SNP - dbSNP |
dbSNP | Type | Alleles | Het | Se(het) | Fxn-class | Gene Name | Assembly | Chr-pos | Sequence | Entrez Gene |
rs339808 | snp | A/T | 0.0479149 | 0.147179 | intron-variant | SPAG16 | GRCh38.p7 | 2:213425003 | CTCTTACTTTGAGTA[A/T]ATCCCTTATTCCTGA | 79582 |
rs339809 | snp | A/G | 0.0535932 | 0.154675 | intron-variant | SPAG16 | GRCh38.p7 | 2:213411043 | ttcaagagcttatca[A/G]tcagttagcccttgt | 79582 |
rs339810 | snp | C/T | 0.0267878 | 0.112589 | intron-variant | SPAG16 | GRCh38.p7 | 2:213413897 | TTTTTTGGGATATTT[C/T]ACAGTGCAAACAAAG | 79582 |
rs339811 | snp | A/G | 0.046775 | 0.145601 | intron-variant | SPAG16 | GRCh38.p7 | 2:213418905 | TTAGGGGCACCATCA[A/G]CTATACAAATTACTG | 79582 |
rs339812 | snp | G/T | 0.0479149 | 0.147179 | intron-variant | SPAG16 | GRCh38.p7 | 2:213419689 | TTTTTTCTTTGAAAA[G/T]AATTCACATTACATG | 79582 |
rs339813 | snp | A/C | 0.046775 | 0.145601 | intron-variant | SPAG16 | GRCh38.p7 | 2:213390088 | tcctcaagcttcatc[A/C]atgttgtggaatttg | 79582 |
rs339814 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | SPAG16 | GRCh38.p7 | 2:213394145 | CTGATCTTGAGATAA[A/G]AAAGGGTTTCTTAAT | 79582 |
rs339815 | snp | A/G | 0.499971 | 0.00379382 | intron-variant, utr-variant-3-prime, downstream-variant-500B | SPAG16 | GRCh38.p7 | 2:213396810 | gactgtaaagaacac[A/G]gataaagggtatgGG | 79582 |
rs339816 | snp | G/T | 0.046775 | 0.145601 | intron-variant, utr-variant-3-prime | SPAG16 | GRCh38.p7 | 2:213397597 | ttcagagagttagaa[G/T]gatcatccatatcaa | 79582 |
rs339817 | snp | A/C/G/T | 0.0456336 | 0.143994 | intron-variant, utr-variant-3-prime | SPAG16 | GRCh38.p7 | 2:213399109 | gaaatacaaataaaa[A/C/G/T]tttttagaattgaaa | 79582 |
rs339818 | snp | C/T | 0.0263992 | 0.111815 | intron-variant, utr-variant-3-prime | SPAG16 | GRCh38.p7 | 2:213399906 | agtaaatttaaaact[C/T]agatgaaatggtcat | 79582 |
rs339819 | snp | A/G | 0.046775 | 0.145601 | intron-variant, utr-variant-3-prime | SPAG16 | GRCh38.p7 | 2:213400339 | aacaaaaattaaaat[A/G]ctacatataaacatc | 79582 |
rs339820 | snp | A/G | 0.0479149 | 0.147179 | intron-variant | SPAG16 | GRCh38.p7 | 2:213430283 | tcttttgaattaatc[A/G]agtcagacaaaagtg | 79582 |
rs339821 | snp | C/T | 0.47934 | 0.0995154 | intron-variant | SPAG16 | GRCh38.p7 | 2:213433689 | aggaattgtattaaa[C/T]ctgtagattgctttg | 79582 |
rs339822 | snp | A/C | 0.35445 | 0.227135 | intron-variant | SPAG16 | GRCh38.p7 | 2:213433944 | gacaagaacgagaca[A/C]tgtctcaaaaaaaaa | 79582 |
rs339823 | snp | A/G | 0.0448719 | 0.142907 | intron-variant | SPAG16 | GRCh38.p7 | 2:213434263 | tatccttctgcatcc[A/G]gctatccaattttcc | 79582 |
rs339824 | snp | C/G | 0.256619 | 0.249912 | intron-variant | SPAG16 | GRCh38.p7 | 2:213434307 | cttgagttgattttt[C/G]tatatgctgagagat | 79582 |
rs339825 | snp | G/T | 0.0479149 | 0.147179 | intron-variant | SPAG16 | GRCh38.p7 | 2:213436163 | AAAATGTGATTAAAT[G/T]ATTTAACATTAAACA | 79582 |
rs714126 | snp | C/T | 0.484841 | 0.0857308 | intron-variant | SPAG16 | GRCh38.p7 | 2:213902193 | CTTTATTCTTTGGTA[C/T]ATCCACAGAAAATAA | 79582 |
rs714567 | snp | G/T | 0.130008 | 0.219321 | intron-variant | SPAG16 | GRCh38.p7 | 2:213767816 | TGTGACATTTATTGG[G/T]CAACAAATGAGCCTG | 79582 |
rs716992 | snp | C/G | | | intron-variant | SPAG16 | GRCh38.p7 | 2:213768793 | gcctataaggcataa[C/G]aaatgtatgtcaata | 79582 |
rs720015 | snp | C/T | 0.479824 | 0.098392 | intron-variant | SPAG16 | GRCh38.p7 | 2:213877347 | CAAGGTCTCACTTTG[C/T]TGTGTAGTCAGGAGT | 79582 |
rs720016 | snp | A/G | 0.479824 | 0.098392 | intron-variant | SPAG16 | GRCh38.p7 | 2:213877472 | ACGCTACCACACCCA[A/G]CTAATTAAAAAATCA | 79582 |
rs721759 | snp | C/T | 0.0825414 | 0.185628 | intron-variant | SPAG16 | GRCh38.p7 | 2:214053307 | TTAATTTTCATTTTT[C/T]TTTGTTCTAGTTAAG | 79582 |
rs723621 | snp | C/T | 0.0103295 | 0.0711199 | intron-variant, utr-variant-5-prime | SPAG16 | GRCh38.p7 | 2:213300561 | AAATGCAGAAAAAAA[C/T]ATGGGGATCTAGCTG | 79582 |
rs723622 | snp | A/G | 0.0652144 | 0.168387 | intron-variant, utr-variant-5-prime | SPAG16 | GRCh38.p7 | 2:213300694 | aattctgtctatgtt[A/G]tctgtgtagaagttt | 79582 |
rs724953 | snp | A/G | 0 | 0 | intron-variant | SPAG16 | GRCh38.p7 | 2:213735421 | AATTTATATTACTGA[A/G]AAATACTCTTCTATA | 79582 |
rs724954 | snp | C/T | 0.474363 | 0.110278 | intron-variant | SPAG16 | GRCh38.p7 | 2:213735568 | ttcccttatcttgtc[C/T]tgactaatggctgga | 79582 |
rs727502 | snp | A/G | 0.480382 | 0.097079 | intron-variant | SPAG16 | GRCh38.p7 | 2:213715266 | TCTATCTATCTATCT[A/G]TCCATTCATCCATCT | 79582 |
rs727503 | snp | C/T | 0.491157 | 0.065903 | intron-variant | SPAG16 | GRCh38.p7 | 2:213715585 | CTTCCTCATGGTATA[C/T]ATTGAGTGAATTACG | 79582 |
rs737690 | snp | C/T | 0.311369 | 0.242351 | intron-variant | SPAG16 | GRCh38.p7 | 2:214043190 | CTCATGCAGTGGGAA[C/T]ATTTAAATTATGAAA | 79582 |
rs759776 | snp | C/T | 0.483418 | 0.0895317 | intron-variant | SPAG16 | GRCh38.p7 | 2:214115986 | GATTCAGGTAGGAGG[C/T]TGCAGAGCCCCAGTG | 79582 |
rs759777 | snp | C/T | 0.280256 | 0.248162 | intron-variant | SPAG16 | GRCh38.p7 | 2:214042615 | ATAAAGATAGTTCAA[C/T]GTTTCCTAAGATTGA | 79582 |
rs766258 | snp | A/G | 0.211212 | 0.246973 | intron-variant | SPAG16 | GRCh38.p7 | 2:213312256 | GTTCTATGAACCACT[A/G]AAAAGTTTCCATTGC | 79582 |
rs766605 | snp | C/T | 0.214843 | 0.247516 | intron-variant | SPAG16 | GRCh38.p7 | 2:214120679 | GAAATAAAATATCCA[C/T]AGGCACCGCTTCTCA | 79582 |
rs769348 | snp | C/G | 0.490007 | 0.0699769 | intron-variant | SPAG16 | GRCh38.p7 | 2:214079844 | TTGAAATTCTCTTTT[C/G]TCTTCTAAACAAGGA | 79582 |
rs769349 | snp | A/T | 0.0329836 | 0.124112 | intron-variant | SPAG16 | GRCh38.p7 | 2:214079843 | TGAAATTCTCTTTTC[A/T]CTTCTAAACAAGGAC | 79582 |
rs878923 | snp | A/G | 0.326035 | 0.238157 | intron-variant | SPAG16 | GRCh38.p7 | 2:213725643 | agaagagggtgcggc[A/G]tgtcttagcaacagt | 79582 |
rs889887 | snp | A/G | 0.0490535 | 0.14873 | intron-variant | SPAG16 | GRCh38.p7 | 2:213607726 | CTTAGATGTATTTTA[A/G]AATGCACATGAGTGG | 79582 |
rs901950 | snp | A/C/G | 0 | 0 | intron-variant | SPAG16 | GRCh38.p7 | 2:213377881 | GAACTAATAGGATGT[A/C/G]TATATATATATATAT | 79582 |
rs905537 | snp | C/T | 0.173643 | 0.238054 | intron-variant | SPAG16 | GRCh38.p7 | 2:213522440 | TTCCCTCTGCCCAGT[C/T]CTCTCTTCCCACCCC | 79582 |
rs907122 | snp | A/T | 0.466721 | 0.124627 | intron-variant | SPAG16 | GRCh38.p7 | 2:213932730 | TTCCTCACCAAAAAG[A/T]TGGATCACTGTGAAG | 79582 |
rs907123 | snp | C/G | 0.120674 | 0.21395 | intron-variant | SPAG16 | GRCh38.p7 | 2:213932827 | CAATTATCTATGACA[C/G]TCAGTCTGAATAATT | 79582 |
rs918327 | snp | A/G | 0.0810805 | 0.184299 | intron-variant | SPAG16 | GRCh38.p7 | 2:214067355 | TATCAAACATTGTGT[A/G]GCACACAATAGAAAT | 79582 |
rs918352 | snp | A/G | 0.499477 | 0.0161657 | intron-variant | SPAG16 | GRCh38.p7 | 2:214220213 | AACACATTTTTAGAA[A/G]GTCTTGAATCCTTGG | 79582 |
rs918353 | snp | C/T | 0.172028 | 0.23753 | intron-variant | SPAG16 | GRCh38.p7 | 2:214248101 | AAACACAAAATAGAG[C/T]AATCTCTAGTTCAGA | 79582 |
rs918354 | snp | A/T | 0.176219 | 0.238865 | intron-variant | SPAG16 | GRCh38.p7 | 2:214251131 | CCTATGATAAGTTAC[A/T]ATGTATATTGTAACA | 79582 |
rs918355 | snp | C/T | 0.26818 | 0.249338 | intron-variant | SPAG16 | GRCh38.p7 | 2:214260208 | TGATAAAAGACTATA[C/T]ATTGGGTACAGTATA | 79582 |
rs918839 | snp | C/T | 0.362104 | 0.223456 | intron-variant | SPAG16 | GRCh38.p7 | 2:213606891 | TCTCATAATATTCTG[C/T]AGATTATTCGCCATT | 79582 |
rs925356 | snp | A/G | 0.401747 | 0.198678 | intron-variant | SPAG16 | GRCh38.p7 | 2:213933681 | CAGAGGGACTTGCAA[A/G]ATTCAACAGCTTCTT | 79582 |
rs925357 | snp | C/T | 0.437965 | 0.164831 | intron-variant | SPAG16 | GRCh38.p7 | 2:213978789 | CAACAGTCACAGGAC[C/T]GAGCTTGAAAACAGA | 79582 |
rs929725 | snp | C/T | 0.348794 | 0.229651 | intron-variant | SPAG16 | GRCh38.p7 | 2:214158335 | CATTCCACTTTTCCT[C/T]GATCCAAAACAGAAA | 79582 |
rs931993 | snp | A/G | 0.391769 | 0.205917 | intron-variant | SPAG16 | GRCh38.p7 | 2:213967645 | TCATAGCAGGGGTTA[A/G]GACATAATTTTCATC | 79582 |
rs933978 | snp | C/T | 0.331874 | 0.236213 | intron-variant | SPAG16 | GRCh38.p7 | 2:213849783 | TTATTATATTAATGA[C/T]AGAGAGTAGATTCTT | 79582 |
rs933979 | snp | C/G | 0.140242 | 0.224618 | intron-variant | SPAG16 | GRCh38.p7 | 2:213725333 | tgagccAACTCTCTG[C/G]TCTTTGTTATTCAAT | 79582 |
rs933980 | snp | A/G | 0.140242 | 0.224618 | intron-variant | SPAG16 | GRCh38.p7 | 2:213725432 | TAAATTCATCATCAT[A/G]GAATGCCCATCCATC | 79582 |
rs933981 | snp | G/T | 0.140242 | 0.224618 | intron-variant | SPAG16 | GRCh38.p7 | 2:213725526 | ttccaacaaaggact[G/T]ccccatagcatccca | 79582 |
rs933982 | snp | C/T | 0.130008 | 0.219321 | intron-variant | SPAG16 | GRCh38.p7 | 2:213726350 | GGATTGATTCCTACC[C/T]TTCATTAGGTACCTT | 79582 |
rs951866 | snp | A/G | 0.405429 | 0.195811 | intron-variant | SPAG16 | GRCh38.p7 | 2:213945976 | TAAAAATATAACAAT[A/G]CTACATTTATATTTG | 79582 |
rs953133 | snp | C/T | 0.498945 | 0.022939 | intron-variant | SPAG16 | GRCh38.p7 | 2:213941351 | TGGAGATTTATAACT[C/T]GTAATGAATGTTAAG | 79582 |
rs953134 | snp | A/T | 0.270892 | 0.249126 | intron-variant | SPAG16 | GRCh38.p7 | 2:213941413 | ATAATTTATTTTAGA[A/T]TTTTGCATACATATA | 79582 |
rs953881 | snp | C/T | 0.362104 | 0.223456 | intron-variant | SPAG16 | GRCh38.p7 | 2:213662571 | TGGCTAAATATGTCA[C/T]ATTATATTCCTATTA | 79582 |
rs956179 | snp | C/T | 0.496483 | 0.0417852 | intron-variant | SPAG16 | GRCh38.p7 | 2:214053273 | ATTTAATATAGATTC[C/T]AAATTTCTCCTCTTA | 79582 |
rs965421 | snp | A/G | 0.482831 | 0.0910472 | intron-variant | SPAG16 | GRCh38.p7 | 2:214263303 | TCATCTGTCCTCTCC[A/G]GTGAATTCTTAATTA | 79582 |
rs974176 | snp | C/T | 0.478354 | 0.101757 | intron-variant | SPAG16 | GRCh38.p7 | 2:214304188 | TGTAAAGGACATAAT[C/T]TTGTTCTTTGTTATT | 79582 |
rs975956 | snp | C/T | 0.370795 | 0.21888 | intron-variant, nc-transcript-variant, utr-variant-5-prime | SPAG16 | GRCh38.p7 | 2:213297049 | GCCCACAAACTAATC[C/T]TGAATTTATTAGAAG | 79582 |
rs976911 | snp | A/G | 0 | 0 | intron-variant | SPAG16 | GRCh38.p7 | 2:214245415 | TCCTGTATCTTAATG[A/G]TACATTTTTATAATT | 79582 |
rs977251 | snp | C/T | 0.192401 | 0.243274 | intron-variant | SPAG16 | GRCh38.p7 | 2:213319976 | AATAGAACTTAAAAT[C/T]TAAAAAATTAGACAA | 79582 |
rs977252 | snp | G/T | 0.0460142 | 0.144533 | intron-variant | SPAG16 | GRCh38.p7 | 2:213320174 | CATTCTTAGAAAATG[G/T]AGAATGAAGTTTTGT | 79582 |
rs1012556 | snp | G/T | 0.211516 | 0.24702 | intron-variant | SPAG16 | GRCh38.p7 | 2:213324867 | gagcaactggaattc[G/T]catgtattcctactg | 79582 |
rs1012557 | snp | A/T | 0.211212 | 0.246973 | intron-variant | SPAG16 | GRCh38.p7 | 2:213324687 | ttcacagcagtttta[A/T]ctttaataaccaact | 79582 |
rs1014450 | snp | C/T | 0.404559 | 0.196498 | intron-variant | SPAG16 | GRCh38.p7 | 2:214130069 | ggggtctggcttcaa[C/T]agagaaaattctcac | 79582 |
rs1014451 | snp | A/G | 0.301681 | 0.2446 | intron-variant | SPAG16 | GRCh38.p7 | 2:214130174 | aagccctgattggCA[A/G]GCTTCCAAGCCCCAA | 79582 |
rs1014452 | snp | A/G | 0.301681 | 0.2446 | intron-variant | SPAG16 | GRCh38.p7 | 2:214130193 | TCCAAGCCCCAAACT[A/G]GAAGTCTCTAGCAGC | 79582 |
rs1015355 | snp | A/G | 0.24449 | 0.249939 | intron-variant | SPAG16 | GRCh38.p7 | 2:214129356 | tggctgacttcattc[A/G]ttttcatctcttgat | 79582 |
rs1015970 | snp | C/G | 0.387263 | 0.208947 | intron-variant | SPAG16 | GRCh38.p7 | 2:214023755 | CCTTTGCATACACAT[C/G]ACAAATATCATTCCT | 79582 |
rs1015971 | snp | G/T | 0.0329836 | 0.124112 | intron-variant | SPAG16 | GRCh38.p7 | 2:214067952 | GTTACTTTGTAAATA[G/T]AATTCAAATTAGAAT | 79582 |
rs1017194 | snp | C/T | 0.243347 | 0.249911 | intron-variant | SPAG16 | GRCh38.p7 | 2:214222478 | AAATGAACCAGCCAC[C/T]TACACAAACTCTTGT | 79582 |
rs1021310 | snp | C/T | 0.194278 | 0.243711 | intron-variant, upstream-variant-2KB | SPAG16 | GRCh38.p7 | 2:213295337 | AATTAGAGTAACTTA[C/T]AGTTTTTGAAAGTCT | 79582 |
rs1023605 | snp | A/G | 0.461923 | 0.132621 | intron-variant | SPAG16 | GRCh38.p7 | 2:214193425 | tgtgtgtgtgtgtgt[A/G]tgagagagagagaga | 79582 |
rs1023606 | snp | A/T | | | intron-variant | SPAG16 | GRCh38.p7 | 2:214193432 | gtgtgtgtatgagag[A/T]gagagagagagagag | 79582 |
rs1023607 | snp | A/T | 0.392881 | 0.205147 | intron-variant | SPAG16 | GRCh38.p7 | 2:214193707 | TCACTAAATGATGGT[A/T]CCTATTTTATATTCA | 79582 |
rs1023608 | snp | C/T | 0.393065 | 0.205018 | intron-variant | SPAG16 | GRCh38.p7 | 2:214193708 | CACTAAATGATGGTT[C/T]CTATTTTATATTCAG | 79582 |
rs1023609 | snp | A/G | 0.499937 | 0.0055907 | intron-variant | SPAG16 | GRCh38.p7 | 2:214230416 | CAGCTCTGGCTGTGC[A/G]CAAATTCTTTTTGCA | 79582 |
rs1024928 | snp | A/G | 0.498392 | 0.028309 | intron-variant | SPAG16 | GRCh38.p7 | 2:214128875 | tgttaggtgggaaag[A/G]agcagtgctcaaact | 79582 |
rs1027939 | snp | C/T | 0.373196 | 0.217538 | intron-variant | SPAG16 | GRCh38.p7 | 2:213937862 | TAAACTTGATGTGAA[C/T]GTTCTTTGATACCAA | 79582 |
rs1027940 | snp | A/C | 0.434398 | 0.168811 | intron-variant | SPAG16 | GRCh38.p7 | 2:213937912 | AAAAAGGTAAATGTC[A/C]TTAGGATTTTAAAAT | 79582 |
rs1027941 | snp | C/T | 0.384785 | 0.210554 | intron-variant | SPAG16 | GRCh38.p7 | 2:213937945 | ATCCCTATTCCTTTC[C/T]ACAGCAAATGCTATT | 79582 |
rs1028137 | snp | C/G | 0.344592 | 0.231414 | intron-variant | SPAG16 | GRCh38.p7 | 2:213670816 | ATATGCGGCATTTGA[C/G]AAATTCAAAAACTAA | 79582 |
rs1030143 | snp | A/G | 0.227074 | 0.248947 | intron-variant | SPAG16 | GRCh38.p7 | 2:214077175 | AAATATTTATTAATA[A/G]TAACAGGCAACCACA | 79582 |
rs1030288 | snp | C/T | 0.132066 | 0.220435 | intron-variant | SPAG16 | GRCh38.p7 | 2:213451701 | tttatataaatgggc[C/T]agtgaggagggtgtg | 79582 |
rs1033065 | snp | G/T | 0.480931 | 0.0957637 | intron-variant | SPAG16 | GRCh38.p7 | 2:213897772 | CCATAGCCAGTAATT[G/T]AGTCCTTACTTAGAG | 79582 |
rs1033066 | snp | A/G | 0.0539704 | 0.155153 | intron-variant | SPAG16 | GRCh38.p7 | 2:213897979 | TGACAATTTTTAAAA[A/G]ACTATTATATGAAGA | 79582 |
rs1033067 | snp | C/T | 0.484841 | 0.0857308 | intron-variant | SPAG16 | GRCh38.p7 | 2:213900369 | ACCAATATCTCGGAA[C/T]GACTGTGATTATACA | 79582 |
rs1033068 | snp | A/C | 0.484841 | 0.0857308 | intron-variant | SPAG16 | GRCh38.p7 | 2:213900391 | GATTATACAAAACAC[A/C]GATATTAAAATAATT | 79582 |
rs1033069 | snp | A/G | 0.484841 | 0.0857308 | intron-variant | SPAG16 | GRCh38.p7 | 2:213900484 | TGTCCTCTCCCTGCA[A/G]CAAACCGGGTCTTCA | 79582 |
rs1033070 | snp | C/T | 0.495634 | 0.0465208 | intron-variant | SPAG16 | GRCh38.p7 | 2:214016024 | GGAGGAGGAGGAGTT[C/T]AGGGTGAGAAACTTT | 79582 |
rs1038662 | snp | C/T | 0.046775 | 0.145601 | intron-variant | SPAG16 | GRCh38.p7 | 2:213324340 | gagtttatccgtttg[C/T]caaaattATATAGCT | 79582 |
rs1039500 | snp | C/T | | | intron-variant | SPAG16 | GRCh38.p7 | 2:213540704 | AACATTCTCCAACTT[C/T]TCCAAATTGTGAAGA | 79582 |
rs1039502 | snp | A/C | 0.0240643 | 0.107019 | intron-variant | SPAG16 | GRCh38.p7 | 2:213497122 | CTGTAAAACTAGCAG[A/C]CTGTATCtttatatt | 79582 |
rs1039503 | snp | C/T | 0.0240643 | 0.107019 | intron-variant | SPAG16 | GRCh38.p7 | 2:213497060 | ACTTATAAGTAATGA[C/T]CACAAGTGTTTCAAT | 79582 |
rs1043646 | snp | G/T | 0.211212 | 0.246973 | utr-variant-3-prime, intron-variant | SPAG16 | GRCh38.p7 | 2:213317597 | AGATGGTACATTTTT[G/T]ATATAACATTCACTT | 79582 |
rs1043647 | snp | A/C | 0.211212 | 0.246973 | utr-variant-3-prime, intron-variant | SPAG16 | GRCh38.p7 | 2:213317604 | ACATTTTTTATATAA[A/C]ATTCACTTCCTTGTG | 79582 |
rs1071875 | snp | C/T | 0.479824 | 0.098392 | intron-variant | SPAG16 | GRCh38.p7 | 2:213883788 | ttgcccttttaaatt[C/T]ttattggcttaaagt | 79582 |
rs1072570 | snp | C/T | 0.287606 | 0.247155 | intron-variant | SPAG16 | GRCh38.p7 | 2:214030137 | aactctctatttccc[C/T]cttccgcaggtccta | 79582 |
rs1072625 | snp | C/T | | | intron-variant | SPAG16 | GRCh38.p7 | 2:213704453 | TGTGTAAGTGGGCTG[C/T]GATGTCACTCTGTGT | 79582 |
rs1107324 | snp | C/T | 0.128288 | 0.218372 | intron-variant | SPAG16 | GRCh38.p7 | 2:213726574 | AAACCGGCGAGCTCC[C/T]GATTTATCTTCATGT | 79582 |
rs1114446 | snp | A/G | 0.472989 | 0.113031 | intron-variant | SPAG16 | GRCh38.p7 | 2:213619507 | aaaaacgggcaaagc[A/G]tatgaatagacattc | 79582 |
rs1114610 | snp | A/G | 0.347694 | 0.230122 | intron-variant | SPAG16 | GRCh38.p7 | 2:213430646 | aaaagcaaaaagttt[A/G]gaaaacctatttaag | 79582 |
rs1116359 | snp | C/T | 0.484771 | 0.0859212 | intron-variant | SPAG16 | GRCh38.p7 | 2:213921913 | gcctgatgggattcc[C/T]tttgtatgtgacctg | 79582 |
rs1116360 | snp | A/T | 0.00279162 | 0.0372561 | intron-variant | SPAG16 | GRCh38.p7 | 2:213922111 | TACAATATCCTGATA[A/T]ATGTTTTCCAAGTTG | 79582 |
rs1116361 | snp | C/G | 0.283947 | 0.247685 | intron-variant | SPAG16 | GRCh38.p7 | 2:213922249 | TTTCTTTATTTTTGT[C/G]TGACTGAGTTATTTC | 79582 |
rs1119234 | snp | C/G | 0.0655868 | 0.168795 | intron-variant | SPAG16 | GRCh38.p7 | 2:213455715 | CATTATATTATCACA[C/G]GAGCGCAAACCCTAT | 79582 |
rs1119235 | snp | G/T | 0.0652144 | 0.168387 | intron-variant | SPAG16 | GRCh38.p7 | 2:213455714 | ATTATATTATCACAG[G/T]AGCGCAAACCCTATT | 79582 |
rs1120124 | snp | A/G | 0.343254 | 0.231956 | intron-variant | SPAG16 | GRCh38.p7 | 2:214046854 | tgttccaggataaaa[A/G]attaatatacaaaaa | 79582 |
rs1120538 | snp | A/G | 0 | 0 | intron-variant | SPAG16 | GRCh38.p7 | 2:213894101 | agtagctatacttat[A/G]tcagataaaataaac | 79582 |
rs1120539 | snp | A/G | 0.479824 | 0.098392 | intron-variant | SPAG16 | GRCh38.p7 | 2:213894270 | ggattcatctcagga[A/G]tgcaaggatggttca | 79582 |
rs1127380 | snp | C/T | 0.211212 | 0.246973 | utr-variant-3-prime, intron-variant | SPAG16 | GRCh38.p7 | 2:213317837 | GTTAACAAATGTATC[C/T]CTCTGTTGGGGGCTA | 79582 |
rs1157387 | snp | G/T | 0.229429 | 0.249152 | intron-variant | SPAG16 | GRCh38.p7 | 2:214184299 | CACCAAGGATTATTT[G/T]TGTCATATAAATGTA | 79582 |
rs1160401 | snp | A/C | 0.44252 | 0.159487 | intron-variant | SPAG16 | GRCh38.p7 | 2:214076702 | TAGTTCTTATTATAG[A/C]ATGTGCCTTGGGCTG | 79582 |
rs1160402 | snp | C/T | 0.45692 | 0.1403 | intron-variant | SPAG16 | GRCh38.p7 | 2:214076993 | TGAACCCAGGCCGCC[C/T]GGAGGAGTGTGCAGC | 79582 |
rs1219969 | snp | A/G | 0.0569829 | 0.158885 | intron-variant, upstream-variant-2KB | SPAG16 | GRCh38.p7 | 2:213295162 | TTCATAACCATTACC[A/G]TGCATTAAAGTGTTT | 79582 |
rs1219987 | snp | A/C | 0.19459 | 0.243782 | intron-variant, upstream-variant-2KB | SPAG16 | GRCh38.p7 | 2:213298006 | AAAAAGGAGTTTCAC[A/C]AATTCCTTCACATTT | 79582 |
rs1238571 | snp | C/G/T | 0 | 0 | intron-variant | SPAG16 | GRCh38.p7 | 2:213904621 | cctttacctactttg[C/G/T]ttttttttttttTTT | 79582 |
rs1238756 | snp | A/G | 0 | 0 | intron-variant | SPAG16 | GRCh38.p7 | 2:214223505 | CAACCTTTTGTTTCA[A/G]AACAATAAAATGCAA | 79582 |
rs1259004 | snp | C/G | 0.00279162 | 0.0372561 | intron-variant | SPAG16 | GRCh38.p7 | 2:213573205 | cagctcccagcgtga[C/G]cgacgcagaagacgg | 79582 |
rs1259005 | snp | A/T | 0.31503 | 0.241394 | intron-variant, downstream-variant-500B | SPAG16 | GRCh38.p7 | 2:213611803 | AATATGAAACAAGAG[A/T]TGTCTTTACTTCTCC | 79582 |
rs1259006 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | SPAG16 | GRCh38.p7 | 2:213602507 | agctgggattacagg[C/T]gtgcaccaccacgcc | 79582 |
rs1259007 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | SPAG16 | GRCh38.p7 | 2:213599863 | aatacaaaaattagc[C/T]ggtcatggtggcagg | 79582 |
rs1271119 | snp | C/T | | | intron-variant | SPAG16 | GRCh38.p7 | 2:213588806 | agagcgagactccgt[C/T]tcaaaaaaaaaaaaa | 79582 |
rs1304727 | snp | A/G | 0.474091 | 0.11083 | intron-variant | SPAG16 | GRCh38.p7 | 2:213610663 | aagcatgtttattaa[A/G]aaagtaaagtggtga | 79582 |
rs1344633 | snp | A/G | 0.470034 | 0.11868 | intron-variant | SPAG16 | GRCh38.p7 | 2:213795064 | TGAGAATAAAAACCT[A/G]TGCAAACTTTTAAAA | 79582 |
rs1344634 | snp | A/G | 0.181978 | 0.240568 | intron-variant | SPAG16 | GRCh38.p7 | 2:213840258 | AATGTAATTGCCACA[A/G]TTCTTTTCTTCAGTA | 79582 |
rs1346329 | snp | C/T | 0.472709 | 0.11358 | intron-variant | SPAG16 | GRCh38.p7 | 2:213885613 | TTTAACATTCCATCT[C/T]AAGGCAATGTGATAG | 79582 |
rs1346330 | snp | A/G | 0.479663 | 0.0987666 | intron-variant | SPAG16 | GRCh38.p7 | 2:213885635 | atgtgatagccatga[A/G]gtctttgtgtgataa | 79582 |
rs1346331 | snp | A/G | 0.140242 | 0.224618 | intron-variant | SPAG16 | GRCh38.p7 | 2:213725071 | tagcctggctctgtc[A/G]cccaggctggagtgc | 79582 |
rs1365814 | snp | A/C | 0.47726 | 0.104176 | intron-variant | SPAG16 | GRCh38.p7 | 2:213869682 | ATTCCAAAAGTAATA[A/C]AGGATCATCATAGAG | 79582 |
rs1365815 | snp | A/C | 0.32885 | 0.23724 | intron-variant | SPAG16 | GRCh38.p7 | 2:213869776 | CTTTGTAAAACCAAC[A/C]TTGCAAGTATTAATT | 79582 |
rs1365816 | snp | C/T | 0.165853 | 0.235413 | intron-variant | SPAG16 | GRCh38.p7 | 2:213869896 | GAGGGAAATTTGGAA[C/T]GGAGAGGATCTTTAG | 79582 |
rs1365817 | snp | A/G | 0.479904 | 0.0982045 | intron-variant | SPAG16 | GRCh38.p7 | 2:213870024 | ATTATAATGCTATGT[A/G]TATTTATGATGCTGC | 79582 |
rs1365818 | snp | A/G | 0.479904 | 0.0982045 | intron-variant | SPAG16 | GRCh38.p7 | 2:213875231 | AGTGTCCCAATTTTA[A/G]TGATAAATTATATGG | 79582 |
rs1365820 | snp | A/G | 0.0711525 | 0.174681 | intron-variant | SPAG16 | GRCh38.p7 | 2:213876351 | AGAAAAAGAATCTTT[A/G]TGTAGTTGAATCCTT | 79582 |
rs1365821 | snp | A/G | 0.479824 | 0.098392 | intron-variant | SPAG16 | GRCh38.p7 | 2:213877116 | ACCTCAGTGCCTTTA[A/G]CATGTACTTTTTCTG | 79582 |
rs1365822 | snp | A/G | 0.479824 | 0.098392 | intron-variant | SPAG16 | GRCh38.p7 | 2:213877691 | TGAGGATACCATAAT[A/G]TCCACTTATGTATTT | 79582 |
rs1365823 | snp | C/T | 0.479824 | 0.098392 | intron-variant | SPAG16 | GRCh38.p7 | 2:213882117 | ttttaattctgttta[C/T]gtgttaaattatatt | 79582 |
rs1365824 | snp | A/G | 0.479824 | 0.098392 | intron-variant | SPAG16 | GRCh38.p7 | 2:213882167 | aatcagccttgcatt[A/G]caggaataaagccta | 79582 |
rs1365825 | snp | A/G | 0.479824 | 0.098392 | intron-variant | SPAG16 | GRCh38.p7 | 2:213882262 | aatttttgtgtctat[A/G]ttcatcagggatact | 79582 |
rs1365826 | snp | A/C | 0.479744 | 0.0985793 | intron-variant | SPAG16 | GRCh38.p7 | 2:213882367 | gagttagggagcagc[A/C]cctggtcctcaattt | 79582 |
rs1365827 | snp | C/T | 0.140242 | 0.224618 | intron-variant | SPAG16 | GRCh38.p7 | 2:213744075 | AAGGTGTATTCATTC[C/T]TTCAGAGGATTTACT | 79582 |
rs1387208 | snp | C/T | 0.358303 | 0.225323 | intron-variant | SPAG16 | GRCh38.p7 | 2:213374622 | AATATTTTATTAATA[C/T]AATATTCTTTTTATA | 79582 |
rs1387209 | snp | A/G | 0.355096 | 0.226837 | intron-variant | SPAG16 | GRCh38.p7 | 2:213377215 | AGGATAGCAATAATT[A/G]CTGTTGGTCTGATTC | 79582 |
rs1393905 | snp | C/T | 0.0452528 | 0.143452 | intron-variant | SPAG16 | GRCh38.p7 | 2:213475005 | AGGGTCCTCCAATGG[C/T]ACTGCTGTTTTTCCA | 79582 |
rs1393906 | snp | A/G | 0.0479149 | 0.147179 | intron-variant | SPAG16 | GRCh38.p7 | 2:213550644 | ACATATAAGTTTAAA[A/G]GAATTTTGTAGATCT | 79582 |
rs1397348 | snp | A/G | 0.0460142 | 0.144533 | intron-variant | SPAG16 | GRCh38.p7 | 2:213929776 | AGCTTGAATTACTAA[A/G]CAATTCAAGTTAGCA | 79582 |
rs1397349 | snp | G/T | | | intron-variant | SPAG16 | GRCh38.p7 | 2:213936753 | CAACCAGGTGTATCA[G/T]CTGGTGATCCAGAAG | 79582 |
rs1397350 | snp | A/G | 0.414741 | 0.188044 | intron-variant | SPAG16 | GRCh38.p7 | 2:213942583 | GGAATAGTCATTCAC[A/G]TGTTTGAAGCTTCAG | 79582 |
rs1397351 | snp | A/G | 0.489083 | 0.0730708 | intron-variant | SPAG16 | GRCh38.p7 | 2:214002408 | ATAAAATGATTAGAT[A/G]ATAAATGGAATTATT | 79582 |
rs1397352 | snp | C/G | 0.489492 | 0.0717183 | intron-variant | SPAG16 | GRCh38.p7 | 2:214002662 | CCAAGGCAGTCAGTG[C/G]TCTAAGTCCTGGTCC | 79582 |
rs1397353 | snp | C/T | 0.489024 | 0.0732638 | intron-variant | SPAG16 | GRCh38.p7 | 2:214002878 | TCTTCTAGAAACACC[C/T]TCACAGACATACCCA | 79582 |
rs1397354 | snp | C/T | 0.484561 | 0.0864924 | intron-variant | SPAG16 | GRCh38.p7 | 2:214051670 | TTTGTGGCTCACCTA[C/T]TCTAGGAGCAAGAAA | 79582 |
rs1397355 | snp | A/C | 0.0829062 | 0.185956 | intron-variant | SPAG16 | GRCh38.p7 | 2:214051617 | CTATTGTAAGTATAA[A/C]TAGAAAAGGCCTAAT | 79582 |
rs1397356 | snp | A/C | 0.381891 | 0.212379 | intron-variant | SPAG16 | GRCh38.p7 | 2:214040736 | tcattgtttttattt[A/C]tttatttattggcta | 79582 |
rs1397357 | snp | C/T | 0.496348 | 0.0425753 | intron-variant | SPAG16 | GRCh38.p7 | 2:214041410 | aaagactctttgcac[C/T]tctacattttaatgg | 79582 |
rs1397358 | snp | A/G | 0.459801 | 0.135955 | intron-variant | SPAG16 | GRCh38.p7 | 2:213949708 | TTATGCAATAAAAAT[A/G]AAGGCCTAAGTAGGC | 79582 |
rs1400015 | snp | A/C | 0.371785 | 0.218331 | intron-variant | SPAG16 | GRCh38.p7 | 2:213598092 | AGAGCATGGCCAAAA[A/C]CAGATGATGATGGTA | 79582 |
rs1400016 | snp | A/C | 0.00716266 | 0.059414 | intron-variant | SPAG16 | GRCh38.p7 | 2:213594531 | AGGTATAGAAAGAGA[A/C]AAAAGAGTGAGCACA | 79582 |
rs1427345 | snp | G/T | 0.47709 | 0.104548 | intron-variant | SPAG16 | GRCh38.p7 | 2:213854874 | GTTACAAAACCAGTT[G/T]GTGGGCTAGGTTTGG | 79582 |
rs1427347 | snp | A/G | 0.144632 | 0.226711 | intron-variant | SPAG16 | GRCh38.p7 | 2:213848506 | GCCAAGGTGAAAATT[A/G]ATGAACATATAAGGC | 79582 |
rs1427348 | snp | G/T | 0.472896 | 0.113214 | intron-variant | SPAG16 | GRCh38.p7 | 2:213861144 | TTCTAGTGAAACATT[G/T]TTTCATTTTTCTCCA | 79582 |
rs1427349 | snp | A/C | 0.16028 | 0.233346 | intron-variant | SPAG16 | GRCh38.p7 | 2:213841537 | AAAGAACAATGCTAA[A/C]GCTATGTAAATTATT | 79582 |
rs1427350 | snp | A/G | 0.472709 | 0.11358 | intron-variant | SPAG16 | GRCh38.p7 | 2:213860323 | AAATGACTTTTGTGG[A/G]TAATTCTACACACAT | 79582 |
rs1427351 | snp | A/C | 0.472709 | 0.11358 | intron-variant | SPAG16 | GRCh38.p7 | 2:213860293 | TTTCAGCAAGGCATA[A/C]AATGTTCTTTAGCTG | 79582 |
rs1427353 | snp | C/T | 0.472803 | 0.113397 | intron-variant | SPAG16 | GRCh38.p7 | 2:213860088 | AAGCAGTTTAAGGGC[C/T]ATGGACCAGAAATAT | 79582 |
rs1427354 | snp | C/G | 0.335101 | 0.23507 | intron-variant | SPAG16 | GRCh38.p7 | 2:213835112 | TTGGACTTGGGTTTC[C/G]TAAATTTCCCACTAA | 79582 |
rs1427355 | snp | C/T | 0.472709 | 0.11358 | intron-variant | SPAG16 | GRCh38.p7 | 2:213869837 | ATAATAATGTCCGTA[C/T]GTATAGTAGTTACCT | 79582 |
rs1427356 | snp | A/G | 0.479904 | 0.0982045 | intron-variant | SPAG16 | GRCh38.p7 | 2:213871339 | TTTTGGAACACAGGA[A/G]CTTAACCAAAGGCTT | 79582 |
rs1427357 | snp | A/C | 0.479904 | 0.0982045 | intron-variant | SPAG16 | GRCh38.p7 | 2:213871510 | GACATATTTCTAAGA[A/C]TATGGAAGGACACAT | 79582 |
rs1427358 | snp | C/T | 0.142947 | 0.22592 | intron-variant | SPAG16 | GRCh38.p7 | 2:213876626 | CTGGAAAAGAGAAAT[C/T]AATAAGAAAGTATTG | 79582 |
rs1427359 | snp | C/T | 0.376394 | 0.215696 | intron-variant | SPAG16 | GRCh38.p7 | 2:213887864 | TTGTACTTTATCTTT[C/T]CCACTTTTTCTATTT | 79582 |
rs1427360 | snp | A/G | 0.472335 | 0.114312 | intron-variant | SPAG16 | GRCh38.p7 | 2:213891336 | GAGTATTATATTGGA[A/G]TAATATTTTATGGCT | 79582 |
rs1427361 | snp | A/G | 0.479824 | 0.098392 | intron-variant | SPAG16 | GRCh38.p7 | 2:213891416 | CTAATACCTAAGTAG[A/G]CAGAGCTGTAGATAC | 79582 |
rs1427362 | snp | G/T | 0.481165 | 0.0951993 | intron-variant | SPAG16 | GRCh38.p7 | 2:213810775 | CCTAGCTCAAATATT[G/T]TGATATTGGTCTAAG | 79582 |
rs1469352 | snp | C/T | 0.479904 | 0.0982045 | intron-variant | SPAG16 | GRCh38.p7 | 2:213868669 | ACAGCATGTAACTCC[C/T]CACATATCTCTATAA | 79582 |
rs1469353 | snp | A/G | 0.144632 | 0.226711 | intron-variant | SPAG16 | GRCh38.p7 | 2:213868931 | TGAAAACCCCTTGAC[A/G]AGTACATTATTTAGA | 79582 |
rs1473227 | snp | A/C | 0.39527 | 0.203462 | intron-variant | SPAG16 | GRCh38.p7 | 2:213810003 | CCCACGCATCGTACG[A/C]AAAGGATAGAAGCCC | 79582 |
rs1474003 | snp | C/T | 0.473726 | 0.111565 | intron-variant | SPAG16 | GRCh38.p7 | 2:213625405 | GCCTGTATCAAAACA[C/T]CTCGTGTACCCCCCG | 79582 |
rs1474004 | snp | A/G | 0.473451 | 0.112115 | intron-variant | SPAG16 | GRCh38.p7 | 2:213625661 | CTTTTTGTTGTTGTT[A/G]CTGTTCTTTTttttg | 79582 |
rs1474005 | snp | C/T | 0.473451 | 0.112115 | intron-variant | SPAG16 | GRCh38.p7 | 2:213625662 | TTTTTGTTGTTGTTA[C/T]TGTTCTTTTttttgt | 79582 |
rs1477256 | snp | C/T | 0.00438332 | 0.0466095 | intron-variant | SPAG16 | GRCh38.p7 | 2:214310862 | CCAAACAGATGACTC[C/T]GCAGTTAGTTGGTTT | 79582 |
rs1477257 | snp | A/G | 0.474992 | 0.108989 | intron-variant | SPAG16 | GRCh38.p7 | 2:214331771 | TCTGCTTTTCTGTGA[A/G]GAAGGTCTCTAGGTC | 79582 |
rs1488971 | snp | A/G | 0.350327 | 0.228986 | intron-variant | SPAG16 | GRCh38.p7 | 2:213309272 | ACATAATATGTAAAC[A/G]AATGGGCATGGGCAT | 79582 |
rs1488972 | snp | C/T | 0.046775 | 0.145601 | intron-variant | SPAG16 | GRCh38.p7 | 2:213373477 | TAAAGTGTGTATTTT[C/T]CATTTTGTTTGTAGA | 79582 |
rs1488975 | snp | C/G | 0.0460142 | 0.144533 | intron-variant | SPAG16 | GRCh38.p7 | 2:213353367 | TCATGGCTTGTATTT[C/G]CAATATAGAGAAATC | 79582 |
rs1488976 | snp | C/T | | | intron-variant | SPAG16 | GRCh38.p7 | 2:213352183 | atagaggttttaggg[C/T]aaaaatatattaaaa | 79582 |
rs1488977 | snp | C/T | 0.218151 | 0.247963 | intron-variant | SPAG16 | GRCh38.p7 | 2:213384304 | ttccacattaattct[C/T]gacctgtgggatata | 79582 |
rs1488978 | snp | C/T | 0.194278 | 0.243711 | intron-variant | SPAG16 | GRCh38.p7 | 2:213383962 | GTGTAGTCATTGATC[C/T]GGCAAATGTGTCTTC | 79582 |
rs1488981 | snp | A/G | 0.194902 | 0.243853 | intron-variant | SPAG16 | GRCh38.p7 | 2:213363296 | CTATTCCTAGAAGCC[A/G]AAAGAATTATAAAtt | 79582 |
rs1488982 | snp | C/T | 0.195214 | 0.243923 | intron-variant | SPAG16 | GRCh38.p7 | 2:213363221 | GAGTTGCTAATGTAG[C/T]ACTGAGAATTCCTGT | 79582 |
rs1488983 | snp | C/G | 0.0463947 | 0.145069 | intron-variant | SPAG16 | GRCh38.p7 | 2:213290336 | CTAGGAATACAGAAC[C/G]TGGCCTGGACTTGGA | 79582 |
rs1488984 | snp | G/T | 0.210301 | 0.246828 | intron-variant | SPAG16 | GRCh38.p7 | 2:213293074 | TAATTGGATCATAGG[G/T]CCAGTTTCCCCCATG | 79582 |
rs1488985 | snp | C/T | 0.325327 | 0.238382 | intron-variant | SPAG16 | GRCh38.p7 | 2:213293386 | TGTAATCCTCACACA[C/T]TGAGTAGACGTGACC | 79582 |
rs1488986 | snp | C/T | 0.210301 | 0.246828 | intron-variant | SPAG16 | GRCh38.p7 | 2:213293395 | CACACACTGAGTAGA[C/T]GTGACCCATGTAACC | 79582 |
rs1488987 | snp | A/G | 0.210301 | 0.246828 | intron-variant | SPAG16 | GRCh38.p7 | 2:213293427 | GTGGGATATTGAAGA[A/G]ATGATGTGTGACTTC | 79582 |
rs1488988 | snp | C/T | 0.395546 | 0.203264 | intron-variant, nc-transcript-variant, missense, utr-variant-5-prime | SPAG16 | GRCh38.p7 | 2:213297125 | TCATTTTTCATGGAT[C/T]TTCAGAATGACATGG | 79582 |
rs1503376 | snp | C/T | 0.0244538 | 0.107838 | intron-variant | SPAG16 | GRCh38.p7 | 2:213482409 | GAATTTGTCTCAGTT[C/T]AAGGAAATGTCAGCA | 79582 |
rs1503377 | snp | A/C | 0.0452528 | 0.143452 | intron-variant | SPAG16 | GRCh38.p7 | 2:213482463 | GGTTTTGACAGTAGT[A/C]AGATTATAAGCATTT | 79582 |
rs1503378 | snp | G/T | 0.0452528 | 0.143452 | intron-variant | SPAG16 | GRCh38.p7 | 2:213482588 | AAAAATGTTCATTTT[G/T]ATTAACTAATAAACT | 79582 |
rs1503379 | snp | G/T | 0.192715 | 0.243348 | intron-variant | SPAG16 | GRCh38.p7 | 2:213459493 | GACTTGACCTACAGG[G/T]ACTAAAGTGAAACTT | 79582 |
rs1503380 | snp | C/T | 0.188631 | 0.242351 | intron-variant | SPAG16 | GRCh38.p7 | 2:213459477 | ACTAAAGTGAAACTT[C/T]GAATCATCTCAATCA | 79582 |
rs1510543 | snp | A/C | 0.237303 | 0.249677 | intron-variant | SPAG16 | GRCh38.p7 | 2:213927987 | AACATATGTGCAAAC[A/C]AACTATTGTGGCAAA | 79582 |
rs1510544 | snp | A/T | 0.237303 | 0.249677 | intron-variant | SPAG16 | GRCh38.p7 | 2:213927991 | TATGTGCAAACCAAC[A/T]ATTGTGGCAAAAACA | 79582 |
rs1510545 | snp | C/G | | | intron-variant | SPAG16 | GRCh38.p7 | 2:213934120 | AGAACAATGGGGAAA[C/G]GTGCTCCTCTGGGGG | 79582 |
rs1510546 | snp | C/G | 0.452597 | 0.146474 | intron-variant | SPAG16 | GRCh38.p7 | 2:213942256 | cagaatcaggctgac[C/G]tgtttcatttcatgt | 79582 |
rs1510547 | snp | A/G | 0.474992 | 0.108989 | intron-variant | SPAG16 | GRCh38.p7 | 2:213994926 | TGCATCTTTTCTTAT[A/G]TGTTCTAAGATCCCT | 79582 |
rs1510548 | snp | A/G | 0.430285 | 0.173197 | intron-variant | SPAG16 | GRCh38.p7 | 2:214006867 | ACTTTCTTCCCTTGA[A/G]CTATGTGAAGACCTA | 79582 |
rs1510549 | snp | C/T | 0.0569829 | 0.158885 | intron-variant | SPAG16 | GRCh38.p7 | 2:214010527 | GTAAGGGCTCTTGGG[C/T]GTAAACAGCAAACGA | 79582 |
rs1510550 | snp | A/G | 0.0256215 | 0.110247 | intron-variant | SPAG16 | GRCh38.p7 | 2:214010599 | GACCTCAGACTTTGC[A/G]GTACTCTAACAGTGA | 79582 |
rs1510551 | snp | A/G | 0.480064 | 0.0978296 | intron-variant | SPAG16 | GRCh38.p7 | 2:214025910 | TAACAAAATTAAACT[A/G]TAAACTTCTGTAAAA | 79582 |
rs1510552 | snp | G/T | 0.317451 | 0.240729 | intron-variant | SPAG16 | GRCh38.p7 | 2:214052678 | ATTAAAATTGGCAGA[G/T]AAATTTTTCAGTTTA | 79582 |
rs1510553 | snp | C/T | 0.418974 | 0.184249 | intron-variant | SPAG16 | GRCh38.p7 | 2:214050135 | CCATATGGCTTCACT[C/T]CTCGCCTCTTCCCAC | 79582 |
rs1510554 | snp | C/T | 0.0807149 | 0.183963 | intron-variant | SPAG16 | GRCh38.p7 | 2:214049365 | TTTAAAAAAGCAACT[C/T]TCATGTTTATAGTCT | 79582 |
rs1510555 | snp | A/G | 0.422158 | 0.181278 | intron-variant | SPAG16 | GRCh38.p7 | 2:214027983 | AACTAATTAAAATAT[A/G]TATTTGTAAAATGAG | 79582 |
rs1510556 | snp | A/G | 0.422 | 0.181428 | intron-variant | SPAG16 | GRCh38.p7 | 2:214028085 | TTTATGATGTGTGAG[A/G]TTGTGGGGAGCTAGC | 79582 |
rs1510557 | snp | A/G | 0.350982 | 0.228698 | intron-variant | SPAG16 | GRCh38.p7 | 2:214032661 | TTCTAGGGAAATCAC[A/G]TGTTGTAAGGCCTTG | 79582 |
rs1515913 | snp | A/G | 0.485255 | 0.0845871 | intron-variant | SPAG16 | GRCh38.p7 | 2:213624742 | TCATACACTTCCTCT[A/G]TACTTGCTGAATGCA | 79582 |
rs1515915 | snp | C/T | 0.444133 | 0.157519 | intron-variant | SPAG16 | GRCh38.p7 | 2:213663117 | GATCATACAGTCACA[C/T]TAAAGTTAATTTTTT | 79582 |
rs1544735 | snp | C/T | 0.0479149 | 0.147179 | intron-variant | SPAG16 | GRCh38.p7 | 2:214265858 | GGCCTTTCCTAATCA[C/T]CCTAGCTAAAGCAGT | 79582 |
rs1549116 | snp | A/T | 0.454182 | 0.144256 | intron-variant | SPAG16 | GRCh38.p7 | 2:214244866 | GACTTTGTTTAGAAG[A/T]TTCTGTAGTCTTAAC | 79582 |
rs1552536 | snp | A/G | | | intron-variant | SPAG16 | GRCh38.p7 | 2:213308347 | TTTTAGGTCTGCTAA[A/G]ATGTTCTGTCAGAAT | 79582 |
rs1552537 | snp | A/G/T | 0 | 0 | intron-variant | SPAG16 | GRCh38.p7 | 2:213308359 | TAAGATGTTCTGTCA[A/G/T]AATACTACATACAGT | 79582 |
rs1552538 | snp | A/G | | | intron-variant | SPAG16 | GRCh38.p7 | 2:213308437 | TTGGATTTTTTTTCA[A/G]ATGTTGGAATATTTG | 79582 |
rs1552539 | snp | A/G | 0.23031 | 0.249223 | intron-variant, utr-variant-3-prime | SPAG16 | GRCh38.p7 | 2:213369906 | GTCCATGACATTAAT[A/G]TCACCGAAGTCCATA | 79582 |
rs1554177 | snp | G/T | 0.475877 | 0.107142 | intron-variant | SPAG16 | GRCh38.p7 | 2:213628877 | AATTCCCTTTATTCA[G/T]TCAGTTTGTGTCTGT | 79582 |
rs1554178 | snp | A/T | 0.485664 | 0.0834419 | intron-variant | SPAG16 | GRCh38.p7 | 2:213629384 | CATTTAGGGAATTAA[A/T]ATGTGAATAATAGTG | 79582 |
rs1559925 | snp | A/T | 0.480931 | 0.0957637 | intron-variant | SPAG16 | GRCh38.p7 | 2:213897592 | TCTTATTTTCTAGAG[A/T]TTGTACCCTCCTCAT | 79582 |
rs1559926 | snp | A/C | 0.480931 | 0.0957637 | intron-variant | SPAG16 | GRCh38.p7 | 2:213897599 | TTCTAGAGATTGTAC[A/C]CTCCTCATCTGCCTA | 79582 |
rs1559927 | snp | A/G | 0.48178 | 0.0936921 | intron-variant | SPAG16 | GRCh38.p7 | 2:213897616 | TCCTCATCTGCCTAT[A/G]TTGGTCTCAGGGCAT | 79582 |
rs1559928 | snp | C/T | 0.479984 | 0.0980171 | intron-variant | SPAG16 | GRCh38.p7 | 2:213874610 | atcaccacaaacaca[C/T]gagtaatgtgtagcc | 79582 |
rs1559929 | snp | G/T | 0.479904 | 0.0982045 | intron-variant | SPAG16 | GRCh38.p7 | 2:213874790 | GCTCAGAGGGAGGGA[G/T]TGTGGGGACTATGAA | 79582 |
rs1582837 | snp | A/G | 0.122411 | 0.214991 | intron-variant | SPAG16 | GRCh38.p7 | 2:213828696 | ttggaccaaaacacc[A/G]aagcctcttcaaata | 79582 |
rs1582838 | snp | C/T | 0.0581099 | 0.160244 | intron-variant | SPAG16 | GRCh38.p7 | 2:213818530 | catacaaagtttatt[C/T]atatatacatggact | 79582 |
rs1582839 | snp | C/T | 0.283684 | 0.24772 | intron-variant | SPAG16 | GRCh38.p7 | 2:213818490 | tgcaaatatgagacc[C/T]aaggcagagccagat | 79582 |
rs1582840 | snp | G/T | 0.00358779 | 0.0422022 | intron-variant | SPAG16 | GRCh38.p7 | 2:213818444 | ACACTCTTCATAGGG[G/T]ACAGGAAAGTGAGAG | 79582 |
rs1586557 | snp | A/G | 0.499767 | 0.0107802 | intron-variant | SPAG16 | GRCh38.p7 | 2:213293568 | agacccacatgggga[A/G]gaactgaggtcttct | 79582 |
rs1588453 | snp | A/G | 0.269809 | 0.249214 | intron-variant | SPAG16 | GRCh38.p7 | 2:213920827 | gtcatactctgccac[A/G]agtgcttaggcacca | 79582 |
rs1588454 | snp | G/T | 0.470424 | 0.117954 | intron-variant | SPAG16 | GRCh38.p7 | 2:213920868 | GCTCTGCATCAGCTG[G/T]CATGCTGCCCCTACC | 79582 |
rs1588455 | snp | C/T | 0.327914 | 0.237549 | intron-variant | SPAG16 | GRCh38.p7 | 2:213927173 | GTATTACAGGGTTCC[C/T]GTGCTCATGACCTTG | 79582 |
rs1588457 | snp | C/T | | | intron-variant | SPAG16 | GRCh38.p7 | 2:213961897 | acttcccaactcatt[C/T]tatgaggttgatatt | 79582 |
rs1593200 | snp | C/T | 0.131381 | 0.220067 | intron-variant | SPAG16 | GRCh38.p7 | 2:213455681 | ttgcaacctagatcc[C/T]tcacatgcacagttc | 79582 |
rs1593201 | snp | A/G | 0.177503 | 0.239258 | intron-variant | SPAG16 | GRCh38.p7 | 2:213442080 | ttgaacctgggaggc[A/G]gatgttgcagtgagc | 79582 |
rs1593202 | snp | G/T | 0.155325 | 0.23138 | intron-variant | SPAG16 | GRCh38.p7 | 2:213442241 | aaaatatgcaccaga[G/T]ctgtatgagaaactc | 79582 |
rs1593688 | snp | C/T | 0.469049 | 0.120489 | intron-variant | SPAG16 | GRCh38.p7 | 2:213796692 | tgtcaacaaacctgc[C/T]gcacttctaatcata | 79582 |
rs1593689 | snp | G/T | 0.479824 | 0.098392 | intron-variant | SPAG16 | GRCh38.p7 | 2:213878981 | GTGATTTAATTTCTG[G/T]GTTCTCTATTCTGTT | 79582 |
rs1593690 | snp | C/T | 0.479824 | 0.098392 | intron-variant | SPAG16 | GRCh38.p7 | 2:213883863 | tttctgtttttatag[C/T]agatctttctctgtc | 79582 |
rs1593691 | snp | A/G | 0.479824 | 0.098392 | intron-variant | SPAG16 | GRCh38.p7 | 2:213883916 | ttacatgtgtgatat[A/G]tctcttgaagacagc | 79582 |
rs1593692 | snp | A/T | 0.470521 | 0.117772 | intron-variant | SPAG16 | GRCh38.p7 | 2:213906606 | atcatactacctgac[A/T]gcaaaatatactaca | 79582 |
rs1593693 | snp | A/G | 0.48491 | 0.0855403 | intron-variant | SPAG16 | GRCh38.p7 | 2:213906665 | ttggtataaaaccag[A/G]cacattagaaaaatg | 79582 |
rs1601955 | snp | A/G | 0.0240643 | 0.107019 | intron-variant, upstream-variant-2KB | SPAG16 | GRCh38.p7 | 2:213315666 | CGTACTCTCAGTTTG[A/G]CTTTTATCTGCATGA | 79582 |
rs1601956 | snp | C/T | 0.298144 | 0.245321 | intron-variant | SPAG16 | GRCh38.p7 | 2:213332264 | TCCAATTTATTGGCA[C/T]GTAGTTGGTCATAGT | 79582 |
rs1604689 | snp | A/G | 0.192715 | 0.243348 | intron-variant | SPAG16 | GRCh38.p7 | 2:213438799 | atcttgcataggtct[A/G]acctaatcagatgca | 79582 |
rs1604690 | snp | C/T | 0.0919752 | 0.193722 | intron-variant | SPAG16 | GRCh38.p7 | 2:213439096 | ACACCTTGATTTCAG[C/T]CTGGGGAGATCATGA | 79582 |
rs1604691 | snp | C/T | 0.111576 | 0.20818 | intron-variant | SPAG16 | GRCh38.p7 | 2:213439113 | TGGGGAGATCATGAA[C/T]AGAGAATCCAGTCAA | 79582 |
rs1604692 | snp | A/G | 0.260227 | 0.249791 | intron-variant | SPAG16 | GRCh38.p7 | 2:213442300 | ATGGAGATTTATTTC[A/G]TGTTCATAATTAGCA | 79582 |
rs1606013 | snp | A/C | 0.178144 | 0.239451 | intron-variant | SPAG16 | GRCh38.p7 | 2:213958595 | attttggaacatcag[A/C]aactgaaaaagttgg | 79582 |
rs1606014 | snp | C/T | 0.416055 | 0.186885 | intron-variant | SPAG16 | GRCh38.p7 | 2:213955501 | tctaataataaacta[C/T]tatatttatagttaa | 79582 |
rs1606936 | snp | A/G | 0.364401 | 0.222289 | intron-variant | SPAG16 | GRCh38.p7 | 2:213634447 | tacttaggattaaag[A/G]agttcacatgccaca | 79582 |
rs1808456 | snp | A/G | 0.00676609 | 0.0577691 | intron-variant | SPAG16 | GRCh38.p7 | 2:213584926 | GCTAGGATTACTGGC[A/G]TGAGCCACCTTGCTG | 79582 |
rs1812884 | snp | C/G | 0.351635 | 0.228408 | intron-variant | SPAG16 | GRCh38.p7 | 2:213425114 | GGATGGTCTCAATCT[C/G]CTGACCTCGTGATCC | 79582 |
rs1813393 | snp | C/T | 0.0689305 | 0.172377 | intron-variant | SPAG16 | GRCh38.p7 | 2:213455542 | CTGGTGCCGAAAAGT[C/T]TGGGGACTGCTGACC | 79582 |
rs1813708 | snp | A/G | 0.138546 | 0.223781 | intron-variant | SPAG16 | GRCh38.p7 | 2:213521184 | cagaaaacatccacc[A/G]accaggccaccttcc | 79582 |
rs1816209 | snp | A/G | 0.153332 | 0.230554 | intron-variant | SPAG16 | GRCh38.p7 | 2:213826559 | aattcaataacaaga[A/G]gaatattggaaacta | 79582 |
rs1816210 | snp | A/C | 0.404035 | 0.196909 | intron-variant | SPAG16 | GRCh38.p7 | 2:213826540 | tattggaaactatac[A/C]aacacatggaaatta | 79582 |
rs1816211 | snp | A/G | 0.479824 | 0.098392 | intron-variant | SPAG16 | GRCh38.p7 | 2:213883018 | CTACAGGCACCCACC[A/G]CCACACCCGGCTAAT | 79582 |
rs1820289 | snp | A/T | 0.0244538 | 0.107838 | intron-variant | SPAG16 | GRCh38.p7 | 2:213451293 | TTAGAAACAAGTACG[A/T]TATCCTCTTTTCCTA | 79582 |
rs1820561 | snp | A/G | 0.470132 | 0.118498 | intron-variant | SPAG16 | GRCh38.p7 | 2:213826050 | tacaggatactatga[A/G]caactatatgccaat | 79582 |
rs1820562 | snp | G/T | 0.473726 | 0.111565 | intron-variant | SPAG16 | GRCh38.p7 | 2:213818960 | TCTGAGACTGGGTAA[G/T]TTATAAACAGAAGAG | 79582 |
rs1820563 | snp | C/T | 0.00199481 | 0.0315187 | intron-variant | SPAG16 | GRCh38.p7 | 2:213838175 | CAAAAAAAAAGAAAT[C/T]AGAGATAAGGACAAA | 79582 |
rs1820564 | snp | A/G | | | intron-variant | SPAG16 | GRCh38.p7 | 2:213877678 | CTTAGGGAGAGGATG[A/G]GGATACCATAATATC | 79582 |
rs1820565 | snp | A/C | 0.479744 | 0.0985793 | intron-variant | SPAG16 | GRCh38.p7 | 2:213893038 | TCAAAAGTCAAGGAC[A/C]AAGAGTGAATCCCAA | 79582 |
rs1820566 | snp | A/G | 0.212122 | 0.247114 | intron-variant, upstream-variant-2KB | SPAG16, MIR4438 | GRCh38.p7 | 2:213757055 | AACTGATATTTGCAT[A/G]TTGATTTTGTGTCCT | 79582 |
rs1820567 | snp | A/G | 0.212122 | 0.247114 | intron-variant, upstream-variant-2KB | SPAG16, MIR4438 | GRCh38.p7 | 2:213756381 | CTGCCTCAGCCTTCC[A/G]AATAGCTGGGACTAC | 79582 |
rs1820568 | snp | A/G | 0.212425 | 0.24716 | intron-variant, upstream-variant-2KB | SPAG16, MIR4438 | GRCh38.p7 | 2:213756301 | TTGAGACGGGGTTTT[A/G]CCACGTTGGCCAGGC | 79582 |
rs1820569 | snp | C/T | 0.140242 | 0.224618 | intron-variant | SPAG16 | GRCh38.p7 | 2:213729458 | TATTATAAGACTTAG[C/T]GTGGCAACAAAGGAG | 79582 |
rs1820570 | snp | A/T | 0.140242 | 0.224618 | intron-variant | SPAG16 | GRCh38.p7 | 2:213729646 | TGTCAGCTTATAAAC[A/T]ACATTGAAATAAGAA | 79582 |
rs1820571 | snp | A/G | 0.140242 | 0.224618 | intron-variant | SPAG16 | GRCh38.p7 | 2:213730265 | GAAACTGCAGTGGCT[A/G]TGGTTGATGGCAAAG | 79582 |
rs1820572 | snp | A/G | 0.0614824 | 0.164198 | intron-variant | SPAG16 | GRCh38.p7 | 2:213730378 | ATATTTTTACCATAA[A/G]AGCAGCTGATTTTGT | 79582 |
rs1827525 | snp | G/T | 0.0221141 | 0.102801 | intron-variant | SPAG16 | GRCh38.p7 | 2:213488205 | TAAATATTATTCAAA[G/T]GAAATAACTATTGAA | 79582 |
rs1828406 | snp | G/T | 0.220544 | 0.248259 | intron-variant | SPAG16 | GRCh38.p7 | 2:214047069 | gatattccatgttca[G/T]ggattgaaagaatca | 79582 |
rs1834161 | snp | A/G | 0.00636936 | 0.0560724 | intron-variant | SPAG16 | GRCh38.p7 | 2:213498643 | ATTTGAGGTGCTCAC[A/G]AGACATGCAAGTTGA | 79582 |
rs1834767 | snp | A/G | | | intron-variant | SPAG16 | GRCh38.p7 | 2:213767711 | TTTATGAATCCTTTA[A/G]GTTACTAAAGGCAGA | 79582 |
rs1834768 | snp | C/T | 0.155987 | 0.23165 | intron-variant | SPAG16 | GRCh38.p7 | 2:213781957 | GAGCTAATAGAGGCA[C/T]GTTTTCTATAGCAAT | 79582 |
rs1834769 | snp | C/T | 0.155987 | 0.23165 | intron-variant | SPAG16 | GRCh38.p7 | 2:213782178 | AACTGTAATAGTCTT[C/T]AGTTTTTTTTTTTTA | 79582 |
rs1834770 | snp | C/T | 0.0236746 | 0.106192 | intron-variant | SPAG16 | GRCh38.p7 | 2:213787313 | ATAATGGTATTGATG[C/T]TTTCTATTTGCTTTT | 79582 |
rs1834771 | snp | A/G | 0.479744 | 0.0985793 | intron-variant | SPAG16 | GRCh38.p7 | 2:213879217 | CAATCTACAGTTTAA[A/G]TGCAATCTCTATCAA | 79582 |
rs1834772 | snp | C/G | 0.479744 | 0.0985793 | intron-variant | SPAG16 | GRCh38.p7 | 2:213891151 | TAATGACAGAAATAA[C/G]CATAGTAAAATTGTT | 79582 |
rs1834773 | snp | C/T | 0.149665 | 0.228982 | intron-variant | SPAG16 | GRCh38.p7 | 2:213812392 | GCAGGTCTAAGTTAG[C/T]AGTTGGAGGCTAAGA | 79582 |
rs1834774 | snp | G/T | 0.46137 | 0.133501 | intron-variant | SPAG16 | GRCh38.p7 | 2:213812754 | TATTTAGCATTTTTT[G/T]TTTTATTACATGTAA | 79582 |
rs1834775 | snp | A/G | 0.0622301 | 0.165053 | intron-variant | SPAG16 | GRCh38.p7 | 2:213722172 | AAAAATGGGAGAAAT[A/G]AGGTTAGATAGGAGT | 79582 |
rs1834776 | snp | A/G | 0.140242 | 0.224618 | intron-variant | SPAG16 | GRCh38.p7 | 2:213729851 | GGCCTTGGTGAGAAC[A/G]GACTAACATCAGTCC | 79582 |
rs1834777 | snp | G/T | 0.140242 | 0.224618 | intron-variant | SPAG16 | GRCh38.p7 | 2:213729952 | TGCTCCTTTTGTAAA[G/T]TAAACAAAATGAGCA | 79582 |
rs1844227 | snp | A/G | 0.213635 | 0.247341 | intron-variant | SPAG16 | GRCh38.p7 | 2:213379580 | TGTCTTGGCAGAAGC[A/G]TTGCTTTTAGGATAG | 79582 |
rs1844228 | snp | C/T | 0.361053 | 0.22398 | intron-variant | SPAG16 | GRCh38.p7 | 2:213379618 | catatccagagtaag[C/T]gtctattccagtaag | 79582 |
rs1844229 | snp | A/G | 0.213635 | 0.247341 | intron-variant | SPAG16 | GRCh38.p7 | 2:213379671 | GATGGAAGAGGTCCA[A/G]TATAATCAATCTGCC | 79582 |
rs1844230 | snp | A/T | 0.213635 | 0.247341 | intron-variant | SPAG16 | GRCh38.p7 | 2:213379939 | AGAACGGGGCATCCT[A/T]TCCACTTGATTATTA | 79582 |
rs1848913 | snp | A/G | 0.308414 | 0.24308 | intron-variant | SPAG16 | GRCh38.p7 | 2:213944905 | TAGCCGGGCGTGGGG[A/G]CGTGCACCTGTAATC | 79582 |
rs1848914 | snp | A/G | 0.12932 | 0.218944 | intron-variant | SPAG16 | GRCh38.p7 | 2:214031157 | ccttctaacagacag[A/G]accctcagctgcagg | 79582 |
rs1848915 | snp | A/C | 0.312593 | 0.242037 | intron-variant | SPAG16 | GRCh38.p7 | 2:214031200 | tgctagaggtccaac[A/C]atgatagactggatt | 79582 |
rs1850130 | snp | G/T | 0.433527 | 0.169758 | intron-variant | SPAG16 | GRCh38.p7 | 2:213679858 | CTAAAGTCTATGGGT[G/T]CTTCCTGTGATAGCC | 79582 |
rs1850131 | snp | A/G | 0.361474 | 0.223771 | intron-variant | SPAG16 | GRCh38.p7 | 2:213616053 | ATCCCAGAACTTAAA[A/G]TATGATAATAATAAC | 79582 |
rs1858252 | snp | C/T | | | intron-variant | SPAG16 | GRCh38.p7 | 2:213894685 | acagaagacaagatt[C/T]tatacttagaaaaac | 79582 |
rs1858253 | snp | G/T | 0.470618 | 0.117591 | intron-variant | SPAG16 | GRCh38.p7 | 2:213894717 | taaagacggcctggc[G/T]cagtggctcacacct | 79582 |
rs1858254 | snp | C/T | 0.479824 | 0.098392 | intron-variant | SPAG16 | GRCh38.p7 | 2:213894860 | ccaggcttggtggca[C/T]gtgcctgtagtccca | 79582 |
rs1858255 | snp | A/G | 0.479824 | 0.098392 | intron-variant | SPAG16 | GRCh38.p7 | 2:213894900 | gaggctgaggcagga[A/G]aatcactgaacctag | 79582 |
rs1862062 | snp | C/T | 0.486464 | 0.0811471 | intron-variant | SPAG16, LOC101928084 | GRCh38.p7 | 2:214085598 | AATGTGTCCTTTACA[C/T]TGCCTTTAAAAATTT | 79582 |
rs1862063 | snp | A/G | 0.496279 | 0.0429702 | intron-variant | SPAG16, LOC101928084 | GRCh38.p7 | 2:214091704 | CTCTCTTGTTTTCTA[A/G]TTTACTTATGCATTT | 79582 |
rs1862944 | snp | A/G | 0.0452528 | 0.143452 | intron-variant | SPAG16 | GRCh38.p7 | 2:213486865 | AATTAACATGCCACT[A/G]GTTGCAGAAATAATA | 79582 |
rs1876837 | snp | A/C | 0.170733 | 0.237101 | intron-variant | SPAG16 | GRCh38.p7 | 2:214213042 | TCAGGCAGCAGATGA[A/C]GGGAATACACAACAC | 79582 |
rs1877049 | snp | A/C | 0.0535932 | 0.154675 | intron-variant | SPAG16 | GRCh38.p7 | 2:213899050 | ATGATCATATATTTT[A/C]TTACCAAGACTTGAA | 79582 |
rs1877050 | snp | A/G | 0.391024 | 0.206427 | intron-variant | SPAG16 | GRCh38.p7 | 2:213965041 | actgaacattgcatt[A/G]tattttctaaaatgt | 79582 |
rs1877051 | snp | A/G | 0.391397 | 0.206172 | intron-variant | SPAG16 | GRCh38.p7 | 2:213964731 | ttttgactctgattg[A/G]tctaggtgtggatct | 79582 |
rs1896274 | snp | G/T | 0.149665 | 0.228982 | | | GRCh38.p7 | 2:213860595 | CACCTTAAACAACTT[G/T]GACTCCTATTCCACA | 79582 |
rs1896275 | snp | C/T | 0.334871 | 0.235153 | | | GRCh38.p7 | 2:213855458 | TTCTCCTATGAGTTA[C/T]GTTTACCACTATCCC | 79582 |
rs1896276 | snp | G/T | 0.333952 | 0.235483 | | | GRCh38.p7 | 2:213851784 | TGCCCTAGAGGGTAG[G/T]CATAAAAGCTAAAGC | 79582 |
rs1896277 | snp | A/G | 0.46974 | 0.119223 | | | GRCh38.p7 | 2:213851726 | CTTCCAACCTTATAC[A/G]TATTGTATATGCCTT | 79582 |
rs1896278 | snp | C/T | 0.479824 | 0.098392 | | | GRCh38.p7 | 2:213881048 | tactgcccaaagcaa[C/T]ttacagattcaatgc | 79582 |
rs1896279 | snp | A/G | 0.479824 | 0.098392 | | | GRCh38.p7 | 2:213880991 | tcttcacagaattag[A/G]aaaaaactattcaaa | 79582 |
rs1896280 | snp | A/G | 0.479824 | 0.098392 | | | GRCh38.p7 | 2:213880720 | GACTCTCTATGTAAT[A/G]AATGGTGCTGCAATA | 79582 |
rs1896281 | snp | C/T | 0.479904 | 0.0982045 | | | GRCh38.p7 | 2:213876096 | ATCTGCAATGCTTTT[C/T]ACAGTAAACTCTCTA | 79582 |
rs1896282 | snp | C/T | 0.143959 | 0.226396 | | | GRCh38.p7 | 2:213876071 | TCTCTACTGGGGAAA[C/T]TGGTATTTTCTTATT | 79582 |
rs1906690 | snp | A/T | 0.046775 | 0.145601 | | | GRCh38.p7 | 2:213360562 | AAACAGTTTCCATTC[A/T]TTAAGTGGTAACCTT | 79582 |
rs1910397 | snp | C/T | 0.155325 | 0.23138 | intron-variant | SPAG16 | GRCh38.p7 | 2:213462652 | GACACACTGAATGCA[C/T]GCAGGGGAAATGTCA | 79582 |
rs1912166 | snp | C/T | 0.328382 | 0.237395 | intron-variant | SPAG16 | GRCh38.p7 | 2:214202080 | ACAAACTTCTGGGCT[C/T]GAGTAATCTCCCTGC | 79582 |
rs1912167 | snp | A/C | 0 | 0 | intron-variant | SPAG16 | GRCh38.p7 | 2:214202675 | CAGTTTTAAGAAGGA[A/C]GTTGCACTTCCCATA | 79582 |
rs1912168 | snp | A/C/T | 0.0248855 | 0.109023 | intron-variant | SPAG16 | GRCh38.p7 | 2:214208663 | tgcctgaggttgcaa[A/C/T]tttttttttagtttt | 79582 |
rs1912169 | snp | A/C | 0.106278 | 0.204558 | intron-variant | SPAG16 | GRCh38.p7 | 2:214316764 | AATATGAGGATTTAT[A/C]TTATGTAACATTGAT | 79582 |
rs1912170 | snp | A/C | 0.0329836 | 0.124112 | intron-variant | SPAG16 | GRCh38.p7 | 2:214315925 | TAGAGGTCTGCACTA[A/C]TTTAAAACATATATT | 79582 |
rs1912171 | snp | A/G | 0.117188 | 0.211804 | intron-variant | SPAG16 | GRCh38.p7 | 2:214313851 | TAGAAGAAAAAAAGC[A/G]GTTAAAAATTAAAAA | 79582 |
rs1912172 | snp | C/T | 0 | 0 | intron-variant | SPAG16 | GRCh38.p7 | 2:214309068 | aatgaacaaaacctc[C/T]gagacatatgggatt | 79582 |
rs1912173 | snp | C/T | 0.0988009 | 0.199095 | intron-variant | SPAG16 | GRCh38.p7 | 2:214308886 | AACCTCAGTAAGACA[C/T]TCCACAAGAAGATCA | 79582 |
rs1912174 | snp | A/G | 0.170408 | 0.236992 | intron-variant | SPAG16 | GRCh38.p7 | 2:214220550 | ATTCACACCTCTCAC[A/G]TCCAATCATAATTAA | 79582 |
rs1912175 | snp | A/G | 0.376791 | 0.215463 | intron-variant | SPAG16 | GRCh38.p7 | 2:214225522 | TATGTAAAATATTAA[A/G]TTACTATCTACTTAA | 79582 |
rs1912176 | snp | C/T | | | intron-variant | SPAG16 | GRCh38.p7 | 2:214225638 | GTTAAGAAAATATTT[C/T]ATATATTTTTCATTG | 79582 |
rs1912177 | snp | C/T | 0.49925 | 0.0193545 | intron-variant | SPAG16 | GRCh38.p7 | 2:214226197 | AAGTTTGCTGGCAGG[C/T]TGGTAGGGGCTAGCC | 79582 |
rs1912178 | snp | C/T | 0.17138 | 0.237316 | intron-variant | SPAG16 | GRCh38.p7 | 2:214227549 | TGCCTCTTTCTCTTC[C/T]TTCCTTGATTAATCA | 79582 |
rs1912180 | snp | C/G | 0.243347 | 0.249911 | intron-variant | SPAG16 | GRCh38.p7 | 2:214229349 | TAATCCATAAAAATA[C/G]CTAAAGATGTGAGAG | 79582 |
rs1912181 | snp | C/T | 0.415563 | 0.18732 | intron-variant | SPAG16 | GRCh38.p7 | 2:214231021 | TTATAATGCCTTCTT[C/T]GGTTGACAAGTTCTA | 79582 |
rs1912182 | snp | C/T | 0.387642 | 0.208697 | intron-variant | SPAG16 | GRCh38.p7 | 2:214232596 | AGGAGTCGGGGGGGG[C/T]TCAGATTG | 79582 |
rs1912183 | snp | A/G | 0.481319 | 0.0948228 | intron-variant | SPAG16 | GRCh38.p7 | 2:214260251 | GTACACCAAAATTTC[A/G]GAAATCATCACTAAA | 79582 |
rs1912184 | snp | A/C | 0.330016 | 0.236849 | intron-variant | SPAG16 | GRCh38.p7 | 2:214327316 | GTCAGAAGACAGACA[A/C]GGATTTGAATCATGG | 79582 |
rs1912185 | snp | G/T | 0.242488 | 0.249887 | intron-variant | SPAG16 | GRCh38.p7 | 2:214329944 | GAAGGGAAGACAGAT[G/T]AAAGAGGCCAGAAAG | 79582 |
rs1912186 | snp | A/G | 0.134119 | 0.221521 | intron-variant | SPAG16 | GRCh38.p7 | 2:214364008 | CCGTTTTACAACCCA[A/G]ACGTATTCTTTCTTT | 79582 |
rs1912187 | snp | C/G | 0.437259 | 0.165632 | intron-variant | SPAG16 | GRCh38.p7 | 2:214364205 | ACTCTACTATAGTAT[C/G]CCCAGTGACTAGTAA | 79582 |
rs1912188 | snp | G/T | 0.471004 | 0.116864 | intron-variant | SPAG16 | GRCh38.p7 | 2:214354143 | TTTTTTTGATTTTTT[G/T]ATTTTAATTTTTTGG | 79582 |
rs1912189 | snp | C/G | 0.479984 | 0.0980171 | intron-variant | SPAG16 | GRCh38.p7 | 2:214353940 | ACTGACATCAGTGAA[C/G]ACAATTGGTTTCTAC | 79582 |
rs1912190 | snp | A/G | 0.479824 | 0.098392 | intron-variant | SPAG16 | GRCh38.p7 | 2:214353933 | TCAGTGAAGACAATT[A/G]GTTTCTACAGCCTAT | 79582 |
rs1912191 | snp | C/T | 0.469642 | 0.119404 | intron-variant | SPAG16 | GRCh38.p7 | 2:214352818 | AGTTAAATGATTAGC[C/T]CACAGGCAGCATAAA | 79582 |
rs1912192 | snp | C/G | 0.497933 | 0.032082 | intron-variant | SPAG16 | GRCh38.p7 | 2:214352809 | ATTAGCTCACAGGCA[C/G]CATAAAAACTGAGGG | 79582 |
rs1912193 | snp | C/T | 0 | 0 | intron-variant | SPAG16 | GRCh38.p7 | 2:214296479 | ttagtaaaacctcta[C/T]ggaaaacagtaggaa | 79582 |
rs1912194 | snp | G/T | 0.48546 | 0.0840147 | intron-variant | SPAG16 | GRCh38.p7 | 2:214292585 | aagataaataaaaat[G/T]attaaagcaatacag | 79582 |
rs1912195 | snp | A/G | 0.344147 | 0.231595 | intron-variant | SPAG16 | GRCh38.p7 | 2:214292322 | AGATCCTATTTAAAA[A/G]AACAATAAATCAAAA | 79582 |
rs1912196 | snp | G/T | 0.294576 | 0.245994 | intron-variant | SPAG16 | GRCh38.p7 | 2:214185796 | AGACCAGAGAGCAGA[G/T]GGACCTGACCACTAT | 79582 |
rs1912197 | snp | A/G | 0.457037 | 0.140127 | intron-variant | SPAG16 | GRCh38.p7 | 2:214285767 | cgccagggctggagt[A/G]tagtggtgtgatctt | 79582 |
rs1912198 | snp | C/T | 0.469642 | 0.119404 | intron-variant | SPAG16 | GRCh38.p7 | 2:214283915 | TGCCCCCTTTATTCA[C/T]TGGTAATTTAAAGAA | 79582 |
rs1912199 | snp | G/T | 0.393434 | 0.20476 | intron-variant | SPAG16 | GRCh38.p7 | 2:214189970 | GAATGAATAAAAATT[G/T]TAATTGACTGAACCA | 79582 |
rs1912200 | snp | A/G | 0.498369 | 0.0285077 | intron-variant | SPAG16 | GRCh38.p7 | 2:214362019 | CAGTAAACAATCCTG[A/G]CTGATAATCCTTCTC | 79582 |
rs1912201 | snp | C/T | 0.471768 | 0.115407 | intron-variant | SPAG16 | GRCh38.p7 | 2:214362010 | ATCCTGACTGATAAT[C/T]CTTCTCTCCAGAAGA | 79582 |
rs1912202 | snp | A/C | 0.442385 | 0.15965 | intron-variant | SPAG16 | GRCh38.p7 | 2:214361854 | TCTTTGTGAAATATA[A/C]TTTGAGGTGAATTTT | 79582 |
rs1912203 | snp | A/G | 0.434831 | 0.168337 | intron-variant | SPAG16 | GRCh38.p7 | 2:214360552 | TTTTAGGATAAATGG[A/G]TTTGCATCTATCTCA | 79582 |
rs1912204 | snp | A/G | | | intron-variant | SPAG16 | GRCh38.p7 | 2:214356498 | TAATTTTTTGCAAGT[A/G]CTGTGTACATAGTTG | 79582 |
rs1912205 | snp | A/G | 0.475613 | 0.107697 | intron-variant | SPAG16 | GRCh38.p7 | 2:214215372 | GGTAGGTTGGAGAAT[A/G]TCTTCCGTGAGGCCA | 79582 |
rs1912206 | snp | C/T | 0.463989 | 0.129263 | intron-variant | SPAG16 | GRCh38.p7 | 2:214215359 | ATATCTTCCGTGAGG[C/T]CAGTCTATTCTATTC | 79582 |
rs1912207 | snp | A/T | 0 | 0 | intron-variant, utr-variant-3-prime | SPAG16 | GRCh38.p7 | 2:214238205 | CTTGATGTTACCTCA[A/T]ATTGAAGTTGCCAAT | 79582 |
rs1912208 | snp | C/T | 0.0475351 | 0.146656 | intron-variant | SPAG16 | GRCh38.p7 | 2:214242555 | TCTCAACTCTAGTCA[C/T]TGAATCTACCAAAAT | 79582 |
rs1912209 | snp | C/T | 0.463018 | 0.130857 | intron-variant | SPAG16 | GRCh38.p7 | 2:214270546 | CGAGCCTCTATGATA[C/T]GGCTCCTGACTACAT | 79582 |
rs1912210 | snp | C/G | 0.302936 | 0.244331 | intron-variant | SPAG16 | GRCh38.p7 | 2:214186226 | GTTGAATAAGCTCCC[C/G]ACTGCCACAGGAGGA | 79582 |
rs1912211 | snp | C/T | 0.465578 | 0.126594 | intron-variant | SPAG16 | GRCh38.p7 | 2:214277664 | aatattgctgcctta[C/T]ccttcttctggaagc | 79582 |
rs1912212 | snp | C/G | 0.445328 | 0.156035 | intron-variant | SPAG16 | GRCh38.p7 | 2:214349128 | GCTCCCTGCAGGTAG[C/G]TGCCATGCAAAAGCA | 79582 |
rs1912213 | snp | C/G | 0.482083 | 0.0929373 | intron-variant | SPAG16 | GRCh38.p7 | 2:214348710 | CTGGGAGATGAGCTG[C/G]TGTGGAGGGTCTGAG | 79582 |
rs1912214 | snp | A/G | 0.46885 | 0.12085 | intron-variant | SPAG16 | GRCh38.p7 | 2:214347592 | agagttttaaataat[A/G]cccttaacattactt | 79582 |
rs1912215 | snp | A/G | 0.499104 | 0.0211472 | intron-variant | SPAG16 | GRCh38.p7 | 2:214347160 | actttccacagctac[A/G]tagccagggtctgct | 79582 |
rs1912216 | snp | G/T | 0.499982 | 0.00299515 | intron-variant | SPAG16 | GRCh38.p7 | 2:214248638 | CATTGCAAAATCAAG[G/T]GCTTAGAATAGTGCC | 79582 |
rs1912217 | snp | C/T | 0.479583 | 0.0989539 | intron-variant | SPAG16 | GRCh38.p7 | 2:214344013 | GAAATGGACACCCAT[C/T]ATTATTAAGGTAAGA | 79582 |
rs1912218 | snp | C/T | 0.478188 | 0.10213 | intron-variant | SPAG16 | GRCh38.p7 | 2:214343710 | TGGGTAGAAACTAGA[C/T]TAACTAAATGGAAAT | 79582 |
rs1912219 | snp | A/C | 0.497416 | 0.0358495 | intron-variant | SPAG16 | GRCh38.p7 | 2:214343703 | AAACTAGACTAACTA[A/C]ATGGAAATAGCTTTT | 79582 |
rs1912220 | snp | A/C | 0.485916 | 0.106024 | intron-variant | SPAG16 | GRCh38.p7 | 2:214342735 | ACCTTTTTGGTACCA[A/C]GGGCCAGTTTCACAG | 79582 |
rs1912221 | snp | A/G | 0.475877 | 0.107142 | intron-variant | SPAG16 | GRCh38.p7 | 2:214342713 | GTTTCACAGAAGACA[A/G]TTTTTCCACTGGGGG | 79582 |
rs1912222 | snp | A/G | 0.479014 | 0.100263 | intron-variant | SPAG16 | GRCh38.p7 | 2:214342392 | GGAGGCAGAACTCAG[A/G]CACTAGTGCAAGAAT | 79582 |
rs1912223 | snp | A/C | 0.130694 | 0.219696 | intron-variant | SPAG16 | GRCh38.p7 | 2:214341673 | ataagttggctggct[A/C]cagaattctagattg | 79582 |
rs1912224 | snp | A/G | 0.347694 | 0.230122 | intron-variant | SPAG16 | GRCh38.p7 | 2:214194925 | TGTGGTAGCCATTGT[A/G]TTAAACTCTGGGGAT | 79582 |
rs1912225 | snp | C/T | 0.347694 | 0.230122 | intron-variant | SPAG16 | GRCh38.p7 | 2:214194932 | GCCATTGTGTTAAAC[C/T]CTGGGGATTTGGGGA | 79582 |
rs1912502 | snp | A/C/G | 0.000399281 | 0.0141238 | intron-variant | SPAG16 | GRCh38.p7 | 2:213964062 | ACAATATTTTTATCA[A/C/G]CCAATCAATGCATAA | 79582 |
rs1912503 | snp | C/T | | | intron-variant | SPAG16 | GRCh38.p7 | 2:213963809 | tcaggcaaaataaac[C/T]tataaaccaaaaatg | 79582 |
rs1912504 | snp | C/T | 0.304966 | 0.247678 | intron-variant | SPAG16 | GRCh38.p7 | 2:213957929 | AATACTCCTCCCAGT[C/T]GGGGCTTTTCTAGAG | 79582 |
rs1912505 | snp | A/T | 0.299664 | 0.245017 | intron-variant | SPAG16 | GRCh38.p7 | 2:213957708 | tttcactactaaaaa[A/T]gtcaactaaacacaa | 79582 |
rs1912506 | snp | A/G | 0.453087 | 0.145793 | intron-variant | SPAG16 | GRCh38.p7 | 2:213953069 | TTCATCATATATGTA[A/G]TATTTCTCACTTTTT | 79582 |
rs1913899 | snp | A/G | 0.479583 | 0.0989539 | intron-variant | SPAG16 | GRCh38.p7 | 2:213660362 | GAATTGCTTGCACCC[A/G]GGAGGCAGAGGTTGC | 79582 |
rs1922789 | snp | C/T | 0.499776 | 0.0105807 | intron-variant | SPAG16 | GRCh38.p7 | 2:213290325 | GCCAGGTTCTGTATT[C/T]CTAGTCATAACCTAG | 79582 |
rs1946413 | snp | C/T | 0.412249 | 0.190198 | intron-variant | SPAG16 | GRCh38.p7 | 2:213788969 | GTTTTTATAGCATCA[C/T]TTGCTTTATAAAGAT | 79582 |
rs1946414 | snp | C/T | 0.296364 | 0.245663 | intron-variant | SPAG16 | GRCh38.p7 | 2:213730776 | ctctgttctctcttc[C/T]tcttcaggtattcca | 79582 |
rs1946415 | snp | C/T | 0.140242 | 0.224618 | intron-variant | SPAG16 | GRCh38.p7 | 2:213730985 | ggcattcttcatttc[C/T]attacatttttttat | 79582 |
rs1946416 | snp | A/G | 0.140242 | 0.224618 | intron-variant | SPAG16 | GRCh38.p7 | 2:213731136 | tctgataattccaac[A/G]tctacattatatctg | 79582 |
rs1946417 | snp | A/G | 0.249038 | 0.249998 | intron-variant | SPAG16 | GRCh38.p7 | 2:213731176 | TTTTTTTTTTTTTGA[A/G]TTGGAGTTTTGCTCT | 79582 |
rs1949049 | snp | A/G | 0.435694 | 0.167385 | intron-variant | SPAG16 | GRCh38.p7 | 2:214359625 | TTTACTCTATTAAAG[A/G]TGTAAATAGAACCCT | 79582 |
rs1960216 | snp | A/G | 0.47726 | 0.104176 | intron-variant | SPAG16 | GRCh38.p7 | 2:213883494 | ACTGAACATTCTACC[A/G]AACAACCACAACATA | 79582 |
rs1961052 | snp | C/T | 0.482905 | 0.0908579 | intron-variant | SPAG16 | GRCh38.p7 | 2:213610782 | cacatctcctcatga[C/T]ctttttttaatccta | 79582 |
rs1964067 | snp | C/T | 0.484701 | 0.0861117 | intron-variant | SPAG16 | GRCh38.p7 | 2:213898406 | TTCCTTGGTGAATAG[C/T]ACAGTCCTGGTGAAG | 79582 |
rs1964673 | snp | A/G | 0.45946 | 0.136478 | intron-variant | SPAG16 | GRCh38.p7 | 2:213498116 | TAAACAGAATAATGA[A/G]TACATGTGTGAATAT | 79582 |
rs1965056 | snp | C/T | 0.498084 | 0.0308911 | intron-variant | SPAG16 | GRCh38.p7 | 2:213772320 | gagatagtcaagatc[C/T]ggcatgttgagggtg | 79582 |
rs1965057 | snp | C/T | 0.152334 | 0.230133 | intron-variant | SPAG16 | GRCh38.p7 | 2:213808657 | AAGATTATGAGTAGG[C/T]CAAGTAGATGACAGG | 79582 |
rs1965058 | snp | C/T | 0.212122 | 0.247114 | intron-variant | SPAG16 | GRCh38.p7 | 2:213756024 | CAGCCATTTAAGTAG[C/T]TGCATAATCTTGGGA | 79582 |
rs1965059 | snp | A/C | 0.137187 | 0.223099 | intron-variant | SPAG16 | GRCh38.p7 | 2:213755897 | ATATTCTTTTCTACT[A/C]TTTTATAATATTTTA | 79582 |
rs1966558 | snp | C/G | 0.482609 | 0.0916147 | intron-variant | SPAG16 | GRCh38.p7 | 2:213836927 | TGTTGGAGGCATAAA[C/G]ATACTAAGATTTGGG | 79582 |
rs1966559 | snp | C/T | 0.485049 | 0.0851591 | intron-variant | SPAG16 | GRCh38.p7 | 2:213836860 | TTGGGAGGCTGAGAC[C/T]GGGGGATCACCTGAG | 79582 |
rs1966560 | snp | C/G | 0.484771 | 0.0859212 | intron-variant | SPAG16 | GRCh38.p7 | 2:213836857 | GGAGGCTGAGACCGG[C/G]GGATCACCTGAGGTC | 79582 |
rs1968345 | snp | A/G | 0.140919 | 0.224948 | intron-variant | SPAG16 | GRCh38.p7 | 2:213742974 | agtggtgagatctcc[A/G]ctcactgcgagctcc | 79582 |
rs1978415 | snp | A/G | 0.318656 | 0.240388 | intron-variant | SPAG16 | GRCh38.p7 | 2:214190390 | AATTTTCTTCTTCAT[A/G]TATGCCCCCAAATTT | 79582 |
rs1978589 | snp | C/G | 0.141596 | 0.225274 | intron-variant | SPAG16 | GRCh38.p7 | 2:213763498 | AAAACCACTATTCAA[C/G]TTTCTGCTTCTATGA | 79582 |
rs1984609 | snp | A/T | 0.449218 | 0.151037 | intron-variant | SPAG16 | GRCh38.p7 | 2:213583506 | ATACTGCATTTTTCC[A/T]CTCACATGTGTGTAT | 79582 |
rs1984610 | snp | C/T | 0.371987 | 0.218218 | intron-variant | SPAG16 | GRCh38.p7 | 2:213583535 | ATAATGCTTCATATA[C/T]TGCTAAATCTTTATA | 79582 |
rs1986978 | snp | A/G | 0.480931 | 0.0957637 | intron-variant | SPAG16 | GRCh38.p7 | 2:213688493 | caggtaatgttacac[A/G]taaaatatttggatt | 79582 |
rs1988858 | snp | C/G | | | intron-variant | SPAG16 | GRCh38.p7 | 2:213467770 | ggtggactgtcccca[C/G]agatgcaggtcactg | 79582 |
rs1990837 | snp | C/G | 0.250168 | 0.25 | intron-variant | SPAG16, LOC101928084 | GRCh38.p7 | 2:214094397 | GAATCACATGGCATG[C/G]TAATTAAAATACAAA | 79582 |
rs1995842 | snp | A/G | 0.47726 | 0.104176 | intron-variant | SPAG16 | GRCh38.p7 | 2:214336782 | AAATAGAGTGTTTTT[A/G]TTGTAAGCTTTTACT | 79582 |
rs1996272 | snp | C/G | 0.0225045 | 0.103662 | intron-variant | SPAG16 | GRCh38.p7 | 2:213665978 | TCTGCCTTCATGGTT[C/G]AACTCTCACATTGTA | 79582 |
rs2003598 | snp | C/T | 0.153 | 0.230415 | intron-variant | SPAG16 | GRCh38.p7 | 2:214114929 | TCTGTTccaagatgg[C/T]caaataggaacagca | 79582 |
rs2005905 | snp | C/T | 0.341909 | 0.232492 | intron-variant | SPAG16 | GRCh38.p7 | 2:214114817 | GTGGGCTGCACCCAC[C/T]GTCCAACCAGTCCCA | 79582 |
rs2007346 | snp | A/G | 0.483995 | 0.0880135 | intron-variant | SPAG16 | GRCh38.p7 | 2:213540251 | catcctggctaacac[A/G]gtgaaaccccgtctc | 79582 |
rs2008939 | snp | C/T | 0.0456336 | 0.143994 | intron-variant | SPAG16 | GRCh38.p7 | 2:213452320 | ACAATCACTGAAATA[C/T]GTACCAAGGTAGTGT | 79582 |
rs2009727 | snp | A/G | 0.13446 | 0.221699 | intron-variant | SPAG16 | GRCh38.p7 | 2:213577808 | GGCATTCTGGAGACA[A/G]ATGCTGAGACTTCTG | 79582 |
rs2013922 | snp | A/G | 0.466927 | 0.124269 | intron-variant | SPAG16 | GRCh38.p7 | 2:213666999 | GAGATCTTGAAGTGA[A/G]TATCAATACATTTCT | 79582 |
rs2013934 | snp | A/G | 0.361684 | 0.223667 | intron-variant | SPAG16 | GRCh38.p7 | 2:213667120 | TAAAACACTTTTTCT[A/G]TAAGAAATCTAAATT | 79582 |
rs2014000 | snp | C/T | 0.45946 | 0.136478 | intron-variant | SPAG16 | GRCh38.p7 | 2:213946239 | CCTGCATCAGCCTCC[C/T]GAGCAGCTGGAACTA | 79582 |
rs2014002 | snp | A/G | 0.45198 | 0.147323 | intron-variant | SPAG16 | GRCh38.p7 | 2:213946208 | CAACCTCTGCCTCCC[A/G]GGTTCAAGCAATTCT | 79582 |
rs2014893 | snp | C/T | | | intron-variant | SPAG16 | GRCh38.p7 | 2:213462355 | GCCATAAAAGCACCT[C/T]AGTGCAATCTCTAGA | 79582 |
rs2015217 | snp | C/T | 0.47934 | 0.0995154 | intron-variant | SPAG16 | GRCh38.p7 | 2:213671784 | GCTGTGAGCAGGGCA[C/T]GTTCATTCAGACAGT | 79582 |
rs2016054 | snp | A/G | 0.491629 | 0.0641526 | intron-variant | SPAG16 | GRCh38.p7 | 2:214114678 | AAACGGGACACTCCC[A/G]CCCAAATACTATGCT | 79582 |
rs2018869 | snp | C/G | 0.32955 | 0.237006 | intron-variant | SPAG16 | GRCh38.p7 | 2:213902560 | catgatgcaaattat[C/G]tcccaccaggtctct | 79582 |
rs2018907 | snp | A/G | 0.474363 | 0.110278 | intron-variant | SPAG16 | GRCh38.p7 | 2:213616080 | TAACAAAAGAAATTA[A/G]TCCATTTTACCGATT | 79582 |
rs2032779 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | SPAG16 | GRCh38.p7 | 2:214183295 | ATGCCCTATTATAGA[C/T]AGACTTTCACTCAGG | 79582 |
rs2032780 | snp | C/T | 0.34659 | 0.230587 | intron-variant | SPAG16 | GRCh38.p7 | 2:214209211 | ACTATGGTAGTGTAG[C/T]TATTATATCTCTTCA | 79582 |
rs2035694 | snp | A/T | 0.21303 | 0.247251 | intron-variant | SPAG16 | GRCh38.p7 | 2:213417408 | AAAATGGTGTCATAC[A/T]TCTAAGAAATTACTT | 79582 |
rs2037179 | snp | A/T | 0.475437 | 0.108066 | intron-variant | SPAG16 | GRCh38.p7 | 2:213653730 | AAAAAATAATGATAG[A/T]CAATTTGAGGAATTG | 79582 |
rs2042784 | snp | A/T | 0.484701 | 0.0861117 | intron-variant | SPAG16 | GRCh38.p7 | 2:213899593 | GTTTCACCATGCTAG[A/T]TTTAAATGTTTTCAA | 79582 |
rs2042785 | snp | A/T | 0.484632 | 0.086302 | intron-variant | SPAG16 | GRCh38.p7 | 2:213900072 | ACCTAGAATGCATCA[A/T]CAAATCAATCCTCCT | 79582 |
rs2042786 | snp | A/G | 0.484841 | 0.0857308 | intron-variant | SPAG16 | GRCh38.p7 | 2:213900158 | TGCAGAAATGGGTAC[A/G]CTGACAAATTTTGCA | 79582 |
rs2042787 | snp | C/T | 0.472709 | 0.11358 | intron-variant | SPAG16 | GRCh38.p7 | 2:213853660 | TTCAAAAATAAAGGC[C/T]CTGTCACAACATTCC | 79582 |
rs2042788 | snp | A/T | 0.481703 | 0.0938806 | intron-variant | SPAG16 | GRCh38.p7 | 2:213887548 | ATATTAACTACTAAA[A/T]GTTTTCATAATTTAA | 79582 |
rs2042789 | snp | G/T | 0.479824 | 0.098392 | intron-variant | SPAG16 | GRCh38.p7 | 2:213887549 | TATTAACTACTAAAT[G/T]TTTTCATAATTTAAA | 79582 |
rs2042790 | snp | C/T | 0.473174 | 0.112665 | intron-variant | SPAG16 | GRCh38.p7 | 2:213862426 | CATTTCATTTATTCA[C/T]ATTCTGAAAACATTT | 79582 |
rs2042791 | snp | A/C | 0.475991 | 0.106901 | missense, nc-transcript-variant | SPAG16 | GRCh38.p7 | 2:213862497 | CAGTGTCTCCATGCA[A/C]CCCCACAAAGACATC | 79582 |
rs2042792 | snp | C/G | 0.47534 | 0.108268 | intron-variant | SPAG16 | GRCh38.p7 | 2:213862643 | GGTCAGTGCACAGGA[C/G]CCCTAGAAATAGCCT | 79582 |
rs2047838 | snp | A/C/T | 0.0460327 | 0.144653 | intron-variant | SPAG16 | GRCh38.p7 | 2:213419835 | ATAATGTAAGAGATC[A/C/T]GTATGAACAAGTAGT | 79582 |
rs2047839 | snp | A/G | | | intron-variant | SPAG16 | GRCh38.p7 | 2:213426301 | AAATCCAAAAAGTAA[A/G]AAGAGTGGTAAATTT | 79582 |
rs2052440 | snp | A/C | 0.455144 | 0.142885 | intron-variant | SPAG16 | GRCh38.p7 | 2:214242832 | CATATGTAGCATCTT[A/C]TAATCAGATGCTAAA | 79582 |
rs2052441 | snp | A/T | 0 | 0 | intron-variant | SPAG16 | GRCh38.p7 | 2:214242874 | AACTATCACTTGGGT[A/T]GCTGCAGCCCTACAT | 79582 |
rs2052442 | snp | C/T | 0.479177 | 0.0998894 | intron-variant | SPAG16 | GRCh38.p7 | 2:214294429 | ttctcttatagatga[C/T]tcatttgaactatga | 79582 |
rs2055866 | snp | A/T | 0.232067 | 0.249356 | intron-variant | SPAG16 | GRCh38.p7 | 2:214020718 | aattcatccactaat[A/T]atgcaaaggaatttt | 79582 |
rs2055867 | snp | C/T | 0.292266 | 0.246401 | intron-variant | SPAG16 | GRCh38.p7 | 2:214020929 | ACTAAAAATATGTGT[C/T]ATCAAATGTTCTATA | 79582 |
rs2058989 | snp | A/G | 0.0422008 | 0.138995 | intron-variant | SPAG16 | GRCh38.p7 | 2:214144068 | gaggctgacgtggaa[A/G]gatcacctgagccca | 79582 |
rs2058990 | snp | A/T | 0.27278 | 0.24896 | intron-variant | SPAG16 | GRCh38.p7 | 2:214176281 | GAAACTTCTTTTTTT[A/T]AAAAAAAAACAATAT | 79582 |
rs2058991 | snp | A/G | 0.156319 | 0.231784 | intron-variant | SPAG16 | GRCh38.p7 | 2:214067856 | ACCAAGTCTGACACC[A/G]TGTTAGCTGTAAGTG | 79582 |
rs2058992 | snp | A/G | 0.17461 | 0.238362 | intron-variant | SPAG16 | GRCh38.p7 | 2:214067935 | ACTATAAAAAATAAT[A/G]TGTTACTTTGTAAAT | 79582 |
rs2077974 | snp | A/G | 0.412082 | 0.190341 | intron-variant | SPAG16 | GRCh38.p7 | 2:213767771 | ACTTTCTCCACTGGA[A/G]TAACTTAAAATTAAT | 79582 |
rs2078429 | snp | A/G | 0.491104 | 0.0660973 | intron-variant | SPAG16 | GRCh38.p7 | 2:213715436 | TCGTGACAAGCGCTT[A/G]CCACCATGAACTGTA | 79582 |
rs2080776 | snp | C/T | 0.496416 | 0.0421803 | intron-variant | SPAG16, LOC101928084 | GRCh38.p7 | 2:214091799 | CTGTTTCCTACAATT[C/T]CTATCTTCTTCCCTT | 79582 |
rs2081313 | snp | A/C | 0.182296 | 0.240658 | intron-variant | SPAG16 | GRCh38.p7 | 2:213472011 | CTGGCATGCAAATAT[A/C]TCACCAATAAGCCCT | 79582 |
rs2081314 | snp | A/T | 0.0244538 | 0.107838 | intron-variant | SPAG16 | GRCh38.p7 | 2:213472065 | CTGGATTTCATCAGT[A/T]TAAGACATGAATGTA | 79582 |
rs2081315 | snp | A/C/G | 0.0456336 | 0.143994 | intron-variant | SPAG16 | GRCh38.p7 | 2:213472087 | ATGAATGTAATGAAC[A/C/G]AGTGTGACATCTTGT | 79582 |
rs2081724 | snp | A/C | 0.248755 | 0.249997 | intron-variant | SPAG16 | GRCh38.p7 | 2:213730586 | gtttctctatagata[A/C]ggcattatttcccct | 79582 |
rs2089762 | snp | C/T | 0.190205 | 0.242744 | intron-variant | SPAG16 | GRCh38.p7 | 2:213941873 | GTCCAGCCAACACCC[C/T]AGCCTCACAGCTCCT | 79582 |
rs2090299 | snp | A/T | 0.475525 | 0.107882 | intron-variant | SPAG16 | GRCh38.p7 | 2:213641058 | agacaaaccatcagg[A/T]cggggcagggttaag | 79582 |
rs2098582 | snp | C/T | 0.32955 | 0.237006 | intron-variant | SPAG16 | GRCh38.p7 | 2:214186849 | ACTGCAACCTCTGCC[C/T]CCTGTGTTCAAGCAA | 79582 |
rs2098977 | snp | A/G | 0.479824 | 0.098392 | intron-variant | SPAG16 | GRCh38.p7 | 2:213879276 | AAAACCATCTCATGC[A/G]CATGAATTGGAAGAA | 79582 |
rs2098978 | snp | G/T | 0.479824 | 0.098392 | intron-variant | SPAG16 | GRCh38.p7 | 2:213879229 | TACTATCCAAAGCAA[G/T]CTACAGTTTAAGTGC | 79582 |
rs2098979 | snp | C/T | 0.140242 | 0.224618 | intron-variant | SPAG16 | GRCh38.p7 | 2:213730448 | TTTATTCCATCTCTT[C/T]CACTtaattttgctg | 79582 |
rs2102521 | snp | C/T | 0.38934 | 0.207568 | intron-variant | SPAG16 | GRCh38.p7 | 2:213942075 | GCCTTCCTCTTCTTT[C/T]CTTCTTCCCCTGAGT | 79582 |
rs2112013 | snp | A/G | 0.251014 | 0.249998 | intron-variant | SPAG16 | GRCh38.p7 | 2:214119001 | cataaagaaatgaca[A/G]gtgtttgaggtgata | 79582 |
rs2112014 | snp | A/G | 0.498084 | 0.0308911 | intron-variant | SPAG16 | GRCh38.p7 | 2:214123086 | CGCTTTAAAAAAGTA[A/G]AGCAAAAGAAAAGCA | 79582 |
rs2112015 | snp | C/G | 0.0452528 | 0.143452 | intron-variant | SPAG16 | GRCh38.p7 | 2:214145584 | TTATTAACTTCATGT[C/G]TATATGGTTTTCTCA | 79582 |
rs2112016 | snp | A/G | 0.0460142 | 0.144533 | intron-variant | SPAG16 | GRCh38.p7 | 2:214148827 | TTTGTTACATCTTCT[A/G]ATGTAGTTAAAATGA | 79582 |
rs2112017 | snp | A/G | 0.171704 | 0.237423 | intron-variant | SPAG16 | GRCh38.p7 | 2:214045758 | ctacatcaaaaaaag[A/G]agaaaaacttcaaac | 79582 |
rs2112119 | snp | A/G | 0.00279162 | 0.0372561 | intron-variant | SPAG16 | GRCh38.p7 | 2:214323124 | CCTATCCTGTTGAGG[A/G]TGGCTGTTGATATTG | 79582 |
rs2113472 | snp | A/G | 0.483199 | 0.0901004 | intron-variant | SPAG16 | GRCh38.p7 | 2:213591461 | GGATCAAAATTAGGG[A/G]TAAAATTCCAATATG | 79582 |
rs2113473 | snp | G/T | 0.360842 | 0.224085 | intron-variant | SPAG16 | GRCh38.p7 | 2:213529781 | ctccattcatgggaa[G/T]tgatctgcacaggta | 79582 |
rs2114638 | snp | A/G | 0.343924 | 0.231686 | intron-variant | SPAG16 | GRCh38.p7 | 2:213780061 | GACTTTGAATAAAAT[A/G]GTACTAGATTATTAA | 79582 |
rs2114639 | snp | C/T | 0.472335 | 0.114312 | intron-variant | SPAG16 | GRCh38.p7 | 2:213881391 | gactatatgatccta[C/T]atataggaaaatctg | 79582 |
rs2114640 | snp | A/G | 0.479824 | 0.098392 | intron-variant | SPAG16 | GRCh38.p7 | 2:213881390 | actatatgatcctac[A/G]tataggaaaatctga | 79582 |
rs2114641 | snp | C/T | 0.479824 | 0.098392 | intron-variant | SPAG16 | GRCh38.p7 | 2:213870774 | ACTTAGAGGCAATAC[C/T]AGTTTTACAGCAAAC | 79582 |
rs2114642 | snp | C/T | 0.479984 | 0.0980171 | intron-variant | SPAG16 | GRCh38.p7 | 2:213870648 | ATGCTTTATATATAT[C/T]TTCTCGTGGAACATT | 79582 |
rs2114643 | snp | C/G | | | intron-variant | SPAG16 | GRCh38.p7 | 2:213864886 | ATAATAAATACAATA[C/G]ACATAGTAATACTCA | 79582 |
rs2130055 | snp | A/G | 0.213635 | 0.247341 | intron-variant | SPAG16 | GRCh38.p7 | 2:213391124 | CGTGCCACCATGCCC[A/G]GCTAATTTTTGTATT | 79582 |
rs2130056 | snp | A/T | 0.327914 | 0.237549 | intron-variant | SPAG16 | GRCh38.p7 | 2:213390969 | TAATTTCTAAAGATC[A/T]AAAGGAATTAAAATA | 79582 |
rs2130057 | snp | C/T | 0.230017 | 0.2492 | intron-variant | SPAG16 | GRCh38.p7 | 2:213385171 | atacaccataaaagg[C/T]caaaaatcccatgag | 79582 |
rs2134602 | snp | A/G | 0.256897 | 0.249905 | intron-variant | SPAG16 | GRCh38.p7 | 2:213431820 | tcatcagcgcatgca[A/G]cattctccaagatag | 79582 |
rs2136514 | snp | A/T | 0 | 0 | intron-variant | SPAG16 | GRCh38.p7 | 2:214240846 | ATTAAATGTAAATGT[A/T]TGCTGAAAAAGTTCA | 79582 |
rs2136777 | snp | G/T | 0.102014 | 0.201495 | intron-variant | SPAG16 | GRCh38.p7 | 2:213935702 | TTTTATGTTAGCATT[G/T]ACCACATTTACTGAT | 79582 |
rs2161020 | snp | A/G | 0.104149 | 0.203046 | intron-variant | SPAG16 | GRCh38.p7 | 2:214118774 | accatatcaatgtcc[A/G]tactgcccaaagtga | 79582 |
rs2161021 | snp | G/T | 0.0444908 | 0.142359 | intron-variant | SPAG16 | GRCh38.p7 | 2:214128644 | ATTTCAATTCAACCA[G/T]ATTTAGTTTCAGATC | 79582 |
rs2161022 | snp | A/G | 0.301177 | 0.244706 | intron-variant | SPAG16 | GRCh38.p7 | 2:214129273 | agtctgctgtgcttt[A/G]tttcagttccctgtc | 79582 |
rs2161023 | snp | A/T | 0.103082 | 0.202275 | intron-variant, downstream-variant-500B | SPAG16 | GRCh38.p7 | 2:214150654 | TTCATGTCTTTGAAT[A/T]TTGAACTCCGAAATT | 79582 |
rs2161081 | snp | A/G | 0 | 0 | intron-variant | SPAG16 | GRCh38.p7 | 2:214181795 | AATTTTTACATTAAA[A/G]TGTAAACAATAGGAA | 79582 |
rs2161082 | snp | A/G | 0.347473 | 0.230215 | intron-variant | SPAG16 | GRCh38.p7 | 2:214181809 | AGTGTAAACAATAGG[A/G]AAAAGACGATTTGAC | 79582 |
rs2161820 | snp | C/T | 0.472709 | 0.11358 | intron-variant | SPAG16 | GRCh38.p7 | 2:213606142 | caaaaaggaataaat[C/T]actaacacccactac | 79582 |
rs2161821 | snp | A/C | 0.193653 | 0.243567 | intron-variant | SPAG16 | GRCh38.p7 | 2:213451934 | TCGCCCCATACCCCG[A/C]CCCCCACCCCATCTC | 79582 |
rs2161822 | snp | C/G | 0.131038 | 0.219882 | intron-variant | SPAG16 | GRCh38.p7 | 2:213452625 | ATGTCAGATCTTTTA[C/G]TGACTTCCCATTGTT | 79582 |
rs2162501 | snp | C/T | 0.498133 | 0.030494 | intron-variant | SPAG16 | GRCh38.p7 | 2:213771363 | ttgtgatctaaccat[C/T]tgataaatgtctaat | 79582 |
rs2162502 | snp | A/G | 0.459801 | 0.135955 | intron-variant | SPAG16 | GRCh38.p7 | 2:213838430 | atcccagcactttgg[A/G]aggccgaggcggatg | 79582 |
rs2162503 | snp | C/T | 0.479824 | 0.098392 | intron-variant | SPAG16 | GRCh38.p7 | 2:213881704 | gcagtttctcccatg[C/T]tgttcttgggatggt | 79582 |
rs2162504 | snp | A/G | 0.479904 | 0.0982045 | intron-variant | SPAG16 | GRCh38.p7 | 2:213873946 | aggagcaatagcaat[A/G]gcaatatgctatagt | 79582 |
rs2162505 | snp | C/T | 0.323197 | 0.239044 | intron-variant | SPAG16 | GRCh38.p7 | 2:213719630 | agatggtatTGTGTC[C/T]AGAATtggtgggtga | 79582 |
rs2162506 | snp | A/G | 0.131038 | 0.219882 | intron-variant | SPAG16 | GRCh38.p7 | 2:213719629 | gatggtatTGTGTCC[A/G]GAATtggtgggtgac | 79582 |
rs2162507 | snp | C/T | 0.131038 | 0.219882 | intron-variant | SPAG16 | GRCh38.p7 | 2:213721348 | AAGTGATCTGCACAC[C/T]TCGGCCTCCCAAAGT | 79582 |
rs2171623 | snp | A/G | 0.0444908 | 0.142359 | intron-variant | SPAG16 | GRCh38.p7 | 2:213348856 | agaagagcaactcca[A/G]gacacataattgtca | 79582 |
rs2171624 | snp | A/G | 0.32768 | 0.237625 | intron-variant | SPAG16 | GRCh38.p7 | 2:213391292 | TTAACAAAATATTAT[A/G]TATCATTTATTTATT | 79582 |
rs2171625 | snp | C/T | 0.192715 | 0.243348 | intron-variant | SPAG16 | GRCh38.p7 | 2:213435452 | TTTCAGCGTAACCAG[C/T]AATTGAATAATGTAC | 79582 |
rs2171626 | snp | C/T | 0.338296 | 0.233889 | intron-variant | SPAG16 | GRCh38.p7 | 2:213334811 | cacacacacacacta[C/T]ccttcccagtctctg | 79582 |
rs2175307 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | SPAG16 | GRCh38.p7 | 2:213998750 | agcttgatagtgata[C/T]ggacactaaggtcca | 79582 |
rs2175308 | snp | A/G | 0.480223 | 0.0974544 | intron-variant | SPAG16 | GRCh38.p7 | 2:213895414 | acagaaatagaaaaa[A/G]caatcataaaattcc | 79582 |
rs2193782 | snp | A/G | 0.00199481 | 0.0315187 | intron-variant | SPAG16 | GRCh38.p7 | 2:214107731 | tttataCAGGTAATA[A/G]TGTTAATGCTGAACT | 79582 |
rs2193783 | snp | C/G | 0.0505692 | 0.150756 | intron-variant | SPAG16 | GRCh38.p7 | 2:214121165 | TACCCAATATCTCCA[C/G]TATGTAGCATAGTTT | 79582 |
rs2193784 | snp | A/G | 0.307919 | 0.243198 | intron-variant | SPAG16 | GRCh38.p7 | 2:214131820 | GAGGGAGGGATGAAT[A/G]GACAGGGCATAGACA | 79582 |
rs2193785 | snp | C/G | 0.0402882 | 0.136092 | intron-variant | SPAG16 | GRCh38.p7 | 2:214162014 | AGCTTTACGTTGGTA[C/G]CTTTTACATTTTAGG | 79582 |
rs2193786 | snp | C/T | 0.353587 | 0.22753 | intron-variant | SPAG16 | GRCh38.p7 | 2:214027178 | TGATAACCTTTCCAA[C/T]TTTTGTATGCTATAG | 79582 |
rs2193787 | snp | C/T | 0.21875 | 0.248039 | intron-variant, downstream-variant-500B | SPAG16, LOC101928084 | GRCh38.p7 | 2:214084543 | CACATTCAGTCTCTC[C/T]CCTTTCTTTCCTTTA | 79582 |
rs2193788 | snp | A/C | 0.394354 | 0.204112 | intron-variant | SPAG16, LOC101928084 | GRCh38.p7 | 2:214102368 | GGTGACCTATTTGTC[A/C]AGTATTGGCATCTGT | 79582 |
rs2195081 | snp | G/T | 0.131038 | 0.219882 | intron-variant | SPAG16 | GRCh38.p7 | 2:213721661 | CTAGTCAGCACTGAA[G/T]CATACTGCATGTGTA | 79582 |
rs2195082 | snp | A/G | 0.131038 | 0.219882 | intron-variant | SPAG16 | GRCh38.p7 | 2:213721670 | ACTGAATCATACTGC[A/G]TGTGTATTTTGTTCT | 79582 |
rs2198849 | snp | A/G/T | 0.733728 | 0.057369 | intron-variant | SPAG16 | GRCh38.p7 | 2:213356440 | GCCTGTTATTGGTCT[A/G/T]TTCAGAGATTCAACT | 79582 |
rs2200758 | snp | C/T | 0.347694 | 0.230122 | intron-variant, utr-variant-3-prime, downstream-variant-500B | SPAG16 | GRCh38.p7 | 2:213396933 | gtacaaagaaagggt[C/T]tggggagtcagaaga | 79582 |
rs2202898 | snp | A/T | 0.47852 | 0.101384 | intron-variant | SPAG16 | GRCh38.p7 | 2:214339592 | ACAAGCTGAGCAGAA[A/T]GCTTTGTTTGGCTGA | 79582 |
rs2202899 | snp | A/G | 0.47852 | 0.101384 | intron-variant | SPAG16 | GRCh38.p7 | 2:214339504 | CCCTAGGATGGTTTG[A/G]CTGTCTTAAAAAGAG | 79582 |
rs2203004 | snp | G/T | | | intron-variant | SPAG16 | GRCh38.p7 | 2:213936765 | TCAGCTGGTGATCCA[G/T]AAGCCATGACAGAAT | 79582 |
rs2216485 | snp | A/T | 0.0807149 | 0.183963 | intron-variant | SPAG16 | GRCh38.p7 | 2:214125773 | AACAAAAGACAGGTT[A/T]ACAAGGGAAAAGTAT | 79582 |
rs2216486 | snp | A/T | 0.446118 | 0.155041 | intron-variant | SPAG16 | GRCh38.p7 | 2:214126487 | ACATGAATCTTGGTA[A/T]TGTAAACATTATGAT | 79582 |
rs2216487 | snp | A/G | 0.109108 | 0.206518 | intron-variant, downstream-variant-500B | SPAG16 | GRCh38.p7 | 2:214151058 | TTTATCAGTCTGAAG[A/G]AATATGATTTCAACC | 79582 |
rs2216488 | snp | C/T | 0 | 0 | intron-variant | SPAG16 | GRCh38.p7 | 2:214162079 | CCATTTTTCCTGCAA[C/T]AACAAAGAAACCCAG | 79582 |
rs2216544 | snp | A/G | 0.492337 | 0.0614248 | intron-variant | SPAG16 | GRCh38.p7 | 2:214318153 | GCCAAATCTGGAAGC[A/G]TCTGTTGCATGCAAT | 79582 |
rs2216545 | snp | A/G | 0.175254 | 0.238565 | intron-variant | SPAG16 | GRCh38.p7 | 2:214253711 | ggttgctgtacactc[A/G]tagtatagtttgaag | 79582 |
rs2217159 | snp | G/T | 0.479824 | 0.098392 | intron-variant | SPAG16 | GRCh38.p7 | 2:213877826 | AATATGGAATTGAGA[G/T]TGGCACATGGAAAAT | 79582 |
rs2217160 | snp | A/T | 0.479824 | 0.098392 | intron-variant | SPAG16 | GRCh38.p7 | 2:213877825 | ATATGGAATTGAGAT[A/T]GGCACATGGAAAATA | 79582 |
rs2217161 | snp | C/T | 0.49934 | 0.0181589 | intron-variant | SPAG16 | GRCh38.p7 | 2:213735275 | TTACCAGATTTGTGA[C/T]TGTGAATTATTTATT | 79582 |
rs2247543 | snp | A/G | 0.130694 | 0.219696 | intron-variant | SPAG16 | GRCh38.p7 | 2:213772225 | aatgggagttaattc[A/G]tgatttggctctctg | 79582 |
rs2248214 | snp | A/G/T | 0.0184039 | 0.0941484 | intron-variant | SPAG16 | GRCh38.p7 | 2:213862481 | TTTCTTTCTCCTCGC[A/G/T]CAGTGTCTCCATGCA | 79582 |
rs2248746 | snp | A/G | 0 | 0 | intron-variant | SPAG16 | GRCh38.p7 | 2:213806935 | ATGGCTAATTAATGC[A/G]TGTTTTCAAAGATCA | 79582 |
rs2250113 | snp | C/T | 0.0566069 | 0.158427 | intron-variant | SPAG16 | GRCh38.p7 | 2:213830741 | TTGCTCAGTACTCCC[C/T]GAATCTCATTTACTT | 79582 |
rs2250198 | snp | A/C | 0.373598 | 0.21731 | intron-variant | SPAG16 | GRCh38.p7 | 2:213830786 | CTTTCAGTCCTTTTC[A/C]ATCACAAATTTCCCA | 79582 |
rs2250423 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | SPAG16 | GRCh38.p7 | 2:213832898 | gcatgaccaagtgat[A/G]ggcgaggaaaggtat | 79582 |
rs2250426 | snp | A/C | 0.379746 | 0.213696 | intron-variant | SPAG16 | GRCh38.p7 | 2:213832960 | CTATCTACAATGCAA[A/C]TTTTAATTCTGCTAT | 79582 |
rs2250780 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | SPAG16 | GRCh38.p7 | 2:213775843 | GGAAGCTGCATTTTT[C/T]GGTTTTATTTGTGTA | 79582 |
rs2251792 | snp | C/T | 0.148661 | 0.22854 | intron-variant | SPAG16 | GRCh38.p7 | 2:213869671 | TTTTTTGTCTAATTC[C/T]AAAAGTAATACAGGA | 79582 |
rs2253644 | snp | C/T | 0.242775 | 0.249896 | intron-variant | SPAG16 | GRCh38.p7 | 2:213752659 | GTTTTGTATTTGCTG[C/T]CTTCTTACTCTTTTT | 79582 |
rs2253646 | snp | C/T | 0.211516 | 0.24702 | intron-variant | SPAG16 | GRCh38.p7 | 2:213752660 | TTTTGTATTTGCTGC[C/T]TTCTTACTCTTTTTC | 79582 |
rs2263042 | snp | A/G | 0.135484 | 0.22223 | intron-variant | SPAG16 | GRCh38.p7 | 2:213761256 | acaatatatcaaaac[A/G]tatgggatgaggaaa | 79582 |
rs2264470 | snp | A/G | 0.473373 | 0.11227 | intron-variant | SPAG16 | GRCh38.p7 | 2:213356431 | CCTGAATAGACCAAT[A/G]ACAGGCTCTGAAATT | 79582 |
rs2266575 | snp | A/G/T | 0.277778 | 0.248452 | intron-variant | SPAG16 | GRCh38.p7 | 2:213356411 | AAGCTATTAATTATC[A/G/T]CCTCAATTTCAGAGC | 79582 |
rs2371889 | snp | C/T | 0.0456336 | 0.143994 | intron-variant | SPAG16 | GRCh38.p7 | 2:213361861 | tcactacttgtggaa[C/T]tgaatttgctgagga | 79582 |
rs2371890 | snp | A/G | 0.353803 | 0.227431 | intron-variant | SPAG16 | GRCh38.p7 | 2:213308727 | gcaaggaagggcagt[A/G]ttctaaagtggtctt | 79582 |
rs2371891 | snp | G/T | 0.0456336 | 0.143994 | intron-variant | SPAG16 | GRCh38.p7 | 2:213308736 | ggcagtgttctaaag[G/T]ggtcttatatctggt | 79582 |
rs2371892 | snp | A/G | 0 | 0 | intron-variant | SPAG16 | GRCh38.p7 | 2:213312314 | TATATGCCTATTTTA[A/G]AATTCTCAATGGGCA | 79582 |
rs2371964 | snp | C/T | 0.14665 | 0.227637 | intron-variant | SPAG16 | GRCh38.p7 | 2:213426477 | TGCAATCTAATGATT[C/T]TTTTTTCCTATGGCT | 79582 |
rs2371965 | snp | A/C | 0.192715 | 0.243348 | intron-variant | SPAG16 | GRCh38.p7 | 2:213432936 | CACTGCCAGGGATAC[A/C]AGGATTGTTCAGCAT | 79582 |
rs2371966 | snp | C/G | 0.0452528 | 0.143452 | intron-variant | SPAG16 | GRCh38.p7 | 2:213433800 | CTAAATAAATTCTAA[C/G]CAAAAAGAATAAAAC | 79582 |
rs2371967 | snp | A/C | 0.0452528 | 0.143452 | intron-variant | SPAG16 | GRCh38.p7 | 2:213474986 | CATCATTGGGGTCCC[A/C]TTTAGGGTCCTCCAA | 79582 |
rs2372094 | snp | A/G | 0 | 0 | intron-variant | SPAG16 | GRCh38.p7 | 2:213715222 | TAGGTAGATCTATCT[A/G]TCTATCTATCTATCT | 79582 |
rs2372095 | snp | G/T | 0.24019 | 0.249807 | intron-variant | SPAG16 | GRCh38.p7 | 2:213719704 | agatgctggagagga[G/T]gtggagaaataggaa | 79582 |
rs2372096 | snp | A/G | 0.141258 | 0.225111 | intron-variant | SPAG16 | GRCh38.p7 | 2:213731302 | GCTAGGATTACAGGC[A/G]CCCACTAACATGCCT | 79582 |
rs2372097 | snp | A/G | 0.140581 | 0.224783 | intron-variant | SPAG16 | GRCh38.p7 | 2:213731306 | GGATTACAGGCACCC[A/G]CTAACATGCCTGGCT | 79582 |
rs2372098 | snp | C/T | 0.0225045 | 0.103662 | intron-variant | SPAG16 | GRCh38.p7 | 2:213736044 | ACTGAGGTAGAATTT[C/T]AATACAGCTTAATAA | 79582 |
rs2372099 | snp | A/G | 0.140242 | 0.224618 | intron-variant | SPAG16 | GRCh38.p7 | 2:213738395 | AGATAGAGCATATGA[A/G]AGTGATGACTGATAA | 79582 |
rs2372100 | snp | C/T | 0.41441 | 0.188333 | intron-variant | SPAG16 | GRCh38.p7 | 2:213777318 | GTGGTGCAATCTCGG[C/T]TTACTGCAACCTCCA | 79582 |
rs2372101 | snp | C/G | 0.484771 | 0.0859212 | intron-variant | SPAG16 | GRCh38.p7 | 2:213913966 | gttgtagagaataat[C/G]agctttactcaacat | 79582 |
rs2372102 | snp | A/G | 0.481473 | 0.0944461 | intron-variant | SPAG16 | GRCh38.p7 | 2:213934683 | GTTAAGTATGTCTGC[A/G]TCACTAAGTTCTATA | 79582 |
rs2372103 | snp | A/G | 0.452965 | 0.145963 | intron-variant | SPAG16 | GRCh38.p7 | 2:213980608 | atatgtatatatgga[A/G]tatatgtatatatat | 79582 |
rs2372104 | snp | A/G | 0.499527 | 0.0153681 | intron-variant | SPAG16 | GRCh38.p7 | 2:213980710 | TATGTGTGTGTGTGT[A/G]TGTATATATATATAT | 79582 |
rs2372105 | snp | A/G | 0.497329 | 0.0364438 | intron-variant | SPAG16 | GRCh38.p7 | 2:213980712 | TGTGTGTGTGTGTGT[A/G]TATATATATATATAG | 79582 |
rs2372106 | snp | G/T | 0 | 0 | intron-variant | SPAG16 | GRCh38.p7 | 2:213980727 | GTATATATATATATA[G/T]AGAGAGAGAGAGAGA | 79582 |
rs2372107 | snp | G/T | 0 | 0 | intron-variant | SPAG16 | GRCh38.p7 | 2:213980729 | ATATATATATATAGA[G/T]AGAGAGAGAGAGAGA | 79582 |
rs2372108 | snp | A/C | 0.47934 | 0.0995154 | intron-variant | SPAG16 | GRCh38.p7 | 2:213981016 | CAAACTGAGTGGCTT[A/C]AACAACAGAAATTTG | 79582 |
rs2372109 | snp | A/G | 0.45198 | 0.147323 | intron-variant | SPAG16 | GRCh38.p7 | 2:213988060 | AAAATCTGGGGATCT[A/G]AAATGATTGTACTGT | 79582 |
rs2372218 | snp | C/G | 0.482683 | 0.0914256 | intron-variant | SPAG16 | GRCh38.p7 | 2:214030203 | gactattttagatac[C/G]tcatctaagtggaat | 79582 |
rs2372219 | snp | C/T | 0.0490535 | 0.14873 | intron-variant | SPAG16 | GRCh38.p7 | 2:214040286 | gaaggactgatatct[C/T]ttTCTTCCAttcttt | 79582 |
rs2372220 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | SPAG16 | GRCh38.p7 | 2:214047265 | aaaactggaggaatc[A/G]cattacctgacttca | 79582 |
rs2372221 | snp | C/T | 0.499295 | 0.0187567 | intron-variant | SPAG16 | GRCh38.p7 | 2:214054941 | GACCCATAATATGCA[C/T]ACACTAATTCCTTTG | 79582 |
rs2372222 | snp | A/G | 0.330482 | 0.236691 | intron-variant | SPAG16 | GRCh38.p7 | 2:214057995 | CTGGATTAAGCTTTG[A/G]CTTAAAAAAAATGTT | 79582 |
rs2372223 | snp | C/T | 0.463343 | 0.130326 | intron-variant | SPAG16 | GRCh38.p7 | 2:214122380 | CTTTTCCTAAGTTGC[C/T]GGTAAGTAGACATAA | 79582 |
rs2372224 | snp | C/T | 0.0460142 | 0.144533 | intron-variant | SPAG16 | GRCh38.p7 | 2:214148444 | TCTGTTTTCCTTCCC[C/T]TTTATCCAATTACCT | 79582 |
rs2372225 | snp | A/G | 0.481473 | 0.0944461 | intron-variant | SPAG16 | GRCh38.p7 | 2:214149063 | TGTGTGTATATATAT[A/G]TGTGTGTGTGTGTGT | 79582 |
rs2372226 | snp | A/G | 0.481473 | 0.0944461 | intron-variant | SPAG16 | GRCh38.p7 | 2:214149077 | TATGTGTGTGTGTGT[A/G]TATATATATATATAT | 79582 |
rs2372227 | snp | A/C | 0.341235 | 0.232758 | intron-variant | SPAG16 | GRCh38.p7 | 2:214169711 | TGATTGGGAGCCTCA[A/C]TACACTGACTTGTTA | 79582 |
rs2372228 | snp | A/G | 0.341235 | 0.232758 | intron-variant | SPAG16 | GRCh38.p7 | 2:214169790 | ATCCTTAAAGCGTTT[A/G]AGCCTGGATTGTATT | 79582 |
rs2372251 | snp | A/C | 0 | 0 | intron-variant | SPAG16 | GRCh38.p7 | 2:214214084 | CCCAGCCATATCAAT[A/C]TTTTTTTATTCTATG | 79582 |
rs2372252 | snp | A/C | 0.469839 | 0.119042 | intron-variant | SPAG16 | GRCh38.p7 | 2:214253707 | TTTTGGTTGCTGTAC[A/C]CTCATAGTATAGTTT | 79582 |
rs2372253 | snp | C/G | 0.470034 | 0.11868 | intron-variant | SPAG16 | GRCh38.p7 | 2:214254074 | GTAGCAATTGTGAAT[C/G]GGAGTCACTGATGAT | 79582 |
rs2372254 | snp | A/G | 0.344592 | 0.231414 | intron-variant | SPAG16 | GRCh38.p7 | 2:214330401 | GGAAATGGAAATGTT[A/G]CAGGAAAATGAAAGG | 79582 |
rs2372255 | snp | C/T | 0.476052 | 0.106772 | intron-variant | SPAG16 | GRCh38.p7 | 2:213814983 | gactttaacaattct[C/T]acccaataatcagca | 79582 |
rs2372256 | snp | A/G | 0.47517 | 0.10862 | intron-variant | SPAG16 | GRCh38.p7 | 2:213832983 | TCTGCTATGAAATTT[A/G]TATATATGTTTCATA | 79582 |
rs2372257 | snp | A/G | 0.319376 | 0.240181 | intron-variant | SPAG16 | GRCh38.p7 | 2:213838088 | GTACTGCATTTCTAG[A/G]CATCATATTCATGAT | 79582 |
rs2372258 | snp | C/T | 0.370568 | 0.219005 | intron-variant | SPAG16 | GRCh38.p7 | 2:213853014 | AAAGCATATGTAATC[C/T]GTGAGTGTGTATTGT | 79582 |
rs2372259 | snp | A/G | 0.472803 | 0.113397 | intron-variant | SPAG16 | GRCh38.p7 | 2:213856785 | CAAGTACCTGGGCCT[A/G]GCTCATGAAACCATT | 79582 |
rs2372260 | snp | A/G | 0.472803 | 0.113397 | intron-variant | SPAG16 | GRCh38.p7 | 2:213856903 | AGTTATCCAGAAGAC[A/G]TAGCTAAGATAATGA | 79582 |
rs2372261 | snp | G/T | 0.472803 | 0.113397 | intron-variant | SPAG16 | GRCh38.p7 | 2:213857001 | TTGGGAGGCCAAGGA[G/T]GATGGGTCACCTAAA | 79582 |
rs2372262 | snp | A/C | 0.472803 | 0.113397 | intron-variant | SPAG16 | GRCh38.p7 | 2:213857050 | GCCTGGCCAACATGG[A/C]GAAACCCTATCTCTA | 79582 |
rs2372263 | snp | C/T | 0.472803 | 0.113397 | intron-variant | SPAG16 | GRCh38.p7 | 2:213857081 | tcaaaaatacaaaaa[C/T]tagccaggcatggtg | 79582 |
rs2372264 | snp | C/T | 0.472803 | 0.113397 | intron-variant | SPAG16 | GRCh38.p7 | 2:213857098 | AGCCAGGCATGGTGG[C/T]GGGCGCCTGAAATCC | 79582 |
rs2372265 | snp | A/C | 0.472803 | 0.113397 | intron-variant | SPAG16 | GRCh38.p7 | 2:213857194 | gagatcactccactg[A/C]actccagcctgggtg | 79582 |
rs2372266 | snp | C/G | 0.472803 | 0.113397 | intron-variant | SPAG16 | GRCh38.p7 | 2:213857205 | actgaactccagcct[C/G]ggtgacagagagaga | 79582 |
rs2372267 | snp | G/T | 0.472896 | 0.113214 | intron-variant | SPAG16 | GRCh38.p7 | 2:213857293 | tttaaaactcttaaa[G/T]ctagagaggtaaagt | 79582 |
rs2372268 | snp | A/T | 0.472896 | 0.113214 | intron-variant | SPAG16 | GRCh38.p7 | 2:213857304 | taaatctagagaggt[A/T]aagtcaatgcttggc | 79582 |
rs2372269 | snp | A/C | 0.472896 | 0.113214 | intron-variant | SPAG16 | GRCh38.p7 | 2:213857310 | tagagaggtaaagtc[A/C]atgcttggcttcaac | 79582 |
rs2372296 | snp | A/G | 0.479984 | 0.0980171 | intron-variant | SPAG16 | GRCh38.p7 | 2:213867145 | ACATGGATAACTTTC[A/G]TCACAGTGTAACTCA | 79582 |
rs2372297 | snp | C/T | 0.327211 | 0.237778 | intron-variant | SPAG16 | GRCh38.p7 | 2:213867162 | CACAGTGTAACTCAT[C/T]ATTATTACATATTTA | 79582 |
rs2372298 | snp | A/G | 0.479984 | 0.0980171 | intron-variant | SPAG16 | GRCh38.p7 | 2:213867188 | ATTTACCACTAGATT[A/G]AGGTCATATATTGGT | 79582 |
rs2372299 | snp | A/G | 0.479984 | 0.0980171 | intron-variant | SPAG16 | GRCh38.p7 | 2:213867263 | GTTGGTAGCTGTTGA[A/G]AGTGATTCATCAATC | 79582 |
rs2372300 | snp | A/G | 0.479904 | 0.0982045 | intron-variant | SPAG16 | GRCh38.p7 | 2:213874405 | tataaatttttctct[A/G]ttttttattttcaaa | 79582 |
rs2372301 | snp | G/T | 0.484841 | 0.0857308 | intron-variant | SPAG16 | GRCh38.p7 | 2:213909877 | GGGTTTAAAGAAACT[G/T]GCATGAAAACAGGCC | 79582 |
rs2372302 | snp | A/G | 0.451856 | 0.147493 | intron-variant | SPAG16 | GRCh38.p7 | 2:213974500 | GAAACATACTCTGAA[A/G]CTAAATTTAACATAA | 79582 |
rs2372303 | snp | A/G | 0.134119 | 0.221521 | intron-variant | SPAG16 | GRCh38.p7 | 2:214368741 | CTGTCATTGGAGTAC[A/G]AGGAATCAAAGACTG | 79582 |
rs2433719 | snp | A/C | 0.304438 | 0.244001 | intron-variant | SPAG16 | GRCh38.p7 | 2:213859217 | AAAAAAAAAAAAAAA[A/C]TCAATGTCCTCTGAC | 79582 |
rs2433720 | snp | A/G | 0.140581 | 0.224783 | intron-variant | SPAG16 | GRCh38.p7 | 2:213742745 | tttagtacagacagc[A/G]tttcaccatgttggc | 79582 |
rs2433721 | snp | A/C | 0.497823 | 0.0427351 | intron-variant | SPAG16 | GRCh38.p7 | 2:213761210 | attgtaagggaaatt[A/C]gaaaatacttggaga | 79582 |
rs2433722 | snp | A/T | 0.15665 | 0.231917 | intron-variant | SPAG16 | GRCh38.p7 | 2:213803298 | TGCATAACTCAAGAT[A/T]ACCCTACTAAAATGT | 79582 |
rs2457181 | snp | C/T | 0.100588 | 0.200439 | intron-variant | SPAG16 | GRCh38.p7 | 2:213826038 | TGAACAACTATATGC[C/T]AATACATTCAAAAAC | 79582 |
rs2457182 | snp | C/T | 0.212122 | 0.247114 | intron-variant | SPAG16 | GRCh38.p7 | 2:213753298 | ATTACACGTGTGAGC[C/T]GCTGCGCCCAGCCTA | 79582 |
rs2457183 | snp | C/G | 0.499527 | 0.0153681 | intron-variant | SPAG16 | GRCh38.p7 | 2:213770608 | ttatcctgataatat[C/G]cttcccctaacaccc | 79582 |
rs2556295 | snp | A/C | 0.155656 | 0.231515 | | | GRCh38.p7 | 2:213801855 | GGAACCAATTGTATA[A/C]TGTGAATAAGAATTA | 79582 |
rs2556296 | snp | C/T | 0.399073 | 0.200692 | | | GRCh38.p7 | 2:213803006 | CTTCAGGGCAGTGTA[C/T]GTAGGAATCTTTTGG | 79582 |
rs2556297 | snp | A/T | 0.111576 | 0.20818 | | | GRCh38.p7 | 2:213764474 | GTTGCAAAATGTAAG[A/T]CCAAGGACACTATAT | 79582 |
rs2556298 | snp | A/T | 0 | 0 | | | GRCh38.p7 | 2:213764160 | ATCTCGTTTACATAG[A/T]CAGCATTTTTCTAAA | 79582 |
rs2556299 | snp | C/G | 0.39121 | 0.2063 | | | GRCh38.p7 | 2:213763359 | CATTGTAATttttag[C/G]tattataaataatac | 79582 |
rs2556300 | snp | C/T | 0.137187 | 0.223099 | | | GRCh38.p7 | 2:213760287 | aaagtctattttgtc[C/T]gttctcagtatagct | 79582 |
rs2556301 | snp | A/T | 0.137187 | 0.223099 | | | GRCh38.p7 | 2:213759448 | atctttatgtattat[A/T]caaaaatataaacat | 79582 |
rs2556302 | snp | A/G | 0.0107246 | 0.0724382 | | | GRCh38.p7 | 2:213758868 | accttttaaagcttt[A/G]attataatgtatttc | 79582 |
rs2556303 | snp | A/T | 0.212122 | 0.247114 | | | GRCh38.p7 | 2:213755006 | GTACCTTTTAGACAT[A/T]TAGAGATTCAATAAT | 79582 |
rs2556304 | snp | G/T | 0.135143 | 0.222054 | | | GRCh38.p7 | 2:213753370 | CAGCAGTGTCAAATT[G/T]TCCTATGCACTTATG | 79582 |
rs2556305 | snp | C/T | 0.139903 | 0.224452 | | | GRCh38.p7 | 2:213748147 | CAACTCTATGTCTAT[C/T]TTTTGTAACCTGAAA | 79582 |
rs2556306 | snp | G/T | 0.140581 | 0.224783 | | | GRCh38.p7 | 2:213746162 | GAAAAATACATATTT[G/T]GTTTCAAGTAATATC | 79582 |
rs2556307 | snp | A/C | 0.140581 | 0.224783 | | | GRCh38.p7 | 2:213745822 | ATCTCTTTTATTATT[A/C]CATTCTAGTATTTAA | 79582 |
rs2556308 | snp | C/T | 0.140242 | 0.224618 | | | GRCh38.p7 | 2:213743524 | ATAAAAGCATTCCTG[C/T]ATGCTGAAAAACATT | 79582 |
rs2556309 | snp | C/T | 0.463451 | 0.130149 | | | GRCh38.p7 | 2:213742983 | gcgggaggtggagct[C/T]gcagtgagtggagat | 79582 |
rs2556310 | snp | A/C | 0.140242 | 0.224618 | | | GRCh38.p7 | 2:213741128 | ATAAAGATTAATAAG[A/C]TTTCTCCTTAAGAAA | 79582 |
rs2556311 | snp | A/G | 0.168785 | 0.236441 | | | GRCh38.p7 | 2:213871244 | CTTCCAGAATGGCAG[A/G]ATAAGGACGTTCAAA | 79582 |
rs2556312 | snp | A/T | 0.0402882 | 0.136092 | | | GRCh38.p7 | 2:213874229 | GTACACTTAGGCTAT[A/T]CTGAATTTGTTTTAA | 79582 |
rs2556313 | snp | A/G | 0.143284 | 0.226079 | | | GRCh38.p7 | 2:213886597 | TTGAGATGCAGTGAC[A/G]AAAGGATTGGTGTAA | 79582 |
rs2556314 | snp | A/G | 0.0558544 | 0.157504 | | | GRCh38.p7 | 2:213889279 | GTGTATAAATATATC[A/G]TCTAAAAGATACCTA | 79582 |
rs2556316 | snp | A/C | 0.188946 | 0.24243 | | | GRCh38.p7 | 2:213847796 | CACTGCAAGAGTAAC[A/C]AGGAGAGGTCCGTGT | 79582 |
rs2556317 | snp | A/G | 0.0704125 | 0.17392 | | | GRCh38.p7 | 2:213845491 | TTAAGAACAAGggcc[A/G]cttgcagtggctcac | 79582 |
rs2556318 | snp | A/C | 0.148326 | 0.228391 | | | GRCh38.p7 | 2:213843304 | CTGGCTTCATGAGAC[A/C]ATTTCTCAAACTATA | 79582 |
rs2556319 | snp | C/T | 0.0566069 | 0.158427 | | | GRCh38.p7 | 2:213842753 | TAATAGCACCTAAAA[C/T]ATAGTTTTTCCAGGT | 79582 |
rs2556320 | snp | C/T | 0.158962 | 0.232835 | | | GRCh38.p7 | 2:213842405 | AAAACATATACACAT[C/T]CTATTTCTTACTACT | 79582 |
rs2556321 | snp | C/T | 0.101658 | 0.201233 | | | GRCh38.p7 | 2:213841312 | AAACTACCCTTATGT[C/T]ATGCCCCACTGGTTT | 79582 |
rs2556322 | snp | C/G | 0.0146672 | 0.084371 | | | GRCh38.p7 | 2:213838274 | tgaggcaggagaatc[C/G]cttgaacccaggagg | 79582 |
rs2556323 | snp | C/T | 0.391954 | 0.205789 | | | GRCh38.p7 | 2:213833812 | ATGGGTCTGAATTAC[C/T]ATGAAGAGACAGAGG | 79582 |
rs2556324 | snp | C/T | 0.377187 | 0.215229 | | | GRCh38.p7 | 2:213831529 | TAAAACAAAAACTAC[C/T]AACACAACAACGACA | 79582 |
rs2556326 | snp | A/C | 0.39527 | 0.203462 | | | GRCh38.p7 | 2:213827636 | aatgagcaataagaa[A/C]tcatctgaagataca | 79582 |
rs2556329 | snp | C/G | 0.0383715 | 0.133092 | | | GRCh38.p7 | 2:213818128 | aggggatctttaaag[C/G]actgcatttctcatg | 79582 |
rs2556330 | snp | A/T | 0.178785 | 0.239642 | | | GRCh38.p7 | 2:213818101 | catggaaagaagttt[A/T]cttagataaggaaat | 79582 |
rs2556331 | snp | G/T | 0 | 0 | | | GRCh38.p7 | 2:213816676 | TGCATAAGAGACATG[G/T]GTAAAGGCTATCTTT | 79582 |
rs2556332 | snp | C/T | 0.0103295 | 0.0711199 | | | GRCh38.p7 | 2:213814656 | attacaggcgtgtgc[C/T]actatgcccaggtaa | 79582 |
rs2556333 | snp | A/G | 0.0905309 | 0.192535 | | | GRCh38.p7 | 2:213810735 | CTGCTCCCCACCCTA[A/G]TACTTCCGCACCACG | 79582 |
rs2556334 | snp | A/G | 0.499968 | 0.00399348 | | | GRCh38.p7 | 2:213776745 | TACTTTTAGAGACTA[A/G]TATAGAGAAATAAAT | 79582 |
rs2556336 | snp | A/G | 0.111928 | 0.208413 | | | GRCh38.p7 | 2:213782542 | AGAAATTACATAGCT[A/G]TTATTCAATAAAGAT | 79582 |
rs2556337 | snp | A/G | 0.0475351 | 0.146656 | | | GRCh38.p7 | 2:213783432 | GAAGGCAGAGTATCT[A/G]TATCTATTATTTTTT | 79582 |
rs2556338 | snp | C/T | 0.375 | 0.216506 | | | GRCh38.p7 | 2:213783788 | AAATAGTGAAAATAT[C/T]TTAGGCATGGGATTT | 79582 |
rs2556339 | snp | G/T | 0.162581 | 0.234218 | | | GRCh38.p7 | 2:213785731 | TATTCTTCAAAAGAA[G/T]TTTAGCCAGGCGCAG | 79582 |
rs2556340 | snp | G/T | 0.102726 | 0.202016 | | | GRCh38.p7 | 2:213786926 | TTCTAATAATTTCAT[G/T]TGGAAAGTGATAAAA | 79582 |
rs2556341 | snp | C/G | 0.10237 | 0.201756 | | | GRCh38.p7 | 2:213792997 | AATGGCGTGATCTCA[C/G]CTCACTGCAATCTCT | 79582 |
rs2556342 | snp | A/G | 0.0509478 | 0.151255 | | | GRCh38.p7 | 2:213794355 | TTTAATATATAAATG[A/G]CTGTTTAAATCCTAA | 79582 |
rs2556343 | snp | A/C | 0.0479149 | 0.147179 | | | GRCh38.p7 | 2:213797393 | TTTTCATTCATAGTG[A/C]CGAGAAAATGTGTAT | 79582 |
rs2634474 | snp | G/T | 0.194278 | 0.243711 | upstream-variant-2KB, intron-variant | SPAG16, LOC100130451 | GRCh38.p7 | 2:213282527 | gcttttacagaaagc[G/T]ttctctttatttcag | 79582 |
rs2634482 | snp | C/T | 0.355525 | 0.226637 | intron-variant | SPAG16 | GRCh38.p7 | 2:213406475 | AAAATTACAACTTAA[C/T]GTATGGTTAAATAAA | 79582 |
rs2654556 | snp | C/T | 0.499609 | 0.0139722 | intron-variant | SPAG16 | GRCh38.p7 | 2:213408550 | ttaaccactgaaaat[C/T]cccctaacccagcag | 79582 |
rs2654557 | snp | C/T | 0.499609 | 0.0139722 | intron-variant | SPAG16 | GRCh38.p7 | 2:213408554 | ccactgaaaatcccc[C/T]taacccagcaggttt | 79582 |
rs2662639 | snp | G/T | 0.411366 | 0.192229 | intron-variant | SPAG16 | GRCh38.p7 | 2:213778485 | AGTATGCTTTATTAC[G/T]GACCATATCAACCCT | 79582 |
rs2662641 | snp | A/G | 0.201908 | 0.246653 | intron-variant | SPAG16 | GRCh38.p7 | 2:213833928 | TTGAGATTTGGGTGC[A/G]GACACAGCCAAACCA | 79582 |
rs2662642 | snp | A/G | 0.491834 | 0.0633738 | intron-variant | SPAG16 | GRCh38.p7 | 2:213752856 | GAATAAGGGAACAGT[A/G]TAGAGAGACTCCAGT | 79582 |
rs2662643 | snp | C/T | 0.490618 | 0.0678448 | intron-variant | SPAG16 | GRCh38.p7 | 2:213753104 | TGCAAGCTCCACCTC[C/T]CAGGTTCATGCCATT | 79582 |
rs2662644 | snp | A/G | 0.184521 | 0.241273 | intron-variant | SPAG16 | GRCh38.p7 | 2:213821876 | aaaaaatgagatccc[A/G]tcacttgcaacaaca | 79582 |
rs2662645 | snp | G/T | 0.372794 | 0.217765 | intron-variant | SPAG16 | GRCh38.p7 | 2:213819112 | GCTCTATTTTATAAA[G/T]AAATGTTCCACTCCT | 79582 |
rs2662646 | snp | C/T | 0.140242 | 0.224618 | intron-variant | SPAG16 | GRCh38.p7 | 2:213741378 | CCAATCAGTATTCTC[C/T]ACCTCCCCAAGTCTG | 79582 |
rs2662647 | snp | C/T | 0.229723 | 0.249176 | intron-variant | SPAG16 | GRCh38.p7 | 2:213883156 | ttagcaatataaact[C/T]tcctcttaacagact | 79582 |
rs2662648 | snp | C/T | 0.490231 | 0.0692021 | intron-variant | SPAG16 | GRCh38.p7 | 2:213753946 | AAAGGATAATTCCAG[C/T]TGCATGTTCAGCAAG | 79582 |
rs2662649 | snp | C/T | 0.0535932 | 0.154675 | intron-variant | SPAG16 | GRCh38.p7 | 2:213884657 | gactctgtctcatta[C/T]ataaacccatatttc | 79582 |
rs2662650 | snp | A/C | 0.0532157 | 0.154195 | intron-variant | SPAG16 | GRCh38.p7 | 2:213898272 | ATCTTATTTCCAGAA[A/C]AACTAAGAGCCATTG | 79582 |
rs2662652 | snp | A/G | 0.495818 | 0.0455352 | intron-variant | SPAG16 | GRCh38.p7 | 2:213759790 | ACCTGCAATCCCTGC[A/G]CTTTGGGAGGCCGAG | 79582 |
rs2662653 | snp | C/T | 0.499642 | 0.0133738 | intron-variant | SPAG16 | GRCh38.p7 | 2:213760214 | aaagatgcaaataga[C/T]tgaaggtagagggac | 79582 |
rs2662654 | snp | C/T | 0.187053 | 0.241946 | intron-variant | SPAG16 | GRCh38.p7 | 2:213845262 | TGCAGTGAGCCGAGA[C/T]TGTGCCACTGCACTC | 79582 |
rs2662655 | snp | C/T | 0.102014 | 0.201495 | intron-variant | SPAG16 | GRCh38.p7 | 2:213844775 | TAAAAATAGTTACTT[C/T]ATGACATTGTTTCCT | 79582 |
rs2662656 | snp | C/G | 0.140581 | 0.224783 | intron-variant | SPAG16 | GRCh38.p7 | 2:213742842 | agctgggattacagg[C/G]gtgagccaccgtgct | 79582 |
rs2662657 | snp | A/C/G | 0.0558544 | 0.157504 | intron-variant | SPAG16 | GRCh38.p7 | 2:213857995 | tgtagcaattgaatc[A/C/G]cattttcaggatgca | 79582 |
rs2662658 | snp | C/T | 0.0865458 | 0.189163 | intron-variant | SPAG16 | GRCh38.p7 | 2:213857022 | GGCTGGTCTCTAATT[C/T]CTGACTTTAGGTGAC | 79582 |
rs2662659 | snp | C/T | 0.40853 | 0.193309 | intron-variant | SPAG16 | GRCh38.p7 | 2:213795857 | TGGCTTCTGCTTCTG[C/T]GGAGTCCTCAGGAAA | 79582 |
rs2662660 | snp | A/G | 0 | 0 | intron-variant | SPAG16 | GRCh38.p7 | 2:213743915 | TTAACTTCCTTTTTA[A/G]ATTTTTCATCTCTGC | 79582 |
rs2662661 | snp | C/G | 0.0584853 | 0.160693 | intron-variant | SPAG16 | GRCh38.p7 | 2:213793538 | TAAAGTTGTCACATA[C/G]AAACAAACTGGTAGC | 79582 |
rs2662662 | snp | A/G | 0.157311 | 0.232183 | intron-variant | SPAG16 | GRCh38.p7 | 2:213800294 | ATCTTGTCTCCCTAT[A/G]TTTCCCTCCCTTTCT | 79582 |
rs2662663 | snp | G/T | 0 | 0 | intron-variant | SPAG16 | GRCh38.p7 | 2:213800620 | ATGTTTTATTGTGTT[G/T]ACTTTATCCCACAGT | 79582 |
rs2662664 | snp | A/C | 0.158632 | 0.232706 | intron-variant | SPAG16 | GRCh38.p7 | 2:213800889 | TGTCATGTGTTTTGC[A/C]GCAGCAGAAAAGATT | 79582 |
rs2662665 | snp | A/C | 0.0517044 | 0.152246 | intron-variant | SPAG16 | GRCh38.p7 | 2:213851302 | ggctggtctcgaact[A/C]ctgacctcaaataat | 79582 |
rs2662666 | snp | C/G | 0.140581 | 0.224783 | intron-variant | SPAG16 | GRCh38.p7 | 2:213745671 | AGCTTTGAATTTTGC[C/G]TACATGTTTCACTTC | 79582 |
rs2662667 | snp | C/T | 0.0569829 | 0.158885 | intron-variant | SPAG16 | GRCh38.p7 | 2:213850425 | CCATTCTTCATCAAA[C/T]CTAAACATAGACAGT | 79582 |
rs2662668 | snp | G/T | 0.39527 | 0.203462 | intron-variant | SPAG16 | GRCh38.p7 | 2:213849448 | TATACTCATCAAACT[G/T]CAGCACTTTCACAAA | 79582 |
rs2662669 | snp | C/T | 0.0513262 | 0.151752 | intron-variant | SPAG16 | GRCh38.p7 | 2:213847625 | tgttgaaatgtaatc[C/T]caatactgaaggtgg | 79582 |
rs2662670 | snp | A/C | 0.483708 | 0.088773 | intron-variant | SPAG16 | GRCh38.p7 | 2:213746682 | cgtggtggtgcgtgc[A/C]tgtagtcccagttac | 79582 |
rs2662671 | snp | C/T | 0.140242 | 0.224618 | intron-variant | SPAG16 | GRCh38.p7 | 2:213746862 | gtacaatacgtaata[C/T]ctgatagtgataata | 79582 |
rs2662672 | snp | C/T | 0.123452 | 0.215605 | intron-variant | SPAG16 | GRCh38.p7 | 2:213875609 | TTTTAAATGTAAGAC[C/T]CAAAAGAGTGAAATT | 79582 |
rs2662673 | snp | C/G | 0 | 0 | intron-variant | SPAG16 | GRCh38.p7 | 2:213871881 | tctctctctctctct[C/G]tgtgtgtgtgtgtgt | 79582 |
rs2662674 | snp | C/T | 0 | 0 | intron-variant | SPAG16 | GRCh38.p7 | 2:213747545 | ccattcttatcttta[C/T]actgtatttttggca | 79582 |
rs2662675 | snp | C/T | | | intron-variant | SPAG16 | GRCh38.p7 | 2:213868649 | TTACATGCTGTTTCA[C/T]ATAATAAGCTGTGGT | 79582 |
rs2662676 | snp | A/C | 0.144296 | 0.226554 | intron-variant | SPAG16 | GRCh38.p7 | 2:213863273 | CAGAGAGTTTTAGAA[A/C]GAAGCAGATCCAAGA | 79582 |
rs2662677 | snp | A/G | | | intron-variant | SPAG16 | GRCh38.p7 | 2:213862049 | AGCCATTATCCAGGA[A/G]AAGATCATGAATCAT | 79582 |
rs2662678 | snp | C/T | 0.378372 | 0.214524 | intron-variant | SPAG16 | GRCh38.p7 | 2:213763147 | aaaattgtaaggata[C/T]agagaaatctgaatc | 79582 |
rs2662679 | snp | C/G | 0.0023933 | 0.0345097 | intron-variant | SPAG16 | GRCh38.p7 | 2:213764203 | ACTAAGTTTTTTTTT[C/G]TCTTTTTCTTCATTT | 79582 |
rs2662680 | snp | A/G | 0.133093 | 0.220981 | intron-variant | SPAG16 | GRCh38.p7 | 2:213765556 | CCTTTTTCTGTCTGC[A/G]TTCTTACATTCCTTA | 79582 |
rs2662681 | snp | A/G | 0.111224 | 0.207945 | intron-variant | SPAG16 | GRCh38.p7 | 2:213773697 | tagctgggattacag[A/G]cacctgccaccacgc | 79582 |
rs2662682 | snp | A/G | 0.131038 | 0.219882 | intron-variant | SPAG16 | GRCh38.p7 | 2:213773899 | GATAGACTCTTGTCT[A/G]TCTGGTCCTCAAATA | 79582 |
rs2662683 | snp | A/T | 0.49934 | 0.0181589 | intron-variant | SPAG16 | GRCh38.p7 | 2:213774982 | tacctgtgtctcagg[A/T]tggatctgtctcGGC | 79582 |
rs2665858 | snp | C/T | 0.322007 | 0.239405 | intron-variant | SPAG16 | GRCh38.p7 | 2:213896591 | ATATACACACACACA[C/T]GCACACACACACACA | 79582 |
rs2708175 | snp | A/G | 0.49975 | 0.0111793 | intron-variant | SPAG16 | GRCh38.p7 | 2:213289260 | AGAAATATCACATGT[A/G]GAGTCCATATCTTTG | 79582 |
rs2888210 | snp | A/G | 0.132409 | 0.220618 | intron-variant | SPAG16 | GRCh38.p7 | 2:213432644 | agaagatagtttgaa[A/G]ttctggttgctgaat | 79582 |
rs2888233 | snp | A/C | 0.0452528 | 0.143452 | intron-variant | SPAG16 | GRCh38.p7 | 2:213552387 | TGGACATTTCTGCAG[A/C]AACTGCTAGAATTCT | 79582 |
rs2888234 | snp | A/T | | | intron-variant | SPAG16 | GRCh38.p7 | 2:213557920 | CTAAAGGGATTTTTT[A/T]AAAAACAAGGAAGTC | 79582 |
rs2888235 | snp | A/C | 0.363985 | 0.222503 | intron-variant | SPAG16 | GRCh38.p7 | 2:213612786 | cctcccaggttcaag[A/C]gattctcctgcctta | 79582 |
rs2888241 | snp | A/G | 0.140242 | 0.224618 | intron-variant | SPAG16 | GRCh38.p7 | 2:213735950 | AGGGAAATGACAGGC[A/G]GAGATACCACTATCC | 79582 |
rs2888260 | snp | A/G | 0.47934 | 0.0995154 | intron-variant | SPAG16 | GRCh38.p7 | 2:214040496 | tctatgtgtccatgt[A/G]ttctcatcatttagc | 79582 |
rs2888266 | snp | C/T | 0.00636936 | 0.0560724 | intron-variant | SPAG16 | GRCh38.p7 | 2:214246736 | TGAACTCCAGAGCTT[C/T]GGGGAATGTTAAATA | 79582 |
rs2888267 | snp | A/C | 0.382279 | 0.212137 | intron-variant | SPAG16 | GRCh38.p7 | 2:214252220 | GGATTTGCTTGCAAA[A/C]CCTAATATGTTGACA | 79582 |
rs2888268 | snp | A/G | 0.463989 | 0.129263 | intron-variant | SPAG16 | GRCh38.p7 | 2:214312872 | TGCTTTTTTTGAAGC[A/G]GATTATCTAAGCTCA | 79582 |
rs2888283 | snp | A/G | | | intron-variant | SPAG16 | GRCh38.p7 | 2:213964805 | gaaaagtccagggtt[A/G]aaagtacaataatta | 79582 |
rs2927242 | snp | A/G | 0.607161 | 0.137716 | intron-variant | SPAG16 | GRCh38.p7 | 2:213356368 | TTTGGCTGTGAATCT[A/G]TCTGATCTTGGACTT | 79582 |
rs3043745 | in-del | -/A | 0 | 0 | intron-variant | SPAG16, LOC101928084 | GRCh38.p7 | 2:214096289 | AATGCAAAAAAAAAA[-/A]TGTAGAATTTTTTTC | 79582 |
rs3043746 | in-del | -/T | | | intron-variant | SPAG16 | GRCh38.p7 | 2:214144433 | TTGGTTCTATAATTG[-/T]TGTTTTAATGGCTTT | 79582 |
rs3043748 | in-del | -/AACT | 0 | 0 | intron-variant | SPAG16 | GRCh38.p7 | 2:214148678 | TTATCAATGCTAACT[-/AACT]GTGAGCATAAAAGCT | 79582 |
rs3043764 | in-del | -/TA/TATA/TATATATACA | 0 | 0 | intron-variant | SPAG16 | GRCh38.p7 | 2:214149097 | atatatatatatata[-/TA/TATA/TATATATACA]CATACATACACATTT | 79582 |
rs3043765 | in-del | -/CA | 0.3748 | 0.216622 | intron-variant | SPAG16 | GRCh38.p7 | 2:214158001 | TATTCATGTCTCCAT[-/CA]GAAAAGGACATTTGA | 79582 |
rs3043766 | in-del | -/AAGGACA | | | intron-variant | SPAG16 | GRCh38.p7 | 2:214158006 | ATGTCTCCATCAGAA[-/AAGGACA]TTTGAATCAGGAACA | 79582 |
rs3043768 | in-del | -/TTG | 0.373799 | 0.217195 | intron-variant | SPAG16 | GRCh38.p7 | 2:214158014 | ATCAGAAAAGGACAT[-/TTG]AATCAGGAACAAACG | 79582 |
rs3044944 | in-del | -/GT/GTGT | 0 | 0 | intron-variant | SPAG16 | GRCh38.p7 | 2:214227739 | TGTGTGTGTGTGTGT[-/GT/GTGT]AAATGTGTATATCTA | 79582 |
rs3044977 | in-del | -/TT | 0.5 | 0 | intron-variant | SPAG16 | GRCh38.p7 | 2:214310166 | TCTTTTTTTTTTTTT[-/TT]GAAATTGCTATTGTT | 79582 |
rs3044978 | in-del | -/AA | 0 | 0 | intron-variant | SPAG16 | GRCh38.p7 | 2:214319517 | AGAAAGATCCACTGG[-/AA]AAAAAAAAAAAAAAC | 79582 |
rs3045010 | in-del | -/TCTC | | | intron-variant | SPAG16 | GRCh38.p7 | 2:213836966 | CTCTCTCTCTCTCTC[-/TCTC]ATAAAAATAAAACAA | 79582 |
rs3045016 | in-del | -/GT | 0 | 0 | intron-variant | SPAG16 | GRCh38.p7 | 2:213856847 | CTCCATAACATAAAA[-/GT]GTATGGTGAAGCAAC | 79582 |
rs3046040 | in-del | -/AT | | | intron-variant | SPAG16 | GRCh38.p7 | 2:213865947 | atactatatatatat[-/AT]GTGCTTAAATTTTTT | 79582 |
rs3046049 | in-del | -/G/TG/TTG/TTT | 0.428786 | 0.174744 | intron-variant | SPAG16 | GRCh38.p7 | 2:213869661 | TTTTTTTTTTTTTTT[-/G/TG/TTG/TTT]GTCTAATTCCAAAAG | 79582 |
rs3073677 | in-del | -/GT | | | intron-variant | SPAG16 | GRCh38.p7 | 2:213462484 | atatgactagactgt[-/GT]ccctacccaaatctc | 79582 |
rs3076744 | in-del | -/TATC/TATCTATCTATCTGTC/TATCTATCTGTC/TGTC | 0 | 0 | intron-variant | SPAG16 | GRCh38.p7 | 2:213715268 | ATCTATCTATCTATC[lengthTooLong]CATTCATCCATCTAA | 79582 |
rs3076768 | in-del | -/TT/TTT | 0 | 0 | intron-variant | SPAG16 | GRCh38.p7 | 2:213737505 | TTCTTTTTTTTTTTT[-/TT/TTT]GAGACGGAGTCTCGC | 79582 |
rs3076788 | snp | A/C | 0.465473 | 0.126772 | intron-variant | SPAG16 | GRCh38.p7 | 2:213761887 | caaaaataaaaacaa[A/C]aaaacaaaacaaaaa | 79582 |
rs3076792 | in-del | -/ACACACA/ACACACAA/ACACACAC | | | intron-variant | SPAG16 | GRCh38.p7 | 2:213932991 | cacacacacacacac[-/ACACACA/ACACACAA/ACACACAC]caGTGTAACCCAGAG | 79582 |
rs3076793 | snp | A/G | | | intron-variant | SPAG16 | GRCh38.p7 | 2:213980477 | agaatatatgtgtgt[A/G]tatatataatatata | 79582 |
rs3076808 | in-del | -/TA | | | intron-variant | SPAG16 | GRCh38.p7 | 2:213980730 | atatatatatagaga[-/TA]gagagagagagagag | 79582 |
rs3108148 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | SPAG16 | GRCh38.p7 | 2:213356647 | TCTCTCCTTTCTTCT[G/T]TATTAGTCTTGTTAG | 79582 |
rs3123639 | snp | C/T | 0.512346 | 0.166209 | intron-variant | SPAG16 | GRCh38.p7 | 2:213356584 | AGGGGATATCACCAC[C/T]GATCCCACAGAACTA | 79582 |
rs3213779 | snp | C/G | 0.233235 | 0.249437 | intron-variant | SPAG16, LOC101928084 | GRCh38.p7 | 2:214096367 | TGTTTAACTCTGTTC[C/G]GCTCAATCACTGTGT | 79582 |
rs3213780 | snp | A/G | 0.233235 | 0.249437 | intron-variant | SPAG16, LOC101928084 | GRCh38.p7 | 2:214096504 | GAATATATATATTCC[A/G]ATACACATATGTATA | 79582 |
rs3213781 | snp | A/G | 0.224709 | 0.248717 | intron-variant | SPAG16, LOC101928084 | GRCh38.p7 | 2:214096557 | TATGCTACTGGGAGC[A/G]TTTTTTTAAACACTC | 79582 |
rs3213782 | snp | C/T | 0.233527 | 0.249457 | intron-variant | SPAG16, LOC101928084 | GRCh38.p7 | 2:214096562 | TACTGGGAGCGTTTT[C/T]TTAAACACTCACTTC | 79582 |
rs3219887 | microsatellite | (CA)17/18/19/20/22/23/24/26 | 0.79228 | 0.0827276 | intron-variant | SPAG16 | GRCh38.p7 | 2:214227699 | AGATATACACATTTA[(CA)17/18/19/20/22/23/24/26]CTTCCACAAGAAAGA | 79582 |
rs3220937 | microsatellite | (CA)14/15/16/17/18 | 0.489984 | 0.248112 | intron-variant | SPAG16 | GRCh38.p7 | 2:213767656 | gagaacaaCATACTT[(CA)14/15/16/17/18]AAATCAGATATAAGA | 79582 |
rs3220958 | microsatellite | (CA)17/19/20/21/22/23/24/26/27/28 | 0.848964 | 0.0675514 | intron-variant | SPAG16 | GRCh38.p7 | 2:214061982 | ATGAATAAAAGCATG[lengthTooLong]GTTANGGTNATTCAG | 79582 |
rs3845645 | snp | A/G | 0.472803 | 0.113397 | intron-variant, downstream-variant-500B | SPAG16 | GRCh38.p7 | 2:213858586 | tgtgatattcacttt[A/G]ttgagattgtctgaa | 79582 |
rs3893331 | snp | A/G | 0.40086 | 0.199352 | intron-variant | SPAG16 | GRCh38.p7 | 2:213932870 | AGGTTTCTGTGAATA[A/G]TTAACAGTAGCTTTT | 79582 |
rs3931235 | snp | C/G | | | intron-variant | SPAG16 | GRCh38.p7 | 2:213417213 | atatGAGTAAAT[C/G] | 79582 |
rs4016161 | snp | A/T | | | intron-variant | SPAG16 | GRCh38.p7 | 2:213833577 | ATATAATATATATAT[A/T]ATATATATATTATAT | 79582 |
rs4016177 | snp | G/T | 0.375 | 0.216506 | intron-variant | SPAG16, LOC101928084 | GRCh38.p7 | 2:214102116 | TGAGGGTGGTTTTTT[G/T]TTTTTTTTTTTTTGC | 79582 |
rs4016237 | snp | C/T | 0.192401 | 0.243274 | intron-variant | SPAG16 | GRCh38.p7 | 2:213467934 | AGCCTGCAAGGCAGC[C/T]ATTAGAGACTGTACC | 79582 |
rs4016238 | snp | C/T | 0.132409 | 0.220618 | intron-variant | SPAG16 | GRCh38.p7 | 2:213468077 | tgcttctgcagcttc[C/T]tcctgataccagggg | 79582 |
rs4016243 | in-del | -/CTGT | | | intron-variant | SPAG16 | GRCh38.p7 | 2:213451135 | AATTATCCACATTGT[-/CTGT]GAAGCACTTTCATGA | 79582 |
rs4055801 | in-del | -/AT | | | intron-variant | SPAG16 | GRCh38.p7 | 2:213468535 | aatacatatatatat[-/AT]nctatatataaatac | 79582 |
rs4073685 | snp | G/T | 0 | 0 | intron-variant | SPAG16 | GRCh38.p7 | 2:214383193 | AGAACCTCTTTCCAG[G/T]GCCATGCAATATGTA | 79582 |
rs4076788 | snp | C/T | 0.282105 | 0.24793 | intron-variant | SPAG16 | GRCh38.p7 | 2:214403425 | AAAATGTACCCAAAA[C/T]GGTATCATATCAACA | 79582 |
rs4113955 | snp | A/G | 0.479904 | 0.0982045 | intron-variant | SPAG16 | GRCh38.p7 | 2:213871363 | AATAAGTGCTCCTTG[A/G]GTTGATGTAAGCCTT | 79582 |
rs4132244 | snp | A/C | 0.406814 | 0.194704 | intron-variant | SPAG16 | GRCh38.p7 | 2:213691803 | AACAATGATTGCCAC[A/C]TTTTAGAGCTTTCAA | 79582 |
rs4132245 | snp | C/G | | | intron-variant | SPAG16 | GRCh38.p7 | 2:213691786 | TTTAGAGCTTTCAAT[C/G]TGGTGGGGACAACAA | 79582 |
rs4143570 | snp | C/G | 0.46137 | 0.133501 | intron-variant | SPAG16 | GRCh38.p7 | 2:213788773 | TGCTGAAAGGAATAA[C/G]ACAACATCTAAACCC | 79582 |
rs4146001 | snp | C/T | 0.0134861 | 0.0810011 | intron-variant | SPAG16 | GRCh38.p7 | 2:213933688 | ACTTGCAAAATTCAA[C/T]AGCTTCTTGACCCCT | 79582 |
rs4146002 | snp | A/G | 0.282369 | 0.247896 | intron-variant | SPAG16 | GRCh38.p7 | 2:213967482 | AAAGATTTTCAAAAA[A/G]CCAGATACTACTATA | 79582 |
rs4146011 | snp | A/T | 0 | 0 | intron-variant | SPAG16 | GRCh38.p7 | 2:213533252 | CATACTATCTTTTTT[A/T]gtatatatgtatata | 79582 |
rs4146048 | snp | A/G | 0.046775 | 0.145601 | intron-variant | SPAG16 | GRCh38.p7 | 2:213364235 | CTAGAGATATTTAAA[A/G]GTGAGTAAGTGGTGG | 79582 |
rs4146049 | snp | A/C | 0.499515 | 0.0155675 | intron-variant | SPAG16 | GRCh38.p7 | 2:213365072 | CATAAAATTAAGCCT[A/C]GGATTTTAGGGTCAT | 79582 |
rs4233993 | snp | C/G | 0.325563 | 0.238307 | intron-variant | SPAG16 | GRCh38.p7 | 2:213769245 | TATTACCAATTCTAT[C/G]TTGAGGAATTTCTCC | 79582 |
rs4267506 | snp | C/T | 0.306927 | 0.243432 | intron-variant | SPAG16 | GRCh38.p7 | 2:214407865 | TTAAGTCACACATTA[C/T]ATGCCGTGTAATAAT | 79582 |
rs4274594 | snp | A/G | 0.278133 | 0.248412 | intron-variant | SPAG16 | GRCh38.p7 | 2:214386653 | gagcacttgagctca[A/G]taattaaagaccagc | 79582 |
rs4275972 | snp | A/G | 0.102014 | 0.201495 | intron-variant | SPAG16 | GRCh38.p7 | 2:213646532 | ATTTTGGACTTAATA[A/G]TGATTAGAGAATTAC | 79582 |
rs4276027 | snp | C/T | 0.282895 | 0.247826 | intron-variant | SPAG16 | GRCh38.p7 | 2:214385993 | ACATGGTCTCTTTTT[C/T]GGGATCTTGATTTTC | 79582 |
rs4276028 | snp | A/C | 0.2768 | 0.248559 | intron-variant | SPAG16 | GRCh38.p7 | 2:214387401 | GCATCTCAGTATATA[A/C]CTGTTGAGGGAAAGA | 79582 |
rs4283423 | snp | C/G | 0 | 0 | intron-variant | SPAG16 | GRCh38.p7 | 2:214390294 | ATTTGGGAGGGTGAA[C/G]TGCCAGTTGTGAATT | 79582 |
rs4286276 | snp | C/T | 0.315758 | 0.241197 | intron-variant | SPAG16 | GRCh38.p7 | 2:214400102 | TCAGAAGGTAGCCCA[C/T]GTAGGAAAGCACCTG | 79582 |
rs4287766 | snp | C/G | 0.0988009 | 0.199095 | intron-variant | SPAG16 | GRCh38.p7 | 2:214390509 | TCTCAGGCTCACTTT[C/G]AGCACAAACTGGTTA | 79582 |
rs4287767 | snp | A/T | 0.304438 | 0.244001 | intron-variant | SPAG16 | GRCh38.p7 | 2:214402391 | TCTCTCTACCTTAGA[A/T]GATTTTACTTTACCA | 79582 |
rs4309528 | snp | C/G | 0.472896 | 0.113214 | intron-variant | SPAG16 | GRCh38.p7 | 2:213858163 | ttcataaacatattt[C/G]ataaagatgtttgag | 79582 |
rs4324320 | snp | A/G | 0.438386 | 0.164349 | intron-variant | SPAG16 | GRCh38.p7 | 2:214395646 | ataagcatagtaccc[A/G]ataggtatttttttc | 79582 |
rs4335945 | snp | C/T | 0.253544 | 0.249975 | intron-variant | SPAG16 | GRCh38.p7 | 2:214407407 | ACATATTTACTTCAA[C/T]ATGAACATTATTAGT | 79582 |
rs4340451 | snp | A/G | 0.473818 | 0.111381 | intron-variant | SPAG16 | GRCh38.p7 | 2:213626374 | CCCGGATTTTTAGGG[A/G]AAAAAAATAGCTGCA | 79582 |
rs4347839 | snp | A/C | 0.305934 | 0.243663 | intron-variant | SPAG16 | GRCh38.p7 | 2:214408278 | ATCAGTGTTTACCCC[A/C]CTTTTCAGCTGTTGT | 79582 |
rs4355057 | snp | A/G | 0.327211 | 0.237778 | intron-variant | SPAG16 | GRCh38.p7 | 2:214328443 | GTTGGGATTACAGGC[A/G]TGAGCCACCATGCCC | 79582 |
rs4361126 | snp | C/T | 0.278133 | 0.248412 | intron-variant | SPAG16 | GRCh38.p7 | 2:214392272 | GCAATCCTCCTACCT[C/T]GGCCTCTAGAGTAGC | 79582 |
rs4371303 | snp | A/G | 0.465052 | 0.127485 | intron-variant | SPAG16 | GRCh38.p7 | 2:213854266 | CTTTAAAAGAAAAAA[A/G]TATGAATGATAGATG | 79582 |
rs4372827 | snp | A/G | 0.192715 | 0.243348 | intron-variant | SPAG16 | GRCh38.p7 | 2:213442439 | ataaagtttatatgg[A/G]tattcaaaagacaga | 79582 |
rs4374320 | snp | A/G | 0 | 0 | intron-variant | SPAG16 | GRCh38.p7 | 2:213345763 | tttggtaccagtacc[A/G]tgctgttttggttac | 79582 |
rs4374321 | snp | C/T | 0.480382 | 0.097079 | intron-variant | SPAG16 | GRCh38.p7 | 2:214138587 | ACCTAGACTTCAGAC[C/T]GAGCAGTTGGCAACT | 79582 |
rs4380236 | snp | C/T | 0.486464 | 0.0811471 | upstream-variant-2KB, intron-variant, downstream-variant-500B | VWC2L, SPAG16 | GRCh38.p7 | 2:214410885 | AATGCAAGCCTCTTC[C/T]GGAACTTTCATCTCT | 79582 |
rs4383277 | snp | A/G | 0.479904 | 0.0982045 | intron-variant | SPAG16 | GRCh38.p7 | 2:213867289 | CAATCATTGAAAATG[A/G]TAAATGAATGGATCA | 79582 |
rs4384723 | snp | A/G | 0.472616 | 0.113763 | intron-variant | SPAG16 | GRCh38.p7 | 2:213854742 | CAAGAATGTCTAGCT[A/G]GCTAACACTGGAACA | 79582 |
rs4384724 | snp | G/T | 0.229429 | 0.249152 | intron-variant | SPAG16 | GRCh38.p7 | 2:214138338 | GAGATTATTTATTCA[G/T]GCCTATTTCAAGGCT | 79582 |
rs4386271 | snp | C/T | 0.473174 | 0.112665 | intron-variant | SPAG16 | GRCh38.p7 | 2:213854568 | ctctCTGTGCTGTGA[C/T]aatgttcactaaatt | 79582 |
rs4393936 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | SPAG16 | GRCh38.p7 | 2:213356583 | GGGGATATCCCCACC[A/G]ATCCCATAGAAATAC | 79582 |
rs4405697 | snp | C/T | 0.472989 | 0.113031 | intron-variant | SPAG16 | GRCh38.p7 | 2:213858245 | aacaatatcacatgc[C/T]acagagaaatctttt | 79582 |
rs4407196 | snp | G/T | 0.479904 | 0.0982045 | intron-variant | SPAG16 | GRCh38.p7 | 2:213871286 | TCATAAAAGCAGAGA[G/T]AATATGGGGGGAGAG | 79582 |
rs4410231 | snp | G/T | 0.209084 | 0.246629 | intron-variant, upstream-variant-2KB | SPAG16, LOC101928084 | GRCh38.p7 | 2:214104384 | ATTCAGCTTTTGTTG[G/T]TTGCTCTAGTGGCGG | 79582 |
rs4422113 | snp | A/T | 0.0471551 | 0.14613 | intron-variant | SPAG16 | GRCh38.p7 | 2:213368283 | taggctcttttttgg[A/T]tccatatgaacttta | 79582 |
rs4427962 | snp | A/G | 0.472616 | 0.113763 | intron-variant | SPAG16 | GRCh38.p7 | 2:213854171 | AACACAGTAATGTAC[A/G]ATGTTTATCAAAACT | 79582 |
rs4427963 | snp | A/G | 0 | 0 | intron-variant | SPAG16 | GRCh38.p7 | 2:214276587 | atgaaattctgggtt[A/G]aaaattcttttaaga | 79582 |
rs4427965 | snp | C/T | 0.45198 | 0.147323 | intron-variant | SPAG16 | GRCh38.p7 | 2:213937804 | ACACATTCAATATGG[C/T]TTTGTATGTGTGAAG | 79582 |
rs4450543 | snp | A/G | 0.473174 | 0.112665 | intron-variant | SPAG16 | GRCh38.p7 | 2:213854564 | ctgtctctctgtgct[A/G]tGAcaatgttcacta | 79582 |
rs4450545 | snp | C/T | 0.172351 | 0.237636 | intron-variant | SPAG16 | GRCh38.p7 | 2:213488267 | GCACGTGTGTGTATA[C/T]GCCATTAACAaagat | 79582 |
rs4453640 | snp | C/T | 0.452597 | 0.146474 | intron-variant | SPAG16 | GRCh38.p7 | 2:213947845 | TTTGATTATTATAAC[C/T]GTATAGTAAGTCTTA | 79582 |
rs4456649 | snp | A/G | 0.490508 | 0.0682328 | intron-variant, downstream-variant-500B | SPAG16 | GRCh38.p7 | 2:213503855 | GAAAGCCAAACACAG[A/G]AGGTGAGGGTTAGTG | 79582 |
rs4458155 | snp | A/G | 0.479824 | 0.098392 | intron-variant | SPAG16 | GRCh38.p7 | 2:213877898 | ATCATGTTACATTCT[A/G]CAACCACACTGTCAC | 79582 |
rs4476297 | snp | A/G | 0.464629 | 0.128197 | intron-variant | SPAG16 | GRCh38.p7 | 2:213854264 | GTCTTTAAAAGAAAA[A/G]AGTATGAATGATAGA | 79582 |
rs4479427 | snp | C/G | 0.418653 | 0.184544 | intron-variant | SPAG16 | GRCh38.p7 | 2:214400050 | TTAGAACATTTTTAG[C/G]ACTTTAGGTGCATTT | 79582 |
rs4483988 | snp | A/C | 0.251014 | 0.249998 | intron-variant | SPAG16 | GRCh38.p7 | 2:214114127 | gaggtccactccaga[A/C]cctgtttgcctgtgt | 79582 |
rs4491895 | snp | C/T | 0 | 0 | intron-variant | SPAG16 | GRCh38.p7 | 2:213356550 | ACTACCATCAGAGAA[C/T]ACTATAAACACCTCT | 79582 |
rs4493195 | snp | C/T | 0 | 0 | intron-variant | SPAG16 | GRCh38.p7 | 2:213922279 | cagagagccagaatt[C/T]gagctcttagattct | 79582 |
rs4494678 | snp | A/G | 0.47802 | 0.102502 | intron-variant | SPAG16 | GRCh38.p7 | 2:213674881 | gcagcatgatttata[A/G]tcctttgggtatata | 79582 |
rs4494679 | snp | A/G | 0.472896 | 0.113214 | intron-variant | SPAG16 | GRCh38.p7 | 2:213858002 | tgaaaatgcgattca[A/G]ttgctacaattttat | 79582 |
rs4494680 | snp | A/G | 0.472989 | 0.113031 | intron-variant | SPAG16 | GRCh38.p7 | 2:213858254 | acatgccacagagaa[A/G]tctttttgaaatgaa | 79582 |
rs4497879 | snp | A/C | 0.282105 | 0.24793 | intron-variant | SPAG16 | GRCh38.p7 | 2:214390687 | GCAGGGGAGCACAGC[A/C]TGAGTTCTAGGGGCA | 79582 |
rs4499373 | snp | A/T | 0 | 0 | intron-variant | SPAG16 | GRCh38.p7 | 2:213433914 | TTTCCTttttctttg[A/T]ctttttttttttttt | 79582 |
rs4499374 | snp | A/G | 0 | 0 | intron-variant | SPAG16 | GRCh38.p7 | 2:213674940 | gtatttctagttcta[A/G]atccctgaggaatca | 79582 |
rs4503943 | snp | A/G | 0.479904 | 0.0982045 | intron-variant | SPAG16 | GRCh38.p7 | 2:213850251 | ATTGTGTGGATTGTC[A/G]GAAAACTAGAAAGAT | 79582 |
rs4507042 | snp | C/T | 0.0456336 | 0.143994 | intron-variant | SPAG16 | GRCh38.p7 | 2:213471346 | tcacgtatataccac[C/T]tccatttgatgatgg | 79582 |
rs4513239 | snp | A/C | 0.45235 | 0.146814 | intron-variant | SPAG16 | GRCh38.p7 | 2:213937829 | GTGAAGAATGGCTCA[A/C]GTAAGTGTCCACTGC | 79582 |
rs4525639 | snp | C/T | 0.102014 | 0.201495 | intron-variant | SPAG16 | GRCh38.p7 | 2:214315396 | GTGTTGGCATTCAGA[C/T]GGAAGAAAAAGCATG | 79582 |
rs4531876 | snp | A/G | 0.0263992 | 0.111815 | intron-variant | SPAG16 | GRCh38.p7 | 2:214069485 | TCCCTTAAACTATGA[A/G]TCAGGCAAAAGCCTG | 79582 |
rs4541202 | snp | C/T | 0.49655 | 0.04139 | intron-variant, upstream-variant-2KB | SPAG16, LOC101928084 | GRCh38.p7 | 2:214104277 | AAGAGCCGAACAATA[C/T]AGGGCCTTAAGACAC | 79582 |
rs4544371 | snp | C/T | 0.499631 | 0.0135733 | intron-variant | SPAG16 | GRCh38.p7 | 2:213956247 | aggcataagccacca[C/T]gccaggcctttattg | 79582 |
rs4550616 | snp | A/C | 0.18134 | 0.240387 | intron-variant | SPAG16 | GRCh38.p7 | 2:214042550 | TTATTTGTTTTCCCC[A/C]TATCTCATCATAGGA | 79582 |
rs4552137 | snp | C/T | 0.0471551 | 0.14613 | intron-variant | SPAG16 | GRCh38.p7 | 2:213348084 | cctgtattaggtgca[C/T]atatatttaggatag | 79582 |
rs4560058 | snp | G/T | 0.194278 | 0.243711 | intron-variant | SPAG16 | GRCh38.p7 | 2:213362456 | catccagaaatgcaa[G/T]ggaaatagggaagaa | 79582 |
rs4585026 | snp | A/G | 0.282632 | 0.247861 | upstream-variant-2KB, intron-variant, downstream-variant-500B | VWC2L, SPAG16 | GRCh38.p7 | 2:214410901 | GGAACTTTCATCTCT[A/G]CAGCCCATCCAAGAA | 79582 |
rs4600591 | snp | C/T | 0.347473 | 0.230215 | intron-variant | SPAG16 | GRCh38.p7 | 2:214191543 | tgtagggaaagccca[C/T]ctccactaaaaatac | 79582 |
rs4602167 | snp | A/G | 0.0777841 | 0.181223 | intron-variant | SPAG16 | GRCh38.p7 | 2:214138531 | ATATACCAATTTGGC[A/G]TATTTGAGGACCATA | 79582 |
rs4608465 | snp | C/T | 0.233235 | 0.249437 | intron-variant | SPAG16 | GRCh38.p7 | 2:213910039 | GAAACCAAAATCATA[C/T]CTTTTACTTATACAA | 79582 |
rs4609995 | snp | C/G | 0.472803 | 0.113397 | intron-variant | SPAG16 | GRCh38.p7 | 2:213854959 | GCTTTCATGCTACAA[C/G]AGCAGAGCTGAAAAG | 79582 |
rs4618051 | snp | C/G | 0.304438 | 0.244001 | intron-variant | SPAG16 | GRCh38.p7 | 2:214407709 | GGCATTTTTTATTTT[C/G]TTTCTGAGAGTACCT | 79582 |
rs4625906 | snp | A/T | 0.358728 | 0.225118 | intron-variant | SPAG16 | GRCh38.p7 | 2:214391256 | ATCATTAGAATGATT[A/T]TGAGCAGTAAATTGG | 79582 |
rs4633868 | snp | G/T | 0.0460142 | 0.144533 | intron-variant | SPAG16 | GRCh38.p7 | 2:213487978 | AAATATAAAAATGTT[G/T]AACTTAATTATATAT | 79582 |
rs4633869 | snp | C/T | 0.470034 | 0.11868 | intron-variant | SPAG16 | GRCh38.p7 | 2:213854206 | GAAAACATCGTTTAA[C/T]TGTAAATATCTACAG | 79582 |
rs4633870 | snp | A/G | 0.472989 | 0.113031 | intron-variant | SPAG16 | GRCh38.p7 | 2:213854231 | CTACAGTTTTAAGTA[A/G]GGAATGTCCTACCCA | 79582 |
rs4638733 | snp | A/T | 0.472803 | 0.113397 | intron-variant, utr-variant-3-prime | SPAG16 | GRCh38.p7 | 2:213858315 | gtcttattttcagaa[A/T]ttgctacaaccatct | 79582 |
rs4638734 | snp | G/T | 0.0588605 | 0.161139 | intron-variant | SPAG16 | GRCh38.p7 | 2:214279335 | CTCTTGACCTTGTGA[G/T]CCGCCCTCCTCAACC | 79582 |
rs4643476 | snp | A/G | 0.116838 | 0.211584 | intron-variant | SPAG16 | GRCh38.p7 | 2:214071249 | TCTCCTGATTTGAAT[A/G]GGCAAGGGCTCAAAG | 79582 |
rs4672678 | snp | A/G | 0.0463947 | 0.145069 | intron-variant | SPAG16 | GRCh38.p7 | 2:213366619 | agcatgggaaaaccc[A/G]cctccatgattcaaa | 79582 |
rs4672679 | snp | A/G | 0.34101 | 0.232846 | intron-variant | SPAG16 | GRCh38.p7 | 2:213373806 | TAAAATTGTACCTAT[A/G]AGTTGTTTAGAATAG | 79582 |
rs4672680 | snp | C/T | 0.0614824 | 0.164198 | intron-variant | SPAG16 | GRCh38.p7 | 2:213476662 | TGTGGCATTTTTGCT[C/T]GCATAGTTTGGTGAG | 79582 |
rs4672682 | snp | G/T | 0.140242 | 0.224618 | intron-variant | SPAG16 | GRCh38.p7 | 2:213734162 | GGTTACCTAACAGTT[G/T]TCATTCTTGATCGAG | 79582 |
rs4672684 | snp | C/T | 0.480144 | 0.097642 | intron-variant | SPAG16 | GRCh38.p7 | 2:213775961 | TCCAAATAGCTATGA[C/T]TGCTTTCTTTCCAAG | 79582 |
rs4672685 | snp | A/G | 0.467642 | 0.123012 | intron-variant | SPAG16 | GRCh38.p7 | 2:213780765 | CTATTTTGTTTCCTG[A/G]AACTGCCTGTATGCT | 79582 |
rs4672687 | snp | A/T | 0.472335 | 0.114312 | intron-variant | SPAG16 | GRCh38.p7 | 2:213876164 | CAGACTTAATGGCAG[A/T]AAATGACATTAAATT | 79582 |
rs4672688 | snp | A/C | 0.475437 | 0.108066 | intron-variant | SPAG16 | GRCh38.p7 | 2:213878394 | ttaagatgctttctc[A/C]ttgtgtttttaactt | 79582 |
rs4672689 | snp | A/G | 0.479744 | 0.0985793 | intron-variant | SPAG16 | GRCh38.p7 | 2:213878652 | gtgcagaagcttttc[A/G]gtttaattaagtcta | 79582 |
rs4672690 | snp | A/G | 0.479824 | 0.098392 | intron-variant | SPAG16 | GRCh38.p7 | 2:213888206 | GCTACATATGTTACT[A/G]TTTCATAATTTCTTT | 79582 |
rs4672691 | snp | A/C | 0.479984 | 0.0980171 | intron-variant | SPAG16 | GRCh38.p7 | 2:213888315 | CTGTTTATAAGTTAG[A/C]GCATTCAGAGATTTA | 79582 |
rs4672692 | snp | A/G | 0.484771 | 0.0859212 | intron-variant | SPAG16 | GRCh38.p7 | 2:213912037 | CTGCAAACTCATAAT[A/G]TTTAGCTAGGTTATT | 79582 |
rs4672693 | snp | A/G | 0.484771 | 0.0859212 | intron-variant | SPAG16 | GRCh38.p7 | 2:213912092 | TTAAAAGTAATTTTA[A/G]TGAGAATAATAGTGT | 79582 |
rs4672694 | snp | C/T | 0.484771 | 0.0859212 | intron-variant | SPAG16 | GRCh38.p7 | 2:213924161 | caggcactgcaacta[C/T]gcctttattcaggtg | 79582 |
rs4672695 | snp | A/G | 0.484841 | 0.0857308 | intron-variant | SPAG16 | GRCh38.p7 | 2:213924204 | ctggtctgctctggg[A/G]ttaaaggcttgtagt | 79582 |
rs4672696 | snp | A/G | 0.48491 | 0.0855403 | intron-variant | SPAG16 | GRCh38.p7 | 2:213924337 | tgtacaggtctctgc[A/G]gagagcatgaatctc | 79582 |
rs4672698 | snp | A/C | 0.371785 | 0.218331 | intron-variant | SPAG16 | GRCh38.p7 | 2:213962641 | tctgggtcttccagc[A/C]tccagaaatgtgaga | 79582 |
rs4672699 | snp | C/T | 0 | 0 | intron-variant | SPAG16 | GRCh38.p7 | 2:213995934 | ATACATACCCCTTTC[C/T]TACTCCAAGGGAATC | 79582 |
rs4672701 | snp | C/T | 0.152001 | 0.229992 | intron-variant | SPAG16 | GRCh38.p7 | 2:214002240 | GTATTAATAAAGAAA[C/T]AGTTTACTATTGCAT | 79582 |
rs4672702 | snp | A/T | 0.144296 | 0.226554 | intron-variant | SPAG16 | GRCh38.p7 | 2:214033294 | ATTCTTTGCTTGAGA[A/T]ATTTATAGTTTTGTG | 79582 |
rs4672703 | snp | G/T | 0.352938 | 0.227824 | intron-variant | SPAG16 | GRCh38.p7 | 2:214033410 | catgatctgattata[G/T]tttcgaagaattact | 79582 |
rs4672704 | snp | A/G | 0.347914 | 0.230028 | intron-variant | SPAG16 | GRCh38.p7 | 2:214038206 | TTTAGGAAAGACTGT[A/G]CTTTTGTTCTAGCAG | 79582 |
rs4672706 | snp | C/T | 0 | 0 | intron-variant | SPAG16 | GRCh38.p7 | 2:214368493 | AATTTATTTTTGTTC[C/T]ATTTCATCCTACCTC | 79582 |
rs4672707 | snp | A/G | 0.390464 | 0.206809 | intron-variant | SPAG16 | GRCh38.p7 | 2:214383580 | CATCTCAAAAAAAAA[A/G]AAAAAAGAAAAAAAA | 79582 |
rs4673737 | snp | A/G | 0.0460142 | 0.144533 | intron-variant | SPAG16 | GRCh38.p7 | 2:213326176 | GGAAGATGAAAAACT[A/G]CCATTTAAAAAATAA | 79582 |
rs4673738 | snp | A/C | 0.0460142 | 0.144533 | intron-variant | SPAG16 | GRCh38.p7 | 2:213326195 | TTTAAAAAATAATGA[A/C]ATACTTTATTTTACA | 79582 |
rs4673739 | snp | G/T | 0.499722 | 0.0117779 | intron-variant | SPAG16 | GRCh38.p7 | 2:213341030 | GTTTAAAGAATACTT[G/T]TCACATAAAATTCAT | 79582 |
rs4673740 | snp | C/T | 0.0471551 | 0.14613 | intron-variant | SPAG16 | GRCh38.p7 | 2:213341353 | AAATCAGCTATAGGA[C/T]AGAGTGTTTTGATGC | 79582 |
rs4673742 | snp | C/T | 0.046775 | 0.145601 | intron-variant | SPAG16 | GRCh38.p7 | 2:213385318 | gccatcctagcttca[C/T]ataaataccagtttc | 79582 |
rs4673744 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | SPAG16 | GRCh38.p7 | 2:213523164 | tggaggcagtaaccc[C/T]gatgctgctgttctc | 79582 |
rs4673748 | snp | C/T | 0.362732 | 0.22314 | intron-variant | SPAG16 | GRCh38.p7 | 2:213605237 | AAGCAAAATCAGACA[C/T]TTTATTTCATCTATA | 79582 |
rs4673750 | snp | A/G | 0 | 0 | intron-variant | SPAG16 | GRCh38.p7 | 2:213643103 | agttttgtcccgcta[A/G]agaactctggctaat | 79582 |
rs4673751 | snp | A/G | 0 | 0 | intron-variant | SPAG16 | GRCh38.p7 | 2:213643105 | ttttgtcccgctaga[A/G]aactctggctaatac | 79582 |
rs4673752 | snp | C/G | 0.0966517 | 0.197444 | intron-variant | SPAG16 | GRCh38.p7 | 2:213672198 | TTTTCATTTCCTTTT[C/G]TGTCTTTCCTTTCCA | 79582 |
rs4673753 | snp | C/T | 0.130694 | 0.219696 | intron-variant | SPAG16 | GRCh38.p7 | 2:213723502 | ATCAAATTGTTGAAT[C/T]GAATGTAGAAGGACA | 79582 |
rs4673754 | snp | G/T | 0.140581 | 0.224783 | intron-variant | SPAG16 | GRCh38.p7 | 2:213734372 | CCCACCAAACCAAGA[G/T]AAAAAAGCATTGAGA | 79582 |
rs4673755 | snp | C/T | 0.110872 | 0.20771 | intron-variant | SPAG16 | GRCh38.p7 | 2:213739009 | CTTTGCTTACTTTTA[C/T]TTAAACAACTGTGAT | 79582 |
rs4673756 | snp | C/T | 0.484491 | 0.0866827 | intron-variant | SPAG16 | GRCh38.p7 | 2:213742238 | CAGATTGTTTACTAA[C/T]TTTGGAGACAGTACA | 79582 |
rs4673760 | snp | A/G | 0.281049 | 0.248064 | intron-variant | SPAG16 | GRCh38.p7 | 2:213792709 | ctgcctcagcctccc[A/G]agtagctggaattac | 79582 |
rs4673761 | snp | C/T | 0.470618 | 0.117591 | intron-variant | SPAG16 | GRCh38.p7 | 2:213809190 | TTGGATTTATGTCAT[C/T]GGGAAATCTGGATTT | 79582 |
rs4673763 | snp | A/G | 0.460925 | 0.134204 | intron-variant | SPAG16 | GRCh38.p7 | 2:213838894 | TGGAACAGAAGCATG[A/G]ATAACTCCATTGTGG | 79582 |
rs4673766 | snp | A/C | 0.479824 | 0.098392 | intron-variant | SPAG16 | GRCh38.p7 | 2:213877915 | AACCACACTGTCACT[A/C]TCTGTTATTTATGGA | 79582 |
rs4673767 | snp | G/T | 0.479824 | 0.098392 | intron-variant | SPAG16 | GRCh38.p7 | 2:213878312 | ATAGTGTATAAGCAT[G/T]TCTTTTCCTTCTTAT | 79582 |
rs4673768 | snp | C/T | 0.479744 | 0.0985793 | intron-variant | SPAG16 | GRCh38.p7 | 2:213878517 | GAATTTTTGTTATTG[C/T]GGAGTTTTTTGAGTT | 79582 |
rs4673772 | snp | A/T | 0.479824 | 0.098392 | intron-variant | SPAG16 | GRCh38.p7 | 2:213886861 | atttaaaattagaac[A/T]aTGGACACTATGCTG | 79582 |
rs4673773 | snp | A/G | 0.479824 | 0.098392 | intron-variant | SPAG16 | GRCh38.p7 | 2:213886862 | tttaaaattagaacA[A/G]TGGACACTATGCTGG | 79582 |
rs4673774 | snp | C/T | 0.479583 | 0.0989539 | intron-variant | SPAG16 | GRCh38.p7 | 2:213888329 | GAGCATTCAGAGATT[C/T]ACTTAGAACTATCCT | 79582 |
rs4673775 | snp | A/G | 0.479583 | 0.0989539 | intron-variant | SPAG16 | GRCh38.p7 | 2:213888361 | AGCTTGGCCACTTCT[A/G]TATGGTTTTGAGAAA | 79582 |
rs4673776 | snp | C/T | 0.483563 | 0.0891524 | intron-variant | SPAG16 | GRCh38.p7 | 2:213888453 | ACTCAACTGAGGTTA[C/T]TCTTTGATGACTGAC | 79582 |
rs4673777 | snp | A/G | 0.470811 | 0.117228 | intron-variant | SPAG16 | GRCh38.p7 | 2:213888580 | AATGTAAGTACACAT[A/G]AAAGTTGGTGGTGGA | 79582 |
rs4673778 | snp | C/T | 0.479824 | 0.098392 | intron-variant | SPAG16 | GRCh38.p7 | 2:213889371 | ATCTAGGTATGTAAT[C/T]ATTATATTAAAATGC | 79582 |
rs4673786 | snp | A/T | 0.329084 | 0.237162 | intron-variant | SPAG16 | GRCh38.p7 | 2:213909387 | actactttaaagttc[A/T]tatggagccaaaaaa | 79582 |
rs4673787 | snp | C/T | 0.243633 | 0.249919 | intron-variant | SPAG16 | GRCh38.p7 | 2:213909530 | gtatcaaaacagaga[C/T]atagatcaatggaac | 79582 |
rs4673788 | snp | A/G | 0.329084 | 0.237162 | intron-variant | SPAG16 | GRCh38.p7 | 2:213919723 | tcattatgtggtaga[A/G]tttagagtatgtgca | 79582 |
rs4673789 | snp | C/T | 0.484632 | 0.086302 | intron-variant | SPAG16 | GRCh38.p7 | 2:213920015 | gttaggtcttctcat[C/T]gaattgaaatctttg | 79582 |
rs4673790 | snp | A/G | 0.255224 | 0.249945 | intron-variant | SPAG16 | GRCh38.p7 | 2:213921264 | tattgccattatata[A/G]tgctcttctttagct | 79582 |
rs4673792 | snp | C/T | 0.484491 | 0.0866827 | intron-variant | SPAG16 | GRCh38.p7 | 2:213922330 | tgctgtttatacttg[C/T]gatttaattatgcaa | 79582 |
rs4673793 | snp | C/T | 0.484771 | 0.0859212 | intron-variant | SPAG16 | GRCh38.p7 | 2:213922474 | tgggttttgctgttt[C/T]cctgtatcttgatga | 79582 |
rs4673794 | snp | C/G | 0.484771 | 0.0859212 | intron-variant | SPAG16 | GRCh38.p7 | 2:213922600 | AGAGGAAAGAAGGTA[C/G]TCTGGCTTTTCAAGT | 79582 |
rs4673795 | snp | C/G | 0.484841 | 0.0857308 | intron-variant | SPAG16 | GRCh38.p7 | 2:213922654 | TTTCTAATTTGTGTG[C/G]GCTGATGTTCCTTCA | 79582 |
rs4673796 | snp | A/C | 0.484771 | 0.0859212 | intron-variant | SPAG16 | GRCh38.p7 | 2:213924168 | tgcaactatgccttt[A/C]ttcaggtgatggcac | 79582 |
rs4673797 | snp | C/T | 0.470424 | 0.117954 | intron-variant | SPAG16 | GRCh38.p7 | 2:213925048 | TAACATTTTACCATG[C/T]TGACTGAATTTAGTA | 79582 |
rs4673798 | snp | A/G | 0.495745 | 0.0459295 | intron-variant | SPAG16 | GRCh38.p7 | 2:213982396 | ATTCTCAATTTTACC[A/G]TTCTTACTAATGAAT | 79582 |
rs4673799 | snp | A/G | 0.461813 | 0.132798 | intron-variant | SPAG16 | GRCh38.p7 | 2:213982475 | CTTTTTGTGTTTTAT[A/G]CTTACATACAACAAA | 79582 |
rs4673800 | snp | A/G | 0.491577 | 0.0643472 | intron-variant | SPAG16 | GRCh38.p7 | 2:213997866 | CAAGCTTGTTTTGTA[A/G]CAACACAGTGGAAAA | 79582 |
rs4673801 | snp | A/G | 0.11963 | 0.213316 | intron-variant | SPAG16 | GRCh38.p7 | 2:213998124 | GTAATTAAAATCCAC[A/G]TAAATCTCAGCAAGT | 79582 |
rs4673804 | snp | A/G | 0.488846 | 0.0738428 | intron-variant | SPAG16 | GRCh38.p7 | 2:214003606 | agttatattctataa[A/G]gtcaccacaaacact | 79582 |
rs4673805 | snp | A/G | 0.453453 | 0.145282 | intron-variant | SPAG16 | GRCh38.p7 | 2:214017954 | ATATGATTCCTAAAT[A/G]TATCATAAATGCATC | 79582 |
rs4673806 | snp | G/T | 0.498392 | 0.028309 | intron-variant | SPAG16 | GRCh38.p7 | 2:214017976 | AAATGCATCATTAAT[G/T]AGAAATAAAGTTCAT | 79582 |
rs4673807 | snp | C/T | 0.495708 | 0.0461266 | intron-variant | SPAG16 | GRCh38.p7 | 2:214020263 | TCTACTTAGTCCCTT[C/T]GAGTTTCTACCACAG | 79582 |
rs4673808 | snp | A/C | 0.0962929 | 0.197165 | intron-variant | SPAG16 | GRCh38.p7 | 2:214033163 | ATAAACCGATAAAGT[A/C]GGTGACAACTGCAGC | 79582 |
rs4673810 | snp | C/G | 0.0916144 | 0.193427 | intron-variant | SPAG16 | GRCh38.p7 | 2:214047295 | aaattatgctccaga[C/G]ctttgattaatcata | 79582 |
rs4673812 | snp | C/T | 0.0810805 | 0.184299 | intron-variant | SPAG16 | GRCh38.p7 | 2:214115660 | GAGGCAGGCAGATCA[C/T]GAGGTCAGGAGATCG | 79582 |
rs4673813 | snp | A/G | 0 | 0 | intron-variant | SPAG16 | GRCh38.p7 | 2:214233344 | GTAAAAATAGATAAT[A/G]ATGATGATGATGATG | 79582 |
rs4673815 | snp | A/G | 0 | 0 | intron-variant | SPAG16 | GRCh38.p7 | 2:214278134 | agccaggcgcaggat[A/G]taatcccctggtgtg | 79582 |
rs4673816 | snp | G/T | 0.469148 | 0.120308 | intron-variant | SPAG16 | GRCh38.p7 | 2:214281427 | TTAAAGTAGGCCTTA[G/T]TCTTAACAACTTTAA | 79582 |
rs4673817 | snp | A/G | 0.482384 | 0.0921818 | intron-variant | SPAG16 | GRCh38.p7 | 2:214295037 | TGCCATCTGTCTAGG[A/G]TCTGGGGAATTTAGG | 79582 |
rs4673819 | snp | C/T | 0.47726 | 0.104176 | intron-variant | SPAG16 | GRCh38.p7 | 2:214336048 | GGCTGTGAGCCACCA[C/T]GCCCAAGCCTATTAT | 79582 |
rs4673820 | snp | A/G | 0.302686 | 0.244385 | intron-variant | SPAG16 | GRCh38.p7 | 2:214356160 | TAACCTGCACATTGT[A/G]CACATGTAACCTAAA | 79582 |
rs4673821 | snp | C/T | 0.483126 | 0.0902898 | intron-variant | SPAG16 | GRCh38.p7 | 2:214379091 | TAGCCTCTTGTGAAT[C/T]ATCCCTAAAATGATG | 79582 |
rs4673822 | snp | A/G | 0.322959 | 0.239117 | intron-variant | SPAG16 | GRCh38.p7 | 2:214379558 | CCAGAACTGGTCCTC[A/G]TGTCCTACAGGGAGG | 79582 |
rs4673823 | snp | G/T | 0.448708 | 0.151707 | intron-variant | SPAG16 | GRCh38.p7 | 2:214384857 | ACTATTGAGTCACTC[G/T]TCTCCATGTCCTTAA | 79582 |
rs4673825 | snp | A/C | 0.307176 | 0.243374 | intron-variant | SPAG16 | GRCh38.p7 | 2:214399572 | TGTACATTAAGAGAA[A/C]AACTCCCAAAATATT | 79582 |
rs5014688 | snp | A/T | | | intron-variant | SPAG16 | GRCh38.p7 | 2:213833567 | TATATAATATATATA[A/T]TATATATATAATATA | 79582 |
rs5015907 | snp | A/G | 0.472989 | 0.113031 | intron-variant | SPAG16 | GRCh38.p7 | 2:213860588 | CAGTTCATGTGGAAT[A/G]GGAGTCCAAGTTGTT | 79582 |
rs5015908 | snp | G/T | | | intron-variant | SPAG16 | GRCh38.p7 | 2:213860482 | ATCTATCTATATATA[G/T]ATATACACACATATG | 79582 |
rs5018577 | snp | A/T | | | intron-variant | SPAG16 | GRCh38.p7 | 2:214390342 | TATGCTTTTTTTTTT[A/T]AAAAAAAAAAAAAAA | 79582 |
rs5020057 | snp | A/T | 0.444444 | 0.157135 | intron-variant | SPAG16 | GRCh38.p7 | 2:214323332 | ATTAAATATATATAT[A/T]TATTTATTTATTTAT | 79582 |
rs5020193 | snp | C/G | 0.444444 | 0.157135 | intron-variant | SPAG16 | GRCh38.p7 | 2:214076543 | TGTGTGTGTGTGTGT[C/G]TGTGTGTGTGTGTGT | 79582 |
rs5838379 | in-del | -/T | 0.100944 | 0.200705 | intron-variant | SPAG16 | GRCh38.p7 | 2:213327164 | TGTCTGTTTGCTGTG[-/T]TTTTTTTTTTTTAAC | 79582 |
rs5838380 | in-del | -/T | | | intron-variant | SPAG16 | GRCh38.p7 | 2:213365475 | AATAACTAAAATGAA[-/T]TTTTTTTTTTTTTGA | 79582 |
rs5838381 | in-del | -/T | 0.486398 | 0.0813386 | intron-variant | SPAG16 | GRCh38.p7 | 2:213417876 | ATTTTTTTTTTTTTT[-/T]GAGACAGTTTTGCTC | 79582 |
rs5838383 | in-del | -/A | | | intron-variant | SPAG16 | GRCh38.p7 | 2:213594509 | ATTTTTGCGGGGAGA[-/A]TGGGGGTGTGCTCAC | 79582 |
rs5838385 | in-del | -/TT/TTT | | | intron-variant | SPAG16 | GRCh38.p7 | 2:213737503 | TTCTTTTTCTTTTCT[-/TT/TTT]TTTTTTTTTTTGAGA | 79582 |
rs5838386 | in-del | -/G | 0.307423 | 0.243316 | intron-variant | SPAG16 | GRCh38.p7 | 2:213743085 | ATTTTTTGTATTTTT[-/G]GTAGAGACAGGGTTT | 79582 |
rs5838389 | in-del | -/CACA/CACACGCACACA | 0 | 0 | intron-variant | SPAG16 | GRCh38.p7 | 2:213767679 | ACACACACACACACA[-/CACA/CACACGCACACA]AAATCAGATATAAGA | 79582 |
rs5838391 | in-del | -/ATA | 0.155987 | 0.23165 | intron-variant | SPAG16 | GRCh38.p7 | 2:213788873 | ACGTCTTTATGAGTG[-/ATA]ATTCTCAAATTATTG | 79582 |
rs5838396 | snp | A/T | | | intron-variant | SPAG16 | GRCh38.p7 | 2:213833557 | atatataatatatat[A/T]atatatataatatat | 79582 |
rs5838398 | in-del | -/C | 0.479744 | 0.0985793 | intron-variant | SPAG16 | GRCh38.p7 | 2:213866977 | GAAGGCATTTAAAAA[-/C]TTGCAAGTCTTCAAA | 79582 |
rs5838399 | in-del | -/A | 0.479744 | 0.0985793 | intron-variant | SPAG16 | GRCh38.p7 | 2:213867016 | TTGCCTCAAAATAAT[-/A]ACTATACACATAACT | 79582 |
rs5838401 | in-del | -/T | 0.480064 | 0.0978296 | intron-variant | SPAG16 | GRCh38.p7 | 2:213875109 | ACCACATCAAACTAA[-/T]TTTTTTTTTTTTTGA | 79582 |
rs5838403 | in-del | -/T | 0.0460142 | 0.144533 | intron-variant | SPAG16 | GRCh38.p7 | 2:213929849 | ATATGCCACTACAAG[-/T]AAAAATAAATCAGAT | 79582 |
rs5838404 | in-del | -/T | 0.497907 | 0.0322805 | intron-variant | SPAG16 | GRCh38.p7 | 2:213994578 | AATGATTTTCCATCC[-/T]TTTTTTTTTTTTTTT | 79582 |
rs5838410 | in-del | -/A | 0.254092 | 0.249967 | intron-variant | SPAG16, LOC101928084 | GRCh38.p7 | 2:214096280 | TGGTTTTTTTAATGC[-/A]AAAAAAAAATGTAGA | 79582 |
rs5838411 | in-del | -/A | 0.336702 | 0.234484 | intron-variant | SPAG16 | GRCh38.p7 | 2:214131376 | CCCTAACTCAAAATT[-/A]AAAAAAAAAAAAAAA | 79582 |
rs5838412 | in-del | -/TA | | | intron-variant | SPAG16 | GRCh38.p7 | 2:214149054 | TGTAGTGTGTGTGTG[-/TA]TATATATATGTGTGT | 79582 |
rs5838415 | in-del | -/ATAAA | | | intron-variant | SPAG16 | GRCh38.p7 | 2:214186038 | GCACTGTACCAGGCA[-/ATAAA]TAAAATAATGTTCAA | 79582 |
rs5838416 | snp | A/T | | | intron-variant, downstream-variant-500B | SPAG16 | GRCh38.p7 | 2:214192637 | TGTATATTCCTTTAT[A/T]TTTTTTGTACTTTTC | 79582 |
rs5838417 | in-del | -/A | | | intron-variant | SPAG16 | GRCh38.p7 | 2:214209552 | TTGCTCTTGCTCTTC[-/A]ACATCTTGAAAGAGT | 79582 |
rs5838419 | snp | A/T | 0.0944967 | 0.195752 | intron-variant | SPAG16 | GRCh38.p7 | 2:214241890 | AAATGTAAGTTGTAT[A/T]AAAAAAAAAAAATTC | 79582 |
rs5838420 | in-del | -/A | 0.414245 | 0.188477 | intron-variant | SPAG16 | GRCh38.p7 | 2:214244395 | TAAGCTGAAGTTCCG[-/A]AAAAAAAAAAAAAGA | 79582 |
rs5838423 | in-del | -/T | 0 | 0 | intron-variant | SPAG16 | GRCh38.p7 | 2:214259494 | ACACACACGTATAGC[-/T]TTTTTTTTTTTTTTT | 79582 |
rs5838424 | in-del | -/TTTC | 0.4862 | 0.0819127 | intron-variant | SPAG16 | GRCh38.p7 | 2:214260548 | ATTAAAAGTCTATTA[-/TTTC]TTTCTTTGGTTATTT | 79582 |
rs5838425 | in-del | -/T | 0.499908 | 0.00678851 | intron-variant | SPAG16 | GRCh38.p7 | 2:214311145 | TGGAGATCAGCACTG[-/T]TACCTGCATTTCCTC | 79582 |
rs5838427 | in-del | -/T/TT | 0 | 0 | intron-variant | SPAG16 | GRCh38.p7 | 2:214325735 | TAGCTTTTTTTTTTT[-/T/TT]ACATGTATTCCAGTT | 79582 |
rs5838428 | in-del | -/A | | | intron-variant | SPAG16 | GRCh38.p7 | 2:214326945 | GTGAGACTAAGTCTC[-/A]AAAAAAAAAAAAAAA | 79582 |
rs5838429 | in-del | -/A | | | intron-variant | SPAG16 | GRCh38.p7 | 2:214330113 | CTCTACCAAAAATAG[-/A]AAAAAAAAAAAAAAG | 79582 |
rs5838431 | in-del | -/CAAC | | | intron-variant | SPAG16 | GRCh38.p7 | 2:214377629 | GGTAACGCTTCCAAC[-/CAAC]AGTAGGCTATTAGTA | 79582 |
rs5838432 | in-del | -/A | 0.329084 | 0.237162 | intron-variant | SPAG16 | GRCh38.p7 | 2:214386874 | GAGAAAAAAAAAAAA[-/A]CAACTATGAAATAGG | 79582 |
rs5838433 | in-del | -/T/TT/TTT/TTTT | 0.5 | 0 | intron-variant | SPAG16 | GRCh38.p7 | 2:214390331 | AATGAATGGGTATGC[-/T/TT/TTT/TTTT]TTTTTTTTTTTTTAA | 79582 |
rs6147167 | in-del | -/TGGCAGGTTCATC | | | intron-variant | SPAG16 | GRCh38.p7 | 2:214219957 | TTTAGCAAAACCTGT[-/TGGCAGGTTCATC]CTCTAGAGATACATT | 79582 |
rs6435766 | snp | C/T | 0.046775 | 0.145601 | intron-variant | SPAG16 | GRCh38.p7 | 2:213304821 | tgattcgtgcagttt[C/T]cttcttgttcaggat | 79582 |
rs6435767 | snp | C/T | 0.0479149 | 0.147179 | intron-variant | SPAG16 | GRCh38.p7 | 2:213307580 | atggtgtatatgtgc[C/T]acattttcttaatcc | 79582 |
rs6435768 | snp | C/T | 0.0471551 | 0.14613 | intron-variant | SPAG16 | GRCh38.p7 | 2:213344311 | ATTTCCACTTCACAG[C/T]GTTGGCTATCTTTTT | 79582 |
rs6435769 | snp | A/G | 0.249038 | 0.249998 | intron-variant | SPAG16 | GRCh38.p7 | 2:213346858 | ttttttttttgttgt[A/G]tctctgccaggcttt | 79582 |
rs6435770 | snp | A/G | 0.350546 | 0.22889 | intron-variant | SPAG16 | GRCh38.p7 | 2:213349573 | aagatatatgaccaa[A/G]aatattacatgactt | 79582 |
rs6435771 | snp | A/G | 0.0471551 | 0.14613 | intron-variant | SPAG16 | GRCh38.p7 | 2:213354475 | acactgtcttccaca[A/G]tggttgaactaattt | 79582 |
rs6435773 | snp | A/G | 0.131038 | 0.219882 | intron-variant | SPAG16 | GRCh38.p7 | 2:213373710 | TTTCTTTCCTCTGAT[A/G]TTACTATATGCATTC | 79582 |
rs6435774 | snp | A/G | 0.354881 | 0.226936 | intron-variant | SPAG16 | GRCh38.p7 | 2:213379389 | aaaaggcaattctac[A/G]gttttatcaatccag | 79582 |
rs6435775 | snp | A/G | 0.338523 | 0.233803 | intron-variant | SPAG16 | GRCh38.p7 | 2:213429256 | ccaaggtgcctgccc[A/G]ttgctcctgaattcc | 79582 |
rs6435777 | snp | A/G | 0.48818 | 0.0759629 | intron-variant | SPAG16 | GRCh38.p7 | 2:213461255 | TTATTAACAGAGGCA[A/G]CAAAAAGGAAGAGGT | 79582 |
rs6435778 | snp | C/T | 0.310632 | 0.242536 | intron-variant | SPAG16 | GRCh38.p7 | 2:213505502 | GTTAATATTTTAAAA[C/T]ATAAGTTAGTATTTA | 79582 |
rs6435779 | snp | C/T | 0.483852 | 0.0883933 | intron-variant | SPAG16 | GRCh38.p7 | 2:213523588 | gagacttggagggct[C/T]agaaaactggaagat | 79582 |
rs6435780 | snp | A/G | 0.413914 | 0.188765 | intron-variant | SPAG16 | GRCh38.p7 | 2:213648423 | CTCAAACCACACTTA[A/G]TGCCAACCAATTAAC | 79582 |
rs6435781 | snp | A/G | 0.046775 | 0.145601 | intron-variant | SPAG16 | GRCh38.p7 | 2:213654336 | TCAATTCTAATGGAC[A/G]CTTGAACATCTATTG | 79582 |
rs6435782 | snp | G/T | 0.468349 | 0.121752 | intron-variant | SPAG16 | GRCh38.p7 | 2:213661475 | TAATATGAATGGAAT[G/T]CTAGGTGTGTACTCA | 79582 |
rs6435783 | snp | C/T | 0.479177 | 0.0998894 | intron-variant | SPAG16 | GRCh38.p7 | 2:213661485 | GGAATGCTAGGTGTG[C/T]ACTCACCAGACTTCT | 79582 |
rs6435784 | snp | A/T | 0.416055 | 0.186885 | intron-variant | SPAG16 | GRCh38.p7 | 2:213661527 | CGATTATACTCAAAC[A/T]TAAATAGATTGATCA | 79582 |
rs6435785 | snp | C/T | 0.36315 | 0.222928 | intron-variant | SPAG16 | GRCh38.p7 | 2:213678248 | tcaaaagccagcaga[C/T]ggcaagaaataacta | 79582 |
rs6435786 | snp | C/T | 0.433527 | 0.169758 | intron-variant | SPAG16 | GRCh38.p7 | 2:213684458 | TTCTTTGAAGACCAT[C/T]CCAGAATTGATTTTA | 79582 |
rs6435787 | snp | A/G | 0.480461 | 0.0968913 | intron-variant | SPAG16 | GRCh38.p7 | 2:213689409 | ttttactttttgggt[A/G]ctggatatttttatt | 79582 |
rs6435788 | snp | C/G/T | 0.145642 | 0.227177 | intron-variant | SPAG16 | GRCh38.p7 | 2:213702376 | ttgcaataaatcttg[C/G/T]tgctgctgtttgggt | 79582 |
rs6435789 | snp | G/T | 0.143284 | 0.226079 | intron-variant | SPAG16 | GRCh38.p7 | 2:213702378 | gcaataaatcttgct[G/T]ctgctgtttgggtcc | 79582 |
rs6435790 | snp | C/T | 0.425586 | 0.17796 | intron-variant | SPAG16 | GRCh38.p7 | 2:213702423 | agctgtaacactcac[C/T]gcgaaggtctgcacc | 79582 |
rs6435791 | snp | G/T | 0.462909 | 0.131034 | intron-variant | SPAG16 | GRCh38.p7 | 2:213705789 | CATGGTGGAGGGTTT[G/T]TTGTTGTTGTTGTTG | 79582 |
rs6435792 | snp | C/T | 0.140242 | 0.224618 | intron-variant | SPAG16 | GRCh38.p7 | 2:213728460 | gaaactgggagatgc[C/T]gtctaaatctgtgtt | 79582 |
rs6435793 | snp | G/T | 0.140242 | 0.224618 | intron-variant | SPAG16 | GRCh38.p7 | 2:213736930 | AGGCTGGTCTTGAAC[G/T]CCTGACCTCAGGTGA | 79582 |
rs6435794 | snp | G/T | 0.489665 | 0.0711382 | intron-variant | SPAG16 | GRCh38.p7 | 2:213737107 | GTCACTAAGATGATG[G/T]TTCTTGATTTATTTT | 79582 |
rs6435795 | snp | A/G | 0.490398 | 0.0686206 | intron-variant | SPAG16 | GRCh38.p7 | 2:213738186 | TTGAACATTTTGTAG[A/G]GCCAGTATAGTTAAG | 79582 |