SNP - dbSNP |
dbSNP | Type | Alleles | Het | Se(het) | Fxn-class | Gene Name | Assembly | Chr-pos | Sequence | Entrez Gene |
rs3143474 | snp | A/C | | | intron-variant | Tbcb | Mm_Celera | 7:30229608 | TATAGCTCTGTATAC[A/C]ATTTTGACCTGTCtt | 66411 |
rs13460270 | snp | C/G | | | downstream-variant-500B, upstream-variant-2KB, missense | Ovol3, Tbcb, Polr2i | Mm_Celera | 7:30233105 | TCTTTCAGTCACACA[C/G]TGCCCGAGCTGAGGA | 66411 |
rs31095719 | snp | C/T | 0.444444 | 0.157135 | intron-variant, upstream-variant-2KB | Tbcb, Polr2i | Mm_Celera | 7:30231313 | AGGCTGTCAGAGGCC[C/T]CCATCTTCAGACTTT | 66411 |
rs31200622 | snp | C/T | 0.444444 | 0.157135 | intron-variant, upstream-variant-2KB | Tbcb, Polr2i | Mm_Celera | 7:30231506 | ACCTTCCCTCCAGCT[C/T]CGCCCACTAGTTTTC | 66411 |
rs31489277 | snp | C/T | 0.5 | 0 | upstream-variant-2KB, intron-variant | Tbcb, Polr2i | GRCm38.p3 | 7:30232733 | GACACTCCTCCCACA[C/T]GCTCTCCCGTCTGCA | 66411 |
rs31604106 | snp | A/G | 0.444444 | 0.157135 | intron-variant | Tbcb | GRCm38.p3 | 7:30227919 | ATCCCTGAAACCAGC[A/G]GCAGAGCTCAGGTCT | 66411 |
rs31610097 | snp | G/T | 0.429688 | 0.173817 | utr-variant-5-prime, upstream-variant-2KB | Tbcb, Polr2i | GRCm38.p3 | 7:30231865 | CTTTCTCCACGGACA[G/T]GCGGATTCTCGGGTA | 66411 |
rs31644606 | snp | A/G | 0.444444 | 0.157135 | intron-variant, upstream-variant-2KB, utr-variant-5-prime | Tbcb, Polr2i | Mm_Celera | 7:30231400 | CCCTCGGCTCTCTGG[A/G]GTGTCTGATTTTTCC | 66411 |
rs31728453 | snp | C/T | 0.444444 | 0.157135 | intron-variant, upstream-variant-2KB | Tbcb, Polr2i | GRCm38.p3 | 7:30231020 | ACTGGGGCTTCCATG[C/T]GGCTAGAGCCTATAC | 66411 |
rs32035890 | snp | C/G | 0 | 0 | intron-variant | Tbcb | Mm_Celera | 7:30224711 | GGCATGCTACTTTGT[C/G]CTGTTACTATATTAT | 66411 |
rs32103993 | snp | A/T | 0.444444 | 0.157135 | utr-variant-3-prime, upstream-variant-2KB, synonymous-codon | Ovol3, Tbcb, Polr2i | GRCm38.p3 | 7:30233308 | GCGCCTGTACTATGT[A/T]TGCACTGCCCCACAC | 66411 |
rs32288175 | snp | C/T | 0.444444 | 0.157135 | intron-variant | Tbcb | GRCm38.p3 | 7:30227554 | GCCCTGCCCTGTCTG[C/T]CCCACTATCTGGACC | 66411 |
rs32298205 | snp | C/T | 0.5 | 0 | downstream-variant-500B, upstream-variant-2KB, synonymous-codon | Ovol3, Tbcb, Polr2i | GRCm38.p3 | 7:30233094 | GGAGGCAGTGTTCTT[C/T]CAGTCACACAGTGCC | 66411 |
rs32320786 | snp | C/G | 0.444444 | 0.157135 | synonymous-codon, upstream-variant-2KB, intron-variant | Ovol3, Tbcb, Polr2i | GRCm38.p3 | 7:30233589 | GGCAAGGTGAGCTTC[C/G]AGGGAACAGCGCTGG | 66411 |
rs32373441 | snp | A/G | 0.5 | 0 | upstream-variant-2KB, intron-variant | Tbcb, Polr2i | GRCm38.p3 | 7:30232419 | GGTGAGGCCCGGGCA[A/G]TAGGTGTGGGAAGGC | 66411 |
rs32496186 | snp | C/T | 0.444444 | 0.157135 | utr-variant-5-prime, upstream-variant-2KB | Tbcb, Polr2i | GRCm38.p3 | 7:30231845 | GCCAGCCAATCGCTG[C/T]TGTTCTTTCTCCACG | 66411 |
rs32527318 | snp | A/G | 0.5 | 0 | synonymous-codon | Tbcb | GRCm38.p3 | 7:30227686 | TCCGAGCCGGACGCC[A/G]CTGTGGTCAATGACC | 66411 |
rs45660308 | snp | C/T | | | intron-variant | Tbcb | GRCm38.p3 | 7:30229213 | GCATCTCAGCGGTGA[C/T]TCATAGAGGATGCTG | 66411 |
rs45712980 | snp | C/T | | | intron-variant | Tbcb | GRCm38.p3 | 7:30230061 | GGAGGAGAAAAACAA[C/T]TGTTGACCTCCAAGC | 66411 |
rs45833221 | snp | C/G | | | intron-variant | Tbcb | Mm_Celera | 7:30229429 | TGTTTTTTAAAGGTG[C/G]TGGTGCACAGTTTTA | 66411 |
rs45847479 | snp | C/T | | | intron-variant | Tbcb | Mm_Celera | 7:30229051 | ACACACACACACACA[C/T]ACCCCGAACTGCATA | 66411 |
rs45934641 | snp | A/G | | | intron-variant | Tbcb | Mm_Celera | 7:30229771 | GCTCAGCAGTTAAGA[A/G]TACCATCTGCTCTTG | 66411 |
rs45959509 | snp | A/C | | | intron-variant, upstream-variant-2KB | Tbcb, Polr2i | Mm_Celera | 7:30230874 | CCCATTCCTCAAGGA[A/C]GCCTCTTCAGATATC | 66411 |
rs45988274 | snp | C/T | | | intron-variant | Tbcb | GRCm38.p3 | 7:30229186 | CTCCCCACATGTTAT[C/T]CTGGGGATTTAGCAT | 66411 |
rs46019021 | snp | C/T | | | intron-variant | Tbcb | Mm_Celera | 7:30225093 | CACCAGGCAGCATTG[C/T]TTGTACCTGCATACG | 66411 |
rs46070500 | snp | C/G | 0.124444 | 0.216185 | intron-variant | Tbcb | Mm_Celera | 7:30228000 | GGATCATCCGGGTCA[C/G]GACAGCCTCCTTTCG | 66411 |
rs46144750 | snp | A/G | | | downstream-variant-500B, upstream-variant-2KB, intron-variant | Ovol3, Tbcb, Polr2i | Mm_Celera | 7:30233159 | GGGTAGGGGTGGGGG[A/G]GACACGCCAGTTTTG | 66411 |
rs46267332 | snp | C/T | | | intron-variant | Tbcb | GRCm38.p3 | 7:30226662 | CCTTTAATCCAGCAC[C/T]TGGGAGGCAGAGTCA | 66411 |
rs46324473 | snp | C/T | | | intron-variant | Tbcb | GRCm38.p3 | 7:30228263 | CGATCTCACTCAAGG[C/T]CGGCCTCCCCAGCAC | 66411 |
rs46368776 | snp | A/G | | | intron-variant | Tbcb | Mm_Celera | 7:30226591 | AAATGGCTATGCTCT[A/G]GATTCTGGAACCATA | 66411 |
rs46383296 | snp | A/C | | | intron-variant | Tbcb | GRCm38.p3 | 7:30229285 | GAACTACAATGAGAG[A/C]GACATCTGTCCTCCT | 66411 |
rs46390739 | snp | A/T | 0.142012 | 0.225474 | intron-variant | Tbcb | Mm_Celera | 7:30228346 | TCTGACTCTGTGATC[A/T]TTTAGCTAAGGCTAC | 66411 |
rs46495119 | snp | C/G | | | intron-variant | Tbcb | Mm_Celera | 7:30229734 | AATTATCTCAAAATA[C/G]AAAAGAGGTGTTGGA | 66411 |
rs46543655 | snp | G/T | | | intron-variant, upstream-variant-2KB | Tbcb, Polr2i | GRCm38.p3 | 7:30230660 | TTGGAAAAAGGAATG[G/T]ACAGAGTTTAGCAGG | 66411 |
rs46610579 | snp | G/T | | | intron-variant | Tbcb | GRCm38.p3 | 7:30225936 | CCGAGTCTGTCCCGT[G/T]GCCCTGATTGATCAG | 66411 |
rs46625115 | snp | A/C | | | intron-variant, upstream-variant-2KB | Tbcb, Polr2i | GRCm38.p3 | 7:30230682 | TTTAGCAGGGAGGGA[A/C]TGAGTAGGGAAGGTG | 66411 |
rs46628757 | snp | C/T | | | intron-variant | Tbcb | GRCm38.p3 | 7:30229176 | CTATAGGACCCTCCC[C/T]ACATGTTATCCTGGG | 66411 |
rs46661248 | snp | A/G | | | intron-variant, upstream-variant-2KB | Tbcb, Polr2i | Mm_Celera | 7:30230500 | GCTGGGATTAAAGGC[A/G]TGTGCCACCTTTTTA | 66411 |
rs46680335 | snp | A/G | | | intron-variant, upstream-variant-2KB | Tbcb, Polr2i | Mm_Celera | 7:30230304 | GTGGGTCCAGGGACT[A/G]AACTCAAGTTGACAG | 66411 |
rs46747141 | snp | C/T | | | intron-variant, upstream-variant-2KB | Tbcb, Polr2i | GRCm38.p3 | 7:30230784 | CGGGCCAGAACTTGA[C/T]GGCTCACCTCAGTTC | 66411 |
rs46779104 | snp | A/G | | | intron-variant | Tbcb | GRCm38.p3 | 7:30227300 | TGACCTGTCCTCAGA[A/G]GCCAGCTTCAAATGC | 66411 |
rs46973811 | snp | A/T | | | intron-variant, upstream-variant-2KB | Tbcb, Polr2i | Mm_Celera | 7:30230339 | CATGACCAGCCTCTG[A/T]CTTTTTTTTTTTTTT | 66411 |
rs47127969 | snp | A/G | | | intron-variant | Tbcb | GRCm38.p3 | 7:30226236 | AGCTTCTCTGTAGGG[A/G]ATGTTCCCAGGGCAA | 66411 |
rs47165955 | snp | A/G | | | intron-variant | Tbcb | GRCm38.p3 | 7:30230049 | AGGACCACAGTGGGA[A/G]GAGAAAAACAATTGT | 66411 |
rs47438183 | snp | A/G | | | intron-variant | Tbcb | GRCm38.p3 | 7:30228996 | TTAGAGCACTATGGA[A/G]GTGGAGGCAAGATGA | 66411 |
rs47529105 | snp | C/T | | | intron-variant | Tbcb | GRCm38.p3 | 7:30224431 | AGCCAGCAGCACAGG[C/T]GGACTTCCACATACA | 66411 |
rs47617975 | snp | A/G | | | downstream-variant-500B | Tbcb | GRCm38.p3 | 7:30223957 | GGGCCACTTCCCAGT[A/G]TTCAGGATATTATTT | 66411 |
rs47631237 | snp | A/G | 0.132653 | 0.220748 | utr-variant-5-prime, upstream-variant-2KB | Tbcb, Polr2i | Mm_Celera | 7:30231995 | GCCGAGTGTAAGTTC[A/G]GCGCATGTGCACTGG | 66411 |
rs47694578 | snp | C/T | | | downstream-variant-500B | Tbcb | Mm_Celera | 7:30223837 | ACATGATTATGCATG[C/T]TGTGTGTGCACAGGA | 66411 |
rs47765894 | snp | C/T | | | intron-variant | Tbcb | Mm_Celera | 7:30226627 | AGACATCTTTCCTTG[C/T]CGGGCGGTGGTGGCT | 66411 |
rs47791157 | snp | A/G | | | intron-variant | Tbcb | GRCm38.p3 | 7:30228265 | ATCTCACTCAAGGTC[A/G]GCCTCCCCAGCACAC | 66411 |
rs47879137 | snp | C/T | | | intron-variant | Tbcb | Mm_Celera | 7:30224972 | CCTCGAACTCAGAAA[C/T]CCACCTGCCTCTGCC | 66411 |
rs47974535 | snp | C/T | | | intron-variant | Tbcb | GRCm38.p3 | 7:30228272 | TCAAGGTCGGCCTCC[C/T]CAGCACACATGGATG | 66411 |
rs48000400 | snp | A/C | | | intron-variant | Tbcb | Mm_Celera | 7:30229385 | GATAACACCAAAGAG[A/C]AAAGAAAAACCCAAA | 66411 |
rs48338410 | snp | C/T | | | intron-variant, upstream-variant-2KB | Tbcb, Polr2i | Mm_Celera | 7:30230178 | TAATTTTTTTCCTGT[C/T]CTCACAATCAAACTT | 66411 |
rs48354177 | snp | G/T | | | synonymous-codon | Tbcb | GRCm38.p3 | 7:30227027 | GTTTCATGAAGGATC[G/T]AACTGTGTCTGTGGG | 66411 |
rs48372007 | snp | C/G | | | intron-variant, upstream-variant-2KB | Tbcb, Polr2i | Mm_Celera | 7:30231504 | CAACCTTCCCTCCAG[C/G]TTCGCCCACTAGTTT | 66411 |
rs48451957 | snp | C/T | | | intron-variant | Tbcb | GRCm38.p3 | 7:30225843 | TAAGGAAGCCCCTAT[C/T]CCTAATCCCGATTAA | 66411 |
rs48591835 | snp | A/G | | | intron-variant | Tbcb | Mm_Celera | 7:30225187 | ATACCAATATAAGAA[A/G]TTATTTGGGGGCCGG | 66411 |
rs48597052 | snp | C/T | | | intron-variant | Tbcb | Mm_Celera | 7:30224981 | CAGAAATCCACCTGC[C/T]TCTGCCTCCTGAGTG | 66411 |
rs48615628 | snp | A/G | 0.426035 | 0.177515 | upstream-variant-2KB, utr-variant-5-prime | Tbcb, Polr2i | GRCm38.p3 | 7:30232142 | GCAGGTTCCGAAATC[A/G]GGAGTGAGTAGCAGA | 66411 |
rs48748049 | snp | C/G | | | intron-variant, upstream-variant-2KB | Tbcb, Polr2i | Mm_Celera | 7:30230320 | AACTCAAGTTGACAG[C/G]CTCCATGACCAGCCT | 66411 |
rs48781509 | snp | A/G | | | downstream-variant-500B, upstream-variant-2KB, intron-variant | Ovol3, Tbcb, Polr2i | Mm_Celera | 7:30233148 | GGTGCTTGGGGGGGT[A/G]GGGGTGGGGGGGACA | 66411 |
rs48834075 | snp | G/T | | | utr-variant-3-prime | Tbcb | GRCm38.p3 | 7:30224227 | GGGGCCTCCTTCCAG[G/T]TACAGTCACATCTCG | 66411 |
rs48865239 | snp | C/G | | | intron-variant | Tbcb | GRCm38.p3 | 7:30227116 | AGCGTCATGAAGAGA[C/G]TCTATTCTGAATGCT | 66411 |
rs48869144 | snp | G/T | | | intron-variant | Tbcb | GRCm38.p3 | 7:30229798 | CTTGCGGAGGACCCA[G/T]GTTTGGTTCTTAGCA | 66411 |
rs49082163 | snp | C/T | | | downstream-variant-500B | Tbcb | GRCm38.p3 | 7:30223934 | AGCAGCAATCACTCT[C/T]AACCACAGGGCCACT | 66411 |
rs49130087 | snp | A/G | | | intron-variant | Tbcb | GRCm38.p3 | 7:30227142 | ATGCTTAGAGCTCTC[A/G]GCAGCTATCCTCAAG | 66411 |
rs49173165 | snp | C/T | 0.375 | 0.216506 | intron-variant, upstream-variant-2KB | Tbcb, Polr2i | GRCm38.p3 | 7:30230818 | ACAGTGTTATACTTT[C/T]GTCCTCTCCATGGAA | 66411 |
rs49183686 | snp | C/T | | | intron-variant | Tbcb | Mm_Celera | 7:30226594 | TGGCTATGCTCTAGA[C/T]TCTGGAACCATAAGT | 66411 |
rs49186771 | snp | C/T | | | intron-variant | Tbcb | GRCm38.p3 | 7:30226181 | TGCCAGCAGTTGACA[C/T]TGAGATGGTTAGCCT | 66411 |
rs49186906 | snp | A/C/T | | | intron-variant | Tbcb | GRCm38.p3 | 7:30226048 | CCTTCTCGCTGGCCT[A/C/T]TCTTTCTGCTTCTGT | 66411 |
rs49410802 | snp | C/T | | | intron-variant | Tbcb | GRCm38.p3 | 7:30225715 | TATGTGGGTAGCTGA[C/T]GCCCTGTCTGGCAAG | 66411 |
rs49412130 | snp | C/G/T | | | intron-variant | Tbcb | GRCm38.p3 | 7:30229669 | GAATAGAGTTACCCA[C/G/T]GGCTACACAGAGTGT | 66411 |
rs49470379 | snp | C/T | | | intron-variant, upstream-variant-2KB | Tbcb, Polr2i | Mm_Celera | 7:30230335 | CCTCCATGACCAGCC[C/T]CTGACTTTTTTTTTT | 66411 |
rs49478835 | snp | C/T | 0.132653 | 0.220748 | intron-variant | Tbcb | Mm_Celera | 7:30224695 | TCACTGCTACCTGTC[C/T]GGCATGCTACTTTGT | 66411 |
rs49480589 | snp | A/G | | | intron-variant | Tbcb | GRCm38.p3 | 7:30226007 | TAGAGTTTGTGTGAC[A/G]ATTTTCAGACCCCAA | 66411 |
rs49564531 | snp | A/G | | | intron-variant, upstream-variant-2KB | Tbcb, Polr2i | GRCm38.p3 | 7:30230617 | CCCACCATAGGCCAC[A/G]GTGGTGGATGACACC | 66411 |
rs49722149 | snp | A/G | | | intron-variant | Tbcb | GRCm38.p3 | 7:30229776 | GCAGTTAAGAATACC[A/G]TCTGCTCTTGCGGAG | 66411 |
rs49780770 | snp | A/G | | | intron-variant, upstream-variant-2KB | Ovol3, Tbcb | GRCm38.p3 | 7:30233937 | TCACAGTGTAGCCCT[A/G]GCTGGCCTGGAACTC | 66411 |
rs49835561 | snp | A/G | | | intron-variant, upstream-variant-2KB | Tbcb, Polr2i | Mm_Celera | 7:30230229 | GGTCTCTCTTTCATT[A/G]TTTTGAGTGTCTGTG | 66411 |
rs49899239 | snp | A/G | | | intron-variant | Tbcb | Mm_Celera | 7:30225590 | AAAAGAAAAGAAAAG[A/G]AAAGAAGGCTATTTG | 66411 |
rs49924948 | snp | A/G | | | intron-variant | Tbcb | GRCm38.p3 | 7:30226098 | ATCCAGAGCAGGGCA[A/G]CACTGCTACTGCTAT | 66411 |
rs49937388 | snp | G/T | | | intron-variant | Tbcb | Mm_Celera | 7:30229732 | GAAATTATCTCAAAA[G/T]ACAAAAGAGGTGTTG | 66411 |
rs50020820 | snp | C/T | | | intron-variant | Tbcb | GRCm38.p3 | 7:30226412 | TCACAGTAAGTGAGG[C/T]TGCCCATGGCTACAG | 66411 |
rs50156291 | snp | A/G | | | intron-variant | Tbcb | Mm_Celera | 7:30225597 | AAGAAAAGAAAAGAA[A/G]GCTATTTGGAATAAG | 66411 |
rs50196857 | snp | A/T | | | intron-variant | Tbcb | Mm_Celera | 7:30226773 | TAGAAAAACAAAAAA[A/T]CAAAAGGAAAAAAAA | 66411 |
rs50245332 | snp | C/T | | | intron-variant | Tbcb | Mm_Celera | 7:30225052 | GCTCTGTATAGTTAG[C/T]CACAATAAGCTCGGA | 66411 |
rs50277166 | snp | C/G | 0.152778 | 0.230321 | intron-variant | Tbcb | Mm_Celera | 7:30227217 | AATTCAGAACTATAG[C/G]GATGCCACCTGTCAC | 66411 |
rs50306817 | snp | A/G | | | intron-variant | Tbcb | Mm_Celera | 7:30225625 | AAGACTTCCATTTTG[A/G]GTGGGGGTCGAGTAA | 66411 |
rs50430269 | snp | C/T | | | intron-variant | Tbcb | GRCm38.p3 | 7:30228282 | CCTCCCCAGCACACA[C/T]GGATGCCAAGCTCTC | 66411 |
rs50501272 | snp | C/T | | | intron-variant, upstream-variant-2KB | Tbcb, Polr2i | Mm_Celera | 7:30230125 | CATAATAAATATAAA[C/T]GAAACAAAAAAAAAG | 66411 |
rs50552396 | snp | A/G | | | intron-variant | Tbcb | GRCm38.p3 | 7:30225716 | ATGTGGGTAGCTGAT[A/G]CCCTGTCTGGCAAGT | 66411 |
rs50588845 | snp | C/T | 0.375 | 0.216506 | synonymous-codon | Tbcb | GRCm38.p3 | 7:30227004 | ATTGTACGGGCCTAG[C/T]TTGCTGCGTTTCATG | 66411 |
rs50914657 | snp | A/G | | | intron-variant, upstream-variant-2KB | Tbcb, Polr2i | GRCm38.p3 | 7:30230688 | AGGGAGGGAATGAGT[A/G]GGGAAGGTGGGGAGA | 66411 |
rs50961883 | snp | C/T | 0.21875 | 0.248039 | synonymous-codon | Tbcb | Mm_Celera | 7:30226995 | GAGTTCTTCATTGTA[C/T]GGGCCTAGCTTGCTG | 66411 |
rs51098521 | snp | C/T | 0.142012 | 0.225474 | intron-variant | Tbcb | GRCm38.p3 | 7:30228014 | ACGACAGCCTCCTTT[C/T]GGGTCTCCCTGTTCT | 66411 |
rs51136504 | snp | C/T | | | intron-variant, upstream-variant-2KB | Tbcb, Polr2i | GRCm38.p3 | 7:30230098 | TCATACCCATGTGTT[C/T]GCACCATGGCACATA | 66411 |
rs51209233 | snp | A/T | | | intron-variant, upstream-variant-2KB | Tbcb, Polr2i | GRCm38.p3 | 7:30230847 | AACATTCTCTAGATA[A/T]CAGCTCAAATACCCA | 66411 |
rs51276028 | snp | C/T | | | intron-variant | Tbcb | Mm_Celera | 7:30225213 | GCCGGAGAGACGGCT[C/T]AGTGGTTAAGAGCAC | 66411 |