SNP - dbSNP |
dbSNP | Type | Alleles | Het | Se(het) | Fxn-class | Gene Name | Assembly | Chr-pos | Sequence | Entrez Gene |
rs26921946 | snp | C/T | 0.473373 | 0.11227 | downstream-variant-500B, utr-variant-3-prime | Rnf222 | GRCm38.p3 | 11:68895465 | CAATGAAACTGGACA[C/T]ATCATCTCTCAGAGT | 320040 |
rs26921947 | snp | G/T | 0.297521 | 0.245442 | utr-variant-3-prime | Rnf222 | Mm_Celera | 11:68894938 | TTTCAGCCGCACACT[G/T]TGGAGGCTACTTCTT | 320040 |
rs26921948 | snp | C/T | 0.489796 | 0.070696 | utr-variant-3-prime | Rnf222 | Mm_Celera | 11:68894885 | CCTTCCGGATCCTGC[C/T]GTGTTTGCGGAGACT | 320040 |
rs26921949 | snp | A/G | 0.497041 | 0.0383476 | utr-variant-3-prime | Rnf222 | Mm_Celera | 11:68894728 | CAGAGGTGCTGTGCC[A/G]ATGTGGAGGGAACAG | 320040 |
rs26921950 | snp | A/G | 0.152778 | 0.230321 | utr-variant-3-prime | Rnf222 | Mm_Celera | 11:68894718 | GGCTAGAGAACAGAG[A/G]TGCTGTGCCAATGTG | 320040 |
rs26921951 | snp | G/T | 0.475309 | 0.108333 | utr-variant-3-prime | Rnf222 | Mm_Celera | 11:68893675 | CCAGACACAAGTTTT[G/T]CTGGCCCGTGTCCTG | 320040 |
rs26921952 | snp | A/G | 0.495868 | 0.0452663 | synonymous-codon | Rnf222 | Mm_Celera | 11:68893106 | CCTGGCAGAGATTTC[A/G]GAGGCATCCCCGGCT | 320040 |
rs26921953 | snp | C/T | 0.124444 | 0.216185 | synonymous-codon | Rnf222 | Mm_Celera | 11:68892678 | GAGAAGTTCCGGGAT[C/T]TGGACGGCGCCAGCA | 320040 |
rs26921954 | snp | A/G | 0.444444 | 0.157135 | intron-variant | Rnf222 | Mm_Celera | 11:68892548 | AAAGGAAAAACTCGC[A/G]GATGTTCACACCCCT | 320040 |
rs26921955 | snp | A/G | 0.497778 | 0.0332592 | intron-variant | Rnf222 | Mm_Celera | 11:68892274 | GGTGAGGCATCAGGC[A/G]CTTCAGGTATCCATC | 320040 |
rs26921956 | snp | C/T | 0.124444 | 0.216185 | utr-variant-5-prime | Rnf222 | Mm_Celera | 11:68891904 | GGAGACGCTGAAGAA[C/T]GCTCGGACATGGCTG | 320040 |
rs26921957 | snp | A/G | 0.124444 | 0.216185 | utr-variant-5-prime | Rnf222 | Mm_Celera | 11:68891898 | ACTTAAGGAGACGCT[A/G]AAGAATGCTCGGACA | 320040 |
rs26921958 | snp | C/G | 0.345679 | 0.230967 | intron-variant, upstream-variant-2KB | Rnf222 | GRCm38.p3 | 11:68886304 | GTCAACCTCTGAGAG[C/G]AAAATGCCCCTGGGG | 320040 |
rs26921959 | snp | A/G | 0.408163 | 0.193609 | intron-variant | Rnf222 | GRCm38.p3 | 11:68885141 | TCAAAGTCCAGCTCC[A/G]TAGAAGGCCAAGTGG | 320040 |
rs26921960 | snp | C/T | 0.32 | 0.24 | intron-variant | Rnf222 | Mm_Celera | 11:68882490 | GTTAGTTTCTCTTGG[C/T]GTCCAAGCTGGGTTT | 320040 |
rs26921961 | snp | G/T | 0.124444 | 0.216185 | intron-variant | Rnf222 | Mm_Celera | 11:68882466 | CTTTCCTGGACACAA[G/T]CCCTCCTTGTTAGTT | 320040 |
rs26921962 | snp | A/G | 0.5 | 0 | utr-variant-5-prime | Rnf222 | GRCm38.p3 | 11:68882105 | CACTGTCCTTGACTC[A/G]GCTGGACCTGCCTCT | 320040 |
rs29383278 | snp | A/T | 0.375 | 0.216506 | utr-variant-3-prime | Rnf222 | GRCm38.p3 | 11:68893542 | TCCATCTGTGACCCC[A/T]TAAGTATCCCTAACA | 320040 |
rs29384027 | snp | C/G | 0.375 | 0.216506 | intron-variant | Rnf222 | Mm_Celera | 11:68891063 | CTCAACCTCAGAGAG[C/G]TATCAGACTTCATCA | 320040 |
rs29386315 | snp | A/T | 0.444444 | 0.157135 | intron-variant | Rnf222 | GRCm38.p3 | 11:68890206 | CAATGCTCCTTTTTT[A/T]AAAAAAAAAAGATCT | 320040 |
rs29388072 | snp | A/T | 0.444444 | 0.157135 | intron-variant | Rnf222 | GRCm38.p3 | 11:68885666 | CTATTGTGATTTTTT[A/T]AAAGATTTATTATTT | 320040 |
rs29390186 | snp | C/T | 0.32 | 0.24 | utr-variant-3-prime | Rnf222 | Mm_Celera | 11:68894036 | TGTAGAATGCCAGGC[C/T]GAAGGAGCAGACCTG | 320040 |
rs29390816 | snp | C/T | 0.375 | 0.216506 | intron-variant | Rnf222 | GRCm38.p3 | 11:68889728 | TACATTGCCCAAGCA[C/T]GAATGGTGTGGCTGT | 320040 |
rs29393585 | snp | A/T | 0.32 | 0.24 | utr-variant-3-prime | Rnf222 | Mm_Celera | 11:68893773 | TGCCCCCAGGAAGAA[A/T]CAGAAGTTGGATGCA | 320040 |
rs29394579 | snp | A/T | 0.375 | 0.216506 | utr-variant-5-prime | Rnf222 | Mm_Celera | 11:68882080 | AAGTTGTTTTTTTTT[A/T]AAACCTTGTCACTGT | 320040 |
rs29404366 | snp | A/G | 0.444444 | 0.157135 | intron-variant | Rnf222 | GRCm38.p3 | 11:68883036 | CCTCCTCTAACCCAG[A/G]GCATCTGTAAGGCAT | 320040 |
rs29416963 | snp | G/T | 0.444444 | 0.157135 | utr-variant-3-prime | Rnf222 | Mm_Celera | 11:68895651 | AGTTATTAACCTTGA[G/T]ATCCAGGGCCTGCGG | 320040 |
rs29419377 | snp | A/C | 0.375 | 0.216506 | intron-variant | Rnf222 | GRCm38.p3 | 11:68890102 | TGACTGATGCTGAAA[A/C]CCTGCCTTCCTCTCT | 320040 |
rs29422056 | snp | A/C | 0.444444 | 0.157135 | intron-variant | Rnf222 | GRCm38.p3 | 11:68890379 | GGGCTACATGAGACC[A/C]TGTCTCCTAGAAATA | 320040 |
rs29425100 | snp | A/G | 0.375 | 0.216506 | upstream-variant-2KB | Rnf222 | Mm_Celera | 11:68881539 | TCTGATACCCTCTCT[A/G]GTCTCCATGGGCACA | 320040 |
rs29425736 | snp | A/G | 0.32 | 0.24 | utr-variant-3-prime | Rnf222 | Mm_Celera | 11:68893921 | CCAGGATGGGGGGCT[A/G]GGGGCAACAGAGAAA | 320040 |
rs29427445 | snp | C/T | 0.375 | 0.216506 | utr-variant-3-prime | Rnf222 | Mm_Celera | 11:68893531 | ATGGCCAACTCTCCA[C/T]CTGTGACCCCATAAG | 320040 |
rs29428315 | snp | C/T | 0.444444 | 0.157135 | downstream-variant-500B | Rnf222 | Mm_Celera | 11:68895968 | GAGGGCGTCAGATCC[C/T]ATTATGGATGGTTGT | 320040 |
rs29429602 | snp | G/T | 0.32 | 0.24 | utr-variant-3-prime | Rnf222 | GRCm38.p3 | 11:68893918 | AGCCCAGGATGGGGG[G/T]CTGGGGGCAACAGAG | 320040 |
rs29432507 | snp | A/G | 0.5 | 0 | intron-variant | Rnf222 | Mm_Celera | 11:68888796 | GTATGAGAGAAAGGA[A/G]AAAGACAGCAAATGT | 320040 |
rs29439618 | snp | G/T | 0.444444 | 0.157135 | intron-variant | Rnf222 | GRCm38.p3 | 11:68884762 | CCACAATTCATTGCT[G/T]AGGAGGTACCTAAGT | 320040 |
rs29442198 | snp | C/T | 0.5 | 0 | utr-variant-3-prime | Rnf222 | Mm_Celera | 11:68894132 | TGAGACCTGAGTCAG[C/T]TGAGAGCTATGTGAG | 320040 |
rs29443901 | snp | C/T | 0.32 | 0.24 | intron-variant | Rnf222 | GRCm38.p3 | 11:68883594 | TCTTGCACAGTGTGC[C/T]CCCATCCTAACCAAC | 320040 |
rs29446212 | snp | A/C | 0.375 | 0.216506 | upstream-variant-2KB | Rnf222 | Mm_Celera | 11:68881525 | TTAAACCCCATGGAT[A/C]TGATACCCTCTCTGG | 320040 |
rs29451246 | snp | C/T | 0.375 | 0.216506 | utr-variant-3-prime | Rnf222 | Mm_Celera | 11:68893565 | CCCTAACAAACAGCT[C/T]CATCTCTAGGCTGGA | 320040 |
rs29456175 | snp | A/T | 0.444444 | 0.157135 | intron-variant | Rnf222 | GRCm38.p3 | 11:68890387 | TGAGACCATGTCTCC[A/T]AGAAATAGGAAAAGA | 320040 |
rs29456519 | snp | C/T | 0.5 | 0 | intron-variant, upstream-variant-2KB | Rnf222 | Mm_Celera | 11:68886326 | CCCCTGGGGACAGGA[C/T]GGTGGTTGACAGGGC | 320040 |
rs29468296 | snp | A/T | 0.444444 | 0.157135 | downstream-variant-500B | Rnf222 | Mm_Celera | 11:68895897 | AGACTTCACTTTGCC[A/T]TTTATGTTTTGGACT | 320040 |
rs29470030 | snp | C/T | 0.444444 | 0.157135 | intron-variant | Rnf222 | GRCm38.p3 | 11:68890638 | AGCAGCCCATTCATT[C/T]AGGTCTATTTGGATG | 320040 |
rs29470907 | snp | G/T | 0.444444 | 0.157135 | intron-variant | Rnf222 | GRCm38.p3 | 11:68890466 | CCCTAGAATATAATC[G/T]CAGTATTTGGTAAAC | 320040 |
rs29475119 | snp | C/G | 0.375 | 0.216506 | upstream-variant-2KB, intron-variant | Rnf222 | Mm_Celera | 11:68887705 | CCCGGCTGATCCTGA[C/G]CTTCTGGTCCTTCTG | 320040 |
rs29480655 | snp | C/T | 0.444444 | 0.157135 | intron-variant | Rnf222 | GRCm38.p3 | 11:68889462 | TCAACACTGGTCTCA[C/T]TTTAACCAGGAAGAC | 320040 |
rs32971250 | snp | A/C | 0.32 | 0.24 | upstream-variant-2KB | Rnf222 | Mm_Celera | 11:68881726 | AGGACCACAAGAATA[A/C]ATAAACAATAAAACC | 320040 |
rs32987858 | snp | C/T | 0.32 | 0.24 | intron-variant | Rnf222 | GRCm38.p3 | 11:68883662 | ATCCCCAGGAGTGGA[C/T]TTGCTAGGTCATTCT | 320040 |
rs33850176 | snp | G/T | 0.48 | 0.0979796 | utr-variant-3-prime | Rnf222 | Mm_Celera | 11:68894094 | GAAATAGAAGACAAG[G/T]GGTGGAGGGGACGGC | 320040 |
rs45958082 | snp | A/G | | | utr-variant-3-prime, downstream-variant-500B | Rnf222 | Mm_Celera | 11:68895010 | GTATATATTTTCTTA[A/G]AGTCCAGAGACCTTT | 320040 |
rs46014907 | snp | A/G | | | synonymous-codon | Rnf222 | Mm_Celera | 11:68893055 | TCGCCACGGGATGCC[A/G]CTGGGGGAACAGGAC | 320040 |
rs46194215 | snp | A/G | | | utr-variant-3-prime | Rnf222 | Mm_Celera | 11:68894456 | TTGTCACTGAAAACA[A/G]CAGAGACTTCCAGCA | 320040 |
rs46311944 | snp | C/T | | | intron-variant | Rnf222 | Mm_Celera | 11:68884154 | GCTTTGTTTTCTTTT[C/T]TTTTTTTTTTTTTTT | 320040 |
rs46344398 | snp | C/G | | | intron-variant | Rnf222 | Mm_Celera | 11:68892290 | CTTCAGGTATCCATC[C/G]CACTCCACACACTTC | 320040 |
rs46445865 | snp | C/T | | | downstream-variant-500B | Rnf222 | Mm_Celera | 11:68895805 | ATTACCTGGAGAAAA[C/T]AGACAAAACAATAAC | 320040 |
rs46568234 | snp | A/G | | | utr-variant-3-prime | Rnf222 | Mm_Celera | 11:68894916 | CTTCCCAAAATGCCT[A/G]CGATGTTTTCAGCCG | 320040 |
rs46582945 | snp | C/T | | | upstream-variant-2KB, intron-variant | Rnf222 | GRCm38.p3 | 11:68887938 | ACACATGTATACAAT[C/T]TTTAATGATTGTATT | 320040 |
rs46828711 | snp | A/G | | | intron-variant | Rnf222 | GRCm38.p3 | 11:68883870 | TGGGGGACTGAGAAG[A/G]AACCCTAGCTGCCAT | 320040 |
rs46845732 | snp | C/T | | | upstream-variant-2KB | Rnf222 | GRCm38.p3 | 11:68881356 | AAGGAGAAAAACCAA[C/T]ATCATGTTTTTCACG | 320040 |
rs47051063 | snp | A/G | | | upstream-variant-2KB, intron-variant, utr-variant-5-prime | Rnf222 | GRCm38.p3 | 11:68888266 | CTTAGGCTCTGACCT[A/G]TTGGCCCGTTCACTC | 320040 |
rs47372931 | snp | A/T | | | missense | Rnf222 | Mm_Celera | 11:68893019 | CAGCCTGCCTCGAGA[A/T]TCACAGATTTTCATC | 320040 |
rs47572528 | snp | C/T | | | upstream-variant-2KB | Rnf222 | Mm_Celera | 11:68880797 | AGAGAGATGGCTCAG[C/T]AGTTACACGTGCTTG | 320040 |
rs47584636 | snp | A/G | | | utr-variant-3-prime | Rnf222 | Mm_Celera | 11:68895535 | CTCCGTGATACAGCT[A/G]TCTAGATGGCTGGTG | 320040 |
rs47731084 | snp | A/G | | | utr-variant-3-prime | Rnf222 | Mm_Celera | 11:68894808 | CAGACTTGTGAGTCT[A/G]TGTCCACCCCAGCCA | 320040 |
rs48002931 | snp | A/G | | | utr-variant-3-prime | Rnf222 | Mm_Celera | 11:68893392 | CTGGACTCAGAGAGG[A/G]CATGGGTGGGGCCAG | 320040 |
rs48083679 | snp | C/G | | | intron-variant | Rnf222 | Mm_Celera | 11:68892314 | ACACTTCCTACCCAA[C/G]CCGAGCACTGCTGGG | 320040 |
rs48234659 | snp | G/T | | | upstream-variant-2KB, intron-variant, utr-variant-5-prime | Rnf222 | GRCm38.p3 | 11:68888327 | TATAGTTTTCCCATG[G/T]TTGGATGGGAAAATC | 320040 |
rs48236891 | snp | A/G | | | intron-variant | Rnf222 | GRCm38.p3 | 11:68885321 | AAAAGCCACACTGAC[A/G]AAGGATCTGAGAACT | 320040 |
rs48991151 | snp | A/G | | | intron-variant | Rnf222 | GRCm38.p3 | 11:68882784 | GGATTACAGACGTGA[A/G]TCACCTGGACCCTGC | 320040 |
rs49094827 | snp | C/T | | | upstream-variant-2KB, intron-variant | Rnf222 | GRCm38.p3 | 11:68887848 | TTACATCCCGGGCCC[C/T]TCGATATCATTTTAA | 320040 |
rs49187351 | snp | A/G | | | upstream-variant-2KB, intron-variant, utr-variant-5-prime | Rnf222 | Mm_Celera | 11:68887987 | ATAAATTCAGATATC[A/G]CTGATAAAAACATTT | 320040 |
rs49188471 | snp | A/G | | | intron-variant | Rnf222 | Mm_Celera | 11:68885840 | TCATTAGACACACCA[A/G]AAGAGGGCGTTAGAT | 320040 |
rs49290458 | snp | C/G | | | utr-variant-3-prime | Rnf222 | Mm_Celera | 11:68894918 | TCCCAAAATGCCTGC[C/G]ATGTTTTCAGCCGCA | 320040 |
rs49408974 | snp | G/T | | | upstream-variant-2KB | Rnf222 | Mm_Celera | 11:68880771 | CATTAAAATCAGGGT[G/T]GAggggctggagaga | 320040 |
rs50192577 | snp | A/G | | | intron-variant | Rnf222 | GRCm38.p3 | 11:68883871 | GGGGGACTGAGAAGA[A/G]ACCCTAGCTGCCATC | 320040 |
rs50426065 | snp | A/C | | | intron-variant | Rnf222 | GRCm38.p3 | 11:68885167 | AGTGGAAAGATACGA[A/C]AGAAACTTAGGAACT | 320040 |
rs50611588 | snp | A/T | | | upstream-variant-2KB | Rnf222 | Mm_Celera | 11:68881421 | CACACACACACACAC[A/T]CACACACACGTTTTT | 320040 |
rs50638386 | snp | A/C | | | upstream-variant-2KB, intron-variant, utr-variant-5-prime | Rnf222 | GRCm38.p3 | 11:68888211 | TGCACATGGGCACAT[A/C]ACACCAAACTTAGTG | 320040 |
rs50656198 | snp | A/G | | | upstream-variant-2KB, intron-variant, utr-variant-5-prime | Rnf222 | GRCm38.p3 | 11:68888071 | ATAATTGATAGTGTC[A/G]ATCACAGTGGTCCAA | 320040 |
rs50892837 | snp | A/G | | | utr-variant-3-prime | Rnf222 | Mm_Celera | 11:68893251 | CAGGCCTGAGTGGCG[A/G]CATGCAGAGGAAAGG | 320040 |
rs51168531 | snp | A/T | | | upstream-variant-2KB | Rnf222 | GRCm38.p3 | 11:68881357 | AGGAGAAAAACCAAT[A/T]TCATGTTTTTCACGT | 320040 |
rs51488944 | snp | C/G | | | upstream-variant-2KB, intron-variant | Rnf222 | Mm_Celera | 11:68887767 | ATGCTACCACACCTG[C/G]TTTATACAGAGCTGG | 320040 |
rs52100180 | snp | G/T | | | downstream-variant-500B | Rnf222 | Mm_Celera | 11:68896070 | AGTTTTTGGTTTTTT[G/T]TTTTTGTTTTTTTTT | 320040 |
rs52171924 | snp | A/G | | | upstream-variant-2KB | Rnf222 | Mm_Celera | 11:68880925 | cacacacacacacac[A/G]cacacgcacacacac | 320040 |
rs52307687 | snp | G/T | | | downstream-variant-500B | Rnf222 | GRCm38.p3 | 11:68896084 | TGTTTTTGTTTTTTT[G/T]TTTTTTTGGTTTTTG | 320040 |
rs52401819 | snp | G/T | | | downstream-variant-500B | Rnf222 | Mm_Celera | 11:68896154 | TTGTTTGTTTTGTTT[G/T]TTTGTTTTTCGAGAC | 320040 |
rs52467421 | snp | G/T | | | downstream-variant-500B | Rnf222 | Mm_Celera | 11:68896128 | TTGTTTGTTTTGTTT[G/T]TTTGTTTTGTTTGTT | 320040 |
rs52522771 | snp | G/T | | | downstream-variant-500B | Rnf222 | Mm_Celera | 11:68896076 | TGGTTTTTTGTTTTT[G/T]TTTTTTTTTTTTTTT | 320040 |
rs52523413 | snp | A/C | | | upstream-variant-2KB | Rnf222 | Mm_Celera | 11:68881009 | AATCCTAAAACAATA[A/C]ACAAAATAAACACCG | 320040 |
rs52542606 | snp | A/G | | | upstream-variant-2KB | Rnf222 | Mm_Celera | 11:68880929 | CACACACACACACAC[A/G]CGCACACACACACAC | 320040 |
rs52550345 | snp | A/G | | | upstream-variant-2KB | Rnf222 | Mm_Celera | 11:68880919 | cacacacacacacac[A/G]cacacacacacgcac | 320040 |
rs52558413 | snp | C/T | | | downstream-variant-500B, utr-variant-3-prime | Rnf222 | Mm_Celera | 11:68895311 | GATTTCTCCATATAG[C/T]CTGGCTGTCCTGGAA | 320040 |
rs52567677 | snp | G/T | | | downstream-variant-500B | Rnf222 | GRCm38.p3 | 11:68896083 | TTGTTTTTGTTTTTT[G/T]TTTTTTTTGGTTTTT | 320040 |
rs52579812 | snp | G/T | | | downstream-variant-500B | Rnf222 | Mm_Celera | 11:68896125 | TTTTTGTTTGTTTTG[G/T]TTGTTTGTTTTGTTT | 320040 |
rs107988094 | snp | A/C | | | intron-variant | Rnf222 | Mm_Celera | 11:68885610 | GCAGACCGATTATGA[A/C]AAAAAAAATCATTTG | 320040 |
rs108131856 | snp | A/G | | | intron-variant | Rnf222 | GRCm38.p3 | 11:68885609 | GGCAGACCGATTATG[A/G]AAAAAAAAATCATTT | 320040 |
rs211770759 | snp | C/T | | | intron-variant | Rnf222 | Mm_Celera | 11:68883011 | GACTGTAATGGCATC[C/T]ATAAAGCCTCCTCCT | 320040 |
rs211831527 | snp | G/T | | | utr-variant-5-prime | Rnf222 | Mm_Celera | 11:68882141 | TGAGGCCTCTTGGCT[G/T]CGGGAGAGCAATCAG | 320040 |
rs211835259 | snp | A/G | | | utr-variant-5-prime | Rnf222 | Mm_Celera | 11:68891858 | TAATCAGGACCTTAG[A/G]ACCTTCTGACAGCCT | 320040 |