SNP - dbSNP |
dbSNP | Type | Alleles | Het | Se(het) | Fxn-class | Gene Name | Assembly | Chr-pos | Sequence | Entrez Gene |
rs6268682 | snp | A/G | 0.32 | 0.24 | intron-variant | Gch1 | Mm_Celera | 14:47160974 | CACATACCTGTGTGC[A/G]CTTCTTCCTGCTCTT | 14528 |
rs6270720 | snp | A/C | 0.5 | 0 | intron-variant | Gch1 | Mm_Celera | 14:47161378 | GTTCTTCTATGAATC[A/C]TGTCTCGTGGTTGGT | 14528 |
rs6310362 | snp | A/G | 0.444444 | 0.157135 | intron-variant | Gch1 | Mm_Celera | 14:47157083 | CGCAAACAAACTTCT[A/G]CAGTGATGCTTAGGA | 14528 |
rs6310999 | snp | C/T | 0.408163 | 0.193609 | intron-variant | Gch1 | Mm_Celera | 14:47157236 | TTTGACCTCCACAAA[C/T]ACAGATACACATGCA | 14528 |
rs6311439 | snp | A/C | 0.5 | 0 | intron-variant | Gch1 | Mm_Celera | 14:47157287 | AATCAGAACAAAAAT[A/C]TTTTCTATCCCTGGC | 14528 |
rs13474611 | snp | G/T | 0.408163 | 0.193609 | utr-variant-3-prime | Gch1 | GRCm38.p3 | 14:47155782 | GCTGAGCTTCCGTGC[G/T]CGAGCCCTGGTTTGC | 14528 |
rs13474612 | snp | C/T | | | utr-variant-3-prime | Gch1 | Mm_Celera | 14:47154210 | GCTATACCTTTATCT[C/T]TCTGGGGGGTTGGTC | 14528 |
rs30112395 | snp | C/G | 0.444444 | 0.157135 | intron-variant | Gch1 | Mm_Celera | 14:47177184 | GCTATTTTAAAATTT[C/G]TTGGTTATTGAATGT | 14528 |
rs30144995 | snp | A/G | 0.5 | 0 | intron-variant | Gch1 | Mm_Celera | 14:47181320 | CAGGACTGATGGGCC[A/G]TTTCTTCAGCAACTA | 14528 |
rs30152228 | snp | C/T | 0.5 | 0 | intron-variant | Gch1 | Mm_Celera | 14:47170959 | AGGCTAGACTTGAAC[C/T]AATCTGCCCAGCTTG | 14528 |
rs30154358 | snp | A/G | 0.5 | 0 | intron-variant | Gch1 | Mm_Celera | 14:47169389 | TTTAAAATAAAAATG[A/G]AAATTAGTTAACTTT | 14528 |
rs30159145 | snp | C/G | 0.49827 | 0.0293608 | intron-variant | Gch1 | Mm_Celera | 14:47177667 | TTATACTTTTTTGTG[C/G]GAGCTTATTGTTTTT | 14528 |
rs30161488 | snp | G/T | 0.375 | 0.216506 | intron-variant | Gch1 | Mm_Celera | 14:47171230 | CATGAGAGAGTTTTT[G/T]GGTAGAAGATAGTGA | 14528 |
rs30165920 | snp | C/T | 0.5 | 0 | intron-variant | Gch1 | Mm_Celera | 14:47181291 | ATAAGCAAAGGCTGA[C/T]GCGGTAGATTCTGCA | 14528 |
rs30207197 | snp | C/T | 0.375 | 0.216506 | intron-variant | Gch1 | Mm_Celera | 14:47159927 | CATCGCTGAGAACAA[C/T]GCAGACAACAGAAGC | 14528 |
rs30214321 | snp | A/G | 0.5 | 0 | upstream-variant-2KB | Gch1 | Mm_Celera | 14:47189567 | CCCGCAGTTACACAA[A/G]ACAAGCTTCTGGTTA | 14528 |
rs30226052 | snp | A/T | 0.375 | 0.216506 | intron-variant | Gch1 | Mm_Celera | 14:47170089 | GGGGATACCCAGTCC[A/T]CGCAGTACAATAAGA | 14528 |
rs30228133 | snp | A/G | 0.5 | 0 | intron-variant | Gch1 | Mm_Celera | 14:47168359 | ATATATAGCCTACAA[A/G]TTTCCTATTGGAAAG | 14528 |
rs30249321 | snp | C/T | 0.444444 | 0.157135 | intron-variant | Gch1 | Mm_Celera | 14:47170001 | TGACAACATTGTATG[C/T]AAGTGTCACCTGTCA | 14528 |
rs30256651 | snp | C/T | 0.375 | 0.216506 | intron-variant | Gch1 | Mm_Celera | 14:47170612 | ATGCATGTTTCTAAA[C/T]GAACTAAGGAAAGCA | 14528 |
rs30284014 | snp | C/T | 0.5 | 0 | intron-variant | Gch1 | Mm_Celera | 14:47166034 | ACCTCCTCTTAAGAT[C/T]CAGGGCTGGACTGGG | 14528 |
rs30288834 | snp | G/T | 0.387812 | 0.208586 | intron-variant | Gch1 | Mm_Celera | 14:47178730 | CATCAGAATCAGGTA[G/T]CTTAGCAACATTTGT | 14528 |
rs30288842 | snp | C/T | 0.375 | 0.216506 | intron-variant | Gch1 | Mm_Celera | 14:47185559 | CCTTCCTCTAGCCTC[C/T]GAGGGCCCCTGTGTA | 14528 |
rs30320316 | snp | G/T | 0.444444 | 0.157135 | intron-variant | Gch1 | Mm_Celera | 14:47188440 | ACCTCAAACTGCTAG[G/T]AAGTCCGAATCCAGA | 14528 |
rs30344934 | snp | A/G | 0.415225 | 0.187619 | intron-variant | Gch1 | Mm_Celera | 14:47176562 | GGTCCACTAGAGCAG[A/G]GAGACCCTTTTCTAC | 14528 |
rs30364363 | snp | C/T | 0.444444 | 0.157135 | intron-variant | Gch1 | Mm_Celera | 14:47156277 | GACAACTCCTTGAAA[C/T]TTCCCAGCTGAGTGG | 14528 |
rs30397367 | snp | C/T | 0.444444 | 0.157135 | intron-variant | Gch1 | Mm_Celera | 14:47188424 | CTCAAGAAAAGTCCA[C/T]ACCTCAAACTGCTAG | 14528 |
rs30406801 | snp | A/G | 0.375 | 0.216506 | intron-variant | Gch1 | GRCm38.p3 | 14:47166822 | CTATACTCAATAAGG[A/G]AAAAAAAAAAATAGG | 14528 |
rs30430198 | snp | C/T | 0.375 | 0.216506 | intron-variant | Gch1 | Mm_Celera | 14:47166798 | AATCTGAAAGCCTGT[C/T]GAGAAAAACTATACT | 14528 |
rs30465580 | snp | A/G | 0.5 | 0 | intron-variant | Gch1 | Mm_Celera | 14:47168330 | ACAAAAAGCAAAGAA[A/G]ATATTAAATATTCAT | 14528 |
rs30502032 | snp | C/G | 0.290657 | 0.246672 | intron-variant | Gch1 | Mm_Celera | 14:47180643 | ACCACTTTCCAGCAT[C/G]TCATCTGACATTATC | 14528 |
rs30509646 | snp | A/G | 0.345679 | 0.230967 | intron-variant | Gch1 | GRCm38.p3 | 14:47180899 | TTACCAGAGTTATAT[A/G]GCTCCTTTTTAAAGG | 14528 |
rs30539140 | snp | G/T | 0.444444 | 0.157135 | intron-variant | Gch1 | Mm_Celera | 14:47177182 | CTGCTATTTTAAAAT[G/T]TGTTGGTTATTGAAT | 14528 |
rs30555154 | snp | C/T | 0.429688 | 0.173817 | intron-variant | Gch1 | Mm_Celera | 14:47177712 | AGAACTGGCAGTGTT[C/T]GCCAGACCTGGGATT | 14528 |
rs30625680 | snp | C/G | 0.375 | 0.216506 | intron-variant | Gch1 | Mm_Celera | 14:47170937 | ATAAGGGCTCACTAA[C/G]TTATCTAGGCTAGAC | 14528 |
rs30636594 | snp | A/G | 0.5 | 0 | intron-variant | Gch1 | Mm_Celera | 14:47171520 | GTATCTCCCAGCCAT[A/G]TCACTCTTCTCAGCT | 14528 |
rs30647503 | snp | A/G | 0.444444 | 0.157135 | intron-variant | Gch1 | Mm_Celera | 14:47178946 | ACGGGAGCCATAACC[A/G]GCGCTGGGATGCTGT | 14528 |
rs30671434 | snp | C/T | 0.401235 | 0.199068 | intron-variant | Gch1 | Mm_Celera | 14:47177226 | ACATGATTTGAGAAG[C/T]TGCACACATAGGCAG | 14528 |
rs30697581 | snp | A/G | 0.444444 | 0.157135 | intron-variant | Gch1 | Mm_Celera | 14:47188404 | ACTTTCAGCAATAAT[A/G]CTAGCTCAAGAAAAG | 14528 |
rs30759615 | snp | A/C | 0.444444 | 0.157135 | intron-variant | Gch1 | Mm_Celera | 14:47156852 | GCTGCCCTCTTTGCT[A/C]TCAAGACACGGCCTG | 14528 |
rs30771204 | snp | A/G | 0.444444 | 0.157135 | intron-variant | Gch1 | Mm_Celera | 14:47176343 | TCTCAGGGCTTCTGA[A/G]CCCCAACCCCTTTCA | 14528 |
rs30773098 | snp | C/T | 0.415225 | 0.187619 | intron-variant | Gch1 | Mm_Celera | 14:47181214 | GAGCAAGCTTCTCAA[C/T]CTGATAATTAGTGCA | 14528 |
rs30792836 | snp | C/T | 0.5 | 0 | intron-variant | Gch1 | Mm_Celera | 14:47182380 | TTGACTTGTACTCTA[C/T]CAAGAAAATCCTGTT | 14528 |
rs30800816 | snp | A/G | 0.415225 | 0.187619 | intron-variant | Gch1 | Mm_Celera | 14:47173832 | GAGCAAAAGCCTCAA[A/G]GTTGTTGGACTTTTA | 14528 |
rs30831587 | snp | A/T | 0.375 | 0.216506 | intron-variant | Gch1 | Mm_Celera | 14:47159683 | TGGGTTCAGTGGTTA[A/T]AAAATGTAGATTTTT | 14528 |
rs30847979 | snp | A/G | 0.444444 | 0.157135 | intron-variant | Gch1 | Mm_Celera | 14:47169976 | CATCTCTGTGATATA[A/G]CCACCGTGTTGACAA | 14528 |
rs30878970 | snp | A/G | 0.5 | 0 | intron-variant | Gch1 | Mm_Celera | 14:47159807 | GTAAGCCTAAATAAG[A/G]CAAAACACTGGTACA | 14528 |
rs30880831 | snp | A/G | 0.444444 | 0.157135 | intron-variant | Gch1 | Mm_Celera | 14:47179813 | CATGCATAAGGCCCC[A/G]GGTCCAATGTCTGAC | 14528 |
rs30899530 | snp | A/T | 0.375 | 0.216506 | intron-variant | Gch1 | Mm_Celera | 14:47183629 | TATTCAGTAAGCACA[A/T]TATCAACTGGGCCAT | 14528 |
rs30911116 | snp | C/T | 0.444444 | 0.157135 | intron-variant | Gch1 | Mm_Celera | 14:47164847 | AGCCAGAGCCTCACA[C/T]GCAGGCTGATCAAAA | 14528 |
rs30919581 | snp | C/T | 0.375 | 0.216506 | intron-variant | Gch1 | Mm_Celera | 14:47164664 | GGTTTGCCACTATGC[C/T]CAGCTTGAAAATAAA | 14528 |
rs30945120 | snp | G/T | 0.5 | 0 | intron-variant | Gch1 | Mm_Celera | 14:47164097 | CCATTTAGGACTATG[G/T]CAAATCTCACTATAA | 14528 |
rs30949981 | snp | C/T | 0.32 | 0.24 | intron-variant | Gch1 | Mm_Celera | 14:47156396 | CCAGAGAGATGCTCA[C/T]GGACATCGGTCATGC | 14528 |
rs30956836 | snp | C/T | 0.32 | 0.24 | intron-variant | Gch1 | Mm_Celera | 14:47170370 | ACAAGCCCCGTCATT[C/T]TCTAAGTAAATAGCC | 14528 |
rs30956838 | snp | C/T | 0.5 | 0 | intron-variant | Gch1 | Mm_Celera | 14:47161932 | GATTCAATATTTCAA[C/T]GATTAGACTTCAATT | 14528 |
rs30961353 | snp | C/T | 0.415225 | 0.187619 | intron-variant | Gch1 | Mm_Celera | 14:47176805 | TCTGCCTTTACAGGT[C/T]GTTATTCTTCTAAGC | 14528 |
rs30993807 | snp | A/G | 0.5 | 0 | intron-variant | Gch1 | Mm_Celera | 14:47186233 | CTGTGTAGCCCTGGC[A/G]GTCCTTGGAACTCAC | 14528 |
rs30995709 | snp | C/T | 0.444444 | 0.157135 | intron-variant | Gch1 | Mm_Celera | 14:47156873 | ACACGGCCTGATAAA[C/T]ACAATCAGCAGTGAT | 14528 |
rs31011424 | snp | A/G | 0.375 | 0.216506 | intron-variant | Gch1 | Mm_Celera | 14:47166792 | AATTCAAATCTGAAA[A/G]CCTGTCGAGAAAAAC | 14528 |
rs31019746 | snp | C/G | 0.5 | 0 | intron-variant | Gch1 | Mm_Celera | 14:47163933 | CCCATAAACACACTT[C/G]CTCCAGCAAGGCCAC | 14528 |
rs31026466 | snp | C/T | 0.5 | 0 | upstream-variant-2KB | Gch1 | Mm_Celera | 14:47189476 | GCGCCGCGAGATATT[C/T]TCATTGGCCGGAGCC | 14528 |
rs31041007 | snp | C/T | 0.5 | 0 | intron-variant | Gch1 | Mm_Celera | 14:47170685 | TTTCACGACTACACA[C/T]GTTAGAGTCAGCCTC | 14528 |
rs31069607 | snp | A/G | 0.5 | 0 | intron-variant | Gch1 | Mm_Celera | 14:47156672 | TGCACAGGGCCTCTG[A/G]GCACTGAGCGGGATA | 14528 |
rs31092667 | snp | C/T | 0.375 | 0.216506 | intron-variant | Gch1 | Mm_Celera | 14:47182434 | TGATTTTACTACGTA[C/T]GGTGATGCTCCAGGT | 14528 |
rs31093938 | snp | C/T | 0.473373 | 0.11227 | intron-variant | Gch1 | Mm_Celera | 14:47177208 | TGAATGTGAGACCCT[C/T]TGACATGATTTGAGA | 14528 |
rs31107782 | snp | C/T | 0.375 | 0.216506 | intron-variant | Gch1 | Mm_Celera | 14:47183142 | GTGTTGCATGCAGTA[C/T]CTGCACCTCCCCATT | 14528 |
rs31120399 | snp | A/T | 0.444444 | 0.157135 | intron-variant | Gch1 | Mm_Celera | 14:47186860 | AGCTCACACCTTTAA[A/T]CTCTTCATTCCAGAG | 14528 |
rs31122206 | snp | A/G | 0.5 | 0 | intron-variant | Gch1 | Mm_Celera | 14:47164039 | TTTAAACCACCACAG[A/G]TTTATACAGATTCCA | 14528 |
rs31136272 | snp | C/T | 0.5 | 0 | intron-variant | Gch1 | Mm_Celera | 14:47171582 | TGACAGATTATTGCC[C/T]TAGGTGTGAAGTTGT | 14528 |
rs31137770 | snp | A/C | 0.5 | 0 | intron-variant | Gch1 | Mm_Celera | 14:47170958 | TAGGCTAGACTTGAA[A/C]CAATCTGCCCAGCTT | 14528 |
rs31140796 | snp | A/G | 0.375 | 0.216506 | intron-variant | Gch1 | Mm_Celera | 14:47178775 | TATAGAATACATCCC[A/G]ACAGGAGTCTGCTCT | 14528 |
rs31145411 | snp | A/G | 0.444444 | 0.157135 | intron-variant | Gch1 | Mm_Celera | 14:47177188 | TTTTAAAATTTGTTG[A/G]TTATTGAATGTGAGA | 14528 |
rs31161557 | snp | C/G/T | 0.5 | 0 | intron-variant | Gch1 | GRCm38.p3 | 14:47177037 | AGAAATGCCAAATTA[C/G/T]TGATAGTCATCGTTG | 14528 |
rs31203907 | snp | C/T | 0.444444 | 0.157135 | intron-variant | Gch1 | Mm_Celera | 14:47181964 | GGCAGCATTGAAGCC[C/T]CGCTTCATGCTGTCA | 14528 |
rs31219116 | snp | A/T | 0.444444 | 0.157135 | upstream-variant-2KB | Gch1 | Mm_Celera | 14:47189629 | GTCTACAAAAAGCCA[A/T]GAATCCGGGGAGCTG | 14528 |
rs31229402 | snp | C/T | 0.415225 | 0.187619 | intron-variant | Gch1 | Mm_Celera | 14:47178321 | CAGAAGCAACTGGGC[C/T]GACAGAACCGGCAAC | 14528 |
rs31232454 | snp | C/T | 0.375 | 0.216506 | intron-variant | Gch1 | Mm_Celera | 14:47171333 | AAAGGATGATAGATA[C/T]CATAGATAAATAGAA | 14528 |
rs31262766 | snp | C/T | 0.401235 | 0.199068 | intron-variant | Gch1 | Mm_Celera | 14:47181089 | GACACTTTAGGCTGA[C/T]TGAGCTTGATGCCAG | 14528 |
rs31277410 | snp | C/T | 0.444444 | 0.157135 | intron-variant | Gch1 | Mm_Celera | 14:47162571 | CAGGAAGACGTGCAC[C/T]ACAGCTGCCTTCACA | 14528 |
rs31310905 | snp | C/T | 0.444444 | 0.157135 | intron-variant | Gch1 | Mm_Celera | 14:47159543 | AGACAGTTTAGAACA[C/T]ACACACCTATACACA | 14528 |
rs31319140 | snp | A/G | 0.493827 | 0.0552116 | intron-variant | Gch1 | Mm_Celera | 14:47165003 | AATAGAAAGGCCTGC[A/G]AACCAGTGTAAGTGC | 14528 |
rs31328753 | snp | C/G | 0.375 | 0.216506 | intron-variant | Gch1 | Mm_Celera | 14:47166399 | CAGTGCTTTTAACCA[C/G]TGAGCCATTGCTCCA | 14528 |
rs31376008 | snp | C/T | 0.444444 | 0.157135 | utr-variant-3-prime | Gch1 | Mm_Celera | 14:47155009 | CCGAGTCAGTACTTA[C/T]AAACTTGAGAAGTAA | 14528 |
rs31376450 | snp | C/G | 0.5 | 0 | intron-variant | Gch1 | Mm_Celera | 14:47176889 | TTAGTGTGATGCCCT[C/G]CTTTCTCTTTTCTTT | 14528 |
rs31382251 | snp | A/T | 0.5 | 0 | intron-variant | Gch1 | Mm_Celera | 14:47156675 | ACAGGGCCTCTGGGC[A/T]CTGAGCGGGATAGAT | 14528 |
rs31411311 | snp | C/T | 0.444444 | 0.157135 | intron-variant | Gch1 | Mm_Celera | 14:47164915 | AAGTGGCTTGGCTCC[C/T]CTTACTGTGTGACCT | 14528 |
rs31436488 | snp | A/G | 0.444444 | 0.157135 | intron-variant | Gch1 | Mm_Celera | 14:47159431 | GTGGTAGTATGGACA[A/G]CCTGTGTGAGGGCAG | 14528 |
rs31437424 | snp | C/T | 0.444444 | 0.157135 | intron-variant | Gch1 | Mm_Celera | 14:47169999 | GTTGACAACATTGTA[C/T]GTAAGTGTCACCTGT | 14528 |
rs31439999 | snp | C/T | 0.5 | 0 | intron-variant | Gch1 | Mm_Celera | 14:47163976 | CCCAAACAGTACCTC[C/T]AACTGGGGACCAAGT | 14528 |
rs31450321 | snp | G/T | 0.5 | 0 | intron-variant | Gch1 | Mm_Celera | 14:47156682 | CTCTGGGCACTGAGC[G/T]GGATAGATGGGTTTT | 14528 |
rs31458211 | snp | A/G | 0.32 | 0.24 | intron-variant | Gch1 | Mm_Celera | 14:47172086 | TTTTTCTTCAATAAT[A/G]AAGTTTTCCAGCTAT | 14528 |
rs31458396 | snp | C/T | 0.5 | 0 | intron-variant | Gch1 | Mm_Celera | 14:47156667 | GGAACTGCACAGGGC[C/T]TCTGGGCACTGAGCG | 14528 |
rs31469169 | snp | C/T | 0.5 | 0 | intron-variant | Gch1 | Mm_Celera | 14:47176707 | AGCTAGGATATAGGG[C/T]AGGGATACATACAGT | 14528 |
rs31509845 | snp | A/G | 0.375 | 0.216506 | intron-variant | Gch1 | Mm_Celera | 14:47177472 | GAAGGAAGGAAGGAA[A/G]GAAGGGAGAGAGAGA | 14528 |
rs31539999 | snp | C/T | 0.5 | 0 | intron-variant | Gch1 | Mm_Celera | 14:47167214 | CACAAGTAAAGCTAT[C/T]TGGGACAAAAGAGTA | 14528 |
rs31542779 | snp | A/G | 0.375 | 0.216506 | intron-variant | Gch1 | Mm_Celera | 14:47182748 | CTGTGGCAGTGGTTT[A/G]AATGAGAATACTTTG | 14528 |
rs33858255 | snp | A/G | 0.48 | 0.0979796 | intron-variant | Gch1 | Mm_Celera | 14:47156405 | TGCTCACGGACATCG[A/G]TCATGCCAACAAATG | 14528 |
rs45639554 | snp | C/G | | | intron-variant | Gch1 | Mm_Celera | 14:47177125 | CTGGGGATGGGGTGG[C/G]GAGGGTAGAAAGGGT | 14528 |
rs45707250 | snp | A/G | 0.391111 | 0.206368 | intron-variant | Gch1 | Mm_Celera | 14:47178186 | TAAGACACTGCTGTG[A/G]ACCAAGGGCTTCTCC | 14528 |
rs45752331 | snp | A/C | | | utr-variant-3-prime | Gch1 | Mm_Celera | 14:47155499 | TCAACCAAATGCATG[A/C]GTTCCCCCTCCTCCC | 14528 |