SNP - dbSNP |
dbSNP | Type | Alleles | Het | Se(het) | Fxn-class | Gene Name | Assembly | Chr-pos | Sequence | Entrez Gene |
rs3023346 | snp | C/T | 0.484877 | 0.0856314 | intron-variant | Trim9 | GRCm38.p3 | 12:70257972 | TGCTTCCTTCCTGCA[C/T]TCCACAGTATAAACA | 94090 |
rs3089042 | snp | A/G | 0.489796 | 0.070696 | intron-variant | Trim9 | GRCm38.p3 | 12:70257941 | CAGAATGCACACTGC[A/G]GTCGTTGTATTTGTG | 94090 |
rs3687368 | snp | C/G | 0.5 | 0 | intron-variant | Trim9 | Mm_Celera | 12:70262358 | CTTTGCAGCTATTCC[C/G]TTAAGATTCTTGATA | 94090 |
rs3689845 | snp | A/G | 0.484429 | 0.0868505 | intron-variant | Trim9 | Mm_Celera | 12:70262731 | AGCATTAGGTGCACG[A/G]GAACTATTGCTTCAG | 94090 |
rs3695792 | snp | A/G | 0.489796 | 0.070696 | intron-variant, utr-variant-3-prime | Trim9 | Mm_Celera | 12:70266539 | AGGTTGTCAGTAGCT[A/G]ATTTGAGCGGTCTAT | 94090 |
rs3696480 | snp | C/T | 0.5 | 0 | intron-variant, utr-variant-3-prime | Trim9 | Mm_Celera | 12:70266677 | ACCACCTTCTGCTCC[C/T]AGGGGCAATGTGGCC | 94090 |
rs6189244 | snp | C/T | 0.489796 | 0.070696 | intron-variant, utr-variant-3-prime, nc-transcript-variant | Trim9 | Mm_Celera | 12:70266414 | TGTGGTACCGGGGAT[C/T]GCAGGTCCACATCTT | 94090 |
rs6327000 | snp | A/C | 0.207612 | 0.24638 | intron-variant | Trim9 | Mm_Celera | 12:70326171 | AGACCCAAACACACA[A/C]ATGAATATCAAATAC | 94090 |
rs6328631 | snp | A/G | 0.444444 | 0.157135 | intron-variant | Trim9 | Mm_Celera | 12:70326471 | GGGTTGTTATTCTAG[A/G]AGGAATGGGAATCAA | 94090 |
rs6351852 | snp | A/G | 0.489796 | 0.070696 | intron-variant | Trim9 | Mm_Celera | 12:70248963 | ACCCCCTGCAGAGAC[A/G]GCCACCTCTCATGAC | 94090 |
rs6352439 | snp | C/T | 0.290657 | 0.246672 | intron-variant | Trim9 | Mm_Celera | 12:70249105 | ACCACAGGGCATCAG[C/T]TCTGCTCTGCACTTA | 94090 |
rs6353498 | snp | C/T | 0.5 | 0 | intron-variant | Trim9 | Mm_Celera | 12:70249305 | CACAATGACTTTGAA[C/T]GAAGACATTAGATTC | 94090 |
rs6366160 | snp | C/T | 0.290657 | 0.246672 | intron-variant | Trim9 | Mm_Celera | 12:70249322 | AAGACATTAGATTCT[C/T]TCTGTAAAATGACAG | 94090 |
rs6366288 | snp | A/C | 0.290657 | 0.246672 | intron-variant | Trim9 | Mm_Celera | 12:70249398 | TTCAGTGGTTTCCAG[A/C]GATCCNAGTATAAAC | 94090 |
rs6366304 | snp | A/G | 0.5 | 0 | intron-variant | Trim9 | Mm_Celera | 12:70249404 | GGTTTCCAGNGATCC[A/G]AGTATAAACACCACC | 94090 |
rs6366766 | snp | A/T | 0.304688 | 0.243945 | intron-variant | Trim9 | Mm_Celera | 12:70249451 | CTTTTGATGCAGCTG[A/T]TGACTGCAGAGCACC | 94090 |
rs13481517 | snp | A/G | 0.448558 | 0.151903 | synonymous-codon, upstream-variant-2KB, nc-transcript-variant | Trim9, Gm32151 | Mm_Celera | 12:70346836 | AGCCGGTGACAGGTG[A/G]GTGGGCGGTGGCGGC | 94090 |
rs29121461 | snp | A/C/G | 0.48 | 0.0979796 | intron-variant | Trim9 | GRCm38.p3 | 12:70331202 | ATCCCCAACAACATC[A/C/G]ATAGTCATCGGAGAC | 94090 |
rs29123104 | snp | C/T | 0.5 | 0 | intron-variant | Trim9 | Mm_Celera | 12:70279404 | TTTCTGTTTTGCTCT[C/T]GATATGGCCTCTTAC | 94090 |
rs29124418 | snp | A/G | 0.487535 | 0.077957 | intron-variant | Trim9 | Mm_Celera | 12:70262860 | GAGGGGGTGCCATGC[A/G]GGTGGACAATTGTTT | 94090 |
rs29125086 | snp | G/T | 0.475309 | 0.108333 | intron-variant | Trim9 | Mm_Celera | 12:70277105 | TCATTATTTCATAAT[G/T]GTCAGATTACATTAA | 94090 |
rs29125366 | snp | A/G | 0.487535 | 0.077957 | intron-variant | Trim9 | Mm_Celera | 12:70322612 | TGCATAGTTCAGAAT[A/G]TTTAGTAAATAATAA | 94090 |
rs29125466 | snp | G/T | 0.495 | 0.0497494 | intron-variant | Trim9 | Mm_Celera | 12:70258166 | ATTGCCATCTTTATC[G/T]GACAACCACTAGAGA | 94090 |
rs29125955 | snp | A/G | 0.487535 | 0.077957 | intron-variant, utr-variant-3-prime, nc-transcript-variant | Trim9 | Mm_Celera | 12:70267281 | GCTTGTAAAATAAAA[A/G]AACATTAACGCCTCA | 94090 |
rs29126673 | snp | A/T | 0.475309 | 0.108333 | upstream-variant-2KB, intron-variant | Trim9, Gm32151 | Mm_Celera | 12:70349655 | GAGTTTAACATTTTT[A/T]AAATTAATTTCTGTT | 94090 |
rs29126949 | snp | A/G | 0.444444 | 0.157135 | intron-variant | Trim9 | Mm_Celera | 12:70311521 | GCCAAGGCCAGCTCT[A/G]GGGATTCTCACCTCC | 94090 |
rs29127164 | snp | A/G | 0.5 | 0 | intron-variant | Trim9 | Mm_Celera | 12:70306773 | TGTGATTGCCTGTGC[A/G]CGCACACACACATGC | 94090 |
rs29127450 | snp | C/T | 0.444444 | 0.157135 | intron-variant | Trim9 | Mm_Celera | 12:70335998 | TGGAAAATGTTTTCC[C/T]ATTACATTCAAGAGC | 94090 |
rs29127518 | snp | C/T | 0.429688 | 0.173817 | intron-variant | Trim9 | Mm_Celera | 12:70313644 | TACATAACTCACTAT[C/T]GTAGGTGTAATTAGC | 94090 |
rs29127527 | snp | A/G | 0.475309 | 0.108333 | intron-variant | Trim9 | Mm_Celera | 12:70251853 | ATTGGGTGTAGAGAA[A/G]ATGAGGTTCTTATAC | 94090 |
rs29128535 | snp | C/T | 0.5 | 0 | intron-variant | Trim9 | Mm_Celera | 12:70297364 | GTTCCTGGAGGCTGG[C/T]GAGCCAGGGAATTGC | 94090 |
rs29129077 | snp | C/T | 0.48 | 0.0979796 | intron-variant | Trim9 | Mm_Celera | 12:70303424 | ACACAGTGTGACCAC[C/T]GCCTCCTGCCCTAGC | 94090 |
rs29129805 | snp | A/G | 0.475309 | 0.108333 | intron-variant | Trim9 | Mm_Celera | 12:70258740 | GCTGTCAGGACTGAT[A/G]GTTTCCTCTTATTCT | 94090 |
rs29130726 | snp | A/G | 0.465374 | 0.126941 | intron-variant | Trim9 | Mm_Celera | 12:70280878 | TTTCTGAAGCAAAGC[A/G]GAATATTTTTTTTTT | 94090 |
rs29130939 | snp | A/C | 0.444444 | 0.157135 | downstream-variant-500B | Trim9 | Mm_Celera | 12:70244063 | AGGACTCAGATGGAG[A/C]AGGCACTTTAGTGAC | 94090 |
rs29132418 | snp | A/C | 0.487535 | 0.077957 | intron-variant | Trim9 | Mm_Celera | 12:70280464 | ACTCTCACTCTGGAT[A/C]GTACAACCTTCATCA | 94090 |
rs29133337 | snp | A/C | 0.465374 | 0.126941 | intron-variant | Trim9 | Mm_Celera | 12:70256362 | CTACCGCAAGTTTTA[A/C]TACTGCAAGGAAGCA | 94090 |
rs29134173 | snp | A/T | 0.493827 | 0.0552116 | upstream-variant-2KB, intron-variant | Trim9, Gm32151 | Mm_Celera | 12:70349453 | TTGTCAGATTAGTGA[A/T]CTGAAGCTAAGAAAA | 94090 |
rs29134889 | snp | G/T | 0.475309 | 0.108333 | upstream-variant-2KB, intron-variant | Trim9, Gm32151 | Mm_Celera | 12:70349352 | GCTTTCCAGATGACT[G/T]CCGTTTGTTGGGAAG | 94090 |
rs29134949 | snp | A/G | 0.48 | 0.0979796 | intron-variant | Trim9 | Mm_Celera | 12:70313645 | ACATAACTCACTATT[A/G]TAGGTGTAATTAGCC | 94090 |
rs29135175 | snp | A/G | 0.5 | 0 | intron-variant | Trim9 | Mm_Celera | 12:70345208 | CATCAAATGGTCATT[A/G]CAGTCTCCATCTGGG | 94090 |
rs29135277 | snp | C/T | 0.5 | 0 | intron-variant | Trim9 | Mm_Celera | 12:70334020 | TTCAAATAATCGTGT[C/T]CTGTACTAGGTACAC | 94090 |
rs29137702 | snp | A/T | 0.444444 | 0.157135 | intron-variant | Trim9 | Mm_Celera | 12:70277873 | AGGTGGATGGACCAG[A/T]CTCAGAAGGGCAGCG | 94090 |
rs29137897 | snp | A/C | 0.475309 | 0.108333 | upstream-variant-2KB, synonymous-codon, nc-transcript-variant | Trim9, Gm32151 | Mm_Celera | 12:70347939 | AGCTTTTTCCCTACC[A/C]GAGGCAAAGGCTCAG | 94090 |
rs29138196 | snp | A/C | 0.495 | 0.0497494 | intron-variant | Trim9 | Mm_Celera | 12:70281792 | CCTACACTCTGCGAT[A/C]TGGGCTATCTGGACC | 94090 |
rs29140714 | snp | A/G | 0.465374 | 0.126941 | intron-variant | Trim9 | Mm_Celera | 12:70334800 | CTGCAATGAAGACCT[A/G]TTTTAGGTAACCGCC | 94090 |
rs29141106 | snp | C/T | 0.444444 | 0.157135 | intron-variant, utr-variant-3-prime, downstream-variant-500B | Trim9 | Mm_Celera | 12:70265790 | GAATGAAATGTGCCC[C/T]TCTGAGACACAGACC | 94090 |
rs29141509 | snp | A/G | 0.484429 | 0.0868505 | intron-variant | Trim9 | Mm_Celera | 12:70340137 | TAGCAACAAGTAGCT[A/G]GTTTGTTGTTGACAC | 94090 |
rs29142803 | snp | A/C | 0.444444 | 0.157135 | intron-variant | Trim9 | Mm_Celera | 12:70284505 | ATTTATAATTTTATT[A/C]TTTAAAGAATAATGT | 94090 |
rs29145912 | snp | A/G | 0.444444 | 0.157135 | intron-variant, utr-variant-3-prime | Trim9 | Mm_Celera | 12:70265111 | GAATTACTTGCATAT[A/G]GGGTGGGAGAGCCAG | 94090 |
rs29146401 | snp | G/T | 0.493827 | 0.0552116 | intron-variant | Trim9 | Mm_Celera | 12:70247194 | TGGAAATCAGGTCCC[G/T]CTGGGCTGTAAGCAG | 94090 |
rs29146643 | snp | C/T | 0.487535 | 0.077957 | intron-variant | Trim9 | Mm_Celera | 12:70279291 | CGCCTGGCCTGGTTT[C/T]TTCAGCTTTCAAGTA | 94090 |
rs29146961 | snp | A/C | 0.475309 | 0.108333 | intron-variant | Trim9 | Mm_Celera | 12:70259032 | TGAGAGGCATGAAGC[A/C]GGCAGGGGAACTGAC | 94090 |
rs29147167 | snp | A/G | 0.497778 | 0.0332592 | intron-variant | Trim9 | Mm_Celera | 12:70301008 | AGCAGTCTGCTGCCT[A/G]ATACTGCTGGGAACA | 94090 |
rs29147254 | snp | A/G | 0.49827 | 0.0293608 | intron-variant | Trim9 | Mm_Celera | 12:70261136 | CAGATGGATGGAGGC[A/G]GATTCTGCTTAGACG | 94090 |
rs29147272 | snp | A/G | 0.475309 | 0.108333 | intron-variant | Trim9 | Mm_Celera | 12:70274227 | TTCCTTGGACTGTCT[A/G]TCTCATTAGCTCCAG | 94090 |
rs29149301 | snp | A/G | 0.484429 | 0.0868505 | intron-variant | Trim9 | Mm_Celera | 12:70313014 | GAAATGATCTTACAC[A/G]TCTTCTAAGCTTGCT | 94090 |
rs29149347 | snp | A/G | 0.455 | 0.143091 | intron-variant | Trim9 | Mm_Celera | 12:70343696 | TGGCCTGTGCCTAAC[A/G]GATATTTATTCACAG | 94090 |
rs29149674 | snp | A/G | 0.336735 | 0.234472 | intron-variant | Trim9 | Mm_Celera | 12:70339843 | GCAGGGTGCACCCAG[A/G]TTCTTACATATAAAC | 94090 |
rs29150284 | snp | C/T | 0.5 | 0 | intron-variant | Trim9 | Mm_Celera | 12:70311759 | TCATTGGCTCATTAC[C/T]GCAAACCCCAACATG | 94090 |
rs29150490 | snp | A/G/T | 0.49827 | 0.0293608 | intron-variant | Trim9 | GRCm38.p3 | 12:70280527 | CCCGCTGGGGACAGC[A/G/T]TGTTGACCCTGGAGA | 94090 |
rs29150577 | snp | C/T | 0.493827 | 0.0552116 | intron-variant | Trim9 | Mm_Celera | 12:70246942 | ACCTTCTTATCTGTA[C/T]CACCCCCATCAAGAG | 94090 |
rs29151006 | snp | C/G | 0.5 | 0 | intron-variant, utr-variant-3-prime, downstream-variant-500B | Trim9 | Mm_Celera | 12:70265898 | CAAACCACCCAGCCA[C/G]CCCAGCAAAACAACA | 94090 |
rs29151083 | snp | A/G | 0.48 | 0.0979796 | intron-variant | Trim9 | Mm_Celera | 12:70296049 | TGTGTCGGAGGGGTC[A/G]GAGGCTCTTGGTTTG | 94090 |
rs29151195 | snp | A/C | 0.444444 | 0.157135 | intron-variant | Trim9 | Mm_Celera | 12:70284478 | CTAGGGTCGCCCTCC[A/C]CAAAGTGTATTATTT | 94090 |
rs29151287 | snp | C/G | 0.5 | 0 | intron-variant | Trim9 | Mm_Celera | 12:70261250 | GCTCAGGTGGACTCT[C/G]GGGGGGAGGCTATGT | 94090 |
rs29152896 | snp | A/C | 0.484429 | 0.0868505 | intron-variant | Trim9 | Mm_Celera | 12:70277737 | GCACTGTGTGCACCG[A/C]TAAGCGAACACGTGA | 94090 |
rs29153014 | snp | G/T | 0.5 | 0 | intron-variant | Trim9 | Mm_Celera | 12:70342419 | TGAAAATATTTACCC[G/T]ATTTTTAAAAAAATA | 94090 |
rs29153514 | snp | A/G | 0.5 | 0 | intron-variant | Trim9 | Mm_Celera | 12:70344039 | CTCTGATATTGACTG[A/G]ACAAATTGAAATGGA | 94090 |
rs29153559 | snp | C/T | 0.487535 | 0.077957 | intron-variant | Trim9 | Mm_Celera | 12:70259517 | GTATGGCAGGCACAG[C/T]TTTGGAACTGAGCAG | 94090 |
rs29153772 | snp | G/T | 0.444444 | 0.157135 | intron-variant | Trim9 | Mm_Celera | 12:70345345 | AGGGAAGGTCCCGGG[G/T]GTTGGCTGAGGAACA | 94090 |
rs29154554 | snp | A/G | 0.498615 | 0.0262793 | intron-variant | Trim9 | Mm_Celera | 12:70328738 | CAGTGTAAGCAGAAT[A/G]TCCAGGCTCTATTCA | 94090 |
rs29154976 | snp | C/G | 0.5 | 0 | intron-variant | Trim9 | Mm_Celera | 12:70306540 | GGATGGCTAGTGGGA[C/G]GGTGCTGAACTAGCC | 94090 |
rs29156112 | snp | C/G | 0.475309 | 0.108333 | intron-variant | Trim9 | Mm_Celera | 12:70255416 | CCCCAGACCAGACAA[C/G]CATTCCAGCACCACT | 94090 |
rs29156968 | snp | A/G | 0.444444 | 0.157135 | intron-variant | Trim9 | Mm_Celera | 12:70247061 | AAAAACTTTGAACGA[A/G]GTTTTTCTTAGATTG | 94090 |
rs29158731 | snp | A/C | 0.5 | 0 | intron-variant | Trim9 | Mm_Celera | 12:70306130 | TAATGCAAAACAAAC[A/C]ACAGGAACAAAGAAA | 94090 |
rs29158975 | snp | A/G | 0.465374 | 0.126941 | intron-variant | Trim9 | Mm_Celera | 12:70343224 | GAACTGCTAAAAATC[A/G]CAAAGTGGTGCTGGC | 94090 |
rs29159206 | snp | C/T | 0.487535 | 0.077957 | intron-variant | Trim9 | Mm_Celera | 12:70277349 | TGTCTCAACTGCAGC[C/T]AGTCAACTGATATTG | 94090 |
rs29159488 | snp | C/T | 0.5 | 0 | intron-variant | Trim9 | Mm_Celera | 12:70263087 | CCCGTGTCATGCTTA[C/T]AGGCACGTGCCACGT | 94090 |
rs29159629 | snp | G/T | 0.5 | 0 | intron-variant | Trim9 | Mm_Celera | 12:70275013 | GAGACATCTTTGGTT[G/T]TCCCTTTATAATGGG | 94090 |
rs29159631 | snp | A/C | 0.5 | 0 | intron-variant | Trim9 | Mm_Celera | 12:70274490 | GAAACAAAAAAAAAA[A/C]CTTGGGGGGAAGAAA | 94090 |
rs29159635 | snp | A/G | 0.498615 | 0.0262793 | intron-variant | Trim9 | Mm_Celera | 12:70333265 | CAGCCTTAGCTTAGA[A/G]CGGCAGACTTTGCTA | 94090 |
rs29159969 | snp | C/T | 0.487535 | 0.077957 | intron-variant | Trim9 | Mm_Celera | 12:70297801 | AGTTGTTAACCCTGG[C/T]TGTGATCCAGGAAAA | 94090 |
rs29160631 | snp | A/C | 0.493827 | 0.0552116 | intron-variant | Trim9 | Mm_Celera | 12:70247886 | GGGGCTACTGCTTCC[A/C]AGCCCTGTTGCACAA | 94090 |
rs29160859 | snp | C/T | 0.475309 | 0.108333 | intron-variant | Trim9 | Mm_Celera | 12:70317332 | ACCGCTGCTCCATAC[C/T]CGGGAACTCAGAGCC | 94090 |
rs29160950 | snp | A/G | 0.5 | 0 | intron-variant | Trim9 | Mm_Celera | 12:70336043 | TTAGTACAACCTTAA[A/G]TTAAAGTGTCTAGTA | 94090 |
rs29161183 | snp | C/T | 0.495 | 0.0497494 | intron-variant | Trim9 | Mm_Celera | 12:70294857 | AACTATCTGATTTCT[C/T]ACATTTCAACCTTAA | 94090 |
rs29161253 | snp | C/T | 0.493827 | 0.0552116 | intron-variant, utr-variant-3-prime, nc-transcript-variant | Trim9 | Mm_Celera | 12:70267341 | CTTCTTCTAGACAGA[C/T]TGTCTCCAATGACCA | 94090 |
rs29161288 | snp | C/G | 0.5 | 0 | intron-variant | Trim9 | Mm_Celera | 12:70274611 | GGCATGTCTAAACTG[C/G]AACCTGTTGCTTATC | 94090 |
rs29161692 | snp | G/T | 0.459184 | 0.136902 | intron-variant | Trim9 | Mm_Celera | 12:70249612 | CACCACCACAGGCAA[G/T]CTTGCTATTTACAAG | 94090 |
rs29165312 | snp | C/T | 0.465374 | 0.126941 | intron-variant | Trim9 | Mm_Celera | 12:70338346 | TTAAGTAAATCTTTA[C/T]CTACCATCCGCTACA | 94090 |
rs29165878 | snp | G/T | 0.487535 | 0.077957 | intron-variant | Trim9 | Mm_Celera | 12:70277590 | AATGCCTAAAGGATT[G/T]TTCTGGATCTTCTAT | 94090 |
rs29169768 | snp | A/G | 0.455 | 0.143091 | intron-variant | Trim9 | Mm_Celera | 12:70343735 | TCAGCAGTAGAAATG[A/G]TTACTATCACAGAAT | 94090 |
rs29169825 | snp | C/T | 0.493827 | 0.0552116 | intron-variant | Trim9 | Mm_Celera | 12:70283649 | CCCATGAAACCAGGG[C/T]AAGCGTTGAGAGTTT | 94090 |
rs29169861 | snp | A/T | 0.48 | 0.0979796 | intron-variant | Trim9 | Mm_Celera | 12:70307537 | ATCCACCAAGGTGCC[A/T]CTTCACACCCACTAG | 94090 |
rs29170250 | snp | C/T | 0.493827 | 0.0552116 | intron-variant | Trim9 | Mm_Celera | 12:70267687 | AGCAAGCAAGAGCTA[C/T]AAAGACACGGAGAAT | 94090 |
rs29170906 | snp | C/T | 0.487535 | 0.077957 | intron-variant | Trim9 | Mm_Celera | 12:70297853 | AGTTCTTAAGGGCAC[C/T]TGAAGCATGTGTGAT | 94090 |
rs29171726 | snp | C/T | 0.375 | 0.216506 | intron-variant | Trim9 | Mm_Celera | 12:70316336 | ACAGCACTGAGCCTC[C/T]CCAGTTCTTATTTAT | 94090 |
rs29172292 | snp | A/C | 0.493827 | 0.0552116 | intron-variant | Trim9 | Mm_Celera | 12:70260945 | CTGGGGTGCTGGCCA[A/C]AGGAATAGGTGACTG | 94090 |
rs29173014 | snp | A/C | 0.455 | 0.143091 | intron-variant | Trim9 | Mm_Celera | 12:70338669 | AAATTTTTCAAGACC[A/C]AAAACACCGAAGAAT | 94090 |
rs29173089 | snp | G/T | 0.487535 | 0.077957 | intron-variant | Trim9 | Mm_Celera | 12:70274529 | AATGTCAGGTCTTGA[G/T]TTTGTCTCATATTTA | 94090 |
rs29173257 | snp | A/T | 0.48 | 0.0979796 | intron-variant | Trim9 | Mm_Celera | 12:70303492 | GGTCTTCAAGTCACA[A/T]CAAATCTTTGCTCCC | 94090 |
rs29173419 | snp | G/T | 0.5 | 0 | upstream-variant-2KB, intron-variant | Trim9, Gm32151 | Mm_Celera | 12:70348175 | AACGAATCGCTATGG[G/T]ACTGAAGATTCCAAA | 94090 |
rs29173597 | snp | C/T | 0.484429 | 0.0868505 | intron-variant | Trim9 | Mm_Celera | 12:70277781 | CGTGGTCTGTGATGC[C/T]CAGCTCTCAGACCTC | 94090 |
rs29174384 | snp | C/T | 0.498615 | 0.0262793 | intron-variant, utr-variant-3-prime | Trim9 | Mm_Celera | 12:70265428 | TGTGTATTTTAGAAC[C/T]AATTTTTTAATGTAT | 94090 |
rs29174674 | snp | C/T | 0.46875 | 0.121031 | intron-variant | Trim9 | Mm_Celera | 12:70328477 | AAAAAATCAGGACAA[C/T]CCTCTTCTGGACTCT | 94090 |
rs29175190 | snp | C/T | 0.5 | 0 | intron-variant, utr-variant-3-prime | Trim9 | Mm_Celera | 12:70266872 | CCCTCTCTGTGGGCA[C/T]AGGTCATGTGAGTGT | 94090 |
rs29175264 | snp | A/T | 0.456747 | 0.140554 | intron-variant | Trim9 | Mm_Celera | 12:70257236 | TACACCATTTTTTTT[A/T]AACTCTTGAACTCGC | 94090 |
rs29177263 | snp | C/T | 0.5 | 0 | intron-variant | Trim9 | Mm_Celera | 12:70343364 | ACTTACACAGAGAAA[C/T]CTCATCTCAAAAACC | 94090 |
rs29177293 | snp | A/C | 0.48 | 0.0979796 | intron-variant | Trim9 | Mm_Celera | 12:70294398 | ATGATGCAGGATTCA[A/C]AGGACAGATTCCTCG | 94090 |
rs29177383 | snp | A/T | 0.475309 | 0.108333 | intron-variant | Trim9 | Mm_Celera | 12:70306017 | GCCTGTAGTTAACAA[A/T]GTTCACAACACCTTG | 94090 |
rs29177667 | snp | G/T | 0.48 | 0.0979796 | intron-variant, downstream-variant-500B | Trim9 | Mm_Celera | 12:70263361 | AAATTCTCAGTAGCT[G/T]GGCATAAAGTGATAT | 94090 |
rs29178138 | snp | C/T | 0.444444 | 0.157135 | intron-variant, utr-variant-3-prime | Trim9 | Mm_Celera | 12:70265086 | TTCTCTTTTTATTTA[C/T]TTACTTATTGAATTA | 94090 |
rs29178251 | snp | A/T | 0.375 | 0.216506 | intron-variant | Trim9 | Mm_Celera | 12:70298674 | TTCAAACTCCTTGTC[A/T]TCTACAAGAAGACAA | 94090 |
rs29178488 | snp | A/C/G | 0.444444 | 0.157135 | intron-variant | Trim9 | GRCm38.p3 | 12:70284200 | TGTAATCTATTTTTC[A/C/G]ACCCCAGTTTAACGC | 94090 |
rs29179261 | snp | C/T | 0.444444 | 0.157135 | intron-variant | Trim9 | Mm_Celera | 12:70275169 | AGGTGTGGCTTGGGG[C/T]TGTTTATGTTCTACA | 94090 |
rs29179948 | snp | A/G | 0.48 | 0.0979796 | intron-variant | Trim9 | Mm_Celera | 12:70313661 | TAGGTGTAATTAGCC[A/G]AGGAACATAATACAA | 94090 |
rs29183845 | snp | C/T | 0.5 | 0 | upstream-variant-2KB, intron-variant | Trim9, Gm32151 | Mm_Celera | 12:70349470 | TGAAGCTAAGAAAAC[C/T]AGAGGAACCTCTCAC | 94090 |
rs29184959 | snp | A/G | 0.375 | 0.216506 | intron-variant | Trim9 | Mm_Celera | 12:70335831 | GGCACCGTGTAAATG[A/G]TCAAGGCCAGCAGAC | 94090 |
rs29185660 | snp | C/T | 0.49827 | 0.0293608 | intron-variant | Trim9 | Mm_Celera | 12:70283838 | GAACTCTCAGGCTTT[C/T]CCAGCAGCCGAGAAC | 94090 |
rs29185698 | snp | C/T | 0.444444 | 0.157135 | intron-variant | Trim9 | Mm_Celera | 12:70308031 | AACTCCTCATTTAGA[C/T]GGCTGTGTTGTTCAT | 94090 |
rs29186384 | snp | A/G | 0.487535 | 0.077957 | intron-variant | Trim9 | Mm_Celera | 12:70295327 | AAGAGCTCTGTCTTC[A/G]TTTAGTATCTAATAT | 94090 |
rs29187017 | snp | C/G | 0.465374 | 0.126941 | upstream-variant-2KB, intron-variant | Trim9, Gm32151 | GRCm38.p3 | 12:70349594 | GAGGTTCTGGTGTAA[C/G]GAACCTGAAATGTTA | 94090 |
rs29187066 | snp | A/G | 0.487535 | 0.077957 | intron-variant | Trim9 | Mm_Celera | 12:70343683 | CTATGTAAGATAATG[A/G]CCTGTGCCTAACGGA | 94090 |
rs29187545 | snp | A/G | 0.5 | 0 | intron-variant | Trim9 | Mm_Celera | 12:70306484 | AAAAGGTTTTTCTCT[A/G]TGAGTCACAGAATGT | 94090 |
rs29187577 | snp | A/G | 0.48 | 0.0979796 | intron-variant | Trim9 | Mm_Celera | 12:70313663 | GGTGTAATTAGCCGA[A/G]GAACATAATACAAAT | 94090 |
rs29187935 | snp | A/G | 0.495 | 0.0497494 | intron-variant, downstream-variant-500B | Trim9 | Mm_Celera | 12:70263426 | TGTATTTACTTCACG[A/G]TGTGATTCTACAAAG | 94090 |
rs29187983 | snp | C/T | 0.475309 | 0.108333 | intron-variant | Trim9 | Mm_Celera | 12:70312404 | TGACTGGGTTGGATC[C/T]GGAAGCTATAAATGA | 94090 |
rs29188632 | snp | C/G | 0.5 | 0 | intron-variant | Trim9 | Mm_Celera | 12:70303271 | GGATACAAATCTCTG[C/G]ATATGCCTATGAGAG | 94090 |
rs29189191 | snp | C/T | 0.444444 | 0.157135 | intron-variant | Trim9 | Mm_Celera | 12:70344542 | CAGCCCACCCACCGA[C/T]GCCACCCCCCCCAAA | 94090 |
rs29189739 | snp | A/G | 0.465374 | 0.126941 | intron-variant | Trim9 | Mm_Celera | 12:70333426 | TCTCTGCTTGGGCCA[A/G]TGGTCCCAACTAGTT | 94090 |
rs29189760 | snp | A/G | 0.493827 | 0.0552116 | intron-variant, synonymous-codon | Trim9 | Mm_Celera | 12:70255117 | AAAGTAGGACCTCCC[A/G]GGGAAGCTGGGTTGT | 94090 |
rs29190236 | snp | C/T | 0.444444 | 0.157135 | intron-variant | Trim9 | Mm_Celera | 12:70284484 | TCGCCCTCCCCAAAG[C/T]GTATTATTTATAATT | 94090 |
rs29191645 | snp | A/G | 0.5 | 0 | intron-variant | Trim9 | Mm_Celera | 12:70328895 | AACAAAAATGAATAG[A/G]GATGAAGCTCAGTGG | 94090 |
rs29192042 | snp | A/G | 0.5 | 0 | intron-variant | Trim9 | Mm_Celera | 12:70306789 | CGCACACACACATGC[A/G]TGTGTGCACATGCAT | 94090 |
rs29192484 | snp | A/G | 0.493827 | 0.0552116 | intron-variant | Trim9 | Mm_Celera | 12:70303803 | CTATGAGTCTGAGAC[A/G]TTTGTTTCTTTGTTA | 94090 |
rs29192529 | snp | A/G | 0.5 | 0 | intron-variant | Trim9 | Mm_Celera | 12:70343330 | TGGTCTACAAAACGA[A/G]GTCCAAGACAGCCAG | 94090 |
rs29192545 | snp | A/G | 0.5 | 0 | intron-variant | Trim9 | Mm_Celera | 12:70259384 | GTGCTTTTAAGCACC[A/G]GGCCACCTCTCCAGC | 94090 |
rs29192654 | snp | A/G | 0.49827 | 0.0293608 | intron-variant | Trim9 | Mm_Celera | 12:70282871 | ACTTCCACTTTCTGA[A/G]CTGATACTTCCTACC | 94090 |
rs29193049 | snp | A/G | 0.49827 | 0.0293608 | intron-variant | Trim9 | Mm_Celera | 12:70281101 | TGGAAGGAGGCCTGC[A/G]AGGCAGAGAGGCTGC | 94090 |
rs29193258 | snp | A/G | 0.465374 | 0.126941 | intron-variant | Trim9 | Mm_Celera | 12:70291450 | GCATAGTTCCTGCCA[A/G]CAAATGCAATGAACG | 94090 |
rs29193778 | snp | C/T | 0.487535 | 0.077957 | intron-variant | Trim9 | Mm_Celera | 12:70313889 | AAATCACCAGTATGG[C/T]TTTAAAGAGAGCGAT | 94090 |
rs29196206 | snp | C/T | 0.493827 | 0.0552116 | intron-variant | Trim9 | Mm_Celera | 12:70274370 | AAACACAAATCTCCC[C/T]GTTAGACAAAGGCAT | 94090 |
rs29196485 | snp | C/T | 0.49827 | 0.0293608 | intron-variant | Trim9 | Mm_Celera | 12:70274666 | GAATTAGTTTTTCTT[C/T]TTCCATATTTATCTA | 94090 |
rs29196964 | snp | C/T | 0.475309 | 0.108333 | intron-variant | Trim9 | Mm_Celera | 12:70268010 | CCAGGCTGCCAGCCA[C/T]GTTAGACGCCACGTA | 94090 |
rs29197181 | snp | C/T | 0.444444 | 0.157135 | intron-variant, utr-variant-3-prime | Trim9 | Mm_Celera | 12:70265082 | AATTTTCTCTTTTTA[C/T]TTACTTACTTATTGA | 94090 |
rs29197600 | snp | C/T | 0.498615 | 0.0262793 | intron-variant | Trim9 | Mm_Celera | 12:70260770 | TCATGCCACGGGTCG[C/T]AGGGTGTCTTCTAAT | 94090 |
rs29198364 | snp | A/G | 0.5 | 0 | intron-variant | Trim9 | Mm_Celera | 12:70297363 | TGTTCCTGGAGGCTG[A/G]TGAGCCAGGGAATTG | 94090 |
rs29200173 | snp | A/G | 0.487535 | 0.077957 | intron-variant | Trim9 | Mm_Celera | 12:70259424 | GGCAAGCTTTAATGT[A/G]CTATTTTGGGGACTC | 94090 |
rs29200326 | snp | G/T | 0.465374 | 0.126941 | intron-variant | Trim9 | Mm_Celera | 12:70338271 | GGCTGATCTATAAAC[G/T]TAAAATGCTGGGATT | 94090 |
rs29201852 | snp | A/G | 0.487535 | 0.077957 | intron-variant | Trim9 | Mm_Celera | 12:70300462 | CACTTATTTCTACCC[A/G]ATGGGCAGTTTTTTT | 94090 |
rs29202693 | snp | A/G | 0.465374 | 0.126941 | intron-variant | Trim9 | Mm_Celera | 12:70338373 | TACATACAAGATATG[A/G]GTAGAGACAAAGATA | 94090 |
rs29203087 | snp | C/T | 0.493827 | 0.0552116 | intron-variant | Trim9 | Mm_Celera | 12:70253047 | TCTTTTCCTTCTTAG[C/T]TTAGCTTTGCTACAG | 94090 |
rs29203347 | snp | A/G | 0.487535 | 0.077957 | intron-variant | Trim9 | Mm_Celera | 12:70300809 | GAAAGGTCTTCCTTG[A/G]GCTAAGTGGTGAGCA | 94090 |
rs29203478 | snp | G/T | 0.493827 | 0.0552116 | intron-variant, utr-variant-3-prime | Trim9 | Mm_Celera | 12:70264346 | ATATGTTTATTTTTA[G/T]AAGTGACTACCTATT | 94090 |
rs29203521 | snp | A/T | 0.5 | 0 | intron-variant | Trim9 | Mm_Celera | 12:70342426 | ATTTACCCGATTTTT[A/T]AAAAAATATTTTTGA | 94090 |
rs29204547 | snp | C/T | 0.5 | 0 | intron-variant | Trim9 | Mm_Celera | 12:70306557 | GTGCTGAACTAGCCC[C/T]GAATAAGGTGGATGT | 94090 |
rs29204778 | snp | A/G | 0.465374 | 0.126941 | intron-variant | Trim9 | Mm_Celera | 12:70333121 | AGCGACACACGACAC[A/G]CAGATAGTAGCGAGC | 94090 |
rs29205877 | snp | A/G | 0.408163 | 0.193609 | intron-variant, utr-variant-3-prime | Trim9 | Mm_Celera | 12:70266873 | CCTCTCTGTGGGCAT[A/G]GGTCATGTGAGTGTT | 94090 |
rs29206142 | snp | C/T | 0.497778 | 0.0332592 | intron-variant | Trim9 | Mm_Celera | 12:70313170 | GAATCCATATTCATC[C/T]GAGAAAGGAACCTGC | 94090 |
rs29207214 | snp | A/G | 0.487535 | 0.077957 | intron-variant | Trim9 | Mm_Celera | 12:70312209 | AGCTTAGGGAAGATC[A/G]GGATTATTGTCTCAT | 94090 |
rs29207277 | snp | C/G | 0.5 | 0 | intron-variant, utr-variant-3-prime, downstream-variant-500B | Trim9 | Mm_Celera | 12:70265816 | AGACCTGTTGTTCTG[C/G]AGTTTGGAAAGACGT | 94090 |
rs29207729 | snp | C/T | 0.48 | 0.0979796 | intron-variant | Trim9 | Mm_Celera | 12:70303333 | TATCCTAAATAGTGG[C/T]ACCATAATAGGCTGA | 94090 |
rs29207916 | snp | C/G | 0.408163 | 0.193609 | intron-variant | Trim9 | Mm_Celera | 12:70277867 | AGGGTCAGGTGGATG[C/G]ACCAGTCTCAGAAGG | 94090 |
rs29207961 | snp | C/T | 0.49827 | 0.0293608 | intron-variant | Trim9 | Mm_Celera | 12:70335152 | CAACACTTTCCAAAG[C/T]GAAGTCCTTAAGGAG | 94090 |
rs29210615 | snp | G/T | 0.444444 | 0.157135 | intron-variant | Trim9 | Mm_Celera | 12:70344834 | TATGTAGTAGAAGAT[G/T]GCCTAGTCGGCCAAC | 94090 |
rs29210817 | snp | A/T | 0.465374 | 0.126941 | intron-variant | Trim9 | Mm_Celera | 12:70338318 | ATCTTCCTCTCACCA[A/T]TTTTTTCCTTTATTA | 94090 |
rs29211038 | snp | A/G | 0.498615 | 0.0262793 | intron-variant | Trim9 | Mm_Celera | 12:70281819 | GACCAGGAAGCGGAA[A/G]CTAGTAAACTGACCT | 94090 |
rs29212666 | snp | C/T | 0.487535 | 0.077957 | intron-variant | Trim9 | Mm_Celera | 12:70260855 | TGCACTGTGGATGAA[C/T]CTTTTATTCTCTCAG | 94090 |
rs29214116 | snp | A/G/T | 0.290657 | 0.246672 | intron-variant | Trim9 | GRCm38.p3 | 12:70304069 | TTACAGGCCAATTTC[A/G/T]GTCTATAATAGCACA | 94090 |
rs29214147 | snp | C/T | 0.465374 | 0.126941 | intron-variant | Trim9 | Mm_Celera | 12:70342216 | CCACCTCCTCCAAAA[C/T]CTGAACTGCTTCTAG | 94090 |
rs29215396 | snp | C/T | 0.475309 | 0.108333 | intron-variant | Trim9 | Mm_Celera | 12:70312516 | CACTCTAAGATCACA[C/T]CAGGGCTCATGGTGA | 94090 |
rs29216123 | snp | A/C | 0.475309 | 0.108333 | intron-variant, upstream-variant-2KB | Trim9, Gm32151 | Mm_Celera | 12:70345528 | ATTCTTTCTCGGTAG[A/C]CCGGGGAGAGACCCT | 94090 |
rs29217954 | snp | C/G | 0.444444 | 0.157135 | intron-variant | Trim9 | Mm_Celera | 12:70299928 | ACAGACACACACACA[C/G]ACACACACACACACA | 94090 |
rs29219478 | snp | A/G | 0.432133 | 0.171253 | intron-variant | Trim9 | Mm_Celera | 12:70334327 | TGAAAGCTATTTATC[A/G]TATTTCCTTGCTACA | 94090 |
rs29220448 | snp | C/T | 0.49827 | 0.0293608 | intron-variant | Trim9 | Mm_Celera | 12:70281405 | GCAACCTGTCTAGTA[C/T]CACTGGGAAAAATAA | 94090 |
rs29220519 | snp | C/T | 0.498615 | 0.0262793 | intron-variant | Trim9 | Mm_Celera | 12:70256661 | ACACATGTATGGATA[C/T]TAGGGACTATCCTGC | 94090 |
rs29221248 | snp | A/G | 0.444444 | 0.157135 | intron-variant | Trim9 | Mm_Celera | 12:70339828 | ACAATAGTAACGAAG[A/G]CAGGGTGCACCCAGG | 94090 |
rs29222625 | snp | A/G | 0.475309 | 0.108333 | intron-variant | Trim9 | Mm_Celera | 12:70247123 | CTGGTGTACAGGCTG[A/G]CCTCTGAAGAATTAG | 94090 |
rs29222639 | snp | A/G | 0.5 | 0 | intron-variant | Trim9 | Mm_Celera | 12:70302672 | TTAGTGGGGGGGGGG[A/G]GAAGCTTTGCCCCCA | 94090 |
rs29222961 | snp | A/G | 0.492188 | 0.0620098 | intron-variant | Trim9 | Mm_Celera | 12:70329688 | GAGTAGGTTATGATA[A/G]TGAAGGAACATCAAT | 94090 |
rs29223824 | snp | C/T | 0.444444 | 0.157135 | intron-variant | Trim9 | Mm_Celera | 12:70284408 | CTCTGAGTGGCCTCA[C/T]GGGGAGCCACAGGGG | 94090 |
rs29483990 | snp | A/G | 0.487535 | 0.077957 | intron-variant | Trim9 | Mm_Celera | 12:70311956 | TAGTTTGGGGACAGG[A/G]TTTCAGAAGGACCTC | 94090 |
rs29484077 | snp | C/T | 0.444444 | 0.157135 | intron-variant | Trim9 | Mm_Celera | 12:70284503 | TTATTTATAATTTTA[C/T]TATTTAAAGAATAAT | 94090 |
rs29485760 | snp | C/T | 0.48 | 0.0979796 | intron-variant, downstream-variant-500B | Trim9 | Mm_Celera | 12:70263690 | TCACACACACACACA[C/T]ATATATGTGAAATAT | 94090 |
rs29489008 | snp | A/G | 0.5 | 0 | intron-variant | Trim9 | Mm_Celera | 12:70280288 | TTCTTTTTAGATAAC[A/G]TCTTACTAGGTAGTC | 94090 |
rs29489162 | snp | C/T | 0.487535 | 0.077957 | intron-variant, utr-variant-3-prime | Trim9 | Mm_Celera | 12:70267192 | CCACGAGTAAGACAA[C/T]ACCCAAAAGTCTCAA | 94090 |
rs29489255 | snp | C/T | 0.489796 | 0.070696 | intron-variant | Trim9 | Mm_Celera | 12:70313138 | AGGCAGCAGGACAGG[C/T]CATGCTGCAGCTCAG | 94090 |
rs29490100 | snp | G/T | 0.475309 | 0.108333 | intron-variant | Trim9 | Mm_Celera | 12:70314216 | GGAAACGGTTGTTAT[G/T]GCCTGAAGCTGTGTG | 94090 |
rs29490883 | snp | A/T | 0.5 | 0 | intron-variant | Trim9 | Mm_Celera | 12:70292972 | TCAGGAACTTTGAGA[A/T]ATTCCACCAGACCCC | 94090 |
rs29491475 | snp | C/T | 0.375 | 0.216506 | intron-variant | Trim9 | Mm_Celera | 12:70335749 | ATTAGATGCTCATAA[C/T]GCATCTGAAGTGTTT | 94090 |
rs32250167 | snp | C/T | 0.231111 | 0.249285 | intron-variant | Trim9 | Mm_Celera | 12:70258762 | TCTTATTCTTCCCTG[C/T]GCTTCTTTCCCTTCC | 94090 |
rs32250170 | snp | A/G | 0.493827 | 0.0552116 | intron-variant | Trim9 | Mm_Celera | 12:70259022 | ATTTAGTAGTTGAGA[A/G]GCATGAAGCCGGCAG | 94090 |
rs32250544 | snp | C/T | 0.124444 | 0.216185 | intron-variant, utr-variant-3-prime | Trim9 | Mm_Celera | 12:70265317 | GTCTGGCTTCATTCA[C/T]GTGTCCATCTTGGAC | 94090 |
rs32250546 | snp | A/G | 0.124444 | 0.216185 | intron-variant, utr-variant-3-prime | Trim9 | Mm_Celera | 12:70265368 | TCAGTGGAGTAACCT[A/G]ACTCGAACCTATGTA | 94090 |
rs32251199 | snp | C/T | 0.48 | 0.0979796 | intron-variant | Trim9 | Mm_Celera | 12:70259670 | ATGTTCTCTGCTCCT[C/T]GGGAAGATTTAAAAA | 94090 |
rs32251202 | snp | C/T | 0.132653 | 0.220748 | intron-variant | Trim9 | Mm_Celera | 12:70260542 | CACTAATTGTAGGAA[C/T]GTCAGAGTTCTGTGG | 94090 |
rs32251466 | snp | A/G | 0.32 | 0.24 | intron-variant | Trim9 | Mm_Celera | 12:70252895 | CAACAGTTTACCGAT[A/G]TGCCCTAGGTTTGCT | 94090 |
rs32251469 | snp | A/G | 0.124444 | 0.216185 | intron-variant | Trim9 | Mm_Celera | 12:70252998 | ACAGCGATTAACAGC[A/G]GCATGACCTGAGTGT | 94090 |
rs32251472 | snp | A/G | 0.231111 | 0.249285 | intron-variant | Trim9 | Mm_Celera | 12:70252999 | CAGCGATTAACAGCG[A/G]CATGACCTGAGTGTT | 94090 |
rs32251474 | snp | A/G | 0.124444 | 0.216185 | intron-variant, utr-variant-3-prime | Trim9 | Mm_Celera | 12:70265565 | CCATTGTGTATCACC[A/G]TGCCCACTTATCAAA | 94090 |
rs32251478 | snp | A/C | 0.124444 | 0.216185 | intron-variant, utr-variant-3-prime, downstream-variant-500B | Trim9 | Mm_Celera | 12:70265925 | AACAAGAAACTTCAG[A/C]GTGAACTTTCCAGAA | 94090 |
rs32251482 | snp | A/G | 0.231111 | 0.249285 | intron-variant, utr-variant-3-prime, nc-transcript-variant | Trim9 | GRCm38.p3 | 12:70266449 | CTAATAATAGACACC[A/G]GTATCTCGTGAACAT | 94090 |
rs32252264 | snp | A/G | 0.231111 | 0.249285 | intron-variant | Trim9 | Mm_Celera | 12:70260596 | CCTAGAAAGGCAAGA[A/G]CACATCTAAGCCACA | 94090 |
rs32252267 | snp | A/C | 0.5 | 0 | intron-variant | Trim9 | Mm_Celera | 12:70260619 | AAGCCACATGCTCAG[A/C]TGTGGCCAGACTGGA | 94090 |
rs32252270 | snp | C/T | 0.231111 | 0.249285 | intron-variant | Trim9 | Mm_Celera | 12:70260745 | TTAGAAGTGTGCAAA[C/T]AGGCAAAGTTCATGC | 94090 |
rs32252357 | snp | A/C | 0.231111 | 0.249285 | intron-variant | Trim9 | Mm_Celera | 12:70253414 | TTACAAGAACTAAGA[A/C]GGCAACTTGTTATCA | 94090 |
rs32252360 | snp | C/T | 0.231111 | 0.249285 | intron-variant | Trim9 | Mm_Celera | 12:70253531 | CTCATGGTTGATTTT[C/T]ATGTTTAATTTCTGC | 94090 |
rs32252363 | snp | A/G | 0.231111 | 0.249285 | intron-variant | Trim9 | Mm_Celera | 12:70253762 | TTCCCATTAATTTAA[A/G]CACAACATTGTACAT | 94090 |
rs32252554 | snp | C/T | 0.124444 | 0.216185 | utr-variant-3-prime | Trim9 | Mm_Celera | 12:70245273 | TGGTGTGGTTTGCAA[C/T]TTCAGAGGCCCGGGG | 94090 |
rs32252557 | snp | G/T | 0.142012 | 0.225474 | utr-variant-3-prime | Trim9 | Mm_Celera | 12:70245465 | GTGGGAAAGCATTGG[G/T]TTGGTACTTGTCTGG | 94090 |
rs32252560 | snp | A/G | 0.142012 | 0.225474 | utr-variant-3-prime | Trim9 | Mm_Celera | 12:70245544 | GTGACACCGTCTTGG[A/G]CATGTTTCCTTACTT | 94090 |
rs32252563 | snp | A/G | 0.124444 | 0.216185 | utr-variant-3-prime | Trim9 | Mm_Celera | 12:70246084 | AAAGTAATTCAACCT[A/G]CGTTAACACAAAAAA | 94090 |
rs32252616 | snp | A/G | 0.124444 | 0.216185 | intron-variant, utr-variant-3-prime | Trim9 | Mm_Celera | 12:70266769 | GTGTTTCAGGAAATG[A/G]GACGACAGCTCTCAA | 94090 |
rs32252621 | snp | C/T | 0.231111 | 0.249285 | intron-variant, utr-variant-3-prime | Trim9 | Mm_Celera | 12:70266893 | ATGTGAGTGTTTCAT[C/T]CTTAACAAACCTCTT | 94090 |
rs32253176 | snp | C/G | 0.124444 | 0.216185 | utr-variant-3-prime | Trim9 | Mm_Celera | 12:70246328 | TTGTACGACTGTCCG[C/G]TGAGGCTGCTGGCTC | 94090 |
rs32253216 | snp | A/G | 0.231111 | 0.249285 | intron-variant | Trim9 | Mm_Celera | 12:70253963 | TGTGGGAAAGCCAGC[A/G]GTGCACAGAAAAACA | 94090 |
rs32253219 | snp | A/G | 0.48 | 0.0979796 | intron-variant | Trim9 | Mm_Celera | 12:70254158 | AGATGTGCATCGTGT[A/G]TATCCATGATTACAA | 94090 |
rs32253222 | snp | C/T | 0.48 | 0.0979796 | intron-variant | Trim9 | Mm_Celera | 12:70254483 | AGGCTTTTGCTTTCC[C/T]TGCTCTGTAGGATGG | 94090 |
rs32253247 | snp | G/T | 0.32 | 0.24 | intron-variant | Trim9 | Mm_Celera | 12:70260884 | AGTAGGGTTGTTCAC[G/T]GGACAGCCGTGCTTA | 94090 |
rs32253250 | snp | C/T | 0.124444 | 0.216185 | intron-variant | Trim9 | Mm_Celera | 12:70260905 | GCCGTGCTTAGGAAC[C/T]GAAAGGCAAATGTGC | 94090 |
rs32253584 | snp | C/T | 0.297521 | 0.245442 | intron-variant, utr-variant-3-prime | Trim9 | Mm_Celera | 12:70266968 | TTGCTTTCGTGGCTA[C/T]GGGTCTTTGGCCCTC | 94090 |
rs32253587 | snp | A/G | 0.231111 | 0.249285 | intron-variant, utr-variant-3-prime | Trim9 | Mm_Celera | 12:70266984 | GGGTCTTTGGCCCTC[A/G]CTGTGGGACTCGGAG | 94090 |
rs32254115 | snp | A/C | 0.231111 | 0.249285 | intron-variant | Trim9 | Mm_Celera | 12:70254507 | AGGATGGGTTCTGCT[A/C]TCTGGCATGTCTTTG | 94090 |
rs32254118 | snp | C/T | 0.48 | 0.0979796 | intron-variant | Trim9 | Mm_Celera | 12:70254720 | GCGTGTGATGAAGAG[C/T]AAGTTTTCCATGGTG | 94090 |
rs32254121 | snp | G/T | 0.48 | 0.0979796 | intron-variant | Trim9 | Mm_Celera | 12:70254760 | GATGCAAAAAGAACA[G/T]CGTCCCACATCCCAA | 94090 |
rs32254217 | snp | A/G | 0.124444 | 0.216185 | intron-variant | Trim9 | Mm_Celera | 12:70248081 | GTAGAGAAGGCGTCT[A/G]TCTCCCGTGGGTGGC | 94090 |
rs32254220 | snp | A/G | 0.32 | 0.24 | intron-variant | Trim9 | Mm_Celera | 12:70248226 | GACTTTGAAGTAGCA[A/G]CCTGAGCAAGCCCTT | 94090 |
rs32254425 | snp | C/G | 0.231111 | 0.249285 | intron-variant | Trim9 | Mm_Celera | 12:70261588 | CCTAGAACATCCCTA[C/G]TGACACCTAGTAGAG | 94090 |
rs32254428 | snp | A/T | 0.124444 | 0.216185 | intron-variant | Trim9 | Mm_Celera | 12:70262230 | TGCCTTAACTGGGGT[A/T]GGATAACTGCTTCCT | 94090 |
rs32254432 | snp | C/T | 0.260355 | 0.249785 | intron-variant | Trim9 | Mm_Celera | 12:70262836 | CACAGAGATGTAGTG[C/T]AGACTGTAGAGGGGG | 94090 |
rs32254730 | snp | C/T | 0.231111 | 0.249285 | intron-variant | Trim9 | Mm_Celera | 12:70269397 | ACCAGGAAAGTAAGT[C/T]AGGAACACAGTTTTG | 94090 |
rs32254733 | snp | A/T | 0.124444 | 0.216185 | intron-variant | Trim9 | Mm_Celera | 12:70269600 | AGCTTAACCGTGACC[A/T]GCAGCTAGGATTTAA | 94090 |
rs32255004 | snp | A/G | 0.231111 | 0.249285 | intron-variant | Trim9 | Mm_Celera | 12:70254971 | CGGATGATAAGAACA[A/G]CACGGGCATTTCAGA | 94090 |
rs32255009 | snp | A/G | 0.124444 | 0.216185 | intron-variant | Trim9 | Mm_Celera | 12:70255384 | GCTGAGGCTGGGAAC[A/G]CCCAGTGGGTCCGGA | 94090 |
rs32255076 | snp | G/T | 0.231111 | 0.249285 | intron-variant | Trim9 | Mm_Celera | 12:70272801 | AAATCTGGTATCAAG[G/T]GACAGAAGCCATGTC | 94090 |
rs32255078 | snp | C/T | 0.231111 | 0.249285 | intron-variant | Trim9 | Mm_Celera | 12:70272850 | GCACATGACATTATA[C/T]TCTCATGGCGGCTGT | 94090 |
rs32255080 | snp | A/G | 0.231111 | 0.249285 | intron-variant | Trim9 | Mm_Celera | 12:70272904 | GTCCACCTGTTTTTC[A/G]GGTCTAGAACAATTT | 94090 |
rs32255082 | snp | A/C/T | 0.48 | 0.0979796 | intron-variant | Trim9 | GRCm38.p3 | 12:70273464 | AAGGCTCCATACTTT[A/C/T]ATCACAGGAGAGAAC | 94090 |
rs32255191 | snp | A/G | 0.231111 | 0.249285 | intron-variant | Trim9 | Mm_Celera | 12:70249540 | AATCCTATCTCAGCA[A/G]AGCACAGACATTTAT | 94090 |
rs32255261 | snp | C/T | 0.124444 | 0.216185 | intron-variant, downstream-variant-500B | Trim9 | Mm_Celera | 12:70263562 | TTTCATAGAAGGCAC[C/T]CCGGATCTGTGGGAC | 94090 |
rs32255715 | snp | C/T | 0.124444 | 0.216185 | intron-variant | Trim9 | Mm_Celera | 12:70270089 | AGAGATTCTGAACAT[C/T]TGTGCACGTGAATCA | 94090 |
rs32255717 | snp | C/G | 0.497041 | 0.0383476 | intron-variant | Trim9 | Mm_Celera | 12:70270330 | GGAGAGAGGAGGCAG[C/G]TGGAGCTCTGAGTTT | 94090 |
rs32255720 | snp | C/T | 0.495868 | 0.0452663 | intron-variant | Trim9 | Mm_Celera | 12:70270417 | GTGGCTTAGTTTAAA[C/T]GTTAAGTTTAGGCTA | 94090 |
rs32255723 | snp | A/G | 0.5 | 0 | intron-variant | Trim9 | Mm_Celera | 12:70270432 | CGTTAAGTTTAGGCT[A/G]GTTTCAAAGTGTCAA | 94090 |
rs32255964 | snp | C/T | 0.32 | 0.24 | intron-variant | Trim9 | Mm_Celera | 12:70255455 | TTTTATGGTTTGCTA[C/T]AACTTTTAGTAACGG | 94090 |
rs32255967 | snp | A/G | 0.124444 | 0.216185 | intron-variant | Trim9 | Mm_Celera | 12:70255730 | TTATTTTAATCCTGG[A/G]ATACCCAAGACTTGA | 94090 |
rs32255970 | snp | A/G | 0.277778 | 0.248452 | intron-variant | Trim9 | Mm_Celera | 12:70255781 | TGCAGAGTGCCCTGG[A/G]AAGTCAGGCCTGACA | 94090 |
rs32255973 | snp | A/G | 0.231111 | 0.249285 | intron-variant | Trim9 | Mm_Celera | 12:70256341 | CTAGAGACCTTATAA[A/G]AAGGGCTACCGCAAG | 94090 |
rs32256134 | snp | G/T | 0.48 | 0.0979796 | intron-variant | Trim9 | Mm_Celera | 12:70273483 | ACAGGAGAGAACATG[G/T]TGAAATTCAAGTTCA | 94090 |
rs32256136 | snp | A/G | 0.497041 | 0.0383476 | intron-variant | Trim9 | Mm_Celera | 12:70273520 | TTTAGGTGAACACAT[A/G]TTAATTATGGAATTA | 94090 |
rs32256139 | snp | A/G | 0.231111 | 0.249285 | intron-variant | Trim9 | Mm_Celera | 12:70273691 | ATAGCTTCAATGCAC[A/G]TGATGCGAAGGTGAG | 94090 |
rs32256142 | snp | A/G | 0.5 | 0 | intron-variant | Trim9 | Mm_Celera | 12:70273798 | GAGCCGAAGGTGATC[A/G]TTTCAGAGCAGGGAG | 94090 |
rs32256176 | snp | C/T | 0.132653 | 0.220748 | intron-variant | Trim9 | Mm_Celera | 12:70249862 | TGGATTTGATATCAA[C/T]ATAAAATGCTTTGTG | 94090 |
rs32256179 | snp | C/T | 0.231111 | 0.249285 | intron-variant | Trim9 | Mm_Celera | 12:70250340 | CAAGAACAAGTGAGT[C/T]CTCATATAAAGCTAT | 94090 |
rs32256181 | snp | C/T | 0.124444 | 0.216185 | intron-variant | Trim9 | Mm_Celera | 12:70250386 | TAACACCAAGTTTCG[C/T]TAATGGCTTCTATTC | 94090 |
rs32256183 | snp | A/G | 0.32 | 0.24 | intron-variant | Trim9 | Mm_Celera | 12:70250859 | AAGACTGTGCGTCCC[A/G]TTCCCTAATGCTGTC | 94090 |
rs32256204 | snp | A/G | 0.132653 | 0.220748 | intron-variant, utr-variant-3-prime | Trim9 | Mm_Celera | 12:70264006 | GCCCCCAAGTTAAAG[A/G]AGAGGGCTGGACTTT | 94090 |
rs32256207 | snp | A/C/G | 0.231111 | 0.249285 | intron-variant, utr-variant-3-prime | Trim9 | GRCm38.p3 | 12:70264077 | ATGACCGAGATGCTC[A/C/G]GTTAGTTGGAGCTTT | 94090 |
rs32256209 | snp | C/T | 0.124444 | 0.216185 | intron-variant, utr-variant-3-prime | Trim9 | Mm_Celera | 12:70264148 | GAGATTTTTGCCTCA[C/T]GCATCATAATTTTGT | 94090 |
rs32256255 | snp | C/T | 0.132653 | 0.220748 | intron-variant | Trim9 | Mm_Celera | 12:70275774 | ACCATCCATTCCCTT[C/T]TACAGTGGCTGAACA | 94090 |
rs32256258 | snp | G/T | 0.132653 | 0.220748 | intron-variant | Trim9 | Mm_Celera | 12:70275802 | ACAATAAAAGCAGCA[G/T]TTAAGCTTTAGAGCA | 94090 |
rs32256261 | snp | A/G | 0.32 | 0.24 | intron-variant | Trim9 | Mm_Celera | 12:70276037 | ATCACTGTCCACTGG[A/G]AAGGCTGGCAATCAT | 94090 |
rs32256446 | snp | C/T | 0.497778 | 0.0332592 | intron-variant | Trim9 | Mm_Celera | 12:70270514 | GGAGCTGAAGACAGA[C/T]AGGGAAGTTCTCAGC | 94090 |
rs32256449 | snp | A/G | 0.489796 | 0.070696 | intron-variant | Trim9 | Mm_Celera | 12:70270584 | CTTGGAAAGGCAATA[A/G]CCTGAGGTGATAACC | 94090 |
rs32256452 | snp | C/T | 0.497041 | 0.0383476 | intron-variant | Trim9 | Mm_Celera | 12:70270737 | AAAGGAAACAAGAGA[C/T]GGGAGAGAGTCTTGA | 94090 |
rs32256635 | snp | C/T | 0.459184 | 0.136902 | intron-variant | Trim9 | Mm_Celera | 12:70286755 | CAGAATAGCAGCAAC[C/T]TCAATTTATATTTCA | 94090 |
rs32256638 | snp | G/T | 0.497778 | 0.0332592 | intron-variant | Trim9 | Mm_Celera | 12:70286823 | TGTAATTTCTTATGT[G/T]GGATACTGTGATAAG | 94090 |
rs32256641 | snp | A/C | 0.48 | 0.0979796 | intron-variant | Trim9 | Mm_Celera | 12:70286837 | TGGGATACTGTGATA[A/C]GTGCTTTTGCATGGC | 94090 |
rs32256828 | snp | A/C | 0.231111 | 0.249285 | intron-variant | Trim9 | Mm_Celera | 12:70256572 | TGTGGCATTTATGGT[A/C]ATTTCTTTGCTCAGA | 94090 |
rs32257025 | snp | C/T | 0.48 | 0.0979796 | intron-variant | Trim9 | Mm_Celera | 12:70273976 | AGCAGGGACAGAAGA[C/T]ATAACTTTAAAGGGC | 94090 |
rs32257028 | snp | A/T | 0.48 | 0.0979796 | intron-variant | Trim9 | Mm_Celera | 12:70274049 | CTACTGAGGGATAAC[A/T]TGAAGTCTATTCGTA | 94090 |
rs32257031 | snp | C/T | 0.132653 | 0.220748 | intron-variant | Trim9 | Mm_Celera | 12:70274075 | TCGTATGTGGAACTT[C/T]TGTTATTAAAACTAT | 94090 |
rs32257104 | snp | A/C | 0.124444 | 0.216185 | intron-variant, utr-variant-3-prime | Trim9 | Mm_Celera | 12:70264445 | TGGTCTACAGTCTAT[A/C]TGGAAAGCAATTTGG | 94090 |
rs32257106 | snp | C/T | 0.124444 | 0.216185 | intron-variant, utr-variant-3-prime | Trim9 | Mm_Celera | 12:70264478 | ACATAGGTCAAGGGT[C/T]TCAAAAATGCCCAGA | 94090 |
rs32257109 | snp | A/T | 0.497041 | 0.0383476 | intron-variant, utr-variant-3-prime | Trim9 | Mm_Celera | 12:70265081 | AAATTTTCTCTTTTT[A/T]TTTACTTACTTATTG | 94090 |
rs32257111 | snp | C/T | 0.124444 | 0.216185 | intron-variant, utr-variant-3-prime | Trim9 | Mm_Celera | 12:70265265 | AAATTCATAGTTGCT[C/T]ATGTTTATATTTCTT | 94090 |
rs32257125 | snp | A/C | 0.497041 | 0.0383476 | intron-variant | Trim9 | Mm_Celera | 12:70270808 | TCTAACAGAAGAAAA[A/C]CAGTCAGGAGGTGGC | 94090 |
rs32257128 | snp | A/G | 0.497041 | 0.0383476 | intron-variant | Trim9 | Mm_Celera | 12:70270981 | ATGCTCCTTTAGGGG[A/G]TCCCAGCATGGGAGC | 94090 |
rs32257131 | snp | A/G | 0.231111 | 0.249285 | intron-variant | Trim9 | Mm_Celera | 12:70271541 | TAGAGATTTGCCCAC[A/G]TTATTCTGTGGACAA | 94090 |
rs32257166 | snp | A/G | 0.231111 | 0.249285 | intron-variant | Trim9 | Mm_Celera | 12:70250884 | GCTGTCTCTATAATA[A/G]GCTATTGAACTAGGC | 94090 |
rs32257168 | snp | A/C | 0.231111 | 0.249285 | intron-variant | Trim9 | Mm_Celera | 12:70251344 | TGGCACACAGTGTCG[A/C]GTTCTCATGCTGCCA | 94090 |
rs32257170 | snp | A/C | 0.231111 | 0.249285 | intron-variant | Trim9 | Mm_Celera | 12:70251371 | GCCATGCAGGAAGGA[A/C]GTATTTGGGGCCAGA | 94090 |
rs32257172 | snp | C/T | 0.231111 | 0.249285 | intron-variant | Trim9 | Mm_Celera | 12:70251497 | TGGCTCAGACTGCAC[C/T]TCCAAACCAGCTGAT | 94090 |
rs32257184 | snp | G/T | 0.231111 | 0.249285 | intron-variant | Trim9 | Mm_Celera | 12:70276117 | GCCTGTACATGTGTA[G/T]GTTCTCTCGCAGCTC | 94090 |
rs32257187 | snp | C/T | 0.124444 | 0.216185 | intron-variant | Trim9 | Mm_Celera | 12:70276161 | GTCAGCTCAGATCGC[C/T]CTGTCCTTGCCTGTG | 94090 |
rs32257190 | snp | A/G | 0.124444 | 0.216185 | intron-variant | Trim9 | Mm_Celera | 12:70276269 | TTAAAGGAATGCACA[A/G]TTACTCGGTCTATGT | 94090 |
rs32257193 | snp | A/G | 0.142012 | 0.225474 | intron-variant | Trim9 | Mm_Celera | 12:70276371 | TTAGCAACATGACTT[A/G]ACTGTTCTCTGTGCT | 94090 |
rs32257384 | snp | A/G | 0.124444 | 0.216185 | intron-variant | Trim9 | Mm_Celera | 12:70286851 | AAGTGCTTTTGCATG[A/G]CCCACAAGGTGAGAA | 94090 |
rs32257387 | snp | C/T | 0.48 | 0.0979796 | intron-variant | Trim9 | Mm_Celera | 12:70286975 | GTATGACCTCTCACC[C/T]AGTCTGTTCTCTGTA | 94090 |
rs32257390 | snp | C/T | 0.345679 | 0.230967 | intron-variant | Trim9 | Mm_Celera | 12:70287122 | CTGGCTTTCCCAGCA[C/T]ACCATGCCTTTTGAA | 94090 |
rs32257393 | snp | C/T | 0.48 | 0.0979796 | intron-variant | Trim9 | Mm_Celera | 12:70287222 | CAGCCAGCAGCAGCT[C/T]TTGGAAATGGAAGAA | 94090 |
rs32257416 | snp | A/G | 0.142012 | 0.225474 | intron-variant | Trim9 | Mm_Celera | 12:70282644 | TACTAGAATAAGGAT[A/G]CCATTCAATACTCTA | 94090 |
rs32257418 | snp | C/G | 0.260355 | 0.249785 | intron-variant | Trim9 | Mm_Celera | 12:70282701 | TCCTTCTTAAGGAGA[C/G]TTGATTCGGGGGCTT | 94090 |
rs32257423 | snp | A/G | 0.18 | 0.24 | intron-variant | Trim9 | GRCm38.p3 | 12:70282932 | TTTAAAAGTATAATC[A/G]CTTTGTAAGGTCTAA | 94090 |
rs32257444 | snp | G/T | 0.132653 | 0.220748 | intron-variant | Trim9 | Mm_Celera | 12:70278825 | TACTTAAATTAAGAG[G/T]TGGAAAATGTAAATA | 94090 |
rs32257447 | snp | C/T | 0.132653 | 0.220748 | intron-variant | Trim9 | Mm_Celera | 12:70279076 | CTTTGAAGAGTACTG[C/T]TTTCATTTTTTAATT | 94090 |
rs32257452 | snp | A/G | 0.231111 | 0.249285 | intron-variant | Trim9 | Mm_Celera | 12:70279791 | CTCAGTGCCATAAAT[A/G]CCACTGCATAGCTGG | 94090 |
rs32257796 | snp | A/G | 0.231111 | 0.249285 | intron-variant | Trim9 | Mm_Celera | 12:70294155 | AATGCTTAAGGGAAC[A/G]TTCATTATGTCCCAT | 94090 |
rs32257799 | snp | A/C | 0.231111 | 0.249285 | intron-variant | Trim9 | Mm_Celera | 12:70294246 | AAAATGAGAATTCTA[A/C]TTCTTGAGTGTGGGC | 94090 |
rs32257864 | snp | C/G | 0.48 | 0.0979796 | intron-variant | Trim9 | Mm_Celera | 12:70274156 | CAAACTGTTGATCTA[C/G]AGATGCGGATGAATC | 94090 |
rs32257867 | snp | C/T | 0.142012 | 0.225474 | intron-variant | Trim9 | Mm_Celera | 12:70274162 | GTTGATCTAGAGATG[C/T]GGATGAATCTTCCTG | 94090 |
rs32257872 | snp | C/T | 0.46281 | 0.131194 | intron-variant | Trim9 | Mm_Celera | 12:70274282 | GATGCTGAGAGCAAG[C/T]GTACACTTCACCAAT | 94090 |
rs32257895 | snp | C/T | 0.231111 | 0.249285 | intron-variant | Trim9 | Mm_Celera | 12:70257301 | CCTTTCATGCCCAAC[C/T]CGATGGGATCTCACC | 94090 |
rs32257898 | snp | A/G | 0.231111 | 0.249285 | intron-variant | Trim9 | Mm_Celera | 12:70257828 | TTTAGCATATGGATC[A/G]TCTTTCTGGTCCTGC | 94090 |
rs32257914 | snp | C/T | 0.132653 | 0.220748 | intron-variant | Trim9 | Mm_Celera | 12:70271674 | GGGCACAGGTCCTGT[C/T]TGATAAAAGGCTCAT | 94090 |
rs32257917 | snp | C/T | 0.142012 | 0.225474 | intron-variant | Trim9 | Mm_Celera | 12:70272121 | GGCTCTGTCACACAG[C/T]TACACTGTCTTTCTG | 94090 |
rs32258086 | snp | A/G | 0.48 | 0.0979796 | intron-variant | Trim9 | Mm_Celera | 12:70287275 | CAAACAAAGTGCTAT[A/G]CTTGGTGAAGATGTC | 94090 |
rs32258089 | snp | A/T | 0.497041 | 0.0383476 | intron-variant | Trim9 | Mm_Celera | 12:70287404 | TGTAGCTATGGTGGC[A/T]GTTCTTAGAAGTGGC | 94090 |
rs32258092 | snp | C/T | 0.48 | 0.0979796 | intron-variant | Trim9 | Mm_Celera | 12:70287419 | AGTTCTTAGAAGTGG[C/T]GAGAGATACAATTAG | 94090 |
rs32258115 | snp | C/G | 0.32 | 0.24 | intron-variant | Trim9 | Mm_Celera | 12:70276401 | TCACATAATCCTAGG[C/G]TGATAGTCTTCGAAG | 94090 |
rs32258118 | snp | C/T | 0.124444 | 0.216185 | intron-variant | Trim9 | Mm_Celera | 12:70276425 | TTCGAAGAAAGTAGA[C/T]GCTCAAAACCTATTC | 94090 |
rs32258121 | snp | C/G | 0.231111 | 0.249285 | intron-variant | Trim9 | Mm_Celera | 12:70276444 | CAAAACCTATTCTCA[C/G]CCATACGGCAGAACC | 94090 |
rs32258334 | snp | A/G | 0.277778 | 0.248452 | intron-variant | Trim9 | Mm_Celera | 12:70251591 | TAAAGGGTGAGGGAT[A/G]TGCTAGGGTGTCTGT | 94090 |
rs32258337 | snp | A/G | 0.231111 | 0.249285 | intron-variant | Trim9 | Mm_Celera | 12:70251610 | TAGGGTGTCTGTGTG[A/G]CCCTGAGGCAGGGAG | 94090 |
rs32258340 | snp | A/G | 0.231111 | 0.249285 | intron-variant | Trim9 | Mm_Celera | 12:70251799 | AAAGCGTTACTCCTA[A/G]AGCTGGCGCGTAATG | 94090 |
rs32258342 | snp | C/T | 0.244898 | 0.249948 | intron-variant | Trim9 | Mm_Celera | 12:70251822 | GCGTAATGTACATGG[C/T]AGAAGCAGTTTGGAC | 94090 |
rs32258424 | snp | C/T | 0.244898 | 0.249948 | intron-variant | Trim9 | Mm_Celera | 12:70279838 | TAAGCACTTTCATTT[C/T]CTTTTGGTGCCGAAC | 94090 |
rs32258427 | snp | C/G | 0.142012 | 0.225474 | intron-variant | Trim9 | Mm_Celera | 12:70279850 | TTTTCTTTTGGTGCC[C/G]AACATAAAAAAAAAT | 94090 |
rs32258430 | snp | C/G | 0.32 | 0.24 | intron-variant | Trim9 | Mm_Celera | 12:70279902 | AGATCTTGCCATATT[C/G]TGCAGTTCCATAAGC | 94090 |
rs32258496 | snp | C/T | 0.48 | 0.0979796 | intron-variant | Trim9 | Mm_Celera | 12:70283319 | AGTCTTCTCTCAGCT[C/T]GCTTACCCATTAGCT | 94090 |
rs32258499 | snp | C/T | 0.231111 | 0.249285 | intron-variant | Trim9 | Mm_Celera | 12:70283353 | TGCTTAGGTTTTCTT[C/T]CTGCTTTTTATTGCT | 94090 |
rs32258502 | snp | A/C | 0.497778 | 0.0332592 | intron-variant | Trim9 | Mm_Celera | 12:70283487 | TGGCACCGTGTTTGC[A/C]GCTGGCAGCAGCCAA | 94090 |
rs32258754 | snp | G/T | 0.132653 | 0.220748 | intron-variant | Trim9 | Mm_Celera | 12:70274310 | AATTACAAAATCAAA[G/T]AATAAGACCATGAAA | 94090 |
rs32258759 | snp | C/T | 0.132653 | 0.220748 | intron-variant | Trim9 | GRCm38.p3 | 12:70274396 | GGCATCATTGAATGA[C/T]TAAGTGAAATGCATG | 94090 |
rs32258761 | snp | C/T | 0.231111 | 0.249285 | intron-variant | Trim9 | Mm_Celera | 12:70274432 | ACATGAAATTAAAAC[C/T]CCGGGGCTTCATTTT | 94090 |
rs32258805 | snp | A/G | 0.426035 | 0.177515 | intron-variant | Trim9 | Mm_Celera | 12:70287467 | ATCATACAGACAGAA[A/G]ACAGAACAGCTTTGC | 94090 |
rs32258808 | snp | A/G | 0.124444 | 0.216185 | intron-variant | Trim9 | Mm_Celera | 12:70287496 | GCTGCCGAGGGCAAC[A/G]GCCAGCCTCCTGTCT | 94090 |
rs32258811 | snp | A/G | 0.473373 | 0.11227 | intron-variant | Trim9 | Mm_Celera | 12:70287559 | GAAATGAGGGCACCA[A/G]TGTCCTCTGCCCAGT | 94090 |
rs32258834 | snp | C/T | 0.124444 | 0.216185 | intron-variant | Trim9 | Mm_Celera | 12:70294435 | ATCTGCTGGAAAACA[C/T]CTTTGTTCACCTTTC | 94090 |
rs32258837 | snp | C/T | 0.32 | 0.24 | intron-variant | Trim9 | Mm_Celera | 12:70294523 | TAGTGAGTCCACCAT[C/T]GTGAAGGGGCCATTC | 94090 |
rs32258840 | snp | C/T | 0.32 | 0.24 | intron-variant | Trim9 | Mm_Celera | 12:70294588 | GGAGTAAATTTTCTC[C/T]TTAAGAGCCATTTCC | 94090 |
rs32258884 | snp | C/T | 0.244898 | 0.249948 | intron-variant | Trim9 | Mm_Celera | 12:70276587 | GTGGCAAACAAAACA[C/T]AGTATGTCAGTTTTA | 94090 |
rs32258887 | snp | G/T | 0.132653 | 0.220748 | intron-variant | Trim9 | Mm_Celera | 12:70276656 | GGTTTGGAAAGAAGG[G/T]TGAAATGGTTTTCTC | 94090 |
rs32258890 | snp | A/G | 0.231111 | 0.249285 | intron-variant | Trim9 | Mm_Celera | 12:70276746 | AGTGTTCTCTAGACA[A/G]AGTTCACCTGCTGAG | 94090 |
rs32258893 | snp | A/G | 0.244898 | 0.249948 | intron-variant | Trim9 | Mm_Celera | 12:70276782 | CAGACCCAGAAAGGG[A/G]CATACTGCTAAGTCC | 94090 |
rs32258945 | snp | C/T | 0.124444 | 0.216185 | intron-variant | Trim9 | Mm_Celera | 12:70258060 | TCAGAGAAGGCTCCT[C/T]GGCTGTTAACTATCG | 94090 |
rs32258949 | snp | G/T | 0.124444 | 0.216185 | intron-variant | Trim9 | Mm_Celera | 12:70258285 | TTAGTGGGAAAGACC[G/T]GCAGAAAGCTGTCCA | 94090 |
rs32258952 | snp | C/T | 0.124444 | 0.216185 | intron-variant | Trim9 | Mm_Celera | 12:70258297 | ACCTGCAGAAAGCTG[C/T]CCACATGGTGGCAGG | 94090 |
rs32258985 | snp | C/T | 0.244898 | 0.249948 | intron-variant | Trim9 | Mm_Celera | 12:70298880 | TAGTCAACTATAGTT[C/T]TTTAAATACTGAGCT | 94090 |
rs32258988 | snp | A/C | 0.124444 | 0.216185 | intron-variant | Trim9 | Mm_Celera | 12:70299285 | CTCAGACTGCCTGAC[A/C]CACAATATGAAGAGG | 94090 |
rs32258991 | snp | C/T | 0.124444 | 0.216185 | intron-variant | Trim9 | Mm_Celera | 12:70299378 | GCAATTATTCTTTTT[C/T]GTGGTTTATGAACTT | 94090 |
rs32258993 | snp | C/G | 0.124444 | 0.216185 | intron-variant | Trim9 | Mm_Celera | 12:70300258 | TGGATAGTCTAATAA[C/G]CAGGCACAGAGGAAA | 94090 |
rs32259117 | snp | A/G | 0.489796 | 0.070696 | intron-variant | Trim9 | Mm_Celera | 12:70283756 | TGAGGGCCACTGCTT[A/G]GGTCAGGACAGGACA | 94090 |
rs32259122 | snp | A/G | 0.231111 | 0.249285 | intron-variant | Trim9 | Mm_Celera | 12:70283968 | AGGCTTGGTGTTAAA[A/G]AAGAGGACTCCACTC | 94090 |
rs32259275 | snp | C/T | 0.32 | 0.24 | intron-variant | Trim9 | Mm_Celera | 12:70280468 | TCACTCTGGATCGTA[C/T]AACCTTCATCACGGG | 94090 |
rs32259277 | snp | C/T | 0.231111 | 0.249285 | intron-variant | Trim9 | Mm_Celera | 12:70280497 | GGGTCATCCACAGTA[C/T]TGCAAGCAGCAGCAC | 94090 |
rs32259282 | snp | C/G/T | 0.231111 | 0.249285 | intron-variant | Trim9 | GRCm38.p3 | 12:70280818 | CTCCTCCAGCCTCAG[C/G/T]GTGCTTGGTGAGAAA | 94090 |
rs32259306 | snp | C/T | 0.231111 | 0.249285 | intron-variant | Trim9 | Mm_Celera | 12:70252112 | CATTGATAAAAAGCA[C/T]GTTTCCTTTGATAGA | 94090 |
rs32259309 | snp | A/G | 0.231111 | 0.249285 | intron-variant | Trim9 | Mm_Celera | 12:70252319 | TTGAAAACAGTTATA[A/G]TGGAGTTAGAATGAC | 94090 |
rs32259312 | snp | C/T | 0.231111 | 0.249285 | intron-variant | Trim9 | Mm_Celera | 12:70252831 | TGAGGACAAATTTGC[C/T]CAATAGAAGTGGAAG | 94090 |
rs32259495 | snp | A/C | 0.336735 | 0.234472 | intron-variant | Trim9 | Mm_Celera | 12:70294896 | ATGTCTGTGAAATGT[A/C]TATTATTATATAAAG | 94090 |
rs32259498 | snp | C/T | 0.48 | 0.0979796 | intron-variant | Trim9 | Mm_Celera | 12:70295236 | TGGCATGTACAAGTG[C/T]ACACACCCACTCAAC | 94090 |
rs32259503 | snp | C/T | 0.32 | 0.24 | intron-variant | Trim9 | Mm_Celera | 12:70295466 | ACAATTGTTTTGATA[C/T]TTGATAAACAGCTAC | 94090 |
rs32259594 | snp | A/G | 0.5 | 0 | intron-variant | Trim9 | Mm_Celera | 12:70287747 | ATCTAGCTACTGCAC[A/G]GGCCATGATGAGATC | 94090 |
rs32259597 | snp | C/T | 0.124444 | 0.216185 | intron-variant | Trim9 | Mm_Celera | 12:70287919 | TCTCATACAGGACAG[C/T]TATAGTCACCTCTAC | 94090 |
rs32259600 | snp | A/C | 0.18 | 0.24 | intron-variant | Trim9 | Mm_Celera | 12:70287975 | AATATTCACTGTGGT[A/C]ACTGTGGTGGTGCCA | 94090 |
rs32259603 | snp | C/T | 0.426035 | 0.177515 | intron-variant | Trim9 | Mm_Celera | 12:70287998 | TGGTGCCAGTTCTTG[C/T]AATGTTTGGTGAAAG | 94090 |
rs32259646 | snp | C/T | 0.46281 | 0.131194 | intron-variant | Trim9 | Mm_Celera | 12:70274604 | AGACAGTGGCATGTC[C/T]AAACTGCAACCTGTT | 94090 |
rs32259652 | snp | C/T | 0.244898 | 0.249948 | intron-variant | Trim9 | Mm_Celera | 12:70274776 | TAAAAGTAGATTTTT[C/T]TTAGTGGTGGCTGTT | 94090 |
rs32259655 | snp | C/G | 0.132653 | 0.220748 | intron-variant | Trim9 | Mm_Celera | 12:70276797 | GCATACTGCTAAGTC[C/G]TTAGCTACAGAGGCA | 94090 |
rs32259657 | snp | A/C | 0.32 | 0.24 | intron-variant | Trim9 | Mm_Celera | 12:70276873 | AGAACTCCATGGACG[A/C]TCACTGCAGACTATC | 94090 |
rs32259659 | snp | C/G | 0.244898 | 0.249948 | intron-variant | Trim9 | Mm_Celera | 12:70276945 | AAACCAGAAAGATGC[C/G]AAAAAAATTTTTTGT | 94090 |
rs32259955 | snp | C/T | 0.408163 | 0.193609 | intron-variant | Trim9 | Mm_Celera | 12:70283979 | TAAAGAAGAGGACTC[C/T]ACTCTCATCTAAGTT | 94090 |
rs32259958 | snp | A/C | 0.124444 | 0.216185 | intron-variant | Trim9 | Mm_Celera | 12:70284000 | CATCTAAGTTTGAAC[A/C]AGGTAAGTTCCCATC | 94090 |
rs32259961 | snp | A/G | 0.32 | 0.24 | intron-variant | Trim9 | Mm_Celera | 12:70284140 | ACTTATAAGTCACCA[A/G]TCTAAATAAATGGCA | 94090 |
rs32260006 | snp | A/G | 0.32 | 0.24 | intron-variant | Trim9 | Mm_Celera | 12:70300408 | ACCCACCAAATTTTA[A/G]AAATTTCTATGCCCT | 94090 |
rs32260010 | snp | A/T | 0.48 | 0.0979796 | intron-variant | Trim9 | Mm_Celera | 12:70300520 | GTCTCAGGACACAGT[A/T]AAAAACAGCCACCTT | 94090 |
rs32260013 | snp | A/G | 0.124444 | 0.216185 | intron-variant | Trim9 | Mm_Celera | 12:70300585 | TGTCTGGTCTCCTTG[A/G]CTCCTTGCTTGGTGT | 94090 |
rs32260054 | snp | C/G | 0.132653 | 0.220748 | intron-variant | Trim9 | Mm_Celera | 12:70289413 | CCTTCATTGTTGAAA[C/G]TTCCTCGGTTCAGCT | 94090 |
rs32260057 | snp | A/G | 0.231111 | 0.249285 | intron-variant | Trim9 | Mm_Celera | 12:70289477 | GGTGTTAGGTAACAG[A/G]CCTGCTGGGTAATAT | 94090 |
rs32260060 | snp | A/G | 0.231111 | 0.249285 | intron-variant | Trim9 | Mm_Celera | 12:70289532 | ACTTCCCTTAAAGTA[A/G]CCCCTGTATCTCCAA | 94090 |
rs32260063 | snp | A/C | 0.244898 | 0.249948 | intron-variant | Trim9 | Mm_Celera | 12:70289575 | CTGGGCCATAACTGT[A/C]TGCTCCCCTCACCAG | 94090 |
rs32260215 | snp | A/G | 0.231111 | 0.249285 | intron-variant | Trim9 | Mm_Celera | 12:70280843 | GAGAAAGACTGTGGC[A/G]TGACTAGAGTGGCCC | 94090 |
rs32260220 | snp | C/T | 0.231111 | 0.249285 | intron-variant | Trim9 | Mm_Celera | 12:70280956 | TTACATGAACTATGC[C/T]CATGCATTTATTACT | 94090 |
rs32260223 | snp | A/G | 0.231111 | 0.249285 | intron-variant | Trim9 | Mm_Celera | 12:70281005 | AACCTTAAAGAATAG[A/G]GTACAGCAGGAACTA | 94090 |
rs32260245 | snp | A/G | 0.124444 | 0.216185 | intron-variant | Trim9 | Mm_Celera | 12:70252844 | GCTCAATAGAAGTGG[A/G]AGAAATCACCAGGTA | 94090 |
rs32260416 | snp | A/G | 0.231111 | 0.249285 | intron-variant | Trim9 | Mm_Celera | 12:70295541 | GCAGAATTCAGCAGC[A/G]GACAGTGAAAATACA | 94090 |
rs32260418 | snp | C/T | 0.124444 | 0.216185 | intron-variant | Trim9 | Mm_Celera | 12:70295575 | GTAGCTATTTATCAG[C/T]AGAAAATGCTGTATT | 94090 |
rs32260421 | snp | A/G | 0.124444 | 0.216185 | intron-variant | Trim9 | Mm_Celera | 12:70295690 | GATCTGTTTTCCTTA[A/G]AGCATTTTAATTCTA | 94090 |
rs32260505 | snp | C/G | 0.231111 | 0.249285 | intron-variant | Trim9 | Mm_Celera | 12:70288024 | GAAAGAGACTCCATT[C/G]GGCAAAAGGTAGGTA | 94090 |
rs32260508 | snp | A/G | 0.48 | 0.0979796 | intron-variant | Trim9 | Mm_Celera | 12:70288033 | TCCATTGGGCAAAAG[A/G]TAGGTACTGAAATGC | 94090 |
rs32260511 | snp | A/G | 0.132653 | 0.220748 | intron-variant | Trim9 | Mm_Celera | 12:70288104 | TCTTTTCCAAAGACA[A/G]CCACAGTTTTATTCT | 94090 |
rs32260513 | snp | A/G | 0.48 | 0.0979796 | intron-variant | Trim9 | Mm_Celera | 12:70288107 | TTTCCAAAGACAGCC[A/G]CAGTTTTATTCTGTA | 94090 |
rs32260715 | snp | C/T | 0.132653 | 0.220748 | intron-variant | Trim9 | Mm_Celera | 12:70274885 | TTTATGGATTGGCCA[C/T]GGATACAGCACAGCA | 94090 |
rs32260718 | snp | A/T | 0.124444 | 0.216185 | intron-variant | Trim9 | Mm_Celera | 12:70274988 | GGTCTTTGCATCTTG[A/T]ATTCATTTGGAGACA | 94090 |
rs32260723 | snp | A/G | 0.132653 | 0.220748 | intron-variant | Trim9 | Mm_Celera | 12:70275081 | TCTCTTGGCCTATAA[A/G]CACAAGCTACAGACT | 94090 |
rs32260784 | snp | C/T | 0.497041 | 0.0383476 | intron-variant | Trim9 | Mm_Celera | 12:70284653 | GGATTTACCTGACAG[C/T]AATTTTTACAAAGAC | 94090 |
rs32260787 | snp | A/G | 0.297521 | 0.245442 | intron-variant | Trim9 | GRCm38.p3 | 12:70284915 | CGCCACCACTGCCCG[A/G]CAATACATACACATT | 94090 |
rs32260790 | snp | A/C | 0.48 | 0.0979796 | intron-variant | Trim9 | Mm_Celera | 12:70285019 | CTCATCGATAATCAC[A/C]GTGTGGAATATGCCA | 94090 |
rs32260793 | snp | A/T | 0.489796 | 0.070696 | intron-variant | Trim9 | Mm_Celera | 12:70285111 | CCTAGGAAGGGAGGA[A/T]TCTGGTGGCATCCTG | 94090 |
rs32260886 | snp | C/T | 0.18 | 0.24 | intron-variant | Trim9 | GRCm38.p3 | 12:70289580 | CCATAACTGTATGCT[C/T]CCCTCACCAGGCCTG | 94090 |
rs32260889 | snp | G/T | 0.48 | 0.0979796 | intron-variant | Trim9 | Mm_Celera | 12:70289761 | ATTCTAGTGGTCAAA[G/T]TCTATATTGAAAAGT | 94090 |
rs32260892 | snp | C/T | 0.396694 | 0.202437 | intron-variant | Trim9 | GRCm38.p3 | 12:70289848 | TTGCCTATGAGTGGC[C/T]ACCCTTATCTAAGCT | 94090 |
rs32260906 | snp | A/C | 0.231111 | 0.249285 | intron-variant | Trim9 | Mm_Celera | 12:70277408 | TGACAGGTAAAAATT[A/C]TTCAGGCTGAATGGG | 94090 |
rs32260909 | snp | A/C | 0.231111 | 0.249285 | intron-variant | Trim9 | Mm_Celera | 12:70277524 | CGAATTAAATTAAGA[A/C]AAAGTGTTAAGAAGA | 94090 |
rs32260931 | snp | A/G | 0.124444 | 0.216185 | downstream-variant-500B | Trim9 | Mm_Celera | 12:70244145 | GATTCACTGAACAGG[A/G]CTAATAATGACGAAA | 94090 |
rs32260933 | snp | A/G | 0.124444 | 0.216185 | downstream-variant-500B | Trim9 | Mm_Celera | 12:70244314 | ATCTCAGTGTTTAGA[A/G]GCACCTGCCGAAGTC | 94090 |
rs32260956 | snp | C/G | 0.124444 | 0.216185 | intron-variant | Trim9 | Mm_Celera | 12:70300653 | ACTGAAGGCAGGAAA[C/G]TTTACTAGGCGTCAG | 94090 |
rs32260959 | snp | A/G | 0.124444 | 0.216185 | intron-variant | Trim9 | Mm_Celera | 12:70300780 | AGGTGCCACGTATGC[A/G]CAACTCGGGCTCAGA | 94090 |
rs32261126 | snp | C/T | 0.231111 | 0.249285 | intron-variant | Trim9 | Mm_Celera | 12:70281056 | AGTGCCACCCTTCTG[C/T]TTCAAGGTGTGGGCA | 94090 |
rs32261131 | snp | C/T | 0.231111 | 0.249285 | intron-variant | Trim9 | Mm_Celera | 12:70281142 | CGTACAGCTTCAGTA[C/T]GCTACCTTCCTGTGG | 94090 |
rs32261235 | snp | A/G | 0.132653 | 0.220748 | intron-variant | Trim9 | Mm_Celera | 12:70305713 | AGACCTGGTCCTAGC[A/G]TTTTCTGCATGAAGC | 94090 |
rs32261238 | snp | A/G | 0.231111 | 0.249285 | intron-variant | Trim9 | Mm_Celera | 12:70305732 | TCTGCATGAAGCAGG[A/G]ACAGAGGGCTGGCCT | 94090 |
rs32261241 | snp | C/T | 0.244898 | 0.249948 | intron-variant | Trim9 | Mm_Celera | 12:70305856 | GCCTGTATGTGCTCA[C/T]GCACCCCACAGTCCA | 94090 |
rs32261364 | snp | A/G | 0.231111 | 0.249285 | intron-variant | Trim9 | Mm_Celera | 12:70295789 | CTGAAGTCTTGAGAG[A/G]GAGAAGGATATGGTT | 94090 |
rs32261366 | snp | C/T | 0.32 | 0.24 | intron-variant | Trim9 | Mm_Celera | 12:70295890 | AGGACAGCGTTATGA[C/T]GAGGCAGCCACAGAC | 94090 |
rs32261369 | snp | A/T | 0.48 | 0.0979796 | intron-variant | Trim9 | Mm_Celera | 12:70296634 | ACAGAAGCGACTGTC[A/T]TAGAGGTCTTGTTGC | 94090 |
rs32261372 | snp | A/G/T | 0.5 | 0 | intron-variant | Trim9 | GRCm38.p3 | 12:70296721 | TGTAGATCTAGGGAT[A/G/T]ATATATTATATACAA | 94090 |
rs32261495 | snp | A/G | 0.124444 | 0.216185 | intron-variant | Trim9 | Mm_Celera | 12:70288666 | TCCCATGAGGTGTTC[A/G]GTGGCCATTCTAGCT | 94090 |
rs32261498 | snp | C/T | 0.48 | 0.0979796 | intron-variant | Trim9 | Mm_Celera | 12:70288784 | TTGCTTCCACTGTGT[C/T]CCTGCCTCCTCTGTA | 94090 |
rs32261501 | snp | C/G | 0.48 | 0.0979796 | intron-variant | Trim9 | Mm_Celera | 12:70288806 | TCCTCTGTACCCCTT[C/G]GCAGCACTGTAACCC | 94090 |
rs32261586 | snp | C/T | 0.396694 | 0.202437 | intron-variant | Trim9 | Mm_Celera | 12:70285450 | AGACTTTCAGATGTA[C/T]TCACATATGGGAGGC | 94090 |
rs32261589 | snp | C/T | 0.48 | 0.0979796 | intron-variant | Trim9 | Mm_Celera | 12:70285506 | AAACTCTGAAAGGGA[C/T]TCTGCACTAATGGCA | 94090 |
rs32261592 | snp | C/T | 0.124444 | 0.216185 | intron-variant | Trim9 | Mm_Celera | 12:70285530 | AATGGCAGGCTGCAA[C/T]CAGTGACACTTGCAG | 94090 |
rs32261706 | snp | A/G | 0.132653 | 0.220748 | downstream-variant-500B | Trim9 | Mm_Celera | 12:70244467 | TTTGCACTTTGCCCC[A/G]AGGAGTGAGGTGCTC | 94090 |
rs32261709 | snp | C/T | 0.48 | 0.0979796 | downstream-variant-500B | Trim9 | Mm_Celera | 12:70244485 | GAGTGAGGTGCTCTG[C/T]GCCCCCAGATGTGTG | 94090 |
rs32261712 | snp | A/G | 0.132653 | 0.220748 | utr-variant-3-prime | Trim9 | Mm_Celera | 12:70244977 | TCTAGCGGGTTCCTG[A/G]CTCAGTGGAAAGTAT | 94090 |
rs32261735 | snp | A/G | 0.124444 | 0.216185 | intron-variant | Trim9 | Mm_Celera | 12:70275111 | TGAAAATTCTCTTGG[A/G]TACAGTGAGCTGTGA | 94090 |
rs32261738 | snp | C/T | 0.124444 | 0.216185 | intron-variant | Trim9 | Mm_Celera | 12:70275233 | CCTTTGGAGGCTGCT[C/T]TCTCCTTATTTAACT | 94090 |
rs32261740 | snp | A/C | 0.142012 | 0.225474 | intron-variant | Trim9 | Mm_Celera | 12:70275306 | GAATTCCTCTGTGGA[A/C]CAAGCTGGAATGTGG | 94090 |
rs32261743 | snp | A/C | 0.142012 | 0.225474 | intron-variant | Trim9 | Mm_Celera | 12:70275704 | CTCCCACTCAGAGCT[A/C]CGGTGTCAGAAGCGC | 94090 |
rs32261767 | snp | C/T | 0.231111 | 0.249285 | intron-variant | Trim9 | Mm_Celera | 12:70290120 | GGAACCTGAGGGAGT[C/T]TGAAGTAAATTGAGG | 94090 |
rs32261770 | snp | C/T | 0.32 | 0.24 | intron-variant | Trim9 | Mm_Celera | 12:70290173 | GTCTGTTCCTGTCGG[C/T]CAGGCCATGTGGGTG | 94090 |
rs32261773 | snp | A/G | 0.489796 | 0.070696 | intron-variant | Trim9 | Mm_Celera | 12:70290180 | CCTGTCGGTCAGGCC[A/G]TGTGGGTGAGGAGGG | 94090 |
rs32261824 | snp | A/C | 0.32 | 0.24 | intron-variant | Trim9 | Mm_Celera | 12:70300848 | GTTTTATTGTTCTAG[A/C]GAGGAAGTCACCGCC | 94090 |
rs32261827 | snp | A/C | 0.32 | 0.24 | intron-variant | Trim9 | Mm_Celera | 12:70300872 | CACCGCCTTTCCACG[A/C]ATGCTGCTGCTCCTG | 94090 |
rs32261832 | snp | C/T | 0.231111 | 0.249285 | intron-variant | Trim9 | Mm_Celera | 12:70301069 | ACGATTTCTTCAGCT[C/T]GTGAGACGAAAAATT | 94090 |
rs32261834 | snp | A/G | 0.231111 | 0.249285 | intron-variant | Trim9 | Mm_Celera | 12:70277639 | GACTCAGGGTGCTCT[A/G]CATTTTAGCTGTAGT | 94090 |
rs32261843 | snp | C/G | 0.489796 | 0.070696 | intron-variant | Trim9 | Mm_Celera | 12:70277869 | GGTCAGGTGGATGGA[C/G]CAGACTCAGAAGGGC | 94090 |
rs32261924 | snp | A/G | 0.132653 | 0.220748 | intron-variant | Trim9 | Mm_Celera | 12:70281233 | CTCTTGGCTGGTTGC[A/G]GAATGTGAATTGGAA | 94090 |
rs32261929 | snp | C/T | 0.48 | 0.0979796 | intron-variant | Trim9 | Mm_Celera | 12:70281705 | GCTCGCGCACACTCC[C/T]TGAGCAGGCAGGTAG | 94090 |
rs32261931 | snp | A/G | 0.489796 | 0.070696 | intron-variant | Trim9 | Mm_Celera | 12:70281726 | AGGCAGGTAGGTTCC[A/G]CTATTGAGCGACAAA | 94090 |
rs32262254 | snp | A/G | 0.297521 | 0.245442 | intron-variant | Trim9 | Mm_Celera | 12:70305867 | CTCATGCACCCCACA[A/G]TCCACCATCCCAGTC | 94090 |
rs32262257 | snp | C/T | 0.124444 | 0.216185 | intron-variant | Trim9 | Mm_Celera | 12:70306005 | GGCATTGTCTAAGCC[C/T]GTAGTTAACAATGTT | 94090 |
rs32262262 | snp | A/G | 0.124444 | 0.216185 | intron-variant | Trim9 | Mm_Celera | 12:70306051 | AAATGAGGCCCTGAC[A/G]CATATAATTGCATCT | 94090 |
rs32262384 | snp | A/G | 0.48 | 0.0979796 | intron-variant | Trim9 | Mm_Celera | 12:70288834 | CCCAGTGACTGAGGA[A/G]AAATGCCTTGTCTGC | 94090 |
rs32262387 | snp | C/T | 0.231111 | 0.249285 | intron-variant | Trim9 | Mm_Celera | 12:70288846 | GGAAAAATGCCTTGT[C/T]TGCATGGAACTTCTT | 94090 |
rs32262389 | snp | A/T | 0.42 | 0.183303 | intron-variant | Trim9 | Mm_Celera | 12:70288879 | GAGCAGTGGGGAGCT[A/T]TTGTTCAGATTTTAG | 94090 |
rs32262391 | snp | A/T | 0.231111 | 0.249285 | intron-variant | Trim9 | Mm_Celera | 12:70288931 | CACACAGGCTCTATA[A/T]CATTAGCATTCTGGG | 94090 |
rs32262393 | snp | A/C | 0.48 | 0.0979796 | intron-variant | Trim9 | Mm_Celera | 12:70289021 | CTTTACCCAAGAATC[A/C]GGGTCCTTAATAACA | 94090 |
rs32262415 | snp | C/T | 0.231111 | 0.249285 | intron-variant | Trim9 | Mm_Celera | 12:70297541 | CTTGGACTAGCACAA[C/T]TGTGTCATAGTCCTA | 94090 |
rs32262418 | snp | C/T | 0.244898 | 0.249948 | intron-variant | Trim9 | Mm_Celera | 12:70297567 | TCCTATGATGAATCC[C/T]TCGCCCATGAACTGA | 94090 |
rs32262421 | snp | C/T | 0.231111 | 0.249285 | intron-variant | Trim9 | Mm_Celera | 12:70297584 | CGCCCATGAACTGAC[C/T]CTTCCTACTTTTTAC | 94090 |
rs32262423 | snp | A/T | 0.231111 | 0.249285 | intron-variant | Trim9 | Mm_Celera | 12:70297683 | AACACTACCCTCCAG[A/T]CACCTTGGTACAAAC | 94090 |
rs32262425 | snp | A/T | 0.231111 | 0.249285 | intron-variant | Trim9 | Mm_Celera | 12:70285595 | GAGGGCGAGGAAAGG[A/T]TTCACACTATGCCAG | 94090 |
rs32262428 | snp | A/G | 0.497041 | 0.0383476 | intron-variant | Trim9 | Mm_Celera | 12:70285601 | GAGGAAAGGATTCAC[A/G]CTATGCCAGGTGCTT | 94090 |
rs32262431 | snp | G/T | 0.48 | 0.0979796 | intron-variant | Trim9 | Mm_Celera | 12:70285642 | CAAGTCTTTCTCCCA[G/T]TGTCCAACCAATTCT | 94090 |
rs32262666 | snp | A/C | 0.231111 | 0.249285 | synonymous-codon, nc-transcript-variant | Trim9 | Mm_Celera | 12:70290301 | ATGCTCCTTGTTGAC[A/C]CGGGCCAGCAGCTGA | 94090 |
rs32262669 | snp | A/G | 0.497778 | 0.0332592 | synonymous-codon, nc-transcript-variant | Trim9 | Mm_Celera | 12:70290340 | TCGGTTTAGGGCATC[A/G]ATGAGCGCATCACAC | 94090 |
rs32262672 | snp | C/T | 0.48 | 0.0979796 | intron-variant | Trim9 | Mm_Celera | 12:70290453 | AGGTAGCCAAGGAAA[C/T]CAGAGAACCCTAGTT | 94090 |
rs32262735 | snp | A/G | 0.231111 | 0.249285 | intron-variant | Trim9 | Mm_Celera | 12:70301082 | CTCGTGAGACGAAAA[A/G]TTTCAGTTGCACAAT | 94090 |
rs32262738 | snp | G/T | 0.124444 | 0.216185 | intron-variant | Trim9 | Mm_Celera | 12:70301088 | AGACGAAAAATTTCA[G/T]TTGCACAATGAGGAT | 94090 |
rs32262741 | snp | G/T | 0.231111 | 0.249285 | intron-variant | Trim9 | Mm_Celera | 12:70301127 | ACCAATTAAAAGCAT[G/T]CGACTAGAAATCAAT | 94090 |
rs32262926 | snp | C/T | 0.231111 | 0.249285 | intron-variant | Trim9 | Mm_Celera | 12:70277916 | GATTGCTCTGCCAGC[C/T]CATCCAAGCATTTCA | 94090 |
rs32262929 | snp | A/T | 0.132653 | 0.220748 | intron-variant | Trim9 | Mm_Celera | 12:70278023 | CTTCCACCAGAAGCC[A/T]TAGCACTGCTCTTTT | 94090 |
rs32262932 | snp | C/T | 0.231111 | 0.249285 | intron-variant | Trim9 | Mm_Celera | 12:70278032 | GAAGCCTTAGCACTG[C/T]TCTTTTATGATGCAG | 94090 |
rs32262964 | snp | C/T | 0.32 | 0.24 | intron-variant | Trim9 | Mm_Celera | 12:70281764 | CAGACTGCTAGATGT[C/T]CCATCTATGTGTCCT | 94090 |
rs32262969 | snp | C/T | 0.231111 | 0.249285 | intron-variant | Trim9 | Mm_Celera | 12:70281954 | ACCACCTAAGGTTGG[C/T]GAGAGAACAGAAAGG | 94090 |
rs32262971 | snp | C/T | 0.231111 | 0.249285 | intron-variant | Trim9 | Mm_Celera | 12:70282211 | ATGTTGAGGTTAGAA[C/T]TCTGTGAATCTGGTG | 94090 |
rs32263164 | snp | C/G | 0.48 | 0.0979796 | intron-variant | Trim9 | Mm_Celera | 12:70285679 | ATTTTATTCCATTCA[C/G]CAGACTGGGCTGGTG | 94090 |
rs32263167 | snp | G/T | 0.495868 | 0.0452663 | intron-variant | Trim9 | Mm_Celera | 12:70285840 | GCAATGGGGGAAAGC[G/T]TGTTACAAGCCGGGA | 94090 |
rs32263170 | snp | A/G | 0.497778 | 0.0332592 | intron-variant | Trim9 | Mm_Celera | 12:70285885 | CTCCCGTTTAGTGAC[A/G]TGACCACATGATAGA | 94090 |
rs32263173 | snp | A/G | 0.48 | 0.0979796 | intron-variant | Trim9 | Mm_Celera | 12:70286189 | CTTACTGTGTAACAA[A/G]AAGGTACATATCAGC | 94090 |
rs32263205 | snp | C/T | 0.124444 | 0.216185 | intron-variant | Trim9 | Mm_Celera | 12:70306072 | AATTGCATCTGTTGT[C/T]GTGCTAGAGAGCTAG | 94090 |
rs32263208 | snp | G/T | 0.277778 | 0.248452 | intron-variant | Trim9 | Mm_Celera | 12:70306640 | TCTCTACAGACACAG[G/T]CCTTTCTCATTCGCT | 94090 |
rs32263211 | snp | C/G | 0.231111 | 0.249285 | intron-variant | Trim9 | Mm_Celera | 12:70306666 | TCGCTCTCCCTTGGG[C/G]TCTGATGCTGAAAAG | 94090 |
rs32263255 | snp | C/T | 0.132653 | 0.220748 | intron-variant | Trim9 | Mm_Celera | 12:70289053 | TGTACCTTTGTTCTC[C/T]GCAAAACCCAGAGAG | 94090 |
rs32263258 | snp | C/T | 0.459184 | 0.136902 | intron-variant | Trim9 | Mm_Celera | 12:70289168 | TGGAAGCATAGCCTG[C/T]TGCTTGCCTCAATCC | 94090 |
rs32263261 | snp | A/G | 0.48 | 0.0979796 | intron-variant | Trim9 | Mm_Celera | 12:70289179 | CCTGCTGCTTGCCTC[A/G]ATCCTGAAGTGTCCC | 94090 |
rs32263409 | snp | C/T | 0.231111 | 0.249285 | intron-variant | Trim9 | Mm_Celera | 12:70297873 | GCATGTGTGATAGAT[C/T]AGAGGGATGTCTGCA | 94090 |
rs32263412 | snp | C/T | 0.231111 | 0.249285 | intron-variant | Trim9 | Mm_Celera | 12:70297909 | AGCTCTCACTTTTCT[C/T]AGACAGTACATGAAG | 94090 |
rs32263454 | snp | C/T | 0.32 | 0.24 | intron-variant | Trim9 | Mm_Celera | 12:70301200 | TTTACATGAGAAGGT[C/T]TTCACTGCTTCCTTC | 94090 |
rs32263457 | snp | C/T | 0.231111 | 0.249285 | intron-variant | Trim9 | Mm_Celera | 12:70301265 | CACTCAACAACCACT[C/T]GAGTTTCCAGAAACA | 94090 |
rs32263460 | snp | G/T | 0.124444 | 0.216185 | intron-variant | Trim9 | Mm_Celera | 12:70301349 | TAACTTTTCTCTTAT[G/T]TCAAAAAGCAGAATT | 94090 |
rs32263463 | snp | C/T | 0.231111 | 0.249285 | intron-variant | Trim9 | Mm_Celera | 12:70301458 | CATTTATATGCAGAT[C/T]CACATGTCCCTAAGT | 94090 |
rs32263545 | snp | C/T | 0.48 | 0.0979796 | intron-variant | Trim9 | Mm_Celera | 12:70291053 | TGTTTAAATTAAATG[C/T]TGGGTATGACATTTT | 94090 |
rs32263548 | snp | A/G | 0.32 | 0.24 | intron-variant | Trim9 | Mm_Celera | 12:70291263 | TGAATTCTCAGAGAA[A/G]GTCCTTCGAGAGGAC | 94090 |
rs32263553 | snp | C/T | 0.32 | 0.24 | intron-variant | Trim9 | Mm_Celera | 12:70291525 | TCAACAGTTCTAACA[C/T]GGGTCTGCACATAAG | 94090 |
rs32263745 | snp | C/T | 0.231111 | 0.249285 | intron-variant | Trim9 | Mm_Celera | 12:70278517 | GTTGCCACAACACGA[C/T]ATTTTAACTTACAAC | 94090 |
rs32263748 | snp | A/G | 0.244898 | 0.249948 | intron-variant | Trim9 | Mm_Celera | 12:70278629 | CAAGAGTAGAGGGTC[A/G]TGAAAAGATGTAGGA | 94090 |
rs32263751 | snp | A/C | 0.132653 | 0.220748 | intron-variant | Trim9 | Mm_Celera | 12:70278685 | CAACACACTGACAGC[A/C]CTAATGGTATTAAAA | 94090 |
rs32263884 | snp | A/G | 0.459184 | 0.136902 | intron-variant | Trim9 | Mm_Celera | 12:70289226 | GTCAAAAGGCAGCAG[A/G]GAAAGGTTTTTGTTC | 94090 |
rs32263896 | snp | A/G | 0.142012 | 0.225474 | intron-variant | Trim9 | Mm_Celera | 12:70286192 | ACTGTGTAACAAGAA[A/G]GTACATATCAGCTTG | 94090 |
rs32263899 | snp | A/T | 0.244898 | 0.249948 | intron-variant | Trim9 | Mm_Celera | 12:70286419 | TGGAAATAATGTAAA[A/T]TTTTGTAAAATACAG | 94090 |
rs32263902 | snp | C/T | 0.345679 | 0.230967 | intron-variant | Trim9 | Mm_Celera | 12:70286550 | AGAACCTGGGAAGGG[C/T]GGTAGCATAACATCT | 94090 |
rs32263954 | snp | A/G | 0.231111 | 0.249285 | intron-variant | Trim9 | Mm_Celera | 12:70302759 | GTACTGAAAAGTTAA[A/G]AGTGACAGAAATTCA | 94090 |
rs32263957 | snp | C/T | 0.32 | 0.24 | intron-variant | Trim9 | Mm_Celera | 12:70302796 | CTAATTGTTTCTTCC[C/T]TGGTTGGTTGTCATC | 94090 |
rs32263960 | snp | G/T | 0.32 | 0.24 | intron-variant | Trim9 | Mm_Celera | 12:70302819 | TTGTCATCTTGGGCA[G/T]ACTCAGTCTTCATAT | 94090 |
rs32263962 | snp | A/G | 0.32 | 0.24 | intron-variant | Trim9 | Mm_Celera | 12:70302831 | GCATACTCAGTCTTC[A/G]TATCTACAGCAACAA | 94090 |
rs32263984 | snp | C/G | 0.231111 | 0.249285 | intron-variant | Trim9 | Mm_Celera | 12:70307168 | TTATAGCTTTTAGTG[C/G]TTCCAGTTCTTTGAC | 94090 |
rs32263987 | snp | C/T | 0.231111 | 0.249285 | intron-variant | Trim9 | Mm_Celera | 12:70307785 | GGCAATCCAAATGAC[C/T]ACAGTGATGAATGGG | 94090 |
rs32263990 | snp | C/T | 0.132653 | 0.220748 | intron-variant | Trim9 | Mm_Celera | 12:70307815 | GTCTGTAGACTGGAA[C/T]GATCTACAGTCAACA | 94090 |
rs32263993 | snp | C/T | 0.231111 | 0.249285 | intron-variant | Trim9 | Mm_Celera | 12:70307861 | ATACAGCAACATGGC[C/T]GAGTAGACAAAGCAA | 94090 |
rs32263995 | snp | A/G | 0.489796 | 0.070696 | intron-variant | Trim9 | Mm_Celera | 12:70311512 | ACACTGAGTGCCAAG[A/G]CCAGCTCTAGGGATT | 94090 |
rs32263998 | snp | A/G | 0.124444 | 0.216185 | intron-variant | Trim9 | Mm_Celera | 12:70311816 | TATTCCAGGAGGAGA[A/G]GCAGGCACACAAGCA | 94090 |
rs32264003 | snp | A/G | 0.244898 | 0.249948 | intron-variant | Trim9 | Mm_Celera | 12:70311981 | GACCTCAGAAGAGCC[A/G]AGGCTCAAAAGATGG | 94090 |
rs32264084 | snp | A/C | 0.231111 | 0.249285 | intron-variant | Trim9 | Mm_Celera | 12:70282356 | AGCTTCCACATGGCT[A/C]CTGGCTGCACTCAAC | 94090 |
rs32264086 | snp | C/T | 0.132653 | 0.220748 | intron-variant | Trim9 | Mm_Celera | 12:70282379 | CACTCAACCCTCTTT[C/T]CTGGCCTGCAGTTTT | 94090 |
rs32264089 | snp | G/T | 0.244898 | 0.249948 | intron-variant | Trim9 | Mm_Celera | 12:70282391 | TTTTCTGGCCTGCAG[G/T]TTTTTTCTAAAGAGT | 94090 |
rs32264092 | snp | C/T | 0.495868 | 0.0452663 | intron-variant | Trim9 | Mm_Celera | 12:70282437 | CCAGGGGCATTTTTT[C/T]CTGGTTGCTACCGTC | 94090 |
rs32264146 | snp | C/T | 0.124444 | 0.216185 | intron-variant | Trim9 | Mm_Celera | 12:70301468 | CAGATCCACATGTCC[C/T]TAAGTAGTGAATATC | 94090 |
rs32264149 | snp | A/G/T | 0.5 | 0 | intron-variant | Trim9 | GRCm38.p3 | 12:70301787 | ATTAACTTCAAAGCT[A/G/T]CAGTGTGATGCTCTC | 94090 |
rs32264152 | snp | C/T | 0.142012 | 0.225474 | intron-variant | Trim9 | Mm_Celera | 12:70301813 | CTCTCTGTACATCAT[C/T]ACAATCTACATAATT | 94090 |
rs32264426 | snp | A/G | 0.48 | 0.0979796 | intron-variant | Trim9 | Mm_Celera | 12:70291576 | GTGATGCTTTGAGAG[A/G]CTGGCGTACATTAGA | 94090 |
rs32264429 | snp | A/G | 0.231111 | 0.249285 | intron-variant | Trim9 | Mm_Celera | 12:70291590 | GGCTGGCGTACATTA[A/G]ACATCCATTTCTGCT | 94090 |
rs32264432 | snp | C/T | 0.231111 | 0.249285 | intron-variant | Trim9 | Mm_Celera | 12:70291624 | ACATGGGTTAAATAG[C/T]CACTGAGAAAGCTGT | 94090 |
rs32264455 | snp | C/T | 0.18 | 0.24 | intron-variant | Trim9 | Mm_Celera | 12:70286643 | GAACTGTTTCTTGGA[C/T]GCTCACAGATGCTTA | 94090 |
rs32264458 | snp | C/T | 0.231111 | 0.249285 | intron-variant | Trim9 | Mm_Celera | 12:70286733 | CTCCCTGCTCATTTT[C/T]AAACCACAGAATAGC | 94090 |
rs32264584 | snp | C/T | 0.231111 | 0.249285 | intron-variant | Trim9 | Mm_Celera | 12:70297930 | GTACATGAAGCTTAC[C/T]ATGTTTATTATGAAT | 94090 |
rs32264587 | snp | A/G | 0.231111 | 0.249285 | intron-variant | Trim9 | Mm_Celera | 12:70298047 | AACCTGCGTACATAA[A/G]CATATAGCAAAAGCT | 94090 |
rs32264590 | snp | A/G | 0.124444 | 0.216185 | intron-variant | Trim9 | Mm_Celera | 12:70298116 | AATTCATATCCAAGT[A/G]TGCCAACTTTTTCTC | 94090 |
rs32264593 | snp | C/T | 0.124444 | 0.216185 | intron-variant | Trim9 | Mm_Celera | 12:70298181 | TCAGATATCAGATAG[C/T]AACAACCAAATCAGA | 94090 |
rs32264764 | snp | A/C/T | 0.142012 | 0.225474 | intron-variant | Trim9 | GRCm38.p3 | 12:70302890 | GGTTCCTGGTTCCTG[A/C/T]TTATCCTGGTGATTT | 94090 |
rs32264767 | snp | C/T | 0.124444 | 0.216185 | intron-variant | Trim9 | Mm_Celera | 12:70303038 | AACCAAAGGGATGCT[C/T]GGACTTCTGGGTGCC | 94090 |
rs32264770 | snp | C/T | 0.231111 | 0.249285 | intron-variant | Trim9 | Mm_Celera | 12:70303072 | CTCCACACCAAGATG[C/T]CAGTTTTCCTTCTGC | 94090 |
rs32264772 | snp | C/G | 0.124444 | 0.216185 | intron-variant | Trim9 | Mm_Celera | 12:70303141 | CAAACGCTATTTCTG[C/G]GAGGCCGAGTCTCTT | 94090 |
rs32264795 | snp | C/G | 0.231111 | 0.249285 | intron-variant | Trim9 | Mm_Celera | 12:70301819 | GTACATCATCACAAT[C/G]TACATAATTAATCTC | 94090 |
rs32264798 | snp | C/T | 0.497778 | 0.0332592 | intron-variant | Trim9 | Mm_Celera | 12:70301927 | TATAAATTATTCCTA[C/T]TTCTAGAGTTGAACA | 94090 |
rs32264801 | snp | A/G | 0.489796 | 0.070696 | intron-variant | Trim9 | Mm_Celera | 12:70301970 | AAGCACTCATATTTA[A/G]AGAGTTTTGAAAATC | 94090 |
rs32264816 | snp | C/G | 0.124444 | 0.216185 | intron-variant | Trim9 | Mm_Celera | 12:70312047 | CAGGAGGTTAAGTGG[C/G]CTAGCTAGGTGGGGC | 94090 |
rs32264819 | snp | A/G | 0.124444 | 0.216185 | intron-variant | Trim9 | Mm_Celera | 12:70312089 | GCTATGGGAAGAGAT[A/G]GTGCAGAAGTGACTG | 94090 |
rs32264821 | snp | C/T | 0.124444 | 0.216185 | intron-variant | Trim9 | Mm_Celera | 12:70312141 | CTGCCATTATTAACT[C/T]GTTATCAAATTTCCC | 94090 |
rs32264865 | snp | C/T | 0.497041 | 0.0383476 | intron-variant | Trim9 | Mm_Celera | 12:70282452 | CCTGGTTGCTACCGT[C/T]GGTAAATGCTACTGG | 94090 |
rs32264868 | snp | A/G | 0.48 | 0.0979796 | intron-variant | Trim9 | Mm_Celera | 12:70282626 | TAATTTATGACATAC[A/G]TATACTAGAATAAGG | 94090 |
rs32264886 | snp | A/C | 0.124444 | 0.216185 | intron-variant | Trim9 | Mm_Celera | 12:70307869 | ACATGGCTGAGTAGA[A/C]AAAGCAAGTTGAAGA | 94090 |
rs32264889 | snp | A/C | 0.231111 | 0.249285 | intron-variant | Trim9 | Mm_Celera | 12:70307940 | GGATAAGAAAAGGAA[A/C]CGTCAGCGGCAGGAG | 94090 |
rs32264891 | snp | A/C | 0.231111 | 0.249285 | intron-variant | Trim9 | Mm_Celera | 12:70308346 | ACCACCAAGCCAACT[A/C]TCATGCGGTTATACA | 94090 |
rs32264914 | snp | C/T | 0.21875 | 0.248039 | intron-variant | Trim9 | Mm_Celera | 12:70314503 | AGTGAACTGCCAGTT[C/T]ACTACCCATAAAGAA | 94090 |
rs32264917 | snp | C/G | 0.32 | 0.24 | intron-variant | Trim9 | Mm_Celera | 12:70314541 | ATGAAGATTACAAAG[C/G]AAGTTGACAGATGCT | 94090 |
rs32264920 | snp | C/T | 0.32 | 0.24 | intron-variant | Trim9 | Mm_Celera | 12:70314865 | TTATGCGATGTTTTA[C/T]TAATGACAACAGAGT | 94090 |
rs32264922 | snp | C/T | 0.32 | 0.24 | intron-variant | Trim9 | Mm_Celera | 12:70315044 | TTCCACCACTCCATG[C/T]ATGATTCATGCAGAC | 94090 |
rs32265185 | snp | C/T | 0.124444 | 0.216185 | intron-variant | Trim9 | Mm_Celera | 12:70291692 | AAAGCTCAAAACAGG[C/T]AAGAAGGTAAATGGT | 94090 |
rs32265188 | snp | C/T | 0.32 | 0.24 | intron-variant | Trim9 | Mm_Celera | 12:70291765 | TCTCCCTTCCAGCTA[C/T]AGTGGGAAATGTATG | 94090 |
rs32265191 | snp | C/G | 0.32 | 0.24 | intron-variant | Trim9 | Mm_Celera | 12:70291796 | CATTCTCGTCTGCTG[C/G]CTGGCCTGCTGGTCA | 94090 |
rs32265478 | snp | A/G | 0.124444 | 0.216185 | intron-variant | Trim9 | Mm_Celera | 12:70322645 | AAACATCACTGAAGC[A/G]TGTCCAGGAACAAAA | 94090 |
rs32265481 | snp | A/G | 0.32 | 0.24 | intron-variant | Trim9 | Mm_Celera | 12:70323309 | TCTCCCACATGTAGA[A/G]TCTAGGCTTAGCTAT | 94090 |
rs32265515 | snp | C/T | 0.231111 | 0.249285 | intron-variant | Trim9 | Mm_Celera | 12:70298366 | CTCTCCTAGTGTTTG[C/T]ATCCTTGGAGCTGCT | 94090 |
rs32265518 | snp | A/G | 0.124444 | 0.216185 | intron-variant | Trim9 | Mm_Celera | 12:70298413 | AACAGACTGCTCTAG[A/G]AATTGCTCTTGTGTG | 94090 |
rs32265520 | snp | C/T | 0.124444 | 0.216185 | intron-variant | Trim9 | Mm_Celera | 12:70298541 | ACTGCAGGTCAACTC[C/T]CAACTCTGCTCAAAC | 94090 |
rs32265594 | snp | A/G | 0.48 | 0.0979796 | intron-variant | Trim9 | Mm_Celera | 12:70302039 | TATCCATAGAAAGTG[A/G]TAAGAGGAATCTTTT | 94090 |
rs32265597 | snp | A/C | 0.48 | 0.0979796 | intron-variant | Trim9 | Mm_Celera | 12:70302071 | AAATAGTATCAATGG[A/C]ACATTTGTATTTGCA | 94090 |
rs32265600 | snp | A/G | 0.124444 | 0.216185 | intron-variant | Trim9 | Mm_Celera | 12:70302329 | TCATATAAAACATTA[A/G]AATGTAGAATCTCAG | 94090 |
rs32265603 | snp | A/C | 0.231111 | 0.249285 | intron-variant | Trim9 | Mm_Celera | 12:70302370 | TAGACTTAAACATTG[A/C]CAGTGTGATATTTAA | 94090 |
rs32265634 | snp | A/G | 0.231111 | 0.249285 | intron-variant | Trim9 | Mm_Celera | 12:70303169 | CTTCCACAAGCACAC[A/G]ATTTTACTTATGCCT | 94090 |
rs32265637 | snp | C/T | 0.231111 | 0.249285 | intron-variant | Trim9 | Mm_Celera | 12:70303180 | ACACGATTTTACTTA[C/T]GCCTAATTGGAAACG | 94090 |
rs32265640 | snp | C/T | 0.231111 | 0.249285 | intron-variant | Trim9 | Mm_Celera | 12:70303199 | TAATTGGAAACGTGG[C/T]TGTGATCCACTGTTT | 94090 |
rs32265642 | snp | A/G | 0.231111 | 0.249285 | intron-variant | Trim9 | Mm_Celera | 12:70303579 | AGGTGATTCTTCAGG[A/G]GAGAGGAGATCTAGA | 94090 |
rs32265674 | snp | C/T | 0.124444 | 0.216185 | intron-variant | Trim9 | Mm_Celera | 12:70312198 | TGTATTGTGCTAGCT[C/T]AGGGAAGATCAGGAT | 94090 |
rs32265678 | snp | C/T | 0.124444 | 0.216185 | intron-variant | Trim9 | Mm_Celera | 12:70312228 | TTATTGTCTCATTAG[C/T]ACACAGGACTCCTTA | 94090 |
rs32265680 | snp | A/C | 0.124444 | 0.216185 | intron-variant | Trim9 | Mm_Celera | 12:70312233 | GTCTCATTAGCACAC[A/C]GGACTCCTTAAGGCA | 94090 |
rs32265683 | snp | A/T | 0.124444 | 0.216185 | intron-variant | Trim9 | Mm_Celera | 12:70312382 | GGTTGAGGAATTTGA[A/T]AGCAGATGACTGGGT | 94090 |
rs32265755 | snp | C/G/T | 0.132653 | 0.220748 | intron-variant | Trim9 | Mm_Celera | 12:70315246 | CAGCATCTATAAAAT[C/G/T]AGATAAGTATTTCCA | 94090 |
rs32265758 | snp | C/T | 0.244898 | 0.249948 | intron-variant | Trim9 | Mm_Celera | 12:70315284 | AGCTATGGCTGACAA[C/T]CCACTCATCTCTGGT | 94090 |
rs32265761 | snp | A/T | 0.32 | 0.24 | intron-variant | Trim9 | Mm_Celera | 12:70315422 | CAGAAGTTTTTTTTT[A/T]AAAGCTCACCTTTCT | 94090 |
rs32265824 | snp | A/G | 0.5 | 0 | intron-variant | Trim9 | Mm_Celera | 12:70331903 | GAGAGTTTCATATTC[A/G]GTCTTTCTGGGGCCC | 94090 |
rs32265827 | snp | A/G | 0.132653 | 0.220748 | intron-variant | Trim9 | Mm_Celera | 12:70331927 | GGGGCCCAGTTGCTA[A/G]GAGCTATATTGGGCC | 94090 |
rs32265830 | snp | C/T | 0.489796 | 0.070696 | intron-variant | Trim9 | Mm_Celera | 12:70331955 | GCCCACTTGGATTCA[C/T]CTCATTAGTACAGAC | 94090 |
rs32265832 | snp | G/T | 0.497041 | 0.0383476 | intron-variant | Trim9 | Mm_Celera | 12:70331989 | GATGTGGGCAAAGGG[G/T]ATCTTATCATTTAGG | 94090 |
rs32265854 | snp | A/C | 0.124444 | 0.216185 | intron-variant | Trim9 | Mm_Celera | 12:70308433 | ATGAGTGCTTTTTTC[A/C]ATGGGTTACAACCTT | 94090 |
rs32265857 | snp | A/G | 0.124444 | 0.216185 | intron-variant | Trim9 | Mm_Celera | 12:70309570 | CCTGGGAAGCTTTCA[A/G]TAACAATTTACATTT | 94090 |
rs32265860 | snp | C/T | 0.124444 | 0.216185 | intron-variant | Trim9 | Mm_Celera | 12:70309709 | AACTGGGCTAATGAG[C/T]ATGCCCTCAGCATGG | 94090 |
rs32265863 | snp | C/T | 0.375 | 0.216506 | intron-variant | Trim9 | Mm_Celera | 12:70309791 | TCAAAGCACACTGAG[C/T]GCCCAGCACAGTGTT | 94090 |
rs32266044 | snp | C/T | 0.32 | 0.24 | intron-variant | Trim9 | Mm_Celera | 12:70292000 | TGGGGCTTAGGGACC[C/T]ATCGGGTTTTAGGAA | 94090 |
rs32266047 | snp | A/G | 0.124444 | 0.216185 | synonymous-codon, nc-transcript-variant | Trim9 | Mm_Celera | 12:70292344 | CGACAATCCATTCAG[A/G]GCCTGGGAGAGCTGG | 94090 |
rs32266050 | snp | C/T | 0.32 | 0.24 | intron-variant | Trim9 | Mm_Celera | 12:70292390 | AAGGAAAGCTTGAGC[C/T]GCCATTATACACAGC | 94090 |
rs32266053 | snp | C/G | 0.231111 | 0.249285 | intron-variant | Trim9 | Mm_Celera | 12:70292432 | TCAGAGTAACAGACT[C/G]CCAATCCCGGGAGCC | 94090 |
rs32266065 | snp | C/G | 0.231111 | 0.249285 | intron-variant | Trim9 | Mm_Celera | 12:70339607 | TCTGCAGCCCTCTAC[C/G]TTTTTAATACTGCCT | 94090 |
rs32266068 | snp | C/T | 0.124444 | 0.216185 | intron-variant | Trim9 | Mm_Celera | 12:70339646 | AATCAAAAGCATTTT[C/T]GAAATAATCTACTTC | 94090 |
rs32266071 | snp | A/C | 0.231111 | 0.249285 | intron-variant | Trim9 | Mm_Celera | 12:70339707 | TAACCTTACACTTGG[A/C]ATTATGGATATAAAG | 94090 |
rs32266125 | snp | A/G | 0.124444 | 0.216185 | intron-variant | Trim9 | Mm_Celera | 12:70328616 | TCAGAATAATTAATT[A/G]GCCAGTCTTCATTAG | 94090 |
rs32266128 | snp | C/T | 0.124444 | 0.216185 | intron-variant | Trim9 | Mm_Celera | 12:70328655 | TTAGATAATAATGTT[C/T]GATTGACTAATCCAA | 94090 |
rs32266131 | snp | A/G | 0.244898 | 0.249948 | intron-variant | Trim9 | Mm_Celera | 12:70328680 | ATCCAATTATTCCCC[A/G]TTTGCAGATGAGATT | 94090 |
rs32266244 | snp | G/T | 0.231111 | 0.249285 | intron-variant | Trim9 | Mm_Celera | 12:70343844 | GGTCATAGCAATTCT[G/T]GCCTGGGAGCATGTT | 94090 |
rs32266247 | snp | C/T | 0.231111 | 0.249285 | intron-variant | Trim9 | Mm_Celera | 12:70343875 | CAGAGACAGAAATAC[C/T]AGGACAGAGTCTAGC | 94090 |
rs32266250 | snp | A/T | 0.231111 | 0.249285 | intron-variant | Trim9 | Mm_Celera | 12:70343965 | GTTAGGTGCTTTTCT[A/T]AAAAAATGAGTATTA | 94090 |
rs32266306 | snp | C/T | 0.497778 | 0.0332592 | intron-variant | Trim9 | Mm_Celera | 12:70302440 | CTAATGATCTTTTCC[C/T]GGCTCGGGAGAAAAT | 94090 |
rs32266424 | snp | C/T | 0.124444 | 0.216185 | intron-variant | Trim9 | Mm_Celera | 12:70323422 | ATTTGCCAGGAAAAA[C/T]GCATTTCGTGAGGGG | 94090 |
rs32266427 | snp | A/G | 0.124444 | 0.216185 | intron-variant | Trim9 | Mm_Celera | 12:70323436 | ACGCATTTCGTGAGG[A/G]GCAGTGACACGTAGC | 94090 |
rs32266430 | snp | A/T | 0.18 | 0.24 | intron-variant | Trim9 | Mm_Celera | 12:70323510 | CCCTTTAAGGTGCTT[A/T]AAAAAAAAAAGGATG | 94090 |
rs32266433 | snp | C/T | 0.124444 | 0.216185 | intron-variant | Trim9 | Mm_Celera | 12:70323753 | TTCATGGGATTGGTA[C/T]ACTATGGTGTGTAGC | 94090 |
rs32266465 | snp | C/T | 0.231111 | 0.249285 | intron-variant | Trim9 | Mm_Celera | 12:70303665 | CTGAGAAGCATTCTT[C/T]TCTTCAGACTGGGAC | 94090 |
rs32266466 | snp | C/T | 0.231111 | 0.249285 | intron-variant | Trim9 | Mm_Celera | 12:70303732 | TTGGCCATATCGAGA[C/T]GCCACTGGTTTGTAA | 94090 |
rs32266468 | snp | C/T | 0.32 | 0.24 | intron-variant | Trim9 | Mm_Celera | 12:70303766 | GAGCATGTGGGCACA[C/T]GTGGTTCATTCCTGT | 94090 |
rs32266473 | snp | G/T | 0.32 | 0.24 | intron-variant | Trim9 | Mm_Celera | 12:70303816 | ACATTTGTTTCTTTG[G/T]TATCAATGGCAAAAC | 94090 |
rs32266474 | snp | C/T | 0.32 | 0.24 | intron-variant | Trim9 | Mm_Celera | 12:70315432 | TTTTTAAAAGCTCAC[C/T]TTTCTAGGTAGATCA | 94090 |
rs32266477 | snp | A/G | 0.244898 | 0.249948 | intron-variant | Trim9 | Mm_Celera | 12:70315572 | CCATTAATTCTATTC[A/G]ATATGACATTCTCAA | 94090 |
rs32266480 | snp | A/G | 0.32 | 0.24 | intron-variant | Trim9 | Mm_Celera | 12:70315632 | AAACAAAACGAAATA[A/G]AGGAACTTACCGTAA | 94090 |
rs32266483 | snp | A/G | 0.231111 | 0.249285 | intron-variant | Trim9 | Mm_Celera | 12:70315802 | GCCCACTCAGAGAAC[A/G]AAGTCACTGACCCAG | 94090 |
rs32266620 | snp | C/T | 0.48 | 0.0979796 | intron-variant | Trim9 | Mm_Celera | 12:70312813 | ATCAGGAGCCTGGGG[C/T]ATGACATGAGTTAAC | 94090 |
rs32266623 | snp | A/G | 0.48 | 0.0979796 | intron-variant | Trim9 | Mm_Celera | 12:70312854 | ATCTGACTGTAGGAA[A/G]CCTGCCCAATGACTG | 94090 |
rs32266646 | snp | A/G | 0.124444 | 0.216185 | intron-variant | Trim9 | Mm_Celera | 12:70309898 | CATGGAGCAATAAGC[A/G]GTCTCAGACATAGAT | 94090 |
rs32266649 | snp | C/T | 0.32 | 0.24 | intron-variant | Trim9 | Mm_Celera | 12:70309953 | GGTACCGCCTGTAGG[C/T]GAGCATTTAACCTGC | 94090 |
rs32266652 | snp | C/T | 0.32 | 0.24 | intron-variant | Trim9 | Mm_Celera | 12:70309989 | CTAGTGGACTTGAGG[C/T]TCTGGGCTCCTGCAC | 94090 |
rs32266675 | snp | A/C | 0.260355 | 0.249785 | intron-variant | Trim9 | Mm_Celera | 12:70332028 | GGCATTATGAGTTCT[A/C]GGCATGAAGGACTAA | 94090 |
rs32266678 | snp | C/T | 0.459184 | 0.136902 | intron-variant | Trim9 | Mm_Celera | 12:70332031 | ATTATGAGTTCTAGG[C/T]ATGAAGGACTAAATC | 94090 |
rs32266681 | snp | C/T | 0.497778 | 0.0332592 | intron-variant | Trim9 | Mm_Celera | 12:70332069 | GACTGTTATACCACA[C/T]TTGAGATAATTGAGA | 94090 |
rs32266796 | snp | A/G | 0.231111 | 0.249285 | intron-variant | Trim9 | Mm_Celera | 12:70292517 | AGGTGGGTTCTGGTA[A/G]CCAGTCAGGCAATGC | 94090 |
rs32266799 | snp | A/C/T | 0.244898 | 0.249948 | intron-variant | Trim9 | GRCm38.p3 | 12:70292844 | GGAAGGCATTCCACC[A/C/T]GACCAAGGTCCTCTT | 94090 |
rs32266802 | snp | G/T | 0.277778 | 0.248452 | intron-variant | Trim9 | Mm_Celera | 12:70293603 | CAAAACTCTCACTCT[G/T]TGCTTCCTGTTGGGA | 94090 |
rs32266915 | snp | C/T | 0.297521 | 0.245442 | intron-variant | Trim9 | Mm_Celera | 12:70339845 | AGGGTGCACCCAGAT[C/T]CTTACATATAAACAT | 94090 |
rs32266919 | snp | A/G | 0.231111 | 0.249285 | intron-variant | Trim9 | Mm_Celera | 12:70340223 | CAACTTTGATGGCTC[A/G]ATACTGCTTATAGAT | 94090 |
rs32266922 | snp | A/C/T | 0.444444 | 0.157135 | intron-variant | Trim9 | GRCm38.p3 | 12:70340851 | ATGGAGAGTTCCAAA[A/C/T]GTATTTATCTATGGA | 94090 |
rs32266924 | snp | A/G | 0.132653 | 0.220748 | intron-variant | Trim9 | Mm_Celera | 12:70328693 | CCATTTGCAGATGAG[A/G]TTTGTAAGTTGTTTT | 94090 |
rs32266928 | snp | C/T | 0.231111 | 0.249285 | intron-variant | Trim9 | Mm_Celera | 12:70329090 | TAAGATGTATGTGAG[C/T]ACACTTTAAATAGCC | 94090 |
rs32266931 | snp | A/G | 0.124444 | 0.216185 | intron-variant | Trim9 | Mm_Celera | 12:70329103 | AGTACACTTTAAATA[A/G]CCCTGATGTGTATGT | 94090 |
rs32267055 | snp | A/G | 0.231111 | 0.249285 | intron-variant | Trim9 | Mm_Celera | 12:70344218 | ATTTCAACTGTACAT[A/G]GAGCTTAGCAGAGAT | 94090 |
rs32267057 | snp | A/G | 0.444444 | 0.157135 | intron-variant | Trim9 | Mm_Celera | 12:70344331 | AACATGTAGCAGTAC[A/G]GTCTTTGCCCAGGCA | 94090 |
rs32267060 | snp | C/T | 0.231111 | 0.249285 | intron-variant, upstream-variant-2KB | Trim9, Gm32151 | Mm_Celera | 12:70345506 | CCCAAGACAACATGT[C/T]AATAGCATTCTTTCT | 94090 |
rs32267076 | snp | A/G | 0.32 | 0.24 | intron-variant | Trim9 | Mm_Celera | 12:70315825 | TGACCCAGGCGCTTG[A/G]TTTGCATCCACAGCT | 94090 |
rs32267078 | snp | C/T | 0.132653 | 0.220748 | intron-variant | Trim9 | Mm_Celera | 12:70315908 | TCCTCGGACTCAGGG[C/T]TTCAACACATTAACT | 94090 |
rs32267081 | snp | A/G | 0.231111 | 0.249285 | intron-variant | Trim9 | Mm_Celera | 12:70316071 | AGCACTGTCAATTAC[A/G]TTTTAGGATGAGGAA | 94090 |
rs32267136 | snp | C/T | 0.124444 | 0.216185 | intron-variant | Trim9 | Mm_Celera | 12:70323801 | CAAGGTTGAGAACTG[C/T]GGCTCCAAACCCATG | 94090 |
rs32267139 | snp | A/G | 0.124444 | 0.216185 | intron-variant | Trim9 | Mm_Celera | 12:70323867 | CAGACACAGTGAGGT[A/G]TAGTGTGGTGTTTTC | 94090 |
rs32267141 | snp | G/T | 0.124444 | 0.216185 | intron-variant | Trim9 | Mm_Celera | 12:70324473 | CTGTGTTTGCAAATG[G/T]CCTGCTTGTGAAATG | 94090 |
rs32267224 | snp | A/G | 0.231111 | 0.249285 | intron-variant | Trim9 | Mm_Celera | 12:70332627 | GGGCTGAGGAGGAAC[A/G]TGAATTGAGCAGAGG | 94090 |
rs32267226 | snp | A/G | 0.32 | 0.24 | intron-variant | Trim9 | Mm_Celera | 12:70332648 | TGAGCAGAGGAAAAG[A/G]TCTGCACCACTGTCG | 94090 |
rs32267229 | snp | A/C | 0.32 | 0.24 | intron-variant | Trim9 | Mm_Celera | 12:70332683 | AGTAGCGAATGTACA[A/C]AGCCAGCAGTATCTA | 94090 |
rs32267232 | snp | C/T | 0.444444 | 0.157135 | intron-variant | Trim9 | Mm_Celera | 12:70332835 | TGGAGGAAGTCCTTG[C/T]ACCGGCTCCTAGAGC | 94090 |
rs32267296 | snp | C/T | 0.124444 | 0.216185 | intron-variant | Trim9 | Mm_Celera | 12:70334530 | AGAGTTGAGCATAAG[C/T]AACGTGGCTTTAGAG | 94090 |
rs32267299 | snp | A/G | 0.124444 | 0.216185 | intron-variant | Trim9 | Mm_Celera | 12:70334545 | CAACGTGGCTTTAGA[A/G]GCATCGTGACTCATT | 94090 |
rs32267302 | snp | A/G | 0.32 | 0.24 | intron-variant | Trim9 | Mm_Celera | 12:70334603 | TAAGCAGCAGATGAT[A/G]TGGGTGTGCGGTACA | 94090 |
rs32267445 | snp | C/T | 0.124444 | 0.216185 | intron-variant | Trim9 | Mm_Celera | 12:70310254 | GGCTGCCTATGCTTC[C/T]GTGTTCAGGACACAC | 94090 |
rs32267448 | snp | C/T | 0.142012 | 0.225474 | intron-variant | Trim9 | Mm_Celera | 12:70310298 | GGACAAGAGGTCTGG[C/T]CTTGAAGTGCAAAGA | 94090 |
rs32267451 | snp | A/G | 0.231111 | 0.249285 | intron-variant | Trim9 | Mm_Celera | 12:70310339 | GGGGTATGACTCAAG[A/G]GTTGTGAGGTCTCAT | 94090 |
rs32267455 | snp | A/G | 0.231111 | 0.249285 | intron-variant | Trim9 | Mm_Celera | 12:70303923 | GCTCTCCCTCTTAAT[A/G]CTGTTTCACAAACAA | 94090 |
rs32267457 | snp | C/G | 0.231111 | 0.249285 | intron-variant | Trim9 | Mm_Celera | 12:70304047 | TAGCTTTGCCAGGAT[C/G]CAGGATTTACAGGCC | 94090 |
rs32267461 | snp | A/G | 0.124444 | 0.216185 | intron-variant | Trim9 | Mm_Celera | 12:70304156 | TTCATTCTCTGCTCA[A/G]TATCTTTATCAGCCT | 94090 |
rs32267462 | snp | G/T | 0.124444 | 0.216185 | intron-variant | Trim9 | Mm_Celera | 12:70304235 | GTTTCCATGACAACT[G/T]TTTTCTCTCAGTGAG | 94090 |
rs32267495 | snp | A/G | 0.48 | 0.0979796 | intron-variant | Trim9 | Mm_Celera | 12:70312871 | CTGCCCAATGACTGC[A/G]TTTTCTGAAGATTCT | 94090 |
rs32267497 | snp | A/G | 0.124444 | 0.216185 | intron-variant | Trim9 | Mm_Celera | 12:70313063 | AAGCTACATATTAGG[A/G]TGCGTTAGAAACTTC | 94090 |
rs32267500 | snp | C/G | 0.48 | 0.0979796 | intron-variant | Trim9 | Mm_Celera | 12:70313071 | TATTAGGGTGCGTTA[C/G]AAACTTCAGTTCCAA | 94090 |
rs32267503 | snp | A/G | 0.35503 | 0.226867 | intron-variant | Trim9 | Mm_Celera | 12:70313080 | GCGTTAGAAACTTCA[A/G]TTCCAACACAAGGGA | 94090 |
rs32267615 | snp | A/G | 0.32 | 0.24 | intron-variant | Trim9 | Mm_Celera | 12:70293648 | CTTCAGTTCAGTGCT[A/G]AGGCTTCCATTCCTT | 94090 |
rs32267618 | snp | C/T | 0.231111 | 0.249285 | intron-variant | Trim9 | Mm_Celera | 12:70293730 | GGCAGACCCTTCTGT[C/T]CCTCAGGCGACACAG | 94090 |
rs32267621 | snp | A/G | 0.32 | 0.24 | intron-variant | Trim9 | Mm_Celera | 12:70293770 | ATTCCTCCTCCTTCC[A/G]GGGCTTTCTTCACAG | 94090 |
rs32267745 | snp | C/T | 0.444444 | 0.157135 | intron-variant | Trim9 | Mm_Celera | 12:70340910 | TCTGCCCTTGAGTAT[C/T]GCTCAGTGGGGTTGG | 94090 |
rs32267748 | snp | A/G | 0.277778 | 0.248452 | intron-variant | Trim9 | Mm_Celera | 12:70341123 | CACACGTGCACATGC[A/G]CACATACACAAATAA | 94090 |
rs32267751 | snp | A/G | 0.408163 | 0.193609 | intron-variant | Trim9 | Mm_Celera | 12:70341154 | AATAATAAACATTCT[A/G]GATTTTTATGCATAA | 94090 |
rs32267834 | snp | C/T | 0.244898 | 0.249948 | intron-variant | Trim9 | Mm_Celera | 12:70329119 | CCCTGATGTGTATGT[C/T]GTAATCTTACTTTAT | 94090 |
rs32267837 | snp | C/T | 0.231111 | 0.249285 | intron-variant | Trim9 | Mm_Celera | 12:70329209 | CCGAGGCAGCGACAC[C/T]AGCTAGGATTTGAGG | 94090 |
rs32267839 | snp | A/G | 0.124444 | 0.216185 | intron-variant | Trim9 | Mm_Celera | 12:70329211 | GAGGCAGCGACACTA[A/G]CTAGGATTTGAGGAG | 94090 |
rs32267841 | snp | C/G | 0.124444 | 0.216185 | intron-variant | Trim9 | Mm_Celera | 12:70329246 | TGTCACTTGGCCTTC[C/G]GTGGGAATGAAGCCA | 94090 |
rs32268044 | snp | A/G | 0.244898 | 0.249948 | intron-variant | Trim9 | Mm_Celera | 12:70316087 | TTTTAGGATGAGGAA[A/G]CAGATATTAGTTAAG | 94090 |
rs32268046 | snp | A/G | 0.132653 | 0.220748 | intron-variant | Trim9 | Mm_Celera | 12:70316120 | AAATTGAGATTTGAG[A/G]CCATGTCTCACACCT | 94090 |
rs32268049 | snp | A/G | 0.32 | 0.24 | intron-variant | Trim9 | Mm_Celera | 12:70316249 | TCATTGTTCTGGAGC[A/G]GTCATTACTAAAGCT | 94090 |
rs32268051 | snp | C/T | 0.244898 | 0.249948 | intron-variant | Trim9 | Mm_Celera | 12:70317039 | ATCCATGAACATGAA[C/T]TAAAGATAGTTTACT | 94090 |
rs32268055 | snp | G/T | 0.231111 | 0.249285 | intron-variant, upstream-variant-2KB | Trim9, Gm32151 | Mm_Celera | 12:70346126 | AAGGGAGACCCGTGC[G/T]AAGGTATTCCTACAA | 94090 |
rs32268058 | snp | A/G | 0.244898 | 0.249948 | intron-variant, upstream-variant-2KB | Trim9, Gm32151 | Mm_Celera | 12:70346226 | GATCTCAAGGCAGAC[A/G]CCGAAGGCACTTGCA | 94090 |
rs32268060 | snp | A/T | 0.231111 | 0.249285 | upstream-variant-2KB, synonymous-codon | Trim9, Gm32151 | Mm_Celera | 12:70347849 | CTCAGAAGCAGCTGG[A/T]GCGCCCGCATCTCTG | 94090 |
rs32268064 | snp | C/T | 0.32 | 0.24 | intron-variant | Trim9 | Mm_Celera | 12:70324512 | CATACAGCACTTCCA[C/T]GGCCATTCACAGATA | 94090 |
rs32268067 | snp | C/T | 0.124444 | 0.216185 | intron-variant | Trim9 | Mm_Celera | 12:70324701 | AGAGCAGGAGAAGAA[C/T]GAATGGGGAGAGTCT | 94090 |
rs32268070 | snp | A/G | 0.124444 | 0.216185 | intron-variant | Trim9 | Mm_Celera | 12:70324991 | TTCCACAGTCTTCAC[A/G]TAGACTTCTCTACCC | 94090 |
rs32268073 | snp | C/T | 0.124444 | 0.216185 | intron-variant | Trim9 | Mm_Celera | 12:70325711 | GTTTTTTTAAAAACG[C/T]TTGCTCTTCAGAACA | 94090 |
rs32268095 | snp | A/G | 0.244898 | 0.249948 | intron-variant | Trim9 | Mm_Celera | 12:70332856 | CTCCTAGAGCACAGC[A/G]TGCTTGGATGTAAGG | 94090 |
rs32268098 | snp | G/T | 0.124444 | 0.216185 | intron-variant | Trim9 | Mm_Celera | 12:70332884 | AGGGGTCAAAGTCAC[G/T]AAAGCTCTGCCCAGG | 94090 |
rs32268101 | snp | G/T | 0.124444 | 0.216185 | intron-variant | Trim9 | Mm_Celera | 12:70332906 | CTGCCCAGGGCTCCC[G/T]CTCAATCTCATTTCC | 94090 |
rs32268115 | snp | A/C | 0.32 | 0.24 | intron-variant | Trim9 | Mm_Celera | 12:70334657 | GATGAGAAGAAATCA[A/C]AGACCATCAGAAAAG | 94090 |
rs32268120 | snp | A/G | 0.231111 | 0.249285 | intron-variant | Trim9 | Mm_Celera | 12:70334813 | CTGTTTTAGGTAACC[A/G]CCTTTGCCCATTTCT | 94090 |
rs32268123 | snp | A/G | 0.231111 | 0.249285 | intron-variant | Trim9 | Mm_Celera | 12:70334987 | AAGTATGGATAAAGA[A/G]GAGGAACAAATATCT | 94090 |
rs32268304 | snp | A/G | 0.124444 | 0.216185 | intron-variant | Trim9 | Mm_Celera | 12:70310525 | GGTATATGGCTTTTA[A/G]TATAATTTCCCATAT | 94090 |
rs32268307 | snp | C/T | 0.124444 | 0.216185 | intron-variant | Trim9 | Mm_Celera | 12:70310541 | TATAATTTCCCATAT[C/T]GTTCAAATGAAAGAA | 94090 |
rs32268310 | snp | C/T | 0.32 | 0.24 | intron-variant | Trim9 | Mm_Celera | 12:70311212 | ATTGAATCCCCTTCA[C/T]AGACCTTGTGTCCGT | 94090 |
rs32268312 | snp | A/G | 0.124444 | 0.216185 | intron-variant | Trim9 | Mm_Celera | 12:70311337 | GTTAAAGTTAGGAAA[A/G]TGAAATTTCAGCTGT | 94090 |
rs32268518 | snp | A/G | 0.124444 | 0.216185 | intron-variant | Trim9 | Mm_Celera | 12:70313201 | CACTGCAGCCCTTTC[A/G]AGATTGGCTTTTGCT | 94090 |
rs32268521 | snp | C/G | 0.124444 | 0.216185 | intron-variant | Trim9 | Mm_Celera | 12:70313302 | CCTTTCTGTTCATGA[C/G]ATTCACTCTTCAAAT | 94090 |
rs32268534 | snp | A/G | 0.444444 | 0.157135 | intron-variant | Trim9 | Mm_Celera | 12:70341196 | TTGCCTTTGAAAACA[A/G]TGTTTATAACTGGCA | 94090 |
rs32268537 | snp | A/G | 0.497778 | 0.0332592 | intron-variant | Trim9 | Mm_Celera | 12:70341231 | TTTGATTGCTGATCC[A/G]GTATGTGCAGGAAAT | 94090 |
rs32268540 | snp | C/T | 0.165289 | 0.235211 | intron-variant | Trim9 | Mm_Celera | 12:70341262 | GGTCCTTTAAGAAAG[C/T]GGCACTCACAAGGCT | 94090 |
rs32268543 | snp | C/T | 0.165289 | 0.235211 | intron-variant | Trim9 | Mm_Celera | 12:70341289 | GGCTATGTAGAGTTC[C/T]TTTAAATAACGTTTC | 94090 |
rs32268724 | snp | A/G | 0.231111 | 0.249285 | intron-variant | Trim9 | Mm_Celera | 12:70304396 | GTAGCTCGAGGTGAC[A/G]GATGGCTGGACCTAC | 94090 |
rs32268727 | snp | C/G | 0.231111 | 0.249285 | intron-variant | Trim9 | Mm_Celera | 12:70304418 | TGGACCTACCCCTGA[C/G]GTCACACAGAGAAAG | 94090 |
rs32268730 | snp | A/T | 0.32 | 0.24 | intron-variant | Trim9 | Mm_Celera | 12:70304436 | CACACAGAGAAAGAG[A/T]CCTGATGCTAGGCAG | 94090 |
rs32268733 | snp | C/T | 0.32 | 0.24 | intron-variant | Trim9 | Mm_Celera | 12:70304533 | TAGAGACAAGGGCTT[C/T]GATCTAAGGACATGT | 94090 |
rs32268854 | snp | A/G | 0.124444 | 0.216185 | intron-variant | Trim9 | Mm_Celera | 12:70329283 | AGCAAGCCAGTGGCT[A/G]AGTGAGGGCAGAGGA | 94090 |
rs32268857 | snp | C/T | 0.124444 | 0.216185 | intron-variant | Trim9 | Mm_Celera | 12:70329301 | TGAGGGCAGAGGATA[C/T]AAGCCATGTGGGGAG | 94090 |
rs32268860 | snp | A/G | 0.32 | 0.24 | intron-variant | Trim9 | Mm_Celera | 12:70329356 | GATTAGCATCTGGCT[A/G]ACCCTACAGACATGC | 94090 |
rs32268862 | snp | C/T | 0.32 | 0.24 | intron-variant | Trim9 | Mm_Celera | 12:70329496 | ACCGCAAAACCACAG[C/T]CACAGTGAACATGAA | 94090 |
rs32268874 | snp | C/T | 0.231111 | 0.249285 | intron-variant | Trim9 | Mm_Celera | 12:70333120 | CAGCGACACACGACA[C/T]GCAGATAGTAGCGAG | 94090 |
rs32268879 | snp | A/G | 0.231111 | 0.249285 | intron-variant | Trim9 | Mm_Celera | 12:70333138 | AGATAGTAGCGAGCA[A/G]CAGGAGAGAATTTAT | 94090 |
rs32268882 | snp | A/G | 0.32 | 0.24 | intron-variant | Trim9 | Mm_Celera | 12:70333221 | CAGATGAGAATGGGG[A/G]CCCAAGGGAGCTTTA | 94090 |
rs32268934 | snp | C/T | 0.244898 | 0.249948 | intron-variant | Trim9 | Mm_Celera | 12:70317137 | AACTATTACAATTAT[C/T]AGGTTTTTAAAGCCA | 94090 |
rs32268937 | snp | A/G | 0.32 | 0.24 | intron-variant | Trim9 | Mm_Celera | 12:70317306 | TGCCAGCCTTTCACC[A/G]TAAGGATTACACCGC | 94090 |
rs32268942 | snp | C/T | 0.32 | 0.24 | intron-variant | Trim9 | Mm_Celera | 12:70317785 | CGTTCAGATTGGATG[C/T]TTAGGGTGCGTCTCC | 94090 |
rs32268956 | snp | A/G | 0.124444 | 0.216185 | intron-variant | Trim9 | Mm_Celera | 12:70325842 | TGCTGCGAGGAATAT[A/G]TAGCATGCTACACAT | 94090 |
rs32268959 | snp | C/T | 0.132653 | 0.220748 | intron-variant | Trim9 | Mm_Celera | 12:70325886 | ACTGAAATTTAATGA[C/T]TTTTTCCTCAGCTGC | 94090 |
rs32268962 | snp | A/G | 0.132653 | 0.220748 | intron-variant | Trim9 | Mm_Celera | 12:70326665 | TCCCCAAGAGTTGAA[A/G]CCCCCCACTGAGAAA | 94090 |
rs32268986 | snp | A/G | 0.132653 | 0.220748 | intron-variant | Trim9 | Mm_Celera | 12:70335039 | GAGTAGAGAATGAGC[A/G]TCCCATGAACGCATC | 94090 |
rs32268989 | snp | A/G | 0.231111 | 0.249285 | intron-variant | Trim9 | Mm_Celera | 12:70335072 | CGGCAGATGAGAATT[A/G]ACCGTCTATGCACCC | 94090 |
rs32268992 | snp | A/C | 0.260355 | 0.249785 | intron-variant | Trim9 | Mm_Celera | 12:70335203 | GGTGGCAGAGACGTG[A/C]GGCTTTGATTTTATG | 94090 |
rs32269135 | snp | C/T | 0.231111 | 0.249285 | upstream-variant-2KB, intron-variant | Trim9, Gm32151 | Mm_Celera | 12:70348138 | ATTTCTGAGTGTTTA[C/T]CGGTTGTTAACTAGC | 94090 |
rs32269140 | snp | G/T | 0.244898 | 0.249948 | upstream-variant-2KB, intron-variant | Trim9, Gm32151 | Mm_Celera | 12:70348998 | GGGGCATCCATGCCC[G/T]TGTATGTTACAATCC | 94090 |
rs32269142 | snp | A/G | 0.244898 | 0.249948 | upstream-variant-2KB, intron-variant | Trim9, Gm32151 | Mm_Celera | 12:70349018 | TGTTACAATCCTTTC[A/G]TGTATTTTGTATTCA | 94090 |
rs32269225 | snp | C/T | 0.231111 | 0.249285 | intron-variant | Trim9 | Mm_Celera | 12:70311354 | GAAATTTCAGCTGTA[C/T]CAAATTACACCCACT | 94090 |
rs32269228 | snp | A/G | 0.231111 | 0.249285 | intron-variant | Trim9 | Mm_Celera | 12:70311455 | TTGCGTTTTAGAACG[A/G]TCTCTGCCTTTTGAA | 94090 |
rs32269336 | snp | A/C | 0.444444 | 0.157135 | intron-variant | Trim9 | Mm_Celera | 12:70341367 | ATCAACTAATAGGAA[A/C]AAACAGGTAGATTTA | 94090 |
rs32269339 | snp | C/T | 0.473373 | 0.11227 | intron-variant | Trim9 | Mm_Celera | 12:70341633 | GAGTGAGGAATTAGT[C/T]GCTCACTGGGGTTTG | 94090 |
rs32269342 | snp | A/G | 0.396694 | 0.202437 | intron-variant | Trim9 | Mm_Celera | 12:70341642 | ATTAGTCGCTCACTG[A/G]GGTTTGGAGATTGTT | 94090 |
rs32269464 | snp | A/G | 0.231111 | 0.249285 | intron-variant | Trim9 | Mm_Celera | 12:70313466 | CCCCCCTGACATCAA[A/G]GGACCTGCGTTGCTC | 94090 |
rs32269470 | snp | C/T | 0.32 | 0.24 | intron-variant | Trim9 | Mm_Celera | 12:70314114 | GATCAACAGCTCCAG[C/T]CCTTAGAGTTATTTC | 94090 |
rs32269472 | snp | C/T | 0.260355 | 0.249785 | intron-variant | Trim9 | Mm_Celera | 12:70314165 | AACATGAAATTTATC[C/T]TTAATCCCTATGGAT | 94090 |
rs32269556 | snp | A/G | 0.124444 | 0.216185 | intron-variant | Trim9 | Mm_Celera | 12:70304598 | AAAGAAGAGGTTTGC[A/G]GAGCTATTCTGAATG | 94090 |
rs32269558 | snp | A/G | 0.124444 | 0.216185 | intron-variant | Trim9 | Mm_Celera | 12:70305038 | ATTTGAGGAGGGGAC[A/G]CATGCACAGCTTCAG | 94090 |
rs32269561 | snp | C/T | 0.124444 | 0.216185 | intron-variant | Trim9 | Mm_Celera | 12:70305389 | TTTCATTTCTGATTG[C/T]CAAACGAGACTGTAG | 94090 |
rs32269687 | snp | C/T | 0.124444 | 0.216185 | intron-variant | Trim9 | Mm_Celera | 12:70333285 | AGACTTTGCTACACG[C/T]GCCATGATGGTTTCA | 94090 |
rs32269690 | snp | C/T | 0.231111 | 0.249285 | intron-variant | Trim9 | Mm_Celera | 12:70333327 | AATTTCATGGGTCAT[C/T]CACGCCAGCATCTTA | 94090 |
rs32269692 | snp | A/G | 0.231111 | 0.249285 | intron-variant | Trim9 | Mm_Celera | 12:70333356 | TAAATTTCCACACAG[A/G]GGCATGCATCTTAGT | 94090 |
rs32269695 | snp | A/C | 0.124444 | 0.216185 | intron-variant | Trim9 | Mm_Celera | 12:70318194 | AAAACACTTCTGCAA[A/C]AAGCCCCGACGTTGC | 94090 |
rs32269697 | snp | A/G | 0.231111 | 0.249285 | intron-variant | Trim9 | Mm_Celera | 12:70318205 | GCAACAAGCCCCGAC[A/G]TTGCTATGGTTACTA | 94090 |
rs32269700 | snp | A/C | 0.124444 | 0.216185 | intron-variant | Trim9 | Mm_Celera | 12:70319634 | ATTAACAATACCATC[A/C]TCATTTGTACAGAGC | 94090 |
rs32269701 | snp | C/T | 0.32 | 0.24 | intron-variant | Trim9 | Mm_Celera | 12:70320325 | ATATGTCATAGTTTT[C/T]CTACTCTATATCTTC | 94090 |
rs32269934 | snp | C/T | 0.231111 | 0.249285 | upstream-variant-2KB, intron-variant | Trim9, Gm32151 | Mm_Celera | 12:70349075 | TAGCAAAGTAAAGAG[C/T]GTCATTCTTCCCAAG | 94090 |
rs32269942 | snp | A/G | 0.124444 | 0.216185 | upstream-variant-2KB, intron-variant | Trim9, Gm32151 | Mm_Celera | 12:70349494 | CTCTCACGATCCAGC[A/G]CCGGTGAGGCTAGGG | 94090 |
rs32269995 | snp | A/C/G | 0.497778 | 0.0332592 | intron-variant | Trim9 | GRCm38.p3 | 12:70341963 | CTCTAACTTGCAAGT[A/C/G]TAAAATCTGTAAATG | 94090 |
rs32269998 | snp | G/T | 0.231111 | 0.249285 | intron-variant | Trim9 | Mm_Celera | 12:70342110 | GACCCAAGGGCTATT[G/T]AAATAGAATGTGTAC | 94090 |
rs32270003 | snp | G/T | 0.444444 | 0.157135 | intron-variant | Trim9 | Mm_Celera | 12:70342538 | TAGCTCCTTCACTGT[G/T]GCCTAGTTCGTTATT | 94090 |
rs32270014 | snp | C/T | 0.32 | 0.24 | intron-variant | Trim9 | Mm_Celera | 12:70329549 | AAGCTGGCTCGCAGA[C/T]AGGTTGGTAGAAACC | 94090 |
rs32270017 | snp | A/T | 0.32 | 0.24 | intron-variant | Trim9 | Mm_Celera | 12:70329577 | ACCAGAAGATTCACA[A/T]GGACCACAGGAGAGT | 94090 |
rs32270020 | snp | G/T | 0.231111 | 0.249285 | intron-variant | Trim9 | Mm_Celera | 12:70329614 | GAATGGTGGGTGGTT[G/T]AAGGCTGATCCTGTT | 94090 |
rs32270023 | snp | A/G | 0.124444 | 0.216185 | intron-variant | Trim9 | Mm_Celera | 12:70329630 | AAGGCTGATCCTGTT[A/G]ACAAAGGTTCTGACT | 94090 |
rs32270175 | snp | G/T | 0.231111 | 0.249285 | intron-variant | Trim9 | Mm_Celera | 12:70335533 | TTGACACGTGGGCTC[G/T]GGAAGATGGCCTCAA | 94090 |
rs32270178 | snp | A/G | 0.231111 | 0.249285 | intron-variant | Trim9 | Mm_Celera | 12:70335629 | TGACTGTTCATGAGT[A/G]GGACTACCCATGGCT | 94090 |
rs32270180 | snp | A/T | 0.231111 | 0.249285 | intron-variant | Trim9 | Mm_Celera | 12:70336569 | ACCCCTGGGTATGGG[A/T]TTGAACACATATTCG | 94090 |
rs32270183 | snp | A/G | 0.497041 | 0.0383476 | intron-variant | Trim9 | Mm_Celera | 12:70337637 | AATATTTAAAAAAAA[A/G]AAGAAGACTGGCTAA | 94090 |
rs32270314 | snp | A/C | 0.231111 | 0.249285 | intron-variant | Trim9 | Mm_Celera | 12:70326739 | CAGCCAGCAGCAGGC[A/C]ATTTTATCTAAGAGA | 94090 |
rs32270317 | snp | A/G | 0.124444 | 0.216185 | intron-variant | Trim9 | Mm_Celera | 12:70326791 | GTCTAGATTCTAATG[A/G]CCCTTGCCTCCAACT | 94090 |
rs32270319 | snp | C/T | 0.244898 | 0.249948 | intron-variant | Trim9 | Mm_Celera | 12:70326846 | CTATGGAAAAACATT[C/T]ATAAATTTGTTGTTA | 94090 |
rs32270322 | snp | A/G | 0.244898 | 0.249948 | intron-variant | Trim9 | Mm_Celera | 12:70326864 | AAATTTGTTGTTAAT[A/G]TGTTGATATCTTGGG | 94090 |
rs32270454 | snp | A/C | 0.124444 | 0.216185 | intron-variant | Trim9 | Mm_Celera | 12:70305420 | TTCAAAGGACTTCCA[A/C]GTGCAGGAACAATGT | 94090 |
rs32270457 | snp | A/G | 0.124444 | 0.216185 | intron-variant | Trim9 | Mm_Celera | 12:70305437 | TGCAGGAACAATGTT[A/G]GTGAGGAAAGGAGTG | 94090 |
rs32270460 | snp | C/T | 0.124444 | 0.216185 | intron-variant | Trim9 | Mm_Celera | 12:70305497 | GGCTAAAAGGCAATC[C/T]TGAGTCAGTCTTGTA | 94090 |
rs32270463 | snp | A/G | 0.132653 | 0.220748 | intron-variant | Trim9 | Mm_Celera | 12:70305586 | CTGAGGCCATTGGCA[A/G]CCTGGCCCTATGAGG | 94090 |
rs32270585 | snp | A/G | 0.32 | 0.24 | intron-variant | Trim9 | Mm_Celera | 12:70333377 | GCATCTTAGTATTAA[A/G]CCAGCCATAGGCAAC | 94090 |
rs32270590 | snp | A/G | 0.32 | 0.24 | intron-variant | Trim9 | Mm_Celera | 12:70333478 | TGGGATTGAGCACTC[A/G]GCCTTCCTTTTTTGC | 94090 |
rs32270593 | snp | C/T | 0.408163 | 0.193609 | intron-variant | Trim9 | Mm_Celera | 12:70333615 | CTGTAGAATTGCATC[C/T]TTCAGATCTTATTCA | 94090 |
rs32270694 | snp | C/T | 0.124444 | 0.216185 | intron-variant | Trim9 | Mm_Celera | 12:70321226 | TGGTTTCCCAGCTGA[C/T]GCCTCCTTCTCCTGG | 94090 |
rs32270697 | snp | A/G | 0.124444 | 0.216185 | intron-variant | Trim9 | Mm_Celera | 12:70321392 | TCCAAGGAGTCTGGA[A/G]AAAAGCAACAGCCAT | 94090 |
rs32270700 | snp | G/T | 0.32 | 0.24 | intron-variant | Trim9 | Mm_Celera | 12:70321743 | CAATTGAAACAAGAT[G/T]GAAGAAGGAAAGCAT | 94090 |
rs32270703 | snp | A/G | 0.124444 | 0.216185 | intron-variant | Trim9 | Mm_Celera | 12:70322389 | GTGAAGGAAGCAAGC[A/G]GAGGTCTATGCCTGT | 94090 |
rs32270766 | snp | C/T | 0.32 | 0.24 | intron-variant | Trim9 | Mm_Celera | 12:70329661 | TACTGAAAGTTTATG[C/T]TCACAGAAATAGAGT | 94090 |
rs32270771 | snp | C/T | 0.277778 | 0.248452 | intron-variant | Trim9 | Mm_Celera | 12:70329689 | AGTAGGTTATGATAG[C/T]GAAGGAACATCAATT | 94090 |
rs32270786 | snp | A/C | 0.444444 | 0.157135 | intron-variant | Trim9 | Mm_Celera | 12:70342808 | AGACATTTTACACAC[A/C]ACTGCTATAACTAAG | 94090 |
rs32270789 | snp | A/G | 0.444444 | 0.157135 | intron-variant | Trim9 | Mm_Celera | 12:70343089 | GACGAATTAGCACGT[A/G]TCTAGGGTAAAAAAG | 94090 |
rs32270792 | snp | A/T | 0.408163 | 0.193609 | intron-variant | Trim9 | Mm_Celera | 12:70343112 | TAAAAAAGAAAAAAA[A/T]TATTTAGCAGCACAA | 94090 |
rs32270866 | snp | A/C | 0.32 | 0.24 | intron-variant | Trim9 | Mm_Celera | 12:70314257 | CTGTCATCACTCAGC[A/C]ATTAGTCCTTGGTTA | 94090 |
rs32270868 | snp | A/T | 0.32 | 0.24 | intron-variant | Trim9 | Mm_Celera | 12:70314393 | AGTGTTTGCTCTACA[A/T]GTGGACAAAATCACC | 94090 |
rs32271036 | snp | C/T | 0.231111 | 0.249285 | intron-variant | Trim9 | Mm_Celera | 12:70337795 | ATTGCTGTGTATTTT[C/T]CTCATGTAATGGATT | 94090 |
rs32271039 | snp | A/G | 0.497041 | 0.0383476 | intron-variant | Trim9 | Mm_Celera | 12:70337833 | AATGAAATTTAGGAG[A/G]AAAATGATTTTTAAC | 94090 |
rs32271041 | snp | C/T | 0.142012 | 0.225474 | intron-variant | Trim9 | Mm_Celera | 12:70337892 | AAAGCACCCCAGCTG[C/T]CCATTAAGGCACAGG | 94090 |
rs32271057 | snp | C/G | 0.32 | 0.24 | upstream-variant-2KB, intron-variant | Trim9, Gm32151 | Mm_Celera | 12:70349606 | TAACGAACCTGAAAT[C/G]TTAATCTTTTGCTAT | 94090 |
rs32271060 | snp | C/T | 0.444444 | 0.157135 | upstream-variant-2KB, intron-variant | Trim9, Gm32151 | Mm_Celera | 12:70349626 | TCTTTTGCTATCCTG[C/T]TTAGCTTCTCTGAGA | 94090 |
rs32271244 | snp | A/C | 0.124444 | 0.216185 | intron-variant | Trim9 | Mm_Celera | 12:70326964 | CAGGTCTTCACACTG[A/C]AACTGTGTCTCTTAT | 94090 |
rs32271246 | snp | C/T | 0.244898 | 0.249948 | intron-variant | Trim9 | Mm_Celera | 12:70327096 | TGTTCTTCCTGAAGT[C/T]ATGGGATGAATTTTT | 94090 |
rs32271249 | snp | A/G | 0.124444 | 0.216185 | intron-variant | Trim9 | Mm_Celera | 12:70327215 | ACTCTGACTTCAGGA[A/G]CTGGGTATCTGGACT | 94090 |
rs32271252 | snp | C/T | 0.32 | 0.24 | intron-variant | Trim9 | Mm_Celera | 12:70327427 | CCACTACAGTCAGAA[C/T]ACTTGCAGGAACACC | 94090 |
rs32271386 | snp | C/T | 0.231111 | 0.249285 | intron-variant | Trim9 | Mm_Celera | 12:70305587 | TGAGGCCATTGGCAG[C/T]CTGGCCCTATGAGGA | 94090 |
rs32271506 | snp | C/T | 0.231111 | 0.249285 | intron-variant | Trim9 | Mm_Celera | 12:70322412 | ATGCCTGTCCAATTA[C/T]GAGGTGCAAGAGTTT | 94090 |
rs32271509 | snp | A/G | 0.124444 | 0.216185 | intron-variant | Trim9 | Mm_Celera | 12:70322490 | GATCACCCTGACAAA[A/G]GAGAAGACTAAGACT | 94090 |
rs32271512 | snp | C/T | 0.32 | 0.24 | intron-variant | Trim9 | Mm_Celera | 12:70322563 | CCAATAATCATACTA[C/T]CCAAGTAAAGGAAGT | 94090 |
rs32271516 | snp | A/G | 0.231111 | 0.249285 | intron-variant | Trim9 | Mm_Celera | 12:70333757 | CTGTGGGAGACTGAA[A/G]TCAATGCAAATCTTG | 94090 |
rs32271519 | snp | C/T | 0.32 | 0.24 | intron-variant | Trim9 | Mm_Celera | 12:70333951 | AAACAAGCTTAATAG[C/T]AGAACATGGGCTAAG | 94090 |
rs32271523 | snp | A/G | 0.32 | 0.24 | intron-variant | Trim9 | Mm_Celera | 12:70334069 | TTTTGGGTCTTCAGC[A/G]AATGGTCAAGTATGG | 94090 |
rs32271625 | snp | C/T | 0.444444 | 0.157135 | intron-variant | Trim9 | Mm_Celera | 12:70343160 | TGAAACATTTACTGA[C/T]TCAGTGATTGGTAAA | 94090 |
rs32271630 | snp | C/T | 0.231111 | 0.249285 | intron-variant | Trim9 | Mm_Celera | 12:70343575 | GTATTACTTATGGAT[C/T]TTCAAGGTCATAAAT | 94090 |
rs32271633 | snp | A/G | 0.231111 | 0.249285 | intron-variant | Trim9 | Mm_Celera | 12:70343650 | TATTAAAACTACTTG[A/G]AAACTATTTTGCCTT | 94090 |
rs32271704 | snp | A/T | 0.124444 | 0.216185 | intron-variant | Trim9 | Mm_Celera | 12:70329834 | AACCCTCTGTGATTA[A/T]AGGTGTCTAGGATTA | 94090 |
rs32271707 | snp | C/T | 0.244898 | 0.249948 | intron-variant | Trim9 | GRCm38.p3 | 12:70329848 | ATAGGTGTCTAGGAT[C/T]ATGGAAGAGTCCCCC | 94090 |
rs32271710 | snp | A/G | 0.244898 | 0.249948 | intron-variant | Trim9 | Mm_Celera | 12:70329884 | AAAAATCCTGTTTCA[A/G]TTGAGCATCATTGAA | 94090 |
rs32271713 | snp | A/G | 0.152778 | 0.230321 | intron-variant | Trim9 | Mm_Celera | 12:70330227 | TATTAATGTATAGTC[A/G]ATAAAATAAAGTTTT | 94090 |
rs32271784 | snp | A/G | 0.132653 | 0.220748 | intron-variant | Trim9 | Mm_Celera | 12:70337914 | AGGCACAGGGATTTA[A/G]GAGACCACAGCATTG | 94090 |
rs32271787 | snp | A/G | 0.231111 | 0.249285 | intron-variant | Trim9 | Mm_Celera | 12:70337931 | AGACCACAGCATTGC[A/G]TTTTACAGGGCATGG | 94090 |
rs32271790 | snp | A/G | 0.444444 | 0.157135 | intron-variant | Trim9 | Mm_Celera | 12:70338179 | GTGCGTGGCTTCTAC[A/G]GTGACTTGCATATAG | 94090 |
rs32271792 | snp | A/G | 0.444444 | 0.157135 | intron-variant | Trim9 | Mm_Celera | 12:70338257 | GATGTTCGCTGGCAG[A/G]CTGATCTATAAACGT | 94090 |
rs32272035 | snp | G/T | 0.142012 | 0.225474 | intron-variant | Trim9 | Mm_Celera | 12:70327449 | AGGAACACCACAGCA[G/T]CCATAAAACCAGCTG | 94090 |
rs32272036 | snp | C/T | 0.124444 | 0.216185 | intron-variant | Trim9 | Mm_Celera | 12:70327508 | ATTTATTGCAACCAT[C/T]CCAATGTCTGGGACT | 94090 |
rs32272038 | snp | C/T | 0.124444 | 0.216185 | intron-variant | Trim9 | Mm_Celera | 12:70327560 | TTCCTCTAGCAGGTA[C/T]GGAGAACTCACCTGA | 94090 |
rs32272041 | snp | C/T | 0.124444 | 0.216185 | intron-variant | Trim9 | Mm_Celera | 12:70327667 | AAGAAGTTGCTGGCT[C/T]CCTCTATTCAAAAGA | 94090 |
rs32272043 | snp | C/T | 0.124444 | 0.216185 | intron-variant | Trim9 | Mm_Celera | 12:70327791 | GAGGAGGGACTCATG[C/T]GCAGGAAACCAGTCA | 94090 |
rs32272205 | snp | A/T | 0.244898 | 0.249948 | intron-variant | Trim9 | Mm_Celera | 12:70322602 | GAGTTTCCAATGCAT[A/T]GTTCAGAATGTTTAG | 94090 |
rs32272315 | snp | A/G | 0.32 | 0.24 | intron-variant | Trim9 | Mm_Celera | 12:70334111 | AAAGAGCTTATTAAA[A/G]CCAACCTGAAGTTCA | 94090 |
rs32272318 | snp | A/G | 0.32 | 0.24 | intron-variant | Trim9 | Mm_Celera | 12:70334320 | AATATGCTGAAAGCT[A/G]TTTATCGTATTTCCT | 94090 |
rs32272323 | snp | C/G | 0.124444 | 0.216185 | intron-variant | Trim9 | Mm_Celera | 12:70334426 | CTCTGCTGTAGAAGA[C/G]TTATTAGATTGGATG | 94090 |
rs32272510 | snp | A/G | 0.231111 | 0.249285 | intron-variant | Trim9 | Mm_Celera | 12:70343712 | GATATTTATTCACAG[A/G]ATTTTCTTCAGCAGT | 94090 |
rs32272636 | snp | A/G | 0.244898 | 0.249948 | intron-variant | Trim9 | Mm_Celera | 12:70330369 | CTGGGAAGGAGTTGG[A/G]CAAATGATGTATAAA | 94090 |
rs32272639 | snp | C/T | 0.244898 | 0.249948 | intron-variant | Trim9 | Mm_Celera | 12:70330391 | ATGTATAAAACCTAG[C/T]ACCTCAATTCTATCA | 94090 |
rs32272642 | snp | C/T | 0.142012 | 0.225474 | intron-variant | Trim9 | Mm_Celera | 12:70330691 | ACATCACAGTGGTAA[C/T]TCTGGGTTAACAGGA | 94090 |
rs32273116 | snp | C/T | 0.124444 | 0.216185 | intron-variant | Trim9 | Mm_Celera | 12:70328326 | GAAATGCCAAGAAAC[C/T]CAAGGACACGTGTAG | 94090 |
rs32273425 | snp | C/G | 0.132653 | 0.220748 | intron-variant | Trim9 | Mm_Celera | 12:70330829 | GAAGTGTCTTCTGCT[C/G]ATCTGAGATGTTCCT | 94090 |
rs32273428 | snp | A/C | 0.132653 | 0.220748 | intron-variant | Trim9 | Mm_Celera | 12:70331042 | ATGATAAGCAAGAGC[A/C]GGGCTCATAATGAAC | 94090 |
rs32273431 | snp | C/T | 0.5 | 0 | intron-variant | Trim9 | Mm_Celera | 12:70331740 | AGAGAGTGGAGCTTG[C/T]GTGTTCTCTGGGAGT | 94090 |
rs32273806 | snp | G/T | 0.231111 | 0.249285 | intron-variant | Trim9 | Mm_Celera | 12:70338685 | AAAACACCGAAGAAT[G/T]TTCTTACCTTTTCCG | 94090 |
rs32273809 | snp | A/G | 0.231111 | 0.249285 | intron-variant | Trim9 | Mm_Celera | 12:70338786 | GCAGCTAAAGCCATC[A/G]TAGTTGTAGAGACTG | 94090 |
rs32273812 | snp | C/G | 0.231111 | 0.249285 | intron-variant | Trim9 | Mm_Celera | 12:70338962 | ACCCAATGGGTAGGA[C/G]ATAGCCGGAAGGTCA | 94090 |
rs32274354 | snp | A/G | 0.132653 | 0.220748 | intron-variant | Trim9 | Mm_Celera | 12:70331813 | AATCTTGCTGTTCAG[A/G]AATTTTTACAGACCT | 94090 |
rs32274515 | snp | C/T | 0.231111 | 0.249285 | intron-variant | Trim9 | Mm_Celera | 12:70339035 | AGGACTGTGACTAGT[C/T]CTAGCCTAACACACT | 94090 |
rs32274518 | snp | G/T | 0.231111 | 0.249285 | intron-variant | Trim9 | Mm_Celera | 12:70339107 | CGAACAAAAATACAG[G/T]GCTCACGTCCCTGAT | 94090 |
rs32274521 | snp | A/G | 0.231111 | 0.249285 | intron-variant | Trim9 | Mm_Celera | 12:70339171 | ACTACAAGTTGGCTC[A/G]AGCAGCTGTGATAAA | 94090 |
rs33844133 | snp | A/T | 0.48 | 0.0979796 | intron-variant | Trim9 | Mm_Celera | 12:70296226 | TGCTCTAACATGGGC[A/T]TGATTTTGCCAGCTG | 94090 |
rs33856475 | snp | A/G | 0.444444 | 0.157135 | intron-variant | Trim9 | Mm_Celera | 12:70289868 | TTATCTAAGCTTTCA[A/G]TCCTGTTCCCAGGAC | 94090 |
rs33857975 | snp | A/C | 0.444444 | 0.157135 | intron-variant | Trim9 | Mm_Celera | 12:70306333 | ACAAAGAAAGTGATA[A/C]ATCAAGGCAAATCTA | 94090 |
rs45688312 | snp | A/G | | | intron-variant | Trim9 | Mm_Celera | 12:70287094 | AGAGAGTACTAAGAC[A/G]CATAAATCCACACTG | 94090 |
rs45705672 | snp | A/G | | | intron-variant | Trim9 | Mm_Celera | 12:70287584 | CCCAGTAGCCCCATG[A/G]CATCCATGTGGCCTT | 94090 |
rs45807988 | snp | A/G | | | intron-variant | Trim9 | Mm_Celera | 12:70286537 | TACCCAGTGGCAGAG[A/G]ACCTGGGAAGGGTGG | 94090 |
rs45819333 | snp | C/G | | | intron-variant | Trim9 | Mm_Celera | 12:70341006 | TCTATATTTGATGGC[C/G]CACAACTGCCTCCAG | 94090 |
rs45940914 | snp | A/G | | | intron-variant | Trim9 | Mm_Celera | 12:70290430 | TCAGGCGCATGCATG[A/G]GGAGCTCAGGTAGCC | 94090 |
rs45951462 | snp | A/G | | | intron-variant | Trim9 | Mm_Celera | 12:70273898 | GTGCCCAGAACATCC[A/G]AATTTGGAGGGAAGT | 94090 |
rs46185808 | snp | A/C | | | intron-variant | Trim9 | Mm_Celera | 12:70287151 | AATTTCGCGCGCGCG[A/C]GCGCACACACACACA | 94090 |
rs46205568 | snp | C/T | | | intron-variant | Trim9 | Mm_Celera | 12:70284203 | AATCTATTTTTCAAC[C/T]CCAGTTTAACGCCCC | 94090 |
rs46206445 | snp | A/T | | | intron-variant | Trim9 | Mm_Celera | 12:70327151 | TCAGGGATTCTTGGA[A/T]AGAATTCAGGGGAGA | 94090 |
rs46287877 | snp | A/G | | | intron-variant | Trim9 | Mm_Celera | 12:70287154 | TTCGCGCGCGCGCGC[A/G]CACACACACACACAC | 94090 |
rs46518987 | snp | C/T | | | intron-variant | Trim9 | Mm_Celera | 12:70342982 | TTTTTGGCTACATAG[C/T]TAGTTAGAGGGCAGC | 94090 |
rs46588381 | snp | A/T | | | intron-variant | Trim9 | Mm_Celera | 12:70326892 | GGGTTCAAGGTAATG[A/T]ATTTATATATTATTC | 94090 |
rs46738063 | snp | A/C | | | intron-variant | Trim9 | Mm_Celera | 12:70283426 | TTTTCATCCCCCTTG[A/C]GATGTGCATTTTTGG | 94090 |
rs46812448 | snp | C/T | | | intron-variant | Trim9 | Mm_Celera | 12:70286529 | TGGGGCTGTACCCAG[C/T]GGCAGAGAACCTGGG | 94090 |
rs46895976 | snp | C/T | | | intron-variant | Trim9 | Mm_Celera | 12:70343252 | GGCAGTGGTGGTGCA[C/T]TCCTTTAATCCCAGC | 94090 |
rs46926175 | snp | A/G | | | intron-variant | Trim9 | Mm_Celera | 12:70286777 | TATATTTCAAAACAG[A/G]CCCAAAATATGGTTC | 94090 |
rs46981909 | snp | C/T | | | intron-variant | Trim9 | Mm_Celera | 12:70312075 | GGCCTGAGGACAAGG[C/T]TATGGGAAGAGATGG | 94090 |
rs47016280 | snp | A/G | | | intron-variant | Trim9 | Mm_Celera | 12:70285961 | CAGCTCCAGAAGGGA[A/G]CGCCTTACATATAAC | 94090 |
rs47055508 | snp | C/G/T | | | intron-variant | Trim9 | GRCm38.p3 | 12:70340630 | ACCAAACCCTGAGTG[C/G/T]GACAGACCAGGATGG | 94090 |
rs47133123 | snp | A/G | | | intron-variant | Trim9 | Mm_Celera | 12:70286551 | GAACCTGGGAAGGGT[A/G]GTAGCATAACATCTT | 94090 |
rs47202442 | snp | A/T | | | intron-variant | Trim9 | Mm_Celera | 12:70326834 | ATTTCTTTCTTCCTA[A/T]GGAAAAACATTTATA | 94090 |
rs47277275 | snp | A/G | | | intron-variant | Trim9 | Mm_Celera | 12:70326583 | GCCCAACAGGGCTGT[A/G]AAGCCCTCGAAGACT | 94090 |
rs47368465 | snp | C/T | | | intron-variant | Trim9 | Mm_Celera | 12:70302154 | GATTAAGAGCACTGA[C/T]TGCTCTCGCAGATGA | 94090 |
rs47370668 | snp | C/T | | | intron-variant | Trim9 | Mm_Celera | 12:70332108 | ACACCAAAACCTATA[C/T]ATAGAGATCTAAGCA | 94090 |
rs47413346 | snp | A/G | | | intron-variant | Trim9 | Mm_Celera | 12:70331875 | CAGAGACCAGGGGGT[A/G]GAGGTAACATATGAG | 94090 |
rs47415023 | snp | C/T | | | intron-variant | Trim9 | Mm_Celera | 12:70289566 | CTTTAACCCCTGGGC[C/T]ATAACTGTATGCTCC | 94090 |
rs47479897 | snp | C/T | | | intron-variant | Trim9 | Mm_Celera | 12:70332206 | ATGATATATCTAATA[C/T]TATAGATTATTAACC | 94090 |
rs47495552 | snp | C/T | | | intron-variant | Trim9 | Mm_Celera | 12:70340713 | AATTTTCATTTAATA[C/T]TTTTGAACGCTGCTT | 94090 |
rs47496309 | snp | A/G | | | intron-variant | Trim9 | Mm_Celera | 12:70290447 | GAGCTCAGGTAGCCA[A/G]GGAAATCAGAGAACC | 94090 |
rs47552710 | snp | A/G | | | intron-variant | Trim9 | Mm_Celera | 12:70289909 | CCCTTTTTGTTTTGC[A/G]AAACAAAACAAAACA | 94090 |
rs47559911 | snp | C/T | | | intron-variant | Trim9 | GRCm38.p3 | 12:70337309 | GGATGGATCACAGGG[C/T]TCCCAATGGAGGAGC | 94090 |
rs47567470 | snp | C/T | | | intron-variant | Trim9 | Mm_Celera | 12:70288276 | AGCAATTCAGCAAGA[C/T]TCTGACTCAAAATCT | 94090 |
rs47666814 | snp | C/T | | | intron-variant | Trim9 | Mm_Celera | 12:70342765 | TGTAATAAATATTAA[C/T]AGAATGTTATCTTAG | 94090 |
rs47679420 | snp | C/T | | | intron-variant | Trim9 | Mm_Celera | 12:70289818 | TTCTATTTATCTACT[C/T]AAGAACATATTTTTT | 94090 |
rs47752943 | snp | A/G | | | intron-variant | Trim9 | Mm_Celera | 12:70270322 | AGCCCTAAGGAGAGA[A/G]GAGGCAGCTGGAGCT | 94090 |
rs47762874 | snp | A/G | | | intron-variant | Trim9 | Mm_Celera | 12:70286640 | CTAGAACTGTTTCTT[A/G]GATGCTCACAGATGC | 94090 |
rs47777405 | snp | G/T | | | intron-variant | Trim9 | Mm_Celera | 12:70332070 | ACTGTTATACCACAT[G/T]TGAGATAATTGAGAA | 94090 |
rs47805606 | snp | C/T | | | intron-variant | Trim9 | Mm_Celera | 12:70301694 | ATCTAACAGGAAGGT[C/T]GAGTTCTAAAGCCAT | 94090 |
rs47961274 | snp | A/T | | | intron-variant | Trim9 | Mm_Celera | 12:70344473 | GAGAACTATTGTTTT[A/T]AATTTTCAAAATTAA | 94090 |
rs47964060 | snp | A/G/T | | | intron-variant | Trim9 | GRCm38.p3 | 12:70337292 | GCTCACAATCAGCTA[A/G/T]TGGATGGATCACAGG | 94090 |
rs48147480 | snp | C/T | | | intron-variant | Trim9 | Mm_Celera | 12:70342968 | GGAATTCAAAGTCAT[C/T]TTTGGCTACATAGCT | 94090 |
rs48171846 | snp | A/G | | | intron-variant | Trim9 | Mm_Celera | 12:70301724 | TAATACTGTTAAGAC[A/G]TAAAGCAGGATTTCC | 94090 |
rs48193675 | snp | G/T | | | intron-variant | Trim9 | Mm_Celera | 12:70285253 | TGAGTCACGTGGCGT[G/T]TAGAGGAAGGAGGCT | 94090 |
rs48218664 | snp | C/T | | | intron-variant | Trim9 | Mm_Celera | 12:70287801 | GAACCAAGTAGGAGG[C/T]AGAGGGGCTCTCATA | 94090 |
rs48352452 | snp | A/G/T | | | intron-variant | Trim9 | GRCm38.p3 | 12:70337868 | CAACATTATTTATAC[A/G/T]TGAGAAATAAAGCAC | 94090 |
rs48369832 | snp | A/G | | | intron-variant | Trim9 | Mm_Celera | 12:70285995 | GGTGGACATACAGAC[A/G]CTCTCCATAGCGAAC | 94090 |
rs48447655 | snp | A/C | | | intron-variant | Trim9 | Mm_Celera | 12:70283859 | AGCCGAGAACCACTC[A/C]GGAGACTGTGTACAC | 94090 |
rs48634947 | snp | A/G | | | intron-variant | Trim9 | Mm_Celera | 12:70286692 | AACTCGGGTCAGTTT[A/G]CAACATCCCAAGACT | 94090 |
rs48786842 | snp | A/C | | | intron-variant | Trim9 | Mm_Celera | 12:70287579 | CTCTGCCCAGTAGCC[A/C]CATGGCATCCATGTG | 94090 |
rs48835992 | snp | C/T | | | intron-variant | Trim9 | GRCm38.p3 | 12:70337310 | GATGGATCACAGGGC[C/T]CCCAATGGAGGAGCT | 94090 |
rs48901888 | snp | A/G | | | intron-variant | Trim9 | Mm_Celera | 12:70330181 | TGCTCCCAACCCCTG[A/G]ACCATCTTTTCAGCC | 94090 |
rs48945063 | snp | C/T | | | intron-variant | Trim9 | Mm_Celera | 12:70287201 | ACACACACACAGCCT[C/T]TTTGTCAGCCAGCAG | 94090 |
rs49036083 | snp | C/T | | | intron-variant | Trim9 | Mm_Celera | 12:70288870 | ACTTCTTGTGAGCAG[C/T]GGGGAGCTATTGTTC | 94090 |
rs49060164 | snp | C/T | | | intron-variant | Trim9 | Mm_Celera | 12:70332165 | GGAAGCAACCATGCT[C/T]ACCACATGTGCATGC | 94090 |
rs49064282 | snp | A/G | | | intron-variant | Trim9 | Mm_Celera | 12:70285139 | CTGTCCATGCAGGGT[A/G]GGGTGGGGTGGGGTG | 94090 |
rs49080494 | snp | A/G | | | intron-variant | Trim9 | Mm_Celera | 12:70285978 | GCCTTACATATAACC[A/G]TGGTGGACATACAGA | 94090 |
rs49097255 | snp | C/T | | | intron-variant | Trim9 | Mm_Celera | 12:70332186 | ATGTGCATGCATAAA[C/T]GAGCATGATATATCT | 94090 |
rs49121189 | snp | C/G | | | intron-variant | Trim9 | Mm_Celera | 12:70319978 | CCTTCTGTTAACACA[C/G]CCGTGAACACTCTTG | 94090 |
rs49125884 | snp | A/G | | | intron-variant | Trim9 | Mm_Celera | 12:70288260 | TTTCAAAGCCAGCCT[A/G]AGCAATTCAGCAAGA | 94090 |
rs49131607 | snp | G/T | | | intron-variant, downstream-variant-500B | Trim9 | Mm_Celera | 12:70263271 | GCTGTCATGTAGCTG[G/T]CATTCTTCATGGAGT | 94090 |
rs49157868 | snp | C/G | | | intron-variant | Trim9 | Mm_Celera | 12:70286662 | CACAGATGCTTATCT[C/G]TCATGTCCTCCGGTA | 94090 |
rs49195294 | snp | C/G | | | intron-variant | Trim9 | Mm_Celera | 12:70284866 | TCAGAAATTTGCCTG[C/G]CTCTGCCTCCCAAGT | 94090 |
rs49289191 | snp | G/T | | | intron-variant | Trim9 | Mm_Celera | 12:70283441 | CGATGTGCATTTTTG[G/T]ACTTTGATGCTGGTG | 94090 |
rs49362773 | snp | A/G | | | intron-variant | Trim9 | Mm_Celera | 12:70284914 | GCGCCACCACTGCCC[A/G]GCAATACATACACAT | 94090 |
rs49395902 | snp | A/G | | | intron-variant | Trim9 | Mm_Celera | 12:70287357 | GGGGAACAGGCAGGG[A/G]CAAAAGAAGAGAGCA | 94090 |
rs49409741 | snp | C/T | | | intron-variant | Trim9 | Mm_Celera | 12:70286725 | ACTCACAGCTCCCTG[C/T]TCATTTTCAAACCAC | 94090 |
rs49450084 | snp | C/T | | | intron-variant | Trim9 | Mm_Celera | 12:70285966 | CCAGAAGGGAACGCC[C/T]TACATATAACCGTGG | 94090 |
rs49594409 | snp | C/T | | | intron-variant | Trim9 | Mm_Celera | 12:70301725 | AATACTGTTAAGACA[C/T]AAAGCAGGATTTCCA | 94090 |
rs49595844 | snp | C/T | | | intron-variant | Trim9 | Mm_Celera | 12:70273554 | TGTGGTCTGCTGCAC[C/T]AACATGCATGTTGTG | 94090 |
rs49654450 | snp | A/T | | | intron-variant | Trim9 | Mm_Celera | 12:70301600 | ACTTAGACAATACTC[A/T]CTATATGCCAGCTAC | 94090 |
rs49661712 | snp | C/G | | | intron-variant | Trim9 | Mm_Celera | 12:70326592 | GGCTGTAAAGCCCTC[C/G]AAGACTTCCAAGGCC | 94090 |
rs49715093 | snp | A/G | | | intron-variant | Trim9 | Mm_Celera | 12:70286601 | AGAACACTGCACAGC[A/G]AACTCACTAATTCCA | 94090 |
rs49731500 | snp | A/G | | | intron-variant | Trim9 | Mm_Celera | 12:70338091 | TTTTCATATGAAGAT[A/G]GGTAGATTATGAAAG | 94090 |
rs49734370 | snp | C/T | | | intron-variant | Trim9 | Mm_Celera | 12:70312076 | GCCTGAGGACAAGGC[C/T]ATGGGAAGAGATGGT | 94090 |
rs49802884 | snp | A/T | | | intron-variant | Trim9 | Mm_Celera | 12:70287374 | AAAAGAAGAGAGCAC[A/T]CAGGGGCTGGTGTCT | 94090 |
rs49826869 | snp | C/T | | | intron-variant | Trim9 | Mm_Celera | 12:70286673 | ATCTCTCATGTCCTC[C/T]GGTAACTCGGGTCAG | 94090 |
rs49836099 | snp | G/T | | | intron-variant | Trim9 | Mm_Celera | 12:70327141 | CTTATGTGAGTCAGG[G/T]ATTCTTGGAAAGAAT | 94090 |
rs49864889 | snp | A/T | | | intron-variant | Trim9 | Mm_Celera | 12:70338089 | CATTTTCATATGAAG[A/T]TGGGTAGATTATGAA | 94090 |
rs49890434 | snp | A/T | | | intron-variant | Trim9 | Mm_Celera | 12:70340699 | TTAAAACTTTGGAAA[A/T]TTTTCATTTAATATT | 94090 |
rs49890749 | snp | G/T | | | intron-variant | Trim9 | Mm_Celera | 12:70285355 | GGGGCAGTAAAGTGT[G/T]CCTCTTCCTCATGGG | 94090 |
rs50004084 | snp | A/G | | | intron-variant | Trim9 | Mm_Celera | 12:70340921 | GTATCGCTCAGTGGG[A/G]TTGGAGAGGTGGCTC | 94090 |
rs50018335 | snp | A/G | | | intron-variant | Trim9 | Mm_Celera | 12:70326593 | GCTGTAAAGCCCTCG[A/G]AGACTTCCAAGGCCT | 94090 |
rs50018997 | snp | G/T | | | intron-variant | Trim9 | Mm_Celera | 12:70289139 | TGACAAGGCTCTCAG[G/T]AGCCCTTCCTGTCTG | 94090 |
rs50019612 | snp | C/T | | | intron-variant | Trim9 | Mm_Celera | 12:70331606 | TTTGGGGAAACTCCC[C/T]TTTAGGTGCGACAGT | 94090 |
rs50050354 | snp | A/G | | | intron-variant | Trim9 | Mm_Celera | 12:70286616 | AAACTCACTAATTCC[A/G]CACACAGGCTAGAAC | 94090 |
rs50073047 | snp | A/C | | | intron-variant | Trim9 | Mm_Celera | 12:70285975 | AACGCCTTACATATA[A/C]CCGTGGTGGACATAC | 94090 |
rs50087506 | snp | A/G | | | intron-variant | Trim9 | Mm_Celera | 12:70286562 | GGGTGGTAGCATAAC[A/G]TCTTGCTTCCTCTGC | 94090 |
rs50144363 | snp | G/T | | | intron-variant | Trim9 | Mm_Celera | 12:70287889 | TCTTCCATAGGGATT[G/T]CTGGCTTCTGTTTCT | 94090 |
rs50157876 | snp | A/G | | | intron-variant | Trim9 | Mm_Celera | 12:70270101 | CATTTGTGCACGTGA[A/G]TCACCTATGAATCGT | 94090 |
rs50281351 | snp | A/G | | | intron-variant | Trim9 | Mm_Celera | 12:70340660 | GTACAGGGGTTCATC[A/G]TGCCACCCAAAATGG | 94090 |
rs50439771 | snp | A/G | | | intron-variant | Trim9 | Mm_Celera | 12:70287884 | TTTCTTCTTCCATAG[A/G]GATTTCTGGCTTCTG | 94090 |
rs50441807 | snp | A/C | | | intron-variant | Trim9 | Mm_Celera | 12:70289725 | TGTCAATGGGACCCC[A/C]GACTTATGCATTAAT | 94090 |
rs50463221 | snp | C/T | | | intron-variant | Trim9 | Mm_Celera | 12:70332015 | TTAGGATATAAGAGG[C/T]ATTATGAGTTCTAGG | 94090 |
rs50478467 | snp | A/G | | | intron-variant | Trim9 | Mm_Celera | 12:70337284 | AAGTGGATGCTCACA[A/G]TCAGCTAGTGGATGG | 94090 |
rs50604740 | snp | C/T | | | intron-variant | Trim9 | Mm_Celera | 12:70283857 | GCAGCCGAGAACCAC[C/T]CAGGAGACTGTGTAC | 94090 |
rs50622227 | snp | G/T | | | intron-variant | Trim9 | Mm_Celera | 12:70341319 | CCCTTGGAGTTGTTT[G/T]CTGACAACTTCACAA | 94090 |
rs50649543 | snp | A/G | | | intron-variant | Trim9 | Mm_Celera | 12:70332151 | AATTTATGAGACATG[A/G]AAGCAACCATGCTCA | 94090 |
rs50660845 | snp | C/T | | | intron-variant | Trim9 | Mm_Celera | 12:70285408 | GGCATCTTGATTCTT[C/T]GGGGACAGTGGGAGC | 94090 |
rs50684531 | snp | C/G | | | intron-variant | Trim9 | Mm_Celera | 12:70270326 | CTAAGGAGAGAGGAG[C/G]CAGCTGGAGCTCTGA | 94090 |
rs50739332 | snp | C/T | | | intron-variant | Trim9 | Mm_Celera | 12:70285643 | AAGTCTTTCTCCCAT[C/T]GTCCAACCAATTCTC | 94090 |
rs50831637 | snp | A/T | | | intron-variant | Trim9 | GRCm38.p3 | 12:70289784 | TGAAAAGTCTACAAT[A/T]TTTTTTAGAAAACAT | 94090 |
rs50851972 | snp | C/T | | | intron-variant | Trim9 | Mm_Celera | 12:70285990 | ACCGTGGTGGACATA[C/T]AGACACTCTCCATAG | 94090 |
rs50877474 | snp | C/T | | | intron-variant | Trim9 | Mm_Celera | 12:70284846 | AGATCAGGCTGGCCT[C/T]GAACTCAGAAATTTG | 94090 |
rs50898782 | snp | C/T | | | intron-variant | Trim9 | Mm_Celera | 12:70302161 | AGCACTGACTGCTCT[C/T]GCAGATGACCTCATT | 94090 |
rs50977894 | snp | A/C | | | intron-variant | Trim9 | Mm_Celera | 12:70338154 | AAGAAAACCAAAATA[A/C]CAAACGGTTGTGCGT | 94090 |
rs51065584 | snp | A/G | | | intron-variant | Trim9 | Mm_Celera | 12:70283792 | ACCTGTTTGGAAAAG[A/G]GGCAGTCTAACAAAG | 94090 |
rs51129358 | snp | A/G | | | intron-variant | Trim9 | Mm_Celera | 12:70285856 | TGTTACAAGCCGGGA[A/G]CACTCAGGAGGTTCT | 94090 |
rs51209716 | snp | C/G | | | intron-variant | Trim9 | Mm_Celera | 12:70341014 | TGATGGCCCACAACT[C/G]CCTCCAGCTTCAGCT | 94090 |
rs51229921 | snp | A/C | | | intron-variant | Trim9 | Mm_Celera | 12:70343275 | ATCCCAGCACTCAGG[A/C]GGCAGAGGCAAGCAG | 94090 |
rs51258384 | snp | C/T | | | intron-variant, downstream-variant-500B | Trim9 | Mm_Celera | 12:70263488 | GCTTTGGGGAATCTG[C/T]TGACTTTTAAATGCT | 94090 |
rs51329118 | snp | A/C | | | intron-variant | Trim9 | Mm_Celera | 12:70283419 | GAGGTCTTTTTCATC[A/C]CCCTTGCGATGTGCA | 94090 |
rs51460661 | snp | C/T | | | intron-variant | Trim9 | Mm_Celera | 12:70341024 | CAACTGCCTCCAGCT[C/T]CAGCTCCACAAGATC | 94090 |
rs51496060 | snp | A/C | | | intron-variant | Trim9 | Mm_Celera | 12:70285348 | GTGAGTTGGGGCAGT[A/C]AAGTGTTCCTCTTCC | 94090 |
rs51508255 | snp | C/G | | | intron-variant | Trim9 | Mm_Celera | 12:70337867 | TCAACATTATTTATA[C/G]GTGAGAAATAAAGCA | 94090 |
rs51654644 | snp | A/G | | | intron-variant | Trim9 | Mm_Celera | 12:70288261 | TTCAAAGCCAGCCTA[A/G]GCAATTCAGCAAGAC | 94090 |
rs51699778 | snp | G/T | | | intron-variant | Trim9 | Mm_Celera | 12:70289697 | GGTGACAGGTAGGGT[G/T]GGTGACCAGTTCTGT | 94090 |
rs51757999 | snp | A/G | | | intron-variant | Trim9 | Mm_Celera | 12:70285251 | AGTGAGTCACGTGGC[A/G]TGTAGAGGAAGGAGG | 94090 |
rs51805732 | snp | A/C | | | intron-variant | Trim9 | Mm_Celera | 12:70287789 | CCAGCAGAGATGGAA[A/C]CAAGTAGGAGGCAGA | 94090 |
rs51848955 | snp | G/T | | | intron-variant | Trim9 | Mm_Celera | 12:70306883 | TCGTTTTGTTTTTTT[G/T]TTTTTTTTTTTTTTT | 94090 |
rs51872521 | snp | A/G | | | intron-variant | Trim9 | Mm_Celera | 12:70301794 | TCAAAGCTTCAGTGT[A/G]ATGCTCTCTGTACAT | 94090 |
rs51912440 | snp | A/G | | | intron-variant | Trim9 | Mm_Celera | 12:70288202 | TATTCTAGAGACTGA[A/G]GCAGAAGTGTCACAA | 94090 |
rs51950081 | snp | C/T | | | intron-variant | Trim9 | Mm_Celera | 12:70284859 | CTTGAACTCAGAAAT[C/T]TGCCTGCCTCTGCCT | 94090 |
rs52090179 | snp | C/T | | | intron-variant | Trim9 | Mm_Celera | 12:70341122 | ACACACGTGCACATG[C/T]GCACATACACAAATA | 94090 |
rs52154080 | snp | A/G | | | intron-variant | Trim9 | Mm_Celera | 12:70341065 | TTCTGGCCTACATGG[A/G]GCATTAACATACATG | 94090 |
rs52180583 | snp | A/G | | | intron-variant | Trim9 | GRCm38.p3 | 12:70271748 | aaggaaggaaggaag[A/G]aagaaagaaagaaag | 94090 |
rs52251408 | snp | G/T | | | intron-variant | Trim9 | Mm_Celera | 12:70270725 | GAAAGGCCAAGAAAA[G/T]GAAACAAGAGATGGG | 94090 |
rs52330294 | snp | G/T | | | intron-variant | Trim9 | Mm_Celera | 12:70289902 | CTACCCCCCCTTTTT[G/T]TTTTGCAAAACAAAA | 94090 |
rs52358649 | snp | A/G | | | intron-variant | Trim9 | Mm_Celera | 12:70342629 | CCCCCACACACACAC[A/G]CACACGCACACGCAC | 94090 |
rs52397509 | snp | C/T | | | intron-variant | Trim9 | Mm_Celera | 12:70305830 | GCGCGTGCGCGCGCG[C/T]GCGCGCGCATGCCTG | 94090 |
rs52537639 | snp | A/T | | | intron-variant | Trim9 | Mm_Celera | 12:70341087 | ACATACATGTGTGTA[A/T]CACACACACACACAA | 94090 |
rs107868766 | snp | C/G | | | intron-variant | Trim9 | Mm_Celera | 12:70299920 | acagacagacagaca[C/G]acagacagacacaca | 94090 |
rs108137445 | snp | A/G | | | intron-variant | Trim9 | Mm_Celera | 12:70340963 | GCACTTGCTGCTTCC[A/G]CAGAGATCTAGAGTT | 94090 |
rs108273402 | snp | G/T | | | intron-variant | Trim9 | GRCm38.p3 | 12:70306893 | TTTTTTTTTTTTTTT[G/T]TTTTTTTTTTTATCA | 94090 |
rs108404633 | snp | C/G | | | intron-variant | Trim9 | Mm_Celera | 12:70292725 | AGTGGGGAGTGAGGG[C/G]CAGAAATAATGAAGA | 94090 |
rs108497843 | snp | A/G | | | intron-variant | Trim9 | Mm_Celera | 12:70289941 | CCAAAACCAAACCAA[A/G]TCAAACCAAAAATGT | 94090 |
rs108534230 | snp | A/C | | | intron-variant | Trim9 | Mm_Celera | 12:70341127 | CGTGCACATGCGCAC[A/C]TACACAAATAAAATA | 94090 |
rs108855745 | snp | G/T | | | intron-variant | Trim9 | Mm_Celera | 12:70281563 | GGAGAAAAGTACAGA[G/T]AATTATGTTTTCATG | 94090 |
rs211704195 | snp | C/T | | | intron-variant | Trim9 | Mm_Celera | 12:70250097 | ACCCCACCCCCAGAG[C/T]CACCAAAGAGAATGT | 94090 |
rs211712921 | snp | C/T | | | intron-variant | Trim9 | Mm_Celera | 12:70300022 | CAGAGTCAGTAGACT[C/T]TAGAGTTTGAAGTCA | 94090 |
rs211741436 | snp | G/T | | | intron-variant | Trim9 | Mm_Celera | 12:70341762 | CCCCGACAAGGCAGA[G/T]TTTGCTGTGTTTTCC | 94090 |
rs211755933 | snp | A/T | | | intron-variant | Trim9 | Mm_Celera | 12:70292188 | TGGCCACTGTGAGTC[A/T]GCCAGTGTAGAGCAG | 94090 |
rs211774348 | snp | C/T | | | intron-variant | Trim9 | Mm_Celera | 12:70291645 | AGAAAGCTGTTTCCC[C/T]GCAAGCAGAGCTAAG | 94090 |
rs211796465 | in-del | -/AAGGCT | | | intron-variant | Trim9 | GRCm38.p3 | 12:70341272 | GAAAGCGGCACTCAC[-/AAGGCT]ATGTAGAGTTCTTTT | 94090 |
rs211835612 | snp | A/G | | | intron-variant | Trim9 | Mm_Celera | 12:70305839 | CGCGCGTGCGCGCGC[A/G]TGCCTGTATGTGCTC | 94090 |
rs211842102 | snp | C/G | | | intron-variant | Trim9 | Mm_Celera | 12:70260047 | GAGCCCATTTCTCTA[C/G]ATCAACATAGAGGCC | 94090 |
rs211853313 | in-del | -/GGGG | | | intron-variant | Trim9 | Mm_Celera | 12:70261249 | GCTCAGGTGGACTCT[-/GGGG]CGGGGGGAGGCTATG | 94090 |
rs211878508 | snp | A/G | | | intron-variant | Trim9 | Mm_Celera | 12:70259266 | ATGCCCACAGAGGCT[A/G]GAAAAGGGCATTTGG | 94090 |
rs211880611 | snp | C/T | | | intron-variant | Trim9 | Mm_Celera | 12:70307145 | TCTCCATCTCTTCAC[C/T]GATGCATTTATAGCT | 94090 |
rs211928656 | snp | A/G | | | intron-variant | Trim9 | Mm_Celera | 12:70313662 | AGGTGTAATTAGCCG[A/G]GGAACATAATACAAA | 94090 |
rs211939895 | in-del | -/CCTCTCCAGCACCATGTCTG | | | intron-variant | Trim9 | Mm_Celera | 12:70320984 | TAGAACTCTCAGCTA[-/CCTCTCCAGCACCATGTCTG]CCTGCATGCCATCAT | 94090 |
rs211957374 | snp | G/T | | | intron-variant | Trim9 | Mm_Celera | 12:70281099 | TTTGGAAGGAGGCCT[G/T]CAAGGCAGAGAGGCT | 94090 |
rs211979412 | snp | C/T | | | intron-variant | Trim9 | Mm_Celera | 12:70322189 | CCTTCTAATACAGTT[C/T]CTCATGTTCTGGTGA | 94090 |
rs212012477 | snp | C/T | | | intron-variant | Trim9 | Mm_Celera | 12:70335878 | GGCCCCCATAAGTTG[C/T]ATATTGCAGTGTTTG | 94090 |
rs212050403 | snp | A/G | | | intron-variant | Trim9 | Mm_Celera | 12:70337679 | TGTCACCCAGCTCTG[A/G]CAGGAAGGCAGGCTG | 94090 |
rs212074869 | snp | A/T | | | intron-variant | Trim9 | Mm_Celera | 12:70314337 | GTGGCTGCCATAACA[A/T]ACACCGACTCCCTCA | 94090 |
rs212093650 | in-del | -/TTT | | | intron-variant | Trim9 | Mm_Celera | 12:70304134 | TTTAACTGCGTATGA[-/TTT]TTTTTTCATTCTCTG | 94090 |
rs212104077 | snp | A/C/T | | | intron-variant | Trim9 | GRCm38.p3 | 12:70306588 | TGGGCCTGTAACATT[A/C/T]CCATGTCTCTGTAGC | 94090 |
rs212143148 | snp | A/T | | | intron-variant | Trim9 | Mm_Celera | 12:70286172 | TGTTGCTTCCAAAAG[A/T]TCTTACTGTGTAACA | 94090 |
rs212158714 | in-del | -/T | | | intron-variant | Trim9 | GRCm38.p3 | 12:70273391 | AGTCTCTTATCAATA[-/T]TTAAAAAAATACAAA | 94090 |
rs212300407 | snp | G/T | | | intron-variant | Trim9 | Mm_Celera | 12:70276198 | GATATATCAAGAGAT[G/T]TTGCATTAAGGAGGA | 94090 |
rs212301356 | snp | C/T | | | intron-variant | Trim9 | Mm_Celera | 12:70294436 | TCTGCTGGAAAACAT[C/T]TTTGTTCACCTTTCC | 94090 |
rs212328752 | snp | C/T | | | intron-variant | Trim9 | Mm_Celera | 12:70344865 | ATTGGGAGGAGAGGC[C/T]CTTGGTCTTGCGAAC | 94090 |
rs212335978 | snp | C/T | | | intron-variant | Trim9 | Mm_Celera | 12:70269422 | GTTTTGGTATCTGCC[C/T]AATCCAGACCTGAAT | 94090 |
rs212366679 | snp | C/T | | | intron-variant | Trim9 | Mm_Celera | 12:70268909 | CTTTCTTTTTCTTTT[C/T]TTTTCTTTTTTTTTT | 94090 |
rs212431688 | snp | A/G | | | intron-variant | Trim9 | Mm_Celera | 12:70261646 | CTTAACCTGCAGGTT[A/G]TGACTCCTTTGGGGG | 94090 |
rs212441708 | snp | C/T | | | intron-variant | Trim9 | Mm_Celera | 12:70323068 | AAATGAACAGGGTCA[C/T]TGGATCCACAGCACA | 94090 |
rs212454598 | snp | C/T | | | intron-variant | Trim9 | Mm_Celera | 12:70307166 | ATTTATAGCTTTTAG[C/T]GCTTCCAGTTCTTTG | 94090 |
rs212455494 | snp | A/G | | | intron-variant | Trim9 | Mm_Celera | 12:70301155 | AATGTAATCCAGCCA[A/G]TCAGTAGTTTTCGGG | 94090 |
rs212493988 | snp | A/G | | | intron-variant | Trim9 | Mm_Celera | 12:70313529 | TGCAGAGGAATTTGG[A/G]CTGAGTTGGGCAAGA | 94090 |
rs212524454 | snp | A/T | | | intron-variant | Trim9 | Mm_Celera | 12:70277515 | AATCAGAATCGAATT[A/T]AATTAAGACAAAGTG | 94090 |
rs212556130 | snp | A/T | | | intron-variant | Trim9 | Mm_Celera | 12:70293835 | GCCTCACTTCCCCTT[A/T]CAGTAAAGAGACAAA | 94090 |
rs212569819 | snp | A/G | | | intron-variant | Trim9 | Mm_Celera | 12:70338919 | AGTTGGGATGTTGAA[A/G]TCTGGCCTAAGAAGG | 94090 |
rs212610259 | snp | A/T | | | intron-variant | Trim9 | Mm_Celera | 12:70325438 | GAGGAGCCACCGAGT[A/T]CCTTAGAGGAATGGT | 94090 |
rs212629659 | snp | G/T | | | intron-variant | Trim9 | Mm_Celera | 12:70338513 | TATTGGGGAGAAGGG[G/T]GAACTGAAGGCAGGG | 94090 |
rs212637211 | snp | C/T | | | intron-variant | Trim9 | Mm_Celera | 12:70331655 | GAACTCAGGAGACAG[C/T]GTACTTGCTGGTTTC | 94090 |
rs212664088 | snp | C/T | | | intron-variant | Trim9 | Mm_Celera | 12:70308639 | ATGTTAGTATGTGGG[C/T]ATATGTGCTGATGTA | 94090 |
rs212666232 | snp | A/T | | | intron-variant, downstream-variant-500B | Trim9 | Mm_Celera | 12:70263546 | TACATAGTTTTAAAA[A/T]TTTCATAGAAGGCAC | 94090 |
rs212670744 | snp | G/T | | | downstream-variant-500B | Trim9 | Mm_Celera | 12:70244049 | TGGGTTCTGGGGAGA[G/T]GACTCAGATGGAGCA | 94090 |
rs212707091 | snp | C/T | | | intron-variant | Trim9 | Mm_Celera | 12:70271687 | GTTTGATAAAAGGCT[C/T]ATCAACAGGGAGAAA | 94090 |
rs212754631 | in-del | -/TT | | | intron-variant | Trim9 | Mm_Celera | 12:70325641 | CGTTAAATGTATTGC[-/TT]TTTTTTTTAAAAATA | 94090 |
rs212828562 | snp | C/G | | | intron-variant | Trim9 | Mm_Celera | 12:70315665 | TAATCCCTCATGGGA[C/G]TCGGGTTACACCAGA | 94090 |
rs212847403 | snp | A/G | | | intron-variant | Trim9 | Mm_Celera | 12:70325904 | TTTCCTCAGCTGCAG[A/G]CTTCAATAATTTTAG | 94090 |
rs212888274 | snp | A/G | | | intron-variant | Trim9 | Mm_Celera | 12:70277948 | AGCCACGAGGCTTCT[A/G]CCTTCTAATTGTCCC | 94090 |
rs212915359 | snp | A/C | | | utr-variant-3-prime | Trim9 | Mm_Celera | 12:70246287 | TAAGGGTGAAGATGG[A/C]GGCTGAGGACCAGCT | 94090 |
rs212918741 | snp | A/G | | | intron-variant | Trim9 | Mm_Celera | 12:70296248 | TGCCAGCTGCAGACA[A/G]TTTCTGCAAGTGTGT | 94090 |
rs212923060 | in-del | -/C | | | intron-variant | Trim9 | Mm_Celera | 12:70295959 | AGCAAGGCCTCCCTT[-/C]CCCCCGCTGGCTTGC | 94090 |
rs212947773 | snp | C/T | | | intron-variant | Trim9 | Mm_Celera | 12:70340194 | CTATTCTGAGAGATA[C/T]AGACTAAGGCTCTCA | 94090 |
rs213037471 | snp | A/C | | | intron-variant | Trim9 | Mm_Celera | 12:70261096 | AAAGGGATTCTAGAC[A/C]TGGTACCTGAGGCCA | 94090 |
rs213058715 | snp | G/T | | | utr-variant-3-prime | Trim9 | Mm_Celera | 12:70245290 | TCAGAGGCCCGGGGT[G/T]GTGACTGGGCCCTGT | 94090 |
rs213076045 | snp | A/T | | | upstream-variant-2KB, utr-variant-5-prime, missense, nc-transcript-variant | Trim9, Gm32151 | Mm_Celera | 12:70347745 | CAGCTTTGGTCTGCA[A/T]GCCGACCCACCCCTT | 94090 |
rs213087041 | snp | A/G | | | intron-variant | Trim9 | Mm_Celera | 12:70295591 | AGAAAATGCTGTATT[A/G]TAAGGATTTATATGT | 94090 |
rs213087217 | snp | C/T | | | intron-variant | Trim9 | Mm_Celera | 12:70303379 | GGAGAAGAGTACCAG[C/T]ATCCATCTTTCGGTG | 94090 |
rs213107172 | snp | A/G | | | intron-variant | Trim9 | Mm_Celera | 12:70262872 | TGCGGGTGGACAATT[A/G]TTTTAATGTGTGAAT | 94090 |
rs213150014 | in-del | -/AG | | | intron-variant | Trim9 | Mm_Celera | 12:70299768 | CACAGATAGACAGAC[-/AG]ACACACACACATAGA | 94090 |
rs213151026 | snp | C/T | | | intron-variant | Trim9 | Mm_Celera | 12:70279285 | CCACCACGCCTGGCC[C/T]GGTTTCTTCAGCTTT | 94090 |
rs213152349 | snp | C/G | | | intron-variant | Trim9 | Mm_Celera | 12:70272977 | TGTGGTATTTTCAGT[C/G]TTGTGAGAGAAATGA | 94090 |
rs213187653 | snp | G/T | | | intron-variant | Trim9 | Mm_Celera | 12:70278785 | TTGCAAAGCATCTAC[G/T]TTTAGGATTTATTTA | 94090 |
rs213203815 | snp | G/T | | | intron-variant | Trim9 | Mm_Celera | 12:70327698 | ATGGTCACACTCAAG[G/T]CCTAGCATGGCCTTT | 94090 |
rs213208987 | snp | C/T | | | intron-variant | Trim9 | Mm_Celera | 12:70315318 | AAGTCCACTTTATTA[C/T]AAGCATGGAAGAGCC | 94090 |
rs213220142 | in-del | -/TAACT | | | intron-variant | Trim9 | Mm_Celera | 12:70282581 | TATCTACCCATTTGC[-/TAACT]TATGGATTTTATTGT | 94090 |