SNP - dbSNP |
dbSNP | Type | Alleles | Het | Se(het) | Fxn-class | Gene Name | Assembly | Chr-pos | Sequence | Entrez Gene |
rs13472184 | snp | A/G | | | utr-variant-3-prime | Trim12c | Mm_Celera | 7:104339306 | TGTGTGTGTATTCTT[A/G]GTGATCACTTTCTTT | 319236 |
rs13479442 | snp | G/T | 0.499882 | 0.0076914 | missense | Trim12c | Mm_Celera | 7:104347976 | TGTTTTGTGGCCCCG[G/T]TGCTCCTGAGATCGC | 319236 |
rs31324035 | snp | C/G | 0.444444 | 0.157135 | intron-variant | Trim12c | Mm_Celera | 7:104348779 | ACCCAGGGACAAAAA[C/G]CATCCAGATGGCTAA | 319236 |
rs31820711 | snp | C/T | 0.415225 | 0.187619 | stop-gained | Trim12c | Mm_Celera | 7:104340787 | ATGTTAAGAGTCTGG[C/T]CAGCAAATTGTCATG | 319236 |
rs31905560 | snp | C/T | 0.375 | 0.216506 | intron-variant | Trim12c | Mm_Celera | 7:104348842 | AGGGCCTCAGAAATC[C/T]GCCTGCCCCTGCCTC | 319236 |
rs31923032 | snp | A/T | 0.260355 | 0.249785 | intron-variant | Trim12c | GRCm38.p3 | 7:104341819 | GGCTACTCTTCCTTG[A/T]CCATATCTAGAAACC | 319236 |
rs31926515 | snp | A/G | 0.124444 | 0.216185 | intron-variant | Trim12c | Mm_Celera | 7:104345153 | ATAAGAAAAGGGAGA[A/G]CCATTAAGTTTGTCA | 319236 |
rs31926518 | snp | G/T | 0.142012 | 0.225474 | intron-variant | Trim12c | GRCm38.p3 | 7:104345442 | AACACACAGACCTCT[G/T]GTCAGCTTTCCTCAG | 319236 |
rs31926523 | snp | A/T | 0.277778 | 0.248452 | intron-variant | Trim12c | Mm_Celera | 7:104346455 | ACCACGCATCCTCCA[A/T]GGTGCCAGCTCCTCA | 319236 |
rs31926524 | snp | A/C | 0.32 | 0.24 | intron-variant, nc-transcript-variant | Trim12c, Gm36430 | Mm_Celera | 7:104351919 | AGCAAAACACACAAA[A/C]TCAACCTTGACAGGA | 319236 |
rs31926527 | snp | C/T | 0.375 | 0.216506 | intron-variant, nc-transcript-variant | Trim12c, Gm36430 | Mm_Celera | 7:104352198 | CTGGGCAACATAAAA[C/T]GTATCCTCTCTCCAA | 319236 |
rs31926647 | snp | C/G | 0.124444 | 0.216185 | missense | Trim12c | Mm_Celera | 7:104341272 | GAGAGTTTTCACAGC[C/G]ATGTTCAAGATTCCT | 319236 |
rs31926650 | snp | C/T | 0.132653 | 0.220748 | intron-variant | Trim12c | Mm_Celera | 7:104341430 | CAGCCTTATCTGTGA[C/T]GTTATTAATAGAAGT | 319236 |
rs31926653 | snp | A/G | 0.244898 | 0.249948 | intron-variant | Trim12c | GRCm38.p3 | 7:104341570 | GAAACATAAGCTCTT[A/G]CAAGACAGTGAGAAG | 319236 |
rs31927295 | snp | A/C | 0.5 | 0 | intron-variant, nc-transcript-variant | Trim12c, Gm36430 | Mm_Celera | 7:104352340 | AACCCAAAGCTTGAA[A/C]AGTACTCTATCACTG | 319236 |
rs31927301 | snp | A/G | 0.375 | 0.216506 | intron-variant, nc-transcript-variant | Trim12c, Gm36430 | Mm_Celera | 7:104352418 | TATTGAGTTGCTGAT[A/G]ATGGCCATCAATTTA | 319236 |
rs31927496 | snp | G/T | 0.124444 | 0.216185 | intron-variant | Trim12c | Mm_Celera | 7:104346519 | ACATCTCCAGCCAGG[G/T]GAACCAGTAGGGAGG | 319236 |
rs31927498 | snp | A/G | 0.336735 | 0.234472 | intron-variant | Trim12c | Mm_Celera | 7:104346609 | GCCCAGGTCCCTCCC[A/G]GGCATCAGGCTGACA | 319236 |
rs31927501 | snp | C/T | 0.132653 | 0.220748 | missense | Trim12c | Mm_Celera | 7:104346660 | TTGCCTCCCAGTAAG[C/T]TCTATCCTTCTGAAG | 319236 |
rs31927516 | snp | A/G | 0.142012 | 0.225474 | intron-variant | Trim12c | Mm_Celera | 7:104341660 | TCTGAAAAGGGGTAA[A/G]AATTTACAATATTAA | 319236 |
rs31927519 | snp | G/T | 0.165289 | 0.235211 | intron-variant | Trim12c | Mm_Celera | 7:104341743 | TTGGAAACCCTAACA[G/T]GGTCCTTTAAAGATG | 319236 |
rs31928184 | snp | G/T | 0.5 | 0 | intron-variant, nc-transcript-variant | Trim12c, Gm36430 | Mm_Celera | 7:104352453 | CCTTCTGCCTCCTGT[G/T]TATCTGGAATCTCAA | 319236 |
rs31928187 | snp | A/C | 0.48 | 0.0979796 | intron-variant, nc-transcript-variant | Trim12c, Gm36430 | Mm_Celera | 7:104352839 | TCCGGTAAAGAACCA[A/C]AGCCCTAAAGTATGC | 319236 |
rs31928190 | snp | C/T | 0.5 | 0 | intron-variant, nc-transcript-variant | Trim12c, Gm36430 | Mm_Celera | 7:104352950 | TGTGGTAGGAAACAA[C/T]GCTCTGGGTCTCGTG | 319236 |
rs31928193 | snp | C/G | 0.5 | 0 | intron-variant | Trim12c, Gm36430 | Mm_Celera | 7:104353029 | TAAACCTGGAAAAAA[C/G]ACAACTTTAAAGTAG | 319236 |
rs31928410 | snp | A/G | 0.124444 | 0.216185 | intron-variant | Trim12c | Mm_Celera | 7:104346862 | CTACCTTTCTTTTAA[A/G]GGATTGTGATATGAA | 319236 |
rs31928413 | snp | C/T | 0.142012 | 0.225474 | intron-variant | Trim12c | Mm_Celera | 7:104346991 | TTGGTCTGGGAAGTT[C/T]ACAGAAACCCAGGGA | 319236 |
rs31929106 | snp | A/G | 0.48 | 0.0979796 | utr-variant-5-prime, intron-variant | Trim12c, Gm36430 | Mm_Celera | 7:104353198 | GATAAACTCACCCAA[A/G]CAAAAGCAATGTTCT | 319236 |
rs31929109 | snp | C/T | 0.32 | 0.24 | utr-variant-5-prime, intron-variant | Trim12c, Gm36430 | Mm_Celera | 7:104353214 | CAAAAGCAATGTTCT[C/T]CTTTCAAAGTCTTCA | 319236 |
rs31929112 | snp | A/G | 0.444444 | 0.157135 | utr-variant-5-prime, intron-variant | Trim12c, Gm36430 | Mm_Celera | 7:104353233 | TCAAAGTCTTCAAAA[A/G]TCTGCCCCCTAAAAT | 319236 |
rs31929346 | snp | A/G | 0.260355 | 0.249785 | intron-variant | Trim12c | Mm_Celera | 7:104347019 | GGAATGGCAACTAGA[A/G]TCTAGGAGTAGGAAG | 319236 |
rs31929349 | snp | C/T | 0.124444 | 0.216185 | intron-variant | Trim12c | Mm_Celera | 7:104347283 | TATAATCAGAGCTTT[C/T]CGTGGACATAAAATC | 319236 |
rs31929351 | snp | A/G | 0.132653 | 0.220748 | intron-variant | Trim12c | Mm_Celera | 7:104347384 | TTAGGATTAAGCTCA[A/G]TGGATAGTCCCATTC | 319236 |
rs31929584 | snp | A/C/T | 0.142012 | 0.225474 | intron-variant | Trim12c | GRCm38.p3 | 7:104342669 | AATGTCTTCTAGTCT[A/C/T]AGAAGAAAATAGTGT | 319236 |
rs31929587 | snp | C/T | 0.244898 | 0.249948 | intron-variant | Trim12c | Mm_Celera | 7:104342814 | GCACATAGGGTGAAC[C/T]ACAATAGAGTTAAGA | 319236 |
rs31929591 | snp | G/T | 0.124444 | 0.216185 | intron-variant | Trim12c | Mm_Celera | 7:104343433 | GTGGTTCTTACATAT[G/T]CCTCACTTCAGTTTG | 319236 |
rs31929785 | snp | C/T | 0.32 | 0.24 | upstream-variant-2KB, intron-variant | Trim12c, Gm36430 | Mm_Celera | 7:104353368 | TTTGAGAGCTGGAAA[C/T]GAAACAGAAACCACA | 319236 |
rs31929788 | snp | A/G | 0.32 | 0.24 | upstream-variant-2KB, intron-variant | Trim12c, Gm36430 | Mm_Celera | 7:104353595 | ACCAGATTATGTATT[A/G]TGTGGCTCAACAGAC | 319236 |
rs31929791 | snp | C/T | 0.444444 | 0.157135 | upstream-variant-2KB, intron-variant | Trim12c, Gm36430 | Mm_Celera | 7:104353621 | CAGACTTAGTCCTTT[C/T]CCAGTGCTGATCTGA | 319236 |
rs31930124 | snp | A/G | 0.391111 | 0.206368 | intron-variant | Trim12c | Mm_Celera | 7:104347405 | AGTCCCATTCTTTCA[A/G]GCCTCAGAAGGTAAC | 319236 |
rs31930127 | snp | A/G | 0.336735 | 0.234472 | intron-variant | Trim12c | Mm_Celera | 7:104347451 | CCAGGTCTGGATTCC[A/G]TGATGATCAGGTCTT | 319236 |
rs31930534 | snp | C/G | 0.48 | 0.0979796 | upstream-variant-2KB, intron-variant | Trim12c, Gm36430 | Mm_Celera | 7:104354335 | GGTGACTGACATCAG[C/G]ATGGCATGGGAAACA | 319236 |
rs31930537 | snp | A/C | 0.375 | 0.216506 | upstream-variant-2KB, intron-variant | Trim12c, Gm36430 | Mm_Celera | 7:104354446 | TCAGTTGTGTGAGTG[A/C]ATGTTGGAGAAGCCA | 319236 |
rs31930540 | snp | C/T | 0.32 | 0.24 | upstream-variant-2KB, intron-variant | Trim12c, Gm36430 | Mm_Celera | 7:104354448 | AGTTGTGTGAGTGAA[C/T]GTTGGAGAAGCCACC | 319236 |
rs31930543 | snp | C/T | 0.32 | 0.24 | upstream-variant-2KB, intron-variant | Trim12c, Gm36430 | GRCm38.p3 | 7:104354739 | GAACCACGGTCCTTG[C/T]GGATGCTGGGCTAGT | 319236 |
rs31930654 | snp | A/C | 0.231111 | 0.249285 | intron-variant | Trim12c | Mm_Celera | 7:104343470 | GTCTGTGACTTCTTC[A/C]GTTAGGCTTTGAGAT | 319236 |
rs31930655 | snp | C/T | 0.32 | 0.24 | intron-variant | Trim12c | Mm_Celera | 7:104343514 | CACAGTCTACTTAAA[C/T]ACATTCTTTACAAGA | 319236 |
rs31930657 | snp | A/G | 0.244898 | 0.249948 | intron-variant | Trim12c | Mm_Celera | 7:104344598 | GCAGTGACTAACTGG[A/G]ATTAGTAAGATACTT | 319236 |
rs31930660 | snp | C/T | 0.124444 | 0.216185 | intron-variant | Trim12c | GRCm38.p3 | 7:104344654 | CTGGTGTCATAAATG[C/T]CCATGGATCCAATAG | 319236 |
rs31930662 | snp | A/G | 0.142012 | 0.225474 | intron-variant | Trim12c | GRCm38.p3 | 7:104344660 | TCATAAATGCCCATG[A/G]ATCCAATAGATCTCC | 319236 |
rs31931020 | snp | A/G | 0.231111 | 0.249285 | missense | Trim12c | Mm_Celera | 7:104348157 | GGCCTCAGATTGCTA[A/G]ACTGGTAACTAAGTC | 319236 |
rs31931023 | snp | A/G | 0.124444 | 0.216185 | synonymous-codon | Trim12c | Mm_Celera | 7:104348174 | CTGGTAACTAAGTCG[A/G]CACACAGGGCAACTG | 319236 |
rs31931229 | snp | C/T | 0.375 | 0.216506 | utr-variant-3-prime | Trim12c | Mm_Celera | 7:104338810 | AAATTGTAAAAACAA[C/T]CAAAAACCTGCAGTT | 319236 |
rs31931232 | snp | G/T | 0.231111 | 0.249285 | utr-variant-3-prime | Trim12c | Mm_Celera | 7:104339048 | AGTCACAGTGATAAG[G/T]TTTCCCAAAGGAATA | 319236 |
rs31931408 | snp | G/T | 0.444444 | 0.157135 | upstream-variant-2KB, downstream-variant-500B, intron-variant | Trim12c, Trim30b, LOC102640171, Gm36430 | Mm_Celera | 7:104355353 | ATTCCCATGGAACAC[G/T]ATTTGAGAGGAAATA | 319236 |
rs31931634 | snp | A/G | 0.132653 | 0.220748 | intron-variant | Trim12c | GRCm38.p3 | 7:104344715 | TCTCTACAAATTCAT[A/G]AAAATAAAATTCCAC | 319236 |
rs31931637 | snp | C/G | 0.124444 | 0.216185 | intron-variant | Trim12c | GRCm38.p3 | 7:104344736 | AAAATTCCACTCCTT[C/G]TTATTTGTGCATGCA | 319236 |
rs31931640 | snp | A/T | 0.132653 | 0.220748 | intron-variant | Trim12c | GRCm38.p3 | 7:104344763 | TGCAGTGATCCCTCC[A/T]GCCTCTGAAACTGAG | 319236 |
rs31931643 | snp | C/G | 0.32 | 0.24 | intron-variant | Trim12c | GRCm38.p3 | 7:104344831 | AGGAAGACCACAGCA[C/G]CAGAGAGGAAGGGCA | 319236 |
rs31931895 | snp | A/C | 0.132653 | 0.220748 | missense | Trim12c | Mm_Celera | 7:104348187 | CGGCACACAGGGCAA[A/C]TGAACATTTCCTTAT | 319236 |
rs31931898 | snp | A/G | 0.231111 | 0.249285 | synonymous-codon | Trim12c | Mm_Celera | 7:104348204 | GAACATTTCCTTATC[A/G]CATTTGGTGGATTCA | 319236 |
rs31931900 | snp | A/C | 0.231111 | 0.249285 | missense | Trim12c | Mm_Celera | 7:104348227 | TGGATTCAAAGTACA[A/C]CGTGATGCAGCCTTG | 319236 |
rs31931903 | snp | G/T | 0.124444 | 0.216185 | synonymous-codon | Trim12c | Mm_Celera | 7:104348237 | GTACACCGTGATGCA[G/T]CCTTGGCAGAAGCTG | 319236 |
rs31932234 | snp | C/T | 0.152778 | 0.230321 | utr-variant-3-prime | Trim12c | Mm_Celera | 7:104339111 | GAAACAATGTAAATC[C/T]TAGTAATAACTCTTA | 319236 |
rs31932237 | snp | C/T | 0.124444 | 0.216185 | utr-variant-3-prime | Trim12c | Mm_Celera | 7:104339268 | ACATGGTACCTTATT[C/T]ATTTGGGGTCTTTAT | 319236 |
rs31932240 | snp | A/C | 0.142012 | 0.225474 | utr-variant-3-prime | Trim12c | Mm_Celera | 7:104339432 | CCATGGTTTCATGGG[A/C]CACTATAACACAGCA | 319236 |
rs31932242 | snp | A/C | 0.359862 | 0.224567 | utr-variant-3-prime | Trim12c | Mm_Celera | 7:104340383 | ATGAAGTTATAGAGA[A/C]CTGACAGAGCTGAGG | 319236 |
rs31932419 | snp | A/C | 0.124444 | 0.216185 | intron-variant | Trim12c | GRCm38.p3 | 7:104344884 | CTCAGACCCTGGGAC[A/C]TCCTGCAGCCTTACC | 319236 |
rs31932422 | snp | C/G | 0.132653 | 0.220748 | intron-variant | Trim12c | GRCm38.p3 | 7:104344887 | AGACCCTGGGACCTC[C/G]TGCAGCCTTACCTGC | 319236 |
rs31932806 | snp | C/G | 0.32 | 0.24 | missense | Trim12c | Mm_Celera | 7:104348250 | CAGCCTTGGCAGAAG[C/G]TGTGACCACAATCTG | 319236 |
rs31932809 | snp | C/G | 0.345679 | 0.230967 | missense | Trim12c | Mm_Celera | 7:104348299 | TCAGGTTCAGACAGA[C/G]AGGACAGGTCACTTC | 319236 |
rs31932812 | snp | C/T | 0.231111 | 0.249285 | utr-variant-5-prime | Trim12c | Mm_Celera | 7:104348385 | ACTGTCCTGACTCCT[C/T]GCACTTCTGCTCAGG | 319236 |
rs31933175 | snp | A/G/T | 0.132653 | 0.220748 | missense | Trim12c | Mm_Celera | 7:104345012 | CTGCCAGTTTGTTGA[A/G/T]AATGTTTTCCTTCTC | 319236 |
rs31933178 | snp | A/G | 0.124444 | 0.216185 | missense | Trim12c | Mm_Celera | 7:104345122 | TCCACATCTTTCTGT[A/G]TTTGATTCTTCAGAG | 319236 |
rs31933224 | snp | A/C | 0.124444 | 0.216185 | utr-variant-3-prime | Trim12c | Mm_Celera | 7:104340495 | ATGAAGAATAAGAGA[A/C]CTTTGCAGCAGTGTT | 319236 |
rs31933228 | snp | A/G | 0.142012 | 0.225474 | synonymous-codon | Trim12c | Mm_Celera | 7:104340862 | AGGAAAGGAAGCTGT[A/G]CAGAATCTGTAGATA | 319236 |
rs31933737 | snp | A/T | 0.244898 | 0.249948 | intron-variant, upstream-variant-2KB | Trim12c, Gm36430 | Mm_Celera | 7:104350053 | ATGAGAAAAAAACAC[A/T]AAAATCAATAATGCA | 319236 |
rs31933739 | snp | C/G | 0.5 | 0 | intron-variant, nc-transcript-variant | Trim12c, Gm36430 | Mm_Celera | 7:104351880 | ACTGGCTTATGAACA[C/G]GGACAAGAAACAGTT | 319236 |
rs45780999 | snp | C/T | | | upstream-variant-2KB, intron-variant | Trim12c, Gm36430 | Mm_Celera | 7:104353491 | AGACTGGGGAGGAGT[C/T]ATGTGCAGAGCCAGG | 319236 |
rs45964500 | snp | C/G | | | intron-variant | Trim12c | Mm_Celera | 7:104342361 | CTTCAAAATGCTTAG[C/G]CAATATGGAGACTAG | 319236 |
rs46012044 | snp | A/G | | | upstream-variant-2KB, intron-variant | Trim12c, Gm36430 | Mm_Celera | 7:104353995 | CCACCACAGTGGAGA[A/G]CCTGATAACAGGCAG | 319236 |
rs46038000 | snp | A/G | | | upstream-variant-2KB, intron-variant | Trim12c, Gm36430 | Mm_Celera | 7:104353962 | GCATTCACAGTTCCT[A/G]TGGGTTAAAGTTCAT | 319236 |
rs46112681 | snp | C/G | | | upstream-variant-2KB, intron-variant | Trim12c, Gm36430 | Mm_Celera | 7:104353657 | CCATTCATTTCCTCC[C/G]TTCTAGGAGTCCCTC | 319236 |
rs46231800 | snp | C/G | | | upstream-variant-2KB, intron-variant | Trim12c, Gm36430 | Mm_Celera | 7:104354027 | GAGCTGGAGCAGGTG[C/G]TGGAGTAGGAAGTGA | 319236 |
rs46249641 | snp | C/T | | | upstream-variant-2KB, downstream-variant-500B, intron-variant | Trim12c, Trim30b, LOC102640171, Gm36430 | Mm_Celera | 7:104355305 | TAACTGTGTACAATA[C/T]ACATTGACATTTATT | 319236 |
rs46278718 | snp | A/T | | | upstream-variant-2KB, intron-variant | Trim12c, Gm36430 | Mm_Celera | 7:104354722 | ttttgacttcagtga[A/T]tgaaccacggtcctt | 319236 |
rs46916837 | snp | A/G | | | upstream-variant-2KB, downstream-variant-500B, intron-variant | Trim12c, Trim30b, LOC102640171, Gm36430 | Mm_Celera | 7:104355302 | TTCTAACTGTGTACA[A/G]TATACATTGACATTT | 319236 |
rs47122765 | snp | C/T | | | upstream-variant-2KB, downstream-variant-500B, nc-transcript-variant | Trim12c, Trim30b, LOC102640171, Gm36430 | Mm_Celera | 7:104355210 | ATTACCCTCTGACCT[C/T]AGTGAAAAGGATGAA | 319236 |
rs47314321 | snp | C/T | | | upstream-variant-2KB, intron-variant | Trim12c, Gm36430 | Mm_Celera | 7:104353908 | CTTCTCTGATAAATA[C/T]CATGACTAGGACAAG | 319236 |
rs47469814 | snp | A/G | | | upstream-variant-2KB, intron-variant | Trim12c, Gm36430 | Mm_Celera | 7:104353758 | CCGGAATTAGAAGGG[A/G]GAAATCTGTAGAGCT | 319236 |
rs47549899 | snp | A/C | | | upstream-variant-2KB, intron-variant | Trim12c, Gm36430 | Mm_Celera | 7:104353570 | GCTCTCCAGCTGCCC[A/C]ATAGTCTCCACCAGA | 319236 |
rs47958124 | snp | C/T | | | upstream-variant-2KB, downstream-variant-500B, nc-transcript-variant | Trim12c, Trim30b, LOC102640171, Gm36430 | Mm_Celera | 7:104355177 | TCTGCAAAGATTAGA[C/T]TTTATATTTAGTCTG | 319236 |
rs48185203 | snp | C/T | | | upstream-variant-2KB, intron-variant | Trim12c, Gm36430 | Mm_Celera | 7:104353927 | GACTAGGACAAGTTA[C/T]AAGGAGAGTGTTTAA | 319236 |
rs48590254 | snp | C/T | | | upstream-variant-2KB, downstream-variant-500B, intron-variant | Trim12c, Trim30b, LOC102640171, Gm36430 | Mm_Celera | 7:104355313 | TACAATATACATTGA[C/T]ATTTATTTCTAACAG | 319236 |
rs48847501 | snp | A/G | | | upstream-variant-2KB, intron-variant | Trim12c, Gm36430 | Mm_Celera | 7:104353573 | CTCCAGCTGCCCAAT[A/G]GTCTCCACCAGATTA | 319236 |
rs48895808 | snp | A/G | | | upstream-variant-2KB, intron-variant | Trim12c, Gm36430 | Mm_Celera | 7:104353992 | TGACCACCACAGTGG[A/G]GAACCTGATAACAGG | 319236 |
rs49030457 | snp | A/T | | | upstream-variant-2KB, intron-variant | Trim12c, Gm36430 | Mm_Celera | 7:104353580 | TGCCCAATAGTCTCC[A/T]CCAGATTATGTATTG | 319236 |
rs49226432 | snp | C/T | | | upstream-variant-2KB, downstream-variant-500B, intron-variant | Trim12c, Trim30b, LOC102640171, Gm36430 | Mm_Celera | 7:104355345 | GGAAAGGGATTCCCA[C/T]GGAACACTATTTGAG | 319236 |
rs49434845 | snp | C/G | | | upstream-variant-2KB, downstream-variant-500B, intron-variant | Trim12c, Trim30b, LOC102640171, Gm36430 | Mm_Celera | 7:104355139 | GCATGAATGTTCTCT[C/G]TAGGCAGAATTCCAC | 319236 |
rs49567120 | snp | C/G | | | upstream-variant-2KB, intron-variant | Trim12c, Gm36430 | Mm_Celera | 7:104353581 | GCCCAATAGTCTCCA[C/G]CAGATTATGTATTGT | 319236 |