SNP - dbSNP |
dbSNP | Type | Alleles | Het | Se(het) | Fxn-class | Gene Name | Assembly | Chr-pos | Sequence | Entrez Gene |
rs6343814 | snp | G/T | 0.5 | 0 | intron-variant | Rnf216 | Mm_Celera | 5:143105799 | TGATATTTCCACTAA[G/T]GATTTTAAAAAGGTA | 108086 |
rs6344312 | snp | A/C | 0.359862 | 0.224567 | intron-variant | Rnf216 | Mm_Celera | 5:143105849 | TATTAAAGTCAGAAG[A/C]TATGAAAACTGGTGT | 108086 |
rs13469727 | snp | A/G | | | utr-variant-3-prime | Rnf216 | Mm_Celera | 5:142991038 | TACAAAAGAAAAAAA[A/G]AAAAAAAAATGAAGT | 108086 |
rs29511785 | snp | G/T | 0.465374 | 0.126941 | intron-variant | Rnf216 | Mm_Celera | 5:143027329 | ACTTGAGGAAAAGTT[G/T]CTTGTCTAATTAATA | 108086 |
rs29513399 | snp | A/G | 0.444444 | 0.157135 | intron-variant | Rnf216 | Mm_Celera | 5:142994254 | CCAGTGACACATGGT[A/G]GCTTACAACCATCTG | 108086 |
rs29525631 | snp | C/T | 0.5 | 0 | utr-variant-3-prime | Rnf216 | Mm_Celera | 5:142992009 | ACTGCCAGGGAACCC[C/T]CAACACCTTAGGAGA | 108086 |
rs29529606 | snp | A/G | 0.493827 | 0.0552116 | intron-variant | Rnf216 | Mm_Celera | 5:143060809 | TCCCAAGCATACATA[A/G]AGAGCAGCTGGAAGC | 108086 |
rs29541003 | snp | C/T | 0.5 | 0 | intron-variant | Rnf216 | Mm_Celera | 5:143058176 | TAGAAACATTCTTTT[C/T]ATAAAATAAGGTATG | 108086 |
rs29544427 | snp | A/G | 0.5 | 0 | intron-variant | Rnf216 | Mm_Celera | 5:143019830 | TTTGTCTTCATGTAT[A/G]TTAAGTGTACCACTT | 108086 |
rs29545251 | snp | A/G | 0.475309 | 0.108333 | intron-variant | Rnf216 | Mm_Celera | 5:143015338 | ATCCCCTAAGTGACT[A/G]AAGTGATTTGTCCAC | 108086 |
rs29546436 | snp | C/T | 0.5 | 0 | intron-variant | Rnf216 | Mm_Celera | 5:142994043 | AGACAAAAAGACTCT[C/T]TATGGTTAGGGCTGG | 108086 |
rs29547443 | snp | C/T | 0.465374 | 0.126941 | intron-variant | Rnf216 | Mm_Celera | 5:143016390 | TGTTTCTAGAAGCAT[C/T]TCAACTGATAAGGAG | 108086 |
rs29560143 | snp | A/T | 0.48 | 0.0979796 | intron-variant | Rnf216 | Mm_Celera | 5:143000827 | ACCAGAGTAGTTTTC[A/T]TTAAGAGCGGAAATG | 108086 |
rs29561174 | snp | A/T | 0.475309 | 0.108333 | intron-variant | Rnf216 | Mm_Celera | 5:142996595 | TAACTGAGCTACCAT[A/T]CAAGCCTCTGTGTGG | 108086 |
rs29562537 | snp | C/T | 0.492188 | 0.0620098 | intron-variant | Rnf216 | Mm_Celera | 5:143000945 | GAGGCAGAGGCTGTG[C/T]CTGCAGGTCAGACAC | 108086 |
rs29562977 | snp | A/T | 0.48 | 0.0979796 | intron-variant | Rnf216 | Mm_Celera | 5:143017891 | AGTGCTGGCATTATA[A/T]AGAATTCTTAAAAAA | 108086 |
rs29581320 | snp | C/T | 0.498615 | 0.0262793 | intron-variant | Rnf216 | Mm_Celera | 5:143001270 | TTCCCAGCTCAGTTG[C/T]GGGACTGCATGAGAA | 108086 |
rs29627777 | snp | C/T | 0.484429 | 0.0868505 | intron-variant | Rnf216 | Mm_Celera | 5:143000622 | AGCAGGCCCCGTACT[C/T]GCAGTAGAGAGAAGC | 108086 |
rs29629865 | snp | A/C | 0.492188 | 0.0620098 | intron-variant | Rnf216 | Mm_Celera | 5:142997896 | CAGCTATGAGCAAGG[A/C]ATGGGGCACAGACCT | 108086 |
rs29675758 | snp | A/G | 0.5 | 0 | intron-variant | Rnf216 | Mm_Celera | 5:142994132 | TCTGTGAGGTTTGTG[A/G]AGGCTACATAGTGAG | 108086 |
rs29684953 | snp | A/T | 0.492188 | 0.0620098 | intron-variant | Rnf216 | GRCm38.p3 | 5:143030861 | CAATGGTGTTGGGAT[A/T]GGACACATCTCAGTG | 108086 |
rs29716169 | snp | C/T | 0.492188 | 0.0620098 | intron-variant | Rnf216 | Mm_Celera | 5:142998419 | GAGCAGGATCACAGG[C/T]CAGTCCTCAAGTTCT | 108086 |
rs29736141 | snp | A/G | 0.465374 | 0.126941 | intron-variant | Rnf216 | GRCm38.p3 | 5:143051498 | GGGATATAAAATTGT[A/G]TTGATGACTAACAGT | 108086 |
rs29767468 | snp | G/T | 0.5 | 0 | intron-variant | Rnf216 | Mm_Celera | 5:143016055 | ATAAATTTCCCAACT[G/T]CCTGGAGACTCAGTT | 108086 |
rs29776669 | snp | A/G | 0.444444 | 0.157135 | intron-variant | Rnf216 | Mm_Celera | 5:143010854 | CCCCTGTTAACTAAC[A/G]GGCTACACCCTTACC | 108086 |
rs29778359 | snp | C/T | 0.5 | 0 | intron-variant | Rnf216 | Mm_Celera | 5:143002614 | GATGGTAGATGCATG[C/T]ACCACCACGCTCGCT | 108086 |
rs33038308 | snp | C/G | 0.5 | 0 | intron-variant | Rnf216 | Mm_Celera | 5:142998504 | TAGTGGATATGGCTA[C/G]AAGAGCTACAATTTT | 108086 |
rs33040711 | snp | C/T | 0.492188 | 0.0620098 | intron-variant | Rnf216 | Mm_Celera | 5:143000507 | CTTAAGAAACAAGCC[C/T]TCAGCTCACCTGAAT | 108086 |
rs33048726 | snp | C/G | 0.5 | 0 | intron-variant | Rnf216 | Mm_Celera | 5:143015491 | TTTCTGATATTCTCC[C/G]TTTTCCCTGTGGCTA | 108086 |
rs33058984 | snp | A/G | 0.48 | 0.0979796 | intron-variant | Rnf216 | Mm_Celera | 5:143030864 | TGGTGTTGGGATTGG[A/G]CACATCTCAGTGTCA | 108086 |
rs33064525 | snp | A/G | 0.5 | 0 | intron-variant | Rnf216 | Mm_Celera | 5:143021265 | GCCTTTTTCGTCTCA[A/G]GCTGCTGTAACTAGT | 108086 |
rs33069809 | snp | C/T | 0.48 | 0.0979796 | intron-variant | Rnf216 | Mm_Celera | 5:142996514 | TCAGTGGCTTTTTTT[C/T]CCTTGAGACAAGTTG | 108086 |
rs33084953 | snp | A/C | 0.484429 | 0.0868505 | intron-variant | Rnf216 | Mm_Celera | 5:143020944 | AGTAGAAACTGCAAA[A/C]AGAAGACTGCTTCTT | 108086 |
rs33097408 | snp | C/T | 0.497778 | 0.0332592 | intron-variant | Rnf216 | Mm_Celera | 5:142998484 | GCCATAGCCACAGGG[C/T]TCAGTAGTGGATATG | 108086 |
rs33098467 | snp | C/G | 0.497778 | 0.0332592 | intron-variant | Rnf216 | Mm_Celera | 5:142997130 | CCAGTTCGTGTACAC[C/G]GTGCATTGTCCTGAA | 108086 |
rs33122533 | snp | C/G/T | 0.475309 | 0.108333 | intron-variant | Rnf216 | GRCm38.p3 | 5:143003124 | TGGGGTGCTGCTGTT[C/G/T]GTGAAGCTGGGCACT | 108086 |
rs33123418 | snp | C/G | 0.5 | 0 | intron-variant | Rnf216 | Mm_Celera | 5:143014222 | CCTTGAAGTCATACA[C/G]ATCTGCCTGCATTGC | 108086 |
rs33153873 | snp | A/G | 0.497778 | 0.0332592 | intron-variant | Rnf216 | Mm_Celera | 5:143000432 | TTAAGGAGAGGGTGA[A/G]GACATACCAGGCTGT | 108086 |
rs33172490 | snp | C/T | 0.48 | 0.0979796 | utr-variant-3-prime | Rnf216 | Mm_Celera | 5:142992609 | GAAGATGAGACTGGG[C/T]CCTCCTGCAGACTCG | 108086 |
rs33174862 | snp | C/T | 0.444444 | 0.157135 | intron-variant | Rnf216 | Mm_Celera | 5:143021339 | CAGCCCCAAGGTTTA[C/T]ACCTGGCAGCTTCTG | 108086 |
rs33175505 | snp | C/G | 0.484429 | 0.0868505 | intron-variant | Rnf216 | Mm_Celera | 5:142997986 | ACAACTCCGAGCAAA[C/G]GGCTGCATCAGATGG | 108086 |
rs33236333 | snp | A/G | 0.444444 | 0.157135 | utr-variant-3-prime | Rnf216 | GRCm38.p3 | 5:142992025 | CAACACCTTAGGAGA[A/G]AGAAGCTGCTCACCC | 108086 |
rs33258775 | snp | G/T | 0.497778 | 0.0332592 | intron-variant | Rnf216 | Mm_Celera | 5:142995182 | AGAGGAGGGCTGTTA[G/T]AGATGGTTCTGGGCT | 108086 |
rs33281610 | snp | A/G | 0.444444 | 0.157135 | intron-variant | Rnf216 | Mm_Celera | 5:143058703 | GGGAGTGGGGGGTGG[A/G]GGGAAGCTGGTCTGT | 108086 |
rs33282766 | snp | C/T | 0.444444 | 0.157135 | intron-variant | Rnf216 | Mm_Celera | 5:142994217 | GCACTGACTGTGCTT[C/T]CAGAGGTCCTGAGTT | 108086 |
rs33342169 | snp | A/G | 0.48 | 0.0979796 | intron-variant | Rnf216 | Mm_Celera | 5:143019435 | GGAGAACATTTGTCA[A/G]GCATGTGTAAGGCCC | 108086 |
rs33358512 | snp | C/T | 0.465374 | 0.126941 | intron-variant | Rnf216 | Mm_Celera | 5:143012279 | CTCTAGAGAAGAACA[C/T]GTTGGTGAATTGCCT | 108086 |
rs33362320 | snp | A/G | 0.484429 | 0.0868505 | intron-variant | Rnf216 | Mm_Celera | 5:142997070 | TCCTCCAGGTCTACA[A/G]TGCTTAAGGGCAGGG | 108086 |
rs33383615 | snp | C/T | 0.5 | 0 | intron-variant | Rnf216 | Mm_Celera | 5:143017158 | TATAGCTCTGGCTGT[C/T]CTGGAACTCACTCTG | 108086 |
rs33389296 | snp | G/T | 0.444444 | 0.157135 | intron-variant | Rnf216 | Mm_Celera | 5:143032312 | ATGAGAGAGCCCATT[G/T]TAAAAAAAGCAAGAT | 108086 |
rs33400285 | snp | C/T | 0.5 | 0 | intron-variant | Rnf216 | Mm_Celera | 5:142997109 | CTTCTCCCCTTAGCC[C/T]GTGAACCAGTTCGTG | 108086 |
rs33406972 | snp | C/G | 0.444444 | 0.157135 | intron-variant | Rnf216 | Mm_Celera | 5:143013674 | GAAATCCGCCTGCCT[C/G]TGTCTCCCGAGTGCT | 108086 |
rs33420197 | snp | C/G | 0.465374 | 0.126941 | intron-variant | Rnf216 | Mm_Celera | 5:143054879 | GTGCTCACCACCCTA[C/G]TCCTTGTTCTCTCCC | 108086 |
rs33423311 | snp | C/G | 0.455 | 0.143091 | intron-variant | Rnf216 | Mm_Celera | 5:143058598 | ACAACATGCTTTCGG[C/G]TGGAAAACAAGCCCT | 108086 |
rs33425556 | snp | A/C | 0.5 | 0 | intron-variant | Rnf216 | Mm_Celera | 5:142998515 | GCTACAAGAGCTACA[A/C]TTTTGGGGCTCCAGC | 108086 |
rs33462514 | snp | C/G | 0.444444 | 0.157135 | intron-variant | Rnf216 | Mm_Celera | 5:143010448 | ATGGTTATGAGCCAC[C/G]ATGTGGTTGCTGGGA | 108086 |
rs33474156 | snp | C/G | 0.497778 | 0.0332592 | intron-variant | Rnf216 | Mm_Celera | 5:142997429 | CTCTGACTTTGTCTA[C/G]ACAGAACCTTGTGTC | 108086 |
rs33487984 | snp | C/T | 0.444444 | 0.157135 | intron-variant | Rnf216 | GRCm38.p3 | 5:143053616 | GTGTGTGTGTGTGTG[C/T]GTGTGTACACATTGT | 108086 |
rs33502030 | snp | A/G | 0.492188 | 0.0620098 | intron-variant | Rnf216 | Mm_Celera | 5:142997726 | TTTGATCACTCCCTG[A/G]GGGGCCAAGGTCCTT | 108086 |
rs33506476 | snp | A/G | 0.432133 | 0.171253 | intron-variant | Rnf216 | GRCm38.p3 | 5:143083981 | TATGAGGCTTAGGGA[A/G]TGGACACCCGGACAA | 108086 |
rs33510887 | snp | C/T | 0.48 | 0.0979796 | intron-variant | Rnf216 | Mm_Celera | 5:143030914 | ATTCTCTCTCTCTCT[C/T]CACTGCTGGCATTCC | 108086 |
rs33534419 | snp | C/G | 0.48 | 0.0979796 | intron-variant | Rnf216 | Mm_Celera | 5:143000026 | AAACCAGCAAACAAA[C/G]AAACAAAAACACTTA | 108086 |
rs33535762 | snp | G/T | 0.5 | 0 | intron-variant | Rnf216 | Mm_Celera | 5:143003300 | TGGGGAATGAGGCAG[G/T]AGGACTGTCAAACGA | 108086 |
rs33551044 | snp | C/T | 0.48 | 0.0979796 | intron-variant | Rnf216 | Mm_Celera | 5:143010858 | TGTTAACTAACAGGC[C/T]ACACCCTTACCACGC | 108086 |
rs33562747 | snp | A/G | 0.492188 | 0.0620098 | intron-variant | Rnf216 | Mm_Celera | 5:143000526 | GCTCACCTGAATTCG[A/G]TGACAATGGGGAAGG | 108086 |
rs33581534 | snp | A/G | 0.46875 | 0.121031 | intron-variant | Rnf216 | Mm_Celera | 5:143022138 | GTTTTTAACTGCTGT[A/G]GCTTGCTGGATCAGA | 108086 |
rs33585300 | snp | A/G | 0.46875 | 0.121031 | intron-variant | Rnf216 | Mm_Celera | 5:143028179 | GTTCGGAAGGCACAG[A/G]CCAGTTTTCTCTTTT | 108086 |
rs33599072 | snp | A/C | 0.5 | 0 | intron-variant | Rnf216 | Mm_Celera | 5:143111057 | AACAAAAACAAAAAA[A/C]AAAAAAAAAACAAAA | 108086 |
rs33610700 | snp | G/T | 0.497778 | 0.0332592 | utr-variant-3-prime | Rnf216 | GRCm38.p3 | 5:142992100 | CCCTTTTGTTTGATG[G/T]CAAGTGTCAGGACTT | 108086 |
rs33630896 | snp | A/C | 0.493827 | 0.0552116 | intron-variant | Rnf216 | Mm_Celera | 5:143021228 | CTGAAGTGTGGCACC[A/C]TGGTCCCTGGTCATT | 108086 |
rs33641476 | snp | C/G | 0.444444 | 0.157135 | intron-variant | Rnf216 | Mm_Celera | 5:143013974 | TGCCACCTCTCCAGT[C/G]TCCCTGTGATACAGA | 108086 |
rs33657472 | snp | G/T | 0.49827 | 0.0293608 | intron-variant | Rnf216 | Mm_Celera | 5:143000898 | TGTCCATGCAGCGGG[G/T]TCTGCACAAAGAAAC | 108086 |
rs33674114 | snp | A/G/T | 0.444444 | 0.157135 | downstream-variant-500B | Rnf216 | GRCm38.p3 | 5:142990632 | ATTTGGGGGGGGGGG[A/G/T]TGGTCCTCCAAGGAC | 108086 |
rs33679167 | snp | A/G | 0.375 | 0.216506 | intron-variant | Rnf216 | Mm_Celera | 5:143036121 | GCATTATGAAGTCCC[A/G]CCCTCTCCATCTTCC | 108086 |
rs33681046 | snp | A/G | 0.484429 | 0.0868505 | intron-variant | Rnf216 | Mm_Celera | 5:142997821 | GCTACCAAAATGATG[A/G]GGCTCATGTATGATT | 108086 |
rs33681395 | snp | C/T | 0.492188 | 0.0620098 | intron-variant | Rnf216 | Mm_Celera | 5:142995340 | ACAAAAGTTCAGTTC[C/T]CATCAAGCATTTTAG | 108086 |
rs33690648 | snp | A/T | 0.484429 | 0.0868505 | intron-variant | Rnf216 | Mm_Celera | 5:142998281 | TGATCTGTAAACAGA[A/T]GGATCTCTGGAGGCC | 108086 |
rs33697804 | snp | C/T | 0.5 | 0 | intron-variant | Rnf216 | Mm_Celera | 5:143055381 | GAGGCAGGCGGATTT[C/T]TAAGTTCGAGGCCAA | 108086 |
rs33698913 | snp | A/G | 0.5 | 0 | intron-variant | Rnf216 | Mm_Celera | 5:142995959 | ACAGGGTTTCTCTGT[A/G]TAGCCCTGGCTGTCC | 108086 |
rs33714939 | snp | C/T | 0.391111 | 0.206368 | intron-variant | Rnf216 | Mm_Celera | 5:143032602 | CCGGCTTAAGCCTAG[C/T]TCAGAGTCAGAACCC | 108086 |
rs33731907 | snp | C/T | 0.5 | 0 | intron-variant | Rnf216 | Mm_Celera | 5:143000435 | AGGAGAGGGTGAGGA[C/T]ATACCAGGCTGTCAT | 108086 |
rs33736984 | snp | A/T | 0.498615 | 0.0262793 | intron-variant | Rnf216 | Mm_Celera | 5:143016258 | TAGTGATTTAAGAAG[A/T]GGGAGCCAAGTCTAT | 108086 |
rs33737273 | snp | A/T | 0.5 | 0 | intron-variant | Rnf216 | Mm_Celera | 5:142996898 | GACTAACCTTGGTTA[A/T]ACAACACCCTAGCTT | 108086 |
rs33741704 | snp | A/T | 0.455 | 0.143091 | intron-variant | Rnf216 | Mm_Celera | 5:143060355 | CCCTAGGATAAGCCA[A/T]TTAGTAAGGGAGTTT | 108086 |
rs33892781 | snp | A/G | 0.444444 | 0.157135 | intron-variant | Rnf216 | Mm_Celera | 5:143057252 | ACTTAGGTTCTCTGC[A/G]AGAGCACCATGTGCT | 108086 |
rs36253070 | snp | C/T | 0.231111 | 0.249285 | intron-variant | Rnf216 | Mm_Celera | 5:143015300 | TGTCCTGTATAACAC[C/T]CCAGATGGCAGAGAA | 108086 |
rs36259365 | snp | C/T | 0.124444 | 0.216185 | intron-variant | Rnf216 | Mm_Celera | 5:143084303 | TTTCCTAGAAGTTTC[C/T]GAGAGGAAGTTAACT | 108086 |
rs36260054 | snp | C/G | 0.124444 | 0.216185 | intron-variant | Rnf216 | Mm_Celera | 5:143023941 | ACACTAAGCACCTCA[C/G]CTCCTTTGTGAAAGA | 108086 |
rs36260379 | snp | A/G | 0.32 | 0.24 | synonymous-codon | Rnf216 | GRCm38.p3 | 5:143068953 | CAGCTCACTGGTTGG[A/G]AAGGAGCACGTGCAG | 108086 |
rs36266209 | snp | C/T | 0.231111 | 0.249285 | intron-variant | Rnf216 | Mm_Celera | 5:143081149 | CTGAGTCTCATCTTC[C/T]CTCACAATGCCAGCT | 108086 |
rs36271611 | snp | C/T | 0.231111 | 0.249285 | intron-variant | Rnf216 | Mm_Celera | 5:143012440 | CCCCATTAACTATCT[C/T]ATTGGCTCTCTTTCA | 108086 |
rs36279147 | snp | C/T | 0.124444 | 0.216185 | intron-variant | Rnf216 | Mm_Celera | 5:143046100 | CAAAACTGTTGTCTT[C/T]TCTGGATCACCAAAA | 108086 |
rs36288845 | snp | A/G | 0.336735 | 0.234472 | intron-variant | Rnf216 | Mm_Celera | 5:143043624 | CTTTATAGTGCTAAT[A/G]TGCTTTCTATAGTAT | 108086 |
rs36291937 | snp | C/T | 0.32 | 0.24 | intron-variant | Rnf216 | Mm_Celera | 5:143037880 | TGAAGGTCACAGTCA[C/T]GAGGTGGATGGTAGA | 108086 |
rs36300826 | snp | C/T | 0.124444 | 0.216185 | intron-variant | Rnf216 | Mm_Celera | 5:143087434 | AAAGCCCTGTGCTAA[C/T]GGCACTTCGCTGCTG | 108086 |
rs36301987 | snp | A/G | 0.32 | 0.24 | intron-variant | Rnf216 | Mm_Celera | 5:143039150 | CTCTTGACTCAGCAG[A/G]CGTCCTAAACACAGA | 108086 |
rs36304543 | snp | C/T | 0.231111 | 0.249285 | intron-variant | Rnf216 | Mm_Celera | 5:143051846 | CTCAATACAATGAAA[C/T]GGAATGAAAGCCTTC | 108086 |
rs36315742 | snp | A/G | 0.132653 | 0.220748 | intron-variant | Rnf216 | Mm_Celera | 5:143101063 | TCAGTCCTCACCCAG[A/G]AGGAAATAGTCACCG | 108086 |
rs36318244 | snp | C/T | 0.231111 | 0.249285 | intron-variant | Rnf216 | Mm_Celera | 5:143034462 | GCTGCTGGTGCTAAA[C/T]GCTACAGGCAGGAGC | 108086 |
rs36323724 | snp | A/C | 0.32 | 0.24 | intron-variant | Rnf216 | Mm_Celera | 5:143098216 | TAAATTTCATTTCTG[A/C]TGCATGTATCATTAT | 108086 |