SNP - dbSNP |
dbSNP | Type | Alleles | Het | Se(het) | Fxn-class | Gene Name | Assembly | Chr-pos | Sequence | Entrez Gene |
rs6178928 | snp | A/G | 0.46875 | 0.121031 | intron-variant | Phip | GRCm38.p3 | 9:82947959 | TTTTACAACAGAAAC[A/G]CTATTCTAGGACTCA | 83946 |
rs6179383 | snp | C/G | 0.46875 | 0.121031 | intron-variant | Phip | GRCm38.p3 | 9:82948020 | ACTGTAACATCTATC[C/G]ATCCTACTATACCTT | 83946 |
rs6208037 | snp | C/G | 0.5 | 0 | intron-variant | Phip | Mm_Celera | 9:82955295 | TTTATAAAAACTCTC[C/G]GAAGGGTTGGCTCAG | 83946 |
rs6208078 | snp | A/G | 0.396694 | 0.202437 | intron-variant | Phip | Mm_Celera | 9:82955325 | GTGAGTTAAGTGTCA[A/G]AGATAGTTCTATTAA | 83946 |
rs6209196 | snp | A/T | 0.5 | 0 | intron-variant | Phip | GRCm38.p3 | 9:82955540 | AGAAGGACAATCCCA[A/T]AATCATTTAATAATC | 83946 |
rs6210165 | snp | G/T | 0.5 | 0 | intron-variant | Phip | GRCm38.p3 | 9:82955682 | ATGTGCAGATTTGTT[G/T]TTTAGTTGTTCTACT | 83946 |
rs6210302 | snp | A/G | 0.391111 | 0.206368 | intron-variant | Phip | GRCm38.p3 | 9:82955766 | AGAAGCAAAGCAGCT[A/G]AAATTTCAGACAGGA | 83946 |
rs6213853 | snp | A/G | 0.5 | 0 | intron-variant | Phip | Mm_Celera | 9:82949858 | ACCTTTAATTTCTGT[A/G]CCAGAATGACAAAAC | 83946 |
rs6303689 | snp | A/G | 0.5 | 0 | intron-variant | Phip | Mm_Celera | 9:82928047 | AGGTCATTCCCATCT[A/G]Caaattataatatta | 83946 |
rs6316826 | snp | A/G | 0.5 | 0 | intron-variant, utr-variant-5-prime | Phip | Mm_Celera | 9:82928248 | GGGGGAAGATCAGAG[A/G]CTCTATCAAAATGTA | 83946 |
rs6317246 | snp | A/C | 0.5 | 0 | intron-variant, utr-variant-5-prime | Phip | GRCm38.p3 | 9:82928307 | CATCTTTATTTACAA[A/C]GTATTCTAATACAGC | 83946 |
rs6317282 | snp | G/T | 0.5 | 0 | intron-variant, utr-variant-5-prime | Phip | GRCm38.p3 | 9:82928324 | TATTCTAATACAGCA[G/T]AAATAGTTNCCTAAG | 83946 |
rs6317298 | snp | A/C | 0.5 | 0 | intron-variant, utr-variant-5-prime | Phip | GRCm38.p3 | 9:82928333 | ACAGCANAAATAGTT[A/C]CCTAAGTCTCTATAA | 83946 |
rs6317828 | snp | G/T | 0.456747 | 0.140554 | intron-variant, utr-variant-5-prime | Phip | GRCm38.p3 | 9:82928440 | TCAAAATGCCTGAAG[G/T]TCACTTGACAAACAG | 83946 |
rs6319001 | snp | A/C | 0.444444 | 0.157135 | intron-variant, upstream-variant-2KB | Phip, LOC105243467 | GRCm38.p3 | 9:82967747 | GGTTTACTCATGTCA[A/C]CAAAATATTCTCTCA | 83946 |
rs6323465 | snp | A/G | 0.5 | 0 | intron-variant | Phip | Mm_Celera | 9:82896199 | AGGAAATAAATCTGT[A/G]CAAAAATTTTACTCT | 83946 |
rs6323931 | snp | C/T | 0.5 | 0 | intron-variant | Phip | Mm_Celera | 9:82896228 | CTCCAGTATTAAAAC[C/T]TTTTACTAGAAAAGC | 83946 |
rs6337766 | snp | C/G | 0.5 | 0 | intron-variant | Phip | GRCm38.p3 | 9:82896479 | AGCAATACTAACTAA[C/G]TAAGACTCTATCCTA | 83946 |
rs6338327 | snp | C/G | 0.304688 | 0.243945 | intron-variant | Phip | GRCm38.p3 | 9:82896582 | TAAACAACCTAACAA[C/G]AGTCTCATTCATTCA | 83946 |
rs13464262 | snp | C/T | | | utr-variant-3-prime | Phip | GRCm38.p3 | 9:82866861 | AACTACTTAATCCCA[C/T]CATGGGATATTTAGA | 83946 |
rs13464263 | snp | A/G | 0.408163 | 0.193609 | utr-variant-3-prime | Phip | Mm_Celera | 9:82867668 | TTTTAATATTTTGTT[A/G]GCGTGAAGTTTATTT | 83946 |
rs13464264 | snp | A/G | | | utr-variant-3-prime | Phip | GRCm38.p3 | 9:82867444 | AGGTTAAAAATTGGG[A/G]AAAGTACACCTTTTG | 83946 |
rs29793861 | snp | A/C | 0.375 | 0.216506 | intron-variant | Phip | Mm_Celera | 9:82894652 | AGTGTACCCCCCCCC[A/C]CCCACACACACACAA | 83946 |
rs29931655 | snp | A/G | 0.32 | 0.24 | intron-variant | Phip | Mm_Celera | 9:82917203 | GCATCCTCTCTCTCA[A/G]AAATCTCGCATTGCA | 83946 |
rs29938732 | snp | C/T | 0.375 | 0.216506 | intron-variant | Phip | Mm_Celera | 9:82973243 | AGTTCAAATTTCAAT[C/T]ACTTTGGACCAAGTA | 83946 |
rs30334702 | snp | A/C | 0.375 | 0.216506 | intron-variant | Phip | Mm_Celera | 9:82894654 | TGTACCCCCCCCCCC[A/C]CACACACACACAAAT | 83946 |
rs33702150 | snp | G/T | 0.444444 | 0.157135 | intron-variant | Phip | Mm_Celera | 9:82956018 | AATGTTATAACTTTT[G/T]GTTGGTGCTAACAGA | 83946 |
rs45649862 | snp | A/G | | | intron-variant | Phip | GRCm38.p3 | 9:82946108 | AAATAAACAATACAA[A/G]TAATTAAGTTCCTTG | 83946 |
rs45664061 | snp | A/C | 0.391111 | 0.206368 | intron-variant | Phip | Mm_Celera | 9:82942679 | TAAAGTAGAGATTGG[A/C]AAAAGATTCAAATTT | 83946 |
rs45669734 | snp | C/T | 0.244898 | 0.249948 | intron-variant | Phip | Mm_Celera | 9:82917077 | AGAAGACAAAGACTT[C/T]ATAACTGCTTCTAGA | 83946 |
rs45674220 | snp | A/T | 0.21875 | 0.248039 | intron-variant | Phip | Mm_Celera | 9:82904674 | GATAGTTGTTTTTGT[A/T]CTTCATTTTTTTTCT | 83946 |
rs45688394 | snp | C/G | 0.142012 | 0.225474 | intron-variant | Phip | Mm_Celera | 9:82886792 | ATTTTAAGATTCACT[C/G]GTACATTAGGATGAA | 83946 |
rs45714856 | snp | A/G | | | intron-variant | Phip | GRCm38.p3 | 9:82972286 | TCTGCTCATATTACT[A/G]TCCAGTTTATCAGTT | 83946 |
rs45730935 | snp | C/T | 0.375 | 0.216506 | intron-variant | Phip | GRCm38.p3 | 9:82889629 | GCTATAGGCTCCAGA[C/T]AGACAAGGACTGTCA | 83946 |
rs45739587 | snp | C/T | 0.336735 | 0.234472 | intron-variant | Phip | GRCm38.p3 | 9:82914791 | CACAAGTTACAAATG[C/T]AAATCTAGATTGTTC | 83946 |
rs45741183 | snp | C/T | 0.473373 | 0.11227 | intron-variant | Phip | GRCm38.p3 | 9:82953072 | ACAGCTGAGCCAAAG[C/T]TTCAAGACCAATGAT | 83946 |
rs45749951 | snp | A/G | 0.244898 | 0.249948 | intron-variant | Phip | GRCm38.p3 | 9:82947029 | ATTCCATAATCTAAC[A/G]CCTGAAACCTCTGAG | 83946 |
rs45755140 | snp | C/T | 0.42 | 0.183303 | intron-variant | Phip | GRCm38.p3 | 9:82946493 | CATCTAACTAAATTA[C/T]TACTGTACTTACTTT | 83946 |
rs45756347 | snp | A/T | | | intron-variant | Phip | GRCm38.p3 | 9:82972366 | CCAAATAATTTTAAA[A/T]TAATTCTTGTTAATT | 83946 |
rs45776001 | snp | C/T | 0.132653 | 0.220748 | missense | Phip | Mm_Celera | 9:82880216 | TCCATGCCTGAATAT[C/T]GTAAGACTGAGCTCT | 83946 |
rs45788551 | snp | C/T | 0.391111 | 0.206368 | intron-variant | Phip | GRCm38.p3 | 9:82940163 | CACTTGCCTGACATG[C/T]ATAAGGCCACTTCAG | 83946 |
rs45793615 | snp | C/G | 0.375 | 0.216506 | intron-variant | Phip | GRCm38.p3 | 9:82968233 | TCTGAGAATCCTGAA[C/G]TGCACATAACTGTTC | 83946 |
rs45820911 | snp | C/T | | | intron-variant | Phip | Mm_Celera | 9:82923227 | GGTATTATTAAAATA[C/T]TGTCTCTAAATATAC | 83946 |
rs45851513 | snp | A/C | 0.336735 | 0.234472 | intron-variant | Phip | GRCm38.p3 | 9:82941688 | TTAAGCTCTCTTCAT[A/C]TGTAATGTTGTTTTC | 83946 |
rs45858975 | snp | C/G | 0.35503 | 0.226867 | intron-variant | Phip | GRCm38.p3 | 9:82885879 | TTTCAGTGCTATATC[C/G]AAGGCTCTAATTCAC | 83946 |
rs45899484 | snp | C/G | 0.375 | 0.216506 | intron-variant | Phip | Mm_Celera | 9:82892757 | TTTGCCAAAATTAAT[C/G]AAGAAAAGCAACATG | 83946 |
rs45906847 | snp | C/T | 0.426035 | 0.177515 | utr-variant-3-prime | Phip | GRCm38.p3 | 9:82867337 | TTTTCATTTGGATCA[C/T]TTTGATAATTATAAT | 83946 |
rs45924118 | snp | A/G | | | intron-variant | Phip | GRCm38.p3 | 9:82957340 | AATGCGTAAGTAATT[A/G]AACAGAGGCGAGAGG | 83946 |
rs45931947 | snp | A/G | | | intron-variant | Phip | GRCm38.p3 | 9:82957483 | GCCTCTTACAGAGCC[A/G]CTATGGAATGCAAAG | 83946 |
rs45946438 | snp | C/T | 0.426035 | 0.177515 | intron-variant | Phip | GRCm38.p3 | 9:82902992 | AGATATAGTTGTAAT[C/T]TTTTCCCATAAAGAC | 83946 |
rs45959334 | snp | C/T | 0.48 | 0.0979796 | intron-variant | Phip | GRCm38.p3 | 9:82896806 | TGACTCATTTATGCT[C/T]GTCCCAAAACAACAC | 83946 |
rs45989337 | snp | C/T | 0.142012 | 0.225474 | intron-variant | Phip | Mm_Celera | 9:82949915 | TTCCCAAGGATTCGT[C/T]TATTTATCTACTTAC | 83946 |
rs45990758 | snp | C/T | 0.459184 | 0.136902 | intron-variant | Phip | GRCm38.p3 | 9:82933775 | ATGATCCGAGGAGTT[C/T]AGAACACCAGTATTT | 83946 |
rs45998373 | snp | A/G | 0.32 | 0.24 | intron-variant | Phip | Mm_Celera | 9:82921155 | TTTATGCCAACAAAT[A/G]AAAGAGATGAAAGAA | 83946 |
rs46069467 | snp | C/T | | | intron-variant | Phip | GRCm38.p3 | 9:82957201 | TCAGAAAACTGAGTA[C/T]CTGATTTCAAATTCA | 83946 |
rs46095271 | snp | C/T | 0.336735 | 0.234472 | intron-variant | Phip | GRCm38.p3 | 9:82910094 | TGATGAGAAGGAGTG[C/T]GTATTTTGTGCTTAT | 83946 |
rs46116477 | snp | C/T | 0.297521 | 0.245442 | intron-variant | Phip | GRCm38.p3 | 9:82890819 | CATCAAGATTTCAGA[C/T]TGATCATCTCCATCA | 83946 |
rs46138548 | snp | A/T | 0.426035 | 0.177515 | intron-variant | Phip | GRCm38.p3 | 9:82936030 | CAGTCCTAAGGGATC[A/T]GACACCCTTCTAAGC | 83946 |
rs46172342 | snp | A/G | 0.391111 | 0.206368 | intron-variant | Phip | GRCm38.p3 | 9:82909745 | TTCTCCAGTGCTGGT[A/G]ATTAGGACGACCTGA | 83946 |
rs46222404 | snp | C/T | 0.336735 | 0.234472 | intron-variant, upstream-variant-2KB | Phip | GRCm38.p3 | 9:82930748 | GCAAAGCAGGTTGTA[C/T]GTTATCAGTATATAG | 83946 |
rs46272729 | snp | C/T | 0.375 | 0.216506 | intron-variant | Phip | GRCm38.p3 | 9:82884660 | GAAAGGCAAGACTTA[C/T]ATTTTTTTCTTTACA | 83946 |
rs46276391 | snp | A/G | 0.391111 | 0.206368 | synonymous-codon | Phip | GRCm38.p3 | 9:82896109 | CTCTTCTAACGTTAG[A/G]CCATTCTCAGTTAGT | 83946 |
rs46281608 | snp | A/G | 0.336735 | 0.234472 | utr-variant-3-prime | Phip | GRCm38.p3 | 9:82867007 | GAAAGTAATCAGCAT[A/G]TGTATCTGCATGTAA | 83946 |
rs46284023 | snp | A/G | 0.473373 | 0.11227 | intron-variant | Phip | Mm_Celera | 9:82920640 | TATATATTACAATCT[A/G]TTAAAAACTTCCTAC | 83946 |
rs46296733 | snp | C/G | 0.124444 | 0.216185 | intron-variant | Phip | Mm_Celera | 9:82872763 | CTGCCATAGCTTTGA[C/G]ATGCCTTACCTAGTC | 83946 |
rs46301810 | snp | A/T | 0.5 | 0 | intron-variant | Phip | Mm_Celera | 9:82901190 | CCTAAAGAACCAGCA[A/T]GCATGTACCACAATA | 83946 |
rs46308089 | snp | G/T | 0.231111 | 0.249285 | intron-variant | Phip | Mm_Celera | 9:82923927 | CAGAGTATGCATTTG[G/T]ATTCCTCAAAGCTTT | 83946 |
rs46310748 | snp | G/T | 0.48 | 0.0979796 | intron-variant | Phip | GRCm38.p3 | 9:82911895 | CAGTCTGGATTTGTA[G/T]TACTCTTGAAATTCG | 83946 |
rs46325512 | snp | C/T | 0.35503 | 0.226867 | intron-variant | Phip | GRCm38.p3 | 9:82883447 | AGCAAAAGTTGAATA[C/T]TGCATCTGGCTTCAA | 83946 |
rs46411348 | snp | A/G | 0.336735 | 0.234472 | intron-variant | Phip | Mm_Celera | 9:82925040 | CAAACTTACCTGATG[A/G]GAGAAAATTCCGAAT | 83946 |
rs46440736 | snp | C/T | 0.459184 | 0.136902 | intron-variant | Phip | GRCm38.p3 | 9:82955215 | ACAACAAAAGAATTT[C/T]ACCCATCACAGAGTC | 83946 |
rs46447984 | snp | A/C | 0.336735 | 0.234472 | intron-variant | Phip | GRCm38.p3 | 9:82890501 | GAACCAGCCTGTCTC[A/C]TCCATCAAATTGGTA | 83946 |
rs46465116 | snp | A/G | 0.391111 | 0.206368 | intron-variant | Phip | GRCm38.p3 | 9:82912146 | GGTATTTTTCAGGGA[A/G]GATGAAGGTATCTAG | 83946 |
rs46467228 | snp | A/G | 0.391111 | 0.206368 | intron-variant | Phip | GRCm38.p3 | 9:82915726 | ATAACTGAACCATAC[A/G]TTCCATCTATTTCCA | 83946 |
rs46469536 | snp | G/T | 0.231111 | 0.249285 | intron-variant | Phip | Mm_Celera | 9:82915765 | TGCCCTTTCTGTAAA[G/T]GCTAAGAACATAGAG | 83946 |
rs46475869 | snp | A/G | 0.21875 | 0.248039 | intron-variant | Phip | GRCm38.p3 | 9:82958719 | ACAAGAGAGTAACAA[A/G]CTACATCAAAAAGTC | 83946 |
rs46498771 | snp | C/T | 0.391111 | 0.206368 | intron-variant | Phip | GRCm38.p3 | 9:82925902 | AGAGGAGGACACATA[C/T]CACTTAATAAGCTGT | 83946 |
rs46502410 | snp | A/T | | | intron-variant | Phip | Mm_Celera | 9:82943243 | AAAACTTCACTTACC[A/T]ATTACAAGGATTTCC | 83946 |
rs46519416 | snp | A/G | 0.408163 | 0.193609 | intron-variant | Phip | GRCm38.p3 | 9:82922480 | TAAAGCTACAATGAT[A/G]CTTTCTTCATGCCAA | 83946 |
rs46544113 | snp | A/C | 0.336735 | 0.234472 | intron-variant | Phip | GRCm38.p3 | 9:82899959 | CAGAGACATATATGC[A/C]TTTACCTCAGAGGAA | 83946 |
rs46621171 | snp | A/T | 0.32 | 0.24 | intron-variant | Phip | Mm_Celera | 9:82920788 | AAACCTGGATCATCC[A/T]GCCTGAACTGACTGA | 83946 |
rs46642056 | snp | A/G | 0.408163 | 0.193609 | intron-variant | Phip | Mm_Celera | 9:82903588 | AAATTAATGATGGAC[A/G]ACAAACTCTATAGTT | 83946 |
rs46647288 | snp | A/C/G | 0.35503 | 0.226867 | intron-variant | Phip | GRCm38.p3 | 9:82895313 | AGGTTCAAGCGTCAG[A/C/G]GCCTAAAGACGAGCC | 83946 |
rs46647394 | snp | C/G | 0.277778 | 0.248452 | intron-variant | Phip | GRCm38.p3 | 9:82889821 | ACTTCTTGCCTTTGC[C/G]TCAAAAATGCTAGGA | 83946 |
rs46694091 | snp | A/C | 0.124444 | 0.216185 | intron-variant | Phip | Mm_Celera | 9:82941622 | ACCAAGAAGCAGAGG[A/C]AACAGCTTTGCCAGT | 83946 |
rs46718593 | snp | A/G | | | intron-variant | Phip | Mm_Celera | 9:82876640 | GCAATATAGGGAATA[A/G]TAAAGGAAGCATTAA | 83946 |
rs46727548 | snp | A/G | 0.132653 | 0.220748 | intron-variant | Phip | Mm_Celera | 9:82935926 | CGGAGCTCAAGACAC[A/G]ACTCAGCAGTTGACA | 83946 |
rs46751480 | snp | C/T | 0.48 | 0.0979796 | intron-variant | Phip | GRCm38.p3 | 9:82938814 | TCAATCATTGTACAA[C/T]AAAAATTTGTAGACT | 83946 |
rs46757282 | snp | C/T | 0.336735 | 0.234472 | intron-variant | Phip | Mm_Celera | 9:82889214 | ATGCCACTTACAAAC[C/T]TTTTGGGCATGGATA | 83946 |
rs46759430 | snp | G/T | 0.497778 | 0.0332592 | intron-variant | Phip | GRCm38.p3 | 9:82920686 | TTTATTTTGTTCATA[G/T]TGTTCCTCTTAATAT | 83946 |
rs46788864 | snp | A/G | 0.408163 | 0.193609 | intron-variant | Phip | Mm_Celera | 9:82905195 | AGCCAGACCATCATA[A/G]GAGCAATTTAATAAC | 83946 |
rs46795180 | snp | C/T | | | intron-variant | Phip | GRCm38.p3 | 9:82948807 | GAAAACCCATTTTGA[C/T]TGTGGATGGGACCAT | 83946 |
rs46855891 | snp | A/T | 0.132653 | 0.220748 | intron-variant | Phip | Mm_Celera | 9:82935721 | TAGAAGACCAAGCAA[A/T]GCTTTGAACCACTGA | 83946 |
rs46870162 | snp | C/T | 0.132653 | 0.220748 | utr-variant-3-prime | Phip | Mm_Celera | 9:82869754 | CCACAGCAGTACATA[C/T]AGAAATACATTCCCC | 83946 |
rs46881630 | snp | C/T | 0.231111 | 0.249285 | intron-variant | Phip | Mm_Celera | 9:82922525 | AGTAAGCTTGCTAAA[C/T]TATACACACTGTGTG | 83946 |
rs46884319 | snp | C/T | 0.426035 | 0.177515 | intron-variant | Phip | GRCm38.p3 | 9:82907907 | AACTGGCATAATGAG[C/T]CATTTAAAAAAAAAG | 83946 |
rs46928938 | snp | C/T | 0.231111 | 0.249285 | intron-variant | Phip | Mm_Celera | 9:82913678 | GACTCCTGTGAAACC[C/T]GAGGCCTACCTGAAG | 83946 |
rs46946447 | snp | C/T | 0.426035 | 0.177515 | intron-variant | Phip | GRCm38.p3 | 9:82968726 | ACCTCCTTCACACTA[C/T]GTAAATGCCCAGCCA | 83946 |
rs46957479 | snp | G/T | 0.459184 | 0.136902 | intron-variant | Phip | GRCm38.p3 | 9:82898678 | GTAAATCACAAATGT[G/T]TATCAATAAATTAGA | 83946 |
rs46966610 | snp | A/G | 0.408163 | 0.193609 | intron-variant | Phip | GRCm38.p3 | 9:82916167 | CACATCTAGGGACTG[A/G]TTTTCAGAAACGTCT | 83946 |
rs47029192 | snp | A/G | 0.48 | 0.0979796 | intron-variant | Phip | GRCm38.p3 | 9:82914620 | CCTAAAGAATCTTTA[A/G]TAACAAAAATTTTAG | 83946 |
rs47038891 | snp | C/T | 0.459184 | 0.136902 | downstream-variant-500B | Phip | GRCm38.p3 | 9:82866122 | CAGTGCAGTAACTTA[C/T]ATATAAACCAATAAC | 83946 |
rs47058033 | snp | A/G | 0.42 | 0.183303 | intron-variant | Phip | GRCm38.p3 | 9:82881029 | TGCAATATTTTCGTA[A/G]AATTTACTGGTTAAG | 83946 |
rs47059432 | snp | G/T | 0.132653 | 0.220748 | intron-variant | Phip | Mm_Celera | 9:82910236 | TACCTACTTACACAT[G/T]AATTTCTGAAAAGTG | 83946 |
rs47085283 | snp | C/T | 0.42 | 0.183303 | intron-variant | Phip | GRCm38.p3 | 9:82881464 | AAAATGAATAATGCA[C/T]TTGACTGGTTTAGTA | 83946 |
rs47085295 | snp | A/G | 0.297521 | 0.245442 | intron-variant, upstream-variant-2KB | Phip, LOC105243467 | GRCm38.p3 | 9:82967427 | GAAAGCTCCAAGACT[A/G]CACATGCATATGTAC | 83946 |
rs47107009 | snp | A/C | 0.132653 | 0.220748 | intron-variant | Phip | Mm_Celera | 9:82895149 | AACTTTCCAGGCCAA[A/C]GAAGGTTATTTCAAA | 83946 |
rs47123790 | snp | C/T | 0.32 | 0.24 | intron-variant | Phip | GRCm38.p3 | 9:82937384 | AAAGCACAGGCCCCT[C/T]CCTGGTAGGTAAAGA | 83946 |
rs47128475 | snp | A/G | 0.48 | 0.0979796 | intron-variant | Phip | GRCm38.p3 | 9:82911928 | GAACCTTGCTGCCAG[A/G]TGTAGATGAGTAACA | 83946 |
rs47134077 | snp | C/T | 0.391111 | 0.206368 | intron-variant | Phip | GRCm38.p3 | 9:82942858 | TCTCTACCCCTACTC[C/T]GCCTTCCTTGGAGAG | 83946 |
rs47147219 | snp | A/G | 0.391111 | 0.206368 | intron-variant | Phip | GRCm38.p3 | 9:82943551 | GGTAAAGCTGTGACT[A/G]AAAGCACTCTAATGC | 83946 |
rs47190483 | snp | A/G | 0.124444 | 0.216185 | intron-variant | Phip | Mm_Celera | 9:82902046 | GAACAAGTATGGCTC[A/G]GTGGTAGGACCACAA | 83946 |
rs47205277 | snp | A/C | 0.42 | 0.183303 | downstream-variant-500B | Phip, LOC102641372 | GRCm38.p3 | 9:82865814 | AATTGTAGATTCTTA[A/C]GAGTTCATAAATATA | 83946 |
rs47230686 | snp | C/T | 0.336735 | 0.234472 | intron-variant, upstream-variant-2KB | Phip | GRCm38.p3 | 9:82929330 | AGTTCCAACTCCCTC[C/T]GTGACTTGCCTATAC | 83946 |
rs47289560 | snp | A/G | 0.132653 | 0.220748 | intron-variant | Phip | Mm_Celera | 9:82934503 | ATAGCACAAGGAGAA[A/G]ACAGCAAGAGCTAGC | 83946 |
rs47321251 | snp | C/T | 0.375 | 0.216506 | intron-variant | Phip | GRCm38.p3 | 9:82887715 | AACATATGTAGTAAG[C/T]AGTGATGAGTTTTCC | 83946 |
rs47341225 | snp | C/T | | | intron-variant | Phip | GRCm38.p3 | 9:82882756 | GGCATTTGAAACTGA[C/T]CTCAGATCGTTAGGT | 83946 |
rs47367580 | snp | C/T | 0.391111 | 0.206368 | intron-variant | Phip | GRCm38.p3 | 9:82941651 | GTTACCATGTGCCCT[C/T]GTCAGTTTCAAAAGT | 83946 |
rs47373670 | snp | C/G | 0.124444 | 0.216185 | intron-variant | Phip | Mm_Celera | 9:82941558 | GTGTTTCATAACCAT[C/G]TCATCTCTCGGCTTG | 83946 |
rs47397076 | snp | C/T | | | intron-variant | Phip | GRCm38.p3 | 9:82957187 | CCTGTAAGTTTCTTT[C/T]AGAAAACTGAGTATC | 83946 |
rs47402813 | snp | A/G | 0.152778 | 0.230321 | intron-variant | Phip | Mm_Celera | 9:82968773 | CCAGGCCTAGTTCAA[A/G]GTAACGCAACTACCC | 83946 |
rs47424913 | snp | C/G | | | intron-variant | Phip | Mm_Celera | 9:82923242 | CTGTCTCTAAATATA[C/G]CCATTTAAATTCTAT | 83946 |
rs47432889 | snp | C/T | 0.408163 | 0.193609 | intron-variant, upstream-variant-2KB | Phip | GRCm38.p3 | 9:82930450 | CCTTCTACAAATTGA[C/T]CTTAAACACAAAATG | 83946 |
rs47445161 | snp | C/T | 0.459184 | 0.136902 | intron-variant | Phip | GRCm38.p3 | 9:82900128 | AAACTGAAGCGTTTG[C/T]ATGCTATCTATATAT | 83946 |
rs47446552 | snp | C/T | 0.391111 | 0.206368 | intron-variant | Phip | GRCm38.p3 | 9:82927591 | TTTCTTGGCTGAGGA[C/T]GCCACAGGGAATGAC | 83946 |
rs47457698 | snp | A/G | 0.124444 | 0.216185 | intron-variant | Phip | Mm_Celera | 9:82936965 | TCCTTCAGCCACTGA[A/G]TAAACAAAGGCTACT | 83946 |
rs47461811 | snp | C/T | 0.489796 | 0.070696 | intron-variant | Phip | GRCm38.p3 | 9:82943484 | GCACTGTTTCATATA[C/T]GCCCTCAGAAACCCA | 83946 |
rs47499348 | snp | A/G | 0.336735 | 0.234472 | intron-variant | Phip | GRCm38.p3 | 9:82926322 | GTTAAAATGGATTTC[A/G]CTTGTGATATGCAGA | 83946 |
rs47515841 | snp | A/G | 0.32 | 0.24 | intron-variant | Phip | Mm_Celera | 9:82916139 | AAGAGGTAAGACTCT[A/G]CCCTGTCTAAAGCAC | 83946 |
rs47528582 | snp | A/C/G/T | 0.35503 | 0.226867 | synonymous-codon | Phip | GRCm38.p3 | 9:82876163 | TTTACCATTCATTTG[A/C/G/T]GCAGCATTATGTCTT | 83946 |
rs47537158 | snp | C/T | 0.336735 | 0.234472 | intron-variant, upstream-variant-2KB | Phip | GRCm38.p3 | 9:82929812 | ATCTAGTGACCCCAA[C/T]TTTCTTTATCAATTT | 83946 |
rs47552090 | snp | A/G | | | intron-variant | Phip | GRCm38.p3 | 9:82972347 | GAAACTACATTTTTA[A/G]TCACCAAATAATTTT | 83946 |
rs47612207 | snp | A/G | 0.231111 | 0.249285 | intron-variant | Phip | Mm_Celera | 9:82924906 | TTCATAGCAATTAAG[A/G]ATTTTTTACAATGAG | 83946 |
rs47672559 | snp | C/T | 0.277778 | 0.248452 | intron-variant | Phip, LOC105243467 | GRCm38.p3 | 9:82964047 | ATGCCATGCTTTCTC[C/T]AGCTTTGAGGTATTA | 83946 |
rs47674011 | snp | A/G | 0.244898 | 0.249948 | intron-variant | Phip | Mm_Celera | 9:82918944 | ATCTAACATCATGAT[A/G]TGCCTCAAGAGTTAT | 83946 |
rs47680255 | snp | A/G | 0.48 | 0.0979796 | intron-variant | Phip | GRCm38.p3 | 9:82941884 | GTTAGATGACTTTCT[A/G]TCAACAAGTTAAATG | 83946 |
rs47727032 | snp | C/T | 0.244898 | 0.249948 | intron-variant | Phip | Mm_Celera | 9:82923682 | AATTAAAGACATACT[C/T]TCTTTCCTATTTTCT | 83946 |
rs47727263 | snp | C/T | 0.336735 | 0.234472 | intron-variant | Phip | Mm_Celera | 9:82879481 | TGTAAGCTCTCGGAA[C/T]TAATATGGAGAAGTA | 83946 |
rs47749065 | snp | A/G | 0.48 | 0.0979796 | synonymous-codon | Phip | GRCm38.p3 | 9:82913818 | AGGGGGAGGCATGAG[A/G]TGAGGTGCCTGCTGC | 83946 |
rs47760758 | snp | C/T | 0.459184 | 0.136902 | intron-variant | Phip | Mm_Celera | 9:82907492 | TTAATCAGTCCACGT[C/T]CTATTCCAGACTACT | 83946 |
rs47807969 | snp | A/G | 0.231111 | 0.249285 | intron-variant | Phip | Mm_Celera | 9:82939740 | ATCGCTGAACTCGAG[A/G]CCTCAGTACCATTCC | 83946 |
rs47821303 | snp | C/T | 0.396694 | 0.202437 | intron-variant | Phip | GRCm38.p3 | 9:82890948 | TGCCTTTTGTCTATT[C/T]TTTATCCAACTGCTA | 83946 |
rs47845494 | snp | A/C | 0.426035 | 0.177515 | intron-variant | Phip | Mm_Celera | 9:82899210 | GTATCACACTGAATC[A/C]TAAGAACACACTTCA | 83946 |
rs47848345 | snp | A/G | 0.473373 | 0.11227 | intron-variant, upstream-variant-2KB | Phip | Mm_Celera | 9:82928925 | GCTGAATACATAAGT[A/G]TTGATTGCACTCAAG | 83946 |
rs47879647 | snp | C/T | 0.244898 | 0.249948 | intron-variant | Phip | GRCm38.p3 | 9:82954639 | TGAAGTTCAGTAATG[C/T]TGAAAAATGTCAGCA | 83946 |
rs47904186 | snp | C/G | 0.336735 | 0.234472 | intron-variant | Phip | GRCm38.p3 | 9:82919376 | ACACTACATGGGTGA[C/G]ATGAATCAATGGGAA | 83946 |
rs47921549 | snp | C/T | 0.408163 | 0.193609 | intron-variant | Phip | GRCm38.p3 | 9:82876459 | GGATCATTGTCAATG[C/T]TACAGTTATATGACA | 83946 |
rs47959731 | snp | A/G | 0.459184 | 0.136902 | intron-variant | Phip | GRCm38.p3 | 9:82934207 | AGCAATGAGTACCAG[A/G]ACCAGATATATTTTC | 83946 |
rs48000472 | snp | C/T | 0.459184 | 0.136902 | intron-variant | Phip | GRCm38.p3 | 9:82910520 | AGGAGGTGTGAGGCC[C/T]GCGTCAGGTTAGTGC | 83946 |
rs48008009 | snp | A/C | 0.244898 | 0.249948 | intron-variant | Phip | Mm_Celera | 9:82926236 | AAAGTAAAACTAAGC[A/C]AGGCATCACAATATA | 83946 |
rs48040348 | snp | G/T | 0.426035 | 0.177515 | intron-variant | Phip | GRCm38.p3 | 9:82903251 | CTAAGAACAGTAGGA[G/T]ATCAAACATCTGACT | 83946 |
rs48085371 | snp | C/T | 0.391111 | 0.206368 | synonymous-codon | Phip | GRCm38.p3 | 9:82932999 | TATTTCAGCAGCATG[C/T]CCTCTTAAAGTAGCT | 83946 |
rs48092615 | snp | A/G | | | intron-variant | Phip | GRCm38.p3 | 9:82957361 | AGGCGAGAGGGTGAT[A/G]TGTAATAGTGACATG | 83946 |
rs48137536 | snp | C/T | 0.444444 | 0.157135 | intron-variant | Phip | GRCm38.p3 | 9:82957423 | GAGAACGCACTGACT[C/T]TGTTACCACTCACCT | 83946 |
rs48240451 | snp | A/T | 0.391111 | 0.206368 | intron-variant, upstream-variant-2KB | Phip | GRCm38.p3 | 9:82928803 | TCTTTATCAAGTTCC[A/T]ACTAAGTTAGACAAA | 83946 |
rs48263389 | snp | C/G | 0.391111 | 0.206368 | intron-variant | Phip | GRCm38.p3 | 9:82900895 | TCTTACAGTCGGCTG[C/G]TTTTAAGACCATTTT | 83946 |
rs48315764 | snp | C/T | 0.336735 | 0.234472 | intron-variant | Phip | GRCm38.p3 | 9:82925549 | GCCTTCAGGAGTTGA[C/T]ATGCATGTGTGGCCT | 83946 |
rs48343057 | snp | A/G | | | intron-variant | Phip | GRCm38.p3 | 9:82957019 | ACTATGGCTTAGCTG[A/G]TGGAATTCGTGTGCT | 83946 |
rs48355488 | snp | C/T | 0.391111 | 0.206368 | intron-variant, upstream-variant-2KB | Phip | GRCm38.p3 | 9:82929382 | CTCAACGTTCCCTTA[C/T]GTCACTGGATTATAT | 83946 |
rs48361482 | snp | A/T | 0.46281 | 0.131194 | intron-variant | Phip | GRCm38.p3 | 9:82918489 | ATTTATTTCATGTTA[A/T]AATAAAATAGTCACA | 83946 |
rs48400999 | snp | C/T | 0.473373 | 0.11227 | intron-variant | Phip | GRCm38.p3 | 9:82939352 | TTCTTCTAAGTATTA[C/T]GTAAAGTGTTGGTAT | 83946 |
rs48433341 | snp | A/C | 0.48 | 0.0979796 | intron-variant | Phip | GRCm38.p3 | 9:82918888 | CTCTTGGCTGTGAAA[A/C]CGTGAAGAGCACTGA | 83946 |
rs48466205 | snp | A/G | | | intron-variant | Phip | GRCm38.p3 | 9:82957068 | TGGAGCCGGAGCACA[A/G]GATAAACCAGGTGTA | 83946 |
rs48509772 | snp | G/T | 0.132653 | 0.220748 | intron-variant | Phip | Mm_Celera | 9:82946444 | AACCCGGAGCTGATC[G/T]GCTTTATATACTGAC | 83946 |
rs48523480 | snp | A/G | 0.32 | 0.24 | intron-variant | Phip | Mm_Celera | 9:82943295 | TATAAACAAGAGTTT[A/G]CTGGAGGTTGAAATA | 83946 |
rs48605419 | snp | A/T | 0.408163 | 0.193609 | intron-variant | Phip | GRCm38.p3 | 9:82906073 | TTAAACCTAATAACT[A/T]GTAGCTCTGACACTT | 83946 |
rs48620162 | snp | C/G | | | utr-variant-3-prime | Phip | GRCm38.p3 | 9:82866669 | CTAGAAGAAATAAAA[C/G]AACATCCGTAAAGCT | 83946 |
rs48682316 | snp | C/T | 0.18 | 0.24 | intron-variant | Phip, LOC105243467 | Mm_Celera | 9:82964936 | ACTCAATGGCATGAC[C/T]AACTCAAGAACCACA | 83946 |
rs48709832 | snp | C/T | 0.231111 | 0.249285 | intron-variant | Phip | Mm_Celera | 9:82925420 | GTACATTGAGCCCAT[C/T]CATGGCAAAAGCCAA | 83946 |
rs48784555 | snp | C/T | 0.391111 | 0.206368 | intron-variant | Phip | GRCm38.p3 | 9:82911807 | CTAAAATGATGACGA[C/T]GCTGAGAAGGTTCTC | 83946 |
rs48816297 | snp | A/C | 0.444444 | 0.157135 | intron-variant | Phip | Mm_Celera | 9:82944161 | TCTCTTAATATTTCT[A/C]CTCCAAAGTATTATT | 83946 |
rs48821963 | snp | A/C | 0.486111 | 0.0821678 | intron-variant | Phip, LOC105243467 | GRCm38.p3 | 9:82965625 | CTGCTTGCCTCCTTA[A/C]GCGTATGTTTAAGTA | 83946 |
rs48841627 | snp | C/T | 0.46281 | 0.131194 | intron-variant | Phip, LOC105243467 | GRCm38.p3 | 9:82961342 | AACTGCTGCGTCATA[C/T]AAGTTTCCACATCAT | 83946 |
rs48877147 | snp | C/T | 0.459184 | 0.136902 | intron-variant | Phip | Mm_Celera | 9:82955823 | AAAAAGCTTCATAAG[C/T]CAAGGACATATCAAA | 83946 |
rs49006530 | snp | A/C | 0.426035 | 0.177515 | downstream-variant-500B | Phip | GRCm38.p3 | 9:82865985 | CACCACCATGCCAAG[A/C]TATAAAACAGCATTC | 83946 |
rs49023792 | snp | A/G | 0.21875 | 0.248039 | intron-variant | Phip | Mm_Celera | 9:82957741 | AATATTAAATTCAAC[A/G]GATCCTTAAAGAAAT | 83946 |
rs49044904 | snp | C/T | 0.124444 | 0.216185 | intron-variant | Phip | Mm_Celera | 9:82884720 | ATGCTGCTGGGACAA[C/T]ACCAACTATGTAAAA | 83946 |
rs49070860 | snp | C/T | 0.426035 | 0.177515 | intron-variant | Phip | GRCm38.p3 | 9:82902857 | AAACTTCTTTACTTT[C/T]ACAATCTGATGCTTA | 83946 |
rs49084322 | snp | A/G | 0.444444 | 0.157135 | intron-variant, upstream-variant-2KB | Phip | Mm_Celera | 9:82929461 | CACACTAAGAGCAAT[A/G]AGCATGAAGTTGTTA | 83946 |
rs49120239 | snp | A/C | 0.231111 | 0.249285 | intron-variant | Phip | Mm_Celera | 9:82900229 | ACACGTTTTGTCATG[A/C]ATATTTCATGTGATG | 83946 |
rs49170285 | snp | C/T | 0.459184 | 0.136902 | intron-variant | Phip | GRCm38.p3 | 9:82952790 | TTGGAAACCAGTGTG[C/T]CCAGCCTTTCACTGC | 83946 |
rs49171011 | snp | A/T | 0.231111 | 0.249285 | intron-variant | Phip | Mm_Celera | 9:82918584 | CTAGTATGCTATTAG[A/T]CATTTTTGGGACATA | 83946 |
rs49182012 | snp | C/T | | | intron-variant | Phip | Mm_Celera | 9:82923243 | TGTCTCTAAATATAC[C/T]CATTTAAATTCTATT | 83946 |
rs49187152 | snp | A/C | 0.132653 | 0.220748 | intron-variant | Phip | Mm_Celera | 9:82931999 | CCTCTCCATCTCTAC[A/C]AATCAAGACTTTAGC | 83946 |
rs49206027 | snp | A/T | 0.18 | 0.24 | intron-variant | Phip | GRCm38.p3 | 9:82888241 | TACTCAAATAAAAAA[A/T]TTTCATCAGAATCAT | 83946 |
rs49207577 | snp | A/G | 0.375 | 0.216506 | intron-variant | Phip | GRCm38.p3 | 9:82907302 | TTTAAATACTGCAAA[A/G]TTATAGCAAGACACC | 83946 |
rs49208653 | snp | A/G | 0.375 | 0.216506 | intron-variant | Phip | Mm_Celera | 9:82882791 | GCGTAGGAAATCCTT[A/G]CCTGCTAAGACATCT | 83946 |
rs49266671 | snp | C/T | 0.391111 | 0.206368 | intron-variant | Phip | GRCm38.p3 | 9:82919052 | TGTCAATTGGCTAGA[C/T]TGACTGGCATGGAAA | 83946 |
rs49280454 | snp | A/G | 0.244898 | 0.249948 | intron-variant | Phip | Mm_Celera | 9:82922337 | TCTAGGACTGGGAAT[A/G]ACGTAATGTCATAAA | 83946 |
rs49305248 | snp | C/T | 0.244898 | 0.249948 | intron-variant | Phip | GRCm38.p3 | 9:82925055 | GGAGAAAATTCCGAA[C/T]CTGTGTTTAACTGAC | 83946 |
rs49316355 | snp | C/T | 0.48 | 0.0979796 | intron-variant | Phip | GRCm38.p3 | 9:82937097 | GCAAAAAGCAGATCT[C/T]ACCAACTGAGAAACC | 83946 |
rs49350909 | snp | A/G | 0.391111 | 0.206368 | intron-variant | Phip | GRCm38.p3 | 9:82935551 | CAGAAAACAGCTGAG[A/G]AAACATTTGTTCAGC | 83946 |
rs49409456 | snp | A/T | 0.142012 | 0.225474 | intron-variant | Phip | Mm_Celera | 9:82907353 | TCCTGCATGTCAAAC[A/T]TGCAATCTATTTAAC | 83946 |
rs49415661 | snp | A/G | 0.132653 | 0.220748 | intron-variant | Phip | Mm_Celera | 9:82931396 | TGAGTTCTGATGCAT[A/G]TAACGATGTACATAC | 83946 |
rs49442400 | snp | A/G | 0.459184 | 0.136902 | synonymous-codon, intron-variant | Phip | GRCm38.p3 | 9:82945914 | CCTTGAAAACAGAGT[A/G]TCCGCTACCAAGAAA | 83946 |
rs49462768 | snp | A/C | 0.408163 | 0.193609 | intron-variant | Phip | GRCm38.p3 | 9:82903207 | TTCACCTTCCTGTGA[A/C]TACAAAGACAGATTT | 83946 |
rs49475810 | snp | A/G | 0.231111 | 0.249285 | intron-variant | Phip | Mm_Celera | 9:82900519 | CTCTGAATTTTTTCG[A/G]TTAGTATTTGTCAAT | 83946 |
rs49505970 | snp | A/G | 0.408163 | 0.193609 | intron-variant | Phip | GRCm38.p3 | 9:82947191 | TCAATCTTATTTTGT[A/G]CACATAAAACTAGCT | 83946 |
rs49517043 | snp | G/T | 0.444444 | 0.157135 | missense | Phip | GRCm38.p3 | 9:82871454 | CTATAGGATCATCTG[G/T]TTTTTTCCGGTTACT | 83946 |
rs49535553 | snp | C/T | 0.336735 | 0.234472 | intron-variant | Phip | Mm_Celera | 9:82920622 | CTTGTGTTTTTACCT[C/T]ACTATATATTACAAT | 83946 |
rs49544095 | snp | C/T | 0.231111 | 0.249285 | intron-variant | Phip | Mm_Celera | 9:82920613 | CTCCCTCAGCTTGTG[C/T]TTTTACCTCACTATA | 83946 |
rs49544786 | snp | C/T | 0.459184 | 0.136902 | intron-variant | Phip | GRCm38.p3 | 9:82947319 | TAATGGCATGCAACC[C/T]AAATGAGGATAGTTA | 83946 |
rs49550800 | snp | C/G | 0.260355 | 0.249785 | intron-variant | Phip | Mm_Celera | 9:82912941 | CTTCAATGTAAATCA[C/G]TCTGCGCTATACTTT | 83946 |
rs49566025 | snp | A/G | 0.375 | 0.216506 | intron-variant | Phip | GRCm38.p3 | 9:82900945 | AGACAGACAGTCAAT[A/G]AGTCAGAAAGATACA | 83946 |
rs49596036 | snp | A/C | 0.48 | 0.0979796 | intron-variant | Phip | GRCm38.p3 | 9:82912175 | AGCACTAACTCTAAA[A/C]GCAGGAACAAAGTCA | 83946 |
rs49599926 | snp | A/T | 0.459184 | 0.136902 | intron-variant | Phip | GRCm38.p3 | 9:82935027 | TATTGATATTGCTGC[A/T]CACTATATAGATCTG | 83946 |
rs49603488 | snp | A/C | 0.48 | 0.0979796 | intron-variant | Phip | Mm_Celera | 9:82895943 | AATATTCTACAAATA[A/C]AGTTTCAAAACCTAT | 83946 |
rs49615845 | snp | C/T | 0.408163 | 0.193609 | intron-variant | Phip | GRCm38.p3 | 9:82902645 | ACTAATAACTTCCTT[C/T]CCCAAGGGTGTATCT | 83946 |
rs49791883 | snp | A/G | 0.48 | 0.0979796 | intron-variant | Phip | GRCm38.p3 | 9:82926661 | TTTACCAATGTCTAA[A/G]CAATAATAGGCTACT | 83946 |
rs49814694 | snp | A/C | 0.375 | 0.216506 | intron-variant | Phip | GRCm38.p3 | 9:82907316 | AATTATAGCAAGACA[A/C]CTTGGGCTTGTGCTA | 83946 |
rs49821048 | snp | G/T | 0.486111 | 0.0821678 | intron-variant | Phip | GRCm38.p3 | 9:82954405 | ATGACAGTAATTTCA[G/T]CATTTCTATCATACA | 83946 |
rs49829771 | snp | C/T | 0.391111 | 0.206368 | intron-variant | Phip | GRCm38.p3 | 9:82919301 | TACTTAGGAAAGCCT[C/T]TTCGGTGCATAAAGC | 83946 |
rs49843573 | snp | C/T | 0.459184 | 0.136902 | intron-variant | Phip | GRCm38.p3 | 9:82901958 | GTGTACCTAGACAGT[C/T]GGAAGGTTGAACTCA | 83946 |
rs49864483 | snp | A/T | | | intron-variant | Phip | Mm_Celera | 9:82942660 | ATTTTATACTTCAAA[A/T]TCTTAAAGTAGAGAT | 83946 |
rs49874875 | snp | A/G | 0.489796 | 0.070696 | intron-variant | Phip | Mm_Celera | 9:82919974 | CTTACTCTCCTCCCA[A/G]CTCTCTGAAAATGAA | 83946 |
rs49906941 | snp | A/G | 0.132653 | 0.220748 | intron-variant | Phip | Mm_Celera | 9:82909457 | AACTTTGACTTTATG[A/G]TTTGAAAATGATATA | 83946 |
rs49908753 | snp | C/T | 0.297521 | 0.245442 | intron-variant | Phip | GRCm38.p3 | 9:82887806 | AAATAAAACGCATCT[C/T]AAAAAGCATATTATT | 83946 |
rs49914532 | snp | C/T | 0.46281 | 0.131194 | intron-variant | Phip | GRCm38.p3 | 9:82946408 | AGTGAAAACAGAAGG[C/T]ATTTAAGGATTCTGA | 83946 |
rs49917201 | snp | C/T | 0.489796 | 0.070696 | intron-variant | Phip | GRCm38.p3 | 9:82945456 | TACAATTTGCCCATG[C/T]TCAGTCTAGACTGAA | 83946 |
rs49922142 | snp | A/T | 0.391111 | 0.206368 | intron-variant | Phip | Mm_Celera | 9:82913418 | AAGTTTTTGAGAGCA[A/T]AGACCAAATTTCCTA | 83946 |
rs49930538 | snp | A/G | 0.48 | 0.0979796 | intron-variant | Phip | GRCm38.p3 | 9:82899979 | CCTCAGAGGAAAAAA[A/G]TTATAAGCTGTCATA | 83946 |
rs49936117 | snp | C/T | 0.48 | 0.0979796 | intron-variant | Phip | Mm_Celera | 9:82940085 | TTTCTGCATGAAGCA[C/T]GTTTACACCACAGAT | 83946 |
rs49980643 | snp | G/T | 0.375 | 0.216506 | intron-variant | Phip | GRCm38.p3 | 9:82892846 | CCATTTACAGTATAC[G/T]CTAACATAGCAAAGA | 83946 |
rs50025677 | snp | A/T | 0.35503 | 0.226867 | intron-variant | Phip | Mm_Celera | 9:82886199 | CACTAGCAGTCAGAG[A/T]ATGTTACCATGAAGA | 83946 |
rs50038108 | snp | A/C | | | intron-variant | Phip | GRCm38.p3 | 9:82949471 | TTGTATTTAATACTG[A/C]TTTGTATTTTAACTA | 83946 |
rs50089106 | snp | A/C | 0.473373 | 0.11227 | intron-variant | Phip | GRCm38.p3 | 9:82922418 | TAAATGCTTTCAGCA[A/C]TTAACTGGCATTTAT | 83946 |
rs50113630 | snp | A/T | 0.18 | 0.24 | intron-variant | Phip | GRCm38.p3 | 9:82889276 | AACCTGATAATCAAG[A/T]GAAAACTATAATCAC | 83946 |
rs50173775 | snp | C/T | 0.35503 | 0.226867 | intron-variant | Phip | GRCm38.p3 | 9:82957319 | AATAGGCACCGCGTG[C/T]ACATGAATGCGTAAG | 83946 |
rs50262941 | snp | C/T | 0.277778 | 0.248452 | intron-variant, downstream-variant-500B | Phip, LOC105243467 | Mm_Celera | 9:82959447 | CTAACAGCACAGTAA[C/T]TAAAAACATTATTTT | 83946 |
rs50310729 | snp | A/G | 0.165289 | 0.235211 | intron-variant | Phip | Mm_Celera | 9:82902713 | ATTAGGACTTTAAAC[A/G]TGTGCAATTCCAGCA | 83946 |
rs50316429 | snp | C/T | 0.408163 | 0.193609 | intron-variant | Phip | GRCm38.p3 | 9:82952805 | TCCAGCCTTTCACTG[C/T]ACTCATTCTCCTCTT | 83946 |
rs50326317 | snp | C/T | 0.142012 | 0.225474 | intron-variant | Phip | Mm_Celera | 9:82968193 | TGCTAATCGAGGTCA[C/T]ATGAGTTAGTATTAA | 83946 |
rs50329823 | snp | A/T | 0.375 | 0.216506 | intron-variant | Phip | GRCm38.p3 | 9:82933139 | TGTTAATATAAAAAA[A/T]GTGTCACCTCCACAT | 83946 |
rs50398429 | snp | C/T | 0.32 | 0.24 | intron-variant | Phip | Mm_Celera | 9:82918912 | GCACTGAAACAGCCA[C/T]TTAGAACCCTACTCA | 83946 |
rs50410246 | snp | C/T | 0.42 | 0.183303 | intron-variant, upstream-variant-2KB | Phip, LOC105243467 | GRCm38.p3 | 9:82967249 | CCCAGTGTGCCATGC[C/T]AGCTGGAGCAGAACC | 83946 |
rs50473320 | snp | C/T | 0.459184 | 0.136902 | intron-variant | Phip | GRCm38.p3 | 9:82901122 | CATTAACTCTGCATA[C/T]AAGAAATGAGGAACG | 83946 |
rs50486408 | snp | C/T | 0.391111 | 0.206368 | intron-variant | Phip | GRCm38.p3 | 9:82872249 | ATTGATAGCAAAAAG[C/T]ACAAATTCCATTATC | 83946 |
rs50490005 | snp | C/T | 0.345679 | 0.230967 | intron-variant, nc-transcript-variant | Phip, LOC105243467 | GRCm38.p3 | 9:82960743 | TGTATACCTGGGATC[C/T]GGTAGTTCACACTGT | 83946 |
rs50493404 | snp | C/T | 0.391111 | 0.206368 | intron-variant | Phip | GRCm38.p3 | 9:82920147 | CCTTTCTGTTCTGAA[C/T]TTCTAGAGCCTCAAA | 83946 |
rs50501417 | snp | A/G | 0.375 | 0.216506 | intron-variant | Phip | Mm_Celera | 9:82907124 | GATTTCCTTTAAAAT[A/G]AGTGTTAGCTCTTAC | 83946 |
rs50563584 | snp | A/G | 0.391111 | 0.206368 | intron-variant | Phip | GRCm38.p3 | 9:82919752 | TATGCTAAGATCACT[A/G]CACATGAACAAGAGA | 83946 |
rs50579751 | snp | C/G | | | intron-variant | Phip | Mm_Celera | 9:82923152 | GAAAACAAAGCAAAA[C/G]AACTTTTTAAAAAAT | 83946 |
rs50582553 | snp | A/G | 0.48 | 0.0979796 | intron-variant | Phip | Mm_Celera | 9:82914330 | TTTTAAATGATTAGG[A/G]TTGTTGTACTTGAGA | 83946 |
rs50627100 | snp | C/G | 0.489796 | 0.070696 | intron-variant | Phip | GRCm38.p3 | 9:82911493 | ATGTAGAGAAAGACA[C/G]AGCTAAATCAAATGT | 83946 |
rs50648941 | snp | C/T | | | utr-variant-3-prime | Phip | GRCm38.p3 | 9:82866945 | AAATGTAACATTGTA[C/T]CTTACTTTTAAATTT | 83946 |
rs50658776 | snp | A/G | 0.459184 | 0.136902 | intron-variant | Phip | GRCm38.p3 | 9:82948088 | ACAAGCAACTGTAAA[A/G]CACCTTAAACAAAGA | 83946 |
rs50684644 | snp | C/T | 0.408163 | 0.193609 | intron-variant, upstream-variant-2KB | Phip | Mm_Celera | 9:82928945 | TTGCACTCAAGACTG[C/T]ACCCATCCAGTTCTT | 83946 |
rs50694054 | snp | A/G | 0.396694 | 0.202437 | intron-variant | Phip | GRCm38.p3 | 9:82956876 | ATTTGCTTTAAGAAA[A/G]TTTACTGTAGCTTTC | 83946 |
rs50709505 | snp | C/T | 0.459184 | 0.136902 | intron-variant | Phip | GRCm38.p3 | 9:82933939 | AGAGAATGCACAAAG[C/T]AGCAAATAACGCACC | 83946 |
rs50727694 | snp | A/G | 0.391111 | 0.206368 | intron-variant, upstream-variant-2KB | Phip | GRCm38.p3 | 9:82929085 | TCCCACCTGTCAAGA[A/G]TAAGAGCATCAGTGT | 83946 |
rs50735438 | snp | A/C | 0.48 | 0.0979796 | intron-variant | Phip | Mm_Celera | 9:82913017 | TTCAAAATCCACTTA[A/C]TTGACTTCAATATTC | 83946 |
rs50744912 | snp | C/G | 0.260355 | 0.249785 | intron-variant | Phip | GRCm38.p3 | 9:82896774 | CCTCTCTTACTAAAA[C/G]TAGTCATTTCATTCT | 83946 |
rs50758789 | snp | C/T | 0.391111 | 0.206368 | intron-variant | Phip | GRCm38.p3 | 9:82912689 | ATTCCAATTTTACAC[C/T]CAATTGTATAACATG | 83946 |
rs50835130 | snp | C/T | 0.391111 | 0.206368 | intron-variant | Phip | GRCm38.p3 | 9:82916348 | ACTGAACTTAATTGG[C/T]TACATTCTAGGAAAT | 83946 |
rs50836088 | snp | A/G | 0.391111 | 0.206368 | intron-variant | Phip | GRCm38.p3 | 9:82923567 | TGAGCCCAGTACCTC[A/G]TGAGTGAGTATTAGG | 83946 |
rs50837032 | snp | A/C | 0.48 | 0.0979796 | intron-variant | Phip | GRCm38.p3 | 9:82937041 | TGGCAGGAATCTGGG[A/C]AAAGGACAAGAAGTA | 83946 |
rs50880876 | snp | C/T | 0.473373 | 0.11227 | intron-variant | Phip | GRCm38.p3 | 9:82954844 | TGCCGGAGTATAACA[C/T]TAGGAAACAAGACTA | 83946 |
rs50885321 | snp | C/T | 0.426035 | 0.177515 | intron-variant | Phip | GRCm38.p3 | 9:82903616 | GTTAATATCTGAAAC[C/T]TATTGAACATTTTTA | 83946 |
rs50890173 | snp | C/T | 0.396694 | 0.202437 | intron-variant | Phip | Mm_Celera | 9:82891785 | AGCACCAGTCAGAGC[C/T]AACCGTCAAATATTC | 83946 |
rs50904308 | snp | C/T | 0.32 | 0.24 | intron-variant | Phip | GRCm38.p3 | 9:82940714 | TGGCTCTGCAGATAG[C/T]ATCTTTATGACCAGA | 83946 |
rs50948171 | snp | C/T | 0.345679 | 0.230967 | intron-variant, nc-transcript-variant | Phip, LOC105243467 | Mm_Celera | 9:82960267 | TGTATACCTGGGATC[C/T]GGTAGTTCACACTGT | 83946 |
rs50952754 | snp | A/G | 0.391111 | 0.206368 | intron-variant | Phip | Mm_Celera | 9:82922362 | CATAAATTTTAGTAC[A/G]CATAGCATATAGCAC | 83946 |
rs50961003 | snp | A/G | 0.336735 | 0.234472 | synonymous-codon, intron-variant | Phip | GRCm38.p3 | 9:82945863 | ATAAACTGCAGTTGG[A/G]ACAAGTCGTTCAAGT | 83946 |
rs50999001 | snp | G/T | 0.444444 | 0.157135 | intron-variant | Phip | GRCm38.p3 | 9:82899045 | TAAAGAGAAAAAATG[G/T]TTAAATTTTAACTCA | 83946 |
rs51017699 | snp | A/G | 0.231111 | 0.249285 | intron-variant | Phip | Mm_Celera | 9:82943913 | GCAGTAGATATAAAC[A/G]TGCCCTGTTACAACT | 83946 |
rs51022899 | snp | A/G | 0.375 | 0.216506 | intron-variant | Phip | GRCm38.p3 | 9:82909976 | AGAAGTCAATAATTA[A/G]GCATGAATTTTACTT | 83946 |
rs51022990 | snp | C/T | 0.391111 | 0.206368 | intron-variant | Phip | GRCm38.p3 | 9:82911907 | GTATTACTCTTGAAA[C/T]TCGTGGAACCTTGCT | 83946 |
rs51046428 | snp | A/T | 0.486111 | 0.0821678 | intron-variant, upstream-variant-2KB | Phip | GRCm38.p3 | 9:82929583 | TCCACAGTGTGATAA[A/T]AATACATATGAAGAA | 83946 |
rs51049328 | snp | A/G | 0.391111 | 0.206368 | intron-variant | Phip | GRCm38.p3 | 9:82925639 | TCTCAGCCTGAAAAT[A/G]ACTGAACTTACAAAA | 83946 |
rs51066247 | snp | G/T | 0.244898 | 0.249948 | intron-variant | Phip | Mm_Celera | 9:82916236 | ATGATTTTCAACAAC[G/T]GTGATTGGATTTCTG | 83946 |
rs51068560 | snp | A/C | 0.48 | 0.0979796 | intron-variant | Phip | GRCm38.p3 | 9:82898424 | AGTTATGGTCACTAT[A/C]GTGAGGAGAGCTAAA | 83946 |
rs51096956 | snp | C/T | | | intron-variant | Phip | GRCm38.p3 | 9:82957349 | GTAATTGAACAGAGG[C/T]GAGAGGGTGATGTGT | 83946 |
rs51244702 | snp | A/G | 0.231111 | 0.249285 | synonymous-codon, utr-variant-5-prime | Phip | Mm_Celera | 9:82926490 | GAGAACTCTAGGATC[A/G]AATGGGTGTGGCTCA | 83946 |
rs51274586 | snp | A/G | 0.132653 | 0.220748 | utr-variant-3-prime | Phip | Mm_Celera | 9:82867998 | GTCAATCAATCATGT[A/G]TCTCCGATGTGGCCT | 83946 |
rs51295358 | snp | C/T | 0.231111 | 0.249285 | intron-variant | Phip | Mm_Celera | 9:82926984 | TACTTATTTAGACTA[C/T]ACTCTACTGTCAGCC | 83946 |
rs51302586 | snp | C/T | 0.231111 | 0.249285 | intron-variant | Phip | Mm_Celera | 9:82913653 | AAGTTTTAAAATCTG[C/T]GAGAACCTTGACTCC | 83946 |
rs51304168 | snp | C/G | 0.48 | 0.0979796 | intron-variant | Phip | Mm_Celera | 9:82899879 | ACCTTCCCTCACCTG[C/G]TATTTTCCTCCACTA | 83946 |
rs51314792 | snp | A/C | 0.391111 | 0.206368 | intron-variant | Phip | Mm_Celera | 9:82925097 | CCTCGTTTCTACAGC[A/C]GTGTAAGATTGTTCT | 83946 |
rs51315658 | snp | C/T | 0.336735 | 0.234472 | intron-variant | Phip | GRCm38.p3 | 9:82877906 | GAGGTCGCAGCACAG[C/T]CCGCACTGCACCTCT | 83946 |
rs51315731 | snp | A/G | 0.244898 | 0.249948 | intron-variant | Phip | Mm_Celera | 9:82946176 | CAAATGCAGCTAAAT[A/G]GTATGTCCAAAGTCA | 83946 |
rs51317620 | snp | A/C | 0.124444 | 0.216185 | utr-variant-3-prime | Phip | Mm_Celera | 9:82870997 | GTGGAACCGAATAAC[A/C]TACCTAAGGGCAATA | 83946 |
rs51359935 | snp | A/G | 0.426035 | 0.177515 | intron-variant | Phip | GRCm38.p3 | 9:82903838 | TTCTATGAGGCTATA[A/G]TTTTTAATACAACTC | 83946 |
rs51413652 | snp | A/G | 0.231111 | 0.249285 | intron-variant | Phip | Mm_Celera | 9:82939086 | TTATTTCAAGCTATC[A/G]TGTCAACAAAGGATA | 83946 |
rs51418214 | snp | C/G | 0.32 | 0.24 | intron-variant | Phip | GRCm38.p3 | 9:82874849 | GCTCAGGGGTTCCAC[C/G]TAAGGTTCAAAGGCC | 83946 |
rs51445771 | snp | A/G | 0.48 | 0.0979796 | intron-variant | Phip | Mm_Celera | 9:82945330 | AATTCAGTGTCAAGG[A/G]TGACAAAATCCTGAG | 83946 |
rs51471424 | snp | C/T | 0.277778 | 0.248452 | intron-variant | Phip | GRCm38.p3 | 9:82885751 | TCAAGGTGAATCCTA[C/T]TGTACTCTGCTCTGA | 83946 |
rs51509452 | snp | A/G | 0.473373 | 0.11227 | intron-variant | Phip | GRCm38.p3 | 9:82934106 | CAAACTAGAAAAGTT[A/G]CCAAGTAGCAAGCTG | 83946 |
rs51577650 | snp | A/G | 0.297521 | 0.245442 | intron-variant | Phip | Mm_Celera | 9:82958890 | GACCTCTAATGCCAC[A/G]TGTTGATATACTGGT | 83946 |
rs51608074 | snp | C/T | 0.391111 | 0.206368 | intron-variant | Phip | GRCm38.p3 | 9:82923662 | TATATTTTAAGAATT[C/T]GTTCAATTAAAGACA | 83946 |
rs51619175 | snp | C/T | 0.408163 | 0.193609 | intron-variant | Phip | GRCm38.p3 | 9:82939598 | CTAAACCTAGACCAA[C/T]ATAAGCATGCTACCT | 83946 |
rs51626505 | snp | A/G | 0.375 | 0.216506 | intron-variant | Phip | GRCm38.p3 | 9:82891412 | AGCTGCATTAAATCA[A/G]AAAAACAAGGTAAAG | 83946 |
rs51653157 | snp | A/G | 0.459184 | 0.136902 | intron-variant | Phip | GRCm38.p3 | 9:82936531 | TTAAGCCTAATTCCA[A/G]CACCACAAATAATAC | 83946 |
rs51666766 | snp | A/G | 0.48 | 0.0979796 | intron-variant | Phip | GRCm38.p3 | 9:82912057 | CCTGCTCCACTCACC[A/G]TGCTATCATGGATGC | 83946 |
rs51688631 | snp | C/T | 0.297521 | 0.245442 | intron-variant | Phip | GRCm38.p3 | 9:82891331 | TCAATCAGTTATCTT[C/T]AAGAAAAGTTTTCTC | 83946 |
rs51695009 | snp | C/T | 0.459184 | 0.136902 | intron-variant | Phip | Mm_Celera | 9:82872710 | AATTAGGACCATTAT[C/T]TGCTGCAGTAATTTA | 83946 |
rs51716852 | snp | A/G | 0.391111 | 0.206368 | intron-variant | Phip | GRCm38.p3 | 9:82939731 | CCAAGGTTTATCGCT[A/G]AACTCGAGACCTCAG | 83946 |
rs51723572 | snp | C/T | 0.459184 | 0.136902 | intron-variant | Phip | Mm_Celera | 9:82872590 | TAGCTTTTCTTCCAT[C/T]TATGAATGTGACAGT | 83946 |
rs51725402 | snp | A/G | 0.48 | 0.0979796 | intron-variant | Phip | GRCm38.p3 | 9:82897952 | AACTAAAGAATGTTG[A/G]GAGCATGACTCCAAG | 83946 |
rs51739547 | snp | C/T | 0.197531 | 0.244432 | intron-variant | Phip | Mm_Celera | 9:82896576 | CACTTCTAAACAACC[C/T]AACAACAGTCTCATT | 83946 |
rs51792360 | snp | A/G | 0.231111 | 0.249285 | intron-variant | Phip | Mm_Celera | 9:82914813 | AGATTGTTCTAACAG[A/G]ATATGTAAAAAGTTG | 83946 |
rs51826361 | snp | A/G | 0.444444 | 0.157135 | intron-variant | Phip | GRCm38.p3 | 9:82889509 | TAAAGACTATTTGTT[A/G]ATGTTACAAAAATGA | 83946 |
rs51832888 | snp | C/T | 0.391111 | 0.206368 | intron-variant | Phip | GRCm38.p3 | 9:82907518 | CTACTTTCTCAATAC[C/T]GGGTCCCTCAAATTT | 83946 |
rs51890300 | snp | A/C | 0.336735 | 0.234472 | intron-variant | Phip | GRCm38.p3 | 9:82916698 | TTACCAGATAAGATA[A/C]ATGATTCATTAATGA | 83946 |
rs51907069 | snp | A/G | 0.231111 | 0.249285 | downstream-variant-500B | Phip | Mm_Celera | 9:82866077 | GTTTTTTGACATGTG[A/G]CCCTCATAAAACTAT | 83946 |
rs51987891 | snp | C/T | 0.231111 | 0.249285 | intron-variant | Phip | Mm_Celera | 9:82914350 | TGTACTTGAGAGGGA[C/T]TGAATATAGAATCCC | 83946 |
rs52010116 | snp | C/T | | | intron-variant | Phip | GRCm38.p3 | 9:82874330 | TGGATCAGAGAAAGA[C/T]TTGACAGAATTGGTC | 83946 |
rs52020102 | snp | C/T | 0.142012 | 0.225474 | intron-variant | Phip | Mm_Celera | 9:82956664 | AGAAAACCTAACAAG[C/T]CAGTCTGAAACACAG | 83946 |
rs52099191 | snp | A/G | | | intron-variant | Phip | GRCm38.p3 | 9:82882551 | ACAGACAGACAGACA[A/G]ACAGACAGACACACA | 83946 |
rs52114224 | snp | A/G | 0.391111 | 0.206368 | intron-variant | Phip | GRCm38.p3 | 9:82916941 | ATAAATGCTACACAA[A/G]ATTACACACACACAA | 83946 |
rs52170421 | snp | C/G | | | intron-variant | Phip | GRCm38.p3 | 9:82882563 | ACAGACAGACAGACA[C/G]ACACATACACATACA | 83946 |
rs52225405 | snp | C/T | | | intron-variant | Phip | GRCm38.p3 | 9:82882557 | AGACAGACAGACAGA[C/T]AGACACACACATACA | 83946 |
rs52258718 | snp | A/C | 0.260355 | 0.249785 | intron-variant | Phip | GRCm38.p3 | 9:82905089 | ATAGAGAAATCTGTA[A/C]ATAAGAAAAAGCAAA | 83946 |
rs52285671 | snp | C/T | 0.231111 | 0.249285 | intron-variant | Phip | Mm_Celera | 9:82926827 | TCTATCAAGTCTGGT[C/T]ATCCAAAGAAGCAAG | 83946 |
rs52320372 | snp | A/T | 0.473373 | 0.11227 | intron-variant | Phip | GRCm38.p3 | 9:82919576 | TAAAGACCAGTTTTT[A/T]AAAAAAATTACCCAA | 83946 |
rs52341927 | snp | A/G/T | 0.391111 | 0.206368 | intron-variant | Phip | GRCm38.p3 | 9:82926881 | TATTATTTTATTTAG[A/G/T]CTACATTCTACAATT | 83946 |
rs52344042 | snp | A/T | 0.391111 | 0.206368 | intron-variant | Phip | Mm_Celera | 9:82924762 | TTTCTTTCCTTCTGT[A/T]AAAAATTGTGATCTC | 83946 |
rs52379724 | snp | A/G | | | intron-variant | Phip | GRCm38.p3 | 9:82882610 | TCATTCTTTAAACAA[A/G]ACAAAACAAAACAAA | 83946 |
rs52400710 | snp | G/T | 0.489796 | 0.070696 | intron-variant | Phip | Mm_Celera | 9:82921954 | TGTGAACACTGTTAG[G/T]TTAGTACTTACTATA | 83946 |
rs52407551 | snp | A/G | 0.391111 | 0.206368 | intron-variant | Phip | GRCm38.p3 | 9:82932263 | ATATCCTTTAAGGAA[A/G]CAACTGGACTTCAGA | 83946 |
rs52537689 | snp | A/G | 0.244898 | 0.249948 | intron-variant | Phip | Mm_Celera | 9:82918425 | AAATATTTAAGGTCT[A/G]TATGTTCTACCTAAA | 83946 |
rs52581237 | snp | C/T | 0.391111 | 0.206368 | synonymous-codon | Phip | GRCm38.p3 | 9:82913860 | TAATACAAAATTGTT[C/T]GCATCACGGATAAGA | 83946 |
rs52583839 | snp | A/G | 0.124444 | 0.216185 | intron-variant | Phip | Mm_Celera | 9:82873131 | AATACAGACAAAATT[A/G]TGAATAACTCTGAAT | 83946 |
rs107728049 | snp | C/T | | | intron-variant | Phip | GRCm38.p3 | 9:82922863 | CCAGCATGTTAGCCC[C/T]TTCCAGGCATATCAT | 83946 |
rs107814785 | snp | A/G | | | downstream-variant-500B | Phip, LOC102641372 | GRCm38.p3 | 9:82865723 | TCTTATGGAGAATAA[A/G]TAGAAACGTGAATTA | 83946 |
rs108082619 | snp | C/T | | | intron-variant, nc-transcript-variant | Phip, LOC105243467 | GRCm38.p3 | 9:82959932 | ATTTGTTCTGTAATG[C/T]TAAGTAAAACAGTTT | 83946 |
rs108747623 | snp | A/G | | | downstream-variant-500B | Phip, LOC102641372 | GRCm38.p3 | 9:82865721 | TTTCTTATGGAGAAT[A/G]AATAGAAACGTGAAT | 83946 |
rs211707464 | snp | C/G | | | intron-variant | Phip | Mm_Celera | 9:82952163 | TGCTTCTTCACTATG[C/G]TCCTCTTCTTCCCTT | 83946 |
rs211756927 | snp | A/G | | | intron-variant | Phip | Mm_Celera | 9:82880931 | TGTGCTTTTAGTACC[A/G]TCATACATCATGAGG | 83946 |
rs211762854 | snp | C/T | | | intron-variant | Phip | Mm_Celera | 9:82881647 | GTATTAATGTAGTAG[C/T]CACAGTGAACTAAGT | 83946 |
rs211780754 | snp | A/G | | | intron-variant | Phip | Mm_Celera | 9:82892164 | TTCTTTATGCATTTA[A/G]ATTAACTATAAACGA | 83946 |
rs211824051 | snp | G/T | | | intron-variant | Phip | Mm_Celera | 9:82940573 | GAATTCTTTTCTTTT[G/T]TTGCACTGGACTCCA | 83946 |
rs211832623 | snp | G/T | | | intron-variant, upstream-variant-2KB | Phip | Mm_Celera | 9:82929918 | ATCAGCACTGGTAGA[G/T]CAAATAAGACTCTGA | 83946 |
rs211854871 | in-del | -/TC | | | intron-variant | Phip | Mm_Celera | 9:82925055 | GGAGAAAATTCCGAA[-/TC]TGTGTTTAACTGACT | 83946 |
rs211877425 | snp | A/G | | | intron-variant | Phip | Mm_Celera | 9:82871880 | GAAAAGAAAAACAGT[A/G]CACTTAATATATAAC | 83946 |
rs211901036 | in-del | -/AGTA | | | intron-variant | Phip | Mm_Celera | 9:82899131 | TGTTGACAGGAATGG[-/AGTA]AGTCTTTCAGAAGGC | 83946 |
rs211963426 | in-del | -/TATA | | | intron-variant | Phip | Mm_Celera | 9:82922224 | TTTGTTAATTCTAAT[-/TATA]TATAATCTATGGTAA | 83946 |
rs211963891 | snp | G/T | | | intron-variant | Phip | Mm_Celera | 9:82920583 | TTCACAAGATTACCT[G/T]AGACTACTGTGAATC | 83946 |
rs211966865 | snp | A/G | | | intron-variant | Phip | Mm_Celera | 9:82872565 | AGATTCAGAAAGAAT[A/G]TACAAATTTTAGCTT | 83946 |
rs211970791 | snp | A/G | | | intron-variant | Phip | Mm_Celera | 9:82930829 | CGAGGGTGGGAGGAG[A/G]CCTATGAATATGTGT | 83946 |
rs212118171 | in-del | -/GAA | | | intron-variant | Phip | Mm_Celera | 9:82917052 | TCAAAATTTTCATGG[-/GAA]AAAAAAAAAAGAAGA | 83946 |
rs212133011 | snp | C/T | | | intron-variant | Phip | Mm_Celera | 9:82928013 | ATCATTTTAACATGA[C/T]TCACAACTTAATAAG | 83946 |
rs212138783 | snp | G/T | | | intron-variant | Phip | Mm_Celera | 9:82910932 | GCTTGTGCTGGTCTT[G/T]TGAGGATTCTAGTTC | 83946 |
rs212177131 | snp | A/C | | | utr-variant-3-prime | Phip | Mm_Celera | 9:82867490 | CTAATTAAGCTACTA[A/C]TGTTAGCAGTATCTT | 83946 |
rs212206795 | snp | A/G | | | intron-variant | Phip | Mm_Celera | 9:82907964 | TTCCAACATACAACC[A/G]TTCAAGTCATATATG | 83946 |
rs212212263 | snp | A/T | | | intron-variant | Phip | Mm_Celera | 9:82918322 | GGGATTTATAAGACT[A/T]TAAATATACATGTGT | 83946 |
rs212234202 | snp | A/G | | | intron-variant | Phip | Mm_Celera | 9:82921362 | TGAAGGATGTTGTGA[A/G]CAAACTTGAAATCCC | 83946 |
rs212298933 | in-del | -/G | | | intron-variant | Phip | Mm_Celera | 9:82901538 | GAGCTTTGAGGGCAT[-/G]GGGGGGGGAAGAGGG | 83946 |
rs212314249 | snp | A/G | | | intron-variant | Phip | GRCm38.p3 | 9:82973848 | TCAATATAAACAAAA[A/G]CTTAAAAGCCAAGGT | 83946 |
rs212346127 | snp | A/G | | | intron-variant | Phip | Mm_Celera | 9:82899972 | GCATTTACCTCAGAG[A/G]AAAAAAGTTATAAGC | 83946 |
rs212393676 | snp | C/G | | | intron-variant | Phip | Mm_Celera | 9:82950817 | ACATTTAAACGTTTA[C/G]AATCCAAGGACTAGA | 83946 |
rs212405007 | snp | A/C/G | | | intron-variant | Phip | Mm_Celera | 9:82909284 | GGACTACACAGAAAA[A/C/G]TCTGCCTCAAAATAA | 83946 |
rs212414114 | snp | C/T | | | intron-variant | Phip | GRCm38.p3 | 9:82919327 | AAAGCTCCAGTGGAG[C/T]TAAGCAACACTAGGA | 83946 |
rs212429533 | snp | A/C | | | intron-variant | Phip, LOC105243467 | Mm_Celera | 9:82962474 | GACAAACAGATAATT[A/C]AGTAGGTAGATTGAT | 83946 |
rs212432480 | snp | A/G | | | intron-variant | Phip | Mm_Celera | 9:82900943 | ACAGACAGACAGTCA[A/G]TGAGTCAGAAAGATA | 83946 |
rs212460616 | in-del | -/T | | | intron-variant | Phip | Mm_Celera | 9:82933139 | GTTAATATAAAAAAA[-/T]GTGTCACCTCCACAT | 83946 |
rs212466987 | in-del | -/A | | | intron-variant | Phip | Mm_Celera | 9:82874617 | AGAGAAGCCAGATTG[-/A]AATCAGTCAGCATGG | 83946 |
rs212477871 | snp | A/C | | | upstream-variant-2KB | Phip | Mm_Celera | 9:82976531 | GAAGGTTATTGAAAG[A/C]GTATATTACAGTTTA | 83946 |
rs212489780 | snp | C/T | | | intron-variant, upstream-variant-2KB | Phip | Mm_Celera | 9:82928821 | TAAGTTAGACAAACA[C/T]ATTTTACCTGTTACT | 83946 |
rs212527506 | in-del | -/AAAAAT | | | intron-variant | Phip | Mm_Celera | 9:82908941 | CTTAGCTTATAACCA[-/AAAAAT]AAAAAATAAAAAATA | 83946 |
rs212541480 | in-del | -/AA | | | intron-variant | Phip | Mm_Celera | 9:82939040 | GGAAAAAAACAAACT[-/AA]AAAAAAAAAAAAATT | 83946 |
rs212562280 | in-del | -/A | | | intron-variant, upstream-variant-2KB | Phip, LOC105243467 | Mm_Celera | 9:82967995 | ACCCTGTCTCAGGGG[-/A]AAAAAAAATCCTACT | 83946 |
rs212574193 | snp | C/T | | | intron-variant | Phip | Mm_Celera | 9:82897683 | ATTATCTTTATAGCA[C/T]TGAAAAGTGTTATGC | 83946 |
rs212590910 | snp | A/T | | | intron-variant | Phip | Mm_Celera | 9:82905865 | TGTTATTATGGAAAT[A/T]CACATATTTAAAATA | 83946 |
rs212591423 | in-del | -/GTTT | | | intron-variant | Phip | Mm_Celera | 9:82888067 | ATTTCTGAAGTAATG[-/GTTT]GTTTCATGTCTACAT | 83946 |
rs212594625 | snp | C/T | | | intron-variant, nc-transcript-variant | Phip, LOC105243467 | Mm_Celera | 9:82960237 | ACTGTATACCTGGGA[C/T]CCCGTAGTTCACACT | 83946 |
rs212636089 | snp | C/T | | | intron-variant | Phip | Mm_Celera | 9:82971409 | AAATGAGCCAAGTGG[C/T]TAATGTCTATAATCC | 83946 |
rs212663517 | in-del | -/AA | | | intron-variant | Phip | Mm_Celera | 9:82904746 | CTAAATCCAAAACAT[-/AA]AAAGACAAAATATTT | 83946 |
rs212679968 | in-del | -/GCA | | | intron-variant, nc-transcript-variant | Phip, LOC105243467 | Mm_Celera | 9:82959907 | CACACACACACGCAC[-/GCA]AAAAAAAATATTTGT | 83946 |
rs212703164 | snp | G/T | | | intron-variant | Phip | Mm_Celera | 9:82948945 | AGCTACTTCAAATTC[G/T]TGTTGCCTTGACTTC | 83946 |
rs212713768 | snp | A/G | | | intron-variant | Phip, LOC105243467 | GRCm38.p3 | 9:82963755 | GAGTTACATGTGGTT[A/G]TAAGCTGCCTTGTGC | 83946 |
rs212717059 | snp | C/T | | | intron-variant | Phip | Mm_Celera | 9:82888796 | GATGGTTCTGAGTTG[C/T]TGTGTGGGAGTTGGG | 83946 |
rs212763276 | snp | G/T | | | intron-variant | Phip | Mm_Celera | 9:82878270 | TTGGAGACCTTTGTG[G/T]TAACAATTTCTACTC | 83946 |
rs212809165 | in-del | -/A | | | intron-variant | Phip | Mm_Celera | 9:82907913 | CATAATGAGTCATTT[-/A]AAAAAAAAGATTATC | 83946 |
rs212813524 | snp | A/G | | | intron-variant | Phip | GRCm38.p3 | 9:82970599 | ATTGATGAGGGGCTA[A/G]CTCACAGTGGGTGGT | 83946 |
rs212831583 | snp | A/C | | | intron-variant | Phip | Mm_Celera | 9:82897035 | AATGGAAATGAATAT[A/C]ATCGTCATCTTCATC | 83946 |
rs212839419 | snp | A/C | | | intron-variant | Phip | Mm_Celera | 9:82937282 | TCTCAGGGCTTGGTC[A/C]CTTTCCCTATTCCTG | 83946 |
rs212850728 | snp | A/G | | | intron-variant | Phip | Mm_Celera | 9:82936207 | GAGGCAGAGGCGGGC[A/G]GATTTCTGAGTTTGA | 83946 |
rs212865686 | snp | A/G | | | intron-variant | Phip | Mm_Celera | 9:82949908 | TAGTTATTTCCCAAG[A/G]ATTCGTTTATTTATC | 83946 |
rs212900519 | snp | G/T | | | downstream-variant-500B | Phip, LOC102641372 | Mm_Celera | 9:82865804 | TTCATCCTAAAATTG[G/T]AGATTCTTAAGAGTT | 83946 |
rs212901049 | snp | C/T | | | intron-variant | Phip | Mm_Celera | 9:82886499 | ATATTTTAACTTGAC[C/T]CCTACGGATTCATGT | 83946 |
rs212911425 | snp | C/T | | | synonymous-codon | Phip | Mm_Celera | 9:82896064 | ACATCTCCTGGGAAG[C/T]GTGTCTGTAATCCAA | 83946 |
rs212912442 | snp | C/T | | | intron-variant | Phip | Mm_Celera | 9:82917021 | CCAGGAATAAGATGT[C/T]TTAGTCCTCAGTTCA | 83946 |
rs213063822 | snp | C/T | | | intron-variant | Phip | Mm_Celera | 9:82940255 | ATCCAGGACAAATAA[C/T]CTCTTAAAAATTTTC | 83946 |
rs213085494 | snp | G/T | | | intron-variant | Phip | Mm_Celera | 9:82875851 | TTCCTAAGCTGCAAC[G/T]TTCTTGTTCTCACTT | 83946 |
rs213087928 | snp | C/T | | | intron-variant | Phip | Mm_Celera | 9:82945567 | TAATGTTACTGTGAT[C/T]ACACTATAACAGGAC | 83946 |
rs213091762 | in-del | -/CCT | | | intron-variant | Phip | Mm_Celera | 9:82944548 | AGATCATGGTGCCCC[-/CCT]CCCCCGAATCTTCTC | 83946 |
rs213103170 | snp | C/T | | | intron-variant | Phip | Mm_Celera | 9:82889801 | TGCAACCCTAGGTTA[C/T]GGTAACTTCTTGCCT | 83946 |
rs213139878 | snp | A/T | | | intron-variant | Phip | Mm_Celera | 9:82934512 | GGAGAAAACAGCAAG[A/T]GCTAGCTAAAACAAA | 83946 |
rs213181346 | snp | C/T | | | synonymous-codon | Phip | Mm_Celera | 9:82877208 | TGATCTCTTGCTTGG[C/T]GTGTATGCTTTAGAA | 83946 |
rs213190276 | in-del | -/AAAA | | | intron-variant | Phip | Mm_Celera | 9:82939156 | TGATTTAAAAAAAGG[-/AAAA]GAAAAAAAAGAACAG | 83946 |
rs213213869 | snp | C/T | | | intron-variant | Phip | Mm_Celera | 9:82916154 | ACCCTGTCTAAAGCA[C/T]ATCTAGGGACTGATT | 83946 |
rs213248761 | snp | A/T | | | intron-variant | Phip | GRCm38.p3 | 9:82925678 | ATTTTTGTGTTAATT[A/T]GCTAATTATACCATC | 83946 |
rs213281847 | snp | A/G | | | intron-variant | Phip | GRCm38.p3 | 9:82879354 | AACCAGTATATATAA[A/G]AATTTTAACAGCTAT | 83946 |
rs213362260 | snp | A/T | | | intron-variant | Phip | Mm_Celera | 9:82885654 | GTAAGGCATTGAATT[A/T]CCAGCAGACAAAACT | 83946 |
rs213368124 | snp | A/G | | | intron-variant | Phip | Mm_Celera | 9:82873797 | ATGAAACCATTCCTC[A/G]CTTTGGGTACAGAAG | 83946 |
rs213382530 | in-del | -/AAAAAAAA | | | intron-variant | Phip | GRCm38.p3 | 9:82908042 | GTGCTATGTTGCTAC[-/AAAAAAAA]AAAAAAAAAATGCAC | 83946 |
rs213429240 | snp | A/C | | | intron-variant | Phip | Mm_Celera | 9:82923851 | GGATGACTAGACATG[A/C]CAAATAATACTCAAA | 83946 |
rs213456355 | snp | C/G | | | intron-variant | Phip | GRCm38.p3 | 9:82933641 | TTAATTCTTTATCTT[C/G]AAATAAATATTACAA | 83946 |
rs213510928 | snp | A/G | | | intron-variant | Phip | GRCm38.p3 | 9:82950248 | TTAGGGGGGAGGAAA[A/G]GCTAACATAAAAATA | 83946 |
rs213511525 | snp | A/G | | | intron-variant | Phip | Mm_Celera | 9:82932195 | TGTTCTCAGTACAAA[A/G]TTAAGCTAAGACAAA | 83946 |
rs213518638 | snp | A/G | | | intron-variant | Phip | Mm_Celera | 9:82903905 | AGTAACAGTCCCCAC[A/G]GTTACTAAAGTACTT | 83946 |
rs213566188 | snp | C/T | | | intron-variant | Phip | GRCm38.p3 | 9:82913182 | AGAGATCTCTGTGAT[C/T]TGAGAGCAGTTTGGA | 83946 |
rs213593577 | snp | A/G | | | intron-variant | Phip | GRCm38.p3 | 9:82904672 | ATGATAGTTGTTTTT[A/G]TACTTCATTTTTTTT | 83946 |
rs213613028 | snp | A/C | | | intron-variant | Phip | Mm_Celera | 9:82956567 | CCACAACGTGGAGAA[A/C]ACCAACTTCTACAAC | 83946 |
rs213626770 | snp | C/T | | | intron-variant | Phip | Mm_Celera | 9:82925163 | CGCATACAGTCACAA[C/T]TAAGTATCAACTGGG | 83946 |
rs213711560 | snp | A/G | | | intron-variant | Phip | Mm_Celera | 9:82910601 | CTACTCTCGCCAGTC[A/G]TACAAATACACTTGA | 83946 |
rs213737026 | in-del | -/T | | | intron-variant | Phip | Mm_Celera | 9:82924323 | TTAGTAATAGTCTTA[-/T]TTTTTAAAAAAATGC | 83946 |
rs213771448 | snp | A/G | | | intron-variant | Phip | Mm_Celera | 9:82921289 | TTCAGGATATTTTAA[A/G]CAGAGAGATTATAGA | 83946 |
rs213773509 | snp | C/T | | | intron-variant | Phip | Mm_Celera | 9:82910361 | TTGTCCTCTATCAAA[C/T]TGCCTATCTTGATTG | 83946 |
rs213841867 | snp | C/T | | | intron-variant | Phip | Mm_Celera | 9:82901296 | TTTCCAGGTTTCCCC[C/T]CTGGAAACTTCTTAT | 83946 |
rs213845263 | in-del | -/AAAA | | | intron-variant | Phip | Mm_Celera | 9:82974083 | AACCAAACAAAGATT[-/AAAA]AAAAAAAAATAAAAT | 83946 |
rs213853786 | snp | A/T | | | intron-variant | Phip | Mm_Celera | 9:82931763 | ATGTCCTTTATCAAT[A/T]GATTCACTGTTCTGC | 83946 |
rs213871597 | snp | A/C | | | intron-variant | Phip | Mm_Celera | 9:82953780 | CCTAATGAATACAAG[A/C]AATGTAGCTGCAGAT | 83946 |
rs213906107 | snp | A/G | | | intron-variant | Phip | Mm_Celera | 9:82882835 | AGCTCTCTCCTCAGC[A/G]TTTCTATCACCCCAC | 83946 |
rs213981571 | snp | C/T | | | intron-variant | Phip | Mm_Celera | 9:82941920 | CCTCTCATACTTGCC[C/T]TCATGTATGTATGCA | 83946 |
rs213983132 | snp | G/T | | | intron-variant | Phip | Mm_Celera | 9:82953279 | TTTTTGGTTTTTTTT[G/T]GGGGGGGGGGGAACG | 83946 |
rs214007751 | snp | A/G | | | intron-variant | Phip | GRCm38.p3 | 9:82891702 | CAAGCTTTGCCCCAC[A/G]GTCAATCAGAGACTG | 83946 |
rs214009648 | snp | C/G | | | intron-variant | Phip | Mm_Celera | 9:82955176 | AGGGCTCCATTAGGA[C/G]ACCATGTCTCAAAAA | 83946 |
rs214011024 | snp | A/G | | | intron-variant | Phip | Mm_Celera | 9:82941167 | AGCTACTGTAACAAG[A/G]CCTTTGGGTGGGTAA | 83946 |
rs214022008 | snp | A/G | | | intron-variant | Phip | Mm_Celera | 9:82873034 | CACATTCAAGGAGCC[A/G]TAGAAGATAAGTAAA | 83946 |
rs214022258 | snp | A/G | | | intron-variant | Phip | Mm_Celera | 9:82884218 | CAATGGGGGAGGGGG[A/G]AGGGACTTGCAACAG | 83946 |
rs214041966 | snp | A/C | | | intron-variant | Phip, LOC105243467 | Mm_Celera | 9:82962113 | CCACTGAGTAATCCT[A/C]ATATGAATTTCTTAA | 83946 |
rs214042060 | snp | A/G | | | intron-variant | Phip | Mm_Celera | 9:82950241 | CTGTTCATTAGGGGG[A/G]AGGAAAAGCTAACAT | 83946 |
rs214060766 | snp | C/G | | | intron-variant | Phip, LOC105243467 | Mm_Celera | 9:82964073 | TATTAAATATAGAAA[C/G]TGAGTTGTCTACTGG | 83946 |
rs214085641 | snp | A/G | | | intron-variant | Phip | Mm_Celera | 9:82879775 | TTCCCTATATGATGG[A/G]CTCTAATCTCTAAAG | 83946 |
rs214098695 | snp | C/T | | | intron-variant | Phip | GRCm38.p3 | 9:82890044 | ACAAACACAAACACA[C/T]GCACGGAAAATGTAA | 83946 |
rs214138455 | snp | C/T | | | intron-variant | Phip | Mm_Celera | 9:82893757 | GACTGTTTTACTTAT[C/T]GAAACAAGAGCCTCT | 83946 |
rs214142860 | snp | A/C | | | intron-variant | Phip | GRCm38.p3 | 9:82895205 | TTGGATAGTCACTAT[A/C]CTACATTTTCCTCCT | 83946 |
rs214145859 | in-del | -/AAAAAAA | | | intron-variant, upstream-variant-2KB | Phip | Mm_Celera | 9:82928882 | GTCCTGTACAAACAG[-/AAAAAAA]AAAAAAAAAACCACA | 83946 |
rs214160705 | snp | C/G | | | intron-variant | Phip | Mm_Celera | 9:82951679 | AGGAATTATAGGAAA[C/G]CGTAAGCAGTGAAGG | 83946 |
rs214196421 | snp | A/G | | | intron-variant | Phip | Mm_Celera | 9:82950754 | ACAACTTTAATATGC[A/G]TTATGCATTATAAAG | 83946 |
rs214206221 | in-del | -/GAG | | | intron-variant | Phip | Mm_Celera | 9:82925888 | CATACACTGATCAAA[-/GAG]GAGGACACATACCAC | 83946 |
rs214211162 | snp | A/G | | | intron-variant | Phip | Mm_Celera | 9:82880895 | CACTGTCCTCACAGA[A/G]GCACTACACCAGCCA | 83946 |
rs214237467 | in-del | -/G | | | intron-variant | Phip, LOC105243467 | Mm_Celera | 9:82964144 | CTCCTGTACTTCTCT[-/G]CCTTCCAAGAGCTGT | 83946 |
rs214267093 | in-del | -/GG | | | intron-variant | Phip | Mm_Celera | 9:82922081 | TGTATATATATATGT[-/GG]GTGTGTATGTATGTA | 83946 |
rs214283123 | snp | G/T | | | intron-variant | Phip | Mm_Celera | 9:82881482 | GACTGGTTTAGTAAA[G/T]TCTCCCCCCATTAAG | 83946 |
rs214337625 | snp | C/T | | | intron-variant | Phip | Mm_Celera | 9:82920431 | CTATATAATTTTTAT[C/T]TTTAAATAACTAAAG | 83946 |
rs214374864 | snp | C/T | | | intron-variant | Phip | Mm_Celera | 9:82901910 | CCAGTAGGAACTCTT[C/T]CAGTAAGCAAATACT | 83946 |
rs214377883 | in-del | -/A | | | intron-variant | Phip | Mm_Celera | 9:82902608 | AATTGCTGAAACAGG[-/A]AAAAAAGAAAAATAA | 83946 |
rs214393357 | snp | A/G | | | intron-variant | Phip, LOC105243467 | GRCm38.p3 | 9:82964895 | CAGGATCTCCACTAC[A/G]CCCAAGGCTGTATCT | 83946 |
rs214394202 | snp | C/T | | | intron-variant | Phip | Mm_Celera | 9:82919630 | CGATCATTCCTATAG[C/T]TTAAACAAAGATAAT | 83946 |
rs214407838 | in-del | -/TA | | | intron-variant | Phip | Mm_Celera | 9:82894554 | AAAAACTCCCCTGTG[-/TA]TATATATATAGAAAA | 83946 |
rs214483128 | snp | C/T | | | intron-variant | Phip | Mm_Celera | 9:82878183 | CTATGTACAAGTGTA[C/T]TGCCCTGCCTGATTT | 83946 |
rs214498534 | snp | G/T | | | intron-variant | Phip | GRCm38.p3 | 9:82938547 | AAAACTTAGTTTTTA[G/T]TTTATAGATGACAAT | 83946 |
rs214531769 | snp | A/T | | | intron-variant | Phip | GRCm38.p3 | 9:82893046 | CTCAAACATAATTGC[A/T]ATTATCAATATTACT | 83946 |
rs214537487 | snp | A/G | | | intron-variant | Phip | Mm_Celera | 9:82917344 | AACTTAAAAACCTCT[A/G]AAACAACAATCATGC | 83946 |
rs214579000 | in-del | -/GCT | | | cds-indel | Phip | Mm_Celera | 9:82867821 | ACTAACTGTGTGAAC[-/GCT]GCTAACATCATGCAG | 83946 |
rs214646474 | snp | A/C | | | utr-variant-3-prime | Phip | Mm_Celera | 9:82868480 | GACCACTCAACTCAG[A/C]CTGAAAACTGGTATC | 83946 |
rs214721930 | snp | G/T | | | intron-variant | Phip | Mm_Celera | 9:82918147 | TAACCACTGTCTTTT[G/T]TAAGTTGCCTAGCTC | 83946 |
rs214746460 | snp | C/T | | | intron-variant | Phip | Mm_Celera | 9:82908907 | CAGGGTGATTAAGTT[C/T]TACTTAGACACTGGC | 83946 |
rs214750461 | snp | A/G | | | intron-variant | Phip | GRCm38.p3 | 9:82891366 | TTAAAAAAAGATTTA[A/G]AAATTTATGCAGATA | 83946 |
rs214764862 | snp | A/G | | | intron-variant | Phip, LOC105243467 | Mm_Celera | 9:82961587 | AGTTTGCCTTTTATT[A/G]CCATTTTCTTTAGTG | 83946 |
rs214766227 | snp | G/T | | | intron-variant | Phip | Mm_Celera | 9:82899877 | GTACCTTCCCTCACC[G/T]GGTATTTTCCTCCAC | 83946 |
rs214795450 | snp | A/G | | | intron-variant, utr-variant-5-prime | Phip | Mm_Celera | 9:82928234 | AAGACAAAAAAGGTG[A/G]GGGAAGATCAGAGAC | 83946 |
rs214822218 | snp | C/T | | | intron-variant | Phip | Mm_Celera | 9:82957042 | cgtgtgctttctgca[C/T]agcactgagttggag | 83946 |
rs214862890 | in-del | -/ACAAG | | | intron-variant | Phip | Mm_Celera | 9:82882606 | CAATTCATTCTTTAA[-/ACAAG]ACAAAACAAAACAAA | 83946 |
rs214954457 | snp | C/T | | | intron-variant | Phip | GRCm38.p3 | 9:82970495 | AAACTCAGTTGTAAA[C/T]GTGACATCTGGGCAA | 83946 |
rs214965561 | in-del | -/TAAAAAA | | | intron-variant | Phip | Mm_Celera | 9:82911386 | AAAAAAGAAAGTCTT[-/TAAAAAA]AAAAAAAAAAAATAC | 83946 |
rs214979211 | snp | A/G | | | intron-variant | Phip | Mm_Celera | 9:82916133 | TTCTGAAAGAGGTAA[A/G]ACTCTACCCTGTCTA | 83946 |
rs214994041 | snp | C/G | | | intron-variant | Phip | Mm_Celera | 9:82969117 | TCTCTTCTGGAGTGT[C/G]TGAAGACAGCTACAG | 83946 |
rs215016201 | snp | A/G | | | intron-variant | Phip | Mm_Celera | 9:82959030 | GGGAGAAAGGCAAGC[A/G]ACAAGATCAACAAGT | 83946 |
rs215020176 | in-del | -/AAAACAAAAC | | | intron-variant | Phip | Mm_Celera | 9:82880277 | CTGAAATTAAAAAAA[-/AAAACAAAAC]AAAACACCTAAGTAG | 83946 |
rs215049002 | snp | A/G | | | intron-variant | Phip | Mm_Celera | 9:82888129 | TAGTGTTGAGAAAGA[A/G]TCTACAAACACACCA | 83946 |
rs215055377 | snp | A/G | | | intron-variant | Phip | Mm_Celera | 9:82907850 | GAAGGAAGCATGAGA[A/G]GACAAAGGGTTAAAA | 83946 |
rs215117684 | snp | C/T | | | intron-variant | Phip | GRCm38.p3 | 9:82949589 | TCTTCTGAAAATAAA[C/T]CAGTAATAAACTGAA | 83946 |
rs215130146 | snp | C/T | | | intron-variant | Phip | GRCm38.p3 | 9:82888742 | TGGTGCCTAGAGGGA[C/T]CAGAGGAGAGGGTTG | 83946 |
rs215132217 | snp | A/C | | | intron-variant | Phip | Mm_Celera | 9:82877441 | AGTTACAGAACTATT[A/C]ATTTCTAAAAACAAA | 83946 |
rs215143134 | snp | C/T | | | intron-variant, upstream-variant-2KB | Phip | Mm_Celera | 9:82929737 | GAAGTAATCCTGCTA[C/T]CTACAATTATAACTG | 83946 |
rs215155651 | snp | A/T | | | intron-variant | Phip | Mm_Celera | 9:82899043 | AATAAAGAGAAAAAA[A/T]GTTTAAATTTTAACT | 83946 |
rs215211538 | snp | A/T | | | intron-variant, upstream-variant-2KB | Phip, LOC105243467 | GRCm38.p3 | 9:82967321 | CAGAAATGTTCTGAC[A/T]AATCTCATTAGTTTC | 83946 |
rs215211600 | snp | C/T | | | intron-variant | Phip | Mm_Celera | 9:82955461 | ATGATTTGGTTCGTA[C/T]CTACAGCACCACCTA | 83946 |
rs215233155 | in-del | -/T | | | intron-variant | Phip | Mm_Celera | 9:82913006 | TTAACAATCATTCAA[-/T]AATCCACTTAATTGA | 83946 |
rs215236737 | snp | A/G | | | intron-variant | Phip | Mm_Celera | 9:82884524 | TCCCCCCTGATCAGA[A/G]CCTTACTATATAAAC | 83946 |
rs215238743 | snp | C/G | | | intron-variant | Phip | Mm_Celera | 9:82895094 | ATAAATTCAACACAG[C/G]CTCTCTGTAAGAGCA | 83946 |
rs215297595 | snp | G/T | | | intron-variant | Phip | Mm_Celera | 9:82894460 | TTTAGAGATTACAAA[G/T]AAAGTCTTACAATGG | 83946 |
rs215317696 | snp | A/C | | | intron-variant | Phip | Mm_Celera | 9:82927730 | GCCTACAATTCCAAC[A/C]TGAGAAGGTGAAGGA | 83946 |
rs215321573 | snp | A/C | | | intron-variant | Phip | Mm_Celera | 9:82885435 | ATGCTAAAAAATTTT[A/C]TAGTATTTCACAATT | 83946 |
rs215343088 | snp | C/T | | | intron-variant | Phip | GRCm38.p3 | 9:82908039 | GTCGTGCTATGTTGC[C/T]ACAAAAAAAAAAAAA | 83946 |
rs215347939 | in-del | -/A | | | intron-variant | Phip | Mm_Celera | 9:82886842 | AATTTATCAACACAC[-/A]AAAAAAAAATAGAGC | 83946 |
rs215355324 | in-del | -/AAAA | | | intron-variant | Phip | Mm_Celera | 9:82911387 | AAAAAAGAAAGTCTT[-/AAAA]AAAAAAAATACCATG | 83946 |
rs215356472 | snp | C/T | | | intron-variant | Phip | Mm_Celera | 9:82905811 | TGAATAAAAATAAAA[C/T]TTAATGATGATAGGC | 83946 |
rs215372250 | snp | G/T | | | intron-variant | Phip | Mm_Celera | 9:82956406 | AAAAAAAGTTGTCAG[G/T]AGGGGAATATAATCC | 83946 |
rs215406859 | snp | A/G | | | utr-variant-3-prime | Phip | Mm_Celera | 9:82867313 | GTACTGTACATAGTT[A/G]AGAATGTCTTTTCAT | 83946 |
rs215415010 | in-del | -/AAA | | | intron-variant | Phip | Mm_Celera | 9:82875093 | AAGGCCAGTTCCTAT[-/AAA]AAAAAAAAACATTAA | 83946 |
rs215456666 | in-del | -/ATATTC | | | intron-variant | Phip | Mm_Celera | 9:82935031 | ATATTGCTGCACACT[-/ATATTC]ATATAGATCTGAGTA | 83946 |
rs215513591 | in-del | -/AAA | | | intron-variant | Phip | Mm_Celera | 9:82875696 | CTAGTAGAAGGCTAC[-/AAA]AAAAAAAAGGTTAAC | 83946 |
rs215551778 | snp | C/G | | | intron-variant | Phip | Mm_Celera | 9:82924136 | GCAATGTAGTGAACA[C/G]AGGGAAAAAGTATGG | 83946 |
rs215562362 | snp | A/G | | | intron-variant | Phip | Mm_Celera | 9:82906737 | TTGGAGAAAGGATAT[A/G]CTGAGAGATAGGAAA | 83946 |
rs215622949 | snp | C/T | | | intron-variant | Phip | Mm_Celera | 9:82973732 | CATTCACCATACTCG[C/T]GTCAGCTCCACGTAT | 83946 |
rs215629590 | snp | C/T | | | intron-variant | Phip | Mm_Celera | 9:82882786 | TTGGGGCGTAGGAAA[C/T]CCTTACCTGCTAAGA | 83946 |
rs215629638 | snp | C/T | | | intron-variant | Phip | GRCm38.p3 | 9:82896991 | CAAGTAATCTGATGA[C/T]AATAGCCTTTATGGT | 83946 |
rs215700784 | snp | C/T | | | intron-variant | Phip | Mm_Celera | 9:82931592 | GAAACAGGCTAAATA[C/T]TCAAAGCTCAGGAGA | 83946 |
rs215713626 | in-del | -/TAGA | | | utr-variant-3-prime | Phip | Mm_Celera | 9:82867697 | ATCAGTTTGTTTTCT[-/TAGA]TAGATAGAAAGCTTG | 83946 |
rs215713930 | snp | G/T | | | intron-variant | Phip | Mm_Celera | 9:82930980 | AGCAAGCCTCACCTG[G/T]GGCTGTCTCAACCCT | 83946 |
rs215748051 | snp | A/T | | | intron-variant | Phip | Mm_Celera | 9:82904940 | TAAAACACTGAACTG[A/T]AAGAGTACTTTCTAA | 83946 |
rs215822252 | in-del | -/ACACAC | | | intron-variant | Phip | Mm_Celera | 9:82896827 | AAACAACACACACAG[-/ACACAC]ACACACACACAGACA | 83946 |
rs215834083 | snp | C/T | | | intron-variant | Phip | Mm_Celera | 9:82922746 | CTCTCTCTAGCTTCA[C/T]TCTTCCCTAGAAGAG | 83946 |
rs215852308 | snp | C/T | | | intron-variant | Phip | Mm_Celera | 9:82896246 | TTACTAGAAAAGCAG[C/T]AGAAGTGACGAAAGT | 83946 |
rs215867882 | snp | G/T | | | intron-variant | Phip | Mm_Celera | 9:82903897 | GCTTCAACAGTAACA[G/T]TCCCCACGGTTACTA | 83946 |
rs215870103 | snp | A/G | | | intron-variant | Phip | Mm_Celera | 9:82885437 | GCTAAAAAATTTTCT[A/G]GTATTTCACAATTTT | 83946 |
rs215891647 | snp | A/C | | | intron-variant | Phip, LOC105243467 | Mm_Celera | 9:82966004 | ACACACACACACTTA[A/C]ACGTACACAAGTAAG | 83946 |
rs215923086 | in-del | -/GTTT | | | intron-variant | Phip | Mm_Celera | 9:82969483 | TTTAAAATCTCCGTA[-/GTTT]GGGGGCATAAACTTA | 83946 |
rs215962425 | in-del | -/T | | | intron-variant | Phip | Mm_Celera | 9:82973077 | AAAAGATGAGTGTGG[-/T]TTTAAAAAAAAAAGC | 83946 |
rs216036911 | in-del | -/TT | | | intron-variant | Phip | Mm_Celera | 9:82945994 | GACTTCTAGAACTCA[-/TT]TTTTTTTTTCATTTA | 83946 |
rs216046958 | snp | A/G | | | intron-variant | Phip | Mm_Celera | 9:82900111 | ACTAACTCAAAAAGT[A/G]AAAACTGAAGCGTTT | 83946 |
rs216047429 | snp | C/G | | | intron-variant | Phip | Mm_Celera | 9:82875655 | CCAGGGCCTCGCTCA[C/G]ACTTGACAAGCCCAG | 83946 |
rs216090249 | snp | A/C | | | intron-variant | Phip | Mm_Celera | 9:82920345 | TCTTTACTCCCTTTC[A/C]CTCCCCAGCCCTCTA | 83946 |
rs216105416 | snp | C/T | | | intron-variant | Phip | Mm_Celera | 9:82974314 | AGCTGGCGAGCGCGC[C/T]CTCCAGGCTTGCGCC | 83946 |
rs216129918 | snp | G/T | | | intron-variant | Phip, LOC105243467 | Mm_Celera | 9:82963857 | GTATTTTAATGTGAC[G/T]TCTAAAACTGCTCAA | 83946 |
rs216142922 | snp | G/T | | | intron-variant | Phip | Mm_Celera | 9:82934601 | ATTCACTTCATTCAT[G/T]TATCCAAAACAATGT | 83946 |
rs216161308 | snp | C/T | | | intron-variant | Phip | Mm_Celera | 9:82947547 | ATCAAGTGTTACTGC[C/T]CTTAAAACAGGATTT | 83946 |
rs216167841 | snp | A/G | | | intron-variant | Phip | GRCm38.p3 | 9:82892213 | CAATATAATTTTAAT[A/G]CTAATTTCTTTTTTT | 83946 |
rs216185264 | in-del | -/AGATAGATAGAT | | | intron-variant | Phip | Mm_Celera | 9:82940096 | GCATGTTTACACCAC[-/AGATAGATAGAT]AGATAGATAGATAGA | 83946 |
rs216202680 | snp | C/T | | | intron-variant | Phip | Mm_Celera | 9:82933287 | ATATAGGTAGTAAAT[C/T]ACAGTCATCAATGGT | 83946 |
rs216244200 | snp | A/C | | | intron-variant | Phip | Mm_Celera | 9:82881824 | TAAAAAACACATTAT[A/C]CATATACATTTAATC | 83946 |
rs216244366 | in-del | -/TACTTAACACAG | | | intron-variant | Phip | Mm_Celera | 9:82947401 | CAATTTTTATAAAAA[-/TACTTAACACAG]TTCAGGTATGAAGAC | 83946 |
rs216245068 | snp | A/G | | | intron-variant | Phip | GRCm38.p3 | 9:82892866 | CATAGCAAAGAGTGG[A/G]TTTGTTTAAATTAAG | 83946 |
rs216298603 | snp | C/T | | | intron-variant | Phip | Mm_Celera | 9:82871913 | GCTTTTTGTTATTGT[C/T]TAGTCCTCCAACTAG | 83946 |
rs216302421 | snp | A/G | | | intron-variant | Phip, LOC105243467 | GRCm38.p3 | 9:82964788 | TATCACCAAAAGTGT[A/G]TGTTCAGGGGTAGAG | 83946 |
rs216353711 | snp | C/T | | | intron-variant | Phip | Mm_Celera | 9:82944382 | GGTACCAGACATGCA[C/T]ATGGTGCACACACAT | 83946 |
rs216360267 | snp | G/T | | | intron-variant | Phip | Mm_Celera | 9:82898879 | ACACTGCGATCCCAG[G/T]TCCTTCTCATTCCCA | 83946 |
rs216361990 | snp | A/T | | | intron-variant | Phip | GRCm38.p3 | 9:82889101 | CTTGTTTTTTTTTTT[A/T]AATCTCTACCTGAGG | 83946 |
rs216377770 | snp | C/T | | | intron-variant | Phip | Mm_Celera | 9:82971456 | GACAGGAAGACAGAG[C/T]ACTAAAAGTCAGTAT | 83946 |
rs216400773 | in-del | -/GT | | | intron-variant | Phip | Mm_Celera | 9:82905434 | TTTTTATAAATTTGA[-/GT]ATGTATATATATGTA | 83946 |
rs216418788 | snp | C/T | | | intron-variant | Phip | Mm_Celera | 9:82897878 | CAAGACTGTCTTTCT[C/T]AGAAGTAACAGAGAA | 83946 |
rs216441536 | snp | C/T | | | intron-variant | Phip | GRCm38.p3 | 9:82889995 | AGCTCTTGCAAACTG[C/T]CCCACTACGTATATG | 83946 |
rs216496820 | snp | A/T | | | intron-variant | Phip, LOC105243467 | GRCm38.p3 | 9:82961425 | TCCAAACTGAGTTAA[A/T]TTAGAACAAATATAT | 83946 |
rs216518103 | snp | C/G | | | intron-variant | Phip | Mm_Celera | 9:82874797 | TGCAAGTGCCTTGGT[C/G]AGAGAACAATTCTGC | 83946 |
rs216553893 | in-del | -/AA | | | intron-variant | Phip | Mm_Celera | 9:82892001 | TTGCTTTATTTCAAT[-/AA]AACAGTATATAAGAG | 83946 |
rs216562245 | snp | A/T | | | intron-variant | Phip | Mm_Celera | 9:82932360 | TAAAAGATCAGATTT[A/T]AAAATTCTAAGCTTA | 83946 |
rs216562945 | snp | C/T | | | intron-variant | Phip | Mm_Celera | 9:82911092 | CTTTTTATGAAACTA[C/T]TTCCATGAAAGTAAC | 83946 |
rs216655998 | snp | C/T | | | intron-variant, upstream-variant-2KB | Phip | Mm_Celera | 9:82928930 | ATACATAAGTATTGA[C/T]TGCACTCAAGACTGT | 83946 |
rs216730565 | snp | G/T | | | intron-variant | Phip | Mm_Celera | 9:82940865 | TTTTCTCACCTCCAA[G/T]TTCTCCTCTTAAACA | 83946 |
rs216806264 | in-del | -/A | | | intron-variant | Phip | Mm_Celera | 9:82916101 | ACTATGTTCCAGTTG[-/A]AAACGCCTTAGCAGT | 83946 |
rs216821009 | snp | C/T | | | intron-variant | Phip | Mm_Celera | 9:82925747 | CAGTAAAGCTAAAAA[C/T]ATGTTGTTTTCTTTC | 83946 |
rs216822329 | snp | A/G | | | intron-variant | Phip | Mm_Celera | 9:82935912 | GCTGAAAAAGCATAC[A/G]GAGCTCAAGACACGA | 83946 |
rs216833067 | snp | A/C | | | intron-variant | Phip | Mm_Celera | 9:82934554 | AGACTCATTTGATCA[A/C]GTTATCTTAACTCTA | 83946 |
rs216879354 | in-del | -/C | | | intron-variant | Phip | Mm_Celera | 9:82891676 | ATTTCTTAGGACTCT[-/C]CCAAGACTGACAAGC | 83946 |
rs216895699 | in-del | -/CA | | | intron-variant, nc-transcript-variant | Phip, LOC105243467 | Mm_Celera | 9:82959891 | GCACCTATTATGTCC[-/CA]CACACACACACGCAC | 83946 |
rs216942836 | snp | A/G | | | intron-variant | Phip | Mm_Celera | 9:82926715 | ATTTGTAATACTCAA[A/G]AATACAATTATTGTA | 83946 |
rs216952172 | snp | A/G | | | intron-variant | Phip | Mm_Celera | 9:82909449 | TGTACTAAAACTTTG[A/G]CTTTATGATTTGAAA | 83946 |
rs217139338 | snp | C/G | | | intron-variant | Phip | Mm_Celera | 9:82904142 | GCAGAGCATATTACT[C/G]TTTACAACTTAAAAT | 83946 |
rs217150757 | snp | A/G | | | intron-variant | Phip | GRCm38.p3 | 9:82912091 | CCTCAGAAGTTAGAA[A/G]CTTTAAGGTAATTAT | 83946 |
rs217210141 | in-del | -/A | | | intron-variant | Phip | Mm_Celera | 9:82920000 | TGAAATAGTGGCTGT[-/A]CAAAACACCACAGGG | 83946 |
rs217241165 | snp | A/T | | | intron-variant | Phip | Mm_Celera | 9:82939783 | CTAACCAGATAGAAC[A/T]CTTTACATTGTAAGT | 83946 |
rs217264952 | snp | A/G | | | intron-variant | Phip | GRCm38.p3 | 9:82904744 | TTCTAAATCCAAAAC[A/G]TAAAAAGACAAAATA | 83946 |
rs217271584 | snp | C/T | | | intron-variant | Phip | Mm_Celera | 9:82968857 | ACTTCTATAGACCTA[C/T]TTAAGAAATTATTTA | 83946 |
rs217279464 | snp | A/G | | | intron-variant | Phip | Mm_Celera | 9:82896867 | CCTGAAAGGAGTACT[A/G]CAAACAGGTTTTTTA | 83946 |
rs217290347 | snp | C/T | | | intron-variant | Phip | GRCm38.p3 | 9:82971465 | ACAGAGCACTAAAAG[C/T]CAGTATAGGCTGCAG | 83946 |
rs217326733 | in-del | -/ATC | | | downstream-variant-500B | Phip, LOC102641372 | Mm_Celera | 9:82865738 | ATAGAAACGTGAATT[-/ATC]ATCCTGTTTAAACTT | 83946 |
rs217328315 | snp | A/G | | | intron-variant | Phip | GRCm38.p3 | 9:82910279 | AACAAACTCTTTGTT[A/G]TCTACTTTGTGTTTG | 83946 |
rs217340437 | snp | A/G | | | intron-variant | Phip | GRCm38.p3 | 9:82952278 | TAAGAGATTGCCTGA[A/G]TCTCAGAAGAGACTC | 83946 |
rs217386499 | in-del | -/AT | | | intron-variant | Phip | Mm_Celera | 9:82901111 | TTGCAAATGTCATTA[-/AT]ACTCTGCATATAAGA | 83946 |
rs217397486 | in-del | -/CT | | | intron-variant | Phip | Mm_Celera | 9:82894126 | ATATTACCTTCTGAA[-/CT]CTTATTCCCCAGCCC | 83946 |
rs217428854 | snp | C/T | | | intron-variant | Phip | GRCm38.p3 | 9:82970374 | GAAGTTACCAGTAAC[C/T]TACTTATTTACTTAC | 83946 |
rs217467360 | snp | C/T | | | intron-variant | Phip | Mm_Celera | 9:82893261 | AATTATGCTAAATAG[C/T]AAATCATTTATAAAG | 83946 |
rs217526992 | snp | C/T | | | intron-variant | Phip | Mm_Celera | 9:82902138 | ACACAAACTGTCTTA[C/T]TATCTGCCATATCTT | 83946 |
rs217533194 | snp | C/T | | | intron-variant | Phip | Mm_Celera | 9:82901091 | TAATTTTAGGAAGCA[C/T]GCTATTTGCAAATGT | 83946 |
rs217554136 | snp | A/G | | | intron-variant | Phip | Mm_Celera | 9:82894009 | CACTCTGTAGACCAG[A/G]CTGGCCTCAAACTCA | 83946 |
rs217573884 | snp | C/T | | | intron-variant | Phip | Mm_Celera | 9:82953423 | GGGATAAAAGGCATG[C/T]GCCACCACTGCCCAC | 83946 |
rs217652328 | snp | C/T | | | intron-variant | Phip | Mm_Celera | 9:82938776 | AACACTGTTTGTCTA[C/T]TGTCACTATTCCTAG | 83946 |
rs217653687 | snp | C/T | | | intron-variant | Phip | GRCm38.p3 | 9:82942233 | TGAATTCCAAACCAG[C/T]CTGTTTTCTGTAGAT | 83946 |
rs217664494 | in-del | -/TAA | | | intron-variant | Phip | Mm_Celera | 9:82958030 | ATGAAAATGGGTATT[-/TAA]AAAAAAAAAAATGTA | 83946 |
rs217684473 | snp | A/G | | | intron-variant | Phip | Mm_Celera | 9:82950124 | CTTTTCCTTTAACTG[A/G]CAGATTCTTTTCTCA | 83946 |
rs217767161 | snp | C/T | | | intron-variant | Phip | Mm_Celera | 9:82907695 | GCAGTGGTATGGTCA[C/T]TGATCAACCGCCAGG | 83946 |
rs217777773 | in-del | -/T | | | intron-variant | Phip | Mm_Celera | 9:82915792 | AGAGCAAAGGTAGCA[-/T]TTTTTTTTTCTTTTT | 83946 |
rs217782121 | snp | C/T | | | intron-variant | Phip | GRCm38.p3 | 9:82931868 | ATAAGTATGTATGTG[C/T]ACTATGTCATGTGTG | 83946 |
rs217816944 | snp | A/G | | | utr-variant-3-prime | Phip | Mm_Celera | 9:82867817 | TGAAACTAACTGTGT[A/G]AACGCTGCTAACATC | 83946 |
rs217821837 | snp | A/C | | | intron-variant | Phip | Mm_Celera | 9:82969161 | AATTAATCAATCAAT[A/C]AATAAATAAATAAAT | 83946 |
rs217841693 | snp | A/G | | | intron-variant | Phip | GRCm38.p3 | 9:82975009 | CCGGGCCGCGGCCCC[A/G]CCGCCGCCGCCGCCC | 83946 |
rs217845071 | snp | C/T | | | intron-variant | Phip | Mm_Celera | 9:82879608 | AAATTGGCACAGTCC[C/T]TACAGGGGATATTTT | 83946 |
rs217860591 | in-del | -/TT | | | intron-variant | Phip | Mm_Celera | 9:82935308 | AATATTCAAATTAAC[-/TT]TTTTTTCCTTTCAAA | 83946 |
rs217865774 | snp | A/G | | | utr-variant-3-prime | Phip | Mm_Celera | 9:82868831 | TCCAAATACGGTCAT[A/G]AATACACAGTGTCTT | 83946 |
rs217873545 | in-del | -/A | | | intron-variant | Phip | Mm_Celera | 9:82887059 | CCTTGGCACCATAAG[-/A]GAAAAAGAAAAAGCC | 83946 |
rs217876992 | snp | C/T | | | utr-variant-3-prime | Phip | Mm_Celera | 9:82867896 | CTACTACACTACAGC[C/T]AAGAGGCAGTTCTGT | 83946 |
rs217913011 | snp | G/T | | | intron-variant | Phip | Mm_Celera | 9:82950728 | TCCATGGCTAGGCTT[G/T]TAATACACCTACAAC | 83946 |
rs217928852 | in-del | -/A | | | intron-variant | Phip | Mm_Celera | 9:82916952 | CAAGATTACACACAC[-/A]ACAAAATTATCTCTA | 83946 |
rs217952318 | snp | A/G | | | intron-variant | Phip | Mm_Celera | 9:82880817 | AGTACTGGGATGTCA[A/G]TTGAGCTGCTTTGTA | 83946 |
rs217984596 | snp | A/C | | | upstream-variant-2KB | Phip | Mm_Celera | 9:82977487 | TTATTTATGTGACTA[A/C]TGTTGTTTTATCTTA | 83946 |
rs218034883 | snp | C/T | | | intron-variant | Phip | Mm_Celera | 9:82905492 | atatatatatacata[C/T]acacatacatatata | 83946 |
rs218052804 | snp | C/T | | | intron-variant | Phip | GRCm38.p3 | 9:82906322 | TTTGAGTAACTAAGC[C/T]CAGGCCCTACCACCT | 83946 |
rs218068403 | snp | A/T | | | intron-variant | Phip | Mm_Celera | 9:82947334 | TAAATGAGGATAGTT[A/T]ACGAGATGTTCTTTA | 83946 |
rs218070274 | snp | A/G | | | intron-variant | Phip | Mm_Celera | 9:82898219 | AGGTCCTCTGGGATG[A/G]AGTGGGTAGAAACAA | 83946 |
rs218072983 | snp | A/G | | | synonymous-codon | Phip | Mm_Celera | 9:82909877 | GAATCATGCTGTCTA[A/G]AGGACTAATATCCTG | 83946 |
rs218084274 | snp | C/T | | | intron-variant | Phip | Mm_Celera | 9:82938303 | GTAGAAAACACTAGC[C/T]ATCAGCTACAGGAAT | 83946 |
rs218094196 | snp | C/T | | | intron-variant | Phip | Mm_Celera | 9:82901387 | CTTGGCTTTCCCCTA[C/T]ACTGGGGCATAGAGC | 83946 |
rs218111515 | snp | C/T | | | synonymous-codon | Phip | Mm_Celera | 9:82877316 | AGTGGCAAAGTCCAT[C/T]GGAGTGTCAATGATG | 83946 |
rs218112058 | snp | G/T | | | utr-variant-3-prime | Phip | Mm_Celera | 9:82868365 | TTTGGTATTGCTGCT[G/T]TTATAGCCCTAGTCT | 83946 |
rs218114172 | in-del | -/A | | | intron-variant | Phip | Mm_Celera | 9:82915886 | TTCTTTTTGGTTTAG[-/A]AAAAAAAAATTCCCT | 83946 |
rs218139421 | snp | C/G | | | intron-variant | Phip | Mm_Celera | 9:82887845 | AATGATTCTTTATAC[C/G]TAGTAAGTGTACTAC | 83946 |
rs218146910 | snp | A/T | | | intron-variant | Phip | Mm_Celera | 9:82900426 | TGGCAATGTTCTGAG[A/T]AAACATTCCTCAGTG | 83946 |
rs218148691 | snp | A/C | | | intron-variant | Phip | Mm_Celera | 9:82910404 | AATAAACCTGGAGAA[A/C]AATGCAGATTTTGAA | 83946 |
rs218178620 | snp | A/C | | | intron-variant | Phip | Mm_Celera | 9:82949567 | TATCTAAATATATTT[A/C]ATCAATTCTTCTGAA | 83946 |
rs218235519 | snp | A/C | | | intron-variant | Phip | Mm_Celera | 9:82899080 | TAACATATTACTTGT[A/C]CCAGTCAATTATTTC | 83946 |
rs218240029 | in-del | -/CTTAGTCCTTTTT | | | intron-variant | Phip | Mm_Celera | 9:82909720 | TAGATCTTCCATTTG[-/CTTAGTCCTTTTT]CTTAGTCCCTTCTCC | 83946 |
rs218270059 | snp | A/G | | | intron-variant | Phip | Mm_Celera | 9:82937581 | GTTTAATTCCCCTTC[A/G]TGTATCACGTGATTT | 83946 |
rs218318791 | snp | A/C | | | intron-variant | Phip | Mm_Celera | 9:82950417 | CCCATAAGAACACTA[A/C]ACTGGAAACCATACA | 83946 |
rs218352008 | in-del | -/ACTTTA | | | intron-variant | Phip | Mm_Celera | 9:82908519 | TGAACCTAATTTGTG[-/ACTTTA]ACACACCCCTATCTC | 83946 |
rs218440718 | in-del | -/AT | | | intron-variant | Phip, LOC105243467 | Mm_Celera | 9:82964944 | CATGACTAACTCAAG[-/AT]AACCACACACAGTCC | 83946 |
rs218442498 | snp | C/T | | | synonymous-codon | Phip | Mm_Celera | 9:82876758 | GGACAGGGAACTGCT[C/T]CTGTTTCGCTTCTTC | 83946 |
rs218466638 | in-del | -/GGGGA | | | intron-variant | Phip | Mm_Celera | 9:82907556 | ATGAAAGGGGGGGGG[-/GGGGA]ATCACAAACTTATAT | 83946 |
rs218478661 | snp | A/G | | | intron-variant | Phip | Mm_Celera | 9:82916179 | CTGATTTTCAGAAAC[A/G]TCTAAAATAGGGAGT | 83946 |
rs218513261 | snp | A/C | | | intron-variant | Phip | Mm_Celera | 9:82906596 | CTTCAATTCCCAGCA[A/C]CCACATGGTGACTCA | 83946 |
rs218645256 | snp | C/G | | | intron-variant | Phip | Mm_Celera | 9:82934045 | TACTACCTAAAACAC[C/G]GCCCCCCACTTGAAT | 83946 |
rs218656688 | snp | A/G | | | intron-variant | Phip | Mm_Celera | 9:82947942 | TCAAAAAGGTGGGTC[A/G]TTTTTACAACAGAAA | 83946 |
rs218675795 | in-del | -/ACATAATGAT | | | intron-variant | Phip | Mm_Celera | 9:82937930 | GCAAATTACAACCAA[-/ACATAATGAT]GCATAGTCATGAAAA | 83946 |
rs218691079 | snp | A/G | | | intron-variant | Phip | Mm_Celera | 9:82944664 | AACTTGGCAATTCAA[A/G]TTGCAATAAGGCTGG | 83946 |
rs218721694 | snp | G/T | | | intron-variant | Phip | Mm_Celera | 9:82934863 | TCAGATGTCCACAAA[G/T]AATATAGAAAAATCT | 83946 |
rs218731295 | snp | A/C | | | intron-variant | Phip | Mm_Celera | 9:82923979 | TAGTTACACTAAACC[A/C]AATAGCTAACCTGAA | 83946 |
rs218771251 | in-del | -/AAAA | | | upstream-variant-2KB | Phip | GRCm38.p3 | 9:82976261 | CTGAAGCGTTCGTTT[-/AAAA]AAAAAAAATGTTTTT | 83946 |
rs218771403 | in-del | -/TGGTT | | | intron-variant | Phip | Mm_Celera | 9:82937504 | ACCAAGTACAACCAA[-/TGGTT]TGGTTTGGTTTTGTC | 83946 |
rs218930760 | snp | A/G | | | intron-variant | Phip | Mm_Celera | 9:82874936 | GTACAAGGAGGCACT[A/G]ACATACAGGTGTCTT | 83946 |
rs218942441 | snp | C/T | | | intron-variant | Phip | Mm_Celera | 9:82873977 | GGTGCAATAGTGGCA[C/T]GTTGTTTATGGGTAA | 83946 |
rs219021603 | snp | C/T | | | synonymous-codon | Phip | Mm_Celera | 9:82886630 | TTCTAACCTGTAAAA[C/T]CTGTTCTCCAGTCTT | 83946 |
rs219046232 | in-del | -/A | | | intron-variant | Phip | Mm_Celera | 9:82932150 | AATTTGAATTATTCT[-/A]AAAAAATAGCATTTA | 83946 |
rs219095575 | snp | C/G | | | intron-variant | Phip | Mm_Celera | 9:82957392 | AATTGAATGCAGAAG[C/G]TGCAAATCATCACCA | 83946 |
rs219122685 | snp | A/G | | | intron-variant | Phip | Mm_Celera | 9:82910493 | AAGTCAGAAGCCAGG[A/G]GACTTAGGTTAAGGA | 83946 |
rs219140056 | in-del | -/G | | | intron-variant | Phip | Mm_Celera | 9:82897146 | GCTGTTGGGTTTTTT[-/G]GGTTTTTTTTTTTTT | 83946 |
rs219145219 | in-del | -/TTTAA | | | intron-variant | Phip | Mm_Celera | 9:82890781 | TAGCTATAGTTTATT[-/TTTAA]TTTTTTATTCCCCAC | 83946 |
rs219160920 | snp | A/C | | | intron-variant | Phip | Mm_Celera | 9:82905103 | AAATAAGAAAAAGCA[A/C]ATAAGAAAAAGTAAA | 83946 |
rs219175678 | in-del | -/T | | | intron-variant | Phip | Mm_Celera | 9:82917311 | AGATTTCCAAAAGAA[-/T]TTTTTTTTGTTGAAA | 83946 |
rs219216212 | snp | A/T | | | intron-variant | Phip | Mm_Celera | 9:82914857 | AATTACAATTTAATT[A/T]TAGTAAAGACTTTAT | 83946 |
rs219217532 | snp | C/T | | | intron-variant | Phip | Mm_Celera | 9:82904424 | ATTATATTATCCCCT[C/T]ATCCTCAGCCCCCAG | 83946 |
rs219223854 | snp | A/T | | | missense | Phip | Mm_Celera | 9:82871856 | GAACATTGTTCTTAC[A/T]CTCTCCTGGAAAAGA | 83946 |
rs219234709 | snp | C/T | | | intron-variant | Phip | GRCm38.p3 | 9:82974799 | CGCTCCCCTCCCCAG[C/T]CCGCCCCGCGCCCCG | 83946 |
rs219246372 | snp | C/T | | | intron-variant | Phip | Mm_Celera | 9:82954832 | CCAACAATATGGTGC[C/T]GGAGTATAACATTAG | 83946 |
rs219254279 | snp | A/C | | | intron-variant | Phip, LOC105243467 | Mm_Celera | 9:82965107 | AGACTGAACCTAACA[A/C]TCAGCTAATACCTTT | 83946 |
rs219296099 | snp | C/T | | | intron-variant, nc-transcript-variant | Phip, LOC105243467 | GRCm38.p3 | 9:82960741 | ACTGTATACCTGGGA[C/T]CTGGTAGTTCACACT | 83946 |
rs219315581 | snp | A/C | | | intron-variant | Phip | Mm_Celera | 9:82903328 | AAACAAATATTTATA[A/C]ATATTATCTATTAAT | 83946 |
rs219349075 | snp | C/T | | | intron-variant | Phip | Mm_Celera | 9:82942856 | CTTCTCTACCCCTAC[C/T]CCGCCTTCCTTGGAG | 83946 |
rs219366100 | snp | C/T | | | intron-variant | Phip, LOC105243467 | Mm_Celera | 9:82965998 | ACCCACACACACACA[C/T]ACTTACACGTACACA | 83946 |
rs219367849 | snp | G/T | | | intron-variant | Phip | Mm_Celera | 9:82911984 | TCTGAGTACAACCGG[G/T]TATTTCTGCTTCTTT | 83946 |
rs219380675 | snp | A/C | | | intron-variant | Phip | Mm_Celera | 9:82941584 | GCTTGACAGGCACTC[A/C]TGCTCTACCTATACA | 83946 |
rs219423244 | snp | A/C | | | intron-variant | Phip | GRCm38.p3 | 9:82873838 | TTCCCCAGACCCTCT[A/C]CCTGCAGCCTATTCT | 83946 |
rs219435970 | snp | C/T | | | intron-variant | Phip | Mm_Celera | 9:82884427 | TGAGGAGCATATACA[C/T]CATGAAGGTAAAGGT | 83946 |
rs219444589 | in-del | -/GG | | | intron-variant | Phip | Mm_Celera | 9:82953161 | AGTTTATTTAAGGAA[-/GG]GGGGGGGAAGTATAC | 83946 |
rs219445895 | snp | A/C | | | intron-variant | Phip | Mm_Celera | 9:82883364 | TACACTGTACTACCT[A/C]ATTTTAAACAGAAGT | 83946 |
rs219494831 | snp | A/T | | | intron-variant | Phip | Mm_Celera | 9:82881089 | ATGAGACACATTTTG[A/T]GCATCAATGCTCAAA | 83946 |
rs219551892 | snp | A/C | | | intron-variant | Phip | Mm_Celera | 9:82956373 | AAAAAATAACCAAAA[A/C]AAAAAACAAAAAAAA | 83946 |
rs219606915 | snp | A/G | | | intron-variant | Phip, LOC105243467 | Mm_Celera | 9:82962798 | CAGTTATACTTCCGA[A/G]GAACTAGATAAACCT | 83946 |
rs219610320 | snp | C/T | | | intron-variant | Phip | GRCm38.p3 | 9:82885347 | AAGGTAAACAACAGA[C/T]TGTTTATAAAACAAA | 83946 |
rs219611065 | snp | C/T | | | intron-variant | Phip | Mm_Celera | 9:82882070 | CCTTTTTCAACAACA[C/T]ACCACTTTTACAGTC | 83946 |
rs219611132 | snp | A/G | | | utr-variant-3-prime | Phip | GRCm38.p3 | 9:82870179 | TATCAATATACACAC[A/G]CACACAGACATGGTT | 83946 |
rs219680189 | in-del | -/A | | | intron-variant | Phip | Mm_Celera | 9:82950662 | TCAATAGTCCTCCTG[-/A]AAAAAAAACAGTAAA | 83946 |
rs219688462 | snp | A/T | | | intron-variant | Phip | Mm_Celera | 9:82920846 | TGTTCTAATTTGTCA[A/T]GCTTCTATTTGATAT | 83946 |
rs219708262 | snp | C/T | | | intron-variant | Phip | Mm_Celera | 9:82952415 | TGTGCCCCACCCCCA[C/T]AGGCTCATGTATTTG | 83946 |
rs219743239 | snp | A/G | | | intron-variant | Phip | Mm_Celera | 9:82951107 | CAGCAATAGAACAGT[A/G]TCTAAGACAGATTGG | 83946 |
rs219809320 | snp | A/G | | | intron-variant | Phip | Mm_Celera | 9:82919945 | GCTTCAAATATACTG[A/G]AATTCTATGGGAACT | 83946 |
rs219811717 | in-del | -/AAACAAAACAAAAACC | | | intron-variant | Phip, LOC105243467 | Mm_Celera | 9:82962717 | GAAGAAAACAAAACA[-/AAACAAAACAAAAACC]AAAACCAAAACAAAA | 83946 |
rs219813215 | snp | A/C | | | intron-variant | Phip | Mm_Celera | 9:82874735 | TCAGAGATGGCAATT[A/C]CATAAGACAGATAAT | 83946 |
rs219819675 | snp | G/T | | | intron-variant, upstream-variant-2KB | Phip | Mm_Celera | 9:82929190 | AGGCCTATTTGATTT[G/T]ATTTTCTTTTATAAC | 83946 |
rs219857995 | snp | A/C | | | intron-variant, utr-variant-5-prime | Phip | Mm_Celera | 9:82928603 | AGAATGTGATGTATT[A/C]CAGTTTTTATCAAAG | 83946 |
rs219891922 | in-del | -/A | | | intron-variant | Phip | Mm_Celera | 9:82917118 | TCTGCAGGTCCACTG[-/A]GGGGGGGGGGGGGGG | 83946 |
rs219921234 | in-del | -/AAA | | | intron-variant | Phip | Mm_Celera | 9:82956696 | AGAGCCTATCTCAAT[-/AAA]AAAAATGAAAGAGAA | 83946 |
rs219927143 | snp | A/G | | | intron-variant | Phip | Mm_Celera | 9:82941873 | TGACACAGTAAGTTA[A/G]ATGACTTTCTATCAA | 83946 |
rs219971733 | in-del | -/T | | | intron-variant | Phip | Mm_Celera | 9:82913106 | ATCTTTAAAAGTTGA[-/T]TGTTTCTAGCCAGGA | 83946 |
rs219980139 | snp | C/T | | | intron-variant | Phip | Mm_Celera | 9:82878701 | AAACAACTAGAACCA[C/T]GAAGTAAATAGCAAA | 83946 |
rs220048263 | in-del | -/A | | | intron-variant | Phip | Mm_Celera | 9:82953168 | TTAAGGAAGGGGGGG[-/A]AAGTATACACACTTA | 83946 |
rs220060520 | snp | C/T | | | intron-variant | Phip | GRCm38.p3 | 9:82917662 | TTGGAATTTGCCCTG[C/T]TTGGTTTGGTTCTTA | 83946 |
rs220103873 | snp | A/T | | | intron-variant | Phip | Mm_Celera | 9:82918887 | TCTCTTGGCTGTGAA[A/T]ACGTGAAGAGCACTG | 83946 |
rs220123759 | snp | A/G | | | intron-variant | Phip | Mm_Celera | 9:82915519 | TGGAAAGATTTAAAA[A/G]TATGCAAACATCCTG | 83946 |
rs220128290 | snp | A/G | | | intron-variant | Phip | Mm_Celera | 9:82926092 | AATTTTGACACTGAT[A/G]TTCTCAAAATGTGTT | 83946 |
rs220132629 | in-del | -/A | | | intron-variant | Phip, LOC105243467 | Mm_Celera | 9:82961740 | TCATAAATTTACTTT[-/A]AAAAAAGTGTTTCAG | 83946 |
rs220206000 | snp | A/G | | | intron-variant | Phip | Mm_Celera | 9:82916432 | TGTTCATGAAACACG[A/G]GTATTAAAATGCAGA | 83946 |
rs220218817 | snp | A/G | | | intron-variant | Phip | GRCm38.p3 | 9:82909625 | TGGTGAAGTCTATAC[A/G]TACTTTAAAAATTCA | 83946 |
rs220235233 | in-del | -/CC | | | intron-variant | Phip | Mm_Celera | 9:82873649 | CAAACAAACAAAAAA[-/CC]CCTCATTGTTGGGTT | 83946 |
rs220242933 | snp | A/G | | | intron-variant | Phip | Mm_Celera | 9:82917451 | CCTGTACATCCTAAC[A/G]TGAGAAGCTGTAATA | 83946 |
rs220247347 | snp | C/T | | | synonymous-codon, missense, downstream-variant-500B | Phip, LOC105243467 | Mm_Celera | 9:82959552 | AACTGGAGACTCTGG[C/T]GGCCTCCCACAGTGC | 83946 |
rs220275570 | snp | A/G | | | intron-variant | Phip | Mm_Celera | 9:82908145 | GATAGGTACACAGTG[A/G]TGTTTCATTGTGGCT | 83946 |
rs220306916 | snp | C/T | | | intron-variant | Phip | Mm_Celera | 9:82891856 | AAGTACAACAGACTA[C/T]GAAGACATAATAATG | 83946 |
rs220343633 | in-del | -/CACACACACA | | | intron-variant | Phip | Mm_Celera | 9:82946699 | GTGCATGCATTCATT[-/CACACACACA]CACACACACACACAC | 83946 |
rs220359671 | snp | A/T | | | intron-variant | Phip | Mm_Celera | 9:82949450 | CCATAGGTAATATAT[A/T]TTGTTTTGTATTTAA | 83946 |
rs220392520 | snp | A/G | | | intron-variant | Phip, LOC105243467 | Mm_Celera | 9:82961769 | AGCCAGGCAGTGGTG[A/G]TGCACGCCCTTAATC | 83946 |
rs220396359 | snp | C/T | | | intron-variant | Phip | Mm_Celera | 9:82948032 | ATCGATCCTACTATA[C/T]CTTAACTGTTCAACT | 83946 |
rs220396706 | snp | C/T | | | intron-variant, nc-transcript-variant | Phip, LOC105243467 | GRCm38.p3 | 9:82960797 | ACTGTATACCTGGGA[C/T]CCGGTAGTTCACACC | 83946 |
rs220412902 | snp | C/G | | | intron-variant | Phip | Mm_Celera | 9:82890659 | TCTAAAATATAACTT[C/G]CATTATTTCTTATAC | 83946 |
rs220430234 | in-del | -/TAA | | | intron-variant | Phip | Mm_Celera | 9:82939872 | CCAAACATTCCTACT[-/TAA]GCACTCCAGCCTTTC | 83946 |
rs220437802 | snp | G/T | | | intron-variant | Phip | Mm_Celera | 9:82972496 | CATATGTACCAATAT[G/T]CTCAAAAACATGACA | 83946 |
rs220445752 | snp | G/T | | | intron-variant | Phip, LOC105243467 | Mm_Celera | 9:82963025 | GGTCCCAGAAAATTC[G/T]GGATCCTGCATACAA | 83946 |
rs220498926 | snp | A/T | | | intron-variant | Phip | Mm_Celera | 9:82894782 | CATATATATATATTT[A/T]TTTTATGTAGCTTAA | 83946 |
rs220518568 | snp | A/T | | | intron-variant | Phip | Mm_Celera | 9:82879951 | GAAGCATAAGCCAGT[A/T]AGTTCTTAACAGGCA | 83946 |
rs220525357 | snp | C/T | | | intron-variant | Phip | Mm_Celera | 9:82888388 | ACAGCAATTGAATTG[C/T]ACCAAATTTAAACAC | 83946 |
rs220525992 | snp | G/T | | | intron-variant | Phip | Mm_Celera | 9:82885983 | AAACTGATCGTAAAA[G/T]AAATTTTAATACAAT | 83946 |
rs220608048 | snp | C/G | | | intron-variant | Phip | Mm_Celera | 9:82889254 | TACTTTTAAAAACTT[C/G]AAACAAAACCTGATA | 83946 |
rs220649931 | snp | C/T | | | synonymous-codon | Phip | Mm_Celera | 9:82875408 | TGCAGAATTATTCTT[C/T]GTAGCATGGCTGAAT | 83946 |
rs220650377 | snp | A/C | | | intron-variant | Phip | Mm_Celera | 9:82887080 | AGAAAAAGCCAAAAA[A/C]CAAAACTTCTGCATA | 83946 |
rs220685625 | in-del | -/A | | | intron-variant | Phip | Mm_Celera | 9:82909141 | ATGAAATCATTACTT[-/A]AAAAAAAAAAAAAAA | 83946 |
rs220694745 | snp | A/G | | | intron-variant, upstream-variant-2KB | Phip, LOC105243467 | Mm_Celera | 9:82967898 | GGTGAGGAGAGGCAG[A/G]GGCAGAGGCAGGTGG | 83946 |
rs220714906 | in-del | -/ATTTTAT | | | intron-variant | Phip | Mm_Celera | 9:82948261 | ATAGAAATTTTTATA[-/ATTTTAT]TAAAGTAGAATATCA | 83946 |
rs220716884 | snp | G/T | | | intron-variant | Phip | Mm_Celera | 9:82971690 | TCAGGACTCTGGGGG[G/T]GGAACCAAGAACACC | 83946 |
rs220726082 | snp | C/T | | | intron-variant, upstream-variant-2KB | Phip, LOC105243467 | Mm_Celera | 9:82966700 | ATTTAGGTAATTCAG[C/T]TGGTTTTATCAATAC | 83946 |
rs220727940 | snp | A/T | | | intron-variant | Phip | Mm_Celera | 9:82925352 | CTAACATATAACTCA[A/T]GTAATCATTTTTCAA | 83946 |
rs220737045 | snp | C/T | | | intron-variant | Phip | Mm_Celera | 9:82943516 | CATTGCAATTATTAT[C/T]CATTCCCCTCTCTGG | 83946 |
rs220753371 | snp | A/G | | | intron-variant | Phip | Mm_Celera | 9:82878826 | ATTCAGGCCAGGCAA[A/G]TGTCTTATTGACCCA | 83946 |
rs220762929 | snp | A/G | | | intron-variant | Phip | Mm_Celera | 9:82888203 | CTGCATGCAATCAAA[A/G]TAACTATGTGTATAT | 83946 |
rs220794509 | in-del | -/A | | | intron-variant | Phip | Mm_Celera | 9:82881182 | ATATGAATCTTCCTC[-/A]AAAAAAATATTTATA | 83946 |
rs220798378 | snp | A/G | | | intron-variant | Phip, LOC105243467 | Mm_Celera | 9:82960934 | CAGACAGCATTATAT[A/G]GTATATTTCAGTTGG | 83946 |
rs220815492 | in-del | -/C | | | intron-variant | Phip | Mm_Celera | 9:82886843 | ATTTATCAACACACA[-/C]AAAAAAAATAGAGCA | 83946 |
rs220833191 | snp | C/T | | | intron-variant | Phip | GRCm38.p3 | 9:82889359 | CTTCCCAGGGCTAAC[C/T]CTCCAACCCCAGTTA | 83946 |
rs220835269 | snp | A/G | | | intron-variant | Phip | Mm_Celera | 9:82958475 | AATGCAGAGGGACAG[A/G]GTGTGAGCAGAAGGG | 83946 |
rs220839238 | snp | C/T | | | intron-variant | Phip | Mm_Celera | 9:82959175 | AAATTTTAAAATACG[C/T]CACTCTATTAAAAGA | 83946 |
rs220840740 | snp | C/T | | | intron-variant | Phip | Mm_Celera | 9:82933949 | CAAAGTAGCAAATAA[C/T]GCACCTAAGTTTTCT | 83946 |
rs220970844 | snp | C/T | | | intron-variant | Phip | GRCm38.p3 | 9:82910954 | TTCTAGTTCAATTCC[C/T]AGCATCCACAGCAGG | 83946 |
rs221013095 | in-del | -/T | | | utr-variant-3-prime | Phip | Mm_Celera | 9:82871195 | TACCTGCGTTACAGA[-/T]TTTTTAAAATGCAAT | 83946 |
rs221019547 | snp | A/G | | | intron-variant | Phip | Mm_Celera | 9:82957890 | GAGCCTGAGTGCATC[A/G]TAACGAGTACTAAAT | 83946 |
rs221026643 | snp | C/T | | | intron-variant | Phip | Mm_Celera | 9:82892939 | CTTAAAAGCATAGGA[C/T]TTCACACTTTCAGAC | 83946 |
rs221033878 | snp | A/C | | | intron-variant | Phip | Mm_Celera | 9:82887208 | AAATACCATAACGAT[A/C]TCCAGTTACCTCAAA | 83946 |
rs221035483 | snp | C/T | | | intron-variant | Phip | Mm_Celera | 9:82926994 | GACTACACTCTACTG[C/T]CAGCCTCAGCAGTAC | 83946 |
rs221064088 | snp | C/T | | | intron-variant | Phip | Mm_Celera | 9:82969255 | TTTCCTTATGGAAAA[C/T]TACACTCCCACACAG | 83946 |
rs221119198 | snp | A/T | | | intron-variant | Phip | Mm_Celera | 9:82883138 | ATAGTCAACTGAAAA[A/T]TACAACCATCAAAAT | 83946 |
rs221127185 | snp | A/G | | | intron-variant | Phip | Mm_Celera | 9:82896363 | CAGACAAAACTAAAA[A/G]CTCTTCTAGCCCCCC | 83946 |
rs221150062 | snp | A/G | | | intron-variant | Phip | Mm_Celera | 9:82931944 | AACTGGAATGTGATA[A/G]GACATAAGATTAATC | 83946 |
rs221162763 | snp | A/G | | | intron-variant | Phip | Mm_Celera | 9:82922467 | ATATTCACTAAAATA[A/G]AGCTACAATGATGCT | 83946 |
rs221169958 | snp | G/T | | | intron-variant | Phip | GRCm38.p3 | 9:82931218 | ACTCAATGTGAATCA[G/T]GTCAACAACAAAATT | 83946 |
rs221207832 | snp | A/G | | | intron-variant | Phip | Mm_Celera | 9:82920082 | ACTTCTAAACTCTCT[A/G]TACTATCTTCTCCCT | 83946 |
rs221211031 | snp | G/T | | | intron-variant, upstream-variant-2KB | Phip | Mm_Celera | 9:82930130 | TGATTTTTATACACC[G/T]AATTCCATAAAAGTA | 83946 |
rs221313627 | snp | G/T | | | intron-variant | Phip | Mm_Celera | 9:82945382 | AAGATTCCCATCACT[G/T]TTTAAAGAGAACTCT | 83946 |
rs221333152 | snp | C/T | | | intron-variant | Phip, LOC105243467 | Mm_Celera | 9:82964244 | AAGGGCCTTAACACT[C/T]TGTAGCATGTACATA | 83946 |
rs221408476 | snp | C/T | | | intron-variant | Phip | Mm_Celera | 9:82912561 | TAAGAAATATTAGCT[C/T]CACATAATAGATTAT | 83946 |
rs221435085 | snp | C/T | | | intron-variant | Phip, LOC105243467 | Mm_Celera | 9:82965181 | GTTAGAAATTTAGAG[C/T]GAAAATTTTGTATAA | 83946 |
rs221438951 | snp | C/G | | | intron-variant | Phip | Mm_Celera | 9:82930814 | AGTGTGTATGTACTA[C/G]GAGGGTGGGAGGAGG | 83946 |
rs221490106 | snp | A/G | | | intron-variant | Phip | GRCm38.p3 | 9:82926190 | TCATTTACATGACTT[A/G]CTAGTCAAACTTTCT | 83946 |
rs221497403 | snp | C/T | | | intron-variant | Phip | Mm_Celera | 9:82895578 | AATACTAGTAGGTAA[C/T]GCTTCTTAAATATGC | 83946 |
rs221602215 | in-del | -/CG | | | intron-variant | Phip | Mm_Celera | 9:82968444 | TAAATTGGTAAAAAA[-/CG]ACAATATTTAACCTA | 83946 |
rs221609302 | snp | C/T | | | intron-variant | Phip | Mm_Celera | 9:82968096 | TGCTAATCGAGGTCA[C/T]ATGAGTTAGTATTAA | 83946 |
rs221646558 | snp | C/T | | | intron-variant | Phip | Mm_Celera | 9:82891622 | ACAGCATTTTTAACT[C/T]TTCCCAGAACATTAC | 83946 |
rs221675212 | snp | A/C | | | intron-variant | Phip | Mm_Celera | 9:82892604 | TCATACCCTCTGATT[A/C]TAACATTTTAAAAGT | 83946 |
rs221751162 | snp | A/G | | | intron-variant | Phip | Mm_Celera | 9:82893308 | TACATCACCTATGGC[A/G]TCTTAATTACCTACC | 83946 |
rs221773538 | snp | C/T | | | intron-variant | Phip | Mm_Celera | 9:82882397 | CTTCCTAAGAGTTAA[C/T]GTGATGGCTCATTAA | 83946 |
rs221783382 | snp | A/T | | | intron-variant | Phip | Mm_Celera | 9:82902479 | AGACATTTGTATACC[A/T]TTATTAAGAGTCATT | 83946 |
rs221808245 | snp | A/G | | | intron-variant | Phip | Mm_Celera | 9:82924430 | AAATTACCCGTAAAA[A/G]AGATATTCATAAAGA | 83946 |
rs221826567 | snp | A/G | | | intron-variant | Phip | Mm_Celera | 9:82932704 | AACAAAGGCACAATG[A/G]CCATGGCACTGCGAG | 83946 |
rs221904966 | snp | A/G | | | intron-variant | Phip | Mm_Celera | 9:82972872 | ACTATTTGGGCCTAT[A/G]AACCACCTCTAAAAT | 83946 |
rs221971242 | snp | G/T | | | intron-variant | Phip, LOC105243467 | GRCm38.p3 | 9:82965319 | TGGGGGGGGGGGGGG[G/T]TTCATCCCCATCAAA | 83946 |
rs221979526 | snp | C/T | | | intron-variant | Phip | Mm_Celera | 9:82924790 | CTCAAATAACCAAGG[C/T]TGGCCTGGATCTCAC | 83946 |
rs221981065 | snp | C/G | | | intron-variant | Phip | Mm_Celera | 9:82933777 | GATCCGAGGAGTTTA[C/G]AACACCAGTATTTCT | 83946 |
rs221995926 | in-del | -/AATCAATA | | | intron-variant | Phip | Mm_Celera | 9:82969158 | TATAATTAATCAATC[-/AATCAATA]AATAAATAAATATTA | 83946 |
rs222011472 | snp | G/T | | | missense | Phip | Mm_Celera | 9:82893401 | CGTCAGGCATATCAT[G/T]GTATCTATTACAAAC | 83946 |
rs222035535 | snp | A/G | | | intron-variant | Phip, LOC105243467 | Mm_Celera | 9:82962623 | GAGGCAGAGGCAGGC[A/G]GATTTCTGAGTTTGA | 83946 |
rs222074344 | snp | A/G | | | intron-variant | Phip, LOC105243467 | GRCm38.p3 | 9:82961775 | GCAGTGGTGGTGCAC[A/G]CCCTTAATCTCAGCA | 83946 |
rs222101157 | snp | A/G | | | intron-variant | Phip | Mm_Celera | 9:82925278 | AACTTTACTGGATTC[A/G]TAAATTTACTTAAAA | 83946 |
rs222145343 | in-del | -/GGAAAAA | | | intron-variant | Phip | Mm_Celera | 9:82873330 | TCAGAAAAGGAAAGG[-/GGAAAAA]AAAAAAAAAACAAAA | 83946 |
rs222154809 | in-del | -/CATCAGTT | | | intron-variant | Phip | Mm_Celera | 9:82891925 | ATGTACTGATGTTTA[-/CATCAGTT]TTCACTCAAAATGAA | 83946 |
rs222190120 | snp | G/T | | | intron-variant | Phip | Mm_Celera | 9:82891765 | CAGTCAGGTTAACAA[G/T]GCGGAGCACCAGTCA | 83946 |
rs222214962 | snp | G/T | | | intron-variant | Phip | Mm_Celera | 9:82974494 | CCGCGGCCCCGGGGC[G/T]CCCGCACCCCCGGCT | 83946 |
rs222257404 | in-del | -/CT | | | intron-variant | Phip | Mm_Celera | 9:82902930 | CCCTGTTAAATATAA[-/CT]CTCAGAAACTCAGTA | 83946 |
rs222288780 | snp | C/T | | | intron-variant | Phip | Mm_Celera | 9:82922150 | TTTAATATATACTAG[C/T]ACTAAGAAACATGGA | 83946 |
rs222315164 | snp | C/T | | | intron-variant | Phip | Mm_Celera | 9:82970744 | TTCAGTTCCTCTGAA[C/T]TCCCACAGAGATGAA | 83946 |
rs222367782 | snp | A/G | | | intron-variant | Phip | Mm_Celera | 9:82901680 | AACTAGCCAAAGTAT[A/G]AAGTTCTTTTCTATT | 83946 |
rs222385331 | snp | A/C | | | intron-variant | Phip | Mm_Celera | 9:82888374 | CAAATTATGAGCTCA[A/C]AGCAATTGAATTGCA | 83946 |
rs222400404 | snp | A/G | | | intron-variant | Phip | Mm_Celera | 9:82902665 | AGGGTGTATCTCCAC[A/G]GACCATTAAAACCTT | 83946 |
rs222412187 | snp | C/G | | | intron-variant | Phip | Mm_Celera | 9:82939941 | AGGTTTCCTCCTTTA[C/G]TTCCTTCCCAGTGAT | 83946 |
rs222414918 | snp | A/G | | | intron-variant, upstream-variant-2KB | Phip, LOC105243467 | Mm_Celera | 9:82966176 | AATTTTATTAAAAAC[A/G]TAGTATTGAAAGTAG | 83946 |
rs222420867 | snp | A/G | | | intron-variant | Phip | Mm_Celera | 9:82894741 | CTACATATGTAGAAA[A/G]CTTTTGAAATCAAAC | 83946 |
rs222446752 | snp | A/T | | | intron-variant | Phip | Mm_Celera | 9:82926303 | AATCATAATAAGGCA[A/T]GAAGTTAAAATGGAT | 83946 |
rs222478311 | snp | A/G | | | intron-variant | Phip | Mm_Celera | 9:82903461 | AGCTAAGAACTGAAC[A/G]CAGGGTTCTGGACTT | 83946 |
rs222506169 | snp | A/G | | | intron-variant | Phip | Mm_Celera | 9:82927417 | GTAAATCCCTCTGCA[A/G]TAACTATCTATGGCT | 83946 |
rs222524813 | snp | G/T | | | intron-variant | Phip | Mm_Celera | 9:82884709 | AAAGAGGATCTATGC[G/T]GCTGGGACAACACCA | 83946 |
rs222527051 | snp | A/C | | | intron-variant | Phip | Mm_Celera | 9:82943225 | ACAATAGTTTCCTAA[A/C]AGAAAACTTCACTTA | 83946 |
rs222550662 | in-del | -/C | | | intron-variant | Phip | Mm_Celera | 9:82974513 | CACCCCCGGCTGCCG[-/C]CCCCCCGCAGCCCCC | 83946 |
rs222562803 | in-del | -/C | | | intron-variant | Phip, LOC105243467 | Mm_Celera | 9:82961568 | TGACTAATAGTAAAA[-/C]TTAAGTTTGCCTTTT | 83946 |
rs222635170 | snp | A/G | | | intron-variant, upstream-variant-2KB | Phip | Mm_Celera | 9:82930449 | CCCTTCTACAAATTG[A/G]CCTTAAACACAAAAT | 83946 |
rs222636992 | snp | A/C | | | intron-variant | Phip | Mm_Celera | 9:82932734 | GTTCATACAGTTCTT[A/C]AAAAAGTACTCTTCT | 83946 |
rs222693580 | snp | A/G | | | intron-variant | Phip | Mm_Celera | 9:82890934 | AGAAAAAGAAAACAT[A/G]CCTTTTGTCTATTCT | 83946 |
rs222700948 | snp | G/T | | | intron-variant | Phip | Mm_Celera | 9:82886939 | AAGCTATTTAAGACA[G/T]TATTTCTAAGATGAC | 83946 |
rs222712664 | snp | C/G | | | intron-variant | Phip | Mm_Celera | 9:82892373 | TTTTTTTTAAAGATT[C/G]ATTCATTTAATGTAT | 83946 |
rs222724918 | snp | C/G | | | intron-variant | Phip | Mm_Celera | 9:82939026 | AGAGAAACCCTGTCT[C/G]GAAAAAAACAAACTA | 83946 |
rs222766384 | snp | C/T | | | downstream-variant-500B | Phip, LOC102641372 | Mm_Celera | 9:82865730 | GAGAATAAATAGAAA[C/T]GTGAATTATCATCCT | 83946 |
rs222808788 | snp | C/T | | | intron-variant, upstream-variant-2KB | Phip | Mm_Celera | 9:82929477 | AGCATGAAGTTGTTA[C/T]ACACACAGAAATATT | 83946 |
rs222836189 | snp | C/T | | | intron-variant | Phip | Mm_Celera | 9:82872091 | GGAGCTCTCTCCTAG[C/T]CTAACACGGGTTCTT | 83946 |
rs222870190 | snp | C/G | | | intron-variant, utr-variant-5-prime | Phip | Mm_Celera | 9:82928330 | AATACAGCAGAAATA[C/G]TTCCCTAAGTCTCTA | 83946 |
rs222874309 | in-del | -/T | | | intron-variant | Phip | Mm_Celera | 9:82971863 | AAAAATGTCCTTTAC[-/T]TTAAAAAAAAAAAAA | 83946 |
rs222879670 | in-del | -/G | | | intron-variant | Phip | Mm_Celera | 9:82885199 | GATTTCTATAGAACA[-/G]GGGCAGACGAGAGAC | 83946 |
rs222886028 | snp | C/G | | | intron-variant | Phip | Mm_Celera | 9:82937544 | GATACATTTCTGTTT[C/G]GTAGCCTTTTTTTAA | 83946 |
rs222913406 | snp | C/T | | | utr-variant-3-prime | Phip | Mm_Celera | 9:82867852 | AGGGCTGAACTTTAT[C/T]TCAATAACCCTTGAA | 83946 |
rs222923198 | snp | A/G | | | intron-variant | Phip | Mm_Celera | 9:82931096 | CCACGTAGCAAGCAC[A/G]TTACCCACTGAGCCA | 83946 |
rs222952238 | in-del | -/TTTGT | | | intron-variant | Phip | Mm_Celera | 9:82888895 | CTTTCTGTTTCTTTC[-/TTTGT]TTTGTTTTGTTTTGT | 83946 |
rs222985402 | snp | A/C/G | | | intron-variant | Phip | GRCm38.p3 | 9:82932346 | GTGAGGCATAAAAAT[A/C/G]AAAGATCAGATTTTA | 83946 |
rs222994977 | snp | C/G | | | intron-variant | Phip | Mm_Celera | 9:82936736 | CACAAGAGTCTAAAG[C/G]GCAAGCAGCCCTTAG | 83946 |
rs223023519 | snp | A/G | | | synonymous-codon | Phip | Mm_Celera | 9:82887526 | TACCTAGTGTCATCA[A/G]CTGATTTATTCCTCC | 83946 |
rs223023659 | snp | C/T | | | intron-variant | Phip | Mm_Celera | 9:82897079 | TGAAACCTAACATTA[C/T]TTATGCAAGAGATAT | 83946 |
rs223083235 | snp | A/C | | | intron-variant | Phip | Mm_Celera | 9:82896475 | GTGTAGCAATACTAA[A/C]TAACTAAGACTCTAT | 83946 |
rs223136714 | snp | C/T | | | intron-variant | Phip | Mm_Celera | 9:82927464 | CCCTCCTTTTACTGT[C/T]CTACTATCCTGACTG | 83946 |
rs223182803 | in-del | -/T | | | utr-variant-3-prime | Phip | Mm_Celera | 9:82868716 | GCTAAATTATAAAAA[-/T]ATAACATCTGTAACT | 83946 |
rs223191490 | in-del | -/AAGCTTCTTAT | | | intron-variant | Phip | Mm_Celera | 9:82912280 | ACTAAATATGTATAA[-/AAGCTTCTTAT]AAGCTATAAAATGGA | 83946 |
rs223243113 | in-del | -/A | | | intron-variant | Phip | Mm_Celera | 9:82893101 | AAAAACAGCTCAGAG[-/A]AAAAAACATTCTAAA | 83946 |
rs223259512 | in-del | -/T | | | intron-variant | Phip | Mm_Celera | 9:82908405 | GAAAGACAGCTGACA[-/T]CCACAACTAAGCTCC | 83946 |
rs223309134 | snp | A/G | | | intron-variant, upstream-variant-2KB | Phip, LOC105243467 | GRCm38.p3 | 9:82966433 | TTGCCTTCTCACAAT[A/G]TCCCCTCCCCCAGTC | 83946 |
rs223312258 | snp | A/T | | | intron-variant | Phip | Mm_Celera | 9:82899459 | TACAAATAACATATT[A/T]ACTTCTAAAGAAAGT | 83946 |
rs223326884 | snp | G/T | | | intron-variant | Phip | GRCm38.p3 | 9:82972052 | GTTAAGAATTCCCTT[G/T]TTCAATCATATATTA | 83946 |
rs223364235 | in-del | -/TTTG | | | intron-variant, upstream-variant-2KB | Phip, LOC105243467 | Mm_Celera | 9:82967264 | AGCTGGAGCAGAACC[-/TTTG]CGACTTCCTTTGGGA | 83946 |
rs223367058 | snp | A/G | | | intron-variant, upstream-variant-2KB | Phip, LOC105243467 | Mm_Celera | 9:82967812 | AGATTTCCTAAATTT[A/G]ACAGTCTTTATCACT | 83946 |
rs223371930 | snp | A/G | | | intron-variant | Phip | Mm_Celera | 9:82905356 | TAACATACTCTATTC[A/G]CAAGGTATTATTCTA | 83946 |
rs223391140 | in-del | -/A | | | intron-variant | Phip | Mm_Celera | 9:82899484 | AAAGTAAAAAAAAAT[-/A]AAAAAATAAAAAATT | 83946 |
rs223403059 | snp | A/T | | | utr-variant-3-prime | Phip | Mm_Celera | 9:82871200 | GCGTTACAGATTTTT[A/T]AAAATGCAATATTTT | 83946 |
rs223407725 | snp | C/T | | | intron-variant | Phip | Mm_Celera | 9:82973361 | ACAGTCACACGGTAA[C/T]CAGTGGTTTATATTA | 83946 |
rs223411527 | snp | C/T | | | intron-variant | Phip | Mm_Celera | 9:82971648 | GCTGCTGGGTTCACA[C/T]CCCACACTGCATAAA | 83946 |
rs223431211 | snp | A/G | | | intron-variant | Phip | Mm_Celera | 9:82897991 | CTCCTAACTTATCAT[A/G]AAAGTACTCATATAT | 83946 |
rs223440437 | snp | A/G | | | intron-variant | Phip | Mm_Celera | 9:82972991 | AAAAAACATAGCATT[A/G]CTTAAAGATTCTTAA | 83946 |
rs223456438 | in-del | -/A | | | intron-variant | Phip | Mm_Celera | 9:82906763 | GGAAATGCAAAAACC[-/A]AAAGTTTTAAGTGAG | 83946 |
rs223467407 | in-del | -/ACTGCCTGTACCT | | | intron-variant | Phip | Mm_Celera | 9:82882475 | ATCAGGTAGTTTACA[-/ACTGCCTGTACCT]TCAGCTCCAGGGGAC | 83946 |
rs223490894 | in-del | -/T | | | intron-variant | Phip | Mm_Celera | 9:82897148 | GTTGGGTTTTTTGGG[-/T]TTTTTTTTTTTTTTA | 83946 |
rs223589927 | snp | A/G | | | intron-variant | Phip | Mm_Celera | 9:82906119 | GAAAGGAAAACACAA[A/G]TCTTGCAAGGGCAGA | 83946 |
rs223593155 | snp | A/G | | | intron-variant, upstream-variant-2KB | Phip | Mm_Celera | 9:82930706 | ATACAAATATATAAT[A/G]AATCAACTTTAAAAA | 83946 |
rs223620177 | snp | C/T | | | intron-variant | Phip | Mm_Celera | 9:82941322 | TTCTAACAGACATGA[C/T]AGGAGGCAAACAAGT | 83946 |
rs223652068 | snp | A/G | | | intron-variant | Phip | Mm_Celera | 9:82897275 | CCCAGACAGCCAAGT[A/G]TACCACTTGCAGGAG | 83946 |
rs223677303 | snp | A/T | | | intron-variant | Phip | Mm_Celera | 9:82947247 | CAAACTATCTTATTC[A/T]AGTACCACAGACCAC | 83946 |
rs223679211 | snp | A/C | | | intron-variant | Phip | Mm_Celera | 9:82935754 | CATCCCTCCAGCTCG[A/C]AGAAAACACTGTCAG | 83946 |
rs223681718 | snp | A/T | | | intron-variant | Phip | Mm_Celera | 9:82931146 | TCTTCTAATACAGCA[A/T]CAAGATAAAACATTC | 83946 |
rs223738213 | snp | C/T | | | intron-variant | Phip | Mm_Celera | 9:82948609 | TATTCAAAATAACCA[C/T]AAATGTCCTCTGATA | 83946 |
rs223741609 | snp | A/G | | | intron-variant | Phip | Mm_Celera | 9:82934541 | AAAAGGCTTCACAAG[A/G]CTCATTTGATCAAGT | 83946 |
rs223765439 | snp | A/G | | | intron-variant | Phip | Mm_Celera | 9:82970865 | ATGGTACTATAAAAA[A/G]CATTTATTCGACTTC | 83946 |
rs223786662 | snp | A/G | | | intron-variant | Phip | Mm_Celera | 9:82897188 | CCTCTGAACTAATAA[A/G]AAATTAAGCTGCACC | 83946 |
rs223884691 | snp | A/G | | | intron-variant | Phip | Mm_Celera | 9:82895363 | CTGACCACCCTGAAG[A/G]TAGCGTTTTCATTTA | 83946 |
rs223898919 | snp | A/G | | | intron-variant | Phip | Mm_Celera | 9:82944919 | ACTCCTCTCATTCCT[A/G]CAATCCTTCTTCCCC | 83946 |
rs223908816 | snp | C/G | | | intron-variant | Phip | Mm_Celera | 9:82936885 | CATCCTGAAGGAGAG[C/G]CTATCACTAAAACCT | 83946 |
rs223942996 | snp | C/T | | | intron-variant | Phip | Mm_Celera | 9:82904350 | AGTGCTTTTAATTGA[C/T]GAGCCATCTTTCCAG | 83946 |
rs223966785 | snp | A/G | | | missense | Phip | Mm_Celera | 9:82875443 | GCGGATCAGGGCTGG[A/G]AAGTGTGCTCAAGGC | 83946 |
rs223968836 | in-del | -/A | | | intron-variant | Phip | Mm_Celera | 9:82899580 | TGGAATTTGGTAGGT[-/A]GGCTAGGCTGGATGC | 83946 |
rs224007401 | snp | A/G | | | intron-variant | Phip | Mm_Celera | 9:82908248 | GATGCCACAGCTTGA[A/G]AGCACCCTTATGCCC | 83946 |
rs224008808 | snp | A/G | | | synonymous-codon | Phip | Mm_Celera | 9:82932942 | TTTATCACAACTTCC[A/G]GCTGCTATCATAGTA | 83946 |
rs224014956 | snp | A/G | | | intron-variant | Phip | GRCm38.p3 | 9:82907666 | TAATGGTTGCTGAGG[A/G]GGAGCTACTTTCTGC | 83946 |
rs224020014 | snp | G/T | | | intron-variant | Phip | Mm_Celera | 9:82874569 | CATTGCTAGAGTTAG[G/T]GTGAGGCCAAGCAGA | 83946 |
rs224119078 | snp | C/G | | | intron-variant | Phip | Mm_Celera | 9:82899541 | TGGGAACAGCAGAGT[C/G]TTTCTATGTAGTCTT | 83946 |
rs224184138 | snp | G/T | | | intron-variant | Phip | Mm_Celera | 9:82914468 | TGTCTAGAGTGTTTG[G/T]GATAATGTAAAATTA | 83946 |
rs224234530 | snp | A/C | | | intron-variant | Phip | Mm_Celera | 9:82941550 | TTAGTCTTGTGTTTC[A/C]TAACCATCTCATCTC | 83946 |
rs224265801 | snp | A/G | | | intron-variant | Phip | Mm_Celera | 9:82873212 | TTACAAAATGGTTTC[A/G]TTTTAGTGCAAATAG | 83946 |
rs224267191 | in-del | -/AG | | | intron-variant | Phip | Mm_Celera | 9:82925254 | GATAGAAAAGAGAAA[-/AG]AAAAAAAAACTTTAC | 83946 |
rs224322848 | snp | C/G | | | intron-variant | Phip | Mm_Celera | 9:82905593 | GTGAATGCAAACAAT[C/G]AAAGTCATATTTAAG | 83946 |
rs224326187 | in-del | -/A | | | intron-variant | Phip | Mm_Celera | 9:82956349 | ATTTTTCTAGAAATC[-/A]AAAAAACTAAAAAAT | 83946 |
rs224339755 | snp | A/G | | | intron-variant | Phip | Mm_Celera | 9:82904694 | ATTTTTTTTCTTAAA[A/G]GGAATGAAAAGAAAC | 83946 |
rs224345745 | snp | A/T | | | synonymous-codon | Phip | Mm_Celera | 9:82877214 | CTTGCTTGGTGTGTA[A/T]GCTTTAGAATTACTG | 83946 |
rs224347148 | snp | A/G | | | intron-variant | Phip | Mm_Celera | 9:82873862 | CTATTCTTATACAAT[A/G]CAGAAGGTACACTGC | 83946 |
rs224374901 | snp | A/G | | | intron-variant | Phip | Mm_Celera | 9:82931892 | ATGTGTGTGCCTGAC[A/G]CTTGTGAAGGACAGA | 83946 |
rs224479786 | in-del | -/C | | | intron-variant | Phip | Mm_Celera | 9:82928050 | CATTCCCATCTGCAA[-/C]ATTATAATATTAAAT | 83946 |
rs224623060 | snp | A/G | | | intron-variant | Phip | Mm_Celera | 9:82903600 | GACGACAAACTCTAT[A/G]GTTAATATCTGAAAC | 83946 |
rs224636874 | snp | A/G | | | intron-variant | Phip | Mm_Celera | 9:82944945 | TCCCCTCTTTCACAG[A/G]ATTCCCCAAGCATCC | 83946 |
rs224664693 | in-del | -/G | | | intron-variant | Phip | Mm_Celera | 9:82917538 | AGGGAGCTATGAACA[-/G]GGAGTTTGCACTAGC | 83946 |
rs224677475 | snp | A/G | | | intron-variant | Phip | Mm_Celera | 9:82943684 | AGAAAACATTGGTTA[A/G]TCCTTTACCAAAATG | 83946 |
rs224757527 | in-del | -/AGTATCAGAA | | | intron-variant | Phip | Mm_Celera | 9:82951297 | GTTGCAGAGGGGAAG[-/AGTATCAGAA]AGTGGCCAAAAGACC | 83946 |
rs224858789 | snp | G/T | | | intron-variant | Phip | Mm_Celera | 9:82910435 | AGATGTAAAAGTTAG[G/T]TGACAAGAAAGGAAA | 83946 |
rs224864859 | in-del | -/AAATA | | | intron-variant | Phip | Mm_Celera | 9:82901056 | TGGAAAAATAAACTT[-/AAATA]AAGAACTTAAGTAAA | 83946 |
rs224866625 | in-del | -/C | | | intron-variant | Phip | Mm_Celera | 9:82893962 | TTTTTCTTTTTTTTT[-/C]CCCTCTGTGTAGCCC | 83946 |
rs224923592 | in-del | -/A | | | intron-variant | Phip | Mm_Celera | 9:82937656 | TTAATATTTTTTTTT[-/A]AATTCTAAACTCTTA | 83946 |
rs224965003 | snp | A/T | | | intron-variant | Phip | Mm_Celera | 9:82902313 | GTTCTACTTCCCAAG[A/T]ACTAGATCAACCTAT | 83946 |
rs225017177 | snp | A/T | | | intron-variant | Phip | Mm_Celera | 9:82910652 | ATTTTACCATAAGGA[A/T]ACACATGATAAAGTT | 83946 |
rs225032601 | in-del | -/AAA | | | intron-variant | Phip | Mm_Celera | 9:82923308 | CAACTTTTCCCAGGG[-/AAA]AAAAAAAAACTTTAA | 83946 |
rs225092973 | snp | C/T | | | intron-variant | Phip | Mm_Celera | 9:82952026 | GGTGCAGAACCAGCC[C/T]GAGAGAAAAGTATGT | 83946 |
rs225101729 | snp | C/T | | | intron-variant | Phip | Mm_Celera | 9:82901426 | GACCAAGGACCTCTC[C/T]TCCCACTGATGACAG | 83946 |
rs225120629 | snp | A/G | | | intron-variant | Phip | Mm_Celera | 9:82940353 | TCCTATAACCATTAC[A/G]TACTTACATGCTTTG | 83946 |
rs225133656 | snp | A/C | | | intron-variant | Phip | Mm_Celera | 9:82950488 | CTGTGTGGGCCATGT[A/C]CATGCTGCTTCAGTC | 83946 |
rs225134201 | snp | C/T | | | intron-variant | Phip | Mm_Celera | 9:82902862 | TCTTTACTTTTACAA[C/T]CTGATGCTTACACAT | 83946 |
rs225135808 | snp | A/G | | | intron-variant | Phip | Mm_Celera | 9:82912729 | AACATTTGATTCTTC[A/G]GTTTTATAGGACCCT | 83946 |
rs225160576 | snp | C/T | | | intron-variant | Phip | Mm_Celera | 9:82953101 | ATTTTAACTAAACAG[C/T]AAAGATATCCCAGTT | 83946 |
rs225167580 | snp | C/T | | | intron-variant | Phip | Mm_Celera | 9:82939622 | GCTACCTTTGCAATA[C/T]TAGAAATTAGAAATC | 83946 |
rs225179611 | in-del | -/CT | | | intron-variant | Phip | Mm_Celera | 9:82911347 | GGCTATGCAGAGAAA[-/CT]CTGTTTCAAACCTCT | 83946 |
rs225215034 | snp | C/T | | | intron-variant | Phip | Mm_Celera | 9:82937708 | ATATTCTTCCCTTGT[C/T]ATTATCCTTTCCCTT | 83946 |
rs225220429 | snp | G/T | | | utr-variant-3-prime | Phip | Mm_Celera | 9:82867957 | CACTGTCCTACGTAA[G/T]TCATTTTCAAGTGAA | 83946 |
rs225222803 | snp | A/G | | | intron-variant | Phip | Mm_Celera | 9:82955188 | GGACACCATGTCTCA[A/G]AAACAAAAGCAACAA | 83946 |
rs225263145 | snp | A/C | | | intron-variant | Phip | GRCm38.p3 | 9:82903673 | CAGGATCTTAAAATT[A/C]GGTACATTTATATTT | 83946 |
rs225280702 | snp | G/T | | | intron-variant | Phip | Mm_Celera | 9:82880040 | TAGGTAATAAAAACA[G/T]GAATGAACTAATGAG | 83946 |
rs225359015 | snp | A/G | | | intron-variant | Phip | Mm_Celera | 9:82880373 | GGGCAAGGCATGCAT[A/G]CTCACACCCATATGT | 83946 |
rs225378073 | snp | A/T | | | intron-variant | Phip | Mm_Celera | 9:82956284 | ATCAAATAAAGAAAA[A/T]TTTGGAACATATAGC | 83946 |
rs225378469 | snp | C/G | | | intron-variant | Phip | GRCm38.p3 | 9:82938800 | TTCCTAGTATAAGCT[C/G]AATCATTGTACAATA | 83946 |
rs225380853 | snp | G/T | | | intron-variant | Phip | Mm_Celera | 9:82947991 | TCCCCTCACATTTGT[G/T]TTATTATACTGTTAC | 83946 |
rs225402430 | in-del | -/G | | | intron-variant | Phip | Mm_Celera | 9:82943295 | ATAAACAAGAGTTTA[-/G]CTGGAGGTTGAAATA | 83946 |
rs225409987 | snp | A/T | | | intron-variant | Phip | Mm_Celera | 9:82877865 | GGTGGGAGAAGAGCT[A/T]CTGCTCACTCCAGGG | 83946 |
rs225435216 | snp | C/T | | | intron-variant | Phip | Mm_Celera | 9:82879295 | ACCTGTCCCCATCCT[C/T]CCTCTGTTTCTCTTC | 83946 |
rs225458840 | snp | A/G | | | utr-variant-3-prime | Phip | Mm_Celera | 9:82868088 | CACCAACCTTTAGTT[A/G]TAGTGAAACACTGCA | 83946 |
rs225469047 | snp | G/T | | | intron-variant | Phip | GRCm38.p3 | 9:82950899 | TGTGTCACTGGGGGT[G/T]GGCTTTGAAATATCA | 83946 |
rs225486430 | in-del | -/G | | | intron-variant | Phip | Mm_Celera | 9:82912538 | GTTCTTAATGCCTGT[-/G]ACTATGCTAAGAAAT | 83946 |
rs225496813 | snp | C/T | | | intron-variant | Phip | Mm_Celera | 9:82881611 | TACATGTAAATCTTA[C/T]TTAGAACTCTATAAT | 83946 |
rs225552353 | in-del | -/G | | | intron-variant | Phip | Mm_Celera | 9:82945932 | CGCTACCAAGAAAAT[-/G]GGGGAATATAAATGG | 83946 |
rs225565061 | snp | A/T | | | intron-variant | Phip | GRCm38.p3 | 9:82919300 | GTACTTAGGAAAGCC[A/T]CTTCGGTGCATAAAG | 83946 |
rs225618685 | snp | C/T | | | utr-variant-3-prime | Phip | Mm_Celera | 9:82869407 | TACTTTTCATTCTTC[C/T]TCAAGACTGACAGTT | 83946 |
rs225623224 | snp | A/G | | | intron-variant | Phip | Mm_Celera | 9:82872296 | ATTCTAACATGTTAG[A/G]AGTTTCGTTTGGATC | 83946 |
rs225640143 | in-del | -/AA | | | intron-variant | Phip | Mm_Celera | 9:82951474 | ACACATATCTGTAAT[-/AA]AAAAAAAAAAGCTAT | 83946 |
rs225674769 | in-del | -/TGTAGCA | | | intron-variant | Phip, LOC105243467 | Mm_Celera | 9:82964245 | AGGGCCTTAACACTT[-/TGTAGCA]TGTACATATTTTACC | 83946 |
rs225689227 | snp | G/T | | | missense | Phip | Mm_Celera | 9:82871521 | TTCTGAATCTAGGTT[G/T]TGAGTTTTCATCTTC | 83946 |
rs225699768 | snp | C/T | | | intron-variant | Phip | Mm_Celera | 9:82910136 | CATTCATAAACCTTA[C/T]GGTAAACAAATTATG | 83946 |
rs225707344 | snp | A/G | | | intron-variant | Phip | Mm_Celera | 9:82908993 | TTCCACATAAATCAA[A/G]TAATTCAATTATCAT | 83946 |
rs225710105 | snp | A/C | | | intron-variant | Phip | Mm_Celera | 9:82873366 | CGGGAAACAGAATCC[A/C]AGTCACATTAAAAGG | 83946 |
rs225711575 | snp | A/G | | | intron-variant | Phip | Mm_Celera | 9:82920187 | TCCAAATGCTGGCTG[A/G]ACATTTCCATAGCAA | 83946 |
rs225723905 | snp | A/G | | | intron-variant | Phip | Mm_Celera | 9:82907388 | GAGCCTTAAAGTAAA[A/G]CCACCAATTACTGAA | 83946 |
rs225734160 | snp | A/G | | | intron-variant | Phip | Mm_Celera | 9:82917571 | CAGAGGGAGAAGTGT[A/G]TTACAGTCAGCAAAC | 83946 |
rs225805440 | in-del | -/T | | | intron-variant | Phip | Mm_Celera | 9:82931427 | AATCTGTGATAACTA[-/T]TATTTAAAATCCTAC | 83946 |
rs225812372 | snp | G/T | | | intron-variant | Phip | Mm_Celera | 9:82950515 | AGTCTCTATGAGTTC[G/T]TATGAGCTTAAGCAA | 83946 |
rs225819409 | in-del | -/A | | | intron-variant | Phip | Mm_Celera | 9:82949586 | AATTCTTCTGAAAAT[-/A]AACCAGTAATAAACT | 83946 |
rs225849188 | snp | A/G | | | intron-variant | Phip | Mm_Celera | 9:82949863 | TAATTTCTGTACCAG[A/G]ATGACAAAACTTTCC | 83946 |
rs225874677 | snp | A/T | | | intron-variant | Phip | Mm_Celera | 9:82878412 | CATAAAGAGACTTTA[A/T]AATTTCACTTTCTAC | 83946 |
rs225937614 | snp | A/G | | | intron-variant | Phip | GRCm38.p3 | 9:82877663 | GACAAAACACCAAAC[A/G]TAAGACCAAAGTATT | 83946 |
rs225940185 | snp | A/G | | | intron-variant | Phip | GRCm38.p3 | 9:82915113 | GCCTGCCTGCCATGA[A/G]TGCTGAAAACCAAAC | 83946 |
rs225972824 | snp | A/T | | | intron-variant | Phip | Mm_Celera | 9:82949388 | TAAACCCACATTTTT[A/T]AATATACCATACTTA | 83946 |
rs226079424 | snp | A/C | | | intron-variant | Phip | Mm_Celera | 9:82888778 | CCTAGAGGCAGATTT[A/C]CAGATGGTTCTGAGT | 83946 |
rs226139645 | snp | A/G | | | intron-variant | Phip | Mm_Celera | 9:82968595 | CAACGTTAATTCTCA[A/G]TCTCTCTCTATCAGA | 83946 |
rs226176089 | snp | C/T | | | intron-variant | Phip | Mm_Celera | 9:82959336 | TAATTTACAGCTGTA[C/T]ATTATGGTTTTATTA | 83946 |
rs226227179 | in-del | -/AA | | | intron-variant | Phip | Mm_Celera | 9:82909140 | ATGAAATCATTACTT[-/AA]AAAAAAAAAAAAAAA | 83946 |
rs226278115 | in-del | -/CAAAAAAAAAAAAAAAA | | | intron-variant | Phip | Mm_Celera | 9:82935482 | AAGGAAATTTGAAAG[-/CAAAAAAAAAAAAAAAA]AAAAAAAAAAAATCA | 83946 |
rs226329142 | snp | A/C | | | intron-variant | Phip | Mm_Celera | 9:82946934 | ATTTCAAAGTAAAAT[A/C]GTCTTATGCTTTTAT | 83946 |
rs226334127 | snp | G/T | | | intron-variant | Phip | Mm_Celera | 9:82912364 | AAGTCTTTCCTTAAT[G/T]TTCTGTGCCTAAAAC | 83946 |
rs226347405 | snp | A/G | | | intron-variant | Phip | Mm_Celera | 9:82906432 | GGAAAATAAGTCTTA[A/G]AATGTACAACTAGTG | 83946 |
rs226361195 | snp | C/T | | | intron-variant | Phip | Mm_Celera | 9:82916889 | ACAAATGTCAGGATT[C/T]CCATCTTAAATGTTC | 83946 |
rs226365461 | snp | C/G | | | intron-variant | Phip | Mm_Celera | 9:82958435 | GCCGGCATGACCATG[C/G]TTCCATGAGGAGAAC | 83946 |
rs226398635 | snp | C/T | | | intron-variant | Phip | Mm_Celera | 9:82914247 | AAGTTTCAATGTAAA[C/T]GTTAAGTAAAATTAC | 83946 |
rs226421145 | snp | C/T | | | intron-variant, nc-transcript-variant | Phip, LOC105243467 | Mm_Celera | 9:82960209 | ACTGTATACCTGGGA[C/T]CTGGTAGTTCACACT | 83946 |
rs226452521 | in-del | -/A/TT | | | intron-variant | Phip | GRCm38.p3 | 9:82894779 | TTCATATATATATAT[-/A/TT]TTTTTTTATGTAGCT | 83946 |
rs226517465 | snp | A/T | | | intron-variant | Phip | Mm_Celera | 9:82885106 | ACTTAGTTTTTTATT[A/T]AGAGAAAACTATATA | 83946 |
rs226532589 | snp | A/G | | | intron-variant | Phip | Mm_Celera | 9:82956738 | AAAAACTCCAAACAC[A/G]CAAAATATAAAACAA | 83946 |
rs226574374 | snp | C/T | | | intron-variant | Phip | Mm_Celera | 9:82884098 | CCTACCTGTAGATCC[C/T]GCACCCCTAAATGGA | 83946 |
rs226578604 | snp | C/T | | | intron-variant | Phip, LOC105243467 | Mm_Celera | 9:82961144 | TATTGTTTTTAGAGA[C/T]AGGGTTTCTCCACTT | 83946 |
rs226611802 | in-del | -/CA | | | intron-variant | Phip | Mm_Celera | 9:82925527 | ACAAGCATTTAATCT[-/CA]CAAATGCCTTCAGGA | 83946 |
rs226613890 | in-del | -/TATT | | | intron-variant | Phip | Mm_Celera | 9:82904471 | TTTTTTCTTTATTAC[-/TATT]TGTTTGTTTGTTTAT | 83946 |
rs226636570 | snp | C/T | | | intron-variant | Phip | Mm_Celera | 9:82875155 | TATTACAAGTAACAT[C/T]TTTTACTTTCACCTT | 83946 |
rs226662622 | snp | A/G | | | intron-variant | Phip | Mm_Celera | 9:82905953 | GTCATCTGGAAACTG[A/G]ACATAGTGGCTCACT | 83946 |
rs226675361 | snp | A/G | | | intron-variant | Phip | Mm_Celera | 9:82958007 | ACTCTAAAAGCACTG[A/G]ATTCCCTATGAAAAT | 83946 |
rs226676582 | in-del | -/GA | | | intron-variant | Phip | Mm_Celera | 9:82901137 | AAGAAATGAGGAACG[-/GA]GTATCACCTTATCAG | 83946 |
rs226680578 | in-del | -/ACACT | | | intron-variant | Phip | Mm_Celera | 9:82925574 | GGCCTCAAAAATCAA[-/ACACT]ACACTACAGGCCTTG | 83946 |
rs226689471 | snp | A/T | | | intron-variant | Phip | Mm_Celera | 9:82886466 | GAAATGCAGAGTACA[A/T]GGGCCTACTCCAACT | 83946 |
rs226715462 | snp | A/C/G | | | intron-variant | Phip | GRCm38.p3 | 9:82944860 | GTGATCCCCCCATGA[A/C/G]CCTAGGTTAGTTGAT | 83946 |
rs226742016 | in-del | -/G | | | intron-variant | Phip | Mm_Celera | 9:82927343 | TACGGCATGGAGTCA[-/G]AAAATCCAAGATTTC | 83946 |
rs226756196 | in-del | -/A | | | intron-variant | Phip | Mm_Celera | 9:82925250 | GAAGATAGAAAAGAG[-/A]AAAAGAAAAAAAAAC | 83946 |
rs226772302 | in-del | -/AAACAAAC | | | intron-variant | Phip | Mm_Celera | 9:82873476 | TAATAAATCTATGAA[-/AAACAAAC]AAACAAACAAACAAA | 83946 |
rs226807138 | snp | A/G | | | intron-variant | Phip | Mm_Celera | 9:82877149 | GCCTTTAGCGACTTG[A/G]CATGCTTGTAACAAA | 83946 |
rs226821064 | snp | A/G | | | intron-variant | Phip | Mm_Celera | 9:82914366 | TGAATATAGAATCCC[A/G]AGCATTCCAAACATG | 83946 |
rs226830256 | snp | A/G | | | intron-variant | Phip | Mm_Celera | 9:82924968 | AGGACCAGAATATCA[A/G]TAAAGCTAAACATGC | 83946 |
rs226869709 | snp | C/G | | | intron-variant | Phip | Mm_Celera | 9:82882900 | GACTTAGTTTCTTCT[C/G]AATTCATCAGCATCT | 83946 |
rs226882335 | snp | G/T | | | intron-variant | Phip | GRCm38.p3 | 9:82892041 | GCTGCTTTTATTTTA[G/T]ATTGTTTCTATCTTG | 83946 |
rs226890684 | snp | C/G | | | intron-variant | Phip | Mm_Celera | 9:82875666 | CTCACACTTGACAAG[C/G]CCAGGAATCAACCTT | 83946 |
rs226905915 | in-del | -/AGAGGC | | | intron-variant, upstream-variant-2KB | Phip, LOC105243467 | Mm_Celera | 9:82967902 | AGGAGAGGCAGAGGC[-/AGAGGC]AGGTGGATTTCTGAG | 83946 |
rs226959954 | snp | A/G | | | intron-variant | Phip | GRCm38.p3 | 9:82954173 | ATAATCTGTAACTAG[A/G]TTTCATTTTAATCTC | 83946 |
rs226966045 | snp | A/G | | | intron-variant | Phip | Mm_Celera | 9:82874213 | CCAAATGGAATAGAG[A/G]CATGCCCCTTAGTAC | 83946 |
rs227008897 | snp | A/T | | | intron-variant | Phip | Mm_Celera | 9:82955981 | TGGTAAAAAGCTTAG[A/T]TATTTTAATTAAAAT | 83946 |
rs227044184 | snp | C/T | | | intron-variant | Phip | Mm_Celera | 9:82885033 | CATCTGACATTTAAG[C/T]TTCATTCTTAAAACA | 83946 |
rs227048594 | snp | C/T | | | intron-variant | Phip | Mm_Celera | 9:82954993 | ATACAAAGTACACAT[C/T]TTAAAGAATATGAAA | 83946 |
rs227137201 | snp | A/G | | | intron-variant | Phip | Mm_Celera | 9:82893723 | AGCGGTAGATGCCTC[A/G]CGTCTCTTCTCCATC | 83946 |
rs227148228 | snp | A/G | | | intron-variant | Phip | Mm_Celera | 9:82923040 | CTGAGAATTCAGTTA[A/G]AAAATTTAAATGGAA | 83946 |
rs227164328 | snp | A/G | | | upstream-variant-2KB | Phip | Mm_Celera | 9:82976714 | AACAAAAATCTTTTC[A/G]TAAATCCTAATGTAA | 83946 |
rs227197222 | snp | A/G | | | intron-variant | Phip | Mm_Celera | 9:82892971 | GTTATGAATAATAAA[A/G]TAATTTTAATGTTAG | 83946 |
rs227203366 | snp | A/G | | | intron-variant | Phip | Mm_Celera | 9:82875545 | GCCAAGGATCGCTAC[A/G]AACCCGGGCTGCTTC | 83946 |
rs227215420 | snp | C/T | | | intron-variant | Phip | Mm_Celera | 9:82952717 | TGCTTTCTCTTGTCA[C/T]AAGAGTTGTCTTAGT | 83946 |
rs227216799 | snp | A/C | | | intron-variant | Phip | GRCm38.p3 | 9:82920966 | GATGTTTTATAATCA[A/C]AAAATAAACAACCAA | 83946 |
rs227220775 | snp | A/T | | | intron-variant | Phip | Mm_Celera | 9:82882173 | CCTTATATTTATTTC[A/T]TAGTCCCTTCCCTTT | 83946 |
rs227230498 | snp | G/T | | | intron-variant | Phip | Mm_Celera | 9:82905248 | CTGCATTTAATTAAT[G/T]TGTCACTATTAAACA | 83946 |
rs227236709 | in-del | -/A | | | intron-variant | Phip | Mm_Celera | 9:82933516 | ATTATGACAACAGCT[-/A]AAAAAATCACTATTC | 83946 |
rs227250253 | snp | A/G | | | intron-variant | Phip | Mm_Celera | 9:82973514 | GCCCTGAAAGCACTA[A/G]TAATCACAACTACCT | 83946 |
rs227270166 | in-del | -/AC | | | intron-variant | Phip | Mm_Celera | 9:82882560 | CAGACAGACAGACAG[-/AC]ACACACATACACATA | 83946 |
rs227273010 | snp | C/G | | | intron-variant | Phip, LOC105243467 | Mm_Celera | 9:82964161 | CTTCCAAGAGCTGTT[C/G]AAACCACCTCAGCCT | 83946 |
rs227302172 | snp | C/G | | | intron-variant | Phip | GRCm38.p3 | 9:82892545 | AGCCATCTCTCCAGC[C/G]CCATCTTTTGTTTCT | 83946 |
rs227329464 | in-del | -/AC | | | intron-variant | Phip | Mm_Celera | 9:82879541 | TTTTTAGTCAATTTG[-/AC]ACAAGAGAGTTATCT | 83946 |
rs227348094 | in-del | -/TC | | | intron-variant | Phip | Mm_Celera | 9:82973648 | ACAACTGTATCAACT[-/TC]TCTCTTAGGCAAAGA | 83946 |
rs227349083 | in-del | -/AC | | | intron-variant | Phip | Mm_Celera | 9:82916268 | ATTAGCAGAATCGGA[-/AC]ACACACACATTATCA | 83946 |
rs227378472 | snp | C/G | | | intron-variant | Phip | Mm_Celera | 9:82920388 | CAAGTGTTACATATA[C/G]GTTTTTTCACTCATA | 83946 |
rs227398562 | snp | A/T | | | intron-variant | Phip, LOC105243467 | Mm_Celera | 9:82961991 | CTAATATATTAAATG[A/T]TAATGGCAAACACCA | 83946 |
rs227399983 | snp | A/G | | | upstream-variant-2KB | Phip | Mm_Celera | 9:82975706 | GGGCGCTTTCTCTAA[A/G]GAGGCCGCGGGCGGG | 83946 |
rs227427897 | in-del | -/TTTC | | | intron-variant | Phip | Mm_Celera | 9:82888887 | CAGTTCCCCTTTCTG[-/TTTC]TTTCTTTGTTTTGTT | 83946 |
rs227455154 | snp | C/T | | | intron-variant | Phip, LOC105243467 | Mm_Celera | 9:82963346 | TTATAATCTCAACAC[C/T]GAGAACAGGGATAGA | 83946 |
rs227502251 | in-del | -/AAG | | | intron-variant | Phip | Mm_Celera | 9:82970466 | AATCTTCATCTTTAC[-/AAG]AAGTATTATAAAAAC | 83946 |
rs227510530 | snp | C/T | | | intron-variant | Phip, LOC105243467 | Mm_Celera | 9:82961355 | TATAAGTTTCCACAT[C/T]ATTTGAAATCATAAT | 83946 |
rs227612604 | snp | C/T | | | intron-variant | Phip | Mm_Celera | 9:82911801 | AGAAATCTAAAATGA[C/T]GACGATGCTGAGAAG | 83946 |
rs227617578 | snp | G/T | | | intron-variant | Phip, LOC105243467 | GRCm38.p3 | 9:82964853 | AGAGTAAAAAATGCT[G/T]TTTTAGACATGTAAA | 83946 |
rs227625861 | snp | A/T | | | intron-variant | Phip | Mm_Celera | 9:82922344 | CTGGGAATGACGTAA[A/T]GTCATAAATTTTAGT | 83946 |
rs227669024 | snp | C/T | | | intron-variant | Phip | Mm_Celera | 9:82888651 | AGATCAAGAGCACTT[C/T]TTACATTACATATTT | 83946 |
rs227698424 | snp | A/G | | | intron-variant | Phip | Mm_Celera | 9:82917931 | GGAATGAGGTAACCT[A/G]AATCAGAATGAAACC | 83946 |
rs227750081 | snp | C/T | | | intron-variant | Phip | Mm_Celera | 9:82889484 | ACTTCCAGTTAGAAG[C/T]TATAGCCCTTAAAGA | 83946 |
rs227766581 | snp | A/T | | | intron-variant | Phip, LOC105243467 | Mm_Celera | 9:82965599 | CAGTTGTAATCATTC[A/T]GATGTTTCCACTGCT | 83946 |
rs227769763 | snp | A/G | | | upstream-variant-2KB | Phip | Mm_Celera | 9:82977340 | TGCCCCTAAACTGGT[A/G]TGGCTAGCCTCAGAA | 83946 |
rs227772484 | snp | C/T | | | intron-variant | Phip | Mm_Celera | 9:82970172 | TTCAAAGTACCCTCA[C/T]ACAGACCGGAAATTC | 83946 |
rs227794793 | snp | C/G | | | intron-variant | Phip | Mm_Celera | 9:82927665 | TAACATGCATAAAAG[C/G]TTGGGACAGAATCCC | 83946 |
rs227804201 | in-del | -/A | | | intron-variant | Phip | Mm_Celera | 9:82895982 | TCAGGTTACTACTTG[-/A]AAAAAATCTTAAACT | 83946 |
rs227861682 | in-del | -/T | | | intron-variant | Phip, LOC105243467 | Mm_Celera | 9:82961062 | TAAAAACAATTAGTA[-/T]TTTTAGGGTCTCATT | 83946 |
rs227872678 | snp | A/T | | | intron-variant | Phip | Mm_Celera | 9:82891287 | TTTTAACAGATAAGT[A/T]AAGATTAATGAATTA | 83946 |
rs227903645 | snp | G/T | | | intron-variant | Phip | Mm_Celera | 9:82918994 | TGGATTTGATTTATA[G/T]CAAAAGAACCAAAAT | 83946 |
rs227904446 | in-del | -/TTTA | | | intron-variant | Phip | Mm_Celera | 9:82924621 | ATCAAGAATAATTGT[-/TTTA]TTTATTTGTTTTTCT | 83946 |
rs227904745 | snp | A/C | | | intron-variant | Phip | Mm_Celera | 9:82887813 | ACGCATCTCAAAAAG[A/C]ATATTATTTAAAACT | 83946 |
rs227914053 | snp | G/T | | | intron-variant, utr-variant-5-prime | Phip | GRCm38.p3 | 9:82928718 | GGAAGAAGACTATAT[G/T]CTGTGTCAAGAATAT | 83946 |
rs227915087 | snp | G/T | | | intron-variant | Phip | GRCm38.p3 | 9:82918017 | TGTCTCCCTCTGCCT[G/T]GTGCTTGTGGATCCT | 83946 |
rs227953040 | snp | C/T | | | intron-variant | Phip | GRCm38.p3 | 9:82959163 | TTGTTCTCTTTGAAA[C/T]TTTAAAATACGCCAC | 83946 |
rs227971287 | snp | A/C | | | intron-variant | Phip, LOC105243467 | Mm_Celera | 9:82961863 | GAGTTCCAGGACAGC[A/C]AGGGCTACACAGAGA | 83946 |
rs227983199 | snp | C/T | | | intron-variant | Phip | Mm_Celera | 9:82881423 | CTAGACCTTATCACT[C/T]GGTAGTTTTTCCTCT | 83946 |
rs228011441 | in-del | -/G | | | intron-variant | Phip | Mm_Celera | 9:82901556 | GGGGGGAAGAGGGAT[-/G]GGGGGGATGGTTGAT | 83946 |
rs228042164 | snp | C/T | | | intron-variant | Phip | Mm_Celera | 9:82880862 | ATTAAACTCAGGCCC[C/T]GAGGCCTGCAGAGGA | 83946 |
rs228043116 | snp | A/T | | | intron-variant | Phip | Mm_Celera | 9:82891925 | AATGTACTGATGTTT[A/T]TTCACTCAAAATGAA | 83946 |
rs228059407 | snp | A/G | | | intron-variant | Phip | GRCm38.p3 | 9:82880782 | AGCAAGCCTCAAGGA[A/G]CCTCCTGCCTTCGCT | 83946 |
rs228071579 | snp | C/G | | | intron-variant, upstream-variant-2KB | Phip | Mm_Celera | 9:82929710 | TCACAGGTGTTTACT[C/G]TCCTTTACCCTGAAG | 83946 |
rs228111699 | snp | C/G | | | intron-variant | Phip | Mm_Celera | 9:82917030 | AGATGTTTTAGTCCT[C/G]AGTTCACTCAAAATT | 83946 |
rs228115282 | snp | A/T | | | intron-variant | Phip, LOC105243467 | Mm_Celera | 9:82961126 | TGCTATACTAACTTT[A/T]GTTATTGTTTTTAGA | 83946 |
rs228158175 | snp | A/G | | | intron-variant | Phip | Mm_Celera | 9:82891182 | GTTGTAACTGAATAT[A/G]TTAGTTGGTTTTCAA | 83946 |
rs228204936 | snp | A/G | | | intron-variant | Phip | Mm_Celera | 9:82950711 | TAACTTTTGATTTAC[A/G]TTCCATGGCTAGGCT | 83946 |
rs228251965 | snp | C/T | | | upstream-variant-2KB | Phip | Mm_Celera | 9:82977642 | TCTAATTCTTCCTCT[C/T]AGATGTTTTGCCCTT | 83946 |
rs228262712 | snp | C/T | | | intron-variant | Phip | Mm_Celera | 9:82971100 | AAGCTAATTGTCACC[C/T]GGCTTCAAGACAACA | 83946 |
rs228322655 | snp | C/G | | | intron-variant | Phip | Mm_Celera | 9:82897403 | CTTGAGAACACAGGA[C/G]AAACAAAAGACTTTG | 83946 |
rs228352159 | snp | A/G | | | intron-variant | Phip | GRCm38.p3 | 9:82934144 | ACTAATATAGAATAT[A/G]AAATAATTGTATGAA | 83946 |
rs228352352 | snp | A/G | | | intron-variant | Phip | Mm_Celera | 9:82925086 | TAAAAACTACTCCTC[A/G]TTTCTACAGCAGTGT | 83946 |
rs228377054 | snp | G/T | | | intron-variant | Phip | Mm_Celera | 9:82888605 | CTTCCTATTTAATAT[G/T]TATAATTACCATATG | 83946 |
rs228413337 | snp | A/G | | | intron-variant | Phip | Mm_Celera | 9:82896875 | GAGTACTGCAAACAG[A/G]TTTTTTACTTTTTAA | 83946 |
rs228464379 | snp | A/G | | | intron-variant | Phip | GRCm38.p3 | 9:82970419 | TTATTCAACAATACA[A/G]AGGTATTCTACAATG | 83946 |
rs228478797 | in-del | -/TA | | | utr-variant-3-prime | Phip | Mm_Celera | 9:82870137 | TTAAGAATGCGTTTG[-/TA]TATATATATATTCAA | 83946 |
rs228511314 | snp | A/T | | | intron-variant, upstream-variant-2KB | Phip, LOC105243467 | Mm_Celera | 9:82967220 | ATCTATCTCCTCCCT[A/T]CCCATGCCAGAAACC | 83946 |
rs228512064 | snp | A/G | | | intron-variant | Phip | Mm_Celera | 9:82933101 | ACATTGATAGAATTA[A/G]TCCCATAAGTAATAA | 83946 |
rs228536849 | snp | A/C | | | intron-variant, downstream-variant-500B | Phip, LOC105243467 | Mm_Celera | 9:82959652 | CAAAAATAACACACA[A/C]AAAAAGTGAGAAGAA | 83946 |