SNP - dbSNP |
dbSNP | Type | Alleles | Het | Se(het) | Fxn-class | Gene Name | Assembly | Chr-pos | Sequence | Entrez Gene |
rs6268367 | snp | C/T | 0.5 | 0 | intron-variant | Bcar1 | GRCm38.p3 | 8:111725323 | GAGTCAACAGCTGGG[C/T]GCTATTTCttttttg | 12927 |
rs6268816 | snp | A/C | 0.5 | 0 | intron-variant | Bcar1 | Mm_Celera | 8:111725379 | atagccctggctgtc[A/C]nggaactcactntgt | 12927 |
rs6268818 | snp | A/T | 0.5 | 0 | intron-variant | Bcar1 | Mm_Celera | 8:111725380 | tagccctggctgtcn[A/T]ggaactcactntgta | 12927 |
rs6268833 | snp | C/T | 0.5 | 0 | intron-variant | Bcar1 | Mm_Celera | 8:111725391 | gtcnnggaactcact[C/T]tgtanaccaggctgg | 12927 |
rs6268835 | snp | C/G | 0.5 | 0 | intron-variant | Bcar1 | Mm_Celera | 8:111725396 | ggaactcactntgta[C/G]accaggctggcctng | 12927 |
rs6268864 | snp | C/G | 0.5 | 0 | intron-variant | Bcar1 | Mm_Celera | 8:111725410 | anaccaggctggcct[C/G]gaactcagaaatctg | 12927 |
rs6268919 | snp | C/G | 0.5 | 0 | intron-variant | Bcar1 | GRCm38.p3 | 8:111725441 | cctgcctctgcctcc[C/G]gagtgctgggattaa | 12927 |
rs6269404 | snp | A/G | 0.5 | 0 | intron-variant | Bcar1 | Mm_Celera | 8:111725539 | AAAGGCAGGGACAGA[A/G]TAAGTCCCTAGGGAG | 12927 |
rs31324156 | snp | A/G | 0.32 | 0.24 | intron-variant | Bcar1 | Mm_Celera | 8:111715421 | GGCACAAAAGAAGGC[A/G]CAGTGACACACTATC | 12927 |
rs31324159 | snp | C/T | 0.231111 | 0.249285 | intron-variant | Bcar1 | Mm_Celera | 8:111715470 | GGATACAGTGGGTCC[C/T]AGAAACCTAGAAACC | 12927 |
rs31324162 | snp | C/T | 0.444444 | 0.157135 | intron-variant | Bcar1 | Mm_Celera | 8:111715608 | GCCTCTGATCCCCAA[C/T]GCTTACCTCCTGGCC | 12927 |
rs31324845 | snp | A/C | 0.391111 | 0.206368 | synonymous-codon, utr-variant-5-prime | Bcar1 | Mm_Celera | 8:111715762 | GCCCTGTCCCACTCG[A/C]GTAGGAACCACCACC | 12927 |
rs31324848 | snp | C/T | 0.124444 | 0.216185 | intron-variant | Bcar1 | Mm_Celera | 8:111716021 | GTCTCTATGGTTGGA[C/T]AACCCAGTAGATTCC | 12927 |
rs31324851 | snp | C/T | 0.32 | 0.24 | intron-variant | Bcar1 | Mm_Celera | 8:111716059 | AGGGTGCAAGTATGG[C/T]TACACACAGTCGACA | 12927 |
rs31324975 | snp | A/G | 0.124444 | 0.216185 | downstream-variant-500B | Bcar1 | Mm_Celera | 8:111710148 | CCAGCTAAGTCTGAT[A/G]AAGACTGGAAGGTGA | 12927 |
rs31324978 | snp | A/G | 0.124444 | 0.216185 | downstream-variant-500B | Bcar1 | Mm_Celera | 8:111710214 | CTCCTTGGGGTACAG[A/G]AGACCCAGAAGGTAT | 12927 |
rs31324981 | snp | C/T | 0.124444 | 0.216185 | utr-variant-3-prime | Bcar1 | Mm_Celera | 8:111710583 | CAGAGGTGTGCACCA[C/T]ACTGTACTTGCCTGT | 12927 |
rs31325534 | snp | A/G | 0.444444 | 0.157135 | intron-variant | Bcar1 | Mm_Celera | 8:111716099 | AGGAAGGGTACAAAG[A/G]CCTGGCTCCAGAGGC | 12927 |
rs31325537 | snp | C/T | 0.244898 | 0.249948 | intron-variant | Bcar1 | Mm_Celera | 8:111716274 | AATCACCATCACCTC[C/T]AGACTCTGGAGGCAA | 12927 |
rs31325540 | snp | C/T | 0.124444 | 0.216185 | intron-variant | Bcar1 | Mm_Celera | 8:111716963 | TCCCAGGCAGCACAT[C/T]TGAGCTAGGCAGTTG | 12927 |
rs31325543 | snp | A/G | 0.152778 | 0.230321 | intron-variant | Bcar1 | Mm_Celera | 8:111717039 | GCCTGGCAGGCTGGT[A/G]TATGCGCCACTGTAG | 12927 |
rs31325794 | snp | C/T | 0.124444 | 0.216185 | synonymous-codon | Bcar1 | Mm_Celera | 8:111711380 | CTCCTGCTCCAGTCG[C/T]TCAAACTGTTTCAGC | 12927 |
rs31325797 | snp | A/G | 0.231111 | 0.249285 | intron-variant | Bcar1 | Mm_Celera | 8:111711425 | CAAGGTTAGGCTCTC[A/G]GCAGACAGACACGTG | 12927 |
rs31325800 | snp | A/G | 0.132653 | 0.220748 | intron-variant | Bcar1 | Mm_Celera | 8:111711428 | GGTTAGGCTCTCGGC[A/G]GACAGACACGTGCAA | 12927 |
rs31325803 | snp | A/G | 0.124444 | 0.216185 | intron-variant | Bcar1 | Mm_Celera | 8:111711440 | GGCAGACAGACACGT[A/G]CAAAAATCTGTACTC | 12927 |
rs31326356 | snp | G/T | 0.231111 | 0.249285 | intron-variant | Bcar1 | Mm_Celera | 8:111717561 | AGGCTTCGCTACTGC[G/T]CAACAGAGAAAGCAG | 12927 |
rs31326359 | snp | C/G | 0.231111 | 0.249285 | intron-variant | Bcar1 | Mm_Celera | 8:111717741 | AACGCACGTTAGGCT[C/G]GGCTGGAGAGAGCTG | 12927 |
rs31326362 | snp | A/G | 0.231111 | 0.249285 | intron-variant | Bcar1 | Mm_Celera | 8:111717802 | GTTTGAAGGAAGAGG[A/G]AGACTGAACCCAGAA | 12927 |
rs31326686 | snp | C/G | 0.124444 | 0.216185 | intron-variant | Bcar1 | Mm_Celera | 8:111711463 | CTGTACTCATGACTG[C/G]AGAGTACTCCACCAA | 12927 |
rs31326689 | snp | A/G | 0.124444 | 0.216185 | intron-variant | Bcar1 | Mm_Celera | 8:111711501 | CGAGCACCAGTATCC[A/G]CAGCATCGCCACTTG | 12927 |
rs31326692 | snp | C/T | 0.124444 | 0.216185 | intron-variant | Bcar1 | Mm_Celera | 8:111711514 | CCGCAGCATCGCCAC[C/T]TGAGGACATGCTGGG | 12927 |
rs31327155 | snp | C/T | 0.32 | 0.24 | intron-variant | Bcar1 | Mm_Celera | 8:111717884 | CTGACTCTACAGGGA[C/T]CAAGGCAGGAATCCA | 12927 |
rs31327158 | snp | G/T | 0.231111 | 0.249285 | intron-variant | Bcar1 | Mm_Celera | 8:111718097 | AATGGAGTGCCAAAG[G/T]GACATCAAGGGGCCT | 12927 |
rs31327161 | snp | C/T | 0.231111 | 0.249285 | intron-variant | Bcar1 | Mm_Celera | 8:111718197 | CACCTTAGTTACTTG[C/T]GTTTCTCTCCCCTGG | 12927 |
rs31327445 | snp | A/G | 0.231111 | 0.249285 | intron-variant | Bcar1 | Mm_Celera | 8:111721359 | GACACAGGTGGTCAT[A/G]AAGGTAGGAGGACGG | 12927 |
rs31327448 | snp | C/T | 0.244898 | 0.249948 | intron-variant | Bcar1 | Mm_Celera | 8:111721476 | AGCAGGGGACCTTTG[C/T]CCTGTCCATCATCAG | 12927 |
rs31327451 | snp | C/G | 0.277778 | 0.248452 | intron-variant | Bcar1 | Mm_Celera | 8:111721516 | GGAGTTGACCCCAGT[C/G]AATCTTTCAGCTGAG | 12927 |
rs31327605 | snp | A/G | 0.32 | 0.24 | intron-variant | Bcar1 | Mm_Celera | 8:111711588 | GGCTTCAAACGTGGC[A/G]CTCCATGGCTACACA | 12927 |
rs31327608 | snp | A/C | 0.32 | 0.24 | intron-variant | Bcar1 | Mm_Celera | 8:111711759 | TCCCAAGCAGTTCAC[A/C]CAGGACTCATTTACT | 12927 |
rs31327611 | snp | C/T | 0.444444 | 0.157135 | intron-variant | Bcar1 | Mm_Celera | 8:111711787 | ACTTCCACCATCACA[C/T]CTGGGAAGCACCTAC | 12927 |
rs31327994 | snp | C/T | 0.132653 | 0.220748 | intron-variant | Bcar1 | Mm_Celera | 8:111718338 | GGGGATTCTGGACCT[C/T]GCTTCCTCCACCTAC | 12927 |
rs31327997 | snp | C/T | 0.231111 | 0.249285 | intron-variant | Bcar1 | Mm_Celera | 8:111718368 | CACTGCAGATGGCCA[C/T]TCTTCCAGGAACGAG | 12927 |
rs31328000 | snp | A/G | 0.142012 | 0.225474 | intron-variant | Bcar1 | Mm_Celera | 8:111718375 | GATGGCCATTCTTCC[A/G]GGAACGAGCTCTCCC | 12927 |
rs31328003 | snp | C/G | 0.231111 | 0.249285 | intron-variant | Bcar1 | Mm_Celera | 8:111718833 | AAATGAAGCAAAAAA[C/G]TATATATATGCATCT | 12927 |
rs31328284 | snp | C/G | 0.32 | 0.24 | intron-variant | Bcar1 | Mm_Celera | 8:111722720 | AGATGTGGGGAGAAA[C/G]TCCCTTAGCCTGAGC | 12927 |
rs31328287 | snp | A/G | 0.345679 | 0.230967 | intron-variant | Bcar1 | GRCm38.p3 | 8:111722773 | AGCGCCAAGGTTCAG[A/G]CCCTTGTGTCCAGGG | 12927 |
rs31328290 | snp | A/G | 0.231111 | 0.249285 | intron-variant | Bcar1 | Mm_Celera | 8:111722808 | GCAATTCTTCCAGAG[A/G]AAAAAAATGATGGGT | 12927 |
rs31328293 | snp | C/G | 0.124444 | 0.216185 | intron-variant | Bcar1 | Mm_Celera | 8:111724023 | GTATGGACCTGACCT[C/G]GCACCACAGACTACC | 12927 |
rs31328494 | snp | A/G | 0.231111 | 0.249285 | intron-variant | Bcar1 | Mm_Celera | 8:111711887 | CCTTCTCTACACCTG[A/G]ACGAGGAGCAGGGAG | 12927 |
rs31328497 | snp | G/T | 0.124444 | 0.216185 | intron-variant | Bcar1 | GRCm38.p3 | 8:111712246 | GTGTTTAGTCCTACA[G/T]TGCTCTGTGCTCTCT | 12927 |
rs31328500 | snp | C/T | 0.231111 | 0.249285 | intron-variant | Bcar1 | Mm_Celera | 8:111712330 | ATGAATCAACTGCTA[C/T]GGCCTCAGCTCTCTG | 12927 |
rs31328503 | snp | A/T | 0.444444 | 0.157135 | intron-variant | Bcar1 | Mm_Celera | 8:111712820 | AGTCCCAGGAAGAGG[A/T]GGCTTCTAAAGGGAG | 12927 |
rs31328836 | snp | A/G | 0.231111 | 0.249285 | intron-variant | Bcar1 | Mm_Celera | 8:111718866 | AAAAGACAAAGAGAG[A/G]AGATGCTAGACAAAA | 12927 |
rs31328839 | snp | A/G | 0.32 | 0.24 | intron-variant | Bcar1 | Mm_Celera | 8:111718991 | TCATGTTCATAAAAT[A/G]AAAGCAGACATCATG | 12927 |
rs31328842 | snp | C/T | 0.142012 | 0.225474 | intron-variant | Bcar1 | Mm_Celera | 8:111719208 | TGTGATAGGTGTGCA[C/T]TGCACTCATATGTGG | 12927 |
rs31329136 | snp | A/C | 0.32 | 0.24 | intron-variant | Bcar1 | GRCm38.p3 | 8:111724098 | TTAGTAGGAATTTGG[A/C]GGAGTTCATACAATC | 12927 |
rs31329139 | snp | C/T | 0.345679 | 0.230967 | intron-variant | Bcar1 | GRCm38.p3 | 8:111724558 | GATACTCCCAGAACG[C/T]ACTTCATGTGGCCCA | 12927 |
rs31329142 | snp | A/G | 0.48 | 0.0979796 | intron-variant | Bcar1 | GRCm38.p3 | 8:111724690 | TGGCCACTGTGACCC[A/G]AGCAGCACTGCTCTT | 12927 |
rs31329426 | snp | A/G | 0.231111 | 0.249285 | intron-variant | Bcar1 | Mm_Celera | 8:111712833 | GGAGGCTTCTAAAGG[A/G]AGCAGCTTGGCCCAG | 12927 |
rs31329428 | snp | A/C | 0.32 | 0.24 | intron-variant | Bcar1 | Mm_Celera | 8:111712932 | TGAAATCAAACCCAA[A/C]CTCTGCCCTTCGCCC | 12927 |
rs31329431 | snp | C/T | 0.231111 | 0.249285 | synonymous-codon | Bcar1 | Mm_Celera | 8:111713630 | GCGGTCCAGGTCTTC[C/T]GGAGTGAATCCTGGA | 12927 |
rs31329745 | snp | C/T | 0.231111 | 0.249285 | intron-variant | Bcar1 | Mm_Celera | 8:111719249 | TGGAGGGGATGAACT[C/T]TGGCCTGTCTCAAGG | 12927 |
rs31329748 | snp | A/G | 0.231111 | 0.249285 | intron-variant | Bcar1 | Mm_Celera | 8:111719342 | GGGCCTTGATTTGAT[A/G]GTAGGCTTCTATGAC | 12927 |
rs31329751 | snp | C/T | 0.32 | 0.24 | intron-variant | Bcar1 | Mm_Celera | 8:111719719 | CCCTATTACCTGCGT[C/T]TCCTTGGTCACGTGA | 12927 |
rs31330035 | snp | C/T | 0.48 | 0.0979796 | intron-variant | Bcar1 | GRCm38.p3 | 8:111724867 | GGCACTCAAGAAGGT[C/T]AGATGCACTCTTCTG | 12927 |
rs31330038 | snp | C/T | 0.244898 | 0.249948 | intron-variant | Bcar1 | Mm_Celera | 8:111724959 | GAAGACAGAGAGAGA[C/T]CTGAACTTAGAAATG | 12927 |
rs31330041 | snp | A/G | 0.124444 | 0.216185 | intron-variant | Bcar1 | Mm_Celera | 8:111725052 | CCCCTGGCCAGGCTG[A/G]TGGTACACAACCTGC | 12927 |
rs31330314 | snp | C/T | 0.32 | 0.24 | synonymous-codon | Bcar1 | Mm_Celera | 8:111713696 | CACCAGTGTCTGGTA[C/T]ACATCCTCCATCTTC | 12927 |
rs31330317 | snp | A/G | 0.124444 | 0.216185 | synonymous-codon | Bcar1 | Mm_Celera | 8:111713780 | ATTGCTCACAGCTCC[A/G]CGGGCGAACTCCAGG | 12927 |
rs31330320 | snp | G/T | 0.124444 | 0.216185 | synonymous-codon | Bcar1 | Mm_Celera | 8:111714211 | TTCCAGGGCCAGGCC[G/T]CCGCAAACCAGGGGG | 12927 |
rs31330323 | snp | C/T | 0.231111 | 0.249285 | intron-variant | Bcar1 | Mm_Celera | 8:111714665 | TAGGTGTAGTGTCCA[C/T]CTCTTACCTGCAGAC | 12927 |
rs31330414 | snp | A/G | 0.132653 | 0.220748 | intron-variant | Bcar1 | Mm_Celera | 8:111719788 | TTAGCGATGGCTGGT[A/G]GTCAGATCCAAGGAA | 12927 |
rs31330417 | snp | A/G | 0.231111 | 0.249285 | intron-variant | Bcar1 | Mm_Celera | 8:111720021 | ACATCATCAGAACAC[A/G]AAACTGCCTTAGCTG | 12927 |
rs31330420 | snp | A/G | 0.231111 | 0.249285 | intron-variant | Bcar1 | Mm_Celera | 8:111720136 | AAGTGACATACACCA[A/G]ACAAGGTTCACACCT | 12927 |
rs31330423 | snp | C/T | 0.32 | 0.24 | intron-variant | Bcar1 | Mm_Celera | 8:111720307 | CTCCCTGTGCTGTCA[C/T]GCTGAGGCTTTTCCT | 12927 |
rs31330624 | snp | A/G | 0.231111 | 0.249285 | intron-variant | Bcar1 | Mm_Celera | 8:111726712 | AGCACCTCATGGACT[A/G]GGCACGTGGCATCAA | 12927 |
rs31330627 | snp | A/G | 0.124444 | 0.216185 | intron-variant | Bcar1 | Mm_Celera | 8:111727409 | CAGCAGGGCAGAAAG[A/G]CATCCAGCCATAATG | 12927 |
rs31330630 | snp | A/G | 0.32 | 0.24 | intron-variant | Bcar1 | Mm_Celera | 8:111727631 | TGACTCCAGAATGGC[A/G]GGTAGGCAGGGGCTG | 12927 |
rs31330633 | snp | A/G | 0.32 | 0.24 | intron-variant | Bcar1 | Mm_Celera | 8:111727923 | CTGGACAGTTGTATG[A/G]CCTATAATGTGCTAA | 12927 |
rs31330926 | snp | A/G | 0.231111 | 0.249285 | intron-variant | Bcar1 | Mm_Celera | 8:111714761 | CTCGCAGGAACTGAC[A/G]GACTTCCTGTTCTTA | 12927 |
rs31330929 | snp | C/T | 0.48 | 0.0979796 | intron-variant | Bcar1 | GRCm38.p3 | 8:111714892 | AGATTTTGTGGTTTC[C/T]TTGCTCATTCCTCTC | 12927 |
rs31330932 | snp | A/C/G | 0.231111 | 0.249285 | synonymous-codon | Bcar1 | GRCm38.p3 | 8:111715301 | ATGATGGCTGGACGA[A/C/G]AGCAGGCCTTTCTCC | 12927 |
rs31330946 | snp | A/C | 0.336735 | 0.234472 | synonymous-codon, utr-variant-5-prime | Bcar1 | Mm_Celera | 8:111720732 | TCCCTCCCATCCGCG[A/C]GTGTCCAGAGATGGA | 12927 |
rs31330949 | snp | C/T | 0.124444 | 0.216185 | missense, utr-variant-5-prime | Bcar1 | Mm_Celera | 8:111720773 | AGATGTCATGCCCTA[C/T]GCCAGCGGAAGGTGG | 12927 |
rs31330952 | snp | A/G | 0.475309 | 0.108333 | missense, utr-variant-5-prime | Bcar1 | GRCm38.p3 | 8:111721129 | CCTGGTCCAGGTCCT[A/G]CTGGCTTCTTATCAT | 12927 |
rs31331276 | snp | C/T | 0.231111 | 0.249285 | intron-variant | Bcar1 | Mm_Celera | 8:111728209 | ACACCATGAAGGCTG[C/T]TGCCTGACTTGCCAA | 12927 |
rs31331279 | snp | A/G | 0.336735 | 0.234472 | intron-variant | Bcar1 | Mm_Celera | 8:111728573 | ACAGGAGCCAAGAGA[A/G]CAGCCCCACAGCCTG | 12927 |
rs31331282 | snp | A/G | 0.231111 | 0.249285 | intron-variant | Bcar1 | Mm_Celera | 8:111728619 | CTCTCATTGCACTGC[A/G]GCCTGAGAAAGCTTC | 12927 |
rs31332095 | snp | C/T | 0.124444 | 0.216185 | intron-variant | Bcar1 | Mm_Celera | 8:111728770 | CCAAACCTGACAACA[C/T]GGCAGGGTGCAAGCT | 12927 |
rs31332098 | snp | A/C | 0.231111 | 0.249285 | intron-variant | Bcar1 | Mm_Celera | 8:111728800 | TGGTGGCTTGGAGTA[A/C]TGAGAAAAGACACTG | 12927 |
rs31332101 | snp | A/C/T | 0.244898 | 0.249948 | intron-variant | Bcar1 | GRCm38.p3 | 8:111728946 | ATGTTCTCAGCGGCC[A/C/T]TAAACCAGCTCAAGG | 12927 |
rs32572929 | snp | C/T | 0.375 | 0.216506 | intron-variant | Bcar1 | Mm_Celera | 8:111721994 | TCTTCTGGACTCTGA[C/T]CCAACACACTCTTCT | 12927 |
rs32576295 | snp | A/G | 0.375 | 0.216506 | intron-variant | Bcar1 | GRCm38.p3 | 8:111735197 | AGTGCAGGCCCCACA[A/G]AGGAGCCATCACTGC | 12927 |
rs32650672 | snp | C/T | 0.32 | 0.24 | upstream-variant-2KB, intron-variant | Bcar1 | GRCm38.p3 | 8:111733382 | CCAGAGCTCCTTCAT[C/T]AGGAGCTAGGCTACA | 12927 |
rs32654415 | snp | A/G | 0.444444 | 0.157135 | intron-variant | Bcar1 | GRCm38.p3 | 8:111719622 | GCTGGGATTAAAGGC[A/G]TGAGCCACCATGTGG | 12927 |
rs32661663 | snp | C/T | 0.375 | 0.216506 | intron-variant | Bcar1 | GRCm38.p3 | 8:111729099 | ACTAAATCTTCAGAA[C/T]GGCCCAGGACAATCA | 12927 |
rs32722768 | snp | A/C | 0.375 | 0.216506 | intron-variant | Bcar1 | GRCm38.p3 | 8:111715264 | GCTCAGCCTTGCCCT[A/C]AGCATCAGTGATCCT | 12927 |
rs32738439 | snp | A/G | 0.444444 | 0.157135 | upstream-variant-2KB, intron-variant | Bcar1 | GRCm38.p3 | 8:111732220 | GCAAATGAGCCGCCG[A/G]GGTGGGCGTGTCGAG | 12927 |
rs32819750 | snp | C/T | 0.444444 | 0.157135 | intron-variant | Bcar1 | GRCm38.p3 | 8:111731582 | GAACAGACACATGGT[C/T]GTTATGTATAGGTGA | 12927 |
rs32830764 | snp | C/T | 0.375 | 0.216506 | intron-variant | Bcar1 | GRCm38.p3 | 8:111736696 | CAGGGCTGGCAGGCA[C/T]GGGGGCTGGAGTCAG | 12927 |