SNP - dbSNP |
dbSNP | Type | Alleles | Het | Se(het) | Fxn-class | Gene Name | Assembly | Chr-pos | Sequence | Entrez Gene |
rs4170132 | snp | A/G | 0.5 | 0 | intron-variant | Rnf168 | Mm_Celera | 16:32281055 | CTGAAGACAGCTACA[A/G]TGTACTTACATATAA | 70238 |
rs4170133 | snp | A/G | 0.444444 | 0.157135 | intron-variant | Rnf168 | GRCm38.p3 | 16:32282226 | TGTCTGTGTGTATAT[A/G]TTTGTGTACTAAGTT | 70238 |
rs4170134 | snp | A/T | 0.387812 | 0.208586 | intron-variant | Rnf168 | GRCm38.p3 | 16:32282572 | AGTATTTGGTTGTGT[A/T]AAGGCATGATTTCAC | 70238 |
rs4170135 | snp | A/C | 0.391111 | 0.206368 | intron-variant | Rnf168 | GRCm38.p3 | 16:32282957 | TTTTTATTTTCAGAG[A/C]GGGACTTGCTGTGTA | 70238 |
rs4170136 | snp | A/G | 0.487535 | 0.077957 | intron-variant | Rnf168 | GRCm38.p3 | 16:32283881 | GCCAGCAGGAGTAGG[A/G]TAGGAACTTCAGAGG | 70238 |
rs4170137 | snp | C/T | 0.444444 | 0.157135 | intron-variant | Rnf168 | GRCm38.p3 | 16:32284574 | ATTCACTTTCCCACA[C/T]GGAGCCACCTAAAGT | 70238 |
rs4170138 | snp | G/T | 0.375 | 0.216506 | intron-variant | Rnf168 | GRCm38.p3 | 16:32285121 | TGTGCCTGTGCCTGT[G/T]CTGCTATGGTGGAAA | 70238 |
rs4170139 | snp | C/T | 0.375 | 0.216506 | intron-variant | Rnf168 | GRCm38.p3 | 16:32285122 | GTGCCTGTGCCTGTG[C/T]TGCTATGGTGGAAAC | 70238 |
rs4170140 | snp | A/G | 0.362812 | 0.2231 | intron-variant | Rnf168 | Mm_Celera | 16:32286081 | CCTGTGCATTCTAGG[A/G]ACTCCCTGTGGAGAT | 70238 |
rs4170141 | snp | C/T | 0.444444 | 0.157135 | intron-variant | Rnf168 | Mm_Celera | 16:32287148 | AGGCGAGCACCACCA[C/T]GCCCGGCTGACTCTT | 70238 |
rs4170142 | snp | C/G | 0.444444 | 0.157135 | intron-variant | Rnf168 | GRCm38.p3 | 16:32289446 | ACAGCGCTGGATTCC[C/G]TAGTACTAGAGTTAC | 70238 |
rs4170143 | snp | C/T | 0.375 | 0.216506 | intron-variant | Rnf168 | GRCm38.p3 | 16:32290878 | AAAAGGAGTCGCCGC[C/T]AGTTGTGGTAGTGTA | 70238 |
rs4170144 | snp | A/T | 0.465374 | 0.126941 | intron-variant | Rnf168 | Mm_Celera | 16:32291756 | CTCAGGGTTTCAAAT[A/T]TTATCTTAGAGTTGA | 70238 |
rs4170145 | snp | A/T | 0.444444 | 0.157135 | intron-variant | Rnf168 | Mm_Celera | 16:32292236 | TTTATTATTAAAAAA[A/T]TTTTTTTATTATTAT | 70238 |
rs4170146 | snp | A/G | 0.32 | 0.24 | intron-variant | Rnf168 | Mm_Celera | 16:32297240 | TCACCAAGGGAAGGA[A/G]GGAGAAGGGAGAGGA | 70238 |
rs4170147 | snp | A/G | 0.432133 | 0.171253 | intron-variant | Rnf168 | Mm_Celera | 16:32298372 | TATATATACTCAGGA[A/G]TTTTGTTTTCTACAG | 70238 |
rs4170148 | snp | A/G | 0.401235 | 0.199068 | utr-variant-3-prime | Rnf168 | GRCm38.p3 | 16:32299504 | AAAGACGGCTAGTAG[A/G]AAACAACCTTGGGAA | 70238 |
rs4170149 | snp | A/G | 0.444444 | 0.157135 | utr-variant-3-prime | Rnf168 | GRCm38.p3 | 16:32300341 | GAACTTAGGACCTTC[A/G]GCAGCACTCTTACCT | 70238 |
rs6282488 | snp | A/T | 0.290657 | 0.246672 | intron-variant | Rnf168 | Mm_Celera | 16:32287546 | GAGGTCAGAGTAGAT[A/T]ATTGAAATTTTGAAT | 70238 |
rs6282933 | snp | A/G | 0.290657 | 0.246672 | intron-variant | Rnf168 | Mm_Celera | 16:32287597 | ATTTTAGAGATGGGT[A/G]AACAATTATGACTTA | 70238 |
rs6283598 | snp | C/T | 0.5 | 0 | intron-variant | Rnf168 | Mm_Celera | 16:32287731 | ctcagtggcagagag[C/T]gctgcttacactcac | 70238 |
rs6284135 | snp | C/T | 0.5 | 0 | intron-variant | Rnf168 | Mm_Celera | 16:32287829 | ccaagtatccaacac[C/T]ctcttctgaacnccc | 70238 |
rs6284157 | snp | C/T | 0.5 | 0 | intron-variant | Rnf168 | Mm_Celera | 16:32287841 | cacnctcttctgaac[C/T]cccctagtgtcaggc | 70238 |
rs6284588 | snp | C/T | 0.5 | 0 | intron-variant | Rnf168 | Mm_Celera | 16:32287884 | cacagacatatgtgt[C/T]ggtaaaatacccata | 70238 |
rs6284621 | snp | C/T | 0.5 | 0 | intron-variant | Rnf168 | Mm_Celera | 16:32287902 | taaaatacccataca[C/T]ataaaataaggaaat | 70238 |
rs32551926 | snp | A/C | 0.32 | 0.24 | upstream-variant-2KB | Rnf168 | Mm_Celera | 16:32277384 | GCAGCCTACAGTAGC[A/C]GAGCGACCAAAAGCG | 70238 |
rs32551928 | snp | G/T | 0.5 | 0 | intron-variant | Rnf168 | Mm_Celera | 16:32281648 | CATTTGAAATGTAAA[G/T]GCAGAAGATTCACCC | 70238 |
rs32551932 | snp | C/T | 0.231111 | 0.249285 | intron-variant | Rnf168 | Mm_Celera | 16:32284182 | GTTTTACTCACCCAG[C/T]ATGACTTGCAAAAAG | 70238 |
rs32552914 | snp | A/G | 0.231111 | 0.249285 | intron-variant | Rnf168 | Mm_Celera | 16:32284258 | CTTCAGACCTGACCC[A/G]GGTTAGCCTTGTCTA | 70238 |
rs32552916 | snp | C/T | 0.231111 | 0.249285 | intron-variant | Rnf168 | Mm_Celera | 16:32284339 | TCAAATGTTTGCTTC[C/T]TGCTTTCTTATTGTG | 70238 |
rs32552918 | snp | C/T | 0.231111 | 0.249285 | intron-variant | Rnf168 | Mm_Celera | 16:32284705 | GACAGGTTGTTATTC[C/T]TGCTGCTGCTGCTAG | 70238 |
rs32552919 | snp | C/G | 0.231111 | 0.249285 | intron-variant | Rnf168 | Mm_Celera | 16:32284974 | GGGCCTAGGGTATTC[C/G]TGCCCTGCTCCACCT | 70238 |
rs32552921 | snp | A/G | 0.231111 | 0.249285 | synonymous-codon | Rnf168 | Mm_Celera | 16:32285384 | GGTGGAGGCTGAGCG[A/G]CAAGCCAGCAAGGAA | 70238 |
rs32552923 | snp | G/T | 0.231111 | 0.249285 | intron-variant | Rnf168 | Mm_Celera | 16:32286061 | ATTGTCTGTCTGTCT[G/T]TAGTCCTGTGCATTC | 70238 |
rs32553795 | snp | C/T | 0.244898 | 0.249948 | intron-variant | Rnf168 | Mm_Celera | 16:32286367 | CAACATTTTTGTGTA[C/T]ATTTACTGTGTATAT | 70238 |
rs32553796 | snp | C/T | 0.231111 | 0.249285 | intron-variant | Rnf168 | Mm_Celera | 16:32287166 | CCGGCTGACTCTTAC[C/T]ATTTATAATGTATTT | 70238 |
rs32553797 | snp | A/T | 0.444444 | 0.157135 | intron-variant | Rnf168 | GRCm38.p3 | 16:32287238 | TGGTTCTAGTTAAAA[A/T]TTATAAAGATACACC | 70238 |
rs32553799 | snp | A/G | 0.231111 | 0.249285 | intron-variant | Rnf168 | Mm_Celera | 16:32287453 | TAGAGTAGTAAGTGG[A/G]TGATAAGTGGAATAG | 70238 |
rs32553802 | snp | C/T | 0.244898 | 0.249948 | intron-variant | Rnf168 | Mm_Celera | 16:32289070 | AGCTTTTTATTTCAT[C/T]AAGTTCTTCTTAATA | 70238 |
rs32555014 | snp | C/G | 0.231111 | 0.249285 | intron-variant | Rnf168 | Mm_Celera | 16:32289274 | CACTTCTCCATTGAT[C/G]GTCTACTGGGTGTTT | 70238 |
rs32555016 | snp | C/T | 0.231111 | 0.249285 | intron-variant | Rnf168 | Mm_Celera | 16:32290242 | GTCTTGGAGACCTTT[C/T]ATAGAACACTTTCTC | 70238 |
rs32555018 | snp | A/G | 0.231111 | 0.249285 | intron-variant | Rnf168 | Mm_Celera | 16:32290974 | ACACATTTAAAAGGA[A/G]GTGGAGGCTAGACTG | 70238 |
rs32555020 | snp | A/G | 0.497778 | 0.0332592 | intron-variant | Rnf168 | Mm_Celera | 16:32291321 | CCTGGGTCCCTGCTG[A/G]CAGAAACAATAAAGC | 70238 |
rs32555022 | snp | A/T | 0.231111 | 0.249285 | intron-variant | Rnf168 | Mm_Celera | 16:32291373 | AAAATAATAGCCAAA[A/T]TTTCTGGTAAGACAA | 70238 |
rs32555704 | snp | C/T | 0.142012 | 0.225474 | intron-variant | Rnf168 | Mm_Celera | 16:32291641 | AAGAATTATAAGATA[C/T]TAAAATGACCTTTTC | 70238 |
rs32555707 | snp | A/G | 0.231111 | 0.249285 | intron-variant | Rnf168 | Mm_Celera | 16:32291777 | TTAGAGTTGACCGGA[A/G]ACCTGGAGATGTTCC | 70238 |
rs32555709 | snp | A/G | 0.231111 | 0.249285 | intron-variant | Rnf168 | Mm_Celera | 16:32291804 | TTCCAGTAAGATAGC[A/G]AGCAAAAATGGTTCA | 70238 |
rs32555711 | snp | G/T | 0.124444 | 0.216185 | intron-variant | Rnf168 | Mm_Celera | 16:32291815 | TAGCAAGCAAAAATG[G/T]TTCATCAACCTTTTA | 70238 |
rs32555713 | snp | A/G | 0.231111 | 0.249285 | synonymous-codon | Rnf168 | Mm_Celera | 16:32291954 | GGCATGTAAGGCTGA[A/G]CTTGAGGAAGACATC | 70238 |
rs32556455 | snp | A/G | 0.231111 | 0.249285 | intron-variant | Rnf168 | Mm_Celera | 16:32292034 | CTGCTGTGCATTACT[A/G]AGACCTGGGCTGTCT | 70238 |
rs32556457 | snp | A/G | 0.231111 | 0.249285 | intron-variant | Rnf168 | Mm_Celera | 16:32296292 | GAGACGCTAAGCAGC[A/G]GCCAAGCAAGAATGT | 70238 |
rs32556459 | snp | A/T | 0.244898 | 0.249948 | intron-variant | Rnf168 | Mm_Celera | 16:32296419 | AGACTACATGGTAAT[A/T]CTCTGTTTCAAAAGT | 70238 |
rs32556461 | snp | C/T | 0.231111 | 0.249285 | intron-variant | Rnf168 | GRCm38.p3 | 16:32297220 | AGCTCCAGGTTTGAT[C/T]CCTATCACCAAGGGA | 70238 |
rs32556463 | snp | C/G | 0.165289 | 0.235211 | intron-variant | Rnf168 | Mm_Celera | 16:32297300 | AATAATTCTCTCTTC[C/G]TTAATATACAAATAA | 70238 |
rs32557235 | snp | C/T | 0.260355 | 0.249785 | intron-variant | Rnf168 | Mm_Celera | 16:32297305 | TTCTCTCTTCCTTAA[C/T]ATACAAATAATTCAG | 70238 |
rs32557238 | snp | A/T | 0.231111 | 0.249285 | missense | Rnf168 | Mm_Celera | 16:32298406 | ACTGATAGGAGTGAC[A/T]CGAAGAGCCCTGTGT | 70238 |
rs45898569 | snp | C/G | | | intron-variant | Rnf168 | GRCm38.p3 | 16:32288870 | TTTTTTTTTTTTTTC[C/G]AGACAGGGTTTCTCT | 70238 |
rs47185961 | snp | G/T | | | intron-variant | Rnf168 | GRCm38.p3 | 16:32283008 | TACAATATACAGTTA[G/T]TGATCCTAAGCATTC | 70238 |
rs48945767 | snp | A/G | | | intron-variant | Rnf168 | Mm_Celera | 16:32279982 | GGAAATGCCTGTGAC[A/G]GGTTTGCTTTTTGAC | 70238 |
rs51903800 | snp | C/G | | | intron-variant | Rnf168 | Mm_Celera | 16:32281064 | GCTACAATGTACTTA[C/G]ATATAATAATAAAGA | 70238 |
rs211715077 | snp | G/T | | | intron-variant | Rnf168 | Mm_Celera | 16:32287770 | CAGAGTTGATTCTTC[G/T]CACCTACATACATGG | 70238 |
rs211751854 | snp | A/G | | | utr-variant-3-prime | Rnf168 | Mm_Celera | 16:32299407 | GTCCTAATATCCTGA[A/G]ATGTCTCACATTCTG | 70238 |
rs211839007 | snp | A/T | | | upstream-variant-2KB | Rnf168 | Mm_Celera | 16:32277437 | TAGGCGGGAACGCAG[A/T]CGCAGCTCCCGGAAG | 70238 |
rs211877661 | snp | C/T | | | intron-variant | Rnf168 | Mm_Celera | 16:32288515 | ACTCTAGTTCCAGGG[C/T]ATCTGACACCTTCAC | 70238 |
rs211960518 | snp | A/G | | | upstream-variant-2KB | Rnf168 | Mm_Celera | 16:32276759 | GCCTCTGCCTGCAAT[A/G]TTTTGGGAACCAGCT | 70238 |
rs212006348 | in-del | -/A | | | intron-variant | Rnf168 | Mm_Celera | 16:32289904 | CCTCTACAGACCATG[-/A]AAGCATACAGTCATA | 70238 |
rs212071762 | snp | A/G | | | upstream-variant-2KB | Rnf168 | GRCm38.p3 | 16:32275592 | CACACGGAGGTGGGG[A/G]TTTTAGATGGTTTGC | 70238 |
rs212093267 | snp | A/T | | | missense | Rnf168 | Mm_Celera | 16:32298583 | GTTGAAACAGTATCA[A/T]CCAGTCCTGATGATT | 70238 |
rs212263037 | snp | A/G | | | intron-variant | Rnf168 | Mm_Celera | 16:32284631 | GTATGTGCACAGAGA[A/G]GTCCTGTCCTGTATA | 70238 |
rs212333438 | snp | C/T | | | intron-variant | Rnf168 | Mm_Celera | 16:32297498 | TTTAATCCCAGCACT[C/T]GGGAGGCAGAGCAGG | 70238 |
rs212773326 | snp | C/T | | | intron-variant | Rnf168 | Mm_Celera | 16:32285903 | TTGTGAGCCACCTGA[C/T]GTGGTTGCTAGGAAG | 70238 |
rs212869599 | snp | C/G | | | intron-variant | Rnf168 | Mm_Celera | 16:32290855 | TGGACATGGTAAGTC[C/G]TTGTCTAAAAAGGAG | 70238 |
rs213078148 | snp | A/G | | | intron-variant | Rnf168 | Mm_Celera | 16:32291582 | ATTTTGAGAAACTTT[A/G]TGGCCTTCCATTGTT | 70238 |
rs213421776 | in-del | -/CCTGAGC | | | intron-variant | Rnf168 | Mm_Celera | 16:32288813 | GCCACCTCTCCAGCT[-/CCTGAGC]CCTGAGCCATCTCAC | 70238 |
rs213450763 | snp | C/G | | | intron-variant | Rnf168 | Mm_Celera | 16:32283215 | GGTACTGGGAGGATA[C/G]TCAGCTGTTTTTGAG | 70238 |
rs213519219 | in-del | -/T | | | intron-variant | Rnf168 | Mm_Celera | 16:32280330 | GCATATAAGACCCCC[-/T]CCCCAAGCTGGGCCT | 70238 |
rs213541831 | in-del | -/TC | | | upstream-variant-2KB | Rnf168 | Mm_Celera | 16:32276111 | ACTCTTTCTTTTTTT[-/TC]TCTCTCTCTTTTTTT | 70238 |
rs213613747 | in-del | -/C | | | intron-variant | Rnf168 | Mm_Celera | 16:32280325 | CCCCCGCATATAAGA[-/C]CCCCCCCCCAAGCTG | 70238 |
rs213694073 | snp | C/T | | | intron-variant | Rnf168 | Mm_Celera | 16:32283577 | TGAGAAACAAAAAGA[C/T]TCAGCAGGCAAGGTG | 70238 |
rs213731437 | snp | A/T | | | intron-variant | Rnf168 | Mm_Celera | 16:32291739 | CAGGCAGTCTTGGAA[A/T]ACTCAGGGTTTCAAA | 70238 |
rs213985318 | snp | A/G | | | intron-variant | Rnf168 | Mm_Celera | 16:32297550 | AGCCTGGTCTACAAA[A/G]TTAGTTCCAGGACAG | 70238 |
rs214033937 | snp | C/T | | | intron-variant | Rnf168 | Mm_Celera | 16:32290925 | TGAAGGAGGCAGATG[C/T]AGGCGATTCACGAGT | 70238 |
rs214251094 | snp | A/T | | | intron-variant | Rnf168 | Mm_Celera | 16:32290014 | TATATATGCCTGTAA[A/T]CTCAGCACTCAGGAG | 70238 |
rs214281339 | in-del | -/G | | | intron-variant | Rnf168 | Mm_Celera | 16:32283895 | GATAGGAACTTCAGA[-/G]GGTAAAGTGGTCTAG | 70238 |
rs214284323 | snp | A/G | | | intron-variant | Rnf168 | Mm_Celera | 16:32289581 | TTTAATTGAAAGCTT[A/G]AGCCAGGTGGTCACA | 70238 |
rs214357464 | in-del | -/TTTTGTTTTATTTTA | | | intron-variant | Rnf168 | Mm_Celera | 16:32296522 | TTTGTTGTTGTTTTG[-/TTTTGTTTTATTTTA]TTTTTAAAAAGTCAC | 70238 |
rs214620943 | snp | A/G | | | downstream-variant-500B | Rnf168 | Mm_Celera | 16:32301696 | GTTGCTAGGCTTAGT[A/G]CCATACTCCCTTTAT | 70238 |
rs214778363 | snp | A/C | | | intron-variant | Rnf168 | Mm_Celera | 16:32280470 | ACACGCTGAGCAAGG[A/C]AGGGGAGTTCAACCC | 70238 |
rs214957652 | snp | A/G | | | intron-variant | Rnf168 | Mm_Celera | 16:32279461 | TTTTTTTTTTTTGAG[A/G]CAGGGTTTCTCTGTG | 70238 |
rs215024057 | snp | C/T | | | intron-variant | Rnf168 | Mm_Celera | 16:32281981 | CTGTCCTGGAACTCA[C/T]TTTGTAGACCAGGCT | 70238 |
rs215353734 | snp | A/G | | | intron-variant | Rnf168 | Mm_Celera | 16:32280734 | GAAACGCTTTAAGTC[A/G]GGGTCTCACATGCCT | 70238 |
rs215445397 | in-del | -/GTGTGTGTGT | | | intron-variant | Rnf168 | Mm_Celera | 16:32288267 | TTCACTATTTGACCA[-/GTGTGTGTGT]GTGTGTGTGTGTGTG | 70238 |
rs215571308 | snp | C/T | | | utr-variant-5-prime | Rnf168 | Mm_Celera | 16:32277529 | TCCGTGGAGCCCGGG[C/T]ACCTGCTCCGGCCGC | 70238 |
rs215585306 | snp | G/T | | | intron-variant | Rnf168 | Mm_Celera | 16:32289462 | TAGTACTAGAGTTAC[G/T]GCTGTCTCGGGGGCC | 70238 |
rs215727859 | snp | A/G | | | intron-variant | Rnf168 | Mm_Celera | 16:32279262 | TTGCAGATACTTCGG[A/G]AGGGAAAACTTGAGA | 70238 |
rs215876111 | snp | C/T | | | intron-variant | Rnf168 | Mm_Celera | 16:32288585 | CAAATAAGTTATTTG[C/T]CTTAGTTGGTATTTT | 70238 |
rs215965118 | snp | A/T | | | intron-variant | Rnf168 | GRCm38.p3 | 16:32290102 | TCTTGAAAAAACAAA[A/T]TCTAATTTTTTTTTT | 70238 |
rs216158378 | snp | A/G | | | intron-variant | Rnf168 | Mm_Celera | 16:32287141 | GGATTAAAGGCGAGC[A/G]CCACCATGCCCGGCT | 70238 |
rs216192734 | snp | A/C/G | | | intron-variant | Rnf168 | GRCm38.p3 | 16:32285961 | GTGATTTAAACCTCT[A/C/G]AGCCATCTCTCCAAC | 70238 |
rs216269622 | snp | A/T | | | upstream-variant-2KB | Rnf168 | Mm_Celera | 16:32276517 | GCCACACCTTCTAAT[A/T]GTCCCATTCCCTGGG | 70238 |