SNP - dbSNP |
dbSNP | Type | Alleles | Het | Se(het) | Fxn-class | Gene Name | Assembly | Chr-pos | Sequence | Entrez Gene |
rs13462441 | snp | A/G | 0.444444 | 0.157135 | missense | Dmwd | Mm_Celera | 7:19080928 | AGGCTGGTGGGCCTA[A/G]TGCATCGATGGAGCC | 13401 |
rs31221333 | snp | A/G | 0.5 | 0 | intron-variant | Dmwd | Mm_Celera | 7:19077775 | GCCCAGGGGACTCTG[A/G]TCCCTGATGCTGTGG | 13401 |
rs31274226 | snp | C/T | 0.48 | 0.0979796 | synonymous-codon | Dmwd | Mm_Celera | 7:19078078 | TCTCAACAAGCCCAT[C/T]GACAAGCGGATCTAC | 13401 |
rs31332721 | snp | A/G | 0.375 | 0.216506 | upstream-variant-2KB | Dmwd | Mm_Celera | 7:19075632 | AGGAAGGGAAGAGCT[A/G]GGCGTGGTGTCTCAG | 13401 |
rs31381551 | snp | C/T | 0.375 | 0.216506 | upstream-variant-2KB, utr-variant-3-prime | Dmpk, Dmwd | Mm_Celera | 7:19082669 | CACTCCTGCCCAAAC[C/T]CCACCCCTTGCTATG | 13401 |
rs31566859 | snp | A/C | 0.375 | 0.216506 | downstream-variant-500B, upstream-variant-2KB | Rsph6a, Dmwd | Mm_Celera | 7:19074463 | GCTGGCTCATCATTC[A/C]TTCTCCATATTCGTT | 13401 |
rs31567533 | snp | A/G | 0.375 | 0.216506 | downstream-variant-500B, upstream-variant-2KB | Rsph6a, Dmwd | Mm_Celera | 7:19074820 | TTACATTTTATTTGC[A/G]GGGGCGGGGGGCTGG | 13401 |
rs31747760 | snp | C/T | 0.375 | 0.216506 | downstream-variant-500B, upstream-variant-2KB | Rsph6a, Dmwd | Mm_Celera | 7:19074455 | CCTGGGCAGCTGGCT[C/T]ATCATTCCTTCTCCA | 13401 |
rs31814483 | snp | A/C | 0.375 | 0.216506 | downstream-variant-500B, upstream-variant-2KB | Rsph6a, Dmwd | Mm_Celera | 7:19074462 | AGCTGGCTCATCATT[A/C]CTTCTCCATATTCGT | 13401 |
rs31896472 | snp | A/G | 0.375 | 0.216506 | utr-variant-3-prime, upstream-variant-2KB, downstream-variant-500B | Rsph6a, Dmwd | Mm_Celera | 7:19074369 | CCTTGAAGGACACAG[A/G]TAGGAAACCACCCAG | 13401 |
rs31907667 | snp | A/C | 0.444444 | 0.157135 | intron-variant | Dmwd | Mm_Celera | 7:19081444 | CCTCTGCTGGCCCAT[A/C]TGGCTCATCCTTAGT | 13401 |
rs31919502 | snp | C/T | 0.444444 | 0.157135 | upstream-variant-2KB, intron-variant | Dmpk, Dmwd | Mm_Celera | 7:19082267 | CCTTTCTCCTCTTGT[C/T]CTCCCCAGGGCATCT | 13401 |
rs32078346 | snp | A/C | 0.375 | 0.216506 | downstream-variant-500B, upstream-variant-2KB | Rsph6a, Dmwd | Mm_Celera | 7:19074777 | TGGGAACTGAAGTTA[A/C]GTCATTCCACCCATT | 13401 |
rs32087814 | snp | C/G | 0.5 | 0 | missense | Dmwd | Mm_Celera | 7:19080577 | GCGCAGAGGAGGCGG[C/G]GTCAGCCAGTGCTGA | 13401 |
rs32090363 | snp | C/T | 0.444444 | 0.157135 | upstream-variant-2KB, downstream-variant-500B | Dmpk, Dmwd | Mm_Celera | 7:19082888 | CCCCATCCCTAGCCC[C/T]GAGCAGAGAGCCCTC | 13401 |
rs32097948 | snp | C/T | 0.48 | 0.0979796 | intron-variant | Dmwd | Mm_Celera | 7:19078016 | TCTTCCTTCCTCTCC[C/T]GCTCTAACCGGTTAA | 13401 |
rs32172250 | snp | C/T | 0.48 | 0.0979796 | intron-variant | Dmwd | Mm_Celera | 7:19078034 | TCTAACCGGTTAACT[C/T]GTCTCCTCCCGCGGT | 13401 |
rs32357079 | snp | C/T | 0.375 | 0.216506 | downstream-variant-500B, upstream-variant-2KB | Rsph6a, Dmwd | Mm_Celera | 7:19074655 | TGTTGTGTATTTGAG[C/T]GTTTGCACGTGTGTG | 13401 |
rs32385712 | snp | C/T | 0.444444 | 0.157135 | intron-variant | Dmwd | Mm_Celera | 7:19076931 | CACGGAGGTGACAGA[C/T]ATTCTGTGGGCTTTG | 13401 |
rs32460915 | snp | C/T | 0.444444 | 0.157135 | synonymous-codon | Dmwd | Mm_Celera | 7:19081103 | GCTCAGTGGTCCTGC[C/T]CCCCGAAGCCGATTG | 13401 |
rs32461663 | snp | A/G | 0.375 | 0.216506 | intron-variant | Dmwd | Mm_Celera | 7:19081553 | GTGATTGAGCTGGGG[A/G]CCCACTTCTGGCCTG | 13401 |
rs45769994 | snp | C/T | | | intron-variant | Dmwd | Mm_Celera | 7:19079323 | TGCCCTCCTCTTCAG[C/T]AGCAGTCTGAGGAGT | 13401 |
rs46497252 | snp | A/C | | | intron-variant | Dmwd | Mm_Celera | 7:19079978 | GAGCTGGGGTCCAGG[A/C]TAAGATGTGGCCTGT | 13401 |
rs47268824 | snp | A/G | | | intron-variant | Dmwd | Mm_Celera | 7:19079349 | GGAGTAGCCTTGCAC[A/G]CCCAGCTGCGGCTGT | 13401 |
rs47281063 | snp | C/T | | | synonymous-codon | Dmwd | Mm_Celera | 7:19080155 | CAACGTCAGTCACCC[C/T]TGCACCTCCACCCCA | 13401 |
rs47446918 | snp | A/G | | | intron-variant | Dmwd | Mm_Celera | 7:19079623 | TGGCTCTGGAAGCCC[A/G]TGGCTTTTGTTGAAA | 13401 |
rs47457013 | snp | A/G | | | upstream-variant-2KB | Dmwd | Mm_Celera | 7:19075138 | CAAGGGGGGCGGGGG[A/G]AGCAAAACAGAACAC | 13401 |
rs47895319 | snp | C/G | | | intron-variant | Dmwd | Mm_Celera | 7:19079667 | TGTGGGCAGAGGAGA[C/G]AGGCTTGGAGGGTTT | 13401 |
rs48081334 | snp | A/G | | | intron-variant | Dmwd | Mm_Celera | 7:19079534 | TGGGGGTGGGGGGTG[A/G]GAGGCAGCTGTATGT | 13401 |
rs48484932 | snp | C/T | | | intron-variant | Dmwd | Mm_Celera | 7:19079751 | GGCATGTCCTCTGAG[C/T]GTTGTTTCAGCTGCT | 13401 |
rs49080398 | snp | G/T | | | intron-variant | Dmwd | Mm_Celera | 7:19077658 | GGAAATCCTAAATTT[G/T]GGGATTTTTGCATCC | 13401 |
rs49344761 | snp | A/G | | | upstream-variant-2KB | Dmwd | Mm_Celera | 7:19076023 | GTTCCCAACAGTCAC[A/G]CCTCGTAGCCAACCA | 13401 |
rs49847833 | snp | A/T | | | intron-variant | Dmwd | Mm_Celera | 7:19077830 | GAAAGACAGGCTCTG[A/T]GGTCTTCACTGGGCG | 13401 |
rs49862451 | snp | A/G | | | upstream-variant-2KB | Dmwd | Mm_Celera | 7:19075139 | AAGGGGGGCGGGGGG[A/G]GCAAAACAGAACACA | 13401 |
rs49908373 | snp | C/G | | | intron-variant | Dmwd | Mm_Celera | 7:19079820 | CCCTGGTGTTCTGGA[C/G]TTGAAGTTCTTGTCT | 13401 |
rs51147681 | snp | G/T | | | synonymous-codon | Dmwd | Mm_Celera | 7:19080407 | CTTTGGGGGTCTGCT[G/T]TGTGTGTGCTGGAGC | 13401 |
rs51448576 | snp | C/T | | | intron-variant | Dmwd | Mm_Celera | 7:19079781 | TGGGGGCCAGACTAG[C/T]GATGAGGATCCTTCC | 13401 |
rs51876975 | snp | C/T | | | synonymous-codon | Dmwd | Mm_Celera | 7:19080149 | CCTCTACAACGTCAG[C/T]CACCCCTGCACCTCC | 13401 |
rs108432880 | snp | A/G | | | intron-variant | Dmwd | Mm_Celera | 7:19079387 | CCGTAGGGTAGAGAC[A/G]ATTGCAGGCCTGGTG | 13401 |
rs211890894 | snp | C/T | | | upstream-variant-2KB | Dmwd | Mm_Celera | 7:19075279 | GAAGTCAAGGCAGGG[C/T]TGTCTCCAGAATAGA | 13401 |
rs212009021 | snp | C/G | | | downstream-variant-500B, upstream-variant-2KB | Rsph6a, Dmwd | Mm_Celera | 7:19074598 | TGCCCCCCACCCCAA[C/G]CCCTGGGATTTAATG | 13401 |
rs212235300 | snp | C/T | | | upstream-variant-2KB, intron-variant | Dmpk, Dmwd | Mm_Celera | 7:19082209 | GGCCTTTGGGTGGCT[C/T]CTTCTCCGGGTTCTG | 13401 |
rs213261214 | snp | A/G | | | intron-variant | Dmwd | Mm_Celera | 7:19077643 | CAGGGAAAAGATGAC[A/G]GAAATCCTAAATTTG | 13401 |
rs213475138 | snp | C/T | | | upstream-variant-2KB | Dmwd | Mm_Celera | 7:19075479 | GACTGTCCCTCATTG[C/T]GATTCTAGGTAGCCT | 13401 |
rs213668047 | in-del | -/T/TA | | | upstream-variant-2KB | Dmwd | Mm_Celera | 7:19075877 | AATGCATTTTTTTTT[-/T/TA]TTATTTAAAAAACAA | 13401 |
rs213694934 | snp | A/G | | | intron-variant | Dmwd | Mm_Celera | 7:19078659 | CTCACAGGGCTTTAA[A/G]CTCATTCACAAGGAT | 13401 |
rs213788108 | snp | A/T | | | upstream-variant-2KB, utr-variant-5-prime | Dmwd | Mm_Celera | 7:19076155 | TCTGGGTGCCAATCG[A/T]AGAGGCGTCACCCGG | 13401 |
rs214451307 | snp | A/T | | | downstream-variant-500B, upstream-variant-2KB | Rsph6a, Dmwd | Mm_Celera | 7:19074533 | CCTGGATGTCCTGGA[A/T]CTCACTCTGTAGACC | 13401 |
rs215454434 | snp | G/T | | | intron-variant | Dmwd | Mm_Celera | 7:19078437 | GAAGAATGCTTTACT[G/T]TTTGGGTTCTCATCC | 13401 |
rs215934268 | snp | C/T | | | upstream-variant-2KB | Dmwd | Mm_Celera | 7:19075384 | CTGACTAGGGAATGG[C/T]ACCTCCCACAATGGA | 13401 |
rs216030848 | in-del | -/T | | | intron-variant | Dmwd | GRCm38.p3 | 7:19079525 | GGGGTGGGGTGGGGG[-/T]GGGGGGTGAGAGGCA | 13401 |
rs216385248 | in-del | -/C | | | intron-variant | Dmwd | Mm_Celera | 7:19077172 | GGGGGTTTGGCAAAA[-/C]TGATGGGAGCTCTGA | 13401 |
rs216481336 | snp | C/T | | | intron-variant | Dmwd | Mm_Celera | 7:19077579 | CCTCTGACCTCTACA[C/T]CTCTACACAACACAC | 13401 |
rs216543485 | snp | A/G | | | upstream-variant-2KB, utr-variant-3-prime | Dmpk, Dmwd | Mm_Celera | 7:19082358 | CCCGGCCTCCTAGCC[A/G]TAACCCTCCCCGCTG | 13401 |
rs216706123 | snp | A/G | | | intron-variant | Dmwd | Mm_Celera | 7:19078838 | GTGAGTGGATTAGAA[A/G]CTCAGGCACCCGTTC | 13401 |
rs217029642 | snp | A/G | | | intron-variant | Dmwd | Mm_Celera | 7:19079603 | TGGCCTGGGCTGTGA[A/G]CACTTGGCTCTGGAA | 13401 |
rs217192654 | snp | A/G | | | intron-variant | Dmwd | Mm_Celera | 7:19077378 | TCCTGGAGTTTAGGG[A/G]CTCCAGGCTGAAGGA | 13401 |
rs217225855 | in-del | -/G | | | intron-variant | Dmwd | Mm_Celera | 7:19078862 | CCCGTTCACAGCAGT[-/G]GACCCTCCTTGCAGA | 13401 |
rs217232693 | snp | C/G | | | missense | Dmwd | Mm_Celera | 7:19076403 | CGACGCGCAGGTCGG[C/G]CCCGACCTCCGCTCA | 13401 |
rs217678892 | snp | A/G | | | upstream-variant-2KB, downstream-variant-500B | Dmpk, Dmwd | Mm_Celera | 7:19083025 | GCTCTCCTTGGGGAG[A/G]GGAGGATGCTGGAAT | 13401 |
rs218721972 | snp | A/C | | | intron-variant | Dmwd | Mm_Celera | 7:19079744 | TTGCTTGGGCATGTC[A/C]TCTGAGTGTTGTTTC | 13401 |
rs219157032 | in-del | -/TCTC | | | upstream-variant-2KB, intron-variant | Dmpk, Dmwd | Mm_Celera | 7:19082030 | AAGTGGACCCCAGTT[-/TCTC]TCTTTTCTCTCCACT | 13401 |
rs220413061 | in-del | -/AATGATGGG | | | intron-variant | Dmwd | Mm_Celera | 7:19077171 | AAGGGGGTTTGGCAA[-/AATGATGGG]AGCTCTGAATTGATG | 13401 |
rs220917121 | snp | A/G | | | intron-variant | Dmwd | Mm_Celera | 7:19079192 | TCCACGAAACAGGAC[A/G]GCCGTTGGGCCATGT | 13401 |
rs221147303 | snp | C/G | | | intron-variant | Dmwd | Mm_Celera | 7:19076859 | TGGGGAGGTTCTCTC[C/G]GGTGGTGAGTGTTCA | 13401 |
rs221275761 | snp | C/G | | | synonymous-codon | Dmwd | Mm_Celera | 7:19076611 | GCCCTCCACGCCCTC[C/G]GGACTGGGCGCGGGA | 13401 |
rs221436603 | snp | A/G | | | upstream-variant-2KB | Dmwd | Mm_Celera | 7:19075731 | GTGAGATGGATCGGC[A/G]GGTAATGGCACTTGC | 13401 |
rs221656758 | snp | A/G | | | upstream-variant-2KB | Dmwd | Mm_Celera | 7:19076008 | TTAGGGTCTAGGGGC[A/G]TTCCCAACAGTCACA | 13401 |
rs222141653 | snp | C/G | | | intron-variant | Dmwd | Mm_Celera | 7:19077012 | TCCTGCCTTCTGGGC[C/G]TGTTGGAGGGAGTCT | 13401 |
rs222549827 | snp | C/T | | | synonymous-codon | Dmwd | Mm_Celera | 7:19081256 | TTGTATCATCACTGC[C/T]TGCCAAGAGGGCCTC | 13401 |
rs222748185 | snp | C/T | | | intron-variant | Dmwd | Mm_Celera | 7:19079916 | TCTTCACTGGCAGCC[C/T]TTCCCAGTATCCCTG | 13401 |
rs222881272 | in-del | -/T | | | utr-variant-3-prime, upstream-variant-2KB, downstream-variant-500B | Rsph6a, Dmwd | Mm_Celera | 7:19074328 | TAGCAACAGATTGTA[-/T]TTTTCCTATTGGTTT | 13401 |
rs222946786 | in-del | -/T | | | downstream-variant-500B, upstream-variant-2KB | Rsph6a, Dmwd | Mm_Celera | 7:19074456 | TGGGCAGCTGGCTCA[-/T]TCATTCCTTCTCCAT | 13401 |
rs223006358 | snp | C/T | | | intron-variant | Dmwd | Mm_Celera | 7:19081323 | CCGCACCTGCCCAAG[C/T]GCTGAGGGGCACCAG | 13401 |
rs223683106 | snp | A/G | | | upstream-variant-2KB | Dmwd | Mm_Celera | 7:19075674 | CAGATGTTGGGTCAA[A/G]TTTGAAAACTGCCTG | 13401 |
rs223699184 | snp | C/T | | | intron-variant | Dmwd | Mm_Celera | 7:19080019 | CACCACTTCCCAACC[C/T]CACCCTGGTGTTCCC | 13401 |
rs223702913 | snp | A/G | | | intron-variant | Dmwd | Mm_Celera | 7:19079164 | CAGAATAGAAGGAAC[A/G]TCTTAGATAAATTCC | 13401 |
rs223713936 | snp | C/T | | | downstream-variant-500B, upstream-variant-2KB | Rsph6a, Dmwd | Mm_Celera | 7:19074864 | TGTTCAGAGCACTGT[C/T]TGCTCTTCCAAAAGA | 13401 |
rs224025633 | snp | C/G | | | intron-variant | Dmwd | Mm_Celera | 7:19078026 | TCTCCTGCTCTAACC[C/G]GTTAACTCGTCTCCT | 13401 |
rs225221332 | snp | C/T | | | upstream-variant-2KB, downstream-variant-500B | Dmpk, Dmwd | Mm_Celera | 7:19083211 | CCAGGCAGCTCCGCC[C/T]TCAACCCCTAAAATG | 13401 |
rs225429728 | in-del | -/TTGTTG | | | upstream-variant-2KB | Dmwd | Mm_Celera | 7:19075047 | GAGTTTGTGGTATTT[-/TTGTTG]TTGTTGTTGTTTTGT | 13401 |
rs226850107 | in-del | -/GTG | | | intron-variant | Dmwd | GRCm38.p3 | 7:19079525 | GGGTGGGGTGGGGGT[-/GTG]GGGGGGTGAGAGGCA | 13401 |
rs227394515 | snp | G/T | | | upstream-variant-2KB | Dmwd | Mm_Celera | 7:19075131 | TGTCTCACAAGGGGG[G/T]CGGGGGGAGCAAAAC | 13401 |
rs227441714 | snp | C/T | | | downstream-variant-500B, upstream-variant-2KB | Rsph6a, Dmwd | Mm_Celera | 7:19074490 | CGTTTTATTTTTGGT[C/T]TTTCAAGACAGGGTT | 13401 |
rs227540276 | in-del | -/AGGT | | | upstream-variant-2KB | Dmwd | Mm_Celera | 7:19075751 | ATGGCACTTGCTGCC[-/AGGT]AGGTAGCTTGAAGAC | 13401 |
rs227562929 | in-del | -/G | | | intron-variant | Dmwd | Mm_Celera | 7:19079520 | ACGGGGGGGTGGGGT[-/G]GGGGTGGGGGGTGAG | 13401 |
rs228380007 | snp | C/T | | | intron-variant | Dmwd | Mm_Celera | 7:19078289 | CTACCCACCCCTGCC[C/T]GCACTAAGCTGCCTG | 13401 |
rs228396085 | snp | A/C | | | intron-variant | Dmwd | Mm_Celera | 7:19077407 | GAAATGAGGCTTTGG[A/C]GATGGATCCCAGGAT | 13401 |
rs228767344 | snp | C/T | | | synonymous-codon | Dmwd | Mm_Celera | 7:19078060 | GCGGTTCAAGTCCAT[C/T]GATCTCAACAAGCCC | 13401 |
rs228825569 | snp | A/G | | | intron-variant | Dmwd | Mm_Celera | 7:19077356 | GCTGGCTGAACCACA[A/G]CAGATGTCCTGGAGT | 13401 |
rs229104408 | snp | A/C | | | upstream-variant-2KB | Dmwd | Mm_Celera | 7:19076074 | TGACCACACCCACAT[A/C]TTGCCTCCGCCCACA | 13401 |
rs229140413 | snp | A/G | | | upstream-variant-2KB | Dmwd | Mm_Celera | 7:19075315 | AAGAAGGGCATGTGT[A/G]CTTGTTTTCTTGTGC | 13401 |
rs229350099 | snp | C/T | | | upstream-variant-2KB, intron-variant | Dmpk, Dmwd | Mm_Celera | 7:19082216 | GGGTGGCTCCTTCTC[C/T]GGGTTCTGGCAGAAG | 13401 |
rs229503755 | snp | A/G | | | upstream-variant-2KB | Dmwd | Mm_Celera | 7:19075199 | AAATACCTTGACAAA[A/G]GGCCGCTTAGGGGAG | 13401 |
rs229708774 | snp | C/T | | | downstream-variant-500B, upstream-variant-2KB | Rsph6a, Dmwd | Mm_Celera | 7:19074547 | ATCTCACTCTGTAGA[C/T]CAGGCTGGCCTCCAA | 13401 |
rs229807007 | snp | C/T | | | synonymous-codon | Dmwd | Mm_Celera | 7:19081163 | GTGCCCTCGGATCCA[C/T]GAGGTGCCACTGCTG | 13401 |
rs229830834 | snp | A/G | | | intron-variant | Dmwd | Mm_Celera | 7:19079749 | TGGGCATGTCCTCTG[A/G]GTGTTGTTTCAGCTG | 13401 |
rs229924543 | in-del | -/A | | | intron-variant | Dmwd | Mm_Celera | 7:19077255 | AAGCAATCCTAGAAG[-/A]GGGGTGACGTGAGGA | 13401 |
rs230027862 | snp | G/T | | | upstream-variant-2KB, intron-variant | Dmpk, Dmwd | Mm_Celera | 7:19082049 | TTTCTCTCCACTGTC[G/T]TCCCCTGTATGCCCA | 13401 |
rs230303130 | snp | C/T | | | intron-variant | Dmwd | Mm_Celera | 7:19078689 | TTTGCTAGCCTGGCT[C/T]CAAAGGAGCCAGGAC | 13401 |