/G]CCCTAATGAAGCTCA | 79582 |
rs114937527 | snp | A/G | 0.0228947 | 0.104514 | intron-variant | SPAG16 | GRCh38.p7 | 2:214406530 | AATATTCAAGTTTTT[A/G]TAACAAATTCAATTG | 79582 |
rs114947335 | snp | A/G | 0.0221141 | 0.102801 | intron-variant | SPAG16 | GRCh38.p7 | 2:214389070 | GTTTTGAAATCAAGA[A/G]AAATATTTCTCTATA | 79582 |
rs114955645 | snp | G/T | 0.00199481 | 0.0315187 | intron-variant | SPAG16 | GRCh38.p7 | 2:214217149 | TAAAAATTCAAAAAG[G/T]TTAACATTTTAGATA | 79582 |
rs114956448 | snp | A/G | 0.0023933 | 0.0345097 | intron-variant | SPAG16 | GRCh38.p7 | 2:213461501 | AAATTTGTTAAGCAG[A/G]GAGACATATTAGAGG | 79582 |
rs114957882 | snp | C/G | 0.00914312 | 0.0669923 | intron-variant | SPAG16 | GRCh38.p7 | 2:213776140 | GGATTTATGTTACCT[C/G]ATATGGCAAAGGAAC | 79582 |
rs114961891 | snp | C/T | 0.00835141 | 0.0640778 | intron-variant, utr-variant-3-prime | SPAG16 | GRCh38.p7 | 2:213398665 | ATCCAATCTAAATTT[C/T]AATGCTGCCTCTAAT | 79582 |
rs114965528 | snp | A/C | 0.0919752 | 0.193722 | intron-variant | SPAG16 | GRCh38.p7 | 2:213953765 | AATTCCATATCCATA[A/C]AAACTGACCCAAATT | 79582 |
rs114972622 | snp | C/T | 0.0566069 | 0.158427 | intron-variant | SPAG16 | GRCh38.p7 | 2:214000244 | TTTGAATTATCAGAG[C/T]GGTTTCCCCCACACT | 79582 |
rs114972818 | snp | A/G | 0.00993419 | 0.0697739 | intron-variant | SPAG16 | GRCh38.p7 | 2:213905540 | TATTGTGTTTCATTC[A/G]TCAAATCATTGATTC | 79582 |
rs114974608 | snp | A/G | 0.00636936 | 0.0560724 | intron-variant | SPAG16 | GRCh38.p7 | 2:214255075 | CTAACACAGTCTTCC[A/G]TTACCAATGCTTATT | 79582 |
rs114975572 | snp | C/T | 0.00438332 | 0.0466095 | intron-variant | SPAG16 | GRCh38.p7 | 2:213848399 | CAGATTATCAGGACT[C/T]ATTTCAGGTCTGTTG | 79582 |
rs114980141 | snp | A/G | 0.0225045 | 0.103662 | intron-variant | SPAG16 | GRCh38.p7 | 2:214163663 | AGAGAAAGAGAGAGA[A/G]AGGAAAAGATTTATT | 79582 |
rs114982026 | snp | C/T | 0.0185938 | 0.0946107 | intron-variant | SPAG16 | GRCh38.p7 | 2:214299564 | TACTTCTGTGTACCA[C/T]AATTGTTTCCAGTCT | 79582 |
rs114982108 | snp | C/T | 0.0532157 | 0.154195 | intron-variant | SPAG16 | GRCh38.p7 | 2:214281201 | TCAAGCCAACCTTCA[C/T]GCCATATTTTGGCAG | 79582 |
rs114986804 | snp | C/T | 0.0283406 | 0.115616 | intron-variant | SPAG16 | GRCh38.p7 | 2:213837066 | TCCTCATTTTAATTC[C/T]GCCTGCTCTTGTTGC | 79582 |
rs114988946 | snp | C/T | 0.0150606 | 0.0854603 | intron-variant | SPAG16 | GRCh38.p7 | 2:213743330 | AATGCCTGGCCCCTA[C/T]AGGAAGCACCAATTA | 79582 |
rs114993570 | snp | A/T | 0.00159617 | 0.0282053 | upstream-variant-2KB, intron-variant, downstream-variant-500B | VWC2L, SPAG16 | GRCh38.p7 | 2:214410671 | AACTGCAGGAAAACC[A/T]GGCTACTTTAAAAAA | 79582 |
rs114993833 | snp | A/C | 0.0178098 | 0.0926698 | intron-variant | SPAG16 | GRCh38.p7 | 2:214243428 | GGGCTCATAAAATTT[A/C]ACTATAGTACCTGGC | 79582 |
rs114999025 | snp | G/T | 0.0923359 | 0.194016 | intron-variant | SPAG16, LOC101928084 | GRCh38.p7 | 2:214095993 | ATAATGTAAAACAAT[G/T]TTCTGAATTTGGGAA | 79582 |
rs115001912 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | SPAG16 | GRCh38.p7 | 2:214258221 | ACTGTACCCAATGTG[A/T]AGTCTTTTATTCCTC | 79582 |
rs115003103 | snp | A/C/T | 0.0490732 | 0.148853 | intron-variant | SPAG16 | GRCh38.p7 | 2:214288122 | TAATTCTATTCTCTG[A/C/T]CTCCATGAGATCAAC | 79582 |
rs115008213 | snp | A/C | 0.00318978 | 0.0398085 | intron-variant | SPAG16 | GRCh38.p7 | 2:213305448 | CAGATCTTGGAGGAA[A/C]GGCTTTCAGGTTTTC | 79582 |
rs115013768 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | SPAG16 | GRCh38.p7 | 2:213704105 | TGTTTATTCACTGGG[C/T]AGCCTTATCATCAGA | 79582 |
rs115014833 | snp | G/T | 0.0182019 | 0.0936463 | intron-variant | SPAG16 | GRCh38.p7 | 2:214269845 | CCAAACAATGACCTC[G/T]GAATCATGGGGGTCA | 79582 |
rs115016359 | snp | A/G | 0.00676609 | 0.0577691 | intron-variant | SPAG16 | GRCh38.p7 | 2:214249146 | ACTGAAGAATGTGAA[A/G]AATTAGGAAAGAAAT | 79582 |
rs115018568 | snp | A/G | 0.040671 | 0.13668 | intron-variant | SPAG16 | GRCh38.p7 | 2:213895719 | AATGGTACTGGGAAA[A/G]CTATATAATTATGTA | 79582 |
rs115019704 | snp | C/T | 0.0170251 | 0.090679 | intron-variant | SPAG16 | GRCh38.p7 | 2:214234174 | TTACCTTACTGAGGA[C/T]AATTGCTTTCAGCAA | 79582 |
rs115021060 | snp | A/G | 0.00199481 | 0.0315187 | intron-variant | SPAG16 | GRCh38.p7 | 2:213770013 | AATATGTACTGTTTT[A/G]TCCCTGGCTTCTTTA | 79582 |
rs115024794 | snp | C/G | 0.0444908 | 0.142359 | intron-variant | SPAG16 | GRCh38.p7 | 2:214235779 | TTTTATTTTTTTATA[C/G]AAACAACATTTATTT | 79582 |
rs115026924 | snp | C/G | 0.0023933 | 0.0345097 | intron-variant, missense | SPAG16 | GRCh38.p7 | 2:214150884 | CATACAGGTCAGTGT[C/G]ATTTTAAGGCCCTTG | 79582 |
rs115027549 | snp | A/G | 0.0221141 | 0.102801 | intron-variant | SPAG16 | GRCh38.p7 | 2:213458430 | AAAAAAAAGTAGCTG[A/G]GCGTGGTGGTGACTG | 79582 |
rs115029005 | snp | C/T | 0.0150606 | 0.0854603 | utr-variant-3-prime, intron-variant | SPAG16 | GRCh38.p7 | 2:213317962 | TCTAAAAATAAAGTT[C/T]ATTAAAAAAAAGTTA | 79582 |
rs115036519 | snp | C/T | 0.0166325 | 0.0896639 | intron-variant | SPAG16 | GRCh38.p7 | 2:213634863 | AGAGGCTTGGTTTTC[C/T]GCTCCTGAGTAACTT | 79582 |
rs115041915 | snp | A/G | 0.0134861 | 0.0810011 | intron-variant | SPAG16 | GRCh38.p7 | 2:214034281 | CTCTGCTGTCTCTCT[A/G]CTGTAAAGCAGAATA | 79582 |
rs115044242 | snp | C/G | 0.00914312 | 0.0669923 | intron-variant | SPAG16 | GRCh38.p7 | 2:214290421 | CTTCTGATAATTTTG[C/G]ATTTGACTTACCCTT | 79582 |
rs115044511 | snp | A/G | 0.0221141 | 0.102801 | intron-variant | SPAG16 | GRCh38.p7 | 2:213656866 | AATAGTTCATGGAGA[A/G]TCTCTGAAGTCTCAG | 79582 |
rs115049917 | snp | A/G | 0.0876345 | 0.190099 | intron-variant | SPAG16 | GRCh38.p7 | 2:214136777 | ATGGTGTAATGAGCT[A/G]TTGCTTAATGCTGCA | 79582 |
rs115050561 | snp | G/T | 0.0225045 | 0.103662 | intron-variant | SPAG16 | GRCh38.p7 | 2:214276946 | TCAAACATAGATTTG[G/T]TTTTTTTCACATAGT | 79582 |
rs115052593 | snp | C/G | 0.228842 | 0.249103 | intron-variant | SPAG16 | GRCh38.p7 | 2:214113425 | AAAGTTTTCCAACTT[C/G]GTTCCATTTTCCCCG | 79582 |
rs115053016 | snp | A/G | 0.0228947 | 0.104514 | intron-variant | SPAG16 | GRCh38.p7 | 2:213963420 | CGATTTCTACGATTT[A/G]ATTTCTTTAAACTTT | 79582 |
rs115053772 | snp | A/G | 0.0236746 | 0.106192 | intron-variant | SPAG16 | GRCh38.p7 | 2:213448077 | ATGATTGCCAGGCCA[A/G]TTCCACCCAAATGTG | 79582 |
rs115058585 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | SPAG16 | GRCh38.p7 | 2:214004064 | GAACATGCACATCAG[A/G]TGACTCAAATTTTTC | 79582 |
rs115059439 | snp | G/T | 0.0182019 | 0.0936463 | intron-variant | SPAG16 | GRCh38.p7 | 2:213698268 | TATTATTATGATGAT[G/T]ATTATTATTTTGAGA | 79582 |
rs115060869 | snp | C/T | 0.0429648 | 0.14013 | intron-variant | SPAG16 | GRCh38.p7 | 2:213292047 | GGAGTATGTAAGTGT[C/T]GATTGATATTTTCTA | 79582 |
rs115061467 | snp | A/G | 0.021333 | 0.101051 | intron-variant | SPAG16 | GRCh38.p7 | 2:213653679 | ATCTCTCAAAATTGT[A/G]TAAAAGTATAGTAGC | 79582 |
rs115061597 | snp | G/T | 0.0333695 | 0.124785 | intron-variant | SPAG16 | GRCh38.p7 | 2:213949117 | TTGAATGAAAATAAT[G/T]TCTACAGTTATTTAT | 79582 |
rs115064750 | snp | A/G | 0.239326 | 0.249772 | intron-variant | SPAG16 | GRCh38.p7 | 2:213759912 | TGGTGGCACATGCCT[A/G]TAGTCCCAGATACTC | 79582 |
rs115066448 | snp | C/G | 0.0178098 | 0.0926698 | intron-variant | SPAG16 | GRCh38.p7 | 2:214226063 | ACAGAATCTGAAAAG[C/G]TTTTCATTTGCAAAT | 79582 |
rs115066952 | snp | A/G | 0.00478085 | 0.0486577 | intron-variant | SPAG16 | GRCh38.p7 | 2:213661073 | TCTGGTCACTCCAAC[A/G]TATAGGTAGCCTTGG | 79582 |
rs115068802 | snp | C/G | 0.0119091 | 0.0762411 | intron-variant | SPAG16 | GRCh38.p7 | 2:214136362 | GTTTAATAACTTAAA[C/G]CTTGGTTGTCTCATT | 79582 |
rs115072293 | snp | C/T | 0.0429648 | 0.14013 | intron-variant | SPAG16 | GRCh38.p7 | 2:213579226 | GTAATAAGGGATTCT[C/T]TGGTATTAAGAGAAA | 79582 |
rs115073964 | snp | C/T | 0.0115144 | 0.0749975 | intron-variant | SPAG16 | GRCh38.p7 | 2:213722211 | AAGTGATGAAAGAGA[C/T]GTTAACTCAAATTTG | 79582 |
rs115077356 | snp | A/G | 0.0279526 | 0.114869 | intron-variant | SPAG16 | GRCh38.p7 | 2:213660740 | CCAGGATCATAGATC[A/G]ATTGCATCTTAAACT | 79582 |
rs115081676 | snp | A/G | 0.0178098 | 0.0926698 | intron-variant | SPAG16 | GRCh38.p7 | 2:214286532 | TGGGCATATCACTTG[A/G]AGCCAGGAGTTGGAG | 79582 |
rs115088731 | snp | A/G | 0.021333 | 0.101051 | intron-variant | SPAG16 | GRCh38.p7 | 2:214198864 | AATTAGGGATATTGA[A/G]CATTTTTTCATATGT | 79582 |
rs115089946 | snp | C/G/T | 0.0240643 | 0.107019 | intron-variant | SPAG16 | GRCh38.p7 | 2:213583611 | AGATATTGACATTTG[C/G/T]GGGGGTGGTAACTGA | 79582 |
rs115093381 | snp | C/G | 0.00279162 | 0.0372561 | intron-variant | SPAG16 | GRCh38.p7 | 2:214261294 | CCGTTCACTCACACA[C/G]AGAGCTAGGCTTCAG | 79582 |
rs115093595 | snp | C/T | 0.0244538 | 0.107838 | intron-variant | SPAG16 | GRCh38.p7 | 2:213291537 | GGTTAGATTTCGTTT[C/T]GAGTCTGTAGCCTGT | 79582 |
rs115101183 | snp | C/T | 0.00835141 | 0.0640778 | intron-variant | SPAG16 | GRCh38.p7 | 2:213354027 | TCTCTTAATGCTATC[C/T]CTGTCCCAGCCCCAC | 79582 |
rs115102543 | snp | A/G | 0.0217236 | 0.101931 | intron-variant | SPAG16 | GRCh38.p7 | 2:213883527 | ATGTTTATTAGGTCC[A/G]TTTGCTTAAGTGTCA | 79582 |
rs115102566 | snp | C/T | 0.0146672 | 0.084371 | intron-variant | SPAG16 | GRCh38.p7 | 2:214134641 | TCAACCTCTTACTTA[C/T]AACAAACTTGAGTAC | 79582 |
rs115103542 | snp | C/T | 0.0923359 | 0.194016 | intron-variant | SPAG16 | GRCh38.p7 | 2:214168114 | CCCACCTCAGCCTTC[C/T]GAATAGCTGGGATTA | 79582 |
rs115106264 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | SPAG16 | GRCh38.p7 | 2:213702522 | TAAGAACTGTAACGC[C/T]GCGAGGGTCCACAGC | 79582 |
rs115107729 | snp | A/G | 0.0329836 | 0.124112 | intron-variant | SPAG16 | GRCh38.p7 | 2:214074327 | AGGTTGTTTTTATGA[A/G]TGATATAGGATCAAT | 79582 |
rs115110187 | snp | A/G | 0.0581099 | 0.160244 | intron-variant | SPAG16 | GRCh38.p7 | 2:214006367 | AACATATGTATGGGA[A/G]ATGCATTTTAAATAA | 79582 |
rs115112875 | snp | C/T | 0.0232847 | 0.105357 | intron-variant | SPAG16 | GRCh38.p7 | 2:213702168 | CAGCTCTCTGTAAAA[C/T]GGACCAATCAGCTGT | 79582 |
rs115112887 | snp | A/G | 0.00795532 | 0.062565 | intron-variant | SPAG16 | GRCh38.p7 | 2:213992203 | GCAACTACTATTTGA[A/G]CCAAGGTGATATTTT | 79582 |
rs115112900 | snp | C/T | 0.0310518 | 0.120672 | intron-variant | SPAG16 | GRCh38.p7 | 2:214030744 | CATTGATACCTCTCC[C/T]CCTAACCTCACGTTT | 79582 |
rs115114968 | snp | C/G/T | 0.0221141 | 0.102801 | intron-variant | SPAG16 | GRCh38.p7 | 2:214011632 | TCTGGGTCGTGGTTT[C/G/T]TTGACCCCTGGTATA | 79582 |
rs115115080 | snp | A/G | 0.0244538 | 0.107838 | intron-variant | SPAG16 | GRCh38.p7 | 2:213449061 | AATAATAATATTAAT[A/G]CCCTGGGAAACGAAT | 79582 |
rs115121000 | snp | A/G | 0.00398564 | 0.0444627 | intron-variant | SPAG16 | GRCh38.p7 | 2:213457060 | CATTATTCATCTGCC[A/G]AAGAGCATAGCTACT | 79582 |
rs115122279 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant, utr-variant-5-prime | SPAG16 | GRCh38.p7 | 2:213296464 | TCCTAGATTCCCACT[A/G]CTCAGTTGAAGCGGA | 79582 |
rs115125124 | snp | A/G | 0.0248432 | 0.108648 | intron-variant | SPAG16 | GRCh38.p7 | 2:213372816 | AGTGGCATGAAGTTA[A/G]GGAGTGGCACAAAGT | 79582 |
rs115125383 | snp | C/T | 0.0197687 | 0.0974348 | intron-variant | SPAG16 | GRCh38.p7 | 2:213883900 | CTTTGAGCCTGAGTC[C/T]TTACATGTGTGATAT | 79582 |
rs115127701 | snp | G/T | 0.0119091 | 0.0762411 | intron-variant | SPAG16 | GRCh38.p7 | 2:214130445 | TGGCCAGAGGCATGC[G/T]TTAACACTAGCAAAC | 79582 |
rs115129138 | snp | A/G | 0.0425829 | 0.139564 | intron-variant | SPAG16 | GRCh38.p7 | 2:213438689 | TGTAAGTATGACGAG[A/G]TGGTACTCCTGGGAT | 79582 |
rs115132339 | snp | A/G | 0.0185938 | 0.0946107 | intron-variant | SPAG16 | GRCh38.p7 | 2:214034998 | TTTTTCAAGTGGATG[A/G]TGAGCAAGGTGAAAA | 79582 |
rs115137639 | snp | A/T | 0.196064 | 0.244113 | intron-variant | SPAG16 | GRCh38.p7 | 2:213356171 | TTTTAATGAGGATTT[A/T]CATCGATGTTCATCA | 79582 |
rs115141252 | snp | A/C | 0.029116 | 0.117091 | intron-variant | SPAG16 | GRCh38.p7 | 2:213918811 | TCAGTTTTGTAACTC[A/C]TTTTTTTTGTCTGTG | 79582 |
rs115146081 | snp | C/T | 0.00358779 | 0.0422022 | intron-variant | SPAG16 | GRCh38.p7 | 2:213573420 | AAAAGAAAACAAAAA[C/T]AAAACTTTCACCAAA | 79582 |
rs115152103 | snp | A/T | 0.0146672 | 0.084371 | intron-variant | SPAG16 | GRCh38.p7 | 2:213762650 | TAAACAGTACTAAAA[A/T]TTTTAACAAAGACCT | 79582 |
rs115157593 | snp | G/T | 0.0166325 | 0.0896639 | intron-variant | SPAG16 | GRCh38.p7 | 2:214265696 | TGGTCATGTAGATTT[G/T]CTTTTATTTATGTTC | 79582 |
rs115158740 | snp | A/C | 0.0123036 | 0.0774623 | intron-variant | SPAG16 | GRCh38.p7 | 2:213592161 | AAAAACAAAAGAAGA[A/C]CTCTAATACCAGCAG | 79582 |
rs115163818 | snp | C/T | 0.021333 | 0.101051 | intron-variant | SPAG16 | GRCh38.p7 | 2:213929507 | CTTCCTTCATCCAAA[C/T]TGCACTCCTGAAGCA | 79582 |
rs115166135 | snp | A/C | 0.021333 | 0.101051 | intron-variant | SPAG16 | GRCh38.p7 | 2:214228653 | TCTGAATCAGAAAGT[A/C]TGCAATTAGGGCCCA | 79582 |
rs115176744 | snp | A/G | 0.00993419 | 0.0697739 | intron-variant | SPAG16 | GRCh38.p7 | 2:213438441 | GCTTATTTTTATATA[A/G]CAAGTTTTATTTGAA | 79582 |
rs115180784 | snp | A/G | 0.0170251 | 0.090679 | intron-variant | SPAG16 | GRCh38.p7 | 2:213886433 | AGGTCAGAGAGGACT[A/G]TTGATTCTGAGGCTG | 79582 |
rs115182741 | snp | C/T | 0.0681886 | 0.171594 | intron-variant | SPAG16 | GRCh38.p7 | 2:213976187 | ATATACATGTATGTG[C/T]GTATGTGTATATATA | 79582 |
rs115183080 | snp | A/C | 0.0228947 | 0.104514 | intron-variant | SPAG16 | GRCh38.p7 | 2:213940464 | GATAATTATATATTT[A/C]TTTTTATTTTTTAGG | 79582 |
rs115185611 | snp | C/T | 0.00279162 | 0.0372561 | intron-variant | SPAG16 | GRCh38.p7 | 2:213991617 | TACCTTGTCCTGATG[C/T]TCTGACTGCTAGGGA | 79582 |
rs115192223 | snp | A/G | 0.0228947 | 0.104514 | intron-variant | SPAG16 | GRCh38.p7 | 2:213958280 | TGGCATGTCTTGGCA[A/G]TCCATGTGGTATATG | 79582 |
rs115192252 | snp | A/G | 0.00795532 | 0.062565 | intron-variant | SPAG16 | GRCh38.p7 | 2:213601043 | TGATTTTAAGCAAGG[A/G]GAGTAAATGATTGTA | 79582 |
rs115192783 | snp | A/G | 0.021333 | 0.101051 | intron-variant | SPAG16 | GRCh38.p7 | 2:213979554 | ATGGAGTGAGTGCAA[A/G]CATGGGAAATGCCAG | 79582 |
rs115194095 | snp | C/T | 0.0341408 | 0.126114 | intron-variant | SPAG16 | GRCh38.p7 | 2:214018780 | GAAATGTGAAAATGA[C/T]CAGTGGATTATATTC | 79582 |
rs115195689 | snp | C/T | 0.0166325 | 0.0896639 | intron-variant | SPAG16 | GRCh38.p7 | 2:213413216 | GAGAAAATGCTATGC[C/T]ATTTCATAGAAGTTC | 79582 |
rs115197299 | snp | A/C | 0.0298908 | 0.118541 | intron-variant | SPAG16 | GRCh38.p7 | 2:213984812 | TGCTGACGCCACTAG[A/C]CTCTGCAGCTCTTCC | 79582 |
rs115199791 | snp | A/T | 0.0134861 | 0.0810011 | intron-variant, upstream-variant-2KB | SPAG16, LOC101928084 | GRCh38.p7 | 2:214103446 | AATAAAAGTGTTTCA[A/T]GAAACAGTTTCTGCT | 79582 |
rs115204947 | snp | C/T | 0.0364509 | 0.129988 | intron-variant | SPAG16 | GRCh38.p7 | 2:213580280 | ACTTCTCCACAAATA[C/T]CCACTTATTCATCAA | 79582 |
rs115206990 | snp | C/T | 0.00279162 | 0.0372561 | intron-variant | SPAG16 | GRCh38.p7 | 2:213636438 | GATCATGTGTGTGCA[C/T]TCATTTTTGGTTCCA | 79582 |
rs115213280 | snp | C/T | 0.00557542 | 0.0525036 | intron-variant | SPAG16 | GRCh38.p7 | 2:213378979 | ATAGTCTGGGCCAAT[C/T]ACCCCAGCCAAGACT | 79582 |
rs115218768 | snp | A/C | 0.0158469 | 0.0875917 | intron-variant | SPAG16 | GRCh38.p7 | 2:213336036 | ACTAGGTGGTTGGCG[A/C]AACCCAGGGAGAGCA | 79582 |
rs115231297 | snp | A/G | 0.0581099 | 0.160244 | intron-variant | SPAG16 | GRCh38.p7 | 2:214000316 | TTATCAGGGGTTTCC[A/G]CTTTTGCATCATCCT | 79582 |
rs115237279 | snp | A/G | 0.00318978 | 0.0398085 | intron-variant | SPAG16 | GRCh38.p7 | 2:213311465 | AGTATACTGTTAACA[A/G]TTCGGTGACTATTGT | 79582 |
rs115238809 | snp | A/G | 0.0189856 | 0.0955633 | intron-variant | SPAG16 | GRCh38.p7 | 2:214297046 | CTATGGTTCATGTAT[A/G]CCCAGCAGAACCACA | 79582 |
rs115238952 | snp | C/T | 0.00438332 | 0.0466095 | intron-variant | SPAG16 | GRCh38.p7 | 2:213703087 | ATGGTCAGTACACAC[C/T]TTGCCATTCTCTTTT | 79582 |
rs115247888 | snp | A/G | 0.0244538 | 0.107838 | intron-variant | SPAG16 | GRCh38.p7 | 2:213446267 | ATGGCTGAAATGACA[A/G]ACATTGGTTCAGAAT | 79582 |
rs115250155 | snp | A/G | 0.0566069 | 0.158427 | intron-variant | SPAG16 | GRCh38.p7 | 2:213992170 | ATAAAGTTTTACTAC[A/G]TACTGTTTTCCAGGA | 79582 |
rs115250798 | snp | C/T | 0.0111196 | 0.0737302 | intron-variant | SPAG16 | GRCh38.p7 | 2:214387863 | ATTCAGTGATCTTCA[C/T]CTGGTCTCTCCCACA | 79582 |
rs115252151 | snp | C/T | 0.00199481 | 0.0315187 | intron-variant | SPAG16 | GRCh38.p7 | 2:213421321 | GGTGGTGCCGACTCA[C/T]CAGTCCCCCGCCATT | 79582 |
rs115253017 | snp | C/T | 0.00358779 | 0.0422022 | intron-variant | SPAG16 | GRCh38.p7 | 2:213445494 | TGGTGAAACTCTCTC[C/T]ACTAAAAATACAAAA | 79582 |
rs115253423 | snp | A/G | 0.0244538 | 0.107838 | intron-variant | SPAG16 | GRCh38.p7 | 2:213496030 | GTATTAGAGGATTTT[A/G]AACAGAAGAATTACA | 79582 |
rs115253475 | snp | A/G | 0.02016 | 0.0983543 | intron-variant | SPAG16 | GRCh38.p7 | 2:213811221 | GTTGGTGTCTAATGT[A/G]GCTCTTGGAAATACA | 79582 |
rs115254716 | snp | C/T | 0.00199481 | 0.0315187 | intron-variant | SPAG16 | GRCh38.p7 | 2:213893384 | TGAAGGTATAAAACC[C/T]ACTGTTATAATTAAG | 79582 |
rs115256830 | snp | C/T | 0.0566069 | 0.158427 | intron-variant | SPAG16 | GRCh38.p7 | 2:213992769 | CTTATATGCATCAGT[C/T]GATATTTCTATCATG | 79582 |
rs115257546 | snp | C/G | 0.030278 | 0.119257 | intron-variant | SPAG16 | GRCh38.p7 | 2:214139571 | TTTATTTTAAATTTC[C/G]CTTTAAAAAATGCAT | 79582 |
rs115258671 | snp | A/G | 0.0425829 | 0.139564 | intron-variant | SPAG16 | GRCh38.p7 | 2:213384733 | ACCAGGCAAGAGATA[A/G]TGACTTTTTACAAGG | 79582 |
rs115263702 | snp | C/G | 0.0452528 | 0.143452 | intron-variant | SPAG16 | GRCh38.p7 | 2:213378802 | CCTTCATTCCTGAAG[C/G]GTCTGGGCCATATGC | 79582 |
rs115266898 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | SPAG16 | GRCh38.p7 | 2:213506529 | TCATTTATGGACCAC[C/T]TTAACTCATGGTGAT | 79582 |
rs115273283 | snp | C/T | 0.0138799 | 0.0821421 | intron-variant | SPAG16, LOC101928084 | GRCh38.p7 | 2:214086331 | TGATAATTTATTATG[C/T]ACCAAGCAAGAAGTA | 79582 |
rs115274561 | snp | C/T | 0.00636936 | 0.0560724 | intron-variant | SPAG16 | GRCh38.p7 | 2:214288090 | CCAATCCCACCCTTC[C/T]AAGCCTCTGGCATCT | 79582 |
rs115274636 | snp | C/T | 0.00199481 | 0.0315187 | intron-variant | SPAG16 | GRCh38.p7 | 2:213541134 | TCATTGTTTCATTTA[C/T]GGTGAAAACGAAAGG | 79582 |
rs115278854 | snp | A/T | 0.00557542 | 0.0525036 | intron-variant | SPAG16 | GRCh38.p7 | 2:214134008 | AAGACCTGGAATTTA[A/T]GAGAGAGTTGTGAAT | 79582 |
rs115281464 | snp | A/T | 0.00795532 | 0.062565 | intron-variant | SPAG16 | GRCh38.p7 | 2:213926626 | TTTCTAAATATATAT[A/T]TTTTTCAGATTTGCA | 79582 |
rs115282317 | snp | A/G | 0.0479149 | 0.147179 | intron-variant | SPAG16 | GRCh38.p7 | 2:213670992 | CCATCACATGGATAC[A/G]TAAAAGTGTCTTTAA | 79582 |
rs115284378 | snp | C/T | 0.00874735 | 0.0655527 | intron-variant | SPAG16 | GRCh38.p7 | 2:213968335 | ACCTGCCACCACACC[C/T]ACACCTGCCACCACA | 79582 |
rs115294222 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | SPAG16 | GRCh38.p7 | 2:214179979 | GCAGTTATTCAGGAA[A/G]AGACTGTCAATTTTA | 79582 |
rs115301011 | snp | A/G | 0.0170251 | 0.090679 | intron-variant | SPAG16 | GRCh38.p7 | 2:213810849 | GCTGTGTTAAAATGT[A/G]TAATAGATAATATTT | 79582 |
rs115303995 | snp | A/G | 0.0236746 | 0.106192 | intron-variant | SPAG16 | GRCh38.p7 | 2:213974179 | AGCCAGATGATCATA[A/G]TTAGTTCTGTCTCTT | 79582 |
rs115316254 | snp | C/T | 0.0142736 | 0.0832652 | intron-variant | SPAG16 | GRCh38.p7 | 2:213386182 | TCTTCCAAACTCCCA[C/T]TGATGCCTTTTTTCC | 79582 |
rs115318682 | snp | G/T | 0.00318978 | 0.0398085 | intron-variant | SPAG16 | GRCh38.p7 | 2:213710352 | TAAAATTACATGTAA[G/T]TCATAAACAATTACG | 79582 |
rs115318699 | snp | A/G | 0.189576 | 0.242588 | intron-variant | SPAG16 | GRCh38.p7 | 2:213950994 | TGGGATTACAGGTGT[A/G]AGCCACCACGCCTAG | 79582 |
rs115328173 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | SPAG16 | GRCh38.p7 | 2:213563876 | TGCTATCACATTTCT[A/G]CACCCTGAATGAGTG | 79582 |
rs115332788 | snp | C/T | 0.0240643 | 0.107019 | intron-variant | SPAG16 | GRCh38.p7 | 2:214304695 | GCGTTAGGGTCTCCC[C/T]GACCAAGCTGGTCTC | 79582 |
rs115339364 | snp | G/T | 0.0267878 | 0.112589 | intron-variant | SPAG16 | GRCh38.p7 | 2:214226287 | GAAGGTGAAAGTACA[G/T]GGGACAAAGTGAAAA | 79582 |
rs115339776 | snp | A/G | 0.0170251 | 0.090679 | intron-variant | SPAG16 | GRCh38.p7 | 2:213684374 | GTTAAAATTAGATCA[A/G]AGCATACACATAGCT | 79582 |
rs115346113 | snp | G/T | 0.0154538 | 0.0865337 | intron-variant | SPAG16 | GRCh38.p7 | 2:214292035 | TGATATCCTTGAGTG[G/T]GAAGTTTGTTTTTTT | 79582 |
rs115347577 | snp | A/G | 0.00318978 | 0.0398085 | intron-variant | SPAG16 | GRCh38.p7 | 2:213695689 | AAGAAGGAGCCAGCC[A/G]TGAGAAGACGTAGAG | 79582 |
rs115350129 | snp | A/G | 0.0205511 | 0.0992634 | intron-variant | SPAG16 | GRCh38.p7 | 2:214176748 | TAAAATTTTCCATGT[A/G]TGCTTACTCTAGAGC | 79582 |
rs115362954 | snp | A/C | 0.0165278 | 0.0893908 | intron-variant | SPAG16 | GRCh38.p7 | 2:214030279 | AATGTCTTCCAGGTT[A/C]ACCCATGTTGTCCCA | 79582 |
rs115370996 | snp | A/C | 0.0240643 | 0.107019 | intron-variant | SPAG16 | GRCh38.p7 | 2:213339302 | CAGAGAAGTAGATTT[A/C]TTCTGTTTCAATCCT | 79582 |
rs115373008 | snp | C/T | 0.0248432 | 0.108648 | intron-variant, utr-variant-3-prime | SPAG16 | GRCh38.p7 | 2:213370559 | CCAAAAATGACTAAA[C/T]AGTCTGAAAAAGAAT | 79582 |
rs115375572 | snp | A/C/G | 0.00795819 | 0.0626103 | intron-variant | SPAG16, LOC101928084 | GRCh38.p7 | 2:214091288 | TTCTCAAAAATCTGT[A/C/G]ATAAAACTACTAATA | 79582 |
rs115380378 | snp | C/T | 0.0221141 | 0.102801 | intron-variant | SPAG16 | GRCh38.p7 | 2:213643596 | CCATTGAATAAACTT[C/T]CTACCCCTATCTCTT | 79582 |
rs115383556 | snp | C/T | 0.0244538 | 0.107838 | intron-variant | SPAG16 | GRCh38.p7 | 2:213566313 | ATTTAAAACGTTATA[C/T]TATTAGTATTTATTT | 79582 |
rs115389680 | snp | A/G | 0.0425829 | 0.139564 | intron-variant, upstream-variant-2KB | SPAG16 | GRCh38.p7 | 2:213342834 | AGGACCGTGATGCCT[A/G]AGAGAAGACAAACAC | 79582 |
rs115390131 | snp | A/G | 0.0456336 | 0.143994 | intron-variant | SPAG16 | GRCh38.p7 | 2:213445607 | AGAGGTGGAGGTTGC[A/G]GTGAGCCAAAAACAT | 79582 |
rs115396376 | snp | A/G | 0.00636936 | 0.0560724 | intron-variant | SPAG16 | GRCh38.p7 | 2:213379507 | GTGCTTTGGTCAGAG[A/G]CAATGCTGTGTGGAA | 79582 |
rs115400573 | snp | C/G | 0.0174175 | 0.0916809 | intron-variant | SPAG16 | GRCh38.p7 | 2:214247032 | TTAGTTTTAATTACA[C/G]CAAGACACAACACTG | 79582 |
rs115401703 | snp | A/G | 0.02016 | 0.0983543 | intron-variant | SPAG16 | GRCh38.p7 | 2:213803741 | TTAAAAATGTATTAT[A/G]TATGTATATATTTAG | 79582 |
rs115402473 | snp | C/T | 0.0228947 | 0.104514 | intron-variant | SPAG16 | GRCh38.p7 | 2:213955819 | AATCATTGTTATTTC[C/T]GTACAATCAACAGTA | 79582 |
rs115405053 | snp | C/T | 0.00279162 | 0.0372561 | intron-variant | SPAG16 | GRCh38.p7 | 2:213765918 | AAACAGATCCAGATC[C/T]CGGTTCCTCAGTAAA | 79582 |
rs115406912 | snp | C/G | 0.0614824 | 0.164198 | intron-variant | SPAG16 | GRCh38.p7 | 2:213742150 | TATTTTTTTTTTACT[C/G]TCTTTTCTTGGTTTC | 79582 |
rs115408828 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | SPAG16 | GRCh38.p7 | 2:213780486 | AATGTTTTTTCAACT[A/G]TGTGGAATCTGGTGT | 79582 |
rs115411398 | snp | A/G | 0.0785177 | 0.181917 | intron-variant | SPAG16 | GRCh38.p7 | 2:214117042 | GATTTTAAAGTGACA[A/G]GGATGTGTCATCTCT | 79582 |
rs115414485 | snp | A/G | 0.0134861 | 0.0810011 | intron-variant, upstream-variant-2KB | SPAG16, LOC101928084 | GRCh38.p7 | 2:214104323 | AGTTCTTTTAGTGCA[A/G]TGATAATTTTTTGGT | 79582 |
rs115414585 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | SPAG16 | GRCh38.p7 | 2:213764804 | AGTATGTAATATATT[C/T]AATATTATAATTCAT | 79582 |
rs115419770 | snp | C/T | 0.00716266 | 0.059414 | intron-variant | SPAG16 | GRCh38.p7 | 2:214037297 | TATTTTCATATTCAC[C/T]CAACTTGTTTAATAA | 79582 |
rs115426485 | snp | C/T | 0.0023933 | 0.0345097 | intron-variant | SPAG16 | GRCh38.p7 | 2:213804901 | GCCTCTTAAGCCAAA[C/T]TAAGAAGCGTTATCT | 79582 |
rs115430324 | snp | A/G | 0.0452528 | 0.143452 | intron-variant | SPAG16 | GRCh38.p7 | 2:213442173 | CAAACCGAAACCACT[A/G]TATCATTTAGATTGG | 79582 |
rs115433158 | snp | A/C | 0.00279162 | 0.0372561 | intron-variant, upstream-variant-2KB | SPAG16 | GRCh38.p7 | 2:213315674 | CAGTTTGGCTTTTAT[A/C]TGCATGACTCTATTG | 79582 |
rs115433427 | snp | A/T | 0.0810805 | 0.184299 | intron-variant | SPAG16 | GRCh38.p7 | 2:214011042 | ACGTGACTTTCAGCA[A/T]TGCCTTTAGTTATAC | 79582 |
rs115436713 | snp | A/C | 0.0174175 | 0.0916809 | intron-variant, utr-variant-3-prime | SPAG16 | GRCh38.p7 | 2:213398781 | TTAACTCATTGTATC[A/C]CTTCCCACTAGAATG | 79582 |
rs115444265 | snp | A/G | 0.0240643 | 0.107019 | intron-variant | SPAG16 | GRCh38.p7 | 2:213558905 | GTTTCAATGCATGTC[A/G]TGACATCATGTCATT | 79582 |
rs115447005 | snp | A/G | 0.0244538 | 0.107838 | intron-variant | SPAG16 | GRCh38.p7 | 2:214382853 | AGCTTCATGAGATCC[A/G]CTTGTTTGGGCTTCT | 79582 |
rs115447919 | snp | G/T | 0.02016 | 0.0983543 | intron-variant | SPAG16 | GRCh38.p7 | 2:214398580 | TGAGAAAGTATGATG[G/T]AGAGAGGCTGAATAA | 79582 |
rs115452643 | snp | A/G | 0.0236746 | 0.106192 | intron-variant | SPAG16 | GRCh38.p7 | 2:213319952 | CTATTTCTCAAATCT[A/G]TCTCATTCAATAGAA | 79582 |
rs115454193 | snp | A/G | 0.00795532 | 0.062565 | intron-variant | SPAG16 | GRCh38.p7 | 2:214167418 | GGGGAGTGTTAGGAT[A/G]CCCATGAGCCAACAA | 79582 |
rs115455314 | snp | A/T | 0.0244538 | 0.107838 | intron-variant | SPAG16 | GRCh38.p7 | 2:213460647 | GAATGCATAGTAAAT[A/T]TGATATACATGTGCA | 79582 |
rs115457230 | snp | A/T | 0.0170251 | 0.090679 | intron-variant, upstream-variant-2KB | SPAG16 | GRCh38.p7 | 2:213297825 | TTTTGATTATAATAC[A/T]ATGAACTAAAAGTGC | 79582 |
rs115457306 | snp | C/T | 0.00358779 | 0.0422022 | intron-variant | SPAG16 | GRCh38.p7 | 2:213380864 | TCCTGTTCTGGACCT[C/T]ACTCAAAACTGGCAG | 79582 |
rs115457590 | snp | A/C | 0.0217236 | 0.101931 | intron-variant | SPAG16 | GRCh38.p7 | 2:213881719 | ACATGGGAGAAACTG[A/C]CCCCATGATTCAATT | 79582 |
rs115458991 | snp | A/C | 0.0130921 | 0.0798413 | intron-variant | SPAG16 | GRCh38.p7 | 2:213771382 | GTTAGATCACAAAAA[A/C]TTTCTCCTATTCTGT | 79582 |
rs115460561 | snp | C/G | 0.00914312 | 0.0669923 | intron-variant | SPAG16 | GRCh38.p7 | 2:213459867 | GTTATTCCACATAAC[C/G]TTGTTCATCATTACT | 79582 |
rs115461121 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | SPAG16 | GRCh38.p7 | 2:213977133 | ATGGGAGGGAACCAT[A/G]CAAAGATGTGAATAA | 79582 |
rs115465904 | snp | A/G | 0.0418186 | 0.138422 | intron-variant | SPAG16 | GRCh38.p7 | 2:213992343 | TTTGCATTTATGGTC[A/G]TCACAGCTATAATGA | 79582 |
rs115469421 | snp | A/T | 0.0217236 | 0.101931 | intron-variant | SPAG16 | GRCh38.p7 | 2:213620827 | ATTATATATATTTAA[A/T]TTTTGCTTATGATAA | 79582 |
rs115470200 | snp | C/T | 0.0329836 | 0.124112 | intron-variant | SPAG16 | GRCh38.p7 | 2:214068925 | ATAATACTTTATTCC[C/T]TAAGAAGTAAAGGTC | 79582 |
rs115470991 | snp | C/T | 0.030665 | 0.119967 | intron-variant | SPAG16 | GRCh38.p7 | 2:213982419 | TAATGAATTATGTTA[C/T]GATTTTATTGCCTTT | 79582 |
rs115473269 | snp | A/T | 1.6569e-05 | 0.00287824 | missense, nc-transcript-variant | SPAG16 | GRCh38.p7 | 2:213490044 | CCAGCAAAATTTGAC[A/T]ACAAGCTGAAAAACA | 79582 |
rs115473998 | snp | A/G | 0.0372196 | 0.131242 | intron-variant | SPAG16 | GRCh38.p7 | 2:213808965 | GGTAGAGTTTTATTG[A/G]AAAAAGGAGAATCTG | 79582 |
rs115476738 | snp | A/C | 0.00636936 | 0.0560724 | intron-variant | SPAG16 | GRCh38.p7 | 2:213377319 | AGAACAGTGAGGTGT[A/C]ATCATAATAACAACT | 79582 |
rs115480007 | snp | G/T | 0.151668 | 0.229849 | intron-variant | SPAG16 | GRCh38.p7 | 2:213991154 | GCTATCTCTCCCCTA[G/T]CCCCCACTCCCCGTC | 79582 |
rs115484135 | snp | C/G | 0.0581099 | 0.160244 | intron-variant | SPAG16 | GRCh38.p7 | 2:214005622 | AGATTTTATTTAGAT[C/G]TCACGTCTCCACTGA | 79582 |
rs115486849 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | SPAG16 | GRCh38.p7 | 2:213408911 | AAGGTTTTCAAGAAA[C/T]GTAGCTTGCTAAAAG | 79582 |
rs115502315 | snp | A/G | 0.0154538 | 0.0865337 | intron-variant | SPAG16 | GRCh38.p7 | 2:214299133 | GGGTGTGTAGTAAGA[A/G]ATGTTATAGTCAGGA | 79582 |
rs115502644 | snp | C/T | 0.0984431 | 0.198823 | intron-variant | SPAG16 | GRCh38.p7 | 2:213981702 | TATTAATGTGAAGAG[C/T]GCAACAAACCCATTA | 79582 |
rs115510886 | snp | C/T | 0.0693013 | 0.172766 | intron-variant | SPAG16 | GRCh38.p7 | 2:213902895 | CAAATGGGAGAAATT[C/T]GTCAAAACAAAGTGG | 79582 |
rs115512207 | snp | A/G | 0.0178098 | 0.0926698 | intron-variant | SPAG16 | GRCh38.p7 | 2:214399356 | TAATGGTGTAGTGAT[A/G]CTGATTTATCACTTA | 79582 |
rs115512313 | snp | A/G | 0.0154538 | 0.0865337 | intron-variant | SPAG16 | GRCh38.p7 | 2:213493393 | AATCATTGATGTATT[A/G]CTAGTTTGCATTTTC | 79582 |
rs115516463 | snp | C/T | 0.0217236 | 0.101931 | intron-variant | SPAG16 | GRCh38.p7 | 2:213424401 | TTTATTTTTTAAACC[C/T]GACTTTATGAACTAA | 79582 |
rs115516880 | snp | C/T | 0.0130921 | 0.0798413 | intron-variant | SPAG16 | GRCh38.p7 | 2:214382897 | TGACTGTTGCTGAAG[C/T]GTTTCATAAAGGAGC | 79582 |
rs115519923 | snp | C/T | 0.0023933 | 0.0345097 | intron-variant | SPAG16 | GRCh38.p7 | 2:214323892 | AAGAAACATTATATG[C/T]AAAGAAAGCTGCATA | 79582 |
rs115520602 | snp | A/G | 0.0322114 | 0.122752 | intron-variant | SPAG16 | GRCh38.p7 | 2:213920463 | CGTACACACATGTTG[A/G]CAATGTGATATATGT | 79582 |
rs115527375 | snp | A/G | 0.0103295 | 0.0711199 | intron-variant | SPAG16 | GRCh38.p7 | 2:214158364 | AATAAAATTTGATAT[A/G]AAAATATTATTTAAA | 79582 |
rs115531622 | snp | A/G | 0.0165278 | 0.0893908 | intron-variant | SPAG16 | GRCh38.p7 | 2:213633644 | TCTCCAGCTATTATT[A/G]TATTGGGACTATCTC | 79582 |
rs115533559 | snp | A/C | 0.00398564 | 0.0444627 | intron-variant | SPAG16 | GRCh38.p7 | 2:213499860 | TGTCTGTTTTCTCAA[A/C]AGTCATCCCCCAATT | 79582 |
rs115533670 | snp | A/G | 0.0023933 | 0.0345097 | intron-variant | SPAG16 | GRCh38.p7 | 2:214376955 | AAACATACACATGCA[A/G]GCACTTACAGACCAT | 79582 |
rs115536036 | snp | A/G | 0.00478085 | 0.0486577 | intron-variant | SPAG16 | GRCh38.p7 | 2:213774433 | CACATGGCATTTTTC[A/G]TGTGTCTGTCTGCAT | 79582 |
rs115539500 | snp | C/T | 0.00953873 | 0.0683987 | intron-variant | SPAG16 | GRCh38.p7 | 2:213711815 | GTGAGCCACCACGCC[C/T]GACCCGTTCTTACAA | 79582 |
rs115549625 | snp | C/G | 0.12932 | 0.218944 | intron-variant | SPAG16 | GRCh38.p7 | 2:213478053 | GTGTCTGGCATTTCC[C/G]CTTCTTGCACTCACT | 79582 |
rs115558987 | snp | C/T | 0.0154538 | 0.0865337 | intron-variant | SPAG16 | GRCh38.p7 | 2:214293420 | AGTAGTGTTCAAGTG[C/T]CAGTGATGGTGAGCT | 79582 |
rs115566555 | snp | C/T | 0.0170251 | 0.090679 | intron-variant | SPAG16 | GRCh38.p7 | 2:214234635 | TTGCATTTCTCTAAT[C/T]ATCAGTGATGTTGAG | 79582 |
rs115568846 | snp | C/T | 0.0166325 | 0.0896639 | intron-variant | SPAG16 | GRCh38.p7 | 2:214276619 | TGTTGAATGTTGTCC[C/T]TCAACCCTCTTCCAG | 79582 |
rs115571179 | snp | A/C | 0.0126979 | 0.078662 | intron-variant | SPAG16 | GRCh38.p7 | 2:213683735 | TTCAGCCTTGTTATG[A/C]CTTAATACTGATTCT | 79582 |
rs115578288 | snp | C/T | 0.00597247 | 0.0543191 | intron-variant | SPAG16 | GRCh38.p7 | 2:214345580 | CAAAAATGTTGAAAC[C/T]CGAAAGTTCTCTGAA | 79582 |
rs115578837 | snp | C/T | 0.0126979 | 0.078662 | intron-variant | SPAG16 | GRCh38.p7 | 2:214384285 | CAATCATTTTTGTTT[C/T]ATAAGTGGAATTTTC | 79582 |
rs115579773 | snp | A/G | 0.00636936 | 0.0560724 | intron-variant | SPAG16, LOC101928084 | GRCh38.p7 | 2:214100491 | TCACCCATGTAATAC[A/G]CATAGTACCTGATAA | 79582 |
rs115582826 | snp | A/T | 0.00993419 | 0.0697739 | intron-variant | SPAG16 | GRCh38.p7 | 2:214082362 | CCCAAAGACACAAGA[A/T]CTTTTACCTTCTCCT | 79582 |
rs115583734 | snp | C/T | 0.0138799 | 0.0821421 | intron-variant | SPAG16, LOC101928084 | GRCh38.p7 | 2:214091124 | CCTACTTCAATCCCA[C/T]TGAGCTAACCAGTGC | 79582 |
rs115583857 | snp | A/G | 0.0182019 | 0.0936463 | intron-variant | SPAG16 | GRCh38.p7 | 2:214267430 | AATGATATTAGGAAT[A/G]CTGGATATTCATATA | 79582 |
rs115590510 | snp | A/G | 0.0333695 | 0.124785 | intron-variant | SPAG16 | GRCh38.p7 | 2:213818217 | AAGCTGTTACCTTGC[A/G]CAGTAGATCTTTCAT | 79582 |
rs115591860 | snp | C/T | 0.00993419 | 0.0697739 | upstream-variant-2KB, intron-variant | SPAG16, LOC100130451 | GRCh38.p7 | 2:213283389 | AAATACTGCATGTTC[C/T]TAGTTGTAAGTGGGA | 79582 |
rs115596529 | snp | C/T | 0.0425829 | 0.139564 | intron-variant | SPAG16 | GRCh38.p7 | 2:214234040 | CTCCCTCCTCCCACC[C/T]GCCACCTTTCAATAG | 79582 |
rs115597882 | snp | A/G | 0.00358779 | 0.0422022 | intron-variant | SPAG16 | GRCh38.p7 | 2:213966304 | ATTTTCTTAAAAATT[A/G]TTTCTTCATTTGGAG | 79582 |
rs115598214 | snp | C/T | 0.0228947 | 0.104514 | intron-variant | SPAG16 | GRCh38.p7 | 2:213948302 | ACAGACACGCAAATG[C/T]ATTTCTGCATATAAT | 79582 |
rs115608598 | snp | A/G | 0.0126979 | 0.078662 | intron-variant | SPAG16 | GRCh38.p7 | 2:213939974 | AAGATGTAGAGTGAC[A/G]TAGTTGTTTTTCATA | 79582 |
rs115609075 | snp | A/C | 0.00835141 | 0.0640778 | intron-variant | SPAG16 | GRCh38.p7 | 2:214151693 | TTTTTTCTAGTCAAA[A/C]CTCTGTGACAGAACT | 79582 |
rs115611521 | snp | A/G | 0.0240643 | 0.107019 | intron-variant | SPAG16 | GRCh38.p7 | 2:213410863 | AATAAGTCGTACCAA[A/G]CTCTCTCTCTCTGCT | 79582 |
rs115621776 | snp | C/T | 0.0217236 | 0.101931 | intron-variant | SPAG16 | GRCh38.p7 | 2:213602045 | TGTGAGAATCTAATG[C/T]CACTACTGATCTGAC | 79582 |
rs115622331 | snp | A/G | 0.121022 | 0.21416 | intron-variant | SPAG16 | GRCh38.p7 | 2:213363269 | TATTCTAAATAAAAA[A/G]TTTATTTTTGAAATT | 79582 |
rs115626188 | snp | G/T | 0.00597247 | 0.0543191 | intron-variant | SPAG16 | GRCh38.p7 | 2:213465503 | TCACAGTCATGTTCA[G/T]GCTTCCCAAGTTTCT | 79582 |
rs115626363 | snp | A/G | 0.0178098 | 0.0926698 | intron-variant | SPAG16 | GRCh38.p7 | 2:214227948 | TGACTATTTGTAAAT[A/G]TAAAAGCAGCTCCCT | 79582 |
rs115627073 | snp | A/G | 0.0228947 | 0.104514 | intron-variant | SPAG16 | GRCh38.p7 | 2:213957695 | TTACTGTCTTCTTTT[A/G]TGTTTAGTTGACTTT | 79582 |
rs115634964 | snp | C/T | 0.0197687 | 0.0974348 | intron-variant | SPAG16 | GRCh38.p7 | 2:214241227 | CCGGGTGTGGCGATG[C/T]GCGACTGTAGTTCCC | 79582 |
rs115639606 | snp | C/G | 0.0248432 | 0.108648 | intron-variant | SPAG16 | GRCh38.p7 | 2:214053050 | GAGTTCACATGGGAC[C/G]AAAAATTGATTTAAG | 79582 |
rs115640695 | snp | A/G | 0.0248432 | 0.108648 | intron-variant | SPAG16 | GRCh38.p7 | 2:213603542 | AATTATCTAATATTC[A/G]CTAAAAGAGATTTAA | 79582 |
rs115641154 | snp | G/T | 0.0244538 | 0.107838 | intron-variant | SPAG16 | GRCh38.p7 | 2:213470570 | CATATTGTGGGCTCA[G/T]TGTTGGTCTCTGCTG | 79582 |
rs115646195 | snp | A/T | 0.0279526 | 0.114869 | intron-variant | SPAG16 | GRCh38.p7 | 2:213578722 | AGTTTTCCTACATTA[A/T]TATGGAGACAGATGA | 79582 |
rs115647255 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | SPAG16 | GRCh38.p7 | 2:213610497 | GTTCTCCCCATCCCA[C/T]AACCTTTTTATCACC | 79582 |
rs115647542 | snp | A/G | 0.0115144 | 0.0749975 | intron-variant | SPAG16 | GRCh38.p7 | 2:213628022 | AAGAGAAAGTAAGAC[A/G]TGAGCCTTAGCATTG | 79582 |
rs115648797 | snp | A/G | 0.0182019 | 0.0936463 | intron-variant | SPAG16 | GRCh38.p7 | 2:214248100 | AAAACACAAAATAGA[A/G]CAATCTCTAGTTCAG | 79582 |
rs115651386 | snp | C/T | 0.00478085 | 0.0486577 | intron-variant | SPAG16 | GRCh38.p7 | 2:213787403 | TTACCTTATTCTAAG[C/T]AATTTTCATATATTA | 79582 |
rs115655395 | snp | C/T | 0.00953873 | 0.0683987 | intron-variant | SPAG16 | GRCh38.p7 | 2:214033926 | AAATTTGTTAACCTG[C/T]CCCAATAGTGCCTTT | 79582 |
rs115655613 | snp | A/G | 0.0267878 | 0.112589 | intron-variant | SPAG16 | GRCh38.p7 | 2:213706894 | AGTCATTAACATGGC[A/G]GTCAAGTTGCTGATG | 79582 |
rs115657980 | snp | C/T | 0.0126979 | 0.078662 | intron-variant | SPAG16 | GRCh38.p7 | 2:213922778 | GACTGGCTTTGATTC[C/T]AGTACACTACTGGGT | 79582 |
rs115663291 | snp | C/T | 0.00993419 | 0.0697739 | intron-variant | SPAG16 | GRCh38.p7 | 2:214385945 | TCAACAATAAAGTCA[C/T]TGTATTGAATTTGCT | 79582 |
rs115664004 | snp | C/G | 0.0248432 | 0.108648 | intron-variant | SPAG16 | GRCh38.p7 | 2:213781446 | GTTTCTTCCTGCCTT[C/G]TTAATGCTTTCATGT | 79582 |
rs115665464 | snp | A/G | 0.0248432 | 0.108648 | intron-variant | SPAG16 | GRCh38.p7 | 2:213389439 | AAAATTTGGGGCATC[A/G]AAAGACTGTCATCAG | 79582 |
rs115666517 | snp | A/T | 0.0154538 | 0.0865337 | intron-variant | SPAG16 | GRCh38.p7 | 2:213805524 | AAGTACCTTTTAGGT[A/T]TTTAGAAGAGTTATC | 79582 |
rs115677452 | snp | C/G | 0.0240643 | 0.107019 | intron-variant, utr-variant-5-prime | SPAG16 | GRCh38.p7 | 2:213296666 | GCGAGCCTGGGTGAG[C/G]AAGAGACAGGATGAA | 79582 |
rs115680536 | snp | A/G | 0.0240643 | 0.107019 | intron-variant | SPAG16 | GRCh38.p7 | 2:213329913 | CAGCCATGACTAAAA[A/G]GGGCCAAGGTACAGC | 79582 |
rs115680712 | snp | A/G | 0.0448719 | 0.142907 | intron-variant | SPAG16 | GRCh38.p7 | 2:213663579 | CAGCAATTTGATAAC[A/G]TATACATAAAACATC | 79582 |
rs115684900 | snp | C/T | 0.0193772 | 0.0965046 | intron-variant | SPAG16 | GRCh38.p7 | 2:214083251 | GTCCAGGGCCTCTCA[C/T]AGACACATCCCCAAA | 79582 |
rs115687795 | snp | A/C | 0.00636936 | 0.0560724 | intron-variant, utr-variant-5-prime | SPAG16 | GRCh38.p7 | 2:213300926 | TAATATAAAAAAGTT[A/C]TCTTGCTATTATGTT | 79582 |
rs115693394 | snp | A/G | 0.00676609 | 0.0577691 | intron-variant | SPAG16 | GRCh38.p7 | 2:214133152 | AAACCTACCATTAGC[A/G]TAGAGCAAGGTTTGG | 79582 |
rs115694552 | snp | A/G | 0.0178098 | 0.0926698 | intron-variant, upstream-variant-2KB | SPAG16, MIR4438 | GRCh38.p7 | 2:213756914 | TTTTGAATGTTTAGC[A/G]TATGAAACCCTTATG | 79582 |
rs115704267 | snp | C/T | 0.00318978 | 0.0398085 | intron-variant | SPAG16 | GRCh38.p7 | 2:213775814 | AATTATCCTTTACCT[C/T]AGATTTATTAAGTGG | 79582 |
rs115714695 | snp | C/T | 0.0178098 | 0.0926698 | intron-variant | SPAG16 | GRCh38.p7 | 2:214401824 | GTAACATGTTCAAAC[C/T]TATAAGTGAATTTTG | 79582 |
rs115717688 | snp | G/T | 0.0228947 | 0.104514 | intron-variant | SPAG16 | GRCh38.p7 | 2:213911649 | CATAAACTGCAAAAA[G/T]AATTTTCAGAGGACT | 79582 |
rs115721005 | snp | C/T | 0.0170251 | 0.090679 | intron-variant | SPAG16 | GRCh38.p7 | 2:214257932 | CTGAAACCATATGGG[C/T]GTATAGTTTTTCTTT | 79582 |
rs115726186 | snp | A/T | 0.0158469 | 0.0875917 | intron-variant | SPAG16 | GRCh38.p7 | 2:213810610 | ATAATTTGAAGATAT[A/T]GAGGACAATTCAGAA | 79582 |
rs115729526 | snp | C/T | 0.0103295 | 0.0711199 | intron-variant | SPAG16 | GRCh38.p7 | 2:213969515 | TTAGGCCTTTATAAA[C/T]GAAGCTTCACATAGC | 79582 |
rs115742741 | snp | C/G | 0.00953873 | 0.0683987 | intron-variant, upstream-variant-2KB | SPAG16 | GRCh38.p7 | 2:213315978 | TTCTTTCTTTACTTT[C/G]ATTTCCCACTGCCTA | 79582 |
rs115746295 | snp | A/G | 0.0391387 | 0.134304 | intron-variant | SPAG16 | GRCh38.p7 | 2:214386232 | ATACAAAACTTAGCC[A/G]GGCATGGTGGCATTC | 79582 |
rs115746723 | snp | A/G | 0.0221141 | 0.102801 | intron-variant | SPAG16 | GRCh38.p7 | 2:213877671 | TTGTGAACTTAGGGA[A/G]AGGATGAGGATACCA | 79582 |
rs115748773 | snp | C/T | 0.0217236 | 0.101931 | intron-variant | SPAG16 | GRCh38.p7 | 2:213900890 | TCCCATAACTATATC[C/T]TGTGTTTTCATATAT | 79582 |
rs115749371 | snp | A/G | 0.0162398 | 0.0886349 | intron-variant | SPAG16 | GRCh38.p7 | 2:213637146 | TATGCTGATTTTGCT[A/G]AGGGTTTAAATCATA | 79582 |
rs115751088 | snp | C/T | 0.0150606 | 0.0854603 | intron-variant | SPAG16 | GRCh38.p7 | 2:214324973 | TCTGCTACCATTTTA[C/T]GCAGGAAATGACATT | 79582 |
rs115752331 | snp | A/G | 0.0295035 | 0.117819 | intron-variant | SPAG16 | GRCh38.p7 | 2:213588945 | TAGAATTGCTGGTTT[A/G]GAAAAATCAGTTCAA | 79582 |
rs115754199 | snp | A/T | 0.0119091 | 0.0762411 | intron-variant | SPAG16 | GRCh38.p7 | 2:213553317 | ATATGGAGAATATCC[A/T]CATAGAATCACTGGT | 79582 |
rs115756890 | snp | A/G | 0.0452528 | 0.143452 | intron-variant | SPAG16 | GRCh38.p7 | 2:213473053 | TTTCACTGAGGGGCC[A/G]TGATTCTCTGTTTTT | 79582 |
rs115757467 | snp | C/T | 0.0165278 | 0.0893908 | intron-variant | SPAG16 | GRCh38.p7 | 2:213679075 | TTCCTTAACGAAGGA[C/T]ACCTTCTCTGCATGC | 79582 |
rs115759158 | snp | A/T | 0.00517822 | 0.0506191 | intron-variant | SPAG16 | GRCh38.p7 | 2:214285121 | TTCTCTTTCCTCATA[A/T]TCTTGCCAATATGTA | 79582 |
rs115759827 | snp | C/T | 0.0146672 | 0.084371 | intron-variant | SPAG16 | GRCh38.p7 | 2:214235491 | ACTTAACTTGTCCTT[C/T]GAGCATTGAGATGTC | 79582 |
rs115759947 | snp | A/T | 0.0119091 | 0.0762411 | intron-variant | SPAG16 | GRCh38.p7 | 2:213388221 | CTGCAAATATCAGGG[A/T]TCTGTGCTCTTATCT | 79582 |
rs115762542 | snp | A/T | 0.00517822 | 0.0506191 | intron-variant | SPAG16 | GRCh38.p7 | 2:214245095 | TCTATCTATAAATTA[A/T]GCATGTCTTCAAATA | 79582 |
rs115765402 | snp | C/T | 0.00716266 | 0.059414 | intron-variant | SPAG16 | GRCh38.p7 | 2:213699164 | TTCTGCTTCACCTTT[C/T]CTATTACTCTTGTAT | 79582 |
rs115765862 | snp | G/T | 0.0644693 | 0.167566 | intron-variant | SPAG16 | GRCh38.p7 | 2:213750916 | CTTCTGGACCACCGA[G/T]GATACATTAACTCCT | 79582 |
rs115767716 | snp | G/T | 0.0178098 | 0.0926698 | intron-variant | SPAG16 | GRCh38.p7 | 2:214227774 | TTTAATTTTCCTATC[G/T]TATTATTTTCTTCCC | 79582 |
rs115769660 | snp | C/T | 0.0142736 | 0.0832652 | intron-variant, upstream-variant-2KB | SPAG16, LOC101928084 | GRCh38.p7 | 2:214103625 | ACAAAGGCGGGAGCA[C/T]TCCAGGCAGTTAGAA | 79582 |
rs115773095 | snp | C/G | 0.00874735 | 0.0655527 | intron-variant | SPAG16 | GRCh38.p7 | 2:213825905 | TTTTCTTTGCTGGGA[C/G]AGTTTTTATTATGGC | 79582 |
rs115775415 | snp | A/G | 0.00318978 | 0.0398085 | intron-variant | SPAG16 | GRCh38.p7 | 2:213322820 | ACCTGAAGAGACTGA[A/G]GGAAAAAGCCAAGTA | 79582 |
rs115778262 | snp | A/G | 0.0119091 | 0.0762411 | intron-variant | SPAG16 | GRCh38.p7 | 2:214308535 | GTAACAATCTTTTCT[A/G]TCCATCTTTAATGCT | 79582 |
rs115781709 | snp | A/G | 0.0228947 | 0.104514 | intron-variant | SPAG16 | GRCh38.p7 | 2:213701441 | GCCTCCTCGGTCTCG[A/G]TGTCCACTCTGGCCA | 79582 |
rs115783396 | snp | A/G | 0.00835141 | 0.0640778 | intron-variant | SPAG16 | GRCh38.p7 | 2:213886374 | GAGGAGAGTGGTGGC[A/G]GGTAGAATGAGCAGC | 79582 |
rs115785239 | snp | C/T | 0.0193772 | 0.0965046 | intron-variant | SPAG16 | GRCh38.p7 | 2:213671562 | TGCTGTCTCCCATCT[C/T]CTCCATAAGATTTCT | 79582 |
rs115787196 | snp | C/T | 0.00159617 | 0.0282053 | intron-variant | SPAG16 | GRCh38.p7 | 2:214176097 | GATAAATTCATCTTT[C/T]AATGTATGGATACCT | 79582 |
rs115789723 | snp | C/T | 0.0138799 | 0.0821421 | intron-variant | SPAG16, LOC101928084 | GRCh38.p7 | 2:214098585 | CTTTGAGCTTGGATT[C/T]CTAGCCTCTACAACT | 79582 |
rs115790316 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | SPAG16 | GRCh38.p7 | 2:214068886 | ACACCTTATCCATTA[A/T]ACTATGAACTTCTTT | 79582 |
rs115794610 | snp | A/G | 0.0142736 | 0.0832652 | intron-variant | SPAG16 | GRCh38.p7 | 2:214044593 | AGGTGAGCATTCAGA[A/G]TACCTGCTTTTAACT | 79582 |
rs115798990 | snp | C/G | 0.030665 | 0.119967 | intron-variant | SPAG16 | GRCh38.p7 | 2:213545510 | GTGAACTCTGCCTTT[C/G]GTATTGTATCAAAAT | 79582 |
rs115800747 | snp | A/G | 0.0410537 | 0.137264 | intron-variant | SPAG16 | GRCh38.p7 | 2:213623645 | TTAAATGGATGAAGA[A/G]ACAAATTGTTCCAGT | 79582 |
rs115804801 | snp | A/G | 0.0452528 | 0.143452 | intron-variant | SPAG16 | GRCh38.p7 | 2:213439291 | TTAAAAAGGGGAGCG[A/G]CTTTGGAACCAGGCA | 79582 |
rs115807246 | snp | C/T | 0.0244538 | 0.107838 | intron-variant | SPAG16 | GRCh38.p7 | 2:213459955 | TGTAGATTTTACCCC[C/T]ACTGAATAATTTCAA | 79582 |
rs115812239 | snp | A/G | 0.0275645 | 0.114116 | intron-variant | SPAG16 | GRCh38.p7 | 2:213362822 | AGAGGTTTATTTGGC[A/G]CATGGTTCTGCAGGC | 79582 |
rs115814562 | snp | A/G | 0.00716266 | 0.059414 | intron-variant | SPAG16 | GRCh38.p7 | 2:213519035 | TGAGCACACATAGAC[A/G]TAAACTTGGGAATAA | 79582 |
rs115816859 | snp | A/C/G | 0.00318978 | 0.0398085 | intron-variant | SPAG16 | GRCh38.p7 | 2:213563402 | TATACTATAGACTAG[A/C/G]TGGCTTTAATAACAG | 79582 |
rs115822680 | snp | C/G | 0.0244538 | 0.107838 | intron-variant | SPAG16 | GRCh38.p7 | 2:213451755 | AACTGGTTAGGACCG[C/G]GTGTGCCGTATGTTG | 79582 |
rs115824678 | snp | G/T | 0.0240643 | 0.107019 | intron-variant | SPAG16 | GRCh38.p7 | 2:213319958 | CTCAAATCTATCTCA[G/T]TCAATAGAACTTAAA | 79582 |
rs115831442 | snp | A/G | 0.0217236 | 0.101931 | intron-variant | SPAG16 | GRCh38.p7 | 2:213564007 | AAGGGAGCTTTGTGA[A/G]TAAAAAGAAGATAAC | 79582 |
rs115833377 | snp | A/G | 0.00835141 | 0.0640778 | intron-variant | SPAG16 | GRCh38.p7 | 2:213499254 | CTAAAGTATGTTTCT[A/G]TACTATACTAGAGCT | 79582 |
rs115833633 | snp | C/T | 0.00318978 | 0.0398085 | intron-variant | SPAG16 | GRCh38.p7 | 2:213562744 | TGATGCCTGGTGAGG[C/T]CAATGTCATATTTAT | 79582 |
rs115839728 | snp | A/T | 0.0562307 | 0.157967 | intron-variant | SPAG16 | GRCh38.p7 | 2:214007420 | GGACAATATAGCAAG[A/T]CTCTATCTCTACAAA | 79582 |
rs115849287 | snp | A/T | 0.0314385 | 0.121371 | upstream-variant-2KB, intron-variant, downstream-variant-500B | VWC2L, SPAG16 | GRCh38.p7 | 2:214410866 | TGCAGATGGCTTAAA[A/T]CTAAATGCAAGCCTC | 79582 |
rs115849789 | snp | A/G | 0.0115144 | 0.0749975 | intron-variant, downstream-variant-500B | SPAG16 | GRCh38.p7 | 2:214238525 | GTGCCAAGTTCATAC[A/G]GCAACACTGTAATTG | 79582 |
rs115852888 | snp | A/G | 0.0566069 | 0.158427 | intron-variant | SPAG16 | GRCh38.p7 | 2:214249105 | GGCAAAGAAATATAA[A/G]TTTATACCCAAACAC | 79582 |
rs115855996 | snp | C/T | 0.0182019 | 0.0936463 | intron-variant | SPAG16 | GRCh38.p7 | 2:213986873 | AGTTTCTAGTCAATT[C/T]GTCTGCCTCTGGTAT | 79582 |
rs115858537 | snp | C/T | 0.0166325 | 0.0896639 | intron-variant | SPAG16 | GRCh38.p7 | 2:213801218 | GAGGAAGGAGCTTTG[C/T]GTGTGTGTGTGCGTG | 79582 |
rs115864007 | snp | G/T | 0.00914312 | 0.0669923 | intron-variant | SPAG16 | GRCh38.p7 | 2:213573897 | CTAAACCAGTGTGAA[G/T]CAGACTTTAATGTGC | 79582 |
rs115881514 | snp | C/T | 0.00318978 | 0.0398085 | intron-variant, utr-variant-3-prime | SPAG16 | GRCh38.p7 | 2:213369789 | TACAGTGATTTTCCA[C/T]ATACCACCTGCCCCC | 79582 |
rs115884673 | snp | C/G/T | 0.00358891 | 0.0422285 | intron-variant | SPAG16 | GRCh38.p7 | 2:213678556 | GCTCTTAACCACTAT[C/G/T]GGTACACCTTCAGAA | 79582 |
rs115886046 | snp | G/T | 0.00557542 | 0.0525036 | intron-variant | SPAG16 | GRCh38.p7 | 2:214134016 | GAATTTAAGAGAGAG[G/T]TGTGAATTGGAGATG | 79582 |
rs115887551 | snp | G/T | 0.00318978 | 0.0398085 | intron-variant | SPAG16 | GRCh38.p7 | 2:213683644 | CATTGAAATACATTC[G/T]GTTCTTATATATTTT | 79582 |
rs115891708 | snp | A/G | 0.0221141 | 0.102801 | intron-variant | SPAG16 | GRCh38.p7 | 2:213849517 | ATTTATAAAATAGAT[A/G]CAAAAAAGTCATTAT | 79582 |
rs115898678 | snp | A/G | 0.00517822 | 0.0506191 | intron-variant | SPAG16 | GRCh38.p7 | 2:214014743 | AAACAAGATCATGAC[A/G]TATTTGATTAAAGTC | 79582 |
rs115901508 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | SPAG16 | GRCh38.p7 | 2:213895893 | TGTGTTTCATACTGT[A/G]AAAGCACAGGCAACT | 79582 |
rs115903502 | snp | A/G | 0.0170251 | 0.090679 | intron-variant | SPAG16 | GRCh38.p7 | 2:214216694 | ATTTTCCAAATTTTG[A/G]GTAAAGACTAATATT | 79582 |
rs115908031 | snp | C/T | 0.102726 | 0.202016 | intron-variant | SPAG16 | GRCh38.p7 | 2:214406578 | ATATTAGTGAAACTA[C/T]TTATTAAAATAAATA | 79582 |
rs115909964 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | SPAG16 | GRCh38.p7 | 2:213839690 | GAATGTGACATTATT[G/T]TTGTACAGCAGTAAA | 79582 |
rs115911488 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | SPAG16 | GRCh38.p7 | 2:213828887 | TTTCTCCTGAATAGA[A/G]TCCCTCTCTCTGTGC | 79582 |
rs115914685 | snp | G/T | 0.00358779 | 0.0422022 | intron-variant | SPAG16 | GRCh38.p7 | 2:213821517 | ATCAAAGTAAATGGG[G/T]TATCCATTCTTTCAA | 79582 |
rs115915142 | snp | C/G | 0.0123036 | 0.0774623 | intron-variant | SPAG16 | GRCh38.p7 | 2:214372640 | TGGAGAGGATTACAT[C/G]GATTTCAGAGACTTA | 79582 |
rs115919148 | snp | C/T | 0.00358779 | 0.0422022 | intron-variant | SPAG16 | GRCh38.p7 | 2:213796515 | CATTCTATGGATATA[C/T]AGTCATGTGCCACCT | 79582 |
rs115921401 | snp | A/G | 0.0158469 | 0.0875917 | intron-variant | SPAG16 | GRCh38.p7 | 2:213828761 | AGTACCCAAAGCCCC[A/G]TAAAGCTGTGGTTCT | 79582 |
rs115926794 | snp | C/T | 0.0379877 | 0.132479 | intron-variant | SPAG16 | GRCh38.p7 | 2:214308723 | ATTGGCCCCCATTCT[C/T]TTCTGGCTTGTAGAG | 79582 |
rs115930594 | snp | A/T | 0.00478085 | 0.0486577 | intron-variant | SPAG16 | GRCh38.p7 | 2:213931073 | CTTTCTTGAAGTTGT[A/T]ATCTCCATGATATTT | 79582 |
rs115941134 | snp | G/T | 0.00159617 | 0.0282053 | intron-variant, upstream-variant-2KB | SPAG16, LOC101928084 | GRCh38.p7 | 2:214104246 | AGTGGTAAAGGATGA[G/T]GTCAGATACAGAGAC | 79582 |
rs115943599 | snp | C/T | 0.0142736 | 0.0832652 | intron-variant | SPAG16 | GRCh38.p7 | 2:214075526 | ACATAAACTCACCAA[C/T]TTAAACGCTTGTGAT | 79582 |
rs115944963 | snp | C/T | 0.0425829 | 0.139564 | intron-variant, utr-variant-3-prime | SPAG16 | GRCh38.p7 | 2:213397523 | TTAAAAAAATTAATC[C/T]CCGTGATATTGTCAC | 79582 |
rs115946325 | snp | G/T | 0.0240643 | 0.107019 | intron-variant | SPAG16 | GRCh38.p7 | 2:213566150 | AATGGGTTGCTGGAG[G/T]GAAGGAGGAGGTAAT | 79582 |
rs115948367 | snp | C/G | 0.00517822 | 0.0506191 | intron-variant | SPAG16 | GRCh38.p7 | 2:213810265 | AAGGTCCAGGATTTT[C/G]TGGTTTAAGAGTATT | 79582 |
rs115954971 | snp | G/T | 0.0165278 | 0.0893908 | intron-variant | SPAG16 | GRCh38.p7 | 2:213614482 | CAACCCTTGATGCCT[G/T]GCTTATTGCAGATAC | 79582 |
rs115955748 | snp | G/T | 0.0178098 | 0.0926698 | intron-variant | SPAG16 | GRCh38.p7 | 2:214271778 | GCACTCCAGCCTGAG[G/T]GGCAAGAGTGAAACT | 79582 |
rs115956215 | snp | C/T | 0.0170251 | 0.090679 | intron-variant | SPAG16 | GRCh38.p7 | 2:214232653 | AAATGCATGTTTGGA[C/T]AGTAGTTCATTTTAA | 79582 |
rs115957310 | snp | G/T | 0.0217236 | 0.101931 | intron-variant | SPAG16 | GRCh38.p7 | 2:213597196 | TATTTTTAATAAAAT[G/T]TATTCATTCATTCAC | 79582 |
rs115959820 | snp | A/C | 0.0150606 | 0.0854603 | intron-variant | SPAG16 | GRCh38.p7 | 2:214292094 | TTTCTCCTGGCCTAA[A/C]AGGTTTCTGCTGAGC | 79582 |
rs115962248 | snp | A/G | 0.00716266 | 0.059414 | intron-variant | SPAG16 | GRCh38.p7 | 2:214127502 | AATACTGGTCTATCC[A/G]AGGAGGAGGAGAGTT | 79582 |
rs115962591 | snp | A/T | 0.0356815 | 0.128715 | intron-variant | SPAG16 | GRCh38.p7 | 2:213502292 | CAGCTATTTAAAAAA[A/T]TTTTTTTTTCTGTAG | 79582 |
rs115963450 | snp | A/G | 0.0130921 | 0.0798413 | intron-variant | SPAG16 | GRCh38.p7 | 2:213915063 | GGCAGAAGGTGAATG[A/G]GAATCAAAGTCACGT | 79582 |
rs115969401 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | SPAG16 | GRCh38.p7 | 2:213636427 | AGTCTTGTTTTGATC[A/G]TGTGTGTGCACTCAT | 79582 |
rs115975361 | snp | A/T | 0.0209421 | 0.100162 | intron-variant | SPAG16 | GRCh38.p7 | 2:213920469 | CACATGTTGGCAATG[A/T]GATATATGTGGTGGC | 79582 |
rs115976339 | snp | C/T | 0.0225045 | 0.103662 | intron-variant | SPAG16 | GRCh38.p7 | 2:213674381 | TGCTCTTTTTTTTTT[C/T]CATTATTTTTTATTA | 79582 |
rs115978658 | snp | A/G | 0.0217236 | 0.101931 | intron-variant | SPAG16 | GRCh38.p7 | 2:213938354 | AAAAATGAAAATCAC[A/G]TTTGTTTTATATTTA | 79582 |
rs115979207 | snp | A/G | 0.0123036 | 0.0774623 | intron-variant | SPAG16 | GRCh38.p7 | 2:214400499 | TACACAGGAGGATAC[A/G]CATAGGTTATATGCA | 79582 |
rs115981530 | snp | C/T | 0.0399052 | 0.1355 | intron-variant | SPAG16 | GRCh38.p7 | 2:214046427 | AGTCAATGTCACTGA[C/T]GAATATTGATACAAA | 79582 |
rs115989117 | snp | A/G | 0.0130921 | 0.0798413 | intron-variant | SPAG16 | GRCh38.p7 | 2:214325913 | AACCACAATTAAACT[A/G]CCCTCCATGAGCATA | 79582 |
rs115991929 | snp | C/G | 0.0232847 | 0.105357 | intron-variant | SPAG16 | GRCh38.p7 | 2:214269435 | TGAGCATAGAATTGT[C/G]TGTGCACACTAATGT | 79582 |
rs115992160 | snp | A/G | 0.039522 | 0.134904 | intron-variant | SPAG16 | GRCh38.p7 | 2:214254922 | AAAGTAAAATAAAAT[A/G]AAATAAAGAACACTG | 79582 |
rs115995957 | snp | A/G | 0.021333 | 0.101051 | intron-variant | SPAG16 | GRCh38.p7 | 2:213902411 | TCAGAATCATGGTGG[A/G]TGCTGAAAGGCACTT | 79582 |
rs115996985 | snp | A/T | 0.00478085 | 0.0486577 | intron-variant | SPAG16 | GRCh38.p7 | 2:214007283 | ATAATTCTTTACAGA[A/T]TGAAATGCCTCAGTT | 79582 |
rs116000313 | snp | C/T | 0.00636936 | 0.0560724 | intron-variant, upstream-variant-2KB | SPAG16 | GRCh38.p7 | 2:213295366 | CTTAAAGCAGTTCTC[C/T]TAGAATTATTTTATG | 79582 |
rs116003052 | snp | A/C | 0.0209421 | 0.100162 | intron-variant | SPAG16 | GRCh38.p7 | 2:214012135 | CATTGCAGAGTTTTG[A/C]CCACTACACTATATT | 79582 |
rs116005979 | snp | A/G | 0.0562307 | 0.157967 | intron-variant | SPAG16 | GRCh38.p7 | 2:214008474 | CTGGGGCTGGGTGTA[A/G]TGGCTCACGCCTGTA | 79582 |
rs116008680 | snp | A/C | 0.0341408 | 0.126114 | intron-variant | SPAG16 | GRCh38.p7 | 2:214020680 | GATGATCTGTACTTA[A/C]CAATGTGCAGGCTGA | 79582 |
rs116010665 | snp | C/G | 0.0418186 | 0.138422 | intron-variant | SPAG16 | GRCh38.p7 | 2:213432759 | CATTCTATTAGGCCA[C/G]TATCTCCCTGATACC | 79582 |
rs116017400 | snp | C/G | 0.030665 | 0.119967 | intron-variant | SPAG16 | GRCh38.p7 | 2:213565084 | ACTCAAATAAGATGT[C/G]TCAGTGTTACTTTCT | 79582 |
rs116023171 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | SPAG16 | GRCh38.p7 | 2:214207537 | CAAAAGGTGGCCTTA[G/T]TTTCATTGATTTCTC | 79582 |
rs116024076 | snp | A/T | 0.0162398 | 0.0886349 | intron-variant | SPAG16 | GRCh38.p7 | 2:214150746 | AATTAATAATAGCCA[A/T]GTATTTTATTGTCAT | 79582 |
rs116030891 | snp | A/C | 0.0023933 | 0.0345097 | intron-variant | SPAG16 | GRCh38.p7 | 2:214347386 | GAAAAAACATAAAGG[A/C]TCAAGGTAGTCTTAT | 79582 |
rs116036608 | snp | A/G | 0.078151 | 0.181571 | intron-variant | SPAG16 | GRCh38.p7 | 2:213901609 | CTCAATATTTAGTCC[A/G]AAGAAAACATGTAAA | 79582 |
rs116041455 | snp | A/G | 0.00318978 | 0.0398085 | intron-variant | SPAG16 | GRCh38.p7 | 2:213696742 | GAAGTTGGTCTGGAG[A/G]GGTGTCATTTGTTAT | 79582 |
rs116050468 | snp | A/G | 0.0150606 | 0.0854603 | intron-variant | SPAG16 | GRCh38.p7 | 2:213471865 | CTTTCTTGGTTGTAG[A/G]TGGGGTCAAATTCAG | 79582 |
rs116058248 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | SPAG16 | GRCh38.p7 | 2:213517242 | AAATACTTAGGAATA[C/T]AGCTAACCAAAGAGG | 79582 |
rs116062135 | snp | A/G | 0.00279162 | 0.0372561 | intron-variant | SPAG16 | GRCh38.p7 | 2:213599179 | CTAAAAACACAAATA[A/G]CCTAATGATTACAGA | 79582 |
rs116062348 | snp | A/G | 0.0872718 | 0.189788 | intron-variant | SPAG16 | GRCh38.p7 | 2:213564517 | AAAAAAAAAAAGAGT[A/G]TGTCATTAACTTTTT | 79582 |
rs116064848 | snp | C/T | 0.00557542 | 0.0525036 | intron-variant | SPAG16 | GRCh38.p7 | 2:214342575 | GCAGGAAAACACGCT[C/T]AGGGCTCCCACTGAG | 79582 |
rs116067379 | snp | C/T | 0.0185938 | 0.0946107 | intron-variant | SPAG16 | GRCh38.p7 | 2:214257071 | TTTAGTGTTCTTTAA[C/T]TTCTCTAAGCAATTT | 79582 |
rs116074009 | snp | G/T | 0.0205511 | 0.0992634 | intron-variant | SPAG16 | GRCh38.p7 | 2:213819748 | TTGTTTGATTGTTTG[G/T]TTGGTTGGTTGGTTG | 79582 |
rs116075104 | snp | C/T | 0.02016 | 0.0983543 | intron-variant | SPAG16 | GRCh38.p7 | 2:214158617 | CTTTACAAATTGCAG[C/T]ATTATGCAGGTGCAG | 79582 |
rs116079915 | snp | A/C | 0.0279526 | 0.114869 | intron-variant | SPAG16 | GRCh38.p7 | 2:214247382 | ACTGGATTAGTGTGG[A/C]TATCTAGAATGTTAG | 79582 |
rs116085995 | snp | A/G | 0.00597247 | 0.0543191 | intron-variant | SPAG16 | GRCh38.p7 | 2:214401081 | TTGATCAGCAGTAAG[A/G]TACAAAATAAACTAA | 79582 |
rs116088743 | snp | C/G | 0.00318978 | 0.0398085 | intron-variant | SPAG16 | GRCh38.p7 | 2:213655717 | ATAAATTTCTTGTTG[C/G]TTCCCCTTGGTTGAT | 79582 |
rs116090845 | snp | A/G | 0.0209421 | 0.100162 | intron-variant | SPAG16 | GRCh38.p7 | 2:213701596 | CCATCGACCTTCCAA[A/G]GGCTGAGGAGTGCAG | 79582 |
rs116094788 | snp | A/G | 0.0134861 | 0.0810011 | intron-variant | SPAG16 | GRCh38.p7 | 2:214310149 | TCTTCTAAAGAAACC[A/G]TCATTTTCTTTCTTT | 79582 |
rs116095108 | snp | C/T | 0.0337553 | 0.125452 | intron-variant | SPAG16 | GRCh38.p7 | 2:214289543 | TAAGTTGGCAATAAA[C/T]ATATGGATTTACTTC | 79582 |
rs116097165 | snp | A/G | 0.0209421 | 0.100162 | intron-variant | SPAG16 | GRCh38.p7 | 2:214346708 | CAAAGCTCAATTCCC[A/G]TGAGACTACAATTTT | 79582 |
rs116100812 | snp | C/T | 0.0111196 | 0.0737302 | intron-variant | SPAG16 | GRCh38.p7 | 2:213848868 | GCTTGTGGCCTATGA[C/T]GCAACTGAAATATGA | 79582 |
rs116102288 | snp | A/G | 0.00478085 | 0.0486577 | intron-variant | SPAG16 | GRCh38.p7 | 2:213825823 | TTGGGATAGTTTTAG[A/G]GGGATTGGTATTAGG | 79582 |
rs116103249 | snp | C/G | 0.0425829 | 0.139564 | intron-variant | SPAG16 | GRCh38.p7 | 2:214244545 | TGATAAAAAACAAAC[C/G]CACAAAAAATCATAC | 79582 |
rs116112130 | snp | A/G | 0.030278 | 0.119257 | intron-variant | SPAG16 | GRCh38.p7 | 2:213482471 | CAGTAGTAAGATTAT[A/G]AGCATTTTCTTATTT | 79582 |
rs116118255 | snp | A/G | 0.00398564 | 0.0444627 | intron-variant | SPAG16 | GRCh38.p7 | 2:213867299 | AAATGGTAAATGAAT[A/G]GATCAATGCAGGGAA | 79582 |
rs116119403 | snp | A/C | 0.021333 | 0.101051 | intron-variant | SPAG16 | GRCh38.p7 | 2:213903441 | GCTTGGAGCTTGCAC[A/C]CTCTGCAAGCCATGG | 79582 |
rs116126965 | snp | C/G | 0.0265466 | 0.11211 | intron-variant | SPAG16 | GRCh38.p7 | 2:213340144 | GCAGTGATTTATAAA[C/G]TTACTATTTTTTTTT | 79582 |
rs116128767 | snp | A/C | 0.00557542 | 0.0525036 | intron-variant | SPAG16 | GRCh38.p7 | 2:213884812 | TTGTATTATGAAATT[A/C]TTGTAGAGAATTTTT | 79582 |
rs116136024 | snp | C/T | 0.0221141 | 0.102801 | intron-variant | SPAG16 | GRCh38.p7 | 2:213487594 | GGGTTTTGCCGCTCT[C/T]GATGTAAATCTTTTT | 79582 |
rs116142495 | snp | A/G | 0.0217236 | 0.101931 | intron-variant | SPAG16 | GRCh38.p7 | 2:213936013 | AAAACTAGAGCACAG[A/G]TGAAAAGGGATAGCA | 79582 |
rs116148664 | snp | A/G | 0.0425829 | 0.139564 | intron-variant | SPAG16 | GRCh38.p7 | 2:213438585 | CAGAAGATGTTTACT[A/G]CTGTTCTAGGTAGAG | 79582 |
rs116157792 | snp | G/T | 0.021333 | 0.101051 | intron-variant | SPAG16 | GRCh38.p7 | 2:213912477 | ATCAAAATTATTTTT[G/T]TAAATTATATGGCTC | 79582 |
rs116161000 | snp | A/G | 0.0566069 | 0.158427 | intron-variant | SPAG16 | GRCh38.p7 | 2:213979407 | TATAAAGAACTGCCC[A/G]TGACTGGGTAATTTA | 79582 |
rs116164627 | snp | C/T | 0.00358779 | 0.0422022 | intron-variant | SPAG16 | GRCh38.p7 | 2:213447751 | ATAGCAAACTTTGGA[C/T]GAATAATCAAACTGT | 79582 |
rs116167456 | snp | C/T | 0.00993419 | 0.0697739 | intron-variant | SPAG16 | GRCh38.p7 | 2:214027441 | AATTGATCTTCTAAA[C/T]AAGAATGCAGAAACA | 79582 |
rs116171178 | snp | A/G | 0.00199481 | 0.0315187 | intron-variant | SPAG16 | GRCh38.p7 | 2:213896416 | AAAATAGAACTACAT[A/G]TGATCCAGCAATTCC | 79582 |
rs116171180 | snp | A/T | 0.0170251 | 0.090679 | intron-variant | SPAG16 | GRCh38.p7 | 2:214221534 | CACTGAATGTCATAG[A/T]TATTAGGAATGGCTT | 79582 |
rs116178007 | snp | C/T | | | intron-variant | SPAG16 | GRCh38.p7 | 2:213848505 | AGCCTTATATGTTCA[C/T]TAATTTTCACCTTGG | 79582 |
rs116180105 | snp | C/G | 0.0162398 | 0.0886349 | intron-variant | SPAG16 | GRCh38.p7 | 2:214351891 | CTTAGTCTGTTTGGT[C/G]TGCTATAACAAAATA | 79582 |
rs116180635 | snp | A/G | 0.0107246 | 0.0724382 | intron-variant | SPAG16 | GRCh38.p7 | 2:213619529 | TAGACATTCCTCAAA[A/G]GAAGATATTCAGATA | 79582 |
rs116181131 | snp | C/T | 0.00676609 | 0.0577691 | intron-variant | SPAG16 | GRCh38.p7 | 2:214278619 | TTTTTCTAAGAAGCA[C/T]TATCTTTGAGAAAAA | 79582 |
rs116181577 | snp | A/G | 0.021333 | 0.101051 | intron-variant | SPAG16 | GRCh38.p7 | 2:213458746 | TTCCATCATCTTCTG[A/G]CTCTCCTTATTCTAT | 79582 |
rs116182228 | snp | C/T | 0.0170251 | 0.090679 | intron-variant | SPAG16 | GRCh38.p7 | 2:214242553 | TCTCTCAACTCTAGT[C/T]ATTGAATCTACCAAA | 79582 |
rs116182699 | snp | C/T | 0.0279526 | 0.114869 | intron-variant | SPAG16 | GRCh38.p7 | 2:213956009 | GAGTTTCGCTCTTGT[C/T]TCCCAGGCAACAATC | 79582 |
rs116183840 | snp | A/G | 0.00636936 | 0.0560724 | intron-variant | SPAG16 | GRCh38.p7 | 2:214283278 | CTTCTTAAAAGTGTA[A/G]AGACTTTGGTCTCTT | 79582 |
rs116184870 | snp | A/T | 0.021333 | 0.101051 | intron-variant | SPAG16 | GRCh38.p7 | 2:213542045 | GACAAATTCTCAATA[A/T]TAAACCTGAGCTATA | 79582 |
rs116185814 | snp | C/G | 0.046775 | 0.145601 | intron-variant | SPAG16 | GRCh38.p7 | 2:213664144 | GCCTTTTCTCCCTCT[C/G]TTTCCACTGTCACAT | 79582 |
rs116187782 | snp | A/G | 0.00636936 | 0.0560724 | intron-variant | SPAG16 | GRCh38.p7 | 2:213428560 | AGAGGGGCTCCCACA[A/G]CCAAAACTGAGAGAT | 79582 |
rs116189664 | snp | A/T | 0.00478085 | 0.0486577 | intron-variant | SPAG16 | GRCh38.p7 | 2:214138729 | CACATGTATATGCAT[A/T]TTACACATTTTCTGA | 79582 |
rs116191234 | snp | C/T | 0.00716266 | 0.059414 | intron-variant | SPAG16 | GRCh38.p7 | 2:213709365 | ACAAGACATTCCCTT[C/T]GAGATTTGGGGGTAT | 79582 |
rs116194902 | snp | C/T | 0.0023933 | 0.0345097 | intron-variant | SPAG16 | GRCh38.p7 | 2:214065881 | TTGACTTCTGTTTGA[C/T]CAGCTCCTCTCTCCA | 79582 |
rs116195717 | snp | A/G | 0.0168055 | 0.0901129 | intron-variant | SPAG16 | GRCh38.p7 | 2:213577828 | TGAGACTTCTGAGAT[A/G]TTGAAAACCATTAGG | 79582 |
rs116202953 | snp | A/G | 0.00557542 | 0.0525036 | intron-variant | SPAG16 | GRCh38.p7 | 2:213809411 | GCAAGCTCATTGTCC[A/G]TGCAACCCACAGGAA | 79582 |
rs116204247 | snp | A/G | 0.0138799 | 0.0821421 | intron-variant | SPAG16 | GRCh38.p7 | 2:214019188 | AGGCAGTAAGAAAAG[A/G]CTCAATGTACATACA | 79582 |
rs116204566 | snp | A/G | 0.0146672 | 0.084371 | intron-variant | SPAG16 | GRCh38.p7 | 2:214059734 | CCTCAGGTTACTTAT[A/G]CCCTTTAAGGTTATT | 79582 |
rs116206501 | snp | A/G | 0.0142736 | 0.0832652 | intron-variant | SPAG16 | GRCh38.p7 | 2:213350850 | AAAATTAGGCCAGGG[A/G]CAGTGGCTCATGCCT | 79582 |
rs116207559 | snp | C/T | 0.00795532 | 0.062565 | intron-variant | SPAG16 | GRCh38.p7 | 2:213302927 | CTTTAGAAATGAGAA[C/T]AGATACACCCTCCTG | 79582 |
rs116211429 | snp | C/T | 0.0448719 | 0.142907 | intron-variant | SPAG16 | GRCh38.p7 | 2:214018050 | AAAAATTTAAATTGA[C/T]AGCTATGTACTGTAA | 79582 |
rs116215891 | snp | G/T | 0.0158469 | 0.0875917 | intron-variant | SPAG16 | GRCh38.p7 | 2:213824747 | TGGCTGCACATAAAT[G/T]TTAGAATTGCTTTTT | 79582 |
rs116219195 | snp | A/G | 0.0178098 | 0.0926698 | intron-variant | SPAG16 | GRCh38.p7 | 2:213655882 | AAGGAAATTGTTTTC[A/G]TTTATTTTAGCTTTA | 79582 |
rs116225129 | snp | A/G | 0.0170251 | 0.090679 | intron-variant | SPAG16 | GRCh38.p7 | 2:213701621 | GTGCAGGTGCGTGGC[A/G]CGGGACTGGTAGGCA | 79582 |
rs116233230 | snp | C/G | 0.0217236 | 0.101931 | intron-variant | SPAG16 | GRCh38.p7 | 2:213881674 | ATAAAACCATCAGAT[C/G]TCTTGTGAGAACTCA | 79582 |
rs116236424 | snp | A/G | 0.132409 | 0.220618 | intron-variant | SPAG16 | GRCh38.p7 | 2:213359142 | CCTGATCCTTCTTCT[A/G]GAAGCTTTGTCCCAG | 79582 |
rs116237456 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | SPAG16 | GRCh38.p7 | 2:213968774 | TTTGTAAAATGTGAA[C/T]CATAATATATATCAC | 79582 |
rs116237897 | snp | A/G | 0.189576 | 0.242588 | intron-variant | SPAG16 | GRCh38.p7 | 2:213950980 | GCCTCCCAAAGTGTT[A/G]GGATTACAGGTGTAA | 79582 |
rs116238116 | snp | C/G | 0.0236746 | 0.106192 | intron-variant | SPAG16 | GRCh38.p7 | 2:213973854 | AATTAATAAGTAAAC[C/G]TGTGAATTATAAGAC | 79582 |
rs116238294 | snp | A/G | 0.0345262 | 0.126772 | intron-variant | SPAG16 | GRCh38.p7 | 2:214304054 | GTTTTGTTCCCCTCT[A/G]TATGTCCATGTATTC | 79582 |
rs116239153 | snp | A/T | 0.0178098 | 0.0926698 | intron-variant | SPAG16 | GRCh38.p7 | 2:214272044 | CTTAATATACAGTAC[A/T]ATAATATTGACAACA | 79582 |
rs116239210 | snp | C/T | 0.0287284 | 0.116357 | intron-variant | SPAG16 | GRCh38.p7 | 2:213954333 | TTGAAAGTTCATCAA[C/T]GTTGTAGTATGTATC | 79582 |
rs116239765 | snp | A/G | 0.0150606 | 0.0854603 | intron-variant | SPAG16 | GRCh38.p7 | 2:214308769 | CCATTATTAGTCAGG[A/G]GCTTCTCTTTGTAGG | 79582 |
rs116240981 | snp | C/T | 0.00279162 | 0.0372561 | intron-variant | SPAG16 | GRCh38.p7 | 2:213755696 | AAAAGCAAACAGAAA[C/T]TTCAAGCTGATGATA | 79582 |
rs116242474 | snp | C/T | 0.00993419 | 0.0697739 | intron-variant | SPAG16 | GRCh38.p7 | 2:213748631 | ATAAGAAAGGAAATC[C/T]GAAAGTAAGCGTAAG | 79582 |
rs116252190 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | SPAG16 | GRCh38.p7 | 2:213415727 | AGGATATTATTAATT[G/T]GTTTATGACGTGAGG | 79582 |
rs116254149 | snp | A/C | 0.0810805 | 0.184299 | intron-variant | SPAG16 | GRCh38.p7 | 2:213954134 | TCTCATAAAGAGTCA[A/C]TCCTATTTTTTTTTT | 79582 |
rs116255082 | snp | A/G | 0.0267878 | 0.112589 | intron-variant | SPAG16 | GRCh38.p7 | 2:214226321 | CACATACTTTTTCAA[A/G]CCTCTGCTTGTGTTA | 79582 |
rs116258190 | snp | C/G | 0.0178098 | 0.0926698 | intron-variant | SPAG16 | GRCh38.p7 | 2:214250188 | GAAAGTCTGTAAAGA[C/G]AGGAACACTCATAGA | 79582 |
rs116258225 | snp | A/G | 0.0189856 | 0.0955633 | intron-variant | SPAG16 | GRCh38.p7 | 2:213965809 | TCTGCCTCTGTCCCT[A/G]GGCAGAATGTCTGCA | 79582 |
rs116263434 | snp | A/G | 0.0287284 | 0.116357 | intron-variant | SPAG16 | GRCh38.p7 | 2:213703448 | TCTCAGAAAACTGTG[A/G]AACAAACCCAGGGCC | 79582 |
rs116265262 | snp | C/T | 0.0240643 | 0.107019 | intron-variant, utr-variant-5-prime | SPAG16 | GRCh38.p7 | 2:213302219 | ACCATGTTTCGCTAG[C/T]TTGTAGATTGCTTGC | 79582 |
rs116266301 | snp | A/T | 0.0221842 | 0.102956 | intron-variant | SPAG16 | GRCh38.p7 | 2:213335845 | ATAACAGTAGAGGTC[A/T]TTTTTAAAAAAATAG | 79582 |
rs116266592 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | SPAG16 | GRCh38.p7 | 2:213293433 | TATTGAAGAAATGAT[A/G]TGTGACTTCTGATGT | 79582 |
rs116266867 | snp | A/G | 0.0138799 | 0.0821421 | intron-variant | SPAG16 | GRCh38.p7 | 2:214349830 | CATTTATTTTATGAC[A/G]AATAAGTTATTTTTT | 79582 |
rs116269570 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | SPAG16 | GRCh38.p7 | 2:214171531 | ATCATTACTTTTCAC[A/G]AACTTGCAAGATGAT | 79582 |
rs116280569 | snp | C/T | 0.0217236 | 0.101931 | intron-variant | SPAG16 | GRCh38.p7 | 2:213545060 | TAAGAAATTACCAAA[C/T]TGTCTTCCAAAGTGG | 79582 |
rs116284509 | snp | A/G | 0.0240643 | 0.107019 | intron-variant | SPAG16 | GRCh38.p7 | 2:213533657 | TGTATTTTTTAGGAA[A/G]GAACTCTATTAATTT | 79582 |
rs116284860 | snp | A/G | 0.0566069 | 0.158427 | intron-variant | SPAG16 | GRCh38.p7 | 2:214004812 | CTGTAGATTTTATAG[A/G]CCAAGCATGAGACCT | 79582 |
rs116288532 | snp | A/C | 0.0130921 | 0.0798413 | intron-variant | SPAG16 | GRCh38.p7 | 2:213841621 | TTTCTGGTTTAAGAT[A/C]GATTTATATTGTTAG | 79582 |
rs116290636 | snp | A/G | 0.0165278 | 0.0893908 | intron-variant | SPAG16 | GRCh38.p7 | 2:214015665 | AGGGAAGCAAGGCTA[A/G]TGGTCATTTTGGAGG | 79582 |
rs116296914 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | SPAG16 | GRCh38.p7 | 2:213690341 | GATTTGGCTCTCCAG[C/T]AAGGGCTGCATCCTC | 79582 |
rs116297893 | snp | G/T | 0.00318978 | 0.0398085 | intron-variant | SPAG16 | GRCh38.p7 | 2:213724077 | GAATAGGGAAGTGTA[G/T]GAGTGAAAACAGACA | 79582 |
rs116307753 | snp | A/G | 0.0422008 | 0.138995 | intron-variant | SPAG16 | GRCh38.p7 | 2:213559362 | AAGAATACAATTATT[A/G]TCACGAGCATCAATG | 79582 |
rs116309405 | snp | C/T | 0.0562307 | 0.157967 | intron-variant | SPAG16 | GRCh38.p7 | 2:214008767 | AAAAAAAAATACATG[C/T]TAGATGTTGTTAATG | 79582 |
rs116312121 | snp | C/T | 0.00398564 | 0.0444627 | intron-variant | SPAG16 | GRCh38.p7 | 2:213550708 | TTATGTTCCAACTTT[C/T]ATATTCCTTATTTCA | 79582 |
rs116315370 | snp | A/G | 0.0185938 | 0.0946107 | intron-variant, upstream-variant-2KB | SPAG16 | GRCh38.p7 | 2:213295446 | TGAATTATGATTGCT[A/G]TATACTTTATATTCA | 79582 |
rs116317427 | snp | A/C | 0.0154538 | 0.0865337 | intron-variant | SPAG16 | GRCh38.p7 | 2:213388197 | TGGGTGGGCAAAAAG[A/C]ATCCTGTCCTGCAAA | 79582 |
rs116319322 | snp | A/T | 0.0248432 | 0.108648 | intron-variant | SPAG16 | GRCh38.p7 | 2:213781109 | ATGTTACTCAGCAAA[A/T]CTCCTTTAAGGTCTT | 79582 |
rs116320277 | snp | A/G | 0.0162398 | 0.0886349 | intron-variant | SPAG16 | GRCh38.p7 | 2:213984401 | TATGCAGTATATCAG[A/G]GCCTTCTCTGTGCTC | 79582 |
rs116321999 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | SPAG16 | GRCh38.p7 | 2:213825798 | GAAAAATTCCCTCCT[C/T]CCCTATTTCTTGGGA | 79582 |
rs116322659 | snp | C/T | 0.00199481 | 0.0315187 | intron-variant | SPAG16 | GRCh38.p7 | 2:214389510 | GCAGATATTAAAGAG[C/T]AGCATGTGTCAGAAG | 79582 |
rs116322976 | snp | A/G | 0.00795532 | 0.062565 | intron-variant | SPAG16 | GRCh38.p7 | 2:213750342 | AATGACAAGAGTTAC[A/G]TCGAAATATGTATCA | 79582 |
rs116330637 | snp | C/T | 0.12932 | 0.218944 | intron-variant | SPAG16 | GRCh38.p7 | 2:213721190 | CTGCAACCTGTGCTT[C/T]CTGGGTTCAAGCTGC | 79582 |
rs116332067 | snp | C/T | 0.0209421 | 0.100162 | intron-variant | SPAG16 | GRCh38.p7 | 2:214384190 | TGGCCACTGAAGATA[C/T]TGGAGTTGTCTGAAA | 79582 |
rs116333390 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | SPAG16 | GRCh38.p7 | 2:214373486 | AAATTATTTATTAAC[A/G]TGAGAAATAGAAATA | 79582 |
rs116347711 | snp | A/G | 0.0314385 | 0.121371 | intron-variant | SPAG16 | GRCh38.p7 | 2:213581743 | AAGCTGCAACACTTA[A/G]AATGTCTGCCACTGT | 79582 |
rs116356371 | snp | G/T | 0.0287284 | 0.116357 | intron-variant | SPAG16 | GRCh38.p7 | 2:213877522 | ATCTCACTATATTGT[G/T]CAAGCTAATCCCAAA | 79582 |
rs116356644 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | SPAG16 | GRCh38.p7 | 2:213713101 | CAGGTCTGGTGAGAA[C/T]TCACTCACTACCATG | 79582 |
rs116357095 | snp | A/G | 0.0182019 | 0.0936463 | intron-variant | SPAG16 | GRCh38.p7 | 2:214213843 | TGCTACCTCTGCTTT[A/G]CAGTTGGACCATAAA | 79582 |
rs116358799 | snp | C/T | 0.0185938 | 0.0946107 | intron-variant, downstream-variant-500B | SPAG16 | GRCh38.p7 | 2:214151073 | GAATATGATTTCAAC[C/T]TGACCTTCCCATCCC | 79582 |
rs116359058 | snp | A/G | 0.0209421 | 0.100162 | intron-variant | SPAG16 | GRCh38.p7 | 2:213388073 | TGGACAGTAAATTAT[A/G]GTTAAGTTGGGTCAA | 79582 |
rs116359101 | snp | G/T | 0.00159617 | 0.0282053 | intron-variant | SPAG16 | GRCh38.p7 | 2:213927964 | AAAAACTAAAATTCT[G/T]AATGACAAACATATG | 79582 |
rs116359481 | snp | C/T | 0.0170251 | 0.090679 | intron-variant | SPAG16 | GRCh38.p7 | 2:214244810 | ACTTTCATTAATGCC[C/T]TTTATTCAACGTATA | 79582 |
rs116360628 | snp | A/G | 0.00716266 | 0.059414 | intron-variant | SPAG16 | GRCh38.p7 | 2:213306258 | GCTAATGTTTTGTCA[A/G]TTTTGTTTATCTTTT | 79582 |
rs116362071 | snp | C/T | 0.0182019 | 0.0936463 | intron-variant, upstream-variant-2KB | SPAG16 | GRCh38.p7 | 2:213295941 | TTAAAGATTAAATTA[C/T]ATATATTTACCAACT | 79582 |
rs116367030 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | SPAG16 | GRCh38.p7 | 2:213327681 | TATACTCAAAATAGA[C/T]GTTCACAAAATTTTA | 79582 |
rs116368503 | snp | A/C | 0.0154538 | 0.0865337 | intron-variant | SPAG16 | GRCh38.p7 | 2:213625497 | CCCCATCTGTAGATT[A/C]TCTTTAATTTCTTTA | 79582 |
rs116371002 | snp | A/T | 0.00755907 | 0.0610114 | intron-variant | SPAG16 | GRCh38.p7 | 2:213565346 | ATAGTCCAGAAGTAA[A/T]TACAAGCTCAATATA | 79582 |
rs116371438 | snp | A/G | 0.0158469 | 0.0875917 | intron-variant | SPAG16 | GRCh38.p7 | 2:213796297 | TTACCCCCGAAAAAA[A/G]TCCATACCTATTCTG | 79582 |
rs116372992 | snp | A/T | 0.00795532 | 0.062565 | intron-variant | SPAG16 | GRCh38.p7 | 2:213577590 | AGACTTATAGGAGGA[A/T]CCAATCCTGACACTT | 79582 |
rs116373618 | snp | C/T | 0.0256215 | 0.110247 | intron-variant | SPAG16 | GRCh38.p7 | 2:213407053 | GAGAAGCCGCGGGAG[C/T]GGGTAGAGTACCTTG | 79582 |
rs116375987 | snp | A/T | 0.0228947 | 0.104514 | intron-variant | SPAG16 | GRCh38.p7 | 2:213945145 | TTAGAGGTACAGAAC[A/T]AATAGGATATATATA | 79582 |
rs116376096 | snp | A/T | 0.021333 | 0.101051 | intron-variant | SPAG16 | GRCh38.p7 | 2:213436915 | AAAATGATAAACTCT[A/T]TTTTTTTTTTCTTTG | 79582 |
rs116378473 | snp | A/G | 0.02016 | 0.0983543 | intron-variant | SPAG16 | GRCh38.p7 | 2:214065128 | AGGTTTAAGAAGGCA[A/G]AATAACTTATCTATG | 79582 |
rs116381072 | snp | A/G | 0.0452528 | 0.143452 | intron-variant | SPAG16 | GRCh38.p7 | 2:214023401 | ATTGCTTCCTAAGGC[A/G]TTCATTAAAAAAAAA | 79582 |
rs116401731 | snp | A/C | 0.0275645 | 0.114116 | intron-variant | SPAG16 | GRCh38.p7 | 2:214391420 | ATTCCTAAAACTTAG[A/C]TTACCTAATTTATTG | 79582 |
rs116401789 | snp | C/T | 0.0168055 | 0.0901129 | intron-variant | SPAG16 | GRCh38.p7 | 2:213658194 | CTTACAAGCCTACTC[C/T]AGTCTCATCTTAAGC | 79582 |
rs116412150 | snp | A/G | 0.0228947 | 0.104514 | intron-variant | SPAG16 | GRCh38.p7 | 2:213943220 | AAGTGGAGTGCTACT[A/G]TTTCAAATACCTGAA | 79582 |
rs116412212 | snp | A/G | 0.0174175 | 0.0916809 | intron-variant | SPAG16 | GRCh38.p7 | 2:214011797 | CTTTGATGAGAAAGG[A/G]AAGTGTTGCTAAATA | 79582 |
rs116412499 | snp | C/G | 0.0174175 | 0.0916809 | intron-variant | SPAG16 | GRCh38.p7 | 2:214235445 | TAAAGAATTTAATGT[C/G]CATTTTCTTCCTCAA | 79582 |
rs116417038 | snp | A/G | 0.0189856 | 0.0955633 | intron-variant | SPAG16 | GRCh38.p7 | 2:213863859 | ATTACTGAAATTAAT[A/G]TGAGGTGAGATACAT | 79582 |
rs116418966 | snp | A/C | 0.0926964 | 0.194308 | intron-variant | SPAG16 | GRCh38.p7 | 2:213674457 | GGTACATATGTATAC[A/C]TGTGACATGCTGGTG | 79582 |
rs116419612 | snp | C/T | 0.0126979 | 0.078662 | intron-variant | SPAG16 | GRCh38.p7 | 2:213671272 | GAAAATTGGACCCTA[C/T]TGTAGGAGCTTGACT | 79582 |
rs116420808 | snp | A/G | 0.00199481 | 0.0315187 | intron-variant | SPAG16 | GRCh38.p7 | 2:214303398 | ATTACTTGTGTCAGG[A/G]TATAAAATTCATGGA | 79582 |
rs116421272 | snp | A/G | 0.0170251 | 0.090679 | intron-variant | SPAG16 | GRCh38.p7 | 2:214335337 | TCTCTGTGACGCCCC[A/G]CAGCATCCGCTACAC | 79582 |
rs116423303 | snp | C/G | 0.00279162 | 0.0372561 | intron-variant | SPAG16 | GRCh38.p7 | 2:213851609 | ATTAGGTCTAAGTCA[C/G]TACATAAGGCCTTTC | 79582 |
rs116425528 | snp | A/C | 0.0232847 | 0.105357 | intron-variant | SPAG16 | GRCh38.p7 | 2:214265567 | GTTTATCTTTTTATT[A/C]TCTTAACATGTCATT | 79582 |
rs116429332 | snp | A/C | 0.0244538 | 0.107838 | intron-variant | SPAG16 | GRCh38.p7 | 2:213444761 | ATTTATATGAAACCA[A/C]AAAATACCCAGAATA | 79582 |
rs116432241 | snp | A/C | 0.0252325 | 0.109451 | intron-variant | SPAG16, LOC101928084 | GRCh38.p7 | 2:214095662 | TTATAGAAAAAAATG[A/C]AAACTTGTATTGGCT | 79582 |
rs116434123 | snp | A/G | 0.0150606 | 0.0854603 | intron-variant | SPAG16 | GRCh38.p7 | 2:214119193 | CCCTGAAAAACTATT[A/G]AATTGAATTTTATTT | 79582 |
rs116437736 | snp | A/G | 0.00953873 | 0.0683987 | intron-variant | SPAG16 | GRCh38.p7 | 2:213959102 | CCTTCTGGCTTCCAT[A/G]GTTTTTGATGAGAAT | 79582 |
rs116440624 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | SPAG16 | GRCh38.p7 | 2:213481074 | CATGACAAGCCATTC[A/T]ATTCAGCAATTTCTA | 79582 |
rs116448147 | snp | C/T | 0.00993419 | 0.0697739 | intron-variant | SPAG16 | GRCh38.p7 | 2:213640624 | TCTCCCAGCTGTAAG[C/T]ACCAGAACCTGCTCT | 79582 |
rs116458318 | snp | C/T | 0.00358779 | 0.0422022 | intron-variant | SPAG16 | GRCh38.p7 | 2:213513716 | ACATAGCGGAATCTC[C/T]GTCACATCGTCTTTC | 79582 |
rs116458697 | snp | C/T | 0.00398564 | 0.0444627 | intron-variant | SPAG16 | GRCh38.p7 | 2:214370462 | ATAATAGAGAAATTA[C/T]ATAAATTTATGGTGT | 79582 |
rs116462670 | snp | C/T | 0.0174175 | 0.0916809 | intron-variant | SPAG16 | GRCh38.p7 | 2:214026257 | ATTATATTATATATA[C/T]ACACACACACAGAAA | 79582 |
rs116462881 | snp | A/C | 0.00478085 | 0.0486577 | intron-variant | SPAG16 | GRCh38.p7 | 2:214067715 | TGAATACATCCGGGT[A/C]TTTTCAAGATGGTCC | 79582 |
rs116462958 | snp | A/C/T | 0.0221141 | 0.102801 | intron-variant | SPAG16 | GRCh38.p7 | 2:213372327 | ATTCCGGATGACCTT[A/C/T]TAGAAATTGTAAATG | 79582 |
rs116473128 | snp | C/T | 0.0178098 | 0.0926698 | intron-variant | SPAG16 | GRCh38.p7 | 2:213413613 | TTTTAAAAGATATTA[C/T]GAGCCAAGCACTTGT | 79582 |
rs116474195 | snp | C/T | 0.00755907 | 0.0610114 | intron-variant | SPAG16 | GRCh38.p7 | 2:213844741 | TTATAGCCAGTTTTT[C/T]ACTGTCTTTACCAAT | 79582 |
rs116482643 | snp | C/T | 0.0158469 | 0.0875917 | intron-variant | SPAG16 | GRCh38.p7 | 2:214290207 | CAGTATTTTAGCATA[C/T]AGTTGTGCATAATGA | 79582 |
rs116482650 | snp | C/T | 0.00318978 | 0.0398085 | intron-variant | SPAG16 | GRCh38.p7 | 2:213695152 | TAGATCTTTTACATA[C/T]CTTTTAACCATATCT | 79582 |
rs116483572 | snp | A/G | 0.0138799 | 0.0821421 | intron-variant | SPAG16 | GRCh38.p7 | 2:214325460 | GGGGGTTAGTGGGTT[A/G]GTTATTATAATGAGA | 79582 |
rs116484631 | snp | A/C | 0.0685596 | 0.171987 | intron-variant | SPAG16 | GRCh38.p7 | 2:214400616 | ATAGATACAGAGGAG[A/C]AACTTATATTTGTTT | 79582 |
rs116492381 | snp | C/T | 0.0119091 | 0.0762411 | intron-variant | SPAG16 | GRCh38.p7 | 2:214305199 | GTGCCTGTTCATATC[C/T]GTTGCTCATTTTTTA | 79582 |
rs116493049 | snp | C/T | 0.00835141 | 0.0640778 | intron-variant | SPAG16 | GRCh38.p7 | 2:213506844 | ACCAAATACCTGATC[C/T]TAACTGTTTTCTGTC | 79582 |
rs116493437 | snp | A/G | 0.00517822 | 0.0506191 | intron-variant | SPAG16 | GRCh38.p7 | 2:214316315 | TGTCAGAGATACCAT[A/G]AGAGGCAATTTGACT | 79582 |
rs116495721 | snp | C/T | 0.0170251 | 0.090679 | intron-variant | SPAG16 | GRCh38.p7 | 2:214244393 | GATAAGCTGAAGTTC[C/T]GAAAAAAAAAAAAAA | 79582 |
rs116498473 | snp | A/T | 0.00159617 | 0.0282053 | intron-variant | SPAG16 | GRCh38.p7 | 2:213710671 | TGTGCAAGGTAAAAT[A/T]GTTTTCCTCTGAGGT | 79582 |
rs116499233 | snp | C/T | 0.0310518 | 0.120672 | intron-variant | SPAG16 | GRCh38.p7 | 2:213549876 | AAAATTTGTGCTTTA[C/T]TTGGATATTTGTTAT | 79582 |
rs116501261 | snp | C/G/T | 0.0240737 | 0.107104 | intron-variant | SPAG16 | GRCh38.p7 | 2:213702680 | GTAATCTATGACACA[C/G/T]AGAAGCTGAGACCTC | 79582 |
rs116502464 | snp | A/C | 0.0126979 | 0.078662 | intron-variant | SPAG16 | GRCh38.p7 | 2:213910166 | AGAACATTGTGACTA[A/C]TAGCCTTTTTATGAA | 79582 |
rs116507637 | snp | C/T | 0.0599851 | 0.162463 | intron-variant | SPAG16 | GRCh38.p7 | 2:214262746 | TAATAAACAATGAAA[C/T]AACCGCAAATACCAC | 79582 |
rs116507711 | snp | C/T | 0.00874735 | 0.0655527 | intron-variant | SPAG16 | GRCh38.p7 | 2:213682951 | AAAAAATAAGTATGG[C/T]TATTTTGTCTTATCT | 79582 |
rs116509310 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | SPAG16 | GRCh38.p7 | 2:213596721 | GTTGAAAGTCAAAGA[C/G]AAAGATTGAGCTCTC | 79582 |
rs116519420 | snp | A/C | 0.0138799 | 0.0821421 | intron-variant | SPAG16 | GRCh38.p7 | 2:213764539 | TTTAAACTCTCTGAA[A/C]AATAGAGAATCTAGA | 79582 |
rs116525764 | snp | A/G | 0.0217236 | 0.101931 | intron-variant | SPAG16 | GRCh38.p7 | 2:213872380 | TGTCACAGCACAAAA[A/G]GAAAACAAATACACT | 79582 |
rs116528025 | snp | A/C | 0.0287284 | 0.116357 | intron-variant | SPAG16 | GRCh38.p7 | 2:213922805 | GGGTCTTGGTGGCAC[A/C]CTCTATGATTACTGT | 79582 |
rs116528412 | snp | C/T | 0.0221141 | 0.102801 | intron-variant | SPAG16 | GRCh38.p7 | 2:213447141 | CTGGGCACCAAAGGG[C/T]TATTTTAAAAAACAA | 79582 |
rs116535664 | snp | G/T | 0.0205511 | 0.0992634 | intron-variant | SPAG16 | GRCh38.p7 | 2:213831356 | CCATGACTTTTTATC[G/T]TTGATTGCAGCTGAT | 79582 |
rs116537338 | snp | A/T | 0.0551013 | 0.156571 | intron-variant | SPAG16 | GRCh38.p7 | 2:214008402 | TCTTGTGTATGGATT[A/T]CATTTTTACCTTTCC | 79582 |
rs116538231 | snp | G/T | 0.00159617 | 0.0282053 | intron-variant | SPAG16 | GRCh38.p7 | 2:213574009 | CATTTCTAATAAGTT[G/T]TCAGGTGATGCCTAA | 79582 |
rs116546490 | snp | G/T | 0.192715 | 0.243348 | intron-variant | SPAG16 | GRCh38.p7 | 2:213945526 | GGGAGGCTAGGCCAG[G/T]CTCGACTTTTCATGT | 79582 |
rs116546512 | snp | C/G | 0.0456336 | 0.143994 | intron-variant | SPAG16 | GRCh38.p7 | 2:213970929 | TACAGTTTTCCTACA[C/G]TAATCATATTAATGT | 79582 |
rs116546580 | snp | C/T | 0.00755907 | 0.0610114 | intron-variant | SPAG16 | GRCh38.p7 | 2:214381763 | CAATCTGTTACTTAA[C/T]CCAATCCAAACAAAG | 79582 |
rs116548302 | snp | C/G | 0.00438332 | 0.0466095 | intron-variant | SPAG16 | GRCh38.p7 | 2:213471078 | GAATTCCCTTTACCA[C/G]TGTCCTTCAGGGATG | 79582 |
rs116549919 | snp | A/T | 0.000798403 | 0.0199641 | intron-variant | SPAG16 | GRCh38.p7 | 2:214128881 | GTGGGAAAGAAGCAG[A/T]GCTCAAACTAGGGCT | 79582 |
rs116551646 | snp | C/T | 0.00318978 | 0.0398085 | intron-variant | SPAG16 | GRCh38.p7 | 2:213319297 | CTTTTCATTGAGAAG[C/T]AGAGAAAATATTTAA | 79582 |
rs116557007 | snp | A/G | 0.0325976 | 0.123435 | intron-variant | SPAG16 | GRCh38.p7 | 2:213421570 | GGGGCCAGGCTCCCA[A/G]TTCCCAGTGGAGTCC | 79582 |
rs116557429 | snp | C/T | 0.0170251 | 0.090679 | intron-variant | SPAG16 | GRCh38.p7 | 2:213534590 | ACACAAAAACACAGA[C/T]GAATCCCAAAAACAT | 79582 |
rs116559663 | snp | C/T | 0.0240643 | 0.107019 | intron-variant | SPAG16 | GRCh38.p7 | 2:213320154 | ATAGCCTGGTTCTAC[C/T]GATACATTCTTAGAA | 79582 |
rs116562920 | snp | C/G | 0.00755907 | 0.0610114 | intron-variant | SPAG16 | GRCh38.p7 | 2:213773621 | GTGCAGTGGCATGAT[C/G]TCGGCTTACTGCAAC | 79582 |
rs116566888 | snp | C/T | 0.00438332 | 0.0466095 | intron-variant | SPAG16 | GRCh38.p7 | 2:213848664 | CTTTATCAAAGCGTT[C/T]TTATAATGCCAGTTT | 79582 |
rs116567247 | snp | C/T | 0.00953873 | 0.0683987 | intron-variant | SPAG16 | GRCh38.p7 | 2:213406474 | TTTTATTTAACCATA[C/T]ATTAAGTTGTAATTT | 79582 |
rs116567817 | snp | A/G | 0.00914312 | 0.0669923 | intron-variant | SPAG16, LOC101928084 | GRCh38.p7 | 2:214086734 | CTAATACAGTTGCCT[A/G]TATTTTCGATGTCTC | 79582 |
rs116568556 | snp | C/G | 0.0275645 | 0.114116 | intron-variant | SPAG16 | GRCh38.p7 | 2:214287859 | TGTAGAATAGGTAAT[C/G]ACCAAGTCAGGTGAT | 79582 |
rs116569547 | snp | A/C/G | 0.00756178 | 0.0610554 | intron-variant | SPAG16 | GRCh38.p7 | 2:214321482 | GAACACAAAGTGTGC[A/C/G]TTCAACCTACACAGT | 79582 |
rs116571516 | snp | A/G | 0.0425829 | 0.139564 | intron-variant | SPAG16 | GRCh38.p7 | 2:213541855 | GAAATTGTTTTTTCC[A/G]TAATTTAAGTCCTAC | 79582 |
rs116576342 | snp | C/T | 0.00835141 | 0.0640778 | intron-variant | SPAG16 | GRCh38.p7 | 2:214397641 | GTCTATTTAACAAAA[C/T]ACTTGAGCTGATTTA | 79582 |
rs116578038 | snp | C/T | 0.046775 | 0.145601 | intron-variant | SPAG16 | GRCh38.p7 | 2:213991655 | ATCATGAGTCATGTA[C/T]CTACTTAGAGCCAGT | 79582 |
rs116578726 | snp | C/T | 0.108402 | 0.206034 | intron-variant | SPAG16 | GRCh38.p7 | 2:213958543 | CAACTTTGAATAGTA[C/T]ACAAAAACTGCCCCT | 79582 |
rs116579386 | snp | A/T | 0.0252325 | 0.109451 | intron-variant | SPAG16 | GRCh38.p7 | 2:214235132 | TTTTGTGATATTCAT[A/T]AAAAGATTGTAACTG | 79582 |
rs116579897 | snp | C/T | 0.0248432 | 0.108648 | intron-variant | SPAG16 | GRCh38.p7 | 2:214245844 | GAATTTTTTTAAATT[C/T]ACCTGATATGTGTTC | 79582 |
rs116580349 | snp | A/G | 0.0722614 | 0.17581 | intron-variant | SPAG16 | GRCh38.p7 | 2:213991324 | ACATTTCTGCAAAGG[A/G]CATGAACTCATTCCT | 79582 |
rs116582571 | snp | A/G | 0.0162398 | 0.0886349 | intron-variant | SPAG16 | GRCh38.p7 | 2:213425315 | AGAGAGTGAGACTCC[A/G]TCTCCAAAAAAAGAA | 79582 |
rs116590084 | snp | A/G | 0.0329836 | 0.124112 | intron-variant | SPAG16 | GRCh38.p7 | 2:214105146 | TGTAGTTAGTAGAGA[A/G]CCTGGCATAGGGCGG | 79582 |
rs116594272 | snp | A/G | 0.00398564 | 0.0444627 | intron-variant | SPAG16 | GRCh38.p7 | 2:213751281 | AAATTTCTCCTCCAC[A/G]TATGGTTGCTTGCAA | 79582 |
rs116601330 | snp | A/T | 0.00119737 | 0.0244387 | intron-variant | SPAG16 | GRCh38.p7 | 2:214135450 | CCCAATAACAAAGTA[A/T]GCATGTTTATGCATC | 79582 |
rs116603970 | snp | C/T | 0.0217236 | 0.101931 | intron-variant | SPAG16 | GRCh38.p7 | 2:213616634 | CATGCAGATTCCTGA[C/T]CTCTGGCCCAAACTA | 79582 |
rs116604502 | snp | C/T | 0.0225045 | 0.103662 | intron-variant | SPAG16 | GRCh38.p7 | 2:213537367 | ATCATACATTAATGA[C/T]TGAACTTTAAATATA | 79582 |
rs116605657 | snp | A/G | 0.0205511 | 0.0992634 | intron-variant | SPAG16 | GRCh38.p7 | 2:213942920 | TTTGGGAATTAATTA[A/G]GTCATGAAGGTAGAG | 79582 |
rs116606934 | snp | A/G | 0.0170251 | 0.090679 | intron-variant | SPAG16 | GRCh38.p7 | 2:213981614 | GAAAATGAAAATAGC[A/G]TACCTATAGGTGGAC | 79582 |
rs116611364 | snp | A/G | 0.0168055 | 0.0901129 | intron-variant | SPAG16 | GRCh38.p7 | 2:213682794 | GTTTATGGTCATGCT[A/G]ACATTAGTCATTAGG | 79582 |
rs116612783 | snp | A/G | 0.0205511 | 0.0992634 | intron-variant | SPAG16 | GRCh38.p7 | 2:213821099 | ATTTTCTTTTCCTCA[A/G]TCTGTGAATTCTTGT | 79582 |
rs116614245 | snp | G/T | 0.00358779 | 0.0422022 | intron-variant | SPAG16 | GRCh38.p7 | 2:213816189 | ATATACTTTTTTGTA[G/T]GTGATTTTTAAAATA | 79582 |
rs116621592 | snp | G/T | 0.0119091 | 0.0762411 | intron-variant, upstream-variant-2KB | SPAG16 | GRCh38.p7 | 2:213294598 | AGGCACTTATTCATG[G/T]TTTACAATAAAATAC | 79582 |
rs116621960 | snp | A/G | 0.030665 | 0.119967 | intron-variant | SPAG16 | GRCh38.p7 | 2:213553693 | GGCTCTGTGACTACA[A/G]TAGGCGTGATCATGT | 79582 |
rs116622235 | snp | C/T | 0.00517822 | 0.0506191 | intron-variant | SPAG16 | GRCh38.p7 | 2:214009479 | GTGTAATTTTACAGT[C/T]GCTTATTATAAGAGA | 79582 |
rs116626794 | snp | A/G | 0.0314385 | 0.121371 | intron-variant | SPAG16 | GRCh38.p7 | 2:213581598 | CTCAGGTCCAAGCTG[A/G]TTTTGACTGGATTAA | 79582 |
rs116629136 | snp | C/G | 0.0221141 | 0.102801 | intron-variant, utr-variant-3-prime | SPAG16 | GRCh38.p7 | 2:213398040 | AGCCAAAAAACTCTA[C/G]AGTCATCCCTGAGAC | 79582 |
rs116630166 | snp | C/T | 0.00755907 | 0.0610114 | intron-variant | SPAG16 | GRCh38.p7 | 2:214390813 | TGTCACAGAGATGAT[C/T]TGAAATGGAGCTGCC | 79582 |
rs116630331 | snp | A/C | 0.00993419 | 0.0697739 | intron-variant | SPAG16 | GRCh38.p7 | 2:214082363 | CCAAAGACACAAGAT[A/C]TTTTACCTTCTCCTC | 79582 |
rs116635074 | snp | C/T | 0.0792508 | 0.182605 | intron-variant | SPAG16 | GRCh38.p7 | 2:214130209 | GAAGTCTCTAGCAGC[C/T]GGTGTGAGAGTTTGA | 79582 |
rs116639408 | snp | C/G | 0.0119091 | 0.0762411 | intron-variant | SPAG16 | GRCh38.p7 | 2:213353497 | AAAATATGAAGGACT[C/G]TTTAAGGGGTTGTCA | 79582 |
rs116640502 | snp | C/G | 0.393987 | 0.204372 | intron-variant | SPAG16 | GRCh38.p7 | 2:214307699 | TCCATGTAATTGTAT[C/G]TTTTTGAGCAAATTT | 79582 |
rs116647929 | snp | C/T | 0.00358779 | 0.0422022 | intron-variant | SPAG16 | GRCh38.p7 | 2:213322800 | AGCAGGGGAGCACAT[C/T]AGAAACCTGAAGAGA | 79582 |
rs116652307 | snp | C/T | 0.00795532 | 0.062565 | intron-variant | SPAG16 | GRCh38.p7 | 2:214118564 | TTCTTCACATGGTGG[C/T]GGCAGAAGTGCTGAG | 79582 |
rs116655313 | snp | A/G | 0.0178098 | 0.0926698 | intron-variant | SPAG16 | GRCh38.p7 | 2:214221774 | TTCATGTTATTTTTC[A/G]TGTTTTCACTTTAGC | 79582 |
rs116655760 | snp | A/C | 0.0174175 | 0.0916809 | intron-variant | SPAG16 | GRCh38.p7 | 2:214254755 | TACAGTCATATTTAT[A/C]ACTAGGCTAGGAGTA | 79582 |
rs116655942 | snp | A/G | 0.00636936 | 0.0560724 | intron-variant | SPAG16 | GRCh38.p7 | 2:213362959 | GATTTGGAGAGGACA[A/G]ATATCCAAACTATAT | 79582 |
rs116660855 | snp | C/T | 0.00199481 | 0.0315187 | intron-variant | SPAG16 | GRCh38.p7 | 2:214167257 | TGTCATTGAATAGCC[C/T]CTACTTGTGCCGCTC | 79582 |
rs116662899 | snp | A/G | 0.00755907 | 0.0610114 | intron-variant | SPAG16 | GRCh38.p7 | 2:214286900 | ACTTCCATGAATCTC[A/G]TCTTCCTCGTCTCTT | 79582 |
rs116664001 | snp | A/G | 0.02016 | 0.0983543 | intron-variant | SPAG16 | GRCh38.p7 | 2:213913465 | TGCCAGAGAAATATA[A/G]TAGAACGAATATGTG | 79582 |
rs116665320 | snp | C/T | 0.0275645 | 0.114116 | intron-variant | SPAG16 | GRCh38.p7 | 2:213855678 | CATGGCAGAAGGCAC[C/T]CCTTCACAGGGCATC | 79582 |
rs116669474 | snp | A/G | 0.0189856 | 0.0955633 | intron-variant | SPAG16 | GRCh38.p7 | 2:213782449 | GATATGTAGTACCAA[A/G]TGTAACAACTTAACA | 79582 |
rs116670745 | snp | A/G | 0.325799 | 0.238232 | intron-variant | SPAG16 | GRCh38.p7 | 2:213718238 | ACATTTATGTGGCCA[A/G]TAAACAAATGAAAAA | 79582 |
rs116675268 | snp | C/T | 0.0726307 | 0.176182 | intron-variant | SPAG16 | GRCh38.p7 | 2:213995103 | CTTCTCATGCGTCCT[C/T]CTCATTTCATAAGCA | 79582 |
rs116675381 | snp | A/G | 0.00597247 | 0.0543191 | intron-variant | SPAG16 | GRCh38.p7 | 2:213372975 | GCACTGGAAGGTACA[A/G]TAAATAGAATTTCTA | 79582 |
rs116676529 | snp | A/G | 0.0425829 | 0.139564 | intron-variant | SPAG16 | GRCh38.p7 | 2:213513237 | TTCTCTATGCCCTAT[A/G]TTTTCAAAGGCTCAT | 79582 |
rs116679531 | snp | A/G | 0.00159617 | 0.0282053 | intron-variant | SPAG16 | GRCh38.p7 | 2:213480498 | TTTGACATTTACTCA[A/G]AGTAATACCATACCT | 79582 |
rs116686713 | snp | A/G | 0.00755907 | 0.0610114 | intron-variant | SPAG16 | GRCh38.p7 | 2:214029863 | GAATTGCACTTGTTT[A/G]ATGTATACAATTTGA | 79582 |
rs116687670 | snp | C/T | 0.00517822 | 0.0506191 | intron-variant | SPAG16 | GRCh38.p7 | 2:213402267 | TTGCAGTAAATATTT[C/T]CTTTCCTCCATTAAT | 79582 |
rs116688844 | snp | A/C | 0.0693013 | 0.172766 | intron-variant | SPAG16 | GRCh38.p7 | 2:213974253 | CTACGATTTAAGCTC[A/C]TGCTTCAGAAGATTA | 79582 |
rs116689760 | snp | A/G | 0.00438332 | 0.0466095 | intron-variant | SPAG16 | GRCh38.p7 | 2:213999310 | GGCTGAAAGGGTCCA[A/G]TGTAGAGCTTGGGCT | 79582 |
rs116692073 | snp | C/T | 0.0189856 | 0.0955633 | intron-variant | SPAG16 | GRCh38.p7 | 2:213587729 | TTAAAATATTTTAAA[C/T]TCTCTCTTTTTACTG | 79582 |
rs116695687 | snp | C/G | 0.0240643 | 0.107019 | intron-variant | SPAG16 | GRCh38.p7 | 2:213534394 | TGCATAAGTATATAC[C/G]CCAATAATTGAAAAC | 79582 |
rs116695743 | snp | C/T | 0.00557542 | 0.0525036 | intron-variant | SPAG16 | GRCh38.p7 | 2:213441361 | TGAATGTCTTCTATA[C/T]GCATAGTATGGAATG | 79582 |
rs116699656 | snp | G/T | 0.00358779 | 0.0422022 | intron-variant | SPAG16 | GRCh38.p7 | 2:213644420 | TAGACATTCTTCAGT[G/T]TCTGGGCATTAAAGA | 79582 |
rs116702557 | snp | A/T | 0.00597247 | 0.0543191 | intron-variant | SPAG16 | GRCh38.p7 | 2:213304365 | TCCTTTGCTGTGCAA[A/T]ACTTTTTAACTGATG | 79582 |
rs116713182 | snp | A/T | 0.0170251 | 0.090679 | intron-variant | SPAG16 | GRCh38.p7 | 2:213699491 | ATTTCTCAAAACATG[A/T]TAGTGACAGACCACC | 79582 |
rs116719977 | snp | A/G | 0.0260105 | 0.111035 | intron-variant | SPAG16 | GRCh38.p7 | 2:213689573 | TCTCACTTCAAAAGT[A/G]TGACCTCTCTAAGAG | 79582 |
rs116726009 | snp | C/G | 0.0283406 | 0.115616 | intron-variant | SPAG16 | GRCh38.p7 | 2:214312731 | GGCTTTTGCAGGAGT[C/G]TATCCTTAGAATACA | 79582 |
rs116731313 | snp | C/T | 0.0023933 | 0.0345097 | intron-variant | SPAG16 | GRCh38.p7 | 2:213793654 | TATTGTAAGCACTAG[C/T]AATAATTCAAAATGA | 79582 |
rs116735922 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | SPAG16 | GRCh38.p7 | 2:214330574 | GGCAACAGAAGCTCA[A/G]TTGATCCTACGGAAC | 79582 |
rs116740055 | snp | C/T | 0.00358779 | 0.0422022 | intron-variant | SPAG16 | GRCh38.p7 | 2:214196513 | TTCAGAATGGAAGAA[C/T]GGTAAATATCACTTA | 79582 |
rs116741198 | snp | A/T | 0.0252325 | 0.109451 | intron-variant | SPAG16 | GRCh38.p7 | 2:213328811 | TAAGATGGTTACCTG[A/T]TGATTGGTTTGGCTG | 79582 |
rs116741530 | snp | A/G | 0.0146672 | 0.084371 | intron-variant | SPAG16 | GRCh38.p7 | 2:213363494 | GTATAATCATATACA[A/G]TGCAAGATGAAATAG | 79582 |
rs116743435 | snp | A/G | 0.029116 | 0.117091 | intron-variant | SPAG16 | GRCh38.p7 | 2:213919698 | CATTTGCTGAGGATT[A/G]TTCTGTGTCTCATTA | 79582 |
rs116744840 | snp | A/G | 0.0126979 | 0.078662 | intron-variant | SPAG16 | GRCh38.p7 | 2:213509185 | ATATTTTTAGAAGAG[A/G]CGGGGTTTCACCATC | 79582 |
rs116749755 | snp | A/C | 0.0150606 | 0.0854603 | intron-variant | SPAG16 | GRCh38.p7 | 2:214042420 | ATCCCATGAAGAAGT[A/C]AAAACAAAAACAAAA | 79582 |
rs116750550 | snp | C/G | 0.0205511 | 0.0992634 | intron-variant | SPAG16 | GRCh38.p7 | 2:213936705 | ATTCTCCTTATACTG[C/G]GACACTAATATAAAC | 79582 |
rs116754446 | snp | A/G | 0.00398564 | 0.0444627 | intron-variant | SPAG16 | GRCh38.p7 | 2:214218783 | ATGAGTTTGGAACAG[A/G]TGGCAAAGCTAGTGG | 79582 |
rs116755055 | snp | C/T | 0.0221141 | 0.102801 | intron-variant | SPAG16 | GRCh38.p7 | 2:213643724 | ATCTTTTGTGTCTTA[C/T]GATTGTGTGTTTTCA | 79582 |
rs116756152 | snp | A/G | 0.00358779 | 0.0422022 | intron-variant | SPAG16 | GRCh38.p7 | 2:214157093 | GGCCTCACTGATTCT[A/G]GAGAAAGGAACTGGA | 79582 |
rs116756466 | snp | C/T | 0.00438332 | 0.0466095 | intron-variant | SPAG16 | GRCh38.p7 | 2:213491455 | ATCCTTCTCATATTT[C/T]ATCACCATAACTAAT | 79582 |
rs116759616 | snp | A/G | 0.0150606 | 0.0854603 | intron-variant | SPAG16 | GRCh38.p7 | 2:213859786 | ATACTGATAGTACCA[A/G]CATCAGTCACTAAGT | 79582 |
rs116761479 | snp | A/C | 0.0142736 | 0.0832652 | intron-variant | SPAG16 | GRCh38.p7 | 2:214108562 | CACATTTTTAAGAGC[A/C]TTTTGTCCAATTTGG | 79582 |
rs116762025 | snp | C/T | 0.0456336 | 0.143994 | intron-variant | SPAG16 | GRCh38.p7 | 2:214007610 | AAAATGTTTTATTCT[C/T]GTTATTGAAGGAATT | 79582 |
rs116765877 | snp | C/T | 0.0562307 | 0.157967 | intron-variant | SPAG16 | GRCh38.p7 | 2:214008139 | TACTATTTTTTCCTT[C/T]AGTACCCAATCTGAT | 79582 |
rs116767275 | snp | A/G | 0.0566069 | 0.158427 | intron-variant | SPAG16 | GRCh38.p7 | 2:213993199 | CCCAACGGGCAGAAT[A/G]TAGAGAAGGTATATT | 79582 |
rs116773843 | snp | A/G | 0.0205511 | 0.0992634 | intron-variant | SPAG16 | GRCh38.p7 | 2:213884960 | CTTCCTTGCCATCCA[A/G]ATTCTGAATTCCTTG | 79582 |
rs116775351 | snp | C/T | 0.00358779 | 0.0422022 | intron-variant | SPAG16 | GRCh38.p7 | 2:213321899 | GAAAAGGAGAGCATA[C/T]GTTTTCTATTGAAAT | 79582 |
rs116778775 | snp | C/T | 0.0236746 | 0.106192 | intron-variant | SPAG16 | GRCh38.p7 | 2:213950830 | CCTCCCATATTAACC[C/T]TCTGAGTAGCTGGGA | 79582 |
rs116787473 | snp | A/G | 0.00478085 | 0.0486577 | intron-variant | SPAG16 | GRCh38.p7 | 2:213646066 | CCTCACAATTGCTGT[A/G]CTCTCCCCACTACTC | 79582 |
rs116789422 | snp | A/G | 0.00874735 | 0.0655527 | intron-variant | SPAG16 | GRCh38.p7 | 2:213535046 | CCCTGCTAACATTTG[A/G]TCTTGAATTTCTACT | 79582 |
rs116791326 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | SPAG16 | GRCh38.p7 | 2:213690684 | CAGGCAGAAGAAGAG[A/G]ATAGGCAGCTTGTTG | 79582 |
rs116793503 | snp | C/T | 0.0182019 | 0.0936463 | intron-variant | SPAG16 | GRCh38.p7 | 2:214284664 | GAGTACAGCTAAATA[C/T]TATGTAAGTTGAAAA | 79582 |
rs116795892 | snp | C/T | 0.00358779 | 0.0422022 | intron-variant | SPAG16 | GRCh38.p7 | 2:213501200 | AATAATTCTTGCAGA[C/T]GCCATTGACAAGTTT | 79582 |
rs116796662 | snp | C/G | 0.0228947 | 0.104514 | intron-variant | SPAG16 | GRCh38.p7 | 2:213991159 | CTCTCCCCTAGCCCC[C/G]ACTCCCCGTCAGGCC | 79582 |
rs116805747 | snp | G/T | 0.0107246 | 0.0724382 | intron-variant | SPAG16 | GRCh38.p7 | 2:214389918 | CCTATGTAAAACGTT[G/T]AAGTGACTGTGAAAT | 79582 |
rs116807835 | snp | A/G | 0.00636936 | 0.0560724 | intron-variant | SPAG16, LOC101928084 | GRCh38.p7 | 2:214100659 | CTGTTCCTTGTTGCT[A/G]TGTTAGTTCACTTAA | 79582 |
rs116807981 | snp | A/C | 0.0178098 | 0.0926698 | intron-variant | SPAG16 | GRCh38.p7 | 2:214281388 | TTACCGTCCCATTGT[A/C]TTCTAAATTTCACTT | 79582 |
rs116811054 | snp | A/G | 0.0205511 | 0.0992634 | intron-variant | SPAG16 | GRCh38.p7 | 2:213797195 | AACAGTTTATAAAGT[A/G]AAAATGTTACAGTAA | 79582 |
rs116811280 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | SPAG16 | GRCh38.p7 | 2:213787413 | CTAAGTAATTTTCAT[A/G]TATTAGCTTCTTTCA | 79582 |
rs116814399 | snp | A/C | 0.0248432 | 0.108648 | intron-variant | SPAG16 | GRCh38.p7 | 2:214234060 | CCTTTCAATAGGCCC[A/C]AGTATGTGTTGTTTC | 79582 |
rs116814580 | snp | A/G | 0.00159617 | 0.0282053 | intron-variant | SPAG16 | GRCh38.p7 | 2:213704891 | TGGGGTAAGGGAATG[A/G]TAGAATTTGTCCAGA | 79582 |
rs116814892 | snp | C/T | 0.00159617 | 0.0282053 | intron-variant, upstream-variant-2KB | SPAG16, MIR4438 | GRCh38.p7 | 2:213757879 | GAGGTGAGTGGTTAT[C/T]GTTGCACCTCTATCC | 79582 |
rs116817297 | snp | A/G | 0.00953873 | 0.0683987 | intron-variant | SPAG16 | GRCh38.p7 | 2:213887339 | CTCCATTGTTTTTTC[A/G]TTTTGTTTTGTTTTG | 79582 |
rs116822560 | snp | G/T | 0.0337553 | 0.125452 | intron-variant | SPAG16 | GRCh38.p7 | 2:214200015 | GATGAGTTTTTAGGG[G/T]TTGCTAGGTAAACGA | 79582 |
rs116825770 | snp | C/T | 0.0154538 | 0.0865337 | intron-variant | SPAG16 | GRCh38.p7 | 2:214306555 | GGTATGTGTCTTCAA[C/T]ACCTCGTTTATTGGA | 79582 |
rs116828719 | snp | A/G | 0.0182019 | 0.0936463 | intron-variant | SPAG16 | GRCh38.p7 | 2:214262068 | ATTTACATTAGATAT[A/G]TAATTAGACTATCTA | 79582 |
rs116838184 | snp | A/G | 0.00874735 | 0.0655527 | intron-variant | SPAG16 | GRCh38.p7 | 2:213673957 | CAACTTTAATACTTA[A/G]TAGTTGCAAGTGTCA | 79582 |
rs116839228 | snp | C/T | 0.00716266 | 0.059414 | intron-variant | SPAG16 | GRCh38.p7 | 2:213603268 | CCCTTGTTTATATCT[C/T]TCGCTCATTTTTCTA | 79582 |
rs116861445 | snp | A/G | 0.00636936 | 0.0560724 | intron-variant | SPAG16 | GRCh38.p7 | 2:213975918 | AACGGGTTCTTGTGA[A/G]GTTGCCATCAGTGTT | 79582 |
rs116876794 | snp | C/T | 0.021333 | 0.101051 | intron-variant | SPAG16 | GRCh38.p7 | 2:214131983 | ACCAATTGTAACAAG[C/T]GTACCACTCTGGTGG | 79582 |
rs116896813 | snp | A/G | 0.0185938 | 0.0946107 | intron-variant | SPAG16 | GRCh38.p7 | 2:213859449 | CTATTGTGTCTGGTG[A/G]TACCCAGCTCTGATA | 79582 |
rs116903309 | snp | C/G | 0.0165278 | 0.0893908 | intron-variant | SPAG16 | GRCh38.p7 | 2:213615863 | TACTTTTTGCAGTAT[C/G]ACAATAATCCTATGA | 79582 |
rs116907694 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | SPAG16 | GRCh38.p7 | 2:214376471 | TCAAACTCTGCCTGC[C/T]TGACCTAAGGAAACC | 79582 |
rs116913638 | snp | C/T | 0.00636936 | 0.0560724 | intron-variant | SPAG16 | GRCh38.p7 | 2:213895612 | AAATCCGTGCATTTG[C/T]ATCCAACTCATCTTT | 79582 |
rs116922552 | snp | A/G | 0.0150606 | 0.0854603 | intron-variant | SPAG16 | GRCh38.p7 | 2:214118029 | GCAAAAAGAAATAAC[A/G]CGCATCCAAATTGGA | 79582 |
rs116954749 | snp | A/G | 0.00438332 | 0.0466095 | intron-variant | SPAG16 | GRCh38.p7 | 2:213357553 | GTTGGTTTTAAAGTC[A/G]TTTTATCAGAGACTA | 79582 |
rs116956357 | snp | A/G | 0.0107246 | 0.0724382 | intron-variant | SPAG16 | GRCh38.p7 | 2:213691034 | GACTAATACAGTGAC[A/G]GAGGAGCCCTGAAGG | 79582 |
rs116989442 | snp | A/G | 0.0197687 | 0.0974348 | intron-variant | SPAG16 | GRCh38.p7 | 2:213424197 | AAGTTGTGAGAAGGA[A/G]TCAAATGTTAGGCAG | 79582 |
rs117010468 | snp | G/T | 0.00398564 | 0.0444627 | intron-variant, upstream-variant-2KB | SPAG16 | GRCh38.p7 | 2:213294921 | GATTTGTAAAATAGA[G/T]TTATAGTTCCAGCCT | 79582 |
rs117010615 | snp | A/C | 0.0197687 | 0.0974348 | intron-variant | SPAG16 | GRCh38.p7 | 2:213837793 | AAACCCAATGTAATC[A/C]CAAGAGTCCATATAA | 79582 |
rs117029482 | snp | A/G | 0.0337553 | 0.125452 | intron-variant | SPAG16 | GRCh38.p7 | 2:214144055 | TTCAACTACTTGGGA[A/G]GCTGACGTGGAAGGA | 79582 |
rs117045437 | snp | A/T | 0.00557542 | 0.0525036 | intron-variant | SPAG16 | GRCh38.p7 | 2:214290560 | CTGTCTCCCACAAGT[A/T]TGGGTATTTTTGTAT | 79582 |
rs117050475 | snp | A/G | 0.0111196 | 0.0737302 | intron-variant | SPAG16 | GRCh38.p7 | 2:213915053 | TCATAATCACGGCAG[A/G]AGGTGAATGAGAATC | 79582 |
rs117057558 | snp | A/G | 0.0165278 | 0.0893908 | intron-variant | SPAG16 | GRCh38.p7 | 2:214221134 | AGGTTCAGGTTCTTT[A/G]GAAGTTTAACTACAG | 79582 |
rs117089916 | snp | C/G | 0.00755907 | 0.0610114 | intron-variant | SPAG16 | GRCh38.p7 | 2:213484723 | CCCAATAGTATTGAT[C/G]AGTGTAAGCAACATT | 79582 |
rs117101707 | snp | C/T | 0.00279162 | 0.0372561 | intron-variant | SPAG16 | GRCh38.p7 | 2:214306100 | CTTTCACCTCCCTAA[C/T]AAGCTGTATTCCTAG | 79582 |
rs117152163 | snp | C/T | 0.0123036 | 0.0774623 | intron-variant | SPAG16 | GRCh38.p7 | 2:213324597 | TAATTTGTTCCTCTT[C/T]ATTGCTAAGTAGTAT | 79582 |
rs117156880 | snp | A/G | 0.00159617 | 0.0282053 | intron-variant | SPAG16 | GRCh38.p7 | 2:213870992 | TGCGAGACCAGAAAT[A/G]TAGTCACTTTCTTTC | 79582 |
rs117235825 | snp | A/T | 0.00279162 | 0.0372561 | intron-variant | SPAG16 | GRCh38.p7 | 2:214336128 | TAGTTATCTTGTTGC[A/T]ATTTGAATTGGCTAT | 79582 |
rs117237204 | snp | C/T | 0.0165278 | 0.0893908 | intron-variant, nc-transcript-variant | SPAG16, LOC101928084 | GRCh38.p7 | 2:214102701 | TACCGACGGCAAATC[C/T]ATAGGTGTCTGGAGC | 79582 |
rs117240134 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | SPAG16 | GRCh38.p7 | 2:214182696 | TATAAATTGGGATAA[A/G]GACCAAAATAATTGC | 79582 |
rs117263662 | snp | G/T | 0.00318978 | 0.0398085 | intron-variant | SPAG16 | GRCh38.p7 | 2:213566347 | GAGATTTTAACTTCA[G/T]GCAAAACATTCAGAG | 79582 |
rs117269236 | snp | G/T | 0.00358779 | 0.0422022 | intron-variant | SPAG16 | GRCh38.p7 | 2:213967058 | CTTTTGAATAACTTA[G/T]TTCAATCTAATTCTA | 79582 |
rs117277231 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | SPAG16 | GRCh38.p7 | 2:213530976 | AATCTAATTAAAGTT[A/G]TTTATAATCTTTTTT | 79582 |
rs117283167 | snp | C/T | 0.00597247 | 0.0543191 | intron-variant | SPAG16 | GRCh38.p7 | 2:214198654 | TGGTAGTTATACTTT[C/T]AGTTCTTTAAGGAGG | 79582 |
rs117298096 | snp | C/T | 0.021333 | 0.101051 | intron-variant | SPAG16 | GRCh38.p7 | 2:214058337 | TTGTCTCTCAGTGAA[C/T]AGAAAGTCCCAAGGA | 79582 |
rs117323118 | snp | A/C | 0.0178098 | 0.0926698 | intron-variant | SPAG16 | GRCh38.p7 | 2:213873609 | TATTTGTTCTTTTTA[A/C]ATGTACCATTTACAT | 79582 |
rs117326014 | snp | G/T | 0.00914312 | 0.0669923 | intron-variant | SPAG16 | GRCh38.p7 | 2:213898456 | CATGTGAAATTCAGA[G/T]GAAAACTGTGATCTT | 79582 |
rs117328811 | snp | C/G | 0.0189856 | 0.0955633 | intron-variant | SPAG16 | GRCh38.p7 | 2:213891780 | GATGGTAAGATAATA[C/G]GACTTCCACATCTGC | 79582 |
rs117334113 | snp | A/G | 0.00716266 | 0.059414 | intron-variant | SPAG16, LOC101928084 | GRCh38.p7 | 2:214097712 | AAATATGTATTAAAT[A/G]CTTCCCACGTGCTAA | 79582 |
rs117362940 | snp | C/T | 0.0577344 | 0.159793 | intron-variant | SPAG16 | GRCh38.p7 | 2:213771763 | TCAGATGATCATAGA[C/T]GTGCAGTCTTATTTC | 79582 |
rs117387746 | snp | A/G | 0.0337553 | 0.125452 | intron-variant | SPAG16 | GRCh38.p7 | 2:214144056 | TCAACTACTTGGGAG[A/G]CTGACGTGGAAGGAT | 79582 |
rs117388944 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | SPAG16 | GRCh38.p7 | 2:213624751 | TCCTCTGTACTTGCT[A/G]AATGCATGATCTTGG | 79582 |
rs117401747 | snp | C/T | 0.0193772 | 0.0965046 | intron-variant | SPAG16 | GRCh38.p7 | 2:213880299 | GTGTCTGTTCATGGC[C/T]TTTGCCCACTTTTTA | 79582 |
rs117410379 | snp | A/G | 0.030665 | 0.119967 | intron-variant | SPAG16 | GRCh38.p7 | 2:213968244 | TAACGGCGAGATCTC[A/G]TCTCACTGCAATCTC | 79582 |
rs117446680 | snp | A/T | 0.00199481 | 0.0315187 | intron-variant | SPAG16 | GRCh38.p7 | 2:213562440 | CAAATATGGATATTG[A/T]CTCTTAAGTTTGTTC | 79582 |
rs117458877 | snp | C/T | 0.0463947 | 0.145069 | intron-variant | SPAG16 | GRCh38.p7 | 2:213713146 | GAACCGCCCCCATGA[C/T]CTAATCACCTCCTCT | 79582 |
rs117472080 | snp | A/G | 0.0471551 | 0.14613 | intron-variant | SPAG16 | GRCh38.p7 | 2:213991309 | TTTCCAGCTTCATCC[A/G]CATTTCTGCAAAGGG | 79582 |
rs117473464 | snp | C/T | 0.00557542 | 0.0525036 | intron-variant, upstream-variant-2KB | SPAG16 | GRCh38.p7 | 2:213316630 | AGACACTCCAGGTAC[C/T]CTGGCTGTTTGTTCT | 79582 |
rs117474492 | snp | A/G | 0.00358779 | 0.0422022 | intron-variant | SPAG16 | GRCh38.p7 | 2:214189924 | CACCTGAAATTTTCC[A/G]AAATTGGGATCATAC | 79582 |
rs117484683 | snp | A/G | 0.00159617 | 0.0282053 | intron-variant | SPAG16 | GRCh38.p7 | 2:214307838 | TACAGTATGTGCCAT[A/G]TTGCAATGAAAAGAA | 79582 |
rs117487444 | snp | C/T | 0.0185938 | 0.0946107 | intron-variant | SPAG16 | GRCh38.p7 | 2:213847614 | TACACCAGGCCCCAC[C/T]TTCAGTATTGGGATT | 79582 |
rs117507994 | snp | C/T | 0.00676609 | 0.0577691 | intron-variant | SPAG16 | GRCh38.p7 | 2:214371009 | TCCCCATCCTCTGTG[C/T]TTGCTCCAGATCGCA | 79582 |
rs117525817 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | SPAG16 | GRCh38.p7 | 2:213646186 | CAGTGCCTCTTTCGA[C/T]GATACAAAGTTACAA | 79582 |
rs117533095 | snp | A/C | 0.0126979 | 0.078662 | intron-variant | SPAG16 | GRCh38.p7 | 2:213553091 | CCTTCACCTTGTGAT[A/C]GTGTGAGTCAATACA | 79582 |
rs117540508 | snp | C/T | 0.00517822 | 0.0506191 | intron-variant | SPAG16 | GRCh38.p7 | 2:214329034 | GGATACAAAGATGGT[C/T]AGAATGTAACTTTGT | 79582 |
rs117546649 | snp | C/T | 0.00478085 | 0.0486577 | intron-variant | SPAG16 | GRCh38.p7 | 2:213523068 | GGTTTGGCTGTGTCA[C/T]CTCCCAGATCTCATC | 79582 |
rs117558747 | snp | C/T | 0.0189856 | 0.0955633 | intron-variant | SPAG16 | GRCh38.p7 | 2:213894961 | GCCATTGCACTCCAG[C/T]GTGGCAACAGAACAA | 79582 |
rs117568860 | snp | A/G | 0.00358779 | 0.0422022 | intron-variant | SPAG16 | GRCh38.p7 | 2:213531485 | ATGGTGAAGAGGCAC[A/G]TGGGGAGTAGCTGCA | 79582 |
rs117581878 | snp | A/G | 0.0166325 | 0.0896639 | intron-variant | SPAG16 | GRCh38.p7 | 2:213329177 | AGTAAATTGGTACCA[A/G]TATAGTGGGCATTGC | 79582 |
rs117602562 | snp | A/G | 0.0107246 | 0.0724382 | intron-variant | SPAG16 | GRCh38.p7 | 2:214048460 | TATGCCAGGCACACA[A/G]AGACAAACTGCATGT | 79582 |
rs117612935 | snp | A/G | 0.0471551 | 0.14613 | intron-variant | SPAG16 | GRCh38.p7 | 2:213975891 | TGGCAGCTCGGCTGG[A/G]TGGTTCTGGTTAACG | 79582 |
rs117617378 | snp | A/C | 0.0138799 | 0.0821421 | intron-variant | SPAG16 | GRCh38.p7 | 2:213819372 | AAGTGGCACTAATTA[A/C]TAGCCAACATTTTAT | 79582 |
rs117619722 | snp | C/G/T | 0.0014238 | 0.0266438 | intron-variant | SPAG16 | GRCh38.p7 | 2:214108274 | AGGGTAAGTTCAGTT[C/G/T]TCCCAGTAAACTGTT | 79582 |
rs117628721 | snp | A/G | 0.00279162 | 0.0372561 | intron-variant | SPAG16 | GRCh38.p7 | 2:213414833 | GTCCCTTCTTAATGG[A/G]CTATATATGTATATA | 79582 |
rs117633650 | snp | A/G | 0.00755907 | 0.0610114 | intron-variant | SPAG16 | GRCh38.p7 | 2:213631260 | ATTTCAAAACAAACA[A/G]ACAAACAAACCATGG | 79582 |
rs117634509 | snp | A/G | 0.0130921 | 0.0798413 | intron-variant | SPAG16 | GRCh38.p7 | 2:214135905 | ATCGGAGGCTGGGCA[A/G]TTTATAAAGAAAAGA | 79582 |
rs117649541 | snp | A/C | 0.0217236 | 0.101931 | intron-variant | SPAG16 | GRCh38.p7 | 2:213611266 | AGAGGGCAAAGGGGA[A/C]GTTTTCCCTTGGCTC | 79582 |
rs117656244 | snp | A/G | 0.0107246 | 0.0724382 | intron-variant | SPAG16 | GRCh38.p7 | 2:213908424 | ACAAATATTCTTAGA[A/G]CTTTCTTGGCCATCG | 79582 |
rs117687669 | snp | C/T | 0.0327778 | 0.123752 | intron-variant | SPAG16 | GRCh38.p7 | 2:213292988 | TGATATGGTTTGGCT[C/T]TGTGTCCCCACCCTA | 79582 |
rs117716960 | snp | A/C | 0.0166325 | 0.0896639 | intron-variant | SPAG16 | GRCh38.p7 | 2:214157402 | AAACTGTTATGCTTT[A/C]TCTGGAAATTTAACT | 79582 |
rs117730121 | snp | C/T | 0.00318978 | 0.0398085 | intron-variant | SPAG16 | GRCh38.p7 | 2:213769187 | TTGGGGTGGATAAAG[C/T]CAACTCTAAGTTAAA | 79582 |
rs117742484 | snp | C/T | 0.00676609 | 0.0577691 | intron-variant | SPAG16 | GRCh38.p7 | 2:213711382 | CATGTTTACATAAGA[C/T]GTTAAAAGTAAAGTA | 79582 |
rs117787855 | snp | C/T | 0.0287284 | 0.116357 | intron-variant | SPAG16 | GRCh38.p7 | 2:213963873 | ACTGTTACTGTTTAA[C/T]GGTGTTTCCTTTCCC | 79582 |
rs117796618 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | SPAG16 | GRCh38.p7 | 2:213838712 | AGCAGAAACAGAGCA[C/G]AAGAAGCTGATTGGC | 79582 |
rs117810996 | snp | C/T | 0.00279162 | 0.0372561 | intron-variant | SPAG16 | GRCh38.p7 | 2:214371060 | TCACTTTAATGGAGG[C/T]ATTGTCAGTTTCAGA | 79582 |
rs117811382 | snp | A/G | 0.00159617 | 0.0282053 | intron-variant, downstream-variant-500B | SPAG16 | GRCh38.p7 | 2:213703573 | GGCTAGGAATCAAAC[A/G]GCTCTTACCATATGT | 79582 |
rs117820882 | snp | A/G | 0.0475351 | 0.146656 | intron-variant | SPAG16 | GRCh38.p7 | 2:213944993 | CAATGAGCCAAGATC[A/G]TGCCATTGCCCTCCA | 79582 |
rs117825210 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant, utr-variant-5-prime | SPAG16 | GRCh38.p7 | 2:213299793 | TTATTAATCTATAAC[A/T]GTTATGTAGTTTGAT | 79582 |
rs117830542 | snp | A/G | 0.00557542 | 0.0525036 | intron-variant | SPAG16 | GRCh38.p7 | 2:214152351 | GAAGAAAAAGAATAT[A/G]GACTATATATTTCAG | 79582 |
rs117831589 | snp | C/T | 0.00159617 | 0.0282053 | intron-variant | SPAG16 | GRCh38.p7 | 2:214293496 | TCAGATGAAAGCTGG[C/T]GAGCAGATTTGTCAT | 79582 |
rs117835776 | snp | C/T | 0.00953873 | 0.0683987 | intron-variant | SPAG16 | GRCh38.p7 | 2:213639573 | AAAGATAGGATCCCA[C/T]CCCTGCTAGCTTACA | 79582 |
rs117847849 | snp | G/T | 0.00119737 | 0.0244387 | intron-variant | SPAG16 | GRCh38.p7 | 2:214117938 | TTCCTCTAAAATCTG[G/T]ACTAAGACAAATATG | 79582 |
rs117854494 | snp | C/T | 0.00398564 | 0.0444627 | intron-variant | SPAG16 | GRCh38.p7 | 2:213429975 | ACAGTAATTCTCTAG[C/T]GACATGTCCTAACTA | 79582 |
rs117888725 | snp | A/G | 0.0209421 | 0.100162 | intron-variant | SPAG16 | GRCh38.p7 | 2:214191435 | GGAAAAACCAGGGCC[A/G]GGCATGGTGGCTCAC | 79582 |
rs117917214 | snp | A/C | 0.00478085 | 0.0486577 | intron-variant | SPAG16 | GRCh38.p7 | 2:214248780 | CAAAAATTAATGCAT[A/C]ATAAGAGAATAGCAA | 79582 |
rs117924462 | snp | C/T | 0.0023933 | 0.0345097 | intron-variant | SPAG16 | GRCh38.p7 | 2:214033296 | TCTTTGCTTGAGATA[C/T]TTATAGTTTTGTGGT | 79582 |
rs117927756 | snp | A/G | 0.0189856 | 0.0955633 | intron-variant | SPAG16 | GRCh38.p7 | 2:213866190 | TTAGTTTCATTACCT[A/G]GCCCAAGGACAGAAA | 79582 |
rs117951038 | snp | A/T | 0.0189856 | 0.0955633 | intron-variant | SPAG16 | GRCh38.p7 | 2:214224445 | TGCAAATACTATAAT[A/T]TTGATGTATAAGTAC | 79582 |
rs117956354 | snp | A/G | 0.0197687 | 0.0974348 | intron-variant | SPAG16 | GRCh38.p7 | 2:213906484 | CTCTATCAAAATACC[A/G]ATTACATTATTCACA | 79582 |
rs117964843 | snp | A/C/T | 0.00239393 | 0.0345281 | intron-variant | SPAG16 | GRCh38.p7 | 2:213911453 | CCCTGCCAATAGTTA[A/C/T]AAGCTCTTATGTTTC | 79582 |
rs117974191 | snp | C/T | 0.00358779 | 0.0422022 | intron-variant | SPAG16 | GRCh38.p7 | 2:214029689 | CAAAAACAAATCTTA[C/T]TCAAACTTAACTCTA | 79582 |
rs117994963 | snp | C/T | 0.0107246 | 0.0724382 | intron-variant, utr-variant-3-prime | SPAG16 | GRCh38.p7 | 2:213400332 | TCCCACAGATGTTTA[C/T]ATGTAGCATTTTAAT | 79582 |
rs117997441 | snp | C/T | 0.00318978 | 0.0398085 | intron-variant | SPAG16 | GRCh38.p7 | 2:213710422 | AGGTATCTTAAGTCT[C/T]TGGAACAAGGGTATA | 79582 |
rs117999118 | snp | G/T | 0.00438332 | 0.0466095 | intron-variant | SPAG16 | GRCh38.p7 | 2:214401704 | CAAAGCTCCATTCCT[G/T]CAGACACATTCCTAC | 79582 |
rs118008181 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | SPAG16 | GRCh38.p7 | 2:213821942 | ACATTATCTTTATCT[A/G]TTGGTCTATTGGTGG | 79582 |
rs118042683 | snp | A/G | 0.00438332 | 0.0466095 | intron-variant | SPAG16 | GRCh38.p7 | 2:213698681 | CACCTGGACAAATAT[A/G]CTCTGTTCTGTACAC | 79582 |
rs118083145 | snp | C/T | 0.0123036 | 0.0774623 | intron-variant | SPAG16 | GRCh38.p7 | 2:214013797 | GCTGAGAATATAAGG[C/T]AGCTATAGAATTTTA | 79582 |
rs118090353 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | SPAG16 | GRCh38.p7 | 2:213468849 | AGGAGAGCCAGTTCA[A/G]GTCCCAAAACTGAAA | 79582 |
rs118105108 | snp | A/G | 0.0182019 | 0.0936463 | intron-variant | SPAG16 | GRCh38.p7 | 2:213862433 | TTTATTCATATTCTG[A/G]AAACATTTGCTATTA | 79582 |
rs118117462 | snp | C/G | 0.00953873 | 0.0683987 | intron-variant | SPAG16 | GRCh38.p7 | 2:213573887 | TTAGGGCAACCTAAA[C/G]CAGTGTGAATCAGAC | 79582 |
rs118125176 | snp | C/T | 0.0165278 | 0.0893908 | intron-variant | SPAG16 | GRCh38.p7 | 2:214009664 | TGATGCTACGGGTAT[C/T]GCAACATACTACATA | 79582 |
rs118136622 | snp | C/T | 0.0189856 | 0.0955633 | intron-variant | SPAG16 | GRCh38.p7 | 2:213879845 | CTGTGTAGTATTCCA[C/T]AGTGTGTGTGTACCA | 79582 |
rs118136691 | snp | A/G/T | 0.00993419 | 0.0697739 | intron-variant | SPAG16 | GRCh38.p7 | 2:214335332 | GAACATCTCTGTGAC[A/G/T]CCCCGCAGCATCCGC | 79582 |
rs118164056 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | SPAG16 | GRCh38.p7 | 2:214116576 | TTGTGCAGGACCTGC[C/T]GGGAAGCACACCTGT | 79582 |
rs118172125 | snp | C/G | 0.0876345 | 0.190099 | intron-variant | SPAG16, LOC101928084 | GRCh38.p7 | 2:214086570 | TTTCCTCCCTTATTC[C/G]CTCTCTTGCTGCCTT | 79582 |
rs118176798 | snp | A/G | 0.0327778 | 0.123752 | intron-variant | SPAG16 | GRCh38.p7 | 2:214195260 | AAAGGCAGAGTGACC[A/G]GGGGAAGATACTGAG | 79582 |
rs118177852 | snp | A/C | 0.0349115 | 0.127424 | intron-variant | SPAG16 | GRCh38.p7 | 2:213609098 | CAGAAATTATTGTAA[A/C]ACTGGTTATTCATCT | 79582 |
rs118186832 | snp | C/T | 0.0178098 | 0.0926698 | intron-variant | SPAG16 | GRCh38.p7 | 2:214149939 | AGTTGCATCTGCATC[C/T]TTAATGATAGAGTTT | 79582 |
rs137855524 | snp | C/T | 0.0023933 | 0.0345097 | intron-variant | SPAG16 | GRCh38.p7 | 2:213365702 | TCTTGAAGTGATCCG[C/T]CTGCCTCAGCCTCCC | 79582 |
rs137855677 | snp | A/G | 0.00517822 | 0.0506191 | intron-variant | SPAG16 | GRCh38.p7 | 2:213324316 | TATATACATTGAAGT[A/G]TATGTCTTAGCTATA | 79582 |
rs137856788 | snp | A/G | 0.00279162 | 0.0372561 | intron-variant | SPAG16 | GRCh38.p7 | 2:213816702 | ATGCACATGATTCCT[A/G]AGGCATATTGTTTTC | 79582 |
rs137857860 | snp | C/T | 0.00358779 | 0.0422022 | intron-variant | SPAG16 | GRCh38.p7 | 2:214351277 | GTATGTTTGTATGTA[C/T]TCAGTAGCATTGTAG | 79582 |
rs137857960 | in-del | -/G | 0.34659 | 0.230587 | intron-variant | SPAG16 | GRCh38.p7 | 2:214199533 | TTGAAGTCGGGTAAT[-/G]TGATGCCTCTAGATT | 79582 |
rs137866011 | in-del | -/TATTCCCAGG | 0.0759472 | 0.179459 | intron-variant, upstream-variant-2KB | SPAG16, LOC101928084 | GRCh38.p7 | 2:214104598 | AAAAAGAGGTATTCT[-/TATTCCCAGG]TTTTTGGTTGCCTTG | 79582 |
rs137870442 | snp | A/G | 0.00159617 | 0.0282053 | intron-variant, utr-variant-3-prime | SPAG16 | GRCh38.p7 | 2:213397322 | GTAACTGTTCTCTCT[A/G]CTCCACTCAAATGTA | 79582 |
rs137871324 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | SPAG16 | GRCh38.p7 | 2:214234761 | TAAATTTTCAACAAA[C/T]TTTTGTTGAGCAAAA | 79582 |
rs137872776 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | SPAG16 | GRCh38.p7 | 2:214268503 | ATTTTTGACAACATG[A/G]ATGCAACTAAGAGGA | 79582 |
rs137874829 | snp | A/C | 0.00199481 | 0.0315187 | intron-variant | SPAG16 | GRCh38.p7 | 2:213479014 | TTATAATAAAAATTT[A/C]CTGTCAGCATTAAAA | 79582 |
rs137880991 | snp | A/G | 0.021333 | 0.101051 | intron-variant | SPAG16 | GRCh38.p7 | 2:213904197 | TACCTTGTCAGCAAC[A/G]TCCCACTCTACTGAT | 79582 |
rs137881683 | snp | C/G | 0.0240643 | 0.107019 | intron-variant | SPAG16 | GRCh38.p7 | 2:214026137 | CTTTAGAAAAGCTAA[C/G]AGCAAACCATACTTA | 79582 |
rs137885774 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | SPAG16 | GRCh38.p7 | 2:213696880 | GACCAAGAAGAGAAA[C/T]AGTAGCTGGAAGAGA | 79582 |
rs137885886 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | SPAG16 | GRCh38.p7 | 2:213643478 | TTTGATTATTAAATG[A/G]CTTGAGGTATTCTTT | 79582 |
rs137889142 | snp | A/G | 0.00358779 | 0.0422022 | intron-variant | SPAG16 | GRCh38.p7 | 2:213932341 | CTGCCTCAGCCTCCC[A/G]AGTAGCTGGGACTAT | 79582 |
rs137891198 | snp | C/T | | | intron-variant | SPAG16 | GRCh38.p7 | 2:213327480 | TTCCTGGGACGAGCA[C/T]AAATAGGCTTCTAAT | 79582 |
rs137898591 | snp | A/G | 0.0170251 | 0.090679 | intron-variant | SPAG16 | GRCh38.p7 | 2:213288409 | TCCCGGATTCGTGCC[A/G]TTCTGCTGCCCCAGC | 79582 |
rs137899900 | snp | C/T | 0.0146672 | 0.084371 | intron-variant | SPAG16 | GRCh38.p7 | 2:213853336 | CTACACACACTCCCT[C/T]CAAAATATCCTCTCG | 79582 |
rs137904339 | snp | A/G | 0.0166325 | 0.0896639 | intron-variant | SPAG16 | GRCh38.p7 | 2:214304214 | TTATTGTTGGGAACA[A/G]GCCCCCCAAAATCTG | 79582 |
rs137915202 | snp | C/G | 0.0103295 | 0.0711199 | intron-variant | SPAG16 | GRCh38.p7 | 2:213632870 | TGTTGAATTCAGTTT[C/G]CTATTACTTTGTTCA | 79582 |
rs137924381 | in-del | -/AT | | | intron-variant | SPAG16 | GRCh38.p7 | 2:214059270 | GTATGTATATATATA[-/AT]TATATAATCAAGAAT | 79582 |
rs137925230 | snp | A/G | 0.00398564 | 0.0444627 | intron-variant | SPAG16 | GRCh38.p7 | 2:213766024 | GGACTTCTGTTTCAT[A/G]TACTGAGAGCTTCGT | 79582 |
rs137928285 | snp | G/T | 0.0209421 | 0.100162 | intron-variant | SPAG16 | GRCh38.p7 | 2:214308849 | TGACCTTGGAGCATA[G/T]GAAGATTATATGTCT | 79582 |
rs137930970 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | SPAG16 | GRCh38.p7 | 2:214106247 | AAATTAACCAAAAAA[C/T]TTCTAAGATAATATA | 79582 |
rs137933426 | snp | G/T | 0.0263992 | 0.111815 | intron-variant | SPAG16 | GRCh38.p7 | 2:214222289 | GCCTGGCTAATTTGT[G/T]TATTTTTAGTAGAGA | 79582 |
rs137940311 | in-del | -/C | | | intron-variant | SPAG16 | GRCh38.p7 | 2:213433909 | TCTTTTTTCCTTTTT[-/C]TTTGTCTTTTTTTTT | 79582 |
rs137943317 | snp | A/G | 0.00318978 | 0.0398085 | intron-variant | SPAG16 | GRCh38.p7 | 2:213566209 | GGTTAGGTCGTTGGA[A/G]GAATTATCCAAATTG | 79582 |
rs137952160 | in-del | -/AT/TGTG | | | intron-variant | SPAG16 | GRCh38.p7 | 2:214149063 | GTGTGTATATATATA[-/AT/TGTG]TGTGTGTGTGTGTGT | 79582 |
rs137952818 | snp | C/T | 0.00438332 | 0.0466095 | intron-variant | SPAG16 | GRCh38.p7 | 2:214226592 | ACCTTTTGTTGTTCA[C/T]CAAAATGTGGTTGCA | 79582 |
rs137953907 | snp | G/T | 0.00874735 | 0.0655527 | intron-variant | SPAG16, LOC101928084 | GRCh38.p7 | 2:214097039 | AATGTTATATAAATT[G/T]CTCTATTGTATTAAA | 79582 |
rs137955664 | snp | A/G | 0.00597247 | 0.0543191 | intron-variant | SPAG16 | GRCh38.p7 | 2:214175078 | CAGCTATAATTCTTG[A/G]GTTGCAGTCAACAGA | 79582 |
rs137956238 | snp | G/T | 0.00953873 | 0.0683987 | intron-variant | SPAG16 | GRCh38.p7 | 2:213682904 | ATCCTGCTCTGTCAA[G/T]TTGTATTGGTTATTT | 79582 |
rs137972716 | snp | A/G | 0.00159617 | 0.0282053 | intron-variant | SPAG16 | GRCh38.p7 | 2:214107730 | TTTTATACAGGTAAT[A/G]ATGTTAATGCTGAAC | 79582 |
rs137974302 | snp | A/G | 0.00199481 | 0.0315187 | intron-variant | SPAG16 | GRCh38.p7 | 2:213353692 | TCCCTCAGGCATCTC[A/G]TCCCTCAGGCACAGA | 79582 |
rs137974609 | snp | C/T | 0.413914 | 0.188765 | intron-variant | SPAG16 | GRCh38.p7 | 2:213980478 | GAATATATGTGTGTA[C/T]ATATATAATATATAT | 79582 |
rs137978764 | snp | A/T | 0.0146672 | 0.084371 | intron-variant | SPAG16 | GRCh38.p7 | 2:214030320 | CCTTCTTTTTATGGC[A/T]AAAAACTGTTGCATT | 79582 |
rs137983233 | in-del | -/TG | 0.0248432 | 0.108648 | intron-variant | SPAG16 | GRCh38.p7 | 2:213388900 | CAAAGACCTTTTTTT[-/TG]CAAAAACATAAAAAC | 79582 |
rs137989619 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | SPAG16 | GRCh38.p7 | 2:214389329 | TTTGTGCAATCTAAC[A/G]TGTGTGACAGAGTTG | 79582 |
rs137993297 | snp | A/G/T | 0.00199529 | 0.0315338 | intron-variant | SPAG16 | GRCh38.p7 | 2:213435515 | GTAACAAAACTGCAC[A/G/T]TGTAACTCTTTAATT | 79582 |
rs137994511 | in-del | -/CTC | 0.0023933 | 0.0345097 | intron-variant, upstream-variant-2KB | SPAG16 | GRCh38.p7 | 2:213299103 | AAGATATATTTTCTT[-/CTC]TGTTAAAGGATACAG | 79582 |
rs138004999 | snp | A/G | 0.0283406 | 0.115616 | intron-variant | SPAG16 | GRCh38.p7 | 2:214079353 | TATATCAATGCCCTC[A/G]AGAATAGTAATTTTC | 79582 |
rs138009210 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | SPAG16 | GRCh38.p7 | 2:213519234 | AAACCTTAAAATTTT[C/G]TACTGATTCATACCC | 79582 |
rs138012670 | snp | G/T | 0.00159617 | 0.0282053 | intron-variant, upstream-variant-2KB | SPAG16 | GRCh38.p7 | 2:213294519 | AAGTATGCAACTATT[G/T]TTTTGTTTAATCATT | 79582 |
rs138018959 | snp | A/T | 0.0023933 | 0.0345097 | intron-variant | SPAG16 | GRCh38.p7 | 2:213985093 | CTAGGAGAGGAGTAG[A/T]TTGTCAGAATTGTAC | 79582 |
rs138019290 | in-del | -/ACACACACACAT | | | intron-variant | SPAG16 | GRCh38.p7 | 2:213665374 | CCATGCTGGATAAAC[-/ACACACACACAT]ACACACACAAACACA | 79582 |
rs138023053 | snp | A/C | 0.0023933 | 0.0345097 | intron-variant | SPAG16 | GRCh38.p7 | 2:213895269 | TGAAAGAAATCAAAG[A/C]GGACAGAAACAAATG | 79582 |
rs138025097 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | SPAG16 | GRCh38.p7 | 2:213523850 | AGCAGAAGAAATTTC[A/G]AAGTGGCAAAGTGTT | 79582 |
rs138029535 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | SPAG16 | GRCh38.p7 | 2:213725460 | ATCCTCATTTCTGTT[C/T]TGTCTAGCCAAACCT | 79582 |
rs138039382 | snp | A/G | 0.461923 | 0.132621 | intron-variant | SPAG16 | GRCh38.p7 | 2:214193423 | TGTGTGTGTGTGTGT[A/G]TATGAGAGAGAGAGA | 79582 |
rs138041501 | snp | A/G | | | intron-variant | SPAG16 | GRCh38.p7 | 2:213668328 | TGCTTTTTTTTTTTT[A/G]AAATACATAGACTAT | 79582 |
rs138055451 | snp | C/T | 0.00199481 | 0.0315187 | intron-variant | SPAG16 | GRCh38.p7 | 2:214328528 | CAAGTATACTTTGGA[C/T]ACCTGAGCTCCCGCA | 79582 |
rs138058542 | snp | C/T | 0.00279162 | 0.0372561 | intron-variant | SPAG16 | GRCh38.p7 | 2:213440633 | AGAGATCCATGCATA[C/T]ATGGTTTATTCATGA | 79582 |
rs138058622 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | SPAG16 | GRCh38.p7 | 2:213314139 | TTTTATGAAATTTCT[A/G]TGCACTTTCTCCCTG | 79582 |
rs138059754 | snp | A/G | 0.00438332 | 0.0466095 | intron-variant | SPAG16 | GRCh38.p7 | 2:213488325 | ACTGGCAGCAGTATA[A/G]TTGGTACAGCTTTTC | 79582 |
rs138061959 | snp | A/G | 0.0146672 | 0.084371 | intron-variant | SPAG16 | GRCh38.p7 | 2:214112165 | GTTTGATTGCACTGT[A/G]GTCTGAGAGACAGTT | 79582 |
rs138064093 | snp | C/T | 0.00159617 | 0.0282053 | intron-variant | SPAG16 | GRCh38.p7 | 2:213660837 | AACCATTACAGCTGT[C/T]GATCATGTGCTTGAT | 79582 |
rs138064570 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | SPAG16 | GRCh38.p7 | 2:213823033 | TAGTGCTGCAATAAA[C/T]GTAAGTGTGCATGTG | 79582 |
rs138065714 | snp | A/T | 0.00597247 | 0.0543191 | intron-variant | SPAG16 | GRCh38.p7 | 2:213576492 | ATACCCAAAGGAATA[A/T]AAATCATTCTGTTAT | 79582 |
rs138066875 | snp | C/G | 0.0023933 | 0.0345097 | intron-variant, utr-variant-3-prime | SPAG16 | GRCh38.p7 | 2:213369454 | GGAAATGTTTTATAT[C/G]TTAATTTTGGTGGTA | 79582 |
rs138073449 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | SPAG16 | GRCh38.p7 | 2:214008006 | GATAACACAATTATA[A/C]TTATGTTAGACCTTG | 79582 |
rs138074351 | in-del | -/TGAAATCTTAAATATAACGT | 0.241053 | 0.24984 | intron-variant | SPAG16 | GRCh38.p7 | 2:213754684 | TTACATTAGTCAAAA[-/TGAAATCTTAAATATAACGT]TGAAATAAAATTAAT | 79582 |
rs138080931 | snp | A/C | 0.00199481 | 0.0315187 | intron-variant | SPAG16 | GRCh38.p7 | 2:214312597 | AACCAATGTATCGAC[A/C]TCCATGTGCCCTAAC | 79582 |
rs138080972 | snp | C/T | 0.00159617 | 0.0282053 | intron-variant | SPAG16 | GRCh38.p7 | 2:214195999 | ACTATATCACAGTAC[C/T]TCCTTAGAAAAATGT | 79582 |
rs138084751 | in-del | -/C | 0.00993419 | 0.0697739 | intron-variant | SPAG16 | GRCh38.p7 | 2:214063606 | GCCCCACCTCTAATA[-/C]TATCACATGAGCAAT | 79582 |
rs138087642 | snp | A/G | 0.00636936 | 0.0560724 | intron-variant | SPAG16 | GRCh38.p7 | 2:214035122 | TGCAGAGAGGAGACC[A/G]TGGGGTAGGTAGCTC | 79582 |
rs138096792 | snp | A/G | 0.00279162 | 0.0372561 | intron-variant | SPAG16 | GRCh38.p7 | 2:214400765 | TGATGTCCATTCAAT[A/G]TTTTATGTTTTCTAA | 79582 |
rs138097806 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | SPAG16 | GRCh38.p7 | 2:213862311 | GATCAGAAAGCTACT[A/G]GTGTTAGAGCTATAG | 79582 |
rs138099032 | snp | G/T | 0.00636936 | 0.0560724 | intron-variant | SPAG16 | GRCh38.p7 | 2:213615378 | GGCAGATCACCTGAG[G/T]CCAGGAATTCGAGAC | 79582 |
rs138108279 | snp | A/G/T | 0.00159617 | 0.0282053 | intron-variant | SPAG16 | GRCh38.p7 | 2:214068378 | AACTCAGAATAAAAG[A/G/T]CATATTTTAACTGGA | 79582 |
rs138112664 | snp | C/T | 0.0158469 | 0.0875917 | intron-variant | SPAG16 | GRCh38.p7 | 2:213991651 | GGCAATCATGAGTCA[C/T]GTACCTACTTAGAGC | 79582 |
rs138119789 | snp | A/G | 0.0119091 | 0.0762411 | intron-variant | SPAG16 | GRCh38.p7 | 2:213441806 | CAAAGTTAATATACA[A/G]AAGTCAACCACTTTC | 79582 |
rs138121820 | snp | G/T | 0.000798403 | 0.0199641 | intron-variant | SPAG16 | GRCh38.p7 | 2:213493023 | CGAATCACAAAGAAA[G/T]AATTTGTGTCAGATC | 79582 |
rs138126828 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | SPAG16 | GRCh38.p7 | 2:213580709 | ACTTGTCTCTTACTA[A/G]CAGTGAGATAGATTA | 79582 |
rs138127751 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | SPAG16 | GRCh38.p7 | 2:214337308 | TAAGAAATCCACTCC[C/T]TAGAATCTTAACCCT | 79582 |
rs138129097 | in-del | -/T | 0.0221141 | 0.102801 | intron-variant | SPAG16 | GRCh38.p7 | 2:213363156 | TATTTGTGAAAAATG[-/T]TATCATTACAATGTA | 79582 |
rs138129307 | in-del | -/TTCACT | 0.0452528 | 0.143452 | intron-variant | SPAG16 | GRCh38.p7 | 2:213436675 | ATTAAATTATATGAA[-/TTCACT]TTCACTTTCTTTAAA | 79582 |
rs138132565 | snp | C/T | 0.00398564 | 0.0444627 | intron-variant | SPAG16 | GRCh38.p7 | 2:213445387 | ACAGATATAGCTGGG[C/T]GTGGCGGCTCATGCC | 79582 |
rs138133225 | snp | A/T | 0.00119737 | 0.0244387 | intron-variant | SPAG16, LOC101928084 | GRCh38.p7 | 2:214094951 | TGCCAATTGGATGAA[A/T]CTTTTGAGAGGACTT | 79582 |
rs138134891 | snp | C/T | 0.00438332 | 0.0466095 | intron-variant | SPAG16 | GRCh38.p7 | 2:214017780 | TGCAAGTCCCATTTG[C/T]ATGACTTTAATCAAC | 79582 |
rs138135964 | in-del | -/G | | | intron-variant | SPAG16 | GRCh38.p7 | 2:213678964 | GGTTTAGGAGAGGCT[-/G]GTTCTGGGGAATGTG | 79582 |
rs138141708 | snp | C/T | 0.0839998 | 0.186933 | intron-variant | SPAG16 | GRCh38.p7 | 2:213913594 | GTACATGTACATATA[C/T]GTATATGTACATGTA | 79582 |
rs138148843 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | SPAG16 | GRCh38.p7 | 2:214207406 | ATTTACTTGATTATG[A/T]GCTCAGTAAAGATAT | 79582 |
rs138149442 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | SPAG16 | GRCh38.p7 | 2:213767999 | GTGCTGCACTGGAAC[A/G]GCTCTTAACTCAGTT | 79582 |
rs138149501 | snp | A/T | 0.0217236 | 0.101931 | intron-variant | SPAG16 | GRCh38.p7 | 2:213827702 | CATTTCTTGTAGGAC[A/T]GGTCTGGTGTTGAAA | 79582 |
rs138149624 | in-del | -/GC | | | intron-variant | SPAG16 | GRCh38.p7 | 2:213325644 | TGTGTGTGTGTGTGT[-/GC]ATATCTATTTTTTGA | 79582 |
rs138159479 | snp | C/T | 0.00159617 | 0.0282053 | intron-variant | SPAG16 | GRCh38.p7 | 2:214360589 | CACTATGCAGTTATA[C/T]ACTTAATTAGTCCAC | 79582 |
rs138160747 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | SPAG16 | GRCh38.p7 | 2:213360557 | AAGTCAAGGTTACCA[C/T]TTAAAGAATGGAAAC | 79582 |
rs138172366 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | SPAG16 | GRCh38.p7 | 2:213837753 | GGAATATTAAGATAA[A/G]GAGGTTTTCCTGGAT | 79582 |
rs138174755 | snp | C/T | 0.00358779 | 0.0422022 | intron-variant | SPAG16 | GRCh38.p7 | 2:213691506 | GCCCAGACTAAAGCC[C/T]TGGCTGATATCTGTC | 79582 |
rs138175468 | snp | A/G | 0.00159617 | 0.0282053 | intron-variant | SPAG16 | GRCh38.p7 | 2:214371098 | GTGGGCTATTACTGG[A/G]ATAATGCATCACATC | 79582 |
rs138179930 | snp | A/G | 0.00159617 | 0.0282053 | intron-variant | SPAG16 | GRCh38.p7 | 2:213745960 | ATGTCTTGATTTCTC[A/G]TACAATTGCTTCATG | 79582 |
rs138181543 | snp | A/G/T | 0.000798403 | 0.0199641 | intron-variant | SPAG16 | GRCh38.p7 | 2:213772302 | GATTTTGTACCCTGA[A/G/T]ACCACCCTCAACATG | 79582 |
rs138183678 | snp | A/G | 0.00953873 | 0.0683987 | intron-variant | SPAG16 | GRCh38.p7 | 2:213622928 | CGATTTGAATAATTT[A/G]TGTAAGTTCTTGGGT | 79582 |
rs138186653 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | SPAG16 | GRCh38.p7 | 2:214279896 | AAAAAACCCATGGAT[C/T]AAAGAAGAAATAAAA | 79582 |
rs138186690 | snp | G/T | 0.00993419 | 0.0697739 | intron-variant | SPAG16 | GRCh38.p7 | 2:214228575 | GTAGACTATATCAAT[G/T]GTTCTCAAAGTGTGC | 79582 |
rs138190310 | snp | A/G | 0.0103295 | 0.0711199 | intron-variant | SPAG16 | GRCh38.p7 | 2:213702591 | TCCGGACACAATAAT[A/G]TTTCATCTTTGTATA | 79582 |
rs138192607 | snp | A/G | 0.00636936 | 0.0560724 | intron-variant | SPAG16 | GRCh38.p7 | 2:214365120 | GATAACTGAGATTTC[A/G]AGCCTGAGTGACAGA | 79582 |
rs138193229 | snp | A/G | 0.00159617 | 0.0282053 | intron-variant | SPAG16 | GRCh38.p7 | 2:213962738 | TCAATCGCTTTACTC[A/G]TTGTAAGTTTATTAA | 79582 |
rs138195554 | snp | C/T | 0.00597247 | 0.0543191 | intron-variant | SPAG16 | GRCh38.p7 | 2:214137307 | GTCATTAATAATCTT[C/T]GGCAATGCCATTATA | 79582 |
rs138198284 | snp | A/C | 0.00755907 | 0.0610114 | intron-variant | SPAG16 | GRCh38.p7 | 2:213423639 | ATTAATCATGATGAC[A/C]ATACTAACACTATTA | 79582 |
rs138205003 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | SPAG16 | GRCh38.p7 | 2:213921570 | GAATTTGATCCTGTC[A/G]TCATATTGTTAGCTG | 79582 |
rs138207589 | in-del | -/TTAT | 0.230896 | 0.249269 | intron-variant, downstream-variant-500B | SPAG16 | GRCh38.p7 | 2:213371713 | AAGACACATTAATTG[-/TTAT]TTAATCTAAATTTAG | 79582 |
rs138209162 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | SPAG16 | GRCh38.p7 | 2:214152358 | AAGAATATAGACTAT[A/G]TATTTCAGACCCTTA | 79582 |
rs138216601 | snp | C/T | 0.00199481 | 0.0315187 | intron-variant | SPAG16 | GRCh38.p7 | 2:213701559 | GGGAGGTGTGGAGGG[C/T]GCTGCTCTGTGGCGC | 79582 |
rs138221699 | snp | C/G | 0.00318978 | 0.0398085 | intron-variant | SPAG16 | GRCh38.p7 | 2:213336087 | ACCCAAGAGCTGTGT[C/G]GGCAAAGGAAGCTTT | 79582 |
rs138222738 | in-del | -/AA | 0.0551013 | 0.156571 | intron-variant | SPAG16 | GRCh38.p7 | 2:214364123 | CACCTTCTCATTTCT[-/AA]AGAGTCACCACTATC | 79582 |
rs138223233 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | SPAG16 | GRCh38.p7 | 2:213494168 | GGCCAGATTTCTGGT[C/T]GATAGGTTGGCCCTA | 79582 |
rs138229170 | snp | A/T | 0.00914312 | 0.0669923 | intron-variant | SPAG16 | GRCh38.p7 | 2:213828381 | ATTTTTCTTTATTAT[A/T]TCAATTTCTTTGTTA | 79582 |
rs138230515 | snp | C/T | 0.0463947 | 0.145069 | intron-variant | SPAG16 | GRCh38.p7 | 2:213344830 | TTGTGAATAGTGCCG[C/T]AATAAACATAACGTG | 79582 |
rs138233624 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant, utr-variant-5-prime | SPAG16 | GRCh38.p7 | 2:213301281 | GTACTCAAAGCCATG[G/T]CTACAGATTATCCAA | 79582 |
rs138245606 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | SPAG16 | GRCh38.p7 | 2:214345399 | ACAATTCAGCCCGCT[C/T]TCATCTCTCCCTTTG | 79582 |
rs138247756 | in-del | -/GAGT | | | intron-variant | SPAG16 | GRCh38.p7 | 2:214352582 | GTGTGTGTATGTGTG[-/GAGT]ACTATCTCCTAACAT | 79582 |
rs138248232 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | SPAG16 | GRCh38.p7 | 2:213807874 | TACACTGGTTGTTTT[A/G]TACTGAAAGACCTGT | 79582 |
rs138256824 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | SPAG16 | GRCh38.p7 | 2:213782326 | ATGATGTAAAAGATT[A/G]TATGGAAACAGGGAA | 79582 |
rs138257266 | snp | A/G | 0.00557542 | 0.0525036 | intron-variant | SPAG16 | GRCh38.p7 | 2:214262090 | GACTATCTATCTGAT[A/G]TTCATTAGATAGCCT | 79582 |
rs138258144 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | SPAG16 | GRCh38.p7 | 2:213473741 | TATGTTTCTTCCACT[A/G]TTATCCCACACCCTT | 79582 |
rs138261117 | snp | A/G | 0.00676609 | 0.0577691 | intron-variant | SPAG16 | GRCh38.p7 | 2:214374508 | ATACCTCTAGCTCTT[A/G]TTGCCTTACAAACTT | 79582 |
rs138264277 | snp | A/G/T | 0.00398564 | 0.0444627 | intron-variant | SPAG16 | GRCh38.p7 | 2:214022185 | ATTAGCTAACATTTC[A/G/T]TGTAATTACTAATGG | 79582 |
rs138264738 | snp | A/G | 0.0023933 | 0.0345097 | intron-variant | SPAG16 | GRCh38.p7 | 2:213927500 | TTTTCCATATTTCAG[A/G]CCATGTTTTTGAAAG | 79582 |
rs138271068 | snp | C/T | 0.00199481 | 0.0315187 | intron-variant | SPAG16 | GRCh38.p7 | 2:213899433 | ACTAGAAGTTTTATA[C/T]AGAGACTGCATGATA | 79582 |
rs138275730 | snp | G/T | | | intron-variant | SPAG16 | GRCh38.p7 | 2:213710409 | ATAACTAAGCGTAAG[G/T]TATCTTAAGTCTCTG | 79582 |
rs138275744 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | SPAG16 | GRCh38.p7 | 2:213668733 | GGCTCACTGCAACCT[C/T]CACCTCCCGGGTTCA | 79582 |
rs138275890 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | SPAG16 | GRCh38.p7 | 2:214045456 | TTCAGCTGAGACTCA[A/G]CACATTCCAAGATGT | 79582 |
rs138280872 | snp | A/T | 0.0283406 | 0.115616 | intron-variant | SPAG16 | GRCh38.p7 | 2:213657274 | AAATAAGTATGTTTT[A/T]AGTCCTTCAATGAAG | 79582 |
rs138283472 | snp | A/C | 0.00953873 | 0.0683987 | intron-variant | SPAG16 | GRCh38.p7 | 2:214124518 | TTAAGATTGTTTTAC[A/C]TAACAGGGATAATGT | 79582 |
rs138283516 | in-del | -/A | 0.00358779 | 0.0422022 | intron-variant | SPAG16 | GRCh38.p7 | 2:214335134 | GCGGTGGCCCTTCAT[-/A]ACTGTTCCAGATCAA | 79582 |
rs138286344 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | SPAG16 | GRCh38.p7 | 2:213884299 | TAAAATTCTTGGTTG[A/G]AATGTCTTTCCTTTA | 79582 |
rs138286481 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | SPAG16 | GRCh38.p7 | 2:213560708 | CACAATGTGAGTTAA[A/G]AATTACTTTTCTTTC | 79582 |
rs138292166 | snp | G/T | 0.00795532 | 0.062565 | intron-variant | SPAG16 | GRCh38.p7 | 2:213790642 | ACCAATTATATACAA[G/T]GTGAGCATACCAGTA | 79582 |
rs138294443 | snp | A/G | 0.00953873 | 0.0683987 | intron-variant | SPAG16 | GRCh38.p7 | 2:213789154 | GGAATTGAAAAATAG[A/G]TTAAAAATCCTTTCA | 79582 |
rs138297038 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | SPAG16 | GRCh38.p7 | 2:213752426 | TACCATTCTTTCCTC[C/T]ACTTCTGTGTTTCTT | 79582 |
rs138297248 | snp | A/C | 0.00159617 | 0.0282053 | intron-variant | SPAG16 | GRCh38.p7 | 2:213678695 | GCAGAAAGCTCACTT[A/C]CTGGCAGTGCCCAGT | 79582 |
rs138298608 | in-del | -/AT | | | intron-variant | SPAG16 | GRCh38.p7 | 2:214298156 | TACACACACACACAC[-/AT]ATACACACACACACA | 79582 |
rs138300607 | snp | C/G | 0.00398564 | 0.0444627 | intron-variant | SPAG16 | GRCh38.p7 | 2:214329257 | ATCAAGTTCAAAACA[C/G]TCAAGTTATTTACAA | 79582 |
rs138302098 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | SPAG16 | GRCh38.p7 | 2:213546917 | TTAAAATACCCTTTG[G/T]AAGTTTAAATTACTA | 79582 |
rs138303445 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | SPAG16 | GRCh38.p7 | 2:213628897 | TTTGTGTCTGTTAAG[C/T]GTGTTGTTTGTATTA | 79582 |
rs138308945 | snp | A/G | 0.00914312 | 0.0669923 | intron-variant | SPAG16 | GRCh38.p7 | 2:214119974 | TATCTTGCATATTTA[A/G]CTTTTAATTTTTCTA | 79582 |
rs138314945 | snp | A/G | 0.0252325 | 0.109451 | intron-variant | SPAG16 | GRCh38.p7 | 2:214250110 | CAGACCAGCAATTAC[A/G]TATCAGTTTCACTCA | 79582 |
rs138324188 | in-del | -/CT | 0.0178098 | 0.0926698 | intron-variant | SPAG16 | GRCh38.p7 | 2:213392355 | CATAATGCAGAGTGA[-/CT]CTGGCATCAACCAAG | 79582 |
rs138332380 | snp | A/G | 0.0126979 | 0.078662 | intron-variant | SPAG16 | GRCh38.p7 | 2:213590740 | TGTGAAAGCAGTTTG[A/G]AGATTTCTCAAAGTA | 79582 |
rs138332439 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | SPAG16 | GRCh38.p7 | 2:213535803 | CATTCTAACTGTAAC[A/C]TTGACCACATTTTTT | 79582 |
rs138336973 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | SPAG16 | GRCh38.p7 | 2:213499151 | TCTATATTCAATGAA[A/C]TCCCTTCATGTGTTC | 79582 |
rs138338361 | snp | A/C | 0.00953873 | 0.0683987 | intron-variant | SPAG16 | GRCh38.p7 | 2:213673080 | GTGTGGATATTCAAA[A/C]ATTTTTAAATCTATT | 79582 |
rs138344577 | snp | A/G | | | intron-variant | SPAG16 | GRCh38.p7 | 2:213306525 | GCATCATAACTTGCC[A/G]AAGAATTACAGTCCA | 79582 |
rs138356919 | snp | A/G | 0.0023933 | 0.0345097 | intron-variant | SPAG16 | GRCh38.p7 | 2:214123726 | AATGCAATGATCAGA[A/G]AGAGATTCTCTGAGA | 79582 |
rs138358705 | snp | A/C | 0.00119737 | 0.0244387 | intron-variant | SPAG16 | GRCh38.p7 | 2:213331565 | ACAAACATCAGACTT[A/C]ATCTGCACCATAGAA | 79582 |
rs138359423 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | SPAG16 | GRCh38.p7 | 2:213766849 | AGAGAGGACTGAATT[C/G]TGGCCTGCAGCTTCC | 79582 |
rs138361871 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | SPAG16 | GRCh38.p7 | 2:214003429 | ACAATCAGGAAGGTA[A/G]TATAATGGTTAAAAG | 79582 |
rs138362302 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | SPAG16 | GRCh38.p7 | 2:214048046 | AGGTAATAACAAACA[C/G]TGGTAAGGATGTGGA | 79582 |
rs138366879 | snp | C/T | 0.0166325 | 0.0896639 | intron-variant | SPAG16 | GRCh38.p7 | 2:213441331 | ATGTAGAAAGCACTG[C/T]AATATGGAGCAAAAT | 79582 |
rs138372584 | snp | C/T | 0.0260105 | 0.111035 | intron-variant | SPAG16 | GRCh38.p7 | 2:213688560 | TTGGAAAGTAAGTCA[C/T]GATATATAGGGTTAA | 79582 |
rs138374886 | snp | A/G | | | intron-variant | SPAG16 | GRCh38.p7 | 2:213986184 | GTGAGATTTGAGGTA[A/G]ACAGTGAAAGTTGGG | 79582 |
rs138378718 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | SPAG16 | GRCh38.p7 | 2:213896182 | TACATATGGCCAAAA[C/G]GTATATGAAAAAAAT | 79582 |
rs138385685 | in-del | -/ATAGCCTTTGTCA | 0.0429648 | 0.14013 | intron-variant | SPAG16 | GRCh38.p7 | 2:213373109 | GTACCTGTTGGTACC[-/ATAGCCTTTGTCA]TTAATAAGCATTAGA | 79582 |
rs138387771 | snp | A/C | 0.00557542 | 0.0525036 | intron-variant | SPAG16 | GRCh38.p7 | 2:213453507 | AAGCAGTTTAATTAT[A/C]TTTTCATAATTTATA | 79582 |
rs138391236 | snp | C/T | 0.00398564 | 0.0444627 | intron-variant | SPAG16 | GRCh38.p7 | 2:213320375 | AGTATTTAGGGTATC[C/T]ATCACCTCAAACATT | 79582 |
rs138394422 | in-del | -/AGAC | | | intron-variant | SPAG16 | GRCh38.p7 | 2:213407894 | GAGGCAGAGAGAGAG[-/AGAC]AGGAGAGAGGCAGAG | 79582 |
rs138396852 | snp | A/G | 0.0154538 | 0.0865337 | intron-variant | SPAG16 | GRCh38.p7 | 2:213524094 | TGGGCTGGGACCAGG[A/G]CCCCCTTGCTGTGTG | 79582 |
rs138398149 | snp | C/T | 0.00953873 | 0.0683987 | intron-variant | SPAG16 | GRCh38.p7 | 2:213457405 | TGAAGTTCTAATTTT[C/T]GTGGTTTCTTGTACT | 79582 |
rs138398435 | snp | C/T | 0.00159617 | 0.0282053 | intron-variant | SPAG16 | GRCh38.p7 | 2:214008950 | TTTATGAACCTTACC[C/T]GTACCCCTATAGTGG | 79582 |
rs138400711 | snp | A/G | 0.00159617 | 0.0282053 | intron-variant | SPAG16 | GRCh38.p7 | 2:213410109 | GGAATCATCACACCC[A/G]AGTCAAGAATGTGCC | 79582 |
rs138402287 | snp | A/G | 0.0023933 | 0.0345097 | intron-variant | SPAG16 | GRCh38.p7 | 2:213714856 | AAAGAGAAGATAAAT[A/G]ATGTAGTTTTCATTA | 79582 |
rs138407172 | snp | A/G | 0.0146672 | 0.084371 | intron-variant | SPAG16 | GRCh38.p7 | 2:214360851 | TAAGCGTCAATGGTT[A/G]AAGCTTAAATACCCT | 79582 |
rs138407974 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | SPAG16 | GRCh38.p7 | 2:213556439 | GAAACCAAAAGATAG[C/T]GGGGATAGCTAAACT | 79582 |
rs138413920 | in-del | -/TTAGAAGA | 0.031825 | 0.122064 | intron-variant | SPAG16 | GRCh38.p7 | 2:214391017 | CAGATGTGATGGTTC[-/TTAGAAGA]TTAGAAGATCTTAAG | 79582 |
rs138433179 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | SPAG16, LOC101928084 | GRCh38.p7 | 2:214101723 | GTCATGACTCTGCCA[C/T]TTTTTATTTGTGGGT | 79582 |
rs138433320 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | SPAG16 | GRCh38.p7 | 2:214181175 | AGAGAACATCTGAGA[A/T]GAAAGAGAAGCAATA | 79582 |
rs138436739 | snp | C/T | 0.0158469 | 0.0875917 | intron-variant | SPAG16 | GRCh38.p7 | 2:213393171 | TATAGCCCTGGATCA[C/T]TTGAAAATGCATAAC | 79582 |
rs138436764 | snp | C/T | 0.00358779 | 0.0422022 | intron-variant | SPAG16 | GRCh38.p7 | 2:214350937 | CCCCAAAACATCAGC[C/T]AAAAGGCAACTTGGA | 79582 |
rs138439346 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | SPAG16 | GRCh38.p7 | 2:213333536 | TCACAAAAGATCCAG[A/C]ATAGGCAAAGCTATC | 79582 |
rs138443153 | snp | A/G | 0.0107246 | 0.0724382 | intron-variant | SPAG16 | GRCh38.p7 | 2:213392378 | TCAACCAAGGATCTG[A/G]GTGCTATTTTGCAGG | 79582 |
rs138445263 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | SPAG16 | GRCh38.p7 | 2:213595188 | AAATGATAGGCTGCT[A/G]TTCCATCAAAATAAA | 79582 |
rs138446266 | snp | A/G | 0.00358779 | 0.0422022 | intron-variant | SPAG16 | GRCh38.p7 | 2:213319685 | TTGCTTGAGTTTGCT[A/G]ATTTTCTTTTAAATA | 79582 |
rs138453557 | snp | C/T | 0.00159617 | 0.0282053 | intron-variant | SPAG16 | GRCh38.p7 | 2:213600462 | TTCCATATATTTGCT[C/T]AACAAATGTTCACTG | 79582 |
rs138462985 | snp | C/T | 0.0023933 | 0.0345097 | intron-variant | SPAG16 | GRCh38.p7 | 2:213970698 | AAGTACATCCTGGCC[C/T]CATTGGAGTATTTTG | 79582 |
rs138465964 | snp | C/T | 0.0333695 | 0.124785 | intron-variant | SPAG16 | GRCh38.p7 | 2:214272903 | ACTAGTTTACAGTCC[C/T]ACCAACAGTGTAAAA | 79582 |
rs138466801 | in-del | -/A | | | intron-variant | SPAG16 | GRCh38.p7 | 2:213597711 | TTTAAGAAAAAAAAA[-/A]TTTTGTTACATATTT | 79582 |
rs138475792 | snp | C/G | 0.0119091 | 0.0762411 | intron-variant | SPAG16 | GRCh38.p7 | 2:213843027 | CTCCCACTTTGGCTT[C/G]CCAAAATGCTGATTA | 79582 |
rs138481950 | snp | C/T | 0.00398564 | 0.0444627 | intron-variant | SPAG16 | GRCh38.p7 | 2:213978514 | GGTTTCAAAATGATT[C/T]CACATATTAGGTATT | 79582 |
rs138487246 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | SPAG16 | GRCh38.p7 | 2:213834316 | AAAGCTCTACATGAC[A/C]TGGGAGCCTTCAGAA | 79582 |
rs138494563 | snp | C/T | | | intron-variant | SPAG16 | GRCh38.p7 | 2:214062333 | CTGAGGCAGGAGAAT[C/T]TCTTGAACCCAGTAG | 79582 |
rs138500780 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | SPAG16 | GRCh38.p7 | 2:213848290 | TTTGCTTGGTTTCAC[A/G]TGAATTAGAAGAAAA | 79582 |
rs138501864 | snp | C/T | 0.00597247 | 0.0543191 | intron-variant | SPAG16 | GRCh38.p7 | 2:214057830 | CTTCTACATCAGCAC[C/T]GGCGCTTCACCTTGC | 79582 |
rs138502945 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | SPAG16 | GRCh38.p7 | 2:213381429 | GGTTTTTCATGGTAC[A/G]GTGCCATAACAACGG | 79582 |
rs138505160 | snp | C/T | 0.0119091 | 0.0762411 | intron-variant | SPAG16 | GRCh38.p7 | 2:213356975 | ATTGATTTCAAAGAA[C/T]GTCTTTATTTCTGCC | 79582 |
rs138505277 | snp | A/C | 0.00358779 | 0.0422022 | intron-variant | SPAG16 | GRCh38.p7 | 2:214309085 | AGGTTTTGTTCATTC[A/C]TTTTCATTCTTTTTT | 79582 |
rs138507286 | snp | C/T | 0.0185938 | 0.0946107 | intron-variant | SPAG16 | GRCh38.p7 | 2:214295578 | GGTGGATTGCTTTAG[C/T]CAAGGAGTTTGAGAC | 79582 |
rs138508751 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | SPAG16 | GRCh38.p7 | 2:214390023 | GTTTGTACTGAAGCC[C/T]GACACTATGTGTAGG | 79582 |
rs138509165 | snp | A/T | 0.00279162 | 0.0372561 | intron-variant | SPAG16 | GRCh38.p7 | 2:214379529 | AATACTCTCCATGTG[A/T]CTTAAGGCTTATTCC | 79582 |
rs138512810 | in-del | -/C | | | intron-variant | SPAG16 | GRCh38.p7 | 2:213387431 | AATGAAATGCATGCT[-/C]TTTTTTTTTTTTTTT | 79582 |
rs138520515 | snp | A/G | | | intron-variant | SPAG16 | GRCh38.p7 | 2:213706180 | GGTGGCAGGGTCACT[A/G]CGTGTTCTCACTACC | 79582 |
rs138522227 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | SPAG16 | GRCh38.p7 | 2:213942709 | AGAACTCATTTAAAC[A/C]TTTACTTACTATTAT | 79582 |
rs138524631 | snp | C/T | 0.00358779 | 0.0422022 | intron-variant | SPAG16 | GRCh38.p7 | 2:214301949 | CACTGAGCTTGCTCT[C/T]TCCTATAGGTTTTGG | 79582 |
rs138528460 | snp | C/T | 0.00953873 | 0.0683987 | intron-variant | SPAG16 | GRCh38.p7 | 2:214254039 | TTGTAAGACGTATTC[C/T]TAGGTATTTTATTCT | 79582 |
rs138530138 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | SPAG16 | GRCh38.p7 | 2:213716001 | TTATCAAGGATTAAT[A/G]TTGCCCTCATCTATT | 79582 |
rs138530942 | snp | A/T | 0.0023933 | 0.0345097 | intron-variant | SPAG16 | GRCh38.p7 | 2:214382785 | AATAGGCTTTTTCTT[A/T]TGAGAGTGATGGAAA | 79582 |
rs138535756 | snp | C/T | 0.0142736 | 0.0832652 | intron-variant | SPAG16 | GRCh38.p7 | 2:213359623 | GCCAGTTGCTAAGAC[C/T]ATGGGAAAAGTGCAG | 79582 |
rs138536701 | snp | C/T | 0.00159617 | 0.0282053 | upstream-variant-2KB | SPAG16, LOC100130451 | GRCh38.p7 | 2:213284251 | CTCCCAGAGCTGCGC[C/T]CGAGCTCTCGCGTTA | 79582 |
rs138545767 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | SPAG16 | GRCh38.p7 | 2:213809159 | TGAGAAGTGGCCTTG[A/G]CAGTAAGGGAATACA | 79582 |
rs138546740 | snp | A/T | 0.000153988 | 0.00877328 | missense, nc-transcript-variant | SPAG16 | GRCh38.p7 | 2:213862517 | ACAAAGACATCCTAG[A/T]CTCCTGTGGCGAGGA | 79582 |
rs138548552 | snp | A/C | 0.00119737 | 0.0244387 | intron-variant | SPAG16 | GRCh38.p7 | 2:214262318 | GAGTTTTTATGTTTA[A/C]AAATGTGCCATATTT | 79582 |
rs138549254 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | SPAG16 | GRCh38.p7 | 2:214185727 | TCCAAGTGTGCCTGC[A/G]TAGTCTGTGACAAAG | 79582 |
rs138549512 | in-del | -/ATAT | 0.362941 | 0.223034 | intron-variant | SPAG16 | GRCh38.p7 | 2:213522798 | AAACTTACATGCCAA[-/ATAT]ATATATATATATATA | 79582 |
rs138553335 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | SPAG16 | GRCh38.p7 | 2:214399419 | AGGAAAGGATGAAGT[G/T]CTAAAATTAGGATGT | 79582 |
rs138560480 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | SPAG16 | GRCh38.p7 | 2:213586726 | TCTCTCCACCTGTGA[A/G]TCTGTGAAATCAGAC | 79582 |
rs138564505 | snp | C/T | 0.0197687 | 0.0974348 | intron-variant | SPAG16 | GRCh38.p7 | 2:213794470 | TTTTCTGCATGTTCC[C/T]TTTCCTGGTCTTTTT | 79582 |
rs138564753 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | SPAG16 | GRCh38.p7 | 2:213679337 | ATTTCCAAGAACCAG[A/G]TAATAATTACAAATT | 79582 |
rs138567836 | in-del | -/T | | | intron-variant | SPAG16 | GRCh38.p7 | 2:213674403 | TTTTTATTATTATAC[-/T]TTTAAGTTTTAGGGT | 79582 |
rs138571372 | snp | G/T | 0.0119091 | 0.0762411 | intron-variant | SPAG16 | GRCh38.p7 | 2:213361998 | ATTCTCATATGTGAG[G/T]TGAGGCTTGAGTCAT | 79582 |
rs138571473 | snp | A/G | 0.00795532 | 0.062565 | intron-variant | SPAG16 | GRCh38.p7 | 2:213445460 | TGAGGTCAGGAGATC[A/G]AGACCAGCCTGGCCA | 79582 |
rs138574756 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | SPAG16 | GRCh38.p7 | 2:214267978 | AACTACTTAATAAGT[A/G]GAAAAACAAATAACC | 79582 |
rs138580390 | snp | A/G | 0.00318978 | 0.0398085 | intron-variant | SPAG16 | GRCh38.p7 | 2:213692000 | TCCCAAAGCCAAAAT[A/G]ATAAATTAAGATGTC | 79582 |
rs138581809 | snp | A/G | 0.00279162 | 0.0372561 | intron-variant | SPAG16 | GRCh38.p7 | 2:214168206 | CATATTGGCCAGGCT[A/G]ATCTCAAACTCCTGA | 79582 |
rs138586251 | in-del | -/TGTA | 0.0248432 | 0.108648 | intron-variant | SPAG16 | GRCh38.p7 | 2:213374429 | GTGTACTTATATATG[-/TGTA]TGTATTATATGTAGA | 79582 |
rs138593775 | in-del | -/AAG | 0.00119737 | 0.0244387 | intron-variant | SPAG16 | GRCh38.p7 | 2:213607069 | ATGTTTGGTAGATGA[-/AAG]AAGAGACTAGTTGGT | 79582 |
rs138596090 | snp | C/T | | | intron-variant | SPAG16 | GRCh38.p7 | 2:214283838 | TTCTAGCTCTGCTTA[C/T]TTGTACAATAGCACT | 79582 |
rs138600951 | in-del | -/AGC | 0.174288 | 0.23826 | intron-variant | SPAG16 | GRCh38.p7 | 2:213936025 | CAGGTGAAAAGGGAT[-/AGC]AGGCATTGGAAAGGG | 79582 |
rs138604494 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | SPAG16 | GRCh38.p7 | 2:213601281 | AGAAAAGGGAATTTC[A/G]GAGACCAACTTCATC | 79582 |
rs138605822 | snp | A/G | 0.00159617 | 0.0282053 | intron-variant | SPAG16 | GRCh38.p7 | 2:214406152 | AATCTCAACCTTAAG[A/G]AGAACTTGGCTACAT | 79582 |
rs138605961 | snp | A/G | 0.0228947 | 0.104514 | intron-variant | SPAG16 | GRCh38.p7 | 2:213955989 | TTTATTTATTTTTTG[A/G]GATGGAGTTTCGCTC | 79582 |
rs138608208 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | SPAG16 | GRCh38.p7 | 2:213816327 | TCTGTTGATGACCCT[A/G]TTGATTTTGTTTTCA | 79582 |
rs138608353 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | SPAG16 | GRCh38.p7 | 2:214127950 | TGTTCTAGAAAAAAG[C/G]GTGGGTTAGAGCAGC | 79582 |
rs138619580 | snp | C/T | 0.0217236 | 0.101931 | intron-variant | SPAG16 | GRCh38.p7 | 2:214276393 | TCTTGCTAGCATTGG[C/T]GGTCTTTACAATTTG | 79582 |
rs138628394 | in-del | -/A | 0.3748 | 0.216622 | intron-variant | SPAG16 | GRCh38.p7 | 2:213325280 | TTTGACATTTTGTTG[-/A]ATATATCATTTTCTA | 79582 |
rs138630868 | in-del | -/AAG | 0.474 | 0.111014 | intron-variant | SPAG16 | GRCh38.p7 | 2:214326556 | ATGAGAAATCATAAT[-/AAG]AAGAGAGAAATTCAG | 79582 |
rs138631441 | snp | A/T | 0.00557542 | 0.0525036 | intron-variant | SPAG16 | GRCh38.p7 | 2:214274155 | TGATTTTGTATCCTG[A/T]GACTTTGCTGAAGTT | 79582 |
rs138641896 | snp | A/C/T | 0.00398564 | 0.0444627 | intron-variant | SPAG16 | GRCh38.p7 | 2:214242675 | AAATATAACACTGAA[A/C/T]AAGTTAATATTACAA | 79582 |
rs138642572 | snp | A/G | 0.0437281 | 0.141251 | intron-variant | SPAG16 | GRCh38.p7 | 2:213727935 | CTCACTGCAACCTCC[A/G]TCTCCTGGGTTCAAG | 79582 |
rs138645448 | snp | A/C | 0.0433465 | 0.140692 | intron-variant | SPAG16 | GRCh38.p7 | 2:214253227 | CCAATGGGTAGATTG[A/C]AAAAATATTCTCCCA | 79582 |
rs138651595 | snp | C/T | 0.00159617 | 0.0282053 | intron-variant | SPAG16 | GRCh38.p7 | 2:213661737 | ACAGCATTTTAATGA[C/T]AATGTTATTGTTTTT | 79582 |
rs138654212 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | SPAG16 | GRCh38.p7 | 2:214356346 | AAAACATTTTCCTAC[A/G]TAGGATTGCATGCAA | 79582 |
rs138656314 | snp | A/G | | | intron-variant | SPAG16 | GRCh38.p7 | 2:213575010 | GTCTACTTCTTATTT[A/G]TCCTGAAATCTTTCT | 79582 |
rs138657812 | snp | A/T | 0.00119737 | 0.0244387 | intron-variant | SPAG16 | GRCh38.p7 | 2:213822347 | TTGAGAAATGTCTAT[A/T]CAAATATTTTGCCCA | 79582 |
rs138659993 | snp | C/T | 0.00914312 | 0.0669923 | intron-variant | SPAG16 | GRCh38.p7 | 2:213655972 | ATGAACTATTTCTGG[C/T]GGGTTTTGAAACTAA | 79582 |
rs138665924 | snp | C/T | 0.00358779 | 0.0422022 | intron-variant | SPAG16 | GRCh38.p7 | 2:214108031 | TCTAGGTCTGTACTA[C/T]TCTGAATAGTAGTTG | 79582 |
rs138675842 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | SPAG16 | GRCh38.p7 | 2:214200197 | TTTTTAACTTTTCCC[C/T]ATTCAGTGTGATGTT | 79582 |
rs138678491 | snp | G/T | 0.00716266 | 0.059414 | intron-variant | SPAG16 | GRCh38.p7 | 2:214378182 | CTTTAGACATCTCCA[G/T]AACTGTAGGATAATA | 79582 |
rs138679682 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | SPAG16 | GRCh38.p7 | 2:214063340 | TGGGTAATTTATAAA[C/T]AATGAAAATTTATTT | 79582 |
rs138680855 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | SPAG16 | GRCh38.p7 | 2:214137003 | ACTTGCCCATTTTGC[A/G]TAGCAGAATTTTAGA | 79582 |
rs138687854 | snp | A/G | 0.00517822 | 0.0506191 | intron-variant | SPAG16 | GRCh38.p7 | 2:213610496 | TGTTCTCCCCATCCC[A/G]TAACCTTTTTATCAC | 79582 |
rs138694935 | snp | C/T | 0.0337553 | 0.125452 | intron-variant | SPAG16 | GRCh38.p7 | 2:214114711 | CCAGGTACAGTCTGT[C/T]ACGGCTTCCCTTGGC | 79582 |
rs138694945 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | SPAG16 | GRCh38.p7 | 2:214068818 | GAGCATTATTTATAA[C/T]GGAGAGCCCAAGAAC | 79582 |
rs138695841 | snp | A/C | 0.0119091 | 0.0762411 | intron-variant | SPAG16 | GRCh38.p7 | 2:214294523 | CCTCTTCCCTTATGA[A/C]AGCCAAAATATTATT | 79582 |
rs138697934 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | SPAG16 | GRCh38.p7 | 2:214052643 | ATAAACTCAATCAAG[A/G]AAAGCTATTTTTAAA | 79582 |
rs138707222 | snp | G/T | 0.00159617 | 0.0282053 | intron-variant | SPAG16 | GRCh38.p7 | 2:213530285 | CAGCACAGTGGGTTT[G/T]TTTACACCAGCATCA | 79582 |
rs138711306 | snp | C/T | 0.00914312 | 0.0669923 | intron-variant | SPAG16 | GRCh38.p7 | 2:213615436 | TCTCTACTAAAAATG[C/T]AAAAATTACCTGGGT | 79582 |
rs138716464 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | SPAG16 | GRCh38.p7 | 2:213474076 | GAGGGGCTGTTGCCA[C/T]TACTGGGCATGGGGA | 79582 |
rs138724685 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | SPAG16 | GRCh38.p7 | 2:213477930 | AATCCCCATAATTCC[C/G]ACATTTTGAGGGTAA | 79582 |
rs138725385 | snp | C/T | 5.09827e-05 | 0.00504864 | missense, upstream-variant-2KB, nc-transcript-variant, utr-variant-5-prime | SPAG16, LOC100130451 | GRCh38.p7 | 2:213284527 | CCGCCGTGAGGGTCC[C/T]GGAAGAGGCGTTGGG | 79582 |
rs138725666 | snp | C/T | 0.00318978 | 0.0398085 | intron-variant | SPAG16 | GRCh38.p7 | 2:213618568 | TATCATAATGCCAAT[C/T]TCTTTAACAGGGGCA | 79582 |
rs138729574 | snp | A/T | 0.0023933 | 0.0345097 | intron-variant | SPAG16 | GRCh38.p7 | 2:214126417 | AGCCATACTTCAGGG[A/T]GTCGTGTTCTGAGCT | 79582 |
rs138731583 | snp | A/G | 0.00636936 | 0.0560724 | intron-variant | SPAG16 | GRCh38.p7 | 2:214159438 | CAAAATTGAATAGAT[A/G]ATCATCTTTAGTCTG | 79582 |
rs138732824 | snp | A/T | 0.0023933 | 0.0345097 | intron-variant | SPAG16 | GRCh38.p7 | 2:213931470 | TCATAAATATTTTTA[A/T]AATAGATTAATGGAA | 79582 |
rs138734182 | snp | C/G | 0.00119737 | 0.0244387 | intron-variant | SPAG16 | GRCh38.p7 | 2:214073480 | GAGCTCATGATTCAC[C/G]TGCCCCGGCCTTCCA | 79582 |
rs138744708 | snp | G/T | 0.0023933 | 0.0345097 | intron-variant | SPAG16 | GRCh38.p7 | 2:214379885 | GTTTCTGGGAATCCT[G/T]TGAGAAACAACACAC | 79582 |
rs138749206 | snp | A/G | 0.00199481 | 0.0315187 | intron-variant | SPAG16 | GRCh38.p7 | 2:213793874 | ATTTATTAATGGGCC[A/G]TGCATAAATGAGACA | 79582 |
rs138752404 | snp | C/T | 0.00755907 | 0.0610114 | intron-variant | SPAG16 | GRCh38.p7 | 2:214366822 | AACTTAGACTACATG[C/T]AGTACCTAAACAGCT | 79582 |
rs138756129 | in-del | -/ACTACCAGTCCTTAACTAG | 0.131038 | 0.219882 | intron-variant | SPAG16 | GRCh38.p7 | 2:213492173 | GTACTCTCATTCTAT[-/ACTACCAGTCCTTAACTAG]ACATAATATAAAACT | 79582 |
rs138756361 | snp | C/T | 0.00159617 | 0.0282053 | intron-variant | SPAG16 | GRCh38.p7 | 2:213586522 | GCATTCAGACCACAG[C/T]GTTTCACCCCGACAC | 79582 |
rs138758088 | snp | A/G | 0.00597247 | 0.0543191 | intron-variant | SPAG16 | GRCh38.p7 | 2:213480151 | CTAATAGTAGAAGTT[A/G]GTTATTTTACTGTGG | 79582 |
rs138760060 | snp | A/G | 0.0221141 | 0.102801 | intron-variant | SPAG16 | GRCh38.p7 | 2:214114818 | TGGGCTGCACCCACT[A/G]TCCAACCAGTCCCAG | 79582 |
rs138760430 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | SPAG16 | GRCh38.p7 | 2:214001486 | GGCACATGAAGGATT[A/G]ACTTTCATAGTTCCA | 79582 |
rs138761845 | in-del | -/AATT | 0.0267878 | 0.112589 | intron-variant | SPAG16 | GRCh38.p7 | 2:213481409 | TGTCATCTTTCAATT[-/AATT]GCTTACATTTTTTGT | 79582 |
rs138761931 | snp | A/T | 0.0170251 | 0.090679 | intron-variant | SPAG16 | GRCh38.p7 | 2:213937328 | TAATACCTGTCTTAT[A/T]TTGCCAAGATCCCCA | 79582 |
rs138762206 | snp | G/T | 0.0023933 | 0.0345097 | intron-variant | SPAG16 | GRCh38.p7 | 2:214040059 | TGGTCGTCAGACATG[G/T]AAAAAACCTGAAAAG | 79582 |
rs138763433 | snp | A/C | 0.00119737 | 0.0244387 | intron-variant | SPAG16 | GRCh38.p7 | 2:213349638 | AGCCCAAACTAAAAT[A/C]CACTCAAGTTTTCAT | 79582 |
rs138764839 | snp | A/G | | | intron-variant | SPAG16 | GRCh38.p7 | 2:213486741 | ATCAAGTCTGCTTCA[A/G]TCAATATCCCAGGAG | 79582 |
rs138766953 | snp | C/G | 0.00953873 | 0.0683987 | intron-variant | SPAG16 | GRCh38.p7 | 2:213855588 | ACATACCTGAGACTG[C/G]GAAATTTATGAAGAA | 79582 |
rs138770303 | snp | A/G | 0.00279162 | 0.0372561 | intron-variant | SPAG16 | GRCh38.p7 | 2:214013552 | AGGTGATTCTAATAT[A/G]TAACCAAGTCGGAGA | 79582 |
rs138771607 | snp | A/G | 0.00159617 | 0.0282053 | intron-variant | SPAG16 | GRCh38.p7 | 2:214025874 | CTATATATAAGGACA[A/G]AAACCTTAAATTTAA | 79582 |
rs138781687 | snp | A/G | 0.00438332 | 0.0466095 | intron-variant | SPAG16 | GRCh38.p7 | 2:213772428 | AACATTTTGTATCCT[A/G]TGTAGCAAATAATCT | 79582 |
rs138783233 | snp | A/C | 0.155656 | 0.231515 | intron-variant | SPAG16 | GRCh38.p7 | 2:213402576 | TGCTATCCCTCCCCC[A/C]TCCCCACACCCCACA | 79582 |
rs138785346 | snp | A/C | 0.0142736 | 0.0832652 | intron-variant | SPAG16 | GRCh38.p7 | 2:214078637 | TCTCTTTAAACAGTT[A/C]AATGAATTTGATTAG | 79582 |
rs138787636 | snp | A/G | 0.00279162 | 0.0372561 | intron-variant | SPAG16 | GRCh38.p7 | 2:213336522 | GGCCACCATCACTGC[A/G]GCTCCAGTTGGCCAT | 79582 |
rs138788445 | snp | C/T | 0.0154538 | 0.0865337 | intron-variant | SPAG16 | GRCh38.p7 | 2:214330201 | AGAATAGCTTGAACC[C/T]GGGAGGTGGAGGTGG | 79582 |
rs138788774 | snp | A/T | 0.0023933 | 0.0345097 | intron-variant | SPAG16 | GRCh38.p7 | 2:213461349 | GATAGGCTTGAGTTA[A/T]CCCTATGGATGATCT | 79582 |
rs138791104 | snp | C/T | 0.00636936 | 0.0560724 | intron-variant, utr-variant-5-prime | SPAG16 | GRCh38.p7 | 2:213301929 | CCTCATCGTCTGTAA[C/T]GTTCAACCTAATAGT | 79582 |
rs138808348 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | SPAG16 | GRCh38.p7 | 2:213969697 | TACATTTATCTTTTT[G/T]TATAAATCATATAAT | 79582 |
rs138813062 | snp | A/G | 0.0111196 | 0.0737302 | intron-variant | SPAG16 | GRCh38.p7 | 2:213883806 | ATTGGCTTAAAGTCT[A/G]TTTTATCAGGTATGA | 79582 |
rs138816304 | snp | A/C | 0.00199481 | 0.0315187 | intron-variant | SPAG16 | GRCh38.p7 | 2:213732027 | CTCCTAGATTTTCTT[A/C]TAGGGTTTATATAGT | 79582 |
rs138817693 | in-del | -/AT | | | intron-variant | SPAG16 | GRCh38.p7 | 2:213584499 | CAGTGAAAAAAAATC[-/AT]AGAATTTTGTGCTCA | 79582 |
rs138819606 | snp | A/G | 0.00438332 | 0.0466095 | intron-variant | SPAG16 | GRCh38.p7 | 2:213870218 | TCCCTTCTCTTCAGA[A/G]CCACATAGCTTTATA | 79582 |
rs138824320 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | SPAG16 | GRCh38.p7 | 2:213863197 | AGACACAGATGGAAA[A/T]CTGCCCATAGTTCCT | 79582 |
rs138826867 | snp | C/T | 0.00159617 | 0.0282053 | intron-variant | SPAG16 | GRCh38.p7 | 2:213306102 | TTTATCCATTTCTTC[C/T]AGGCTTTCCAATTTA | 79582 |
rs138835600 | snp | C/T | 0.0295035 | 0.117819 | intron-variant | SPAG16 | GRCh38.p7 | 2:213720616 | GCACTCCAGCCTGGG[C/T]GACAGAGAAAGACTC | 79582 |
rs138836241 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | SPAG16 | GRCh38.p7 | 2:214333045 | TTTTTTCCCATTATC[A/G]GAGGAAATGGCTGTA | 79582 |
rs138845692 | snp | A/C/G | 0.0115254 | 0.0751417 | intron-variant | SPAG16 | GRCh38.p7 | 2:213615484 | AAATCCCAGCTACTC[A/C/G]GGAGGCTGAGGCAGG | 79582 |
rs138850424 | snp | A/G | 0.0614824 | 0.164198 | intron-variant | SPAG16 | GRCh38.p7 | 2:213736531 | GACCTCAGATGATCC[A/G]CCTGCCTCGGCCTCC | 79582 |
rs138851043 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | SPAG16 | GRCh38.p7 | 2:213338909 | CATTAGGAAAAATAG[C/T]GAACGTATGCTGCGC | 79582 |
rs138852036 | snp | A/G | 0.0146672 | 0.084371 | intron-variant | SPAG16 | GRCh38.p7 | 2:213289992 | CTCCCCCTCATACCA[A/G]TTGGCACCTCAAGCT | 79582 |
rs138853916 | snp | A/G | 0.00199481 | 0.0315187 | intron-variant | SPAG16 | GRCh38.p7 | 2:214284779 | AAACTCATTTTTAAG[A/G]TTGAATAATATTTTA | 79582 |
rs138855385 | in-del | -/TG | 0.373196 | 0.217538 | intron-variant | SPAG16 | GRCh38.p7 | 2:213896648 | TATGATATTCTATTA[-/TG]TGTGTGTTTATATAT | 79582 |
rs138855934 | snp | C/T | 0.0256215 | 0.110247 | intron-variant | SPAG16 | GRCh38.p7 | 2:213380737 | CCTTGCTCCATAATC[C/T]AAGAGGCCTCCGCTG | 79582 |
rs138860068 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | SPAG16 | GRCh38.p7 | 2:213852722 | CTCCCCCAAATTATT[A/G]TATCACTTTACTACA | 79582 |
rs138864931 | snp | C/T | 0.00199481 | 0.0315187 | intron-variant | SPAG16 | GRCh38.p7 | 2:214201257 | ATTCCTGACTAAACA[C/T]TTTCGATTAGTTTCT | 79582 |
rs138870931 | snp | C/T | 0.0023933 | 0.0345097 | intron-variant | SPAG16 | GRCh38.p7 | 2:214317656 | AATTCATCAGTTTAA[C/T]AATGTCAGGGTTCTG | 79582 |
rs138871158 | snp | A/G | 0.00557542 | 0.0525036 | intron-variant | SPAG16 | GRCh38.p7 | 2:213777226 | CTTCAGCAAGTGTCC[A/G]GTTTGTAGGAATTTT | 79582 |
rs138874174 | snp | A/G | 0.0023933 | 0.0345097 | intron-variant | SPAG16 | GRCh38.p7 | 2:214216655 | GAAATCTTGGAGCAC[A/G]GTACATTTTTGCAGT | 79582 |
rs138879918 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | SPAG16 | GRCh38.p7 | 2:214058153 | ATTCATAACTTGGCT[G/T]TTTAGCATAAGACAC | 79582 |
rs138883697 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | SPAG16 | GRCh38.p7 | 2:213979348 | CAAGACATTACCAAG[A/G]CAATTGAAACCTAAC | 79582 |
rs138886326 | snp | A/C | 0.0130921 | 0.0798413 | intron-variant | SPAG16 | GRCh38.p7 | 2:213836897 | GGGATTACAGGCATG[A/C]GCCACCAGGCCCAGC | 79582 |
rs138888161 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | SPAG16 | GRCh38.p7 | 2:213619372 | AAGCAAGGTGAATAG[A/G]CAGCCTGTAGAATAA | 79582 |
rs138892943 | snp | A/T | 0.00795532 | 0.062565 | intron-variant | SPAG16 | GRCh38.p7 | 2:213710760 | CATTGTTGTTAGGAG[A/T]CCATATTAAGGGCCT | 79582 |
rs138894850 | snp | A/T | 0.00557542 | 0.0525036 | intron-variant | SPAG16 | GRCh38.p7 | 2:214169309 | GTTAAAAAAGAACAC[A/T]ATCATAATTTGACTC | 79582 |
rs138898111 | snp | C/T | 0.00279162 | 0.0372561 | intron-variant | SPAG16 | GRCh38.p7 | 2:214147363 | CTCAAATTTTAATAT[C/T]CAATGGGATAAAGTA | 79582 |
rs138898180 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | SPAG16 | GRCh38.p7 | 2:214206531 | ATCTGTTGATGGACA[C/T]TTAAGCTGATTCCAT | 79582 |
rs138898923 | snp | C/T | 0.0479149 | 0.147179 | intron-variant | SPAG16 | GRCh38.p7 | 2:213724741 | GAAAAAGCACCACTG[C/T]ACTCCAGCCTGGGTG | 79582 |
rs138905081 | snp | A/G | 0.0142736 | 0.0832652 | intron-variant | SPAG16, LOC101928084 | GRCh38.p7 | 2:214092255 | CACATCATTTTAAAT[A/G]TTAATAGATGTTACC | 79582 |
rs138907670 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | SPAG16 | GRCh38.p7 | 2:214073946 | ATTGCAATGGATTGA[A/C]TGTTTGTGTCCCTTC | 79582 |
rs138908349 | snp | A/C | 0.00636936 | 0.0560724 | intron-variant | SPAG16 | GRCh38.p7 | 2:213604804 | TGCTTCAAGAAAAAA[A/C]CCTAAATTTGTAATA | 79582 |
rs138908459 | snp | A/G | 0.00199481 | 0.0315187 | intron-variant | SPAG16 | GRCh38.p7 | 2:213838136 | AAGAAAGAGACAAAT[A/G]ACAAAAATAAAAGGC | 79582 |
rs138920439 | snp | A/G/T | 0.0138799 | 0.0821421 | intron-variant | SPAG16 | GRCh38.p7 | 2:213591501 | TTTTAATAACTATTT[A/G/T]AAATCATTTTATGTT | 79582 |
rs138927285 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | SPAG16 | GRCh38.p7 | 2:214187093 | CAGGAGGGATAAATA[C/G]AAGCTTTCAAAGTTT | 79582 |
rs138930639 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | SPAG16 | GRCh38.p7 | 2:213923096 | GTTTCCAGGGCAACA[A/G]GAGCCTGCCTGCACC | 79582 |
rs138936579 | snp | C/G | 0.0126979 | 0.078662 | intron-variant | SPAG16 | GRCh38.p7 | 2:213462528 | AAACCCCATAATCCC[C/G]ACATTTTGAGGGTGG | 79582 |
rs138940147 | snp | A/G | 0.0119091 | 0.0762411 | intron-variant | SPAG16 | GRCh38.p7 | 2:213467572 | GGAGGGGAGGCCTGG[A/G]CTGGAGAGGAGAACA | 79582 |
rs138944043 | snp | A/G | 0.00358779 | 0.0422022 | intron-variant | SPAG16 | GRCh38.p7 | 2:213502496 | TTTGTTCACCCTACT[A/G]TAAAGTCATTTAGAT | 79582 |
rs138944626 | in-del | -/C | | | intron-variant | SPAG16 | GRCh38.p7 | 2:214154499 | GCAAAAAGTATCAGA[-/C]CCCCCCCCCCCATTT | 79582 |
rs138945551 | snp | C/T | 0.00119737 | 0.0244387 | upstream-variant-2KB, intron-variant, downstream-variant-500B | VWC2L, SPAG16 | GRCh38.p7 | 2:214410644 | GAGATTGATTTTTAA[C/T]GTTAGAGAACAAACT | 79582 |
rs138946038 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | SPAG16 | GRCh38.p7 | 2:213682727 | CATGTTTCTGGTTGG[A/G]TGGAGATTTATCTCA | 79582 |
rs138946629 | in-del | -/T | 0.131381 | 0.220067 | intron-variant | SPAG16 | GRCh38.p7 | 2:213652318 | TTGAATTTTTTCTTG[-/T]TTTTTTTAATGAATA | 79582 |
rs138947127 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | SPAG16 | GRCh38.p7 | 2:213519784 | AAAAAAAATGAAAGC[A/G]CACATGTTTTCATAG | 79582 |
rs138963164 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | SPAG16 | GRCh38.p7 | 2:214189493 | AGTCAGGTAAACAGT[C/G]TTCTTTTCTCTGGAC | 79582 |
rs138966436 | snp | A/G | 0.00478085 | 0.0486577 | intron-variant | SPAG16 | GRCh38.p7 | 2:214221103 | TTTTAGAATTTCCCC[A/G]TAAGAAATATTTATC | 79582 |
rs138966871 | snp | A/G | 0.00438332 | 0.0466095 | intron-variant | SPAG16 | GRCh38.p7 | 2:213293753 | CCCAGAGAAACTACA[A/G]TATAATAAATGCTTA | 79582 |
rs138971420 | in-del | -/TT | 0.040671 | 0.13668 | intron-variant | SPAG16 | GRCh38.p7 | 2:214157943 | CAATACCCACAAATC[-/TT]TTCTCTGAGTCTAGA | 79582 |
rs138981596 | snp | A/G | 0.0505692 | 0.150756 | intron-variant | SPAG16 | GRCh38.p7 | 2:213345813 | TTGAAGTCAGGTAGC[A/G]TGATGCTTCCAGCTT | 79582 |
rs138981964 | snp | C/T | 0.0119091 | 0.0762411 | intron-variant | SPAG16 | GRCh38.p7 | 2:213551822 | ACCATTTTGAAGAAC[C/T]AGCTGAAATAATGCC | 79582 |
rs138989315 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | SPAG16, LOC101928084 | GRCh38.p7 | 2:214095478 | TTTGGATTTAAATAT[A/G]CTATTAACTCTAGTA | 79582 |
rs138999252 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | SPAG16 | GRCh38.p7 | 2:214018365 | TATATGTTGTCTGTA[A/T]AATATGGAATTGTTA | 79582 |
rs139005763 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | SPAG16 | GRCh38.p7 | 2:213421222 | TCTGGCCTTTCCCTG[A/C]TCCTGGCACCCACTT | 79582 |
rs139012796 | snp | A/C | 0.00517822 | 0.0506191 | intron-variant | SPAG16 | GRCh38.p7 | 2:213623327 | TAAATCGAAGGTAAA[A/C]TTATGTTTTTTTCCT | 79582 |
rs139015790 | snp | A/G | 0.00358779 | 0.0422022 | intron-variant | SPAG16 | GRCh38.p7 | 2:213554718 | AAAATACGATGCAAT[A/G]GAAAGTGTCAAAGCA | 79582 |
rs139018814 | snp | A/C/T | 0.0023933 | 0.0345097 | intron-variant | SPAG16 | GRCh38.p7 | 2:213964741 | CTAGATCAATCAGAG[A/C/T]CAAAATGTTCCAACC | 79582 |
rs139018954 | snp | C/G | 0.00318978 | 0.0398085 | intron-variant | SPAG16 | GRCh38.p7 | 2:213424527 | GGCTAATTTACTGGA[C/G]TTATCTTTTTCTTAG | 79582 |
rs139022650 | snp | C/G | 0.0119091 | 0.0762411 | intron-variant | SPAG16 | GRCh38.p7 | 2:213878393 | TTTAAGATGCTTTCT[C/G]CTTGTGTTTTTAACT | 79582 |
rs139026481 | snp | A/G | 0.00755907 | 0.0610114 | intron-variant | SPAG16 | GRCh38.p7 | 2:214380113 | GGATGGTGAGATGGT[A/G]GTGAAGTGCACTAGA | 79582 |
rs139038580 | in-del | -/T | 0.0689305 | 0.172377 | intron-variant | SPAG16 | GRCh38.p7 | 2:214206183 | ACTCTGTCTCAAAAA[-/T]ATATATATATATTGA | 79582 |
rs139042713 | snp | A/G | 0.0107246 | 0.0724382 | intron-variant | SPAG16 | GRCh38.p7 | 2:214128535 | TGCTGTGCCAAAATC[A/G]ATTAATATGCATCCA | 79582 |
rs139043723 | snp | C/G | 0.00279162 | 0.0372561 | intron-variant | SPAG16 | GRCh38.p7 | 2:213708713 | ATCACTTGAACCCAG[C/G]AGGCAGAGGCTGCAG | 79582 |
rs139044078 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | SPAG16 | GRCh38.p7 | 2:214298345 | GTCTTTTGGAAGAGT[C/T]TTAGGGTTTCTAGGT | 79582 |
rs139046422 | snp | A/G | 0.00438332 | 0.0466095 | intron-variant | SPAG16 | GRCh38.p7 | 2:213753878 | GGCCAGATTATCAGG[A/G]ATCAGGAAAATGCTC | 79582 |
rs139051743 | snp | C/T | 0.00478085 | 0.0486577 | intron-variant | SPAG16 | GRCh38.p7 | 2:214054390 | TAAAATCTCAGAGAG[C/T]GTTCATAATTCAAGC | 79582 |
rs139053856 | snp | C/T | 0.00795532 | 0.062565 | intron-variant | SPAG16 | GRCh38.p7 | 2:214334249 | CCAGGAGGGGAGCTA[C/T]AGATAGATCCTGAGG | 79582 |
rs139059035 | snp | C/G | 0.0023933 | 0.0345097 | intron-variant | SPAG16 | GRCh38.p7 | 2:214368591 | AACTTAATCTCACCT[C/G]AATCAACAACCTCTG | 79582 |
rs139059527 | snp | G/T | 0.00159617 | 0.0282053 | intron-variant, downstream-variant-500B | SPAG16, LOC101928084 | GRCh38.p7 | 2:214084795 | CATTCAGTTACTAAT[G/T]TCTTCATCATTCATT | 79582 |
rs139061168 | snp | C/T | 0.0126979 | 0.078662 | intron-variant | SPAG16 | GRCh38.p7 | 2:214254381 | TTTTCAAAGGGAATG[C/T]TTCCAGTTTTTGCCC | 79582 |
rs139062369 | in-del | -/A | | | intron-variant | SPAG16 | GRCh38.p7 | 2:213604804 | TGCTTCAAGAAAAAA[-/A]CCTAAATTTGTAATA | 79582 |
rs139065638 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | SPAG16 | GRCh38.p7 | 2:213545852 | AGAATGCCAAATGTT[C/G]ATGTCCATAGGTCTT | 79582 |
rs139066560 | snp | C/T | 0.021333 | 0.101051 | intron-variant | SPAG16 | GRCh38.p7 | 2:214213122 | TTCCAGATTTGCAAA[C/T]CATTCCAGAGTTGTG | 79582 |
rs139076169 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | SPAG16 | GRCh38.p7 | 2:213628114 | TTAACACTAGCTTGA[A/G]ATTTCATCTCTCAGT | 79582 |
rs139077664 | snp | A/G | 0.00199481 | 0.0315187 | intron-variant | SPAG16 | GRCh38.p7 | 2:213670099 | GCCTCCGGGGTTCAC[A/G]CCCTTCTGCCTCAGC | 79582 |
rs139078961 | snp | C/T | 0.00318978 | 0.0398085 | intron-variant | SPAG16 | GRCh38.p7 | 2:213626801 | TACAGGTGCATGCCA[C/T]CACACCTGGCTACTT | 79582 |
rs139079629 | snp | C/T | 0.00159617 | 0.0282053 | intron-variant | SPAG16 | GRCh38.p7 | 2:214204880 | AAATCGATTATTAAG[C/T]TAATCCAAAAGGCAC | 79582 |
rs139081628 | in-del | -/CA | 0.0471551 | 0.14613 | intron-variant | SPAG16 | GRCh38.p7 | 2:213597421 | CGTTCTTGCCAACCA[-/CA]GTTCTACAAACAACA | 79582 |
rs139088260 | snp | A/G | 0.00318978 | 0.0398085 | intron-variant | SPAG16 | GRCh38.p7 | 2:214117605 | GATGCAAAAACTCTC[A/G]AGAAAACACTAGCAA | 79582 |
rs139092557 | snp | C/T | 0.0107246 | 0.0724382 | intron-variant | SPAG16 | GRCh38.p7 | 2:213462852 | ACTAATACAGTAAAT[C/T]GGTACCACAGAGAGT | 79582 |
rs139096097 | snp | G/T | 0.000798403 | 0.0199641 | intron-variant | SPAG16 | GRCh38.p7 | 2:214167456 | TTATGTGTTCAGCTT[G/T]GCCTTATCACATTTT | 79582 |
rs139096292 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | SPAG16 | GRCh38.p7 | 2:213873863 | TGCAAACATTGGAGC[A/G]TGTACTTACACAAAC | 79582 |
rs139099269 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | SPAG16 | GRCh38.p7 | 2:213421645 | ATGGCCACCCAAGGA[C/G]CAATCAGCACGTATT | 79582 |
rs139099706 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | SPAG16 | GRCh38.p7 | 2:213779865 | GAAAGTGGAATACTT[G/T]ATAAGCCACCAGTGG | 79582 |
rs139099920 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | SPAG16, LOC101928084 | GRCh38.p7 | 2:214090226 | AGATAAAGATGAAGA[C/T]GAAGAAAAAAAGAAG | 79582 |
rs139101032 | snp | A/T | 0.00119737 | 0.0244387 | intron-variant | SPAG16, LOC101928084 | GRCh38.p7 | 2:214086460 | GTTGGGGGAGGGACC[A/T]TATGGAGGTGATGAG | 79582 |
rs139102900 | snp | A/G | 0.0111196 | 0.0737302 | intron-variant | SPAG16 | GRCh38.p7 | 2:214216950 | TTAATATATAAAACT[A/G]TGATTAAGATAACAT | 79582 |
rs139103770 | snp | C/G | 0.00159617 | 0.0282053 | intron-variant | SPAG16 | GRCh38.p7 | 2:213537648 | ATGTCTCTATTTTTG[C/G]CAAAGCCACCTCTTA | 79582 |
rs139104937 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | SPAG16 | GRCh38.p7 | 2:214164278 | ATTTGCCAAGTGGTG[A/G]TAAGTCTTATGAAAA | 79582 |
rs139128292 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | SPAG16 | GRCh38.p7 | 2:214187256 | TCCTGTTTTAATCCA[C/T]AGTAATCTCTTGTTT | 79582 |
rs139129720 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | SPAG16 | GRCh38.p7 | 2:213498635 | AGGACATTTCAACTT[G/T]CATGTCTTGTGAGCA | 79582 |
rs139129835 | in-del | -/A | 0.499977 | 0.00339449 | intron-variant | SPAG16 | GRCh38.p7 | 2:214254116 | CTGTTATTGGTGTCT[-/A]GGTTTTGCACATTAA | 79582 |
rs139142577 | snp | C/G | 0.00279162 | 0.0372561 | intron-variant | SPAG16 | GRCh38.p7 | 2:213855964 | ATCATGTCCTTCCCA[C/G]TCCCCCAAAGTCTCA | 79582 |
rs139142901 | snp | G/T | 0.00318978 | 0.0398085 | intron-variant | SPAG16 | GRCh38.p7 | 2:213629850 | TCTCTAGAAGCTGCT[G/T]TGTCTCCTTCCTGGG | 79582 |
rs139143609 | snp | A/G | 0.00279162 | 0.0372561 | intron-variant | SPAG16 | GRCh38.p7 | 2:214385673 | ACATGGCGAAATCCC[A/G]TCTCTACTGAAAATA | 79582 |
rs139143816 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | SPAG16 | GRCh38.p7 | 2:213501509 | CTTATGCAAAACACT[A/G]TCAGGGAACTGACAT | 79582 |
rs139148556 | in-del | -/GA | 0.0221141 | 0.102801 | intron-variant | SPAG16 | GRCh38.p7 | 2:214005051 | GATGTAGGAAGTGTT[-/GA]GTTATAAAGCTGTTT | 79582 |
rs139151214 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | SPAG16 | GRCh38.p7 | 2:213500371 | TCAATAAGACCACCA[A/G]TAGGAGGAAGATAAT | 79582 |
rs139152665 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | SPAG16 | GRCh38.p7 | 2:213712274 | TTATTATTTATTCAA[C/G]AAATATTTATGTTCA | 79582 |
rs139156630 | snp | A/G | | | intron-variant | SPAG16 | GRCh38.p7 | 2:214006471 | TCAGTTACCAAAATA[A/G]CAAATTAAAGCAGCA | 79582 |
rs139163758 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | SPAG16 | GRCh38.p7 | 2:213521492 | AGAGCTTTTGCTTTT[C/T]ATTCTCTTGCTCCAC | 79582 |
rs139169643 | in-del | -/ATATAAAGG | | | intron-variant | SPAG16 | GRCh38.p7 | 2:214229192 | ACTATAGAAGAAAGT[-/ATATAAAGG]ATGTAAAGGTCACTA | 79582 |
rs139181218 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | SPAG16 | GRCh38.p7 | 2:213924716 | AAGTTTAGTGTGCCT[C/T]GTGTAAAAATCATAT | 79582 |
rs139185496 | snp | C/T | 0.00795532 | 0.062565 | intron-variant | SPAG16 | GRCh38.p7 | 2:213839707 | TGTACAGCAGTAAAG[C/T]TGACATGTACAGTAT | 79582 |
rs139189739 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | SPAG16 | GRCh38.p7 | 2:213290951 | TCTCTACACTGCACT[A/G]TTCTTTTTATGAGAA | 79582 |
rs139191770 | snp | A/G | 0.00199481 | 0.0315187 | intron-variant | SPAG16 | GRCh38.p7 | 2:214044617 | TTTAACTTCATACTG[A/G]AAGAGGCACTGAAAA | 79582 |
rs139194848 | snp | C/T | 0.00517822 | 0.0506191 | intron-variant | SPAG16 | GRCh38.p7 | 2:214042707 | TTCTGTGCTTCTCAT[C/T]CCTGATTTGTGTTAC | 79582 |
rs139194956 | snp | A/C | 0.00636936 | 0.0560724 | intron-variant | SPAG16, LOC101928084 | GRCh38.p7 | 2:214093260 | TGTGGTTTCTCTTCA[A/C]CAGTGATATAATAAT | 79582 |
rs139195631 | snp | A/G | 0.0275645 | 0.114116 | intron-variant | SPAG16 | GRCh38.p7 | 2:213388270 | CATAGAGGTGCAGAC[A/G]AAGAGGGTTATAGCA | 79582 |
rs139198012 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | SPAG16 | GRCh38.p7 | 2:213795498 | GCCTTCAAAAAATAC[A/G]CCAATCCTTTAATTA | 79582 |
rs139202294 | snp | A/G | | | intron-variant | SPAG16 | GRCh38.p7 | 2:214383705 | TGTTAAGGCTGAGAG[A/G]TGGGAGTTGGGTGAG | 79582 |
rs139207701 | in-del | -/A | 0.185788 | 0.241613 | intron-variant | SPAG16 | GRCh38.p7 | 2:213519767 | CTGTAGCAATCATAC[-/A]AAAAAAAAATGAAAG | 79582 |
rs139210209 | snp | A/C | 0.00636936 | 0.0560724 | intron-variant | SPAG16 | GRCh38.p7 | 2:213434360 | AGACCTGATACTATT[A/C]AAATACTAGAAAAAG | 79582 |
rs139212981 | snp | C/T | 0.00159617 | 0.0282053 | intron-variant | SPAG16 | GRCh38.p7 | 2:213505065 | CATTCATTCAAAATA[C/T]CATTTGTATCAGTGA | 79582 |
rs139216978 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | SPAG16 | GRCh38.p7 | 2:213450766 | TTTATGTATGTTTTA[A/G]TCAATATTCACCTGC | 79582 |
rs139220438 | in-del | -/CC | | | intron-variant | SPAG16 | GRCh38.p7 | 2:214126058 | CTTCCTTCCTTCCTT[-/CC]TTTTTTTTTTTTTTT | 79582 |
rs139223370 | snp | C/T | 0.00517822 | 0.0506191 | intron-variant | SPAG16 | GRCh38.p7 | 2:213592491 | GTTGAAAAGTGCAAG[C/T]ATTTTTAAAACTAAA | 79582 |
rs139226804 | snp | C/T | 0.00478085 | 0.0486577 | intron-variant | SPAG16 | GRCh38.p7 | 2:213291622 | GATTTGATTTACCTG[C/T]TATTAATATAACACT | 79582 |
rs139231043 | in-del | -/G | 0.0260105 | 0.111035 | intron-variant | SPAG16 | GRCh38.p7 | 2:213988347 | GATAGACTGTATCTT[-/G]GGCCATAAAACAAGA | 79582 |
rs139234634 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | SPAG16 | GRCh38.p7 | 2:214047037 | CAAGAATTTGAAGAG[A/G]ATGCCAAAAATGGAA | 79582 |
rs139235524 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | SPAG16 | GRCh38.p7 | 2:214143055 | TTTAAAAATCGTTTT[A/T]TAGCCTCACTCTGTC | 79582 |
rs139239504 | snp | C/T | 0.172351 | 0.237636 | intron-variant | SPAG16 | GRCh38.p7 | 2:213367375 | CCACACTGTCTTTCA[C/T]AATGGCTGAACTAGT | 79582 |
rs139239972 | snp | C/G | 0.0205511 | 0.0992634 | intron-variant | SPAG16 | GRCh38.p7 | 2:213935107 | CTTGGGAGGCTGAGG[C/G]AGAAGGATGGCATGA | 79582 |
rs139242451 | snp | A/G | 0.00636936 | 0.0560724 | intron-variant | SPAG16 | GRCh38.p7 | 2:213616259 | TATGATTGAAAAGAA[A/G]CATGCTTCCACAAAT | 79582 |
rs139250470 | in-del | -/TA | 0.0107246 | 0.0724382 | intron-variant | SPAG16 | GRCh38.p7 | 2:213593069 | AACTCAATCCGTATG[-/TA]TATATATATATTTTT | 79582 |
rs139250728 | snp | C/G | 0.00438332 | 0.0466095 | intron-variant | SPAG16 | GRCh38.p7 | 2:213959977 | TCTTTAAATATCTCT[C/G]TTACCCTTTCTCTCT | 79582 |
rs139251266 | snp | C/G | 0.0314385 | 0.121371 | intron-variant | SPAG16 | GRCh38.p7 | 2:213818799 | GAGTTCTCATGAGAT[C/G]TGATGGTTTAAAAGT | 79582 |
rs139251896 | snp | A/G | 0.0260105 | 0.111035 | intron-variant | SPAG16 | GRCh38.p7 | 2:214257225 | GTGATAGATTTTTAT[A/G]TACTTAGCTCATACC | 79582 |
rs139252343 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | SPAG16 | GRCh38.p7 | 2:213722534 | GTAGTAAACATGGTT[A/G]TGTGCAGAGCATGGG | 79582 |
rs139253543 | snp | C/T | 0.00398564 | 0.0444627 | intron-variant | SPAG16 | GRCh38.p7 | 2:213739283 | TTTTATAACTACTTA[C/T]TTTATAATGTAGGTT | 79582 |
rs139259365 | snp | A/G | 0.00199481 | 0.0315187 | intron-variant | SPAG16 | GRCh38.p7 | 2:213685289 | AGACCCCAATCCAAT[A/G]TGACGCGTGTTCTTG | 79582 |
rs139259803 | snp | A/C | 0.0119091 | 0.0762411 | intron-variant | SPAG16 | GRCh38.p7 | 2:213313706 | TAATTTAGAATTCAA[A/C]TTTGTGCCTATTTTC | 79582 |
rs139261394 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | SPAG16 | GRCh38.p7 | 2:214029607 | GGTTAGAGAAAATTA[A/G]ACACACAAAAGAAAA | 79582 |
rs139272834 | snp | G/T | 0.00318978 | 0.0398085 | intron-variant | SPAG16 | GRCh38.p7 | 2:213483214 | TTATTTGAAATTTAG[G/T]TGTTTCTAGTCCTTC | 79582 |
rs139283458 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | SPAG16 | GRCh38.p7 | 2:214031970 | GAGAATTACAATTCA[A/T]CATGAGAACTGGGTG | 79582 |
rs139284663 | snp | G/T | 0.00358779 | 0.0422022 | intron-variant | SPAG16 | GRCh38.p7 | 2:213800583 | ACTCACTAAGTTGCC[G/T]AGGCTGGCATTTATT | 79582 |
rs139287788 | snp | C/T | 0.000354931 | 0.0133169 | missense, nc-transcript-variant, utr-variant-5-prime | SPAG16 | GRCh38.p7 | 2:213340200 | AAAATTCAGAAAGAA[C/T]GTGATTTTCATCGAA | 79582 |
rs139291891 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | SPAG16 | GRCh38.p7 | 2:213892453 | ATGATTTCCCCAAAC[A/G]TAAAAAACAAGGAAT | 79582 |
rs139303683 | snp | A/G | 0.0182019 | 0.0936463 | intron-variant | SPAG16 | GRCh38.p7 | 2:213355587 | TCCTTTACATCCCTT[A/G]TAAGTTGGATTCCTA | 79582 |
rs139307708 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | SPAG16 | GRCh38.p7 | 2:214392181 | TTTTCTTCTTTTTTT[A/G]AGATAGGGTTTCACT | 79582 |
rs139308931 | snp | A/T | 0.0123036 | 0.0774623 | intron-variant | SPAG16 | GRCh38.p7 | 2:213943744 | AACCAAAACTTAGAG[A/T]TTTGGAAAATTCTTA | 79582 |
rs139321730 | in-del | -/A | 0.109461 | 0.206758 | intron-variant | SPAG16 | GRCh38.p7 | 2:213818628 | CATTCCCTTTCCTAC[-/A]AAGGCATGCATAAAT | 79582 |
rs139323298 | snp | A/G | 0.00159617 | 0.0282053 | intron-variant | SPAG16 | GRCh38.p7 | 2:214138130 | ATTTTACATTTACAT[A/G]AGGATTTTCATCAGA | 79582 |
rs139325041 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | SPAG16 | GRCh38.p7 | 2:213746859 | TGTGTACAATACGTA[A/G]TACCTGATAGTGATA | 79582 |
rs139330867 | snp | A/G | 0.0162398 | 0.0886349 | intron-variant | SPAG16 | GRCh38.p7 | 2:214344548 | TTTTGAAAGTTCAGC[A/G]TTTCTATAATTTTTT | 79582 |
rs139332371 | in-del | -/C | 0.193966 | 0.243639 | intron-variant, utr-variant-3-prime | SPAG16 | GRCh38.p7 | 2:213397224 | TCACTGAATAAGGAG[-/C]CTGGGACTTGATGTC | 79582 |
rs139335751 | snp | G/T | 0.0120078 | 0.0765488 | intron-variant | SPAG16 | GRCh38.p7 | 2:213297396 | GTCTATAGTTTAGTG[G/T]TAGTGCTTTTTATAT | 79582 |
rs139336224 | snp | G/T | | | intron-variant | SPAG16 | GRCh38.p7 | 2:214341852 | ACTCATTCCAGGATG[G/T]CAATGAAGAAATCTT | 79582 |
rs139336295 | snp | A/G | 0.00835141 | 0.0640778 | intron-variant | SPAG16 | GRCh38.p7 | 2:213437146 | CCTCGTGATCTGCCC[A/G]TCTCAGCCTTCCAAA | 79582 |
rs139343144 | snp | A/G | 0.00636936 | 0.0560724 | intron-variant | SPAG16 | GRCh38.p7 | 2:214207802 | AACAAAGCAGAGAAG[A/G]AGGTATGACAAGCTG | 79582 |
rs139345270 | snp | A/C | 0.00199481 | 0.0315187 | intron-variant | SPAG16 | GRCh38.p7 | 2:214120290 | TTCTTTAGCTGAATC[A/C]TGTTTAATTTTATTC | 79582 |
rs139345494 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | SPAG16 | GRCh38.p7 | 2:214261390 | TCTTTTCTAGTCTGG[C/T]GGCTAAGAAAGCTCT | 79582 |
rs139350517 | snp | C/G | 1.66405e-05 | 0.00288443 | missense, nc-transcript-variant, utr-variant-5-prime, intron-variant | SPAG16 | GRCh38.p7 | 2:213350622 | ATGCTGACCTCCTTG[C/G]AAAGAGACAAAGTAG | 79582 |
rs139354362 | in-del | -/CT | | | intron-variant | SPAG16 | GRCh38.p7 | 2:214030124 | ATATTCATTGACTAA[-/CT]CTCTATTTCCCCCTT | 79582 |
rs139368558 | snp | A/T | 0.324855 | 0.23853 | intron-variant | SPAG16 | GRCh38.p7 | 2:213621056 | TAGTACTAAAACTAA[A/T]AACTAGTTTTAGTAC | 79582 |
rs139378759 | snp | C/T | | | intron-variant | SPAG16 | GRCh38.p7 | 2:213318250 | AAGTCATGGAATCAA[C/T]GTAAGTGTCCATCAG | 79582 |
rs139381895 | snp | C/T | 0.00358779 | 0.0422022 | intron-variant | SPAG16 | GRCh38.p7 | 2:213676584 | TTTGTTGAGAGTTTT[C/T]AGCATGAAGGGTTGT | 79582 |
rs139382996 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | SPAG16 | GRCh38.p7 | 2:214211874 | ACCCTACATTCCACC[C/G]ATCAGCAAGTCCTGC | 79582 |
rs139383604 | snp | A/C/T | 0.00239401 | 0.0345304 | intron-variant | SPAG16 | GRCh38.p7 | 2:214330700 | GCCTTAGGAAAGGGA[A/C/T]AAACTCTTGAGCAAG | 79582 |
rs139385898 | in-del | -/AT | 0.214239 | 0.247429 | intron-variant | SPAG16 | GRCh38.p7 | 2:213361415 | AAAAACTAAATCTAA[-/AT]ATATATATATATATT | 79582 |
rs139386702 | snp | A/G | 0.0142736 | 0.0832652 | intron-variant, nc-transcript-variant | SPAG16, LOC101928084 | GRCh38.p7 | 2:214084972 | TAGCACTGAAAGACT[A/G]TTAGAAGACAAAGCA | 79582 |
rs139393975 | snp | A/G | 0.00159617 | 0.0282053 | intron-variant | SPAG16 | GRCh38.p7 | 2:213664252 | AGGATTTATCTTCCC[A/G]TCTTGAAATCCTTTA | 79582 |
rs139396521 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant, upstream-variant-2KB | SPAG16 | GRCh38.p7 | 2:213316458 | GCTAGACTAATCCCT[G/T]TAAAACATAAATCTG | 79582 |
rs139399770 | snp | G/T | 0.00438332 | 0.0466095 | intron-variant | SPAG16 | GRCh38.p7 | 2:214198354 | ATTATACAAAATTTG[G/T]TTTTTCCATTCCTGA | 79582 |
rs139411137 | snp | A/C/G | 0.000399281 | 0.0141238 | intron-variant | SPAG16 | GRCh38.p7 | 2:214403489 | TTACATTCTTTCTTC[A/C/G]TTTGAAACCTGGTGA | 79582 |
rs139411199 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | SPAG16 | GRCh38.p7 | 2:213416409 | AGCCAAAACTAGGTC[A/G]TAGCCTATATTGGTT | 79582 |
rs139414408 | snp | C/T | 0.00199481 | 0.0315187 | intron-variant | SPAG16 | GRCh38.p7 | 2:213866626 | CAGGTGAATGTCAAA[C/T]CTGGATGCCATGAAG | 79582 |
rs139421818 | snp | C/T | 0.0023933 | 0.0345097 | intron-variant | SPAG16 | GRCh38.p7 | 2:214314912 | AAGTAGCTACTGCAT[C/T]CAGCCTGATGGGTAG | 79582 |
rs139423585 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | SPAG16 | GRCh38.p7 | 2:213431116 | CCATCATTAAAACAC[A/G]TTAAAGGATAAGATT | 79582 |
rs139423803 | snp | A/G | 0.00953873 | 0.0683987 | intron-variant | SPAG16 | GRCh38.p7 | 2:213532327 | GAACTATGAATTCTA[A/G]TTTAATTTTTATATA | 79582 |
rs139424471 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | SPAG16 | GRCh38.p7 | 2:214293081 | ACCTTGAGCCGTAGA[A/G]CAATGTATGCTGGCT | 79582 |
rs139425280 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | SPAG16 | GRCh38.p7 | 2:213304412 | TTACTTGTCTTGGAT[A/G]CCTGTGCTTGTGAAG | 79582 |
rs139429571 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | SPAG16 | GRCh38.p7 | 2:213974122 | AATAGAATCCTGTTT[A/T]ATGAGTATGTAGGCT | 79582 |
rs139429823 | snp | A/C/G | 0.0126979 | 0.078662 | intron-variant | SPAG16 | GRCh38.p7 | 2:214069446 | AGATAGCATCTAAGG[A/C/G]GATTTTATTGTCTGG | 79582 |
rs139434050 | snp | G/T | 0.00279162 | 0.0372561 | intron-variant | SPAG16 | GRCh38.p7 | 2:213950287 | TCTTTATTCTTCTAA[G/T]AATTAAGAAAAACGA | 79582 |
rs139437287 | snp | A/C | 1.65787e-05 | 0.00287907 | missense, nc-transcript-variant, utr-variant-5-prime, intron-variant | SPAG16 | GRCh38.p7 | 2:213350581 | GGGTGTTACATGAGA[A/C]ACACCACACTTTACT | 79582 |
rs139442585 | snp | C/T | 0.00279162 | 0.0372561 | intron-variant | SPAG16 | GRCh38.p7 | 2:214340655 | CTTAGCAGCTTCAGA[C/T]AACACATATTTACTA | 79582 |
rs139443815 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | SPAG16 | GRCh38.p7 | 2:214332052 | AGGTCAGGAGTTCAA[C/G]ATCAGCATGGCCAAC | 79582 |
rs139443821 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | SPAG16 | GRCh38.p7 | 2:213885609 | CATATTTAACATTCC[A/G]TCTTAAGGCAATGTG | 79582 |
rs139460415 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | SPAG16 | GRCh38.p7 | 2:213320635 | GAGATCAACTATTTT[A/G]GCTTCCACATGAGTA | 79582 |
rs139464501 | snp | A/C | 0.00318978 | 0.0398085 | intron-variant | SPAG16 | GRCh38.p7 | 2:213778074 | TATAAGCTGTCCAAC[A/C]CAGGAAATCTAAATA | 79582 |
rs139466202 | in-del | -/A | | | intron-variant | SPAG16 | GRCh38.p7 | 2:214184497 | ATGACAGCAAAAAAA[-/A]GACATTTCTTTTGTC | 79582 |
rs139470904 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | SPAG16, LOC101928084 | GRCh38.p7 | 2:214097859 | GTACTTGCTTTGTCA[C/T]GGGCAGCAATCAAAG | 79582 |
rs139471714 | snp | C/T | 0.0107246 | 0.0724382 | intron-variant | SPAG16 | GRCh38.p7 | 2:213734628 | ATAACTAATTTTATC[C/T]AGTTGCAATAAAGGG | 79582 |
rs139478099 | snp | A/G | 0.0178098 | 0.0926698 | intron-variant | SPAG16 | GRCh38.p7 | 2:213843746 | GTTCCAGCTACTTGG[A/G]AGGCTGAGGCAGGAG | 79582 |
rs139483105 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | SPAG16 | GRCh38.p7 | 2:213747882 | TCATCTGATGATCAA[A/C]ATCTTGCCACAATAA | 79582 |
rs139483729 | snp | C/T | 0.0205511 | 0.0992634 | intron-variant | SPAG16 | GRCh38.p7 | 2:213835001 | CAAAATATATTTGAA[C/T]TCTATCCCAGTTTCC | 79582 |
rs139484867 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant, downstream-variant-500B | SPAG16 | GRCh38.p7 | 2:214238705 | TCTAGCTACCTCTTC[A/C]CACAAAATCTACATC | 79582 |
rs139486081 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | SPAG16 | GRCh38.p7 | 2:214208494 | TGAATCTTTTTCAAA[C/T]TATTTCAGTTGAAGA | 79582 |
rs139486218 | snp | A/C | | | intron-variant | SPAG16 | GRCh38.p7 | 2:214292193 | TTCTCTTTAATACTG[A/C]CTTTAGATGGTTGGA | 79582 |
rs139486780 | in-del | -/TTTTG | | | intron-variant | SPAG16 | GRCh38.p7 | 2:213668625 | AATATAATAGTGTTT[-/TTTTG]TTTTGTTTTGTTTTG | 79582 |
rs139488402 | in-del | -/T | | | intron-variant | SPAG16 | GRCh38.p7 | 2:214068865 | AGTCTCATTTTTTTT[-/T]CCCTGACACCTTATC | 79582 |
rs139491952 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | SPAG16 | GRCh38.p7 | 2:213515428 | CTCCCTAGCTAGTCT[A/G]TTGCCCTGTTGCTCT | 79582 |
rs139494386 | snp | C/G | 0.00119737 | 0.0244387 | intron-variant | SPAG16 | GRCh38.p7 | 2:213967897 | TAAATGATAATGCTG[C/G]TTTATAGGGATTGTG | 79582 |
rs139494799 | in-del | -/ATAATAATA | | | intron-variant | SPAG16 | GRCh38.p7 | 2:214301029 | CCTAAAACTTAAAGT[-/ATAATAATA]ATAATAATAATAATA | 79582 |
rs139498637 | snp | A/G | 0.131038 | 0.219882 | intron-variant | SPAG16 | GRCh38.p7 | 2:213625937 | TCAGGTTATCCACCC[A/G]CCTCGGTCTCCCAAA | 79582 |
rs139502464 | snp | C/T | 0.0103295 | 0.0711199 | intron-variant | SPAG16 | GRCh38.p7 | 2:213703303 | AGATTATTAGGAACT[C/T]GGCTGTCCTGTTCTC | 79582 |
rs139504002 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | SPAG16 | GRCh38.p7 | 2:213698236 | GGCTTTTTCTTGGTG[A/C]AATTTTTTAAATTTA | 79582 |
rs139506067 | snp | A/G | 0.0182019 | 0.0936463 | intron-variant | SPAG16 | GRCh38.p7 | 2:213645049 | GTATTCGGCTGAGCT[A/G]GCTCTCAAATCACTT | 79582 |
rs139510920 | snp | C/T | 0.116138 | 0.211142 | intron-variant | SPAG16 | GRCh38.p7 | 2:213425608 | AGTGAGCCGAGATGG[C/T]GCCACTGCATTCCAG | 79582 |
rs139513934 | snp | C/T | 0.0023933 | 0.0345097 | intron-variant | SPAG16 | GRCh38.p7 | 2:213509960 | GAAGAATCAAATAGA[C/T]GCAATACAAAATGAT | 79582 |
rs139515119 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | SPAG16 | GRCh38.p7 | 2:214082375 | GATCTTTTACCTTCT[C/T]CTCCACTTCTTACTG | 79582 |
rs139518713 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | SPAG16 | GRCh38.p7 | 2:213650057 | ATTTGTTCTCAAGGA[G/T]AACTCTCAAGGAGAA | 79582 |
rs139520191 | snp | G/T | 0.000798403 | 0.0199641 | intron-variant | SPAG16 | GRCh38.p7 | 2:213830381 | TGAGGGGTAGTGTTG[G/T]CAAATCAAGACTGTC | 79582 |
rs139520780 | snp | C/T | 0.00676609 | 0.0577691 | intron-variant | SPAG16 | GRCh38.p7 | 2:213379298 | AATGCTGATTCAGAG[C/T]ATACACACCTTCTGG | 79582 |
rs139524684 | in-del | -/TATA | | | intron-variant | SPAG16 | GRCh38.p7 | 2:213869272 | AAAAAAAATATATAT[-/TATA]ATATATATGTATATA | 79582 |
rs139525219 | snp | G/T | 0.0023933 | 0.0345097 | intron-variant | SPAG16 | GRCh38.p7 | 2:214243919 | AGGGCCTGGGTCAGG[G/T]TTTACCCCCAAGACA | 79582 |
rs139525349 | snp | C/T | 0.00874735 | 0.0655527 | intron-variant | SPAG16 | GRCh38.p7 | 2:214107226 | TTATCACAAAATGCC[C/T]ATCTCCTCCACTAGA | 79582 |
rs139527943 | snp | A/C | 0.00159617 | 0.0282053 | intron-variant | SPAG16 | GRCh38.p7 | 2:213495592 | ATTGATTGAAGGAAG[A/C]GGTAATAAGCCAATA | 79582 |
rs139529621 | in-del | -/A/CA | | | intron-variant | SPAG16 | GRCh38.p7 | 2:214108483 | ACACACACACACCCC[-/A/CA]CACACACACCCCAAG | 79582 |
rs139530735 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | SPAG16 | GRCh38.p7 | 2:213890305 | GTGTTAAATCTGAAA[A/G]CATATTAGTAAGTGA | 79582 |
rs139537256 | snp | C/T | 0.00993419 | 0.0697739 | intron-variant | SPAG16 | GRCh38.p7 | 2:213303531 | CATTAACCATCCCCT[C/T]TCCCCTCCCCAGCCT | 79582 |
rs139540939 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | SPAG16 | GRCh38.p7 | 2:213382917 | CTTTGTCATGTAAAG[G/T]CAATTTGGATTAACT | 79582 |
rs139541134 | snp | C/T | | | intron-variant | SPAG16 | GRCh38.p7 | 2:213308965 | GCTGGGACCCAGTTA[C/T]AAACATGAAATTCAT | 79582 |
rs139541447 | snp | A/C | 0.00358779 | 0.0422022 | intron-variant | SPAG16 | GRCh38.p7 | 2:213913948 | TGGAAGAAGCCCACT[A/C]ATGTTGTAGAGAATA | 79582 |
rs139543283 | snp | A/G | 0.00318978 | 0.0398085 | intron-variant | SPAG16 | GRCh38.p7 | 2:214262977 | ATTGTATACATTTAA[A/G]GTACACACGTGATAT | 79582 |
rs139550467 | in-del | -/CACA | | | intron-variant | SPAG16 | GRCh38.p7 | 2:214061982 | ATGAATAAAAGCATG[-/CACA]CACACACACACACAC | 79582 |
rs139555516 | in-del | -/CTA | | | intron-variant | SPAG16 | GRCh38.p7 | 2:213323072 | TGCTCAATGTTACTA[-/CTA]ATTGTCAAGGAAATC | 79582 |
rs139556736 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | SPAG16 | GRCh38.p7 | 2:213612598 | CATAAAATCAACCAC[C/T]AATTGATCACAACCT | 79582 |
rs139564128 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | SPAG16 | GRCh38.p7 | 2:214347645 | AAGGTATTATCCTGA[C/T]GATATTATCACAGTG | 79582 |
rs139568832 | snp | A/C | 0.000798403 | 0.0199641 | intron-variant | SPAG16 | GRCh38.p7 | 2:213811521 | TAATGAAATTGGAAG[A/C]TTCTCTCTTCTTTTG | 79582 |
rs139570610 | snp | C/G | 0.00358779 | 0.0422022 | intron-variant | SPAG16 | GRCh38.p7 | 2:213522083 | AGAGGTTCTAAAGAT[C/G]TATAGCATTGCTATC | 79582 |
rs139573308 | snp | A/G | 0.0023933 | 0.0345097 | intron-variant | SPAG16 | GRCh38.p7 | 2:213680541 | CTAAACCTGTATTCT[A/G]TGTTCTCCAAGAGCA | 79582 |
rs139577546 | in-del | -/AT | 0.29432 | 0.24604 | intron-variant | SPAG16 | GRCh38.p7 | 2:213759330 | TTAATATATATATAT[-/AT]TTAAATTTGTATAAA | 79582 |
rs139579325 | snp | G/T | 0.00478085 | 0.0486577 | intron-variant, upstream-variant-2KB | SPAG16, LOC101928084 | GRCh38.p7 | 2:214103096 | TTTTTCCTTTCTCCA[G/T]TGGCATGTGCCCCCC | 79582 |
rs139580026 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | SPAG16 | GRCh38.p7 | 2:213742442 | TTCAATTACTAGTTT[A/G]TAAATTTACTCACGT | 79582 |
rs139582171 | snp | C/G | 0.00119737 | 0.0244387 | intron-variant | SPAG16 | GRCh38.p7 | 2:214024534 | TAAGATAAATGAATT[C/G]TAAAACATAATTACT | 79582 |
rs139583588 | snp | C/T | | | intron-variant | SPAG16 | GRCh38.p7 | 2:213475209 | CTCTATATAACTGTC[C/T]GGGTCATCTGAAAAC | 79582 |
rs139587698 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | SPAG16 | GRCh38.p7 | 2:213755937 | CTGTGGCTGCATTTA[A/G]CCATCTAAATATATC | 79582 |
rs139590538 | snp | C/T | 0.00636936 | 0.0560724 | intron-variant | SPAG16 | GRCh38.p7 | 2:214213903 | CCATTAGAAGTAAAA[C/T]TGTAGATGAGTGTGA | 79582 |
rs139592367 | snp | C/T | 0.0115144 | 0.0749975 | intron-variant | SPAG16 | GRCh38.p7 | 2:213562709 | TTTTCTCTGTCCTCA[C/T]GTGGTGGAAGGGGCA | 79582 |
rs139602569 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | SPAG16 | GRCh38.p7 | 2:213976249 | ACGTGTGTATACATA[C/T]GTGTATATACACACA | 79582 |
rs139604041 | snp | A/T | 0.00358779 | 0.0422022 | intron-variant | SPAG16 | GRCh38.p7 | 2:213886326 | CCATGGGGAACGGAT[A/T]TTCAGAAACTAGAAT | 79582 |
rs139607437 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | SPAG16 | GRCh38.p7 | 2:213630032 | ATTTGACTTCTCAAT[A/G]TTCCCATCATCCATA | 79582 |
rs139611583 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | SPAG16 | GRCh38.p7 | 2:213351524 | ATACCTTTGGCATAA[A/T]AATTTAAGAAAAAGA | 79582 |
rs139612862 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | SPAG16 | GRCh38.p7 | 2:213324383 | ATTCATCTCAAGGTA[G/T]AACATTTTTATCTAT | 79582 |
rs139615259 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant, downstream-variant-500B | SPAG16 | GRCh38.p7 | 2:214192611 | GTTCTGTTTATTGCA[C/T]TTAGTAGTATTGTAT | 79582 |
rs139617876 | snp | A/G | 0.0588605 | 0.161139 | intron-variant | SPAG16 | GRCh38.p7 | 2:214274449 | TCATAAATAGCTCTT[A/G]CTATTTTGAGATATG | 79582 |
rs139618905 | snp | A/T | 0.000798403 | 0.0199641 | intron-variant | SPAG16 | GRCh38.p7 | 2:214109648 | GCTTGTGTCATTGTC[A/T]GGCCTGGGAATTTTA | 79582 |
rs139619135 | snp | A/T | | | intron-variant | SPAG16 | GRCh38.p7 | 2:213437639 | CTTATTCTGCTACAG[A/T]GACCTTTACTTTTTA | 79582 |
rs139620169 | snp | A/T | 0.00636936 | 0.0560724 | intron-variant | SPAG16 | GRCh38.p7 | 2:214356375 | AAGTGATCCCAATTG[A/T]CACAATATGGAAGAC | 79582 |
rs139629167 | snp | C/G | 0.0785177 | 0.181917 | intron-variant | SPAG16 | GRCh38.p7 | 2:214129633 | GTTGGCAGTATGTTT[C/G]AAGAAGACCTTAATT | 79582 |
rs139629946 | snp | A/G | 0.0023933 | 0.0345097 | intron-variant | SPAG16 | GRCh38.p7 | 2:213389406 | AACAATAGAAAAACT[A/G]GACTTTATAAACATT | 79582 |
rs139632933 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | SPAG16 | GRCh38.p7 | 2:213525676 | ACTAATAAATCTGAT[A/G]ATGTTACAATTTTTA | 79582 |
rs139633567 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | SPAG16 | GRCh38.p7 | 2:214218890 | CACTCTTGTTGGGTG[A/T]ACTTCTCCTAAAATA | 79582 |
rs139643342 | snp | G/T | 0.000798403 | 0.0199641 | intron-variant | SPAG16 | GRCh38.p7 | 2:214065026 | TACTGTGCTAAGAGC[G/T]TTAAATATTTTTTCT | 79582 |
rs139646755 | snp | C/T | 0.0452528 | 0.143452 | intron-variant | SPAG16 | GRCh38.p7 | 2:213988363 | GGCCATAAAACAAGA[C/T]CAATAAAATTAAGAT | 79582 |
rs139659148 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | SPAG16 | GRCh38.p7 | 2:213373770 | TAGTGTGACCTTCAC[A/G]AGATTATTTACATAA | 79582 |
rs139660447 | snp | A/G | | | intron-variant | SPAG16 | GRCh38.p7 | 2:213310606 | TTTATTTATAGTGTA[A/G]TGGCTTGTCTTTTTC | 79582 |
rs139662687 | in-del | -/A | | | intron-variant | SPAG16 | GRCh38.p7 | 2:214013172 | AGACTGGGTATGAGT[-/A]TTTTGTCTTTTTTTT | 79582 |
rs139665775 | snp | A/C | 0.0260105 | 0.111035 | intron-variant | SPAG16 | GRCh38.p7 | 2:213689048 | CACTGCAACCTCCAC[A/C]ACCCTGGTTCAAGCA | 79582 |
rs139669055 | snp | A/G | 0.00636936 | 0.0560724 | intron-variant | SPAG16 | GRCh38.p7 | 2:213334096 | TAATAACCAGAATAT[A/G]TAAGAAACTCTATAG | 79582 |
rs139670282 | snp | A/C | 0.0158469 | 0.0875917 | intron-variant | SPAG16 | GRCh38.p7 | 2:214311192 | TTGGCAGTCTGCATT[A/C]CCCCTCTCTCCCTCT | 79582 |
rs139676713 | snp | A/C | 0.0166325 | 0.0896639 | intron-variant | SPAG16 | GRCh38.p7 | 2:213911388 | GAGCTCAAGCAATCT[A/C]CCTGCCTTGGCCTCC | 79582 |
rs139678809 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | SPAG16 | GRCh38.p7 | 2:213967150 | TTATATTCAATATAC[C/T]TTATATAGTTATTGT | 79582 |
rs139680588 | snp | A/G | 0.00159617 | 0.0282053 | intron-variant | SPAG16 | GRCh38.p7 | 2:213577773 | AGAATGCAACATGTT[A/G]CAGAAATGAAGTCCA | 79582 |
rs139683493 | snp | C/T | 0.00398564 | 0.0444627 | intron-variant | SPAG16 | GRCh38.p7 | 2:213658280 | CCTGTGCCCAGAATA[C/T]TCTCCTCAGCAATCC | 79582 |
rs139689116 | snp | A/T | | | intron-variant | SPAG16 | GRCh38.p7 | 2:214336907 | AATTTTCTAACAGTA[A/T]AAAGACTAAGAGCTA | 79582 |
rs139691214 | snp | G/T | 0.00279162 | 0.0372561 | intron-variant | SPAG16 | GRCh38.p7 | 2:213769344 | GGTAGTACATCCTTA[G/T]TTCATTTGCGGTAGA | 79582 |
rs139694142 | snp | A/T | 0.0107246 | 0.0724382 | intron-variant | SPAG16 | GRCh38.p7 | 2:213639805 | TAGCTAGGCCAGGGA[A/T]GTTTTCCTTGATTAT | 79582 |
rs139702415 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | SPAG16 | GRCh38.p7 | 2:213988986 | TTGCAGCTATGGAAG[C/T]AGGCAGTGCAAGGCT | 79582 |
rs139705514 | snp | A/G | | | intron-variant | SPAG16 | GRCh38.p7 | 2:213553340 | TCACTGGTAAGAACA[A/G]CATACCCAAGTACCT | 79582 |
rs139707015 | snp | C/T | 0.00199481 | 0.0315187 | intron-variant | SPAG16 | GRCh38.p7 | 2:213442890 | CATGAACGAAAGAAT[C/T]GATAATTAATTTTAA | 79582 |
rs139707575 | snp | A/C | 0.0023933 | 0.0345097 | intron-variant | SPAG16 | GRCh38.p7 | 2:214224347 | AAAACAGTGAATGTC[A/C]CATAAATATATGTAC | 79582 |
rs139714675 | snp | A/G/T | 0.00557901 | 0.0525714 | intron-variant | SPAG16 | GRCh38.p7 | 2:213526369 | GGGGTTATTTTCATT[A/G/T]TTTTCTCTTGTTTAA | 79582 |
rs139717204 | snp | C/T | 0.00438332 | 0.0466095 | intron-variant | SPAG16 | GRCh38.p7 | 2:214049745 | AAGTTGGACGCAGCC[C/T]TGGGGACTCCTGTGA | 79582 |
rs139717561 | snp | G/T | 0.00676609 | 0.0577691 | intron-variant | SPAG16 | GRCh38.p7 | 2:214020181 | TGACAGGGTGAGAAC[G/T]CAGGCTGCCTCTCCA | 79582 |
rs139720174 | snp | C/T | 0.00795532 | 0.062565 | intron-variant | SPAG16 | GRCh38.p7 | 2:213454389 | TTGTGTGTTAGTCTA[C/T]AGGATAATAACAAGA | 79582 |
rs139721306 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | SPAG16 | GRCh38.p7 | 2:213829844 | GACTTTACCCAGTGC[A/G]TTATCCTACTGCGGC | 79582 |
rs139728001 | snp | G/T | 0.046775 | 0.145601 | intron-variant | SPAG16 | GRCh38.p7 | 2:213638876 | ATTGTGTTATCTATC[G/T]CATTTCTTAGGTCTA | 79582 |
rs139745699 | snp | C/T | 0.0170251 | 0.090679 | intron-variant | SPAG16 | GRCh38.p7 | 2:213334393 | CTGTGAAGAACAGTT[C/T]GCAGTTCCTCAAAAA | 79582 |
rs139748854 | snp | G/T | 0.00953873 | 0.0683987 | intron-variant | SPAG16 | GRCh38.p7 | 2:214232273 | GCTAGAAATATCTCA[G/T]AGAGTATAGTATCTT | 79582 |
rs139751132 | snp | A/G | 0.0244538 | 0.107838 | intron-variant | SPAG16 | GRCh38.p7 | 2:214236639 | CCTGGGTGACAGAGC[A/G]AGACTCCGTTTCAAA | 79582 |
rs139765330 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | SPAG16 | GRCh38.p7 | 2:213395699 | CATTTTACCTCCCTG[A/T]TTCCACCTTTCAGAG | 79582 |
rs139765784 | snp | A/G | 0.00953873 | 0.0683987 | intron-variant, nc-transcript-variant | SPAG16, LOC101928084 | GRCh38.p7 | 2:214098361 | TCAGTATCTTGGAAG[A/G]TGACTGTATTTGGAG | 79582 |
rs139770913 | snp | G/T | 0.00914312 | 0.0669923 | intron-variant | SPAG16 | GRCh38.p7 | 2:214368189 | ACTTTTTTCATCATC[G/T]CACTAGTTATATGTT | 79582 |
rs139770973 | in-del | -/TA | 0.342134 | 0.232404 | intron-variant | SPAG16 | GRCh38.p7 | 2:213794754 | CTTCGAAAAATACAC[-/TA]AAACTATGCCCTGCA | 79582 |
rs139773178 | snp | A/G | 0.00318978 | 0.0398085 | intron-variant | SPAG16 | GRCh38.p7 | 2:213694010 | CTAATAAATACTGAA[A/G]TGTACTTCATTCTTT | 79582 |
rs139775477 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | SPAG16 | GRCh38.p7 | 2:213425759 | ATTAACATTTTATGA[G/T]ATTTCTCAGTATACT | 79582 |
rs139778744 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | SPAG16 | GRCh38.p7 | 2:213905646 | TTTCCTGCCCCCTAT[A/G]TATTACATTCTATTG | 79582 |
rs139780930 | snp | C/T | 0.122064 | 0.214785 | intron-variant | SPAG16 | GRCh38.p7 | 2:213337310 | AAAGCCAGAGTGCCT[C/T]TTCTCCTCCAAATGA | 79582 |
rs139782655 | in-del | -/AA | 0.0279526 | 0.114869 | intron-variant | SPAG16 | GRCh38.p7 | 2:213308122 | AAAATGACAGCACTC[-/AA]GAGACGATGATTGTT | 79582 |
rs139787985 | snp | C/T | 0.144969 | 0.226867 | intron-variant | SPAG16 | GRCh38.p7 | 2:214258494 | ATATATATATATACA[C/T]ACACACATATATGTA | 79582 |
rs139794677 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | SPAG16 | GRCh38.p7 | 2:214170070 | TTTTATACCACTTGA[C/T]TCCACATGCATTATG | 79582 |
rs139803706 | snp | C/T | 0.00676609 | 0.0577691 | intron-variant, upstream-variant-2KB | SPAG16, LOC101928084 | GRCh38.p7 | 2:214103020 | GTGTTTTCCTTACCC[C/T]TTGGAATTGAGCACA | 79582 |
rs139804947 | snp | C/G | | | intron-variant | SPAG16 | GRCh38.p7 | 2:213589556 | TTTCTTTAAACATTT[C/G]CTGTGCCAGGGTAGG | 79582 |
rs139807310 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | SPAG16 | GRCh38.p7 | 2:213671629 | AATAACTTAATGACT[A/G]TGGTGTTTCCCTATG | 79582 |
rs139807525 | snp | A/G | 0.0197687 | 0.0974348 | intron-variant | SPAG16 | GRCh38.p7 | 2:214023928 | ATAATGACTATGTCC[A/G]TTGAAAAATAAATAT | 79582 |
rs139807667 | snp | C/T | 0.00398564 | 0.0444627 | intron-variant | SPAG16 | GRCh38.p7 | 2:213968232 | CAGGCTGGAGTGTAA[C/T]GGCGAGATCTCATCT | 79582 |
rs139808310 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | SPAG16 | GRCh38.p7 | 2:213712071 | TTACATAGACTGCAA[C/T]ATAAATGGCCTAGGA | 79582 |
rs139813238 | snp | A/G | 0.00318978 | 0.0398085 | intron-variant | SPAG16 | GRCh38.p7 | 2:214175976 | TTAGCCATTTTATAT[A/G]TTGTGATTTACTTGG | 79582 |
rs139815380 | snp | A/G | 0.105214 | 0.203807 | intron-variant | SPAG16 | GRCh38.p7 | 2:213675657 | AATCCTTTCCCCAAT[A/G]CTTGTTTTTCTCAGG | 79582 |
rs139818535 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | SPAG16 | GRCh38.p7 | 2:214121844 | ATGTATAAGGTATAT[A/G]TGAAACATAAATTAA | 79582 |
rs139828362 | snp | G/T | 0.000798403 | 0.0199641 | intron-variant | SPAG16 | GRCh38.p7 | 2:213996977 | GTTAGATGGCTAGAA[G/T]GCTCTAGGGTCTGGA | 79582 |
rs139836952 | snp | A/G | 0.00676609 | 0.0577691 | intron-variant | SPAG16 | GRCh38.p7 | 2:213593214 | TCAATATGCTTCTTG[A/G]TATTTTCCTGTGTGG | 79582 |
rs139837963 | in-del | -/GAA | | | intron-variant, downstream-variant-500B | SPAG16 | GRCh38.p7 | 2:213371419 | AAAAAAAAAAAAAAA[-/GAA]AAGAAAAGACGATTT | 79582 |
rs139843811 | snp | A/T | 0.00636936 | 0.0560724 | intron-variant | SPAG16 | GRCh38.p7 | 2:213596294 | TGTAATATCCTTGTC[A/T]TTCTCATGAAATATG | 79582 |
rs139844329 | snp | A/G | 0.00874735 | 0.0655527 | intron-variant | SPAG16 | GRCh38.p7 | 2:213325330 | TCTGTGTTTTCTTCT[A/G]AAACGCTTAAAATAT | 79582 |
rs139844958 | snp | C/T | 0.00318978 | 0.0398085 | intron-variant | SPAG16 | GRCh38.p7 | 2:213542293 | TTACATGAAACCTAG[C/T]TAATATAATTATTTT | 79582 |
rs139852494 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | SPAG16 | GRCh38.p7 | 2:213998449 | CCTCCATAAGAAGTG[C/G]CTTTCACCTCCTGCC | 79582 |
rs139858606 | snp | G/T | 0.00119737 | 0.0244387 | intron-variant | SPAG16 | GRCh38.p7 | 2:213906624 | AAAATATACTACAAA[G/T]CTATAGTAACAATGA | 79582 |
rs139859442 | snp | A/C | 0.0785177 | 0.181917 | intron-variant | SPAG16 | GRCh38.p7 | 2:214124846 | AGCAGGATGGGCTGG[A/C]ATTTCCTGGAGCACC | 79582 |
rs139862440 | snp | A/T | 0.00119737 | 0.0244387 | intron-variant | SPAG16 | GRCh38.p7 | 2:213455131 | TGTTCAGAGTTTGAC[A/T]TTTTATTCATTTTCT | 79582 |
rs139864968 | snp | G/T | 0.00398564 | 0.0444627 | intron-variant | SPAG16 | GRCh38.p7 | 2:214353258 | TAATTCAACATTTCT[G/T]AAGTTTACTACTAAA | 79582 |
rs139868100 | in-del | -/ATA | 0.0387552 | 0.1337 | intron-variant | SPAG16 | GRCh38.p7 | 2:214065859 | TAGTTAAGCAAACTC[-/ATA]ATGTTTGACTTCTGT | 79582 |
rs139869448 | snp | A/T | 0.000798403 | 0.0199641 | intron-variant | SPAG16 | GRCh38.p7 | 2:213459090 | TTTACTTTGTACCTT[A/T]TATTCTTTTCTATAT | 79582 |
rs139869571 | snp | G/T | 0.00159617 | 0.0282053 | intron-variant | SPAG16 | GRCh38.p7 | 2:213411749 | GGTGTACTTATTCTT[G/T]TCAAGTGCTGTGTCA | 79582 |
rs139877972 | snp | A/G | 0.00358779 | 0.0422022 | intron-variant | SPAG16 | GRCh38.p7 | 2:213774531 | ATATTAAGCAATTTT[A/G]TATGCAATGGTGTTA | 79582 |
rs139878499 | snp | C/T | 0.00318978 | 0.0398085 | intron-variant | SPAG16 | GRCh38.p7 | 2:213547561 | TTGATTTTTAAATCA[C/T]GACATTTTAAATCAT | 79582 |
rs139890450 | in-del | -/TT | 0.0256215 | 0.110247 | intron-variant | SPAG16 | GRCh38.p7 | 2:214004699 | TCCCCAGGCAGGATC[-/TT]AAATGGGGCTGGGTC | 79582 |
rs139895364 | in-del | -/AT | | | intron-variant | SPAG16 | GRCh38.p7 | 2:213634938 | GCCATTATTTCACTC[-/AT]ATATATATATATTCC | 79582 |
rs139899643 | in-del | -/T | 0.0505692 | 0.150756 | intron-variant | SPAG16 | GRCh38.p7 | 2:214280581 | TTGTTCGTTTTTTTT[-/T]AAATTTATCGTCTTT | 79582 |
rs139903441 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | SPAG16 | GRCh38.p7 | 2:213448997 | GCAGAGAGCCTATAA[A/G]CAGTTGTGCAAGTAG | 79582 |
rs139903724 | snp | A/G | 0.00557542 | 0.0525036 | intron-variant | SPAG16 | GRCh38.p7 | 2:213394561 | GCCAGAGGATCCCTG[A/G]TGTTGCCCTTTTATA | 79582 |
rs139905151 | snp | G/T | 0.00438332 | 0.0466095 | intron-variant, utr-variant-3-prime | SPAG16 | GRCh38.p7 | 2:213399835 | TGTAATGTAATAGAA[G/T]TTATTTCTTCCTTAA | 79582 |
rs139905226 | snp | A/G | 0.0023933 | 0.0345097 | intron-variant | SPAG16 | GRCh38.p7 | 2:214357475 | CTTTAGCTATGTCTA[A/G]TCTGCTCTACCCCCT | 79582 |
rs139906687 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | SPAG16 | GRCh38.p7 | 2:213992147 | AAAATAAACACAAAG[C/G]CCCGTTTATAAAGTT | 79582 |
rs139907728 | snp | A/G | 0.00716266 | 0.059414 | intron-variant | SPAG16 | GRCh38.p7 | 2:213929319 | GTGCCCGAGCCTGAC[A/G]CCTACCCATTTCTTA | 79582 |
rs139908624 | snp | C/G | 0.0197687 | 0.0974348 | intron-variant | SPAG16 | GRCh38.p7 | 2:214371419 | GGCCTGTAATCCCAG[C/G]TACTCGGGAGTCTGA | 79582 |
rs139914304 | snp | C/T | 0.00358779 | 0.0422022 | intron-variant | SPAG16 | GRCh38.p7 | 2:213846012 | CTCTTGAGTGTGATA[C/T]ATTTACTAGCATCTC | 79582 |
rs139920327 | snp | C/T | 0.0256215 | 0.110247 | intron-variant | SPAG16 | GRCh38.p7 | 2:213446730 | GGAAATCTATACTAA[C/T]GATAGTGTGTGGATG | 79582 |
rs139926715 | in-del | -/A/AA | 0.0752897 | 0.18061 | intron-variant | SPAG16 | GRCh38.p7 | 2:214366848 | AGCTTGATATAGTTG[-/A/AA]AAAAAAAAACACATT | 79582 |
rs139933806 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | SPAG16 | GRCh38.p7 | 2:213850195 | TGGTATTTCTTTCAC[G/T]TATTAGAAAGTTGAA | 79582 |
rs139933935 | snp | A/G | 0.0596104 | 0.162024 | intron-variant | SPAG16 | GRCh38.p7 | 2:214299275 | TTTTTTTTTGAGACG[A/G]GGTCTTGCTGTGTCA | 79582 |
rs139936009 | snp | C/T | 0.0023933 | 0.0345097 | intron-variant | SPAG16 | GRCh38.p7 | 2:214381053 | CTTTGCAAGGGAAAG[C/T]AGAATGCTACCTTTT | 79582 |
rs139949938 | snp | C/T | 0.021333 | 0.101051 | intron-variant | SPAG16 | GRCh38.p7 | 2:213910413 | AGTCTTAACTAGAGA[C/T]AACAAGAGAATTTTT | 79582 |
rs139949954 | snp | C/T | 0.00318978 | 0.0398085 | intron-variant | SPAG16 | GRCh38.p7 | 2:213856123 | TGGTAAATATACCCA[C/T]TCCAAATGGGAGAAA | 79582 |
rs139954452 | snp | C/T | 0.00398564 | 0.0444627 | intron-variant | SPAG16 | GRCh38.p7 | 2:213933332 | TACTCAACCATTGCC[C/T]TCAATGAGATTACAA | 79582 |
rs139956967 | snp | C/G | 0.0693013 | 0.172766 | intron-variant | SPAG16 | GRCh38.p7 | 2:213701993 | TATAAATGCACCAAT[C/G]AGCACTTTGTGTCTA | 79582 |
rs139962840 | snp | C/G | 0.000798403 | 0.0199641 | intron-variant | SPAG16 | GRCh38.p7 | 2:214225223 | AGATGCGTGGAGCAA[C/G]GGAGATGGAGCCAAA | 79582 |
rs139962945 | snp | C/T | 0.00279162 | 0.0372561 | intron-variant | SPAG16 | GRCh38.p7 | 2:213330243 | GAATGATGGATCCAC[C/T]GACAGCTTGCACTGT | 79582 |
rs139963469 | snp | A/C | 0.0142736 | 0.0832652 | intron-variant, utr-variant-3-prime | SPAG16 | GRCh38.p7 | 2:213398654 | TTTTCATAGCCATCC[A/C]ATCTAAATTTTAATG | 79582 |
rs139964488 | snp | A/C | 0.0142736 | 0.0832652 | intron-variant | SPAG16 | GRCh38.p7 | 2:213634703 | TGGTGCACCTATAAC[A/C]CGAGCAGTGTACACT | 79582 |
rs139969945 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | SPAG16 | GRCh38.p7 | 2:214245799 | ATTTGACATTTGCAC[A/T]GTTTTATTGGGTTAG | 79582 |
rs139978096 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | SPAG16 | GRCh38.p7 | 2:213797660 | GGACACGTTTCTCAG[A/C]TCATATTCCCATCAT | 79582 |
rs139984052 | snp | C/G/T | 0.000399281 | 0.0141238 | intron-variant | SPAG16 | GRCh38.p7 | 2:214384891 | TATCCCTGAGTCAAG[C/G/T]TGAATTCCTAAAGTC | 79582 |
rs139985135 | in-del | -/C | 0.0150606 | 0.0854603 | intron-variant | SPAG16, LOC101928084 | GRCh38.p7 | 2:214090914 | GATGAGATTAATAAA[-/C]AAAAAATGAGAACAA | 79582 |
rs139986109 | snp | A/C | 0.00358779 | 0.0422022 | intron-variant | SPAG16 | GRCh38.p7 | 2:213709269 | TTTCTCGTTTGAAAT[A/C]TGGATGTAACAGGTG | 79582 |
rs139991913 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | SPAG16 | GRCh38.p7 | 2:214310740 | CCTTCAGTTCAGATA[C/G]TCACTGTCCTTTATC | 79582 |
rs139993983 | snp | A/G | 0.0123036 | 0.0774623 | intron-variant | SPAG16 | GRCh38.p7 | 2:213354637 | TTTCTCTGATGACCA[A/G]TGATGATGAGCATTT | 79582 |
rs139997689 | snp | A/T | 0.0422008 | 0.138995 | intron-variant | SPAG16 | GRCh38.p7 | 2:213454032 | TTCTCCATGACTCGC[A/T]ATAACCTCTGATTCT | 79582 |
rs139998898 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | SPAG16 | GRCh38.p7 | 2:213768477 | AGACTTCACAAGACA[A/G]CACTATATATGAATA | 79582 |
rs140007506 | snp | A/G | 0.00358779 | 0.0422022 | intron-variant | SPAG16 | GRCh38.p7 | 2:213784681 | CTCCGTGATAGAACT[A/G]TATGCTGTTTGCTCT | 79582 |
rs140009796 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | SPAG16 | GRCh38.p7 | 2:214358260 | CCGACCCTTGCATCT[A/G]CCCAAGCTTGGTTTT | 79582 |
rs140010909 | snp | G/T | 0.000798403 | 0.0199641 | intron-variant | SPAG16 | GRCh38.p7 | 2:214193633 | CGTCTGTCATGGGTA[G/T]CTACCTGAGGATTAT | 79582 |
rs140017747 | snp | A/G | 0.0785177 | 0.181917 | intron-variant | SPAG16 | GRCh38.p7 | 2:214110108 | GGCAAGATAACAGAT[A/G]TGAGGTTTAGGTGTC | 79582 |
rs140019800 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | SPAG16 | GRCh38.p7 | 2:214032739 | AGATAAAGTAAAACC[C/G]CAAATTCTATATTAA | 79582 |
rs140023115 | snp | C/T | 0.00199481 | 0.0315187 | intron-variant | SPAG16 | GRCh38.p7 | 2:213829128 | TAAGAGAAACAAGTT[C/T]TCCTGGGCTCTAACT | 79582 |
rs140026653 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | SPAG16 | GRCh38.p7 | 2:213692453 | ACTGATTTATTGTGT[C/T]TGGTGTCCAAGAACA | 79582 |
rs140030575 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | SPAG16 | GRCh38.p7 | 2:214139086 | TTAATCATTCTTTCT[G/T]CTGTCTAGGTCTCAT | 79582 |
rs140030705 | snp | C/T | 0.00597247 | 0.0543191 | intron-variant | SPAG16 | GRCh38.p7 | 2:214197327 | GTTTATATTCCCATT[C/T]TGGCGTTAATATCAT | 79582 |
rs140032276 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | SPAG16 | GRCh38.p7 | 2:213372959 | GAGTGGGTAAAATTT[A/G]GCACTGGAAGGTACA | 79582 |
rs140032724 | snp | A/C | 0.00438332 | 0.0466095 | intron-variant | SPAG16 | GRCh38.p7 | 2:214065443 | TATGAAAGTTCTCAT[A/C]TAATATTCTAAATCT | 79582 |
rs140036817 | snp | C/T | 0.0146672 | 0.084371 | intron-variant | SPAG16 | GRCh38.p7 | 2:214290926 | GTTTAAATCTACTGT[C/T]TCTATTAAAAGTGCA | 79582 |
rs140042712 | snp | C/T | 0.00358779 | 0.0422022 | intron-variant | SPAG16 | GRCh38.p7 | 2:214375080 | CAGAACAGGGTATCT[C/T]ACCTTAATCAGCCAC | 79582 |
rs140046610 | snp | A/G | 0.00478085 | 0.0486577 | intron-variant | SPAG16 | GRCh38.p7 | 2:214149813 | TCCACAATGATATAA[A/G]TATTATCAATTAGAT | 79582 |
rs140047183 | snp | A/G | 0.126564 | 0.217402 | intron-variant | SPAG16 | GRCh38.p7 | 2:213612920 | TCCGGCAATCCGCTC[A/G]CCTTGACCTCCCAAA | 79582 |
rs140051696 | snp | G/T | 0.0414363 | 0.137845 | intron-variant | SPAG16 | GRCh38.p7 | 2:213475456 | GGAGTGCAGGCTGCA[G/T]GTGGTTTGTTACCCA | 79582 |
rs140052666 | snp | C/T | 0.00159617 | 0.0282053 | intron-variant | SPAG16 | GRCh38.p7 | 2:214069214 | TGGTTTTAATCATTC[C/T]GATACGTGTATATTG | 79582 |
rs140056649 | snp | A/T | 0.0554779 | 0.157039 | intron-variant | SPAG16 | GRCh38.p7 | 2:214111839 | TTGAAGAGGTCCTTC[A/T]TATCCCTTGTGAGTT | 79582 |
rs140060401 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | SPAG16 | GRCh38.p7 | 2:213335257 | ATCTCATAATGAACT[C/T]GAGAAAATTACATCC | 79582 |
rs140065569 | snp | C/T | 0.00159617 | 0.0282053 | intron-variant | SPAG16 | GRCh38.p7 | 2:213621451 | TTGGTTTGATTAGTG[C/T]GACAAACTTCATGAT | 79582 |
rs140071726 | snp | A/G | | | intron-variant | SPAG16 | GRCh38.p7 | 2:213862134 | ACCACTGGTCCAAAT[A/G]TCCCAACATAAAAAT | 79582 |
rs140073103 | snp | C/T | 0.0693013 | 0.172766 | intron-variant | SPAG16 | GRCh38.p7 | 2:213702115 | AAATGCACCAATCAG[C/T]GCTCTGTGTCTAGCT | 79582 |
rs140079916 | snp | C/T | 0.0023933 | 0.0345097 | intron-variant | SPAG16 | GRCh38.p7 | 2:213580198 | ACAAAGAAGAATCTA[C/T]ACAAACAGGCCTATG | 79582 |
rs140081957 | snp | G/T | 0.0182019 | 0.0936463 | intron-variant | SPAG16 | GRCh38.p7 | 2:213772067 | TTTCAAAACATTGAT[G/T]CTTCCTGTCTGAGCA | 79582 |
rs140083330 | snp | C/T | 0.00676609 | 0.0577691 | intron-variant | SPAG16 | GRCh38.p7 | 2:214153031 | ATAACTGCGGGCAAG[C/T]CTGACTAGTGTCAGG | 79582 |
rs140086543 | snp | C/G | 0.00398564 | 0.0444627 | intron-variant | SPAG16 | GRCh38.p7 | 2:213432697 | ACTGAAACCCATCCT[C/G]CAGAAACTCTTTCAA | 79582 |
rs140087090 | snp | A/T | 0.153332 | 0.230554 | intron-variant | SPAG16 | GRCh38.p7 | 2:214111236 | atggtattccctagg[A/T]tttcctctagggttt | 79582 |
rs140088322 | snp | A/G | 0.0023933 | 0.0345097 | intron-variant | SPAG16 | GRCh38.p7 | 2:213660331 | CTTGAGTGCCGTGGC[A/G]CAATCTCAGCTCACT | 79582 |
rs140089144 | snp | C/T | 0.0023933 | 0.0345097 | intron-variant | SPAG16 | GRCh38.p7 | 2:213703098 | ACACTTTGCCATTCT[C/T]TTTTTCCCTCTCCTG | 79582 |
rs140099323 | snp | G/T | 0.0130921 | 0.0798413 | intron-variant | SPAG16 | GRCh38.p7 | 2:214028223 | AAAATGGTGGTGAGT[G/T]TGTGATGAAATGACA | 79582 |
rs140103507 | snp | C/T | 0.00318978 | 0.0398085 | intron-variant | SPAG16 | GRCh38.p7 | 2:213934488 | TTCTTTTTTTGGTTG[C/T]GGAGAGAAGAAAGTC | 79582 |
rs140109828 | in-del | -/C | | | intron-variant | SPAG16 | GRCh38.p7 | 2:214191235 | GTGAGAAAAAAGGCA[-/C]CAGCCACTTTCAATA | 79582 |
rs140114042 | snp | C/T | 0.00993419 | 0.0697739 | intron-variant | SPAG16 | GRCh38.p7 | 2:213416866 | TCAGGAGGCAAAACA[C/T]AGGAGCAAGGGAAAA | 79582 |
rs140118515 | snp | C/G | 0.00159617 | 0.0282053 | intron-variant | SPAG16 | GRCh38.p7 | 2:213491567 | TTGGCTGATGGGAGT[C/G]GCCAATGCTGGTCTA | 79582 |
rs140119100 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | SPAG16 | GRCh38.p7 | 2:214014871 | GGAAAATAAATTCCT[C/T]ATAAGGGGTTACAGT | 79582 |
rs140123144 | in-del | -/AT | | | intron-variant | SPAG16 | GRCh38.p7 | 2:213938105 | TTCTGATAAAAGCGA[-/AT]ATATATATATATATT | 79582 |
rs140130885 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | SPAG16 | GRCh38.p7 | 2:213578349 | AGTGTGAGAAAACTA[C/G]TTTGTAAATTAATGT | 79582 |
rs140135617 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | SPAG16 | GRCh38.p7 | 2:213445087 | TCACCATATATAAAA[A/G]TCAAATTAAGGACAG | 79582 |
rs140139628 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | SPAG16 | GRCh38.p7 | 2:213528654 | AGCCTGAGCAAGCTG[A/G]AAACCTTTCCTGTAA | 79582 |
rs140142192 | in-del | -/TAC | 0.0142736 | 0.0832652 | intron-variant | SPAG16 | GRCh38.p7 | 2:214057176 | AGAAGGTTTTCAGTT[-/TAC]TTTTTTTTTTTTTTT | 79582 |
rs140142877 | snp | C/T | 0.00398564 | 0.0444627 | intron-variant | SPAG16 | GRCh38.p7 | 2:214037038 | TAAATTATTTCCTTT[C/T]TTGTGTTGTCGTTTA | 79582 |
rs140143236 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | SPAG16 | GRCh38.p7 | 2:214319742 | TGTAACCCCAGAATA[A/T]CTCATACAATGCCTG | 79582 |
rs140144899 | snp | A/T | 0.00119737 | 0.0244387 | intron-variant | SPAG16 | GRCh38.p7 | 2:213583795 | TAATATAATTGACAA[A/T]GAAAGACAATTTTGT | 79582 |
rs140147589 | snp | A/G | 0.0333695 | 0.124785 | intron-variant | SPAG16 | GRCh38.p7 | 2:214408615 | GGGGGTAAAATTTGT[A/G]ATTAAATATTTCACT | 79582 |
rs140165436 | snp | G/T | 0.000798403 | 0.0199641 | intron-variant | SPAG16 | GRCh38.p7 | 2:213958737 | TAAGACTAGCTTTTT[G/T]ACTTTTTTTTAATGT | 79582 |
rs140167435 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | SPAG16 | GRCh38.p7 | 2:213873032 | AAGAGACATGGGTGA[A/T]GCCTTTTTCAGGTTT | 79582 |
rs140176426 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | SPAG16 | GRCh38.p7 | 2:213288051 | GCGGGGACTGCAGAT[A/G]TGCGGCACCATACCC | 79582 |
rs140187451 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | SPAG16 | GRCh38.p7 | 2:213824467 | TGCATATGGATATTC[A/G]GTTTTCCCAGCACTA | 79582 |
rs140190029 | snp | C/T | 0.00755907 | 0.0610114 | intron-variant | SPAG16 | GRCh38.p7 | 2:214113312 | TGGGGTTGCTCTTCT[C/T]GAGGAGTGTCTTTGT | 79582 |
rs140196717 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | SPAG16 | GRCh38.p7 | 2:213726637 | TACACTGGTCTTGAA[C/T]TGGTATTTGGCATTT | 79582 |
rs140198215 | snp | A/G | | | intron-variant | SPAG16 | GRCh38.p7 | 2:213446365 | ATGATTGAAGAGTTT[A/G]AAGATGGCATAGCCA | 79582 |
rs140213141 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | SPAG16 | GRCh38.p7 | 2:214240427 | ATCAGGCTTTATCAT[C/T]GTCTAGCATATGGTG | 79582 |
rs140218417 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | SPAG16 | GRCh38.p7 | 2:214115419 | TAGACATTCATGTTG[C/T]GTTACCATTTAAAGT | 79582 |
rs140220328 | snp | A/G | | | intron-variant | SPAG16 | GRCh38.p7 | 2:214155886 | AGAGACAAAGCATTA[A/G]CAGGCCCACTGTCAC | 79582 |
rs140221461 | snp | A/G | 0.00557542 | 0.0525036 | intron-variant | SPAG16 | GRCh38.p7 | 2:214320673 | CAAAGGGGGCAGGGC[A/G]CCTTATAAAACCATC | 79582 |
rs140222750 | snp | A/T | 0.00835141 | 0.0640778 | intron-variant | SPAG16 | GRCh38.p7 | 2:214076035 | TTTTTACATGTGAAC[A/T]TCTCTTTTATATATT | 79582 |
rs140228906 | snp | A/G | 0.00159617 | 0.0282053 | intron-variant | SPAG16 | GRCh38.p7 | 2:214000246 | TGAATTATCAGAGCG[A/G]TTTCCCCCACACTGT | 79582 |
rs140238067 | snp | A/G | 0.00517822 | 0.0506191 | intron-variant | SPAG16 | GRCh38.p7 | 2:213993467 | AAGTAAACCCCCTAA[A/G]GCATAATTACAATAG | 79582 |
rs140238900 | in-del | -/A/GATA/GATAGATAGATA/GATAGATAGATAGATA | 0.130694 | 0.219696 | intron-variant | SPAG16 | GRCh38.p7 | 2:214195303 | AGATAGATGAGAGAT[lengthTooLong]GATAGATAGATAGAT | 79582 |
rs140247635 | snp | G/T | 0.00119737 | 0.0244387 | intron-variant | SPAG16 | GRCh38.p7 | 2:213947098 | TATTTATTCACTCCT[G/T]GAAGGATATCTGGAA | 79582 |
rs140254552 | snp | A/G | 0.00159617 | 0.0282053 | intron-variant | SPAG16 | GRCh38.p7 | 2:213359872 | ACACTGGGAGCTGCA[A/G]ACGGGAGCTGTTCCT | 79582 |
rs140258225 | snp | C/T | 0.00398564 | 0.0444627 | intron-variant | SPAG16 | GRCh38.p7 | 2:213496409 | GACATGTTAAATGAT[C/T]GATGGTAATTAAACT | 79582 |
rs140264791 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | SPAG16 | GRCh38.p7 | 2:213903469 | TGGCCCAAGCTCTAC[A/G]TTGGCCCCTTTCATC | 79582 |
rs140268098 | snp | C/T | | | intron-variant | SPAG16 | GRCh38.p7 | 2:213954900 | TGATTTTAATTTGCA[C/T]TTTCCTGATAGTAAC | 79582 |
rs140270743 | snp | A/G | | | intron-variant, upstream-variant-2KB | SPAG16 | GRCh38.p7 | 2:213342576 | ATCCAAATTAATGAC[A/G]TTTATAAATACTGCT | 79582 |
rs140270935 | snp | A/G | 0.00716266 | 0.059414 | intron-variant | SPAG16 | GRCh38.p7 | 2:214405183 | AGAATGGAGTGTAAC[A/G]GTGGGAATAGCTCAC | 79582 |
rs140273138 | in-del | -/TATC | 0.0023933 | 0.0345097 | intron-variant | SPAG16 | GRCh38.p7 | 2:214328724 | TGACAATTTTCAATT[-/TATC]TATCTTTTGATGATG | 79582 |
rs140277686 | in-del | -/T | 0.0130921 | 0.0798413 | intron-variant | SPAG16 | GRCh38.p7 | 2:213974549 | CTACCAGAAAGTTAC[-/T]TATTAAAATACCATT | 79582 |
rs140278946 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | SPAG16 | GRCh38.p7 | 2:213924336 | TTGTACAGGTCTCTG[C/T]AGAGAGCATGAATCT | 79582 |
rs140285600 | snp | A/G | 0.00517822 | 0.0506191 | intron-variant | SPAG16 | GRCh38.p7 | 2:213586055 | ATTTTTAGAGATTAC[A/G]TAAGAAAGAAGTAGT | 79582 |
rs140287841 | snp | C/T | 0.00358779 | 0.0422022 | intron-variant | SPAG16 | GRCh38.p7 | 2:214372944 | ACCAGCAAATGGGGC[C/T]ACCTGCATTTCCTGA | 79582 |
rs140288794 | snp | G/T | 0.00716266 | 0.059414 | intron-variant | SPAG16 | GRCh38.p7 | 2:213365355 | GGACTTAATGGAAAA[G/T]ACTAATAAGTGAACA | 79582 |
rs140289545 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant, splice-acceptor-variant | SPAG16 | GRCh38.p7 | 2:213368812 | TCAAATCCCATTCAC[A/G]GTTGCTTCAAAGAGA | 79582 |
rs140291393 | snp | A/G | | | intron-variant | SPAG16 | GRCh38.p7 | 2:213820649 | CTGTTAGTGACTGCA[A/G]TAAAGACTTCTAAAT | 79582 |
rs140291668 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | SPAG16 | GRCh38.p7 | 2:214408834 | TTCTATACCTAGGGT[A/G]TCATTATGAGCAAGT | 79582 |
rs140312966 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | SPAG16 | GRCh38.p7 | 2:213908577 | TCTACCTCTCTCATT[C/T]GACGAGAATTCATAA | 79582 |
rs140316453 | in-del | -/TAATC | 0.0248432 | 0.108648 | intron-variant | SPAG16 | GRCh38.p7 | 2:213339726 | ATTATCAGAACTGAA[-/TAATC]TAGTATATTCTCTTT | 79582 |
rs140317843 | snp | A/G | 0.00438332 | 0.0466095 | intron-variant | SPAG16 | GRCh38.p7 | 2:213736288 | TCCTAATTGCTGTAG[A/G]TTCAGATTTTTTTTT | 79582 |
rs140318218 | snp | C/G | 0.00279162 | 0.0372561 | intron-variant | SPAG16 | GRCh38.p7 | 2:214019927 | TCTTAAAATAATGTA[C/G]TAATTGCTATATATT | 79582 |
rs140325283 | snp | G/T | 0.0185938 | 0.0946107 | intron-variant | SPAG16 | GRCh38.p7 | 2:214288942 | CCCGGCTAATATTTT[G/T]AATTTTTAGTAGAGA | 79582 |
rs140326450 | snp | A/G | 0.00557542 | 0.0525036 | intron-variant | SPAG16 | GRCh38.p7 | 2:214375346 | CTGGAAACTTATTAC[A/G]GTTGCCAATAACCAG | 79582 |
rs140326457 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | SPAG16 | GRCh38.p7 | 2:213786390 | ATTACACTTTAGTGA[C/G]TATTAGAAGAAAGAA | 79582 |
rs140326504 | snp | C/T | 0.00517822 | 0.0506191 | intron-variant | SPAG16 | GRCh38.p7 | 2:213470441 | ACACAAACCCATATC[C/T]GGAGTAAGTGTGTAT | 79582 |
rs140326739 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | SPAG16 | GRCh38.p7 | 2:213311315 | TAGATGATTAATTTA[C/T]AGTGCTAATAAAGTG | 79582 |
rs140331569 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | SPAG16 | GRCh38.p7 | 2:213338713 | CCATGTCCTTTGTAG[C/T]GACATGGATGGAGTT | 79582 |
rs140340212 | snp | G/T | 0.00318978 | 0.0398085 | intron-variant | SPAG16 | GRCh38.p7 | 2:213667054 | ATTGAGGAGGTAATG[G/T]AGAAAAGGTTAAATC | 79582 |
rs140346416 | snp | G/T | | | intron-variant | SPAG16 | GRCh38.p7 | 2:213672153 | TGAAGGTTCATTTCC[G/T]GAATCTACTGAATTT | 79582 |
rs140347252 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | SPAG16 | GRCh38.p7 | 2:213618571 | CATAATGCCAATCTC[C/T]TTAACAGGGGCACAG | 79582 |
rs140353004 | in-del | -/T | 0.0558544 | 0.157504 | intron-variant | SPAG16 | GRCh38.p7 | 2:214339629 | AGAAAAACATGCTTA[-/T]TTGTTCTTACTTGCA | 79582 |
rs140357540 | snp | C/T | 0.00835141 | 0.0640778 | intron-variant | SPAG16 | GRCh38.p7 | 2:213743659 | ATTTGTCTGTCTTCT[C/T]GGGCTACTACTAAAA | 79582 |
rs140365569 | snp | A/G | 0.00438332 | 0.0466095 | intron-variant | SPAG16 | GRCh38.p7 | 2:214374238 | ATCTGCTTGGCAGCA[A/G]TATACCAGGAAGGGA | 79582 |
rs140366440 | snp | C/T | 0.0182019 | 0.0936463 | intron-variant | SPAG16 | GRCh38.p7 | 2:214205763 | TTTATGGAATACATG[C/T]GATATTTTGATACAT | 79582 |
rs140374974 | snp | G/T | 0.0107246 | 0.0724382 | intron-variant | SPAG16 | GRCh38.p7 | 2:213346890 | GTATCAGGATGATGC[G/T]GGCCTCATAAAATGA | 79582 |
rs140381366 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | SPAG16 | GRCh38.p7 | 2:213622107 | AACAATTAAAGATGA[A/G]TGCATTTTTTTTCCT | 79582 |
rs140383028 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | SPAG16 | GRCh38.p7 | 2:214251704 | CTGTGTCCAAGAAAC[A/G]TACTCCTATAAAGTG | 79582 |
rs140385355 | snp | A/G | 0.0103295 | 0.0711199 | intron-variant | SPAG16 | GRCh38.p7 | 2:214151541 | CACATTCATTTGAAT[A/G]TACCTTTATTTATTC | 79582 |
rs140388731 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | SPAG16 | GRCh38.p7 | 2:214209404 | AGTAAACAAAGTTCT[C/T]ATTTATGTGAAACTT | 79582 |
rs140390010 | snp | C/G | 0.00159617 | 0.0282053 | intron-variant | SPAG16 | GRCh38.p7 | 2:214122247 | AACCTGAGCTAAATC[C/G]TACTAAAAAAATAGG | 79582 |
rs140392321 | snp | A/T | 0.00119737 | 0.0244387 | intron-variant | SPAG16 | GRCh38.p7 | 2:214047521 | CTAGACCCTGTCTCT[A/T]GCCATACACAGAAAT | 79582 |
rs140397436 | snp | A/G | 0.00199481 | 0.0315187 | intron-variant | SPAG16 | GRCh38.p7 | 2:214360205 | AGCTCTCCCAGCCAA[A/G]TAACTGATGGATTAT | 79582 |
rs140398502 | snp | G/T | 0.00597247 | 0.0543191 | intron-variant | SPAG16 | GRCh38.p7 | 2:213787061 | GTTTAATGTCTCATA[G/T]CCAAGTCGAGTACTA | 79582 |
rs140398709 | snp | A/G | 0.0325976 | 0.123435 | intron-variant | SPAG16 | GRCh38.p7 | 2:214078767 | GATAAATATCTTTAG[A/G]GGTTGTTGTTTTCAG | 79582 |
rs140400240 | snp | C/T | 0.00398564 | 0.0444627 | intron-variant | SPAG16 | GRCh38.p7 | 2:214248862 | ATATAGTTAAATTTA[C/T]AGAAAAACTGGAACG | 79582 |
rs140400604 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | SPAG16 | GRCh38.p7 | 2:213456049 | GCCTGCCTTTCGCCA[C/T]ACCTTGCCTCTCATG | 79582 |
rs140408572 | snp | A/C | 0.00676609 | 0.0577691 | intron-variant | SPAG16 | GRCh38.p7 | 2:214034802 | GCTCCTAGGTCTGGG[A/C]TCCCCTAAGGGCTGC | 79582 |
rs140412569 | snp | A/G | 0.0023933 | 0.0345097 | intron-variant | SPAG16 | GRCh38.p7 | 2:214007594 | GGTTTTATTTATCTA[A/G]AAAATGTTTTATTCT | 79582 |
rs140415689 | snp | A/T | 0.00279162 | 0.0372561 | intron-variant | SPAG16 | GRCh38.p7 | 2:213913268 | CTTTTCCCACATATT[A/T]TTTATCCATGTTTGT | 79582 |
rs140418353 | snp | A/G | 0.0154538 | 0.0865337 | intron-variant | SPAG16 | GRCh38.p7 | 2:214331365 | CTTTTCTTCTGGGCC[A/G]TTGGCATGATGAGCC | 79582 |
rs140420209 | in-del | -/A | 0.490673 | 0.0676508 | intron-variant | SPAG16 | GRCh38.p7 | 2:214273738 | TAGTGTGATACTTCC[-/A]AGCTTTGTTCTTTTT | 79582 |
rs140420224 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | SPAG16 | GRCh38.p7 | 2:213791757 | ATGGTTAAGACAGGC[A/C]CTTATCATTTAATGG | 79582 |
rs140425069 | snp | A/G | | | intron-variant | SPAG16 | GRCh38.p7 | 2:213642845 | AAAAAAAAAAAAAAA[A/G]AAAAGAGAGACTGGT | 79582 |
rs140431471 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | SPAG16 | GRCh38.p7 | 2:214184668 | ATTGCCTGATAGCTC[A/G]CAGACATCTGTCAGC | 79582 |
rs140433673 | snp | A/G | 0.17654 | 0.238964 | intron-variant | SPAG16 | GRCh38.p7 | 2:213934974 | TTGGGAGGCTGAGGC[A/G]GGCCGATCACGAGGT | 79582 |
rs140435109 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | SPAG16 | GRCh38.p7 | 2:213729908 | ATATTTAATGTCTAG[A/G]TGAACTCTCTATCAC | 79582 |
rs140436481 | snp | A/G | 0.00398564 | 0.0444627 | intron-variant | SPAG16 | GRCh38.p7 | 2:214083352 | TTATTCCTCTCCTGA[A/G]TTAAGGAGGCAGTTT | 79582 |
rs140444947 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | SPAG16 | GRCh38.p7 | 2:214382586 | TGGTGGAGAGATTCT[C/T]AGAGATGGCACCATC | 79582 |
rs140447789 | snp | A/G | 0.00199481 | 0.0315187 | intron-variant | SPAG16 | GRCh38.p7 | 2:213603703 | GGATGAGATCTATTC[A/G]TAAAATGATTCAGTG | 79582 |
rs140450141 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | SPAG16 | GRCh38.p7 | 2:214129875 | GCAAGGATTTATTTT[C/T]AACACCTGGTTTTTC | 79582 |
rs140450857 | snp | A/G | 0.0322114 | 0.122752 | intron-variant | SPAG16 | GRCh38.p7 | 2:214056890 | AGCATCTTCCCCAGG[A/G]GTAGATTCCATCTCC | 79582 |
rs140453987 | in-del | -/CAAA | 0.148661 | 0.22854 | intron-variant | SPAG16 | GRCh38.p7 | 2:214321399 | GCATAGAAGGCAAAG[-/CAAA]CAAACATTCTTTGCT | 79582 |
rs140455193 | in-del | -/TA | | | intron-variant | SPAG16 | GRCh38.p7 | 2:214133128 | ATAAATAAATAATAA[-/TA]TAAAAAAAAAACCTA | 79582 |
rs140456525 | in-del | -/AG | 0.0267878 | 0.112589 | intron-variant | SPAG16 | GRCh38.p7 | 2:213338861 | ACACTGGCGCCTGTC[-/AG]GGGGTGGAGTATGTG | 79582 |
rs140459320 | snp | A/T | 0.0154538 | 0.0865337 | intron-variant | SPAG16 | GRCh38.p7 | 2:214313135 | ACTTTAAAAAAAAAC[A/T]GGTAAGTCAAATCAA | 79582 |
rs140461560 | snp | C/G | 0.00517822 | 0.0506191 | intron-variant | SPAG16 | GRCh38.p7 | 2:214255963 | AGTGTTTTCATTTCT[C/G]GTGAGTAAACACTGA | 79582 |
rs140464184 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant, upstream-variant-2KB, utr-variant-5-prime | SPAG16, LOC100130451 | GRCh38.p7 | 2:213285855 | CCAGTGATATTCCTC[C/T]TTAACAACGATTTTC | 79582 |
rs140473692 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | SPAG16 | GRCh38.p7 | 2:213466834 | CACTTTACCAAACAG[G/T]TGGGGGCTGTCTCAG | 79582 |
rs140477413 | snp | A/G | 0.00159617 | 0.0282053 | intron-variant | SPAG16 | GRCh38.p7 | 2:213920392 | CTGGTCTGTATACTG[A/G]CAGGTTAGGATGCAT | 79582 |
rs140478214 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | SPAG16 | GRCh38.p7 | 2:214179474 | CACCTCTTTTCTCAG[A/T]GGAGCATTCCCTCTT | 79582 |
rs140478222 | snp | C/G | 0.00119737 | 0.0244387 | intron-variant | SPAG16 | GRCh38.p7 | 2:214229781 | ATGGGAGACAGCTTT[C/G]AATATGGTGTAGAAT | 79582 |
rs140479638 | snp | G/T | 0.0225045 | 0.103662 | intron-variant | SPAG16 | GRCh38.p7 | 2:213893318 | AAAATACCAAAGAGA[G/T]TTCTTCCATCTGAAA | 79582 |
rs140480838 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | SPAG16 | GRCh38.p7 | 2:213553537 | AAAGAGGGGCTGCAC[A/G]CTCCTCCCCTTCAAG | 79582 |
rs140480973 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant, upstream-variant-2KB | SPAG16, LOC101928084 | GRCh38.p7 | 2:214104849 | GCTAGCACAGCAGCC[A/G]GGGACTCGCAACAAT | 79582 |
rs140484898 | snp | A/T | 0.021333 | 0.101051 | intron-variant | SPAG16 | GRCh38.p7 | 2:213799699 | AGAAAATATAACATA[A/T]ATGATTACTTGTCAG | 79582 |
rs140486125 | in-del | -/A/CACACA/CACACACACA/CACACACACACA/CACACACACACACA/CACACACACACACACACA/CACACC | | | intron-variant | SPAG16 | GRCh38.p7 | 2:214319200 | TGCACACACACACAC[lengthTooLong]CACACACACACACAC | 79582 |
rs140486156 | snp | A/G | 0.00199481 | 0.0315187 | intron-variant | SPAG16 | GRCh38.p7 | 2:213513623 | TGGGATGGGAGTTTT[A/G]TGGCCAGCCCTGGGA | 79582 |
rs140491652 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | SPAG16 | GRCh38.p7 | 2:213639270 | ATATGAGGTACTATT[C/T]TATTCACCATGCCAT | 79582 |
rs140495022 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | SPAG16 | GRCh38.p7 | 2:214017155 | GCAGAAGTCAAGGGG[A/G]CATTGTGGAAAGAGT | 79582 |
rs140498537 | in-del | -/CAGC | 0.00755907 | 0.0610114 | intron-variant | SPAG16 | GRCh38.p7 | 2:213923908 | GGGTGGGGTCATGTG[-/CAGC]CAGCCTCCTGCCACC | 79582 |
rs140499204 | snp | A/G/T | 0.00119737 | 0.0244387 | intron-variant | SPAG16 | GRCh38.p7 | 2:213344382 | TTCACTGGAGTTTTT[A/G/T]TCTTTTTTTTTTGTA | 79582 |
rs140499779 | snp | G/T | 0.00199481 | 0.0315187 | intron-variant | SPAG16 | GRCh38.p7 | 2:213718023 | AAACTAAATAGCTTC[G/T]GCACAGCAAAAGAAA | 79582 |
rs140504139 | snp | C/G | 0.00755907 | 0.0610114 | intron-variant | SPAG16 | GRCh38.p7 | 2:213744572 | AGCTAGAGACTCCAT[C/G]TGACAATGGAATCAT | 79582 |
rs140506160 | snp | A/G | 0.0130921 | 0.0798413 | intron-variant | SPAG16 | GRCh38.p7 | 2:213423380 | TTTTAAATAGGGTTA[A/G]GTTACCTTAAAATTA | 79582 |
rs140507277 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | SPAG16 | GRCh38.p7 | 2:214207187 | GGGTACCATTCTTCT[A/T]TTCCTGCTTGCCCTG | 79582 |
rs140514900 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | SPAG16 | GRCh38.p7 | 2:213672701 | TTTATAATATTTATA[A/T]GGGTATCACATTATT | 79582 |
rs140515518 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | SPAG16 | GRCh38.p7 | 2:214183684 | TCAGCCCTATCACTC[C/T]TGTCTCATTTTAGCT | 79582 |
rs140515650 | in-del | -/TT | 0.0239001 | 0.106672 | upstream-variant-2KB, intron-variant | VWC2L, SPAG16 | GRCh38.p7 | 2:214410099 | CACTTGAAATAAAAC[-/TT]TGATTCATTCTCTCT | 79582 |
rs140522975 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | SPAG16 | GRCh38.p7 | 2:213877057 | ATCAAAGATCTTGTA[C/T]ATCATAGAAGATTCT | 79582 |
rs140527994 | snp | A/G | 0.00478085 | 0.0486577 | intron-variant | SPAG16 | GRCh38.p7 | 2:214188802 | CCACACTTCTTAAGC[A/G]ACACATCTATTTTTT | 79582 |
rs140534603 | snp | A/G | 0.00279162 | 0.0372561 | intron-variant | SPAG16 | GRCh38.p7 | 2:213978055 | TTTTTTCACCACAGA[A/G]TACTATGAGACACCC | 79582 |
rs140537292 | snp | G/T | | | intron-variant | SPAG16 | GRCh38.p7 | 2:214107604 | GTAGTTAATTTTAAT[G/T]TTAGCTATTATTTGG | 79582 |
rs140538230 | snp | G/T | 0.00597247 | 0.0543191 | intron-variant | SPAG16 | GRCh38.p7 | 2:214388553 | TTATTAAAATCACCT[G/T]CATCAAGACAGAATT | 79582 |
rs140545694 | snp | A/G | | | intron-variant | SPAG16 | GRCh38.p7 | 2:214307442 | CTAGCTTTAGGATTT[A/G]TTTGCCCTTGTTTCT | 79582 |
rs140547245 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | SPAG16 | GRCh38.p7 | 2:213432824 | TATAGACAAATATCC[C/T]GAGTGAACAAAGATA | 79582 |
rs140547395 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | SPAG16 | GRCh38.p7 | 2:213654463 | GCACTTTGGGAGGCC[A/G]GGGCGGGTGGATCAC | 79582 |
rs140549119 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | SPAG16 | GRCh38.p7 | 2:213381101 | CGTAAAATAGACTTA[C/T]ACCACAACACTGTTG | 79582 |
rs140550048 | snp | A/G | 0.00159617 | 0.0282053 | intron-variant | SPAG16 | GRCh38.p7 | 2:213512467 | GGAACTGCTTCCTAT[A/G]TAATTACTGGAAAAA | 79582 |
rs140550700 | snp | A/G | 0.0310518 | 0.120672 | intron-variant | SPAG16 | GRCh38.p7 | 2:213727212 | GCCTTTACTGTTTCA[A/G]TCAATTAATCATTTG | 79582 |
rs140551216 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | SPAG16 | GRCh38.p7 | 2:213517666 | AATAAAGCCACACAC[A/G]TCTGATCTTTGGCAA | 79582 |
rs140553959 | snp | C/T | 0.00636936 | 0.0560724 | intron-variant | SPAG16 | GRCh38.p7 | 2:213608915 | GTCTCGATCTCCTGA[C/T]CTTGTGATCTGCCCG | 79582 |
rs140556924 | snp | G/T | 0.00398564 | 0.0444627 | intron-variant | SPAG16 | GRCh38.p7 | 2:214062061 | ACTGCTACAGTGATA[G/T]GTTAAAATGTATTAT | 79582 |
rs140557641 | snp | A/C | 0.000798403 | 0.0199641 | intron-variant | SPAG16 | GRCh38.p7 | 2:213984898 | TCTACATGGCTTATT[A/C]CCTCACTTCATTCAA | 79582 |
rs140558437 | snp | A/T | 0.0425829 | 0.139564 | intron-variant | SPAG16 | GRCh38.p7 | 2:213643982 | GATGGAGTTTCACCA[A/T]GTTGGCCAGGCTGGT | 79582 |
rs140561873 | snp | A/T | 0.0111196 | 0.0737302 | intron-variant | SPAG16 | GRCh38.p7 | 2:213713995 | GTTCTATAACATGAG[A/T]AAAAAAGGATGTTAT | 79582 |
rs140564655 | snp | A/G | 0.0166325 | 0.0896639 | intron-variant | SPAG16 | GRCh38.p7 | 2:213515907 | TTTCAGCCCTCCGGT[A/G]TGAAGTAGGAATTGC | 79582 |
rs140565903 | snp | C/T | 0.00358779 | 0.0422022 | intron-variant | SPAG16 | GRCh38.p7 | 2:213406928 | CCGAGCTCTCAGCGA[C/T]GCGGATTTAAAAAAA | 79582 |
rs140567315 | snp | C/T | 0.0023933 | 0.0345097 | intron-variant | SPAG16 | GRCh38.p7 | 2:213983201 | TGTTTTACAAATATA[C/T]GATTGATAACATTAT | 79582 |
rs140570168 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | SPAG16 | GRCh38.p7 | 2:213602290 | TCCCCATTAAGTGAC[C/T]CAGATCTATAATTTA | 79582 |
rs140579100 | snp | A/G | 0.00438332 | 0.0466095 | intron-variant | SPAG16 | GRCh38.p7 | 2:213837294 | TACTATATAGGCCTT[A/G]TACCAAGTATAAAAG | 79582 |
rs140584779 | in-del | -/TG | | | intron-variant | SPAG16 | GRCh38.p7 | 2:214351388 | GATTGTCTGTGTGTC[-/TG]TGTGTGTGTGTGTGT | 79582 |
rs140589305 | snp | A/G | 0.00279162 | 0.0372561 | intron-variant | SPAG16 | GRCh38.p7 | 2:213807271 | TTTTTAGTCTATTTG[A/G]AGGGGGAGATTCTTG | 79582 |
rs140591751 | snp | C/T | 0.000399281 | 0.0141238 | upstream-variant-2KB, intron-variant | SPAG16, LOC100130451 | GRCh38.p7 | 2:213282692 | CAGGAATGAATTACC[C/T]GACTATTATATCTGT | 79582 |
rs140606081 | snp | C/G | 0.0360663 | 0.129354 | intron-variant | SPAG16 | GRCh38.p7 | 2:213348639 | CCTTCACTTATGAAG[C/G]TTAGTTTGGCTGGAT | 79582 |
rs140608718 | in-del | -/G | | | intron-variant | SPAG16 | GRCh38.p7 | 2:214230843 | CAAGCAGTTGTGGCA[-/G]GTTTTTTGAGTTAAA | 79582 |
rs140609458 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | SPAG16 | GRCh38.p7 | 2:213384890 | CGTTCTATGGTTCAG[G/T]ATATCCTGATAGCCC | 79582 |
rs140611702 | snp | C/T | 0.00478085 | 0.0486577 | intron-variant | SPAG16 | GRCh38.p7 | 2:213841197 | TTTGTATGTCACAAC[C/T]CACCCCTAAAAAAAT | 79582 |
rs140614611 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant, upstream-variant-2KB | SPAG16 | GRCh38.p7 | 2:213316682 | TCCTTGGTTCAGGGC[C/T]ATTGCATTTACTTTT | 79582 |
rs140615489 | snp | A/G | 0.00597247 | 0.0543191 | intron-variant | SPAG16 | GRCh38.p7 | 2:214374439 | AACATGAACCTCTCG[A/G]TATTTCATGAAAAAT | 79582 |
rs140622214 | snp | A/G | 0.0185938 | 0.0946107 | intron-variant | SPAG16 | GRCh38.p7 | 2:214289761 | TTTTTAATTCTGTGG[A/G]AAGTGACATTCTTAC | 79582 |
rs140623413 | in-del | -/T | | | intron-variant | SPAG16 | GRCh38.p7 | 2:213417877 | TTTATTGTGTTTCAA[-/T]TTTTTTTTTTTTTGA | 79582 |
rs140625983 | snp | A/G | 0.00835141 | 0.0640778 | intron-variant | SPAG16 | GRCh38.p7 | 2:213463727 | GTTTGCTGCAGGGGC[A/G]GAGCCCTCATGGAGA | 79582 |
rs140632556 | snp | C/T | 0.0722614 | 0.17581 | intron-variant | SPAG16 | GRCh38.p7 | 2:213925527 | CGGCTAATTTTTGTA[C/T]TTTTAGTAGGGATAT | 79582 |
rs140635235 | in-del | -/T | 0.00438332 | 0.0466095 | intron-variant | SPAG16 | GRCh38.p7 | 2:213976687 | CATTTGGGGCCCATA[-/T]GAAAGGCTTGAAGAG | 79582 |
rs140637000 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | SPAG16 | GRCh38.p7 | 2:213678557 | CTCTTAACCACTATC[A/G]GTACACCTTCAGAAT | 79582 |
rs140641739 | snp | A/G | 0.00199481 | 0.0315187 | intron-variant | SPAG16 | GRCh38.p7 | 2:214221501 | ATAAACCTACAAAGC[A/G]GTTAAAGTAAGATGT | 79582 |
rs140644068 | snp | A/G | 0.021333 | 0.101051 | intron-variant | SPAG16 | GRCh38.p7 | 2:214059096 | GCAAGAGAATCTCTT[A/G]AACCCAGGAGGCAGA | 79582 |
rs140644334 | in-del | -/A | 0.0150606 | 0.0854603 | intron-variant | SPAG16 | GRCh38.p7 | 2:214210514 | AAAATTTATGTGTGG[-/A]TTTTCTATTTCCTGG | 79582 |
rs140644918 | snp | A/G | 0.00755907 | 0.0610114 | intron-variant | SPAG16 | GRCh38.p7 | 2:213331087 | CTAATACACCTCTCC[A/G]TCTATCAGGGGTAGA | 79582 |
rs140645246 | in-del | -/G | 0.021333 | 0.101051 | intron-variant | SPAG16 | GRCh38.p7 | 2:213944670 | AGAAGGACATGAATT[-/G]GTGGGGGGCTGGGAA | 79582 |
rs140646206 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | SPAG16 | GRCh38.p7 | 2:214132575 | TTGTGTCACTTAGAG[A/G]ACTTTAGAAGAAGTT | 79582 |
rs140652255 | in-del | -/ACACACAC | 0.0463947 | 0.145069 | intron-variant | SPAG16 | GRCh38.p7 | 2:213417206 | TATAGAAAAGTACAG[-/ACACACAC]ACACACACAATACAA | 79582 |
rs140656220 | snp | A/T | 0.0154538 | 0.0865337 | intron-variant | SPAG16 | GRCh38.p7 | 2:213919013 | CTTTGTAATTTCTAA[A/T]TGTTTTTATTTGGAT | 79582 |
rs140659866 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | SPAG16 | GRCh38.p7 | 2:214359276 | ATTTTTCAAGTTTGT[A/G]TAGGTAATGATGATA | 79582 |
rs140660080 | snp | C/T | 0.0023933 | 0.0345097 | intron-variant | SPAG16 | GRCh38.p7 | 2:213765489 | ATTATGGAATGCCTT[C/T]TATGTCCTCTTGAGT | 79582 |
rs140661486 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | SPAG16 | GRCh38.p7 | 2:213724409 | CCTGGAATTTCTAGT[A/G]AGGGAGACAATATTT | 79582 |
rs140663346 | snp | C/G | 0.00199481 | 0.0315187 | intron-variant | SPAG16 | GRCh38.p7 | 2:213687725 | AATATAATGTATCTT[C/G]ACATAGTTTTCTTCA | 79582 |
rs140664236 | snp | A/G | 0.00835141 | 0.0640778 | intron-variant | SPAG16 | GRCh38.p7 | 2:213554884 | TATTCAAGTTATAAG[A/G]GTTTAAGAAGGTGAG | 79582 |
rs140670365 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | SPAG16 | GRCh38.p7 | 2:213690417 | GGGCAAGAGAGAGAC[A/G]CTCCCTCTATCCACT | 79582 |
rs140676837 | snp | C/T | 0.0103295 | 0.0711199 | intron-variant | SPAG16 | GRCh38.p7 | 2:213358449 | TTCTTGGAGGCTTTG[C/T]TCATTTCTTTTTACT | 79582 |
rs140677891 | snp | A/T | 0.00159617 | 0.0282053 | intron-variant | SPAG16 | GRCh38.p7 | 2:213293555 | GCAGCCTGTGGAGAG[A/T]CCCACATGGGGAAGA | 79582 |
rs140678001 | snp | A/C | 0.00318978 | 0.0398085 | intron-variant | SPAG16 | GRCh38.p7 | 2:214072435 | CATACCACTCCTACA[A/C]CCCGAACAATCCCAC | 79582 |
rs140679465 | snp | A/T | 0.00159617 | 0.0282053 | intron-variant | SPAG16 | GRCh38.p7 | 2:213770058 | TTTGAAGATTTGTCC[A/T]TGTTGTTGCTTATAT | 79582 |
rs140685150 | snp | C/G | 0.00199481 | 0.0315187 | intron-variant | SPAG16 | GRCh38.p7 | 2:213410676 | CCAAGATGCAAATGC[C/G]TAGTTGGAATGGATC | 79582 |
rs140686597 | snp | A/C | 0.0023933 | 0.0345097 | intron-variant | SPAG16 | GRCh38.p7 | 2:214134947 | GCTCTGACATTGTGC[A/C]GTTTTCGATAAAAAT | 79582 |
rs140687726 | snp | G/T | 0.0267878 | 0.112589 | intron-variant | SPAG16 | GRCh38.p7 | 2:214226317 | AATGCACATACTTTT[G/T]CAAACCTCTGCTTGT | 79582 |
rs140690431 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | SPAG16 | GRCh38.p7 | 2:213821431 | AAATTTTTAATTGTG[C/T]GTATAGTAGGTATAC | 79582 |
rs140694048 | snp | C/T | 0 | 0 | intron-variant | SPAG16 | GRCh38.p7 | 2:213618060 | CTTGTTTTGTGAAAA[C/T]GTAGCAGAGATAAAT | 79582 |
rs140697849 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | SPAG16 | GRCh38.p7 | 2:213560016 | CCTGTTCCCTACCCC[A/G]CCCAGCCTGGATATG | 79582 |
rs140707873 | snp | C/T | 0.00716266 | 0.059414 | intron-variant | SPAG16 | GRCh38.p7 | 2:213699096 | TTCTAATGTCTCCTA[C/T]AACGTTTGATGTTCA | 79582 |
rs140708272 | snp | C/G | 0.0174175 | 0.0916809 | intron-variant | SPAG16 | GRCh38.p7 | 2:213574280 | TTACTTTCCATGACT[C/G]TTTTCTTGATGTTCT | 79582 |
rs140709344 | snp | A/T | 0.00795532 | 0.062565 | intron-variant | SPAG16 | GRCh38.p7 | 2:214394604 | TAGATCAGTTTTAGT[A/T]TCACAGAAAAATTGA | 79582 |
rs140713412 | in-del | -/GTGTGTGTGTGC/TG | | | intron-variant | SPAG16 | GRCh38.p7 | 2:214193396 | AAAGAGATCTTTTAT[-/GTGTGTGTGTGC/TG]GTGTGTGTGTGTGTG | 79582 |
rs140715712 | snp | A/T | 0.00517822 | 0.0506191 | intron-variant | SPAG16 | GRCh38.p7 | 2:214021511 | TCATGAGAGCAGCAC[A/T]GAAAAGACCTGCCCC | 79582 |
rs140730584 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | SPAG16 | GRCh38.p7 | 2:213429292 | GAGATGGTGCTTTTA[C/T]ACACCATTGCAGGGC | 79582 |
rs140731733 | snp | C/T | 0.0023933 | 0.0345097 | intron-variant | SPAG16 | GRCh38.p7 | 2:213640373 | TCTCATTTGGGTAGA[C/T]TATGTCAGTGGAAAG | 79582 |
rs140735083 | in-del | -/A | 0.0441095 | 0.141807 | intron-variant | SPAG16 | GRCh38.p7 | 2:214126319 | ACTCATTCATGGGAG[-/A]AGGAGGGTCGGAAGA | 79582 |
rs140736561 | snp | G/T | 0.00676609 | 0.0577691 | intron-variant | SPAG16 | GRCh38.p7 | 2:214025309 | TTTCAAGAACTAAGT[G/T]ACTACAATTCATTGC | 79582 |
rs140739722 | in-del | -/A | 0.0463947 | 0.145069 | intron-variant | SPAG16 | GRCh38.p7 | 2:213420026 | AAGTATATACAAGAT[-/A]TTTTTTTATACCTTT | 79582 |
rs140740208 | snp | A/C | 0.00478085 | 0.0486577 | intron-variant | SPAG16 | GRCh38.p7 | 2:213813151 | ACTTTTTCTGAACCC[A/C]TCAGAGAACTGAAGT | 79582 |
rs140740528 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | SPAG16 | GRCh38.p7 | 2:213494802 | GGCTGCATGCTCTCC[C/T]ACTCTCCCTTGCCCT | 79582 |
rs140744090 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | SPAG16 | GRCh38.p7 | 2:213486084 | TATAAATGTTTGAAT[C/T]ATTCTCTTCTAGCTA | 79582 |
rs140745511 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | SPAG16 | GRCh38.p7 | 2:214402307 | TAACAAGTTTCATGC[C/T]TCTCAGTGGTTTTTC | 79582 |
rs140772037 | snp | A/T | 0.081446 | 0.184634 | intron-variant | SPAG16 | GRCh38.p7 | 2:214118131 | TGAAAAACTGTTAGA[A/T]CTAATAAATTCAGTA | 79582 |
rs140776442 | in-del | -/AAAAAACCC | | | intron-variant | SPAG16 | GRCh38.p7 | 2:213808340 | TAAAAAACGAAAGAA[-/AAAAAACCC]CAGCCACTCGTTTAC | 79582 |
rs140777584 | snp | A/G | 0.00438332 | 0.0466095 | intron-variant | SPAG16 | GRCh38.p7 | 2:214364346 | AATAGCTCAAGTCAC[A/G]CTTTCTCCTTAAAAT | 79582 |
rs140777901 | snp | A/G | 0.00159617 | 0.0282053 | intron-variant | SPAG16 | GRCh38.p7 | 2:213534737 | CATGAAGGGGAAAGG[A/G]AATGAAAGGAAAGAG | 79582 |
rs140777965 | snp | C/G | 0.079617 | 0.182947 | intron-variant | SPAG16 | GRCh38.p7 | 2:213908929 | CCCTCCCTCCTCCCC[C/G]CCACCACACAACAGT | 79582 |
rs140783470 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | SPAG16 | GRCh38.p7 | 2:214397925 | TTGGGTAGTTCTCCG[C/T]ATGCACTCTCACTTG | 79582 |
rs140793295 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | SPAG16 | GRCh38.p7 | 2:213362957 | GAGATTTGGAGAGGA[A/C]AAATATCCAAACTAT | 79582 |
rs140795030 | snp | A/T | 0.0142736 | 0.0832652 | intron-variant | SPAG16 | GRCh38.p7 | 2:214038194 | TTTCTTTTGGTGTTT[A/T]GGAAAGACTGTACTT | 79582 |
rs140796955 | snp | A/T | 0.00119737 | 0.0244387 | intron-variant | SPAG16 | GRCh38.p7 | 2:213946276 | CATGCCACCACACCC[A/T]TCTAATTTTTCTATT | 79582 |
rs140797736 | snp | A/G | 0.00874735 | 0.0655527 | intron-variant | SPAG16 | GRCh38.p7 | 2:213286393 | GGTTTAGTCATTTCA[A/G]CTCTCAGTTGAAATG | 79582 |
rs140814862 | snp | C/G | 0.00557542 | 0.0525036 | intron-variant | SPAG16 | GRCh38.p7 | 2:214001147 | AAATATTTTAGAAGA[C/G]GTTTTTGAATTTAGA | 79582 |
rs140821985 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | SPAG16 | GRCh38.p7 | 2:213540646 | TAAAGGAATATTTCC[A/G]TATTATGAAAAATAA | 79582 |
rs140824029 | snp | G/T | 0.00279162 | 0.0372561 | intron-variant | SPAG16 | GRCh38.p7 | 2:213622697 | TAGACTGTCACCATA[G/T]TAAGTAGGACTCTTC | 79582 |
rs140835560 | snp | G/T | 0.0023933 | 0.0345097 | intron-variant | SPAG16 | GRCh38.p7 | 2:214126135 | GGCAGGTCCCACCTC[G/T]AATCACGTCTTCAAA | 79582 |
rs140835638 | snp | C/T | 0.0479149 | 0.147179 | intron-variant | SPAG16 | GRCh38.p7 | 2:213402441 | AAATTTTATTATTAT[C/T]ATACTTTAAGTTTTA | 79582 |
rs140835662 | snp | C/T | 0.00716266 | 0.059414 | intron-variant | SPAG16 | GRCh38.p7 | 2:213452085 | GTATGTGAAGTTTGG[C/T]GATTACCCAGGACAC | 79582 |
rs140837086 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | SPAG16 | GRCh38.p7 | 2:214352745 | ATTCTTTTTTTATTT[A/T]TATTTTTGCTCTTTT | 79582 |
rs140847384 | snp | A/G | 0.00676609 | 0.0577691 | intron-variant | SPAG16 | GRCh38.p7 | 2:214332182 | ACTTGAACCTGGGAG[A/G]TGGAGGTTGCAGTGA | 79582 |
rs140848326 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | SPAG16 | GRCh38.p7 | 2:213538049 | TGAGGTTTTTGTCTA[C/T]AAGATTAGGTAACAA | 79582 |
rs140852194 | snp | G/T | 0.000798403 | 0.0199641 | intron-variant | SPAG16 | GRCh38.p7 | 2:214006509 | AGAAAAGAGAGGAGA[G/T]GAAAGGAAATAAAGG | 79582 |
rs140864608 | in-del | -/C | 0.499784 | 0.0103811 | intron-variant | SPAG16 | GRCh38.p7 | 2:213776827 | CAGCGTTCTATGCCA[-/C]CCCCCCCCCACCCCA | 79582 |
rs140868381 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | SPAG16 | GRCh38.p7 | 2:213912813 | CTAAGTGGCCCAGCT[A/G]ACCTACAAATCATAA | 79582 |
rs140869531 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | SPAG16 | GRCh38.p7 | 2:213306759 | TGTAAAAAATTCCAT[A/T]ATTACTACAGTCTCC | 79582 |
rs140873992 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | SPAG16 | GRCh38.p7 | 2:214199716 | TTTTCACAATATTGT[A/C]TCTTCCCATCCATGA | 79582 |
rs140874843 | in-del | -/T | 0.0718919 | 0.175435 | intron-variant | SPAG16 | GRCh38.p7 | 2:214167408 | ATTCACTGTGGGGAG[-/T]TGTTAGGATGCCCAT | 79582 |
rs140874861 | snp | A/T | 0.00398564 | 0.0444627 | intron-variant | SPAG16 | GRCh38.p7 | 2:213766636 | TCGAGAAAGCACCAA[A/T]CAAAAAGGCTCTAGT | 79582 |
rs140877392 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | SPAG16, LOC101928084 | GRCh38.p7 | 2:214087224 | ATGCAGATTTTTTTG[C/T]TATCTTAACTTTAAG | 79582 |
rs140877989 | snp | C/G | 0.00159617 | 0.0282053 | intron-variant | SPAG16 | GRCh38.p7 | 2:214333693 | TACCACTCTGCCATC[C/G]CCACACTGAGACTTG | 79582 |
rs140886221 | snp | A/G | 0.00478085 | 0.0486577 | intron-variant | SPAG16 | GRCh38.p7 | 2:213835156 | ACACACAGACACAAA[A/G]CTTAGAGATTTTACA | 79582 |
rs140888057 | snp | C/G | 0.0248432 | 0.108648 | intron-variant | SPAG16 | GRCh38.p7 | 2:214254264 | CCTCTCTTCCTGTTT[C/G]AATGCCCTTTATTTC | 79582 |
rs140890160 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | SPAG16 | GRCh38.p7 | 2:214198703 | AATGGTTAACTAGTT[C/T]ACATTCCCACCAGCA | 79582 |
rs140892220 | snp | C/T | | | intron-variant | SPAG16 | GRCh38.p7 | 2:213418582 | ATGAATGCAGTATAT[C/T]CTTCAAGGGTAATAA | 79582 |
rs140893897 | snp | A/G | | | intron-variant | SPAG16 | GRCh38.p7 | 2:214191727 | TCAAAAAAAAAAAAA[A/G]AAAAAAAAAAAAAAA | 79582 |
rs140896125 | snp | C/T | 0.0178098 | 0.0926698 | intron-variant | SPAG16 | GRCh38.p7 | 2:214283378 | GGTGTTAAATACATG[C/T]CAGCCCCATATTAGC | 79582 |
rs140898839 | snp | A/G | 0.00279162 | 0.0372561 | intron-variant | SPAG16 | GRCh38.p7 | 2:213407157 | GTGTGGATGGTGACA[A/G]GTCCTACTGCTGGAC | 79582 |
rs140900647 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | SPAG16 | GRCh38.p7 | 2:213331338 | TTGGCAGGATTTACC[A/G]TCATAAGAATGTCAT | 79582 |
rs140902374 | snp | C/T | 0.00557542 | 0.0525036 | intron-variant | SPAG16 | GRCh38.p7 | 2:213735190 | GTTATCTTTTATAAA[C/T]CACCAAACTAAATAT | 79582 |
rs140904299 | snp | A/G | 0.00478085 | 0.0486577 | intron-variant | SPAG16 | GRCh38.p7 | 2:214405389 | GCCTTGGCCTCTCAA[A/G]GCATTGGGATTATAG | 79582 |
rs140906171 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | SPAG16 | GRCh38.p7 | 2:213861657 | GTAAGGCATAGATGA[A/T]ACTTTATACAAATAA | 79582 |
rs140907375 | snp | C/T | 0.00636936 | 0.0560724 | intron-variant | SPAG16 | GRCh38.p7 | 2:213664683 | CTATACTCAAGGAAG[C/T]TCATTATACTCAAGG | 79582 |
rs140908358 | snp | A/C | 0.0185938 | 0.0946107 | intron-variant | SPAG16 | GRCh38.p7 | 2:214311487 | TCTGGGTTGATTGAT[A/C]GGGGAACCCCGACAG | 79582 |
rs140910386 | snp | A/G | 0.000399281 | 0.0141238 | upstream-variant-2KB, intron-variant | SPAG16, LOC100130451 | GRCh38.p7 | 2:213283550 | CGAAATAAGTTATAT[A/G]CCAAACCCCTGCGAC | 79582 |
rs140912348 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | SPAG16 | GRCh38.p7 | 2:213334690 | GTTATGTTAAGTGAA[A/G]TAACCCAGGCATGGA | 79582 |
rs140912688 | snp | A/T | 0.00358779 | 0.0422022 | intron-variant | SPAG16 | GRCh38.p7 | 2:213770655 | TGTGTGTTATTCATC[A/T]CCTTGTGTTCATGTG | 79582 |
rs140913856 | in-del | -/TTAAG | 0.128632 | 0.218563 | intron-variant | SPAG16 | GRCh38.p7 | 2:213514851 | TAAAATGGAATCCTA[-/TTAAG]TTATTTTACTATGAT | 79582 |
rs140916625 | snp | A/G | 0.00159617 | 0.0282053 | intron-variant | SPAG16 | GRCh38.p7 | 2:213734185 | TGATCGAGTGATGGG[A/G]GGAAAGAATTGCAAG | 79582 |
rs140926495 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | SPAG16 | GRCh38.p7 | 2:213897687 | GAGCTCATCACACGC[A/G]GTGCTAATCTATACC | 79582 |
rs140928891 | snp | A/G | 0.00676609 | 0.0577691 | intron-variant | SPAG16 | GRCh38.p7 | 2:214116517 | CAGTGAGACAGGTTC[A/G]TCAGCTGCTGTCACA | 79582 |
rs140930649 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | SPAG16 | GRCh38.p7 | 2:214203942 | GTTGGAGCAAGTTCT[C/T]AGCTCTGCCTACCCA | 79582 |
rs140934242 | snp | C/T | 0.00279162 | 0.0372561 | intron-variant | SPAG16 | GRCh38.p7 | 2:214343871 | AATAATAAAGTAGAA[C/T]GAACAATGGAATAGA | 79582 |
rs140936296 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | SPAG16, LOC101928084 | GRCh38.p7 | 2:214100674 | ATGTTAGTTCACTTA[A/G]GATAATGACCTCCAG | 79582 |
rs140944009 | in-del | -/TT | 0.0821764 | 0.185298 | intron-variant | SPAG16 | GRCh38.p7 | 2:214239605 | ATAATCAGAGCAAAC[-/TT]TCATTTATTTAGCTA | 79582 |
rs140946373 | in-del | -/T | 0.0584853 | 0.160693 | intron-variant | SPAG16 | GRCh38.p7 | 2:213992445 | ATTTTGAAAAACACA[-/T]TTTTTTGATATATAT | 79582 |
rs140949640 | in-del | -/TT | 0.0364509 | 0.129988 | intron-variant | SPAG16 | GRCh38.p7 | 2:213579097 | AATATATGTATTGAA[-/TT]TTAGGTATTTAACAT | 79582 |
rs140951197 | in-del | -/C | 0.0126979 | 0.078662 | intron-variant | SPAG16 | GRCh38.p7 | 2:213512893 | CAAGACTGGAAATAG[-/C]CCCAAACTGCTGCTG | 79582 |
rs140951780 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | SPAG16 | GRCh38.p7 | 2:213751471 | AGCCTAAGTGGTAAC[A/G]CTCATAGGCCTTAAT | 79582 |
rs140955802 | snp | C/G | 0.00318978 | 0.0398085 | intron-variant | SPAG16 | GRCh38.p7 | 2:214294214 | TTTCTAGGCTCGTGG[C/G]TGCCGAGGGGCTTGC | 79582 |
rs140957330 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | SPAG16 | GRCh38.p7 | 2:213702520 | TTTAAGAACTGTAAC[A/G]CCGCGAGGGTCCACA | 79582 |
rs140958595 | snp | G/T | 0.0287284 | 0.116357 | intron-variant | SPAG16 | GRCh38.p7 | 2:213532662 | GAGATGTGGTTTCAC[G/T]ATGTTGTCCAGGCTG | 79582 |
rs140959137 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | SPAG16 | GRCh38.p7 | 2:214180541 | TATTTAATTACCAAC[A/T]AACTTTTTCTTTGTA | 79582 |
rs140961912 | snp | C/T | | | intron-variant | SPAG16 | GRCh38.p7 | 2:214211757 | TTTTCTTATCATGGC[C/T]AGCAAATTGTCAAGT | 79582 |
rs140965605 | snp | C/T | 0.00398564 | 0.0444627 | intron-variant | SPAG16 | GRCh38.p7 | 2:214249671 | AATAATGGAAAAGCA[C/T]GTAAACATTTAAAAC | 79582 |
rs140965647 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | SPAG16 | GRCh38.p7 | 2:214294205 | CTATGTTAGTTTCTA[A/G]GCTCGTGGGTGCCGA | 79582 |
rs140966239 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | SPAG16 | GRCh38.p7 | 2:213969608 | ATCTTGGAAGCAGAT[A/G]CTAGGACCTCATCAA | 79582 |
rs140968868 | snp | A/G | | | intron-variant | SPAG16 | GRCh38.p7 | 2:213616667 | GAATCTCAGTCTAAC[A/G]GCAGAGTTCCTAATG | 79582 |
rs140969358 | snp | C/G | 0.00953873 | 0.0683987 | intron-variant | SPAG16 | GRCh38.p7 | 2:213513280 | GTGGTCATACACTGT[C/G]GCTGAACCATATTCT | 79582 |
rs140972487 | snp | A/G | 0.00676609 | 0.0577691 | intron-variant | SPAG16 | GRCh38.p7 | 2:213599264 | TATATGCTGCTTCTT[A/G]CTTGCTTTCTTGATA | 79582 |
rs140974219 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | SPAG16 | GRCh38.p7 | 2:213846857 | CTCAATGGCTTCTGC[C/T]GCTTAGAATCTCAGC | 79582 |
rs140978272 | snp | C/T | | | intron-variant | SPAG16 | GRCh38.p7 | 2:213321991 | GTTGCAGAGATTTGG[C/T]GGTTGACACCAACAT | 79582 |
rs140981387 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | SPAG16 | GRCh38.p7 | 2:214158271 | AAAATTTAAATGCTC[C/T]TCTATGCTATTTTAA | 79582 |
rs140984463 | snp | A/T | 0.000798403 | 0.0199641 | intron-variant | SPAG16 | GRCh38.p7 | 2:214052300 | TTTACTTCAGCTATC[A/T]GGCGACCTTCTTTGT | 79582 |
rs140986943 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | SPAG16 | GRCh38.p7 | 2:213620851 | ATGATAAGACTATTA[A/G]AGTCTGCAGATAAAT | 79582 |
rs140997577 | snp | C/T | 0.0275645 | 0.114116 | intron-variant | SPAG16 | GRCh38.p7 | 2:213789007 | AAACAGGAGTCTGAA[C/T]GTTTTTCCTGTTTTC | 79582 |
rs141000503 | snp | A/G | 0.00597247 | 0.0543191 | intron-variant | SPAG16 | GRCh38.p7 | 2:213380581 | CTAGATGTGTCAGAA[A/G]GCATCCAGTTCACGA | 79582 |
rs141003228 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | SPAG16 | GRCh38.p7 | 2:213461208 | TATGCAATGACACAA[C/T]TGCAATGTTCTGTAA | 79582 |
rs141005490 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | SPAG16 | GRCh38.p7 | 2:213627426 | TATCAGGTCTTTCTT[C/T]TTTCAATACCTGGAG | 79582 |
rs141009368 | snp | A/G | 0.145305 | 0.227022 | intron-variant | SPAG16 | GRCh38.p7 | 2:213705018 | AGCACTTTGGGAGGC[A/G]GAGGCAGGCGGATCA | 79582 |
rs141015694 | snp | A/G | 0.0383715 | 0.133092 | intron-variant | SPAG16 | GRCh38.p7 | 2:213833296 | AATGAGTAGAGATCC[A/G]CCAGACTGTTTCCTA | 79582 |
rs141018004 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | SPAG16 | GRCh38.p7 | 2:214233222 | AGGGTTATCTTCTGG[A/G]GTGTTGGCAATAGTC | 79582 |
rs141018171 | snp | A/G | 0.0142736 | 0.0832652 | intron-variant | SPAG16 | GRCh38.p7 | 2:214075739 | CATGATGATAATTAA[A/G]TGAAACTGATTTATT | 79582 |
rs141025209 | snp | A/G | 0.00636936 | 0.0560724 | intron-variant | SPAG16 | GRCh38.p7 | 2:213704933 | GTCTGCCTGAACTAC[A/G]GTAGTGGCAACAGGA | 79582 |
rs141025564 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | SPAG16 | GRCh38.p7 | 2:213661033 | ACTCTGCCAGATTTC[A/G]TAGCCCCCACTGCCT | 79582 |
rs141026177 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | SPAG16 | GRCh38.p7 | 2:213364730 | TTACTATGAGTCCTT[A/G]GCTGAGGCTGCAATA | 79582 |
rs141032528 | snp | C/T | 0.0271762 | 0.113356 | intron-variant | SPAG16 | GRCh38.p7 | 2:213404669 | ACTTCATGTCTAAAA[C/T]ACCAAAAGCAATGGC | 79582 |
rs141034655 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | SPAG16 | GRCh38.p7 | 2:213491266 | TCGTGACTTTTTCTT[A/C]TATGTCTATCGTTTG | 79582 |
rs141038013 | snp | C/G | | | intron-variant | SPAG16 | GRCh38.p7 | 2:213815406 | AGGGTAGTTACAGGA[C/G]TGTGTGAATTTGTCC | 79582 |
rs141044162 | snp | C/G | 0.00398564 | 0.0444627 | intron-variant | SPAG16 | GRCh38.p7 | 2:214350195 | TTACTGGTTTCTTAC[C/G]TCTGAAACTTATATC | 79582 |
rs141046136 | snp | C/T | 0.00199481 | 0.0315187 | intron-variant | SPAG16 | GRCh38.p7 | 2:214105220 | CAGCACCCATGTCCA[C/T]AAGAGCTCTTTAAGA | 79582 |
rs141047433 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | SPAG16 | GRCh38.p7 | 2:213646881 | CAAGTGGCTGAATAT[C/T]ATGTAATATGCTGTT | 79582 |
rs141047492 | in-del | -/TAGTAGCTAGGTTGAA | 0.436408 | 0.16659 | intron-variant | SPAG16 | GRCh38.p7 | 2:214314753 | AATGTTTAAAAAAAG[-/TAGTAGCTAGGTTGAA]TGGGTTCACATTATG | 79582 |
rs141048371 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | SPAG16 | GRCh38.p7 | 2:214025651 | TGTAAGGTAAAACAA[C/T]ACCTCTTGTTATATA | 79582 |
rs141052679 | snp | A/G | 0.00676609 | 0.0577691 | intron-variant | SPAG16 | GRCh38.p7 | 2:213681866 | TTCTTTCCACTCCCC[A/G]TCTGTATTTTTGACA | 79582 |
rs141052930 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | SPAG16 | GRCh38.p7 | 2:214157213 | ATGCTTCCTTTTTCA[A/G]TCACCGCAGCACATG | 79582 |
rs141054172 | snp | C/T | 0.00199481 | 0.0315187 | intron-variant | SPAG16 | GRCh38.p7 | 2:214080948 | GGGATGTAAGTTTTT[C/T]AAGTTCTCAGGTGAT | 79582 |
rs141065039 | in-del | -/T | 0.0134861 | 0.0810011 | intron-variant | SPAG16 | GRCh38.p7 | 2:214352245 | GCAATGAGTTAGTAC[-/T]TTTTCAGTTAACAAA | 79582 |
rs141069282 | snp | C/T | 0.00279162 | 0.0372561 | intron-variant | SPAG16 | GRCh38.p7 | 2:213564922 | GCTCCTGAGCCTGCA[C/T]ATTTAATTACATCAC | 79582 |
rs141069671 | snp | A/T | 0.00636936 | 0.0560724 | intron-variant | SPAG16 | GRCh38.p7 | 2:213940144 | ATTATATAACAGCCA[A/T]AACTACCATTAAAAA | 79582 |
rs141069717 | snp | A/T | 0.00159617 | 0.0282053 | intron-variant | SPAG16 | GRCh38.p7 | 2:214005030 | TCTGCTTAAATTATA[A/T]TGTAAGATGTAGGAA | 79582 |
rs141072403 | snp | A/G | 0.00438332 | 0.0466095 | intron-variant | SPAG16 | GRCh38.p7 | 2:213433412 | GTAAAGTTTTATTAT[A/G]CAAAATCAATTTACA | 79582 |
rs141073847 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | SPAG16 | GRCh38.p7 | 2:213691128 | AGAGGGCACATTCAA[A/G]CCATAGCACTCTTCA | 79582 |
rs141074123 | snp | A/C | 0.00398564 | 0.0444627 | intron-variant | SPAG16 | GRCh38.p7 | 2:213730895 | CACTTCGGGTTGGGA[A/C]GTTTCTAATGACCAA | 79582 |
rs141074183 | snp | G/T | 0.0107246 | 0.0724382 | intron-variant | SPAG16 | GRCh38.p7 | 2:214195691 | TTTCTACTTTTGCCC[G/T]GTCTTCTTCATCTCA | 79582 |
rs141075511 | snp | C/G | 0.00119737 | 0.0244387 | intron-variant | SPAG16 | GRCh38.p7 | 2:213518346 | GATCATCGCTTACTG[C/G]AACCGCAAAGTCCTG | 79582 |
rs141079054 | snp | A/G/T | 0.00517822 | 0.0506191 | intron-variant | SPAG16 | GRCh38.p7 | 2:213585469 | CTTAGTAGAGATGGG[A/G/T]TTTCACCATGTTGAC | 79582 |
rs141084611 | snp | A/G | 0.00318978 | 0.0398085 | intron-variant | SPAG16 | GRCh38.p7 | 2:213760394 | AGTATAAACATTTAT[A/G]AACCTAGTAACAGAT | 79582 |
rs141087666 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | SPAG16 | GRCh38.p7 | 2:213326211 | ATACTTTATTTTACA[A/G]TCTGCCAGAGAGTAT | 79582 |
rs141091140 | snp | A/G | 0.00755907 | 0.0610114 | intron-variant | SPAG16 | GRCh38.p7 | 2:214165458 | TTTTAAAAATGCTTT[A/G]CATCACCATCCTTTT | 79582 |
rs141096051 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | SPAG16 | GRCh38.p7 | 2:213978904 | TCACAGGACTTCCTA[C/T]AAGAAAAAAACGATA | 79582 |
rs141098796 | snp | A/T | 0.00597247 | 0.0543191 | intron-variant | SPAG16 | GRCh38.p7 | 2:213312572 | TTGAAAACAGAGTTT[A/T]AATTTTTTTTCTTTC | 79582 |
rs141099471 | snp | A/G | 0.00279162 | 0.0372561 | intron-variant | SPAG16 | GRCh38.p7 | 2:214114251 | CTGTCAGCCCCTACC[A/G]GGAGGTGTCTCCCAG | 79582 |
rs141106216 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | SPAG16 | GRCh38.p7 | 2:213385081 | CAACTGAGCTTCTCA[A/G]TGATGTTGCTGCTCC | 79582 |
rs141111992 | snp | A/C | 0.000798403 | 0.0199641 | intron-variant | SPAG16 | GRCh38.p7 | 2:213831383 | TGATATTTCTCCCTG[A/C]CAAAATGCTTTTCAA | 79582 |
rs141114188 | snp | A/G | 0.00636936 | 0.0560724 | intron-variant | SPAG16 | GRCh38.p7 | 2:213632037 | GTAATTGGTATTTTC[A/G]TAGGGATTGCATTGA | 79582 |
rs141115731 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | SPAG16 | GRCh38.p7 | 2:214279418 | GAAGGAACCCAGAGA[A/G]ATGAAAAACACAGTG | 79582 |
rs141128251 | snp | A/G | 0.00874735 | 0.0655527 | intron-variant | SPAG16 | GRCh38.p7 | 2:214228362 | CACAGCTGATCAAGT[A/G]ATTTATCATGTTAAC | 79582 |
rs141133275 | in-del | -/ATTG | 0.084728 | 0.187577 | intron-variant | SPAG16 | GRCh38.p7 | 2:214111739 | GGTCATTTTCACAAT[-/ATTG]ATTCTTCCTATCCGT | 79582 |
rs141134810 | snp | A/G/T | 0.000399281 | 0.0141238 | intron-variant | SPAG16 | GRCh38.p7 | 2:213447802 | TATACACTTGTGTTA[A/G/T]CTCCTGTTTTGCTTC | 79582 |
rs141135867 | snp | A/G | 0.00199481 | 0.0315187 | intron-variant | SPAG16 | GRCh38.p7 | 2:213615047 | ACTTTATTGATAACT[A/G]ATCTGAGAGTCTCAG | 79582 |
rs141141930 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | SPAG16 | GRCh38.p7 | 2:213696084 | AGAGTATATCTAGAG[C/G]GTAAAGCCAAAAGAT | 79582 |
rs141142858 | snp | C/G | 0.00953873 | 0.0683987 | intron-variant | SPAG16 | GRCh38.p7 | 2:213666837 | CAGGAGTTCAGATTA[C/G]AAGAGACACATCCAT | 79582 |
rs141143012 | snp | A/G | 0.0154538 | 0.0865337 | intron-variant | SPAG16 | GRCh38.p7 | 2:214043242 | ACACTAGTATAGCCT[A/G]TTTCACATTTTCCAG | 79582 |
rs141147573 | snp | A/G | 0.0023933 | 0.0345097 | intron-variant | SPAG16 | GRCh38.p7 | 2:214311892 | TATGCCCCACTCTAC[A/G]TAGCATACTTAGAGT | 79582 |
rs141152673 | snp | A/C | | | missense, nc-transcript-variant, intron-variant, utr-variant-5-prime | SPAG16 | GRCh38.p7 | 2:213375086 | AGCCAGGGAACAAAA[A/C]AAATGTAAAACAAAG | 79582 |
rs141156457 | snp | C/G | 0.00676609 | 0.0577691 | intron-variant | SPAG16 | GRCh38.p7 | 2:214283172 | GTCAGTAAATTGATT[C/G]TACACAGGTTTACTG | 79582 |
rs141157244 | in-del | -/C | | | intron-variant | SPAG16 | GRCh38.p7 | 2:213567165 | TAATCAACACAGATT[-/C]TTTTTTTTTTTTTTT | 79582 |
rs141157821 | snp | A/G | 0.0023933 | 0.0345097 | intron-variant | SPAG16 | GRCh38.p7 | 2:213642223 | GCCACTTCTTCCAAA[A/G]GGTTTGTGAATTATT | 79582 |
rs141158842 | snp | C/T | 0.0573587 | 0.15934 | intron-variant | SPAG16 | GRCh38.p7 | 2:213991128 | CATCTACATTAGGTA[C/T]GTCTCCTAATGCTAT | 79582 |
rs141166279 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | SPAG16 | GRCh38.p7 | 2:214199088 | GTTTCTTTTGCTGTG[C/T]GGAGGCTTTTTCATT | 79582 |
rs141166805 | snp | C/T | 0.0263992 | 0.111815 | intron-variant | SPAG16 | GRCh38.p7 | 2:214182370 | TAAATACCGTCTATG[C/T]CTTTTCAAAGTATAT | 79582 |
rs141179371 | snp | A/C | 0.00159617 | 0.0282053 | intron-variant, utr-variant-3-prime, downstream-variant-500B | SPAG16 | GRCh38.p7 | 2:213397106 | AATGTTTTAACAATC[A/C]ACTCTTTGGAAGAAG | 79582 |
rs141181912 | in-del | -/A | 0.317451 | 0.240729 | intron-variant | SPAG16 | GRCh38.p7 | 2:213743504 | TTTCATCCTAAAAAA[-/A]TGTTTTTCAGCATAC | 79582 |
rs141184041 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | SPAG16 | GRCh38.p7 | 2:213477941 | TTCCCACATTTTGAG[A/G]GTAAAAGAGGTGGAG | 79582 |
rs141184410 | snp | A/G | 0.00318978 | 0.0398085 | intron-variant | SPAG16 | GRCh38.p7 | 2:214297632 | TGCTGACATTGGAAA[A/G]TATAAGTTGGTCGTA | 79582 |
rs141189282 | snp | A/G | 0.00636936 | 0.0560724 | intron-variant | SPAG16 | GRCh38.p7 | 2:213514430 | AATATAATTTGCTTC[A/G]TTAAAAATTACTATT | 79582 |
rs141193044 | snp | A/G | 0.00159617 | 0.0282053 | intron-variant | SPAG16 | GRCh38.p7 | 2:214134013 | CTGGAATTTAAGAGA[A/G]AGTTGTGAATTGGAG | 79582 |
rs141195641 | snp | C/T | 0.0111196 | 0.0737302 | intron-variant | SPAG16 | GRCh38.p7 | 2:214054304 | TGTGAGCCACTGTGC[C/T]CAGCCCTCACTTCCC | 79582 |
rs141198300 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | SPAG16 | GRCh38.p7 | 2:213973124 | TGTGGACATCAGCCA[A/G]TGATGAAAGCTTAAG | 79582 |
rs141199754 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | SPAG16 | GRCh38.p7 | 2:213617033 | TCATGTGTTGGTCCC[A/G]TGTGTAATGGGTAGG | 79582 |
rs141203259 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | SPAG16 | GRCh38.p7 | 2:213324031 | TAGGTAAACAAAAAT[C/G]AGTGCTACAGATTTG | 79582 |
rs141204183 | snp | A/C | 0.0248432 | 0.108648 | intron-variant | SPAG16 | GRCh38.p7 | 2:214254266 | TCTCTTCCTGTTTGA[A/C]TGCCCTTTATTTCTT | 79582 |
rs141204798 | snp | G/T | 0.00517822 | 0.0506191 | intron-variant | SPAG16 | GRCh38.p7 | 2:213554126 | ACAGATTCCCCTTAG[G/T]AACAACTTCTCTGGT | 79582 |
rs141215779 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | SPAG16 | GRCh38.p7 | 2:213382683 | AGCATTATCTTACCA[C/T]GTTCCAGGCTTCAGA | 79582 |
rs141217901 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | SPAG16 | GRCh38.p7 | 2:213601318 | TTTGGAAGAGATGGA[A/G]GGGAGAGAGACCTTG | 79582 |
rs141220011 | snp | G/T | 0.00398564 | 0.0444627 | intron-variant | SPAG16 | GRCh38.p7 | 2:213918335 | TTGGAACAGTTTCAG[G/T]AAGAGTGATAGGAGC | 79582 |
rs141227401 | snp | C/T | 0.00597247 | 0.0543191 | intron-variant | SPAG16 | GRCh38.p7 | 2:213708423 | AAGTATTGGGGTGGC[C/T]GGGCATGGTGGCTCA | 79582 |
rs141234698 | snp | A/G | 0.00318978 | 0.0398085 | intron-variant | SPAG16 | GRCh38.p7 | 2:213697120 | AGAAAGAAAGGGGAT[A/G]GGTAGAAGTTTAGGT | 79582 |
rs141236549 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | SPAG16 | GRCh38.p7 | 2:214021292 | TTAATCTGTTTTCAC[A/G]CTGCTGATAAAGACA | 79582 |
rs141241297 | snp | G/T | 0.00478085 | 0.0486577 | intron-variant | SPAG16 | GRCh38.p7 | 2:214039637 | GGATTCTGTGGCACT[G/T]AAAACTGTTTTTCCA | 79582 |
rs141243229 | in-del | -/AA | 0.0023933 | 0.0345097 | intron-variant | SPAG16 | GRCh38.p7 | 2:213912380 | AAATATTTGCTATAT[-/AA]GAGAGAAACTATGAG | 79582 |
rs141249482 | snp | A/G | 0.00199481 | 0.0315187 | intron-variant | SPAG16 | GRCh38.p7 | 2:214352115 | TTCCTATTGCCATTC[A/G]TGAAGACTTTGCCCT | 79582 |
rs141249741 | snp | C/T | 0.00199481 | 0.0315187 | intron-variant | SPAG16 | GRCh38.p7 | 2:213423725 | TAAGATATGTTATTC[C/T]CATTTTTTAGGTAAA | 79582 |
rs141251304 | snp | G/T | | | intron-variant | SPAG16 | GRCh38.p7 | 2:213734725 | GGACATGTTTTTTTT[G/T]GGTATGAACATGAAT | 79582 |
rs141254508 | snp | A/G | 0.00438332 | 0.0466095 | intron-variant | SPAG16 | GRCh38.p7 | 2:214235400 | AATAAATATTATACC[A/G]TATTTATTGGTATGA | 79582 |
rs141259004 | snp | A/G | 0.00199481 | 0.0315187 | intron-variant | SPAG16 | GRCh38.p7 | 2:213698940 | CACATCAAGTACAAC[A/G]CATAGTACCTGGCAT | 79582 |
rs141260097 | snp | A/C | 0.131723 | 0.220251 | intron-variant | SPAG16 | GRCh38.p7 | 2:213472587 | ATGACTTCCATTTGG[A/C]CTTTCCCACCATAAT | 79582 |
rs141262318 | snp | A/G | | | intron-variant | SPAG16 | GRCh38.p7 | 2:213566915 | CTTTTTAAATTTTCT[A/G]AACACATCTTTTGAC | 79582 |
rs141267547 | snp | G/T | 0.0023933 | 0.0345097 | intron-variant | SPAG16 | GRCh38.p7 | 2:213649322 | GGAGGAAAGTTAAAC[G/T]GGAAAGATAGGTCTG | 79582 |
rs141268234 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | SPAG16 | GRCh38.p7 | 2:213558192 | CTATGTGAAAATTAG[C/T]CCCATAGCCACATTC | 79582 |
rs141269817 | snp | A/G | 0.0130921 | 0.0798413 | intron-variant | SPAG16 | GRCh38.p7 | 2:213905090 | GGAATTTGGTCCACT[A/G]ACATGATTTTGTGAA | 79582 |
rs141272982 | snp | A/T | 0.00279162 | 0.0372561 | intron-variant | SPAG16 | GRCh38.p7 | 2:213366921 | TAGATATATCTCCTA[A/T]TGGTATCCCTCCCCA | 79582 |
rs141274456 | snp | G/T | 0.000798403 | 0.0199641 | intron-variant | SPAG16 | GRCh38.p7 | 2:214024686 | TATGAATAGAAGGTT[G/T]ATAGAGAGCTAAAAC | 79582 |
rs141277057 | snp | G/T | 0.0023933 | 0.0345097 | intron-variant | SPAG16 | GRCh38.p7 | 2:213883714 | TGGGTGCATATATAT[G/T]TGGGGTAGGCAAGTC | 79582 |
rs141281083 | snp | A/G | 0.00279162 | 0.0372561 | intron-variant | SPAG16 | GRCh38.p7 | 2:214377508 | GGTATTTTCTCTTTC[A/G]TATTATTTTCTTAAT | 79582 |
rs141282179 | snp | A/G | 0.0217236 | 0.101931 | intron-variant | SPAG16 | GRCh38.p7 | 2:213789468 | GTTCAGATTTATCTG[A/G]GAGTATGTGTGGCAT | 79582 |
rs141282398 | snp | A/C/T | 0.00279242 | 0.0372774 | intron-variant | SPAG16 | GRCh38.p7 | 2:214106767 | GTGAATGAGAGTAGA[A/C/T]GAAGACTTTTGAGTG | 79582 |
rs141297299 | snp | C/T | 0.0162398 | 0.0886349 | intron-variant | SPAG16 | GRCh38.p7 | 2:213348355 | GTCTGTGTCTTTTAA[C/T]GGGAGCATTTAGCCC | 79582 |
rs141301417 | snp | A/G | 0.00557542 | 0.0525036 | intron-variant | SPAG16 | GRCh38.p7 | 2:214332885 | TACGTCCATGGCCAC[A/G]TGTAACCTGGAATGG | 79582 |
rs141301549 | snp | C/T | 0.00279162 | 0.0372561 | intron-variant | SPAG16 | GRCh38.p7 | 2:213793430 | AGGTACATGCCACTC[C/T]TTCTGCTTACCTTCC | 79582 |
rs141302891 | in-del | -/AT | 0.0603597 | 0.1629 | intron-variant | SPAG16 | GRCh38.p7 | 2:213951016 | CACGCCTAGCCTGAC[-/AT]AGTTTTTTTTTTTTT | 79582 |
rs141303453 | snp | G/T | 0.00636936 | 0.0560724 | intron-variant | SPAG16 | GRCh38.p7 | 2:213306037 | ATTGGTCTGTTTGGC[G/T]TTTGGATTTCTTCAT | 79582 |
rs141303554 | snp | A/C | 0.00517822 | 0.0506191 | intron-variant | SPAG16 | GRCh38.p7 | 2:213351893 | CTGTGTCCCCATCCA[A/C]ATCTCACCTTGAATT | 79582 |
rs141303946 | snp | A/C | 0.00358779 | 0.0422022 | intron-variant, nc-transcript-variant | SPAG16, LOC101928084 | GRCh38.p7 | 2:214088568 | ATGAAAGGCCAGGGC[A/C]CAACAAAGACAGATG | 79582 |
rs141310984 | snp | A/G | 0.00517822 | 0.0506191 | intron-variant | SPAG16 | GRCh38.p7 | 2:213762057 | CAACATAGCAAAGTC[A/G]ATCAATGAAATACAC | 79582 |
rs141314722 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | SPAG16 | GRCh38.p7 | 2:213437134 | TCGATTTCCTGACCT[C/T]GTGATCTGCCCGTCT | 79582 |
rs141323443 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | SPAG16 | GRCh38.p7 | 2:213886819 | AAAGAAACTGTGGAT[A/G]AAGGACTCATGAAGA | 79582 |
rs141325418 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | SPAG16 | GRCh38.p7 | 2:213719631 | CACCCACCAATTCTG[A/G]ACACAATACCATCTC | 79582 |
rs141328352 | snp | A/G | | | intron-variant | SPAG16 | GRCh38.p7 | 2:213603252 | TCTACTTTCTGTGAA[A/G]CCCTTGTTTATATCT | 79582 |
rs141334350 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | SPAG16 | GRCh38.p7 | 2:213287393 | GACTGCCTAGTTCCA[A/G]TTGGAAGGCCAGCAT | 79582 |
rs141337329 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | SPAG16 | GRCh38.p7 | 2:213328558 | ACTCAGTAAGGATGA[C/T]GCCAAACAGTCTGCC | 79582 |
rs141343807 | snp | C/T | 0.00398564 | 0.0444627 | intron-variant | SPAG16 | GRCh38.p7 | 2:214315726 | TTGTAGAGTTGGGGT[C/T]TCACTATGTTGTCCA | 79582 |
rs141344228 | snp | A/T | 0.0142736 | 0.0832652 | intron-variant | SPAG16, LOC101928084 | GRCh38.p7 | 2:214094090 | TCACACTGATTTGTG[A/T]AAGCAGAATACGCAC | 79582 |
rs141349748 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | SPAG16 | GRCh38.p7 | 2:214016641 | CAGCATGTTTATTTG[C/T]TTATGGGTAAGATCG | 79582 |
rs141350162 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | SPAG16 | GRCh38.p7 | 2:214404384 | GTTGGATCTAAAACA[A/G]AACAAAACCTGAGAA | 79582 |
rs141354564 | snp | C/T | 0.0130921 | 0.0798413 | intron-variant | SPAG16 | GRCh38.p7 | 2:213600924 | ATACAAATTTATTAG[C/T]GTGCAGGGAGGAAAA | 79582 |
rs141358672 | snp | A/G | | | intron-variant | SPAG16 | GRCh38.p7 | 2:213643965 | TTTGTATTTTTAGTA[A/G]AGATGGAGTTTCACC | 79582 |
rs141358760 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | SPAG16 | GRCh38.p7 | 2:213723470 | GGGTGTTATTTTGCA[A/C]TGAATTACCACAAAG | 79582 |
rs141365648 | snp | A/G | 0.0182019 | 0.0936463 | intron-variant | SPAG16 | GRCh38.p7 | 2:214272729 | CAAGTCTTTGCTATC[A/G]TGAATAGTGCTGCAA | 79582 |
rs141386686 | snp | C/T | 0.0217236 | 0.101931 | intron-variant | SPAG16 | GRCh38.p7 | 2:213712191 | TATACGTGTAATAGC[C/T]GCAGGTATTTCAGTC | 79582 |
rs141389054 | snp | A/T | 0.0158469 | 0.0875917 | intron-variant | SPAG16 | GRCh38.p7 | 2:213961826 | GATATTTATCAGCAG[A/T]TTTGATCTATGGTTT | 79582 |
rs141389083 | snp | A/G | 0.0166325 | 0.0896639 | intron-variant | SPAG16 | GRCh38.p7 | 2:213506570 | TCCTCATCTTATCTC[A/G]AACCCTCATCTCAGC | 79582 |
rs141396310 | snp | A/G | 0.00199481 | 0.0315187 | intron-variant | SPAG16 | GRCh38.p7 | 2:213604539 | TCATCATATTGCCTA[A/G]GTTCAGTATCTTCCA | 79582 |
rs141399789 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | SPAG16 | GRCh38.p7 | 2:214009785 | GAGACAACAAATCTG[A/G]ATAGAAGTCAGTGCC | 79582 |
rs141401682 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | SPAG16 | GRCh38.p7 | 2:213875878 | GATGTCTTTGATTGA[C/T]GCAAAACTCAATAAG | 79582 |
rs141402156 | snp | A/G | 0.00676609 | 0.0577691 | intron-variant | SPAG16 | GRCh38.p7 | 2:213458186 | TTTAGATATACTCAC[A/G]TATTTACCTATGCCA | 79582 |
rs141402376 | snp | A/C | 0.0134861 | 0.0810011 | intron-variant | SPAG16 | GRCh38.p7 | 2:214130875 | ATGTAAGGAACTTCC[A/C]TTTCTCCTTGAATAA | 79582 |
rs141404604 | snp | C/T | | | intron-variant, upstream-variant-2KB | SPAG16 | GRCh38.p7 | 2:213315695 | GACTCTATTGAAAAC[C/T]TTTTTTTTTTTAATA | 79582 |
rs141405030 | in-del | -/AC | | | intron-variant | SPAG16 | GRCh38.p7 | 2:214170202 | GGTGTGTATACATAT[-/AC]ACACACACTTAGGTG | 79582 |
rs141406064 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | SPAG16 | GRCh38.p7 | 2:213546160 | AGACTAGTCAATTTC[C/T]CTACTTTTACTTTAA | 79582 |
rs141407872 | snp | C/T | 0.000798403 | 0.0199641 | upstream-variant-2KB, intron-variant, downstream-variant-500B | VWC2L, SPAG16 | GRCh38.p7 | 2:214410907 | TTCATCTCTGCAGCC[C/T]ATCCAAGAACGCGTT | 79582 |
rs141410090 | snp | A/G/T | 0.000798403 | 0.0199641 | intron-variant | SPAG16 | GRCh38.p7 | 2:214197690 | TCAGATTTTTGTTTC[A/G/T]TCAGAGTTCTACTTC | 79582 |
rs141418929 | snp | C/T | 0.00159617 | 0.0282053 | intron-variant | SPAG16 | GRCh38.p7 | 2:214057833 | CTACATCAGCACTGG[C/T]GCTTCACCTTGCACT | 79582 |
rs141421257 | snp | C/T | 0.00358779 | 0.0422022 | intron-variant | SPAG16 | GRCh38.p7 | 2:213531699 | TTTTTCTGTTTGATA[C/T]AATGAAGACTTCAGT | 79582 |
rs141426432 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | SPAG16 | GRCh38.p7 | 2:213864465 | GATTTTTTAATGAAT[A/G]CAGTTATAGTCTTCA | 79582 |
rs141428234 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant, utr-variant-3-prime | SPAG16 | GRCh38.p7 | 2:213369156 | AAAATGTAGACATTT[G/T]AAGATGCAGGCAAGC | 79582 |
rs141428394 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | SPAG16 | GRCh38.p7 | 2:213336774 | AGGGGCAGCTACGGT[A/G]TCATGGATCAGTGGT | 79582 |
rs141434268 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant, upstream-variant-2KB | SPAG16 | GRCh38.p7 | 2:213294159 | TTTTTTAGATTCCAC[A/G]TATAAGTGAGACTAT | 79582 |
rs141436443 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | SPAG16 | GRCh38.p7 | 2:213416013 | CACAAACATGGAAGA[C/T]TGTGAAGATGAGATG | 79582 |
rs141438017 | snp | A/T | | | intron-variant | SPAG16 | GRCh38.p7 | 2:213826766 | GTCCATTTGTTCTAT[A/T]GTATGGATTATCAAA | 79582 |
rs141441763 | snp | G/T | 0.000798403 | 0.0199641 | intron-variant | SPAG16 | GRCh38.p7 | 2:213880014 | CAGTAATAAGATAGC[G/T]AGGTCAAATGGTAGC | 79582 |
rs141445886 | snp | A/C | 0.0166325 | 0.0896639 | intron-variant, upstream-variant-2KB | SPAG16 | GRCh38.p7 | 2:213298886 | CAGTATTATGCTGAA[A/C]ATTCACAGAAGTTGT | 79582 |
rs141455567 | snp | C/T | 0.00199481 | 0.0315187 | intron-variant | SPAG16 | GRCh38.p7 | 2:214119764 | ATTTTATCTTGCTAA[C/T]GATAGTCTCTCATAG | 79582 |
rs141462328 | in-del | -/G/GT | | | intron-variant | SPAG16 | GRCh38.p7 | 2:214176825 | TGTGTGTGTGTGTGT[-/G/GT]TTTATATATGTATCT | 79582 |
rs141463058 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | SPAG16 | GRCh38.p7 | 2:213291181 | CTTAATCATATTTCT[A/G]TAATGCTATTTCCTT | 79582 |
rs141466674 | in-del | -/GT | | | intron-variant | SPAG16 | GRCh38.p7 | 2:213856848 | TCCATAACATAAAAG[-/GT]TATGGTGAAGCAACA | 79582 |
rs141467412 | in-del | -/A | 0.0414363 | 0.137845 | intron-variant | SPAG16 | GRCh38.p7 | 2:214047840 | CTCAAACAACTCTAT[-/A]AAAAAATTCTAATAC | 79582 |
rs141469976 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | SPAG16 | GRCh38.p7 | 2:213781998 | TCTGTGTTTTCACCT[C/T]TTCAGAGGCTAATAA | 79582 |
rs141472974 | snp | G/T | 0.0158469 | 0.0875917 | intron-variant | SPAG16 | GRCh38.p7 | 2:214324058 | CTTTAATTAATGAAT[G/T]CATGGAACACATTTA | 79582 |
rs141492793 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant, upstream-variant-2KB, utr-variant-5-prime | SPAG16, LOC100130451 | GRCh38.p7 | 2:213284788 | TCTTCCTGAGAGCCA[C/G]TCACTGAATTTCTCG | 79582 |
rs141496110 | snp | G/T | 0.00597247 | 0.0543191 | intron-variant | SPAG16 | GRCh38.p7 | 2:213705359 | AGTGTCACACTGGTT[G/T]GGACACTTCATCTGG | 79582 |
rs141497604 | in-del | -/AAAAC | 0.211346 | 0.246994 | intron-variant | SPAG16 | GRCh38.p7 | 2:213314393 | GTCAGGATATTTGTT[-/AAAAC]AAAACAAAACAAAAC | 79582 |
rs141498228 | in-del | -/A | 0.00358779 | 0.0422022 | intron-variant | SPAG16 | GRCh38.p7 | 2:213557202 | TGCCAGCTAATGGCT[-/A]TCTCTATAATAATGA | 79582 |
rs141499213 | in-del | -/T | | | intron-variant | SPAG16 | GRCh38.p7 | 2:213812866 | GTTTCATATGTTATC[-/T]TTTTTTTTTTGAGTT | 79582 |
rs141504141 | snp | A/C | 0.00755907 | 0.0610114 | intron-variant | SPAG16 | GRCh38.p7 | 2:214215225 | TTTGCCTCAGAAATG[A/C]CTAATGGAACTGCTT | 79582 |
rs141507437 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | SPAG16 | GRCh38.p7 | 2:214399817 | TTTGTGATGGCTTAT[C/T]GAATCCTCAGAACTG | 79582 |
rs141509332 | snp | A/G | 0.00358779 | 0.0422022 | intron-variant | SPAG16 | GRCh38.p7 | 2:213809375 | GTAAGTTGGAAAAAG[A/G]AAAAACTCACCCAGG | 79582 |
rs141509510 | snp | C/G | 0.000798403 | 0.0199641 | intron-variant | SPAG16 | GRCh38.p7 | 2:214346866 | CTGAATGATCTCTGT[C/G]GACATCATTAAAAAT | 79582 |
rs141514039 | snp | A/C | 0.0023933 | 0.0345097 | intron-variant | SPAG16 | GRCh38.p7 | 2:213462736 | TAAGTTTCCTGAGGC[A/C]TGCCTAGTGATGTGA | 79582 |
rs141530882 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | SPAG16 | GRCh38.p7 | 2:214262460 | CTTAACAATAATGTG[A/G]TATTTATGTTTTAAT | 79582 |
rs141537307 | snp | C/T | 0.00318978 | 0.0398085 | intron-variant | SPAG16 | GRCh38.p7 | 2:214300894 | GGACTAAGGATTCCT[C/T]CCTAACTCATTTAAA | 79582 |
rs141537995 | snp | A/G | 0.00279162 | 0.0372561 | intron-variant, upstream-variant-2KB | SPAG16 | GRCh38.p7 | 2:213342287 | ATTACATACATATGT[A/G]TATATATATGACATA | 79582 |
rs141539239 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | SPAG16 | GRCh38.p7 | 2:213758951 | ATAAGGAATAATCAG[C/T]AAGATTATCAGTATA | 79582 |
rs141546993 | snp | C/T | 0.0115144 | 0.0749975 | intron-variant | SPAG16 | GRCh38.p7 | 2:214174727 | CCAGGATGGCAAAGG[C/T]TGTTCCATTTTCAGT | 79582 |
rs141549599 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | SPAG16, LOC101928084 | GRCh38.p7 | 2:214090438 | GTGCCTCAGAGAGAG[G/T]CACCTTCACTGTATG | 79582 |
rs141551941 | snp | G/T | 0.127599 | 0.217986 | intron-variant | SPAG16 | GRCh38.p7 | 2:213631446 | AAGTGATATGGTTTG[G/T]CTCTGTGTCCCCACC | 79582 |
rs141552119 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | SPAG16 | GRCh38.p7 | 2:213927114 | TCACAATGCAGGGAG[C/T]GAGTTAACTCCAGTC | 79582 |
rs141554697 | snp | A/T | 0.00119737 | 0.0244387 | intron-variant | SPAG16 | GRCh38.p7 | 2:213679338 | TTTCCAAGAACCAGA[A/T]AATAATTACAAATTT | 79582 |
rs141555162 | snp | A/G | 0.00795532 | 0.062565 | intron-variant | SPAG16 | GRCh38.p7 | 2:213841779 | AAACCCATAATAAAT[A/G]CTGTATATCAATGTT | 79582 |
rs141556804 | snp | A/G | 0.0119091 | 0.0762411 | intron-variant | SPAG16 | GRCh38.p7 | 2:213900365 | ATTTACCAATATCTC[A/G]GAACGACTGTGATTA | 79582 |
rs141560632 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | SPAG16 | GRCh38.p7 | 2:213594991 | TATCTACATTAGCTC[A/G]AGGTTTTATATTTAT | 79582 |
rs141560795 | snp | A/G | | | intron-variant | SPAG16 | GRCh38.p7 | 2:214247135 | TAGTCTACTCTTTGT[A/G]GCTTTAATCCTAGCC | 79582 |
rs141561193 | in-del | -/T | 0.00557542 | 0.0525036 | intron-variant | SPAG16 | GRCh38.p7 | 2:214276769 | TGACAATTATGTGTC[-/T]TGGGGTTGCTCTTCT | 79582 |
rs141562167 | snp | C/T | 0.0107246 | 0.0724382 | intron-variant | SPAG16 | GRCh38.p7 | 2:213710107 | AACATGGTGAAACCT[C/T]GTCTCTACTAAAAAA | 79582 |
rs141562371 | snp | C/T | 0.00279162 | 0.0372561 | intron-variant | SPAG16 | GRCh38.p7 | 2:214374812 | AACATCACAAAATCA[C/T]TTAGCTCATTAGATG | 79582 |
rs141566408 | snp | A/G | 0.00398564 | 0.0444627 | intron-variant | SPAG16 | GRCh38.p7 | 2:214049132 | CTAGAGATGAGGTCT[A/G]CTATGTTGCCCAGGC | 79582 |
rs141567231 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | SPAG16 | GRCh38.p7 | 2:214212927 | CACACAGCACAGACT[C/T]CTCACCTGCCCGTTA | 79582 |
rs141567507 | snp | C/G/T | 0.00279162 | 0.0372561 | intron-variant | SPAG16 | GRCh38.p7 | 2:214124213 | ATACTTTGCAGACTC[C/G/T]CCATGATTGTTTTGA | 79582 |
rs141569080 | snp | A/C | 0.00159617 | 0.0282053 | intron-variant | SPAG16 | GRCh38.p7 | 2:214268230 | GTGGTATTGCAAATT[A/C]ATACAGCCATTTTGG | 79582 |
rs141570326 | snp | C/T | 0.00358779 | 0.0422022 | intron-variant | SPAG16 | GRCh38.p7 | 2:214306749 | TTGGTGGACAAACTT[C/T]CTGATGTGCTGCTAG | 79582 |
rs141577838 | snp | C/T | 0.0166325 | 0.0896639 | intron-variant | SPAG16 | GRCh38.p7 | 2:214250896 | AGATTTTGATTATTT[C/T]GATGGTTTGTTCCAC | 79582 |
rs141594696 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | SPAG16 | GRCh38.p7 | 2:214220131 | AATAGAAGACTGTAA[A/G]TAGGATTTTTATACC | 79582 |
rs141599785 | in-del | -/T | 0.295226 | 0.245875 | intron-variant | SPAG16 | GRCh38.p7 | 2:213836253 | AATTACTTCTTATAA[-/T]TTTTTTTTCCTTTAG | 79582 |
rs141601579 | snp | A/G | 0.00358779 | 0.0422022 | intron-variant | SPAG16 | GRCh38.p7 | 2:214350939 | CCAAAACATCAGCTA[A/G]AAGGCAACTTGGAAT | 79582 |
rs141601918 | snp | A/G | 0.0023933 | 0.0345097 | intron-variant | SPAG16 | GRCh38.p7 | 2:213753281 | CCTCCCAAAGTGCTG[A/G]GATTACACGTGTGAG | 79582 |
rs141602469 | snp | G/T | 0.02016 | 0.0983543 | intron-variant | SPAG16 | GRCh38.p7 | 2:213789890 | ATTTCTCCAATTTTC[G/T]GTAACGATATCATTA | 79582 |
rs141608894 | in-del | -/TTATAT | 0.0551013 | 0.156571 | intron-variant | SPAG16 | GRCh38.p7 | 2:214007152 | ATAACACAAATGTAC[-/TTATAT]TTATAATAATGTTGC | 79582 |
rs141614967 | snp | C/G | 0.0287284 | 0.116357 | intron-variant | SPAG16 | GRCh38.p7 | 2:213501797 | TAGATATTGGACTTA[C/G]TATATACTAAAGCTT | 79582 |
rs141617093 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | SPAG16 | GRCh38.p7 | 2:213590360 | CTTTCCCTCCATTCA[C/T]CCTCCCCATTTTTGG | 79582 |
rs141619823 | snp | G/T | 0.000798403 | 0.0199641 | intron-variant | SPAG16 | GRCh38.p7 | 2:214384352 | CCATTTTTCCCTAGA[G/T]ATGCTACAGATAATC | 79582 |
rs141635125 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | SPAG16 | GRCh38.p7 | 2:214030356 | TATATACCATATGAT[A/C]CAGCACTCCCATGTT | 79582 |
rs141635166 | snp | A/G | | | intron-variant | SPAG16 | GRCh38.p7 | 2:213605806 | GAATGCATTTCTGAA[A/G]GAGAACTTTTAGGGC | 79582 |
rs141636346 | snp | C/G | 0.0252325 | 0.109451 | intron-variant | SPAG16 | GRCh38.p7 | 2:214172137 | TTTAGGTTACATGTG[C/G]ACAATGTGCAGGTTA | 79582 |
rs141637932 | snp | A/G | 0.00874735 | 0.0655527 | intron-variant | SPAG16, LOC101928084 | GRCh38.p7 | 2:214094183 | AATATTTATACCATG[A/G]CAGTTTGCAAATGCT | 79582 |
rs141638549 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | SPAG16 | GRCh38.p7 | 2:213936296 | AATGAGTATGTACAT[A/G]TAATAGAGGGCCTTA | 79582 |
rs141640468 | snp | A/G | 0.00438332 | 0.0466095 | intron-variant | SPAG16 | GRCh38.p7 | 2:213688266 | TAGTGGCTGCCATTA[A/G]AGACAATAGATGACA | 79582 |
rs141642898 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | SPAG16 | GRCh38.p7 | 2:214222430 | CTTGCTATTCTTGAG[C/T]ACATTGTAGTAAAAT | 79582 |
rs141655094 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | SPAG16 | GRCh38.p7 | 2:214132460 | TAAAGTACTCAGTAG[C/T]CACATGTATTAAACA | 79582 |
rs141657667 | snp | C/G | 0.00119737 | 0.0244387 | intron-variant | SPAG16 | GRCh38.p7 | 2:214128064 | AGTTGAATCACCCAT[C/G]ATCATGGGTTGTTTT | 79582 |
rs141658010 | snp | C/T | 0.00557542 | 0.0525036 | intron-variant | SPAG16 | GRCh38.p7 | 2:213895488 | CAAAAAGAACAGAGC[C/T]GGAGTCACACTACCT | 79582 |
rs141659154 | in-del | -/ACATAT | | | intron-variant | SPAG16 | GRCh38.p7 | 2:214298154 | CATACACACACACAC[-/ACATAT]ACACACACACACACA | 79582 |
rs141663029 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | SPAG16 | GRCh38.p7 | 2:213801239 | TGTGTGCGTGCGCGC[A/G]TGCCCACATGTGTTT | 79582 |
rs141663405 | snp | G/T | 0.00159617 | 0.0282053 | intron-variant | SPAG16 | GRCh38.p7 | 2:214216807 | TTTAAAATTTTCAAT[G/T]TTCTGAACATCTAAC | 79582 |
rs141664359 | snp | C/T | 0.00159617 | 0.0282053 | intron-variant | SPAG16 | GRCh38.p7 | 2:213468994 | CACACTGGCAGCTGA[C/T]TAGATTGTGCCCACC | 79582 |
rs141666164 | snp | C/T | 0.00438332 | 0.0466095 | intron-variant | SPAG16 | GRCh38.p7 | 2:214340330 | TTTCACCTGCCCCAG[C/T]GTTATCCATTTTTGC | 79582 |
rs141666448 | snp | A/G | 0.00159617 | 0.0282053 | intron-variant | SPAG16 | GRCh38.p7 | 2:213556144 | ACCAAATCAGTAAAG[A/G]AGACAGCTAAAAAAT | 79582 |
rs141670270 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | SPAG16, LOC101928084 | GRCh38.p7 | 2:214097652 | AAGGGTGCATTTACC[A/G]AACTTGCAATGTGTG | 79582 |
rs141671840 | snp | C/T | 1.64955e-05 | 0.00287184 | missense, nc-transcript-variant, intron-variant | SPAG16 | GRCh38.p7 | 2:213930106 | ATTTTGTGGCTTCCT[C/T]CTCACTGGATAAAAC | 79582 |
rs141675870 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | SPAG16 | GRCh38.p7 | 2:214047721 | TTAAAAAGCTTCTAC[A/C]CAGCAAAGGAAATAA | 79582 |
rs141677783 | snp | A/T | 0.0023933 | 0.0345097 | intron-variant | SPAG16, LOC101928084 | GRCh38.p7 | 2:214098906 | TAGCTTGTATTGGTC[A/T]ATGAGACTTTTTTTT | 79582 |
rs141678416 | snp | C/T | 0.00318978 | 0.0398085 | intron-variant | SPAG16 | GRCh38.p7 | 2:214019403 | GTTGCTGACATTTTG[C/T]CTCTTGCCATGAGTC | 79582 |
rs141678839 | snp | G/T | 0.0023933 | 0.0345097 | intron-variant | SPAG16 | GRCh38.p7 | 2:213629399 | AATGTGAATAATAGT[G/T]AAATTCAATATATAT | 79582 |
rs141678938 | snp | A/G | 0.0197687 | 0.0974348 | intron-variant | SPAG16 | GRCh38.p7 | 2:213682834 | TGGGGCTGGATTTAC[A/G]CGGTTTTTAATCAAG | 79582 |
rs141680026 | snp | G/T | 0.00993419 | 0.0697739 | intron-variant | SPAG16 | GRCh38.p7 | 2:213962119 | GTAATTCTATTTGGA[G/T]ATAAGGCATTTAAAG | 79582 |
rs141683349 | snp | A/T | 0.00279162 | 0.0372561 | intron-variant | SPAG16 | GRCh38.p7 | 2:213747631 | ATATTCGGTATGGTA[A/T]CATGCTATACAGGTT | 79582 |
rs141684646 | snp | A/T | 0.00318978 | 0.0398085 | intron-variant | SPAG16 | GRCh38.p7 | 2:213320286 | ATACATATGTATCAA[A/T]TACATTTGTACATAT | 79582 |
rs141697771 | snp | A/G | 0.00279162 | 0.0372561 | intron-variant | SPAG16 | GRCh38.p7 | 2:213967763 | ATATACAATGTAGGA[A/G]TATAGTAGTTTATGG | 79582 |
rs141705358 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | SPAG16 | GRCh38.p7 | 2:214200282 | GCCAATGTCGTTGAG[A/G]GTTTTGATCATAAAG | 79582 |
rs141709412 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | SPAG16 | GRCh38.p7 | 2:214069152 | AAATGCAAAATCTTT[A/G]AAGGACACTTAAATC | 79582 |
rs141709802 | snp | C/T | | | intron-variant | SPAG16 | GRCh38.p7 | 2:214114810 | GCCCTCTGTGGGCTG[C/T]ACCCACTGTCCAACC | 79582 |
rs141710670 | snp | G/T | 0.00755907 | 0.0610114 | intron-variant | SPAG16 | GRCh38.p7 | 2:213656816 | TTTAATTTCAGGGAT[G/T]TGTACTTTAAATATG | 79582 |
rs141711431 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | SPAG16 | GRCh38.p7 | 2:213992151 | TAAACACAAAGCCCC[A/G]TTTATAAAGTTTTAC | 79582 |
rs141712741 | snp | A/C | 0.0023933 | 0.0345097 | intron-variant | SPAG16 | GRCh38.p7 | 2:214191086 | CCTCAATTATCCATT[A/C]TTCTTCTGAATTCTA | 79582 |
rs141714606 | snp | A/T | 0.000798403 | 0.0199641 | intron-variant | SPAG16 | GRCh38.p7 | 2:213728172 | GTTCTTAAATCTCAC[A/T]GGCTTAATGCAATAA | 79582 |
rs141716602 | snp | A/G | 0.00159617 | 0.0282053 | intron-variant | SPAG16 | GRCh38.p7 | 2:214079761 | TTTTTGTCTCAGAAG[A/G]ATCTGGGAATGGGAG | 79582 |
rs141722512 | in-del | -/ACTC | 0.0930568 | 0.194599 | intron-variant | SPAG16 | GRCh38.p7 | 2:214295411 | TATTTTTTTAATCTT[-/ACTC]ACAATAAATAATTTA | 79582 |
rs141727168 | snp | C/T | 0.247337 | 0.249986 | intron-variant | SPAG16 | GRCh38.p7 | 2:214146856 | ATACAAAAAATTAGC[C/T]GGGTGTGGTGGCAGG | 79582 |
rs141727403 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | SPAG16 | GRCh38.p7 | 2:214391466 | GGAAAATTGGCACTA[C/T]ATTTTATCCACCAAA | 79582 |
rs141733944 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | SPAG16 | GRCh38.p7 | 2:213573856 | ATATTTATGAAATAC[A/G]TAAAGCTCTTAAAGT | 79582 |
rs141735408 | snp | A/G | 0.00358779 | 0.0422022 | intron-variant | SPAG16 | GRCh38.p7 | 2:213530495 | TCAAAATTTATATAC[A/G]CCTTTAAAAAGTCAA | 79582 |
rs141739533 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | SPAG16 | GRCh38.p7 | 2:213615454 | AAATTACCTGGGTGG[G/T]ATGGCATGCACCTGA | 79582 |
rs141742763 | snp | C/T | 0.046775 | 0.145601 | intron-variant, downstream-variant-500B | SPAG16 | GRCh38.p7 | 2:213611841 | AATTGAAACCACAGA[C/T]TTATTTACTTAAAAA | 79582 |
rs141747443 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | SPAG16 | GRCh38.p7 | 2:213858228 | TGGGTAAAATGCTAT[C/T]AAACAATATCACATG | 79582 |
rs141751174 | snp | C/T | 0.0023933 | 0.0345097 | intron-variant | SPAG16 | GRCh38.p7 | 2:213480325 | GCCAATTGGTTGGGA[C/T]AGTACTATTAGGCAT | 79582 |
rs141751288 | snp | A/C | 0.00199481 | 0.0315187 | intron-variant | SPAG16 | GRCh38.p7 | 2:213535248 | CAAATGAGTACAAAA[A/C]CATCAATCATCTATA | 79582 |
rs141753015 | snp | C/T | 0.00159617 | 0.0282053 | intron-variant | SPAG16 | GRCh38.p7 | 2:214073534 | GCCACCACGCCCGGC[C/T]GGATATTTTAAAAGA | 79582 |
rs141757522 | snp | C/T | | | intron-variant | SPAG16 | GRCh38.p7 | 2:213409881 | CAATTTCTTAGAAAT[C/T]ATATACTTGGTTTAT | 79582 |
rs141757916 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | SPAG16 | GRCh38.p7 | 2:214137323 | GGCAATGCCATTATA[A/C]TAGTTTAGTTATATA | 79582 |
rs141759786 | snp | A/G | 0.00993419 | 0.0697739 | intron-variant | SPAG16 | GRCh38.p7 | 2:213493198 | ATGCATGACAAGCAC[A/G]ACCTAGGATAATTGC | 79582 |
rs141764192 | snp | A/C | 0.0146672 | 0.084371 | intron-variant | SPAG16 | GRCh38.p7 | 2:214110822 | TGTTTAATGATTGCC[A/C]TTCTAACTGGTGTGA | 79582 |
rs141764608 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | SPAG16 | GRCh38.p7 | 2:213360897 | CCAAACTTTAGGATG[C/T]GAGTTAAGAGCAGTA | 79582 |
rs141766231 | snp | A/T | 0.0174175 | 0.0916809 | intron-variant | SPAG16 | GRCh38.p7 | 2:214033982 | GTATTGCATTCAGTT[A/T]GTTGTCTTGTCTCTT | 79582 |
rs141767831 | in-del | -/G | 0.0298908 | 0.118541 | intron-variant | SPAG16 | GRCh38.p7 | 2:213831763 | ATTGTAATCATAAAT[-/G]ACATTTAGCATTTTA | 79582 |
rs141768868 | snp | A/G | 0.0023933 | 0.0345097 | intron-variant | SPAG16 | GRCh38.p7 | 2:213475116 | TGTCTGCTTCTCAGC[A/G]GTAGTCAGGATTCGA | 79582 |
rs141777110 | snp | C/T | 0.00159617 | 0.0282053 | intron-variant | SPAG16 | GRCh38.p7 | 2:213717310 | ACTACAGGCGCCCGC[C/T]ACCAAGCCTGGCTAA | 79582 |
rs141778090 | in-del | -/A | 0.0718919 | 0.175435 | intron-variant | SPAG16 | GRCh38.p7 | 2:214394440 | ATTATGTAATTGAGT[-/A]AAAAAAACTTTAAAA | 79582 |
rs141784808 | snp | C/T | 0.0248432 | 0.108648 | intron-variant | SPAG16 | GRCh38.p7 | 2:213440415 | AAAAATTTAGCTGGG[C/T]GTGGCGGCGGGCGCC | 79582 |
rs141786534 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant, upstream-variant-2KB, utr-variant-5-prime | SPAG16, LOC100130451 | GRCh38.p7 | 2:213285620 | CAAGCCGATTAACCT[C/G]TCCTGACTCAGGCTC | 79582 |
rs141789644 | snp | C/T | 0.0119091 | 0.0762411 | intron-variant, utr-variant-3-prime | SPAG16 | GRCh38.p7 | 2:213398865 | AGTGCCAGAAAAATG[C/T]CTGGCAAATAGTAAT | 79582 |
rs141804447 | snp | C/G | 0.00755907 | 0.0610114 | intron-variant | SPAG16 | GRCh38.p7 | 2:214385504 | AGTTCTTTATATAAA[C/G]ACTTGTGAGAGAATA | 79582 |
rs141806737 | snp | C/G | 0.0126979 | 0.078662 | intron-variant | SPAG16 | GRCh38.p7 | 2:213855774 | CTCACTTACTGTCAT[C/G]AGAACAACATGGGGG | 79582 |
rs141808838 | snp | G/T | 0.00676609 | 0.0577691 | intron-variant | SPAG16 | GRCh38.p7 | 2:213354736 | TCTTGTAAATTTGTT[G/T]AAGTTATTTGTAGAT | 79582 |
rs141810006 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | SPAG16 | GRCh38.p7 | 2:213989968 | TGATTTTAGAATAGC[C/T]ACTAATTTTATATCA | 79582 |
rs141814117 | snp | A/C/T | 0.0023933 | 0.0345097 | intron-variant | SPAG16 | GRCh38.p7 | 2:213898814 | TCAAAATATTAGAGA[A/C/T]GGTCTTACTTGTCCT | 79582 |
rs141818607 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | SPAG16 | GRCh38.p7 | 2:214148139 | TTTTAATGTGGCCAA[C/T]ACTCATTCAATTTGT | 79582 |
rs141840570 | snp | A/T | 0.00318978 | 0.0398085 | intron-variant | SPAG16 | GRCh38.p7 | 2:213490674 | GCATATATAAACCTT[A/T]TAATTCCATGGTACA | 79582 |
rs141844780 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | SPAG16 | GRCh38.p7 | 2:213577149 | TCAATTAATAAAGGG[C/T]ACATTTTAATAGAGG | 79582 |
rs141849589 | snp | A/G | 0.0402882 | 0.136092 | intron-variant | SPAG16 | GRCh38.p7 | 2:213910479 | TAAAAATTTGCTTTT[A/G]TAAGAATTCTTTTTT | 79582 |
rs141850302 | snp | A/G | 0.00159617 | 0.0282053 | intron-variant | SPAG16 | GRCh38.p7 | 2:213938126 | ATATATATATTTTAT[A/G]ACATGATACATTTCT | 79582 |
rs141852731 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | SPAG16 | GRCh38.p7 | 2:213824056 | TTTGGGTTTTACATA[C/T]AAGTCTTTAATCCAT | 79582 |
rs141853118 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | SPAG16 | GRCh38.p7 | 2:213443185 | TGAGAGTACCTAATA[C/T]CTACTTTCTTAGCAA | 79582 |
rs141853397 | snp | C/T | 0.00159617 | 0.0282053 | intron-variant | SPAG16 | GRCh38.p7 | 2:213318348 | AAATCAGGCCTTTTG[C/T]AGCAACATGGGTGGA | 79582 |
rs141855907 | snp | C/T | 0.00636936 | 0.0560724 | intron-variant | SPAG16 | GRCh38.p7 | 2:213372068 | AAGGGTCATATGTAT[C/T]GAATATTTACATGAC | 79582 |
rs141856937 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant, upstream-variant-2KB | SPAG16 | GRCh38.p7 | 2:213295604 | TTTTGTTCATTCACA[A/G]TACTTTAAACCAAAT | 79582 |
rs141859189 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | SPAG16 | GRCh38.p7 | 2:214349542 | GAATAGTTATGAACA[C/G]TCTTGCCAAATACTT | 79582 |
rs141869538 | snp | C/T | 0.102014 | 0.201495 | intron-variant | SPAG16 | GRCh38.p7 | 2:213323178 | CGGCGCGGTGGCTTA[C/T]GCCTGTAATCCCAGC | 79582 |
rs141898797 | snp | C/T | | | intron-variant | SPAG16 | GRCh38.p7 | 2:214390915 | ATGAGAAAGGAGTCT[C/T]GAAACAAGTGCAGAG | 79582 |
rs141900628 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | SPAG16 | GRCh38.p7 | 2:213801574 | TGTCTTCCAAGCCAA[A/G]TAGACCTATGTGCTA | 79582 |
rs141908388 | in-del | -/TTTG | | | intron-variant | SPAG16 | GRCh38.p7 | 2:213654354 | TGAACATCTATTGTT[-/TTTG]TTTGTTTGTTTGTTT | 79582 |
rs141910006 | snp | C/T | 0.0103295 | 0.0711199 | intron-variant | SPAG16 | GRCh38.p7 | 2:213847589 | ACCTAGCTCCGTGAT[C/T]CAAACACCCTACACC | 79582 |
rs141919263 | snp | C/T | 0.0103295 | 0.0711199 | intron-variant | SPAG16 | GRCh38.p7 | 2:213624831 | AGTCTTGATCTGTTG[C/T]CCAGGCTGGAGTGCA | 79582 |
rs141921910 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | SPAG16 | GRCh38.p7 | 2:214242597 | AAAAATAAGAAAAAA[A/G]TATTGCATTTTTCTA | 79582 |
rs141924636 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | SPAG16 | GRCh38.p7 | 2:213306113 | CTTCTAGGCTTTCCA[A/G]TTTACTGGCACGTAG | 79582 |
rs141935787 | snp | C/G | 0.00358779 | 0.0422022 | intron-variant | SPAG16 | GRCh38.p7 | 2:213834063 | AATAAGTCTCATGAG[C/G]TCTGATGGGTCTATC | 79582 |
rs141938981 | in-del | -/TTT | 0.188 | 0.24219 | intron-variant | SPAG16 | GRCh38.p7 | 2:213958856 | GTAATGAAATCTTTA[-/TTT]CTTAATGTGGCTTTG | 79582 |
rs141952059 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | SPAG16 | GRCh38.p7 | 2:214280786 | CTAGATTCTCTCATA[C/T]AGCAGCATGAGCTTT | 79582 |
rs141952934 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | SPAG16 | GRCh38.p7 | 2:214321690 | CCAATAAGTCTGGGA[C/T]ATAATTTCCTTTGTT | 79582 |
rs141952959 | snp | A/G | 0.00279162 | 0.0372561 | intron-variant | SPAG16 | GRCh38.p7 | 2:213780377 | ATTTTTCTCTGACTT[A/G]TGTGAAATATATACA | 79582 |
rs141961395 | in-del | -/T | 0.0189856 | 0.0955633 | intron-variant | SPAG16 | GRCh38.p7 | 2:213973087 | AGCTCTGGCCCAACC[-/T]TTACTTCCTACTTGT | 79582 |
rs141963037 | snp | C/T | 0.00953873 | 0.0683987 | intron-variant | SPAG16 | GRCh38.p7 | 2:214216361 | GGAGTCTTGCTCTGT[C/T]GCCAGGCTGGAATGC | 79582 |
rs141964163 | snp | A/T | 1.65236e-05 | 0.00287429 | stop-gained, nc-transcript-variant, intron-variant, upstream-variant-2KB, missense, utr-variant-5-prime | SPAG16 | GRCh38.p7 | 2:213296104 | AGATGACTATGAATA[A/T]GAAGAGGTAACATGT | 79582 |
rs141969738 | snp | A/G | 0.00795532 | 0.062565 | intron-variant | SPAG16 | GRCh38.p7 | 2:213655064 | GTACATGTCATCATA[A/G]ATTTGTCCAAACCCA | 79582 |
rs141971240 | in-del | -/AACTT | 0.00755907 | 0.0610114 | intron-variant | SPAG16 | GRCh38.p7 | 2:214351734 | CAAAAAAAACAACAA[-/AACTT]AAATATTGACAGTGA | 79582 |
rs141972707 | in-del | -/TATAA | 0.0217236 | 0.101931 | intron-variant | SPAG16 | GRCh38.p7 | 2:213496653 | TTATATATGGATATG[-/TATAA]TATAAGCTTTAAGTA | 79582 |
rs141972870 | in-del | -/T | 0.0696718 | 0.173152 | intron-variant | SPAG16 | GRCh38.p7 | 2:213975350 | ATACCACATTCTCAA[-/T]TTTTCACTAACACAA | 79582 |
rs141975028 | snp | C/T | 0.0023933 | 0.0345097 | intron-variant | SPAG16 | GRCh38.p7 | 2:213616031 | AACCTGCATGTTCTG[C/T]ACATGTATCCCAGAA | 79582 |
rs141982386 | snp | C/G | 0.0142736 | 0.0832652 | intron-variant | SPAG16 | GRCh38.p7 | 2:214333561 | CTGCCACTACCTTCC[C/G]AGTGTCATTGGTGTC | 79582 |
rs141982737 | snp | A/G | 3.38181e-05 | 0.00411192 | missense, nc-transcript-variant, utr-variant-5-prime, intron-variant | SPAG16 | GRCh38.p7 | 2:213350544 | TTGAAGTTACATTAT[A/G]CATCTTATGAACCGA | 79582 |
rs141985135 | snp | A/C/T | 0.00199481 | 0.0315187 | intron-variant | SPAG16 | GRCh38.p7 | 2:214236646 | GACAGAGCGAGACTC[A/C/T]GTTTCAAAAAAAAAA | 79582 |
rs141989677 | snp | C/G | 0.00716266 | 0.059414 | intron-variant | SPAG16 | GRCh38.p7 | 2:214327929 | CTTATCTAATTGATA[C/G]TAGAGTATCAGCAGG | 79582 |
rs141997144 | in-del | -/AAAAA | 0.0228947 | 0.104514 | intron-variant | SPAG16 | GRCh38.p7 | 2:213970802 | GAGTGAATGCAAAAT[-/AAAAA]TGTATGGAGTGAATA | 79582 |
rs142001917 | snp | A/C | | | intron-variant, nc-transcript-variant | SPAG16, LOC101928084 | GRCh38.p7 | 2:214091362 | TAGCAACTTACCAAG[A/C]TGGGAAAGTCACACA | 79582 |
rs142009529 | snp | A/T | 0.00874735 | 0.0655527 | intron-variant | SPAG16 | GRCh38.p7 | 2:214189067 | TTCACTTTCAGAACT[A/T]ACAAATCCATTTGTA | 79582 |
rs142009676 | snp | A/C | 0.00398564 | 0.0444627 | intron-variant | SPAG16 | GRCh38.p7 | 2:214247144 | CTTTGTGGCTTTAAT[A/C]CTAGCCTTCTTGAAT | 79582 |
rs142010816 | snp | A/C | 0.00755907 | 0.0610114 | intron-variant | SPAG16 | GRCh38.p7 | 2:214370613 | GTCTACTCTCTTGGC[A/C]AATTTCAAGTATACA | 79582 |
rs142019280 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | SPAG16 | GRCh38.p7 | 2:213420530 | AAAGGCCAAGAAAAT[A/G]TTTTAGAATTTGCAC | 79582 |
rs142019378 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | SPAG16 | GRCh38.p7 | 2:214203263 | TTTCTGGTTCTGGTA[G/T]ATTTCTAAGTTCTTT | 79582 |
rs142021603 | snp | C/T | 0.00953873 | 0.0683987 | intron-variant | SPAG16 | GRCh38.p7 | 2:213958343 | TGTCCCATGGGCAGG[C/T]GGTTGTCAGGAGGTA | 79582 |
rs142030271 | snp | A/G | 0.00358779 | 0.0422022 | intron-variant | SPAG16 | GRCh38.p7 | 2:213524051 | TCTCATCTCAGGCCC[A/G]GAGACTTAGGATGAA | 79582 |
rs142032617 | snp | A/T | 0.000798403 | 0.0199641 | intron-variant | SPAG16 | GRCh38.p7 | 2:213738864 | AACAGACATATCTTC[A/T]GGCCAGATTTCATTG | 79582 |
rs142033370 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | SPAG16 | GRCh38.p7 | 2:213837827 | AAAGAGAGAGGTAGA[C/T]GAGTCTAGGAGGTGT | 79582 |
rs142035940 | snp | A/T | 0.00676609 | 0.0577691 | intron-variant | SPAG16 | GRCh38.p7 | 2:213659943 | ATTTTCAACAAACCC[A/T]CTCTGTGAGTCCATT | 79582 |
rs142035994 | snp | G/T | 0.000798403 | 0.0199641 | intron-variant | SPAG16 | GRCh38.p7 | 2:213610361 | AATGTAGGAAAGATT[G/T]ACTGAAAGTTTAACA | 79582 |
rs142038953 | snp | A/G | 0.0023933 | 0.0345097 | intron-variant | SPAG16 | GRCh38.p7 | 2:214047308 | GAGCTTTGATTAATC[A/G]TAACCAAAGCAGCAT | 79582 |
rs142040858 | snp | A/G | | | intron-variant | SPAG16 | GRCh38.p7 | 2:213621809 | AAGTGTGATCTAAAG[A/G]TAGATCACATAATAA | 79582 |
rs142044695 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | SPAG16 | GRCh38.p7 | 2:213702333 | TTGGGTCTCTTTTCA[G/T]GCTGTGGAAGGTTTG | 79582 |
rs142048563 | snp | A/G | 0.00557542 | 0.0525036 | intron-variant | SPAG16 | GRCh38.p7 | 2:214195461 | CATTAGATATGAGGA[A/G]ACCACTGATGGGGCT | 79582 |
rs142050909 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | SPAG16 | GRCh38.p7 | 2:213387885 | GGTGTTTTAAAATAT[C/T]ATAAAGATCTAGTAA | 79582 |
rs142056125 | snp | A/T | 0.00358779 | 0.0422022 | intron-variant | SPAG16 | GRCh38.p7 | 2:213506191 | CTTAATTTAAGGAAA[A/T]AAGGACAATAGATGA | 79582 |
rs142057754 | snp | A/G | 0.00438332 | 0.0466095 | intron-variant | SPAG16 | GRCh38.p7 | 2:214147527 | AAAAATTTCCATTCT[A/G]TGACTTCTCTCAGAT | 79582 |
rs142063263 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | SPAG16 | GRCh38.p7 | 2:213912848 | TACCCCCAAAAAACA[A/G]ATTATCATGTTAAAT | 79582 |
rs142063611 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | SPAG16 | GRCh38.p7 | 2:214243401 | TTTTAATAAACCTCT[C/G]TCTCTGAGTCAGGGC | 79582 |
rs142068674 | in-del | -/GATCAA | | | intron-variant | SPAG16 | GRCh38.p7 | 2:213467296 | TGGTGGTTGTGGCTT[-/GATCAA]TTTTCCCTTGAGCTG | 79582 |
rs142074438 | snp | A/G | 0.0158469 | 0.0875917 | intron-variant | SPAG16 | GRCh38.p7 | 2:213579959 | ATTGTTTATCTAAAT[A/G]CTGATGGGGTTCAAA | 79582 |
rs142078600 | snp | C/T | 0.0228947 | 0.104514 | intron-variant | SPAG16 | GRCh38.p7 | 2:213700969 | CCTGGTGGCCAGGCA[C/T]GGTGGCTCATGCCTG | 79582 |
rs142082745 | snp | C/T | 0.0154538 | 0.0865337 | intron-variant, downstream-variant-500B | SPAG16 | GRCh38.p7 | 2:213376440 | CATTCTGATATTTAA[C/T]GTAATACCTACAGCA | 79582 |
rs142088993 | snp | A/G | 0.0134861 | 0.0810011 | intron-variant | SPAG16 | GRCh38.p7 | 2:213335052 | TATCTCATATACTCC[A/G]TGAATATATACATCT | 79582 |
rs142097695 | snp | C/T | | | intron-variant | SPAG16 | GRCh38.p7 | 2:214131262 | TGGTCCTAGTTGCTT[C/T]GGGAAGTTGAAGTGG | 79582 |
rs142099575 | snp | C/T | 0.0142736 | 0.0832652 | intron-variant | SPAG16, LOC101928084 | GRCh38.p7 | 2:214092496 | CTGTGTTACTATGAA[C/T]ATATATATAAATATA | 79582 |
rs142102853 | snp | C/T | 0.00159617 | 0.0282053 | intron-variant | SPAG16 | GRCh38.p7 | 2:213991067 | CGTGCAGGTTTGCTA[C/T]GTAGGTATACACGTG | 79582 |
rs142117829 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | SPAG16 | GRCh38.p7 | 2:214015313 | TTTTGAAAGGGCTGG[G/T]TTCGGCTGGGTGCAG | 79582 |
rs142133850 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | SPAG16 | GRCh38.p7 | 2:213834909 | TCTGTTTCTATTCTT[A/G]TGGGGTTGGGCAGAT | 79582 |
rs142136382 | snp | C/T | 0.00636936 | 0.0560724 | intron-variant | SPAG16 | GRCh38.p7 | 2:213552204 | TCTTGAATTTGCTCC[C/T]TGCTTTAGTATACAG | 79582 |
rs142137624 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | SPAG16 | GRCh38.p7 | 2:214368358 | GATTTCCTAGTCTGT[A/G]GTCAAGAAAAACCTC | 79582 |
rs142140410 | snp | A/G | 0.00398564 | 0.0444627 | intron-variant | SPAG16 | GRCh38.p7 | 2:213632804 | TTAAACCATCCTTGC[A/G]TTCTAGGGATAAATC | 79582 |
rs142145629 | in-del | -/A | 0.0225045 | 0.103662 | intron-variant | SPAG16 | GRCh38.p7 | 2:213949890 | TTCTGCTCCTTTGGC[-/A]AAATCTTTCCTGAAT | 79582 |
rs142148604 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | SPAG16 | GRCh38.p7 | 2:213504633 | TTTGAAAAGGGGGCA[A/G]TTTAAAACAACTAGC | 79582 |
rs142154070 | in-del | -/TTG | 0.0926964 | 0.194308 | intron-variant | SPAG16 | GRCh38.p7 | 2:213742909 | ATTTAACATGCCGTA[-/TTG]TTGTTTTTTTGAGAC | 79582 |
rs142154980 | snp | G/T | 0.0134861 | 0.0810011 | intron-variant | SPAG16 | GRCh38.p7 | 2:214018558 | TTTGCAACATCAACT[G/T]AATCCATGGTATACT | 79582 |
rs142155905 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | SPAG16 | GRCh38.p7 | 2:213594197 | CTCATCATACCTAGC[A/G]CAGATTTTAGGAGTC | 79582 |
rs142156397 | snp | C/T | 0.00993419 | 0.0697739 | intron-variant | SPAG16 | GRCh38.p7 | 2:213427867 | GCTATCAGTAAAATA[C/T]TCAGTGTAGATTTAA | 79582 |
rs142166269 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | SPAG16 | GRCh38.p7 | 2:213513104 | TGATCCTCTTTTCCA[C/G]TGTCACGTGTGTATG | 79582 |
rs142169621 | in-del | -/T | 0.0510073 | 0.151334 | intron-variant | SPAG16 | GRCh38.p7 | 2:213632718 | CTTTTACAGCATCAA[-/T]TGAAATGATCATATG | 79582 |
rs142184690 | snp | A/G | 0.00438332 | 0.0466095 | intron-variant | SPAG16 | GRCh38.p7 | 2:214218636 | TTTACTATACTACAT[A/G]AGGAGAGTGGGGAAT | 79582 |
rs142186588 | snp | A/C | 0.02016 | 0.0983543 | intron-variant | SPAG16 | GRCh38.p7 | 2:214051355 | AAGGAATTGCCAAGA[A/C]AAGCTTTTACTAATG | 79582 |
rs142192677 | snp | A/G | 0.00478085 | 0.0486577 | intron-variant | SPAG16 | GRCh38.p7 | 2:213913595 | TACATGTACATATAT[A/G]TATATGTACATGTAC | 79582 |
rs142196020 | snp | A/G | 0.00398564 | 0.0444627 | intron-variant | SPAG16 | GRCh38.p7 | 2:214335101 | GCCTCAGCTGATCCT[A/G]TAGGAAGTTTTGAAG | 79582 |
rs142197587 | snp | C/G | 0.000798403 | 0.0199641 | intron-variant | SPAG16 | GRCh38.p7 | 2:213373466 | TAAAATTTTATTAAA[C/G]TGTGTATTTTCCATT | 79582 |
rs142203140 | snp | C/T | 0.0023933 | 0.0345097 | intron-variant | SPAG16 | GRCh38.p7 | 2:213878761 | AGTTTTCTCTGTTTT[C/T]ATCATTTTAATAGTT | 79582 |
rs142205593 | snp | G/T | 0.00438332 | 0.0466095 | intron-variant | SPAG16 | GRCh38.p7 | 2:213377817 | TGGCAAAATCAGAAA[G/T]CTTTTATCCTGATGA | 79582 |
rs142206930 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | SPAG16 | GRCh38.p7 | 2:213424728 | CATGCTAGAGATGCT[A/G]TAGTCCTTACATTTT | 79582 |
rs142212147 | snp | G/T | 0.0162398 | 0.0886349 | intron-variant | SPAG16 | GRCh38.p7 | 2:213456702 | ATCAGTCAAGGATCT[G/T]TTTCTCCAAATTCTT | 79582 |
rs142216613 | snp | C/T | 0.00835141 | 0.0640778 | intron-variant | SPAG16 | GRCh38.p7 | 2:213981222 | CAGATCAGTGCTTCA[C/T]CCTTAAGAACTCATT | 79582 |
rs142220398 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | SPAG16 | GRCh38.p7 | 2:213891907 | AACCATCTTCCCCAT[A/C]ATATTGGGTAGCCTG | 79582 |
rs142227235 | snp | A/G/T | 0.0142791 | 0.083329 | intron-variant | SPAG16 | GRCh38.p7 | 2:213460658 | AAATTTGATATACAT[A/G/T]TGCATGGCTAGAAGT | 79582 |
rs142231854 | snp | C/T | 0.00716266 | 0.059414 | intron-variant | SPAG16, LOC101928084 | GRCh38.p7 | 2:214094003 | TCTGTGCACAAGGAA[C/T]GACCATATCACCTGG | 79582 |
rs142231951 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant, upstream-variant-2KB | SPAG16 | GRCh38.p7 | 2:213315932 | AAGCAGTGTAGTGTT[C/T]ATGGCTCACTCCTAG | 79582 |
rs142233407 | snp | C/G | 0.26078 | 0.249767 | intron-variant | SPAG16 | GRCh38.p7 | 2:213915394 | GTTTGGTTTTCTGTT[C/G]CTGTTTTAGTGTGCT | 79582 |
rs142238856 | snp | G/T | 0.0115144 | 0.0749975 | intron-variant | SPAG16 | GRCh38.p7 | 2:213839016 | AAGACAATATAGAAA[G/T]GTGTTTTAGCTTTCC | 79582 |
rs142239468 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | SPAG16 | GRCh38.p7 | 2:213832447 | CATCCCTCTTTCTCC[C/T]CTGAAGCAAGTGACA | 79582 |
rs142239748 | snp | A/C | 0.000798403 | 0.0199641 | intron-variant | SPAG16 | GRCh38.p7 | 2:214365127 | GAGATTTCAAGCCTG[A/C]GTGACAGAAGGCGCG | 79582 |
rs142240131 | snp | A/G | 0.00358779 | 0.0422022 | intron-variant | SPAG16 | GRCh38.p7 | 2:214288296 | CCTTTGTGTAAATAT[A/G]CTGTATTTTTAAAAA | 79582 |
rs142244776 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | SPAG16 | GRCh38.p7 | 2:213964994 | GTCCTTTCTCTTGCC[A/G]TTTTCTTTGCCTGTG | 79582 |
rs142248989 | snp | A/G | 0.00199481 | 0.0315187 | intron-variant, utr-variant-5-prime | SPAG16 | GRCh38.p7 | 2:213302293 | AGTTAGTTAAAAGCC[A/G]TAATGAGAGTTGTAT | 79582 |
rs142252479 | snp | C/G | 0.00835141 | 0.0640778 | intron-variant | SPAG16 | GRCh38.p7 | 2:214112876 | TTTATGATGTTAGCT[C/G]GTTATTTTGCCCATT | 79582 |
rs142259760 | snp | C/T | 0.0130921 | 0.0798413 | intron-variant | SPAG16 | GRCh38.p7 | 2:213378870 | ACCTTAATCACAGGG[C/T]ATGGCAATACTAAGA | 79582 |
rs142261518 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | SPAG16 | GRCh38.p7 | 2:214314884 | ATAAAAAATGAATGC[A/T]GTTGAAGCAAGAAAG | 79582 |
rs142262322 | snp | A/G | 0.031825 | 0.122064 | intron-variant | SPAG16 | GRCh38.p7 | 2:213773624 | CAGTGGCATGATCTC[A/G]GCTTACTGCAACCTC | 79582 |
rs142268680 | in-del | -/T | 0.335788 | 0.23482 | intron-variant | SPAG16 | GRCh38.p7 | 2:213850689 | AGAAGAGAAATTCTG[-/T]TTTTTTTTTTATGAT | 79582 |
rs142270478 | snp | A/G | 0.00438332 | 0.0466095 | intron-variant | SPAG16 | GRCh38.p7 | 2:214231496 | GTTTATAAGTATTGT[A/G]TAACGATACTCATGC | 79582 |
rs142273339 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | SPAG16 | GRCh38.p7 | 2:213380489 | TACTTGTGCCTTCGG[A/G]ACCTGCTTGAGCCCG | 79582 |
rs142273433 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | SPAG16 | GRCh38.p7 | 2:213336122 | CCCAGCCAAAGGAGG[C/T]GGTGAGGGATTGTGC | 79582 |
rs142273568 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | SPAG16 | GRCh38.p7 | 2:213993154 | AGCTTACAGAGAATG[A/G]CACCCTGCAGGTAGC | 79582 |
rs142274084 | snp | C/T | 0.420733 | 0.18262 | intron-variant | SPAG16 | GRCh38.p7 | 2:213676431 | tatgttgaataggag[C/T]ggtgagagagggcat | 79582 |
rs142276017 | in-del | -/A | 0.0217236 | 0.101931 | intron-variant | SPAG16 | GRCh38.p7 | 2:213618985 | AAAGTTAAACATTTT[-/A]TTTTAAAACAAGTTT | 79582 |
rs142278699 | snp | G/T | 0.000798403 | 0.0199641 | intron-variant | SPAG16 | GRCh38.p7 | 2:214369304 | AAAAGAAGAAGTTTG[G/T]TCTAACATGGACCAG | 79582 |
rs142280868 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | SPAG16 | GRCh38.p7 | 2:213776661 | ATTCTCCCATGTTTA[A/G]TTCGCTAGGTTAGTT | 79582 |
rs142284024 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | SPAG16 | GRCh38.p7 | 2:213970334 | TTTTTATAGATAGCA[C/T]CTTATTGTGTTACCC | 79582 |
rs142284690 | snp | C/T | 0.00636936 | 0.0560724 | intron-variant | SPAG16 | GRCh38.p7 | 2:213644946 | TTTTCTTCAGGGTGG[C/T]GATGTCCCTCAGGCC | 79582 |
rs142286594 | snp | C/T | 0.00318978 | 0.0398085 | intron-variant | SPAG16 | GRCh38.p7 | 2:213338273 | AAACACACTGAAGTA[C/T]ACAGACCAGTGACAA | 79582 |
rs142288270 | in-del | -/TGAG | 0.453331 | 0.145452 | intron-variant | SPAG16 | GRCh38.p7 | 2:214352584 | GTGTGTATGTGTGAC[-/TGAG]TATCTCCTAACATTT | 79582 |
rs142289485 | snp | C/T | 0.0209421 | 0.100162 | intron-variant | SPAG16 | GRCh38.p7 | 2:213829209 | AAATTTCCCTGAAAC[C/T]GTAAGACAAAGTTCT | 79582 |
rs142289722 | in-del | -/A | 0.0475351 | 0.146656 | intron-variant | SPAG16 | GRCh38.p7 | 2:213994841 | TTCAGTTAATCATAT[-/A]ATTTAAAGGTTATTG | 79582 |
rs142289799 | snp | G/T | 0.0130921 | 0.0798413 | intron-variant | SPAG16 | GRCh38.p7 | 2:213883846 | CTCCTGTACTTTTAT[G/T]CTTTCTGTTTTTATA | 79582 |
rs142290920 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | SPAG16 | GRCh38.p7 | 2:214184009 | GTGGTCTTTACTATA[C/T]ATGTATTTATAGTAC | 79582 |
rs142299406 | snp | C/T | 0.0023933 | 0.0345097 | intron-variant | SPAG16 | GRCh38.p7 | 2:214069219 | TTAATCATTCCGATA[C/T]GTGTATATTGTTAAG | 79582 |
rs142302293 | snp | A/C | 0.00517822 | 0.0506191 | intron-variant | SPAG16 | GRCh38.p7 | 2:214299794 | TCAAGTCAATGATTT[A/C]TCTATGCCTGTAGAT | 79582 |
rs142303470 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant, utr-variant-3-prime | SPAG16 | GRCh38.p7 | 2:213399646 | AGTCACTGTCTTTTT[A/C]TAATTTTAGTATCAT | 79582 |
rs142306366 | snp | A/G | 0.00159617 | 0.0282053 | intron-variant | SPAG16 | GRCh38.p7 | 2:214382428 | ATTTTGTGGGCCCCT[A/G]TCCAGTGACTCAACA | 79582 |
rs142307821 | snp | A/G | 0.00716266 | 0.059414 | intron-variant | SPAG16 | GRCh38.p7 | 2:213696893 | AATAGTAGCTGGAAG[A/G]GAATGTGGGCTAAAG | 79582 |
rs142318154 | in-del | -/TT | 0.0150606 | 0.0854603 | intron-variant | SPAG16 | GRCh38.p7 | 2:213390566 | AAAAGAAAAAATAAC[-/TT]ATGTTTTGGGAAATA | 79582 |
rs142321593 | in-del | -/AG | 0.0410537 | 0.137264 | intron-variant | SPAG16 | GRCh38.p7 | 2:213750336 | GTGTAAAATGACAAG[-/AG]TTACATCGAAATATG | 79582 |
rs142326670 | snp | A/G | 0.00358779 | 0.0422022 | intron-variant | SPAG16 | GRCh38.p7 | 2:213721599 | CTTTAAACGGTAATA[A/G]CCATTCATTGCAAAT | 79582 |
rs142329254 | snp | A/C | 0.00438332 | 0.0466095 | intron-variant | SPAG16 | GRCh38.p7 | 2:213853505 | CCTGGTATATTGTTT[A/C]ACAAAACATTTTATG | 79582 |
rs142329393 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | SPAG16 | GRCh38.p7 | 2:214304319 | ACCCACACTGGAAGG[C/T]TGTGGGTTTACCGGA | 79582 |
rs142330269 | snp | A/G | 0.00993419 | 0.0697739 | intron-variant | SPAG16 | GRCh38.p7 | 2:213976615 | TCTTCTGCTGGAGTC[A/G]GGAGAGGTATAGCAG | 79582 |
rs142330864 | in-del | -/A | | | intron-variant | SPAG16 | GRCh38.p7 | 2:214195788 | AGATGAAATTCAAGT[-/A]AAAAAAAACTAGCTA | 79582 |
rs142335694 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | SPAG16 | GRCh38.p7 | 2:213761609 | GCTCACGCCTGTAAT[C/T]TCAGCACTTTGGGAG | 79582 |
rs142337032 | snp | A/C/T | 0.00636936 | 0.0560724 | intron-variant | SPAG16 | GRCh38.p7 | 2:213805867 | GGTTGTTATAATGCC[A/C/T]AAGGCATGGTAAAAA | 79582 |
rs142337422 | in-del | -/AATT | 0.0217236 | 0.101931 | intron-variant | SPAG16 | GRCh38.p7 | 2:213623961 | TTTAACAATGTAATA[-/AATT]AATTAAGTTAAACAC | 79582 |
rs142338629 | snp | G/T | 0.00398564 | 0.0444627 | intron-variant | SPAG16 | GRCh38.p7 | 2:213934846 | GCTGCTTGAAGTAAA[G/T]CCACCCCTGTTTTGT | 79582 |
rs142341616 | snp | C/T | 0.00795532 | 0.062565 | intron-variant | SPAG16 | GRCh38.p7 | 2:214217451 | CTGACTATGTTATGC[C/T]GATGCTTTAAATATC | 79582 |
rs142342827 | snp | C/G | 0.00199481 | 0.0315187 | intron-variant | SPAG16 | GRCh38.p7 | 2:213850976 | CAAAATAGTATTACT[C/G]TTATTTAATAATTAA | 79582 |
rs142345192 | snp | A/G | 0.00159617 | 0.0282053 | intron-variant | SPAG16 | GRCh38.p7 | 2:213594641 | GTGATTACTCCTGTG[A/G]GTTCCCAGTAAATGT | 79582 |
rs142349141 | snp | G/T | 0.00597247 | 0.0543191 | intron-variant | SPAG16 | GRCh38.p7 | 2:213709944 | GCTATTGAAATCAAT[G/T]TGTAAGTGCAAGTTA | 79582 |
rs142357329 | snp | C/T | 6.59033e-05 | 0.00573997 | missense, nc-transcript-variant, intron-variant | SPAG16 | GRCh38.p7 | 2:213930054 | TTTGAAGGACACAGC[C/T]GCGCAGTGTGGTCCT | 79582 |
rs142360570 | snp | A/G | 0.00993419 | 0.0697739 | intron-variant | SPAG16 | GRCh38.p7 | 2:213355492 | TGATTGTTCCTATCC[A/G]TGAGCATGGAATGTT | 79582 |
rs142360668 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | SPAG16 | GRCh38.p7 | 2:214056362 | TTTATAAGCATACCT[C/T]GGAGATACTGCAGTT | 79582 |
rs142363323 | snp | C/G | 0.00398564 | 0.0444627 | intron-variant | SPAG16 | GRCh38.p7 | 2:214348193 | AACCTAGAAACTGAA[C/G]CTAAAGCATCTCCTT | 79582 |
rs142364749 | snp | A/T | 0.0023933 | 0.0345097 | intron-variant | SPAG16 | GRCh38.p7 | 2:213517473 | ATCCTAAAATTCATA[A/T]GGAACCAAAGAAGAG | 79582 |
rs142369862 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | SPAG16 | GRCh38.p7 | 2:213798728 | CTTATGTTTAGGTCC[A/G]TGATCCATTTTTATT | 79582 |
rs142371740 | in-del | -/ATAAT | | | intron-variant | SPAG16 | GRCh38.p7 | 2:213624237 | GAATATCAATGGTTG[-/ATAAT]AAGATCAGGCTATTT | 79582 |
rs142372618 | in-del | -/T | 0.0232847 | 0.105357 | intron-variant | SPAG16 | GRCh38.p7 | 2:213648978 | TAGTCTGAAAAAAAA[-/T]AATCTAAATGAATAA | 79582 |
rs142377407 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | SPAG16 | GRCh38.p7 | 2:214264417 | TTTGCCTAGACTGCC[C/T]TGCCCCTGCCTGTGG | 79582 |
rs142378218 | snp | A/G | 0.00438332 | 0.0466095 | intron-variant | SPAG16 | GRCh38.p7 | 2:214116906 | CAGTAAAGCCAGACT[A/G]TGAAGACTGGAACAA | 79582 |
rs142384747 | snp | C/T | 0.0023933 | 0.0345097 | intron-variant | SPAG16 | GRCh38.p7 | 2:213327737 | TGTTACTAATATTCA[C/T]ATATCCTAATATTTT | 79582 |
rs142385057 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | SPAG16 | GRCh38.p7 | 2:213698661 | TATTTGACACTCTTA[A/G]TACTCACCTGGACAA | 79582 |
rs142386400 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | SPAG16 | GRCh38.p7 | 2:214041810 | ACACACAGGGAAGAT[A/G]TTTTCTGAAATATTT | 79582 |
rs142390035 | in-del | -/ATG | 0.00279162 | 0.0372561 | intron-variant | SPAG16 | GRCh38.p7 | 2:214136466 | GTACAAGTTATTGTA[-/ATG]ATGATGTAGTGCTGT | 79582 |
rs142390658 | snp | A/T | | | intron-variant | SPAG16 | GRCh38.p7 | 2:213457529 | AGGCAACATGCAAAA[A/T]CTTTTGAATTGTTAT | 79582 |
rs142391401 | snp | C/T | 0.00716266 | 0.059414 | intron-variant | SPAG16 | GRCh38.p7 | 2:213779825 | ACTTAAAAATTGAAA[C/T]GTGTTATTTTATCCC | 79582 |
rs142393212 | snp | A/C | 0.00119737 | 0.0244387 | intron-variant | SPAG16 | GRCh38.p7 | 2:214240050 | TGAGGTGGTCATTAA[A/C]GAATGATGAGGAAAG | 79582 |
rs142398408 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | SPAG16 | GRCh38.p7 | 2:214144557 | AAACAAACAAAACAA[A/T]GTTCCTTCACTTAGT | 79582 |
rs142403495 | snp | A/G | 0.00478085 | 0.0486577 | intron-variant | SPAG16 | GRCh38.p7 | 2:213587889 | AATATTCGAATTAGC[A/G]TACCCATTATATGAT | 79582 |
rs142406471 | snp | A/G | 0.0126979 | 0.078662 | intron-variant | SPAG16 | GRCh38.p7 | 2:214000106 | TTCAAATGTGAGGAC[A/G]TGAGATTTGGAGGGG | 79582 |
rs142407679 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | SPAG16 | GRCh38.p7 | 2:213908181 | AAATAATTCAGTTGA[A/G]GATGAGTAAGCAACT | 79582 |
rs142409313 | snp | A/G | 0.00199481 | 0.0315187 | intron-variant | SPAG16 | GRCh38.p7 | 2:214126244 | TTATGGCTTTCTTTG[A/G]GGGAGAGAAGTTTCC | 79582 |
rs142409582 | in-del | -/A | 0.00597247 | 0.0543191 | intron-variant | SPAG16 | GRCh38.p7 | 2:213663948 | GTATAAACTTAGTTT[-/A]AAAACAGCACAAATT | 79582 |
rs142413225 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | SPAG16 | GRCh38.p7 | 2:214214100 | TTTTTTTATTCTATG[A/G]AAACAATTTGCTTTC | 79582 |
rs142418020 | in-del | -/GGGGGG | | | intron-variant | SPAG16 | GRCh38.p7 | 2:214332433 | TGGAAGATACTGGCT[-/GGGGGG]GTTGTCAAACGGCTA | 79582 |
rs142421534 | snp | A/T | 0.00914312 | 0.0669923 | intron-variant | SPAG16 | GRCh38.p7 | 2:214308855 | TGGAGCATATGAAGA[A/T]TATATGTCTTGGGGA | 79582 |
rs142422878 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | SPAG16 | GRCh38.p7 | 2:214107556 | TAGGTCCATCTTTCC[C/T]GGAAACATTTAAACT | 79582 |
rs142440288 | in-del | -/GATTATG | 0.0295035 | 0.117819 | intron-variant | SPAG16 | GRCh38.p7 | 2:214060433 | AAGATAATTCAGTAA[-/GATTATG]GGTTACTATAATGAA | 79582 |
rs142442358 | snp | C/G | 0.00398564 | 0.0444627 | intron-variant | SPAG16 | GRCh38.p7 | 2:213438794 | AGGCTATCTTGCATA[C/G]GTCTAACCTAATCAG | 79582 |
rs142444591 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | SPAG16 | GRCh38.p7 | 2:213653137 | TTACAGCTCCGGGAT[A/G]TGGATAGGTGTTTCA | 79582 |
rs142454589 | snp | C/G | 0.00358779 | 0.0422022 | intron-variant | SPAG16 | GRCh38.p7 | 2:213856408 | AACCTACCATTCTGG[C/G]GTCTGAAGGACAGTG | 79582 |
rs142460395 | snp | C/G | 0.00279162 | 0.0372561 | intron-variant | SPAG16 | GRCh38.p7 | 2:213681056 | CAGAGAGAGAGAGCA[C/G]GTTATAAAATGTTTC | 79582 |
rs142467655 | in-del | -/TGTGTGTGTGTGTG | | | intron-variant | SPAG16 | GRCh38.p7 | 2:214284798 | AATAATATTTTACTC[-/TGTGTGTGTGTGTG]TGTGTGTGTGTGTGT | 79582 |
rs142471769 | snp | A/C | 0.00636936 | 0.0560724 | intron-variant | SPAG16 | GRCh38.p7 | 2:214175192 | GAGGAACCAGGAATA[A/C]AGAAATATATATATA | 79582 |
rs142475995 | snp | A/C | 0.0103295 | 0.0711199 | intron-variant | SPAG16 | GRCh38.p7 | 2:213522645 | CATCTGCTGTTTGCA[A/C]ACCCCAACACTGGGC | 79582 |
rs142479373 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | SPAG16 | GRCh38.p7 | 2:214362270 | AGTAAGTCACAGAGT[C/G]ATTCCTAAGTACATC | 79582 |
rs142488780 | in-del | -/TG | | | intron-variant | SPAG16 | GRCh38.p7 | 2:213765604 | GTCACGTGTGTGTGT[-/TG]GTGTGTGTGTTATTT | 79582 |
rs142490535 | snp | A/C/G | | | intron-variant | SPAG16 | GRCh38.p7 | 2:213665402 | CACACACAAACACAC[A/C/G]TGCACATAAATTAGG | 79582 |
rs142491903 | snp | A/G | 0.0150606 | 0.0854603 | intron-variant | SPAG16 | GRCh38.p7 | 2:213638004 | CCTCGTGATCCGCCC[A/G]TCTTGGCCTCCCAGA | 79582 |
rs142492085 | snp | C/T | 0.00438332 | 0.0466095 | intron-variant | SPAG16 | GRCh38.p7 | 2:213592496 | AAAGTGCAAGTATTT[C/T]TAAAACTAAATATAT | 79582 |
rs142493584 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | SPAG16 | GRCh38.p7 | 2:214011826 | TAATTTACATACATA[G/T]TCATATACATGCAAA | 79582 |
rs142495745 | snp | A/C | 0.00279162 | 0.0372561 | intron-variant | SPAG16 | GRCh38.p7 | 2:213734661 | TATATGCAAATACAC[A/C]AGAATGCTATGGGTT | 79582 |
rs142496463 | snp | C/G | 0.0244538 | 0.107838 | intron-variant | SPAG16 | GRCh38.p7 | 2:213915227 | GGTGGTTTGCTGCAC[C/G]CATCAACCCATCATC | 79582 |
rs142499489 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | SPAG16 | GRCh38.p7 | 2:213715188 | TAATGAAAGTGGGAT[A/G]GATGGAAAAGATTCA | 79582 |
rs142506778 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | SPAG16 | GRCh38.p7 | 2:214067600 | AAAGATAAGAAAAGG[A/C]TTTTTAGGCATATGG | 79582 |
rs142507201 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | SPAG16 | GRCh38.p7 | 2:213460235 | GGATTTGATTTTCCC[C/T]GAGTCCAAATTATTT | 79582 |
rs142512026 | snp | A/G | 0.00318978 | 0.0398085 | intron-variant | SPAG16 | GRCh38.p7 | 2:214151806 | CTGTGCTCTTGGACT[A/G]TTGAAAACACACATG | 79582 |
rs142513377 | snp | A/C | 0.00636936 | 0.0560724 | intron-variant | SPAG16 | GRCh38.p7 | 2:213417743 | AATTTAGAAACTTAC[A/C]TTTTTACTTATCTAT | 79582 |
rs142518009 | snp | A/T | 0.000798403 | 0.0199641 | intron-variant | SPAG16 | GRCh38.p7 | 2:214108805 | AAAACTGATGACAAA[A/T]CAAAAATATTTTATC | 79582 |
rs142524249 | in-del | -/AT | 0.149665 | 0.228982 | intron-variant | SPAG16 | GRCh38.p7 | 2:213976335 | TACGCATGTGTGCAC[-/AT]ATATATATATATCAG | 79582 |
rs142531898 | snp | C/T | 0.0146672 | 0.084371 | intron-variant | SPAG16 | GRCh38.p7 | 2:214032050 | TGCTCATAGTGTTCC[C/T]ATAGCATACCCTTTA | 79582 |
rs142535640 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | SPAG16 | GRCh38.p7 | 2:213337902 | ACATGAGAAGATCAA[A/G]CAAAAGACACATAAT | 79582 |
rs142543692 | snp | C/T | 0.0429648 | 0.14013 | intron-variant | SPAG16 | GRCh38.p7 | 2:213293125 | GAGTATCGCAAGATC[C/T]CATGGTTTTGTAAGT | 79582 |
rs142545053 | snp | C/G | 0.0325976 | 0.123435 | intron-variant | SPAG16 | GRCh38.p7 | 2:214070560 | ATTTGTTTTACTCCA[C/G]TATTAGGAATATTTT | 79582 |
rs142557709 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | SPAG16 | GRCh38.p7 | 2:213931203 | TTCCGTTTCCTGACA[A/T]GTCCTTGAAAGATCC | 79582 |
rs142560006 | snp | C/T | 0.00557542 | 0.0525036 | intron-variant | SPAG16 | GRCh38.p7 | 2:213993647 | TGCTTAATAGGAAAA[C/T]GGTGTTTTCTCACGT | 79582 |
rs142565034 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | SPAG16 | GRCh38.p7 | 2:214035168 | CTTATCATCATCTCC[A/T]CAAGTCTGGCTGAGT | 79582 |
rs142574921 | snp | G/T | 0.00557542 | 0.0525036 | intron-variant | SPAG16 | GRCh38.p7 | 2:214121535 | TTATTTAGCTCATCT[G/T]TAAAATGAGTGACAA | 79582 |
rs142575469 | snp | A/C | 0.00318978 | 0.0398085 | intron-variant, utr-variant-3-prime, downstream-variant-500B | SPAG16 | GRCh38.p7 | 2:213396956 | CTTTGTACTCTATTG[A/C]ATTCAAGGTCAGTCA | 79582 |
rs142580539 | snp | C/T | 0.0126979 | 0.078662 | intron-variant | SPAG16 | GRCh38.p7 | 2:213879561 | ACATGTGCAAGGTTA[C/T]TGCATGGGTTCATTG | 79582 |
rs142580936 | snp | C/T | 0.0174175 | 0.0916809 | intron-variant | SPAG16 | GRCh38.p7 | 2:213477561 | TGGAACTTTAAGGTT[C/T]AATGACTGCCCTGTT | 79582 |
rs142586315 | snp | A/T | 0.00557542 | 0.0525036 | intron-variant | SPAG16 | GRCh38.p7 | 2:214327804 | GGTATAGATTCTTTT[A/T]TATTCAAATGCCCAT | 79582 |
rs142588250 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | SPAG16 | GRCh38.p7 | 2:213483516 | TGTTTGCTAAATTTC[G/T]AAAGATGGGTTGTTG | 79582 |
rs142607217 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | SPAG16 | GRCh38.p7 | 2:214309773 | TGGAGTTCACTTTGC[C/T]GGGGGAACCAAAGTG | 79582 |
rs142608175 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | SPAG16 | GRCh38.p7 | 2:214382872 | GTTTGGGCTTCTGCC[G/T]CTCTAAGCATGACTG | 79582 |
rs142609592 | snp | A/C | 0.0119091 | 0.0762411 | intron-variant | SPAG16 | GRCh38.p7 | 2:213384330 | TGGAAGTTCTGCAAA[A/C]TACCAAGTATGTTCT | 79582 |
rs142611526 | snp | A/T | 0.00318978 | 0.0398085 | intron-variant | SPAG16 | GRCh38.p7 | 2:213465355 | ATAGTGTCATTCAGG[A/T]TGACTACTGTGTATT | 79582 |
rs142612914 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | SPAG16 | GRCh38.p7 | 2:213442009 | TTTAAAAAGTTAGCC[A/G]TAGTGGCACATGCCT | 79582 |
rs142615242 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | SPAG16 | GRCh38.p7 | 2:213900753 | CATTTTTCCTCTCCT[A/G]TTTTTACATTGTGAA | 79582 |
rs142617263 | in-del | -/C | | | intron-variant | SPAG16 | GRCh38.p7 | 2:214318373 | GAGTGAGAGTGAATT[-/C]TTTTTTTTTTTTTTT | 79582 |
rs142625161 | snp | C/T | | | intron-variant | SPAG16 | GRCh38.p7 | 2:213394165 | CTCAAGATCAGAGTA[C/T]TATGTTCATATCTTT | 79582 |
rs142625311 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | SPAG16 | GRCh38.p7 | 2:213445388 | CAGATATAGCTGGGC[A/G]TGGCGGCTCATGCCT | 79582 |
rs142626433 | snp | A/G | 0.0166325 | 0.0896639 | intron-variant | SPAG16 | GRCh38.p7 | 2:213353058 | GTTACTTGTCTATCC[A/G]TATAGCTTAAAGTCT | 79582 |
rs142629381 | snp | C/T | 0.00318978 | 0.0398085 | intron-variant | SPAG16 | GRCh38.p7 | 2:213529869 | ATTTTTTTCTATTTT[C/T]AAAATGCTTTATAAT | 79582 |
rs142635834 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | SPAG16 | GRCh38.p7 | 2:214177626 | ATTATGACAGAAGGT[A/G]GGTTTTTTGTGAAAC | 79582 |
rs142636833 | snp | A/G | 0.00716266 | 0.059414 | intron-variant, utr-variant-3-prime | SPAG16 | GRCh38.p7 | 2:213400444 | TTTACATATGCATGG[A/G]TTTTGGGTTATTTTT | 79582 |
rs142640522 | snp | G/T | 0.0879971 | 0.190408 | intron-variant | SPAG16 | GRCh38.p7 | 2:213355926 | ATTGGAGTGGTGAGA[G/T]AGGGCATCGTTGTCT | 79582 |
rs142640631 | snp | A/C | 0.00953873 | 0.0683987 | intron-variant | SPAG16 | GRCh38.p7 | 2:213856400 | TGTCAGTAAACCTAC[A/C]ATTCTGGGGTCTGAA | 79582 |
rs142642439 | snp | A/T | | | intron-variant | SPAG16 | GRCh38.p7 | 2:213800333 | CCCTCCCTCCCTCCC[A/T]CTCTCCCTCTCTCCC | 79582 |
rs142647906 | snp | G/T | 0.00835141 | 0.0640778 | intron-variant | SPAG16 | GRCh38.p7 | 2:214376116 | ATAAAAAAGAAGAAG[G/T]AATAAAAAATAATAA | 79582 |
rs142648612 | snp | A/C | 0.00119737 | 0.0244387 | intron-variant | SPAG16 | GRCh38.p7 | 2:214387713 | TGGTAGAAGGGGAAG[A/C]AAACACATCCTTCTT | 79582 |
rs142663306 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | SPAG16 | GRCh38.p7 | 2:213710460 | ATCTATGTATTAAAT[A/G]GTAATGAAACATTTC | 79582 |
rs142668274 | snp | A/G | 0.00438332 | 0.0466095 | intron-variant | SPAG16 | GRCh38.p7 | 2:214051018 | TTTCCCTGAAGACTA[A/G]TTATGACTGTCTTTT | 79582 |
rs142671652 | snp | A/G | 0.00159617 | 0.0282053 | intron-variant | SPAG16 | GRCh38.p7 | 2:214137280 | TATTTTCATTGAACT[A/G]CATATTTTTTCGTCA | 79582 |
rs142672451 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | SPAG16 | GRCh38.p7 | 2:214023956 | TATAGATTAGCTTTA[C/T]GAGATTATTTTAATT | 79582 |
rs142682879 | snp | A/C | 0.0174175 | 0.0916809 | intron-variant | SPAG16 | GRCh38.p7 | 2:213929064 | TGTTGCCCAGGCTGC[A/C]GTGCAGTGGTGCGAT | 79582 |
rs142685032 | in-del | -/TC | 0.487082 | 0.0793231 | intron-variant | SPAG16 | GRCh38.p7 | 2:213931094 | ATGATATTTTAATGT[-/TC]TCTTTTCCCTTTTTT | 79582 |
rs142685469 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant, utr-variant-3-prime | SPAG16 | GRCh38.p7 | 2:213397768 | ATACTGAGGTGTTTC[A/C]AGGCTCAGTTCTTGA | 79582 |
rs142688403 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | SPAG16 | GRCh38.p7 | 2:213470632 | GCCAGGTCAGCCTTG[A/G]TGAGTGAAAATCCAT | 79582 |
rs142689839 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | SPAG16 | GRCh38.p7 | 2:213995980 | CCTTGTCCTTGAAAG[C/T]TTCCCTAAAGCCTTC | 79582 |
rs142693195 | snp | A/G | 0.0260105 | 0.111035 | intron-variant | SPAG16 | GRCh38.p7 | 2:213610609 | GTTCTTGGATCTTGC[A/G]CAAGAAAGAATTCAG | 79582 |
rs142694019 | in-del | -/T | | | intron-variant | SPAG16 | GRCh38.p7 | 2:213457879 | TTCCCTCTTCTTTTA[-/T]TTTTTTTTTTCCTTC | 79582 |
rs142699715 | snp | A/C | | | intron-variant | SPAG16 | GRCh38.p7 | 2:214068061 | AATGTCCTGTTGTAT[A/C]AGGATGGAACACAGA | 79582 |
rs142699895 | snp | A/T | 0.00119737 | 0.0244387 | intron-variant | SPAG16 | GRCh38.p7 | 2:213561262 | AAATGTATATTAGTT[A/T]GAATTACCTTTAATT | 79582 |
rs142700612 | snp | A/G | 0.0252325 | 0.109451 | intron-variant | SPAG16 | GRCh38.p7 | 2:214252471 | CCACGACAGACCACA[A/G]TATGTGATGTTCCCC | 79582 |
rs142701388 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | SPAG16 | GRCh38.p7 | 2:213850076 | TGGAAGTAGTTCACC[A/T]GTTTCATTGATTGTC | 79582 |
rs142703383 | snp | A/G | 0.00199481 | 0.0315187 | intron-variant | SPAG16 | GRCh38.p7 | 2:213904446 | GACTTATTCACTACC[A/G]TTAGAATAGTATGGG | 79582 |
rs142705875 | snp | A/G | 0.00318978 | 0.0398085 | intron-variant | SPAG16 | GRCh38.p7 | 2:213928659 | CTTGCATGCATTTCT[A/G]TATTTACTTACTCTA | 79582 |
rs142706755 | snp | C/T | 0.00438332 | 0.0466095 | intron-variant | SPAG16 | GRCh38.p7 | 2:213351066 | AGAATCATTTGAACC[C/T]GGGAGTGGAGGTTGC | 79582 |
rs142706889 | in-del | -/AT | 0.32955 | 0.237006 | intron-variant | SPAG16 | GRCh38.p7 | 2:213889719 | TATATATACATATGC[-/AT]ATATATATACATATA | 79582 |
rs142711242 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | SPAG16 | GRCh38.p7 | 2:213755369 | AAATGTGAAGTCATA[A/G]GTGTCTGTGTAATGG | 79582 |
rs142720619 | snp | A/G | 0.00358779 | 0.0422022 | intron-variant | SPAG16 | GRCh38.p7 | 2:213885780 | GGCTTAATCTATGAG[A/G]TAAACCTTACAGTAT | 79582 |
rs142722504 | in-del | -/TTAGTGCCA | 0.271162 | 0.249103 | intron-variant | SPAG16 | GRCh38.p7 | 2:214180588 | CCTTTAAATGACAAG[-/TTAGTGCCA]TAAAAACAAGGTAGC | 79582 |
rs142726835 | snp | A/G/T | 0.000399281 | 0.0141238 | intron-variant | SPAG16 | GRCh38.p7 | 2:213885229 | CAGAAGGGTATATTA[A/G/T]CAAAGTATTTTTGGT | 79582 |
rs142729168 | snp | A/C | 0.0170251 | 0.090679 | intron-variant | SPAG16 | GRCh38.p7 | 2:213430686 | GATGAAAACTTCACT[A/C]GGCTAGCAATATATT | 79582 |
rs142731418 | snp | A/G | 0.0126979 | 0.078662 | intron-variant | SPAG16 | GRCh38.p7 | 2:213597775 | TCTTTTGCCCCCCCA[A/G]AAACTTCTCTGACAT | 79582 |
rs142738976 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | SPAG16 | GRCh38.p7 | 2:214374565 | AACTCTTTTATCAAA[C/T]AGAACGGAGTGAAGC | 79582 |
rs142739037 | snp | C/T | 0.02016 | 0.0983543 | intron-variant | SPAG16 | GRCh38.p7 | 2:214326667 | CACAGTACTTCCGGC[C/T]GGGCGCGGTGGCTCA | 79582 |
rs142739837 | snp | C/T | 0.00159617 | 0.0282053 | intron-variant | SPAG16 | GRCh38.p7 | 2:214332080 | AACATGGTGAAATCC[C/T]ACCTCTGCTAAAAAT | 79582 |
rs142745716 | snp | A/T | 0.000798403 | 0.0199641 | intron-variant | SPAG16 | GRCh38.p7 | 2:214025996 | TTCTTTTGAAGGGAA[A/T]TTGACAATGTAAGAA | 79582 |
rs142746595 | snp | C/G | 0.410905 | 0.191336 | intron-variant | SPAG16 | GRCh38.p7 | 2:213783597 | CCAAAATCTCACCCC[C/G]AAATAAATGATTAAA | 79582 |
rs142751370 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | SPAG16 | GRCh38.p7 | 2:214075533 | CTCACCAACTTAAAC[A/G]CTTGTGATTTCAGCA | 79582 |
rs142752699 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | SPAG16 | GRCh38.p7 | 2:214245189 | TATTCTGACTATACA[A/G]CAGCATTCTGAAATC | 79582 |
rs142762077 | snp | A/C/T | 0.000399281 | 0.0141238 | intron-variant | SPAG16 | GRCh38.p7 | 2:213308150 | TGTTTTATTTTTTTA[A/C/T]TTTTATTTTTATTGA | 79582 |
rs142763185 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | SPAG16 | GRCh38.p7 | 2:213353496 | TAAAATATGAAGGAC[A/T]CTTTAAGGGGTTGTC | 79582 |
rs142763325 | snp | A/G | 0.0111196 | 0.0737302 | intron-variant | SPAG16 | GRCh38.p7 | 2:213434578 | CTATGCATCTGATAG[A/G]GGACTGATATCCAGA | 79582 |
rs142772701 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | SPAG16 | GRCh38.p7 | 2:213889820 | ATGACATCAAATGTT[G/T]CCTATGGGAAGCCTC | 79582 |
rs142772704 | snp | C/G/T | 0.0130921 | 0.0798413 | intron-variant | SPAG16 | GRCh38.p7 | 2:214333860 | AGCACTTATAAATTC[C/G/T]AAATCTCCAGATTTC | 79582 |
rs142776486 | snp | A/T | 0.0263992 | 0.111815 | intron-variant | SPAG16 | GRCh38.p7 | 2:214275036 | TTGGGAGGGTGTATA[A/T]GTCCAGGAATTTATC | 79582 |
rs142776957 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | SPAG16 | GRCh38.p7 | 2:213795974 | CAGTGAAAGAATGGA[C/G]TAATACACTTTGTAT | 79582 |
rs142782595 | snp | C/T | | | intron-variant | SPAG16 | GRCh38.p7 | 2:214357953 | CCAAACTCTTAGGAA[C/T]GTGAGTTTATGATTA | 79582 |
rs142783748 | snp | G/T | 0.00358779 | 0.0422022 | intron-variant | SPAG16 | GRCh38.p7 | 2:213657786 | TTCTCTATAAAGAGA[G/T]AAAAGATATAGTCCA | 79582 |
rs142785544 | snp | G/T | 0.00199481 | 0.0315187 | intron-variant | SPAG16 | GRCh38.p7 | 2:213720652 | AAAAACTTAAATAAA[G/T]AAAGAAAAAAAATAT | 79582 |
rs142786014 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | SPAG16 | GRCh38.p7 | 2:213878310 | CAATAGTGTATAAGC[A/G]TTTCTTTTCCTTCTT | 79582 |
rs142790086 | snp | A/C | 0.00676609 | 0.0577691 | intron-variant, downstream-variant-500B | SPAG16 | GRCh38.p7 | 2:214192680 | TCTAATATTTTATGG[A/C]ATTTGGGATGGTTTT | 79582 |
rs142792457 | snp | G/T | 0.0154538 | 0.0865337 | intron-variant | SPAG16 | GRCh38.p7 | 2:213869724 | AAAGAAAATAAATAT[G/T]TCTCACAGTCCTACA | 79582 |
rs142795492 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | SPAG16 | GRCh38.p7 | 2:214406154 | TCTCAACCTTAAGGA[A/G]AACTTGGCTACATGA | 79582 |
rs142800200 | snp | C/T | 0.132751 | 0.2208 | intron-variant | SPAG16 | GRCh38.p7 | 2:213344860 | GTGCATGTGTATTTA[C/T]AGCAGCATGATTTAT | 79582 |
rs142800297 | snp | A/G | 0.00318978 | 0.0398085 | intron-variant | SPAG16 | GRCh38.p7 | 2:214250228 | AGCATTCTCTCTGCC[A/G]CATTTATTGACAGTT | 79582 |
rs142801968 | snp | A/G | 0.324855 | 0.23853 | intron-variant | SPAG16 | GRCh38.p7 | 2:213621055 | CTAGTACTAAAACTA[A/G]AAACTAGTTTTAGTA | 79582 |
rs142802258 | in-del | -/A | 0.0295035 | 0.117819 | intron-variant | SPAG16 | GRCh38.p7 | 2:213958478 | TGGTATGATAAAATT[-/A]AAACCTATATTCAAA | 79582 |
rs142821876 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | SPAG16 | GRCh38.p7 | 2:214187146 | AGGACACTATATGGG[C/T]GTACTCTCATTTGCA | 79582 |
rs142825296 | snp | A/G | 0.0174175 | 0.0916809 | intron-variant | SPAG16 | GRCh38.p7 | 2:214274184 | TTGCTTCTCAGCTTA[A/G]GGAGATTTTGCGCTG | 79582 |
rs142831863 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | SPAG16 | GRCh38.p7 | 2:213525765 | AATATATCCATGTCT[A/G]TGTATATCTACATCT | 79582 |
rs142834312 | in-del | -/T | | | intron-variant | SPAG16 | GRCh38.p7 | 2:213819765 | TGGTTGGTTGGTTGG[-/T]TTTTTTTTTGAGACA | 79582 |
rs142836708 | snp | A/T | 0.12932 | 0.218944 | intron-variant | SPAG16 | GRCh38.p7 | 2:213728637 | TCCCAGCACTTTGGG[A/T]GGCCGAAGCGGGCGG | 79582 |
rs142842300 | snp | A/G | 0.00159617 | 0.0282053 | intron-variant | SPAG16 | GRCh38.p7 | 2:214032547 | GGAATACAGCTTCTC[A/G]GAGGCTAGGATCTGA | 79582 |
rs142844613 | snp | A/C | 0.00478085 | 0.0486577 | intron-variant | SPAG16 | GRCh38.p7 | 2:213358084 | GTGTCGAATATTGGC[A/C]CCCACTCTCTTCTGG | 79582 |
rs142846282 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | SPAG16 | GRCh38.p7 | 2:214343123 | CAAAAAAAAGTATAA[A/T]AACTATTTTATTTAA | 79582 |
rs142850293 | snp | C/T | 0.00874735 | 0.0655527 | intron-variant, utr-variant-5-prime | SPAG16 | GRCh38.p7 | 2:213301578 | TATCCTTCTCTTTAC[C/T]TTCATCCTCACTTAG | 79582 |
rs142850954 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | SPAG16 | GRCh38.p7 | 2:213768878 | CATCTGAACACAAAA[A/T]CTTTAGAAAAGAGAA | 79582 |
rs142852614 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | SPAG16 | GRCh38.p7 | 2:213442487 | AAGGAGAACAAAGTT[A/G]CAAGACTGTGACACT | 79582 |
rs142854733 | snp | A/C | 0.0150606 | 0.0854603 | intron-variant | SPAG16 | GRCh38.p7 | 2:214225427 | GGATGCTTGGATCAG[A/C]GTGAAAGCAGGGAAG | 79582 |
rs142855558 | snp | C/T | 0.0126979 | 0.078662 | intron-variant | SPAG16 | GRCh38.p7 | 2:213822678 | TAAGTACACGTGTGC[C/T]ATGGTGGTTTGCTGA | 79582 |
rs142859842 | snp | A/G | | | intron-variant | SPAG16 | GRCh38.p7 | 2:213689606 | GTGCCCAATAGCCAT[A/G]TGAATTAATAAGATT | 79582 |
rs142867722 | snp | A/G | 0.0023933 | 0.0345097 | intron-variant | SPAG16 | GRCh38.p7 | 2:213724950 | TTTATTCAGTCAACA[A/G]ATAGGCCAGTATGCA | 79582 |
rs142878148 | snp | C/G | 0.00557542 | 0.0525036 | intron-variant | SPAG16 | GRCh38.p7 | 2:213321529 | TGCTGTCATCTCTAA[C/G]TTTTTATTAATCACA | 79582 |
rs142878681 | snp | A/C | 0.00318978 | 0.0398085 | intron-variant | SPAG16 | GRCh38.p7 | 2:214197247 | GTTCAGTCATTTTGA[A/C]ATCTGTGAATAAATC | 79582 |
rs142884187 | snp | A/C | 0.0138799 | 0.0821421 | intron-variant | SPAG16, LOC101928084 | GRCh38.p7 | 2:214099451 | AGTGTTTATACGAAT[A/C]AGAGATAGTATCAAT | 79582 |
rs142887197 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | SPAG16 | GRCh38.p7 | 2:213661882 | ATTATCCAGAAGAAC[C/T]TGGTTTCTATAGAAG | 79582 |
rs142887925 | in-del | -/T | | | intron-variant | SPAG16 | GRCh38.p7 | 2:213731154 | ACATTATATCTGAGT[-/T]TTTTTTTTTTTTTTT | 79582 |
rs142889153 | in-del | -/AAAC | | | intron-variant | SPAG16 | GRCh38.p7 | 2:213292692 | AAAAAAACAAAAAAA[-/AAAC]AACAAAACTATCAGA | 79582 |
rs142889720 | snp | A/G | 0.00358779 | 0.0422022 | intron-variant | SPAG16 | GRCh38.p7 | 2:213557639 | ATTAAAAAAAATTGA[A/G]TTGAAGTCTCACTCT | 79582 |
rs142892554 | snp | C/T | 0.0023933 | 0.0345097 | intron-variant | SPAG16 | GRCh38.p7 | 2:213750913 | CAGCTTCTGGACCAC[C/T]GATGATACATTAACT | 79582 |
rs142893500 | snp | C/G | 0.00676609 | 0.0577691 | intron-variant | SPAG16 | GRCh38.p7 | 2:213639390 | ATATTTTGAGGATTT[C/G]TTTCAAGATTTAGAG | 79582 |
rs142896983 | snp | A/G | 0.10237 | 0.201756 | intron-variant | SPAG16 | GRCh38.p7 | 2:213677297 | GTAAATGGACTAAAT[A/G]CTCCAATTAAAAGAC | 79582 |
rs142902344 | snp | C/G | 0.000798403 | 0.0199641 | intron-variant | SPAG16 | GRCh38.p7 | 2:214082109 | TGGCTCTTCTTGCCC[C/G]TCGCTTTTGGCTTGG | 79582 |
rs142905288 | snp | C/T | 0.0023933 | 0.0345097 | intron-variant | SPAG16 | GRCh38.p7 | 2:214006190 | CATAATTCTATTAGC[C/T]ACATTTTGTTGACCT | 79582 |
rs142905643 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | SPAG16 | GRCh38.p7 | 2:214181269 | TGTGTCCCTCTCTGC[A/C]TAGTACTAACAGACA | 79582 |
rs142907137 | snp | A/G | 0.00358779 | 0.0422022 | intron-variant | SPAG16 | GRCh38.p7 | 2:214190155 | ACTACAATGTTACTA[A/G]AATATGCTCCACGTC | 79582 |
rs142907495 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | SPAG16 | GRCh38.p7 | 2:213729209 | AATAGACAATATCAC[A/G]TAGCTAATATTCCAA | 79582 |
rs142915102 | snp | C/T | 0.0535932 | 0.154675 | intron-variant | SPAG16 | GRCh38.p7 | 2:214276471 | TGCTTCCTTCAGGAG[C/T]TCTTTTAAGGCAGGC | 79582 |
rs142920301 | snp | C/T | 0.00279162 | 0.0372561 | intron-variant | SPAG16 | GRCh38.p7 | 2:214049755 | CAGCCCTGGGGACTC[C/T]TGTGAGCAGTATCTC | 79582 |
rs142921820 | snp | G/T | 0.00953873 | 0.0683987 | intron-variant | SPAG16 | GRCh38.p7 | 2:214194745 | CAAAATTTGCATCCT[G/T]ATCATATTGTTAGAT | 79582 |
rs142923058 | snp | C/T | 0.00159617 | 0.0282053 | intron-variant | SPAG16 | GRCh38.p7 | 2:213606288 | CTTTTGGTGGATGTA[C/T]GCTCAACAAAGTGGG | 79582 |
rs142931090 | in-del | -/AG | | | intron-variant | SPAG16 | GRCh38.p7 | 2:214002527 | GAACCAATAGGAGAA[-/AG]AGAGAGAGAGAGATA | 79582 |
rs142934000 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | SPAG16 | GRCh38.p7 | 2:213829922 | CTCCTCTCATGAAGT[A/G]GAAGGAAGGGGTCTC | 79582 |
rs142935072 | snp | A/G | | | intron-variant | SPAG16 | GRCh38.p7 | 2:213614206 | TGCTAAAACAAAATG[A/G]AAGTTCTCAGCATTC | 79582 |
rs142935391 | snp | C/T | 0.00874735 | 0.0655527 | intron-variant | SPAG16 | GRCh38.p7 | 2:213688856 | ATATTAATAATTCTA[C/T]CACCAGACATTTTAT | 79582 |
rs142941997 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | SPAG16 | GRCh38.p7 | 2:214140334 | TTTAATTGCATCATC[A/G]TCATAAAATGTGGCC | 79582 |
rs142946868 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | SPAG16 | GRCh38.p7 | 2:214159835 | ATTTTGAAATAATGA[C/T]AAGCATCTTTGAATA | 79582 |
rs142947190 | snp | C/T | 0.00199481 | 0.0315187 | intron-variant | SPAG16 | GRCh38.p7 | 2:213411346 | CAATATTTTGGTGGG[C/T]GACCATTAATAAAAA | 79582 |
rs142951420 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | SPAG16 | GRCh38.p7 | 2:213363612 | GACATGTTTAATAAA[A/G]TAGAGAATATATGTG | 79582 |
rs142952132 | snp | C/T | 0.00279162 | 0.0372561 | intron-variant | SPAG16 | GRCh38.p7 | 2:213595688 | AATTGCTACCTTAAG[C/T]AATATGGTGGATTTT | 79582 |
rs142952522 | snp | A/C | 0.0138799 | 0.0821421 | intron-variant | SPAG16 | GRCh38.p7 | 2:213286756 | GACAATGAGCTATCA[A/C]TATCGAGCAAGACTT | 79582 |
rs142958252 | snp | A/G | 0.00318978 | 0.0398085 | intron-variant | SPAG16 | GRCh38.p7 | 2:214053424 | GACTGTGTGCTTAGT[A/G]CTTACCATATCTCAG | 79582 |
rs142959655 | in-del | -/CCCCC | | | intron-variant | SPAG16 | GRCh38.p7 | 2:213683023 | CATCTCAACATCTCA[-/CCCCC]CAGCCACAAACTGGA | 79582 |
rs142963200 | snp | A/G | 0.0119091 | 0.0762411 | intron-variant, downstream-variant-500B | SPAG16, LOC101928084 | GRCh38.p7 | 2:214084886 | CAATATCTCTTTTCA[A/G]TGAGCTTATATTATA | 79582 |
rs142964307 | in-del | -/ATATAT/ATATATATATAT/ATATATATATATATAT | | | intron-variant | SPAG16 | GRCh38.p7 | 2:213896573 | AATGGATAAAATGTG[lengthTooLong]ATATATACACACACA | 79582 |
rs142965574 | snp | A/T | 0.00914312 | 0.0669923 | intron-variant | SPAG16 | GRCh38.p7 | 2:213694466 | TTTTTCAAGTTCCAT[A/T]TGCGTTGCTTTCTAG | 79582 |
rs142991651 | snp | C/T | 0.00517822 | 0.0506191 | intron-variant | SPAG16 | GRCh38.p7 | 2:213476100 | TCAGGTTTACACTCC[C/T]GATAACTAAGCCAAG | 79582 |
rs142992363 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | SPAG16 | GRCh38.p7 | 2:213628239 | CTTATGAGGTCAGGA[A/G]ATTCTTGAGTGTTTT | 79582 |
rs142992767 | snp | C/T | 0.0240643 | 0.107019 | intron-variant | SPAG16 | GRCh38.p7 | 2:213564387 | GTAATCCCAGCTACT[C/T]GAGAGGCTGAGGCAG | 79582 |
rs142994328 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | SPAG16 | GRCh38.p7 | 2:213583227 | AAAACAGGCTCCTTT[A/C]CAAATGGAATGAAAC | 79582 |
rs143003751 | snp | A/T | 0.00993419 | 0.0697739 | intron-variant | SPAG16 | GRCh38.p7 | 2:213379120 | CGTTCCTCCCTCTGG[A/T]ACTAAGACCTCTAGG | 79582 |
rs143004830 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | SPAG16 | GRCh38.p7 | 2:214040457 | CCTTTACCCTCCCAA[A/T]ATCCCCGGTGTGTAT | 79582 |
rs143005602 | in-del | -/G | 0.0966517 | 0.197444 | intron-variant | SPAG16 | GRCh38.p7 | 2:214263071 | TTTATTCTATAGTGA[-/G]AACAATTAAGATCTA | 79582 |
rs143005966 | snp | C/G | 0.0130921 | 0.0798413 | intron-variant | SPAG16 | GRCh38.p7 | 2:213458842 | CTACATTTAAAATTT[C/G]CCCTTTATCTGTAAT | 79582 |
rs143005981 | snp | C/G/T | 0.000399281 | 0.0141238 | intron-variant | SPAG16 | GRCh38.p7 | 2:213513807 | TATACTTAAGCTGGT[C/G/T]CCCTTCATATTTATG | 79582 |
rs143007118 | snp | A/G | 0.00318978 | 0.0398085 | intron-variant | SPAG16 | GRCh38.p7 | 2:213586523 | CATTCAGACCACAGC[A/G]TTTCACCCCGACACT | 79582 |
rs143015905 | snp | C/G | 0.00159617 | 0.0282053 | intron-variant | SPAG16 | GRCh38.p7 | 2:213462390 | GGATGGCTTCCCATT[C/G]TAAGCCTTTTTGAGG | 79582 |
rs143018101 | snp | C/T | 0.00636936 | 0.0560724 | intron-variant | SPAG16 | GRCh38.p7 | 2:214276377 | ATTAATTGATGTAGT[C/T]TCTTGCTAGCATTGG | 79582 |
rs143019098 | snp | A/G | | | intron-variant | SPAG16 | GRCh38.p7 | 2:213337375 | GCTGAGGCTGAGATG[A/G]ATGAATTGACAGAAG | 79582 |
rs143026872 | snp | A/T | 0.00874735 | 0.0655527 | intron-variant, downstream-variant-500B | SPAG16 | GRCh38.p7 | 2:214151152 | TGTGTGAGAAATTAC[A/T]GTCATAAGGATTTTC | 79582 |
rs143040242 | in-del | -/ATAG/ATATAG | | | intron-variant | SPAG16 | GRCh38.p7 | 2:213860482 | TCTATCTATATATAT[-/ATAG/ATATAG]ATATACACACATATG | 79582 |
rs143049126 | snp | C/T | 0.00199481 | 0.0315187 | intron-variant | SPAG16 | GRCh38.p7 | 2:214014820 | ACATAATCGGATTTA[C/T]CTTGTCAACTGAAGA | 79582 |
rs143049308 | snp | C/T | 0.0023933 | 0.0345097 | intron-variant | SPAG16 | GRCh38.p7 | 2:214034673 | TGCAGCCAGACCAGA[C/T]ATCCTGAAAGCAGCT | 79582 |
rs143049997 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | SPAG16 | GRCh38.p7 | 2:213498714 | CCTCATCTTCATGCT[C/T]ACCAACTTTCTCCCA | 79582 |
rs143053733 | snp | A/C | 0.00358779 | 0.0422022 | intron-variant | SPAG16 | GRCh38.p7 | 2:213770656 | GTGTGTTATTCATCT[A/C]CTTGTGTTCATGTGT | 79582 |
rs143056328 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | SPAG16 | GRCh38.p7 | 2:213917096 | AAGTTGAACATGTGT[A/G]GCATTATTTCTGGGC | 79582 |
rs143059054 | snp | C/T | 0.00835141 | 0.0640778 | intron-variant | SPAG16 | GRCh38.p7 | 2:214408001 | GTAAACTTGAAAAAC[C/T]GCATAATAAATTTGC | 79582 |
rs143060939 | snp | A/G | 0.0240643 | 0.107019 | intron-variant | SPAG16 | GRCh38.p7 | 2:214136603 | GCATAGGAAAGAAGT[A/G]TACACCCAAAATTAC | 79582 |
rs143063940 | snp | A/G | 0.00159617 | 0.0282053 | intron-variant | SPAG16 | GRCh38.p7 | 2:214227361 | ATATACCTAAAATCT[A/G]CTTTAGACAAGAGAG | 79582 |
rs143065661 | snp | C/G | 0.0244538 | 0.107838 | intron-variant | SPAG16 | GRCh38.p7 | 2:213359482 | AAGCCTCAGCAATGG[C/G]AGACGCCCCTCCTCC | 79582 |
rs143071951 | snp | A/G | 0.00795532 | 0.062565 | intron-variant | SPAG16 | GRCh38.p7 | 2:213899969 | TTTGTACAACTCTTA[A/G]TACCAAAGCAGAGAT | 79582 |
rs143074045 | snp | G/T | 0.00716266 | 0.059414 | intron-variant | SPAG16 | GRCh38.p7 | 2:213690831 | ACCTCCCAGGGGCTC[G/T]TGGGCCTATGGCCTC | 79582 |
rs143079276 | snp | A/C | 0.000798403 | 0.0199641 | intron-variant | SPAG16 | GRCh38.p7 | 2:213641972 | CATGATAAGTCACTC[A/C]CTATCATGAGAACAG | 79582 |
rs143082867 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | SPAG16 | GRCh38.p7 | 2:213341522 | AATTTTACAGTATTT[C/T]TTTGTTTGTTGTTTT | 79582 |
rs143084154 | snp | A/G | 0.00676609 | 0.0577691 | intron-variant | SPAG16, LOC101928084 | GRCh38.p7 | 2:214102159 | AATCTCCATGTAAGT[A/G]TGCTTACTTTTTCAT | 79582 |
rs143092882 | snp | G/T | 0.00279162 | 0.0372561 | intron-variant | SPAG16 | GRCh38.p7 | 2:214017834 | ATGGCAAATTAAAAT[G/T]TATATCACTACAATT | 79582 |
rs143095644 | snp | C/G | 0.089084 | 0.191327 | intron-variant | SPAG16 | GRCh38.p7 | 2:213753047 | AGACGGAGTCTCGCT[C/G]TGTCACCCAGGCTGG | 79582 |
rs143098372 | snp | A/G | 0.00279162 | 0.0372561 | intron-variant | SPAG16 | GRCh38.p7 | 2:213922371 | ATGTTTCTTATCTCT[A/G]TTAGATGAGTTTGGT | 79582 |
rs143098486 | snp | A/G | | | intron-variant | SPAG16 | GRCh38.p7 | 2:213871632 | CAGGAGGTAAAGGCT[A/G]AGGCTAAGTTGTAAA | 79582 |
rs143099958 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | SPAG16 | GRCh38.p7 | 2:214371200 | TCGACAGGGAAAATG[C/T]GTTGTCCCTGTGTAA | 79582 |
rs143100343 | snp | A/G | 0.00318978 | 0.0398085 | intron-variant | SPAG16 | GRCh38.p7 | 2:213560989 | CTGTCTCAGCCTCCC[A/G]AGTAACTGGGATTAC | 79582 |
rs143101132 | snp | C/T | 0.00597247 | 0.0543191 | intron-variant | SPAG16 | GRCh38.p7 | 2:214044918 | CCTTAACACTGTGGG[C/T]GGAAGTGCTCTGGGG | 79582 |
rs143105173 | snp | G/T | 0.00159617 | 0.0282053 | intron-variant | SPAG16 | GRCh38.p7 | 2:213957091 | ACTTAAGAAGAATGT[G/T]TATGTAGCTGCTGGT | 79582 |
rs143108279 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | SPAG16 | GRCh38.p7 | 2:213778276 | TACTTAACTATAAAA[A/G]TTAAAATAAGAAAGT | 79582 |
rs143109028 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | SPAG16 | GRCh38.p7 | 2:213906000 | TTGAGATGAATAAAT[A/G]AATTTCCTGTCTTGA | 79582 |
rs143110204 | in-del | -/ATAATGTCTGCC | | | intron-variant | SPAG16 | GRCh38.p7 | 2:214187671 | TTAGTCATGTAAACA[-/ATAATGTCTGCC]ATAACAAACCTCAGG | 79582 |
rs143114963 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | SPAG16 | GRCh38.p7 | 2:213969292 | TCCAGATTATGGCTG[A/G]TTGATACCTATGACT | 79582 |
rs143118272 | snp | A/G | 0.00159617 | 0.0282053 | intron-variant | SPAG16 | GRCh38.p7 | 2:213538316 | AGGATTAGGTAGGAT[A/G]TGATGTTACAGCCTG | 79582 |
rs143119035 | snp | A/G | | | intron-variant | SPAG16 | GRCh38.p7 | 2:214196646 | AGTGAAACACAAAGA[A/G]TGAAACCAGTCTATA | 79582 |
rs143124408 | snp | C/G | 0.0182019 | 0.0936463 | intron-variant | SPAG16 | GRCh38.p7 | 2:213675970 | GAATCTATAAATTAC[C/G]TTGGGTAGTATGGCC | 79582 |
rs143128392 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | SPAG16 | GRCh38.p7 | 2:214084048 | CATACAGTTTTGAGA[A/G]AACCATATAACATTT | 79582 |
rs143134797 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant, utr-variant-3-prime | SPAG16 | GRCh38.p7 | 2:213369967 | ACGTTCTGTGGAATT[C/T]AACACATTTATGACG | 79582 |
rs143134936 | snp | A/C | 0.000798403 | 0.0199641 | intron-variant | SPAG16 | GRCh38.p7 | 2:213330035 | GTGTGTGGCCTCTGC[A/C]TAGATTTTAAAAGAT | 79582 |
rs143136815 | in-del | -/T | 0.0973687 | 0.197999 | intron-variant | SPAG16 | GRCh38.p7 | 2:213346842 | TGGTCTAAAATTCTC[-/T]TTTTTTTTTTGTTGT | 79582 |
rs143137506 | snp | A/G | | | intron-variant | SPAG16 | GRCh38.p7 | 2:213414119 | AACCACTCTTTTCCA[A/G]TGTAGACAGTAGGAA | 79582 |
rs143138113 | in-del | -/ACAG | | | intron-variant | SPAG16 | GRCh38.p7 | 2:213871878 | CACACACACACACAC[-/ACAG]AGAGAGAGAGAGAGA | 79582 |
rs143138630 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | SPAG16 | GRCh38.p7 | 2:213498334 | CTTATTTTTTTTATG[A/G]TGAATGGGTTGTAAA | 79582 |
rs143140613 | snp | C/G | 0.00716266 | 0.059414 | intron-variant | SPAG16 | GRCh38.p7 | 2:214280050 | ATTGATGACACCAAC[C/G]ATCACTTTAAGACAC | 79582 |
rs143150079 | snp | A/C | 0.0352966 | 0.128072 | intron-variant | SPAG16 | GRCh38.p7 | 2:214357301 | GGAATAATTTCTCTC[A/C]ATATCCTATGATCTC | 79582 |
rs143155693 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | SPAG16 | GRCh38.p7 | 2:213823102 | CTCAGCAATGGGTTG[A/C]TGGGTCAAATGGTAT | 79582 |
rs143156484 | in-del | -/AT | 0.0283406 | 0.115616 | intron-variant | SPAG16 | GRCh38.p7 | 2:213667717 | AAGAGAGAAATAAAC[-/AT]ATTTATATTCCAAAT | 79582 |
rs143157361 | snp | C/T | 0.0383715 | 0.133092 | intron-variant | SPAG16 | GRCh38.p7 | 2:213948029 | TCTAGTTAATTTCTG[C/T]ACTTTTTTAAAATTT | 79582 |
rs143157426 | snp | A/T | | | intron-variant | SPAG16 | GRCh38.p7 | 2:213305649 | CATTCTTTTGTTATG[A/T]TGTATCACATTGATA | 79582 |
rs143160303 | snp | A/G | 0.00159617 | 0.0282053 | intron-variant | SPAG16 | GRCh38.p7 | 2:213288761 | TAGATACATGTGTTA[A/G]CCACTTTTTCTTCTG | 79582 |
rs143165641 | snp | C/T | 0.00914312 | 0.0669923 | intron-variant | SPAG16 | GRCh38.p7 | 2:213366752 | CCATTGATAGATGAA[C/T]GGATAAGCAAAATGT | 79582 |
rs143166026 | snp | C/T | 0.0126979 | 0.078662 | intron-variant | SPAG16 | GRCh38.p7 | 2:214208725 | GTAGGATATAAATAA[C/T]TCCCACATGCTTAGG | 79582 |
rs143167105 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | SPAG16 | GRCh38.p7 | 2:213669837 | TTCTCACCTCCTGCA[A/G]TAGAAACTTTGCCTC | 79582 |
rs143175004 | snp | C/G | 0.0614824 | 0.164198 | intron-variant | SPAG16 | GRCh38.p7 | 2:213739774 | GGCCAGCTAATTTTT[C/G]TGTTTTTAGTAGAGG | 79582 |
rs143175927 | snp | C/T | 0.00199481 | 0.0315187 | intron-variant | SPAG16 | GRCh38.p7 | 2:213615423 | TGGTGAGACCCTGTC[C/T]CTACTAAAAATGCAA | 79582 |
rs143176809 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | SPAG16 | GRCh38.p7 | 2:213904660 | TTAGGGATGAGACTG[A/G]AATTTAGATAGGCCT | 79582 |
rs143180531 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | SPAG16 | GRCh38.p7 | 2:213697028 | AAGTTCATTAGAAAG[C/T]GAGTCGCAGATGGAG | 79582 |
rs143182285 | snp | A/C | | | intron-variant | SPAG16 | GRCh38.p7 | 2:213350983 | ACAAAAAAAAAAAAA[A/C]AAAAAACAAATAGCC | 79582 |
rs143184727 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | SPAG16 | GRCh38.p7 | 2:213542650 | GTATAAGAATATTGC[A/G]AATTAAAAGATGCAG | 79582 |
rs143201823 | snp | A/C | 0.000399281 | 0.0141238 | upstream-variant-2KB, intron-variant | VWC2L, SPAG16 | GRCh38.p7 | 2:214410077 | TTCATTGCTTATAAA[A/C]TGTGAACACTTGAAA | 79582 |
rs143210643 | snp | A/C | 0.00835141 | 0.0640778 | intron-variant | SPAG16 | GRCh38.p7 | 2:214082637 | TCAACTCTGGCTGCA[A/C]ATTAGAATTACCTGG | 79582 |
rs143211127 | snp | C/T | 0.00953873 | 0.0683987 | intron-variant | SPAG16 | GRCh38.p7 | 2:213566684 | TTATTTTTGCAACAT[C/T]TGCATAACAATCTAA | 79582 |
rs143212410 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | SPAG16 | GRCh38.p7 | 2:214125058 | TTCTTTTTTTTTAAG[A/G]TTTAGCAAATATTCC | 79582 |
rs143212605 | snp | A/C | | | intron-variant | SPAG16 | GRCh38.p7 | 2:214006803 | GCCAGGGATGCCCCA[A/C]ACCTTAAGCCAGTGA | 79582 |
rs143218088 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | SPAG16 | GRCh38.p7 | 2:213964037 | AAATGGAAGTACATA[C/T]AAAACAAGGTTATGC | 79582 |
rs143229287 | snp | A/C | 0.00119737 | 0.0244387 | intron-variant | SPAG16 | GRCh38.p7 | 2:213389970 | CACAGTAGCTGAAAC[A/C]TGGAGACAATTCAGT | 79582 |
rs143229524 | snp | A/T | 0.00199481 | 0.0315187 | utr-variant-3-prime, intron-variant | SPAG16 | GRCh38.p7 | 2:213317683 | GGCTAATTTCTGAAA[A/T]AATAATTAAATTTAT | 79582 |
rs143229995 | in-del | -/AGTG | | | intron-variant | SPAG16 | GRCh38.p7 | 2:213531883 | TGGAATCTTACAATC[-/AGTG]AGTGAACCATCCCTG | 79582 |
rs143231907 | snp | C/G | 0.0023933 | 0.0345097 | intron-variant | SPAG16 | GRCh38.p7 | 2:213411768 | AGTGCTGTGTCATAC[C/G]ATACATCCGTAAGTA | 79582 |
rs143235392 | snp | A/G | 0.00159617 | 0.0282053 | intron-variant | SPAG16 | GRCh38.p7 | 2:214048571 | AAGGGGGTAGTAGAC[A/G]GGTGGCGGGGGGAAG | 79582 |
rs143239054 | snp | C/T | 0.00835141 | 0.0640778 | intron-variant | SPAG16 | GRCh38.p7 | 2:214208039 | GGCTTCCTACCTCCT[C/T]AGTTTGCAGACTGCT | 79582 |
rs143242130 | snp | C/T | 0.000563231 | 0.0167719 | missense, nc-transcript-variant, intron-variant, utr-variant-5-prime | SPAG16 | GRCh38.p7 | 2:213310095 | TCAAAGCATGCAGTA[C/T]CTGAAGTAATAGAAG | 79582 |
rs143246508 | snp | A/T | 0.0287284 | 0.116357 | intron-variant | SPAG16 | GRCh38.p7 | 2:213457592 | CCCTTTTCTTTTTTT[A/T]AAAACCCTTGTATTA | 79582 |
rs143247403 | snp | A/G | 0.0119091 | 0.0762411 | intron-variant | SPAG16 | GRCh38.p7 | 2:213313725 | GTGCCTATTTTCTAT[A/G]TTGGTTTGAGGAATC | 79582 |
rs143252860 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | SPAG16 | GRCh38.p7 | 2:213702890 | GTACTAGCACTCAGA[C/T]CCAAGGAGGTGGGCT | 79582 |
rs143254623 | snp | A/C | 0.000798403 | 0.0199641 | intron-variant | SPAG16 | GRCh38.p7 | 2:214011382 | CTCAAAAAAGATTAA[A/C]TGTCATAAGTAAAAC | 79582 |
rs143265667 | in-del | -/C | | | intron-variant | SPAG16 | GRCh38.p7 | 2:213977443 | AGAGGCAGGTTACTG[-/C]CCCCCCCCATACCCA | 79582 |
rs143275706 | in-del | -/C | 0.0244538 | 0.107838 | intron-variant | SPAG16 | GRCh38.p7 | 2:213437703 | TTTTTTAAAAACATA[-/C]TCAGAGAAACATGGA | 79582 |
rs143282078 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | SPAG16 | GRCh38.p7 | 2:214290810 | CAAACTATGGTTTAT[C/T]CTGAAGAATGTTCCA | 79582 |
rs143286213 | snp | A/G | 0.02016 | 0.0983543 | intron-variant | SPAG16 | GRCh38.p7 | 2:213747177 | AAAAGTTCAAGCAGT[A/G]AAAGATAACAGTTTT | 79582 |
rs143289759 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | SPAG16 | GRCh38.p7 | 2:214167318 | AGGTTCTTCCATCTA[C/T]TACTGCCAGCAGACA | 79582 |
rs143290465 | in-del | -/TATA | 0.0448719 | 0.142907 | intron-variant | SPAG16 | GRCh38.p7 | 2:213981819 | ACATACACACATGCT[-/TATA]TATAATAATCAAATG | 79582 |
rs143297920 | in-del | -/TAAA | | | intron-variant | SPAG16 | GRCh38.p7 | 2:214227739 | GTGTGTGTGTGTGTG[-/TAAA]TGTGTATATCTAAAA | 79582 |
rs143299333 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | SPAG16 | GRCh38.p7 | 2:214404530 | GAATTAATATAGGTA[G/T]ATTTAAAAGTAAAAA | 79582 |
rs143307138 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | SPAG16 | GRCh38.p7 | 2:214369970 | CCCTCACCTCAGTAA[C/T]GAATGTTGAAAACTC | 79582 |
rs143312171 | snp | G/T | 0.00517822 | 0.0506191 | intron-variant | SPAG16 | GRCh38.p7 | 2:214255766 | GAATCTTTTGTGTAA[G/T]ATTTCTTCATATGTG | 79582 |
rs143316429 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | SPAG16 | GRCh38.p7 | 2:213513916 | ACTTCTCTCTCAATC[A/G]TAGATTGCAAATCTT | 79582 |
rs143322781 | snp | A/T | 0.0150606 | 0.0854603 | intron-variant | SPAG16 | GRCh38.p7 | 2:214295027 | ACGGTCACAGTGCCA[A/T]CTGTCTAGGGTCTGG | 79582 |
rs143328357 | snp | A/G | 0.00199481 | 0.0315187 | intron-variant | SPAG16 | GRCh38.p7 | 2:213848592 | ATTGTAGTTATATCT[A/G]TCTGGTTGCCACCCC | 79582 |
rs143329963 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | SPAG16 | GRCh38.p7 | 2:214211973 | CGGGCTACTGTGACA[C/T]TTGGTGCCTATTTGG | 79582 |
rs143330004 | snp | C/T | 0.00914312 | 0.0669923 | intron-variant | SPAG16 | GRCh38.p7 | 2:214152662 | ACTACCACCAATGCG[C/T]GGAGACCAGTAGTGG | 79582 |
rs143334722 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | SPAG16 | GRCh38.p7 | 2:213323782 | CATTCATGCAATGCA[A/G]TACTACTCATCCTTT | 79582 |
rs143340608 | snp | C/T | 0.0130921 | 0.0798413 | intron-variant | SPAG16 | GRCh38.p7 | 2:213430442 | CAAATTCGTAAACTT[C/T]CTGAAAACATTATGA | 79582 |
rs143345054 | snp | C/G | 0.0134861 | 0.0810011 | intron-variant | SPAG16 | GRCh38.p7 | 2:213704976 | AAATTAAATAGGCTA[C/G]GCGCATGGGCTTGCG | 79582 |
rs143347051 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | SPAG16 | GRCh38.p7 | 2:213929762 | CAGTTTCTCTCTTCA[A/G]CTTGAATTACTAAGC | 79582 |
rs143349666 | in-del | -/A | | | intron-variant | SPAG16 | GRCh38.p7 | 2:213672313 | CCCCAAAGAAAAAAA[-/A]TGTTTCTTTCAGCTC | 79582 |
rs143350095 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | SPAG16 | GRCh38.p7 | 2:213623705 | GCACTTTAAAAAGCT[A/G]TAGTAATACATGCAA | 79582 |
rs143350577 | snp | A/T | 0.000798403 | 0.0199641 | intron-variant | SPAG16 | GRCh38.p7 | 2:214353839 | TCCAACCTGCTTCTA[A/T]CACACTTGTGGTTCA | 79582 |
rs143351230 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | SPAG16 | GRCh38.p7 | 2:213394627 | AACCCCAGGAAACCA[C/T]TAATCTTTTCTTCAT | 79582 |
rs143357310 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | SPAG16 | GRCh38.p7 | 2:213475210 | TCTATATAACTGTCC[A/G]GGTCATCTGAAAACC | 79582 |
rs143358365 | snp | C/G | 0.00398564 | 0.0444627 | intron-variant | SPAG16 | GRCh38.p7 | 2:213703046 | TCCATAGAAGTGGAG[C/G]GTGTCACTTCCTGGA | 79582 |
rs143360944 | snp | A/G | 0.0463947 | 0.145069 | intron-variant | SPAG16 | GRCh38.p7 | 2:213348112 | TAGTTAGCTCTTGTC[A/G]AATTGATCCCTTTAC | 79582 |
rs143368926 | snp | A/G | 0.00279162 | 0.0372561 | intron-variant | SPAG16 | GRCh38.p7 | 2:214307263 | TGATTGTGATTATTT[A/G]CTCTTCTCTCTTTTC | 79582 |
rs143380924 | snp | A/C | 0.00199481 | 0.0315187 | intron-variant | SPAG16 | GRCh38.p7 | 2:214220832 | TATGACATGTGCTGA[A/C]GGTATTTTATATTCT | 79582 |
rs143381939 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | SPAG16 | GRCh38.p7 | 2:213984247 | AATATGCTTCAAATT[A/G]ACATTGCATACTGGA | 79582 |
rs143386803 | snp | A/G | 0.0134861 | 0.0810011 | intron-variant | SPAG16 | GRCh38.p7 | 2:214106359 | TTCTTAGCATAATTG[A/G]TTTAAAGTTATAACA | 79582 |
rs143387723 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | SPAG16 | GRCh38.p7 | 2:213933340 | CATTGCCTTCAATGA[A/G]ATTACAAGTAATTTA | 79582 |
rs143394221 | snp | A/C | 0.00636936 | 0.0560724 | intron-variant | SPAG16 | GRCh38.p7 | 2:213431838 | TTCTCCAAGATAGAC[A/C]ATATGTTAGGCCACA | 79582 |
rs143394576 | in-del | -/TCC | 0.0685596 | 0.171987 | intron-variant | SPAG16 | GRCh38.p7 | 2:213929348 | AAACTAGCTTTTGTG[-/TCC]TCCACCACTTGGAAG | 79582 |
rs143395545 | snp | C/T | 0.00279162 | 0.0372561 | intron-variant | SPAG16 | GRCh38.p7 | 2:214381368 | AATGATACCTTTCCA[C/T]GTGGGCAAGTTCTTT | 79582 |
rs143397711 | snp | A/G | 0.0209421 | 0.100162 | intron-variant | SPAG16 | GRCh38.p7 | 2:213793175 | TCAGGTGATCCACCC[A/G]CCTCGGCCTCTCAAA | 79582 |
rs143397812 | snp | C/T | 0.00199481 | 0.0315187 | intron-variant | SPAG16 | GRCh38.p7 | 2:213713524 | GAAGTCACAAGTACC[C/T]TACAAAAGAAAAAAC | 79582 |
rs143399164 | snp | C/T | 0.0452528 | 0.143452 | intron-variant | SPAG16 | GRCh38.p7 | 2:214173629 | AGATGGATTCACAGA[C/T]GAATTCTACCAGAGC | 79582 |
rs143399507 | snp | A/G | 0.00398564 | 0.0444627 | intron-variant | SPAG16 | GRCh38.p7 | 2:213850417 | CAGGGAAAACTGTCT[A/G]TGTTTAGATTTGATG | 79582 |
rs143403078 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | SPAG16, LOC101928084 | GRCh38.p7 | 2:214095426 | CTGGTGTTCACTTTG[A/G]AGTGTGGACTCTGTT | 79582 |
rs143406177 | in-del | -/G | 0.040671 | 0.13668 | intron-variant | SPAG16, LOC101928084 | GRCh38.p7 | 2:214094971 | GAGAGGACTTGGGGA[-/G]GGGGCTGCATGTGGG | 79582 |
rs143406246 | in-del | -/GACAAGA | 0.181022 | 0.240296 | intron-variant | SPAG16 | GRCh38.p7 | 2:213546580 | AACTCCATTCTTGTG[-/GACAAGA]GATAATAAACAAATA | 79582 |
rs143406632 | snp | A/G | 0.0023933 | 0.0345097 | intron-variant | SPAG16 | GRCh38.p7 | 2:213841600 | TATTTTAAAGGTTTC[A/G]TTATTTTTCTGGTTT | 79582 |
rs143407801 | snp | A/T | 0.00478085 | 0.0486577 | intron-variant | SPAG16 | GRCh38.p7 | 2:214290178 | AGGAATTCATCCATT[A/T]CTTCTAGGTTTTCCA | 79582 |
rs143409561 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | SPAG16 | GRCh38.p7 | 2:213515496 | CTGTGTCCCTGATGC[A/G]AGCATAAAGTATGTG | 79582 |
rs143412380 | snp | C/T | 0.02016 | 0.0983543 | intron-variant | SPAG16 | GRCh38.p7 | 2:214374732 | AATCATTATATGAAA[C/T]AGAACATTAGATTTC | 79582 |
rs143417652 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | SPAG16 | GRCh38.p7 | 2:213635304 | GCTCCCAAAGTGCTC[A/G]GATTACAGGCGTGAG | 79582 |
rs143417875 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | SPAG16 | GRCh38.p7 | 2:213648138 | CTTCATTTGCAAGAC[A/G]TAACCATTTTTTATA | 79582 |
rs143423951 | snp | A/G | 0.00159617 | 0.0282053 | intron-variant | SPAG16 | GRCh38.p7 | 2:214058755 | TGTAGTAAAGGAAGG[A/G]AAACAAACAATATAT | 79582 |
rs143424070 | snp | C/T | 0.00358779 | 0.0422022 | intron-variant | SPAG16 | GRCh38.p7 | 2:213519312 | TATGATTTGGCTTGG[C/T]GTCCCCACCCAAATC | 79582 |
rs143428911 | snp | C/G | 0.0103295 | 0.0711199 | intron-variant | SPAG16 | GRCh38.p7 | 2:213351605 | TATATAAAACTGCAA[C/G]TATGCTTAACATTCT | 79582 |
rs143439287 | snp | A/C/G | | | intron-variant | SPAG16 | GRCh38.p7 | 2:213797842 | GGTAGATAACTAGGA[A/C/G]TAGAGCTGCTGTCTT | 79582 |
rs143442843 | snp | C/T | 0.00159617 | 0.0282053 | intron-variant | SPAG16 | GRCh38.p7 | 2:214199369 | CAGGGTGTCCTTTCC[C/T]CAATTTGTGTTTTTG | 79582 |
rs143452004 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | SPAG16 | GRCh38.p7 | 2:213868465 | AGAGTTACATAATCA[A/G]TATTCAGGTTAATAA | 79582 |
rs143453156 | snp | G/T | 0.000798403 | 0.0199641 | intron-variant | SPAG16 | GRCh38.p7 | 2:213534193 | TTTTTCTACAATGGT[G/T]TTAATCTTTGGGCTA | 79582 |
rs143455266 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | SPAG16 | GRCh38.p7 | 2:214317067 | ACATCCCAGGTTGCC[G/T]TGCCTGCTGCTGATT | 79582 |
rs143455640 | snp | C/T | 0.0023933 | 0.0345097 | intron-variant | SPAG16 | GRCh38.p7 | 2:214254540 | CTTAAAACAATCGGT[C/T]AGCTTAGTCAGTCAG | 79582 |
rs143456103 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | SPAG16 | GRCh38.p7 | 2:213775692 | TTATGAGTTTGGCTA[C/T]TTTAGATTCTTCATA | 79582 |
rs143458037 | snp | A/C | 0.00557542 | 0.0525036 | intron-variant | SPAG16 | GRCh38.p7 | 2:214405286 | TGCCACCATACCTGG[A/C]TAATTTTCTTTTAAA | 79582 |
rs143463313 | snp | C/T | 0.00676609 | 0.0577691 | intron-variant | SPAG16 | GRCh38.p7 | 2:214072051 | TCACAAATTGAACTT[C/T]TTTAAAAGCATTATT | 79582 |
rs143466008 | in-del | -/ACTT | 0.0146672 | 0.084371 | intron-variant | SPAG16 | GRCh38.p7 | 2:214369266 | CAAAGTACTGTCTCA[-/ACTT]ACTTAAAGACTGTAT | 79582 |
rs143466718 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | SPAG16 | GRCh38.p7 | 2:213995433 | TGCCATGAATAGCAT[A/G]TATGGAATTACTTTT | 79582 |
rs143467939 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | SPAG16 | GRCh38.p7 | 2:213709619 | ACACTATCAAAAGCT[A/G]TGTTGTGGACCTTAC | 79582 |
rs143471116 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | SPAG16 | GRCh38.p7 | 2:213386651 | TATCTTTTATAACAT[C/T]ATAAATCACATTTTA | 79582 |
rs143483337 | snp | A/G | 0.00398564 | 0.0444627 | intron-variant | SPAG16 | GRCh38.p7 | 2:213402058 | TAATTTATAAAGACA[A/G]TGCTTATTTCAATTT | 79582 |
rs143485127 | snp | A/G | | | intron-variant | SPAG16 | GRCh38.p7 | 2:214186125 | CAACAAGCATTACTG[A/G]ATAAACTGGGGAATT | 79582 |
rs143491658 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | SPAG16 | GRCh38.p7 | 2:213853324 | TTCACCATACACCTA[C/G]ACACACTCCCTCCAA | 79582 |
rs143494671 | snp | A/C/G | 0.0123036 | 0.0774623 | intron-variant | SPAG16 | GRCh38.p7 | 2:213723984 | TGGTCATCAGGGTGA[A/C/G]AGAGAGAAAGAAAGA | 79582 |
rs143495886 | snp | C/T | 0.00159617 | 0.0282053 | intron-variant | SPAG16 | GRCh38.p7 | 2:214258771 | TAGTATATCTTCAGC[C/T]GCCTTCCTTTCTTCA | 79582 |
rs143497966 | snp | A/C | 0.0103295 | 0.0711199 | intron-variant | SPAG16 | GRCh38.p7 | 2:214205599 | TTGAAGCACATCTCA[A/C]CTAAAGATATTTATG | 79582 |
rs143503951 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | SPAG16 | GRCh38.p7 | 2:214131433 | CTATTTGTTTGTATA[A/G]GGTAACATGTTATAA | 79582 |
rs143512813 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | SPAG16 | GRCh38.p7 | 2:213800786 | TTTGTATAAACATAA[C/G]GTCCCAATTCTGCTT | 79582 |
rs143519373 | snp | A/G | 0.00716266 | 0.059414 | intron-variant | SPAG16 | GRCh38.p7 | 2:213924101 | CTAGAAGCTGGTGCT[A/G]AGCCCCATCTGGCAA | 79582 |
rs143523932 | snp | A/G | 0.00398564 | 0.0444627 | intron-variant | SPAG16 | GRCh38.p7 | 2:213985178 | CTATTAAAAGAATGA[A/G]TAAATTAAGAAGTGG | 79582 |
rs143524193 | snp | G/T | 0.00438332 | 0.0466095 | intron-variant | SPAG16 | GRCh38.p7 | 2:213605298 | TTGAGATGGAGTCTC[G/T]CACTGTCACCCAGGC | 79582 |
rs143524809 | snp | G/T | 0.0023933 | 0.0345097 | intron-variant | SPAG16 | GRCh38.p7 | 2:213589741 | AGGCTGGACAACATG[G/T]TGAAATCCCGTCTGT | 79582 |
rs143526453 | snp | C/T | 0.00199481 | 0.0315187 | intron-variant | SPAG16 | GRCh38.p7 | 2:214044612 | CTGCTTTTAACTTCA[C/T]ACTGAAAGAGGCACT | 79582 |
rs143528768 | snp | A/G | 0.00398564 | 0.0444627 | intron-variant | SPAG16 | GRCh38.p7 | 2:214341114 | AGTGCCTAAAAGGGA[A/G]CAACTTGAAAAAGAA | 79582 |
rs143532529 | snp | A/C | 0.00716266 | 0.059414 | intron-variant | SPAG16 | GRCh38.p7 | 2:213672229 | GGGGCCTAGTACTAT[A/C]ATGACATGTCTTGTT | 79582 |
rs143533135 | snp | C/T | 0.00199481 | 0.0315187 | intron-variant | SPAG16 | GRCh38.p7 | 2:213671968 | TTTATCTGAAAATAT[C/T]TATTATGCATCATCA | 79582 |
rs143535244 | snp | C/G | 0.00358779 | 0.0422022 | intron-variant | SPAG16 | GRCh38.p7 | 2:213919794 | GGGGAGAGTTCTGTA[C/G]ATATCTATCAGGTCC | 79582 |
rs143537843 | snp | A/G | | | intron-variant | SPAG16 | GRCh38.p7 | 2:214291175 | GACATAAGCATAGCT[A/G]CTCCTGCTCGCTTTT | 79582 |
rs143540740 | snp | C/T | 0.126564 | 0.217402 | intron-variant | SPAG16 | GRCh38.p7 | 2:213612962 | ACAGGCGTGAACCAC[C/T]GTGCCCGGCCCGAAT | 79582 |
rs143541294 | snp | A/G | 0.0166325 | 0.0896639 | intron-variant | SPAG16 | GRCh38.p7 | 2:214242989 | GACTTGGGAAAATCA[A/G]TAATTGGAAAGATAA | 79582 |
rs143542358 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | SPAG16 | GRCh38.p7 | 2:213559546 | AAATTATGTTTTAGA[C/T]TTTGAATATTTGTTA | 79582 |
rs143546713 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | SPAG16 | GRCh38.p7 | 2:213693013 | ACATATAACTGGAAT[A/C]TTTATTACAAAAGAA | 79582 |
rs143549958 | snp | C/T | 0.0103295 | 0.0711199 | intron-variant | SPAG16 | GRCh38.p7 | 2:213346669 | TTGGCTCTGTTTATA[C/T]GCTGGATTATGTTTA | 79582 |
rs143551069 | snp | C/T | 0.00318978 | 0.0398085 | intron-variant | SPAG16 | GRCh38.p7 | 2:214119047 | CTGATTTGAGCATTA[C/T]TCAATGTACCCATGT | 79582 |
rs143551547 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | SPAG16 | GRCh38.p7 | 2:213393005 | TTCTGTGCTAAGTAG[A/G]AAATCAAATAAACAG | 79582 |
rs143551634 | in-del | -/T | 0.00676609 | 0.0577691 | intron-variant | SPAG16 | GRCh38.p7 | 2:213434460 | TAATAAAAACAAAAA[-/T]AGATAAGTGGGACTT | 79582 |
rs143554566 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | SPAG16 | GRCh38.p7 | 2:213452396 | CCTTGTTGCTCCTCT[A/G]CATCCCTCACTCTAT | 79582 |
rs143557940 | snp | C/G | | | intron-variant | SPAG16 | GRCh38.p7 | 2:213927869 | GAAAGATAGATTTGA[C/G]AAAGAAGCATGCTTA | 79582 |
rs143559366 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | SPAG16 | GRCh38.p7 | 2:213781092 | TACATTACAGACATT[A/G]TATGTTACTCAGCAA | 79582 |
rs143564474 | in-del | -/AG | 0.0205511 | 0.0992634 | intron-variant | SPAG16 | GRCh38.p7 | 2:213829438 | CAGAAAAGCCATCTA[-/AG]AGAGTCAAGGCCTGA | 79582 |
rs143567941 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | SPAG16 | GRCh38.p7 | 2:214375119 | TTTTCAGGCAGGTAC[A/G]TGTTAAAGATTAGGG | 79582 |
rs143571112 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | SPAG16 | GRCh38.p7 | 2:213343993 | TTCAAATTATTTACT[C/T]AGGAAGACTGGAGTT | 79582 |
rs143571752 | snp | C/T | 0.00438332 | 0.0466095 | intron-variant | SPAG16 | GRCh38.p7 | 2:213843340 | CAGAACCGTACAATC[C/T]ACAGTGACTAATCTA | 79582 |
rs143573242 | snp | C/T | 0.0023933 | 0.0345097 | intron-variant | SPAG16 | GRCh38.p7 | 2:214001973 | GAGGAGGCTTCACAA[C/T]TGTGGCTGAATGTGA | 79582 |
rs143573914 | in-del | -/TG | | | intron-variant | SPAG16 | GRCh38.p7 | 2:213913499 | GTGTGTCTGTGTGTC[-/TG]TGTGTGTGTGTGTGT | 79582 |
rs143576939 | in-del | -/TA | 0.0138799 | 0.0821421 | intron-variant | SPAG16 | GRCh38.p7 | 2:214170532 | TCCCTTGCTGGGTTG[-/TA]TATACATAAAAAGGG | 79582 |
rs143579030 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | SPAG16 | GRCh38.p7 | 2:214139244 | AATGCCATTTTGCTG[A/C]AGAATTAACAGTGAA | 79582 |
rs143579471 | snp | G/T | 0.345037 | 0.231231 | intron-variant | SPAG16 | GRCh38.p7 | 2:213367814 | CCATTTGTCAATTTT[G/T]GCTTTTGTTGCCATT | 79582 |
rs143585797 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | SPAG16 | GRCh38.p7 | 2:213689114 | ACAGGCTCCTGCCAC[A/G]GTGCCTGGTTAGTGT | 79582 |
rs143589519 | snp | C/T | 0.00953873 | 0.0683987 | intron-variant | SPAG16 | GRCh38.p7 | 2:213333092 | TGTTTGCAGATGATA[C/T]GATCTTATATTTGGA | 79582 |
rs143600859 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | SPAG16 | GRCh38.p7 | 2:213475665 | ATAGTCATGCTTACC[C/T]GCACTCTGTCCTAGC | 79582 |
rs143602373 | in-del | -/CA | | | intron-variant | SPAG16 | GRCh38.p7 | 2:214168508 | GCACGCACACACATG[-/CA]CACACACACACATTC | 79582 |
rs143604727 | snp | A/C | 0.00119737 | 0.0244387 | intron-variant | SPAG16 | GRCh38.p7 | 2:213563505 | GAACTCTCTTTCTGG[A/C]TTGCAGATTACTGCC | 79582 |
rs143609886 | snp | A/G | 0.00159617 | 0.0282053 | intron-variant | SPAG16 | GRCh38.p7 | 2:213768012 | ACAGCTCTTAACTCA[A/G]TTTGGCAATGGTGGG | 79582 |
rs143610115 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | SPAG16 | GRCh38.p7 | 2:213828107 | TAAATTTTCTACCCC[A/G]TCTCTCTCTTTCTCT | 79582 |
rs143621172 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | SPAG16 | GRCh38.p7 | 2:214142421 | TATATTAGCTTTAGA[G/T]CTCCTTGCATGTTAT | 79582 |
rs143629213 | snp | A/G | 0.00636936 | 0.0560724 | intron-variant | SPAG16 | GRCh38.p7 | 2:214013773 | TTTATGCTACTAATC[A/G]TATAAAGTGCTGAGA | 79582 |
rs143639556 | snp | C/T | 0.00318978 | 0.0398085 | intron-variant | SPAG16 | GRCh38.p7 | 2:214024708 | AGCTAAAACCAAAGA[C/T]TGATGGAAAGTTGAA | 79582 |
rs143640051 | snp | A/G/T | 0.00637439 | 0.0561611 | intron-variant | SPAG16 | GRCh38.p7 | 2:213887426 | TCTCATATCGTATTC[A/G/T]TCTGATGTTTTCTCC | 79582 |
rs143642366 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | SPAG16 | GRCh38.p7 | 2:213668671 | TTGCGATGGAGTCTT[A/G]CTCTGTCACCCAGAG | 79582 |
rs143648392 | in-del | -/GGGGGGGT | | | intron-variant | SPAG16 | GRCh38.p7 | 2:213959866 | CTAGAAGAGTGGCTG[-/GGGGGGGT]TTTTGGTTTATGAGT | 79582 |
rs143649230 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | SPAG16 | GRCh38.p7 | 2:213352523 | TATACCATGTACAAT[A/G]TTTGTGTTTCAAGTT | 79582 |
rs143651586 | snp | A/C | 0.00398564 | 0.0444627 | intron-variant | SPAG16 | GRCh38.p7 | 2:213432887 | ATCCAAGAGCACTCC[A/C]AAAAGATAATACACC | 79582 |
rs143653112 | snp | C/T | 0.00318978 | 0.0398085 | intron-variant | SPAG16 | GRCh38.p7 | 2:213691727 | TTATCATTTAACATA[C/T]TATATGATTTGTGAT | 79582 |
rs143654662 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | SPAG16, LOC101928084 | GRCh38.p7 | 2:214091003 | AGTTTAAGTCTGTCT[C/T]GAGGTCATAAAATGT | 79582 |
rs143660514 | snp | A/C | 0.00478085 | 0.0486577 | intron-variant | SPAG16 | GRCh38.p7 | 2:213420306 | TAATCCATCAAAAGA[A/C]ACTGTCAGTGTATCC | 79582 |
rs143664362 | snp | G/T | 0.0115144 | 0.0749975 | intron-variant | SPAG16 | GRCh38.p7 | 2:213333308 | CAAATAAATGAAATA[G/T]CTCTACAATGAAAAC | 79582 |
rs143664415 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | SPAG16 | GRCh38.p7 | 2:214228579 | ACTATATCAATGGTT[A/C]TCAAAGTGTGCAGTA | 79582 |
rs143669254 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | SPAG16 | GRCh38.p7 | 2:213432717 | AACTCTTTCAAAAAA[C/T]TGAGGTGGTGGGAAT | 79582 |
rs143669351 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | SPAG16 | GRCh38.p7 | 2:213482639 | ATTATGTTCTTCTTA[G/T]GTAATTATAAACCAT | 79582 |
rs143679267 | snp | C/G | | | intron-variant | SPAG16 | GRCh38.p7 | 2:214028318 | CACTGCTGTCAATGT[C/G]TTAGTTCCTAAAAGC | 79582 |
rs143682583 | snp | A/G | 0.00159617 | 0.0282053 | intron-variant | SPAG16 | GRCh38.p7 | 2:213311971 | TCACTCCTCAAGCAG[A/G]AAATGCAATAGATCC | 79582 |
rs143700488 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | SPAG16 | GRCh38.p7 | 2:213772314 | TGAGACCACCCTCAA[C/G]ATGCCAGATCTTGAC | 79582 |
rs143711613 | snp | C/T | 0.00318978 | 0.0398085 | intron-variant, upstream-variant-2KB | SPAG16, LOC101928084 | GRCh38.p7 | 2:214103085 | CCATCTGAGGTTTTT[C/T]CCTTTCTCCAGTGGC | 79582 |
rs143714356 | snp | C/T | | | intron-variant | SPAG16 | GRCh38.p7 | 2:214211649 | TGACTAGAGAGGGGA[C/T]CTGCAACCAAGACTG | 79582 |
rs143717030 | snp | C/G | 0.000798403 | 0.0199641 | intron-variant | SPAG16 | GRCh38.p7 | 2:214106927 | AGAAAAACTCCCTTC[C/G]TATACTTTGGCTATA | 79582 |
rs143723629 | snp | G/T | 0.0154538 | 0.0865337 | intron-variant | SPAG16 | GRCh38.p7 | 2:214328546 | CTGAGCTCCCGCAAT[G/T]TCCTTGCATGAGCTA | 79582 |
rs143728226 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | SPAG16 | GRCh38.p7 | 2:213892660 | CTGAGAAATACATAA[A/G]CTGAAGTAAAAAATT | 79582 |
rs143737827 | in-del | -/ATA | | | intron-variant | SPAG16 | GRCh38.p7 | 2:214301029 | CCTAAAACTTAAAGT[-/ATA]ATAATAATAATAATA | 79582 |
rs143757044 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | SPAG16 | GRCh38.p7 | 2:214235002 | TATTGAGGTCATAGT[C/T]TGGAATATTATGAAA | 79582 |
rs143761374 | snp | G/T | 0.00318978 | 0.0398085 | intron-variant | SPAG16 | GRCh38.p7 | 2:213562178 | GTCTTTCAGAATTCA[G/T]AGTTGCTAATATGAA | 79582 |
rs143770547 | snp | G/T | | | intron-variant | SPAG16 | GRCh38.p7 | 2:214335483 | GAATATATATATATA[G/T]AGATATATATATAAT | 79582 |
rs143772132 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | SPAG16 | GRCh38.p7 | 2:213723527 | AGGACAGAGAGCTTA[A/C]CCAGTCTCAAATTTT | 79582 |
rs143773904 | snp | A/G | 0.0142736 | 0.0832652 | intron-variant | SPAG16 | GRCh38.p7 | 2:213954706 | GATCCCACAGTGACT[A/G]TAGGTTAATGTTTAA | 79582 |
rs143774027 | snp | G/T | 0.000798403 | 0.0199641 | intron-variant | SPAG16 | GRCh38.p7 | 2:213416944 | AGGACAGACTTAACA[G/T]TTTAGAATTGGCTAG | 79582 |
rs143774680 | snp | A/G | 0.00438332 | 0.0466095 | intron-variant | SPAG16 | GRCh38.p7 | 2:214396003 | CACACGTGTGCATGT[A/G]TCTTTATGGTAGAGT | 79582 |
rs143779745 | in-del | -/A | 0.089084 | 0.191327 | intron-variant | SPAG16 | GRCh38.p7 | 2:213933196 | TCAGAAAATAGCTAT[-/A]AAAAATAATTTGTAT | 79582 |
rs143780281 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | SPAG16 | GRCh38.p7 | 2:214319911 | AGGATATGCTTTTCA[A/C]ATAGCTGCCTTCATC | 79582 |
rs143784588 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | SPAG16 | GRCh38.p7 | 2:213364860 | ATTGCAAATCTGGCC[A/G]TGCCTGGGTGGAAAG | 79582 |
rs143785591 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | SPAG16 | GRCh38.p7 | 2:213673168 | AAAATTATCAGACTG[C/T]CACAGCATTTGGTAA | 79582 |
rs143787485 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | SPAG16 | GRCh38.p7 | 2:214066458 | CTTAAAATTAAGCAT[G/T]TCCATAAAACTTTAC | 79582 |
rs143791056 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | SPAG16 | GRCh38.p7 | 2:213499987 | CTATTTGGCCTTCTC[A/G]ATTCTAAATTTTGAC | 79582 |
rs143791880 | snp | A/G | 0.00199481 | 0.0315187 | intron-variant | SPAG16 | GRCh38.p7 | 2:214120101 | AATTTTTCAGCCATT[A/G]TGTTATTAAATATTG | 79582 |
rs143793350 | in-del | -/A | 0.0189856 | 0.0955633 | intron-variant | SPAG16 | GRCh38.p7 | 2:213871030 | CAGAAGGTATTATGT[-/A]ATTTTAGGGACATAC | 79582 |
rs143806977 | snp | C/T | 0.00636936 | 0.0560724 | intron-variant | SPAG16 | GRCh38.p7 | 2:214025437 | AGCTTGTCACTGTTA[C/T]TCATTCTTTTATACA | 79582 |
rs143808606 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | SPAG16 | GRCh38.p7 | 2:213931175 | TTATTATTGTTACAA[C/T]GATAGGTGCAAGTTC | 79582 |
rs143809565 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | SPAG16 | GRCh38.p7 | 2:213959042 | AGAAAGTTCGTTGAC[A/G]GTTTTTGTTTTTCCT | 79582 |
rs143814263 | snp | C/T | 0.00199481 | 0.0315187 | intron-variant | SPAG16 | GRCh38.p7 | 2:214378825 | CTGTGCCCTCAGTCA[C/T]AGACCTAGGAAACAA | 79582 |
rs143814918 | snp | C/T | 0.00159617 | 0.0282053 | intron-variant | SPAG16 | GRCh38.p7 | 2:214408647 | TAGCTTTTATGGTGA[C/T]ATAATTCTAGAATTC | 79582 |
rs143817084 | snp | C/T | 0.0283406 | 0.115616 | intron-variant | SPAG16 | GRCh38.p7 | 2:213819915 | GTGCCTGCCACCACA[C/T]CCGGCTAATTTTTCT | 79582 |
rs143819585 | snp | A/C | 0.00318978 | 0.0398085 | intron-variant | SPAG16 | GRCh38.p7 | 2:213681584 | TGCTTCTGAGACAGG[A/C]ATCCATTCTTATTAT | 79582 |
rs143819590 | snp | A/T | 0.00358779 | 0.0422022 | intron-variant | SPAG16 | GRCh38.p7 | 2:214126576 | TATGTGACTGTACTT[A/T]TGCACATATTAAGAG | 79582 |
rs143822111 | snp | A/C | 0.00199481 | 0.0315187 | intron-variant | SPAG16 | GRCh38.p7 | 2:213449282 | GATGTTTATCAAGAC[A/C]ATACATGCACCACTG | 79582 |
rs143823965 | snp | A/G | 0.00358779 | 0.0422022 | intron-variant | SPAG16 | GRCh38.p7 | 2:213536126 | TTAAATTTTGACTTA[A/G]TCTTTTGTATAGTTC | 79582 |
rs143827159 | snp | A/T | 0.000798403 | 0.0199641 | intron-variant | SPAG16 | GRCh38.p7 | 2:213591173 | TAGGTTATAGGAAGC[A/T]TTATGATCTGTCACT | 79582 |
rs143834548 | snp | A/T | 0.00914312 | 0.0669923 | intron-variant | SPAG16 | GRCh38.p7 | 2:213541242 | AAACCTGTAGTCTCT[A/T]GAGGAAAATCCCTCA | 79582 |
rs143834780 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | SPAG16 | GRCh38.p7 | 2:214333217 | AAGAGATCTTGGCTT[C/T]TTATTGGTGCTTCTG | 79582 |
rs143834911 | snp | C/T | 0.00557542 | 0.0525036 | intron-variant | SPAG16 | GRCh38.p7 | 2:213794197 | GTTCTCCTGTTGTAT[C/T]CTAAAAAGACTCGCT | 79582 |
rs143841826 | snp | A/C | 0.000798403 | 0.0199641 | intron-variant | SPAG16 | GRCh38.p7 | 2:214215885 | GTCTAGATCCTAATC[A/C]ATTCAGACTTTTTCC | 79582 |
rs143843919 | snp | A/C | | | intron-variant | SPAG16 | GRCh38.p7 | 2:213600270 | ACACATACGTTATGC[A/C]TCTCAGATTTGCAAC | 79582 |
rs143844398 | snp | A/T | 0.0023933 | 0.0345097 | intron-variant | SPAG16 | GRCh38.p7 | 2:214004085 | CAAATTTTTCAAGCT[A/T]CTGCCCATGCCTGTG | 79582 |
rs143850926 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | SPAG16 | GRCh38.p7 | 2:213891104 | ATTAAACATCATTTT[A/G]TAAACACAGAATATA | 79582 |
rs143851150 | snp | A/C | 0.00159617 | 0.0282053 | intron-variant | SPAG16 | GRCh38.p7 | 2:213368388 | TGCTAAAAACTCTCA[A/C]AAATTCGTTATTGAT | 79582 |
rs143856032 | snp | A/T | 0.0107246 | 0.0724382 | intron-variant | SPAG16 | GRCh38.p7 | 2:213797131 | CAGCTGTACAATGTA[A/T]GTTTTAAGCTAACTG | 79582 |
rs143864316 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | SPAG16, LOC101928084 | GRCh38.p7 | 2:214093696 | TAAGAGAGTATAGCT[A/G]TTAACTTAATGCTCT | 79582 |
rs143868924 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | SPAG16 | GRCh38.p7 | 2:214188520 | GGACTTATTAAACTA[A/G]ATATCTGGATCTATT | 79582 |
rs143876862 | snp | A/G | 0.0126979 | 0.078662 | intron-variant | SPAG16 | GRCh38.p7 | 2:213742880 | TTATTTCTTAATTCT[A/G]CAAATTTGCCAGTAT | 79582 |
rs143878054 | snp | A/G | 0.00993419 | 0.0697739 | intron-variant | SPAG16 | GRCh38.p7 | 2:213314947 | CTTAATCTTCAGGAT[A/G]TTCTATGGGGGGGTC | 79582 |
rs143886626 | snp | A/G | 0.0150606 | 0.0854603 | intron-variant | SPAG16 | GRCh38.p7 | 2:213727067 | ATATTATCAAATCAC[A/G]ATCCCCAACTTCTCA | 79582 |
rs143886862 | snp | A/T | 0.0185938 | 0.0946107 | intron-variant | SPAG16 | GRCh38.p7 | 2:213633148 | CTTCAATCTTGTTAC[A/T]TGTTATTGGTCAGTT | 79582 |
rs143887331 | snp | A/T | 0.0154538 | 0.0865337 | intron-variant | SPAG16 | GRCh38.p7 | 2:213453597 | GCAGGATGAACCACT[A/T]AAGTAAGGGAGACCC | 79582 |
rs143888545 | in-del | -/AATA | 0.00636936 | 0.0560724 | intron-variant | SPAG16 | GRCh38.p7 | 2:214171448 | AGATGCTAGCATATC[-/AATA]AATAGTTTATATATT | 79582 |
rs143888958 | in-del | -/ATA | | | intron-variant | SPAG16 | GRCh38.p7 | 2:213992679 | AGGTGCAAAAATTGC[-/ATA]ATAAGTTATTTAGCT | 79582 |
rs143892007 | snp | A/T | 0.0111196 | 0.0737302 | intron-variant, utr-variant-5-prime | SPAG16 | GRCh38.p7 | 2:213296306 | ATTTAAATTGGAAAA[A/T]ACATCTGATTCTTTT | 79582 |
rs143892800 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | SPAG16 | GRCh38.p7 | 2:213410129 | AAGAATGTGCCACCC[C/T]CTCCAGAGTCGTGGG | 79582 |
rs143898713 | in-del | -/G | 0.272241 | 0.249009 | intron-variant | SPAG16 | GRCh38.p7 | 2:213826502 | CTTCCTTGACCCACT[-/G]GATCATTCAGGAGCA | 79582 |
rs143904882 | snp | A/G | 0.00159617 | 0.0282053 | intron-variant | SPAG16 | GRCh38.p7 | 2:214084438 | TTTCTCACACCTTAC[A/G]ACATGAACTCCCCCT | 79582 |
rs143906562 | snp | C/T | 0.0023933 | 0.0345097 | intron-variant | SPAG16 | GRCh38.p7 | 2:214193671 | AAAATGTGTGTCAAG[C/T]TGCTGACAAAAGGGA | 79582 |
rs143910780 | snp | C/T | 0.00636936 | 0.0560724 | intron-variant | SPAG16 | GRCh38.p7 | 2:213333764 | GGAAAAGGCAGTCTC[C/T]TCAATAAATGGTGCT | 79582 |
rs143916986 | snp | A/G | 0.00279162 | 0.0372561 | intron-variant | SPAG16 | GRCh38.p7 | 2:213336608 | CCACAGCGCAGCACA[A/G]CAGCTGTGTCAGTTC | 79582 |
rs143919424 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | SPAG16 | GRCh38.p7 | 2:214314515 | CTACAGTCAGTCTCT[A/G]TGGGTTTGAATCCCA | 79582 |
rs143925088 | snp | A/G | 0.000139968 | 0.00836447 | missense, nc-transcript-variant, utr-variant-5-prime | SPAG16 | GRCh38.p7 | 2:213340170 | TTTTTCAGCAAAGCT[A/G]GAGAAGATTTGCTGA | 79582 |
rs143925882 | in-del | -/TTG | | | intron-variant | SPAG16 | GRCh38.p7 | 2:213705787 | ATCATGGTGGAGGGT[-/TTG]TTGTTGTTGTTGTTG | 79582 |
rs143926269 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | SPAG16 | GRCh38.p7 | 2:213414767 | AACCGCTGATAAACT[A/G]TTTGACCTAGAGTCT | 79582 |
rs143931930 | snp | C/T | 0.0263992 | 0.111815 | intron-variant | SPAG16 | GRCh38.p7 | 2:213948873 | AGTTAAATTACTTCT[C/T]TAATACTCTTCTCTT | 79582 |
rs143933954 | snp | A/G | 0.0138799 | 0.0821421 | intron-variant | SPAG16 | GRCh38.p7 | 2:213863434 | TATTTTATCTTTGCT[A/G]TGAATGTCTATGAAA | 79582 |
rs143938074 | snp | A/G | 0.00159617 | 0.0282053 | intron-variant | SPAG16 | GRCh38.p7 | 2:214401860 | TTTTTGCTAGTGTAT[A/G]TGTTACGTGTTTAGA | 79582 |
rs143947286 | snp | A/G | 0.000185938 | 0.00964025 | upstream-variant-2KB, missense, nc-transcript-variant | VWC2L, SPAG16 | GRCh38.p7 | 2:214410304 | GACGGCACAGTTCGA[A/G]CGTGGTCTTGACCGT | 79582 |
rs143948307 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | SPAG16 | GRCh38.p7 | 2:214346399 | GAAGAATGCCTGATT[C/G]AAATCTCTTGTTCAT | 79582 |
rs143952727 | snp | A/C | 0.0023933 | 0.0345097 | intron-variant | SPAG16 | GRCh38.p7 | 2:213703111 | CTCTTTTTCCCTCTC[A/C]TGTGATAATAGACAT | 79582 |
rs143953734 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | SPAG16 | GRCh38.p7 | 2:213690211 | CTAGACTTAACTCTT[C/T]GTCTTAGTCTTAGTC | 79582 |
rs143953809 | snp | C/T | 0.00557542 | 0.0525036 | intron-variant | SPAG16, LOC101928084 | GRCh38.p7 | 2:214086605 | AGAGATGCCTTCCAC[C/T]GTGATTATGTTTCCT | 79582 |
rs143957390 | snp | C/T | 0.00159617 | 0.0282053 | intron-variant | SPAG16 | GRCh38.p7 | 2:213584997 | AGTTCAAGATCAGCC[C/T]GGCCAACATGGCGAA | 79582 |
rs143960122 | snp | A/G | 0.00199481 | 0.0315187 | intron-variant | SPAG16 | GRCh38.p7 | 2:214022833 | TCCATTTATATTAAC[A/G]CCAAGCCATAGTACA | 79582 |
rs143965399 | in-del | -/T | 0.0217236 | 0.101931 | intron-variant | SPAG16 | GRCh38.p7 | 2:213897149 | TTTGATCTTTACCAA[-/T]TATATGAGTGTATTA | 79582 |
rs143966101 | snp | A/T | 0.00953873 | 0.0683987 | intron-variant | SPAG16 | GRCh38.p7 | 2:214296601 | CTGGTGTGATGTGTT[A/T]TCTTATTGTGGTTTT | 79582 |
rs143967844 | snp | A/G | 0.00318978 | 0.0398085 | intron-variant | SPAG16 | GRCh38.p7 | 2:213708735 | AGGCTGCAGTGAGCC[A/G]AGACCATGCCATTGC | 79582 |
rs143971000 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | SPAG16 | GRCh38.p7 | 2:214379580 | ACAGGGAGGCTAAGA[A/G]GTCTGAAGACATCGG | 79582 |
rs143972730 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | SPAG16 | GRCh38.p7 | 2:213473752 | CACTATTATCCCACA[C/T]CCTTAATATCCATTC | 79582 |
rs143972731 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | SPAG16 | GRCh38.p7 | 2:213791557 | GGGATTAGACTAGTG[C/T]TCTCTCAGCAGTGGT | 79582 |
rs143972867 | snp | A/G | | | intron-variant | SPAG16 | GRCh38.p7 | 2:213848532 | TTGGCTGAATTGGCC[A/G]CCCAATCCTTCCCCT | 79582 |
rs143974072 | in-del | -/G | 0.170733 | 0.237101 | intron-variant | SPAG16 | GRCh38.p7 | 2:213496270 | ATTTTCTGTTGGGCT[-/G]GTTGTGGAGTGAAAG | 79582 |
rs143983682 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | SPAG16 | GRCh38.p7 | 2:214164643 | CTCAATTTTTTAAAT[A/G]CATGTACATTTGATG | 79582 |
rs143984275 | snp | A/G | 0.0248432 | 0.108648 | intron-variant | SPAG16 | GRCh38.p7 | 2:214212703 | ACCCCAGCTAGCTCT[A/G]CTCTTTCTATTTTTC | 79582 |
rs143987183 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | SPAG16 | GRCh38.p7 | 2:214296205 | ATGGCCCCCAACTTT[A/G]CTCATGTAGCTACAG | 79582 |
rs143987348 | in-del | -/AAGA | 0.144632 | 0.226711 | intron-variant | SPAG16 | GRCh38.p7 | 2:213705262 | CTCTGTCTCAAAAAT[-/AAGA]AAGAAAGAGAGAGAG | 79582 |
rs143991707 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | SPAG16 | GRCh38.p7 | 2:213954916 | TTTCCTGATAGTAAC[A/G]TTGTGTTTTCCATTC | 79582 |
rs143992863 | snp | A/G | 0.00279162 | 0.0372561 | intron-variant | SPAG16 | GRCh38.p7 | 2:213500636 | ACTAGTACAACCTAG[A/G]GATCCAATTATTGAC | 79582 |
rs143994570 | snp | C/T | | | intron-variant | SPAG16 | GRCh38.p7 | 2:213567149 | GTTGGATGCTCATTT[C/T]TAATCAACACAGATT | 79582 |
rs144003996 | snp | A/G | 0.00199481 | 0.0315187 | intron-variant | SPAG16 | GRCh38.p7 | 2:214169630 | CTTCTTTTGTCTAGC[A/G]GAGAGTATGGTAATA | 79582 |
rs144009217 | snp | A/G | 0.0244538 | 0.107838 | intron-variant | SPAG16 | GRCh38.p7 | 2:214042784 | TCCTAAGAGTCTCCT[A/G]CAAATTTATCTACCC | 79582 |
rs144009256 | snp | A/G | 0.00636936 | 0.0560724 | intron-variant | SPAG16, LOC101928084 | GRCh38.p7 | 2:214093286 | ATAATTCATAAATTA[A/G]GTTGGGTTATTTGTA | 79582 |
rs144009785 | snp | A/T | | | intron-variant | SPAG16 | GRCh38.p7 | 2:213557142 | AGTCAGGTGATTGAG[A/T]AATGGACCATGTCAG | 79582 |
rs144011272 | in-del | -/T | 0.0884829 | 0.19082 | intron-variant | SPAG16 | GRCh38.p7 | 2:213820354 | TGATTTTTGGTAACC[-/T]CTTTTTTTTGTGTGT | 79582 |
rs144018782 | snp | A/G | 0.0023933 | 0.0345097 | intron-variant | SPAG16 | GRCh38.p7 | 2:213664431 | AAAATTAAAGAGGGC[A/G]TTATTAATAATTATT | 79582 |
rs144018855 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | SPAG16 | GRCh38.p7 | 2:213707191 | TGGTTTTCATTTACT[C/T]TGGGATAAAGTTCAA | 79582 |
rs144024183 | in-del | -/CTTAAATATAACGTTGAAAT | | | intron-variant | SPAG16 | GRCh38.p7 | 2:213754671 | ACCTACGATAGTCTT[-/CTTAAATATAACGTTGAAAT]ACATTAGTCAAAATG | 79582 |
rs144024850 | snp | C/T | 0.00835141 | 0.0640778 | intron-variant | SPAG16 | GRCh38.p7 | 2:214162127 | GAAGCATTTGTTTCT[C/T]GTTCCCTTATCAGAA | 79582 |
rs144026043 | snp | C/T | 0.0252325 | 0.109451 | intron-variant | SPAG16 | GRCh38.p7 | 2:213357506 | ATCCCTTTACCATTA[C/T]GTAATGGCCTTCTTT | 79582 |
rs144026327 | snp | C/G | 0.000798403 | 0.0199641 | intron-variant, stop-gained | SPAG16 | GRCh38.p7 | 2:213368836 | AAAGAGAATAAAATA[C/G]CTAAGAATCCAACTT | 79582 |
rs144026520 | snp | A/G | 0.00159617 | 0.0282053 | intron-variant | SPAG16 | GRCh38.p7 | 2:213451485 | ACATGAACTCATAGT[A/G]TCTCCCATCTCTACT | 79582 |
rs144028725 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | SPAG16 | GRCh38.p7 | 2:214047203 | AATATTCATATGGAA[C/T]CACAAAAGACCTAGA | 79582 |
rs144037657 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | SPAG16 | GRCh38.p7 | 2:213960807 | CTGGCCTTTTAAATG[C/T]CCTAGAAGTTATTGT | 79582 |
rs144039388 | in-del | -/A | | | intron-variant | SPAG16 | GRCh38.p7 | 2:213590459 | CAACAAAACAACAAG[-/A]AAAAAAAAAAAACAA | 79582 |
rs144046628 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | SPAG16 | GRCh38.p7 | 2:214400915 | ATACTCTATGTTTTA[C/T]ACTTTGACATCAACT | 79582 |
rs144059093 | snp | A/G | 0.00398564 | 0.0444627 | intron-variant | SPAG16 | GRCh38.p7 | 2:214359469 | TAATACAACTTTAGA[A/G]CACGAGAGAGAATAT | 79582 |
rs144059755 | snp | A/T | 0.000798403 | 0.0199641 | intron-variant | SPAG16 | GRCh38.p7 | 2:213795221 | TGTTATGTTTAGCAA[A/T]GATTAAGAATTGTTA | 79582 |
rs144063263 | snp | A/G | 0.0869089 | 0.189476 | intron-variant | SPAG16 | GRCh38.p7 | 2:213825464 | ATCAAATACTTTTTC[A/G]GCATCAATTGAAATG | 79582 |
rs144082647 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | SPAG16 | GRCh38.p7 | 2:213982246 | GGCTCCCATGTGCCC[A/G]TGTATTTGGATACAT | 79582 |
rs144089091 | snp | A/C | 0.00318978 | 0.0398085 | intron-variant | SPAG16 | GRCh38.p7 | 2:213437200 | CACTGTGCCTGGCCA[A/C]AAATGAGAAACTCTT | 79582 |
rs144089731 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | SPAG16 | GRCh38.p7 | 2:214342427 | AGATCAGTGGCAGCA[C/T]AGATTCCCACAGGAA | 79582 |
rs144099393 | snp | G/T | 0.00159617 | 0.0282053 | intron-variant | SPAG16 | GRCh38.p7 | 2:214269620 | GCCAAACTACAAATT[G/T]TAATGCCATAAGAAT | 79582 |
rs144101052 | in-del | -/A | 0.046775 | 0.145601 | intron-variant | SPAG16 | GRCh38.p7 | 2:213411933 | AAGAAAACTATAAAG[-/A]AATACAAGGGGAAGG | 79582 |
rs144103748 | snp | A/G | 0.0023933 | 0.0345097 | intron-variant | SPAG16 | GRCh38.p7 | 2:214141815 | GGTAAATATCTCTTC[A/G]TCCATAATATCCCAC | 79582 |
rs144104445 | snp | G/T | 0.000798403 | 0.0199641 | intron-variant | SPAG16 | GRCh38.p7 | 2:213840573 | TCCTTTCAAGGTAGA[G/T]TAAGGTAAATTCCAT | 79582 |
rs144109559 | in-del | -/A | 0.00438332 | 0.0466095 | intron-variant | SPAG16 | GRCh38.p7 | 2:214229916 | AAAATGCAGCACAGT[-/A]AATGTTAAACTATTC | 79582 |
rs144110193 | snp | C/T | 0.00159617 | 0.0282053 | intron-variant | SPAG16 | GRCh38.p7 | 2:213743725 | GTGTTGTATTTGTTG[C/T]GCATTTCTTTTTTAA | 79582 |
rs144113275 | snp | A/G | 0.0103295 | 0.0711199 | intron-variant, upstream-variant-2KB | SPAG16 | GRCh38.p7 | 2:213316570 | CTGTTTTCCTGACTC[A/G]TCTTTCACCATTCTC | 79582 |
rs144115856 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | SPAG16 | GRCh38.p7 | 2:214168284 | GGTGTGAGCCACTGC[A/G]CCTAGACAGTTCCTT | 79582 |
rs144116152 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | SPAG16 | GRCh38.p7 | 2:214256860 | CGGTTAGAAGTCCTC[C/T]AAAGCTGTTTTTCTT | 79582 |
rs144129562 | snp | A/G | 0.00199481 | 0.0315187 | intron-variant | SPAG16 | GRCh38.p7 | 2:213749526 | CCAGAGAAAAGCTAC[A/G]TTAAATCTCTGTCCT | 79582 |
rs144131957 | snp | C/T | 0.00159617 | 0.0282053 | intron-variant | SPAG16 | GRCh38.p7 | 2:214209816 | TAGTCAATAAGGTTA[C/T]ATAATTGATTAATTT | 79582 |
rs144134073 | snp | A/G | 0.00478085 | 0.0486577 | intron-variant | SPAG16 | GRCh38.p7 | 2:214293288 | GTTGGTGTTGGTGTT[A/G]TCAGTGGCTGCAACA | 79582 |
rs144134423 | snp | C/T | 0.00517822 | 0.0506191 | intron-variant | SPAG16 | GRCh38.p7 | 2:213817372 | AACAGAGAAACACTA[C/T]ATACACTGTTAGTGG | 79582 |
rs144134906 | snp | A/C | 0.0256215 | 0.110247 | intron-variant | SPAG16 | GRCh38.p7 | 2:214347151 | GTGGAAGAAAGCAGA[A/C]CCTGGCTACGTAGCT | 79582 |
rs144135013 | in-del | -/A | 0.0383715 | 0.133092 | intron-variant | SPAG16 | GRCh38.p7 | 2:213819014 | ACCTGACTAAGTATT[-/A]AAAGTGTACATTCAT | 79582 |
rs144135262 | snp | A/G | 0.102726 | 0.202016 | intron-variant | SPAG16 | GRCh38.p7 | 2:213668916 | GCCTCCCTAAGTGCT[A/G]GGATTACAGGCATGA | 79582 |
rs144140277 | snp | A/G | 0.00517822 | 0.0506191 | intron-variant | SPAG16 | GRCh38.p7 | 2:214351896 | TCTGTTTGGTCTGCT[A/G]TAACAAAATACCATA | 79582 |
rs144150676 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | SPAG16 | GRCh38.p7 | 2:213704197 | CATCCTTAATTCTGT[C/G]AGGATTTTGAAATGA | 79582 |
rs144150820 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | SPAG16 | GRCh38.p7 | 2:214213757 | GTGATAACTCAAAAA[A/G]TCAATTCTATCTACT | 79582 |
rs144151816 | snp | C/G | 0.0178098 | 0.0926698 | intron-variant | SPAG16 | GRCh38.p7 | 2:214156967 | ATAAAATACAAGAGA[C/G]AAAAGGTGACCAGGT | 79582 |
rs144154753 | snp | C/T | 0.00358779 | 0.0422022 | intron-variant | SPAG16 | GRCh38.p7 | 2:214298933 | GCCTAGTCAGGGGTA[C/T]AGTATGAACAAATTT | 79582 |
rs144156518 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | SPAG16 | GRCh38.p7 | 2:213683982 | GTTTTGTGTAGTTTT[A/G]TAAGTTCTTTCTTCA | 79582 |
rs144160607 | snp | C/T | 0.0123036 | 0.0774623 | intron-variant | SPAG16 | GRCh38.p7 | 2:214026663 | TATCTCCTTAGATAA[C/T]AGCAATTGATAAATA | 79582 |
rs144162089 | in-del | -/GATG | | | intron-variant | SPAG16 | GRCh38.p7 | 2:214233392 | GATGATGGTAGAATA[-/GATG]GATGGATGGATACAT | 79582 |
rs144163701 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | SPAG16 | GRCh38.p7 | 2:214020062 | TATAAAATCTACATA[A/G]CTTACTGGAATCTGA | 79582 |
rs144167254 | snp | A/G | 0.00318978 | 0.0398085 | intron-variant | SPAG16 | GRCh38.p7 | 2:213932483 | GCTGGGGTTACAGGC[A/G]TGAACCACTGCGCCT | 79582 |
rs144170854 | snp | A/C | 0.00557542 | 0.0525036 | intron-variant | SPAG16 | GRCh38.p7 | 2:213626833 | TTGTAATTTTAATAG[A/C]GACGGTGTTTCACCA | 79582 |
rs144177672 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | SPAG16 | GRCh38.p7 | 2:214107252 | CTAGAATATAAGGTC[C/T]GTGAGAATAAGGTTC | 79582 |
rs144178060 | snp | C/T | 0.00676609 | 0.0577691 | intron-variant | SPAG16 | GRCh38.p7 | 2:214247368 | TTCTGTTTTTACATA[C/T]TGGATTAGTGTGGAT | 79582 |
rs144179160 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | SPAG16 | GRCh38.p7 | 2:213479710 | GTCCTCTACAGCCAT[C/T]ACCACCACACTTGTC | 79582 |
rs144180039 | snp | C/T | 0.00795532 | 0.062565 | intron-variant | SPAG16 | GRCh38.p7 | 2:213603892 | TTTCTTTTCTCTTTC[C/T]GTATTATCCATCTCT | 79582 |
rs144182376 | in-del | -/TGA | | | intron-variant | SPAG16 | GRCh38.p7 | 2:213859994 | ATCATTACCATTAGT[-/TGA]TGATGATGATGATGA | 79582 |
rs144182556 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant, upstream-variant-2KB | SPAG16 | GRCh38.p7 | 2:213342918 | ACAGTTTGACCAGAT[A/G]TAACCCAAGCAGAGC | 79582 |
rs144184865 | snp | A/C | 0.00318978 | 0.0398085 | intron-variant | SPAG16 | GRCh38.p7 | 2:213726237 | TGTAAATAAATACCC[A/C]ATCTCTCTCATCCCT | 79582 |
rs144186378 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | SPAG16 | GRCh38.p7 | 2:213422034 | TTTCATGTACCTCAT[C/T]CTTCCTGGATGTGGA | 79582 |
rs144186451 | snp | A/T | 0.00279162 | 0.0372561 | intron-variant | SPAG16 | GRCh38.p7 | 2:214328033 | AGGCTCTATGATAGG[A/T]TCCAGTTTATAAATA | 79582 |
rs144187732 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | SPAG16 | GRCh38.p7 | 2:214129194 | CCTCTTCTGTACACT[C/T]TGCCTCGCAAATTCT | 79582 |
rs144187962 | in-del | -/AG | 0.35574 | 0.226537 | intron-variant | SPAG16 | GRCh38.p7 | 2:213705473 | AATTGGCATCTCTTA[-/AG]AGGGAGCTGGAGGTA | 79582 |
rs144193471 | snp | C/G | 0.0248432 | 0.108648 | intron-variant | SPAG16 | GRCh38.p7 | 2:214218279 | CGGCCTCGAGGTCCC[C/G]TTAAACAGTCTGGGG | 79582 |
rs144196117 | snp | G/T | 0.00636936 | 0.0560724 | intron-variant | SPAG16 | GRCh38.p7 | 2:214187872 | AAACTTTCGGACAAA[G/T]TAGTACTTTGAGCTA | 79582 |
rs144200458 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | SPAG16 | GRCh38.p7 | 2:213517736 | TAAATAGTGCTGGGA[A/C]AATCGGCCCGTTATA | 79582 |
rs144207448 | snp | A/G | 0.00398564 | 0.0444627 | intron-variant | SPAG16 | GRCh38.p7 | 2:213522085 | AGGTTCTAAAGATCT[A/G]TAGCATTGCTATCTT | 79582 |
rs144211767 | in-del | -/TAC | 0.211516 | 0.24702 | intron-variant | SPAG16 | GRCh38.p7 | 2:213323067 | AAAAATGCTCAATGT[-/TAC]TACTAATTGTCAAGG | 79582 |
rs144212727 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | SPAG16 | GRCh38.p7 | 2:213607758 | TACAATTGGGATTCT[A/G]TCTAGGAGGGTTTCA | 79582 |
rs144214300 | snp | C/G | 0.000798403 | 0.0199641 | intron-variant | SPAG16 | GRCh38.p7 | 2:213879878 | TTTTATTTATCCAAT[C/G]CACCGTTGGTGGGCA | 79582 |
rs144221465 | snp | C/T | 0.0209421 | 0.100162 | intron-variant | SPAG16 | GRCh38.p7 | 2:214152573 | GTCTCTCCCTGTGTG[C/T]GGCGACGAGAGAGTG | 79582 |
rs144226736 | snp | A/G | | | intron-variant | SPAG16 | GRCh38.p7 | 2:213786639 | AGAAGATGATGTAGA[A/G]CTATGCAAACTGTGT | 79582 |
rs144229265 | snp | A/G | 0.00557542 | 0.0525036 | intron-variant | SPAG16 | GRCh38.p7 | 2:214060014 | CAGGACCTGCGGGCA[A/G]TGCAGCCCAGTAATG | 79582 |
rs144231276 | snp | A/C | 0.00159617 | 0.0282053 | intron-variant | SPAG16 | GRCh38.p7 | 2:214109963 | TTTTATTTTGGCAAG[A/C]AATATAATAACTGCA | 79582 |
rs144233969 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | SPAG16 | GRCh38.p7 | 2:213330337 | CCTTGTAAAGCCACA[A/G]GGGTGGAGCTTCCCA | 79582 |
rs144235920 | snp | A/C | 0.00636936 | 0.0560724 | intron-variant | SPAG16 | GRCh38.p7 | 2:214361342 | TGGTTGGGACACTAA[A/C]CATTATTTAGAAATC | 79582 |
rs144237112 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | SPAG16 | GRCh38.p7 | 2:213828932 | CTGGAGGATGGGTGA[C/T]ACAATCACCCCTGTG | 79582 |
rs144237396 | snp | C/G | 0.00953873 | 0.0683987 | intron-variant | SPAG16 | GRCh38.p7 | 2:213983537 | ACTGTATAATTCAGA[C/G]TAAAATTTAACATAA | 79582 |
rs144243018 | snp | C/T | 0.0228947 | 0.104514 | intron-variant | SPAG16 | GRCh38.p7 | 2:214250479 | TTTCTCAAACCTAAT[C/T]ATATTGAATAAATTC | 79582 |
rs144247170 | snp | G/T | 0.00159617 | 0.0282053 | intron-variant | SPAG16 | GRCh38.p7 | 2:214277471 | ACCAATGGGGTTTTG[G/T]TGTGGATGTCCTTTT | 79582 |
rs144247372 | snp | C/T | 0.0146672 | 0.084371 | intron-variant | SPAG16 | GRCh38.p7 | 2:214035952 | GTGTCATGCAGTGGC[C/T]GCTGTAGATTAACCA | 79582 |
rs144248553 | snp | C/T | 0.0463947 | 0.145069 | intron-variant | SPAG16 | GRCh38.p7 | 2:213347596 | TTGTATCTTTGTTCT[C/T]ATTGGTTTCAAAGAA | 79582 |
rs144248873 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant, upstream-variant-2KB | SPAG16 | GRCh38.p7 | 2:213297978 | TTCAGTGTTTAACCC[C/T]TTTACTACAGAGAAA | 79582 |
rs144250647 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | SPAG16 | GRCh38.p7 | 2:213425697 | TGTTGCAGGAAAAGT[C/T]GTGTATTTCCATTTC | 79582 |
rs144256175 | snp | A/G | 0.00159617 | 0.0282053 | intron-variant | SPAG16 | GRCh38.p7 | 2:213389500 | AATATCTGTAATCAT[A/G]TATCTGGCAAGGAAT | 79582 |
rs144257054 | snp | C/T | 0.00835141 | 0.0640778 | intron-variant | SPAG16 | GRCh38.p7 | 2:214331514 | GAAAAATTCTGCAAT[C/T]GGGCCCTTGGGAAGT | 79582 |
rs144261192 | snp | C/T | | | intron-variant | SPAG16 | GRCh38.p7 | 2:213304239 | ATTACTTTTTTTCTT[C/T]AGAGTTGTTTGAGCT | 79582 |
rs144262156 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | SPAG16 | GRCh38.p7 | 2:213471724 | GTTGCAGAGCCTTCT[C/G]CTGTTCTGGAGCCCA | 79582 |
rs144264966 | snp | A/T | 0.00199481 | 0.0315187 | intron-variant | SPAG16 | GRCh38.p7 | 2:213792097 | CAGAAATGTTGTTTA[A/T]AAGTGTTACCAATTA | 79582 |
rs144265812 | snp | C/T | 0.00755907 | 0.0610114 | intron-variant | SPAG16 | GRCh38.p7 | 2:214231097 | CTTGGTGTCCTATGT[C/T]GTTGGATCCAGACAT | 79582 |
rs144266929 | snp | A/G | | | intron-variant | SPAG16 | GRCh38.p7 | 2:213336677 | TTTTTCTCACTGGGT[A/G]AGGCCTCTCTGTGGG | 79582 |
rs144272122 | snp | C/T | 0.00318978 | 0.0398085 | intron-variant | SPAG16 | GRCh38.p7 | 2:214065267 | TAATTCTTCTGATCA[C/T]CTTTAAAAATAAATA | 79582 |
rs144274605 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | SPAG16 | GRCh38.p7 | 2:213988599 | GCAAGGTTACAGAAT[C/T]CAAAGTCAACACACA | 79582 |
rs144277893 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | SPAG16 | GRCh38.p7 | 2:213582569 | ACTTTAAAAAGAGGA[A/G]TTTTTGATATTCAGT | 79582 |
rs144282136 | snp | A/T | 0.0217236 | 0.101931 | intron-variant | SPAG16 | GRCh38.p7 | 2:213662199 | TTTGGAAAGATAGAC[A/T]TCATTCATTACAAGG | 79582 |
rs144282817 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | SPAG16 | GRCh38.p7 | 2:213773213 | TTCAGGCAGTTTCTA[C/T]GGAATTCTGTTTTAT | 79582 |
rs144285435 | snp | C/T | 0.00953873 | 0.0683987 | intron-variant | SPAG16 | GRCh38.p7 | 2:213659978 | TTCTTTCTCTTTTCT[C/T]TCTTTTTTTTAAGAT | 79582 |
rs144286239 | snp | A/G | 0.0023933 | 0.0345097 | intron-variant | SPAG16 | GRCh38.p7 | 2:213692380 | AATCTGCTGGAGATT[A/G]ACTTGTGTTTGTACT | 79582 |
rs144291382 | snp | C/T | 0.129664 | 0.219133 | intron-variant | SPAG16 | GRCh38.p7 | 2:213644072 | AGGCATGAGACACCA[C/T]GCCCGGCCCAAGCTC | 79582 |
rs144295802 | snp | A/G | 0.00159617 | 0.0282053 | intron-variant | SPAG16 | GRCh38.p7 | 2:213730571 | CTAATTCTTATTATC[A/G]TTTCTCTATAGATAA | 79582 |
rs144303739 | snp | A/G | 0.0023933 | 0.0345097 | intron-variant | SPAG16 | GRCh38.p7 | 2:213445958 | CAGCCCCTTAGGGTT[A/G]GAACACACAGCCCAG | 79582 |
rs144309431 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | SPAG16 | GRCh38.p7 | 2:214198720 | CATTCCCACCAGCAA[C/T]ACTGCTGGTGGCAGT | 79582 |
rs144309456 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | SPAG16 | GRCh38.p7 | 2:213734248 | CCAGCAAGAAAAGAG[A/G]TAAATGCTAGATGGA | 79582 |
rs144311115 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | SPAG16 | GRCh38.p7 | 2:213530874 | TGATTTTATGTACCA[A/G]TCATGTGTTTGTATA | 79582 |
rs144313376 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | SPAG16 | GRCh38.p7 | 2:213972364 | TGGAGGCTGAGCAGT[C/T]CCATGACTTCTGTCT | 79582 |
rs144322890 | snp | C/T | 0.00914312 | 0.0669923 | intron-variant | SPAG16 | GRCh38.p7 | 2:214377291 | ACCGTTGGACCCATA[C/T]GAAGTGCCACTAGTG | 79582 |
rs144324258 | snp | A/G | 0.0023933 | 0.0345097 | intron-variant | SPAG16 | GRCh38.p7 | 2:213629310 | GCCATTGCAACCAAG[A/G]ACTACACGTGTTACC | 79582 |
rs144328898 | snp | A/G | 0.00199481 | 0.0315187 | intron-variant | SPAG16 | GRCh38.p7 | 2:213846374 | TGCCAGTAGTACCTG[A/G]AGAAACTCCTCTTAG | 79582 |
rs144330706 | snp | C/T | 0.00478085 | 0.0486577 | intron-variant | SPAG16 | GRCh38.p7 | 2:214162376 | GTTATAAACCAAGTA[C/T]AAAACCACTGAGATG | 79582 |
rs144332374 | in-del | -/AC | 0.328616 | 0.237317 | intron-variant | SPAG16 | GRCh38.p7 | 2:213322356 | AAAAAAAAAAAAAAA[-/AC]AAAAAACTCGTTTGG | 79582 |
rs144334980 | in-del | -/TT | 0.293037 | 0.246268 | intron-variant | SPAG16 | GRCh38.p7 | 2:213733518 | TTTTTTTTTTTTTTT[-/TT]GGTGTGTGTCTTCAT | 79582 |
rs144339667 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | SPAG16 | GRCh38.p7 | 2:213834535 | ACCCATCTGGAATGA[A/G]GATTGTATGACTCAC | 79582 |
rs144342847 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | SPAG16 | GRCh38.p7 | 2:213382328 | TTGCTTGGTGTTATA[A/T]GTCCTCAGTATCTGT | 79582 |
rs144349138 | snp | A/C | 0.00874735 | 0.0655527 | intron-variant | SPAG16 | GRCh38.p7 | 2:214281715 | GAGAAACAAAAACAT[A/C]TGTCCATACAAAGAC | 79582 |
rs144354010 | snp | A/G | 0.00199481 | 0.0315187 | intron-variant | SPAG16 | GRCh38.p7 | 2:214040948 | TCCATTATTTTACTT[A/G]TATTCCTTGGAGACT | 79582 |
rs144354255 | snp | A/C | 0.00279162 | 0.0372561 | intron-variant | SPAG16 | GRCh38.p7 | 2:213951862 | ATGTTTTGAGATTCG[A/C]TAAAACCAAATATTA | 79582 |
rs144358295 | snp | C/G | 0.00199481 | 0.0315187 | intron-variant | SPAG16 | GRCh38.p7 | 2:213733797 | TGCCTAGTGACTTCA[C/G]TTCTCTGATAGGTTC | 79582 |
rs144363667 | snp | G/T | 0.00517822 | 0.0506191 | intron-variant | SPAG16 | GRCh38.p7 | 2:213598389 | AAGATGCCTTTTGAG[G/T]TATCAAATTAATATT | 79582 |
rs144365397 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | SPAG16 | GRCh38.p7 | 2:213698405 | TAGCTGGGACTATAG[A/G]TGCATGCTACCACAC | 79582 |
rs144366125 | in-del | -/A | 0.0248432 | 0.108648 | intron-variant | SPAG16 | GRCh38.p7 | 2:213467937 | TGCAAGGCAGCTATT[-/A]AGAGACTGTACCTTT | 79582 |
rs144369888 | snp | A/G | 0.00279162 | 0.0372561 | intron-variant | SPAG16 | GRCh38.p7 | 2:214051891 | CCTACATCATTAGAC[A/G]TACTTCATAAATTTT | 79582 |
rs144371917 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | SPAG16 | GRCh38.p7 | 2:213680623 | CTTGCAAGTAGGGAG[C/T]TACTTACACTTTCTC | 79582 |
rs144378735 | snp | G/T | 0.00119737 | 0.0244387 | intron-variant | SPAG16 | GRCh38.p7 | 2:213499922 | ACACTGGTTTCTTTA[G/T]TATTCCTAAGACTTT | 79582 |
rs144379319 | in-del | -/CCCC | | | intron-variant | SPAG16 | GRCh38.p7 | 2:213313453 | TCTAGCAGGTAGCCA[-/CCCC]CAGCCATATTTCTAT | 79582 |
rs144382929 | snp | C/T | 0.0023933 | 0.0345097 | intron-variant | SPAG16 | GRCh38.p7 | 2:213587237 | AAATCTAGATAGAAG[C/T]AGCCACATTCCCACA | 79582 |
rs144383120 | snp | A/C | 0.00953873 | 0.0683987 | intron-variant | SPAG16 | GRCh38.p7 | 2:213331104 | CTATCAGGGGTAGAG[A/C]GTTTTTCTTTTACTT | 79582 |
rs144383393 | snp | C/T | 0.00159617 | 0.0282053 | intron-variant | SPAG16 | GRCh38.p7 | 2:213374551 | ATGTTACAACTATTT[C/T]GAATATTACCCTGTG | 79582 |
rs144385703 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | SPAG16 | GRCh38.p7 | 2:213616666 | TGAATCTCAGTCTAA[C/T]GGCAGAGTTCCTAAT | 79582 |
rs144387873 | snp | C/T | | | intron-variant | SPAG16 | GRCh38.p7 | 2:214118661 | TAGCATGAGGGTAAC[C/T]GCCCCCATGATTAAA | 79582 |
rs144388256 | in-del | -/ATGAGAGA | | | intron-variant | SPAG16 | GRCh38.p7 | 2:214193425 | TGTGTGTGTGTGTGT[-/ATGAGAGA]GAGAGAGAGAGAGAG | 79582 |
rs144401850 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | SPAG16 | GRCh38.p7 | 2:214183735 | GCTGATAATATTTTC[A/G]TCATCTGTGTAGTCC | 79582 |
rs144402821 | in-del | -/A | 0.0581099 | 0.160244 | intron-variant | SPAG16 | GRCh38.p7 | 2:213999943 | ACCCCTATTGTATCT[-/A]GGAAGTAACTAGCTT | 79582 |
rs144405969 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | SPAG16 | GRCh38.p7 | 2:214270712 | TGCTTGATTAGTCCC[A/G]TGGTTGTCTCCATAG | 79582 |
rs144409984 | snp | C/T | 0.172997 | 0.237846 | intron-variant | SPAG16 | GRCh38.p7 | 2:213367381 | TGTCTTTCATAATGG[C/T]TGAACTAGTTTACAG | 79582 |
rs144416633 | snp | A/G | 0.00159617 | 0.0282053 | intron-variant | SPAG16 | GRCh38.p7 | 2:213474500 | ATGGTCAAAGGTATT[A/G]TATATATAGTCACTT | 79582 |
rs144418318 | snp | A/G | 0.00676609 | 0.0577691 | intron-variant | SPAG16 | GRCh38.p7 | 2:214362869 | ATAAAAAAATGCCAT[A/G]ATAACACAAGATAGG | 79582 |
rs144420224 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | SPAG16 | GRCh38.p7 | 2:213928721 | CATGAGGCTTGGTGC[C/T]GTAGAAACAGAGATG | 79582 |
rs144420793 | snp | A/G | 0.00159617 | 0.0282053 | intron-variant | SPAG16 | GRCh38.p7 | 2:213510532 | ATATTAAATTTCAAC[A/G]TAATATGGAATATAT | 79582 |
rs144421364 | snp | A/G | 0.00557542 | 0.0525036 | intron-variant | SPAG16 | GRCh38.p7 | 2:213460763 | GTTACATAATGCTAC[A/G]GTTGGTCATAGTAAA | 79582 |
rs144425552 | snp | C/G | 0.0178098 | 0.0926698 | intron-variant | SPAG16 | GRCh38.p7 | 2:213548755 | ATTTATTTTTGTATG[C/G]TATAAACTTTAAATA | 79582 |
rs144427024 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | SPAG16 | GRCh38.p7 | 2:214375830 | GAACTAAGCACAGTG[C/G]TTACCTCTGGAATGA | 79582 |
rs144427765 | snp | A/G | 0.0209421 | 0.100162 | intron-variant | SPAG16 | GRCh38.p7 | 2:213602389 | CTGTAATCCCAGCCC[A/G]TTGGGAGGCTGAGGC | 79582 |
rs144437714 | snp | A/G | 0.00159617 | 0.0282053 | intron-variant | SPAG16 | GRCh38.p7 | 2:214050857 | TTGTAAAAAAAGATC[A/G]ACCTGCAAAAGAGAT | 79582 |
rs144441032 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | SPAG16 | GRCh38.p7 | 2:213393266 | ATACTTACATTAGCT[A/G]TATTTCAACTGTTGA | 79582 |
rs144442631 | in-del | -/CTGA | 0.0236746 | 0.106192 | intron-variant | SPAG16 | GRCh38.p7 | 2:213819001 | ATAGCAGTGTGAAAC[-/CTGA]CTAAGTATTAAAAGT | 79582 |
rs144443149 | snp | A/T | 0.00318978 | 0.0398085 | intron-variant | SPAG16 | GRCh38.p7 | 2:213350250 | TCATGGGTAGCAGCA[A/T]TCTTCTGAGTACATA | 79582 |
rs144443298 | snp | A/G | 0.0023933 | 0.0345097 | intron-variant | SPAG16 | GRCh38.p7 | 2:214129369 | TCGTTTTCATCTCTT[A/G]ATGATTATTGCCCTT | 79582 |
rs144444036 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | SPAG16 | GRCh38.p7 | 2:213792336 | GCAACAGTTGTGCCT[C/T]CCTCAGTGTGTTGAA | 79582 |
rs144448427 | snp | C/T | | | intron-variant | SPAG16 | GRCh38.p7 | 2:213334624 | GGAGAACTGTTCAAC[C/T]GTAAAAATGAATGAG | 79582 |
rs144453020 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | SPAG16 | GRCh38.p7 | 2:213460090 | GTCTTCCTGTTTCTT[A/C]ATGGTCTTCTGCCAC | 79582 |
rs144453191 | in-del | -/T | | | intron-variant | SPAG16 | GRCh38.p7 | 2:213618709 | TCATGAGGATTTCTG[-/T]TTTTTTTTTTTCTTT | 79582 |
rs144454987 | snp | A/G | 0.00199481 | 0.0315187 | intron-variant | SPAG16 | GRCh38.p7 | 2:213867291 | ATCATTGAAAATGGT[A/G]AATGAATGGATCAAT | 79582 |
rs144456753 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | SPAG16 | GRCh38.p7 | 2:214368249 | TATCCCATGTTCTTC[G/T]TTACTCACACCTGCA | 79582 |
rs144459993 | in-del | -/CAA | | | intron-variant | SPAG16 | GRCh38.p7 | 2:213904600 | TAAGGATAAATTTTG[-/CAA]AAAAAAAAAAAAAAA | 79582 |
rs144461208 | in-del | -/CA | | | intron-variant | SPAG16 | GRCh38.p7 | 2:214187208 | ACACACACACACACA[-/CA]AAGTTCCGGTATATT | 79582 |
rs144463020 | snp | C/T | 0.00755907 | 0.0610114 | intron-variant | SPAG16 | GRCh38.p7 | 2:213774374 | TTTGCTTATAATCTT[C/T]CATGTTTTTGTCTTG | 79582 |
rs144470954 | snp | A/C | 0.000798403 | 0.0199641 | intron-variant | SPAG16 | GRCh38.p7 | 2:214233031 | CCAAAGAATACATAT[A/C]CTATGATTCTTTTTT | 79582 |
rs144474074 | snp | C/G | 0.00358779 | 0.0422022 | intron-variant | SPAG16 | GRCh38.p7 | 2:214304133 | TCTGTTCCTATGTTA[C/G]TTTGCTAAAGATAAT | 79582 |
rs144488020 | snp | A/G | 0.0107246 | 0.0724382 | intron-variant | SPAG16 | GRCh38.p7 | 2:213464101 | TCCTGCAGGAAATGG[A/G]CCAAAGAACTTACAT | 79582 |
rs144492253 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | SPAG16 | GRCh38.p7 | 2:214016321 | CAGCATGCAAGAGAG[C/T]ATGTGCCGGGGAACT | 79582 |
rs144492637 | snp | C/T | 0.00438332 | 0.0466095 | intron-variant | SPAG16 | GRCh38.p7 | 2:214384218 | AAAGGACTTGCTATT[C/T]ATGAAGGCATGACAA | 79582 |
rs144503538 | snp | C/T | 0.00557542 | 0.0525036 | intron-variant | SPAG16 | GRCh38.p7 | 2:213711215 | TTTATGTACTTTCCT[C/T]TCAGTTATCAGATGG | 79582 |
rs144504289 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | SPAG16 | GRCh38.p7 | 2:213919275 | TTCAGTGGTTTTTTC[A/T]TATCTCAATCTCCTT | 79582 |
rs144505645 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | SPAG16 | GRCh38.p7 | 2:214058516 | CCATCATAACAGATA[C/T]AATAATAATGAAAAA | 79582 |
rs144506648 | in-del | -/C | 0.0138799 | 0.0821421 | intron-variant | SPAG16 | GRCh38.p7 | 2:213760560 | ACATTAAAAAAAAAA[-/C]AATTAGACCTAACTC | 79582 |
rs144507440 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | SPAG16 | GRCh38.p7 | 2:214184928 | TAGAAATGAAAATTT[C/T]GTCTTTAAAAATTTT | 79582 |
rs144516595 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | SPAG16 | GRCh38.p7 | 2:214169364 | AATTCAAAGTGTTGC[G/T]CTTAAAAGTGAGTTG | 79582 |
rs144528764 | snp | C/T | 0.0221141 | 0.102801 | intron-variant | SPAG16 | GRCh38.p7 | 2:213850872 | AAATGTAAATCTTTA[C/T]ATTTTTATTTTCACT | 79582 |
rs144542288 | snp | C/T | 0.00159617 | 0.0282053 | intron-variant | SPAG16 | GRCh38.p7 | 2:213874752 | TATATGGCACATGAC[C/T]GTGCCTTATTCCATT | 79582 |
rs144544111 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | SPAG16 | GRCh38.p7 | 2:213924570 | ATACAAGCTGCTTCT[C/T]GTCTGCCATCTTGGC | 79582 |
rs144544154 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | SPAG16 | GRCh38.p7 | 2:213553030 | TTTGGGACTTGGACT[A/G]GCTTCCTTGCTCCTC | 79582 |
rs144545669 | snp | A/G | 0.00318978 | 0.0398085 | intron-variant, utr-variant-3-prime | SPAG16 | GRCh38.p7 | 2:213399241 | TTCAACACAAGGAAT[A/G]ATATTTATTGTCTTT | 79582 |
rs144545906 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | SPAG16 | GRCh38.p7 | 2:213324486 | TAGATTAGTTTTGTT[C/T]GAGAATTTCATAAAT | 79582 |
rs144548763 | snp | A/C/T | 0.00914312 | 0.0669923 | intron-variant | SPAG16 | GRCh38.p7 | 2:214356372 | TGCAAGTGATCCCAA[A/C/T]TGACACAATATGGAA | 79582 |
rs144549330 | snp | C/G | 0.0111196 | 0.0737302 | intron-variant | SPAG16 | GRCh38.p7 | 2:214318673 | GAGCCACCGCGCCCA[C/G]CCCAGAGAGTGGACT | 79582 |
rs144557458 | snp | A/G | 0.00358779 | 0.0422022 | intron-variant | SPAG16 | GRCh38.p7 | 2:213645926 | AGGCACTCAAGTTCT[A/G]ATGGCTGTGATCCAG | 79582 |
rs144565551 | snp | C/T | 0.00279162 | 0.0372561 | intron-variant | SPAG16 | GRCh38.p7 | 2:214077976 | GCTGCTCTGGGCTTG[C/T]ATCTCTTAAGTAAAG | 79582 |
rs144567849 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | SPAG16 | GRCh38.p7 | 2:214001190 | ATACTTCTTTATCAA[C/T]TTACAGTTAACAATG | 79582 |
rs144582656 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | SPAG16 | GRCh38.p7 | 2:214036823 | AACATATAGTCCAAC[C/T]ATGGTTAGATCTTCT | 79582 |
rs144585430 | snp | A/G | 0.0134861 | 0.0810011 | intron-variant | SPAG16 | GRCh38.p7 | 2:214108392 | AGGAATTAGTTGTAA[A/G]CAATAGGAAAAGTCT | 79582 |
rs144586375 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | SPAG16 | GRCh38.p7 | 2:214190270 | AAAAGGGAATATGAG[C/T]GGGACCTTTACAAGC | 79582 |
rs144589162 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | SPAG16 | GRCh38.p7 | 2:213327848 | GTCTGTTTTACTATA[C/T]TGAATAGCAGTATTA | 79582 |
rs144590262 | snp | C/T | 0.00874735 | 0.0655527 | intron-variant | SPAG16 | GRCh38.p7 | 2:213945434 | CAAGGAGACCCAGTC[C/T]GAGTCTCAAAACTGA | 79582 |
rs144590357 | in-del | -/TTTTC | 0.432352 | 0.184056 | intron-variant | SPAG16 | GRCh38.p7 | 2:213508984 | ATTTTCTATACAATA[-/TTTTC]TTTTCTTTTCTTTTC | 79582 |
rs144594605 | snp | C/T | 0.00953873 | 0.0683987 | intron-variant | SPAG16 | GRCh38.p7 | 2:213857618 | CTGGTCACTCAAGAA[C/T]TGTGATGAAGATGTA | 79582 |
rs144595663 | snp | C/T | 0.00676609 | 0.0577691 | intron-variant | SPAG16 | GRCh38.p7 | 2:214264510 | ATTGGACAGAAGGTA[C/T]AGGAAGTTTTCATAT | 79582 |
rs144601471 | snp | C/G | 0.0433465 | 0.140692 | intron-variant | SPAG16 | GRCh38.p7 | 2:213358598 | TCGTGCTGTGGTTTT[C/G]AGCTCCATCAGGTCA | 79582 |
rs144602251 | snp | C/T | 0.0023933 | 0.0345097 | intron-variant | SPAG16 | GRCh38.p7 | 2:214309560 | TTGCTGACCTTTGGA[C/T]AGGTTTTTTTTTTCT | 79582 |
rs144603426 | snp | A/T | 3.29685e-05 | 0.00405995 | missense, nc-transcript-variant, intron-variant | SPAG16 | GRCh38.p7 | 2:213930094 | ACTCCTGCGGCAATT[A/T]TGTGGCTTCCTCCTC | 79582 |
rs144604252 | in-del | -/AC | | | intron-variant | SPAG16 | GRCh38.p7 | 2:214299242 | AAACAAGTGTAGTAT[-/AC]TTTTTTTTTTTTTTT | 79582 |
rs144604555 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | SPAG16 | GRCh38.p7 | 2:213767543 | GGCGGTTGAGAGGTC[A/G]CTTGAGCCTGGGAGG | 79582 |
rs144605882 | snp | A/G | 0.00279162 | 0.0372561 | intron-variant | SPAG16 | GRCh38.p7 | 2:213407209 | CAGTTCTACCTTGGC[A/G]GAGCGGCCAGAGAGG | 79582 |
rs144607252 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | SPAG16 | GRCh38.p7 | 2:214389773 | AATATTACAAAAATA[C/T]CTTTTAGTCATTTGC | 79582 |
rs144612650 | snp | C/T | 0.00636936 | 0.0560724 | intron-variant | SPAG16, LOC101928084 | GRCh38.p7 | 2:214097935 | ATGTAGATACTATAT[C/T]ATTTCTATTTTACAG | 79582 |
rs144616621 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | SPAG16 | GRCh38.p7 | 2:213638712 | ATGAATAGAATGTAT[A/G]TTCTACAGTTGCTAG | 79582 |
rs144618774 | snp | A/G | 0.00676609 | 0.0577691 | intron-variant | SPAG16 | GRCh38.p7 | 2:214064225 | GCTATAATTAATTGC[A/G]TCTGTCTAGAGAGTA | 79582 |
rs144628667 | snp | C/T | 0.00874735 | 0.0655527 | intron-variant | SPAG16 | GRCh38.p7 | 2:213716534 | TTAACCAGGAAGCTA[C/T]TGTCTTAAACTGCTG | 79582 |
rs144628926 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | SPAG16 | GRCh38.p7 | 2:213942700 | CAATGAACAAGAACT[A/C]ATTTAAACCTTTACT | 79582 |
rs144630732 | snp | A/C | 0.00517822 | 0.0506191 | intron-variant | SPAG16 | GRCh38.p7 | 2:214402457 | AAATTAAGTTGAGAT[A/C]TTTCAGCAAAACAAG | 79582 |
rs144631987 | snp | A/G/T | 0.00398564 | 0.0444627 | upstream-variant-2KB, intron-variant | SPAG16, LOC100130451 | GRCh38.p7 | 2:213283667 | GCTTCTGATACATAC[A/G/T]CGATATAACCTGAGG | 79582 |
rs144632395 | snp | C/G | 0.00517822 | 0.0506191 | intron-variant | SPAG16 | GRCh38.p7 | 2:214348539 | CTGCTTTTTTATTTG[C/G]TGAAATGTTCACTTT | 79582 |
rs144633769 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | SPAG16 | GRCh38.p7 | 2:213987515 | TTTTATTTCCAAATT[C/T]AGCTCCCTAAATACT | 79582 |
rs144635921 | in-del | -/C | | | intron-variant | SPAG16 | GRCh38.p7 | 2:214035964 | GCCGCTGTAGATTAA[-/C]CCACCACTGCCATGA | 79582 |
rs144637340 | snp | C/G | 0.00358779 | 0.0422022 | intron-variant | SPAG16 | GRCh38.p7 | 2:214311698 | TTCCACTTGGGTCAT[C/G]ATTATTCACCTGCAA | 79582 |
rs144645789 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | SPAG16 | GRCh38.p7 | 2:214177242 | TTGCCTAAGCTCAAA[G/T]TCCCTGAATTTTCCT | 79582 |
rs144645922 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | SPAG16 | GRCh38.p7 | 2:213524671 | GACTTCCTGACTGGA[C/T]TTCGGACTTGCATGG | 79582 |
rs144655498 | snp | C/T | 0.0193772 | 0.0965046 | intron-variant | SPAG16 | GRCh38.p7 | 2:213946362 | TCGAGATCTACCTGC[C/T]TCGGCCTCCCAGAGT | 79582 |
rs144656591 | in-del | -/AA | 0.00755907 | 0.0610114 | intron-variant | SPAG16 | GRCh38.p7 | 2:214401928 | AACATAAAGAAATTT[-/AA]AGTTTTGATAGATAT | 79582 |
rs144662804 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | SPAG16 | GRCh38.p7 | 2:213446093 | TAAAAGCAGAAAGGC[C/T]GATTCCAAAGACAGA | 79582 |
rs144664778 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | SPAG16 | GRCh38.p7 | 2:213322119 | GTAAAAAAAAAAGAT[G/T]ATAAAACACCACTTA | 79582 |
rs144665952 | snp | A/T | 0.00279162 | 0.0372561 | intron-variant | SPAG16 | GRCh38.p7 | 2:213861676 | TTATACAAATAAGAT[A/T]AAAGCATTGCCATAG | 79582 |
rs144666590 | snp | A/G | 0.0115144 | 0.0749975 | intron-variant | SPAG16 | GRCh38.p7 | 2:213363105 | AAAACTAAAAATATG[A/G]CCTGTAGTTCATAAT | 79582 |
rs144667572 | in-del | -/T | 0.031825 | 0.122064 | intron-variant | SPAG16 | GRCh38.p7 | 2:214176947 | AATTTTATGCTAAGC[-/T]TTTTTTTAAAAAAAT | 79582 |
rs144667825 | snp | C/T | 0.00159617 | 0.0282053 | intron-variant | SPAG16 | GRCh38.p7 | 2:214398775 | CTTAACTTTCTGGCA[C/T]AACTACTTTTGTTTC | 79582 |
rs144668358 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | SPAG16 | GRCh38.p7 | 2:214115352 | ATATATAGAAGGCAA[A/C]AATTTTAGTTATTTG | 79582 |
rs144669033 | snp | C/G | | | intron-variant | SPAG16 | GRCh38.p7 | 2:214352893 | TTCTCCTAACATTTA[C/G]AGAGAGACCTTACAC | 79582 |
rs144670393 | snp | C/T | 0.00358779 | 0.0422022 | intron-variant | SPAG16 | GRCh38.p7 | 2:214202264 | TTTACAACCTAAATA[C/T]ATTAAATTGATGGCT | 79582 |
rs144676353 | snp | G/T | 0.000798403 | 0.0199641 | intron-variant | SPAG16 | GRCh38.p7 | 2:213818742 | TAGTGGGAGGTGATT[G/T]TACCATGGGGGTGGT | 79582 |
rs144678309 | snp | A/T | | | intron-variant | SPAG16 | GRCh38.p7 | 2:213324813 | TGTATGAACTGCTCG[A/T]ACATATTCCCACATT | 79582 |
rs144678344 | snp | C/T | 0.00438332 | 0.0466095 | intron-variant | SPAG16 | GRCh38.p7 | 2:213758756 | AACTTGAAGAAACAA[C/T]GGATAGAACCTTTCC | 79582 |
rs144680008 | snp | C/T | 0.00358779 | 0.0422022 | intron-variant | SPAG16 | GRCh38.p7 | 2:214318665 | ACAGGCATGAGCCAC[C/T]GCGCCCAGCCCAGAG | 79582 |
rs144680463 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | SPAG16 | GRCh38.p7 | 2:214181419 | TCAAGGCATCCCAAG[C/G]CATCCCAGGGGAGCT | 79582 |
rs144684654 | snp | G/T | 0.00557542 | 0.0525036 | intron-variant | SPAG16 | GRCh38.p7 | 2:213719649 | ACAATACCATCTCAT[G/T]CTAGTTAGATCGGCA | 79582 |
rs144688555 | snp | C/T | 0.00199481 | 0.0315187 | intron-variant | SPAG16 | GRCh38.p7 | 2:213287394 | ACTGCCTAGTTCCAA[C/T]TGGAAGGCCAGCATG | 79582 |
rs144689897 | in-del | -/AC | | | intron-variant | SPAG16 | GRCh38.p7 | 2:213842572 | TTTTTTGCCAAACTA[-/AC]ATTTTGTTTGTTTTG | 79582 |
rs144697688 | snp | A/G | 0.0205511 | 0.0992634 | intron-variant | SPAG16 | GRCh38.p7 | 2:213997737 | CTAGTGATAGCTGAT[A/G]AGGTTATAAAAAAAT | 79582 |
rs144699399 | snp | A/C | 0.0217236 | 0.101931 | intron-variant | SPAG16 | GRCh38.p7 | 2:213957661 | TACCTTATAAATATT[A/C]TTTTCTTTATTTCCA | 79582 |
rs144704597 | snp | A/G | 0.00358779 | 0.0422022 | intron-variant | SPAG16 | GRCh38.p7 | 2:213815868 | GAAATAAATTTACAT[A/G]ATATTGACTCATAAT | 79582 |
rs144705435 | snp | C/G | 0.00159617 | 0.0282053 | intron-variant | SPAG16 | GRCh38.p7 | 2:213681067 | AGCAGGTTATAAAAT[C/G]TTTCTTATCAGACCT | 79582 |
rs144707213 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | SPAG16 | GRCh38.p7 | 2:214187586 | ATCTCCCCTAGCTTG[A/G]ACGGAAGCTGAGAAA | 79582 |
rs144707356 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | SPAG16 | GRCh38.p7 | 2:213725655 | GGCGTGTCTTAGCAA[C/T]AGTGAGAAAAGAGAT | 79582 |
rs144716173 | snp | A/G | 0.00159617 | 0.0282053 | intron-variant, upstream-variant-2KB | SPAG16 | GRCh38.p7 | 2:213295169 | CCATTACCATGCATT[A/G]AAGTGTTTAATTCAC | 79582 |
rs144716287 | snp | A/C | 0.00119737 | 0.0244387 | intron-variant | SPAG16 | GRCh38.p7 | 2:214074604 | CCATTCATTAACGCC[A/C]TTATGAACTGAAAAG | 79582 |
rs144718575 | snp | G/T | 0.00835141 | 0.0640778 | intron-variant | SPAG16 | GRCh38.p7 | 2:214316225 | CTGTAGGTAGCCTAT[G/T]GTGCAGAGTTGCAAT | 79582 |
rs144719998 | in-del | -/AC | 0.37778 | 0.214877 | intron-variant | SPAG16 | GRCh38.p7 | 2:214163587 | TGTGTATATATATAT[-/AC]ACACACACATATATA | 79582 |
rs144721121 | snp | A/C | 0.0166325 | 0.0896639 | intron-variant | SPAG16 | GRCh38.p7 | 2:213856077 | AAAAGCAAGTTAGTT[A/C]CTTCCTAGACACACT | 79582 |
rs144721708 | snp | G/T | 0.039522 | 0.134904 | intron-variant | SPAG16 | GRCh38.p7 | 2:214219271 | GGTTTAGAAATCTTT[G/T]GTTAAATCTATTTTT | 79582 |
rs144722955 | snp | C/T | 0.00398564 | 0.0444627 | intron-variant | SPAG16 | GRCh38.p7 | 2:213535633 | TATTCAGAACTCTAA[C/T]TGTTTTGTTACCCAT | 79582 |
rs144724411 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | SPAG16 | GRCh38.p7 | 2:214267338 | GAGCCCAGAAATAAA[C/T]CCATACATTTATGGT | 79582 |
rs144724884 | snp | C/T | 0.0103295 | 0.0711199 | intron-variant | SPAG16 | GRCh38.p7 | 2:213619518 | AAGCGTATGAATAGA[C/T]ATTCCTCAAAAGAAG | 79582 |
rs144727077 | snp | A/G | 0.00318978 | 0.0398085 | intron-variant | SPAG16 | GRCh38.p7 | 2:213823122 | TCAAATGGTATTTCT[A/G]GTTCTAGATCCTTGA | 79582 |
rs144728196 | in-del | -/ACAA | 0.0126979 | 0.078662 | intron-variant | SPAG16 | GRCh38.p7 | 2:214311346 | ACCCATAACAGATAC[-/ACAA]ACAGTGTGGTCCCTG | 79582 |
rs144728906 | snp | G/T | 0.00716266 | 0.059414 | intron-variant | SPAG16 | GRCh38.p7 | 2:214274935 | TGGTCCTAAACTTTT[G/T]TTGGTTGGTAGGCTA | 79582 |
rs144737206 | snp | A/G | 0.00914312 | 0.0669923 | intron-variant | SPAG16 | GRCh38.p7 | 2:213607090 | AGACTAGTTGGTAAA[A/G]TGTCTTGAAAATTGA | 79582 |
rs144741572 | snp | C/G | 0.00279162 | 0.0372561 | intron-variant | SPAG16 | GRCh38.p7 | 2:213689144 | TTTGTATTTTTAGTA[C/G]AGTCAGGGTTTCACC | 79582 |
rs144742127 | snp | A/G | 0.0023933 | 0.0345097 | intron-variant | SPAG16 | GRCh38.p7 | 2:214129662 | TTATAGTTCTGCTTG[A/G]ACCATGAATTTCATG | 79582 |
rs144743441 | snp | G/T | 0.029116 | 0.117091 | intron-variant | SPAG16 | GRCh38.p7 | 2:213938708 | GAAACAAATCAAATG[G/T]CCAAGGACATCAAAT | 79582 |
rs144761489 | snp | A/C | 0.0256215 | 0.110247 | intron-variant | SPAG16 | GRCh38.p7 | 2:214253124 | AGGATCTGTTCATAT[A/C]CTTCACCCACTTTTT | 79582 |
rs144761725 | snp | A/G | 0.00279162 | 0.0372561 | intron-variant | SPAG16 | GRCh38.p7 | 2:214018729 | ACCTCAATGTGATCA[A/G]TTACTATTGAGACAC | 79582 |
rs144766032 | snp | A/G | 0.00199481 | 0.0315187 | intron-variant | SPAG16 | GRCh38.p7 | 2:213923702 | GTAGGACTGCTGGGC[A/G]GGAAGCTCTAGCACA | 79582 |
rs144768173 | snp | G/T | 0.00953873 | 0.0683987 | intron-variant | SPAG16 | GRCh38.p7 | 2:213592454 | TTTATAAAAGCTTTA[G/T]AGTTAGTAAATCAAA | 79582 |
rs144768352 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | SPAG16 | GRCh38.p7 | 2:213762931 | AGAACTCCTACAACT[C/G]AATAGTTAAAAAAAC | 79582 |
rs144768458 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | SPAG16 | GRCh38.p7 | 2:213684919 | CAAAATTGCAGCTCT[A/G]CATGTGCTATGAAGG | 79582 |
rs144774878 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | SPAG16 | GRCh38.p7 | 2:214070614 | TTTCCTCACCTAGTA[A/G]GTATTGTTTTTTGTC | 79582 |
rs144778078 | snp | A/C/T | 0.00199481 | 0.0315187 | intron-variant | SPAG16 | GRCh38.p7 | 2:214120817 | TATTTAAACTTGTAA[A/C/T]TTTTAATTTTATTTA | 79582 |
rs144780112 | snp | C/T | 0.0123036 | 0.0774623 | intron-variant | SPAG16 | GRCh38.p7 | 2:214046655 | GATGCCTACTTTCAC[C/T]GTTATTCAACATAGT | 79582 |
rs144780963 | snp | C/T | 0.00199481 | 0.0315187 | intron-variant | SPAG16 | GRCh38.p7 | 2:213616808 | GGTACTCTGTCTGCA[C/T]AGGGTACTCTGGCTA | 79582 |
rs144782348 | in-del | -/ATAAA | 0.254105 | 0.249966 | intron-variant | SPAG16 | GRCh38.p7 | 2:213449818 | ATAAAAATAAAATAG[-/ATAAA]ATAAAATGTAAATTA | 79582 |
rs144789283 | snp | A/G | 0.00398564 | 0.0444627 | intron-variant | SPAG16 | GRCh38.p7 | 2:213785157 | TCTCAGGTAACCATC[A/G]TTAGCATTTTGATTC | 79582 |
rs144789320 | snp | C/T | 0.00358779 | 0.0422022 | intron-variant | SPAG16 | GRCh38.p7 | 2:214327178 | ATAAAATGTTCACAT[C/T]ATAATCAAACTGGAC | 79582 |
rs144792418 | snp | C/T | 0.00358779 | 0.0422022 | intron-variant | SPAG16 | GRCh38.p7 | 2:213346393 | TCTCCTGCCTGATTG[C/T]CCTGGCCAGAACTTC | 79582 |
rs144795292 | in-del | -/TAA | | | intron-variant | SPAG16 | GRCh38.p7 | 2:213814805 | AAACAATAATAATAA[-/TAA]TAATAAAGAGGGACA | 79582 |
rs144797390 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | SPAG16 | GRCh38.p7 | 2:213454266 | TTTTCTTGATGTTAG[A/C]AAACTATGGATCATA | 79582 |
rs144800575 | snp | C/T | | | intron-variant | SPAG16 | GRCh38.p7 | 2:214005591 | TTATGGTAGAGCTTG[C/T]GGCAGACTCCATGGT | 79582 |
rs144801466 | snp | C/G | 0.0252325 | 0.109451 | intron-variant | SPAG16 | GRCh38.p7 | 2:213674490 | CTGCACCCACTAACT[C/G]GTCATCTAGCATTAG | 79582 |
rs144802798 | in-del | -/T | | | intron-variant | SPAG16 | GRCh38.p7 | 2:213855497 | TCTCATTTTATCGCA[-/T]TTCACTTTGTTGCAT | 79582 |
rs144803268 | snp | A/G | 0.00597247 | 0.0543191 | intron-variant | SPAG16 | GRCh38.p7 | 2:214286369 | GATCCCAAAAAGTTT[A/G]TATGAATGCTTATGT | 79582 |
rs144812093 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | SPAG16 | GRCh38.p7 | 2:213878783 | TTAATAGTTTCGAGT[A/G]TTACATTTAAATTCT | 79582 |
rs144813314 | snp | C/T | 0.00557542 | 0.0525036 | intron-variant | SPAG16 | GRCh38.p7 | 2:214204587 | ATAAATAACAATCAC[C/T]GCAGTTTGGCTCTCA | 79582 |
rs144816233 | snp | C/T | 0.0138799 | 0.0821421 | intron-variant | SPAG16 | GRCh38.p7 | 2:213728801 | AGAATGGCACGAACT[C/T]GGGAGGCAGAGCTTG | 79582 |
rs144817530 | snp | A/G | 0.0150606 | 0.0854603 | intron-variant | SPAG16 | GRCh38.p7 | 2:213532674 | CACTATGTTGTCCAG[A/G]CTGATCTCGAACTCC | 79582 |
rs144818118 | in-del | -/G | 0.0166325 | 0.0896639 | intron-variant | SPAG16 | GRCh38.p7 | 2:213713011 | GCAATCATGGCAGAA[-/G]GGCATCTCTTCACAG | 79582 |
rs144826278 | snp | C/T | 0.00953873 | 0.0683987 | intron-variant, utr-variant-5-prime | SPAG16 | GRCh38.p7 | 2:213302313 | GAGAGTTGTATATAA[C/T]GTATAATAGGGATAA | 79582 |
rs144827634 | snp | G/T | 0.00636936 | 0.0560724 | intron-variant, utr-variant-3-prime | SPAG16 | GRCh38.p7 | 2:213400733 | TGTGTGTTTGTGGAA[G/T]TACCTTTCAGAAATA | 79582 |
rs144829788 | snp | A/G | 0.00914312 | 0.0669923 | intron-variant | SPAG16 | GRCh38.p7 | 2:213483536 | ATGGGTTGTTGAGCA[A/G]ATGGATTCTCAAACT | 79582 |
rs144838337 | in-del | -/A | 0.0402882 | 0.136092 | intron-variant | SPAG16 | GRCh38.p7 | 2:214069783 | GAACCTAAATTTTCT[-/A]AAAAAAAATCATAGA | 79582 |
rs144839419 | snp | A/G | 0.00159617 | 0.0282053 | intron-variant | SPAG16 | GRCh38.p7 | 2:213658854 | CATCCTGGCCAACAT[A/G]GTGAAACCCTGTCTC | 79582 |
rs144841441 | in-del | -/G | 0.0217236 | 0.101931 | intron-variant | SPAG16 | GRCh38.p7 | 2:213881789 | GGGATTACAATTTAA[-/G]ATGTGATTTGGGTGG | 79582 |
rs144847368 | in-del | -/TGTG | | | intron-variant | SPAG16 | GRCh38.p7 | 2:213980697 | TATATATAGAATATA[-/TGTG]TGTGTGTGTGTGTAT | 79582 |
rs144854983 | snp | A/C/G | 3.37116e-05 | 0.00410547 | missense, nc-transcript-variant, utr-variant-5-prime | SPAG16 | GRCh38.p7 | 2:213340228 | GAATGCATCATAAGC[A/C/G]AATAGTCCAGGAAAA | 79582 |
rs144857662 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | SPAG16 | GRCh38.p7 | 2:213334333 | GGATATGGAGAAAAG[A/G]GAACCCTTGTACGCT | 79582 |
rs144857995 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | SPAG16 | GRCh38.p7 | 2:213410915 | TGCGGGTCAGCCCCC[A/G]AGGGCCATCCAGCTT | 79582 |
rs144861268 | snp | A/G | 0.00517822 | 0.0506191 | intron-variant | SPAG16 | GRCh38.p7 | 2:213585540 | CCATGGCCTCCCAAA[A/G]TTCTGGGATTATGAT | 79582 |
rs144864755 | snp | A/T | 0.00159617 | 0.0282053 | intron-variant | SPAG16 | GRCh38.p7 | 2:213666930 | CTGGATACAATGGTG[A/T]CTCTACAAATGGAGC | 79582 |
rs144865590 | snp | A/G | 0.02016 | 0.0983543 | intron-variant | SPAG16 | GRCh38.p7 | 2:214075934 | TCTGCCTTGATTACA[A/G]CTAATTAGCAAATAA | 79582 |
rs144866050 | snp | C/T | 0.00914312 | 0.0669923 | intron-variant | SPAG16 | GRCh38.p7 | 2:214253973 | TTGTATCCTCTTTTA[C/T]TTCTTTGAGCAGTGG | 79582 |
rs144873373 | snp | A/G | 0.00557542 | 0.0525036 | intron-variant | SPAG16 | GRCh38.p7 | 2:214334665 | CCAGCAATAGCCATG[A/G]GGTTTCAGAGTCCTT | 79582 |
rs144878230 | in-del | -/TT | | | intron-variant | SPAG16 | GRCh38.p7 | 2:213957464 | GAACTTTTTTTTTTT[-/TT]CACTTTCAATCTACT | 79582 |
rs144888312 | in-del | -/A | 0.131038 | 0.219882 | intron-variant | SPAG16 | GRCh38.p7 | 2:213472759 | TTACCTGACCTCCAT[-/A]ACCCCCTACTTTAAC | 79582 |
rs144898229 | snp | A/G | 0.00199481 | 0.0315187 | intron-variant | SPAG16 | GRCh38.p7 | 2:213491499 | TAACAAACACAACTG[A/G]CTTATAAACAGGTTT | 79582 |
rs144898903 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | SPAG16 | GRCh38.p7 | 2:214320773 | CTCCACCTGGTCTCT[A/C]CCTTGACACATGAAG | 79582 |
rs144900593 | snp | C/T | 0.00199481 | 0.0315187 | intron-variant | SPAG16 | GRCh38.p7 | 2:214205080 | CTAAAAATACAAAAA[C/T]TAGCTGAGCATGTTG | 79582 |
rs144901246 | snp | C/G | 0.0785177 | 0.181917 | intron-variant | SPAG16 | GRCh38.p7 | 2:214118562 | CCTTCTTCACATGGT[C/G]GCGGCAGAAGTGCTG | 79582 |
rs144902313 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | SPAG16 | GRCh38.p7 | 2:214033504 | TTGGTGGACTAGGGA[A/C]AAGATGGTAGCAGTG | 79582 |
rs144905384 | snp | A/G | | | intron-variant | SPAG16 | GRCh38.p7 | 2:213996028 | CTAGCATGAGCTTAG[A/G]GTTTCATAAAAGATG | 79582 |
rs144905709 | snp | G/T | | | intron-variant | SPAG16 | GRCh38.p7 | 2:213723418 | CATGCTACGCCTTCT[G/T]TCTGTCTCATTTGCT | 79582 |
rs144910288 | snp | A/G | 0.00318978 | 0.0398085 | intron-variant | SPAG16 | GRCh38.p7 | 2:213671140 | CTTTGATAATTGTGT[A/G]CTCATTTTAACATAC | 79582 |
rs144911152 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | SPAG16 | GRCh38.p7 | 2:213960919 | GGAAGCAGCAATCAG[C/T]AATCAGAGCACAAAT | 79582 |
rs144911792 | snp | A/G | 0.00716266 | 0.059414 | intron-variant | SPAG16 | GRCh38.p7 | 2:213448036 | AGTGGCATTACACCA[A/G]TCTGTTCAAATGGCT | 79582 |
rs144915256 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | SPAG16 | GRCh38.p7 | 2:213874473 | GCCTACACAGGGTCA[A/G]GATCATTAATATCAC | 79582 |
rs144916351 | snp | C/G | 0.00478085 | 0.0486577 | intron-variant | SPAG16 | GRCh38.p7 | 2:214409505 | CAAATACCCTGTGCT[C/G]TATTTAGCCATCTTA | 79582 |
rs144918022 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | SPAG16 | GRCh38.p7 | 2:213940194 | AAAATTAGCTGTGCT[A/G]AAATATCTGACAAGT | 79582 |
rs144924026 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | SPAG16 | GRCh38.p7 | 2:213534757 | AAAGGAAAGAGACAC[A/G]TTTATTTGTCACAAA | 79582 |
rs144927561 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant, utr-variant-3-prime | SPAG16 | GRCh38.p7 | 2:214151021 | GACAACACGTATGAA[C/T]GAGGGACTCTAATGA | 79582 |
rs144928334 | snp | A/G | 0.00874735 | 0.0655527 | intron-variant | SPAG16 | GRCh38.p7 | 2:213727774 | GACTTACATTTTACT[A/G]TGATCTAACTGGCTA | 79582 |
rs144930416 | snp | A/G | 0.0126979 | 0.078662 | intron-variant | SPAG16 | GRCh38.p7 | 2:214077241 | CCTTGTGAGGGACTG[A/G]AGCCAGGAATGAGAA | 79582 |
rs144930629 | snp | C/T | 0.00199481 | 0.0315187 | intron-variant | SPAG16 | GRCh38.p7 | 2:213297466 | CTCAGTCATCTGTTA[C/T]ATCATTTTCATCTCT | 79582 |
rs144935531 | snp | A/C | 0.0225045 | 0.103662 | intron-variant | SPAG16 | GRCh38.p7 | 2:213825576 | CTTGGGATAAATCCC[A/C]CTTGGTCATGATGAG | 79582 |
rs144942385 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | SPAG16 | GRCh38.p7 | 2:213537744 | TGTGTTTTTTCTGCT[G/T]CTTGGTTTTACAGTC | 79582 |
rs144949523 | snp | A/G | 0.00993419 | 0.0697739 | intron-variant | SPAG16 | GRCh38.p7 | 2:213491734 | TGGAGAAGAAACAGA[A/G]GGAAACATTTAGCTC | 79582 |
rs144950263 | snp | A/G | | | intron-variant | SPAG16 | GRCh38.p7 | 2:214034545 | AAGTGGAGCAGCAAG[A/G]GGTGTGTGAGAGAGA | 79582 |
rs144950929 | snp | A/C | 0.000798403 | 0.0199641 | intron-variant | SPAG16 | GRCh38.p7 | 2:214394682 | CTCCTTGATTATCAA[A/C]ATCCCCTGCCAGAGT | 79582 |
rs144951446 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | SPAG16 | GRCh38.p7 | 2:213942254 | ATCAGAATCAGGCTG[A/G]CCTGTTTCATTTCAT | 79582 |
rs144953005 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | SPAG16 | GRCh38.p7 | 2:213898665 | CTTTCTTTTATTTAT[A/G]CTTTAAGGATGAAGA | 79582 |
rs144953946 | snp | A/G | 0.0119091 | 0.0762411 | intron-variant | SPAG16 | GRCh38.p7 | 2:213926567 | CTCATATGCTATTTA[A/G]CCCATCCATTGATTT | 79582 |
rs144956620 | snp | G/T | 0.00199481 | 0.0315187 | intron-variant | SPAG16 | GRCh38.p7 | 2:213609495 | TCTTCTGGATGCTAA[G/T]TTGGTTTTCTTACAT | 79582 |
rs144961503 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | SPAG16 | GRCh38.p7 | 2:213375899 | TTTTCTCTCTAAAAC[A/G]TGCATTGGATTCTGG | 79582 |
rs144965557 | snp | C/G/T | 0.0891392 | 0.19158 | intron-variant | SPAG16 | GRCh38.p7 | 2:213344907 | ACCCAGTAATGGGAT[C/G/T]GCTGGGTCAAATGGT | 79582 |
rs144975958 | snp | G/T | 0.0193772 | 0.0965046 | intron-variant | SPAG16 | GRCh38.p7 | 2:213925419 | TGCAGTGTCACAATC[G/T]TGGCTCACTGCAACC | 79582 |
rs144977900 | snp | A/G | 0.00636936 | 0.0560724 | intron-variant | SPAG16 | GRCh38.p7 | 2:213471630 | GCATCCCTATCTGCC[A/G]CTGTCACCTCAAGCA | 79582 |
rs144983073 | snp | A/G | 0.0126979 | 0.078662 | intron-variant | SPAG16 | GRCh38.p7 | 2:213804552 | GTTGGGCGTGGTGGC[A/G]GGCGCCTGTAGTCCC | 79582 |
rs144983259 | snp | C/T | 0.00199481 | 0.0315187 | intron-variant | SPAG16 | GRCh38.p7 | 2:214342626 | ATAATTATTTCATTA[C/T]ATATTGCAATGTAAT | 79582 |
rs144985545 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | SPAG16 | GRCh38.p7 | 2:213472662 | AGCCTGCTAAGTATG[C/T]CTATGCCAATTATGT | 79582 |
rs144993692 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | SPAG16 | GRCh38.p7 | 2:213883731 | GGGGTAGGCAAGTCT[A/G]CTTGTTGGATTGCAC | 79582 |
rs144994367 | snp | A/G | 0.00159617 | 0.0282053 | intron-variant | SPAG16 | GRCh38.p7 | 2:214020746 | TTTTGTTAAAATTTT[A/G]TTAGGGTTTCCTCTT | 79582 |
rs144994987 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | SPAG16 | GRCh38.p7 | 2:214054887 | GTATTCTATTGGGGA[A/G]AGCTGAAAATAATTT | 79582 |
rs144995073 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | SPAG16 | GRCh38.p7 | 2:213974652 | ATGATGTTAATTTAT[A/G]TATGCTTTCTATAAG | 79582 |
rs145011368 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | SPAG16 | GRCh38.p7 | 2:214122599 | AATGCAAACAACAAT[G/T]AGGTCATACAGTGAT | 79582 |
rs145011991 | snp | C/T | 0.0295035 | 0.117819 | intron-variant | SPAG16 | GRCh38.p7 | 2:213426572 | AAAATATTCTTGATA[C/T]TTGTATTATGTATTA | 79582 |
rs145012204 | snp | C/T | 0.0228947 | 0.104514 | intron-variant | SPAG16 | GRCh38.p7 | 2:213347894 | AGTTCTGTAGATGTC[C/T]ATTAGGTCTGCTTGG | 79582 |
rs145012738 | snp | C/T | 0.00199481 | 0.0315187 | intron-variant | SPAG16 | GRCh38.p7 | 2:214283262 | ACGTGTGTGAACCAG[C/T]CTTCTTAAAAGTGTA | 79582 |
rs145012791 | snp | C/T | 0.00914312 | 0.0669923 | intron-variant | SPAG16 | GRCh38.p7 | 2:213380047 | AGAGGTGTCCATCCA[C/T]GTACCTCTTTCCTGA | 79582 |
rs145013637 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | SPAG16 | GRCh38.p7 | 2:214329995 | GTTTAGGCTGGGTGC[A/G]GTGGCTCATGCTTGT | 79582 |
rs145014052 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | SPAG16 | GRCh38.p7 | 2:214209926 | TACAGTGTTTGTCAT[A/G]TGACCTTTTACCAGC | 79582 |
rs145015100 | snp | C/G | | | intron-variant | SPAG16 | GRCh38.p7 | 2:213594136 | CACATATTTTTCAAT[C/G]CATCACATTCTTTCC | 79582 |
rs145016331 | in-del | -/ATACAT | | | intron-variant | SPAG16 | GRCh38.p7 | 2:213971736 | CAGATGCTGGTACAC[-/ATACAT]ATGTTTAACTTTTTG | 79582 |
rs145023185 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant, utr-variant-5-prime | SPAG16 | GRCh38.p7 | 2:213301870 | TTGCCTCAGATGTTT[C/T]CTTGCCTTGAATATT | 79582 |
rs145023746 | snp | A/T | 0.00398564 | 0.0444627 | intron-variant | SPAG16 | GRCh38.p7 | 2:213348396 | AAGGTTAATATTCTT[A/T]TGTGTGAATTTGATC | 79582 |
rs145026301 | snp | A/G | 0.0221141 | 0.102801 | intron-variant | SPAG16 | GRCh38.p7 | 2:213677029 | GGACTCTTTTTGGTT[A/G]GTAAGCTGTTGATTA | 79582 |
rs145028499 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | SPAG16 | GRCh38.p7 | 2:213882260 | GGAATTTTTGTGTCT[A/G]TATTCATCAGGGATA | 79582 |
rs145030025 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | SPAG16 | GRCh38.p7 | 2:213306059 | TTTCTTCATGTTACA[A/G]TCTTGGTAGGTTGTA | 79582 |
rs145034396 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | SPAG16 | GRCh38.p7 | 2:214333044 | CTTTTTTCCCATTAT[C/T]GGAGGAAATGGCTGT | 79582 |
rs145034931 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | SPAG16 | GRCh38.p7 | 2:213788041 | GGCACTCTTAGGCAC[C/T]ATTGGATTGAATCAT | 79582 |
rs145040046 | snp | A/G | 0.0162398 | 0.0886349 | intron-variant | SPAG16 | GRCh38.p7 | 2:213918513 | AGGGACCTGGTGGGA[A/G]GTAATTGAATTAAGG | 79582 |
rs145046190 | snp | A/C | 0.00159617 | 0.0282053 | intron-variant | SPAG16 | GRCh38.p7 | 2:213835005 | ATATATTTGAACTCT[A/C]TCCCAGTTTCCTGAT | 79582 |
rs145047055 | snp | C/T | 0.00199481 | 0.0315187 | intron-variant | SPAG16 | GRCh38.p7 | 2:214083700 | TAAATTCAAGTTTTA[C/T]TCTAGATTTGGGGGT | 79582 |
rs145048005 | snp | C/G | 0.00557542 | 0.0525036 | intron-variant | SPAG16 | GRCh38.p7 | 2:214368765 | ATGACAGAAATTCAA[C/G]TCAGTTTAGAAACTA | 79582 |
rs145050564 | snp | A/G | 0.00358779 | 0.0422022 | intron-variant | SPAG16 | GRCh38.p7 | 2:213886866 | AAATTAGAACAATGG[A/G]CACTATGCTGGTATA | 79582 |
rs145054537 | snp | A/G | 0.00199481 | 0.0315187 | intron-variant | SPAG16 | GRCh38.p7 | 2:213731848 | TACTACATTTTCTTT[A/G]TCCACTCTTGATGGT | 79582 |
rs145055319 | snp | A/G | 0.00636936 | 0.0560724 | intron-variant | SPAG16 | GRCh38.p7 | 2:213309707 | CACCACCCTAAATAC[A/G]TAGCAACCCAGCTTC | 79582 |
rs145057088 | in-del | -/AAG | 0.0573587 | 0.15934 | intron-variant | SPAG16 | GRCh38.p7 | 2:213964906 | TTTGTTTAATTATTT[-/AAG]AAGTGTGACTTTGTT | 79582 |
rs145061557 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | SPAG16 | GRCh38.p7 | 2:213736436 | GGCATTACATGCACC[C/T]ACCACCACACCCGGC | 79582 |
rs145064739 | snp | A/G | | | intron-variant | SPAG16 | GRCh38.p7 | 2:213311613 | TAAAATTGGTATAAC[A/G]CATTTCTTTATGAGT | 79582 |
rs145067616 | snp | A/G | 0.00199481 | 0.0315187 | intron-variant | SPAG16 | GRCh38.p7 | 2:213383048 | TATGGCACAGCCCAT[A/G]TGTTCCAGATCTTTA | 79582 |
rs145070080 | snp | A/G | 0.0115144 | 0.0749975 | intron-variant | SPAG16 | GRCh38.p7 | 2:213836861 | TCAGGTGATCCCCCG[A/G]TCTCAGCCTCCCAAA | 79582 |
rs145079039 | snp | G/T | 0.00557542 | 0.0525036 | intron-variant | SPAG16 | GRCh38.p7 | 2:214200283 | CCAATGTCGTTGAGG[G/T]TTTTGATCATAAAGG | 79582 |
rs145079203 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | SPAG16 | GRCh38.p7 | 2:214284456 | TTGGTTGAGCATTAA[A/G]TATTATAATATACAC | 79582 |
rs145082080 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | SPAG16 | GRCh38.p7 | 2:214336475 | AGTGTATACCTTTTT[A/G]GAGATTAGAAAAATA | 79582 |
rs145084004 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | SPAG16 | GRCh38.p7 | 2:213543609 | ATTTAATGTAGCAAT[C/T]CTGTTCATATTGGTA | 79582 |
rs145084810 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | SPAG16 | GRCh38.p7 | 2:213838449 | AAGTGCTGGGATTAC[A/C]GGCGTGAGCCACTGC | 79582 |
rs145084841 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | SPAG16 | GRCh38.p7 | 2:213780353 | CTTTCTGATTCCAGG[C/T]CTCTTCCCATTTTTC | 79582 |
rs145084919 | snp | C/T | 0.00914312 | 0.0669923 | intron-variant | SPAG16 | GRCh38.p7 | 2:214372784 | TATTTTGCCAACATG[C/T]AGTAGAAAATCCCAA | 79582 |
rs145094456 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | SPAG16 | GRCh38.p7 | 2:213681940 | TTTGAAATATAAAGA[C/G]ATTACCCAGATCCAG | 79582 |
rs145103360 | snp | A/G | 0.00159617 | 0.0282053 | intron-variant | SPAG16 | GRCh38.p7 | 2:214287013 | TATATTTGGAGATTA[A/G]TAAAGTTCTTCAGGA | 79582 |
rs145105892 | snp | A/G | 0.00159617 | 0.0282053 | intron-variant | SPAG16 | GRCh38.p7 | 2:214127194 | TATCTTGGAGAATAT[A/G]AAAGGACTGACTTCC | 79582 |
rs145106544 | snp | C/T | 0.00597247 | 0.0543191 | intron-variant | SPAG16 | GRCh38.p7 | 2:214185611 | GTATTTTTTAAATTT[C/T]GAAGAATGGACAACT | 79582 |
rs145115357 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | SPAG16 | GRCh38.p7 | 2:213698943 | ATCAAGTACAACGCA[C/T]AGTACCTGGCATATA | 79582 |
rs145126010 | snp | C/T | 0.00358779 | 0.0422022 | intron-variant | SPAG16 | GRCh38.p7 | 2:214130893 | TCTCCTTGAATAAAA[C/T]GTTAGTTTCAAAAAT | 79582 |
rs145126810 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | SPAG16 | GRCh38.p7 | 2:213305559 | TTTTTGAGGGTTTCT[A/G]TCATGAAGGGATGTT | 79582 |
rs145128068 | snp | A/G | 0.00478085 | 0.0486577 | intron-variant | SPAG16 | GRCh38.p7 | 2:214058071 | AACAGCAATAAGGCT[A/G]TGTCACTATCATTTG | 79582 |
rs145144072 | snp | C/T | 0.00557542 | 0.0525036 | intron-variant | SPAG16 | GRCh38.p7 | 2:214246701 | GACTTTAAGCTAAAA[C/T]CACCCAGCCAAGTCC | 79582 |
rs145144864 | snp | G/T | 0.00755907 | 0.0610114 | intron-variant | SPAG16 | GRCh38.p7 | 2:213413527 | ACTGTCATATGAAAT[G/T]TAAGAACTTTCTTAT | 79582 |
rs145147129 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | SPAG16 | GRCh38.p7 | 2:213893956 | TAAAAGGCATAGAAT[A/G]GCTGAATGAGTAAAG | 79582 |
rs145149816 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | SPAG16 | GRCh38.p7 | 2:213604590 | TTTGTTAAAAACTTA[A/T]GGGCACTGTCTTATT | 79582 |
rs145151704 | snp | A/G | 0.00318978 | 0.0398085 | intron-variant | SPAG16 | GRCh38.p7 | 2:213923038 | GGTCCATCTGGCTAT[A/G]GGAGGCAGGGGTGAG | 79582 |
rs145151727 | snp | A/C | 0.000798403 | 0.0199641 | intron-variant | SPAG16 | GRCh38.p7 | 2:213551809 | ATTTGACCTGAATAC[A/C]ATTTTGAAGAACTAG | 79582 |
rs145153112 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | SPAG16 | GRCh38.p7 | 2:213355855 | ATCGAATCCCCTTTA[C/T]TTCTTTCTCTTGCCT | 79582 |
rs145153305 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | SPAG16 | GRCh38.p7 | 2:213437783 | AAGTGCTCTCCCTGC[A/G]TATTTATATTATTCT | 79582 |
rs145155713 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | SPAG16 | GRCh38.p7 | 2:213686828 | AGCTGGGACAACAGG[C/T]GCGTGCCACCACACC | 79582 |
rs145163257 | in-del | -/T | 0.0524604 | 0.153226 | intron-variant | SPAG16 | GRCh38.p7 | 2:214385885 | AAAACTCTAAACTTA[-/T]TTTTTTGAGTTGGCT | 79582 |
rs145163695 | snp | G/T | 0.00199481 | 0.0315187 | intron-variant | SPAG16 | GRCh38.p7 | 2:213764098 | GTGTTACACAAATAT[G/T]AGTTAGATATCTTGT | 79582 |
rs145165263 | snp | G/T | 0.00119737 | 0.0244387 | intron-variant | SPAG16 | GRCh38.p7 | 2:214134801 | AAACACATAAGAACT[G/T]TTTTTACATCATATG | 79582 |
rs145174261 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | SPAG16 | GRCh38.p7 | 2:214061545 | GCAGTCTTGATGCAG[A/G]ATTTTCTCTTACATG | 79582 |
rs145175227 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | SPAG16 | GRCh38.p7 | 2:214018016 | TTATTTTCTAAAAAT[A/G]TTTTCAAACCAAGTA | 79582 |
rs145176600 | snp | C/T | 0.0189856 | 0.0955633 | intron-variant | SPAG16 | GRCh38.p7 | 2:213785879 | GGGCATGGTGGCACT[C/T]GCCTATAGTCCCAGC | 79582 |
rs145185572 | snp | C/G | 0.000798403 | 0.0199641 | intron-variant | SPAG16 | GRCh38.p7 | 2:213983769 | GTACCATCACAATAG[C/G]GGGTGTTGAAGAAGC | 79582 |
rs145186621 | snp | A/G | 0.00318978 | 0.0398085 | intron-variant | SPAG16, LOC101928084 | GRCh38.p7 | 2:214094102 | GTGAAAGCAGAATAC[A/G]CACAACTCTTCCCAA | 79582 |
rs145190763 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | SPAG16 | GRCh38.p7 | 2:213634618 | ATTTGTTTATTATTT[C/T]GATAGTTTTAGGGGA | 79582 |
rs145191979 | snp | A/G | 0.0788843 | 0.182262 | intron-variant | SPAG16 | GRCh38.p7 | 2:214133157 | TACCATTAGCATAGA[A/G]CAAGGTTTGGCAATA | 79582 |
rs145205334 | snp | A/T | 0.00279162 | 0.0372561 | intron-variant, upstream-variant-2KB | SPAG16 | GRCh38.p7 | 2:213316785 | AGATATCACTTTGTC[A/T]GTCATGTTTGTCATT | 79582 |
rs145207018 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | SPAG16 | GRCh38.p7 | 2:213947462 | TAGACATCTTATTAT[A/G]TACATACTTGCCACC | 79582 |
rs145210714 | snp | C/G | 0.00159617 | 0.0282053 | intron-variant | SPAG16 | GRCh38.p7 | 2:213553908 | CTGCTTTACAAACAC[C/G]CTTTCTTTGAATACT | 79582 |
rs145214611 | snp | A/G | 0.0185938 | 0.0946107 | intron-variant | SPAG16 | GRCh38.p7 | 2:213635252 | ATGCTAGCCAGGATG[A/G]TCTCGATCTCCTGAC | 79582 |
rs145214783 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | SPAG16 | GRCh38.p7 | 2:213841301 | CACTTGGTACAAAAC[C/G]AGTGGGGCATGACAT | 79582 |
rs145220287 | snp | C/T | 0.00199481 | 0.0315187 | intron-variant | SPAG16 | GRCh38.p7 | 2:213360503 | GGCACAGAATATAGT[C/T]CTAGTCCTGTCAGCT | 79582 |
rs145227659 | snp | A/G | | | intron-variant | SPAG16 | GRCh38.p7 | 2:213620411 | CATTCTCCTGCCTCA[A/G]ACTCCTGAGTAGCTG | 79582 |
rs145232827 | snp | C/T | 0.00438332 | 0.0466095 | intron-variant | SPAG16 | GRCh38.p7 | 2:213553413 | GCTATCAGCATGGTT[C/T]ATTGACAGGAACCGC | 79582 |
rs145233153 | snp | A/C | 0.00953873 | 0.0683987 | intron-variant | SPAG16 | GRCh38.p7 | 2:214224858 | TAGAACTGTCCCTGA[A/C]CTCATAGGGCTTATC | 79582 |
rs145235415 | snp | A/G | 0.00438332 | 0.0466095 | intron-variant | SPAG16 | GRCh38.p7 | 2:214347916 | CCAAGGAAAGCATCA[A/G]GACCTCAGAGGACAG | 79582 |
rs145237875 | in-del | -/TT | | | intron-variant | SPAG16 | GRCh38.p7 | 2:213416543 | GCAGCATTACTTGAC[-/TT]TTGTTTTTTCTTTTT | 79582 |
rs145238139 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | SPAG16 | GRCh38.p7 | 2:213422928 | CTTAGACTTCTAAGT[A/G]CTTTTCTCTTCCCTG | 79582 |
rs145239304 | snp | A/G | 0.00279162 | 0.0372561 | intron-variant | SPAG16 | GRCh38.p7 | 2:213445182 | CTAAAAATCTTCTGC[A/G]CAACAATGAGAACAA | 79582 |
rs145241389 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | SPAG16 | GRCh38.p7 | 2:213497365 | ATTGCATGTGTTTGT[C/T]TTCAACTTTAAAGTA | 79582 |
rs145245046 | snp | G/T | 0.00119737 | 0.0244387 | intron-variant | SPAG16 | GRCh38.p7 | 2:213903655 | TGTCCTCATTGTCTT[G/T]GGGATTAATTCCGCT | 79582 |
rs145248112 | in-del | -/ATGT | | | intron-variant | SPAG16 | GRCh38.p7 | 2:214037863 | TATTCCCAGAAGCCT[-/ATGT]GGTGTGTGTGTGTGT | 79582 |
rs145249353 | snp | G/T | 0.0240643 | 0.107019 | intron-variant | SPAG16 | GRCh38.p7 | 2:213365517 | GGCTGGAGTGCAGTG[G/T]CATGATCTCAGCTCA | 79582 |
rs145252320 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | SPAG16 | GRCh38.p7 | 2:213556992 | ATATCAAAAGTCAAG[A/G]AAGTATTTCACTGAC | 79582 |
rs145253383 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | SPAG16 | GRCh38.p7 | 2:213816481 | ATATATTTAGCTTTA[C/T]TCTGTAATTTTTTTC | 79582 |
rs145255263 | in-del | -/GTG | | | intron-variant | SPAG16 | GRCh38.p7 | 2:213286889 | GCCAGGATCCATCTT[-/GTG]GGGGACATTAATGAA | 79582 |
rs145255933 | snp | C/T | 0.00597247 | 0.0543191 | intron-variant | SPAG16 | GRCh38.p7 | 2:213639018 | CTTTGTCTTTTTTAA[C/T]TGCTGTCACTTTAAA | 79582 |
rs145268027 | snp | A/C | 0.000798403 | 0.0199641 | intron-variant | SPAG16 | GRCh38.p7 | 2:214020507 | AGAAAAGATGACTCA[A/C]TATGCTTATATTTTC | 79582 |
rs145270147 | snp | C/T | 0.00159617 | 0.0282053 | intron-variant | SPAG16 | GRCh38.p7 | 2:214351165 | GGGTTTAATATTTAA[C/T]GTAAGGGCTGAAAAA | 79582 |
rs145287719 | snp | C/T | 0.00159617 | 0.0282053 | intron-variant, upstream-variant-2KB | SPAG16, LOC101928084 | GRCh38.p7 | 2:214104365 | AGGAGCGTGACATGG[C/T]CTGATTCAGCTTTTG | 79582 |
rs145305005 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | SPAG16 | GRCh38.p7 | 2:213305142 | TAACTATTTGTAAAT[A/G]TGTTTTCTTTCTTGA | 79582 |
rs145314097 | snp | A/G | 0.0368353 | 0.130617 | intron-variant | SPAG16 | GRCh38.p7 | 2:213832045 | TCTGTCACCCAGGAT[A/G]GAGTGCAGTGGCACA | 79582 |
rs145316599 | snp | A/G | 0.00199481 | 0.0315187 | intron-variant | SPAG16 | GRCh38.p7 | 2:213327374 | TACTGAATAGACTTC[A/G]TTGTGCAAACAGAAA | 79582 |
rs145323819 | snp | A/G | 0.00716266 | 0.059414 | intron-variant | SPAG16 | GRCh38.p7 | 2:213690530 | GATGGCTGATGAAGC[A/G]TGTTAATAGATGTGT | 79582 |
rs145334303 | snp | A/G | 0.00398564 | 0.0444627 | intron-variant | SPAG16 | GRCh38.p7 | 2:213908600 | ATTCATAATACCTAT[A/G]TATAGTGCTGTCCTC | 79582 |
rs145335532 | snp | A/G | 0.00398564 | 0.0444627 | intron-variant | SPAG16 | GRCh38.p7 | 2:213998952 | CAGTAAAACTCAAGC[A/G]ATGACTTGGGTGCTG | 79582 |
rs145336806 | snp | A/C | 0.0185938 | 0.0946107 | intron-variant | SPAG16 | GRCh38.p7 | 2:213764053 | TGAATCTCTAAGATA[A/C]CCTCAAAGACTCAGG | 79582 |
rs145340025 | snp | C/T | 0.00358779 | 0.0422022 | intron-variant | SPAG16 | GRCh38.p7 | 2:214306833 | CTGAAGTTTTGTTTT[C/T]TGTTTTGTTTTGTTT | 79582 |
rs145340192 | snp | C/T | 0.00517822 | 0.0506191 | intron-variant | SPAG16 | GRCh38.p7 | 2:213682835 | GGGGCTGGATTTACG[C/T]GGTTTTTAATCAAGG | 79582 |
rs145344228 | snp | C/T | 0.0205511 | 0.0992634 | intron-variant | SPAG16 | GRCh38.p7 | 2:213820944 | GATCTGGGCATAAAA[C/T]GCTCCAAAAATATAA | 79582 |
rs145344491 | snp | G/T | | | intron-variant | SPAG16 | GRCh38.p7 | 2:213760783 | ATATAAAAATGTTTT[G/T]TCCTCACAGTTTTGG | 79582 |
rs145352527 | snp | G/T | | | intron-variant | SPAG16 | GRCh38.p7 | 2:213687863 | TTATTTCTCCTTTCC[G/T]TTAGAGACTCCCATT | 79582 |
rs145364262 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | SPAG16 | GRCh38.p7 | 2:213856146 | GGGAGAAATTGGCCA[A/G]AACAAAGGGGCTACA | 79582 |
rs145376304 | snp | A/G | 0.00716266 | 0.059414 | intron-variant | SPAG16 | GRCh38.p7 | 2:213330309 | CATGAAAGCACCCAG[A/G]AGGGAGGGTGTACCT | 79582 |
rs145376455 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | SPAG16 | GRCh38.p7 | 2:214403732 | TATTATCCACTGATA[C/T]TGATTATATCTTCCT | 79582 |
rs145381550 | snp | C/T | 0.00398564 | 0.0444627 | intron-variant | SPAG16 | GRCh38.p7 | 2:214143915 | ATAATCCCAGCACTT[C/T]GGCAGGTCAAGGTGG | 79582 |
rs145392103 | in-del | -/TAT | 0.0178098 | 0.0926698 | intron-variant | SPAG16 | GRCh38.p7 | 2:214287586 | ATCTATTTGAGGCAG[-/TAT]TATTTTTTTGAGTTT | 79582 |
rs145396545 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | SPAG16 | GRCh38.p7 | 2:214353529 | TAAATTCTTTCTTTA[A/C]TTCTAGAGGGAGTTT | 79582 |
rs145396645 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | SPAG16 | GRCh38.p7 | 2:213819587 | TCTACTTCTGTCACC[C/T]AGGCTAAAGTGCAAT | 79582 |
rs145398748 | in-del | -/A | 0.157311 | 0.232183 | intron-variant | SPAG16 | GRCh38.p7 | 2:214266807 | ACAACAGACTGCCTG[-/A]AAAAAAAATTAAGAA | 79582 |
rs145406149 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | SPAG16 | GRCh38.p7 | 2:214392779 | GCCTAAGAGAAATAC[C/T]TCCATAGAAATGTGT | 79582 |
rs145408837 | snp | A/G | 0.0023933 | 0.0345097 | intron-variant | SPAG16 | GRCh38.p7 | 2:214029739 | AGCCTTCAAAGAAGC[A/G]ACAAATTACTCAGTC | 79582 |
rs145409618 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | SPAG16 | GRCh38.p7 | 2:213573277 | CTTCTCTAATCAACA[C/T]AGATTCTAATCACCT | 79582 |
rs145418435 | snp | A/G | 0.0126979 | 0.078662 | intron-variant | SPAG16 | GRCh38.p7 | 2:214310873 | ACTCTGCAGTTAGTT[A/G]GTTTACACTGTTTTG | 79582 |
rs145419178 | snp | C/T | 0.0103295 | 0.0711199 | intron-variant | SPAG16 | GRCh38.p7 | 2:213685999 | GTGAAATTTAATAAA[C/T]TTTGACATATAATTA | 79582 |
rs145419379 | snp | A/T | 0.0023933 | 0.0345097 | intron-variant | SPAG16 | GRCh38.p7 | 2:213618655 | TTAAACAGAATCGTG[A/T]TTATAGTTTGCTGAA | 79582 |
rs145420888 | snp | C/T | 0.00358779 | 0.0422022 | intron-variant | SPAG16 | GRCh38.p7 | 2:213907385 | ACAAAATAAAAATGC[C/T]GGTGAGAATGCAGAG | 79582 |
rs145429710 | snp | C/T | 0.00199481 | 0.0315187 | intron-variant | SPAG16 | GRCh38.p7 | 2:214206127 | CTTGAACCCAGGAGG[C/T]GGAGTTTGCAGTGAG | 79582 |
rs145432023 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | SPAG16 | GRCh38.p7 | 2:213483435 | AGCACCTGTACAAAT[G/T]TACATGGTATATATA | 79582 |
rs145432073 | in-del | -/CA/CCG | | | intron-variant | SPAG16 | GRCh38.p7 | 2:214271852 | GGAAACCCCCCCCCC[-/CA/CCG]AAAAAAAAAGAAAGA | 79582 |
rs145433250 | snp | C/T | 0.00318978 | 0.0398085 | intron-variant | SPAG16 | GRCh38.p7 | 2:214289279 | TGTTATAGTTCTCTG[C/T]GCTTTTGGGGTCTTA | 79582 |
rs145436198 | snp | C/T | 0.00438332 | 0.0466095 | intron-variant | SPAG16 | GRCh38.p7 | 2:213713050 | GAGAGAGAATGAGTG[C/T]CGAGCGCAGTGGGGG | 79582 |
rs145449910 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | SPAG16 | GRCh38.p7 | 2:213718224 | CTTCTCAAAAGCAGA[C/T]ATTTATGTGGCCAAT | 79582 |
rs145452450 | snp | A/G | 0.00358779 | 0.0422022 | intron-variant | SPAG16 | GRCh38.p7 | 2:214179622 | CACTAGATAACTTAA[A/G]AGGTGAAATAAAATG | 79582 |
rs145456336 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | SPAG16 | GRCh38.p7 | 2:214263237 | TGCAATGACCCCACA[C/T]ATGCATAAATTTTAT | 79582 |
rs145459178 | snp | G/T | 0.00279162 | 0.0372561 | intron-variant | SPAG16 | GRCh38.p7 | 2:213967975 | GATGTACTTCAATGT[G/T]TAAAGGTAGAATACT | 79582 |
rs145465479 | in-del | -/TTTATTTA | | | intron-variant | SPAG16 | GRCh38.p7 | 2:214315502 | TCCAGCCCCATCTTT[-/TTTATTTA]TTTATTTATTTATTT | 79582 |
rs145467785 | snp | A/G | | | intron-variant | SPAG16, LOC101928084 | GRCh38.p7 | 2:214100208 | CCTTCTGCCATGATT[A/G]TAAGTTTCCTGAGGC | 79582 |
rs145469762 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | SPAG16 | GRCh38.p7 | 2:214155567 | GGTCTGGAACTCCTG[A/G]GTGCAAGCAATCTTC | 79582 |
rs145471509 | snp | A/C | 0.00119737 | 0.0244387 | intron-variant | SPAG16 | GRCh38.p7 | 2:214251971 | GACTAATAATCTTAA[A/C]TGAATTGATCTGATG | 79582 |
rs145473311 | in-del | -/AT | 0.00478085 | 0.0486577 | intron-variant | SPAG16 | GRCh38.p7 | 2:214407305 | CTGTTCAGAAATTAC[-/AT]GTTACAAGACAATAT | 79582 |
rs145475865 | in-del | -/G | 0.0209421 | 0.100162 | intron-variant | SPAG16 | GRCh38.p7 | 2:213489007 | CTGAATCCGGAAGGC[-/G]GAGGTTGCAGTGAGC | 79582 |
rs145478602 | snp | A/G | 0.00159617 | 0.0282053 | intron-variant | SPAG16 | GRCh38.p7 | 2:213914793 | ATGTCTTCTTTTGGA[A/G]AGAGTCTGTTCTTGT | 79582 |
rs145479759 | snp | G/T | 0.00398564 | 0.0444627 | intron-variant | SPAG16 | GRCh38.p7 | 2:213703477 | CCTAGTATAATTCAC[G/T]GTATTTTTGCAGATT | 79582 |
rs145480036 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | SPAG16 | GRCh38.p7 | 2:214364879 | GTTTGTGAGCAGAGA[A/G]GTGTACCTTTCTCAA | 79582 |
rs145482325 | snp | C/T | 0.00159617 | 0.0282053 | intron-variant | SPAG16 | GRCh38.p7 | 2:213700882 | CCAGGCGTGGTGGCT[C/T]ACACATATAATCCCA | 79582 |
rs145486860 | snp | A/G | 0.00318978 | 0.0398085 | intron-variant | SPAG16 | GRCh38.p7 | 2:213664823 | TGTGTGTCTGTATGC[A/G]TGCATATATATACAT | 79582 |
rs145492732 | snp | A/T | | | intron-variant | SPAG16 | GRCh38.p7 | 2:214078973 | GAAAAAGGCAGCAAC[A/T]ACCAACGAGAAGCTG | 79582 |
rs145496595 | snp | C/T | | | intron-variant | SPAG16 | GRCh38.p7 | 2:213394507 | ATCAAGATTAGGATG[C/T]TGACATTGATATAAT | 79582 |
rs145498268 | snp | G/T | 0.00199481 | 0.0315187 | intron-variant | SPAG16 | GRCh38.p7 | 2:214038377 | ATTTCAGTTCTGTTA[G/T]TTCTACTTTGTCAGA | 79582 |
rs145501879 | snp | G/T | | | intron-variant | SPAG16 | GRCh38.p7 | 2:213578656 | TCGCTTCTACACTTT[G/T]TGGCTAAAATCAAGT | 79582 |
rs145503293 | snp | A/C | 0.0115144 | 0.0749975 | intron-variant | SPAG16 | GRCh38.p7 | 2:213774840 | GCTTTAGTTAGATTC[A/C]CTTCTCAGGCTTCAA | 79582 |
rs145507896 | snp | A/G | 0.0379877 | 0.132479 | intron-variant | SPAG16 | GRCh38.p7 | 2:214110974 | TGCCCACTTTTTGAT[A/G]GGATTTTTTTTTTCC | 79582 |
rs145513798 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | SPAG16 | GRCh38.p7 | 2:214034362 | ATCCCATGTGTTCTC[C/T]AGATTTCACCTATTA | 79582 |
rs145514048 | in-del | -/TTTTATT | 0.0693013 | 0.172766 | intron-variant | SPAG16 | GRCh38.p7 | 2:214388194 | TTTTTATATTTTATA[-/TTTTATT]AACAAATAACAAGCT | 79582 |
rs145517715 | snp | A/G | 0.00279162 | 0.0372561 | intron-variant | SPAG16 | GRCh38.p7 | 2:213994691 | TTCATGACTGCTTTG[A/G]TTAAATACCATCTAT | 79582 |
rs145519647 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | SPAG16 | GRCh38.p7 | 2:213903291 | GTTTTCCATGGGCAT[C/G]CCACCCCTGCAGCAA | 79582 |
rs145525300 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | SPAG16 | GRCh38.p7 | 2:214151675 | ATTAGTTATGTCTAA[A/C]CATTTTTTCTAGTCA | 79582 |
rs145531868 | snp | A/C | 0.00636936 | 0.0560724 | intron-variant | SPAG16 | GRCh38.p7 | 2:213337838 | CTCAACCTAGCAAGA[A/C]AGGCCAGTGTTCAAA | 79582 |
rs145539569 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | SPAG16 | GRCh38.p7 | 2:213622489 | ATGAGCTCCCATGGC[C/T]TCTGCTGCAGCACCC | 79582 |
rs145539717 | snp | G/T | 0.00636936 | 0.0560724 | intron-variant | SPAG16 | GRCh38.p7 | 2:213942973 | CCTTATATAGGAAGG[G/T]ACAAGAGACCTTACT | 79582 |
rs145545252 | snp | A/C | 0.00318978 | 0.0398085 | intron-variant | SPAG16 | GRCh38.p7 | 2:213432564 | AAAATCCTAAACAGA[A/C]CAATAATGAGTAATG | 79582 |
rs145547624 | snp | A/T | 0.0138799 | 0.0821421 | intron-variant | SPAG16 | GRCh38.p7 | 2:213702471 | TGAGACCACGAACTC[A/T]CCAAAAGGAACAAAC | 79582 |
rs145548125 | snp | A/G | 0.00557542 | 0.0525036 | intron-variant | SPAG16 | GRCh38.p7 | 2:214299738 | GAAACTTTTTAATAA[A/G]GAATCTCAGGTTAAA | 79582 |
rs145550524 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant, upstream-variant-2KB | SPAG16, MIR4438 | GRCh38.p7 | 2:213757178 | GGAGACTAAAGACTT[A/G]TTCTCTGAAAACTAC | 79582 |
rs145553121 | snp | A/G | 0.00159617 | 0.0282053 | intron-variant | SPAG16 | GRCh38.p7 | 2:214251361 | TAATAGGCAAAAGAT[A/G]AAGACTAGAAGAACT | 79582 |
rs145554246 | snp | C/T | 0.00199481 | 0.0315187 | intron-variant | SPAG16, LOC101928084 | GRCh38.p7 | 2:214087911 | GAAAAATACTAAAAA[C/T]AGTATTCTGCACAAA | 79582 |
rs145555100 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | SPAG16 | GRCh38.p7 | 2:213443188 | GAGTACCTAATATCT[A/G]CTTTCTTAGCAAATT | 79582 |
rs145564225 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | SPAG16 | GRCh38.p7 | 2:213976445 | CACACAAATATATCC[C/T]ATTGGACCTTTCAAG | 79582 |