SNP - dbSNP |
dbSNP | Type | Alleles | Het | Se(het) | Fxn-class | Gene Name | Assembly | Chr-pos | Sequence | Entrez Gene |
rs8152721 | snp | A/G | | | intron-variant | Abl2, Fam20b | Rn_Celera | 13:74287552 | TGAATTCTGAGTTTT[A/G]GGCGACCTGCGTCTG | 304883 |
rs8169271 | snp | C/G | | | intron-variant | Abl2, Tor3a | Rn_Celera | 13:74250336 | ACTACACAGCTTTTC[C/G]TGATTAAAAAAGACA | 304883 |
rs64718927 | snp | A/T | 0 | 0 | intron-variant | Abl2, Fam20b | Rn_Celera | 13:74330839 | TTGTTTTTGCCTTTT[A/T]AAAAAAAAAATTCCT | 304883 |
rs65251654 | snp | C/T | 0 | 0 | intron-variant, upstream-variant-2KB | Abl2, Fam20b | Rn_Celera | 13:74331450 | GTTGGGGATTTAGCT[C/T]AGTGGTAGAGTGCTT | 304883 |
rs104921618 | snp | G/T | 0 | 0 | intron-variant | Abl2, Fam20b | Rn_Celera | 13:74312821 | TTGTCTAGGTGGCTC[G/T]AAGTTTGATCACTTT | 304883 |
rs104963143 | snp | C/T | 0 | 0 | intron-variant | Abl2, Fam20b | Rn_Celera | 13:74309636 | AGGAACCATAGGTAC[C/T]AAAGGGCCGAAGGTT | 304883 |
rs104984297 | snp | C/T | 0 | 0 | intron-variant | Abl2 | Rn_Celera | 13:74172584 | TTACTACTACTACTA[C/T]TATTATTATTATTAT | 304883 |
rs105043007 | snp | C/T | 0 | 0 | intron-variant | Abl2, Fam20b | Rn_Celera | 13:74312409 | GTACATAAACCACCA[C/T]TAATAGCTGTTATAG | 304883 |
rs105574055 | snp | A/C | 0 | 0 | intron-variant | Abl2 | Rn_Celera | 13:74184053 | CCTGACACTATTGAT[A/C]TCCTGCCATACTTGG | 304883 |
rs105586482 | snp | A/G | 0 | 0 | intron-variant | Abl2 | Rn_Celera | 13:74237525 | ACACACAGGAAGAGT[A/G]TGGGCACACACAGTT | 304883 |
rs105610191 | snp | C/T | 0 | 0 | utr-variant-3-prime, upstream-variant-2KB, intron-variant, utr-variant-5-prime | Abl2, Fam20b | Rn_Celera | 13:74333108 | CCGACACCAGCTTAG[C/T]TTGACAGGAGGACGA | 304883 |
rs105706910 | snp | C/T | 0 | 0 | intron-variant | Abl2, Fam20b | Rn_Celera | 13:74307242 | TCAAGACAGAGGTGT[C/T]AAAACGTACAATTCA | 304883 |
rs105808157 | snp | C/G | 0 | 0 | intron-variant | Abl2 | Rn_Celera | 13:74183985 | CGGAGATGAGGGACG[C/G]CCCACCCAGTGACTA | 304883 |
rs105955696 | snp | A/T | 0 | 0 | intron-variant | Abl2 | Rn_Celera | 13:74183802 | ATTATTGGTTACTAG[A/T]GGGGGGAAGTCTTGA | 304883 |
rs106041072 | snp | C/T | 0 | 0 | intron-variant | Abl2 | Rn_Celera | 13:74183921 | TAGACCATAAACCCT[C/T]CTACCTACAATTTTG | 304883 |
rs106056088 | snp | A/T | 0 | 0 | intron-variant | Abl2 | Rn_Celera | 13:74165795 | AAAAAAGAAAAAAAA[A/T]TTGTGATTTGGGTTC | 304883 |
rs106337331 | snp | C/T | 0 | 0 | intron-variant | Abl2, Fam20b | Rn_Celera | 13:74288507 | CCCCAGGCTCATCCG[C/T]TAAGGCACTAGAGGC | 304883 |
rs106442709 | snp | A/C | 0 | 0 | intron-variant | Abl2 | Rn_Celera | 13:74183917 | CCCCTAGACCATAAA[A/C]CCTCCTACCTACAAT | 304883 |
rs106443995 | snp | A/G | 0 | 0 | intron-variant | Abl2 | Rn_Celera | 13:74183892 | CTTCCCAGCGGAGGG[A/G]CCGGGCACACCACCC | 304883 |
rs106463302 | snp | A/T | 0 | 0 | intron-variant | Abl2, Fam20b | Rn_Celera | 13:74312022 | AAGCTACCGGTATTT[A/T]AAAAAAAAAAAATCT | 304883 |
rs106468161 | snp | G/T | 0.5 | 0 | intron-variant | Abl2 | Rn_Celera | 13:74185337 | TTTTTTTTTTTNTGG[G/T]TCTTCTTTTCGGAGC | 304883 |
rs106498181 | snp | A/C | 0 | 0 | intron-variant | Abl2, Fam20b | Rn_Celera | 13:74311895 | CTATCTCACACAAAA[A/C]TCAGAAATACAGCAT | 304883 |
rs106519975 | snp | A/T | 0 | 0 | intron-variant | Abl2, Fam20b | Rn_Celera | 13:74313011 | GAGACCTTTATGGTT[A/T]AAAGCATTTCTTCTG | 304883 |
rs106684423 | snp | G/T | 0.5 | 0 | intron-variant | Abl2 | Rn_Celera | 13:74171423 | TTTTTTTTTTTTTGG[G/T]TCTTTTTTTCGGAGC | 304883 |
rs106689534 | snp | C/T | 0 | 0 | intron-variant | Abl2, Fam20b | Rn_Celera | 13:74311593 | TTCTGAGCTTAGGCA[C/T]ATTGAGAGTCATTCA | 304883 |
rs106938321 | snp | C/T | 0 | 0 | intron-variant | Abl2, Fam20b | Rn_Celera | 13:74312710 | TGGCCCCTTAGTTTC[C/T]GCCCCTATGTTCCAT | 304883 |
rs107022010 | snp | C/T | 0 | 0 | intron-variant | Abl2, Fam20b | Rn_Celera | 13:74311539 | GCTGGCTTTGCAGCT[C/T]CTTTGGATCAGAAAG | 304883 |
rs107108375 | snp | A/C | 0 | 0 | intron-variant | Abl2 | Rn_Celera | 13:74183962 | ATGTGCCCGGAGTAA[A/C]CGTGACCCGGAGATG | 304883 |
rs107159772 | snp | C/G | 0 | 0 | intron-variant | Abl2, Fam20b | Rn_Celera | 13:74310180 | GCATTCTCAAAGTAG[C/G]ACTGCATGCCCGCCC | 304883 |
rs107214991 | snp | G/T | 0 | 0 | intron-variant, utr-variant-3-prime | Abl2, Fam20b | Rn_Celera | 13:74281206 | ATCCATCTATGCAGA[G/T]GTTCAGTTGGCTAAA | 304883 |
rs107388676 | snp | C/T | 0 | 0 | intron-variant | Abl2, Fam20b | Rn_Celera | 13:74310264 | AGCTACACACGGTCA[C/T]TTGTTCTCATGTTTG | 304883 |
rs107472846 | snp | A/G | 0 | 0 | intron-variant | Abl2, Fam20b | Rn_Celera | 13:74312310 | AAACCCGGTATACAA[A/G]AAAGAGACAAACATT | 304883 |
rs107506886 | snp | C/T | 0 | 0 | intron-variant | Abl2, Fam20b | Rn_Celera | 13:74312746 | GTCAGTGTGTCAAGC[C/T]TACAAACCACAAGAA | 304883 |
rs196998953 | snp | A/G | 0 | 0 | intron-variant | Abl2, Fam20b | Rn_Celera | 13:74287597 | CTGTCAGGGTTCACA[A/G]GGGTTCTGGGCTAGA | 304883 |
rs197001600 | snp | A/G | 0 | 0 | intron-variant | Abl2, Fam20b | Rn_Celera | 13:74301245 | CTACCACTGAGCTAA[A/G]TCCCCAACCCCTCCT | 304883 |
rs197010947 | snp | A/T | 0 | 0 | intron-variant | Abl2, Fam20b | Rn_Celera | 13:74329731 | GGTCTCTGGGCAATC[A/T]CAACATGGCTACAAG | 304883 |
rs197015571 | snp | C/T | 0 | 0 | intron-variant | Tor3a, Abl2 | Rn_Celera | 13:74253438 | TGGCTACTCTGAGCA[C/T]AGTGATTGTGGCTGT | 304883 |
rs197021842 | snp | C/T | 0 | 0 | intron-variant | Tor3a, Abl2 | Rn_Celera | 13:74265953 | CACCGACTGCTCTTC[C/T]AGAGGTCCTGAGTTC | 304883 |
rs197035800 | snp | G/T | 0 | 0 | intron-variant | Abl2 | Rn_Celera | 13:74172926 | TGCGTGCGTGTGCAT[G/T]CGTGCGTGTGCCTGC | 304883 |
rs197037756 | snp | C/T | 0 | 0 | intron-variant | Abl2, Fam20b | Rn_Celera | 13:74305079 | ACCGAACAAACAAAG[C/T]CCCAGAGCAATCGAC | 304883 |
rs197053875 | snp | G/T | 0 | 0 | intron-variant | Abl2, Fam20b | Rn_Celera | 13:74299381 | CGTTTTCTCTTACAT[G/T]TGTAAAAACACACAG | 304883 |
rs197055719 | snp | C/T | 0 | 0 | intron-variant | Abl2, Fam20b | Rn_Celera | 13:74308270 | CTAAAGTCTGGCTAA[C/T]TGACTTTGATTTTAT | 304883 |
rs197065365 | snp | A/G | 0 | 0 | intron-variant, utr-variant-3-prime | Abl2 | Rn_Celera | 13:74243593 | TTATGGAAGCTAATA[A/G]AGTAACATGGAGCAG | 304883 |
rs197074948 | snp | A/T | 0 | 0 | intron-variant | Tor3a, Abl2 | Rn_Celera | 13:74257496 | ATGCTTCCCTTGAGA[A/T]AAGAGGGTCACTGGG | 304883 |
rs197081804 | snp | A/G | 0 | 0 | intron-variant | Tor3a, Abl2 | Rn_Celera | 13:74255051 | CTTCGGAGTCACTGC[A/G]TGCCCTTCCCTAGCT | 304883 |
rs197113480 | snp | C/T | 0 | 0 | intron-variant | Abl2, Fam20b | Rn_Celera | 13:74297864 | TTTTTTATTTATTTA[C/T]TTTCATGTGGTGGGG | 304883 |
rs197124558 | snp | A/G | 0 | 0 | intron-variant, utr-variant-3-prime | Abl2, Fam20b | Rn_Celera | 13:74282974 | CCATTGAAAGGGGGG[A/G]AAAGGTGTGTGTGGG | 304883 |
rs197157494 | snp | C/T | 0 | 0 | intron-variant | Abl2 | Rn_Celera | 13:74169803 | AAAGGAGCACAGGAC[C/T]TTTCTATTTATTTAC | 304883 |
rs197193875 | snp | C/T | 0 | 0 | intron-variant | Tor3a, Abl2 | Rn_Celera | 13:74267398 | TGGGAGGGACTTCCT[C/T]ACTTTCTAAGTCTCA | 304883 |
rs197268846 | snp | G/T | 0 | 0 | intron-variant | Abl2 | Rn_Celera | 13:74182750 | TTTTTTTTTTTTTGG[G/T]TCTTTTTTTCGGAGC | 304883 |
rs197283345 | snp | C/G | 0 | 0 | intron-variant | Tor3a, Abl2 | Rn_Celera | 13:74271484 | AAAGACAGACAGACA[C/G]ACACACACACACACA | 304883 |
rs197293366 | snp | C/T | 0 | 0 | intron-variant | Abl2, Fam20b | Rn_Celera | 13:74291525 | TAGTCACTGGGAATA[C/T]ACCTGGAAGAGGAGA | 304883 |
rs197294592 | snp | A/C | 0 | 0 | intron-variant | Abl2 | Rn_Celera | 13:74165098 | AGCATGTCAGGATGC[A/C]TTTGCAAGTTGGGAA | 304883 |
rs197321853 | snp | C/T | 0 | 0 | intron-variant, upstream-variant-2KB | Abl2, Fam20b | Rn_Celera | 13:74332432 | TTAATGAATGACAGT[C/T]TTGACTTTACCCGAT | 304883 |
rs197336985 | snp | G/T | 0 | 0 | intron-variant | Abl2 | Rn_Celera | 13:74182217 | ATGCATTAAGAAAAG[G/T]GTGTGTGTGTGTGTG | 304883 |
rs197340847 | snp | C/T | 0 | 0 | intron-variant | Abl2, Fam20b | Rn_Celera | 13:74290554 | GGAACTAGAAGATTT[C/T]TTAAAAAGAATTTAT | 304883 |
rs197372419 | snp | A/G | 0 | 0 | intron-variant | Abl2 | Rn_Celera | 13:74162438 | AAGATTGCATTTACT[A/G]TGCAAAGACACCTCA | 304883 |
rs197380320 | snp | C/T | 0 | 0 | intron-variant | Tor3a, Abl2 | Rn_Celera | 13:74258152 | GCATATGCAAACCAT[C/T]ACATTCCACTCCCTG | 304883 |
rs197417340 | snp | C/T | 0 | 0 | intron-variant | Tor3a, Abl2 | Rn_Celera | 13:74270270 | AGACACAGACAGGAT[C/T]TCTCTTGTGCAGCCC | 304883 |
rs197430634 | snp | A/G | 0 | 0 | intron-variant, utr-variant-3-prime, nc-transcript-variant | Abl2, Tor3a | Rn_Celera | 13:74247811 | CTGTGCATTGCTAAG[A/G]GGACACAGTGCCCAG | 304883 |
rs197505935 | snp | A/G | 0 | 0 | intron-variant | Abl2, Fam20b | Rn_Celera | 13:74290301 | TGAGAGGGTACAGAC[A/G]GGGTTCCTGCCAATA | 304883 |
rs197514295 | snp | C/T | 0 | 0 | intron-variant | Abl2, Fam20b | Rn_Celera | 13:74325946 | TACAGAGGACCTAGA[C/T]TTGGTTCCCAACATC | 304883 |
rs197531504 | snp | A/C | 0 | 0 | intron-variant | Tor3a, Abl2 | Rn_Celera | 13:74274073 | AGGTCTCTTATCGAA[A/C]CCAGAGCTCCGGTTT | 304883 |
rs197571923 | snp | A/G | 0 | 0 | intron-variant | Tor3a, Abl2 | Rn_Celera | 13:74264265 | TGGGGAGGACAAACA[A/G]TGGTGGGATTTTAGG | 304883 |
rs197573070 | snp | A/T | 0 | 0 | intron-variant | Abl2 | Rn_Celera | 13:74178707 | GCTTGGCATTGTTGT[A/T]CATATGGGGTCTCGA | 304883 |
rs197582166 | snp | C/T | 0 | 0 | intron-variant, utr-variant-3-prime, downstream-variant-500B | Abl2, Tor3a | Rn_Celera | 13:74246070 | CCGAGGCGTGTGAGG[C/T]GGTGCGTCCGAAAGC | 304883 |
rs197582996 | snp | C/T | 0 | 0 | intron-variant | Abl2, Fam20b | Rn_Celera | 13:74312673 | AATGATCCTCTTACC[C/T]GGGGCTACAACCAGG | 304883 |
rs197602502 | snp | C/T | 0 | 0 | upstream-variant-2KB, intron-variant | Tor3a, Abl2 | Rn_Celera | 13:74278073 | AGCTCAGTGGTAGAG[C/T]GCTTGCCTAGGAAGC | 304883 |
rs197602840 | snp | A/G | 0 | 0 | intron-variant | Tor3a, Abl2 | Rn_Celera | 13:74259051 | ATTTCACCTCAGTGA[A/G]GCTGATCTTTCTTAG | 304883 |
rs197654883 | snp | A/T | 0 | 0 | intron-variant | Abl2, Fam20b | Rn_Celera | 13:74304128 | TTTTGAAAGGGTTGT[A/T]AGGATAAGCAGGTGT | 304883 |
rs197660461 | snp | C/T | 0 | 0 | intron-variant | Abl2 | Rn_Celera | 13:74167575 | TCAGAGACATGCCTT[C/T]ACCGCCTCCCAAGTG | 304883 |
rs197688346 | snp | C/T | 0 | 0 | intron-variant | Abl2, Tor3a | Rn_Celera | 13:74249832 | ACTACGCAAAACAGT[C/T]TCTGACACTGGTGCC | 304883 |
rs197723495 | snp | A/G | 0 | 0 | intron-variant | Tor3a, Abl2 | Rn_Celera | 13:74261017 | GGGATTTAGCTCAGC[A/G]GTAGAGCACTTGCCT | 304883 |
rs197735630 | snp | C/G | 0 | 0 | intron-variant | Tor3a, Abl2 | Rn_Celera | 13:74276539 | CTTAGAGAAATCAGG[C/G]CAGGTGAAGGGCGGC | 304883 |
rs197742225 | snp | C/G | 0 | 0 | intron-variant | Tor3a, Abl2 | Rn_Celera | 13:74254748 | TGCCACCCAGCTGAG[C/G]CTTGTCTGACTCCAC | 304883 |
rs197759643 | snp | G/T | 0 | 0 | intron-variant | Abl2, Fam20b | Rn_Celera | 13:74305108 | ACACAGCTCTGGTCG[G/T]AGGCTCAGCTGTTGG | 304883 |
rs197764349 | snp | C/T | 0 | 0 | intron-variant | Abl2, Fam20b | Rn_Celera | 13:74304832 | CCCCCTGGAAGTCTG[C/T]TCTCTATCCTACCTC | 304883 |
rs197789534 | snp | A/G | 0 | 0 | intron-variant | Abl2, Fam20b | Rn_Celera | 13:74293209 | GCATCACAGAGCTCC[A/G]CCTGGGACGTGATGC | 304883 |
rs197818254 | snp | A/G | 0 | 0 | intron-variant | Abl2, Fam20b | Rn_Celera | 13:74312039 | AAAAAAAAAAATCTA[A/G]TTCCTATAAGTCCAA | 304883 |
rs197849043 | snp | C/G | 0 | 0 | intron-variant, nc-transcript-variant | Tor3a, Abl2 | Rn_Celera | 13:74252275 | AGAGAACGAGTCTTC[C/G]TAAGATCTTAGTAAG | 304883 |
rs197852425 | snp | A/G | 0 | 0 | intron-variant | Abl2, Fam20b | Rn_Celera | 13:74296028 | GTCAGGGGACTGTAC[A/G]ATGCCTAGCATGCAA | 304883 |
rs197856653 | snp | G/T | 0 | 0 | intron-variant | Tor3a, Abl2 | Rn_Celera | 13:74265154 | ACTATGTTAATAGAT[G/T]AATACTGTGAAATGA | 304883 |
rs197875334 | snp | C/T | 0 | 0 | intron-variant | Abl2 | Rn_Celera | 13:74187028 | GCTGCTTTGTAAAAA[C/T]TAAATTCTTGGGACA | 304883 |
rs197876210 | snp | C/T | 0 | 0 | intron-variant | Abl2, Fam20b | Rn_Celera | 13:74309101 | GGAAGTGTGCTTTCA[C/T]GCTTGTGACTCATGA | 304883 |
rs197962970 | snp | C/T | 0 | 0 | intron-variant | Tor3a, Abl2 | Rn_Celera | 13:74255982 | TGACTTCTGGGTGCA[C/T]GGTAAGAGGACAGCA | 304883 |
rs197970070 | snp | A/G | 0 | 0 | synonymous-codon, intron-variant, nc-transcript-variant | Tor3a, Abl2 | Rn_Celera | 13:74270687 | ATACTTGGGGTGTGG[A/G]AAATGGAAGGTAGAG | 304883 |
rs197973315 | snp | C/T | 0 | 0 | intron-variant | Abl2, Fam20b | Rn_Celera | 13:74290409 | AATGTGGAACACTTG[C/T]CCACTGAGGAAAGCA | 304883 |
rs197975304 | snp | A/G | 0 | 0 | intron-variant | Abl2 | Rn_Celera | 13:74180496 | TGGACTTGCAATCCT[A/G]GGATTGAAGGGGCAG | 304883 |
rs197990772 | snp | A/G | 0 | 0 | intron-variant | Abl2, Fam20b | Rn_Celera | 13:74288033 | CTGGACCATAACTGT[A/G]GGGCCACACGTGAGT | 304883 |
rs197996568 | snp | G/T | 0 | 0 | intron-variant | Abl2, Fam20b | Rn_Celera | 13:74306765 | TGAAGCAAGTGCAAG[G/T]CCCTGGGTTCGGTCC | 304883 |
rs198005992 | snp | G/T | 0 | 0 | intron-variant | Tor3a, Abl2 | Rn_Celera | 13:74266539 | TCACAATGGAAATCA[G/T]TGTGGAGACTCCTTG | 304883 |
rs198008793 | snp | C/T | 0 | 0 | intron-variant, utr-variant-3-prime | Abl2 | Rn_Celera | 13:74245384 | CAGTATTACCGCTGG[C/T]GTGAGGCAGTGTTCA | 304883 |
rs198016127 | snp | G/T | 0 | 0 | intron-variant | Abl2, Fam20b | Rn_Celera | 13:74301438 | TGGATAGGCTGGTTT[G/T]TTTTTTTTTTTTTTT | 304883 |
rs198057165 | snp | C/T | 0 | 0 | intron-variant, utr-variant-3-prime | Abl2 | Rn_Celera | 13:74243691 | TAACTTTGTGAACAC[C/T]CTTTTCATTCTTCAA | 304883 |
rs198059110 | snp | A/G | 0 | 0 | intron-variant | Abl2, Fam20b | Rn_Celera | 13:74299869 | AATTTACTATGCTGG[A/G]TATACTGATCCAGAA | 304883 |
rs198100077 | snp | C/G | 0 | 0 | intron-variant | Abl2, Fam20b | Rn_Celera | 13:74312113 | ACAACCATACACTAT[C/G]TATAAAATAAGACAC | 304883 |
rs198128504 | snp | A/G | 0 | 0 | intron-variant | Abl2 | Rn_Celera | 13:74182333 | GGTTCAATCACGGAA[A/G]CCCCATCTCTTATTT | 304883 |
rs198141290 | snp | A/T | 0 | 0 | intron-variant | Tor3a, Abl2 | Rn_Celera | 13:74259493 | TGCTCTTCATGAGAC[A/T]ACCGGAGAACAAAAT | 304883 |
rs198150452 | snp | G/T | 0 | 0 | intron-variant, upstream-variant-2KB | Abl2, Fam20b | Rn_Celera | 13:74332480 | AGTCCTAGAGCTCAA[G/T]AGTGAAAAGATCGCA | 304883 |
rs198163283 | snp | C/T | 0 | 0 | intron-variant | Tor3a, Abl2 | Rn_Celera | 13:74269115 | AGGTTATACGGAACC[C/T]GAGGGTCACCACATG | 304883 |