SNP - dbSNP |
dbSNP | Type | Alleles | Het | Se(het) | Fxn-class | Gene Name | Assembly | Chr-pos | Sequence | Entrez Gene |
rs4222407 | snp | A/C | 0.40625 | 0.270633 | upstream-variant-2KB, downstream-variant-500B | Vwc2l, Spag16 | GRCm38.p3 | 1:70725148 | TGGGTGAAAAAAAAA[A/C]ACACACACAGAAAAA | 66722 |
rs4222408 | snp | C/G | 0.21875 | 0.248039 | upstream-variant-2KB, downstream-variant-500B | Vwc2l, Spag16 | Mm_Celera | 1:70725142 | AAAAAAAAACACACA[C/G]ACAGAAAAATGAACA | 66722 |
rs4222409 | snp | A/G | 0.21875 | 0.248039 | upstream-variant-2KB, utr-variant-3-prime | Vwc2l, Spag16 | GRCm38.p3 | 1:70725104 | ATAATTTTTATTTGA[A/G]ATAGTATGGTCCATA | 66722 |
rs4222410 | snp | A/G | 0.21875 | 0.248039 | upstream-variant-2KB, synonymous-codon | Vwc2l, Spag16 | GRCm38.p3 | 1:70724912 | AATGGTGCCGTCAGA[A/G]CCTCCAGAATACAGA | 66722 |
rs4222411 | snp | A/C | 0.21875 | 0.248039 | upstream-variant-2KB, synonymous-codon | Vwc2l, Spag16 | GRCm38.p3 | 1:70724888 | ATACAGATTTTCCCC[A/C]AGGTGGGAAAACACC | 66722 |
rs4222412 | snp | C/T | 0.21875 | 0.248039 | upstream-variant-2KB, synonymous-codon | Vwc2l, Spag16 | GRCm38.p3 | 1:70724876 | CCCCAGGTGGGAAAA[C/T]ACCACACTGTGCACT | 66722 |
rs6155277 | snp | A/G | 0.5 | 0 | intron-variant | Spag16 | Mm_Celera | 1:69919361 | GTTGATCTTTGAAAC[A/G]TAATAATTTCTCTGA | 66722 |
rs6155929 | snp | A/T | 0.5 | 0 | intron-variant | Spag16 | Mm_Celera | 1:69853224 | ACCCTGGTAAATAAT[A/T]CTTGAGAAAAATATT | 66722 |
rs6157079 | snp | A/C | 0.5 | 0 | intron-variant | Spag16 | Mm_Celera | 1:69853458 | TAAACCATTATGTAG[A/C]TAAGTAGTACTCCAG | 66722 |
rs6157504 | snp | C/T | 0.5 | 0 | intron-variant | Spag16 | Mm_Celera | 1:70482327 | TTAACCATAAGGTGA[C/T]TGAAATGTCATATCT | 66722 |
rs6157606 | snp | C/T | 0.5 | 0 | intron-variant | Spag16 | Mm_Celera | 1:69853546 | TGAGGgcttcagttt[C/T]ttttcttgttgctgt | 66722 |
rs6158155 | snp | C/T | 0.359862 | 0.224567 | intron-variant | Spag16 | Mm_Celera | 1:70482459 | CCTTATGCACTTAAG[C/T]ACTATCTTGCTCCAT | 66722 |
rs6158192 | snp | C/T | 0.5 | 0 | intron-variant | Spag16 | Mm_Celera | 1:69853645 | catggtgccgtccat[C/T]gtgatggggacatca | 66722 |
rs6168512 | snp | A/T | 0.5 | 0 | intron-variant | Spag16 | Mm_Celera | 1:69919498 | GAAGATCATGAGTTC[A/T]TTTTTGGAGCACTTT | 66722 |
rs6169118 | snp | C/T | 0.5 | 0 | intron-variant, downstream-variant-500B, missense | Spag16 | Mm_Celera | 1:69919615 | ttcttctaagttatc[C/T]tggagtcataaanta | 66722 |
rs6169523 | snp | A/G | 0.5 | 0 | intron-variant, downstream-variant-500B, splice-donor-variant | Spag16 | Mm_Celera | 1:69919628 | tcntggagtcataaa[A/G]taattagtatttctc | 66722 |
rs6169582 | snp | C/T | 0.5 | 0 | intron-variant, downstream-variant-500B | Spag16 | Mm_Celera | 1:69919657 | tccctatccttttag[C/T]gatggcaggntccat | 66722 |
rs6169597 | snp | A/G | 0.5 | 0 | intron-variant, downstream-variant-500B | Spag16 | Mm_Celera | 1:69919667 | tttagngatggcagg[A/G]tccattgtgatttcc | 66722 |
rs6170147 | snp | A/T | 0.5 | 0 | intron-variant, downstream-variant-500B | Spag16 | Mm_Celera | 1:69919762 | atgggtgtttatcag[A/T]tttactgattccttt | 66722 |
rs6171233 | snp | A/G | 0.5 | 0 | intron-variant, downstream-variant-500B | Spag16 | Mm_Celera | 1:69919926 | GCTATTTTATAGTCT[A/G]CAGGACAGGCAACAA | 66722 |
rs6185691 | snp | A/G | 0.304688 | 0.243945 | intron-variant | Spag16 | Mm_Celera | 1:69926904 | ATCAAGTCTCTCCAA[A/G]ATAGTTTACTTGAAA | 66722 |
rs6186110 | snp | A/T | 0.290657 | 0.246672 | intron-variant | Spag16 | Mm_Celera | 1:69926957 | GTACATTTTCCCATC[A/T]CCTAAGTTCACATGG | 66722 |
rs6186795 | snp | A/G | 0.290657 | 0.246672 | intron-variant | Spag16 | Mm_Celera | 1:69927111 | ATTTATTATACCTGT[A/G]CATGTGTAATTTTAT | 66722 |
rs6187291 | snp | C/G | 0.5 | 0 | intron-variant | Spag16 | Mm_Celera | 1:69927163 | atgtgagaaaacatg[C/G]aatatttgtctaaga | 66722 |
rs6191382 | snp | A/G | 0.415225 | 0.187619 | intron-variant | Spag16 | Mm_Celera | 1:69888523 | gaacagaatctctac[A/G]gtgtgtcattcctct | 66722 |
rs6191979 | snp | A/G | 0.5 | 0 | intron-variant | Spag16 | Mm_Celera | 1:69888637 | cctaaattccttctg[A/G]tattgaatttaacag | 66722 |
rs6194296 | snp | C/T | 0.5 | 0 | intron-variant | Spag16 | Mm_Celera | 1:70083952 | TCAGTGCAAGGTCCA[C/T]CTCCAAAAGCCACCA | 66722 |
rs6194818 | snp | C/T | 0.5 | 0 | intron-variant | Spag16 | Mm_Celera | 1:70084048 | AAAGCTTACTGGATG[C/T]ACAGATTCCTAGGTA | 66722 |
rs6194861 | snp | C/G | 0.5 | 0 | intron-variant | Spag16 | Mm_Celera | 1:70084075 | GGTACCAGCTGAAAT[C/G]ATTAAACCTGCtgaa | 66722 |
rs6195345 | snp | A/G | 0.5 | 0 | intron-variant | Spag16 | Mm_Celera | 1:70084163 | ttaccccagagggat[A/G]gaaggaagggattaa | 66722 |
rs6206027 | snp | A/G | 0.5 | 0 | intron-variant | Spag16 | Mm_Celera | 1:70591656 | ataaaaccactgtcc[A/G]aatcaatctgattaa | 66722 |
rs6206460 | snp | C/G | 0.415225 | 0.187619 | intron-variant | Spag16 | Mm_Celera | 1:69888995 | ACTTGTTTTAAAAAT[C/G]GAAAAGAGGAGGCTC | 66722 |
rs6206526 | snp | C/T | 0.5 | 0 | intron-variant | Spag16 | Mm_Celera | 1:70591727 | aatctactctcctag[C/T]aactttcagtatatc | 66722 |
rs6207061 | snp | C/T | 0.5 | 0 | intron-variant | Spag16 | Mm_Celera | 1:70591853 | GCACAGGTACAGTTG[C/T]CCCACACNTGAGTAA | 66722 |
rs6207068 | snp | A/G | 0.5 | 0 | intron-variant | Spag16 | Mm_Celera | 1:70591861 | ACAGTTGNCCCACAC[A/G]TGAGTAAATTTCTCA | 66722 |
rs6210186 | snp | A/G | 0.207612 | 0.24638 | intron-variant | Spag16 | Mm_Celera | 1:70525026 | CAGGTGTGAAATAAA[A/G]CACTCAGTGTTCAAA | 66722 |
rs6210868 | snp | A/C | 0.5 | 0 | intron-variant | Spag16 | Mm_Celera | 1:70525201 | CTCTAAGAGCTCTGC[A/C]ATATATNCATTGGCT | 66722 |
rs6210876 | snp | A/G | 0.5 | 0 | intron-variant | Spag16 | Mm_Celera | 1:70525208 | AGCTCTGCNATATAT[A/G]CATTGGCTGATAGGA | 66722 |
rs6224224 | snp | A/G | 0.207612 | 0.24638 | intron-variant | Spag16 | Mm_Celera | 1:70525353 | CAATTAAAAGGAGAG[A/G]TAGAAGGTTTCTAAT | 66722 |
rs6224810 | snp | C/T | 0.359862 | 0.224567 | intron-variant | Spag16 | Mm_Celera | 1:70525456 | ATTTCAGTTATACAT[C/T]ACTGTGCATATATCA | 66722 |
rs6243544 | snp | C/T | 0.290657 | 0.246672 | intron-variant | Spag16 | Mm_Celera | 1:69897871 | TATTCTCATAATTGG[C/T]AGTGCTTGTGTTTGT | 66722 |
rs6252364 | snp | G/T | 0.5 | 0 | intron-variant | Spag16 | Mm_Celera | 1:70414374 | CCTAATTATTTTTGG[G/T]NTTTTTTTGGtttat | 66722 |
rs6252365 | snp | G/T | 0.5 | 0 | intron-variant | Spag16 | GRCm38.p3 | 1:70414374 | CTAATTATTTTTGGN[G/T]TTTTTTTGGtttatt | 66722 |
rs6252867 | snp | A/G | 0.5 | 0 | intron-variant | Spag16 | Mm_Celera | 1:70414495 | gaccaggctggcctc[A/G]aactcagaaatcctc | 66722 |
rs6252985 | snp | C/T | 0.5 | 0 | intron-variant | Spag16 | Mm_Celera | 1:70414561 | tgtgccaccactgcc[C/T]ggcTGCCCCTAATTA | 66722 |
rs6253437 | snp | C/T | 0.5 | 0 | intron-variant | Spag16 | Mm_Celera | 1:70414617 | TGCTATTTATGACAT[C/T]GTCTAATGTATGGTC | 66722 |
rs6253990 | snp | A/T | 0.5 | 0 | intron-variant | Spag16 | Mm_Celera | 1:70414716 | TGGGGCTGTGGTAGA[A/T]GCTTGNTTTTTCCTA | 66722 |
rs6254009 | snp | G/T | 0.5 | 0 | intron-variant | Spag16 | Mm_Celera | 1:70414722 | TGTGGTAGANGCTTG[G/T]TTTTTCCTATCTATG | 66722 |
rs6254739 | snp | G/T | 0.5 | 0 | intron-variant | Spag16 | Mm_Celera | 1:69930491 | tcattcagagatgat[G/T]canctaaccntcaag | 66722 |
rs6254741 | snp | A/C | 0.5 | 0 | intron-variant | Spag16 | Mm_Celera | 1:69930494 | ttcagagatgatnca[A/C]ctaaccntcaagaga | 66722 |
rs6254754 | snp | A/C | 0.5 | 0 | intron-variant | Spag16 | Mm_Celera | 1:69930501 | atgatncanctaacc[A/C]tcaagagactggagg | 66722 |
rs6254878 | snp | A/T | 0.359862 | 0.224567 | intron-variant | Spag16 | Mm_Celera | 1:70009494 | TATCCAGAAGTAACT[A/T]TGTTGAGTTTAGTCA | 66722 |
rs6255266 | snp | A/G | 0.5 | 0 | intron-variant | Spag16 | Mm_Celera | 1:69930567 | tgggggcatccacct[A/G]gagacagtgggatgg | 66722 |
rs6255343 | snp | A/T | 0.5 | 0 | intron-variant | Spag16 | Mm_Celera | 1:69930617 | gagcagtcagagggt[A/T]tatggggggcangga | 66722 |
rs6255765 | snp | A/G | 0.5 | 0 | intron-variant | Spag16 | Mm_Celera | 1:69930629 | ggtntatggggggca[A/G]ggaatggaatangga | 66722 |
rs6255789 | snp | C/T | 0.5 | 0 | intron-variant | Spag16 | Mm_Celera | 1:69930641 | gcanggaatggaata[C/T]ggagtgtaaagaata | 66722 |
rs6255907 | snp | C/T | 0.359862 | 0.224567 | intron-variant | Spag16 | Mm_Celera | 1:69930706 | GATTGAGGTAGTAAC[C/T]ATGATATGAATGAAT | 66722 |
rs6256356 | snp | A/C/G | 0.359862 | 0.224567 | intron-variant | Spag16 | GRCm38.p3 | 1:69930740 | GTTTTTAGAAGTATT[A/C/G]AAGAAAATGTGTGTA | 66722 |
rs6257499 | snp | A/T | 0.5 | 0 | intron-variant | Spag16 | Mm_Celera | 1:69898101 | TTCTCACTTGGTTTC[A/T]NTGTTGCTCTATGCG | 66722 |
rs6257500 | snp | A/T | 0.5 | 0 | intron-variant | Spag16 | Mm_Celera | 1:69898102 | TCTCACTTGGTTTCN[A/T]TGTTGCTCTATGCGG | 66722 |
rs6257531 | snp | C/T | 0.290657 | 0.246672 | intron-variant | Spag16 | Mm_Celera | 1:69898123 | CTCTATGCGGACTGC[C/T]TGTTTTGTTTTCCTG | 66722 |
rs6262228 | snp | C/T | 0.359862 | 0.224567 | intron-variant | Spag16 | Mm_Celera | 1:70567184 | AAATATTTCATCAAC[C/T]ACTGAAGACTGGAAA | 66722 |
rs6262810 | snp | A/C | 0.5 | 0 | intron-variant | Spag16 | Mm_Celera | 1:70567305 | AATATCCCTAAGCAA[A/C]AGTTCCCAAAATGTA | 66722 |
rs6262835 | snp | C/T | 0.5 | 0 | intron-variant | Spag16 | Mm_Celera | 1:70567322 | GTTCCCAAAATGTAC[C/T]CCCCCCCCCCGACTG | 66722 |
rs6263310 | snp | A/C | 0.304688 | 0.243945 | intron-variant | Spag16 | Mm_Celera | 1:70567365 | GCACCTGGGAACTAA[A/C]AAGAAAAGCACAGTG | 66722 |
rs6263620 | snp | C/T | 0.5 | 0 | intron-variant | Spag16 | Mm_Celera | 1:70333673 | ctgggtatagtagcc[C/T]aggctgccatttgtg | 66722 |
rs6263676 | snp | A/C/G | 0.5 | 0 | intron-variant | Spag16 | GRCm38.p3 | 1:70333710 | tagggtctgcaagac[A/C/G]tctgtccaagatttt | 66722 |
rs6263851 | snp | G/T | 0.207612 | 0.24638 | intron-variant | Spag16 | Mm_Celera | 1:70567480 | ATGGACATGAAGGTT[G/T]GCCAGCCTTACATTT | 66722 |
rs6263912 | snp | C/T | 0.304688 | 0.243945 | intron-variant | Spag16 | Mm_Celera | 1:70567518 | CAGTCACTTTTGCTA[C/T]GGCAAGGTCACTTCA | 66722 |
rs6264428 | snp | A/G | 0.5 | 0 | intron-variant | Spag16 | Mm_Celera | 1:70567606 | agattaaaagctttt[A/G]tggctcttcaaggag | 66722 |
rs6264689 | snp | G/T | 0.5 | 0 | intron-variant | Spag16 | Mm_Celera | 1:70333903 | tctatatgatggtct[G/T]taggcttcttgtatg | 66722 |
rs6265162 | snp | G/T | 0.5 | 0 | intron-variant | Spag16 | Mm_Celera | 1:70333965 | ttcttctatgatttt[G/T]ttcaagatgttttct | 66722 |
rs6265402 | snp | A/G | 0.5 | 0 | intron-variant | Spag16 | Mm_Celera | 1:70567779 | tGCACACATGTGTac[A/G]nacacacacacacac | 66722 |
rs6265403 | snp | C/T | 0.5 | 0 | intron-variant | Spag16 | GRCm38.p3 | 1:70567779 | GCACACATGTGTacn[C/T]acacacacacacaca | 66722 |
rs6265689 | snp | G/T | 0.5 | 0 | intron-variant | Spag16 | Mm_Celera | 1:70334062 | tgtcctaaatttcct[G/T]gatgcttttggttag | 66722 |
rs6265774 | snp | A/G | 0.5 | 0 | intron-variant | Spag16 | Mm_Celera | 1:70334114 | ttctttgtctgttct[A/G]ttaatatcttatgtg | 66722 |
rs6265800 | snp | G/T | 0.5 | 0 | intron-variant | Spag16 | Mm_Celera | 1:70300985 | GGGAGAGAAAATTCA[G/T]CTAGCAGGTACCTCT | 66722 |
rs6266393 | snp | C/T | 0.5 | 0 | intron-variant | Spag16 | Mm_Celera | 1:70301099 | CTGATTTCAGCCATT[C/T]CAACTGTGGAAACCT | 66722 |
rs6267007 | snp | C/T | 0.5 | 0 | intron-variant | Spag16 | Mm_Celera | 1:70301216 | gtttgtttgtttTTG[C/T]TTTGGGTTTTTTTCT | 66722 |
rs6268099 | snp | A/T | 0.5 | 0 | intron-variant | Spag16 | Mm_Celera | 1:70301389 | CGTAATTGCCTTTGT[A/T]GTTTTAGTTGGTGTT | 66722 |
rs6268132 | snp | C/T | 0.391111 | 0.206368 | intron-variant | Spag16 | Mm_Celera | 1:70301412 | TTGGTGTTTGTAGGT[C/T]TGTCCTGAAGGAACT | 66722 |
rs6268540 | snp | C/T | 0.32 | 0.24 | intron-variant | Spag16 | Mm_Celera | 1:70301444 | TGTCTGTCCTTACTA[C/T]TCTTTTCCTATTAGT | 66722 |
rs6268599 | snp | A/C | 0.5 | 0 | intron-variant | Spag16 | Mm_Celera | 1:70301473 | GTTAGTAAACAAGTT[A/C]CATAGTTGACAGTCC | 66722 |
rs6295153 | snp | A/C | 0.5 | 0 | intron-variant | Spag16 | Mm_Celera | 1:69834906 | GAGAAGATGACAGTG[A/C]TATTTGCTATTTATA | 66722 |
rs6295183 | snp | C/G | 0.5 | 0 | intron-variant | Spag16 | Mm_Celera | 1:69834922 | TATTTGCTATTTATA[C/G]CACCCTTTCTGTTAG | 66722 |
rs6299309 | snp | A/T | 0.290657 | 0.246672 | intron-variant | Spag16 | Mm_Celera | 1:70503129 | CAAAGGTAGCTTTGA[A/T]ATATGGCAAATTAAT | 66722 |
rs6299411 | snp | A/G | 0.5 | 0 | intron-variant | Spag16 | Mm_Celera | 1:70503197 | ACTTTGAATTTTTCC[A/G]AGGAATGNAGTTGAG | 66722 |
rs6299423 | snp | C/T | 0.5 | 0 | intron-variant | Spag16 | Mm_Celera | 1:70503205 | TTTTTCCNAGGAATG[C/T]AGTTGAGAAACCTAA | 66722 |
rs6309537 | snp | C/G | 0.5 | 0 | intron-variant | Spag16 | Mm_Celera | 1:69835226 | CATTGATTTCTGCCC[C/G]TGGCTCATTTGCAGA | 66722 |
rs6310053 | snp | A/G | 0.375 | 0.216506 | intron-variant | Spag16 | Mm_Celera | 1:69835323 | GGCACCTGGTCTTGA[A/G]GCTGGGTCTTCTGTG | 66722 |
rs6310085 | snp | A/G | 0.5 | 0 | intron-variant | Spag16 | Mm_Celera | 1:69835344 | GTCTTCTGTGCTACT[A/G]TAATTANGTCCCTGT | 66722 |
rs6310097 | snp | C/T | 0.5 | 0 | intron-variant | Spag16 | Mm_Celera | 1:69835351 | GTGCTACTNTAATTA[C/T]GTCCCTGTTCCATGA | 66722 |
rs6312289 | snp | A/G | 0.5 | 0 | intron-variant | Spag16 | Mm_Celera | 1:70503300 | ATTCAGTGCACACAT[A/G]CTATGTGGTCCAGAG | 66722 |
rs6331251 | snp | C/T | 0.5 | 0 | intron-variant | Spag16 | Mm_Celera | 1:69902545 | tgcaggaatagaaac[C/T]ctgactaagacGGTA | 66722 |
rs6331327 | snp | A/G | 0.359862 | 0.224567 | intron-variant | Spag16 | Mm_Celera | 1:70504517 | ACCCCTCTCTCCTAG[A/G]AAATCCCTCCTTCAT | 66722 |
rs6331719 | snp | C/T | 0.5 | 0 | intron-variant | Spag16 | Mm_Celera | 1:70504536 | TCCCTCCTTCATTCA[C/T]CTTCCCATTTGCTTA | 66722 |
rs6331756 | snp | C/T | 0.359862 | 0.224567 | intron-variant | Spag16 | Mm_Celera | 1:69902641 | TGCAATTACAGACAA[C/T]ACCTGATGAAGCTTA | 66722 |
rs6332333 | snp | A/G | 0.5 | 0 | intron-variant | Spag16 | Mm_Celera | 1:70504663 | TGGCTAGAAAGTTGA[A/G]TGGAGAGGTTGATGG | 66722 |
rs6342495 | snp | A/G | 0.5 | 0 | intron-variant | Spag16 | Mm_Celera | 1:69843298 | AGGAACCTTCCCATC[A/G]TCCTGGCTGTTCTTA | 66722 |
rs6342594 | snp | C/G | 0.5 | 0 | intron-variant | Spag16 | Mm_Celera | 1:69843360 | AAACTCAGGCCTCTG[C/G]TTTCTTCTATCCTTC | 66722 |
rs6342618 | snp | C/T | 0.336735 | 0.234472 | intron-variant | Spag16 | Mm_Celera | 1:69843388 | TTCACTTTAGCTCTG[C/T]AAAACATGCTCCTGT | 66722 |
rs6343617 | snp | A/G | 0.260355 | 0.249785 | intron-variant | Spag16 | Mm_Celera | 1:69843529 | AGAGCCTGGCAGCCC[A/G]TGGCNTAGGCAGGCA | 66722 |
rs6343621 | snp | C/T | 0.5 | 0 | intron-variant | Spag16 | Mm_Celera | 1:69843534 | CTGGCAGCCCNTGGC[C/T]TAGGCAGGCAAGAGG | 66722 |
rs6344278 | snp | A/G | 0.5 | 0 | intron-variant | Spag16 | Mm_Celera | 1:69843685 | GATGCTTTTTATTTA[A/G]TTGCATAATTTACTT | 66722 |
rs6371631 | snp | C/G | 0.5 | 0 | intron-variant | Spag16 | Mm_Celera | 1:70467362 | gactgtcacggtcct[C/G]tcagtggagtgttgg | 66722 |
rs6372144 | snp | A/G | 0.5 | 0 | intron-variant | Spag16 | Mm_Celera | 1:70467480 | TTCTTCATTCTGGTA[A/G]TACAGTCCATTTGCC | 66722 |
rs6372706 | snp | A/G | 0.5 | 0 | intron-variant | Spag16 | Mm_Celera | 1:70467605 | TCCCATGACTTCTAT[A/G]AAACTATGTTTTGAA | 66722 |
rs6373127 | snp | C/T | 0.5 | 0 | intron-variant | Spag16 | Mm_Celera | 1:70467644 | CATTATCAATTGCAG[C/T]TATGTTTTTACCCTA | 66722 |
rs6377208 | snp | C/T | 0.290657 | 0.246672 | intron-variant | Spag16 | Mm_Celera | 1:70061409 | TTAATCATTTCTGCT[C/T]CATTCAGGGATCATT | 66722 |
rs6378191 | snp | A/G | 0.231111 | 0.249285 | intron-variant | Spag16 | Mm_Celera | 1:70061520 | TTTGGGTCACTATCC[A/G]AGACTGGAATGGAGA | 66722 |
rs6378331 | snp | C/T | 0.5 | 0 | intron-variant | Spag16 | Mm_Celera | 1:70061603 | TTAGAACAATTTTCT[C/T]CTGAGACTAGGTCCT | 66722 |
rs6389654 | snp | A/G | 0.290657 | 0.246672 | intron-variant | Spag16 | Mm_Celera | 1:70101358 | TATAGATTACCTGTT[A/G]TGTTTTTAAACTGTT | 66722 |
rs6390191 | snp | C/G/T | 0.5 | 0 | intron-variant | Spag16 | Mm_Celera | 1:70101448 | CTTCATCTATCTACC[C/G/T]GAGACTGCTGATATG | 66722 |
rs6390747 | snp | A/T | 0.5 | 0 | intron-variant | Spag16 | Mm_Celera | 1:70101564 | GTTTTGTGTTCTTCC[A/T]CTTTCTNAGTAATAT | 66722 |
rs6390760 | snp | C/T | 0.5 | 0 | intron-variant | Spag16 | Mm_Celera | 1:70101571 | GTTCTTCCNCTTTCT[C/T]AGTAATATTAAAAAT | 66722 |
rs6390780 | snp | C/T | 0.5 | 0 | intron-variant | Spag16 | Mm_Celera | 1:70101593 | ATTAAAAATTGTTTT[C/T]CATATAAATAATGAG | 66722 |
rs6391218 | snp | C/T | 0.231111 | 0.249285 | intron-variant | Spag16 | Mm_Celera | 1:70061627 | AGGTCCTGAGCTCTG[C/T]AGTCAGCTGTGTGGG | 66722 |
rs6391282 | snp | A/G | 0.5 | 0 | intron-variant | Spag16 | Mm_Celera | 1:70061650 | TGTGTGGGGCTTCAC[A/G]GTCCTGAAGAGCGAT | 66722 |
rs6391844 | snp | A/G | 0.5 | 0 | intron-variant | Spag16 | Mm_Celera | 1:70061755 | ACTTCTGGACCTCTC[A/G]TGTCCACAGTGATAT | 66722 |
rs6392400 | snp | A/G | 0.5 | 0 | intron-variant | Spag16 | Mm_Celera | 1:70061854 | CTAGATGTTTTTCGG[A/G]TTTTTANTAATTTCA | 66722 |
rs6392411 | snp | C/G | 0.5 | 0 | intron-variant | Spag16 | Mm_Celera | 1:70061861 | TTTTTCGGNTTTTTA[C/G]TAATTTCACTTTTGA | 66722 |
rs6393022 | snp | A/G | 0.231111 | 0.249285 | intron-variant | Spag16 | Mm_Celera | 1:70061952 | TAAGTGGGAGAAAAC[A/G]ATTACTNTCCATTGG | 66722 |
rs6393039 | snp | A/T | 0.5 | 0 | intron-variant | Spag16 | Mm_Celera | 1:70061959 | GAGAAAACNATTACT[A/T]TCCATTGGCAAAGAA | 66722 |
rs6393122 | snp | A/G | 0.5 | 0 | intron-variant | Spag16 | Mm_Celera | 1:70062011 | AATGCCTGAAACTGT[A/G]TCAGCTGGATGAAAG | 66722 |
rs6393600 | snp | C/T | 0.5 | 0 | intron-variant | Spag16 | Mm_Celera | 1:70062069 | TATTTCTGTTTCATC[C/T]TCTGTATTACTTGTT | 66722 |
rs6393637 | snp | C/G | 0.5 | 0 | intron-variant | Spag16 | Mm_Celera | 1:70062092 | TACTTGTTTCAAAGT[C/G]ATGCATACAACTAAT | 66722 |
rs6395215 | snp | G/T | 0.5 | 0 | intron-variant | Spag16 | Mm_Celera | 1:70062350 | TCTGTTTATTTAAAT[G/T]TGTTCATTTACATAG | 66722 |
rs13475912 | snp | A/G | 0.314099 | 0.241643 | intron-variant | Spag16 | Mm_Celera | 1:69869980 | CAATAAATGTGCACT[A/G]TGCACATATCTTGCA | 66722 |
rs13475913 | snp | A/G | 0.0739645 | 0.177515 | intron-variant | Spag16 | Mm_Celera | 1:70080595 | CTACAGCCATGGGGG[A/G]GGGGGGACGTAAATA | 66722 |
rs29242127 | snp | A/G | 0.375 | 0.216506 | intron-variant | Spag16 | Mm_Celera | 1:70666606 | GTTAGAACATCTTCT[A/G]GATATATGCCCAGGA | 66722 |
rs29518202 | snp | A/G | 0.444444 | 0.157135 | intron-variant | Spag16 | Mm_Celera | 1:70094702 | CATTTTTTTGGCTGG[A/G]AGACTATTAATGACT | 66722 |
rs29731100 | snp | C/T | 0.375 | 0.216506 | intron-variant | Spag16 | Mm_Celera | 1:70666654 | TCCAGTTGTACTATG[C/T]CCAATTTTCTGAGGA | 66722 |
rs30137249 | snp | A/G | 0.375 | 0.216506 | intron-variant | Spag16 | Mm_Celera | 1:70542873 | TGCAACTAGAGACAC[A/G]GCTCTGGGGGCGGGG | 66722 |
rs30445404 | snp | A/T | 0.231111 | 0.249285 | intron-variant | Spag16 | Mm_Celera | 1:69879042 | GAGTGAAGTTCTGAA[A/T]CTAAGAGTCTGTAAA | 66722 |
rs30445407 | snp | C/T | 0.244898 | 0.249948 | intron-variant | Spag16 | Mm_Celera | 1:69879129 | ATAGAGACAAACCAC[C/T]TGCCTTTAAGACTAA | 66722 |
rs30445410 | snp | A/G | 0.231111 | 0.249285 | intron-variant | Spag16 | Mm_Celera | 1:69879311 | ATCTATCTGCTAGAG[A/G]TCATGTGAATCCTTC | 66722 |
rs30445413 | snp | A/T | 0.231111 | 0.249285 | intron-variant | Spag16 | Mm_Celera | 1:69879372 | CATGATGTGTAAAAA[A/T]GTTAAGTGCTTAGCA | 66722 |
rs30446376 | snp | A/C | 0.244898 | 0.249948 | intron-variant | Spag16 | Mm_Celera | 1:69879453 | CATTTTCTGTCCTTA[A/C]TTTCTGGTGTTATAT | 66722 |
rs30446379 | snp | A/G | 0.231111 | 0.249285 | intron-variant | Spag16 | Mm_Celera | 1:69879473 | TGGTGTTATATGTCA[A/G]CCTTGGCCAGTTTTT | 66722 |
rs30446382 | snp | A/T | 0.231111 | 0.249285 | intron-variant | Spag16 | Mm_Celera | 1:69879573 | GGTCTATGTTTCTGG[A/T]CTAGTATTTTAAATG | 66722 |
rs30447095 | snp | A/G | 0.142012 | 0.225474 | intron-variant | Spag16 | Mm_Celera | 1:69879822 | TATTAACAGCTCTAC[A/G]TACTTCTATTGAAGT | 66722 |
rs30447098 | snp | C/T | 0.132653 | 0.220748 | intron-variant | Spag16 | Mm_Celera | 1:69880006 | AAACTATGTGATATG[C/T]TTCTCCTTTCCTTCA | 66722 |
rs30447101 | snp | G/T | 0.142012 | 0.225474 | intron-variant | Spag16 | Mm_Celera | 1:69880018 | ATGTTTCTCCTTTCC[G/T]TCAAGTCAAATCACC | 66722 |
rs30447103 | snp | A/C | 0.231111 | 0.249285 | intron-variant | Spag16 | Mm_Celera | 1:69880039 | TCAAATCACCTTTCT[A/C]TGATTGCTCCTTTCT | 66722 |
rs30447965 | snp | C/G | 0.231111 | 0.249285 | intron-variant | Spag16 | Mm_Celera | 1:69880137 | GGAAACCATGCCATG[C/G]CCCTATTTGTCTCAA | 66722 |
rs30447967 | snp | A/G | 0.231111 | 0.249285 | intron-variant | Spag16 | Mm_Celera | 1:69880152 | GCCCTATTTGTCTCA[A/G]CAATACCACACCCAT | 66722 |
rs30447969 | snp | A/G | 0.231111 | 0.249285 | intron-variant | Spag16 | Mm_Celera | 1:69882054 | TCCACACCCATTCTT[A/G]CAGACTAACTTCTAA | 66722 |
rs30447971 | snp | C/G | 0.231111 | 0.249285 | intron-variant | Spag16 | Mm_Celera | 1:69882178 | GTTAGGATTTAGAGT[C/G]AGCTTTCCTCTTAGC | 66722 |
rs30447973 | snp | A/G | 0.444444 | 0.157135 | intron-variant | Spag16 | Mm_Celera | 1:69882366 | TACATGATTACTCAC[A/G]CCAACACATTTTATT | 66722 |
rs30448725 | snp | C/T | 0.231111 | 0.249285 | intron-variant | Spag16 | Mm_Celera | 1:69882412 | TCAAATGATTGAATT[C/T]GCTTACACAACAATG | 66722 |
rs30448727 | snp | C/T | 0.231111 | 0.249285 | intron-variant | Spag16 | Mm_Celera | 1:69882423 | AATTCGCTTACACAA[C/T]AATGTGCTTAACACA | 66722 |
rs30448729 | snp | C/T | 0.132653 | 0.220748 | intron-variant | Spag16 | Mm_Celera | 1:69882492 | AAGAAGTAGATAATT[C/T]ATAATTTGTTGAACT | 66722 |
rs30448731 | snp | A/G | 0.231111 | 0.249285 | intron-variant | Spag16 | Mm_Celera | 1:69882774 | CTGTGGTCACTGGTT[A/G]ATCTTCTGACCTAAA | 66722 |
rs30448733 | snp | C/T | 0.231111 | 0.249285 | intron-variant | Spag16 | Mm_Celera | 1:69882798 | ACCTAAACCAATTAC[C/T]ATGTCATGAAGCCAC | 66722 |
rs30449485 | snp | A/G | 0.231111 | 0.249285 | intron-variant | Spag16 | Mm_Celera | 1:69883607 | ATCCGCATCTTAGTG[A/G]CATTTAACTTACTAT | 66722 |
rs30449487 | snp | C/T | 0.231111 | 0.249285 | intron-variant | Spag16 | Mm_Celera | 1:69883679 | AGAATTTACAATCTT[C/T]CAAATGAAAAAAGTC | 66722 |
rs30449489 | snp | C/T | 0.231111 | 0.249285 | intron-variant | Spag16 | Mm_Celera | 1:69883712 | TGGGAATTTCATACA[C/T]GAGTACTGTACTAGG | 66722 |
rs30449491 | snp | C/G | 0.231111 | 0.249285 | intron-variant | Spag16 | Mm_Celera | 1:69883749 | TCCATCTCTTCCTCA[C/G]TGCAGATTATCCCAT | 66722 |
rs30449493 | snp | A/T | 0.124444 | 0.216185 | intron-variant | Spag16 | Mm_Celera | 1:69883809 | TCTGCTTTGATTTTG[A/T]TTGTTGCGTGCACAC | 66722 |
rs30449635 | snp | C/T | 0.132653 | 0.220748 | intron-variant | Spag16 | Mm_Celera | 1:69939312 | GACAAGGAACAAGGT[C/T]GTTTGAAAAGGCCTC | 66722 |
rs30449638 | snp | A/G | 0.132653 | 0.220748 | intron-variant | Spag16 | Mm_Celera | 1:69939363 | CATTTAAACTAGTTG[A/G]ATGTACAGTATTTTC | 66722 |
rs30449641 | snp | A/C | 0.21875 | 0.248039 | intron-variant | Spag16 | Mm_Celera | 1:69939401 | AATACTTAGAAGTAT[A/C]ATAGTTTTGTATAAT | 66722 |
rs30449675 | snp | C/T | 0.244898 | 0.249948 | intron-variant | Spag16 | Mm_Celera | 1:69887273 | ACACTTCAAATACTT[C/T]GTATGGTGGATTAGT | 66722 |
rs30449677 | snp | A/G | 0.132653 | 0.220748 | intron-variant | Spag16 | Mm_Celera | 1:69887302 | GTGGTTGCACGTGGA[A/G]TTGAATTTTAATTAA | 66722 |
rs30449679 | snp | G/T | 0.132653 | 0.220748 | intron-variant | Spag16 | Mm_Celera | 1:69887331 | AAAACAATGCTTTCT[G/T]CTAAAGTTTATGTTC | 66722 |
rs30449681 | snp | C/T | 0.152778 | 0.230321 | intron-variant | Spag16 | Mm_Celera | 1:69887351 | AGTTTATGTTCAATG[C/T]TTTATAACTTAAAGG | 66722 |
rs30449683 | snp | A/G/T | 0.260355 | 0.249785 | intron-variant | Spag16 | GRCm38.p3 | 1:69887397 | GATTAATATTTTTTG[A/G/T]TATTTTGCAATCAAT | 66722 |
rs30449695 | snp | C/T | 0.124444 | 0.216185 | intron-variant | Spag16 | Mm_Celera | 1:69894497 | ACTGTGGCTTCCAGC[C/T]GCTCATTGTGGACAT | 66722 |
rs30449697 | snp | A/C | 0.124444 | 0.216185 | intron-variant | Spag16 | Mm_Celera | 1:69894520 | GTGGACATTGCTGTG[A/C]ATGACCTTTGTAGCT | 66722 |
rs30449699 | snp | A/G | 0.444444 | 0.157135 | intron-variant | Spag16 | Mm_Celera | 1:69894570 | AATTATCTAAAAAAA[A/G]AGAAAAAAATTAATT | 66722 |
rs30449701 | snp | A/G | 0.444444 | 0.157135 | intron-variant | Spag16 | Mm_Celera | 1:69894726 | GATTCCAGGGATCAA[A/G]CTTTGGTCACCAGGC | 66722 |
rs30449703 | snp | C/T | 0.124444 | 0.216185 | intron-variant | Spag16 | Mm_Celera | 1:69894747 | GTCACCAGGCTAACA[C/T]GACCAGTGCATTGAT | 66722 |
rs30449765 | snp | C/T | 0.231111 | 0.249285 | intron-variant | Spag16 | Mm_Celera | 1:69905785 | TGCAGTGAAGACAGC[C/T]CTGGGGTGCTCCTCA | 66722 |
rs30449767 | snp | C/T | 0.32 | 0.24 | intron-variant | Spag16 | Mm_Celera | 1:69905821 | GGACACTCTCAGACT[C/T]TGAGGATGACATGTG | 66722 |
rs30449769 | snp | A/G | 0.391111 | 0.206368 | intron-variant | Spag16 | Mm_Celera | 1:69905865 | TGGATAAGGATGGGA[A/G]GATTCTGATCTCTTC | 66722 |
rs30449771 | snp | C/T | 0.32 | 0.24 | intron-variant | Spag16 | Mm_Celera | 1:69905926 | TGACTACCCTGGGAA[C/T]AGCCAAACAGTTTCC | 66722 |
rs30449773 | snp | A/G | 0.231111 | 0.249285 | intron-variant | Spag16 | Mm_Celera | 1:69906089 | TGCAGTTGTAATCCT[A/G]CCATCATTGTCGTAA | 66722 |
rs30450465 | snp | A/G | 0.260355 | 0.249785 | intron-variant | Spag16 | Mm_Celera | 1:69884091 | AATTTATAATCTTAA[A/G]GAATGAAAGTACACA | 66722 |
rs30450467 | snp | C/T | 0.231111 | 0.249285 | intron-variant | Spag16 | Mm_Celera | 1:69884141 | GTAAGCATTTAAATT[C/T]CTTTGGTACATAATA | 66722 |
rs30450469 | snp | A/G | 0.231111 | 0.249285 | intron-variant | Spag16 | Mm_Celera | 1:69884296 | GTTAGTTTTGAAAGT[A/G]TCTGGGAAATATTTT | 66722 |
rs30450471 | snp | A/C | 0.152778 | 0.230321 | intron-variant | Spag16 | Mm_Celera | 1:69884349 | AATTCACAAAATCCA[A/C]AATGCATTTGGTTTG | 66722 |
rs30450473 | snp | G/T | 0.231111 | 0.249285 | intron-variant | Spag16 | Mm_Celera | 1:69884376 | TTTGTAAGTGCATAG[G/T]TATGGATGGTTAATA | 66722 |
rs30450535 | snp | A/T | 0.124444 | 0.216185 | intron-variant | Spag16 | Mm_Celera | 1:69894765 | CCAGTGCATTGATCC[A/T]CTGGGCTATCTTGTC | 66722 |
rs30450537 | snp | C/T | 0.124444 | 0.216185 | intron-variant | Spag16 | Mm_Celera | 1:69894780 | ACTGGGCTATCTTGT[C/T]AACTTCCTCTGTCTG | 66722 |
rs30450539 | snp | A/G | 0.124444 | 0.216185 | intron-variant | Spag16 | Mm_Celera | 1:69894860 | TTACCTGTGTCCTCA[A/G]AGTTTTTTTTCCCTC | 66722 |
rs30450541 | snp | A/G | 0.124444 | 0.216185 | intron-variant | Spag16 | Mm_Celera | 1:69894894 | CAATTTCAGAGCTTC[A/G]CATCTTTTAAGGTCT | 66722 |
rs30450543 | snp | A/G | 0.444444 | 0.157135 | intron-variant | Spag16 | Mm_Celera | 1:69894933 | CCCTGAACTGATTTC[A/G]CTACAGAGAAAAGAG | 66722 |
rs30450565 | snp | A/G | 0.165289 | 0.235211 | missense | Spag16 | Mm_Celera | 1:69887530 | GAAGAACATAGACAT[A/G]GGACATATTCAGGTT | 66722 |
rs30450567 | snp | C/T | 0.231111 | 0.249285 | intron-variant | Spag16 | Mm_Celera | 1:69887758 | GACTCCTGGTCAGAG[C/T]GAGATGGGACTTCCT | 66722 |
rs30450569 | snp | C/T | 0.231111 | 0.249285 | intron-variant | Spag16 | Mm_Celera | 1:69887763 | CTGGTCAGAGTGAGA[C/T]GGGACTTCCTGGTGG | 66722 |
rs30450571 | snp | C/T | 0.244898 | 0.249948 | intron-variant | Spag16 | Mm_Celera | 1:69887813 | TATATCAAAGTATAA[C/T]TAAAGTGTAGCTGAA | 66722 |
rs30450573 | snp | A/G | 0.35503 | 0.226867 | intron-variant | Spag16 | Mm_Celera | 1:69887864 | GCAAACATACAGTAC[A/G]GGTCAAGAAGACACA | 66722 |
rs30450584 | snp | C/T | 0.32 | 0.24 | intron-variant | Spag16 | Mm_Celera | 1:69940157 | TTAATTTATATTAAG[C/T]ATAATTTGAGGTTAT | 66722 |
rs30450587 | snp | A/G | 0.231111 | 0.249285 | intron-variant | Spag16 | Mm_Celera | 1:69940291 | GTGGGATATGTGGGT[A/G]GAACTGAGCATTGTG | 66722 |
rs30450590 | snp | C/T | 0.124444 | 0.216185 | intron-variant | Spag16 | Mm_Celera | 1:69946809 | CAGTATACATTTTAC[C/T]GAGTTATCCTTTATT | 66722 |
rs30450593 | snp | A/G | 0.21875 | 0.248039 | intron-variant | Spag16 | Mm_Celera | 1:69947025 | CAGATTTAAACACCT[A/G]CACTTTATCGTATAG | 66722 |
rs30450605 | snp | A/G | 0.124444 | 0.216185 | intron-variant | Spag16 | Mm_Celera | 1:69906101 | CCTGCCATCATTGTC[A/G]TAATACAAAGCTTGG | 66722 |
rs30450607 | snp | C/G | 0.124444 | 0.216185 | intron-variant | Spag16 | Mm_Celera | 1:69906177 | CTGCTTGCAAAGAAA[C/G]GTATCAAGTCCTCTT | 66722 |
rs30450609 | snp | C/T | 0.32 | 0.24 | intron-variant | Spag16 | Mm_Celera | 1:69906233 | AACTGTTTTCATAAG[C/T]CTGTAGCATTTAAAA | 66722 |
rs30450611 | snp | A/G | 0.444444 | 0.157135 | intron-variant | Spag16 | Mm_Celera | 1:69906452 | AAGTAGCCTTTAAAA[A/G]ACTTAGCGTATACCA | 66722 |
rs30450613 | snp | A/T | 0.375 | 0.216506 | intron-variant | Spag16 | Mm_Celera | 1:69906544 | TCTAGCTCCTTTGGA[A/T]ATTAAAAGTGAGGTG | 66722 |
rs30451005 | snp | C/T | 0.32 | 0.24 | intron-variant | Spag16 | Mm_Celera | 1:69899006 | TCAGGCCATGCTCTT[C/T]GCTACAACTCTAGGT | 66722 |
rs30451007 | snp | C/T | 0.32 | 0.24 | intron-variant | Spag16 | Mm_Celera | 1:69899114 | TCTTGTTGTTATAGA[C/T]TGCAGGTTAGCAATC | 66722 |
rs30451009 | snp | C/G | 0.32 | 0.24 | intron-variant | Spag16 | Mm_Celera | 1:69899255 | AATAGCACTCACATG[C/G]GAGCTTTGTCTAGAG | 66722 |
rs30451011 | snp | A/T | 0.231111 | 0.249285 | intron-variant | Spag16 | Mm_Celera | 1:69899267 | ATGCGAGCTTTGTCT[A/T]GAGAGGTTCCTGGCA | 66722 |
rs30451013 | snp | C/G | 0.231111 | 0.249285 | intron-variant | Spag16 | Mm_Celera | 1:69899391 | GCAAGTAGCCTGATA[C/G]CTCTTCTGGAAAGCA | 66722 |
rs30451145 | snp | C/G | 0.231111 | 0.249285 | intron-variant | Spag16 | Mm_Celera | 1:69885034 | AAAATCTGCTGAGGT[C/G]TTGTTCCTGCATATG | 66722 |
rs30451147 | snp | G/T | 0.231111 | 0.249285 | intron-variant | Spag16 | Mm_Celera | 1:69885055 | CCTGCATATGAGAGA[G/T]GTTAAATGAAAAGTA | 66722 |
rs30451149 | snp | C/T | 0.336735 | 0.234472 | intron-variant | Spag16 | Mm_Celera | 1:69885393 | AAAGCTAAAAGCTTT[C/T]AGTAGCCAGGTATCT | 66722 |
rs30451151 | snp | A/T | 0.244898 | 0.249948 | intron-variant | Spag16 | Mm_Celera | 1:69885442 | GTTTCTTGTTCTGAG[A/T]CTCTGTTAACAGAGT | 66722 |
rs30451153 | snp | C/T | 0.35503 | 0.226867 | intron-variant | Spag16 | Mm_Celera | 1:69886235 | GTGCCTTCCTAAATC[C/T]CTAATTCTAGTTTAG | 66722 |
rs30451225 | snp | A/C | 0.231111 | 0.249285 | intron-variant | Spag16 | Mm_Celera | 1:69887897 | ACATACAGAAAAATG[A/C]AGACTGAGTTCCACA | 66722 |
rs30451227 | snp | A/G | 0.244898 | 0.249948 | intron-variant | Spag16 | Mm_Celera | 1:69887930 | CAACCATGGAATCAT[A/G]TCTAAGAAACCTTCC | 66722 |
rs30451229 | snp | G/T | 0.231111 | 0.249285 | intron-variant | Spag16 | Mm_Celera | 1:69888065 | CAGAGGAGTTAGAAT[G/T]AAGAGTGTCTGCTCC | 66722 |
rs30451231 | snp | C/T | 0.132653 | 0.220748 | intron-variant | Spag16 | Mm_Celera | 1:69888197 | ACTAGACATTTTTCA[C/T]GTCAATCCTGATAGG | 66722 |
rs30451233 | snp | A/T | 0.444444 | 0.157135 | intron-variant | Spag16 | Mm_Celera | 1:69888461 | ATCAGCCAAAAATTA[A/T]ACTGCTTTTTTAATT | 66722 |
rs30451265 | snp | C/T | 0.132653 | 0.220748 | intron-variant | Spag16 | Mm_Celera | 1:69895028 | TAGAGTAATAACTCA[C/T]AGTATTGTCTATTGT | 66722 |
rs30451267 | snp | A/G | 0.336735 | 0.234472 | intron-variant | Spag16 | Mm_Celera | 1:69895147 | TCAATTAGATATAGA[A/G]CATAAGTCATATGTA | 66722 |
rs30451269 | snp | A/G | 0.244898 | 0.249948 | intron-variant | Spag16 | Mm_Celera | 1:69895168 | GTCATATGTACCTAT[A/G]TATGTGTGTATAAAG | 66722 |
rs30451271 | snp | C/T | 0.124444 | 0.216185 | intron-variant | Spag16 | Mm_Celera | 1:69895204 | TGAATACAAAAGTCT[C/T]TTCTTCTCACTTCTT | 66722 |
rs30451273 | snp | A/G | 0.124444 | 0.216185 | intron-variant | Spag16 | Mm_Celera | 1:69895465 | TACAGCAATTTGATT[A/G]TGCTGCGATTAAAGA | 66722 |
rs30451376 | snp | A/G | 0.32 | 0.24 | intron-variant | Spag16 | Mm_Celera | 1:69947066 | TTTCTTCAGGATCAA[A/G]GTCTCCTGAATCTAT | 66722 |
rs30451379 | snp | A/G | 0.21875 | 0.248039 | intron-variant | Spag16 | Mm_Celera | 1:69947115 | TATATTTCGGTTCAC[A/G]CATTTTCTTTAAATC | 66722 |
rs30451382 | snp | A/T | 0.244898 | 0.249948 | intron-variant | Spag16 | Mm_Celera | 1:69947136 | TCTTTAAATCTGGGT[A/T]TGTTAAGCCAATCCT | 66722 |
rs30451585 | snp | C/T | 0.375 | 0.216506 | intron-variant | Spag16 | Mm_Celera | 1:69906616 | TTCCTTTAGTTCTTT[C/T]GCAATTTTTCCTCTT | 66722 |
rs30451587 | snp | C/T | 0.375 | 0.216506 | intron-variant | Spag16 | Mm_Celera | 1:69906937 | ACACATATTCCTCTT[C/T]TCTAGCACAGTTCCT | 66722 |
rs30451589 | snp | A/C | 0.444444 | 0.157135 | intron-variant | Spag16 | Mm_Celera | 1:69916241 | CTCCATGTCTTTTTC[A/C]ATATAACACTCAGCC | 66722 |
rs30451591 | snp | C/T | 0.444444 | 0.157135 | intron-variant, synonymous-codon | Spag16 | Mm_Celera | 1:69917508 | AGCTGTGTGTTCTGG[C/T]TTAGAGCCTCCTGGG | 66722 |
rs30451593 | snp | G/T | 0.444444 | 0.157135 | intron-variant | Spag16 | Mm_Celera | 1:69917544 | GGAAGTTCTATCTCT[G/T]GTTATAGCAGGCCTC | 66722 |
rs30451905 | snp | A/G | 0.32 | 0.24 | intron-variant | Spag16 | Mm_Celera | 1:69899424 | ATATAGTGTTCTTTC[A/G]AAAAAGTAACATGGA | 66722 |
rs30451907 | snp | A/C | 0.32 | 0.24 | intron-variant | Spag16 | Mm_Celera | 1:69899482 | TGTGTTTGGGGAAAA[A/C]TTTTAATTTAATGTC | 66722 |
rs30451909 | snp | A/G | 0.231111 | 0.249285 | intron-variant | Spag16 | Mm_Celera | 1:69899571 | TCATTTTTATTGTTC[A/G]TTTGTATCCCTTCTT | 66722 |
rs30451911 | snp | A/G | 0.124444 | 0.216185 | intron-variant | Spag16 | Mm_Celera | 1:69899603 | CCACTTTTAAATCTG[A/G]TAAGATGTACAGTTT | 66722 |
rs30451913 | snp | G/T | 0.124444 | 0.216185 | intron-variant | Spag16 | Mm_Celera | 1:69899616 | TGGTAAGATGTACAG[G/T]TTACCTTCTCAAAAC | 66722 |
rs30452035 | snp | A/G | 0.124444 | 0.216185 | intron-variant | Spag16 | Mm_Celera | 1:69886267 | CATGGGGGAAGGGAA[A/G]CATTCACACTCATGT | 66722 |
rs30452037 | snp | C/G | 0.391111 | 0.206368 | intron-variant | Spag16 | Mm_Celera | 1:69886551 | TGTAAAAATGTGTGC[C/G]TGGGTGTGGGACACA | 66722 |
rs30452039 | snp | A/T | 0.336735 | 0.234472 | intron-variant | Spag16 | Mm_Celera | 1:69886585 | TATTTCCCAGCACTG[A/T]ATCAATCACTATTGT | 66722 |
rs30452041 | snp | A/G | 0.231111 | 0.249285 | intron-variant | Spag16 | Mm_Celera | 1:69886599 | GAATCAATCACTATT[A/G]TATGATGTTTACAAT | 66722 |
rs30452043 | snp | C/T | 0.124444 | 0.216185 | intron-variant | Spag16 | Mm_Celera | 1:69886652 | AATCCATTCGCCTTC[C/T]GAAGAAACTGATCTG | 66722 |
rs30452095 | snp | C/T | 0.132653 | 0.220748 | intron-variant | Spag16 | Mm_Celera | 1:69888522 | TGAACAGAATCTCTA[C/T]GGTGTGTCATTCCTC | 66722 |
rs30452098 | snp | C/T | 0.444444 | 0.157135 | intron-variant | Spag16 | Mm_Celera | 1:69888918 | TTAGTCATCTTTTAA[C/T]ATATATTTGTTAAAA | 66722 |
rs30452101 | snp | A/G | 0.260355 | 0.249785 | intron-variant | Spag16 | Mm_Celera | 1:69889195 | TGTCATGCTTGCCTT[A/G]GTTATTACATTTTAT | 66722 |
rs30452103 | snp | C/T | 0.260355 | 0.249785 | intron-variant | Spag16 | Mm_Celera | 1:69889200 | TGCTTGCCTTAGTTA[C/T]TACATTTTATTATTC | 66722 |
rs30452175 | snp | A/G | 0.124444 | 0.216185 | intron-variant | Spag16 | Mm_Celera | 1:69895472 | ATTTGATTGTGCTGC[A/G]ATTAAAGACTGTTTC | 66722 |
rs30452177 | snp | A/G | 0.336735 | 0.234472 | intron-variant | Spag16 | Mm_Celera | 1:69895594 | TTAAAGCACTTTAGA[A/G]TGTTAGTATATTTTG | 66722 |
rs30452179 | snp | A/G | 0.142012 | 0.225474 | intron-variant | Spag16 | Mm_Celera | 1:69895596 | AAAGCACTTTAGAAT[A/G]TTAGTATATTTTGGT | 66722 |
rs30452181 | snp | A/G | 0.244898 | 0.249948 | intron-variant | Spag16 | Mm_Celera | 1:69896328 | TTTGAGTGCACGCTA[A/G]CCTGTCTCATGAGCC | 66722 |
rs30452183 | snp | C/T | 0.132653 | 0.220748 | intron-variant | Spag16 | Mm_Celera | 1:69896368 | CATATATTATTCAGA[C/T]AAATTTTAATACTTT | 66722 |
rs30452255 | snp | C/T | 0.444444 | 0.157135 | intron-variant | Spag16 | Mm_Celera | 1:69947210 | TCTCAAAAGTGTCTA[C/T]AACTGAGGACATCTG | 66722 |
rs30452257 | snp | A/G | 0.32 | 0.24 | intron-variant | Spag16 | Mm_Celera | 1:69947522 | CACGTTAGCAGAATG[A/G]TCTTCAGAGAAAATC | 66722 |
rs30452260 | snp | A/G | 0.408163 | 0.193609 | intron-variant | Spag16 | Mm_Celera | 1:69947555 | ATCCCTAGTAGTTTC[A/G]AGTCACAGTAATGAT | 66722 |
rs30452263 | snp | C/T | 0.408163 | 0.193609 | intron-variant | Spag16 | Mm_Celera | 1:69947637 | TGACTGAGTCTTACT[C/T]CTGTTTTCCCATTCG | 66722 |
rs30452495 | snp | C/T | 0.231111 | 0.249285 | intron-variant | Spag16 | Mm_Celera | 1:69917699 | AGATCCCATGTCTGC[C/T]GAGCTCTGTGGTGGG | 66722 |
rs30452497 | snp | C/T | 0.132653 | 0.220748 | intron-variant | Spag16 | Mm_Celera | 1:69917998 | TAATTTTATACATTG[C/T]TTTGTAATGTGAGAT | 66722 |
rs30452499 | snp | C/T | 0.231111 | 0.249285 | intron-variant | Spag16 | Mm_Celera | 1:69918008 | CATTGTTTTGTAATG[C/T]GAGATCATCATATTT | 66722 |
rs30452501 | snp | C/T | 0.32 | 0.24 | intron-variant | Spag16 | Mm_Celera | 1:69918058 | AGAAGTTAGTTTTCA[C/T]TGTTTCAGAGTTTGA | 66722 |
rs30452503 | snp | A/T | 0.277778 | 0.248452 | intron-variant | Spag16 | Mm_Celera | 1:69918309 | AATACAAGTTATTAT[A/T]TTATGCTAAATATAT | 66722 |
rs30452825 | snp | C/T | 0.32 | 0.24 | intron-variant | Spag16 | Mm_Celera | 1:69899703 | GGGAATGACTTCATC[C/T]ATTTTATCATGATCA | 66722 |
rs30452827 | snp | A/C | 0.231111 | 0.249285 | intron-variant | Spag16 | Mm_Celera | 1:69899775 | TATTTATTTCCTATT[A/C]ACCATTGACTGTGCT | 66722 |
rs30452829 | snp | A/T | 0.32 | 0.24 | intron-variant | Spag16 | Mm_Celera | 1:69900267 | ACTCCTTAAAGACTA[A/T]AATTTTGCCTTTAAA | 66722 |
rs30452831 | snp | C/T | 0.124444 | 0.216185 | intron-variant | Spag16 | Mm_Celera | 1:69900350 | ATTTTGTTTTATTAC[C/T]TTTTTCTTCAATTTG | 66722 |
rs30452833 | snp | C/T | 0.244898 | 0.249948 | intron-variant | Spag16 | Mm_Celera | 1:69900370 | TCTTCAATTTGTGAT[C/T]TTTTTTTTTTTTGAG | 66722 |
rs30452975 | snp | A/T | 0.297521 | 0.245442 | intron-variant | Spag16 | Mm_Celera | 1:69886748 | TTTATTTTATTTTTT[A/T]GATTTAAATGTACTG | 66722 |
rs30452977 | snp | C/T | 0.444444 | 0.157135 | intron-variant | Spag16 | Mm_Celera | 1:69886795 | GAGAAATACGTACAT[C/T]TGTATGTAATTAAAT | 66722 |
rs30452979 | snp | A/C | 0.336735 | 0.234472 | intron-variant | Spag16 | Mm_Celera | 1:69886866 | ATGAGACAGCTTTAA[A/C]GGTTGAATATTAAAT | 66722 |
rs30452981 | snp | A/C/G | 0.132653 | 0.220748 | intron-variant | Spag16 | Mm_Celera | 1:69887064 | GTTTGTAGATAGAAG[A/C/G]ACAAATTGCCATAGT | 66722 |
rs30452983 | snp | C/T | 0.132653 | 0.220748 | intron-variant | Spag16 | Mm_Celera | 1:69887261 | GCTGTGAGATACACA[C/T]TTCAAATACTTTGTA | 66722 |
rs30453095 | snp | C/G | 0.124444 | 0.216185 | missense | Spag16 | Mm_Celera | 1:69896475 | TTTCTCTTGAAGCTG[C/G]TCACAGTTGTGAGAA | 66722 |
rs30453097 | snp | A/G | 0.124444 | 0.216185 | synonymous-codon | Spag16 | Mm_Celera | 1:69896506 | AGAAAACAGTTCAGA[A/G]GGCCCAACTCAGAAA | 66722 |
rs30453099 | snp | A/T | 0.124444 | 0.216185 | missense | Spag16 | Mm_Celera | 1:69896558 | GAAGTTGGATATAAA[A/T]CAAAGTTGAAGAATG | 66722 |
rs30453101 | snp | A/G | 0.124444 | 0.216185 | intron-variant | Spag16 | Mm_Celera | 1:69896638 | TTGGGATTGTTACAG[A/G]ACAGCGATTGTACAG | 66722 |
rs30453103 | snp | A/C | 0.231111 | 0.249285 | intron-variant | Spag16 | Mm_Celera | 1:69896697 | TAGAGTTTATTTATT[A/C]CAAGCTCTTTTACAG | 66722 |
rs30453125 | snp | A/G | 0.244898 | 0.249948 | intron-variant | Spag16 | Mm_Celera | 1:69889809 | ATATGGAAATTATGG[A/G]AAAAAATGATTTTAG | 66722 |
rs30453127 | snp | C/T | 0.124444 | 0.216185 | intron-variant | Spag16 | Mm_Celera | 1:69889847 | TAGAGGAAATAAGTA[C/T]CATGTAGAGAGCAAA | 66722 |
rs30453129 | snp | A/G | 0.124444 | 0.216185 | intron-variant | Spag16 | Mm_Celera | 1:69889930 | ATTCCTCACTCAACA[A/G]TTCAGGGTACTCCTT | 66722 |
rs30453131 | snp | A/G | 0.124444 | 0.216185 | intron-variant | Spag16 | Mm_Celera | 1:69890014 | AGAATTGTTCTATGT[A/G]ATGCTCGTTTCTTAC | 66722 |
rs30453133 | snp | A/G | 0.444444 | 0.157135 | intron-variant | Spag16 | Mm_Celera | 1:69890021 | TTCTATGTAATGCTC[A/G]TTTCTTACATTGGCA | 66722 |
rs30453216 | snp | A/G | 0.32 | 0.24 | intron-variant | Spag16 | Mm_Celera | 1:69947695 | CCTTACCCTTAGTGG[A/G]TTTTGCATAACCCCT | 66722 |
rs30453219 | snp | C/T | 0.277778 | 0.248452 | intron-variant | Spag16 | Mm_Celera | 1:69947823 | CATGAAGAAACATGC[C/T]ATTACAAAATGTCAG | 66722 |
rs30453222 | snp | A/G | 0.32 | 0.24 | intron-variant | Spag16 | Mm_Celera | 1:69947870 | TGCAGCAATTATGGA[A/G]TTGATGATTTTTAAG | 66722 |
rs30453444 | snp | A/G | 0.231111 | 0.249285 | intron-variant | Spag16 | Mm_Celera | 1:69918349 | GAACTGAACCTAAAT[A/G]TGTATCACAATATAA | 66722 |
rs30453446 | snp | A/G | 0.231111 | 0.249285 | intron-variant | Spag16 | Mm_Celera | 1:69918856 | AGTCTCTTGTAACTT[A/G]TCTTTGCATTTTGTT | 66722 |
rs30453448 | snp | C/T | 0.231111 | 0.249285 | intron-variant | Spag16 | Mm_Celera | 1:69918892 | GTTTCTGTGACTTTT[C/T]CCTGATATGGCTGTA | 66722 |
rs30453450 | snp | C/T | 0.231111 | 0.249285 | intron-variant | Spag16 | Mm_Celera | 1:69920176 | TATTTGTTTCCATCT[C/T]CCAACTCATTCAAGA | 66722 |
rs30453452 | snp | A/G | 0.231111 | 0.249285 | intron-variant | Spag16 | Mm_Celera | 1:69920278 | ACAACTGAAAATCAA[A/G]ACAATACCAAGAGGC | 66722 |
rs30453460 | snp | A/G | 0.124444 | 0.216185 | intron-variant | Spag16 | Mm_Celera | 1:69877920 | TTCTTTATTCATAGT[A/G]AGTGACACCCTTTCC | 66722 |
rs30453635 | snp | C/T | 0.231111 | 0.249285 | intron-variant | Spag16 | Mm_Celera | 1:69900533 | CTATGAGCTCTATGT[C/T]AGTGGGTAAGTGTCT | 66722 |
rs30453637 | snp | A/C | 0.124444 | 0.216185 | intron-variant | Spag16 | Mm_Celera | 1:69900599 | GAGCAGGGTGCTACA[A/C]TATCCCTGGCTACAA | 66722 |
rs30453639 | snp | C/T | 0.32 | 0.24 | intron-variant | Spag16 | Mm_Celera | 1:69900903 | TCTGACATTTAGCAT[C/T]TTCACTCAGATCAAA | 66722 |
rs30453641 | snp | A/G | 0.32 | 0.24 | intron-variant | Spag16 | Mm_Celera | 1:69901144 | GGAAGATGGGGTCAT[A/G]TGGTAGAGATTGAAG | 66722 |
rs30453643 | snp | A/G | 0.444444 | 0.157135 | intron-variant | Spag16 | Mm_Celera | 1:69901182 | ACCAGACTTGGTAAA[A/G]CTGCCTAAGTGGACA | 66722 |
rs30453885 | snp | C/T | 0.231111 | 0.249285 | intron-variant | Spag16 | Mm_Celera | 1:69896790 | GGGGTAAGGACAGCT[C/T]CATGAGTCTCAGTGC | 66722 |
rs30453887 | snp | C/T | 0.32 | 0.24 | intron-variant | Spag16 | Mm_Celera | 1:69896841 | CTACTTACAGTTGCC[C/T]CTGTCATAAAGAAAA | 66722 |
rs30453889 | snp | C/T | 0.231111 | 0.249285 | intron-variant | Spag16 | Mm_Celera | 1:69896887 | TGTGGGGTAACATAA[C/T]TTCCCTAGTCTTCCT | 66722 |
rs30453891 | snp | C/T | 0.132653 | 0.220748 | intron-variant | Spag16 | Mm_Celera | 1:69896904 | TCCCTAGTCTTCCTT[C/T]TAAATGCATAGAAGA | 66722 |
rs30453893 | snp | A/G | 0.32 | 0.24 | intron-variant | Spag16 | Mm_Celera | 1:69896929 | AGAAGAGAATTGTGC[A/G]CCATTTAAGAATAAG | 66722 |
rs30453955 | snp | A/T | 0.444444 | 0.157135 | intron-variant | Spag16 | Mm_Celera | 1:69890039 | TCTTACATTGGCAGG[A/T]AGACAATATAGTCTA | 66722 |
rs30453957 | snp | A/C | 0.124444 | 0.216185 | intron-variant | Spag16 | Mm_Celera | 1:69890132 | TTTTTTTTTGACTTT[A/C]AGTTACATGTGTGAT | 66722 |
rs30453959 | snp | C/T | 0.124444 | 0.216185 | intron-variant | Spag16 | Mm_Celera | 1:69890292 | GTGGACTTGGAGATT[C/T]GCAATGTTAGGTGTT | 66722 |
rs30453961 | snp | G/T | 0.124444 | 0.216185 | intron-variant | Spag16 | Mm_Celera | 1:69890354 | ACTTATCCCAGGACC[G/T]GAGCATGTTCAGTTA | 66722 |
rs30453963 | snp | A/G | 0.124444 | 0.216185 | intron-variant | Spag16 | Mm_Celera | 1:69890391 | GTTAAATGTGTATCT[A/G]TATAAAGGAGAGTTG | 66722 |
rs30454044 | snp | A/T | 0.244898 | 0.249948 | intron-variant | Spag16 | Mm_Celera | 1:69947942 | CTCATTTCTTCAGGA[A/T]CTCTTCCCTTCGCTG | 66722 |
rs30454047 | snp | A/G | 0.244898 | 0.249948 | intron-variant | Spag16 | Mm_Celera | 1:69947954 | GGAACTCTTCCCTTC[A/G]CTGTTGACAATATCT | 66722 |
rs30454050 | snp | A/C | 0.444444 | 0.157135 | intron-variant | Spag16 | Mm_Celera | 1:69948361 | GGTAATCAGTTAATT[A/C]TGCTTTCATGATTCT | 66722 |
rs30454053 | snp | C/T | 0.444444 | 0.157135 | intron-variant | Spag16 | Mm_Celera | 1:69948471 | TAGCTGGCTAGTGGC[C/T]GTCTGCCTTTATGAT | 66722 |
rs30454294 | snp | C/T | 0.336735 | 0.234472 | intron-variant | Spag16 | Mm_Celera | 1:69921528 | GGCAGGAAGATTTTT[C/T]ATCTTTTCTGATGAT | 66722 |
rs30454296 | snp | G/T | 0.231111 | 0.249285 | intron-variant | Spag16 | Mm_Celera | 1:69921547 | TTTTCTGATGATCTT[G/T]CTTTGAGGTTTAAGC | 66722 |
rs30454298 | snp | A/C | 0.231111 | 0.249285 | intron-variant | Spag16 | Mm_Celera | 1:69921924 | AGTCAGCTTGCCATT[A/C]TATTTATTTCTTTTG | 66722 |
rs30454300 | snp | A/C | 0.244898 | 0.249948 | intron-variant | Spag16 | Mm_Celera | 1:69922037 | TTCTATAGGCAACAT[A/C]TCTCTTAATACAATT | 66722 |
rs30454302 | snp | G/T | 0.426035 | 0.177515 | intron-variant | Spag16 | Mm_Celera | 1:69922146 | TGCACACCACAATTT[G/T]TTAGGTGGTGCTTTT | 66722 |
rs30454465 | snp | C/T | 0.231111 | 0.249285 | intron-variant | Spag16 | Mm_Celera | 1:69901363 | TGAACTGTGATCCCT[C/T]TCCATCTTTGAGTAC | 66722 |
rs30454467 | snp | C/G | 0.231111 | 0.249285 | intron-variant | Spag16 | Mm_Celera | 1:69901488 | TCCTGCTATTTTGAG[C/G]TGCTTTAATTTCCCT | 66722 |
rs30454469 | snp | A/C | 0.124444 | 0.216185 | intron-variant | Spag16 | Mm_Celera | 1:69901616 | AGTTTATCCCAGTAA[A/C]TGAGAGCAAAGTAGA | 66722 |
rs30454471 | snp | A/T | 0.124444 | 0.216185 | intron-variant | Spag16 | Mm_Celera | 1:69901829 | ATACTTCTGTTTCTG[A/T]GGACCATTGGTTTTC | 66722 |
rs30454473 | snp | A/G/T | 0.124444 | 0.216185 | intron-variant | Spag16 | Mm_Celera | 1:69901839 | TTCTGAGGACCATTG[A/G/T]TTTTCATGATTGTGA | 66722 |
rs30454785 | snp | A/G | 0.32 | 0.24 | intron-variant | Spag16 | Mm_Celera | 1:69897314 | GGATAGAATACCCAC[A/G]GAGAGCAATGCAAAG | 66722 |
rs30454787 | snp | C/G | 0.124444 | 0.216185 | intron-variant | Spag16 | Mm_Celera | 1:69897419 | TATGCTGTGCCTAGT[C/G]ACAGCTGGTCCCCTG | 66722 |
rs30454789 | snp | C/T | 0.231111 | 0.249285 | intron-variant | Spag16 | Mm_Celera | 1:69897432 | GTGACAGCTGGTCCC[C/T]TGTATACACATATTC | 66722 |
rs30454791 | snp | A/T | 0.231111 | 0.249285 | intron-variant | Spag16 | Mm_Celera | 1:69897461 | TCTCTTTCAGGTGGT[A/T]TGCTATGCTTAATGA | 66722 |
rs30454793 | snp | C/G | 0.231111 | 0.249285 | intron-variant | Spag16 | Mm_Celera | 1:69897526 | ATGCAAGGCTGGCAT[C/G]TTATTTGACAGAAAA | 66722 |
rs30454805 | snp | C/T | 0.336735 | 0.234472 | intron-variant | Spag16 | Mm_Celera | 1:69890408 | ATAAAGGAGAGTTGG[C/T]GAGTTTAGCATGAGA | 66722 |
rs30454807 | snp | A/G | 0.124444 | 0.216185 | intron-variant | Spag16 | Mm_Celera | 1:69892672 | TTAATGCTGTGTGAA[A/G]TCTGCTCAGATTCCT | 66722 |
rs30454809 | snp | A/G | 0.124444 | 0.216185 | intron-variant | Spag16 | Mm_Celera | 1:69892702 | TGCAAGTGTCTGTTT[A/G]AGAGCTTGCTGTGTC | 66722 |
rs30454811 | snp | C/G/T | 0.124444 | 0.216185 | intron-variant | Spag16 | Mm_Celera | 1:69892727 | TGTGTCTTCTTTCTT[C/G/T]AATCTCCATCTGTAT | 66722 |
rs30454813 | snp | A/C | 0.444444 | 0.157135 | intron-variant | Spag16 | Mm_Celera | 1:69892762 | ATCACTGCACCAGTT[A/C]TTTTCTCATATATAA | 66722 |
rs30454984 | snp | G/T | 0.408163 | 0.193609 | intron-variant | Spag16 | Mm_Celera | 1:69922191 | TCTAGTATATCTTTG[G/T]CATTTAGCTATTATC | 66722 |
rs30454986 | snp | A/G | 0.231111 | 0.249285 | intron-variant | Spag16 | Mm_Celera | 1:69922212 | AGCTATTATCAAAAT[A/G]TGTTGGCATTTCATT | 66722 |
rs30454988 | snp | G/T | 0.231111 | 0.249285 | intron-variant | Spag16 | Mm_Celera | 1:69922295 | AGTTCCTGGTCAGCA[G/T]GTCCACCTGACTCTG | 66722 |
rs30454990 | snp | A/G | 0.231111 | 0.249285 | intron-variant | Spag16 | Mm_Celera | 1:69922362 | CAGTAGAGCACAGAT[A/G]CTTACCTCATTGAGC | 66722 |
rs30454992 | snp | C/T | 0.231111 | 0.249285 | intron-variant | Spag16 | Mm_Celera | 1:69922377 | ACTTACCTCATTGAG[C/T]TAGAGAGCTGAAAAA | 66722 |
rs30454996 | snp | C/G | 0.5 | 0 | intron-variant | Spag16 | Mm_Celera | 1:69948628 | CATTTTTGGTTGTGA[C/G]CCTAACCTTTAATGG | 66722 |
rs30454999 | snp | A/G | 0.444444 | 0.157135 | intron-variant | Spag16 | Mm_Celera | 1:69948842 | CAGAAGACATTTGGT[A/G]TTAAAAATAAGATAG | 66722 |
rs30455001 | snp | A/G | 0.444444 | 0.157135 | intron-variant | Spag16 | Mm_Celera | 1:69948929 | TTATTTCTCTATCCC[A/G]GTTCATTTAACTTCT | 66722 |
rs30455315 | snp | C/T | 0.124444 | 0.216185 | intron-variant | Spag16 | Mm_Celera | 1:69902029 | ACTGTAATAATCGAA[C/T]TTTTGGTAAGATACT | 66722 |
rs30455317 | snp | C/T | 0.124444 | 0.216185 | intron-variant | Spag16 | Mm_Celera | 1:69902048 | TGGTAAGATACTCTT[C/T]GACTCATTGAAAGTT | 66722 |
rs30455320 | snp | C/T | 0.124444 | 0.216185 | intron-variant | Spag16 | Mm_Celera | 1:69902674 | GTACTTCTATGCCAT[C/T]TAATCAGGTCCACAA | 66722 |
rs30455322 | snp | C/T | 0.32 | 0.24 | intron-variant | Spag16 | Mm_Celera | 1:69903142 | CACACATGTTGAATG[C/T]CCAAAGAGGATATCT | 66722 |
rs30455685 | snp | A/C | 0.32 | 0.24 | intron-variant | Spag16 | Mm_Celera | 1:69892855 | ACAGCAGCAGTCATT[A/C]GGTAAAAGATAAATC | 66722 |
rs30455687 | snp | A/C | 0.124444 | 0.216185 | intron-variant | Spag16 | Mm_Celera | 1:69892983 | TTGCAAAGGGCCTGT[A/C]ACTGCTGCTCTCCCT | 66722 |
rs30455689 | snp | A/C | 0.124444 | 0.216185 | intron-variant | Spag16 | Mm_Celera | 1:69893029 | CTTGGGCTCCATTGT[A/C]TTTGGGACCCTGATA | 66722 |
rs30455691 | snp | A/G | 0.231111 | 0.249285 | intron-variant | Spag16 | Mm_Celera | 1:69893041 | TGTATTTGGGACCCT[A/G]ATATGCAGAATTGCT | 66722 |
rs30455693 | snp | A/T | 0.124444 | 0.216185 | intron-variant | Spag16 | Mm_Celera | 1:69893045 | TTTGGGACCCTGATA[A/T]GCAGAATTGCTAAAG | 66722 |
rs30455695 | snp | A/G | 0.32 | 0.24 | intron-variant | Spag16 | Mm_Celera | 1:69897587 | ATCAATGCTTTGTCC[A/G]TTTCTCCTGGTGATG | 66722 |
rs30455697 | snp | C/T | 0.124444 | 0.216185 | intron-variant | Spag16 | Mm_Celera | 1:69897629 | TTAAAGAAGCACCTC[C/T]GTGGTAAAGAGTTGA | 66722 |
rs30455699 | snp | A/G | 0.231111 | 0.249285 | intron-variant | Spag16 | Mm_Celera | 1:69897697 | CCTTTCTTTCCTCTA[A/G]GATCACTTACTTTTA | 66722 |
rs30455701 | snp | A/C | 0.124444 | 0.216185 | intron-variant | Spag16 | Mm_Celera | 1:69897797 | TGGCACTTATGGACT[A/C]TGTTATAGAAAAATA | 66722 |
rs30455864 | snp | C/T | 0.48 | 0.0979796 | intron-variant | Spag16 | Mm_Celera | 1:69948974 | GATGTGCCATAGAAT[C/T]CTTACTATGATAGTA | 66722 |
rs30455867 | snp | C/T | 0.375 | 0.216506 | intron-variant | Spag16 | Mm_Celera | 1:69949076 | TTTTTTGACTATCTT[C/T]TATAAAGACTATACT | 66722 |
rs30455870 | snp | A/T | 0.277778 | 0.248452 | intron-variant | Spag16 | Mm_Celera | 1:69949107 | AGTTTCCATTAAAAA[A/T]TGCAGAACTTAATTT | 66722 |
rs30455873 | snp | A/T | 0.32 | 0.24 | intron-variant | Spag16 | Mm_Celera | 1:69949289 | TGTTTATAAGTGTCA[A/T]TTTTTTATACATTTA | 66722 |
rs30455944 | snp | A/G | 0.124444 | 0.216185 | intron-variant | Spag16 | Mm_Celera | 1:69922392 | CTAGAGAGCTGAAAA[A/G]GACAGAGAGGCACAG | 66722 |
rs30455946 | snp | A/G | 0.231111 | 0.249285 | intron-variant | Spag16 | Mm_Celera | 1:69922440 | AAGACATACTCATAG[A/G]GCTCCACTTCCTCTG | 66722 |
rs30455948 | snp | G/T | 0.231111 | 0.249285 | intron-variant | Spag16 | Mm_Celera | 1:69922454 | GGGCTCCACTTCCTC[G/T]GACTATATCCAGCTA | 66722 |
rs30455950 | snp | C/T | 0.231111 | 0.249285 | intron-variant | Spag16 | Mm_Celera | 1:69922531 | CAGTAGATAGTTGGC[C/T]AGATCAGATCCTTTT | 66722 |
rs30455952 | snp | A/C | 0.244898 | 0.249948 | intron-variant | Spag16 | Mm_Celera | 1:69923066 | ATTTTATCAGAGTAC[A/C]TTATATACAAATCAG | 66722 |
rs30456234 | snp | C/G | 0.124444 | 0.216185 | intron-variant | Spag16 | Mm_Celera | 1:69903400 | GGGATCTTTCTAGCC[C/G]CAGGACTAGTAAGTA | 66722 |
rs30456236 | snp | C/G | 0.32 | 0.24 | intron-variant | Spag16 | Mm_Celera | 1:69903418 | GGACTAGTAAGTACA[C/G]TTTTAAACTGACGTT | 66722 |
rs30456238 | snp | C/T | 0.32 | 0.24 | intron-variant | Spag16 | Mm_Celera | 1:69903528 | AAGCATCCATGAAGT[C/T]AGTGGTAATAACCTA | 66722 |
rs30456240 | snp | A/G | 0.231111 | 0.249285 | intron-variant | Spag16 | Mm_Celera | 1:69903555 | CCTAGTAGGTAGTGT[A/G]CTGGTTTGCTCCAGT | 66722 |
rs30456242 | snp | C/T | 0.231111 | 0.249285 | intron-variant | Spag16 | Mm_Celera | 1:69903673 | CAATTTCTTTTGTTT[C/T]CTGAGACTTTCATAA | 66722 |
rs30456475 | snp | G/T | 0.124444 | 0.216185 | intron-variant | Spag16 | Mm_Celera | 1:69893054 | CTGATATGCAGAATT[G/T]CTAAAGGAGGATAGA | 66722 |
rs30456477 | snp | C/T | 0.124444 | 0.216185 | intron-variant | Spag16 | Mm_Celera | 1:69893108 | GATAGATATTCTAGT[C/T]TGTGTTATCATGTGT | 66722 |
rs30456479 | snp | G/T | 0.124444 | 0.216185 | intron-variant | Spag16 | Mm_Celera | 1:69893123 | CTGTGTTATCATGTG[G/T]TCATTTTTAATATTT | 66722 |
rs30456481 | snp | C/T | 0.132653 | 0.220748 | intron-variant | Spag16 | Mm_Celera | 1:69893165 | AAGAACTGTACAGGT[C/T]AGCAGACTTAGGTTA | 66722 |
rs30456483 | snp | C/T | 0.124444 | 0.216185 | intron-variant | Spag16 | Mm_Celera | 1:69893214 | CATGTGCCTCCTTGC[C/T]CTTGCCATCTCTAGT | 66722 |
rs30456516 | snp | G/T | 0.231111 | 0.249285 | intron-variant | Spag16 | Mm_Celera | 1:69929149 | AGGACTTTCTGTGTC[G/T]GCCTGTGTTAACTCT | 66722 |
rs30456519 | snp | G/T | 0.32 | 0.24 | intron-variant | Spag16 | Mm_Celera | 1:69929214 | TCTATGGATCAAAAT[G/T]GGGCATCATCTGCTT | 66722 |
rs30456522 | snp | A/C | 0.124444 | 0.216185 | intron-variant | Spag16 | Mm_Celera | 1:69929270 | GTGTTCTGGCAAATG[A/C]TTATTCTTACAACAA | 66722 |
rs30456524 | snp | A/G | 0.231111 | 0.249285 | missense, intron-variant | Spag16 | Mm_Celera | 1:69923870 | GAAAAAGACCACCGA[A/G]GACCTCTTGTCTCCA | 66722 |
rs30456527 | snp | A/C | 0.231111 | 0.249285 | stop-gained, intron-variant, missense | Spag16 | Mm_Celera | 1:69923897 | TCCATCAGCATGAGT[A/C]AAATGGAAGATTCTG | 66722 |
rs30456530 | snp | C/T | 0.231111 | 0.249285 | utr-variant-3-prime, intron-variant, synonymous-codon | Spag16 | Mm_Celera | 1:69923923 | TTCTGAGCAATACAA[C/T]TTCCTAGCTTTCCCT | 66722 |
rs30456533 | snp | A/G | 0.231111 | 0.249285 | utr-variant-3-prime, intron-variant, missense | Spag16 | Mm_Celera | 1:69923967 | CTTTTATCAATACCC[A/G]GACTCTTATTCCTTG | 66722 |
rs30456634 | snp | A/G | 0.408163 | 0.193609 | intron-variant | Spag16 | Mm_Celera | 1:69923310 | TTTTTCTTCAATGGT[A/G]TTATATTTGTTTTTA | 66722 |
rs30456636 | snp | A/T | 0.231111 | 0.249285 | intron-variant | Spag16 | Mm_Celera | 1:69923384 | TCATTATTTTCCTTG[A/T]GACTTTTATAGAAAG | 66722 |
rs30456638 | snp | A/T | 0.231111 | 0.249285 | intron-variant | Spag16 | Mm_Celera | 1:69923448 | GGTTGGATCTTTCAA[A/T]GCTCAAATGCCTGTG | 66722 |
rs30456641 | snp | C/T | 0.231111 | 0.249285 | intron-variant | Spag16 | Mm_Celera | 1:69923472 | GCCTGTGTTTAATTG[C/T]TGACCAGGAACTCAA | 66722 |
rs30456696 | snp | A/G | 0.444444 | 0.157135 | intron-variant | Spag16 | Mm_Celera | 1:69949421 | ATTCAAATTTCTGAG[A/G]ACTAAATGCACGTAC | 66722 |
rs30456699 | snp | C/G | 0.408163 | 0.193609 | intron-variant | Spag16 | Mm_Celera | 1:69949468 | ATGATGCTTTGAAGC[C/G]ATTCGCTGTGTAGCT | 66722 |
rs30456702 | snp | A/G | 0.277778 | 0.248452 | upstream-variant-2KB, intron-variant | Spag16 | Mm_Celera | 1:69949653 | CATGCGATTATGTCA[A/G]GACAGATCCTCCTCA | 66722 |
rs30456784 | snp | C/T | 0.124444 | 0.216185 | intron-variant | Spag16 | Mm_Celera | 1:69897930 | ATTAGTAGGCAAATT[C/T]AATAAAACACCATTT | 66722 |
rs30456787 | snp | G/T | 0.124444 | 0.216185 | intron-variant | Spag16 | Mm_Celera | 1:69898317 | ATCTTAGATGCTGCT[G/T]CTGTTTGCTTTTGGA | 66722 |
rs30456789 | snp | A/G | 0.124444 | 0.216185 | intron-variant | Spag16 | Mm_Celera | 1:69898370 | TAACCAATGCTGTAT[A/G]TGTTGCAATACACTA | 66722 |
rs30456791 | snp | A/G | 0.231111 | 0.249285 | intron-variant | Spag16 | Mm_Celera | 1:69898388 | TTGCAATACACTAAT[A/G]TGCCAATATTTTGAA | 66722 |
rs30456793 | snp | A/G | 0.231111 | 0.249285 | intron-variant | Spag16 | Mm_Celera | 1:69898527 | AGGAACTTTCAGGCT[A/G]ATTGGCGAAGTCATT | 66722 |
rs30457024 | snp | A/C | 0.32 | 0.24 | intron-variant | Spag16 | Mm_Celera | 1:69903684 | GTTTTCTGAGACTTT[A/C]ATAATGCAGTGCAAA | 66722 |
rs30457026 | snp | A/G | 0.231111 | 0.249285 | intron-variant | Spag16 | Mm_Celera | 1:69903857 | AGAGAGCTAGCCATT[A/G]GTTCATGTATAAGCT | 66722 |
rs30457028 | snp | A/G | 0.124444 | 0.216185 | intron-variant | Spag16 | Mm_Celera | 1:69904127 | TTCACAAGTGAGAAT[A/G]TCCACCTGAGGAGAC | 66722 |
rs30457030 | snp | A/T | 0.124444 | 0.216185 | intron-variant | Spag16 | Mm_Celera | 1:69904632 | CAGCTGCCAAATATA[A/T]TCTTTCAATGACATG | 66722 |
rs30457032 | snp | C/G | 0.231111 | 0.249285 | intron-variant | Spag16 | Mm_Celera | 1:69904769 | TGGATTTAAGCAAAG[C/G]GTACACTGGGGAGGA | 66722 |
rs30457155 | snp | C/T | 0.124444 | 0.216185 | intron-variant | Spag16 | Mm_Celera | 1:69893235 | CATCTCTAGTTTCTG[C/T]AACCACAGGGTGAGG | 66722 |
rs30457157 | snp | A/T | 0.32 | 0.24 | intron-variant | Spag16 | Mm_Celera | 1:69893629 | AATGTAAAAATATTA[A/T]GCATTTGGGCATACC | 66722 |
rs30457159 | snp | C/G | 0.124444 | 0.216185 | intron-variant | Spag16 | Mm_Celera | 1:69893638 | ATATTAAGCATTTGG[C/G]CATACCACTCCTTTG | 66722 |
rs30457161 | snp | G/T | 0.32 | 0.24 | intron-variant | Spag16 | Mm_Celera | 1:69894478 | GTCTCCTTTCTGTGT[G/T]TTCACTGTGGCTTCC | 66722 |
rs30457346 | snp | C/T | 0.231111 | 0.249285 | utr-variant-3-prime, intron-variant | Spag16 | Mm_Celera | 1:69924725 | TATATGTCTTTGTCA[C/T]GCCATATGTGTGGTG | 66722 |
rs30457349 | snp | C/G | 0.244898 | 0.249948 | utr-variant-3-prime, intron-variant | Spag16 | Mm_Celera | 1:69924772 | CCAACAAATTCATGA[C/G]TGTAATGATCCCAGG | 66722 |
rs30457352 | snp | C/T | 0.231111 | 0.249285 | utr-variant-3-prime, intron-variant | Spag16 | Mm_Celera | 1:69924844 | GTACCCAACAGTCCA[C/T]TTGAAAGCTGACCAA | 66722 |
rs30457404 | snp | A/C | 0.244898 | 0.249948 | intron-variant | Spag16 | Mm_Celera | 1:69923582 | GTTTGTGTGAAATGT[A/C]ATTCTACATATTTTT | 66722 |
rs30457407 | snp | C/G | 0.231111 | 0.249285 | missense, intron-variant | Spag16 | Mm_Celera | 1:69923767 | TCCTTCCATCAGCAG[C/G]AGTCAAGAGGGAACT | 66722 |
rs30457410 | snp | C/T | 0.231111 | 0.249285 | missense, intron-variant | Spag16 | Mm_Celera | 1:69923783 | AGTCAAGAGGGAACT[C/T]TCCAACTTGGAATAA | 66722 |
rs30457425 | snp | A/C | 0.277778 | 0.248452 | upstream-variant-2KB, intron-variant | Spag16 | Mm_Celera | 1:69949768 | TCACAGAGCACATCG[A/C]AGTAGAGAGAGGCAA | 66722 |
rs30457428 | snp | A/G | 0.32 | 0.24 | upstream-variant-2KB, intron-variant | Spag16 | Mm_Celera | 1:69949836 | ATAAACGTTTGCATT[A/G]ATTTAAATGCAGGTA | 66722 |
rs30457575 | snp | A/T | 0.32 | 0.24 | intron-variant | Spag16 | Mm_Celera | 1:69929388 | ATAGTACAAAGTGGA[A/T]CACAGATCTTTGTCT | 66722 |
rs30457578 | snp | C/T | 0.260355 | 0.249785 | intron-variant | Spag16 | Mm_Celera | 1:69929467 | GGAAGAATTTAATGA[C/T]AATGATTATTTTCCT | 66722 |
rs30457581 | snp | C/T | 0.231111 | 0.249285 | intron-variant | Spag16 | Mm_Celera | 1:69929486 | GATTATTTTCCTTGC[C/T]TACTTGGGAATCTTC | 66722 |
rs30457695 | snp | C/G | 0.124444 | 0.216185 | intron-variant | Spag16 | Mm_Celera | 1:69898626 | GGGTACAGAAAGCAT[C/G]CTCAGATTAGTGACT | 66722 |
rs30457697 | snp | A/C/G | 0.231111 | 0.249285 | intron-variant | Spag16 | Mm_Celera | 1:69898656 | TTAGAATTAGAAAAC[A/C/G]GAGTGTCCAGTTTTA | 66722 |
rs30457699 | snp | A/G | 0.32 | 0.24 | intron-variant | Spag16 | Mm_Celera | 1:69898748 | GGTTGAAGTTGGAAG[A/G]GGAAAAGGATTTAAG | 66722 |
rs30457701 | snp | G/T | 0.124444 | 0.216185 | intron-variant | Spag16 | Mm_Celera | 1:69898776 | AAGAGGAATAGAGAA[G/T]TCAGGCTTTCACTTG | 66722 |
rs30457934 | snp | C/T | 0.231111 | 0.249285 | intron-variant | Spag16 | Mm_Celera | 1:69904827 | TAAACAGCTTTACAA[C/T]GAAACTGGAGATATG | 66722 |
rs30457936 | snp | G/T | 0.124444 | 0.216185 | intron-variant | Spag16 | Mm_Celera | 1:69904828 | AAACAGCTTTACAAT[G/T]AAACTGGAGATATGT | 66722 |
rs30457938 | snp | G/T | 0.132653 | 0.220748 | intron-variant | Spag16 | Mm_Celera | 1:69904842 | TGAAACTGGAGATAT[G/T]TATGTATGTATGTAT | 66722 |
rs30457940 | snp | G/T | 0.408163 | 0.193609 | intron-variant | Spag16 | Mm_Celera | 1:69904878 | TATGTATGTATGTAT[G/T]TATTTATTATTCTTT | 66722 |
rs30457942 | snp | G/T | 0.375 | 0.216506 | intron-variant | Spag16 | Mm_Celera | 1:69905422 | AAAAAATATTTAGGG[G/T]AGTAACTAAAATGTA | 66722 |
rs30458175 | snp | C/T | 0.231111 | 0.249285 | utr-variant-3-prime, intron-variant | Spag16 | Mm_Celera | 1:69924883 | ACTGATTTCCTGACA[C/T]AGTTGTCTTTCTTTA | 66722 |
rs30458178 | snp | G/T | 0.142012 | 0.225474 | utr-variant-3-prime, intron-variant | Spag16 | Mm_Celera | 1:69925730 | ATAAAAATGTGTTCT[G/T]AGAAAGTAATATAAA | 66722 |
rs30458181 | snp | C/T | 0.142012 | 0.225474 | utr-variant-3-prime, intron-variant | Spag16 | Mm_Celera | 1:69925790 | GCCTTGTTAATCTCT[C/T]CTTTCATATAGATAG | 66722 |
rs30458384 | snp | C/T | 0.32 | 0.24 | intron-variant | Spag16 | Mm_Celera | 1:69929720 | CCTTACAGGTGACTA[C/T]ACTTACCATCTCTGT | 66722 |
rs30458387 | snp | C/T | 0.142012 | 0.225474 | intron-variant | Spag16 | Mm_Celera | 1:69929785 | TAAGTTAATTCTTGG[C/T]GAGCTTTCATTCTCT | 66722 |
rs30458390 | snp | C/T | 0.32 | 0.24 | intron-variant | Spag16 | Mm_Celera | 1:69929887 | TAGTTATAGATAAAG[C/T]ACTTTGGGCTTAGAG | 66722 |
rs30458393 | snp | C/T | 0.142012 | 0.225474 | intron-variant | Spag16 | Mm_Celera | 1:69929940 | AGATGATGCTCTGTT[C/T]GCTTGAGGCTAAGCA | 66722 |
rs30458594 | snp | A/G | 0.124444 | 0.216185 | intron-variant | Spag16 | Mm_Celera | 1:69905633 | TAATGTTGAACAAAT[A/G]TCTTCAGTAAGCACT | 66722 |
rs30458596 | snp | G/T | 0.336735 | 0.234472 | intron-variant | Spag16 | Mm_Celera | 1:69905682 | ATGTAATTCAGTGAC[G/T]GTCTAGTCAGTCATT | 66722 |
rs30458598 | snp | C/T | 0.32 | 0.24 | intron-variant | Spag16 | Mm_Celera | 1:69905696 | CTGTCTAGTCAGTCA[C/T]TGCACGCTTGCTAGA | 66722 |
rs30458600 | snp | A/G | 0.124444 | 0.216185 | intron-variant | Spag16 | Mm_Celera | 1:69905758 | AAGTACAGCACAGAT[A/G]TGTTCTGCAAGTGCA | 66722 |
rs30458602 | snp | C/T | 0.231111 | 0.249285 | intron-variant | Spag16 | Mm_Celera | 1:69905762 | ACAGCACAGATGTGT[C/T]CTGCAAGTGCAGTGA | 66722 |
rs30458944 | snp | A/T | 0.231111 | 0.249285 | utr-variant-3-prime, intron-variant | Spag16 | Mm_Celera | 1:69925804 | TTCTTTCATATAGAT[A/T]GTAGCTGTGGTGGGA | 66722 |
rs30458947 | snp | A/G | 0.231111 | 0.249285 | utr-variant-3-prime, intron-variant | Spag16 | Mm_Celera | 1:69925862 | ATGAATGATGACGAT[A/G]ATTCCCCTCATCTAA | 66722 |
rs30458950 | snp | C/T | 0.231111 | 0.249285 | utr-variant-3-prime, intron-variant | Spag16 | Mm_Celera | 1:69926085 | TTTATCTTTGAAATA[C/T]ATTAGTGGCAAATTG | 66722 |
rs30458953 | snp | A/T | 0.244898 | 0.249948 | downstream-variant-500B, intron-variant | Spag16 | Mm_Celera | 1:69926278 | GTGCGCTTTGGTTTG[A/T]GGAGTGTTGGGTCTC | 66722 |
rs30459326 | snp | C/T | 0.231111 | 0.249285 | intron-variant | Spag16 | Mm_Celera | 1:69929949 | TCTGTTCGCTTGAGG[C/T]TAAGCAGTGCCAGTA | 66722 |
rs30459329 | snp | A/G | 0.32 | 0.24 | intron-variant | Spag16 | Mm_Celera | 1:69929964 | CTAAGCAGTGCCAGT[A/G]TGTGTATGTTCTCTA | 66722 |
rs30459332 | snp | A/G | 0.32 | 0.24 | intron-variant | Spag16 | Mm_Celera | 1:69929992 | CTACTCCCTTTCTTC[A/G]GTGATGAGAATATAA | 66722 |
rs30459796 | snp | A/G | 0.124444 | 0.216185 | downstream-variant-500B, intron-variant | Spag16 | Mm_Celera | 1:69926288 | GTTTGAGGAGTGTTG[A/G]GTCTCACTATTACTC | 66722 |
rs30459799 | snp | G/T | 0.231111 | 0.249285 | downstream-variant-500B, intron-variant | Spag16 | Mm_Celera | 1:69926309 | ACTATTACTCTTATC[G/T]CGTGCTTCCTTTCTA | 66722 |
rs30459802 | snp | G/T | 0.124444 | 0.216185 | downstream-variant-500B, intron-variant | Spag16 | Mm_Celera | 1:69926375 | GAGATTCCTAAAGTT[G/T]ATGTTCTTTTGAAAT | 66722 |
rs30460205 | snp | A/T | 0.32 | 0.24 | intron-variant | Spag16 | Mm_Celera | 1:69930015 | GAATATAAGGAGGAA[A/T]AACTTAGGTGATTAA | 66722 |
rs30460212 | snp | C/G | 0.124444 | 0.216185 | intron-variant | Spag16 | Mm_Celera | 1:69930867 | CTTCAGGGTTCGTCT[C/G]TGCCCAGAGCTGATC | 66722 |
rs30460404 | snp | A/G | 0.5 | 0 | upstream-variant-2KB, intron-variant | Spag16 | Mm_Celera | 1:69949924 | TTAGGAAAAAAAAAG[A/G]AAAAGAGTTCCAGTC | 66722 |
rs30460407 | snp | A/T | 0.277778 | 0.248452 | upstream-variant-2KB, intron-variant | Spag16 | Mm_Celera | 1:69949953 | TCAGAAACCCTGAAA[A/T]GTATTGCTAATATAA | 66722 |
rs30460410 | snp | A/G | 0.32 | 0.24 | upstream-variant-2KB, intron-variant | Spag16 | Mm_Celera | 1:69949956 | GAAACCCTGAAAAGT[A/G]TTGCTAATATAAACT | 66722 |
rs30460413 | snp | A/G | 0.277778 | 0.248452 | upstream-variant-2KB, intron-variant | Spag16 | Mm_Celera | 1:69950405 | GAACTGGAGTAGACA[A/G]TGACCCAATTGTACT | 66722 |
rs30460695 | snp | A/G | 0.231111 | 0.249285 | downstream-variant-500B, intron-variant | Spag16 | Mm_Celera | 1:69926507 | TGCTTAGAAGATTTT[A/G]TATTATGACATCTGG | 66722 |
rs30460698 | snp | A/G | 0.132653 | 0.220748 | downstream-variant-500B, intron-variant | Spag16 | Mm_Celera | 1:69926551 | TAATATAGAACTATG[A/G]CGGTTATTTGTTCTT | 66722 |
rs30460701 | snp | A/G | 0.132653 | 0.220748 | downstream-variant-500B, intron-variant | Spag16 | Mm_Celera | 1:69926598 | GTTATAAAGCAACAA[A/G]CTTACATTAATTTAG | 66722 |
rs30460905 | snp | C/T | 0.244898 | 0.249948 | intron-variant | Spag16 | Mm_Celera | 1:69976010 | CAAGTTCCCTTATGC[C/T]AAGGAACATTATTAG | 66722 |
rs30460908 | snp | C/G | 0.231111 | 0.249285 | intron-variant | Spag16 | Mm_Celera | 1:69976014 | TTCCCTTATGCCAAG[C/G]AACATTATTAGGATT | 66722 |
rs30460911 | snp | A/G | 0.231111 | 0.249285 | intron-variant | Spag16 | Mm_Celera | 1:69976270 | GCATTAGAGATAGAA[A/G]TGTGTTTCTTCACTG | 66722 |
rs30461235 | snp | A/C | 0.142012 | 0.225474 | intron-variant | Spag16 | GRCm38.p3 | 1:69930892 | CTGATCCTGTGCTAT[A/C]ATGCCCAGAGCTGAT | 66722 |
rs30461238 | snp | C/G | 0.32 | 0.24 | intron-variant | Spag16 | Mm_Celera | 1:69934965 | GCAACTGCTCAGTTT[C/G]TTCTTCAGCCCATGG | 66722 |
rs30461241 | snp | A/G | 0.231111 | 0.249285 | intron-variant | Spag16 | Mm_Celera | 1:69935175 | TGTTCTGTGCTAGTG[A/G]GATTTTCTAACACTC | 66722 |
rs30461266 | snp | C/G | 0.277778 | 0.248452 | upstream-variant-2KB, intron-variant | Spag16 | Mm_Celera | 1:69950419 | AGTGACCCAATTGTA[C/G]TGTCCTCTATAACAC | 66722 |
rs30461269 | snp | C/T | 0.244898 | 0.249948 | upstream-variant-2KB, intron-variant | Spag16 | Mm_Celera | 1:69950593 | CATCCTCTGACAGTG[C/T]GCATAGAAAACAAGA | 66722 |
rs30461272 | snp | A/G | 0.408163 | 0.193609 | upstream-variant-2KB, intron-variant | Spag16 | Mm_Celera | 1:69950738 | AGGGAGCCCATGTGA[A/G]GGAGGAAGTGGATCT | 66722 |
rs30461594 | snp | C/G | 0.142012 | 0.225474 | downstream-variant-500B, intron-variant | Spag16 | Mm_Celera | 1:69926674 | TTCAGCAGCCAGTGG[C/G]TCTACTGTTACAGCG | 66722 |
rs30461597 | snp | C/T | 0.231111 | 0.249285 | downstream-variant-500B, intron-variant | Spag16 | Mm_Celera | 1:69926707 | TTCTTTTGTGTGAGC[C/T]TTTACCCCATATCCA | 66722 |
rs30461764 | snp | A/G | 0.231111 | 0.249285 | intron-variant | Spag16 | Mm_Celera | 1:69976300 | GTACTCTAGGTTCTC[A/G]GGGCCTAAAGGGAAG | 66722 |
rs30461767 | snp | A/G | 0.231111 | 0.249285 | intron-variant | Spag16 | Mm_Celera | 1:69976314 | CGGGGCCTAAAGGGA[A/G]GCCTCAGTTGATTAG | 66722 |
rs30461770 | snp | C/T | 0.459184 | 0.136902 | intron-variant | Spag16 | Mm_Celera | 1:69976335 | AGTTGATTAGCCCAG[C/T]CCTCAACTCTTCTCC | 66722 |
rs30461773 | snp | C/T | 0.260355 | 0.249785 | intron-variant | Spag16 | Mm_Celera | 1:69976666 | TAAAATTGGAATGAG[C/T]AATTCTCAGGCTGTG | 66722 |
rs30462204 | snp | C/T | 0.231111 | 0.249285 | intron-variant | Spag16 | Mm_Celera | 1:69935191 | GATTTTCTAACACTC[C/T]AATTCATGGACAGAC | 66722 |
rs30462207 | snp | A/C | 0.32 | 0.24 | intron-variant | Spag16 | Mm_Celera | 1:69937067 | AATGCCAGGGACTAA[A/C]ATAGAAATCAATGTA | 66722 |
rs30462210 | snp | A/T | 0.124444 | 0.216185 | intron-variant | Spag16 | Mm_Celera | 1:69937128 | TCTGCTTTCTCTGGG[A/T]TCAGTCATGTTTTCT | 66722 |
rs30462213 | snp | A/C/T | 0.124444 | 0.216185 | intron-variant | Spag16 | GRCm38.p3 | 1:69937231 | AAAGTTCCCTGGATA[A/C/T]GATAATGAAGCCCAT | 66722 |
rs30462285 | snp | A/G | 0.408163 | 0.193609 | upstream-variant-2KB, intron-variant | Spag16 | Mm_Celera | 1:69950839 | TGTAGGCACAGTGTG[A/G]TAGGGTCTTCATGGA | 66722 |
rs30462288 | snp | A/T | 0.444444 | 0.157135 | upstream-variant-2KB, intron-variant | Spag16 | Mm_Celera | 1:69951519 | GCTTTGGTTCTTGAC[A/T]GTATGGGCCTCTTTT | 66722 |
rs30462291 | snp | C/T | 0.408163 | 0.193609 | utr-variant-5-prime, intron-variant | Spag16 | Mm_Celera | 1:69951624 | TCAACCGCCTTTATT[C/T]CTCCCGGATGTTAAC | 66722 |
rs30462446 | snp | C/T | 0.231111 | 0.249285 | intron-variant | Spag16 | Mm_Celera | 1:69976727 | CCATTATGTTTGTCT[C/T]TCTTCACTTTGCTCT | 66722 |
rs30462449 | snp | C/T | 0.124444 | 0.216185 | intron-variant | Spag16 | Mm_Celera | 1:69976747 | CACTTTGCTCTCATC[C/T]TCAGACCCTTTGCAA | 66722 |
rs30462452 | snp | A/G | 0.124444 | 0.216185 | intron-variant | Spag16 | Mm_Celera | 1:69976818 | CCCTTAGCAACCCTG[A/G]ACTCTAGACTAGCAT | 66722 |
rs30462596 | snp | A/G | 0.32 | 0.24 | intron-variant | Spag16 | Mm_Celera | 1:69937383 | CAAGATGAAAGGGAA[A/G]ACTCAACAGAAATTC | 66722 |
rs30462599 | snp | G/T | 0.231111 | 0.249285 | intron-variant | Spag16 | Mm_Celera | 1:69938902 | TACATGCTCATAGAA[G/T]CTTGAAGACTTGAGT | 66722 |
rs30462602 | snp | A/T | 0.124444 | 0.216185 | intron-variant | Spag16 | Mm_Celera | 1:69938910 | CATAGAATCTTGAAG[A/T]CTTGAGTTAGGCAAA | 66722 |
rs30462866 | snp | A/G | 0.231111 | 0.249285 | intron-variant | Spag16 | Mm_Celera | 1:69927562 | AATATATTGAAATTA[A/G]AGAGCTTTGGTATCA | 66722 |
rs30462869 | snp | C/T | 0.444444 | 0.157135 | intron-variant | Spag16 | Mm_Celera | 1:69927802 | CATTTTCCTGTACTA[C/T]ATATGTCATCTTAGG | 66722 |
rs30462872 | snp | G/T | 0.231111 | 0.249285 | intron-variant | Spag16 | Mm_Celera | 1:69927838 | GAGATATTCCTGCTA[G/T]TGACATAACTTGACC | 66722 |
rs30463114 | snp | A/T | 0.444444 | 0.157135 | utr-variant-5-prime, intron-variant | Spag16 | Mm_Celera | 1:69951637 | TTTCTCCCGGATGTT[A/T]ACTCTGACACAATGA | 66722 |
rs30463117 | snp | G/T | 0.244898 | 0.249948 | utr-variant-5-prime, intron-variant | Spag16 | Mm_Celera | 1:69951755 | TGCTTTCCCAGAGAC[G/T]CACTTTCTGCCTGAG | 66722 |
rs30463120 | snp | C/T | 0.408163 | 0.193609 | intron-variant | Spag16 | Mm_Celera | 1:69951845 | GTGCTTATTGGGCTT[C/T]TGCCTCAGCCGGTCC | 66722 |
rs30463123 | snp | G/T | 0.32 | 0.24 | intron-variant | Spag16 | Mm_Celera | 1:69952954 | GATATAAGAGTGTAG[G/T]ACAATTTTAAGACTA | 66722 |
rs30463275 | snp | A/G | 0.375 | 0.216506 | intron-variant | Spag16 | Mm_Celera | 1:69976849 | TTGTTCTTTAAGAGG[A/G]ATCGAATGATTCTCT | 66722 |
rs30463278 | snp | A/G | 0.124444 | 0.216185 | intron-variant | Spag16 | Mm_Celera | 1:69977129 | TTGTTAGTATTTAAC[A/G]TGTATATGTGGGTTA | 66722 |
rs30463281 | snp | A/G | 0.345679 | 0.230967 | intron-variant | Spag16 | Mm_Celera | 1:69977168 | TAGCAATTATATTTA[A/G]TACTAATTACAGATA | 66722 |
rs30463375 | snp | C/T | 0.124444 | 0.216185 | intron-variant | Spag16 | Mm_Celera | 1:69938947 | TTCAATTTGTCTTGA[C/T]AGCAATGCTTTCCCC | 66722 |
rs30463378 | snp | A/G | 0.231111 | 0.249285 | intron-variant | Spag16 | Mm_Celera | 1:69938999 | CCTTTTGGATAGGCA[A/G]CCTGTGCATGGCTCT | 66722 |
rs30463381 | snp | C/T | 0.231111 | 0.249285 | intron-variant | Spag16 | Mm_Celera | 1:69939092 | CATATATTTTTATTG[C/T]GTATGATTTTAGGTA | 66722 |
rs30463383 | snp | A/G | 0.32 | 0.24 | intron-variant | Spag16 | Mm_Celera | 1:69939163 | TGGAGCTTCTAGCTC[A/G]AAATCTTCAGATGTG | 66722 |
rs30463575 | snp | C/T | 0.244898 | 0.249948 | intron-variant | Spag16 | Mm_Celera | 1:69927910 | AAACACTGAATTCTC[C/T]ATCATTTTGTACAAA | 66722 |
rs30463577 | snp | C/T | 0.231111 | 0.249285 | intron-variant | Spag16 | Mm_Celera | 1:69927960 | ATACACAATTTTTCT[C/T]TGCTTGCAATTATGT | 66722 |
rs30463580 | snp | A/G | 0.124444 | 0.216185 | intron-variant | Spag16 | Mm_Celera | 1:69928056 | ACCTGCGCATACAGT[A/G]TGCTTAAAATGATGG | 66722 |
rs30463583 | snp | A/G | 0.231111 | 0.249285 | intron-variant | Spag16 | Mm_Celera | 1:69928094 | GAACCAAGGGGAAGC[A/G]ATTCCTGAAGAAATA | 66722 |
rs30463786 | snp | C/T | 0.444444 | 0.157135 | intron-variant | Spag16 | Mm_Celera | 1:69952999 | CTGTGATGTCACACA[C/T]TGCTTCTAAGGAATT | 66722 |
rs30463789 | snp | C/T | 0.21875 | 0.248039 | intron-variant | Spag16 | Mm_Celera | 1:69953350 | TTTTAAATTAATCCT[C/T]TCAACCATGCTGAAC | 66722 |
rs30463792 | snp | C/T | 0.48 | 0.0979796 | intron-variant | Spag16 | Mm_Celera | 1:69953641 | GGAAAGTTATGTCAG[C/T]GCATCAATATATGAG | 66722 |
rs30463936 | snp | A/C | 0.32 | 0.24 | intron-variant | Spag16 | Mm_Celera | 1:69955610 | TTTATTTCTTTTCTG[A/C]TAGTGTATGACAGGC | 66722 |
rs30463939 | snp | A/C | 0.244898 | 0.249948 | intron-variant | Spag16 | Mm_Celera | 1:69955649 | TACTGATAAGCAGGT[A/C]ACTCACAGAGCAATT | 66722 |
rs30463942 | snp | A/G/T | 0.244898 | 0.249948 | intron-variant | Spag16 | Mm_Celera | 1:69955860 | TTGAGTTATCTTTCT[A/G/T]ATGTCTGCCTTTTGA | 66722 |
rs30464124 | snp | C/T | 0.231111 | 0.249285 | intron-variant | Spag16 | Mm_Celera | 1:69977253 | TTAAATGAAGTTAGT[C/T]TTGTCAATAGAGATG | 66722 |
rs30464127 | snp | A/G | 0.244898 | 0.249948 | intron-variant | Spag16 | Mm_Celera | 1:69977348 | ATTCTTGAGTAACTA[A/G]TATTTTATTACATTA | 66722 |
rs30464130 | snp | C/G | 0.124444 | 0.216185 | intron-variant | Spag16 | Mm_Celera | 1:69977487 | TTTATGATATGAAAT[C/G]GCCCACAATTATTTC | 66722 |
rs30464133 | snp | A/T | 0.231111 | 0.249285 | intron-variant | Spag16 | Mm_Celera | 1:69977495 | ATGAAATGGCCCACA[A/T]TTATTTCTTTCATCA | 66722 |
rs30464275 | snp | A/G | 0.132653 | 0.220748 | intron-variant | Spag16 | Mm_Celera | 1:69939229 | GGAGAGGGGAACAGC[A/G]GGATACAGGGGATGT | 66722 |
rs30464278 | snp | C/G | 0.124444 | 0.216185 | intron-variant | Spag16 | Mm_Celera | 1:69939306 | AAGAGAGACAAGGAA[C/G]AAGGTCGTTTGAAAA | 66722 |
rs30464376 | snp | C/T | 0.124444 | 0.216185 | intron-variant | Spag16 | Mm_Celera | 1:69991115 | GCTTAGCTTTCCTTG[C/T]ATTTGTACCTTGTCA | 66722 |
rs30464379 | snp | A/G | 0.124444 | 0.216185 | intron-variant | Spag16 | Mm_Celera | 1:69991156 | TTGGTGATGGCTAGG[A/G]ATAGTTGAAAGCTTT | 66722 |
rs30464382 | snp | C/T | 0.124444 | 0.216185 | intron-variant | Spag16 | Mm_Celera | 1:69991223 | AGAATTTTACATTGA[C/T]CTTCCTGATTCTTTG | 66722 |
rs30464384 | snp | C/T | 0.231111 | 0.249285 | intron-variant | Spag16 | Mm_Celera | 1:70004079 | CCCAGGCTTTTATTT[C/T]GCTTTTACCTAGTTG | 66722 |
rs30464387 | snp | G/T | 0.124444 | 0.216185 | intron-variant | Spag16 | Mm_Celera | 1:70004099 | TTACCTAGTTGATGA[G/T]ATGCACAGCAGTGCT | 66722 |
rs30464390 | snp | A/G | 0.32 | 0.24 | intron-variant | Spag16 | Mm_Celera | 1:70004404 | AATGCAAGAAACACT[A/G]CATAATATTTATATC | 66722 |
rs30464392 | snp | C/T | 0.391111 | 0.206368 | intron-variant | Spag16 | Mm_Celera | 1:70004500 | TTCATTTGCAGGCAG[C/T]TGGCATTTACTTGAG | 66722 |
rs30464504 | snp | A/G | 0.231111 | 0.249285 | intron-variant | Spag16 | Mm_Celera | 1:69979214 | AAGGAATGTCTTGGC[A/G]AAAGCTTTAAAACAT | 66722 |
rs30464507 | snp | C/T | 0.32 | 0.24 | intron-variant | Spag16 | Mm_Celera | 1:69979277 | TAAAAATGTAAAGAA[C/T]GATTAGTATTTTAGT | 66722 |
rs30464510 | snp | A/T | 0.231111 | 0.249285 | intron-variant | Spag16 | Mm_Celera | 1:69979303 | TTAGTAGCACTAAAT[A/T]AAAAAAAATGCTTGC | 66722 |
rs30464513 | snp | A/G | 0.391111 | 0.206368 | intron-variant | Spag16 | Mm_Celera | 1:69979350 | TTTCGAAAATGTGCC[A/G]CCTTTTTCTAACATC | 66722 |
rs30464556 | snp | C/T | 0.336735 | 0.234472 | intron-variant | Spag16 | Mm_Celera | 1:69929050 | AGAATAATATGCTTC[C/T]TATTTAAAAACCAAA | 66722 |
rs30464559 | snp | C/T | 0.231111 | 0.249285 | intron-variant | Spag16 | Mm_Celera | 1:69929113 | CAAAATGAATGCCAC[C/T]GAATTTGTGAGTGTA | 66722 |
rs30464685 | snp | A/G | 0.277778 | 0.248452 | intron-variant | Spag16 | Mm_Celera | 1:69953655 | GTGCATCAATATATG[A/G]GAAGGTTTTGCCAAT | 66722 |
rs30464688 | snp | G/T | 0.244898 | 0.249948 | intron-variant | Spag16 | Mm_Celera | 1:69953674 | GGTTTTGCCAATAAT[G/T]TCATAAGCACTACTC | 66722 |
rs30464691 | snp | C/T | 0.32 | 0.24 | intron-variant | Spag16 | Mm_Celera | 1:69953684 | ATAATGTCATAAGCA[C/T]TACTCTCATTAATAG | 66722 |
rs30464725 | snp | G/T | 0.124444 | 0.216185 | intron-variant | Spag16 | Mm_Celera | 1:70001131 | GCAGTTTACTAACCT[G/T]CATGAGGCTTAGGTT | 66722 |
rs30464728 | snp | C/T | 0.124444 | 0.216185 | intron-variant | Spag16 | Mm_Celera | 1:70001182 | TATTGATTTATTGTA[C/T]GCTTTTTAAGGTAAG | 66722 |
rs30464731 | snp | G/T | 0.32 | 0.24 | intron-variant | Spag16 | Mm_Celera | 1:70001232 | AAGGGTTAATTTTGC[G/T]TTTGTTTGTCAATAT | 66722 |
rs30464944 | snp | A/C | 0.277778 | 0.248452 | intron-variant | Spag16 | Mm_Celera | 1:69956086 | CAAGCATATGCTCCT[A/C]ATGGATATCTTCAGA | 66722 |
rs30464947 | snp | A/T | 0.48 | 0.0979796 | intron-variant | Spag16 | Mm_Celera | 1:69956355 | ACATTTACTAAGGAA[A/T]GTGTCATAAATTGAA | 66722 |
rs30464950 | snp | A/G | 0.32 | 0.24 | intron-variant | Spag16 | Mm_Celera | 1:69956511 | TTATATTTTTCCTGT[A/G]CTTCCATTTTATTTA | 66722 |
rs30464953 | snp | G/T | 0.277778 | 0.248452 | intron-variant | Spag16 | Mm_Celera | 1:69956578 | TATGTGATAATGCTA[G/T]TCCTAAAGAAAACAA | 66722 |
rs30465036 | snp | A/G | 0.231111 | 0.249285 | intron-variant | Spag16 | Mm_Celera | 1:69977578 | AGCCAGGTGTGCTGA[A/G]TTTTGAAACCTGGGT | 66722 |
rs30465039 | snp | A/G | 0.124444 | 0.216185 | intron-variant | Spag16 | Mm_Celera | 1:69977664 | GGCAAAAGAACTGGT[A/G]GAAGCAGGCCATTGA | 66722 |
rs30465042 | snp | C/T | 0.231111 | 0.249285 | intron-variant | Spag16 | Mm_Celera | 1:69977673 | ACTGGTGGAAGCAGG[C/T]CATTGACTGGCATAG | 66722 |
rs30465295 | snp | A/T | 0.124444 | 0.216185 | intron-variant | Spag16 | Mm_Celera | 1:69991351 | TATCTAGGTCTTCTC[A/T]TGGTTGTTTTTGTAA | 66722 |
rs30465298 | snp | C/T | 0.142012 | 0.225474 | intron-variant | Spag16 | Mm_Celera | 1:69991690 | CTTTCAGTGTTAACA[C/T]AGCAATATGCATGTG | 66722 |
rs30465301 | snp | C/T | 0.391111 | 0.206368 | intron-variant | Spag16 | Mm_Celera | 1:69991844 | AATTATTTATACTTC[C/T]GAAAGTGTGTATGTG | 66722 |
rs30465306 | snp | A/C | 0.124444 | 0.216185 | intron-variant | Spag16 | Mm_Celera | 1:69979393 | AATGTAAACATAAAT[A/C]AAGGTCAAGAGGGCA | 66722 |
rs30465309 | snp | A/G | 0.391111 | 0.206368 | intron-variant | Spag16 | Mm_Celera | 1:69979405 | AATAAAGGTCAAGAG[A/G]GCAAACAAATGTATA | 66722 |
rs30465312 | snp | C/T | 0.124444 | 0.216185 | intron-variant | Spag16 | Mm_Celera | 1:69979423 | AAACAAATGTATAAG[C/T]AATGCTTTTTCTGGC | 66722 |
rs30465325 | snp | A/T | 0.391111 | 0.206368 | intron-variant | Spag16 | Mm_Celera | 1:70004665 | TGAAAAGACAGCATG[A/T]AGCAGAGATCCTGCA | 66722 |
rs30465328 | snp | C/G | 0.142012 | 0.225474 | intron-variant | Spag16 | Mm_Celera | 1:70004772 | CCCAGTATCCCAGGG[C/G]AAACAGGTAATGCAG | 66722 |
rs30465331 | snp | G/T | 0.124444 | 0.216185 | intron-variant | Spag16 | Mm_Celera | 1:70004827 | AGACTCAGCAGAGAC[G/T]TGTTAGGAAGTTGAA | 66722 |
rs30465333 | snp | A/G | 0.124444 | 0.216185 | intron-variant | Spag16 | Mm_Celera | 1:70004904 | CTTTCTTTTGTAACC[A/G]GGAAATGTTGGAAAT | 66722 |
rs30465564 | snp | A/G | 0.32 | 0.24 | intron-variant | Spag16 | Mm_Celera | 1:69953831 | TCTTTAGGTGGCTGT[A/G]AATGTTTTCAGACCA | 66722 |
rs30465567 | snp | C/T | 0.375 | 0.216506 | intron-variant | Spag16 | Mm_Celera | 1:69953863 | AGAGTACTCTAACAT[C/T]TTTCTATCCCTAAAA | 66722 |
rs30465570 | snp | C/T | 0.244898 | 0.249948 | intron-variant | Spag16 | Mm_Celera | 1:69953889 | TAAAATTCGAGGACA[C/T]CCCTTCCACATTAAT | 66722 |
rs30465573 | snp | A/C | 0.244898 | 0.249948 | intron-variant | Spag16 | Mm_Celera | 1:69953953 | TCTTGGTGCTCTAGA[A/C]GTTTCTTTCTATTTT | 66722 |
rs30465604 | snp | A/T | 0.231111 | 0.249285 | intron-variant | Spag16 | Mm_Celera | 1:70001255 | GTCAATATCAGTGGG[A/T]CATGTTCTTAAGCTA | 66722 |
rs30465607 | snp | A/C/T | 0.142012 | 0.225474 | intron-variant | Spag16 | GRCm38.p3 | 1:70001260 | TATCAGTGGGACATG[A/C/T]TCTTAAGCTATAGTT | 66722 |
rs30465610 | snp | A/G | 0.32 | 0.24 | intron-variant | Spag16 | Mm_Celera | 1:70001298 | TCCAACAGTAGTAGT[A/G]TGGCCATTAATACTG | 66722 |
rs30465613 | snp | C/T | 0.336735 | 0.234472 | intron-variant | Spag16 | Mm_Celera | 1:70001389 | CACCTTCCTAATATA[C/T]ACTATCTCTGGTCAT | 66722 |
rs30465875 | snp | A/T | 0.260355 | 0.249785 | intron-variant | Spag16 | Mm_Celera | 1:69977679 | GGAAGCAGGCCATTG[A/T]CTGGCATAGGCCACA | 66722 |
rs30465878 | snp | A/C | 0.231111 | 0.249285 | intron-variant | Spag16 | Mm_Celera | 1:69977768 | TACTAGGGCATTAAC[A/C]AGAGGAACTTTCCAT | 66722 |
rs30465881 | snp | A/G | 0.231111 | 0.249285 | intron-variant | Spag16 | Mm_Celera | 1:69977804 | CTGATGTTGACAGAT[A/G]GAAGTCAGTTTCCAA | 66722 |
rs30465916 | snp | A/T | 0.375 | 0.216506 | intron-variant | Spag16 | Mm_Celera | 1:69956650 | AACATTGTCATAATT[A/T]AAAAATTGAGCAACT | 66722 |
rs30465919 | snp | A/G | 0.21875 | 0.248039 | intron-variant | Spag16 | Mm_Celera | 1:69956779 | TTATTTTTCGATTTG[A/G]AAGCCTGCCAACTGG | 66722 |
rs30465922 | snp | A/G | 0.244898 | 0.249948 | intron-variant | Spag16 | Mm_Celera | 1:69956813 | CTTTATTAGGCATCC[A/G]GGGCAACTGACAAGT | 66722 |
rs30466115 | snp | C/T | 0.124444 | 0.216185 | intron-variant | Spag16 | Mm_Celera | 1:69979490 | TTAGCTCAAGCAAGT[C/T]TAGCTGATAATGTCA | 66722 |
rs30466118 | snp | C/G | 0.231111 | 0.249285 | intron-variant | Spag16 | Mm_Celera | 1:69979493 | GCTCAAGCAAGTCTA[C/G]CTGATAATGTCAGCT | 66722 |
rs30466121 | snp | G/T | 0.231111 | 0.249285 | intron-variant | Spag16 | Mm_Celera | 1:69979588 | AAGGAAATAATGAGG[G/T]CACAGAAACCTCAGA | 66722 |
rs30466315 | snp | A/G | 0.124444 | 0.216185 | intron-variant | Spag16 | Mm_Celera | 1:70005832 | CCAGGTGTTGTCCTG[A/G]CACTTTCATCAGAAA | 66722 |
rs30466318 | snp | C/T | 0.124444 | 0.216185 | intron-variant | Spag16 | Mm_Celera | 1:70005867 | GTATCTGCCATTTCC[C/T]GTAAAAAGAAAAAAA | 66722 |
rs30466321 | snp | A/G | 0.444444 | 0.157135 | intron-variant | Spag16 | Mm_Celera | 1:70005958 | ATGAGTTATTAAACC[A/G]TGAAACAATATAAAG | 66722 |
rs30466344 | snp | C/G | 0.124444 | 0.216185 | intron-variant | Spag16 | Mm_Celera | 1:69991926 | TAGTAGCATTGAATA[C/G]CACAAAAGATACAAA | 66722 |
rs30466347 | snp | G/T | 0.408163 | 0.193609 | intron-variant | Spag16 | Mm_Celera | 1:69991936 | GAATACCACAAAAGA[G/T]ACAAAAATAATAGAA | 66722 |
rs30466350 | snp | A/T | 0.124444 | 0.216185 | intron-variant | Spag16 | Mm_Celera | 1:69995664 | GAATGATTTTCAAAA[A/T]GAAAGCAAACCATGG | 66722 |
rs30466353 | snp | G/T | 0.231111 | 0.249285 | intron-variant | Spag16 | Mm_Celera | 1:69995712 | CTAAGGTGAAGAAAA[G/T]AAATTAAATAGTTCT | 66722 |
rs30466416 | snp | A/T | 0.32 | 0.24 | intron-variant | Spag16 | Mm_Celera | 1:69954147 | AAAATGGCAGTCTAT[A/T]GATATATTTTGATTG | 66722 |
rs30466419 | snp | A/G | 0.46875 | 0.121031 | intron-variant | Spag16 | Mm_Celera | 1:69955027 | GTGGTTAGATGCCAC[A/G]AAGTAGGTAGCAATG | 66722 |
rs30466422 | snp | A/G | 0.277778 | 0.248452 | intron-variant | Spag16 | Mm_Celera | 1:69955095 | TTCCATCCTTGTCAA[A/G]GGAAGTGCTAACCTT | 66722 |
rs30466566 | snp | C/T | 0.32 | 0.24 | intron-variant | Spag16 | Mm_Celera | 1:70001424 | CAGTTATCTTCTCTC[C/T]GTTTTTAGCAGACAC | 66722 |
rs30466569 | snp | A/G | 0.244898 | 0.249948 | intron-variant | Spag16 | Mm_Celera | 1:70001452 | CACAGATAAACAGAT[A/G]ACACACACACATGGA | 66722 |
rs30466572 | snp | A/G | 0.231111 | 0.249285 | intron-variant | Spag16 | Mm_Celera | 1:70001552 | AATATAGTTTAAGAT[A/G]AAAGAAAAGACTAAA | 66722 |
rs30466714 | snp | C/T | 0.124444 | 0.216185 | intron-variant | Spag16 | Mm_Celera | 1:69977909 | ATATTTTAAGATGCC[C/T]ACTATGGTGTTGCTT | 66722 |
rs30466717 | snp | C/T | 0.391111 | 0.206368 | intron-variant | Spag16 | Mm_Celera | 1:69978047 | CATTGCCAGCCCTAT[C/T]AATCTGCCTTCTCTC | 66722 |
rs30466720 | snp | A/G | 0.124444 | 0.216185 | intron-variant | Spag16 | Mm_Celera | 1:69978107 | TAGGCTCTATTTTTG[A/G]CCTATTTAGTTTAAC | 66722 |
rs30466723 | snp | A/G | 0.231111 | 0.249285 | intron-variant | Spag16 | Mm_Celera | 1:69978134 | TAACCAAGCTTACCA[A/G]TGTAACCAATGGATA | 66722 |
rs30466895 | snp | A/C | 0.244898 | 0.249948 | intron-variant | Spag16 | Mm_Celera | 1:69956817 | ATTAGGCATCCAGGG[A/C]AACTGACAAGTCACT | 66722 |
rs30466898 | snp | C/T | 0.277778 | 0.248452 | intron-variant | Spag16 | Mm_Celera | 1:69956836 | TGACAAGTCACTCCA[C/T]GGGGAGCTGTTTGCT | 66722 |
rs30466901 | snp | G/T | 0.32 | 0.24 | intron-variant | Spag16 | Mm_Celera | 1:69957030 | GAGAAATTAATAAAA[G/T]CTTGGGACATCTTTA | 66722 |
rs30466994 | snp | A/G | 0.124444 | 0.216185 | intron-variant | Spag16 | Mm_Celera | 1:69979661 | TAATAAAAGAAAAGA[A/G]ATGTCTCATTAAAAT | 66722 |
rs30466997 | snp | C/T | 0.231111 | 0.249285 | intron-variant | Spag16 | Mm_Celera | 1:69979695 | TTTCAATTTAGTTCA[C/T]TTTTAATAAATTATA | 66722 |
rs30467000 | snp | C/T | 0.231111 | 0.249285 | intron-variant | Spag16 | Mm_Celera | 1:69980141 | GTCTTCATTATTGTT[C/T]CATCCTTCTTTTGAC | 66722 |
rs30467003 | snp | C/T | 0.231111 | 0.249285 | intron-variant | Spag16 | Mm_Celera | 1:69980146 | CATTATTGTTCCATC[C/T]TTCTTTTGACTTTTA | 66722 |
rs30467154 | snp | A/T | 0.132653 | 0.220748 | intron-variant | Spag16 | Mm_Celera | 1:70006188 | AAAAAGAGAAAAAAA[A/T]GTACTCATAATTCCT | 66722 |
rs30467157 | snp | A/C | 0.124444 | 0.216185 | intron-variant | Spag16 | Mm_Celera | 1:70006277 | TTTTAACATTTGATA[A/C]CCAAGTGCTAAGGTG | 66722 |
rs30467160 | snp | A/T | 0.391111 | 0.206368 | intron-variant | Spag16 | Mm_Celera | 1:70006294 | CAAGTGCTAAGGTGT[A/T]AGGTAGGTCCCATTA | 66722 |
rs30467163 | snp | C/T | 0.244898 | 0.249948 | intron-variant | Spag16 | Mm_Celera | 1:70006631 | TCTCTCTCTCTCTCT[C/T]GGTTAACTTACAGCT | 66722 |
rs30467265 | snp | C/G/T | 0.277778 | 0.248452 | intron-variant | Spag16 | GRCm38.p3 | 1:69955124 | TTCTCTCCTTTCACA[C/G/T]GACACTAAAGTTCAT | 66722 |
rs30467268 | snp | C/T | 0.277778 | 0.248452 | intron-variant | Spag16 | Mm_Celera | 1:69955202 | CATGTACAATTCATT[C/T]TAACTATCAGAACAT | 66722 |
rs30467271 | snp | A/C | 0.32 | 0.24 | intron-variant | Spag16 | Mm_Celera | 1:69955211 | TTCATTCTAACTATC[A/C]GAACATGCATACCTC | 66722 |
rs30467306 | snp | A/C | 0.391111 | 0.206368 | intron-variant | Spag16 | Mm_Celera | 1:69996035 | AAAAAGTTTGAGTAT[A/C]AAAACAAATATATGG | 66722 |
rs30467309 | snp | A/T | 0.124444 | 0.216185 | utr-variant-5-prime, synonymous-codon | Spag16 | Mm_Celera | 1:69996795 | GGATTCAGAATTTCC[A/T]GTAGATATGCAACCA | 66722 |
rs30467312 | snp | A/G | 0.231111 | 0.249285 | intron-variant | Spag16 | Mm_Celera | 1:69996966 | CCTGTCTAAACTGTG[A/G]TGTTCTCTTAACTAT | 66722 |
rs30467388 | snp | C/T | 0.444444 | 0.157135 | intron-variant | Spag16 | Mm_Celera | 1:70009939 | CAAGGAAACTTCATT[C/T]ACAATGGTCAACAAT | 66722 |
rs30467391 | snp | C/T | 0.35503 | 0.226867 | intron-variant | Spag16 | Mm_Celera | 1:70010304 | TATTTTTCCATTTTA[C/T]ATTTCTATTGCAGCT | 66722 |
rs30467445 | snp | C/T | 0.231111 | 0.249285 | intron-variant | Spag16 | Mm_Celera | 1:70001563 | AGATGAAAGAAAAGA[C/T]TAAACCCACAATTGT | 66722 |
rs30467448 | snp | A/T | 0.231111 | 0.249285 | intron-variant | Spag16 | Mm_Celera | 1:70001675 | TTTAGGGTAAAATCC[A/T]ATTTTTCTCTCTTGA | 66722 |
rs30467451 | snp | C/G | 0.231111 | 0.249285 | intron-variant | Spag16 | Mm_Celera | 1:70001705 | AGAATCATGACCTAG[C/G]ATAATTGCTTTATAG | 66722 |
rs30467596 | snp | A/G | 0.495868 | 0.0452663 | intron-variant | Spag16 | Mm_Celera | 1:69978953 | ATAAGTATTTCTTAA[A/G]ATAATAATTCCTTTT | 66722 |
rs30467599 | snp | C/T | 0.231111 | 0.249285 | intron-variant | Spag16 | Mm_Celera | 1:69978979 | CTTTTATGAAAATTG[C/T]TATAAATATTAAGTA | 66722 |
rs30467602 | snp | C/T | 0.231111 | 0.249285 | intron-variant | Spag16 | Mm_Celera | 1:69979120 | GACAAAGTTGTACAG[C/T]TTTCAAGTATAGTTT | 66722 |
rs30467836 | snp | C/T | 0.231111 | 0.249285 | intron-variant | Spag16 | Mm_Celera | 1:69980175 | TATCTACTTATCCAC[C/T]CATCTATGTATCAAA | 66722 |
rs30467839 | snp | A/C | 0.231111 | 0.249285 | intron-variant | Spag16 | Mm_Celera | 1:69980188 | ACCCATCTATGTATC[A/C]AACCATCCATCTTTA | 66722 |
rs30467842 | snp | A/G | 0.231111 | 0.249285 | intron-variant | Spag16 | Mm_Celera | 1:69980237 | AAGTACCATTAATAA[A/G]ATTACATCAACTCAG | 66722 |
rs30467864 | snp | A/G | 0.32 | 0.24 | intron-variant | Spag16 | Mm_Celera | 1:69957098 | TCTTAAACATATTAC[A/G]TCCTTTATTGATAAA | 66722 |
rs30467867 | snp | A/G | 0.244898 | 0.249948 | intron-variant | Spag16 | Mm_Celera | 1:69957504 | TCATATTTTCAAAAG[A/G]GCAGCTTTATCTAAG | 66722 |
rs30467870 | snp | A/G | 0.244898 | 0.249948 | intron-variant | Spag16 | Mm_Celera | 1:69957825 | ACTTTAAGTAACTCA[A/G]CTGAGCAAAGCGTAT | 66722 |
rs30467873 | snp | A/G | 0.489796 | 0.070696 | intron-variant | Spag16 | Mm_Celera | 1:69957873 | GCCACTGTTGGGCTA[A/G]CAATGGGGTTTTGCT | 66722 |
rs30467966 | snp | C/T | 0.132653 | 0.220748 | intron-variant | Spag16 | Mm_Celera | 1:70006884 | CAACAATGCATAAAA[C/T]CCTACTTATTAACTA | 66722 |
rs30467969 | snp | G/T | 0.124444 | 0.216185 | intron-variant | Spag16 | Mm_Celera | 1:70006966 | TTTTGAAAAGCCAAG[G/T]CATTTAATTTGTGCA | 66722 |
rs30467972 | snp | C/T | 0.124444 | 0.216185 | intron-variant | Spag16 | Mm_Celera | 1:70007161 | AAATGGAGTTCAAAG[C/T]GAAGGTGACCCAGAT | 66722 |
rs30468044 | snp | C/T | 0.408163 | 0.193609 | intron-variant | Spag16 | Mm_Celera | 1:69955289 | CATCTCACTTCCTTT[C/T]GTTTCTTTAAGTTGA | 66722 |
rs30468047 | snp | C/T | 0.444444 | 0.157135 | intron-variant | Spag16 | Mm_Celera | 1:69955376 | CCATATTCAAGCCTT[C/T]GCTACAGGTCAGATC | 66722 |
rs30468050 | snp | A/G | 0.444444 | 0.157135 | intron-variant | Spag16 | Mm_Celera | 1:69955389 | TTTGCTACAGGTCAG[A/G]TCCACCTTCTCTGTG | 66722 |
rs30468052 | snp | G/T | 0.244898 | 0.249948 | intron-variant | Spag16 | Mm_Celera | 1:69955490 | TATTCCTCCATTTTG[G/T]TTCTTTCCATAGAAG | 66722 |
rs30468144 | snp | C/T | 0.124444 | 0.216185 | intron-variant | Spag16 | Mm_Celera | 1:70012580 | TCACTTTCACATTCT[C/T]AGCTTTGGAATCATG | 66722 |
rs30468147 | snp | A/G | 0.124444 | 0.216185 | intron-variant | Spag16 | Mm_Celera | 1:70012603 | GAATCATGGTAAAGA[A/G]GACATTGGCTGGGAC | 66722 |
rs30468150 | snp | C/G | 0.124444 | 0.216185 | intron-variant | Spag16 | Mm_Celera | 1:70012777 | AATTAGACACTCTGG[C/G]TGAAGGACCTTCAAA | 66722 |
rs30468152 | snp | A/G | 0.124444 | 0.216185 | intron-variant | Spag16 | Mm_Celera | 1:70012794 | GAAGGACCTTCAAAG[A/G]ATACCCACTGTCCTC | 66722 |
rs30468165 | snp | A/G | 0.124444 | 0.216185 | intron-variant | Spag16 | Mm_Celera | 1:69997010 | GATCTGTGAAAATAG[A/G]TGCTTTAGCTTCTCA | 66722 |
rs30468168 | snp | A/G | 0.444444 | 0.157135 | intron-variant | Spag16 | Mm_Celera | 1:69997160 | AACTTACAAGAACAC[A/G]CATGGATTTAAGAGA | 66722 |
rs30468171 | snp | G/T | 0.231111 | 0.249285 | intron-variant | Spag16 | Mm_Celera | 1:69997464 | TATTTTTCTTTTAGA[G/T]AAGAATGTTTCTGTC | 66722 |
rs30468225 | snp | A/T | 0.124444 | 0.216185 | intron-variant | Spag16 | Mm_Celera | 1:69979150 | TATGGCTATCTCCTT[A/T]ATTTTTGTTCCCTTT | 66722 |
rs30468228 | snp | G/T | 0.124444 | 0.216185 | intron-variant | Spag16 | Mm_Celera | 1:69979169 | TTTGTTCCCTTTTTT[G/T]CCTCAGCCTGGTTTG | 66722 |
rs30468230 | snp | C/T | 0.124444 | 0.216185 | intron-variant | Spag16 | Mm_Celera | 1:69979213 | TAAGGAATGTCTTGG[C/T]GAAAGCTTTAAAACA | 66722 |
rs30468274 | snp | A/G | 0.231111 | 0.249285 | intron-variant | Spag16 | Mm_Celera | 1:70001923 | AGTGCAATTACATAG[A/G]TCAAAAATCCAGAAG | 66722 |
rs30468277 | snp | A/C | 0.124444 | 0.216185 | intron-variant | Spag16 | Mm_Celera | 1:70002185 | TCTTGCCATTCTCCA[A/C]CACTGGAGATCCTAT | 66722 |
rs30468280 | snp | A/C/T | 0.231111 | 0.249285 | intron-variant | Spag16 | GRCm38.p3 | 1:70002220 | ATTGGTTCCTTGATG[A/C/T]GCTATCATGACAAGA | 66722 |
rs30468283 | snp | C/G | 0.231111 | 0.249285 | intron-variant | Spag16 | Mm_Celera | 1:70002661 | GTTTTTAATAACCTA[C/G]CAGTGGTCTGGGCCA | 66722 |
rs30468456 | snp | C/T | 0.444444 | 0.157135 | intron-variant | Spag16 | Mm_Celera | 1:69957976 | CCAAGAACTGGCACA[C/T]TTGTTCTGGTGTCTC | 66722 |
rs30468458 | snp | C/T | 0.444444 | 0.157135 | intron-variant | Spag16 | Mm_Celera | 1:69958016 | GACCAGAGGTACTCC[C/T]ATGTTTTTGGCAATT | 66722 |
rs30468460 | snp | G/T | 0.48 | 0.0979796 | intron-variant | Spag16 | Mm_Celera | 1:69958030 | CCATGTTTTTGGCAA[G/T]TAATGAGGTAAATCA | 66722 |
rs30468463 | snp | C/G | 0.48 | 0.0979796 | intron-variant | Spag16 | Mm_Celera | 1:69958161 | CTGGGTCAATATGGT[C/G]AAGAATTAGATTATA | 66722 |
rs30468675 | snp | C/T | 0.231111 | 0.249285 | intron-variant | Spag16 | Mm_Celera | 1:69980350 | CTTATCTCTTCACCT[C/T]AATATTCTGTACATA | 66722 |
rs30468678 | snp | A/G | 0.231111 | 0.249285 | intron-variant | Spag16 | Mm_Celera | 1:69980370 | TTCTGTACATATTTG[A/G]CCTCTAGCTTTTAAA | 66722 |
rs30468681 | snp | A/G | 0.231111 | 0.249285 | intron-variant | Spag16 | Mm_Celera | 1:69980420 | TTTGTGTAGGTGCAC[A/G]TGTGTGTGCTGGTAT | 66722 |
rs30468755 | snp | A/G | 0.391111 | 0.206368 | intron-variant | Spag16 | Mm_Celera | 1:70007234 | CTTTTCCTCGTGAAC[A/G]ATTTGCTTATTTTTG | 66722 |
rs30468758 | snp | A/G | 0.32 | 0.24 | intron-variant | Spag16 | Mm_Celera | 1:70007285 | TGTTTAAATAATTAG[A/G]AACACTATATGACAT | 66722 |
rs30468761 | snp | A/T | 0.124444 | 0.216185 | intron-variant | Spag16 | Mm_Celera | 1:70007683 | AAATAGCCCATTTTA[A/T]CTTGCATACATGTGA | 66722 |
rs30468815 | snp | G/T | 0.124444 | 0.216185 | intron-variant | Spag16 | Mm_Celera | 1:70012861 | GTCTTACCTGGTTGT[G/T]GCTTCTTTAACTCTT | 66722 |
rs30468818 | snp | A/C | 0.124444 | 0.216185 | intron-variant | Spag16 | Mm_Celera | 1:70013220 | ACCAGACTTTTCACT[A/C]TAGTGTTCTGGTGTG | 66722 |
rs30468821 | snp | A/G | 0.124444 | 0.216185 | intron-variant | Spag16 | Mm_Celera | 1:70013246 | GTGTGCATAATGACA[A/G]CGTGGGTGGCTCTGA | 66722 |
rs30468904 | snp | C/T | 0.260355 | 0.249785 | intron-variant | Spag16 | Mm_Celera | 1:69997474 | TTAGAGAAGAATGTT[C/T]CTGTCAGTAATTTAT | 66722 |
rs30468907 | snp | C/T | 0.231111 | 0.249285 | intron-variant | Spag16 | Mm_Celera | 1:69998409 | TTTTCACATATTTAA[C/T]TTATACTTCATCGGT | 66722 |
rs30468910 | snp | A/G | 0.124444 | 0.216185 | intron-variant | Spag16 | Mm_Celera | 1:69998522 | AGCCCAGGCAATGGT[A/G]AGAATATGCAGATTT | 66722 |
rs30468913 | snp | G/T | 0.231111 | 0.249285 | intron-variant | Spag16 | Mm_Celera | 1:69998530 | CAATGGTGAGAATAT[G/T]CAGATTTGATTTGAT | 66722 |
rs30469044 | snp | A/G | 0.132653 | 0.220748 | intron-variant | Spag16 | Mm_Celera | 1:70024834 | GGAGACATTTCATTT[A/G]AGTGGGCACCCATGA | 66722 |
rs30469047 | snp | G/T | 0.336735 | 0.234472 | intron-variant | Spag16 | Mm_Celera | 1:70025184 | CTTCCAGTCATGGAA[G/T]AGAAGTCTTTCTTGA | 66722 |
rs30469050 | snp | A/G | 0.124444 | 0.216185 | intron-variant | Spag16 | Mm_Celera | 1:70025234 | CACTTTGTGGTAGAG[A/G]ACTGAGCATCTGAAC | 66722 |
rs30469053 | snp | G/T | 0.124444 | 0.216185 | intron-variant | Spag16 | Mm_Celera | 1:70025290 | TAGAGTCAGGAAGGA[G/T]ATATCAGACTAGTAT | 66722 |
rs30469065 | snp | A/G | 0.32 | 0.24 | intron-variant | Spag16 | Mm_Celera | 1:70017353 | GGCTACTAATCCAGG[A/G]TCAGGTGTAAATTTC | 66722 |
rs30469068 | snp | G/T | 0.32 | 0.24 | intron-variant | Spag16 | Mm_Celera | 1:70017782 | CCTCACTGAATATTT[G/T]CTACCACCTGTTTTC | 66722 |
rs30469071 | snp | A/T | 0.124444 | 0.216185 | intron-variant | Spag16 | Mm_Celera | 1:70018059 | GCTTTGGTAGTTTAA[A/T]TGGTAAGTAAAAATA | 66722 |
rs30469086 | snp | A/G | 0.142012 | 0.225474 | intron-variant | Spag16 | Mm_Celera | 1:70028784 | AAATGTACTCCACCT[A/G]TGTTCACACACCTAG | 66722 |
rs30469089 | snp | C/T | 0.32 | 0.24 | intron-variant | Spag16 | Mm_Celera | 1:70028890 | ACTTTGACGTGCACA[C/T]TTTGCTGCTGATTTA | 66722 |
rs30469092 | snp | A/C | 0.152778 | 0.230321 | intron-variant | Spag16 | Mm_Celera | 1:70028936 | ATATAAAGGGAATCC[A/C]TCCCTTCAAAGTGCT | 66722 |
rs30469095 | snp | A/T | 0.231111 | 0.249285 | intron-variant | Spag16 | Mm_Celera | 1:70031117 | ATTCTTAATTTAAAG[A/T]GCTTGTTTTAGCCCA | 66722 |
rs30469098 | snp | C/T | 0.124444 | 0.216185 | intron-variant | Spag16 | Mm_Celera | 1:70031126 | TTAAAGTGCTTGTTT[C/T]AGCCCACTCTCTGTG | 66722 |
rs30469101 | snp | A/G | 0.142012 | 0.225474 | intron-variant | Spag16 | Mm_Celera | 1:70031510 | AGTGTAAGGTCAAAA[A/G]CCAACAAAAGGGTTA | 66722 |
rs30469126 | snp | A/G | 0.231111 | 0.249285 | intron-variant | Spag16 | Mm_Celera | 1:70002680 | TGGTCTGGGCCACTC[A/G]TAGCTTCTCACTTTC | 66722 |
rs30469129 | snp | C/T | 0.231111 | 0.249285 | intron-variant | Spag16 | Mm_Celera | 1:70002698 | GCTTCTCACTTTCTT[C/T]ACCAGTCAGGTACTG | 66722 |
rs30469132 | snp | C/T | 0.408163 | 0.193609 | intron-variant | Spag16 | Mm_Celera | 1:70002786 | TCCTGGATTTCCTCT[C/T]GACTTCCATGTTCCT | 66722 |
rs30469305 | snp | A/G | 0.32 | 0.24 | intron-variant | Spag16 | Mm_Celera | 1:69958649 | CTTTTATTAACATGT[A/G]AAATTAGAATGAATG | 66722 |
rs30469308 | snp | C/T | 0.444444 | 0.157135 | intron-variant | Spag16 | Mm_Celera | 1:69961076 | TTTTTTCTGGTTTTG[C/T]TGATTTTTTTAAATT | 66722 |
rs30469311 | snp | A/C | 0.124444 | 0.216185 | intron-variant | Spag16 | Mm_Celera | 1:69975203 | ATTTCTGCTTTCTCT[A/C]ATTTCTTATATGATG | 66722 |
rs30469355 | snp | C/T | 0.124444 | 0.216185 | intron-variant | Spag16 | Mm_Celera | 1:70048099 | CATGAAACTACACAC[C/T]GACAACTGGAAAAGT | 66722 |
rs30469358 | snp | A/T | 0.336735 | 0.234472 | intron-variant | Spag16 | Mm_Celera | 1:70048244 | TCCTCTCAAAATCAC[A/T]GTTTGGTGAGGAAAG | 66722 |
rs30469361 | snp | G/T | 0.396694 | 0.202437 | intron-variant | Spag16 | Mm_Celera | 1:70048330 | TGCTAATTTTCAGAT[G/T]TTTTTTTTCATCTGC | 66722 |
rs30469376 | snp | C/G | 0.32 | 0.24 | intron-variant | Spag16 | Mm_Celera | 1:70043812 | TCAGTGATAAAATTA[C/G]AAGTCAGAGAAGTAT | 66722 |
rs30469379 | snp | C/T | 0.35503 | 0.226867 | intron-variant | Spag16 | Mm_Celera | 1:70044043 | TGTTGGTTAATACTA[C/T]GAAAACACAACAGAT | 66722 |
rs30469382 | snp | C/T | 0.32 | 0.24 | intron-variant | Spag16 | Mm_Celera | 1:70044234 | GAGTCATAATTACCT[C/T]GCCAGCCGTTTCTCT | 66722 |
rs30469385 | snp | A/G | 0.142012 | 0.225474 | intron-variant | Spag16 | Mm_Celera | 1:70063630 | TGTTGACAGTTCCTG[A/G]AAATTCGTTTCCTAG | 66722 |
rs30469388 | snp | A/C | 0.142012 | 0.225474 | intron-variant | Spag16 | Mm_Celera | 1:70063719 | AAGTTCTTTGGTTGT[A/C]GTCTATTGCTGGAGA | 66722 |
rs30469390 | snp | C/G | 0.142012 | 0.225474 | intron-variant | Spag16 | Mm_Celera | 1:70063766 | GCTTGTGGTGAACAT[C/G]CTATTCTGTGCCCTC | 66722 |
rs30469393 | snp | C/G | 0.142012 | 0.225474 | intron-variant | Spag16 | Mm_Celera | 1:70063788 | TGTGCCCTCCAGAAT[C/G]CTCACTCACTTTTGC | 66722 |
rs30469394 | snp | A/C | 0.444444 | 0.157135 | intron-variant | Spag16 | Mm_Celera | 1:70036527 | AATGTGAAGTAAATA[A/C]ATTAATTAGCGAAAA | 66722 |
rs30469397 | snp | C/T | 0.231111 | 0.249285 | intron-variant | Spag16 | Mm_Celera | 1:70036735 | AAATTACTTGAAATA[C/T]TTGGATGATATCGTC | 66722 |
rs30469399 | snp | A/G/T | 0.231111 | 0.249285 | intron-variant | Spag16 | GRCm38.p3 | 1:70036775 | CACAGTAACTCGGTG[A/G/T]CTTCCCTGTTCCAAA | 66722 |
rs30469402 | snp | A/T | 0.231111 | 0.249285 | intron-variant | Spag16 | Mm_Celera | 1:70036861 | CTTGGGACCTCATAT[A/T]AAGTTTGCACACAGA | 66722 |
rs30469404 | snp | C/T | 0.244898 | 0.249948 | intron-variant | Spag16 | Mm_Celera | 1:70052588 | GCTTTTTTCTTTCAG[C/T]ACTAAAATTGACTTC | 66722 |
rs30469407 | snp | A/C | 0.165289 | 0.235211 | intron-variant | Spag16 | Mm_Celera | 1:70052740 | TTTGAATTACTGTTT[A/C]CTCTCATATAGTGTA | 66722 |
rs30469410 | snp | A/G | 0.336735 | 0.234472 | intron-variant | Spag16 | Mm_Celera | 1:70052998 | CTCCATGTAAGTGAA[A/G]CAATTTCATAGCAGC | 66722 |
rs30469413 | snp | A/G | 0.260355 | 0.249785 | intron-variant | Spag16 | Mm_Celera | 1:70053126 | GGAAGGACATGGGGA[A/G]TGCATAGCAGCATGC | 66722 |
rs30469414 | snp | A/T | 0.231111 | 0.249285 | intron-variant | Spag16 | Mm_Celera | 1:69980448 | TATGCACATATGTGT[A/T]TGCATGCAGAGGTGG | 66722 |
rs30469417 | snp | A/C | 0.124444 | 0.216185 | intron-variant | Spag16 | Mm_Celera | 1:69980483 | TAGACGCTCACCCTG[A/C]GTAGTGCTCGTCATG | 66722 |
rs30469420 | snp | G/T | 0.132653 | 0.220748 | intron-variant | Spag16 | Mm_Celera | 1:69980493 | CCCTGAGTAGTGCTC[G/T]TCATGTCAGATCTGT | 66722 |
rs30469423 | snp | A/G | 0.231111 | 0.249285 | intron-variant | Spag16 | Mm_Celera | 1:69981133 | GGAATATGACTCTAG[A/G]ATAGGACAAACATAT | 66722 |
rs30469436 | snp | A/G | 0.231111 | 0.249285 | intron-variant | Spag16 | Mm_Celera | 1:70057626 | CAACACCCTCATTTT[A/G]GAAGAAAAGGTACAA | 66722 |
rs30469439 | snp | A/T | 0.444444 | 0.157135 | intron-variant | Spag16 | Mm_Celera | 1:70057650 | GGTACAACATTCTAC[A/T]TTGGAGTAATCTTGA | 66722 |
rs30469442 | snp | C/T | 0.231111 | 0.249285 | intron-variant | Spag16 | Mm_Celera | 1:70057740 | GAAGGGCAGAAACTG[C/T]TTACAAGAAGGATGT | 66722 |
rs30469504 | snp | C/T | 0.124444 | 0.216185 | intron-variant | Spag16 | Mm_Celera | 1:70007762 | TTTTATTTTTTTCTC[C/T]AACTTCATATGTCTT | 66722 |
rs30469507 | snp | A/C | 0.124444 | 0.216185 | intron-variant | Spag16 | Mm_Celera | 1:70007811 | CTTCCATAAAGTAGT[A/C]GGTGATGCCTGTCTT | 66722 |
rs30469510 | snp | A/G | 0.124444 | 0.216185 | intron-variant | Spag16 | Mm_Celera | 1:70007845 | ACTCATTTAACCACT[A/G]TCCTTACCACTTTAT | 66722 |
rs30469513 | snp | A/G | 0.391111 | 0.206368 | intron-variant | Spag16 | Mm_Celera | 1:70007955 | ATAGCCTGAGTGAAT[A/G]TATCAGCCTCTGAAC | 66722 |
rs30469564 | snp | G/T | 0.231111 | 0.249285 | intron-variant | Spag16 | Mm_Celera | 1:70013725 | TTATGAGTGATAATG[G/T]CTTACCATGTTCTAA | 66722 |
rs30469567 | snp | A/G | 0.124444 | 0.216185 | intron-variant | Spag16 | Mm_Celera | 1:70014113 | GCTGCAGAGTATCAA[A/G]CAGGAGACATTGGCT | 66722 |
rs30469570 | snp | A/G | 0.231111 | 0.249285 | intron-variant | Spag16 | Mm_Celera | 1:70014147 | AAAAGCTGGCATCTT[A/G]CAAGTTCTCTTTGGT | 66722 |
rs30469573 | snp | C/T | 0.231111 | 0.249285 | intron-variant | Spag16 | Mm_Celera | 1:70014433 | CAGCTAGGAGTTGTT[C/T]ACTTTTATGGCTAAT | 66722 |
rs30469766 | snp | C/T | 0.231111 | 0.249285 | intron-variant | Spag16 | Mm_Celera | 1:69999925 | GCTCAAGCAATGAGA[C/T]ATAGCCAGCATTTCT | 66722 |
rs30469769 | snp | A/G | 0.124444 | 0.216185 | intron-variant | Spag16 | Mm_Celera | 1:70000001 | TGGATGTTGAAGGAG[A/G]AGCCTTTATTCAATG | 66722 |
rs30469772 | snp | C/T | 0.32 | 0.24 | intron-variant | Spag16 | Mm_Celera | 1:70000055 | TTGCTTTGTGAATAA[C/T]AGGAATCCAGATTTC | 66722 |
rs30469844 | snp | C/T | 0.32 | 0.24 | intron-variant | Spag16 | Mm_Celera | 1:70066473 | TCTTAATTGTATAAA[C/T]AATGAACAAAGGAAT | 66722 |
rs30469847 | snp | A/G | 0.124444 | 0.216185 | intron-variant | Spag16 | Mm_Celera | 1:70066755 | ATGGCTCTTGCTCAT[A/G]ACAAGAAACAACACT | 66722 |
rs30469850 | snp | C/T | 0.231111 | 0.249285 | intron-variant | Spag16 | Mm_Celera | 1:70066767 | CATGACAAGAAACAA[C/T]ACTCAAAAGACTACA | 66722 |
rs30469853 | snp | G/T | 0.391111 | 0.206368 | intron-variant | Spag16 | Mm_Celera | 1:70066790 | AGACTACAAGGGACT[G/T]CTTTTGAAACAGTAT | 66722 |
rs30469934 | snp | A/T | 0.297521 | 0.245442 | intron-variant | Spag16 | Mm_Celera | 1:70018172 | TATAAATGTACTTTA[A/T]TAATATCTCTGAGAG | 66722 |
rs30469937 | snp | C/T | 0.18 | 0.24 | intron-variant | Spag16 | Mm_Celera | 1:70018176 | AATGTACTTTATTAA[C/T]ATCTCTGAGAGATTC | 66722 |
rs30469940 | snp | C/T | 0.244898 | 0.249948 | intron-variant | Spag16 | Mm_Celera | 1:70018458 | ACTCGAGAGGAGTTC[C/T]GGCTTACTATACATG | 66722 |
rs30469943 | snp | A/G | 0.231111 | 0.249285 | intron-variant | Spag16 | Mm_Celera | 1:70018480 | CTATACATGGAAAGG[A/G]CCTTCAAGCTTAGCC | 66722 |
rs30469966 | snp | C/T | 0.231111 | 0.249285 | intron-variant | Spag16 | Mm_Celera | 1:70025309 | TCAGACTAGTATGTG[C/T]TTTAAGTATGACAGA | 66722 |
rs30469969 | snp | A/C | 0.124444 | 0.216185 | intron-variant | Spag16 | Mm_Celera | 1:70026824 | TTACATACCATTGAC[A/C]CTGTGTCCTCAGCAA | 66722 |
rs30469972 | snp | C/G | 0.231111 | 0.249285 | intron-variant | Spag16 | Mm_Celera | 1:70027230 | TACTGTTTCTTAAAG[C/G]CTACCAGAAACATAG | 66722 |
rs30469984 | snp | C/G | 0.142012 | 0.225474 | intron-variant | Spag16 | Mm_Celera | 1:70031515 | AAGGTCAAAAGCCAA[C/G]AAAAGGGTTATCTCT | 66722 |
rs30469987 | snp | A/G | 0.124444 | 0.216185 | intron-variant | Spag16 | Mm_Celera | 1:70031554 | GAAAGGAAGAAGACA[A/G]AGAGGGACAAGTAGG | 66722 |
rs30469990 | snp | A/G | 0.231111 | 0.249285 | intron-variant | Spag16 | Mm_Celera | 1:70031824 | TTAGAACACAAACAC[A/G]TCTTAGAAGTGCAAA | 66722 |
rs30469993 | snp | C/T | 0.231111 | 0.249285 | intron-variant | Spag16 | Mm_Celera | 1:70031859 | AAGACAGTCCCTGTC[C/T]ACGAGCCCAGCATAA | 66722 |
rs30470005 | snp | C/T | 0.32 | 0.24 | intron-variant | Spag16 | Mm_Celera | 1:70028940 | AAAGGGAATCCCTCC[C/T]TTCAAAGTGCTCAAA | 66722 |
rs30470008 | snp | A/T | 0.32 | 0.24 | intron-variant | Spag16 | Mm_Celera | 1:70028964 | GCTCAAAACACAAGC[A/T]GCTTGCAGAAACAGC | 66722 |
rs30470011 | snp | A/G | 0.231111 | 0.249285 | intron-variant | Spag16 | Mm_Celera | 1:70028983 | TGCAGAAACAGCATG[A/G]TCACCATGTTTGGGC | 66722 |
rs30470065 | snp | C/T | 0.231111 | 0.249285 | intron-variant | Spag16 | Mm_Celera | 1:70002968 | ATCTTGATATTTTCC[C/T]TAAGTGTGAACATTT | 66722 |
rs30470067 | snp | C/G | 0.124444 | 0.216185 | intron-variant | Spag16 | Mm_Celera | 1:70003008 | CTCCAGCTCTCATAT[C/G]CAAAGAAGAAATTTG | 66722 |
rs30470069 | snp | C/G | 0.231111 | 0.249285 | intron-variant | Spag16 | Mm_Celera | 1:70003075 | ATCATTATAAAAGAA[C/G]CACAGTGTATAAAAA | 66722 |
rs30470071 | snp | A/T | 0.336735 | 0.234472 | intron-variant | Spag16 | Mm_Celera | 1:70003101 | AAAAATATATTAGCT[A/T]AAGTCCCACAAATAA | 66722 |
rs30470224 | snp | A/G | 0.231111 | 0.249285 | intron-variant | Spag16 | Mm_Celera | 1:69975231 | ATGAGCAAGATGTAA[A/G]AGACTTCAGTTTTTC | 66722 |
rs30470227 | snp | A/G | 0.231111 | 0.249285 | intron-variant | Spag16 | Mm_Celera | 1:69975257 | TTTTCCTTATAGTTT[A/G]ACTGTCACTACATAT | 66722 |
rs30470230 | snp | C/T | 0.231111 | 0.249285 | intron-variant | Spag16 | Mm_Celera | 1:69975376 | ACTGGAGTTGTGGAG[C/T]AGAAGGTGCTGATAC | 66722 |
rs30470233 | snp | G/T | 0.231111 | 0.249285 | intron-variant | Spag16 | Mm_Celera | 1:69975414 | CCCTGGTGCAATGAC[G/T]ATACTCTTCTTTCTA | 66722 |
rs30470246 | snp | A/G | 0.32 | 0.24 | intron-variant | Spag16 | Mm_Celera | 1:70053206 | GTATTTACAGTTTGG[A/G]CATGTGAGGGAGGGA | 66722 |
rs30470249 | snp | A/G | 0.375 | 0.216506 | intron-variant | Spag16 | Mm_Celera | 1:70053240 | AACATATTCATAGGC[A/G]TGATTGTTCTAGTTC | 66722 |
rs30470252 | snp | A/G | 0.124444 | 0.216185 | intron-variant | Spag16 | Mm_Celera | 1:70053630 | GTATATATGTGGAAG[A/G]GTGTTCAGATGGGCA | 66722 |
rs30470256 | snp | A/G | 0.231111 | 0.249285 | intron-variant | Spag16 | Mm_Celera | 1:69981179 | AACATAGTGTTTCAC[A/G]TGGTCTACACGCTGA | 66722 |
rs30470259 | snp | G/T | 0.231111 | 0.249285 | intron-variant | Spag16 | Mm_Celera | 1:69981271 | GAACATTGGTTCAGT[G/T]GAAAAAATAATGATA | 66722 |
rs30470262 | snp | C/T | 0.231111 | 0.249285 | intron-variant | Spag16 | Mm_Celera | 1:69981304 | AAAATGGAAGAAAGA[C/T]CTTTGCTAAGAAGTC | 66722 |
rs30470306 | snp | A/G | 0.231111 | 0.249285 | intron-variant | Spag16 | Mm_Celera | 1:70008010 | TTTCTTTGTATTACC[A/G]TCATAAGAATCTTTT | 66722 |
rs30470309 | snp | A/C | 0.132653 | 0.220748 | intron-variant | Spag16 | Mm_Celera | 1:70008288 | TTTTCTTCAGACAGT[A/C]ATGCACTTTACCCCT | 66722 |
rs30470312 | snp | C/T | 0.231111 | 0.249285 | intron-variant | Spag16 | Mm_Celera | 1:70008301 | GTAATGCACTTTACC[C/T]CTGTATTAGTTTGCA | 66722 |
rs30470335 | snp | C/T | 0.124444 | 0.216185 | intron-variant | Spag16 | Mm_Celera | 1:70044246 | CCTCGCCAGCCGTTT[C/T]TCTCCTCCTGTCTTC | 66722 |
rs30470338 | snp | C/T | 0.124444 | 0.216185 | intron-variant | Spag16 | Mm_Celera | 1:70044354 | ATTGAAAATCATGTG[C/T]AATGCAGTTACATTT | 66722 |
rs30470341 | snp | A/G | 0.32 | 0.24 | intron-variant | Spag16 | Mm_Celera | 1:70044402 | GAGGAGAGAGGGAAA[A/G]GAACCTGAGGCTAAT | 66722 |
rs30470345 | snp | C/T | 0.124444 | 0.216185 | intron-variant | Spag16 | Mm_Celera | 1:70058024 | AAGTGCCTGGTGTGC[C/T]AACACTTTTCTTGCT | 66722 |
rs30470348 | snp | A/G | 0.124444 | 0.216185 | intron-variant | Spag16 | Mm_Celera | 1:70058100 | TGTTATTAGCTTTCT[A/G]AAAGTGTTGTTTATC | 66722 |
rs30470351 | snp | C/T | 0.231111 | 0.249285 | intron-variant | Spag16 | Mm_Celera | 1:70058107 | AGCTTTCTAAAAGTG[C/T]TGTTTATCTGTGCAG | 66722 |
rs30470405 | snp | A/T | 0.124444 | 0.216185 | intron-variant | Spag16 | Mm_Celera | 1:70037240 | CCTTTTTCTTCACTG[A/T]GTAATACAGGTCTCT | 66722 |
rs30470407 | snp | A/G | 0.231111 | 0.249285 | intron-variant | Spag16 | Mm_Celera | 1:70037382 | ATAGTTAGATACATA[A/G]AAGCCATCATTAATG | 66722 |
rs30470410 | snp | G/T | 0.124444 | 0.216185 | intron-variant | Spag16 | Mm_Celera | 1:70037480 | AACTTACTTTCTAAC[G/T]GTGCTATAGTCTGTA | 66722 |
rs30470413 | snp | A/G | 0.32 | 0.24 | intron-variant | Spag16 | Mm_Celera | 1:70037498 | GCTATAGTCTGTAAA[A/G]CTGCCTTTCATTTTG | 66722 |
rs30470474 | snp | C/G | 0.231111 | 0.249285 | intron-variant | Spag16 | Mm_Celera | 1:70048380 | GTTTGCACGGTAGTT[C/G]TGTGTGAAGAGCCAC | 66722 |
rs30470477 | snp | G/T | 0.231111 | 0.249285 | intron-variant | Spag16 | Mm_Celera | 1:70048445 | GTGAGGCTAAACTTA[G/T]GGAAAAGTAAAGTCT | 66722 |
rs30470480 | snp | G/T | 0.124444 | 0.216185 | intron-variant | Spag16 | Mm_Celera | 1:70048446 | TGAGGCTAAACTTAT[G/T]GAAAAGTAAAGTCTG | 66722 |
rs30470482 | snp | A/C | 0.32 | 0.24 | intron-variant | Spag16 | Mm_Celera | 1:70048471 | AGTCTGTAAAGAAAC[A/C]TTCATCATTTGTGAA | 66722 |
rs30470506 | snp | C/T | 0.391111 | 0.206368 | intron-variant | Spag16 | Mm_Celera | 1:70014556 | GCAAATTAAAATACT[C/T]GGAGGATCCAGAGAG | 66722 |
rs30470509 | snp | A/T | 0.444444 | 0.157135 | intron-variant | Spag16 | Mm_Celera | 1:70014817 | AATAATATACAAAAA[A/T]TTTAAAAGAAAATGG | 66722 |
rs30470512 | snp | A/T | 0.132653 | 0.220748 | intron-variant | Spag16 | Mm_Celera | 1:70014894 | TTGTATTAGGATAGG[A/T]GGCCATCTGAGATGT | 66722 |
rs30470565 | snp | A/C | 0.152778 | 0.230321 | intron-variant | Spag16 | Mm_Celera | 1:70063865 | TTTTCTGGAATGCAT[A/C]TAAGTCCATTTCAAA | 66722 |
rs30470567 | snp | A/G | 0.35503 | 0.226867 | intron-variant | Spag16 | Mm_Celera | 1:70063891 | TCAAAAAAAAAAAAG[A/G]ATGATATGGTACAAT | 66722 |
rs30470570 | snp | C/T | 0.152778 | 0.230321 | intron-variant | Spag16 | Mm_Celera | 1:70063906 | AATGATATGGTACAA[C/T]ATAAGTGAGAAAATA | 66722 |
rs30470573 | snp | A/C | 0.142012 | 0.225474 | intron-variant | Spag16 | Mm_Celera | 1:70064158 | TTTCCTTCAGAAAGA[A/C]GAGTGAATTTTGTAC | 66722 |
rs30470725 | snp | A/G | 0.32 | 0.24 | intron-variant | Spag16 | Mm_Celera | 1:70000090 | TACATTCTTTCCAGC[A/G]TCTACAGAGCCAGCT | 66722 |
rs30470728 | snp | C/T | 0.32 | 0.24 | intron-variant | Spag16 | Mm_Celera | 1:70000105 | ATCTACAGAGCCAGC[C/T]GCCCCATAACCACTA | 66722 |
rs30470731 | snp | A/G | 0.32 | 0.24 | intron-variant | Spag16 | Mm_Celera | 1:70000174 | ATTTTATTAGGAGAG[A/G]GGCTCTGTCTTTATG | 66722 |
rs30470766 | snp | C/T | 0.231111 | 0.249285 | intron-variant | Spag16 | Mm_Celera | 1:70066862 | TCTCATCACCTGTTC[C/T]AGTGTACATAACAGT | 66722 |
rs30470768 | snp | A/T | 0.260355 | 0.249785 | intron-variant | Spag16 | Mm_Celera | 1:70066949 | ATGAATATACATCTT[A/T]CTTAGACATAAAACT | 66722 |
rs30470771 | snp | C/T | 0.231111 | 0.249285 | intron-variant | Spag16 | Mm_Celera | 1:70066985 | TTTAGAATTCTGTGC[C/T]GAGAATGTTTTTCAG | 66722 |
rs30470885 | snp | A/C | 0.124444 | 0.216185 | intron-variant | Spag16 | Mm_Celera | 1:70027275 | ATTATTACAATTTTT[A/C]ACTTTTCAATTTTAA | 66722 |
rs30470888 | snp | A/G | 0.231111 | 0.249285 | intron-variant | Spag16 | Mm_Celera | 1:70027309 | CTTAATCTAAAATAC[A/G]ATTTATAACATTGAA | 66722 |
rs30470891 | snp | A/T | 0.244898 | 0.249948 | intron-variant | Spag16 | Mm_Celera | 1:70027511 | TGTTCTAAAGTTGAT[A/T]TAATGTGATGAATTA | 66722 |
rs30470914 | snp | G/T | 0.124444 | 0.216185 | intron-variant | Spag16 | Mm_Celera | 1:70029023 | TTGGGCCCAGGAACA[G/T]TGAAATCCCAAAACT | 66722 |
rs30470916 | snp | G/T | 0.444444 | 0.157135 | intron-variant | Spag16 | Mm_Celera | 1:70029042 | AATCCCAAAACTCCT[G/T]ATGTAAGTTGTGTTC | 66722 |
rs30470919 | snp | A/G | 0.124444 | 0.216185 | intron-variant | Spag16 | Mm_Celera | 1:70029076 | CACACTCCTGAATAA[A/G]TATGTTAGGTGAGAA | 66722 |
rs30470922 | snp | C/G | 0.124444 | 0.216185 | intron-variant | Spag16 | Mm_Celera | 1:70029104 | GAAAGGGAACTTCGG[C/G]AAGAGGAGAATTTCA | 66722 |
rs30470925 | snp | C/T | 0.142012 | 0.225474 | intron-variant | Spag16 | Mm_Celera | 1:70031861 | GACAGTCCCTGTCCA[C/T]GAGCCCAGCATAATA | 66722 |
rs30470928 | snp | A/C | 0.231111 | 0.249285 | intron-variant | Spag16 | Mm_Celera | 1:70031956 | TCCTTAAAACACATA[A/C]TTTGCTGGGCTGTAT | 66722 |
rs30470931 | snp | C/T | 0.244898 | 0.249948 | intron-variant | Spag16 | Mm_Celera | 1:70031958 | CTTAAAACACATAAT[C/T]TGCTGGGCTGTATTG | 66722 |
rs30470965 | snp | A/C/T | 0.124444 | 0.216185 | intron-variant | Spag16 | GRCm38.p3 | 1:70018556 | CTCCTAGGATTGGCA[A/C/T]TGATGGAAAATGCTC | 66722 |
rs30470968 | snp | A/T | 0.231111 | 0.249285 | intron-variant | Spag16 | Mm_Celera | 1:70018580 | AATGCTCAGAGAAAT[A/T]AGAAGACAAGCATGG | 66722 |
rs30470971 | snp | C/T | 0.408163 | 0.193609 | intron-variant | Spag16 | Mm_Celera | 1:70018616 | GGTCTCTCCAGGAGA[C/T]GAGTCTAAATTCTTT | 66722 |
rs30471094 | snp | A/G | 0.231111 | 0.249285 | intron-variant | Spag16 | Mm_Celera | 1:70003161 | ATTCTACTATTAAAT[A/G]TTCCAGTCATGAAGA | 66722 |
rs30471096 | snp | A/G | 0.444444 | 0.157135 | intron-variant | Spag16 | Mm_Celera | 1:70003185 | ATGAAGATGTAGCTC[A/G]GAGGTAGTACCCTTG | 66722 |
rs30471099 | snp | C/T | 0.391111 | 0.206368 | intron-variant | Spag16 | Mm_Celera | 1:70003291 | ATTTTCATTTTCTAT[C/T]TCTAATACTAGTAGT | 66722 |
rs30471102 | snp | A/T | 0.124444 | 0.216185 | intron-variant | Spag16 | Mm_Celera | 1:70003335 | GTACAAAAGGCTAAT[A/T]ATTTTCTCACCATAC | 66722 |
rs30471105 | snp | C/T | 0.231111 | 0.249285 | intron-variant | Spag16 | Mm_Celera | 1:69981328 | AGAAGTCTGGATTAA[C/T]GTGTGGCCTAAGAGA | 66722 |
rs30471108 | snp | A/G | 0.231111 | 0.249285 | intron-variant | Spag16 | Mm_Celera | 1:69981329 | GAAGTCTGGATTAAC[A/G]TGTGGCCTAAGAGAA | 66722 |
rs30471111 | snp | A/G | 0.231111 | 0.249285 | intron-variant | Spag16 | Mm_Celera | 1:69981728 | AATCATAGGTAGACC[A/G]TGAAGCTTGGACCTA | 66722 |
rs30471136 | snp | A/G | 0.408163 | 0.193609 | intron-variant | Spag16 | Mm_Celera | 1:69975551 | TTATTATCAGCCATT[A/G]AAAAGTTATGTCTAT | 66722 |
rs30471139 | snp | C/T | 0.231111 | 0.249285 | intron-variant | Spag16 | Mm_Celera | 1:69975629 | TGTTGATAAAAAATT[C/T]AATCTAATAAAACAC | 66722 |
rs30471142 | snp | C/G | 0.391111 | 0.206368 | intron-variant | Spag16 | Mm_Celera | 1:69975891 | CTACTCTGCTTCTCT[C/G]TCCTGAACCAGCAAG | 66722 |
rs30471195 | snp | C/T | 0.375 | 0.216506 | intron-variant | Spag16 | Mm_Celera | 1:70053706 | TAGGAGAAAAGAGAA[C/T]GTTTTTCACTGAAAA | 66722 |
rs30471198 | snp | C/G | 0.35503 | 0.226867 | intron-variant | Spag16 | Mm_Celera | 1:70053734 | AAAGAAAATAGAGTA[C/G]ACTTAGACTAAGCCT | 66722 |
rs30471201 | snp | C/T | 0.32 | 0.24 | intron-variant | Spag16 | Mm_Celera | 1:70053772 | TCTGCTTGAGACAAT[C/T]CACCCTTTTACTTCA | 66722 |
rs30471225 | snp | A/G | 0.124444 | 0.216185 | intron-variant | Spag16 | Mm_Celera | 1:70008403 | ACTAGGTACACATAA[A/G]ACTGGGCATAAAAAC | 66722 |
rs30471228 | snp | C/T | 0.124444 | 0.216185 | intron-variant | Spag16 | Mm_Celera | 1:70008651 | CCTGTAATTGACATA[C/T]TTTAGGCATAGGAAG | 66722 |
rs30471231 | snp | C/T | 0.391111 | 0.206368 | intron-variant | Spag16 | Mm_Celera | 1:70008702 | AGAATTAGTGTTTAC[C/T]TCTTCATTTTCCCAA | 66722 |
rs30471274 | snp | C/T | 0.375 | 0.216506 | intron-variant | Spag16 | Mm_Celera | 1:70044678 | AAAAATATAAAAGGG[C/T]CCCGAAATGCAATTT | 66722 |
rs30471277 | snp | A/G | 0.124444 | 0.216185 | intron-variant | Spag16 | Mm_Celera | 1:70044774 | GAGAAACCATATCAA[A/G]TACATACAAACACAG | 66722 |
rs30471280 | snp | C/T | 0.35503 | 0.226867 | intron-variant | Spag16 | Mm_Celera | 1:70044992 | TCATATTTTCCATAT[C/T]GAAGAAGATTGCTTT | 66722 |
rs30471283 | snp | A/G | 0.32 | 0.24 | intron-variant | Spag16 | Mm_Celera | 1:70045469 | AAAAGTAGCTTTTTT[A/G]GAAGTGTGATTTTAA | 66722 |
rs30471284 | snp | A/C | 0.444444 | 0.157135 | intron-variant | Spag16 | Mm_Celera | 1:70058178 | ACTCTTCAGAAAATC[A/C]ATACATAACAGTGTC | 66722 |
rs30471287 | snp | C/T | 0.124444 | 0.216185 | intron-variant | Spag16 | Mm_Celera | 1:70058192 | CCATACATAACAGTG[C/T]CCAAAATTCATCACA | 66722 |
rs30471290 | snp | C/T | 0.231111 | 0.249285 | intron-variant | Spag16 | Mm_Celera | 1:70058212 | AATTCATCACAGTAG[C/T]TTAAATATCATAATG | 66722 |
rs30471293 | snp | C/T | 0.124444 | 0.216185 | intron-variant | Spag16 | Mm_Celera | 1:70058764 | CTGTGTCTCATGTGT[C/T]AGGACCTGGCCCTTT | 66722 |
rs30471356 | snp | A/G | 0.124444 | 0.216185 | intron-variant | Spag16 | Mm_Celera | 1:70037569 | CACAGATGAACTTGC[A/G]AGGCTCTGCCTTCTG | 66722 |
rs30471359 | snp | C/T | 0.124444 | 0.216185 | intron-variant | Spag16 | Mm_Celera | 1:70037917 | GTTTGGGTGATGATC[C/T]AGTGGCAGTGGGCAC | 66722 |
rs30471362 | snp | C/T | 0.32 | 0.24 | intron-variant | Spag16 | Mm_Celera | 1:70037938 | CAGTGGGCACTGTCC[C/T]TGGCAGCCACTCTGC | 66722 |
rs30471415 | snp | A/G | 0.124444 | 0.216185 | intron-variant | Spag16 | Mm_Celera | 1:70014944 | GAAGCCCTGTGCTGG[A/G]TGTGGGTCAGTGTGA | 66722 |
rs30471418 | snp | A/G | 0.231111 | 0.249285 | intron-variant | Spag16 | Mm_Celera | 1:70014961 | GTGGGTCAGTGTGAT[A/G]CAGACATGTTGGCCA | 66722 |
rs30471421 | snp | A/G | 0.124444 | 0.216185 | intron-variant | Spag16 | Mm_Celera | 1:70015027 | ATACCCTTACTTTAC[A/G]GTCTGCTCTCAGATT | 66722 |
rs30471504 | snp | A/G | 0.244898 | 0.249948 | intron-variant | Spag16 | Mm_Celera | 1:70048491 | TCATTTGTGAAGTCC[A/G]CAACATAACATGCTC | 66722 |
rs30471507 | snp | C/T | 0.32 | 0.24 | intron-variant | Spag16 | Mm_Celera | 1:70048502 | GTCCGCAACATAACA[C/T]GCTCAAGAATTAGCA | 66722 |
rs30471509 | snp | A/T | 0.32 | 0.24 | intron-variant | Spag16 | Mm_Celera | 1:70048573 | TAACACATTTGTTTC[A/T]AATTTGGCAACATTA | 66722 |
rs30471512 | snp | C/T | 0.260355 | 0.249785 | intron-variant | Spag16 | Mm_Celera | 1:70049504 | GTTACTCTTTTCTCA[C/T]CTGTAAGTTGATAAA | 66722 |
rs30471606 | snp | A/G | 0.142012 | 0.225474 | intron-variant | Spag16 | Mm_Celera | 1:70064217 | CCCATGGATGGAGAT[A/G]CTTACTCTGAAAGGA | 66722 |
rs30471609 | snp | A/C | 0.260355 | 0.249785 | intron-variant | Spag16 | Mm_Celera | 1:70064248 | AGTTAACTATTACTG[A/C]AAATCCCAAACAGAA | 66722 |
rs30471612 | snp | A/T | 0.142012 | 0.225474 | intron-variant | Spag16 | Mm_Celera | 1:70064486 | ATCATGGAATTCTTG[A/T]TGTATGGAGATTCTG | 66722 |
rs30471624 | snp | A/C | 0.124444 | 0.216185 | intron-variant | Spag16 | Mm_Celera | 1:70000177 | TTATTAGGAGAGGGG[A/C]TCTGTCTTTATGGCT | 66722 |
rs30471627 | snp | C/G | 0.124444 | 0.216185 | intron-variant | Spag16 | Mm_Celera | 1:70000344 | CACCATTTCTTCCTT[C/G]CTTTGTGTTGCTGTG | 66722 |
rs30471630 | snp | C/T | 0.124444 | 0.216185 | intron-variant | Spag16 | Mm_Celera | 1:70000382 | TCTATTTTATTCTTT[C/T]AACTCTTCCCGTTTA | 66722 |
rs30471633 | snp | C/T | 0.124444 | 0.216185 | intron-variant | Spag16 | Mm_Celera | 1:70000392 | TCTTTCAACTCTTCC[C/T]GTTTATCCTGTTTTA | 66722 |
rs30471694 | snp | C/G | 0.32 | 0.24 | intron-variant | Spag16 | Mm_Celera | 1:70027548 | TTCACTTATCAGCAT[C/G]AAGGGCCTGTAAATT | 66722 |
rs30471697 | snp | C/T | 0.244898 | 0.249948 | intron-variant | Spag16 | Mm_Celera | 1:70027669 | AGTGGATAAGACATA[C/T]AATTATGAAATGAAC | 66722 |
rs30471700 | snp | G/T | 0.124444 | 0.216185 | intron-variant | Spag16 | Mm_Celera | 1:70027743 | CACTTACTATCTGAT[G/T]CAATGTAAACTTATT | 66722 |
rs30471703 | snp | A/G | 0.124444 | 0.216185 | intron-variant | Spag16 | Mm_Celera | 1:70027810 | ACTTATACTGTAGGC[A/G]CTGATGAAAATTCTT | 66722 |
rs30471714 | snp | G/T | 0.231111 | 0.249285 | intron-variant | Spag16 | Mm_Celera | 1:70032280 | CTTAGGAAGCAGAAG[G/T]AGTTGACTGAGTGAA | 66722 |
rs30471717 | snp | A/T | 0.231111 | 0.249285 | intron-variant | Spag16 | Mm_Celera | 1:70032295 | GAGTTGACTGAGTGA[A/T]TGTGAAACCATCATA | 66722 |
rs30471720 | snp | A/G | 0.231111 | 0.249285 | intron-variant | Spag16 | Mm_Celera | 1:70032308 | GAATGTGAAACCATC[A/G]TAAACTTTAACAGAG | 66722 |
rs30471723 | snp | A/G | 0.231111 | 0.249285 | intron-variant | Spag16 | Mm_Celera | 1:70032560 | ATATACTCATACAAA[A/G]TGTCTCATAATTTCT | 66722 |
rs30471734 | snp | G/T | 0.124444 | 0.216185 | intron-variant | Spag16 | Mm_Celera | 1:70067052 | AACAGTGACTATGAA[G/T]AGTGAGTGTTTTATT | 66722 |
rs30471737 | snp | A/C | 0.32 | 0.24 | intron-variant | Spag16 | Mm_Celera | 1:70067149 | GCACAGGGAACACTG[A/C]ACTGTCTTTTCCTTC | 66722 |
rs30471740 | snp | A/G | 0.32 | 0.24 | intron-variant | Spag16 | Mm_Celera | 1:70067208 | CTCCCGTGGTCAGGA[A/G]GCATTTTGTTCTCTG | 66722 |
rs30471743 | snp | C/T | 0.244898 | 0.249948 | intron-variant | Spag16 | Mm_Celera | 1:70067306 | TCAGTCTCAATATCC[C/T]CTTAATTTCTCTCTG | 66722 |
rs30471764 | snp | A/G | 0.277778 | 0.248452 | intron-variant | Spag16 | Mm_Celera | 1:70018624 | CAGGAGATGAGTCTA[A/G]ATTCTTTATACTGAG | 66722 |
rs30471767 | snp | C/T | 0.32 | 0.24 | intron-variant | Spag16 | Mm_Celera | 1:70018800 | AAGGTTGATTCATGA[C/T]GGCTGTTCTTTAGGG | 66722 |
rs30471770 | snp | A/G | 0.124444 | 0.216185 | intron-variant | Spag16 | Mm_Celera | 1:70019117 | GCTATGCATGAGAAT[A/G]AAAGGCTGAGGATCA | 66722 |
rs30471773 | snp | C/T | 0.231111 | 0.249285 | intron-variant | Spag16 | Mm_Celera | 1:70019637 | TCAGGTCCCGTGACG[C/T]TTCTGTATGTCCCAT | 66722 |
rs30471835 | snp | C/T | 0.32 | 0.24 | intron-variant | Spag16 | Mm_Celera | 1:70029188 | ATTAATGAATTAAGT[C/T]CAGCATGACAGCTAT | 66722 |
rs30471838 | snp | G/T | 0.124444 | 0.216185 | intron-variant | Spag16 | Mm_Celera | 1:70029253 | ACTTAACATGTTTGT[G/T]GTTTTCTATGGACTC | 66722 |
rs30471841 | snp | C/T | 0.124444 | 0.216185 | intron-variant | Spag16 | Mm_Celera | 1:70029258 | ACATGTTTGTGGTTT[C/T]CTATGGACTCAAACC | 66722 |
rs30472024 | snp | A/G | 0.124444 | 0.216185 | intron-variant | Spag16 | Mm_Celera | 1:69981766 | ATTGTTTTGGGTCAA[A/G]TAGAGATGGTCAGTA | 66722 |
rs30472027 | snp | A/G | 0.391111 | 0.206368 | intron-variant | Spag16 | Mm_Celera | 1:69981847 | TAGGCTGCTTTCAAG[A/G]GAATATTGAACCTCT | 66722 |
rs30472030 | snp | A/C | 0.35503 | 0.226867 | intron-variant | Spag16 | Mm_Celera | 1:69981950 | TATTATGGACCACTA[A/C]CTATAGATATAAACA | 66722 |
rs30472033 | snp | G/T | 0.132653 | 0.220748 | intron-variant | Spag16 | Mm_Celera | 1:69991086 | TTGAGAGCCACCAGC[G/T]GTTGAAGCTGAGAGC | 66722 |
rs30472054 | snp | C/T | 0.336735 | 0.234472 | intron-variant | Spag16 | Mm_Celera | 1:70053896 | GTCTAATCGGTCATG[C/T]AGAAACATTTGAAAA | 66722 |
rs30472057 | snp | C/T | 0.32 | 0.24 | intron-variant | Spag16 | Mm_Celera | 1:70053986 | TTTGAATGGAATTGC[C/T]TGTAGGTTACTCTGG | 66722 |
rs30472060 | snp | A/G | 0.48 | 0.0979796 | intron-variant | Spag16 | Mm_Celera | 1:70054165 | CATCTCATATATTAG[A/G]AAGTATTTTCAGAAC | 66722 |
rs30472063 | snp | A/C | 0.32 | 0.24 | intron-variant | Spag16 | Mm_Celera | 1:70054248 | ATATTGGGAAATTGA[A/C]CCTCTGACTTGCTTC | 66722 |
rs30472095 | snp | C/T | 0.124444 | 0.216185 | intron-variant | Spag16 | Mm_Celera | 1:69975894 | CTCTGCTTCTCTCTC[C/T]TGAACCAGCAAGTCA | 66722 |
rs30472098 | snp | A/G | 0.32 | 0.24 | intron-variant | Spag16 | Mm_Celera | 1:69975916 | AGCAAGTCACTCTTC[A/G]GAGAGAAAGAGGACA | 66722 |
rs30472115 | snp | G/T | 0.244898 | 0.249948 | intron-variant | Spag16 | Mm_Celera | 1:70003500 | TTCTTTTGGACACTT[G/T]TTGTCATTCCTTCCA | 66722 |
rs30472118 | snp | A/G | 0.391111 | 0.206368 | intron-variant | Spag16 | Mm_Celera | 1:70003559 | CTGTGGACACTCATT[A/G]CTGCATCATCAGACA | 66722 |
rs30472121 | snp | A/G | 0.244898 | 0.249948 | intron-variant | Spag16 | Mm_Celera | 1:70003612 | GTCAAGATTGCAAGT[A/G]TTGCACATCTGCTTC | 66722 |
rs30472154 | snp | G/T | 0.124444 | 0.216185 | intron-variant | Spag16 | Mm_Celera | 1:70008813 | CCTACAAGGATTCTC[G/T]CTCAATTGTTGCTAT | 66722 |
rs30472157 | snp | A/T | 0.244898 | 0.249948 | intron-variant | Spag16 | Mm_Celera | 1:70008891 | TTTCGTTTTAAAGAT[A/T]TATTTATTCTATTTA | 66722 |
rs30472160 | snp | A/G | 0.124444 | 0.216185 | intron-variant | Spag16 | Mm_Celera | 1:70009296 | TGAGTAGCTGTCTTC[A/G]GAGGAGGCTAGATAT | 66722 |
rs30472196 | snp | G/T | 0.32 | 0.24 | intron-variant | Spag16 | Mm_Celera | 1:70045498 | AAACTGAGGAATAGT[G/T]TTAATTTGAGGACTA | 66722 |
rs30472199 | snp | G/T | 0.152778 | 0.230321 | intron-variant | Spag16 | Mm_Celera | 1:70045610 | TTCAACCTGGTTTTT[G/T]TTTTTAACCTGAAAG | 66722 |
rs30472202 | snp | C/T | 0.32 | 0.24 | intron-variant | Spag16 | Mm_Celera | 1:70045641 | TAGCCATTAGTATAC[C/T]TTGTGTAGCCATCAA | 66722 |
rs30472206 | snp | A/C/G | 0.124444 | 0.216185 | intron-variant | Spag16 | GRCm38.p3 | 1:70058775 | GTGTTAGGACCTGGC[A/C/G]CTTTGTCAGTCACTG | 66722 |
rs30472209 | snp | G/T | 0.231111 | 0.249285 | intron-variant | Spag16 | Mm_Celera | 1:70059072 | TGCATATAAATAAAA[G/T]TTCACAGATGAAAGT | 66722 |
rs30472212 | snp | A/G/T | 0.32 | 0.24 | intron-variant | Spag16 | GRCm38.p3 | 1:70059338 | ATAATCTACATTAAG[A/G/T]TCTTATTACCCCCTT | 66722 |
rs30472255 | snp | A/G | 0.124444 | 0.216185 | intron-variant | Spag16 | Mm_Celera | 1:70038077 | ACTCTCCTCCTGACA[A/G]ACAGTTCCTTTGTAC | 66722 |
rs30472258 | snp | A/G | 0.231111 | 0.249285 | intron-variant | Spag16 | Mm_Celera | 1:70038125 | TATGAAAAAATCCTA[A/G]CTTGTAGAAAAATGT | 66722 |
rs30472261 | snp | A/G | 0.32 | 0.24 | intron-variant | Spag16 | Mm_Celera | 1:70038184 | TAAATGTGGTAGACA[A/G]TTACAATTTTTCTTT | 66722 |
rs30472263 | snp | C/T | 0.124444 | 0.216185 | intron-variant | Spag16 | Mm_Celera | 1:70038332 | ATTAAACAAAAAAGT[C/T]ATTGTACTAGTGACA | 66722 |
rs30472314 | snp | A/T | 0.231111 | 0.249285 | intron-variant | Spag16 | Mm_Celera | 1:70015304 | ACGCAGAATGTCAGA[A/T]CTAATAGCTGCAGTG | 66722 |
rs30472317 | snp | A/G | 0.124444 | 0.216185 | intron-variant | Spag16 | Mm_Celera | 1:70015316 | AGAACTAATAGCTGC[A/G]GTGGAAGGAGATTTA | 66722 |
rs30472320 | snp | A/G | 0.231111 | 0.249285 | intron-variant | Spag16 | Mm_Celera | 1:70015463 | GTATCTGTGGGTTCT[A/G]CACTGGAAGATTGAA | 66722 |
rs30472323 | snp | C/T | 0.444444 | 0.157135 | intron-variant | Spag16 | Mm_Celera | 1:70015514 | AGCCTTTGTTGGTCG[C/T]ATCTGAACACTAAGA | 66722 |
rs30472485 | snp | C/G | 0.132653 | 0.220748 | intron-variant | Spag16 | Mm_Celera | 1:70049677 | AAGTGCTTATTCTAT[C/G]CCTGTCCTTATTTTG | 66722 |
rs30472487 | snp | A/G | 0.32 | 0.24 | intron-variant | Spag16 | Mm_Celera | 1:70049750 | ACCTGTCTAAAAAAA[A/G]TGCAAGATGAAGAAA | 66722 |
rs30472490 | snp | A/T | 0.336735 | 0.234472 | intron-variant | Spag16 | Mm_Celera | 1:70050255 | GTTTCCTGTGAATCA[A/T]ATAGTTTTCAGATGC | 66722 |
rs30472493 | snp | A/T | 0.124444 | 0.216185 | intron-variant | Spag16 | Mm_Celera | 1:70050314 | TAGAAGGTCAGCAAA[A/T]ATATGCACCTTTAAC | 66722 |
rs30472505 | snp | A/C | 0.32 | 0.24 | intron-variant | Spag16 | Mm_Celera | 1:70064522 | AACAAATAACAAAGC[A/C]GGCTTTTCCTGAGGT | 66722 |
rs30472508 | snp | A/G | 0.231111 | 0.249285 | intron-variant | Spag16 | Mm_Celera | 1:70064567 | GATACTACTGTCTTT[A/G]AGGTTTCAGTAAGTC | 66722 |
rs30472511 | snp | A/G | 0.124444 | 0.216185 | intron-variant | Spag16 | Mm_Celera | 1:70064609 | GTCTTCCAAAACCTA[A/G]GGAAAAAGATGTTTC | 66722 |
rs30472546 | snp | A/G | 0.231111 | 0.249285 | intron-variant | Spag16 | Mm_Celera | 1:70000421 | TAACTATCAGTCATC[A/G]GCCAGCCATAAAATA | 66722 |
rs30472549 | snp | G/T | 0.32 | 0.24 | intron-variant | Spag16 | Mm_Celera | 1:70000453 | AATTCCAAAGTAATA[G/T]TTAGTGTTTCTCTAG | 66722 |
rs30472552 | snp | C/T | 0.142012 | 0.225474 | intron-variant | Spag16 | Mm_Celera | 1:70000710 | ACACACAAATGCATG[C/T]ACAGTAAATAAATGA | 66722 |
rs30472596 | snp | C/T | 0.231111 | 0.249285 | intron-variant | Spag16 | Mm_Celera | 1:70033028 | GGGCTATCCACAACA[C/T]CTTCTGCAGTATGAG | 66722 |
rs30472599 | snp | C/T | 0.124444 | 0.216185 | intron-variant | Spag16 | Mm_Celera | 1:70033087 | TAACAACATTCAGAA[C/T]ACTTTTATAACTTAT | 66722 |
rs30472602 | snp | A/G | 0.231111 | 0.249285 | intron-variant | Spag16 | Mm_Celera | 1:70033243 | TCAGCAAGCTCTTTC[A/G]TAAGCCTGGACTCCA | 66722 |
rs30472616 | snp | A/T | 0.32 | 0.24 | intron-variant | Spag16 | Mm_Celera | 1:70027860 | ATCAAGTGGCATCCT[A/T]GTATTGTTCTCATAT | 66722 |
rs30472619 | snp | A/T | 0.231111 | 0.249285 | intron-variant | Spag16 | Mm_Celera | 1:70027887 | ATATTGCTGACTTCC[A/T]AATATGAAAGGAAGA | 66722 |
rs30472622 | snp | A/G | 0.124444 | 0.216185 | intron-variant | Spag16 | Mm_Celera | 1:70027973 | AATTAGCCTTTGGGA[A/G]TTCCTTAGGCATGCA | 66722 |
rs30472656 | snp | C/T | 0.124444 | 0.216185 | intron-variant | Spag16 | Mm_Celera | 1:70067408 | ATTTAGATGCCAAAA[C/T]ATGTGCTGGAAAGCC | 66722 |
rs30472659 | snp | A/G | 0.124444 | 0.216185 | intron-variant | Spag16 | Mm_Celera | 1:70067419 | AAAACATGTGCTGGA[A/G]AGCCATGGGTCCCAG | 66722 |
rs30472661 | snp | A/G | 0.124444 | 0.216185 | intron-variant | Spag16 | Mm_Celera | 1:70067512 | CCATGGAAAAAGATC[A/G]CCCTCTGTACTTTGT | 66722 |
rs30472746 | snp | A/G | 0.124444 | 0.216185 | intron-variant | Spag16 | Mm_Celera | 1:70020128 | CACTTTATGAAACCC[A/G]AGATCCTATTTATTC | 66722 |
rs30472748 | snp | C/T | 0.124444 | 0.216185 | intron-variant | Spag16 | Mm_Celera | 1:70020321 | AGCATGGTGAGAGTT[C/T]AGCATGGCCTGTCTT | 66722 |
rs30472751 | snp | C/T | 0.32 | 0.24 | intron-variant | Spag16 | Mm_Celera | 1:70020352 | TCACTTGATTCAACT[C/T]TATTTATAGTTGATG | 66722 |
rs30472764 | snp | C/T | 0.231111 | 0.249285 | intron-variant | Spag16 | Mm_Celera | 1:70029293 | ATTGTTTTATTGACT[C/T]AATCCCTTTGAGCTG | 66722 |
rs30472767 | snp | G/T | 0.231111 | 0.249285 | intron-variant | Spag16 | Mm_Celera | 1:70029546 | TAAAACTTTTGAAGC[G/T]TGTTATTGTGATTGG | 66722 |
rs30472770 | snp | C/T | 0.124444 | 0.216185 | intron-variant | Spag16 | Mm_Celera | 1:70029590 | CACCAGAATCCCTGA[C/T]TGTAGAAAAGGCGTT | 66722 |
rs30472773 | snp | G/T | 0.231111 | 0.249285 | intron-variant | Spag16 | Mm_Celera | 1:70029607 | GTAGAAAAGGCGTTT[G/T]GCCACACTGTGGCAT | 66722 |
rs30472926 | snp | C/T | 0.197531 | 0.244432 | intron-variant | Spag16 | Mm_Celera | 1:70054354 | GCTGTTGGACATATA[C/T]TAGGAAGAAAAATAT | 66722 |
rs30472929 | snp | A/C/G | 0.444444 | 0.157135 | intron-variant | Spag16 | GRCm38.p3 | 1:70054429 | AAATATTACTCAGAG[A/C/G]AAATTTATTAGTATA | 66722 |
rs30472932 | snp | A/T | 0.124444 | 0.216185 | intron-variant | Spag16 | Mm_Celera | 1:70054580 | CAGTTTTCCCAGTTA[A/T]GGATAGAACCAGAAG | 66722 |
rs30473014 | snp | G/T | 0.124444 | 0.216185 | intron-variant | Spag16 | Mm_Celera | 1:70003691 | AAACATAACTGCTAT[G/T]CTACCTCTCATTTCC | 66722 |
rs30473017 | snp | A/C | 0.426035 | 0.177515 | intron-variant | Spag16 | Mm_Celera | 1:70003758 | AAATACATTTCAAAT[A/C]CTATTTTATTGGCTT | 66722 |
rs30473135 | snp | A/G | 0.32 | 0.24 | intron-variant | Spag16 | Mm_Celera | 1:70060376 | ACCTCCCTGTGGCAG[A/G]ATAAGTTCAGGTACC | 66722 |
rs30473138 | snp | A/G | 0.124444 | 0.216185 | intron-variant | Spag16 | Mm_Celera | 1:70061367 | ATTTTTACTTTTTGA[A/G]CCATGAAAACTTCAA | 66722 |
rs30473141 | snp | A/G | 0.124444 | 0.216185 | intron-variant | Spag16 | Mm_Celera | 1:70061391 | ACTTCAACAGAGAAC[A/G]TTTTAATCATTTCTG | 66722 |
rs30473155 | snp | C/T | 0.32 | 0.24 | intron-variant | Spag16 | Mm_Celera | 1:70045903 | CTGTCTGTCATTATA[C/T]TCTGAATTTTCTTGT | 66722 |
rs30473158 | snp | A/G | 0.21875 | 0.248039 | intron-variant | Spag16 | Mm_Celera | 1:70045952 | TTGTAGTTAAAAATT[A/G]TCAAAACACCTTTTT | 66722 |
rs30473161 | snp | A/C | 0.244898 | 0.249948 | intron-variant | Spag16 | Mm_Celera | 1:70046065 | TCTTCTGAGAATAGA[A/C]CTGTACCAAAATATT | 66722 |
rs30473206 | snp | C/T | 0.124444 | 0.216185 | intron-variant | Spag16 | Mm_Celera | 1:70015947 | TGTCAGTTTGAATGA[C/T]TTACTCTGTCATTTG | 66722 |
rs30473209 | snp | A/G | 0.260355 | 0.249785 | intron-variant | Spag16 | Mm_Celera | 1:70016051 | AAGCAATATTACAAA[A/G]TATAAAGAATTGTTT | 66722 |
rs30473212 | snp | G/T | 0.124444 | 0.216185 | intron-variant | Spag16 | Mm_Celera | 1:70016166 | TCAAAACTGAAAATA[G/T]GGTCCATGATTCAAT | 66722 |
rs30473276 | snp | A/C/T | 0.124444 | 0.216185 | intron-variant | Spag16 | Mm_Celera | 1:70038698 | CTCTGCTGTGACTTA[A/C/T]GACAAATATTTTACC | 66722 |
rs30473279 | snp | A/C | 0.231111 | 0.249285 | intron-variant | Spag16 | Mm_Celera | 1:70038700 | CTGCTGTGACTTACG[A/C]CAAATATTTTACCTT | 66722 |
rs30473282 | snp | A/T | 0.124444 | 0.216185 | intron-variant | Spag16 | Mm_Celera | 1:70038859 | TGTGTCCACATGGAG[A/T]AGGGAAAAATGCTCT | 66722 |
rs30473285 | snp | C/T | 0.375 | 0.216506 | intron-variant | Spag16 | Mm_Celera | 1:70137552 | AAGCCCTATTCAATG[C/T]TAGGCTGTGTCTTAG | 66722 |
rs30473384 | snp | C/G | 0.336735 | 0.234472 | intron-variant | Spag16 | Mm_Celera | 1:70064665 | TTTTTTTTTTTTTGT[C/G]GAGTATTGGTTTAAA | 66722 |
rs30473387 | snp | A/G | 0.231111 | 0.249285 | intron-variant | Spag16 | Mm_Celera | 1:70064727 | ATAAACAAAGAGAAG[A/G]AAATGTGCCTTTTAC | 66722 |
rs30473390 | snp | A/G | 0.32 | 0.24 | intron-variant | Spag16 | Mm_Celera | 1:70064747 | GTGCCTTTTACAGCC[A/G]AAATATGGTTGGAAT | 66722 |
rs30473393 | snp | C/T | 0.244898 | 0.249948 | intron-variant | Spag16 | Mm_Celera | 1:70064767 | ATGGTTGGAATTATT[C/T]TCTTCTGTTCCCATA | 66722 |
rs30473406 | snp | A/G | 0.132653 | 0.220748 | intron-variant | Spag16 | Mm_Celera | 1:70050333 | TGCACCTTTAACCTT[A/G]GGAAGATAATGTGCC | 66722 |
rs30473409 | snp | A/G | 0.244898 | 0.249948 | intron-variant | Spag16 | Mm_Celera | 1:70050349 | GGAAGATAATGTGCC[A/G]TGCAGGTCTTCAGAG | 66722 |
rs30473412 | snp | C/T | 0.336735 | 0.234472 | intron-variant | Spag16 | Mm_Celera | 1:70050483 | TAATGCTAGAGTTTC[C/T]ATTTGCTTGTCTGAC | 66722 |
rs30473495 | snp | C/G | 0.124444 | 0.216185 | intron-variant | Spag16 | Mm_Celera | 1:70033384 | AGCAATAAAAGCATT[C/G]CTTATGTACTCTCTC | 66722 |
rs30473498 | snp | G/T | 0.124444 | 0.216185 | intron-variant | Spag16 | Mm_Celera | 1:70033410 | CTCTCATCTGTGTTT[G/T]TGCGTGTGAGTCTTA | 66722 |
rs30473501 | snp | A/G | 0.231111 | 0.249285 | intron-variant | Spag16 | Mm_Celera | 1:70033412 | CTCATCTGTGTTTGT[A/G]CGTGTGAGTCTTAAA | 66722 |
rs30473503 | snp | A/T | 0.124444 | 0.216185 | intron-variant | Spag16 | Mm_Celera | 1:70033425 | GTGCGTGTGAGTCTT[A/T]AAGGTTTGAACATTG | 66722 |
rs30473525 | snp | C/G | 0.32 | 0.24 | intron-variant | Spag16 | Mm_Celera | 1:70028101 | CATTGCATTATTGAA[C/G]CTGCAGCTGTTTGGC | 66722 |
rs30473528 | snp | A/G | 0.124444 | 0.216185 | intron-variant | Spag16 | Mm_Celera | 1:70028118 | TGCAGCTGTTTGGCT[A/G]TGTGCTTCTGAAATG | 66722 |
rs30473531 | snp | C/T | 0.32 | 0.24 | intron-variant | Spag16 | Mm_Celera | 1:70028159 | AGTGTAAATGAATGG[C/T]AGGAAAGTAGAGAAT | 66722 |
rs30473676 | snp | C/T | 0.231111 | 0.249285 | intron-variant | Spag16 | Mm_Celera | 1:70029768 | TATATTATTCTGTGG[C/T]CTAAAGTGTGAGGAT | 66722 |
rs30473678 | snp | A/T | 0.260355 | 0.249785 | intron-variant | Spag16 | Mm_Celera | 1:70029798 | TTATCTACTTAATTA[A/T]CATTTAATTCTTATA | 66722 |
rs30473681 | snp | G/T | 0.231111 | 0.249285 | intron-variant | Spag16 | Mm_Celera | 1:70029885 | ATGAAGACAATTTTA[G/T]TGTATTGACCAGAAG | 66722 |
rs30473714 | snp | A/G | 0.231111 | 0.249285 | intron-variant | Spag16 | Mm_Celera | 1:70067672 | GAGTCATGGTGAAAC[A/G]GCTGCCATCTCAAAG | 66722 |
rs30473720 | snp | A/C | 0.231111 | 0.249285 | intron-variant | Spag16 | Mm_Celera | 1:70068039 | CATTGTCATAACAGG[A/C]AGTGATCTTGACAAA | 66722 |
rs30473723 | snp | G/T | 0.124444 | 0.216185 | intron-variant | Spag16 | Mm_Celera | 1:70068073 | TTGTTAATGTTTTCA[G/T]TTCCTTCCCATTTTT | 66722 |
rs30473744 | snp | C/T | 0.231111 | 0.249285 | intron-variant | Spag16 | Mm_Celera | 1:70020610 | GAACCGTACTATCAC[C/T]GCCTATCTGTGTGAC | 66722 |
rs30473747 | snp | C/T | 0.124444 | 0.216185 | intron-variant | Spag16 | Mm_Celera | 1:70022131 | CATTATTATTGGAGC[C/T]AAAGTTTGAAACACT | 66722 |
rs30473750 | snp | A/G | 0.231111 | 0.249285 | intron-variant | Spag16 | Mm_Celera | 1:70022827 | TGAGTGATTTGGAAA[A/G]GATTCACTGCTGAGA | 66722 |
rs30473753 | snp | C/T | 0.124444 | 0.216185 | intron-variant | Spag16 | Mm_Celera | 1:70022849 | CTGCTGAGACAAGTC[C/T]TTTGTATTATGCTAA | 66722 |
rs30473835 | snp | C/G | 0.336735 | 0.234472 | intron-variant | Spag16 | Mm_Celera | 1:70054636 | ATAGAGGGCTTGTTG[C/G]AACTGTCTTTAGCAA | 66722 |
rs30473838 | snp | A/G | 0.142012 | 0.225474 | intron-variant | Spag16 | Mm_Celera | 1:70054680 | AAACAGGAAAATTCT[A/G]GTCATACTCAGACCA | 66722 |
rs30473841 | snp | A/G | 0.244898 | 0.249948 | intron-variant | Spag16 | Mm_Celera | 1:70054746 | ATCCCTAGGAAGCAC[A/G]AAAGCTTGGGCAGTG | 66722 |
rs30473945 | snp | A/G | 0.124444 | 0.216185 | intron-variant | Spag16 | Mm_Celera | 1:70038901 | TAAAATGCAAAGATC[A/G]GCCTGGAGAATTGAG | 66722 |
rs30473948 | snp | A/C | 0.231111 | 0.249285 | intron-variant | Spag16 | Mm_Celera | 1:70039047 | AAGACGCCTTCAGCG[A/C]CAAATGAAAAGTTAA | 66722 |
rs30473951 | snp | C/T | 0.244898 | 0.249948 | intron-variant | Spag16 | Mm_Celera | 1:70039091 | TGGGTAGGACTCATT[C/T]TGTAAAAATTGGGAG | 66722 |
rs30473995 | snp | A/T | 0.35503 | 0.226867 | intron-variant | Spag16 | Mm_Celera | 1:70050639 | GAGAGGTTTAACAAG[A/T]ATAATATGGCTAAAA | 66722 |
rs30473998 | snp | A/C | 0.473373 | 0.11227 | intron-variant | Spag16 | Mm_Celera | 1:70050672 | AACTCACATCTTGTA[A/C]ATTTCCATTGGCTTT | 66722 |
rs30474001 | snp | A/G | 0.244898 | 0.249948 | intron-variant | Spag16 | Mm_Celera | 1:70050694 | ATTGGCTTTTTAAGT[A/G]TAAAGATGTAATTTC | 66722 |
rs30474024 | snp | A/G | 0.5 | 0 | intron-variant | Spag16 | Mm_Celera | 1:70046086 | CCAAAATATTCAGAT[A/G]GGAAATTTATAATGG | 66722 |
rs30474027 | snp | C/T | 0.42 | 0.183303 | intron-variant | Spag16 | Mm_Celera | 1:70046119 | ATTTGAAACAATCTA[C/T]CAGTAGTTTTTCTCT | 66722 |
rs30474030 | snp | C/T | 0.244898 | 0.249948 | intron-variant | Spag16 | Mm_Celera | 1:70046182 | TCATATCCCAAATTG[C/T]CTTTTTCTGATAATA | 66722 |
rs30474032 | snp | C/T | 0.375 | 0.216506 | intron-variant | Spag16 | Mm_Celera | 1:70046219 | ATAGAACTTTTCTTC[C/T]TTTATTTTCTTCTAA | 66722 |
rs30474036 | snp | C/G | 0.231111 | 0.249285 | intron-variant | Spag16 | Mm_Celera | 1:70064795 | ATATGTTATAGCCTA[C/G]CTCTTATTATGCTAG | 66722 |
rs30474039 | snp | C/T | 0.124444 | 0.216185 | intron-variant | Spag16 | Mm_Celera | 1:70064836 | TCTTCTCTAAGAAGG[C/T]TGTGAGTCACCAAAA | 66722 |
rs30474042 | snp | C/G | 0.231111 | 0.249285 | intron-variant | Spag16 | Mm_Celera | 1:70064972 | GTAGGTCATTTTGCT[C/G]TATGTGAGGCATATA | 66722 |
rs30474146 | snp | A/G | 0.142012 | 0.225474 | intron-variant | Spag16 | Mm_Celera | 1:70061467 | GTACCTCAGTGCTGT[A/G]GACAACAAGTCCACG | 66722 |
rs30474149 | snp | C/T | 0.142012 | 0.225474 | intron-variant | Spag16 | Mm_Celera | 1:70061478 | CTGTAGACAACAAGT[C/T]CACGTATGTGTAGAC | 66722 |
rs30474275 | snp | A/G | 0.336735 | 0.234472 | intron-variant | Spag16 | Mm_Celera | 1:70016188 | TGATTCAATGATATT[A/G]TGTAGTAGTGAGTTA | 66722 |
rs30474278 | snp | C/G | 0.132653 | 0.220748 | intron-variant | Spag16 | Mm_Celera | 1:70016604 | TTTCATAAACATGAG[C/G]TATAAATATGAATTT | 66722 |
rs30474281 | snp | C/T | 0.124444 | 0.216185 | intron-variant | Spag16 | Mm_Celera | 1:70016725 | AAGTTTACTCTTAGC[C/T]TGTCGCCATCGTTGA | 66722 |
rs30474286 | snp | A/G | 0.142012 | 0.225474 | intron-variant | Spag16 | Mm_Celera | 1:70022885 | CGAGGAATATGTCTT[A/G]TAATATGATGATAAC | 66722 |
rs30474289 | snp | A/T | 0.32 | 0.24 | intron-variant | Spag16 | Mm_Celera | 1:70023049 | GCTATGAAAAATAGT[A/T]GAACTTTAAAAGCAT | 66722 |
rs30474292 | snp | C/T | 0.124444 | 0.216185 | intron-variant | Spag16 | Mm_Celera | 1:70023182 | GGGAGAAAAGAGAAA[C/T]AATCATTCAATCTTT | 66722 |
rs30474354 | snp | C/T | 0.231111 | 0.249285 | intron-variant | Spag16 | Mm_Celera | 1:70029964 | TATTCTGATTTTCTA[C/T]GTGTTTTGGTGATAA | 66722 |
rs30474357 | snp | A/T | 0.231111 | 0.249285 | intron-variant | Spag16 | Mm_Celera | 1:70029987 | GGTGATAATAGCATA[A/T]TTTCCATTCTCTTTC | 66722 |
rs30474359 | snp | C/T | 0.231111 | 0.249285 | intron-variant | Spag16 | Mm_Celera | 1:70030240 | TGAATATAACCACAG[C/T]AATTATTCTCAGATC | 66722 |
rs30474362 | snp | C/T | 0.231111 | 0.249285 | intron-variant | Spag16 | Mm_Celera | 1:70030266 | AGATCTTAGTTTCTT[C/T]GAACCTATATTTTGT | 66722 |
rs30474406 | snp | A/G | 0.132653 | 0.220748 | intron-variant | Spag16 | Mm_Celera | 1:70071418 | TACCTGGTTTTGCTG[A/G]TATGTTTCTCACTCA | 66722 |
rs30474409 | snp | C/T | 0.142012 | 0.225474 | intron-variant | Spag16 | Mm_Celera | 1:70071421 | CTGGTTTTGCTGGTA[C/T]GTTTCTCACTCAGTT | 66722 |
rs30474412 | snp | C/G | 0.124444 | 0.216185 | intron-variant | Spag16 | Mm_Celera | 1:70071603 | ATCTATGAACAAATG[C/G]AAAGTGACTATCATT | 66722 |
rs30474444 | snp | C/T | 0.231111 | 0.249285 | intron-variant | Spag16 | Mm_Celera | 1:70054751 | TAGGAAGCACAAAAG[C/T]TTGGGCAGTGGAGGA | 66722 |
rs30474447 | snp | C/T | 0.244898 | 0.249948 | intron-variant | Spag16 | Mm_Celera | 1:70054836 | GAGTGAGGAAGAATT[C/T]CATACCATGTCACTG | 66722 |
rs30474450 | snp | C/T | 0.132653 | 0.220748 | intron-variant | Spag16 | Mm_Celera | 1:70054963 | TGGCAGATTTAAAAT[C/T]GAGAAGCAAAGCATC | 66722 |
rs30474453 | snp | A/G | 0.277778 | 0.248452 | intron-variant | Spag16 | Mm_Celera | 1:70055136 | TAATATAATCCAAGG[A/G]CTGGGCCTTTTCAAT | 66722 |
rs30474464 | snp | C/T | 0.336735 | 0.234472 | intron-variant | Spag16 | Mm_Celera | 1:70028201 | AGTAATGTTTGTAAC[C/T]TTGTTTTTAAGAAGG | 66722 |
rs30474467 | snp | A/C | 0.32 | 0.24 | intron-variant | Spag16 | Mm_Celera | 1:70028214 | ACCTTGTTTTTAAGA[A/C]GGTTAAGGAAGTTAA | 66722 |
rs30474470 | snp | A/G | 0.32 | 0.24 | intron-variant | Spag16 | Mm_Celera | 1:70028246 | AAAGGAAAGGGTTGC[A/G]GTGTAGCTAAAACAG | 66722 |
rs30474473 | snp | C/T | 0.124444 | 0.216185 | intron-variant | Spag16 | Mm_Celera | 1:70028504 | AAAACCAAATGAATC[C/T]GTGTTCCTAAGAAAT | 66722 |
rs30474506 | snp | C/G | 0.32 | 0.24 | intron-variant | Spag16 | Mm_Celera | 1:70033482 | TGTTGAAATTTTGAT[C/G]TGCTCTTTTCAAAAG | 66722 |
rs30474509 | snp | A/T | 0.124444 | 0.216185 | intron-variant | Spag16 | Mm_Celera | 1:70033495 | ATCTGCTCTTTTCAA[A/T]AGCACACATTCTTTT | 66722 |
rs30474512 | snp | C/T | 0.231111 | 0.249285 | intron-variant | Spag16 | Mm_Celera | 1:70033541 | CTTTTCTTATTGTCT[C/T]ACACAAAGTTCCATA | 66722 |
rs30474545 | snp | A/C | 0.32 | 0.24 | intron-variant | Spag16 | Mm_Celera | 1:70068294 | TCTTCACAGAGTCAC[A/C]CATATTTCCCTACCC | 66722 |
rs30474548 | snp | C/T | 0.124444 | 0.216185 | intron-variant | Spag16 | Mm_Celera | 1:70068826 | AGCTCATAGTGCTCC[C/T]TACTATATACTAGAA | 66722 |
rs30474551 | snp | G/T | 0.231111 | 0.249285 | intron-variant | Spag16 | Mm_Celera | 1:70068988 | AGTTCTTAAAGTTCA[G/T]TTGAATTAATAATCA | 66722 |
rs30474553 | snp | A/G | 0.231111 | 0.249285 | intron-variant | Spag16 | Mm_Celera | 1:70069039 | TAGAAAACCACAGCC[A/G]CATGCATAAGTCAGT | 66722 |
rs30474834 | snp | A/G | 0.132653 | 0.220748 | intron-variant | Spag16 | Mm_Celera | 1:70050717 | GTAATTTCCCAGTAG[A/G]GCATTAGATTAAGGA | 66722 |
rs30474837 | snp | A/G | 0.231111 | 0.249285 | intron-variant | Spag16 | Mm_Celera | 1:70050744 | AGGATTCAGAGAGAC[A/G]ATGTTTTTCTAATTA | 66722 |
rs30474840 | snp | C/G | 0.336735 | 0.234472 | intron-variant | Spag16 | Mm_Celera | 1:70050832 | CATGGGAGCACTTAA[C/G]ATAATTAGTCTTACA | 66722 |
rs30474843 | snp | C/T | 0.231111 | 0.249285 | intron-variant | Spag16 | Mm_Celera | 1:70051010 | GCAGGCAGTTTCCTA[C/T]CCCTCTTCATTCTGA | 66722 |
rs30474874 | snp | C/G | 0.32 | 0.24 | intron-variant | Spag16 | Mm_Celera | 1:70039250 | GCACCACTGGCTGCC[C/G]TTCTTAAATCATTAC | 66722 |
rs30474877 | snp | A/G | 0.124444 | 0.216185 | intron-variant | Spag16 | Mm_Celera | 1:70040881 | AATATTTTGGGCTTG[A/G]GTCATTCTACAGTCG | 66722 |
rs30474880 | snp | C/G/T | 0.32 | 0.24 | intron-variant | Spag16 | Mm_Celera | 1:70040938 | CCACCTGTGTGTTGT[C/G/T]CTGAGATTTTGTCTG | 66722 |
rs30474883 | snp | A/T | 0.459184 | 0.136902 | intron-variant | Spag16 | Mm_Celera | 1:70041748 | TACTAATTAACAATT[A/T]TCTTAGTTCTTTTCA | 66722 |
rs30474935 | snp | A/G | 0.132653 | 0.220748 | intron-variant | Spag16 | Mm_Celera | 1:70065002 | ATGTCCCTTGTGTCT[A/G]CAACTCAGAAAAAAA | 66722 |
rs30474938 | snp | A/T | 0.46875 | 0.121031 | intron-variant | Spag16 | Mm_Celera | 1:70065048 | CAATCAAAGTAGAAA[A/T]TTTTCTTTTGTAAAG | 66722 |
rs30474941 | snp | C/T | 0.32 | 0.24 | intron-variant | Spag16 | Mm_Celera | 1:70065326 | TTCTGATGCCTTGAC[C/T]GTCCCTAACAAGTCT | 66722 |
rs30475046 | snp | C/T | 0.142012 | 0.225474 | intron-variant | Spag16 | Mm_Celera | 1:70061930 | AGGCATGTGACATGA[C/T]CTTGTTTAAGTGGGA | 66722 |
rs30475051 | snp | C/T | 0.142012 | 0.225474 | intron-variant | Spag16 | Mm_Celera | 1:70061979 | TTGGCAAAGAAGCTG[C/T]TAGGCCGTCTGTATT | 66722 |
rs30475064 | snp | A/G | 0.124444 | 0.216185 | intron-variant | Spag16 | Mm_Celera | 1:70016852 | TGTCTCTTGAGCCGT[A/G]CTATTATCCATTTGA | 66722 |
rs30475067 | snp | C/T | 0.231111 | 0.249285 | intron-variant | Spag16 | Mm_Celera | 1:70016968 | TACATTAGTAGTAAG[C/T]CAATTTGGTTTAGAA | 66722 |
rs30475070 | snp | C/T | 0.124444 | 0.216185 | intron-variant | Spag16 | Mm_Celera | 1:70017203 | TTATCCACTGATCAG[C/T]TTTAAAGGGGGCCAG | 66722 |
rs30475175 | snp | C/T | 0.124444 | 0.216185 | intron-variant | Spag16 | Mm_Celera | 1:70046313 | ACTGTGGGCTTAGGA[C/T]ACCTTATGTGCTAGA | 66722 |
rs30475178 | snp | A/G | 0.260355 | 0.249785 | intron-variant | Spag16 | Mm_Celera | 1:70046840 | TATTAATTTAAATGT[A/G]CAAATGAGGTGTTGA | 66722 |
rs30475181 | snp | C/T | 0.444444 | 0.157135 | intron-variant | Spag16 | Mm_Celera | 1:70047167 | TGCCTAAGGCAAGAC[C/T]ATTAATATTTCTCTG | 66722 |
rs30475183 | snp | G/T | 0.132653 | 0.220748 | intron-variant | Spag16 | Mm_Celera | 1:70047346 | CTATGTGTGTTTATT[G/T]TGTTGTCTACATTCT | 66722 |
rs30475215 | snp | A/G | 0.231111 | 0.249285 | intron-variant | Spag16 | Mm_Celera | 1:70023307 | TACAACAGTGAAGCA[A/G]TCTTTCAGTATCACT | 66722 |
rs30475218 | snp | C/T | 0.124444 | 0.216185 | intron-variant | Spag16 | Mm_Celera | 1:70024139 | CTTTCTAGAACTTTC[C/T]GTCTTTTGTAGTATC | 66722 |
rs30475221 | snp | C/T | 0.124444 | 0.216185 | intron-variant | Spag16 | Mm_Celera | 1:70024198 | AAGAGATGCCAACAG[C/T]CAACATACATTTTTT | 66722 |
rs30475265 | snp | A/G | 0.231111 | 0.249285 | intron-variant | Spag16 | Mm_Celera | 1:70030306 | TTATGTGTGTTTGAA[A/G]TTTGTGTATATGCAG | 66722 |