SNP - dbSNP |
dbSNP | Type | Alleles | Het | Se(het) | Fxn-class | Gene Name | Assembly | Chr-pos | Sequence | Entrez Gene |
rs6178713 | snp | A/T | 0.5 | 0 | intron-variant | Wdr20 | Mm_Celera | 12:110738471 | GGCAGCGCTGCCTCC[A/T]AGGGGAGGAGGGGGC | 69641 |
rs6294292 | snp | C/G/T | 0.5 | 0 | intron-variant | Wdr20 | Mm_Celera | 12:110790352 | CAGATTAAGAGGCAT[C/G/T]TTCTAGCTGCCCTCC | 69641 |
rs6295453 | snp | A/T | 0.375 | 0.216506 | intron-variant | Wdr20 | GRCm38.p3 | 12:110790571 | GCTCTGGAGGGAACA[A/T]AATTTGTTACAGTCT | 69641 |
rs6296763 | snp | C/T | 0.304688 | 0.243945 | intron-variant | Wdr20 | Mm_Celera | 12:110790841 | AGTCATGCACATGTG[C/T]TATGAGTGCCTTCAC | 69641 |
rs6307936 | snp | C/T | 0.5 | 0 | utr-variant-3-prime | Wdr20 | Mm_Celera | 12:110803750 | atatatatatatata[C/T]ncacacatatataca | 69641 |
rs6307937 | snp | A/G | 0.5 | 0 | utr-variant-3-prime | Wdr20 | GRCm38.p3 | 12:110803750 | tatatatatatatan[A/G]cacacatatatacat | 69641 |
rs29122096 | snp | C/T | 0.375 | 0.216506 | intron-variant | Wdr20 | GRCm38.p3 | 12:110759067 | AGTTAGGAGATGAGA[C/T]GGGCCTTTGAAGTCA | 69641 |
rs29122678 | snp | A/T | 0.32 | 0.24 | intron-variant | Wdr20 | Mm_Celera | 12:110755197 | CCTTCTAAATCAGCT[A/T]AATCAGAGTGTGAAA | 69641 |
rs29126578 | snp | C/T | 0.5 | 0 | intron-variant | Wdr20 | Mm_Celera | 12:110776665 | AATGGTATCTGATGC[C/T]CTCTTATAGCACACA | 69641 |
rs29129612 | snp | A/G | 0.46875 | 0.121031 | intron-variant | Wdr20 | Mm_Celera | 12:110780322 | GGAATGAAATGACAT[A/G]GTGGTGACATGTCCT | 69641 |
rs29131099 | snp | C/T | 0.46875 | 0.121031 | intron-variant, upstream-variant-2KB | Wdr20 | Mm_Celera | 12:110778655 | CTTATGGTCAGCAGA[C/T]CTGGGATCCAAATCC | 69641 |
rs29131655 | snp | A/G | 0.375 | 0.216506 | intron-variant | Wdr20 | Mm_Celera | 12:110773886 | TTGTAGACCAGGCTG[A/G]CCTCAAACTCAGAAA | 69641 |
rs29131935 | snp | A/G | 0.32 | 0.24 | utr-variant-3-prime | Wdr20 | Mm_Celera | 12:110803487 | GCTCCCAGGCTCCCC[A/G]GACACGCGTGGACCG | 69641 |
rs29132412 | snp | C/T | 0.375 | 0.216506 | intron-variant | Wdr20 | Mm_Celera | 12:110773840 | TGAGACAGGGTTTCT[C/T]TGTATAGCCTTGGCT | 69641 |
rs29132477 | snp | C/T | 0.5 | 0 | intron-variant | Wdr20 | Mm_Celera | 12:110761116 | GGAGGCAGAGGCAGG[C/T]GGATTTCTGAGTTCC | 69641 |
rs29132566 | snp | G/T | 0.5 | 0 | intron-variant | Wdr20 | Mm_Celera | 12:110775194 | TTTTTTTTGTTTTTT[G/T]TTTTTTTTTTTCGAG | 69641 |
rs29135997 | snp | C/T | 0.492188 | 0.0620098 | intron-variant, upstream-variant-2KB | Wdr20 | Mm_Celera | 12:110778676 | ATCCAAATCCAGCTC[C/T]GACATTTGCCAGGTG | 69641 |
rs29136494 | snp | A/G | 0.487535 | 0.077957 | intron-variant | Wdr20 | Mm_Celera | 12:110784645 | GGGAACCAAGACAAC[A/G]GCTTCTAGGCAGAGC | 69641 |
rs29138152 | snp | C/G | 0.375 | 0.216506 | intron-variant, utr-variant-5-prime | Wdr20 | Mm_Celera | 12:110788989 | GTTGCTCCCAATGCT[C/G]CCTTGCTTGACTTTT | 69641 |
rs29138437 | snp | A/T | 0.5 | 0 | intron-variant | Wdr20 | Mm_Celera | 12:110786343 | GGCAATAACTGGAGG[A/T]TTCCCACTTTTCTGT | 69641 |
rs29138986 | snp | C/T | 0.375 | 0.216506 | intron-variant | Wdr20 | Mm_Celera | 12:110766073 | GTCAGTGTTTGGGTC[C/T]TTGACTACAAGACAG | 69641 |
rs29139975 | snp | C/T | 0.401235 | 0.199068 | intron-variant | Wdr20 | Mm_Celera | 12:110796219 | AGGCTAGAAATAAAA[C/T]ACTCTGTGCAGTTTC | 69641 |
rs29140206 | snp | C/T | 0.375 | 0.216506 | intron-variant | Wdr20 | Mm_Celera | 12:110765819 | GTAAAACCAAAAATG[C/T]CATCACTTAATATAA | 69641 |
rs29144073 | snp | A/C | 0.444444 | 0.157135 | intron-variant, utr-variant-5-prime | Wdr20 | Mm_Celera | 12:110789052 | TCTTTATACCCTTCT[A/C]CCCTTCTCCCCACCC | 69641 |
rs29144286 | snp | A/C | 0.444444 | 0.157135 | intron-variant | Wdr20 | Mm_Celera | 12:110762658 | TGTTATAAACAGTAC[A/C]CTTGTCTATTCTGAC | 69641 |
rs29144709 | snp | C/T | 0.32 | 0.24 | intron-variant, downstream-variant-500B | Wdr20 | Mm_Celera | 12:110742428 | CAGCTAGCTGTTCCC[C/T]CCCACCCCCAATTAA | 69641 |
rs29145431 | snp | C/G | 0.32 | 0.24 | intron-variant | Wdr20 | Mm_Celera | 12:110755201 | CTAAATCAGCTAAAT[C/G]AGAGTGTGAAAATGA | 69641 |
rs29150705 | snp | C/T | 0.498615 | 0.0262793 | intron-variant | Wdr20 | Mm_Celera | 12:110791293 | TGACCTTCAACTTTC[C/T]CACCTGTAGTAGAGT | 69641 |
rs29151998 | snp | C/T | 0.375 | 0.216506 | downstream-variant-500B | Wdr20 | Mm_Celera | 12:110804396 | TCGGAGAAGTCTTGG[C/T]TCTGGGCCAAGTCCA | 69641 |
rs29152011 | snp | C/T | 0.32 | 0.24 | intron-variant | Wdr20 | Mm_Celera | 12:110770631 | GTGTGTATACTTATA[C/T]TTGGCTCTTTACATA | 69641 |
rs29152358 | snp | C/T | 0.32 | 0.24 | intron-variant | Wdr20 | Mm_Celera | 12:110770615 | GTGTGTGTGCGCGCG[C/T]GTGTGTATACTTATA | 69641 |
rs29154509 | snp | C/G | 0.498615 | 0.0262793 | intron-variant, utr-variant-5-prime, downstream-variant-500B | Wdr20 | Mm_Celera | 12:110779545 | TTACTCAGAGGGAGC[C/G]GGCCTTTTCACAGTT | 69641 |
rs29154923 | snp | A/G | 0.375 | 0.216506 | intron-variant | Wdr20 | Mm_Celera | 12:110791507 | AGGCTCCGGAGAGCT[A/G]GATGTCTCTTCATTT | 69641 |
rs29156634 | snp | C/T | 0.32 | 0.24 | intron-variant | Wdr20 | Mm_Celera | 12:110773940 | TGCTGGGATTAAAGG[C/T]GTGCGCCACCACAGC | 69641 |
rs29156960 | snp | A/G | 0.49827 | 0.0293608 | intron-variant, upstream-variant-2KB | Wdr20 | Mm_Celera | 12:110787090 | TAAAGATTTATTCGT[A/G]TGTGTCTATGCATGT | 69641 |
rs29158862 | snp | C/T | 0.444444 | 0.157135 | intron-variant | Wdr20 | Mm_Celera | 12:110744641 | AGGCCCCCCTCTACC[C/T]CAGATCTCCCTTTTT | 69641 |
rs29159807 | snp | A/G | 0.432133 | 0.171253 | utr-variant-3-prime, intron-variant | Wdr20 | Mm_Celera | 12:110794894 | ACTTAGGAACAAAGC[A/G]TTCATCAGGGTTGAT | 69641 |
rs29162121 | snp | C/T | 0.415225 | 0.187619 | intron-variant | Wdr20 | Mm_Celera | 12:110780991 | GGCAGATGCTGTCTG[C/T]AGTCCACGATCATTC | 69641 |
rs29162577 | snp | C/T | 0.444444 | 0.157135 | intron-variant | Wdr20 | Mm_Celera | 12:110776664 | TAATGGTATCTGATG[C/T]CCTCTTATAGCACAC | 69641 |
rs29164319 | snp | A/G | 0.444444 | 0.157135 | intron-variant | Wdr20 | Mm_Celera | 12:110773588 | AATAAAAAAATGGGG[A/G]AAAAAAAAAAAGAAA | 69641 |
rs29165983 | snp | A/C | 0.375 | 0.216506 | upstream-variant-2KB | Wdr20 | Mm_Celera | 12:110736547 | AAAAAAAAACCACCA[A/C]AAAAAAAAAAAAAAA | 69641 |
rs29168692 | snp | A/T | 0.5 | 0 | intron-variant | Wdr20 | Mm_Celera | 12:110773246 | CATATAAATAAAAAA[A/T]AAATAAATCTTTAAA | 69641 |
rs29170399 | snp | C/T | 0.5 | 0 | intron-variant, upstream-variant-2KB | Wdr20 | Mm_Celera | 12:110778840 | ATTTCTAGAGCAGGG[C/T]CTGCAGCAGGGCTTG | 69641 |
rs29170860 | snp | A/C | 0.375 | 0.216506 | upstream-variant-2KB | Wdr20 | Mm_Celera | 12:110736542 | GAAAAAAAAAAAAAC[A/C]ACCAAAAAAAAAAAA | 69641 |
rs29172033 | snp | A/G | 0.46875 | 0.121031 | intron-variant | Wdr20 | Mm_Celera | 12:110776441 | CCATGAAGTATTAGA[A/G]AAGGGACTTCTGTAT | 69641 |
rs29173207 | snp | A/G | 0.5 | 0 | intron-variant | Wdr20 | Mm_Celera | 12:110773275 | AAGAAAAAAAAAAAA[A/G]GGGAGCTAGAGAAAG | 69641 |
rs29173857 | snp | A/C | 0.375 | 0.216506 | intron-variant | Wdr20 | Mm_Celera | 12:110755562 | CCCCCCCTCCCCCCC[A/C]GACAGGGTCTCTCTG | 69641 |
rs29175868 | snp | C/T | 0.375 | 0.216506 | intron-variant | Wdr20 | Mm_Celera | 12:110771017 | TGGTAGCCCACACAG[C/T]GGCACGATTAGGAGG | 69641 |
rs29177377 | snp | A/C/G | 0.375 | 0.216506 | intron-variant | Wdr20 | GRCm38.p3 | 12:110790974 | TCCCAGGGCCGGAAC[A/C/G]TAACAGTGAGGATGG | 69641 |
rs29177556 | snp | C/T | 0.375 | 0.216506 | intron-variant | Wdr20 | Mm_Celera | 12:110755554 | GTCCGTTCCCCCCCC[C/T]CCCCCCCAGACAGGG | 69641 |
rs29178737 | snp | A/G | 0.493827 | 0.0552116 | intron-variant | Wdr20 | Mm_Celera | 12:110784497 | AGAAGTTCTGTCAGA[A/G]CAAGTGGTGTGCTTC | 69641 |
rs29180288 | snp | G/T | 0.32 | 0.24 | intron-variant | Wdr20 | Mm_Celera | 12:110770884 | GAGGTAGAAGGAGGT[G/T]TGACTGCTGACATCT | 69641 |
rs29180894 | snp | A/G | 0.375 | 0.216506 | intron-variant | Wdr20 | Mm_Celera | 12:110766262 | AAACAGAAATCTGCA[A/G]CCAATGAAAATGCAG | 69641 |
rs29180924 | snp | C/T | 0.375 | 0.216506 | intron-variant | Wdr20 | Mm_Celera | 12:110744166 | GCTGCAAATAAGAGA[C/T]AGTGAGTACTAGAAA | 69641 |
rs29181162 | snp | A/G | 0.5 | 0 | upstream-variant-2KB | Wdr20 | GRCm38.p3 | 12:110735676 | GAGGCAGAAGCAGGC[A/G]GATTTCTGAGTTCGA | 69641 |
rs29183079 | snp | C/T | 0.32 | 0.24 | intron-variant | Wdr20 | Mm_Celera | 12:110772660 | AGTCACACATGTCAG[C/T]GTATGGGGGCCAAAT | 69641 |
rs29183851 | snp | A/C | 0.5 | 0 | intron-variant | Wdr20 | Mm_Celera | 12:110796499 | ATCAAGGGGAAATAG[A/C]TAGGATGCTGACAGT | 69641 |
rs29185675 | snp | A/G | 0.375 | 0.216506 | intron-variant | Wdr20 | Mm_Celera | 12:110771226 | ATGCTTCCCACTATG[A/G]TGATAATGGACCAAA | 69641 |
rs29185956 | snp | A/G | 0.401235 | 0.199068 | intron-variant | Wdr20 | Mm_Celera | 12:110759137 | TACAGGCTGCTGTAT[A/G]GGAAAACCAAATCTA | 69641 |
rs29188680 | snp | C/T | 0.387812 | 0.208586 | intron-variant, utr-variant-5-prime | Wdr20 | Mm_Celera | 12:110788834 | TAGTCCTTAGGAAGC[C/T]GGCTGTTTAATGGAG | 69641 |
rs29188745 | snp | C/T | 0.32 | 0.24 | intron-variant | Wdr20 | Mm_Celera | 12:110742910 | TTTCTTTCTTTCTTT[C/T]TTTTTTTTCTTTTCT | 69641 |
rs29190051 | snp | A/T | 0.32 | 0.24 | intron-variant | Wdr20 | Mm_Celera | 12:110773953 | GGTGTGCGCCACCAC[A/T]GCCCGACTCCTCTTG | 69641 |
rs29193331 | snp | A/G | 0.426035 | 0.177515 | intron-variant | Wdr20 | Mm_Celera | 12:110747390 | ATGAATGTCAGTCGC[A/G]TTTTTAAGATTTAAT | 69641 |
rs29193398 | snp | A/T | 0.297521 | 0.245442 | intron-variant, downstream-variant-500B | Wdr20 | Mm_Celera | 12:110742787 | TCTGAGCATAAAAAA[A/T]TTATTTTAGACTAAT | 69641 |
rs29193511 | snp | C/T | 0.5 | 0 | intron-variant | Wdr20 | Mm_Celera | 12:110775336 | CGTGCACCACCACGC[C/T]CGGCAAGAAAGTTTT | 69641 |
rs29194145 | snp | A/G | 0.48 | 0.0979796 | intron-variant | Wdr20 | GRCm38.p3 | 12:110797665 | TTCTGCCTCCAGATT[A/G]GCCTACACAGGGCAG | 69641 |
rs29194511 | snp | C/T | 0.444444 | 0.157135 | intron-variant | Wdr20 | Mm_Celera | 12:110754162 | ATTGAAGCAAGGTCT[C/T]ATGTGTCTCAGGCTG | 69641 |
rs29195900 | snp | A/G | 0.5 | 0 | intron-variant | Wdr20 | Mm_Celera | 12:110757329 | AAGTTTGGTCACACA[A/G]TAACACCTCTATTCC | 69641 |
rs29199644 | snp | C/T | 0.444444 | 0.157135 | intron-variant | Wdr20 | Mm_Celera | 12:110776759 | CAACAACAACAAAAA[C/T]ACCTTTCTCATCCAT | 69641 |
rs29200339 | snp | C/T | 0.46875 | 0.121031 | intron-variant, upstream-variant-2KB | Wdr20 | Mm_Celera | 12:110778640 | TTTTCTCCTTGTCTG[C/T]TTATGGTCAGCAGAC | 69641 |
rs29201161 | snp | C/T | 0.475309 | 0.108333 | synonymous-codon, intron-variant | Wdr20 | Mm_Celera | 12:110793761 | GAACTCTACAGACAG[C/T]CGCCCTGTAAGTGTT | 69641 |
rs29204796 | snp | A/G | 0.375 | 0.216506 | intron-variant | Wdr20 | Mm_Celera | 12:110790969 | TCAGTTCCCAGGGCC[A/G]GAACGTAACAGTGAG | 69641 |
rs29205188 | snp | C/G/T | 0.444444 | 0.157135 | intron-variant | Wdr20 | GRCm38.p3 | 12:110744187 | GTACTAGAAAGTAAA[C/G/T]GGGTTGCTGCAGGTT | 69641 |
rs29210718 | snp | A/G | 0.444444 | 0.157135 | intron-variant | Wdr20 | Mm_Celera | 12:110755954 | AAATTAGCAATGGTA[A/G]GGTCCAGCAGAAACC | 69641 |
rs29211249 | snp | C/T | 0.46281 | 0.131194 | intron-variant | Wdr20 | Mm_Celera | 12:110749200 | AACCAGTTTATCTAG[C/T]TGCAGTTCTCCAAGG | 69641 |
rs29211822 | snp | G/T | 0.32 | 0.24 | intron-variant | Wdr20 | Mm_Celera | 12:110747568 | CTGTCTGTACCCGTG[G/T]TGCCATCTCCCCACC | 69641 |
rs29216681 | snp | C/T | 0.444444 | 0.157135 | downstream-variant-500B, intron-variant | Wdr20 | Mm_Celera | 12:110795439 | GCTGAGAGTCCAGGA[C/T]TCTTGGAGACAGCAC | 69641 |
rs29217111 | snp | C/T | 0.375 | 0.216506 | intron-variant | Wdr20 | Mm_Celera | 12:110802605 | GCCAGCTCTTCCCTA[C/T]CGCCCTCCCAGCCCA | 69641 |
rs29217537 | snp | C/T | 0.32 | 0.24 | intron-variant | Wdr20 | Mm_Celera | 12:110773904 | TCAAACTCAGAAATC[C/T]GCCTGCCTCTGCCTC | 69641 |
rs29218491 | snp | A/T | 0.5 | 0 | intron-variant | Wdr20 | Mm_Celera | 12:110780582 | AATATATCAGGACTT[A/T]TACAGAGCAGACAGA | 69641 |
rs29218775 | snp | A/G | 0.5 | 0 | intron-variant | Wdr20 | Mm_Celera | 12:110801014 | GAGGTACTGTCAGAT[A/G]TTTATGGCCAAAGGT | 69641 |
rs29220011 | snp | C/T | 0.32 | 0.24 | intron-variant | Wdr20 | Mm_Celera | 12:110744152 | TTAACTTTCTTAAAG[C/T]TGCAAATAAGAGACA | 69641 |
rs29220176 | snp | C/T | 0.387812 | 0.208586 | intron-variant | Wdr20 | Mm_Celera | 12:110790995 | GTGAGGATGGCATAC[C/T]GCAGCACGTGGTATG | 69641 |
rs29220532 | snp | C/T | 0.32 | 0.24 | intron-variant | Wdr20 | Mm_Celera | 12:110748734 | CCTGTCCTGGAACTC[C/T]GTAGTCGAGGCTGGC | 69641 |
rs29221472 | snp | C/T | 0.444444 | 0.157135 | intron-variant | Wdr20 | Mm_Celera | 12:110746513 | AGTGTGCTGTGTAGC[C/T]CAGGCTGGCCTGGAG | 69641 |
rs29222960 | snp | A/G | 0.487535 | 0.077957 | intron-variant | Wdr20 | Mm_Celera | 12:110784583 | CAGGCCATTTCTGCA[A/G]TAGGGGTGGCAGGTA | 69641 |
rs29488592 | snp | C/T | 0.32 | 0.24 | intron-variant | Wdr20 | Mm_Celera | 12:110770607 | TGGATGCCGTGTGTG[C/T]GCGCGCGCGTGTGTA | 69641 |
rs29489911 | snp | A/G | 0.415225 | 0.187619 | intron-variant | Wdr20 | Mm_Celera | 12:110775341 | ACCACCACGCTCGGC[A/G]AGAAAGTTTTAAAGT | 69641 |
rs33355096 | snp | C/T | 0.459184 | 0.136902 | upstream-variant-2KB, utr-variant-5-prime, nc-transcript-variant | Wdr20 | Mm_Celera | 12:110737700 | CTCTTAGGGATCGGG[C/T]CCCTCAGCGAAGCTG | 69641 |
rs33355099 | snp | A/T | 0.396694 | 0.202437 | intron-variant | Wdr20 | Mm_Celera | 12:110738952 | TAGGGAGGTTGGAAT[A/T]ATGTTTTCAAATAGG | 69641 |
rs33355102 | snp | C/T | 0.18 | 0.24 | intron-variant | Wdr20 | Mm_Celera | 12:110739368 | TGTTCCCAGGGATGG[C/T]TATATCCAAAGTCAG | 69641 |
rs33355615 | snp | A/T | 0.444444 | 0.157135 | intron-variant | Wdr20 | Mm_Celera | 12:110753962 | TGGGTTCTTTTTAAA[A/T]GCATGTCGAGTGCTG | 69641 |
rs33355618 | snp | C/T | 0.197531 | 0.244432 | intron-variant | Wdr20 | Mm_Celera | 12:110753969 | TTTTTAAAAGCATGT[C/T]GAGTGCTGACTTGTG | 69641 |
rs33355621 | snp | C/T | 0.345679 | 0.230967 | intron-variant | Wdr20 | Mm_Celera | 12:110753979 | CATGTCGAGTGCTGA[C/T]TTGTGTGCGCTGCTC | 69641 |
rs33355636 | snp | C/T | 0.124444 | 0.216185 | intron-variant | Wdr20 | Mm_Celera | 12:110785876 | ATTGTAAGTTCTTCA[C/T]ATGTACTGGAAATAA | 69641 |
rs33355639 | snp | A/T | 0.124444 | 0.216185 | intron-variant | Wdr20 | Mm_Celera | 12:110785942 | AATTTCAAAGGTAAT[A/T]TTTTTTGCCTGCAAA | 69641 |
rs33355642 | snp | A/G | 0.124444 | 0.216185 | intron-variant | Wdr20 | Mm_Celera | 12:110785957 | ATTTTTTGCCTGCAA[A/G]TTAGAACTGTAAGAA | 69641 |
rs33355874 | snp | A/C | 0.497778 | 0.0332592 | intron-variant | Wdr20 | Mm_Celera | 12:110777478 | GTCCTCAGACTCCGT[A/C]CAGCTGCCCTGTGTC | 69641 |
rs33355877 | snp | A/G | 0.444444 | 0.157135 | intron-variant, upstream-variant-2KB | Wdr20 | Mm_Celera | 12:110777548 | TTTGTTTGAGCCAGT[A/G]TTCACCATACACTTC | 69641 |
rs33355880 | snp | A/G | 0.396694 | 0.202437 | intron-variant, upstream-variant-2KB | Wdr20 | Mm_Celera | 12:110777552 | TTTGAGCCAGTGTTC[A/G]CCATACACTTCAGTG | 69641 |