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 |