SNP - dbSNP |
dbSNP | Type | Alleles | Het | Se(het) | Fxn-class | Gene Name | Assembly | Chr-pos | Sequence | Entrez Gene |
rs13467314 | snp | A/G | 0.487535 | 0.077957 | synonymous-codon | Dcaf13 | Mm_Celera | 15:39146715 | GCCTGGATCTGTGCC[A/G]ATTGTGTCAGAGAGG | 223499 |
rs13467315 | snp | A/C | | | missense | Dcaf13 | Mm_Celera | 15:39143680 | GAAATGGACTTCTGA[A/C]AGCAAGTACATTATG | 223499 |
rs13482529 | snp | A/G | 0.494201 | 0.053533 | intron-variant | Dcaf13 | GRCm38.p3 | 15:39124218 | CAAAATGTGGTGGGA[A/G]AAGAGGAAAGAAGTT | 223499 |
rs31574050 | snp | C/T | 0.387812 | 0.208586 | intron-variant | Dcaf13 | Mm_Celera | 15:39115377 | CATGGCCCTCTAATA[C/T]CTGTTTATGTGATAT | 223499 |
rs31592584 | snp | C/T | 0.444444 | 0.157135 | intron-variant, upstream-variant-2KB | Slc25a32, Dcaf13 | Mm_Celera | 15:39112218 | CCAGGTAACGCAGGG[C/T]GCACAGCATCATCTT | 223499 |
rs31609752 | snp | A/T | 0.375 | 0.216506 | intron-variant | Dcaf13 | Mm_Celera | 15:39128594 | ACATATAAAAGAAAA[A/T]TTTTTTTTCCAGCTA | 223499 |
rs31634450 | snp | G/T | 0.444444 | 0.157135 | intron-variant | Dcaf13 | Mm_Celera | 15:39121144 | ATCAACAGATGAATA[G/T]ATATAGAAATTTTTG | 223499 |
rs31640619 | snp | C/T | 0.444444 | 0.157135 | intron-variant | Dcaf13 | Mm_Celera | 15:39141980 | GGATGTTTCCCTAAT[C/T]TCTTTCTCAGCCTGT | 223499 |
rs31649888 | snp | C/T | 0.5 | 0 | intron-variant, upstream-variant-2KB | Slc25a32, Dcaf13 | Mm_Celera | 15:39111939 | GCAAACTAAAGAAAC[C/T]TTAGTGAATATTTTA | 223499 |
rs31673177 | snp | A/G | 0.444444 | 0.157135 | intron-variant | Dcaf13 | Mm_Celera | 15:39136626 | ATGTATGGCTCCAGA[A/G]CAGCAAAGCGGCAGG | 223499 |
rs31749227 | snp | G/T | 0.5 | 0 | intron-variant | Dcaf13 | GRCm38.p3 | 15:39122922 | TATTATAATAATATG[G/T]TTTTTGTTCTGATTT | 223499 |
rs31749973 | snp | A/T | 0.33241 | 0.236027 | intron-variant | Dcaf13 | Mm_Celera | 15:39140136 | GATTGATAATATGAC[A/T]CAAAGATATATGACT | 223499 |
rs31763486 | snp | C/G | 0.401235 | 0.199068 | intron-variant, upstream-variant-2KB | Slc25a32, Dcaf13 | Mm_Celera | 15:39112285 | TAATGTCTCTTCTGC[C/G]TGTAAGTGCTTCGCT | 223499 |
rs31770897 | snp | A/T | 0.444444 | 0.157135 | intron-variant | Dcaf13 | Mm_Celera | 15:39136768 | TTTGAATTAAAACTA[A/T]AATTCAGATCTGCAA | 223499 |
rs31773663 | snp | A/G | 0.48 | 0.0979796 | intron-variant | Dcaf13 | Mm_Celera | 15:39144073 | AGCTTAGTTGAATTG[A/G]ACACCTGTCTCCAGA | 223499 |
rs31779733 | snp | A/G | 0.387812 | 0.208586 | intron-variant | Dcaf13 | Mm_Celera | 15:39121559 | CAAAGAATTAAAACT[A/G]TTGTATGAAATAATC | 223499 |
rs31783878 | snp | C/T | 0.33241 | 0.236027 | downstream-variant-500B | Dcaf13 | Mm_Celera | 15:39147033 | TCTTGTCAGAGCATT[C/T]GATGCTACTGCTATG | 223499 |
rs31794487 | snp | G/T | 0.188366 | 0.242283 | intron-variant | Dcaf13 | GRCm38.p3 | 15:39121622 | AGTCTCCTTCCCAAA[G/T]AGTTCCTTAGGTACC | 223499 |
rs31795206 | snp | C/T | 0.444444 | 0.157135 | intron-variant | Dcaf13 | Mm_Celera | 15:39130522 | CCCTTTGCACAGTTC[C/T]TGCTATGGTGCGCTT | 223499 |
rs31803113 | snp | C/T | 0.444444 | 0.157135 | intron-variant | Dcaf13 | Mm_Celera | 15:39131919 | TATTTTTGAAATATT[C/T]TTGTTGGCTGTCATG | 223499 |
rs31816087 | snp | A/G | 0.33241 | 0.236027 | intron-variant | Dcaf13 | Mm_Celera | 15:39139206 | AGCATATTTACTACC[A/G]TTCCTGTCTTTAAGA | 223499 |
rs31820068 | snp | A/C | 0.33241 | 0.236027 | intron-variant | Dcaf13 | Mm_Celera | 15:39115359 | ACCCTGTTTACAGAC[A/C]AACATGGCCCTCTAA | 223499 |
rs31822920 | snp | A/G | 0.375 | 0.216506 | intron-variant | Dcaf13 | Mm_Celera | 15:39131299 | CTGGAGAGATGGCTC[A/G]GCAGTTTAGAGGACG | 223499 |
rs31896936 | snp | A/G | 0.5 | 0 | intron-variant | Dcaf13 | Mm_Celera | 15:39143874 | TGTGATGGAAGGCTG[A/G]GGGGCTGGCTTGTTT | 223499 |
rs31912487 | snp | C/T | 0.444444 | 0.157135 | intron-variant | Dcaf13 | GRCm38.p3 | 15:39125121 | ATCTTTTTCTGAATA[C/T]ATAACAAGAAATGAC | 223499 |
rs31917696 | snp | C/G | 0.387812 | 0.208586 | intron-variant | Dcaf13 | GRCm38.p3 | 15:39123498 | GTGTTCTTTGTAATA[C/G]AGTCTGATTTCTCTG | 223499 |
rs31919384 | snp | G/T | 0.48 | 0.0979796 | intron-variant | Dcaf13 | Mm_Celera | 15:39145584 | AGCCTGGTCAGCAGA[G/T]CGAGCTCCAGGACAG | 223499 |
rs31921013 | snp | C/T | 0.375 | 0.216506 | intron-variant | Dcaf13 | Mm_Celera | 15:39146038 | CCAGCCCCCACCCTT[C/T]CTCCTGTAGAACGCC | 223499 |
rs31937878 | snp | A/G | 0.487535 | 0.077957 | intron-variant | Dcaf13 | Mm_Celera | 15:39145324 | GTCATCTCTGTCATC[A/G]CCATCACCAAGCAGA | 223499 |
rs31946189 | snp | A/G | 0.375 | 0.216506 | intron-variant | Dcaf13 | Mm_Celera | 15:39137562 | TAATCAGGTTCTCCT[A/G]AGGGCTCTCTTCTAG | 223499 |
rs31974144 | snp | G/T | 0.375 | 0.216506 | intron-variant | Dcaf13 | Mm_Celera | 15:39139705 | AGGCAACTTGGGGAG[G/T]AAAGAGTTTATTTGG | 223499 |
rs31987593 | snp | C/T | 0.444444 | 0.157135 | intron-variant | Dcaf13 | Mm_Celera | 15:39121362 | AAGACGTTCTGAGAA[C/T]GTACACTTTGAGATG | 223499 |
rs31989408 | snp | C/T | 0.46281 | 0.131194 | synonymous-codon | Dcaf13 | Mm_Celera | 15:39130293 | TGCAGCAAATGAAGA[C/T]TATAAGTAAGGTCTC | 223499 |
rs31993203 | snp | A/G | 0.375 | 0.216506 | intron-variant | Dcaf13 | Mm_Celera | 15:39115311 | AGCCTGGTCTACATA[A/G]TGAGTTCCAGGCCAG | 223499 |
rs31996013 | snp | A/C/T | 0.304498 | 0.276817 | intron-variant, upstream-variant-2KB | Slc25a32, Dcaf13 | Mm_Celera | 15:39112165 | TTTATGGTTAGGAGA[A/C/T]ACAGGGAAAGCCGGG | 223499 |
rs31996636 | snp | G/T | 0.498615 | 0.0262793 | intron-variant | Dcaf13 | GRCm38.p3 | 15:39124565 | AACATTTTCTACATT[G/T]ACTTTCTAGCATTTA | 223499 |
rs32046230 | snp | A/T | 0.33241 | 0.236027 | intron-variant | Dcaf13 | Mm_Celera | 15:39143515 | TTGAATTGTCCTTTT[A/T]TACTTCCTCCAGACA | 223499 |
rs32099108 | snp | A/G | 0.498615 | 0.0262793 | intron-variant | Dcaf13 | GRCm38.p3 | 15:39123571 | AGGGGTTGCAATGAA[A/G]TAGTTCTTAAAGGAA | 223499 |
rs32107025 | snp | A/C | 0.487535 | 0.077957 | intron-variant | Dcaf13 | Mm_Celera | 15:39145975 | TGAATTCCTGGGCTC[A/C]AGTGGTTCTTCTTCT | 223499 |
rs32114201 | snp | A/G | 0.375 | 0.216506 | intron-variant | Dcaf13 | Mm_Celera | 15:39132699 | CGTTGGAACCCTGGC[A/G]AAGGTTGACTGTAAG | 223499 |
rs32116061 | snp | A/G | 0.375 | 0.216506 | intron-variant | Dcaf13 | Mm_Celera | 15:39131455 | AGTGCACATAGAGAT[A/G]AGGAAGCACACACAC | 223499 |
rs32150897 | snp | A/G | 0.444444 | 0.157135 | intron-variant | Dcaf13 | Mm_Celera | 15:39122309 | GGGATTGCTCTTCTT[A/G]CTTGCAGGGGAAATG | 223499 |
rs32151420 | snp | A/G | 0.487535 | 0.077957 | intron-variant | Dcaf13 | Mm_Celera | 15:39140267 | AAGTGGCCTAGACTT[A/G]CTTGACAAAACTGTA | 223499 |
rs32174737 | snp | C/T | 0.375 | 0.216506 | intron-variant | Dcaf13 | Mm_Celera | 15:39124033 | AGACTAGGAATTTCA[C/T]AGCAAACTTGGTTTC | 223499 |
rs32184073 | snp | A/C | 0.359862 | 0.224567 | upstream-variant-2KB, intron-variant | Slc25a32, Dcaf13 | Mm_Celera | 15:39113629 | ACAGTGCATTGCTGG[A/C]TGGAGCTGTCATGGT | 223499 |
rs32212546 | snp | A/G | 0.444444 | 0.157135 | intron-variant | Dcaf13 | GRCm38.p3 | 15:39122673 | AGCACCAAGTTCTTA[A/G]CCTCGGAGTTTTCTC | 223499 |
rs32220397 | snp | A/G | 0.359862 | 0.224567 | intron-variant | Dcaf13 | Mm_Celera | 15:39121395 | AGAAGAAGTAAATGT[A/G]TGTGACGCATTAATA | 223499 |
rs32220849 | snp | A/C | 0.444444 | 0.157135 | intron-variant | Dcaf13 | Mm_Celera | 15:39142151 | AAGTAACCTTGGTTT[A/C]TGTTGCTTCTGTTCT | 223499 |
rs32223925 | snp | C/T | 0.444444 | 0.157135 | intron-variant | Dcaf13 | Mm_Celera | 15:39121401 | AGTAAATGTATGTGA[C/T]GCATTAATAGAAATG | 223499 |
rs32226467 | snp | C/T | 0.498615 | 0.0262793 | intron-variant | Dcaf13 | GRCm38.p3 | 15:39124693 | AGACAGACCTTGGAT[C/T]GCACAGACTGGTCTT | 223499 |
rs32251083 | snp | C/T | 0.444444 | 0.157135 | intron-variant | Dcaf13 | GRCm38.p3 | 15:39122638 | TCTGATAAGGAAACC[C/T]AGCCCCAGCCCTCTG | 223499 |
rs32316482 | snp | C/T | 0.48 | 0.0979796 | intron-variant | Dcaf13 | Mm_Celera | 15:39136210 | GTTCCTAGCTCCTGA[C/T]GTGCCTCACTGCTGA | 223499 |
rs32328148 | snp | C/T | 0.231111 | 0.249285 | intron-variant | Dcaf13 | GRCm38.p3 | 15:39117097 | CAGCTCAAGAGCTGT[C/T]GATGTCAGTGTGAAC | 223499 |
rs32342756 | snp | A/G | 0.375 | 0.216506 | intron-variant | Dcaf13 | Mm_Celera | 15:39145020 | GGACAAGGGGGAAGA[A/G]GTACTTCCTAAATTT | 223499 |
rs32343561 | snp | A/T | 0.444444 | 0.157135 | intron-variant | Dcaf13 | Mm_Celera | 15:39122305 | TCTAGGGATTGCTCT[A/T]CTTGCTTGCAGGGGA | 223499 |
rs32352116 | snp | A/G | 0.487535 | 0.077957 | intron-variant | Dcaf13 | Mm_Celera | 15:39144468 | GTTGATATTTTCTAA[A/G]TGTCCACTTTCCTGT | 223499 |
rs32353187 | snp | C/T | 0.375 | 0.216506 | intron-variant | Dcaf13 | Mm_Celera | 15:39132480 | AAGGCTGGCCTGAGG[C/T]AAAAAATTTATCTAT | 223499 |
rs32386047 | snp | G/T | 0.444444 | 0.157135 | upstream-variant-2KB, intron-variant | Slc25a32, Dcaf13 | Mm_Celera | 15:39113347 | CCAGCCTGGTCTACA[G/T]AGTGAGTTCCAGGAC | 223499 |
rs32395303 | snp | A/C | 0.375 | 0.216506 | intron-variant | Dcaf13 | Mm_Celera | 15:39138719 | TTCACAACCATGCTG[A/C]TTAAGCCAATTACAA | 223499 |
rs32403597 | snp | C/G | 0.401235 | 0.199068 | intron-variant, upstream-variant-2KB | Slc25a32, Dcaf13 | Mm_Celera | 15:39112179 | ACACAGGGAAAGCCG[C/G]GGTCCCCTTCCTAAA | 223499 |
rs32408918 | snp | A/G | 0.426035 | 0.177515 | intron-variant | Dcaf13 | Mm_Celera | 15:39131642 | GCAATGCCCAGCCGC[A/G]TTGAAGCCTTTGCTT | 223499 |
rs32409278 | snp | C/T | 0.487535 | 0.077957 | intron-variant | Dcaf13 | Mm_Celera | 15:39145990 | CAGTGGTTCTTCTTC[C/T]TCATCCTCTGAGAGC | 223499 |
rs32424465 | snp | A/C | 0.493827 | 0.0552116 | intron-variant | Dcaf13 | GRCm38.p3 | 15:39125151 | CCCTCATTGTCCAGA[A/C]GACTCAGTTAAGATG | 223499 |
rs32449650 | snp | A/G | 0.375 | 0.216506 | intron-variant | Dcaf13 | Mm_Celera | 15:39140322 | CATTGTAGGTGGTGG[A/G]AAAGAGAAGGAGAAA | 223499 |
rs32460615 | snp | C/T | 0.375 | 0.216506 | intron-variant | Dcaf13 | Mm_Celera | 15:39135123 | ACTGTGTGTCAGTGC[C/T]CCGCCCCGCAGCAGC | 223499 |
rs32474686 | snp | A/G | 0.487535 | 0.077957 | intron-variant | Dcaf13 | Mm_Celera | 15:39139158 | GCTGGGAGATTTAGT[A/G]CTGAGCCATCCATTT | 223499 |
rs32477466 | snp | C/T | 0.48 | 0.0979796 | intron-variant | Dcaf13 | Mm_Celera | 15:39126188 | CTTTTTTTTTTTAAT[C/T]TTATGAATTGACTTA | 223499 |
rs32505409 | snp | C/T | 0.375 | 0.216506 | intron-variant | Dcaf13 | Mm_Celera | 15:39130882 | TCTTCTTCACAAGTA[C/T]TTGTGACTCCTCCAG | 223499 |
rs32513692 | snp | G/T | 0.345679 | 0.230967 | intron-variant | Dcaf13 | GRCm38.p3 | 15:39123471 | AATATGAACAACTCT[G/T]TGTAGTAGAGTGTGT | 223499 |
rs32514426 | snp | C/G | 0.32 | 0.24 | intron-variant | Dcaf13 | Mm_Celera | 15:39145730 | TCAGTTGTAATATAG[C/G]TATTATTATGACATA | 223499 |
rs45676578 | snp | A/T | 0.197531 | 0.244432 | intron-variant, upstream-variant-2KB | Slc25a32, Dcaf13 | Mm_Celera | 15:39111031 | TAATAAATGCCTATT[A/T]TACATTCAATCAAAG | 223499 |
rs45719826 | snp | A/G | 0.142012 | 0.225474 | intron-variant | Dcaf13 | Mm_Celera | 15:39118234 | AAGGGAGCAAATGTA[A/G]AGTTATGTTCTATAG | 223499 |
rs45733311 | snp | A/G | 0.152778 | 0.230321 | intron-variant | Dcaf13 | Mm_Celera | 15:39128526 | TGTAGTATTGCTAGA[A/G]CAGAAGAAGGGGTAG | 223499 |
rs45778046 | snp | A/G | | | intron-variant | Dcaf13 | Mm_Celera | 15:39134042 | GCCTTGTAACTTTAT[A/G]GCAATAGTACATCAG | 223499 |
rs45790149 | snp | A/G | | | intron-variant, upstream-variant-2KB | Slc25a32, Dcaf13 | Mm_Celera | 15:39111022 | TAAAGGTCATAATAA[A/G]TGCCTATTATACATT | 223499 |
rs45816172 | snp | A/G | 0.32 | 0.24 | intron-variant | Dcaf13 | Mm_Celera | 15:39144346 | TGCAAGTCCTAAGAG[A/G]TCATCTGATGGCAAA | 223499 |
rs45868293 | snp | A/G | 0.124444 | 0.216185 | intron-variant | Dcaf13 | Mm_Celera | 15:39139030 | TTGAAAAGCAGATGT[A/G]GCTGTGCTGTTGAGG | 223499 |
rs45877302 | snp | A/G | 0.124444 | 0.216185 | intron-variant | Dcaf13 | Mm_Celera | 15:39140438 | TGCACCTACTAACTT[A/G]CCAGAGATTGGAATA | 223499 |
rs45881489 | snp | A/C | | | intron-variant | Dcaf13 | Mm_Celera | 15:39131602 | TTTCCCAGACTGAGA[A/C]GGAGCAGAGGTGATT | 223499 |
rs45955062 | snp | A/G | | | intron-variant | Dcaf13 | Mm_Celera | 15:39127257 | AGGAGATGGAGAGAC[A/G]ACTCAGTAGGTAAGC | 223499 |
rs45993314 | snp | A/G | 0.21875 | 0.248039 | intron-variant | Dcaf13 | Mm_Celera | 15:39126711 | TTGTTTGCAATAGGA[A/G]GTAACATTAGGCAGA | 223499 |
rs46078174 | snp | A/C | | | intron-variant | Dcaf13 | Mm_Celera | 15:39134785 | ATGAGGTTATATATC[A/C]AATCTATTTTACACG | 223499 |
rs46097483 | snp | A/G | | | intron-variant | Dcaf13 | Mm_Celera | 15:39117832 | GGAGAAAAGGGGAGC[A/G]TTACTGTTGATTTCA | 223499 |
rs46127774 | snp | A/T | 0.124444 | 0.216185 | intron-variant | Dcaf13 | Mm_Celera | 15:39124168 | GCCAACCCGGTGACT[A/T]TCAAATGTAGGCAAC | 223499 |
rs46150774 | snp | A/G | 0.124444 | 0.216185 | intron-variant | Dcaf13 | Mm_Celera | 15:39145040 | TTCCTAAATTTTTAC[A/G]CTCAAGAAAACTATA | 223499 |
rs46178700 | snp | A/C/T | | | upstream-variant-2KB, intron-variant | Slc25a32, Dcaf13 | GRCm38.p3 | 15:39114502 | TCCCAAGTGCTGGGA[A/C/T]TAAAGGCGTGCGCCG | 223499 |
rs46246850 | snp | A/G | 0.32 | 0.24 | intron-variant | Dcaf13 | Mm_Celera | 15:39145270 | GTATGTGTTGAGACC[A/G]TTGACTCTTCGCTTA | 223499 |
rs46427933 | snp | C/G | 0.124444 | 0.216185 | downstream-variant-500B | Dcaf13 | Mm_Celera | 15:39147186 | TGTAATTCAAGCCTA[C/G]GCTAATCTACACACA | 223499 |
rs46428312 | snp | C/T | 0.32 | 0.24 | intron-variant | Dcaf13 | Mm_Celera | 15:39118513 | ACTTGTACAGGACTA[C/T]ATATTTCATGATTTT | 223499 |
rs46437450 | snp | A/G | 0.124444 | 0.216185 | intron-variant | Dcaf13 | Mm_Celera | 15:39121335 | TTGGAAGCTACAGGG[A/G]AAGAGGCTAAGAAGA | 223499 |
rs46441387 | snp | C/G | 0.124444 | 0.216185 | intron-variant | Dcaf13 | Mm_Celera | 15:39120581 | GAGAGGAAGGGTCTG[C/G]TGTGATGAACTGGAC | 223499 |
rs46443765 | snp | C/T | 0.132653 | 0.220748 | intron-variant | Dcaf13 | Mm_Celera | 15:39129050 | CTCATTTGTGTGATA[C/T]GTGAACGCCACTGTC | 223499 |
rs46469951 | snp | A/G | 0.277778 | 0.248452 | intron-variant | Dcaf13 | Mm_Celera | 15:39131876 | TGTCTCTTAAAAGAA[A/G]TAGCTGCTAGTTTTC | 223499 |
rs46495507 | snp | A/G | 0.21875 | 0.248039 | intron-variant | Dcaf13 | Mm_Celera | 15:39114905 | GATTTAGAAGATAAA[A/G]TGAATATTTTCAAGG | 223499 |
rs46538359 | snp | C/T | 0.497041 | 0.0383476 | upstream-variant-2KB | Slc25a32, Dcaf13 | Mm_Celera | 15:39112831 | GAGACTACGGAACGC[C/T]GCGAGGTCCAGCTGA | 223499 |
rs46566897 | snp | C/T | | | upstream-variant-2KB, intron-variant | Slc25a32, Dcaf13 | Mm_Celera | 15:39113672 | GCCCAGGGAGTGGCC[C/T]TGTTGGAGTAGGTGT | 223499 |
rs46661534 | snp | C/T | 0.142012 | 0.225474 | utr-variant-5-prime, upstream-variant-2KB | Slc25a32, Dcaf13 | Mm_Celera | 15:39112540 | CGGCGTCCAGCGCCG[C/T]CGACGTGGGGCGTGA | 223499 |
rs46708669 | snp | A/T | 0.32 | 0.24 | intron-variant | Dcaf13 | Mm_Celera | 15:39117642 | CAATGAGACATACAG[A/T]CTAAAGGTTTGAGGA | 223499 |
rs46794162 | snp | C/G | 0.444444 | 0.157135 | intron-variant | Dcaf13 | Mm_Celera | 15:39132069 | TGTGCTGTCTGTTTT[C/G]TATCTTCATTTTTTT | 223499 |
rs46864761 | snp | C/T | 0.18 | 0.24 | intron-variant | Dcaf13 | Mm_Celera | 15:39131592 | GCTCTCAGGATTTCC[C/T]AGACTGAGACGGAGC | 223499 |