SNP - dbSNP |
dbSNP | Type | Alleles | Het | Se(het) | Fxn-class | Gene Name | Assembly | Chr-pos | Sequence | Entrez Gene |
rs6212143 | snp | C/T | 0.290657 | 0.246672 | intron-variant | Ercc6 | Mm_Celera | 14:32545579 | GGCTCATTTGTCTGA[C/T]TGTGTGTCTGTCTGT | 319955 |
rs30685558 | snp | C/G | 0.444444 | 0.157135 | intron-variant | Ercc6 | Mm_Celera | 14:32525540 | CAACGCATATATATT[C/G]TGTAGTGTGTAAATT | 319955 |
rs45640292 | snp | C/T | 0.32 | 0.24 | intron-variant | Ercc6 | Mm_Celera | 14:32575923 | ATGTTGTCACTGATG[C/T]GGTGTCATTTGATAC | 319955 |
rs45675478 | snp | C/T | 0.124444 | 0.216185 | intron-variant, downstream-variant-500B | Ercc6 | Mm_Celera | 14:32574167 | TTATTGATGCAGATA[C/T]TCAGGGAAGTGAACT | 319955 |
rs45687495 | snp | C/T | 0.124444 | 0.216185 | intron-variant | Ercc6 | Mm_Celera | 14:32527280 | AAAAAAGCTGAAACG[C/T]GTGTTTTAGCATATG | 319955 |
rs45689133 | snp | A/T | 0.124444 | 0.216185 | intron-variant, upstream-variant-2KB | Ercc6 | Mm_Celera | 14:32546151 | AATAGTTCTTTTTTT[A/T]ACATCTGTTAATTTG | 319955 |
rs45714470 | snp | C/G | 0.124444 | 0.216185 | intron-variant, upstream-variant-2KB | Ercc6 | Mm_Celera | 14:32547751 | GCAGTGATGGAGTTA[C/G]CAGGTGGATCTGTGT | 319955 |
rs45738398 | snp | A/G | 0.391111 | 0.206368 | intron-variant | Ercc6 | Mm_Celera | 14:32556499 | CTTAGCTCCGTGCTC[A/G]TGTTTGCAAGACTGT | 319955 |
rs45754785 | snp | A/G | 0.124444 | 0.216185 | intron-variant, upstream-variant-2KB | Ercc6 | Mm_Celera | 14:32541052 | AGTAAGAATTGACTC[A/G]AGGGGGCACGAGACA | 319955 |
rs45774275 | snp | C/T | 0.165289 | 0.235211 | intron-variant | Ercc6 | Mm_Celera | 14:32526119 | TCTTTGAGAGTTTTA[C/T]TCGAGTCTTCATTGT | 319955 |
rs45791449 | snp | C/T | 0.124444 | 0.216185 | intron-variant, upstream-variant-2KB | Ercc6 | Mm_Celera | 14:32541637 | AGCCTCTGCATCAAA[C/T]TATGTTTTTGCTCTT | 319955 |
rs45844480 | snp | C/T | 0.231111 | 0.249285 | intron-variant | Ercc6 | Mm_Celera | 14:32521266 | AATAAAATGTTAACC[C/T]GGTTCTTTCTGGTGG | 319955 |
rs45868239 | snp | G/T | 0.142012 | 0.225474 | intron-variant | Ercc6 | Mm_Celera | 14:32552434 | TTTCCCCACTATAGC[G/T]TTTTTCCTTAAAGAA | 319955 |
rs45904162 | snp | A/G | 0.231111 | 0.249285 | intron-variant | Ercc6 | Mm_Celera | 14:32556391 | TGGGGTTCATAGTGA[A/G]GCTCAGGAGTGGAGT | 319955 |
rs45920677 | snp | A/G | 0.231111 | 0.249285 | intron-variant | Ercc6 | Mm_Celera | 14:32575118 | ACAAGAAGTTCCCTC[A/G]GGGGCCATTGTGTTG | 319955 |
rs45930778 | snp | A/C | 0.124444 | 0.216185 | intron-variant | Ercc6 | Mm_Celera | 14:32550070 | ATATAGATAACAACT[A/C]GGTTTTATTCTCACT | 319955 |
rs45954639 | snp | A/C | 0.124444 | 0.216185 | intron-variant | Ercc6 | Mm_Celera | 14:32534133 | TGAAGATATTACAGA[A/C]GCTGTACAAATGAGA | 319955 |
rs45975944 | snp | C/T | 0.142012 | 0.225474 | intron-variant | Ercc6 | Mm_Celera | 14:32528303 | ATTGCCACCAAAATA[C/T]GATAGCTCTTAAAAT | 319955 |
rs46008197 | snp | C/T | 0.132653 | 0.220748 | utr-variant-3-prime | Ercc6 | Mm_Celera | 14:32579273 | GGCTAGTCCATCATC[C/T]GCCACCACTCCAAAT | 319955 |
rs46019879 | snp | C/T | 0.124444 | 0.216185 | intron-variant | Ercc6 | Mm_Celera | 14:32545632 | GTTTCAAGGCAGACC[C/T]GGAACTCCTGGAATT | 319955 |
rs46034911 | snp | C/T | 0.124444 | 0.216185 | intron-variant | Ercc6 | Mm_Celera | 14:32539268 | CTCCCTGCAGAATTA[C/T]TAAAGATAAATGCCA | 319955 |
rs46066030 | snp | A/G | 0.391111 | 0.206368 | intron-variant | Ercc6 | Mm_Celera | 14:32536581 | AGGACATAGGCTGAT[A/G]GCTGGATATTCAGTT | 319955 |
rs46097826 | snp | C/T | 0.32 | 0.24 | intron-variant | Ercc6 | Mm_Celera | 14:32567655 | TGCAGAGAAGGTGCC[C/T]GCAGAAGGACAGCTT | 319955 |
rs46106876 | snp | C/G | 0.124444 | 0.216185 | intron-variant | Ercc6 | Mm_Celera | 14:32563561 | GCTAGGAAAGCCCAG[C/G]CTGCCAGGGTTTGTG | 319955 |
rs46114841 | snp | C/T | 0.391111 | 0.206368 | intron-variant | Ercc6 | Mm_Celera | 14:32555540 | CTTTTAATTTGAAAC[C/T]GCCCGAGATGATTTG | 319955 |
rs46117628 | snp | C/G | 0.152778 | 0.230321 | intron-variant | Ercc6 | Mm_Celera | 14:32513700 | CGTCTAGCCTTCTGC[C/G]GCGGAGCCCGTCCGA | 319955 |
rs46144731 | snp | A/G | 0.391111 | 0.206368 | intron-variant | Ercc6 | Mm_Celera | 14:32535560 | GTGGCCACCACTGGC[A/G]TCATCGGACTGGGTT | 319955 |
rs46179938 | snp | A/G | 0.32 | 0.24 | intron-variant, utr-variant-3-prime | Ercc6 | Mm_Celera | 14:32573419 | GGTATGGGTAATGAA[A/G]TTTGTCAAAGGTGTT | 319955 |
rs46217485 | snp | A/G | 0.124444 | 0.216185 | intron-variant | Ercc6 | Mm_Celera | 14:32556769 | ACGGGGTCTCACTGT[A/G]TAGCTGAAACCCTAG | 319955 |
rs46222921 | snp | A/G | 0.32 | 0.24 | intron-variant | Ercc6 | Mm_Celera | 14:32536489 | GCCTAAGTCTACTTG[A/G]CCAGGAACAGCTTCC | 319955 |
rs46231585 | snp | C/T | 0.124444 | 0.216185 | intron-variant, utr-variant-5-prime | Ercc6 | Mm_Celera | 14:32519959 | AGGTGTCTCTGTTTG[C/T]GGCTGACTGAATGCA | 319955 |
rs46250893 | snp | G/T | 0.132653 | 0.220748 | downstream-variant-500B | Ercc6 | Mm_Celera | 14:32581364 | GTACACAGAGCATAT[G/T]CCACATGAAAACCAG | 319955 |
rs46313272 | snp | A/C/T | 0.124444 | 0.216185 | intron-variant | Ercc6 | GRCm38.p3 | 14:32549348 | CGCTGAGCACACTGA[A/C/T]TTTTTACTTGAGCAT | 319955 |
rs46328794 | snp | A/G | 0.124444 | 0.216185 | intron-variant | Ercc6 | Mm_Celera | 14:32543903 | ATCCAACAATTCTGT[A/G]TGGTTATTGTCTGAT | 319955 |
rs46364985 | snp | A/G | 0.132653 | 0.220748 | intron-variant | Ercc6 | Mm_Celera | 14:32563044 | TGTCCAGTAAACACT[A/G]GCAGACCACTGCCAT | 319955 |
rs46391327 | snp | A/G | 0.124444 | 0.216185 | intron-variant | Ercc6 | Mm_Celera | 14:32558903 | TGAGCAGTCATGGAG[A/G]AGATTGAGCAGTTCT | 319955 |
rs46392015 | snp | A/G | 0.124444 | 0.216185 | intron-variant | Ercc6 | Mm_Celera | 14:32554117 | TGGCTTGTAGATTGA[A/G]AGTTTTGATAGTTTT | 319955 |
rs46438626 | snp | C/T | 0.124444 | 0.216185 | intron-variant | Ercc6 | Mm_Celera | 14:32556679 | AGTTTCTCTTTATCC[C/T]TCTTTAAACTCCTTT | 319955 |
rs46451247 | snp | A/G | 0.124444 | 0.216185 | intron-variant | Ercc6 | Mm_Celera | 14:32543697 | CCCAGGGAGTCAGGA[A/G]GCACAGTTTTCCATT | 319955 |
rs46466008 | snp | A/G | 0.391111 | 0.206368 | utr-variant-3-prime | Ercc6 | Mm_Celera | 14:32579208 | CACCTAGTTTCCTCA[A/G]TATAAATGAAAGACA | 319955 |
rs46482287 | snp | C/T | 0.124444 | 0.216185 | intron-variant | Ercc6 | Mm_Celera | 14:32557747 | CGTGCTTGTGTATCT[C/T]TGCGGTGTGCTTTAG | 319955 |
rs46500122 | snp | C/T | 0.124444 | 0.216185 | intron-variant, upstream-variant-2KB | Ercc6 | Mm_Celera | 14:32547447 | TTAGATGTGTGCTCA[C/T]CCTCTTGGAGTGAAA | 319955 |
rs46501963 | snp | G/T | 0.124444 | 0.216185 | intron-variant | Ercc6 | Mm_Celera | 14:32534041 | CAGGATCCTGTAACT[G/T]TGGGCAGTTCTCATG | 319955 |
rs46526463 | snp | C/G | 0.32 | 0.24 | intron-variant, utr-variant-5-prime | Ercc6 | Mm_Celera | 14:32520427 | TCGGAAGGCCACATA[C/G]CTGAGTTCTCATAAT | 319955 |
rs46534505 | snp | A/G | 0.124444 | 0.216185 | intron-variant | Ercc6 | Mm_Celera | 14:32562988 | TATCAGGCCATGGTT[A/G]TCAAGATGCACAAGT | 319955 |
rs46560694 | snp | A/C | 0.152778 | 0.230321 | intron-variant | Ercc6 | Mm_Celera | 14:32513662 | CTCGGGCTCTCCATG[A/C]GGCTGTGGCCCCGCG | 319955 |
rs46570505 | snp | C/T | 0.32 | 0.24 | intron-variant, utr-variant-5-prime | Ercc6 | Mm_Celera | 14:32520213 | TGGGTCATGGCCTGA[C/T]CTAATTATATTCTGT | 319955 |
rs46571540 | snp | A/T | 0.124444 | 0.216185 | intron-variant | Ercc6 | Mm_Celera | 14:32528723 | GCTCAGTCTTGGATG[A/T]TCCCTTCCTGTGCAT | 319955 |
rs46576923 | snp | C/T | 0.124444 | 0.216185 | intron-variant | Ercc6 | Mm_Celera | 14:32532319 | CAAATGAAGACTAAT[C/T]CCGCTCCCTGCTCTG | 319955 |
rs46634734 | snp | C/T | 0.391111 | 0.206368 | intron-variant | Ercc6 | Mm_Celera | 14:32528833 | AGAAGCTGATGTTTG[C/T]GGGCTCTTGCTCTTG | 319955 |
rs46640634 | snp | C/T | 0.124444 | 0.216185 | intron-variant | Ercc6 | Mm_Celera | 14:32533177 | GTCTGTATGTTTGTA[C/T]AGAAGGCCTCTGTGT | 319955 |
rs46686303 | snp | A/G | 0.124444 | 0.216185 | intron-variant | Ercc6 | Mm_Celera | 14:32544334 | GAGATTCAGTTCCTG[A/G]GCTGCATTGTAACTA | 319955 |
rs46703501 | snp | C/G | 0.124444 | 0.216185 | intron-variant, upstream-variant-2KB | Ercc6 | Mm_Celera | 14:32547097 | GGAGAAATTAAACAT[C/G]TAACACTTGTAATGA | 319955 |
rs46707883 | snp | C/T | 0.152778 | 0.230321 | intron-variant | Ercc6 | Mm_Celera | 14:32513641 | GCCGGGTGAGAGTAC[C/T]TGCGCCTCGGGCTCT | 319955 |
rs46720869 | snp | A/G | 0.336735 | 0.234472 | intron-variant | Ercc6 | Mm_Celera | 14:32575198 | TGCTTTCTAGAGATA[A/G]CTTTTCTGGGGAAGA | 319955 |
rs46737330 | snp | C/G | 0.124444 | 0.216185 | intron-variant | Ercc6 | Mm_Celera | 14:32537018 | TGTATGAGGAGTTAG[C/G]AGCTCTGCCAGGGAA | 319955 |
rs46738531 | snp | G/T | | | missense, nc-transcript-variant | Ercc6 | Mm_Celera | 14:32569773 | GACACCCAAATGCCA[G/T]TTAAAAAAAAGGACT | 319955 |
rs46828259 | snp | A/G | 0.124444 | 0.216185 | intron-variant | Ercc6 | Mm_Celera | 14:32559502 | CTAATCAGATGGGGA[A/G]GTGCCTCATGGGTCC | 319955 |
rs46833560 | snp | C/T | 0.142012 | 0.225474 | intron-variant | Ercc6 | Mm_Celera | 14:32545915 | TTTATTACTTAAACA[C/T]AAAACAGACCTTAGA | 319955 |
rs46843053 | snp | C/T | 0.124444 | 0.216185 | intron-variant | Ercc6 | Mm_Celera | 14:32571880 | TGGTGTGAAAAATGA[C/T]TTGTAGGAGATGGAG | 319955 |
rs46847470 | snp | A/T | 0.124444 | 0.216185 | intron-variant | Ercc6 | Mm_Celera | 14:32552771 | CAAATGTGCTTATGT[A/T]TATTTCTTTCATTTT | 319955 |
rs46865645 | snp | C/T | 0.124444 | 0.216185 | intron-variant | Ercc6 | Mm_Celera | 14:32571093 | TTTGTCATTCACATG[C/T]ATATGTAAAGTAAAT | 319955 |
rs46866473 | snp | C/G | 0.244898 | 0.249948 | intron-variant | Ercc6 | Mm_Celera | 14:32522181 | TGGTAACTTATCCAG[C/G]AGTATCTTAAATGCT | 319955 |
rs46873581 | snp | A/G | 0.124444 | 0.216185 | intron-variant | Ercc6 | Mm_Celera | 14:32550739 | TGTCTGGTGAGAAGG[A/G]CCAGCTCTCTCAAGG | 319955 |
rs46892126 | snp | A/G | 0.124444 | 0.216185 | intron-variant | Ercc6 | Mm_Celera | 14:32553567 | GTGGAACAACTATAA[A/G]TGCTGTCTCTAGTCC | 319955 |
rs46900250 | snp | C/T | 0.231111 | 0.249285 | intron-variant | Ercc6 | Mm_Celera | 14:32530533 | GGGTTCTCCAAAAGC[C/T]TTCCTGTGTGCCTTG | 319955 |
rs46921960 | snp | G/T | | | intron-variant | Ercc6 | Mm_Celera | 14:32569694 | ACATAATCAGCTGCA[G/T]AAGAATTCTGCAGAG | 319955 |
rs46922715 | snp | C/T | 0.124444 | 0.216185 | intron-variant | Ercc6 | Mm_Celera | 14:32528642 | TCTAAGGTTCTGGCT[C/T]ACCTGCTCTAGAACT | 319955 |
rs46938007 | snp | C/T | 0.336735 | 0.234472 | intron-variant | Ercc6 | Mm_Celera | 14:32529787 | AAAGAAGTGCTGATA[C/T]AGTCAAATCAAGGCT | 319955 |
rs46949338 | snp | A/C | 0.152778 | 0.230321 | intron-variant, upstream-variant-2KB | Ercc6 | Mm_Celera | 14:32518522 | ACACCATGAAGGTTA[A/C]TGTTACAGTAGAGGA | 319955 |
rs46951255 | snp | A/G | 0.231111 | 0.249285 | intron-variant | Ercc6 | Mm_Celera | 14:32575043 | AACATGCTTGCAAGG[A/G]GTTCCAGTGGTTGAG | 319955 |
rs46970771 | snp | G/T | 0.124444 | 0.216185 | intron-variant | Ercc6 | Mm_Celera | 14:32553584 | GCTGTCTCTAGTCCA[G/T]GTGTTTCATATTGTT | 319955 |
rs46980758 | snp | C/G | 0.132653 | 0.220748 | intron-variant | Ercc6 | Mm_Celera | 14:32550987 | AGCGATTGGAGGGGA[C/G]AAGACACCCAGATTT | 319955 |
rs46991562 | snp | A/G | 0.244898 | 0.249948 | intron-variant | Ercc6 | Mm_Celera | 14:32552429 | CAGATTTTCCCCACT[A/G]TAGCTTTTTTCCTTA | 319955 |
rs47004016 | snp | C/T | 0.391111 | 0.206368 | intron-variant | Ercc6 | Mm_Celera | 14:32576562 | CTCGGATGGCGACCA[C/T]GCCCTCTCCCGCATC | 319955 |
rs47004610 | snp | C/G | 0.124444 | 0.216185 | intron-variant | Ercc6 | Mm_Celera | 14:32557125 | ACAGCGTGCAGGCAG[C/G]TTAGTTTTTGAACTC | 319955 |
rs47013137 | snp | C/T | 0.132653 | 0.220748 | utr-variant-3-prime | Ercc6 | Mm_Celera | 14:32580229 | TCTTTACCAATAAAC[C/T]ATTTTTAATCATGTA | 319955 |
rs47049339 | snp | C/T | 0.152778 | 0.230321 | intron-variant | Ercc6 | Mm_Celera | 14:32521902 | GGCTTTAGATTTGCT[C/T]CTAAAGTTCAGTCTC | 319955 |
rs47070041 | snp | C/T | 0.124444 | 0.216185 | intron-variant, upstream-variant-2KB | Ercc6 | Mm_Celera | 14:32546656 | GGACCAGAACCTAAC[C/T]AGATGACTAATTCAT | 319955 |
rs47083139 | snp | C/T | 0.132653 | 0.220748 | intron-variant | Ercc6 | Mm_Celera | 14:32521992 | AGGGGATCTTCCCTG[C/T]CTGTCTGAAGCCTGA | 319955 |
rs47085544 | snp | A/G | 0.231111 | 0.249285 | intron-variant | Ercc6 | Mm_Celera | 14:32539179 | GAGTGAAACTGTACT[A/G]TGTAGTGTGGCAAGG | 319955 |
rs47106703 | snp | G/T | 0.152778 | 0.230321 | upstream-variant-2KB | Ercc6 | Mm_Celera | 14:32512517 | GGTTGGGTAAAGAAT[G/T]TTACTACTTGGCTTA | 319955 |
rs47185936 | snp | A/G | 0.124444 | 0.216185 | missense, nc-transcript-variant | Ercc6 | Mm_Celera | 14:32557864 | TTCGAGATATTGTTT[A/G]TTGTCATGGAGTTTT | 319955 |
rs47228947 | snp | C/T | 0.124444 | 0.216185 | intron-variant | Ercc6 | Mm_Celera | 14:32563435 | AGAGGTGAGGGTGTT[C/T]ATTACGTAAGAGGAC | 319955 |
rs47245975 | snp | C/T | 0.124444 | 0.216185 | intron-variant | Ercc6 | Mm_Celera | 14:32534541 | TAGATCTGACTAGCC[C/T]AGGTGTGCATTGCGT | 319955 |
rs47262004 | snp | G/T | 0.124444 | 0.216185 | intron-variant | Ercc6 | Mm_Celera | 14:32542098 | CCAGTCTCCTCACTT[G/T]CAGAGGCTTTAGCTG | 319955 |
rs47279748 | snp | C/T | 0.124444 | 0.216185 | intron-variant | Ercc6 | Mm_Celera | 14:32529502 | CTTTGTGTTTTAGCA[C/T]GGTGGACAGATGTTT | 319955 |
rs47326452 | snp | A/G | 0.32 | 0.24 | intron-variant | Ercc6 | Mm_Celera | 14:32556250 | TCTACCTATTGCATG[A/G]CTTGGGATGCCCTTT | 319955 |
rs47331493 | snp | C/G | 0.391111 | 0.206368 | intron-variant, upstream-variant-2KB | Ercc6 | Mm_Celera | 14:32547717 | ACGGATATGTTCTAG[C/G]AGGTTTATCTAATGA | 319955 |
rs47338833 | snp | C/T | 0.35503 | 0.226867 | intron-variant, utr-variant-5-prime | Ercc6 | Mm_Celera | 14:32520400 | TTTTCTGCATGAAGA[C/T]AGTTGAAGCTTTCGG | 319955 |
rs47353692 | snp | A/G | 0.124444 | 0.216185 | intron-variant | Ercc6 | Mm_Celera | 14:32571015 | AAATTAGCATGAAGA[A/G]CATATGAACTCTGCT | 319955 |
rs47357473 | snp | C/T | | | downstream-variant-500B | Ercc6 | Mm_Celera | 14:32581020 | CTTTAATACCCTTCC[C/T]TAGTTTGGTGAAGTA | 319955 |
rs47370012 | snp | A/G | 0.124444 | 0.216185 | intron-variant | Ercc6 | Mm_Celera | 14:32567217 | TGGTTTGGGAAGTGG[A/G]CATAAAAGATTTAGA | 319955 |
rs47375885 | snp | C/T | 0.231111 | 0.249285 | intron-variant | Ercc6 | Mm_Celera | 14:32553864 | CCCACCTTTTCCTGA[C/T]ATGTAGGATCCAGTG | 319955 |
rs47393821 | snp | A/G | 0.124444 | 0.216185 | intron-variant | Ercc6 | Mm_Celera | 14:32539821 | GTGGTCTAGGTGCGC[A/G]GGAAGGAACTGTTGT | 319955 |
rs47406514 | snp | A/C | 0.124444 | 0.216185 | intron-variant | Ercc6 | Mm_Celera | 14:32546100 | CTTGAGTGCTTTAAA[A/C]TACTAAAAGACCTAT | 319955 |
rs47409089 | snp | A/T | 0.142012 | 0.225474 | intron-variant | Ercc6 | Mm_Celera | 14:32514002 | TGGGAGGGACAGAGC[A/T]GTAAGTGCTGTAACC | 319955 |
rs47424392 | snp | A/G | 0.142012 | 0.225474 | upstream-variant-2KB | Ercc6 | Mm_Celera | 14:32511707 | GTACAGTTAGGAAAC[A/G]AAGTCCTTGACGGGC | 319955 |
rs47469102 | snp | A/G | 0.124444 | 0.216185 | intron-variant | Ercc6 | Mm_Celera | 14:32554262 | TGGTAGCTGAGAAGG[A/G]TGGTCCCAAAGACTG | 319955 |
rs47482011 | snp | A/G | 0.391111 | 0.206368 | missense, nc-transcript-variant | Ercc6 | Mm_Celera | 14:32575776 | TTCGGTCAGAAAAGG[A/G]ACTCCAGCCTCCCTG | 319955 |