SNP - dbSNP |
dbSNP | Type | Alleles | Het | Se(het) | Fxn-class | Gene Name | Assembly | Chr-pos | Sequence | Entrez Gene |
rs6359318 | snp | A/T | 0.290657 | 0.246672 | intron-variant | Btbd1 | Mm_Celera | 7:81819093 | AAATTAACCTGGGTA[A/T]ATGTTAGCTGCTCAC | 83962 |
rs6359920 | snp | G/T | 0.5 | 0 | intron-variant | Btbd1 | Mm_Celera | 7:81819224 | ggttttcaagacagg[G/T]tttctctgtgtagcc | 83962 |
rs6360444 | snp | C/T | 0.290657 | 0.246672 | intron-variant | Btbd1 | Mm_Celera | 7:81819328 | CCCTTTGCTTATAGC[C/T]TTACTTTTCTCCCCA | 83962 |
rs6373413 | snp | A/G/T | 0.359862 | 0.224567 | intron-variant | Btbd1 | GRCm38.p3 | 7:81819374 | TTTCTAAAAACTCCC[A/G/T]CCTTGTTCTTGATTA | 83962 |
rs6373452 | snp | G/T | 0.290657 | 0.246672 | intron-variant | Btbd1 | Mm_Celera | 7:81819401 | ATTATTCCTTTTTCT[G/T]CCCTTCACAACTATG | 83962 |
rs6396311 | snp | C/T | 0.290657 | 0.246672 | intron-variant | Btbd1 | Mm_Celera | 7:81814725 | ttttaaaaCATTTCC[C/T]GTTGTAAATGAGAGG | 83962 |
rs6398388 | snp | C/G | 0.290657 | 0.246672 | intron-variant | Btbd1 | Mm_Celera | 7:81815039 | CTCTATCGTCTGGAG[C/G]CATCAGCCAGCTCTT | 83962 |
rs31097088 | snp | C/T | 0.444444 | 0.157135 | intron-variant | Btbd1 | Mm_Celera | 7:81797465 | CTATCTATCTATCTA[C/T]CTATCTATCTACCTA | 83962 |
rs31100910 | snp | C/T | 0.5 | 0 | intron-variant | Btbd1 | Mm_Celera | 7:81797840 | ATCCGCCACTATGCC[C/T]GGCTTGTATTTTAAA | 83962 |
rs31159808 | snp | G/T | 0.444444 | 0.157135 | intron-variant, utr-variant-3-prime | Btbd1 | Mm_Celera | 7:81798462 | CCAAACACATGGGAT[G/T]TCAGAAAGAAATGTT | 83962 |
rs31179951 | snp | A/G | 0.345679 | 0.230967 | utr-variant-3-prime, upstream-variant-2KB | Btbd1, 3110040N11Rik | GRCm38.p3 | 7:81792354 | GACCCATAAGATCAT[A/G]GTACCAGAGCAGACT | 83962 |
rs31249402 | snp | C/T | 0.32 | 0.24 | intron-variant | Btbd1 | Mm_Celera | 7:81817775 | CAGAATTCATTCATC[C/T]TTAAAGAAATTTAGT | 83962 |
rs31291821 | snp | A/G | 0.444444 | 0.157135 | intron-variant, downstream-variant-500B | Btbd1 | Mm_Celera | 7:81798186 | AAGTTTAGAGAGGCA[A/G]ATAATCCTCATCACC | 83962 |
rs31320279 | snp | C/T | 0.375 | 0.216506 | intron-variant, utr-variant-3-prime | Btbd1 | Mm_Celera | 7:81799989 | CTAGATTTTTAATTT[C/T]TTTTTAATAGTCTAT | 83962 |
rs31324699 | snp | C/T | 0.5 | 0 | intron-variant | Btbd1 | Mm_Celera | 7:81816920 | TGAGAACAGCAAATG[C/T]GCTTTAACTGCCGAG | 83962 |
rs31337975 | snp | C/T | 0.375 | 0.216506 | intron-variant | Btbd1 | Mm_Celera | 7:81796933 | AAACTTGTTTTTTTG[C/T]TAGGACAGTATTTAC | 83962 |
rs31338344 | snp | A/G | 0.375 | 0.216506 | intron-variant | Btbd1 | Mm_Celera | 7:81805345 | TACACCAAATGGCAC[A/G]TATATGAATGTACTT | 83962 |
rs31350702 | snp | A/C | 0.5 | 0 | intron-variant | Btbd1 | Mm_Celera | 7:81811869 | GAGTCCTGGGCTAGC[A/C]CCGGCCAACAGCCCA | 83962 |
rs31383513 | snp | C/T | 0.277778 | 0.248452 | intron-variant, utr-variant-3-prime | Btbd1 | Mm_Celera | 7:81799220 | GTGAAGATGCAGATA[C/T]CCTTCTCTACCTTAG | 83962 |
rs31555633 | snp | C/T | 0.444444 | 0.157135 | intron-variant | Btbd1 | Mm_Celera | 7:81797469 | CTATCTATCTATCTA[C/T]CTATCTACCTACCTA | 83962 |
rs31572220 | snp | A/G | 0.444444 | 0.157135 | intron-variant | Btbd1 | Mm_Celera | 7:81808585 | CACACACACACACAC[A/G]CACACACACACACAC | 83962 |
rs31576758 | snp | A/T | 0.375 | 0.216506 | intron-variant | Btbd1 | Mm_Celera | 7:81805062 | TGTAAATGCTGGGGA[A/T]GCACTCCAGGCTGTA | 83962 |
rs31622706 | snp | C/T | 0.444444 | 0.157135 | intron-variant | Btbd1 | Mm_Celera | 7:81812489 | GGACAGCCAGGGCTA[C/T]ACAGAGAAACCCTGT | 83962 |
rs31724710 | snp | C/T | 0.375 | 0.216506 | utr-variant-3-prime, upstream-variant-2KB | Btbd1, 3110040N11Rik | Mm_Celera | 7:81792199 | AAAGCACAAGGCATG[C/T]GAATGCCCCAATGGT | 83962 |
rs31808485 | snp | A/T | 0.375 | 0.216506 | intron-variant | Btbd1 | Mm_Celera | 7:81797191 | TACTGAATTTTACTT[A/T]AAAAAAAAAAGCCTA | 83962 |
rs31812486 | snp | C/T | 0.290657 | 0.246672 | synonymous-codon | Btbd1 | GRCm38.p3 | 7:81797017 | ATTCACTTGATAATC[C/T]GTGGGCCCGTGAATA | 83962 |
rs31917054 | snp | C/T | 0.32 | 0.24 | intron-variant | Btbd1 | Mm_Celera | 7:81823036 | AACAAAGTATGGGCA[C/T]ATTTAAGTTTTAATA | 83962 |
rs31967010 | snp | A/G | 0.444444 | 0.157135 | intron-variant | Btbd1 | Mm_Celera | 7:81808451 | ACAAACATGCTATGT[A/G]CTCACTTATTATGTG | 83962 |
rs31989427 | snp | C/T | 0.444444 | 0.157135 | intron-variant, utr-variant-3-prime | Btbd1 | Mm_Celera | 7:81798637 | CAATTTACTGCAATA[C/T]AGTAAAATATAAATT | 83962 |
rs32022129 | snp | C/T | 0.33241 | 0.236027 | intron-variant | Btbd1 | Mm_Celera | 7:81794445 | TAAAGCATAAGATGA[C/T]CAGAAAATGGCTCTG | 83962 |
rs32038867 | snp | A/C | 0.375 | 0.216506 | intron-variant | Btbd1 | Mm_Celera | 7:81797312 | AGTCAAAGGATTGTA[A/C]CCTAAACAACTACTT | 83962 |
rs32085560 | snp | C/G | 0.375 | 0.216506 | intron-variant | Btbd1 | Mm_Celera | 7:81817145 | CTTTAGAGACCTGAA[C/G]CTCAACAGCTGAGGG | 83962 |
rs32129657 | snp | A/G | 0.375 | 0.216506 | intron-variant | Btbd1 | Mm_Celera | 7:81800938 | TCCACTCCATGTCAC[A/G]CCCACACTCCGACAG | 83962 |
rs32171061 | snp | A/G | 0.375 | 0.216506 | upstream-variant-2KB | Btbd1 | Mm_Celera | 7:81830689 | CAAGCCTGATGACCC[A/G]AGTTTAATCCCAAGC | 83962 |
rs32210345 | snp | C/T | 0.375 | 0.216506 | intron-variant | Btbd1 | Mm_Celera | 7:81801542 | TGTGGAAACAGACAA[C/T]CACATATAGTAAATT | 83962 |
rs32223436 | snp | G/T | 0.5 | 0 | intron-variant | Btbd1 | Mm_Celera | 7:81811058 | GGATGGAGAGATGGC[G/T]CAGAGGTTAAAAGCA | 83962 |
rs32232828 | snp | A/G | 0.336735 | 0.234472 | intron-variant | Btbd1 | Mm_Celera | 7:81801422 | ACTTAATACTTGTCT[A/G]AGGCTATAACTGAAC | 83962 |
rs32253068 | snp | C/T | 0.444444 | 0.157135 | intron-variant, downstream-variant-500B | Btbd1 | Mm_Celera | 7:81798250 | ATATTAAAACTTTAA[C/T]TTCCCAGTGGGTAAT | 83962 |
rs32331015 | snp | A/G | 0.375 | 0.216506 | intron-variant | Btbd1 | Mm_Celera | 7:81795017 | CAGTGTTTCCTCTGT[A/G]AGGAGGGTGGAAGGA | 83962 |
rs32335188 | snp | A/C | 0.375 | 0.216506 | intron-variant | Btbd1 | Mm_Celera | 7:81805634 | TTATCTTGAACAGCT[A/C]TTTTGAGAATTAAAT | 83962 |
rs32358119 | snp | C/T | 0.444444 | 0.157135 | intron-variant | Btbd1 | Mm_Celera | 7:81797473 | CTATCTATCTATCTA[C/T]CTACCTACCTACCTA | 83962 |
rs32441911 | snp | C/T | 0.375 | 0.216506 | intron-variant | Btbd1 | Mm_Celera | 7:81816800 | GTATTGTCTGTGTGC[C/T]TGGCACCCGTAAAAA | 83962 |
rs32460576 | snp | A/G | 0.375 | 0.216506 | intron-variant | Btbd1 | GRCm38.p3 | 7:81795634 | CTCTTGGTAGTGCAC[A/G]GCTCTCGCTTCAGAG | 83962 |
rs32497124 | snp | G/T | 0.32 | 0.24 | intron-variant | Btbd1 | Mm_Celera | 7:81815713 | ATCCCATGAAGATGG[G/T]GAACAATCTTAGTTA | 83962 |
rs32527833 | snp | C/G | 0.444444 | 0.157135 | intron-variant | Btbd1 | Mm_Celera | 7:81797454 | TATCTATCTATCTAT[C/G]TATCTATCTATCTAT | 83962 |
rs36242919 | snp | C/G | 0.231111 | 0.249285 | intron-variant | Btbd1 | Mm_Celera | 7:81824179 | TCTGGCTAATTAAAA[C/G]AATGTTATGCATATG | 83962 |
rs36247985 | snp | A/G | 0.375 | 0.216506 | intron-variant, utr-variant-3-prime | Btbd1 | Mm_Celera | 7:81799786 | AAATTGTGACACTAT[A/G]AATTTCAAGTCAGTA | 83962 |
rs36252304 | snp | C/T | 0.231111 | 0.249285 | intron-variant | Btbd1 | Mm_Celera | 7:81818767 | TTGTTTAAAACCTTT[C/T]GTAGCCATTCCAGAA | 83962 |
rs36255808 | snp | C/T | 0.231111 | 0.249285 | intron-variant | Btbd1 | Mm_Celera | 7:81824824 | TACACGATTCCCATT[C/T]ACCATTAATCAGCAA | 83962 |
rs36267580 | snp | C/T | 0.35503 | 0.226867 | intron-variant | Btbd1 | Mm_Celera | 7:81796633 | AAGAGGTGTCCTTAG[C/T]GCCCTATCTCAAAGA | 83962 |
rs36300290 | snp | A/G | 0.5 | 0 | intron-variant | Btbd1 | Mm_Celera | 7:81797341 | TTTTATTATAATGGT[A/G]GACTCTGTGCTACAC | 83962 |
rs36321265 | snp | A/C | 0.277778 | 0.248452 | intron-variant, downstream-variant-500B | Btbd1 | Mm_Celera | 7:81798218 | GTTGTAGTACGTTCA[A/C]GTTTCATTTTTGTTT | 83962 |
rs36368218 | snp | A/G | 0.231111 | 0.249285 | intron-variant | Btbd1 | Mm_Celera | 7:81812887 | TCATATCCGTGTTAA[A/G]ATGATTCTTTCTCCT | 83962 |
rs36387012 | snp | A/T | 0.277778 | 0.248452 | intron-variant | Btbd1 | Mm_Celera | 7:81805161 | CATCATGAGCAGAAG[A/T]GTTAGGGAAGACTGT | 83962 |
rs36391565 | snp | A/G | 0.35503 | 0.226867 | intron-variant, utr-variant-3-prime | Btbd1 | Mm_Celera | 7:81799651 | TTGCCTGCTAGTGTC[A/G]TACCCAAAGTCTATG | 83962 |
rs36401632 | snp | A/G | 0.231111 | 0.249285 | intron-variant | Btbd1 | Mm_Celera | 7:81818814 | GGATTAGAGTGCTTT[A/G]GAGGTAAAATAATTT | 83962 |
rs36429908 | snp | A/G | 0.132653 | 0.220748 | intron-variant | Btbd1 | Mm_Celera | 7:81816403 | ATAAAGAGATCCTAA[A/G]TTTTTTTTTTTTTAA | 83962 |
rs36432336 | snp | G/T | 0.124444 | 0.216185 | intron-variant | Btbd1 | Mm_Celera | 7:81817632 | AGTCTCACATAACTT[G/T]AATCATTTGGTAAAT | 83962 |
rs36455963 | snp | G/T | 0.124444 | 0.216185 | intron-variant | Btbd1 | Mm_Celera | 7:81810910 | CACATATATGACACT[G/T]TCAAAAATAAAAGGT | 83962 |
rs36459180 | snp | C/T | 0.231111 | 0.249285 | intron-variant | Btbd1 | Mm_Celera | 7:81818971 | GTGTGGTTTTAAGCA[C/T]AGTATCATGGTGTGA | 83962 |
rs36488374 | snp | C/T | 0.231111 | 0.249285 | intron-variant | Btbd1 | Mm_Celera | 7:81826372 | AGTTTTCTCTGGTAT[C/T]ATTTCCTTCCAAACC | 83962 |
rs36490113 | snp | A/G | 0.132653 | 0.220748 | intron-variant, upstream-variant-2KB | Btbd1, 3110040N11Rik | Mm_Celera | 7:81792015 | AACTTTAATTAGCTG[A/G]AACTTTTGTTCTAAA | 83962 |
rs36492623 | snp | C/T | 0.124444 | 0.216185 | intron-variant | Btbd1 | Mm_Celera | 7:81794110 | ATGGAAGCCAGGAGC[C/T]TCCTGAGTGCATAGC | 83962 |
rs36503016 | snp | A/C | 0.231111 | 0.249285 | intron-variant | Btbd1 | Mm_Celera | 7:81826288 | TCTACTCAAACCTCG[A/C]TAGTTTACTCTTGTA | 83962 |
rs36517054 | snp | A/G | 0.231111 | 0.249285 | intron-variant | Btbd1 | Mm_Celera | 7:81813180 | AATACAACACCGGAT[A/G]TTAAACAAATCAGCA | 83962 |
rs36520123 | snp | C/G | 0.35503 | 0.226867 | intron-variant, downstream-variant-500B | Btbd1 | Mm_Celera | 7:81798375 | TACTTTTTCATATTT[C/G]AGCTGCTCCTCTCTT | 83962 |
rs36520897 | snp | A/G | 0.124444 | 0.216185 | intron-variant | Btbd1 | Mm_Celera | 7:81825239 | ATTAAATGAGCTAGG[A/G]TACAAATTTGCCTGA | 83962 |
rs36541940 | snp | A/G | 0.231111 | 0.249285 | intron-variant | Btbd1 | Mm_Celera | 7:81811862 | AGCACCTGAGTCCTG[A/G]GCTAGCACCGGCCAA | 83962 |
rs36544766 | snp | A/G | 0.277778 | 0.248452 | intron-variant, utr-variant-3-prime | Btbd1 | Mm_Celera | 7:81800151 | CTGCTGTGATGAGCT[A/G]TATTACTGACCTACT | 83962 |
rs36549021 | snp | A/T | 0.35503 | 0.226867 | intron-variant | Btbd1 | Mm_Celera | 7:81802342 | CATGATAATTCAAAA[A/T]CCTGTGGCAAGAGAA | 83962 |
rs36552522 | snp | A/G | 0.260355 | 0.249785 | intron-variant, utr-variant-3-prime | Btbd1 | Mm_Celera | 7:81798711 | AAGTCTTGGGTTTCC[A/G]CACTGTGGCAATACA | 83962 |
rs36567494 | snp | C/T | 0.124444 | 0.216185 | intron-variant | Btbd1 | Mm_Celera | 7:81814047 | AGGTAGTGACTCCTG[C/T]CGAGTGTAAATGAAC | 83962 |
rs36572075 | snp | C/T | 0.396694 | 0.202437 | intron-variant | Btbd1 | Mm_Celera | 7:81797535 | CAACCAACCAGAAAG[C/T]GGTCCAGATATGGAG | 83962 |
rs36585705 | snp | A/G | 0.165289 | 0.235211 | intron-variant | Btbd1 | Mm_Celera | 7:81797378 | AAATCTCTCTCATGA[A/G]TATGCTAATCATTAA | 83962 |
rs36625827 | snp | C/T | 0.124444 | 0.216185 | intron-variant | Btbd1 | Mm_Celera | 7:81806363 | CTATGGAGACAGAGG[C/T]GGAAGTGTAGCAGAG | 83962 |
rs36637430 | snp | C/T | 0.231111 | 0.249285 | intron-variant | Btbd1 | Mm_Celera | 7:81816074 | CTTCCTCAGACTGTG[C/T]ACAAAGTTGATACTG | 83962 |
rs36639520 | snp | G/T | 0.231111 | 0.249285 | intron-variant | Btbd1 | Mm_Celera | 7:81816114 | ACAATTGCTATTTAT[G/T]CAAAATACTGAGAAT | 83962 |
rs36656705 | snp | A/T | 0.165289 | 0.235211 | intron-variant | Btbd1 | Mm_Celera | 7:81796804 | GTTCCGGTATGCTTA[A/T]ACTTTTGTAAAGGAC | 83962 |
rs36658066 | snp | A/G | 0.142012 | 0.225474 | intron-variant | Btbd1 | Mm_Celera | 7:81806630 | AAACACGCTGTAACT[A/G]ACTGGTGAGGTAGAA | 83962 |
rs36666251 | snp | A/C | 0.152778 | 0.230321 | intron-variant | Btbd1 | Mm_Celera | 7:81800621 | TAAAGAACTGCTTCG[A/C]GGATGGTTTGTTTGT | 83962 |
rs36695618 | snp | A/G | 0.165289 | 0.235211 | intron-variant | Btbd1 | Mm_Celera | 7:81804602 | TATGGAACCAAGTAG[A/G]GACATACTTTCAACC | 83962 |
rs36718749 | snp | G/T | 0.231111 | 0.249285 | intron-variant | Btbd1 | Mm_Celera | 7:81825259 | AATTTGCCTGAAGGG[G/T]AAAGGAACAGTGATT | 83962 |
rs36727205 | snp | A/G | 0.231111 | 0.249285 | intron-variant | Btbd1 | Mm_Celera | 7:81811713 | CCTTAGAACAAAGTA[A/G]GGGTTCAATAATATG | 83962 |
rs36735574 | snp | A/T | 0.231111 | 0.249285 | intron-variant | Btbd1 | Mm_Celera | 7:81824995 | TCAAGCTCGCTGAAA[A/T]GACCTCAAACCACTG | 83962 |
rs36743741 | snp | G/T | 0.152778 | 0.230321 | intron-variant | Btbd1 | Mm_Celera | 7:81822326 | TAATAAAAATTTCAC[G/T]TTAGTAATAACCTTT | 83962 |
rs36755390 | snp | C/T | 0.277778 | 0.248452 | intron-variant, utr-variant-3-prime | Btbd1 | Mm_Celera | 7:81799051 | TATTAGCCTTAATCA[C/T]ATCCTATTTAAAAAC | 83962 |
rs36768782 | snp | C/T | 0.32 | 0.24 | intron-variant | Btbd1 | Mm_Celera | 7:81794597 | AGAGGGAAGAATCTG[C/T]CCTCCTTGTTTAGCC | 83962 |
rs36776115 | snp | A/G | 0.152778 | 0.230321 | intron-variant | Btbd1 | Mm_Celera | 7:81801605 | TAAGTTTACAGAATT[A/G]ATGCTGTTCCCTTAT | 83962 |
rs36792734 | snp | A/G | 0.231111 | 0.249285 | intron-variant | Btbd1 | Mm_Celera | 7:81818435 | AACTTTAATGAGCAA[A/G]CAAACAAAAGAAAAA | 83962 |
rs36798990 | snp | G/T | 0.260355 | 0.249785 | intron-variant, utr-variant-3-prime | Btbd1 | Mm_Celera | 7:81799539 | GCTTTCAGCCAGTAG[G/T]TAAGCTCAGATATGT | 83962 |
rs36813854 | snp | G/T | 0.165289 | 0.235211 | intron-variant | Btbd1 | Mm_Celera | 7:81795587 | TCTCTAATACTGTCA[G/T]TTATGTGTTAATAGA | 83962 |
rs36822067 | snp | A/G | 0.152778 | 0.230321 | intron-variant | Btbd1 | Mm_Celera | 7:81804722 | TTTAGAATGTATTTT[A/G]TAGATATGTGATTAA | 83962 |
rs36841232 | snp | A/G | 0.124444 | 0.216185 | intron-variant | Btbd1 | Mm_Celera | 7:81816333 | ATATGCTGCTGTCTA[A/G]TACTTAAAACTTCAA | 83962 |
rs36844302 | snp | G/T | 0.197531 | 0.244432 | intron-variant | Btbd1 | Mm_Celera | 7:81824050 | AGCTAAGGCTATATT[G/T]AATACAATTTAAGAA | 83962 |
rs36885127 | snp | A/C | 0.35503 | 0.226867 | intron-variant | Btbd1 | Mm_Celera | 7:81796530 | GATCACTGCATAGTT[A/C]ATAAATGACTTGTTT | 83962 |
rs36899264 | snp | A/T | 0.231111 | 0.249285 | intron-variant | Btbd1 | Mm_Celera | 7:81818743 | CATTTATTTCTTGGT[A/T]TCAGAATCTTGTTTA | 83962 |
rs36932306 | snp | C/T | 0.124444 | 0.216185 | utr-variant-3-prime, upstream-variant-2KB | Btbd1, 3110040N11Rik | Mm_Celera | 7:81792288 | GTCTTTACTTCTCTT[C/T]AGTTAAGCAGAATCA | 83962 |
rs36936481 | snp | A/C | 0.231111 | 0.249285 | intron-variant | Btbd1 | Mm_Celera | 7:81825935 | CCGCCTAGTTTGCTT[A/C]TCGCTCCCTTTCCCT | 83962 |
rs36960053 | snp | C/G | 0.231111 | 0.249285 | intron-variant | Btbd1 | Mm_Celera | 7:81817610 | TAAATTTCCTACCAA[C/G]GAGGACAGTCTCACA | 83962 |
rs36972042 | snp | G/T | 0.231111 | 0.249285 | intron-variant | Btbd1 | Mm_Celera | 7:81793745 | AATGAAAATAAACAA[G/T]TCAGTGGCTGTCAGT | 83962 |