SNP - dbSNP |
dbSNP | Type | Alleles | Het | Se(het) | Fxn-class | Gene Name | Assembly | Chr-pos | Sequence | Entrez Gene |
rs4187160 | snp | C/G | 0.444444 | 0.157135 | intron-variant | Cblb | Mm_Celera | 16:52063467 | TTATTTGATGCACTC[C/G]TGTGAATCAACTTTG | 208650 |
rs4187161 | snp | C/T | 0.48 | 0.0979796 | intron-variant | Cblb | Mm_Celera | 16:52080929 | ACACACACACACACA[C/T]ACACATACACACACA | 208650 |
rs4187162 | snp | C/T | 0.48 | 0.0979796 | intron-variant | Cblb | GRCm38.p3 | 16:52080935 | ACACACACACACACA[C/T]ACACACACACACACA | 208650 |
rs4187163 | snp | C/T | 0.444444 | 0.157135 | intron-variant | Cblb | Mm_Celera | 16:52103058 | GTAGTGAATCTGCTT[C/T]TCAGAGATGACTGCT | 208650 |
rs4187164 | snp | C/T | 0.32 | 0.24 | intron-variant | Cblb | Mm_Celera | 16:52146766 | GTTCAGACGTAGTTT[C/T]TACTTTAAACTCACT | 208650 |
rs4187165 | snp | A/G | 0.255 | 0.24995 | intron-variant | Cblb | Mm_Celera | 16:52159130 | GCTTAGTGTCTGTGC[A/G]TCTGGCACTCTTCCC | 208650 |
rs4231217 | snp | A/T | 0.244898 | 0.249948 | utr-variant-3-prime | Cblb | Mm_Celera | 16:52207788 | GGTATATTTTAAATA[A/T]TGATGCAGGTACTTT | 208650 |
rs4231218 | snp | A/T | 0.244898 | 0.249948 | utr-variant-3-prime | Cblb | Mm_Celera | 16:52207974 | TTTATTCTTTTTTCA[A/T]TTCTGGATATGTAAC | 208650 |
rs4231219 | snp | A/G | 0.244898 | 0.249948 | downstream-variant-500B | Cblb | Mm_Celera | 16:52208131 | TTCCATAGGATTATG[A/G]AAATGGCACTAGAAA | 208650 |
rs6157995 | snp | C/T | 0.207612 | 0.24638 | intron-variant | Cblb | Mm_Celera | 16:52085669 | GGAGTAAAAGTGGAC[C/T]ACAGCTCTCTTGTGT | 208650 |
rs6162069 | snp | A/C | 0.5 | 0 | intron-variant | Cblb | GRCm38.p3 | 16:52086389 | CAAATTTGACTTTAC[A/C]CATTAATGAATGATG | 208650 |
rs6162462 | snp | C/G | 0.5 | 0 | intron-variant | Cblb | GRCm38.p3 | 16:52086415 | TGATGTATGTCCAGG[C/G]TGCCGGTGCTCAGTG | 208650 |
rs6162534 | snp | C/T | 0.304688 | 0.243945 | intron-variant | Cblb | GRCm38.p3 | 16:52086459 | CATGTGGCTGCATCC[C/T]GACATACCATTAATG | 208650 |
rs6162565 | snp | A/G | 0.359862 | 0.224567 | intron-variant | Cblb | GRCm38.p3 | 16:52086484 | TTAATGCTGTACCTA[A/G]AGGGCCAGTTGCACA | 208650 |
rs6176773 | snp | A/G | 0.5 | 0 | intron-variant | Cblb | Mm_Celera | 16:52086746 | AAGTCTCCTAGAGAT[A/G]TATGGGATTTCTCTA | 208650 |
rs6222478 | snp | C/T | 0.359862 | 0.224567 | intron-variant | Cblb | Mm_Celera | 16:52101671 | TAAAAATGAAGGCCT[C/T]TAGATGAGCTAATGA | 208650 |
rs6223096 | snp | C/T | 0.359862 | 0.224567 | intron-variant | Cblb | Mm_Celera | 16:52101801 | AAATTGAAAATATGG[C/T]GGCAGCATTCTCCTT | 208650 |
rs6223132 | snp | C/T | 0.359862 | 0.224567 | intron-variant | Cblb | GRCm38.p3 | 16:52101828 | CCTTGCACTTTAGCA[C/T]GGTTTGTAAAGTTCA | 208650 |
rs6223620 | snp | A/C/G | 0.304688 | 0.243945 | intron-variant | Cblb | GRCm38.p3 | 16:52101874 | CTTCAGGGCAGACTT[A/C/G]TCTAGGTACCTCCTG | 208650 |
rs6223674 | snp | C/T | 0.359862 | 0.224567 | intron-variant | Cblb | GRCm38.p3 | 16:52101908 | ACAAGAAAATGTTAA[C/T]CCTCCCACTGCCTGT | 208650 |
rs6249508 | snp | C/T | 0.415225 | 0.187619 | intron-variant | Cblb | GRCm38.p3 | 16:52136475 | CGTCCAAGAAATCAT[C/T]CCTCACGGGCAAATA | 208650 |
rs6250033 | snp | A/C | 0.456747 | 0.140554 | intron-variant | Cblb | GRCm38.p3 | 16:52136584 | TCAATGACATCTAAG[A/C]AATAGTCAATAATAC | 208650 |
rs6264851 | snp | C/T | 0.5 | 0 | intron-variant | Cblb | Mm_Celera | 16:52137120 | CTTATGAACAGATAT[C/T]CACTNGCTTTGTAAA | 208650 |
rs6264856 | snp | C/T | 0.375 | 0.216506 | intron-variant | Cblb | Mm_Celera | 16:52137125 | GAACAGATATNCACT[C/T]GCTTTGTAAAATATC | 208650 |
rs6317860 | snp | G/T | 0.459184 | 0.136902 | intron-variant | Cblb | GRCm38.p3 | 16:52146393 | GGAAGATTTCTGAGT[G/T]TCGGAGCTCTGGGCT | 208650 |
rs6326302 | snp | C/T | 0.5 | 0 | intron-variant | Cblb | GRCm38.p3 | 16:52192017 | ATGCGCCCCAGGCTT[C/T]GCAGCCCTACCTCAC | 208650 |
rs6326402 | snp | A/G | 0.290657 | 0.246672 | intron-variant | Cblb | GRCm38.p3 | 16:52192079 | CAATATTAACATCTC[A/G]ATTCAATTTTAAGAT | 208650 |
rs6327458 | snp | A/G | 0.359862 | 0.224567 | intron-variant | Cblb | GRCm38.p3 | 16:52192272 | AAGGTTGACAGAGGA[A/G]TCACATAAGTGATGT | 208650 |
rs6327490 | snp | C/T | 0.5 | 0 | intron-variant | Cblb | GRCm38.p3 | 16:52192294 | AAGTGATGTCAACTG[C/T]GGTGTCCTTCCCGTG | 208650 |
rs6331206 | snp | A/G | 0.5 | 0 | intron-variant | Cblb | GRCm38.p3 | 16:52080220 | AATGGTGCATGGAGC[A/G]CTCATGACAACGGGA | 208650 |
rs6331258 | snp | A/G/T | 0.359862 | 0.224567 | intron-variant | Cblb | GRCm38.p3 | 16:52080251 | ATGGGAACTATGATC[A/G/T]CTGTCTTTATCCTTA | 208650 |
rs6331760 | snp | G/T | 0.5 | 0 | intron-variant | Cblb | GRCm38.p3 | 16:52080343 | TACACATGTTGGTTC[G/T]TAGAGGAACATGTCA | 208650 |
rs6332355 | snp | A/G | 0.5 | 0 | intron-variant | Cblb | GRCm38.p3 | 16:52080467 | TTTTTTTTTTAAAAA[A/G]AAAGACAaaacaaaa | 208650 |
rs6332387 | snp | A/C | 0.5 | 0 | intron-variant | Cblb | GRCm38.p3 | 16:52080484 | AAGACAaaacaaaac[A/C]aancaaacaaacaaa | 208650 |
rs6332391 | snp | A/C | 0.5 | 0 | intron-variant | Cblb | GRCm38.p3 | 16:52080487 | ACAaaacaaaacnaa[A/C]caaacaaacaaacaa | 208650 |
rs6332907 | snp | C/T | 0.290657 | 0.246672 | intron-variant | Cblb | GRCm38.p3 | 16:52080555 | AGCTCTAGCTGGCCT[C/T]TTATTTTTATTTAtg | 208650 |
rs6333328 | snp | A/G | 0.5 | 0 | intron-variant | Cblb | GRCm38.p3 | 16:52080598 | tgtttgtctgtgaat[A/G]tgtgtgtgtgtgtgt | 208650 |
rs6364053 | snp | A/G | 0.492188 | 0.0620098 | intron-variant | Cblb | GRCm38.p3 | 16:52161130 | CAGGATGGCCACACT[A/G]CTTCTCTCAGAGAAT | 208650 |
rs6364136 | snp | C/G | 0.290657 | 0.246672 | intron-variant | Cblb | GRCm38.p3 | 16:52161177 | CACATGTTTCATTTT[C/G]AGTTTCTTCCCAGTG | 208650 |
rs6364717 | snp | C/T | 0.290657 | 0.246672 | intron-variant | Cblb | GRCm38.p3 | 16:52161273 | TATGCTGCATTGGTT[C/T]TATACCATGTGCTTC | 208650 |
rs6365196 | snp | C/T | 0.290657 | 0.246672 | intron-variant | Cblb | GRCm38.p3 | 16:52161309 | ACCTTTTGCTTATTA[C/T]TGAAATGGGGCAGTG | 208650 |
rs6365258 | snp | A/G | 0.5 | 0 | intron-variant | Cblb | GRCm38.p3 | 16:52161344 | AGATAAGGAAGAATA[A/G]AGAACATTAACTNTC | 208650 |
rs6365275 | snp | A/G | 0.5 | 0 | intron-variant | Cblb | GRCm38.p3 | 16:52161357 | TANAGAACATTAACT[A/G]TCTGTGCCTAACCAT | 208650 |
rs6369065 | snp | C/T | 0.5 | 0 | intron-variant | Cblb | GRCm38.p3 | 16:52115712 | CAAACCAGAGCCCTG[C/T]TCTCTGCCTGNGTAG | 208650 |
rs6369080 | snp | C/T | 0.5 | 0 | intron-variant | Cblb | Mm_Celera | 16:52115723 | CCTGNTCTCTGCCTG[C/T]GTAGCAGCCATTAGC | 208650 |
rs6369663 | snp | C/T | 0.5 | 0 | intron-variant | Cblb | GRCm38.p3 | 16:52115848 | ATTTCAAAAGTTCAG[C/T]CTTATCTTTACTTCC | 208650 |
rs6370096 | snp | C/T | 0.5 | 0 | intron-variant | Cblb | GRCm38.p3 | 16:52115875 | TTCCTATTATTCTAT[C/T]CACCAGGAGATAATA | 208650 |
rs6370147 | snp | A/G | 0.5 | 0 | intron-variant | Cblb | GRCm38.p3 | 16:52115909 | ATATGTAGTAAAAGA[A/G]CATTATTGAAGAAAT | 208650 |
rs6370188 | snp | A/G | 0.5 | 0 | intron-variant | Cblb | Mm_Celera | 16:52115940 | CTGTCAAAGTAAGTT[A/G]TACAAATCTTCANAT | 208650 |
rs6370593 | snp | A/T | 0.5 | 0 | intron-variant | Cblb | GRCm38.p3 | 16:52115953 | TTNTACAAATCTTCA[A/T]ATTTTGTAATAATGT | 208650 |
rs6373093 | snp | A/G | 0.5 | 0 | intron-variant | Cblb | GRCm38.p3 | 16:52037101 | ATCTCTAAATTGCCC[A/G]AGAACTCTCTCTTGT | 208650 |
rs6373156 | snp | A/G | 0.5 | 0 | intron-variant | Cblb | GRCm38.p3 | 16:52037145 | GGCTTTGAACTTATG[A/G]CCCTCNTCAGACTCC | 208650 |
rs6373157 | snp | C/G | 0.5 | 0 | intron-variant | Cblb | GRCm38.p3 | 16:52037151 | GAACTTATGNCCCTC[C/G]TCAGACTCCATAGTA | 208650 |
rs6373665 | snp | A/G | 0.5 | 0 | intron-variant | Cblb | GRCm38.p3 | 16:52037241 | CTGTCAGCTTTCCAG[A/G]GCATTAATAAAGGGA | 208650 |
rs6374749 | snp | A/C | 0.5 | 0 | intron-variant | Cblb | Mm_Celera | 16:52037418 | AATTTGTGCTGACAC[A/C]ATTGGCTTGATTCTA | 208650 |
rs6374787 | snp | A/G | 0.5 | 0 | intron-variant | Cblb | GRCm38.p3 | 16:52037442 | GATTCTAAAGTTTGC[A/G]ACTAGTGACACCTGG | 208650 |
rs6378148 | snp | A/C | 0.5 | 0 | intron-variant | Cblb | GRCm38.p3 | 16:52161427 | CATTGTGTGTAACTT[A/C]TGAATAATACTNTAT | 208650 |
rs6378168 | snp | C/T | 0.304688 | 0.243945 | intron-variant | Cblb | GRCm38.p3 | 16:52161439 | CTTNTGAATAATACT[C/T]TATACTAGCTATTTT | 208650 |
rs6403775 | snp | C/T | 0.290657 | 0.246672 | intron-variant | Cblb | GRCm38.p3 | 16:52085130 | ACCACATTTGAAGTG[C/T]AGCGTCTCACATGTG | 208650 |
rs32629994 | snp | C/G | 0 | 0 | intron-variant | Cblb | Mm_Celera | 16:52142914 | GTACTGCCTTGTTGT[C/G]TGTCCCGTTCACACT | 208650 |
rs45653952 | snp | A/C | 0.142012 | 0.225474 | intron-variant | Cblb | Mm_Celera | 16:52132101 | CATCCTTATAAAGTG[A/C]TTACAATCCTAGTTA | 208650 |
rs45655321 | snp | A/G | 0.35503 | 0.226867 | intron-variant | Cblb | GRCm38.p3 | 16:52132642 | GTAGTTATCATTTAC[A/G]ACCTAAAGCTCCTGA | 208650 |
rs45668333 | snp | A/C | 0.244898 | 0.249948 | intron-variant | Cblb | GRCm38.p3 | 16:52198134 | AAGTTAGGACATAAT[A/C]AAAAATAACAGCTTT | 208650 |
rs45672619 | snp | C/T | 0.132653 | 0.220748 | intron-variant | Cblb | Mm_Celera | 16:52197102 | TTGAACAGATTGTTA[C/T]ATGGGTAATGGGTTT | 208650 |
rs45680451 | snp | C/G | 0.124444 | 0.216185 | intron-variant | Cblb | Mm_Celera | 16:52102927 | CACATTTGGCCCTTG[C/G]CTTTAAAAAAAATAA | 208650 |
rs45695417 | snp | C/T | 0.231111 | 0.249285 | intron-variant | Cblb | GRCm38.p3 | 16:52174699 | AACTTAGCCTAACCT[C/T]CATCGAAGCAGAGGG | 208650 |
rs45700470 | snp | A/G | 0.124444 | 0.216185 | utr-variant-3-prime | Cblb | Mm_Celera | 16:52205932 | TCTGTAATGTGCGTT[A/G]CACTCTTGTGGGCTT | 208650 |
rs45701184 | snp | C/T | 0.244898 | 0.249948 | intron-variant | Cblb | GRCm38.p3 | 16:52159096 | AGTCCCACGGCCACG[C/T]GTCTCAGTCTAGCTT | 208650 |
rs45702256 | snp | C/T | 0.231111 | 0.249285 | intron-variant | Cblb | GRCm38.p3 | 16:52082781 | TGAGTGGTCTCTCAA[C/T]AGTACCATGAATTTG | 208650 |
rs45706431 | snp | C/G | 0.124444 | 0.216185 | intron-variant | Cblb | Mm_Celera | 16:52153801 | GTCGCATAAAATCAT[C/G]TCAGTGAATGCACTA | 208650 |
rs45708498 | snp | A/T | 0.124444 | 0.216185 | intron-variant | Cblb | Mm_Celera | 16:52193614 | GAATTAACTATTCAG[A/T]GAGACAACCTGAGAA | 208650 |
rs45715032 | snp | A/G | 0.408163 | 0.193609 | intron-variant | Cblb | GRCm38.p3 | 16:52130790 | GTCTATCTTCAGCAT[A/G]CAAATAAAGAGTTCA | 208650 |
rs45719342 | snp | A/G | 0.132653 | 0.220748 | intron-variant | Cblb | Mm_Celera | 16:52061281 | TGGTTCCTGTTTCTC[A/G]GGCCAGTGTTGGGTT | 208650 |
rs45726572 | snp | G/T | 0.124444 | 0.216185 | intron-variant | Cblb | Mm_Celera | 16:52101209 | ATAGCTGAGGGTAGT[G/T]TTATTGACTTGAGGA | 208650 |
rs45748226 | snp | C/T | 0.124444 | 0.216185 | intron-variant | Cblb | Mm_Celera | 16:52175478 | GGATGGTTTGCAAAT[C/T]ATAAACAAGGTTTAT | 208650 |
rs45749769 | snp | A/G | 0.391111 | 0.206368 | intron-variant | Cblb | Mm_Celera | 16:52167863 | TGTAGTTGACACCAC[A/G]GCCAGTTCTTTGAAG | 208650 |
rs45753149 | snp | A/G | 0.244898 | 0.249948 | intron-variant | Cblb | Mm_Celera | 16:52094553 | TAGGCATCTGAAATG[A/G]TAATGGAAAGTGATG | 208650 |
rs45757716 | snp | C/T | 0.244898 | 0.249948 | intron-variant | Cblb | Mm_Celera | 16:52071557 | TACAAGGCTACTGTC[C/T]AGCAGTCTCAAAATA | 208650 |
rs45758843 | snp | A/G | 0.132653 | 0.220748 | intron-variant | Cblb | Mm_Celera | 16:52198207 | GTAAAACAGAGGAAG[A/G]GCCATGAAGGACGAG | 208650 |
rs45761364 | snp | G/T | 0.32 | 0.24 | intron-variant | Cblb | GRCm38.p3 | 16:52101132 | GCCCGCAGAGAGGTT[G/T]TAATGACTGTGGTGA | 208650 |
rs45764227 | snp | A/T | 0.124444 | 0.216185 | upstream-variant-2KB | Cblb | Mm_Celera | 16:52030414 | TCAAGGTGTGAGGTG[A/T]ATCCATACTACCAAT | 208650 |
rs45766480 | snp | G/T | 0.444444 | 0.157135 | intron-variant | Cblb | GRCm38.p3 | 16:52173652 | ACTTACAAACTTTAA[G/T]AGGTCCATAGCCTTG | 208650 |
rs45771962 | snp | A/T | 0.231111 | 0.249285 | intron-variant | Cblb | GRCm38.p3 | 16:52182953 | AATTGTACACATCTT[A/T]TGTTAAAGCTTTATT | 208650 |
rs45785570 | snp | C/T | 0.32 | 0.24 | intron-variant | Cblb | GRCm38.p3 | 16:52167311 | AGTGCCATGTACTTA[C/T]GTGTGTGTGTTTGTG | 208650 |
rs45786307 | snp | C/T | 0.124444 | 0.216185 | intron-variant | Cblb | Mm_Celera | 16:52137764 | GACTGGTTTTAGAAA[C/T]GCCATCATGAAACAA | 208650 |
rs45789094 | snp | G/T | 0.444444 | 0.157135 | intron-variant, utr-variant-5-prime | Cblb | GRCm38.p3 | 16:52049238 | CCTTGAACTCTTGAT[G/T]CTCCTGAGTCTCCCC | 208650 |
rs45803168 | snp | A/G | | | intron-variant | Cblb | GRCm38.p3 | 16:52055497 | CCTCTCCAGGAGGGC[A/G]TGCTGCCATGTCTCT | 208650 |
rs45803952 | snp | C/T | 0.124444 | 0.216185 | utr-variant-3-prime | Cblb | Mm_Celera | 16:52205521 | AGGCTTGCAGGAGAC[C/T]GCTTGTACTCCAGTA | 208650 |
rs45811247 | snp | G/T | 0.132653 | 0.220748 | intron-variant | Cblb | Mm_Celera | 16:52153681 | TGGAGAAAAATAGAA[G/T]ATAGGAAGTTATTTT | 208650 |
rs45817138 | snp | C/T | 0.32 | 0.24 | intron-variant | Cblb | Mm_Celera | 16:52156495 | TTCATGCATGCTCTT[C/T]CTGTTTTGTAAGCAT | 208650 |
rs45822693 | snp | A/G | 0.231111 | 0.249285 | intron-variant | Cblb | Mm_Celera | 16:52181435 | TCTGCCTATAGAGAC[A/G]TCCTGGTCTTTGCAG | 208650 |
rs45849586 | snp | A/C | 0.444444 | 0.157135 | intron-variant, utr-variant-5-prime | Cblb | GRCm38.p3 | 16:52048413 | GAAATGTTCTACCTT[A/C]AACCTACACAGTGTG | 208650 |
rs45854544 | snp | C/T | 0.444444 | 0.157135 | intron-variant | Cblb | GRCm38.p3 | 16:52129082 | TCTGCAGTTGTATGG[C/T]AGAGGAAAATTTTAG | 208650 |
rs45858675 | snp | A/G | 0.124444 | 0.216185 | intron-variant | Cblb | Mm_Celera | 16:52173396 | TGTTTATATAACCAA[A/G]AATCTAAGCAGTGGA | 208650 |
rs45869589 | snp | A/G | 0.244898 | 0.249948 | intron-variant | Cblb | GRCm38.p3 | 16:52174075 | CCCTATTCTTGTGAT[A/G]TAATCTGATCGTTCC | 208650 |
rs45879302 | snp | C/G | 0.124444 | 0.216185 | intron-variant | Cblb | Mm_Celera | 16:52153846 | CTGGTTAAGTTAGAG[C/G]ACTGACCTTATGAAC | 208650 |
rs45890113 | snp | G/T | 0.32 | 0.24 | intron-variant | Cblb | GRCm38.p3 | 16:52102970 | GATCAATGTAATGGC[G/T]TTTGAGTGATGTTTT | 208650 |
rs45901816 | snp | A/G | 0.124444 | 0.216185 | intron-variant | Cblb | Mm_Celera | 16:52076036 | ACAAGCAGTTGACTA[A/G]CACAGGAGAACAGTT | 208650 |
rs45902539 | snp | G/T | 0.32 | 0.24 | intron-variant | Cblb | GRCm38.p3 | 16:52084713 | ACCCTGTCTAGTGGA[G/T]CCATATTGTGAACAG | 208650 |
rs45915487 | snp | A/G | 0.132653 | 0.220748 | intron-variant | Cblb | GRCm38.p3 | 16:52067465 | TTAGTAACTATACCT[A/G]ACTTAAACCATAAGC | 208650 |
rs45923984 | snp | C/T | 0.32 | 0.24 | intron-variant | Cblb | GRCm38.p3 | 16:52100475 | AGAACTACAATACTC[C/T]TTGTCAGAAGCCTCA | 208650 |
rs45934581 | snp | C/G | 0.124444 | 0.216185 | intron-variant | Cblb | Mm_Celera | 16:52124369 | GAAAAATGTGTATCA[C/G]AAACGCTTTCGGTGT | 208650 |
rs45943398 | snp | G/T | 0.124444 | 0.216185 | intron-variant | Cblb | Mm_Celera | 16:52152507 | TTTGTTGTCTTTGTT[G/T]CAGGAGTCTGATGGC | 208650 |
rs45953009 | snp | A/G | 0.132653 | 0.220748 | intron-variant | Cblb | Mm_Celera | 16:52061251 | TGTCCCTCTATGTAA[A/G]GAAAGCCTCAGCATT | 208650 |
rs45953554 | snp | G/T | 0.124444 | 0.216185 | intron-variant | Cblb | Mm_Celera | 16:52152147 | TTGCTTAGATTACTA[G/T]TAATTATTGCTCTAG | 208650 |
rs45957353 | snp | C/T | 0.124444 | 0.216185 | intron-variant | Cblb | Mm_Celera | 16:52190060 | TAACAAGGTAGCTCT[C/T]CTAAATGTTTGTGTT | 208650 |
rs45970243 | snp | A/G | 0.231111 | 0.249285 | intron-variant | Cblb | Mm_Celera | 16:52195996 | AAGCATGGGACTGGT[A/G]CCCTGTGTTACACAC | 208650 |
rs45976442 | snp | A/G | 0.244898 | 0.249948 | intron-variant | Cblb | GRCm38.p3 | 16:52164924 | ACAGACTGCGCTTCA[A/G]CCCAGGAAATTAATT | 208650 |
rs45979293 | snp | C/T | 0.142012 | 0.225474 | intron-variant | Cblb | Mm_Celera | 16:52085133 | ACATTTGAAGTGCAG[C/T]GTCTCACATGTGTCT | 208650 |
rs45980477 | snp | A/G | 0.32 | 0.24 | intron-variant | Cblb | GRCm38.p3 | 16:52190186 | TGAAGAGACTAAAGG[A/G]AACCCTCTGCACATC | 208650 |
rs45982026 | snp | A/T | 0.124444 | 0.216185 | intron-variant | Cblb | Mm_Celera | 16:52078662 | CCTCTTCAAATGTGA[A/T]TCCTGGGTACCGAGA | 208650 |
rs45986631 | snp | A/G | 0.244898 | 0.249948 | intron-variant | Cblb | GRCm38.p3 | 16:52167482 | ACAGGCATCATACTA[A/G]AGCCGAGAGCATTAG | 208650 |
rs45986806 | snp | C/G | 0.244898 | 0.249948 | intron-variant | Cblb | Mm_Celera | 16:52165131 | GGACTTATAGTCTAG[C/G]ATTGCCAAAGAGTAC | 208650 |
rs45995617 | snp | C/T | 0.231111 | 0.249285 | intron-variant | Cblb | GRCm38.p3 | 16:52170006 | TGTGCACACGGGCCT[C/T]ATTTGCAGTGTCCTA | 208650 |
rs45999646 | snp | C/T | 0.124444 | 0.216185 | intron-variant | Cblb | Mm_Celera | 16:52106111 | TCCAGGATGAGGAAA[C/T]TGATTTCAAAAGGCT | 208650 |
rs46001745 | snp | A/C/G | 0.231111 | 0.249285 | intron-variant | Cblb | GRCm38.p3 | 16:52102585 | AAGCGACTTGAGAAC[A/C/G]TATTCTTTCTCGACC | 208650 |
rs46013280 | snp | C/T | 0.32 | 0.24 | intron-variant | Cblb | Mm_Celera | 16:52115774 | GGAACACAGAATGCC[C/T]ATGACAAGGGGAATA | 208650 |
rs46016024 | snp | C/T | 0.124444 | 0.216185 | intron-variant | Cblb | GRCm38.p3 | 16:52163023 | GTTAGTACAAGAAAA[C/T]AATCCACCAAGTGTT | 208650 |
rs46027262 | snp | C/T | 0.489796 | 0.070696 | intron-variant | Cblb | GRCm38.p3 | 16:52160064 | ATTTAGAGATTAAAG[C/T]GGCTATTCACCAGCC | 208650 |
rs46029306 | snp | C/T | 0.124444 | 0.216185 | intron-variant | Cblb | Mm_Celera | 16:52196273 | AAAACCTGACCTAGA[C/T]ACTATGTGCCTTCAC | 208650 |
rs46031423 | snp | G/T | 0.444444 | 0.157135 | intron-variant | Cblb | GRCm38.p3 | 16:52090049 | TGCAGTTACTATACC[G/T]TGGACCTAGGGCAGT | 208650 |
rs46041349 | snp | G/T | 0.244898 | 0.249948 | intron-variant | Cblb | Mm_Celera | 16:52176263 | ACCCAGCAGTTACAA[G/T]CACGCTGTCATACAG | 208650 |
rs46047358 | snp | A/G | 0.231111 | 0.249285 | intron-variant | Cblb | GRCm38.p3 | 16:52171800 | AAGCTACAGTCCATC[A/G]ATACAATTCATGAAG | 208650 |
rs46050490 | snp | C/T | 0.124444 | 0.216185 | intron-variant | Cblb | Mm_Celera | 16:52191040 | GTAATGTACTCTCGA[C/T]TTAATACCCGACTGG | 208650 |
rs46059630 | snp | A/G | 0.124444 | 0.216185 | synonymous-codon | Cblb | Mm_Celera | 16:52131188 | TGATTACATCTCAGT[A/G]TTTGAATTTGATATT | 208650 |
rs46061116 | snp | A/G | 0.231111 | 0.249285 | intron-variant | Cblb | GRCm38.p3 | 16:52191712 | ATAATTCCCACTAAC[A/G]TGCTCGAGCCTTCCT | 208650 |
rs46105622 | snp | A/G | 0.142012 | 0.225474 | intron-variant | Cblb | GRCm38.p3 | 16:52162059 | GTATGGCGGTCACTA[A/G]CATTGTGTCTTACGT | 208650 |
rs46118776 | snp | C/G | 0.124444 | 0.216185 | intron-variant | Cblb | Mm_Celera | 16:52202966 | CTAGCTGGTCACCAA[C/G]TCTCCTTTCTTAGAT | 208650 |
rs46126445 | snp | A/G | 0.48 | 0.0979796 | intron-variant | Cblb | GRCm38.p3 | 16:52092194 | CACCACAAAACTGGA[A/G]GAAAAACAACACAAC | 208650 |
rs46131004 | snp | A/C | 0.391111 | 0.206368 | intron-variant | Cblb | GRCm38.p3 | 16:52197167 | CACAAGGTGTAGAGA[A/C]CTGTTTAAGTTATTG | 208650 |
rs46150142 | snp | A/G | 0.165289 | 0.235211 | intron-variant | Cblb | Mm_Celera | 16:52061919 | ACCTCTGCTGTGTGT[A/G]TGGCTTCATCCTAAC | 208650 |
rs46154432 | snp | C/G | 0.32 | 0.24 | intron-variant | Cblb | GRCm38.p3 | 16:52089073 | TCAAGACTGTTGCCA[C/G]CACTTTTTAAAATTT | 208650 |
rs46162668 | snp | A/G | 0.124444 | 0.216185 | intron-variant | Cblb | Mm_Celera | 16:52073086 | AATAAAGCAAAATCC[A/G]GGAGAGTGTATTTGC | 208650 |
rs46165819 | snp | A/G | 0.132653 | 0.220748 | intron-variant | Cblb | GRCm38.p3 | 16:52201665 | TGTATCTCTTCAGTG[A/G]GGTTTCCTATTTTAC | 208650 |
rs46168852 | snp | A/G | 0.444444 | 0.157135 | intron-variant | Cblb | GRCm38.p3 | 16:52052315 | CCAGTTGGTTTGGGG[A/G]ATGCAAGAGACATAA | 208650 |
rs46179353 | snp | A/C | 0.124444 | 0.216185 | intron-variant | Cblb | Mm_Celera | 16:52075281 | TTTTCCTGTGTTCAA[A/C]TGAAACATTGCTCCT | 208650 |
rs46179499 | snp | C/T | 0.231111 | 0.249285 | intron-variant | Cblb | Mm_Celera | 16:52131435 | GCTTGTATATCGGGT[C/T]ATGTGATCCTGGTAG | 208650 |
rs46180601 | snp | A/G | 0.124444 | 0.216185 | intron-variant | Cblb | Mm_Celera | 16:52173822 | CCCCACTGATAAAAC[A/G]TTGGCTCTGAGCTTT | 208650 |
rs46186602 | snp | C/T | 0.165289 | 0.235211 | intron-variant | Cblb | Mm_Celera | 16:52143141 | TCTTGCCGTTAGTGT[C/T]ATGATGACGCCAAGA | 208650 |
rs46189106 | snp | A/T | 0.142012 | 0.225474 | intron-variant | Cblb | GRCm38.p3 | 16:52154406 | TACTTGAAAAATCTT[A/T]CATGTGCAGGTAGGT | 208650 |
rs46194012 | snp | A/G | 0.444444 | 0.157135 | intron-variant | Cblb | Mm_Celera | 16:52167991 | TGAAAAGTGGGATGA[A/G]GACTTCCTTTGGGTA | 208650 |
rs46196476 | snp | C/T | 0.124444 | 0.216185 | intron-variant | Cblb | Mm_Celera | 16:52159413 | CATTCTGTAATATCT[C/T]GTTACCCAAATGGTA | 208650 |
rs46229043 | snp | A/C/T | 0.244898 | 0.249948 | intron-variant | Cblb | GRCm38.p3 | 16:52177365 | ATTGCAGAAGCCATC[A/C/T]TGAGATGAACTATCG | 208650 |
rs46230560 | snp | G/T | 0.32 | 0.24 | intron-variant | Cblb | Mm_Celera | 16:52196413 | GATAGTAGCTTACTC[G/T]TCCATGAACTATGAA | 208650 |
rs46232858 | snp | A/T | | | intron-variant | Cblb | GRCm38.p3 | 16:52174756 | CCAGCCTTCTTCTTT[A/T]TGACTTTATCTCACT | 208650 |
rs46239014 | snp | A/G | 0.32 | 0.24 | intron-variant | Cblb | GRCm38.p3 | 16:52100534 | AAATCTAAGACTTAT[A/G]CTAGGTATGGTTTTC | 208650 |
rs46253224 | snp | A/C | 0.231111 | 0.249285 | intron-variant | Cblb | GRCm38.p3 | 16:52153973 | AGATCTCAGACTGCC[A/C]TTTGTATAGAAATAC | 208650 |
rs46253639 | snp | C/T | 0.124444 | 0.216185 | intron-variant | Cblb | Mm_Celera | 16:52176716 | CTTAGTTAATTTGCA[C/T]GTTACATATTAGCCA | 208650 |
rs46254448 | snp | C/T | 0.32 | 0.24 | intron-variant | Cblb | GRCm38.p3 | 16:52188503 | TTTGACACTAAATTA[C/T]CTGTGCATGGTGTGA | 208650 |
rs46254489 | snp | C/G | 0.124444 | 0.216185 | intron-variant | Cblb | Mm_Celera | 16:52192242 | GGGGCTAATCAGAGA[C/G]CTCGTGCCATCTGCA | 208650 |
rs46265583 | snp | C/G/T | 0.124444 | 0.216185 | intron-variant | Cblb | GRCm38.p3 | 16:52066260 | GCATCTTGTGACTGA[C/G/T]GAGCCTTTCTTTTAA | 208650 |
rs46281828 | snp | A/G | 0.231111 | 0.249285 | intron-variant | Cblb | Mm_Celera | 16:52138541 | GTTATTAAATGTAGC[A/G]ACAAACCATCCTGTA | 208650 |
rs46282150 | snp | A/G | 0.231111 | 0.249285 | intron-variant | Cblb | GRCm38.p3 | 16:52106169 | AAGGATATGGACCCA[A/G]TAATAACAGACTACA | 208650 |
rs46291840 | snp | C/T | 0.165289 | 0.235211 | intron-variant | Cblb | Mm_Celera | 16:52145308 | ACCACTAGTGAGTAC[C/T]GTTATCTTAAACAGA | 208650 |
rs46299273 | snp | A/G | 0.32 | 0.24 | downstream-variant-500B | Cblb | GRCm38.p3 | 16:52208394 | TTGTAATCATTGGAT[A/G]TGGCCAGGGATTTAA | 208650 |
rs46312786 | snp | A/T | 0.32 | 0.24 | intron-variant | Cblb | GRCm38.p3 | 16:52177203 | TAATACATGAGAGGA[A/T]ATGTTTAACTTAAAT | 208650 |
rs46315545 | snp | A/G | 0.231111 | 0.249285 | intron-variant | Cblb | GRCm38.p3 | 16:52156746 | ATAGAGAACTGAGCC[A/G]ACTGTAGTTTCCCGT | 208650 |
rs46317561 | snp | A/G | 0.142012 | 0.225474 | intron-variant | Cblb | Mm_Celera | 16:52146117 | GTTCAAAGCCTTCCA[A/G]TTAGTGCATGAGCAG | 208650 |
rs46327145 | snp | A/G | 0.473373 | 0.11227 | intron-variant | Cblb | GRCm38.p3 | 16:52184302 | GGAGACTGCAAGGCC[A/G]TCAGTCATCCACGCC | 208650 |
rs46334810 | snp | A/C | 0.231111 | 0.249285 | intron-variant | Cblb | GRCm38.p3 | 16:52201344 | ACATCTGGAGAGAGA[A/C]CGCTATGGTGAACAT | 208650 |
rs46343181 | snp | A/G | 0.408163 | 0.193609 | intron-variant | Cblb | Mm_Celera | 16:52167509 | TTAGTTGCGAACCAC[A/G]GTTGCCAGTGAGCTG | 208650 |
rs46346728 | snp | A/C | 0.124444 | 0.216185 | intron-variant | Cblb | Mm_Celera | 16:52067381 | TGCTATTTCTATTAC[A/C]TTCTTTGATGTTCAG | 208650 |
rs46354539 | snp | A/C | 0.132653 | 0.220748 | upstream-variant-2KB | Cblb | GRCm38.p3 | 16:52030024 | TGGAGAAGCCTGCAC[A/C]ATCTACATATATAAA | 208650 |
rs46356005 | snp | A/G | 0.244898 | 0.249948 | intron-variant | Cblb | Mm_Celera | 16:52133649 | AAGTAGTAGAATAGA[A/G]AAATATCTGAGAGGA | 208650 |
rs46362086 | snp | A/G | 0.497778 | 0.0332592 | intron-variant | Cblb | GRCm38.p3 | 16:52156149 | ATAAATTCTTTCTGA[A/G]TAGTTGGAAAAATAT | 208650 |
rs46374836 | snp | A/C | | | intron-variant | Cblb | Mm_Celera | 16:52062290 | TCCATTTGCCAAAGG[A/C]TAAGCTGTGTTCACC | 208650 |
rs46395861 | snp | A/G | 0.124444 | 0.216185 | intron-variant | Cblb | GRCm38.p3 | 16:52162613 | GTTAAATGCCAGGGT[A/G]TCTATTCAAAGCACC | 208650 |
rs46402596 | snp | G/T | 0.244898 | 0.249948 | intron-variant | Cblb | GRCm38.p3 | 16:52061341 | ACTGTTTTTCTCATC[G/T]TGTAACCCTGGAGGT | 208650 |
rs46407703 | snp | G/T | 0.124444 | 0.216185 | intron-variant | Cblb | Mm_Celera | 16:52135299 | AGAGGGCCTCATTGA[G/T]GAAGAGTTGGTAGTC | 208650 |
rs46411975 | snp | G/T | 0.124444 | 0.216185 | intron-variant | Cblb | GRCm38.p3 | 16:52053746 | AAGAAACTTAATTCC[G/T]AGGGTTGATTCACTG | 208650 |
rs46414002 | snp | C/T | 0.32 | 0.24 | intron-variant | Cblb | GRCm38.p3 | 16:52201678 | TGAGGTTTCCTATTT[C/T]ACATGCTTTCATGAT | 208650 |
rs46426093 | snp | A/G | 0.124444 | 0.216185 | intron-variant | Cblb | Mm_Celera | 16:52071475 | GTTAGCTGTAACCCA[A/G]TCAGAGAAAAGCCCA | 208650 |
rs46432185 | snp | C/T | 0.124444 | 0.216185 | intron-variant | Cblb | GRCm38.p3 | 16:52072323 | CAGCTGTTCAGTTCT[C/T]TAGACATTGCTACTC | 208650 |
rs46433825 | snp | A/G | 0.142012 | 0.225474 | intron-variant | Cblb | Mm_Celera | 16:52204296 | ATTCTGCAATAAGTA[A/G]CTAACAAATAAAAAG | 208650 |
rs46439305 | snp | C/T | 0.231111 | 0.249285 | intron-variant | Cblb | Mm_Celera | 16:52082379 | GTTCAACGCATGCTA[C/T]AGTAAACTGAAAAGA | 208650 |
rs46443269 | snp | G/T | 0.32 | 0.24 | utr-variant-3-prime | Cblb | GRCm38.p3 | 16:52204704 | ATAGCAGCCAGAACT[G/T]CAGACACCAAAGGGC | 208650 |
rs46444400 | snp | C/T | 0.444444 | 0.157135 | intron-variant | Cblb | GRCm38.p3 | 16:52092219 | CACAACAAGCCAGCT[C/T]TCTTTTCAGCTCTAG | 208650 |
rs46449295 | snp | A/G | 0.152778 | 0.230321 | intron-variant | Cblb | Mm_Celera | 16:52180741 | ATTTTTTATATTTCA[A/G]TACAAATGGCACATA | 208650 |
rs46455949 | snp | A/G | 0.124444 | 0.216185 | intron-variant | Cblb | Mm_Celera | 16:52071486 | CCCAATCAGAGAAAA[A/G]CCCACCTGTTCCATC | 208650 |
rs46456656 | snp | C/T | 0.32 | 0.24 | intron-variant | Cblb | GRCm38.p3 | 16:52133730 | TTGAGACCCCTCTTC[C/T]AGCATAACACAGTGC | 208650 |
rs46464167 | snp | C/G | 0.32 | 0.24 | intron-variant | Cblb | GRCm38.p3 | 16:52204415 | TTCACTGGTATCTGT[C/G]TTTGACAATCTCCAC | 208650 |
rs46472948 | snp | C/G | 0.124444 | 0.216185 | intron-variant | Cblb | Mm_Celera | 16:52068731 | CTGTTAGCACTGCTC[C/G]ACTCAGCCCTCCATG | 208650 |
rs46490170 | snp | A/G | 0.32 | 0.24 | intron-variant | Cblb | GRCm38.p3 | 16:52076246 | TCTGTTGAAACATCA[A/G]GAGTGTTTGCTTCCA | 208650 |
rs46492415 | snp | C/T | 0.124444 | 0.216185 | intron-variant | Cblb | Mm_Celera | 16:52154263 | ACAGTTGGGAAAGAG[C/T]AGGTGCAGAGTCCAG | 208650 |
rs46503281 | snp | A/G | 0.124444 | 0.216185 | intron-variant | Cblb | Mm_Celera | 16:52105298 | TTATAAAGCTATTAG[A/G]CAAAATAAAGGTGGG | 208650 |
rs46503465 | snp | A/G | 0.124444 | 0.216185 | intron-variant | Cblb | Mm_Celera | 16:52148012 | TTTGCTTTTAAGACC[A/G]TTTCAAACGTACATT | 208650 |
rs46503496 | snp | C/T | 0.231111 | 0.249285 | utr-variant-3-prime | Cblb | GRCm38.p3 | 16:52206713 | GTCTGTTGGGCTTCA[C/T]GTAGCTTGCCAGCAA | 208650 |
rs46511844 | snp | A/G | 0.124444 | 0.216185 | intron-variant | Cblb | Mm_Celera | 16:52191965 | AAGCACTGAGTCTTA[A/G]TCCCACCCTGCATGG | 208650 |
rs46512408 | snp | A/G | 0.142012 | 0.225474 | intron-variant | Cblb | Mm_Celera | 16:52056123 | TGTTTTAATTTTTAA[A/G]AGCCATTCTCTACTT | 208650 |
rs46513745 | snp | A/G | 0.244898 | 0.249948 | intron-variant | Cblb | GRCm38.p3 | 16:52057406 | TACAAGCAGAAGGCA[A/G]GAGAATCTTTGGTCA | 208650 |
rs46518669 | snp | G/T | 0.32 | 0.24 | intron-variant | Cblb | GRCm38.p3 | 16:52082311 | GTTAAGCTCGGTAGG[G/T]TCTTTCCTAAGACTC | 208650 |
rs46530418 | snp | C/T | 0.5 | 0 | intron-variant | Cblb | GRCm38.p3 | 16:52093532 | GTCATGAGCTGCTGT[C/T]TCATAGGGAAATAGC | 208650 |
rs46534510 | snp | C/T | 0.124444 | 0.216185 | intron-variant | Cblb | Mm_Celera | 16:52173782 | CCAGCATTACCACTG[C/T]GCCTGTAAACCGGAA | 208650 |
rs46538647 | snp | A/G | 0.124444 | 0.216185 | intron-variant | Cblb | Mm_Celera | 16:52100713 | GAAGTTATGCATAAC[A/G]TGCAGTGCTGCTCTG | 208650 |
rs46540115 | snp | C/T | 0.46875 | 0.121031 | intron-variant | Cblb | GRCm38.p3 | 16:52094252 | AGGCTACACTAACGT[C/T]TTTCTCTTGATTATT | 208650 |
rs46543300 | snp | G/T | 0.124444 | 0.216185 | intron-variant | Cblb | Mm_Celera | 16:52152418 | AGATATACCCATCAT[G/T]GATCCACAGACTTGT | 208650 |
rs46548556 | snp | A/T | 0.124444 | 0.216185 | intron-variant | Cblb | Mm_Celera | 16:52138930 | TTGGAAAATATTTGA[A/T]TGGCAGGTTGTGTAG | 208650 |
rs46549435 | snp | C/T | 0.124444 | 0.216185 | downstream-variant-500B | Cblb | Mm_Celera | 16:52208218 | CCACGTAACTTGAGA[C/T]GATCTAAAGTCAGTC | 208650 |
rs46549739 | snp | A/T | 0.152778 | 0.230321 | intron-variant | Cblb | GRCm38.p3 | 16:52143138 | CCGTCTTGCCGTTAG[A/T]GTCATGATGACGCCA | 208650 |
rs46549822 | snp | A/G | 0.124444 | 0.216185 | intron-variant | Cblb | Mm_Celera | 16:52119271 | CTGTCCTTTTGTCTA[A/G]AGTGTGTGCCTGTGA | 208650 |
rs46554163 | snp | C/T | 0.132653 | 0.220748 | intron-variant | Cblb | GRCm38.p3 | 16:52160309 | CGTGTATAAGTTTAT[C/T]GCCTGCTCAGCGTTT | 208650 |
rs46575686 | snp | A/G | 0.244898 | 0.249948 | intron-variant | Cblb | GRCm38.p3 | 16:52163329 | CACTTGGCGGGCAGT[A/G]TGTAGCTCTCCGCTT | 208650 |
rs46582901 | snp | C/T | 0.497778 | 0.0332592 | intron-variant | Cblb | GRCm38.p3 | 16:52177508 | ACTACATAATATCCA[C/T]GCAATTTATTATTAA | 208650 |
rs46585438 | snp | A/G | 0.124444 | 0.216185 | intron-variant | Cblb | Mm_Celera | 16:52174493 | GTCCATACCTAATAT[A/G]GGAAAGAATGTTTTT | 208650 |
rs46589562 | snp | C/T | 0.297521 | 0.245442 | intron-variant | Cblb | GRCm38.p3 | 16:52145138 | GAAATTGGGGAAGTG[C/T]GTGCACGATCAAGCA | 208650 |
rs46595146 | snp | C/T | 0.132653 | 0.220748 | intron-variant | Cblb | GRCm38.p3 | 16:52056405 | ACTCAAAGCAGTGCG[C/T]TGTGTACAATTTTAA | 208650 |
rs46600610 | snp | A/G | 0.142012 | 0.225474 | intron-variant | Cblb | Mm_Celera | 16:52154730 | TAAAGGGAGCAGTGA[A/G]CCAGCTCTGTAACAG | 208650 |
rs46601438 | snp | A/G/T | 0.132653 | 0.220748 | intron-variant | Cblb | GRCm38.p3 | 16:52141879 | TTCATTCATAAGTTG[A/G/T]CATGGGTTATTTGGT | 208650 |
rs46605844 | snp | A/G | 0.165289 | 0.235211 | intron-variant | Cblb | GRCm38.p3 | 16:52143816 | CATGGTACCTGTGCA[A/G]CTTGTGGATTGGTGA | 208650 |
rs46613337 | snp | A/C/T | 0.32 | 0.24 | intron-variant | Cblb | GRCm38.p3 | 16:52073130 | AGATGCCCACATGTA[A/C/T]GTCTGCTCATGTTTG | 208650 |
rs46614896 | snp | A/C | 0.32 | 0.24 | intron-variant | Cblb | Mm_Celera | 16:52181990 | TCAGCCACACTGACC[A/C]AAAAGTGAAATCATT | 208650 |
rs46617116 | snp | C/G | 0.142012 | 0.225474 | intron-variant | Cblb | GRCm38.p3 | 16:52177122 | GTTCCATGTCTTACC[C/G]TAGCATTTATTAATT | 208650 |
rs46620082 | snp | C/T | 0.142012 | 0.225474 | intron-variant | Cblb | Mm_Celera | 16:52130890 | CATGAACTAGGATTC[C/T]TAGCAAACACAGAAT | 208650 |
rs46630397 | snp | A/G | 0.231111 | 0.249285 | intron-variant | Cblb | Mm_Celera | 16:52135518 | ACAAATTCTCTATTG[A/G]CTGTCTACTTGGTTT | 208650 |
rs46637053 | snp | C/T | 0.277778 | 0.248452 | intron-variant | Cblb | Mm_Celera | 16:52096123 | GTTCTAGCAGAGACA[C/T]GGAGGTTTGCTTTGT | 208650 |
rs46638187 | snp | C/T | 0.32 | 0.24 | intron-variant | Cblb | Mm_Celera | 16:52155721 | ATAGGACTCTAGTAC[C/T]ACAAACTGAGAATGG | 208650 |
rs46647626 | snp | C/G | 0.132653 | 0.220748 | intron-variant | Cblb | Mm_Celera | 16:52147414 | CGCGGGCACCCCTCT[C/G]ACTTTCACCTGTCAC | 208650 |
rs46669443 | snp | A/C | 0.408163 | 0.193609 | intron-variant | Cblb | Mm_Celera | 16:52158641 | AAAATAATTGAGAAG[A/C]GTTAACAACTTACAT | 208650 |
rs46670344 | snp | A/G | 0.124444 | 0.216185 | intron-variant | Cblb | Mm_Celera | 16:52196305 | GTCTCTTCTTGTCAA[A/G]GGCCCTACTAAATGG | 208650 |
rs46676060 | snp | A/C | 0.124444 | 0.216185 | intron-variant | Cblb | Mm_Celera | 16:52077591 | GTTTATTTAGTTGCC[A/C]GATTTCACCTGTCTG | 208650 |
rs46677509 | snp | A/C | 0.132653 | 0.220748 | intron-variant | Cblb | Mm_Celera | 16:52162314 | TTCTGAGGGTACTAA[A/C]GGTGGCAGAGACCCA | 208650 |
rs46680362 | snp | A/G | 0.18 | 0.24 | intron-variant | Cblb | GRCm38.p3 | 16:52142285 | TCAGGCAGCAAGCAC[A/G]CATGAGGAACGAACG | 208650 |
rs46685911 | snp | A/G | 0.124444 | 0.216185 | intron-variant | Cblb | Mm_Celera | 16:52104123 | TAGGGGTCAGGTAAA[A/G]TGGAGCCTTCACAGT | 208650 |
rs46693504 | snp | C/G | 0.152778 | 0.230321 | intron-variant | Cblb | Mm_Celera | 16:52130885 | ATATCCATGAACTAG[C/G]ATTCCTAGCAAACAC | 208650 |
rs46696362 | snp | A/G | 0.231111 | 0.249285 | intron-variant | Cblb | GRCm38.p3 | 16:52154115 | AGACATGACTACTCA[A/G]CCACATCCCTCTGAG | 208650 |
rs46697716 | snp | A/T | 0.444444 | 0.157135 | intron-variant | Cblb | GRCm38.p3 | 16:52133227 | TAGAAAGCAGTGAAG[A/T]ACCCAAGAGATGAAG | 208650 |
rs46701445 | snp | A/G | 0.497778 | 0.0332592 | intron-variant | Cblb | GRCm38.p3 | 16:52178804 | AAAATCAGACGTGGG[A/G]CAGGATGACTAGTGA | 208650 |
rs46703579 | snp | A/G | 0.48 | 0.0979796 | intron-variant | Cblb | GRCm38.p3 | 16:52093119 | GCTTTGAAACTAAAA[A/G]TGTCCTGACAGAAGA | 208650 |
rs46717054 | snp | G/T | 0.132653 | 0.220748 | intron-variant | Cblb | Mm_Celera | 16:52063542 | CATGAATTAACTTTT[G/T]ATTACAGCATGGAGA | 208650 |
rs46726769 | snp | A/G | 0.124444 | 0.216185 | intron-variant | Cblb | Mm_Celera | 16:52169905 | TATAACTTTTTGTGT[A/G]AGGAAGCACATGTTC | 208650 |
rs46729349 | snp | C/G | 0.132653 | 0.220748 | intron-variant | Cblb | Mm_Celera | 16:52062697 | CTAAGTTGGAGTCAC[C/G]TGAGAACATGTTTTG | 208650 |
rs46729355 | snp | C/T | 0.32 | 0.24 | intron-variant | Cblb | Mm_Celera | 16:52204396 | TTCATTTTTATCTCA[C/T]TGTTTCACTGGTATC | 208650 |
rs46740269 | snp | A/G | 0.32 | 0.24 | intron-variant | Cblb | Mm_Celera | 16:52130977 | CAATGCAAGCCTGCT[A/G]CTGCTGATGTTATGG | 208650 |
rs46742497 | snp | G/T | 0.444444 | 0.157135 | intron-variant | Cblb | GRCm38.p3 | 16:52042770 | TTTAGCAGTAATCCA[G/T]CTGATGAAGTGCACA | 208650 |
rs46758062 | snp | G/T | 0.152778 | 0.230321 | intron-variant | Cblb | Mm_Celera | 16:52146235 | GTGAAAAAACGTTCA[G/T]TAACAAGCCCCTGTT | 208650 |
rs46761636 | snp | C/G | 0.124444 | 0.216185 | intron-variant | Cblb | Mm_Celera | 16:52107633 | AATGCTTTTTTCATG[C/G]TAAAGTTTTTTTGTA | 208650 |
rs46767167 | snp | A/C | 0.124444 | 0.216185 | intron-variant | Cblb | Mm_Celera | 16:52129562 | ATTGCTAAATACTTT[A/C]CTTGTGCTTTTATGA | 208650 |
rs46769211 | snp | A/G | 0.32 | 0.24 | intron-variant | Cblb | Mm_Celera | 16:52153915 | AAAAGAATCAGCGTG[A/G]CAGTTGAATAATTTA | 208650 |
rs46771951 | snp | A/T | 0.32 | 0.24 | intron-variant | Cblb | GRCm38.p3 | 16:52089265 | GTTTCTAAGGAACTC[A/T]CAAAAATGCCTCACT | 208650 |
rs46776988 | snp | A/T | 0.152778 | 0.230321 | intron-variant | Cblb | GRCm38.p3 | 16:52062541 | TTCACAGATAAGATC[A/T]TGGAACCCAGCTGGG | 208650 |
rs46784402 | snp | G/T | 0.132653 | 0.220748 | intron-variant | Cblb | Mm_Celera | 16:52123742 | ATGGCAGAATGCAAT[G/T]GGGCAAGTGCATCCC | 208650 |
rs46801370 | snp | C/T | 0.231111 | 0.249285 | intron-variant | Cblb | GRCm38.p3 | 16:52193507 | TCAGTCTACTATTCA[C/T]GCTTCACAGTTTTAC | 208650 |
rs46808470 | snp | A/T | 0.444444 | 0.157135 | intron-variant | Cblb | Mm_Celera | 16:52052196 | TGTTTTTGGGAAGAG[A/T]TATGTAGTGAAGTGT | 208650 |
rs46831158 | snp | A/G | 0.32 | 0.24 | intron-variant | Cblb | GRCm38.p3 | 16:52099937 | CTTCCCTTTTAGTCA[A/G]TGTCAGGAGCTGCTC | 208650 |
rs46839926 | snp | A/T | 0.231111 | 0.249285 | intron-variant | Cblb | GRCm38.p3 | 16:52129637 | CCTAAATGGCCTCTG[A/T]TGTGGTGCCTCTCTT | 208650 |
rs46842294 | snp | C/T | 0.32 | 0.24 | intron-variant | Cblb | GRCm38.p3 | 16:52177245 | TCTTTTGAGCTTCTG[C/T]TCCCTATGCAGCAAT | 208650 |
rs46852119 | snp | A/G | 0.132653 | 0.220748 | intron-variant | Cblb | Mm_Celera | 16:52174552 | AAATAGAAGGAAATC[A/G]GTAAAGACAGAAGCG | 208650 |
rs46859580 | snp | A/G | 0.391111 | 0.206368 | intron-variant | Cblb | GRCm38.p3 | 16:52132889 | TGTAGTTTCACTTAA[A/G]AATGGCCAAGTAGCC | 208650 |
rs46864623 | snp | G/T | 0.124444 | 0.216185 | intron-variant | Cblb | GRCm38.p3 | 16:52163938 | TGCTTCTGATGAAAA[G/T]CATTTAGCTTCAGGA | 208650 |
rs46875528 | snp | C/T | 0.124444 | 0.216185 | intron-variant | Cblb | Mm_Celera | 16:52167243 | AGGCCGACAGGGCAA[C/T]GTGAGACCCTGTGTC | 208650 |
rs46884374 | snp | C/G | 0.497778 | 0.0332592 | intron-variant | Cblb | GRCm38.p3 | 16:52124494 | GTAGTCCTATAGCAT[C/G]TGCATGACCCCAGTG | 208650 |
rs46887581 | snp | A/G | 0.231111 | 0.249285 | intron-variant | Cblb | GRCm38.p3 | 16:52128694 | TGGCATCATCTTATG[A/G]CAATTGATAATCAAC | 208650 |
rs46889146 | snp | A/G | 0.165289 | 0.235211 | intron-variant | Cblb | Mm_Celera | 16:52143198 | CAGTCAGCTCACGTC[A/G]TGCTCCTGGGAAGAT | 208650 |
rs46893532 | snp | A/C | 0.124444 | 0.216185 | intron-variant | Cblb | Mm_Celera | 16:52196850 | AGTTTGAATTCCTTG[A/C]GCATTCCATAATGCC | 208650 |
rs46898217 | snp | C/T | | | intron-variant | Cblb | Mm_Celera | 16:52142733 | TTCATGCTAGTAAAC[C/T]ATTAACCGCCGGCCC | 208650 |
rs46913615 | snp | A/G | 0.32 | 0.24 | intron-variant | Cblb | GRCm38.p3 | 16:52067235 | GGATTCCTTCAGGAT[A/G]GCACGAGGAGTATAG | 208650 |
rs46918388 | snp | C/T | 0.444444 | 0.157135 | intron-variant | Cblb | GRCm38.p3 | 16:52144432 | TGAACTGAGAAGAAG[C/T]CAAGTTGTATCGCTT | 208650 |
rs46924501 | snp | C/G | 0.244898 | 0.249948 | intron-variant | Cblb | GRCm38.p3 | 16:52162979 | ATCATAGAAAAGTCA[C/G]TTCTAAATTTGGTTT | 208650 |
rs46935279 | snp | A/G | 0.124444 | 0.216185 | intron-variant | Cblb | Mm_Celera | 16:52154438 | GACATCACCAGTGTC[A/G]CTATGCTCCAATTCA | 208650 |
rs46943648 | snp | A/G | 0.244898 | 0.249948 | intron-variant | Cblb | GRCm38.p3 | 16:52079452 | TTATGGCTATAACAA[A/G]TATAAACAGCAGTGA | 208650 |
rs46957238 | snp | C/G | 0.124444 | 0.216185 | utr-variant-3-prime | Cblb | Mm_Celera | 16:52206297 | ACCTAGTCTCACATA[C/G]AGAGATGCCTCGGAT | 208650 |
rs46959174 | snp | A/C | 0.231111 | 0.249285 | intron-variant | Cblb | Mm_Celera | 16:52134568 | TGCCAGGAACATGAA[A/C]AAGTTTCAAAACAAA | 208650 |
rs46966200 | snp | A/G | 0.231111 | 0.249285 | intron-variant | Cblb | GRCm38.p3 | 16:52071743 | GCTACAAAGAAACAA[A/G]GGCCTGTCACTGCAT | 208650 |
rs46986037 | snp | C/T | 0.32 | 0.24 | intron-variant | Cblb | GRCm38.p3 | 16:52072363 | TCACTATGTTGTATG[C/T]TGATTAAACAACAGG | 208650 |
rs46991570 | snp | C/T | 0.391111 | 0.206368 | intron-variant | Cblb | Mm_Celera | 16:52170961 | ACGAGACTAACGTGA[C/T]CAGCGATGCGGATTT | 208650 |
rs46992802 | snp | A/T | 0.165289 | 0.235211 | intron-variant | Cblb | Mm_Celera | 16:52144730 | TTAATACACTCTGCA[A/T]ATGTAGCTTACCTTG | 208650 |
rs46994348 | snp | A/G | 0.32 | 0.24 | intron-variant | Cblb | GRCm38.p3 | 16:52177932 | CTGGGTGATTATGTG[A/G]CTCTTTCTACACACT | 208650 |
rs46995911 | snp | C/T | | | intron-variant | Cblb | GRCm38.p3 | 16:52115423 | TTTTATTTAATCTAC[C/T]GGTGACTTTAAACTT | 208650 |
rs46997358 | snp | A/G | 0.124444 | 0.216185 | intron-variant | Cblb | Mm_Celera | 16:52192295 | AGTGATGTCAACTGC[A/G]GTGTCCTTCCCGTGT | 208650 |
rs46999368 | snp | A/G | 0.489796 | 0.070696 | intron-variant | Cblb | GRCm38.p3 | 16:52164898 | TGCAGGTTACTCAGA[A/G]GACGGATCATACAGA | 208650 |
rs47007951 | snp | C/G | | | intron-variant | Cblb | GRCm38.p3 | 16:52055054 | GTACATCAGTCTATA[C/G]ATGTGCTCGTTTCGA | 208650 |
rs47010951 | snp | C/G | 0.231111 | 0.249285 | intron-variant | Cblb | GRCm38.p3 | 16:52101197 | ATTCCACAGCCAATA[C/G]CTGAGGGTAGTTTTA | 208650 |
rs47018355 | snp | A/C | 0.391111 | 0.206368 | intron-variant | Cblb | GRCm38.p3 | 16:52133685 | GCCATCAGTGATACC[A/C]AGCCTTCAAGGAGTG | 208650 |
rs47032455 | snp | A/G | 0.231111 | 0.249285 | intron-variant | Cblb | GRCm38.p3 | 16:52195255 | GAAGAGGTGCTAGAT[A/G]TAATAGTTGCATAAT | 208650 |
rs47038192 | snp | A/G | 0.124444 | 0.216185 | intron-variant | Cblb | Mm_Celera | 16:52197035 | TAAGGGGAATGAGCT[A/G]CAGTGCTGTGTCCTT | 208650 |
rs47038927 | snp | C/T | 0.132653 | 0.220748 | intron-variant | Cblb | Mm_Celera | 16:52160278 | AGTACAGTCAGCCAT[C/T]CCTGTAACTGTGCTC | 208650 |
rs47043028 | snp | C/T | 0.231111 | 0.249285 | intron-variant | Cblb | GRCm38.p3 | 16:52134376 | GGGCCAGTGTCTCTG[C/T]TGCTAGTGTTCTTGG | 208650 |
rs47044949 | snp | G/T | 0.32 | 0.24 | intron-variant | Cblb | GRCm38.p3 | 16:52075249 | CCATGGCAGTTCTGT[G/T]CTTTTATGTTACATG | 208650 |
rs47046767 | snp | C/T | 0.231111 | 0.249285 | intron-variant | Cblb | Mm_Celera | 16:52158472 | CATCAAACTTACAAC[C/T]GCCTTCATTTTGATA | 208650 |
rs47047488 | snp | C/T | 0.124444 | 0.216185 | intron-variant | Cblb | Mm_Celera | 16:52070258 | CAGCCAAAAGGGAAT[C/T]GGCATGTACCAAACT | 208650 |
rs47047805 | snp | C/T | 0.231111 | 0.249285 | intron-variant | Cblb | GRCm38.p3 | 16:52201700 | TTTCATGATGGTGAT[C/T]ACATTTCTTTCACTT | 208650 |
rs47068548 | snp | C/T | 0.32 | 0.24 | intron-variant | Cblb | GRCm38.p3 | 16:52103378 | ATGTTGCAGAATCAG[C/T]AGTGGGGTGAGCTGG | 208650 |
rs47095270 | snp | G/T | 0.124444 | 0.216185 | intron-variant | Cblb | GRCm38.p3 | 16:52135987 | TAGGGAAAGCAGGAA[G/T]ACTGACTGAGAGGGT | 208650 |
rs47113268 | snp | A/T | 0.489796 | 0.070696 | intron-variant | Cblb | GRCm38.p3 | 16:52092079 | CAGCATTTTCATGGG[A/T]TACTGAATTTTTATT | 208650 |
rs47115999 | snp | C/G | 0.231111 | 0.249285 | intron-variant | Cblb | GRCm38.p3 | 16:52124348 | GGCACAGGCTTCTTT[C/G]AATAGGAAAAATGTG | 208650 |
rs47122361 | snp | A/G | 0.408163 | 0.193609 | intron-variant | Cblb | Mm_Celera | 16:52163853 | ACTCCCAGAGAGGAC[A/G]AAGACCGTGACGCAG | 208650 |
rs47138106 | snp | C/T | 0.244898 | 0.249948 | intron-variant | Cblb | GRCm38.p3 | 16:52060268 | TTTAAAAGAAAGGCA[C/T]GTGGGTAAATAGATT | 208650 |
rs47158192 | snp | A/T | 0.5 | 0 | intron-variant | Cblb | Mm_Celera | 16:52093067 | TCTATACTATGAAAA[A/T]AGAAGCAAATTACTT | 208650 |
rs47161198 | snp | A/G | 0.231111 | 0.249285 | intron-variant | Cblb | GRCm38.p3 | 16:52178858 | TGGTCCTGAGGAAAG[A/G]CCTCTCTGAAAGGCG | 208650 |
rs47169548 | snp | C/T | 0.142012 | 0.225474 | intron-variant | Cblb | GRCm38.p3 | 16:52079092 | GTTTGTGTCCAAATG[C/T]GCAAATGTCAGACTT | 208650 |
rs47170687 | snp | C/G | 0.124444 | 0.216185 | intron-variant | Cblb | Mm_Celera | 16:52129909 | CCCTCAAAGCCAGAG[C/G]TGGTGTTAGGCCTTT | 208650 |
rs47191430 | snp | A/G | 0.375 | 0.216506 | intron-variant, upstream-variant-2KB | Cblb | Mm_Celera | 16:52046833 | ATACAGAAAAGTAGC[A/G]TCTTAAAATTAGATA | 208650 |
rs47194054 | snp | A/G | 0.375 | 0.216506 | intron-variant | Cblb | GRCm38.p3 | 16:52128564 | AAGCTCAAGTTGGCC[A/G]CTTTGTGCTTCTCTC | 208650 |
rs47196891 | snp | C/T | 0.132653 | 0.220748 | intron-variant | Cblb | Mm_Celera | 16:52055722 | TCCTAAGTTGGCTAC[C/T]TCTGCAGAGACACTA | 208650 |
rs47224465 | snp | A/G | 0.124444 | 0.216185 | intron-variant | Cblb | Mm_Celera | 16:52195145 | ATGTAGGGAAACCCC[A/G]TCTCCAAACAAACTA | 208650 |
rs47224976 | snp | C/T | 0.277778 | 0.248452 | intron-variant | Cblb | GRCm38.p3 | 16:52093025 | TGTGTTGACCAGTCA[C/T]AGAATTTCTGAGTTT | 208650 |
rs47228875 | snp | G/T | 0.32 | 0.24 | intron-variant | Cblb | GRCm38.p3 | 16:52067649 | TCTCCTATCTTTTCA[G/T]TCTCTATCTTCCTGT | 208650 |
rs47229177 | snp | A/G | 0.497778 | 0.0332592 | intron-variant | Cblb | GRCm38.p3 | 16:52194003 | TGAATGAGTTTGAAA[A/G]CTGCACAGTCCATTT | 208650 |
rs47246077 | snp | C/T | 0.132653 | 0.220748 | intron-variant | Cblb | Mm_Celera | 16:52161097 | CCACAGTGGACTAAC[C/T]ATGTCTTAGTGAGGC | 208650 |
rs47254589 | snp | C/G/T | 0.142012 | 0.225474 | utr-variant-5-prime, upstream-variant-2KB | Cblb | GRCm38.p3 | 16:52031677 | GGCGGGCGTGGAGCT[C/G/T]TTTGCACGGTAATTG | 208650 |
rs47258156 | snp | C/G | 0.18 | 0.24 | intron-variant | Cblb | Mm_Celera | 16:52143393 | AACAGGCAATTTCCA[C/G]TTTTGAAAAACGTAA | 208650 |
rs47261219 | snp | A/G | 0.124444 | 0.216185 | intron-variant | Cblb | Mm_Celera | 16:52076697 | TTTCCAGTACCACCC[A/G]TCACCTTTCCCATCT | 208650 |
rs47264800 | snp | C/T | 0.32 | 0.24 | intron-variant | Cblb | GRCm38.p3 | 16:52099822 | TCTTATCTAGGCTTA[C/T]GTCAAATATGGTTAT | 208650 |
rs47274845 | snp | A/C | 0.231111 | 0.249285 | intron-variant | Cblb | GRCm38.p3 | 16:52133697 | ACCAAGCCTTCAAGG[A/C]GTGTCTGACTAGATT | 208650 |
rs47275461 | snp | G/T | 0.32 | 0.24 | intron-variant | Cblb | GRCm38.p3 | 16:52180125 | ATAACAGTGTAAATG[G/T]GTGTAAATGGATGCA | 208650 |
rs47283023 | snp | A/G | 0.231111 | 0.249285 | intron-variant | Cblb | GRCm38.p3 | 16:52078338 | AAAAGTAGCAATAAA[A/G]TGGAGAGTTAATGGG | 208650 |
rs47293508 | snp | G/T | 0.489796 | 0.070696 | intron-variant | Cblb | GRCm38.p3 | 16:52167406 | TGGTGAAAACTTTGC[G/T]TCCTAACATCACTCC | 208650 |
rs47297147 | snp | G/T | | | intron-variant | Cblb | GRCm38.p3 | 16:52197314 | CACACAGCTCCAGTT[G/T]AAAACCTCGGGGCTG | 208650 |
rs47299448 | snp | C/G | 0.124444 | 0.216185 | intron-variant | Cblb | Mm_Celera | 16:52152489 | TTGGTTTGAGCCAGT[C/G]AGTTTGTTGTCTTTG | 208650 |
rs47300856 | snp | A/G | 0.375 | 0.216506 | intron-variant, utr-variant-5-prime | Cblb | Mm_Celera | 16:52047634 | TGAGCCAATGGTCTT[A/G]CTATTCTCTGGACTC | 208650 |
rs47315788 | snp | A/T | 0.124444 | 0.216185 | intron-variant | Cblb | Mm_Celera | 16:52192854 | TTAAATAATTTATTG[A/T]ATCCAGTCCCTTCTT | 208650 |
rs47345252 | snp | A/G | 0.231111 | 0.249285 | intron-variant | Cblb | Mm_Celera | 16:52136799 | ACACAGTTTTCTCAA[A/G]TCAAAGCCAAGAGTT | 208650 |
rs47348723 | snp | C/T | 0.391111 | 0.206368 | intron-variant | Cblb | Mm_Celera | 16:52169754 | TTGAGAGTCTGAGGA[C/T]CCAGCTGATTCTTAG | 208650 |
rs47352447 | snp | G/T | 0.375 | 0.216506 | intron-variant | Cblb | Mm_Celera | 16:52204103 | ACTTTTATTCTGAAC[G/T]TCAACTGTTATTGCA | 208650 |
rs47355812 | snp | A/G | 0.489796 | 0.070696 | intron-variant | Cblb | Mm_Celera | 16:52198016 | TCAGCCCAATAAAAT[A/G]TAAGTTGATTTCAAC | 208650 |
rs47360614 | snp | C/T | 0.426035 | 0.177515 | intron-variant | Cblb | GRCm38.p3 | 16:52170042 | CAACACATGAAGACA[C/T]GCTCTCTAGATTGTG | 208650 |
rs47369213 | snp | A/G | 0.497778 | 0.0332592 | intron-variant | Cblb | GRCm38.p3 | 16:52135335 | ATTGGTTGGGATTTG[A/G]AAAATTCAAAGATCC | 208650 |
rs47374450 | snp | A/G | 0.260355 | 0.249785 | intron-variant | Cblb | Mm_Celera | 16:52146008 | CACTAGTGAAAACTC[A/G]ATAATCAGTAAAGGT | 208650 |
rs47383068 | snp | A/G | 0.32 | 0.24 | intron-variant | Cblb | GRCm38.p3 | 16:52197501 | GCTCCAAAATTAATT[A/G]ACAGTGCATATATTT | 208650 |
rs47392782 | snp | C/T | 0.32 | 0.24 | intron-variant | Cblb | GRCm38.p3 | 16:52180198 | CCTACTTTGTTCCTC[C/T]GGGACCCTGGAGGAA | 208650 |
rs47392816 | snp | C/T | 0.244898 | 0.249948 | intron-variant | Cblb | GRCm38.p3 | 16:52159885 | CATGAAGCCACTAAA[C/T]GCAACACAACTTATT | 208650 |
rs47402695 | snp | C/T | 0.142012 | 0.225474 | intron-variant | Cblb | Mm_Celera | 16:52140019 | AACTCTTTGCTCTGT[C/T]TGTTACTGTGTGAGA | 208650 |
rs47405933 | snp | C/T | 0.231111 | 0.249285 | intron-variant | Cblb | GRCm38.p3 | 16:52100587 | TTTAGCAAACCATTC[C/T]AAACTCGGTGGTGTG | 208650 |
rs47406533 | snp | G/T | 0.32 | 0.24 | intron-variant | Cblb | GRCm38.p3 | 16:52100792 | CTCCCAATGAAGCCC[G/T]GGAGCACGTGCAGAG | 208650 |
rs47408862 | snp | A/T | 0.231111 | 0.249285 | intron-variant | Cblb | Mm_Celera | 16:52195869 | AGAAACACCCATATA[A/T]CGGGACTAAACTAGG | 208650 |
rs47411085 | snp | A/C | 0.473373 | 0.11227 | intron-variant | Cblb | Mm_Celera | 16:52156235 | TAGACTTATTACAGA[A/C]GACTATAAGTGCTAA | 208650 |
rs47415557 | snp | C/T | 0.231111 | 0.249285 | intron-variant | Cblb | Mm_Celera | 16:52137668 | CTGAGAGAAATAAAT[C/T]GCTCTTAAGTGTCAT | 208650 |
rs47418324 | snp | A/G | 0.124444 | 0.216185 | intron-variant | Cblb | Mm_Celera | 16:52185605 | AGAGGGCCAGCGTTT[A/G]TTAAACATAGTGGTT | 208650 |
rs47424421 | snp | A/G | 0.124444 | 0.216185 | downstream-variant-500B | Cblb | GRCm38.p3 | 16:52208540 | CTATTCAGGGAACTC[A/G]GTCTATATCACGAAT | 208650 |
rs47430219 | snp | C/T | 0.231111 | 0.249285 | intron-variant | Cblb | GRCm38.p3 | 16:52071787 | CAGAAGTCGCTTAAG[C/T]GGTCTGAGAGGCTTC | 208650 |
rs47432732 | snp | A/G | 0.408163 | 0.193609 | intron-variant | Cblb | Mm_Celera | 16:52064539 | CAGGGAAAGCACACC[A/G]TGTGGTTTCAGCGCT | 208650 |
rs47440673 | snp | C/T | 0.336735 | 0.234472 | intron-variant | Cblb | Mm_Celera | 16:52164790 | TATTATCAAATGGTA[C/T]TTTACACTTACTTTC | 208650 |
rs47442309 | snp | A/G | 0.32 | 0.24 | intron-variant | Cblb | Mm_Celera | 16:52183664 | TCAAAAGGTCCAAGC[A/G]TATATATCATGAAGA | 208650 |
rs47456671 | snp | C/T | 0.32 | 0.24 | intron-variant | Cblb | GRCm38.p3 | 16:52102047 | TGTCCCCATTATATG[C/T]TGGTATTCTTTTAAC | 208650 |
rs47462488 | snp | A/C | 0.231111 | 0.249285 | intron-variant | Cblb | GRCm38.p3 | 16:52134735 | GATGGAGCAAGCTGC[A/C]AGTGCTCTGGGATAA | 208650 |
rs47465607 | snp | A/C | 0.32 | 0.24 | intron-variant | Cblb | GRCm38.p3 | 16:52156581 | CGATGTGCATCACTG[A/C]CCAACAGGAAGATTC | 208650 |
rs47479320 | snp | A/G | 0.124444 | 0.216185 | intron-variant | Cblb | Mm_Celera | 16:52069979 | TAAAATCCGAAGCAA[A/G]CTTTTAGATGGCCAC | 208650 |
rs47481158 | snp | A/G | 0.244898 | 0.249948 | intron-variant | Cblb | GRCm38.p3 | 16:52089351 | GGAAATGAAACATGG[A/G]CATTCATAGTAAAAC | 208650 |
rs47490737 | snp | A/T | 0.32 | 0.24 | downstream-variant-500B | Cblb | GRCm38.p3 | 16:52208285 | CGTAATGAGGACCCT[A/T]ATTTGTGAAAAGGCT | 208650 |
rs47492149 | snp | C/T | 0.124444 | 0.216185 | intron-variant | Cblb | Mm_Celera | 16:52124564 | TTTTTTCCTTAGCGA[C/T]GGAGCAGTGGATCAA | 208650 |
rs47493733 | snp | C/T | 0.152778 | 0.230321 | intron-variant | Cblb | Mm_Celera | 16:52140355 | CAGTATACTTATGAA[C/T]GAAAATCCCTTATTG | 208650 |
rs47502026 | snp | C/T | 0.391111 | 0.206368 | intron-variant | Cblb | Mm_Celera | 16:52170421 | CAATAGATTGCACAG[C/T]CCACATTGGAGGGCT | 208650 |
rs47502318 | snp | A/C | 0.231111 | 0.249285 | intron-variant | Cblb | GRCm38.p3 | 16:52173495 | TAAAAATATATCTCA[A/C]CCATCTGGGCTCATT | 208650 |
rs47504149 | snp | A/G | 0.231111 | 0.249285 | intron-variant | Cblb | Mm_Celera | 16:52133147 | ATAATCATCATACGC[A/G]AGGCTTTAAATAAGA | 208650 |
rs47505125 | snp | C/G | 0.391111 | 0.206368 | intron-variant | Cblb | Mm_Celera | 16:52171095 | CACTATTCACAAACA[C/G]GTCCTCCAGATTCCT | 208650 |
rs47506772 | snp | C/G | 0.32 | 0.24 | intron-variant | Cblb | GRCm38.p3 | 16:52199956 | TTCTCTGGCTGAGAC[C/G]GCAAGGCTTCCTTTT | 208650 |
rs47517656 | snp | C/G | 0.375 | 0.216506 | intron-variant | Cblb | GRCm38.p3 | 16:52096197 | TTCTTCAACAAAGTT[C/G]GTAGGTGTGCATAAA | 208650 |
rs47520584 | snp | C/T | 0.18 | 0.24 | intron-variant | Cblb | Mm_Celera | 16:52140974 | CACTGAAGCCTCATA[C/T]ATTAAAATAATATGG | 208650 |
rs47546256 | snp | C/T | 0.408163 | 0.193609 | intron-variant | Cblb | GRCm38.p3 | 16:52132753 | AGATAGATGATGTTT[C/T]AGTGTGGATGTCAAG | 208650 |
rs47547412 | snp | C/T | 0.231111 | 0.249285 | intron-variant | Cblb | Mm_Celera | 16:52196439 | ATGAAAAGAACAGTT[C/T]TAAAGATTCAGAAAC | 208650 |
rs47556017 | snp | C/T | 0.231111 | 0.249285 | intron-variant | Cblb | GRCm38.p3 | 16:52081678 | GTAAAGCATTACTGA[C/T]AGTGCTTGTTCAACA | 208650 |
rs47556657 | snp | C/T | 0.32 | 0.24 | intron-variant | Cblb | GRCm38.p3 | 16:52183726 | ACTAGGTCAACCTGC[C/T]TAAGAATTTTTCTTC | 208650 |
rs47558498 | snp | C/T | 0.124444 | 0.216185 | intron-variant | Cblb | Mm_Celera | 16:52076827 | GGAGAGAGCAGATTG[C/T]CAGAAGTGGTGCGGG | 208650 |
rs47561521 | snp | A/G | 0.132653 | 0.220748 | utr-variant-3-prime | Cblb | Mm_Celera | 16:52206363 | ACATCAGACAGATCC[A/G]ATGGAGCTGCCATTG | 208650 |
rs47563303 | snp | A/T | 0.124444 | 0.216185 | intron-variant | Cblb | Mm_Celera | 16:52158567 | TCTATTTCTGTGCCT[A/T]TGTTTCCTACATTTG | 208650 |
rs47569056 | snp | A/G | 0.124444 | 0.216185 | intron-variant | Cblb | Mm_Celera | 16:52133670 | TCTGAGAGGAAGGAA[A/G]CCATCAGTGATACCA | 208650 |
rs47571713 | snp | C/T | 0.5 | 0 | intron-variant | Cblb | Mm_Celera | 16:52042975 | ACAACTGCATGATCC[C/T]GTTCCTTTACCCTGG | 208650 |
rs47574997 | snp | C/T | 0.124444 | 0.216185 | intron-variant | Cblb | Mm_Celera | 16:52068903 | CTATGCCACTCAATG[C/T]GTTGTCTCTTAGGTC | 208650 |
rs47578870 | snp | C/T | 0.32 | 0.24 | intron-variant | Cblb | GRCm38.p3 | 16:52102257 | TACTGTAGGTGTTTT[C/T]CTCGGTTTCTTTGCC | 208650 |
rs47590693 | snp | A/G | 0.124444 | 0.216185 | intron-variant | Cblb | Mm_Celera | 16:52201740 | GGAATTCTTATACCT[A/G]TTTGGAAGCCGTCTA | 208650 |
rs47608857 | snp | A/T | 0.142012 | 0.225474 | intron-variant | Cblb | Mm_Celera | 16:52132177 | ATTTGTATGCTAAAG[A/T]ATTGTTTTAAACTTC | 208650 |
rs47610945 | snp | C/T | 0.124444 | 0.216185 | intron-variant | Cblb | Mm_Celera | 16:52159674 | AGCAGTAATTGTTTG[C/T]TCATTGTTCTGTCTG | 208650 |
rs47631387 | snp | A/G | 0.231111 | 0.249285 | intron-variant | Cblb | GRCm38.p3 | 16:52134639 | GTGCCTGTTTCAGCA[A/G]CTTGAAGTTGGGGAC | 208650 |
rs47631895 | snp | A/G | 0.32 | 0.24 | intron-variant | Cblb | GRCm38.p3 | 16:52087277 | CAGGCGATTGTGACT[A/G]GAGGTGGAGTCCTGG | 208650 |
rs47633300 | snp | A/C | 0.244898 | 0.249948 | intron-variant | Cblb | GRCm38.p3 | 16:52123249 | CCAGATGTTAATGAA[A/C]TTTCTGAGAAAAGGC | 208650 |
rs47634750 | snp | C/T | 0.391111 | 0.206368 | intron-variant | Cblb | GRCm38.p3 | 16:52187286 | CTGTTTCTCCTCTTG[C/T]GCTTGAATTCTACGT | 208650 |
rs47635377 | snp | C/T | 0.124444 | 0.216185 | intron-variant | Cblb | Mm_Celera | 16:52151621 | CAGTGGTAGATTCCA[C/T]ATGAGCAAGTCAAGA | 208650 |
rs47647848 | snp | A/T | 0.132653 | 0.220748 | intron-variant | Cblb | Mm_Celera | 16:52138595 | AGTTTTTTTTAGTGC[A/T]CTCTATTTATCAATA | 208650 |
rs47650619 | snp | C/T | 0.124444 | 0.216185 | intron-variant | Cblb | Mm_Celera | 16:52107727 | TGATGTTGGCTAGAA[C/T]AAGCTAAACTACTTA | 208650 |
rs47651070 | snp | A/G | | | intron-variant, utr-variant-5-prime | Cblb | Mm_Celera | 16:52048450 | GTAACTGTTCAGACT[A/G]GTTTCTTGCTGGTCT | 208650 |
rs47652447 | snp | A/T | 0.124444 | 0.216185 | intron-variant | Cblb | Mm_Celera | 16:52171807 | AGTCCATCAATACAA[A/T]TCATGAAGCCATTAG | 208650 |
rs47653820 | snp | A/G | 0.124444 | 0.216185 | intron-variant | Cblb | Mm_Celera | 16:52201336 | AACTGTTTACATCTG[A/G]AGAGAGACCGCTATG | 208650 |
rs47662790 | snp | A/G | 0.391111 | 0.206368 | intron-variant | Cblb | Mm_Celera | 16:52169915 | TGTGTGAGGAAGCAC[A/G]TGTTCATGCATATGA | 208650 |
rs47668936 | snp | C/T | 0.21875 | 0.248039 | intron-variant | Cblb | Mm_Celera | 16:52092856 | GCCTGCTTCTAACAA[C/T]TTGAGCACTTAAAAA | 208650 |
rs47677694 | snp | C/T | 0.132653 | 0.220748 | intron-variant | Cblb | Mm_Celera | 16:52159563 | TTAAGCGTTAAATAA[C/T]TTAGGTAAGTTTATG | 208650 |
rs47680429 | snp | A/T | 0.231111 | 0.249285 | intron-variant | Cblb | GRCm38.p3 | 16:52078421 | TGAGTCCAATAGAGT[A/T]TTAAACATAGACTGT | 208650 |
rs47699065 | snp | C/T | 0.32 | 0.24 | utr-variant-3-prime | Cblb | Mm_Celera | 16:52205188 | TTTCTCCCATTCACA[C/T]GGCACGCTAGTCTGA | 208650 |
rs47702590 | snp | C/G | 0.408163 | 0.193609 | intron-variant | Cblb | Mm_Celera | 16:52171194 | GACAGCCAAATTCTG[C/G]TTTGATGAAATGGGT | 208650 |
rs47708856 | snp | C/T | 0.244898 | 0.249948 | intron-variant | Cblb | GRCm38.p3 | 16:52162201 | CGTGGAAGATGTAAA[C/T]TTAGGAGATGAGGTT | 208650 |
rs47711661 | snp | C/G | 0.32 | 0.24 | intron-variant | Cblb | GRCm38.p3 | 16:52182612 | GTTTTATTCGTTGCA[C/G]TTAGGTATTACACTT | 208650 |
rs47716104 | snp | G/T | 0.391111 | 0.206368 | intron-variant | Cblb | Mm_Celera | 16:52171148 | TCAGCTAGGAGATGG[G/T]CGTGTACTCCACTCT | 208650 |
rs47716837 | snp | G/T | 0.277778 | 0.248452 | intron-variant | Cblb | Mm_Celera | 16:52147024 | TGTGTTCAAGAAAGT[G/T]CATTTTTAGCAAGTT | 208650 |
rs47718385 | snp | A/C | 0.231111 | 0.249285 | intron-variant | Cblb | Mm_Celera | 16:52148349 | GAGTGGTGGGATTGC[A/C]GACAGGTGCCACTTA | 208650 |
rs47721206 | snp | C/T | 0.124444 | 0.216185 | intron-variant | Cblb | Mm_Celera | 16:52202687 | GGCTAATTAGTTATT[C/T]CTGCTTTTATGTGGT | 208650 |
rs47722968 | snp | A/G | 0.408163 | 0.193609 | intron-variant | Cblb | Mm_Celera | 16:52167200 | TCCCAATGGGGATGA[A/G]AAGTTTAAGGTTACT | 208650 |
rs47723638 | snp | A/G | 0.231111 | 0.249285 | intron-variant | Cblb | GRCm38.p3 | 16:52170043 | AACACATGAAGACAT[A/G]CTCTCTAGATTGTGG | 208650 |
rs47729123 | snp | C/T | 0.124444 | 0.216185 | intron-variant | Cblb | Mm_Celera | 16:52148054 | CTTCTACTGTCTCTT[C/T]TCTGGGTTAGTGTGA | 208650 |
rs47734394 | snp | C/T | 0.260355 | 0.249785 | intron-variant | Cblb | Mm_Celera | 16:52151341 | CTTTTTACAATGTAA[C/T]ACTAATCTTAGTGTA | 208650 |
rs47741725 | snp | A/T | 0.444444 | 0.157135 | intron-variant | Cblb | GRCm38.p3 | 16:52050018 | CTGAATTAATTTACC[A/T]CTCAGTATTTAAGTT | 208650 |
rs47749744 | snp | A/G | 0.124444 | 0.216185 | intron-variant | Cblb | GRCm38.p3 | 16:52102185 | CATTAGGTTCATAAC[A/G]TTTGCAGCTTTTCTT | 208650 |
rs47751799 | snp | C/T | | | intron-variant | Cblb | GRCm38.p3 | 16:52174755 | TCCAGCCTTCTTCTT[C/T]ATGACTTTATCTCAC | 208650 |
rs47760222 | snp | C/T | 0.132653 | 0.220748 | intron-variant | Cblb | Mm_Celera | 16:52057385 | TTCATCCGCTTCATT[C/T]TCATGTACAAGCAGA | 208650 |
rs47774405 | snp | C/T | 0.244898 | 0.249948 | missense | Cblb | Mm_Celera | 16:52166214 | CAGGTGATGGGATGT[C/T]GCATCCTCGGGGATG | 208650 |
rs47774729 | snp | A/G/T | 0.124444 | 0.216185 | intron-variant | Cblb | GRCm38.p3 | 16:52198298 | GCCCCTCCCTGGGTC[A/G/T]GCTACTCTCTCATAT | 208650 |
rs47774814 | snp | A/G | 0.124444 | 0.216185 | intron-variant | Cblb | Mm_Celera | 16:52165932 | GAAGGTCTTTTCAAT[A/G]CATGGTACAAACAAC | 208650 |
rs47783243 | snp | C/T | | | intron-variant | Cblb | GRCm38.p3 | 16:52115251 | GTTTTTCTGTCGTCC[C/T]TGTGCTTTTTGACTT | 208650 |
rs47789819 | snp | C/T | 0.444444 | 0.157135 | intron-variant | Cblb | Mm_Celera | 16:52051350 | AGGTACATTCTCGCC[C/T]GTGGAGCCCTGTGGC | 208650 |
rs47796395 | snp | A/G | 0.32 | 0.24 | utr-variant-3-prime | Cblb | Mm_Celera | 16:52207666 | CATTTCCTGCAGTTT[A/G]AACGTGACTTTGCCT | 208650 |
rs47812568 | snp | A/T | 0.124444 | 0.216185 | intron-variant | Cblb | Mm_Celera | 16:52162670 | TTAATGGTGGTTAGA[A/T]TCTCTTGGTATAGTG | 208650 |
rs47813885 | snp | C/T | 0.444444 | 0.157135 | intron-variant | Cblb | GRCm38.p3 | 16:52052709 | TGGGTTCTCTTTCAG[C/T]TTTTTTGTACACCAG | 208650 |
rs47817707 | snp | C/G | 0.32 | 0.24 | intron-variant | Cblb | Mm_Celera | 16:52180372 | ACAAAAGTTTGGATA[C/G]AATGCATAGACTTTG | 208650 |
rs47819257 | snp | A/G | 0.142012 | 0.225474 | intron-variant | Cblb | Mm_Celera | 16:52157087 | GTTGGAGTTTTCTCT[A/G]TTATTACAGGGACAA | 208650 |
rs47820902 | snp | G/T | 0.32 | 0.24 | intron-variant | Cblb | GRCm38.p3 | 16:52107904 | AAGAGTGTCGGGGCA[G/T]CATCGGTGATGGCCT | 208650 |
rs47827225 | snp | C/T | 0.32 | 0.24 | intron-variant | Cblb | Mm_Celera | 16:52095341 | TTATTGAAGCAATAT[C/T]CACACTGCAGTGTTT | 208650 |
rs47829261 | snp | A/G | 0.124444 | 0.216185 | intron-variant | Cblb | GRCm38.p3 | 16:52082703 | ATTCTGGACAAAACT[A/G]TGGGATCTCCCAGGC | 208650 |
rs47830647 | snp | A/G | 0.132653 | 0.220748 | intron-variant | Cblb | Mm_Celera | 16:52064585 | GACACGTGGCCTCAC[A/G]TTATAGCTGCAGGTG | 208650 |
rs47840496 | snp | A/T | | | intron-variant | Cblb | GRCm38.p3 | 16:52114936 | TGAATTATGAATTTT[A/T]GACACTTTGGGTTTT | 208650 |
rs47844631 | snp | A/C | 0.32 | 0.24 | intron-variant | Cblb | GRCm38.p3 | 16:52065733 | CTTCTTGTGACAAAA[A/C]TGTGGGAAAGACCAT | 208650 |
rs47847209 | snp | A/G | 0.124444 | 0.216185 | intron-variant | Cblb | Mm_Celera | 16:52160352 | CTAGGTGGTATCTGA[A/G]AAGTCCCAGAGCAGA | 208650 |
rs47850853 | snp | C/G | 0.32 | 0.24 | intron-variant | Cblb | GRCm38.p3 | 16:52072495 | ATTTTCCCATTGTAT[C/G]AAAAGGGTCCTTGTT | 208650 |
rs47851384 | snp | C/T | 0.142012 | 0.225474 | intron-variant | Cblb | GRCm38.p3 | 16:52162514 | AATCTGTATGGTCTT[C/T]TCTTTAAAGTCTAAT | 208650 |
rs47856570 | snp | C/T | 0.32 | 0.24 | intron-variant | Cblb | GRCm38.p3 | 16:52197435 | TGTTTCACTGAAAAC[C/T]TTATGTGAACTCACA | 208650 |
rs47862934 | snp | C/T | 0.32 | 0.24 | intron-variant | Cblb | GRCm38.p3 | 16:52190117 | GTCTTCAACGGGAAA[C/T]AAATACAGTTTTCTA | 208650 |
rs47872496 | snp | C/T | 0.124444 | 0.216185 | intron-variant | Cblb | Mm_Celera | 16:52100317 | TATGCATGATGACAG[C/T]ATGGTAAATTATCCA | 208650 |
rs47878721 | snp | A/G | 0.32 | 0.24 | intron-variant | Cblb | Mm_Celera | 16:52193968 | TTGGAAGTAAATGGA[A/G]TAGCTCTCGCCTGAA | 208650 |
rs47897034 | snp | A/G | 0.244898 | 0.249948 | intron-variant | Cblb | Mm_Celera | 16:52166537 | GCTCACTTAACGTTG[A/G]ACACGAGGGAAGGGA | 208650 |
rs47898170 | snp | C/T | 0.497778 | 0.0332592 | intron-variant | Cblb | GRCm38.p3 | 16:52191902 | TAGGCATTTCTACAG[C/T]TTTGCTTAAGGCAAA | 208650 |
rs47900265 | snp | A/C | 0.231111 | 0.249285 | intron-variant | Cblb | Mm_Celera | 16:52136910 | AAAAAGTCAGAGTCC[A/C]ATTGACGCCCTCTCT | 208650 |
rs47901006 | snp | G/T | 0.231111 | 0.249285 | intron-variant | Cblb | Mm_Celera | 16:52155916 | CACATCTCTCAATGA[G/T]TCTGTGACCTTCAGT | 208650 |
rs47914744 | snp | C/T | 0.48 | 0.0979796 | intron-variant | Cblb | Mm_Celera | 16:52094981 | CACGGGTGATGTGAT[C/T]GGGCTTCTAGCCTGC | 208650 |
rs47914860 | snp | A/C | 0.391111 | 0.206368 | intron-variant | Cblb | Mm_Celera | 16:52171373 | ATTAGGAAGAACTAC[A/C]CAGAATTTCATGTGT | 208650 |
rs47931191 | snp | C/T | 0.32 | 0.24 | intron-variant | Cblb | Mm_Celera | 16:52180903 | CAGATGCTCTCTGAC[C/T]AACAAAAGAGTGAGT | 208650 |
rs47931254 | snp | A/C | 0.124444 | 0.216185 | intron-variant | Cblb | Mm_Celera | 16:52070202 | TTTTCTCTGTTTACG[A/C]ATCATACTTGAGCTC | 208650 |
rs47933704 | snp | C/T | 0.231111 | 0.249285 | utr-variant-3-prime | Cblb | GRCm38.p3 | 16:52205909 | AATCTATGGATATCT[C/T]TTGACCATCTGTAAT | 208650 |
rs47954895 | snp | A/C/G | 0.124444 | 0.216185 | intron-variant | Cblb | Mm_Celera | 16:52174192 | ATCTGTGATATGGTA[A/C/G]ATCACCACTGATCCT | 208650 |
rs47958859 | snp | A/G | 0.124444 | 0.216185 | intron-variant | Cblb | GRCm38.p3 | 16:52136142 | TTTGTTGGGTACACA[A/G]TGTTCCTGCTCAAAC | 208650 |
rs47986395 | snp | C/T | 0.152778 | 0.230321 | intron-variant | Cblb | GRCm38.p3 | 16:52186778 | AAAAAGTACTTAACT[C/T]TGTTTTAAGCTACAT | 208650 |
rs47988544 | snp | G/T | 0.124444 | 0.216185 | intron-variant | Cblb | Mm_Celera | 16:52185425 | ACTAAGCTAGGAGCT[G/T]AAGGGCAAGTGTGTT | 208650 |
rs47992582 | snp | C/T | 0.231111 | 0.249285 | intron-variant | Cblb | Mm_Celera | 16:52135395 | CTGGTAGAAAGGCCA[C/T]TGGGGCTACACCAAG | 208650 |
rs47996623 | snp | A/G | 0.124444 | 0.216185 | intron-variant | Cblb | Mm_Celera | 16:52104293 | GGACAAACTCAGCGA[A/G]AGAAATTAGGAAAGG | 208650 |
rs47997244 | snp | A/G | 0.231111 | 0.249285 | intron-variant | Cblb | GRCm38.p3 | 16:52195759 | ATGCGAGTATTGTGG[A/G]GTCAATAGCATCATT | 208650 |
rs48003779 | snp | A/G | 0.124444 | 0.216185 | intron-variant | Cblb | GRCm38.p3 | 16:52161831 | CTTAGCAGATGTCTC[A/G]CCATTTCCATAATAA | 208650 |
rs48013564 | snp | G/T | 0.32 | 0.24 | intron-variant | Cblb | GRCm38.p3 | 16:52179309 | TCTGCCATTAGTTGC[G/T]TGAACAGAGATCTTC | 208650 |
rs48018784 | snp | A/G | | | intron-variant, utr-variant-5-prime | Cblb | GRCm38.p3 | 16:52048217 | CTTCACTGCTGGGCC[A/G]TCTTTGCTTTAGTGT | 208650 |
rs48028557 | snp | C/T | | | intron-variant, utr-variant-5-prime | Cblb | GRCm38.p3 | 16:52049000 | CACCCTACAAGTTCT[C/T]GTGTAGCCCAGGATG | 208650 |
rs48030768 | snp | A/G | 0.5 | 0 | intron-variant, utr-variant-5-prime | Cblb | GRCm38.p3 | 16:52049268 | CGCTGATGCTACTGG[A/G]ATATCACTCTGACTC | 208650 |
rs48031517 | snp | A/T | 0.231111 | 0.249285 | intron-variant | Cblb | GRCm38.p3 | 16:52201502 | TTTACAGAGGGCTTC[A/T]CTTGCTCCCTGCAGT | 208650 |
rs48038288 | snp | C/G | 0.32 | 0.24 | intron-variant | Cblb | GRCm38.p3 | 16:52079178 | GTTTCTTAGAGTCTC[C/G]TCTCATTTATCTTAA | 208650 |
rs48043451 | snp | A/G | 0.32 | 0.24 | intron-variant | Cblb | GRCm38.p3 | 16:52178402 | ACTGTAGAAAGCTGA[A/G]GAATAATTTCTTTAT | 208650 |
rs48044966 | snp | A/G | 0.497778 | 0.0332592 | intron-variant | Cblb | GRCm38.p3 | 16:52078197 | CCTCTGCAATTCAGG[A/G]AAAAGCCTAATTAAG | 208650 |
rs48046566 | snp | A/G | 0.132653 | 0.220748 | intron-variant | Cblb | Mm_Celera | 16:52159764 | GTTCCTTTAATTCCC[A/G]AGTGTTCTTGCTTCT | 208650 |
rs48047742 | snp | C/T | 0.124444 | 0.216185 | missense | Cblb | GRCm38.p3 | 16:52186179 | ATGGAACTCATGGTG[C/T]GCCTTCAGAGATGAA | 208650 |
rs48056207 | snp | C/T | 0.32 | 0.24 | intron-variant | Cblb | Mm_Celera | 16:52132278 | ATACTATGGATTTTT[C/T]ACTTTACCTCTGGCT | 208650 |
rs48060424 | snp | C/T | 0.32 | 0.24 | intron-variant | Cblb | GRCm38.p3 | 16:52181475 | AGATTGATGTCTGTC[C/T]CCAAGAATTTAGTGT | 208650 |
rs48066810 | snp | C/T | 0.244898 | 0.249948 | intron-variant | Cblb | GRCm38.p3 | 16:52159582 | GGTAAGTTTATGGTA[C/T]ACTTATTTTCTGTAT | 208650 |
rs48072038 | snp | C/T | | | intron-variant | Cblb | GRCm38.p3 | 16:52115037 | ACAGGTCAAGTACTC[C/T]CCCTACCTCCTCAGC | 208650 |
rs48073304 | snp | A/G | 0.244898 | 0.249948 | intron-variant | Cblb | Mm_Celera | 16:52198047 | AATTTTTAGTAAGGT[A/G]TTCAAACATTTATTC | 208650 |
rs48077668 | snp | C/T | 0.124444 | 0.216185 | intron-variant | Cblb | Mm_Celera | 16:52151536 | AATGCGTTTCTCAAC[C/T]CAAAGTATTTTACCA | 208650 |
rs48120045 | snp | A/C | 0.124444 | 0.216185 | intron-variant | Cblb | Mm_Celera | 16:52174865 | ATGGAGTTTTTTCCT[A/C]TCCAGTTAAGCCTCC | 208650 |
rs48127879 | snp | A/C | 0.152778 | 0.230321 | intron-variant | Cblb | Mm_Celera | 16:52204301 | GCAATAAGTAACTAA[A/C]AAATAAAAAGAGTTG | 208650 |
rs48147398 | snp | A/G | 0.152778 | 0.230321 | intron-variant | Cblb | Mm_Celera | 16:52140746 | TTTAAACAGTTTTAG[A/G]ATAGGCTATAACTCA | 208650 |
rs48148789 | snp | A/G | 0.132653 | 0.220748 | intron-variant | Cblb | GRCm38.p3 | 16:52164043 | TTAAGGCTGATCTCC[A/G]TTCCTAGTTTTCCCT | 208650 |
rs48152091 | snp | C/T | 0.165289 | 0.235211 | intron-variant | Cblb | Mm_Celera | 16:52147449 | AGGCAGAGAAAACAT[C/T]TCCATGCAGAGTCCC | 208650 |
rs48163513 | snp | C/T | 0.231111 | 0.249285 | intron-variant | Cblb | Mm_Celera | 16:52136375 | ACCCACTTCTTTACA[C/T]CTTCAAAGTGTTATG | 208650 |
rs48164403 | snp | A/G | 0.124444 | 0.216185 | upstream-variant-2KB | Cblb | GRCm38.p3 | 16:52029695 | TCCATGATGCACTTT[A/G]CTCCGCAGGCCATTC | 208650 |
rs48171346 | snp | G/T | 0.231111 | 0.249285 | intron-variant | Cblb | GRCm38.p3 | 16:52197287 | GTAGTTGATGCCACT[G/T]GAAAACCTTCACACA | 208650 |
rs48173706 | snp | C/T | 0.231111 | 0.249285 | intron-variant | Cblb | GRCm38.p3 | 16:52169823 | GGACATTACAGATGA[C/T]CTTATGTAGAACAAT | 208650 |
rs48174411 | snp | A/G | 0.124444 | 0.216185 | intron-variant | Cblb | Mm_Celera | 16:52156339 | GTGCATCTTCTGTCT[A/G]AGGGTGGTTACCTGA | 208650 |
rs48178559 | snp | A/G | 0.124444 | 0.216185 | intron-variant | Cblb | Mm_Celera | 16:52155889 | GAAGGATGCTCTCCT[A/G]CATTCTTGGCTCACA | 208650 |
rs48180028 | snp | A/G | 0.142012 | 0.225474 | intron-variant | Cblb | Mm_Celera | 16:52162872 | AGGGAAACATTATCA[A/G]TTACAAAGAATGTGC | 208650 |
rs48181960 | snp | C/G | 0.231111 | 0.249285 | intron-variant | Cblb | GRCm38.p3 | 16:52105315 | AAAATAAAGGTGGGA[C/G]TCATAATATAATGCT | 208650 |
rs48183493 | snp | C/G | 0.124444 | 0.216185 | intron-variant | Cblb | Mm_Celera | 16:52069232 | AACGAAAGCTTAAAA[C/G]TATGGATTTGATATT | 208650 |
rs48183664 | snp | C/G | 0.497778 | 0.0332592 | intron-variant | Cblb | GRCm38.p3 | 16:52171659 | CTGTAGTCTGAAATA[C/G]ATACAATATTGCATT | 208650 |
rs48186102 | snp | A/T | 0.231111 | 0.249285 | intron-variant | Cblb | GRCm38.p3 | 16:52190712 | CACCTGGTTTGATAA[A/T]GTAGAGACATTGGAG | 208650 |
rs48203952 | snp | A/G | 0.231111 | 0.249285 | intron-variant | Cblb | GRCm38.p3 | 16:52151684 | TTGAGTCAGAACTGA[A/G]CTAAGTCAACTGAAC | 208650 |
rs48212047 | snp | G/T | 0.231111 | 0.249285 | intron-variant | Cblb | Mm_Celera | 16:52137532 | ATGTTAATCACACCA[G/T]TTTGCAGAACAAGGT | 208650 |
rs48227248 | snp | A/G | 0.444444 | 0.157135 | intron-variant | Cblb | GRCm38.p3 | 16:52149039 | TAGTTTCAACTTGCA[A/G]TGTTCATTTGCGTGC | 208650 |
rs48228680 | snp | C/T | 0.244898 | 0.249948 | intron-variant | Cblb | Mm_Celera | 16:52126021 | TCAGAATATTAGTGG[C/T]CCCTCCTCTGAGAAC | 208650 |
rs48237980 | snp | C/T | 0.18 | 0.24 | intron-variant | Cblb | Mm_Celera | 16:52143054 | AAATTGATAGCTTTG[C/T]TGCGTTTTATATTGT | 208650 |
rs48245748 | snp | A/G | 0.32 | 0.24 | intron-variant | Cblb | GRCm38.p3 | 16:52106144 | GTAACGTAAGACTTC[A/G]TAGCAGAGTAAGGAT | 208650 |
rs48246791 | snp | A/G | 0.231111 | 0.249285 | intron-variant | Cblb | Mm_Celera | 16:52157043 | TGCTGTGAGCCCCAG[A/G]AAGTAGTATAGGTAT | 208650 |
rs48249209 | snp | C/T | 0.32 | 0.24 | intron-variant | Cblb | GRCm38.p3 | 16:52072185 | GTGTCAGCCAGCAGT[C/T]GGTTTGAGAGGAGCA | 208650 |
rs48280896 | snp | A/G | 0.124444 | 0.216185 | intron-variant | Cblb | Mm_Celera | 16:52133990 | ATATTTCTGCAATAA[A/G]AAGCTGCCCTCTGGC | 208650 |
rs48289512 | snp | C/T | 0.48 | 0.0979796 | intron-variant | Cblb | GRCm38.p3 | 16:52091078 | GAGAAAGGGTCAGTT[C/T]TCAGTGTTGAAAGAG | 208650 |
rs48289712 | snp | C/G | 0.124444 | 0.216185 | intron-variant | Cblb | GRCm38.p3 | 16:52067126 | TTAACCTCAAGACCT[C/G]AAAGAGCTGAAAGGG | 208650 |
rs48294343 | snp | A/G | 0.32 | 0.24 | intron-variant | Cblb | GRCm38.p3 | 16:52089406 | AATTCAGGAAATTAA[A/G]GAGGTAGATTTAGAA | 208650 |
rs48299398 | snp | A/G | 0.231111 | 0.249285 | intron-variant | Cblb | GRCm38.p3 | 16:52193880 | GAAATGCATGGGTAG[A/G]GATAGAAATTTGAGT | 208650 |
rs48300062 | snp | C/T | 0.124444 | 0.216185 | intron-variant | Cblb | Mm_Celera | 16:52107331 | CCCAAAGCAGAACAT[C/T]CTCATGAAGTTTGGA | 208650 |
rs48315952 | snp | A/G | 0.497041 | 0.0383476 | intron-variant | Cblb | GRCm38.p3 | 16:52139343 | TGATAACACTAAGGT[A/G]CAGTAGTGTTAGATT | 208650 |
rs48319922 | snp | C/T | 0.32 | 0.24 | utr-variant-3-prime | Cblb | GRCm38.p3 | 16:52205614 | CACCGCCTGGAAATA[C/T]GTTAATATGCCTTTA | 208650 |
rs48320917 | snp | G/T | 0.32 | 0.24 | intron-variant | Cblb | GRCm38.p3 | 16:52105758 | CCTTTTAGGTGTAGT[G/T]AACTGCCTCTTTGAG | 208650 |
rs48323995 | snp | A/T | 0.32 | 0.24 | intron-variant | Cblb | GRCm38.p3 | 16:52189925 | ATAGGAGAAGCACAA[A/T]CTTTAGGTTCTCAAT | 208650 |
rs48327277 | snp | A/T | 0.124444 | 0.216185 | intron-variant | Cblb | Mm_Celera | 16:52191068 | TGGTGAAGCCTCTGT[A/T]CAGTGGGCTCCCTTA | 208650 |
rs48329165 | snp | A/G | 0.260355 | 0.249785 | intron-variant | Cblb | Mm_Celera | 16:52167760 | GCTTGTCATGGGAAG[A/G]GCCTTGAAACAAGCT | 208650 |
rs48333724 | snp | A/C | | | intron-variant | Cblb | GRCm38.p3 | 16:52114781 | GAAAATGTATAGAAC[A/C]GGTTGTTCACAGAAA | 208650 |
rs48335044 | snp | C/G | 0.497778 | 0.0332592 | intron-variant | Cblb | GRCm38.p3 | 16:52191821 | GCAACTGCTGGCATA[C/G]GTGCCTTTTTCTCTT | 208650 |
rs48336251 | snp | C/T | 0.408163 | 0.193609 | intron-variant | Cblb | GRCm38.p3 | 16:52118746 | GCAAAGGATAGTCTT[C/T]GCCCAGCAATTGTGT | 208650 |
rs48344915 | snp | C/T | | | intron-variant | Cblb | GRCm38.p3 | 16:52115064 | CAGCCCTCCCACCGC[C/T]TGCTGAGTCTACAGA | 208650 |
rs48345144 | snp | G/T | 0.408163 | 0.193609 | intron-variant | Cblb | GRCm38.p3 | 16:52065274 | TTGGACTTCCTGAGT[G/T]TATAGGTAATCCAAG | 208650 |
rs48346215 | snp | A/G | 0.124444 | 0.216185 | intron-variant | Cblb | Mm_Celera | 16:52134878 | ATTAGATTAAGAGAG[A/G]TTGATGGCAAACACA | 208650 |
rs48346693 | snp | A/G | 0.486111 | 0.0821678 | intron-variant | Cblb | GRCm38.p3 | 16:52145519 | GGGATCGCTTTGCAT[A/G]TTCATGTCCGTGCAT | 208650 |
rs48349528 | snp | C/T | 0.32 | 0.24 | intron-variant | Cblb | GRCm38.p3 | 16:52188956 | ATAATTTTTGCTTGG[C/T]ACTGTGGTTTGATTA | 208650 |
rs48356391 | snp | A/T | 0.165289 | 0.235211 | intron-variant | Cblb | Mm_Celera | 16:52140097 | CTAATATTGATTACT[A/T]TGCTGTTTGTAGACA | 208650 |
rs48373419 | snp | C/T | 0.132653 | 0.220748 | intron-variant | Cblb | GRCm38.p3 | 16:52159218 | GACAATAGAATCATG[C/T]GGAAGGCAAGCATCA | 208650 |
rs48381030 | snp | A/G | 0.124444 | 0.216185 | utr-variant-3-prime | Cblb | GRCm38.p3 | 16:52205463 | CATCCACCCAGGAGT[A/G]TCATAATGCTGTAAA | 208650 |
rs48382852 | snp | A/T | 0.32 | 0.24 | intron-variant | Cblb | GRCm38.p3 | 16:52100219 | GAAGATCTTTAGGCC[A/T]TGTAAATTGGTAGTA | 208650 |
rs48384563 | snp | C/G | 0.32 | 0.24 | intron-variant | Cblb | Mm_Celera | 16:52126503 | CCTTTTTTCTCATGA[C/G]CAGTGAAGTGGAGAC | 208650 |
rs48386388 | snp | C/T | 0.132653 | 0.220748 | intron-variant | Cblb | Mm_Celera | 16:52062586 | GCTTGTGAGGAAATA[C/T]TTTGGATCTAATGTT | 208650 |
rs48391657 | snp | A/T | 0.124444 | 0.216185 | intron-variant | Cblb | Mm_Celera | 16:52132924 | GATTCTGAGGTTTGC[A/T]TATCTTGTGTGTGTT | 208650 |
rs48392788 | snp | A/C | 0.391111 | 0.206368 | intron-variant | Cblb | GRCm38.p3 | 16:52170311 | AACCTTAGACAATAT[A/C]GTCGAAGTCACAGGA | 208650 |
rs48396947 | snp | C/T | 0.124444 | 0.216185 | intron-variant | Cblb | Mm_Celera | 16:52078673 | GTGAATCCTGGGTAC[C/T]GAGAGTGAAAATTAG | 208650 |
rs48397474 | snp | A/G | 0.132653 | 0.220748 | intron-variant | Cblb | Mm_Celera | 16:52143036 | TACTATGTTGAATGC[A/G]TAAAATTGATAGCTT | 208650 |
rs48404266 | snp | C/T | 0.244898 | 0.249948 | intron-variant | Cblb | Mm_Celera | 16:52064228 | GGTTTTGGAAAGTCA[C/T]GGACATTGTCTTTGA | 208650 |
rs48408363 | snp | C/T | 0.231111 | 0.249285 | intron-variant | Cblb | GRCm38.p3 | 16:52121922 | TTTGAAGCAGAGATC[C/T]AGTCTGTTGAGCCCT | 208650 |
rs48440283 | snp | G/T | 0.124444 | 0.216185 | intron-variant | Cblb | Mm_Celera | 16:52136204 | GTACTTAAGACAAAA[G/T]TAAGTAGTTTACTTA | 208650 |
rs48452073 | snp | G/T | 0.231111 | 0.249285 | intron-variant | Cblb | GRCm38.p3 | 16:52164525 | GCAGGCAGTTCTCTG[G/T]GCTTTCTGTGTACCT | 208650 |
rs48460186 | snp | A/T | 0.124444 | 0.216185 | intron-variant | Cblb | Mm_Celera | 16:52201534 | TTAGGAGACCTGTTA[A/T]TGGAAATTGTTTTAC | 208650 |
rs48461245 | snp | A/C | 0.244898 | 0.249948 | upstream-variant-2KB | Cblb | GRCm38.p3 | 16:52030509 | TAGAGAGAATCATGG[A/C]ACTTGTCTAATGTGT | 208650 |
rs48463304 | snp | C/T | 0.124444 | 0.216185 | intron-variant | Cblb | Mm_Celera | 16:52184047 | TGTTTTGAAATATGT[C/T]TGTCTCTAAGCAAAA | 208650 |
rs48465702 | snp | A/T | 0.32 | 0.24 | intron-variant | Cblb | GRCm38.p3 | 16:52071375 | TTTTTGTATTCAGGC[A/T]CGAGAATTTCTGTCC | 208650 |
rs48472732 | snp | C/G | 0.124444 | 0.216185 | intron-variant | Cblb | Mm_Celera | 16:52068545 | TCACTGCATTTGCGT[C/G]TCCACTCTTGCTTTC | 208650 |
rs48482891 | snp | G/T | 0.231111 | 0.249285 | intron-variant | Cblb | Mm_Celera | 16:52135316 | AAGAGTTGGTAGTCA[G/T]CTGATTGGTTGGGAT | 208650 |
rs48491162 | snp | C/G | 0.124444 | 0.216185 | intron-variant | Cblb | Mm_Celera | 16:52132509 | TTCTAGTGGCTTAAT[C/G]GTTGTTCTCCTTGAT | 208650 |
rs48501033 | snp | C/T | 0.152778 | 0.230321 | intron-variant | Cblb | Mm_Celera | 16:52141862 | AGCAGGATGCTCAGG[C/T]GTTCATTCATAAGTT | 208650 |
rs48513549 | snp | A/G | 0.132653 | 0.220748 | intron-variant | Cblb | Mm_Celera | 16:52064555 | TGTGGTTTCAGCGCT[A/G]TGTTGGTTGGGGTAG | 208650 |
rs48521372 | snp | C/T | 0.444444 | 0.157135 | intron-variant | Cblb | Mm_Celera | 16:52043883 | ATGTGAGGCTGCCCT[C/T]TTTACAAGTTAATAA | 208650 |
rs48524783 | snp | A/G | 0.231111 | 0.249285 | intron-variant | Cblb | GRCm38.p3 | 16:52076844 | AGAAGTGGTGCGGGC[A/G]CCAAGTGGTAATGGC | 208650 |
rs48525417 | snp | G/T | 0.124444 | 0.216185 | intron-variant | Cblb | Mm_Celera | 16:52080119 | TGTAGCTATCATGTA[G/T]TAATAAGTCCTAGAT | 208650 |
rs48539719 | snp | A/G | 0.132653 | 0.220748 | intron-variant | Cblb | GRCm38.p3 | 16:52064709 | TTTATAGACTTTACC[A/G]GCAAACATATCAGAG | 208650 |
rs48559954 | snp | A/G | 0.124444 | 0.216185 | intron-variant | Cblb | Mm_Celera | 16:52137036 | AGTTCATTCAATGAA[A/G]CCAATACTAGAAAGC | 208650 |
rs48561307 | snp | G/T | 0.231111 | 0.249285 | intron-variant | Cblb | GRCm38.p3 | 16:52132413 | ATTTTACTTTATCAC[G/T]ATTGAGAAACCATGA | 208650 |
rs48589144 | snp | A/G | 0.391111 | 0.206368 | intron-variant | Cblb | Mm_Celera | 16:52167951 | TTCCAGAGCAAGGCT[A/G]TTAACTTTTTCAGAT | 208650 |
rs48590625 | snp | C/T | 0.231111 | 0.249285 | intron-variant | Cblb | GRCm38.p3 | 16:52184248 | TTCAGACACTGTTAG[C/T]GGCTGAGCTGCCTGG | 208650 |
rs48596157 | snp | C/T | 0.124444 | 0.216185 | intron-variant | Cblb | Mm_Celera | 16:52184602 | CTGCAAAGACGATAA[C/T]GGAGAGTGTTACCCT | 208650 |
rs48596635 | snp | A/T | 0.124444 | 0.216185 | intron-variant | Cblb | Mm_Celera | 16:52075967 | CCTTTTGGTTTTGCC[A/T]GTGGTCTTGTTTATT | 208650 |
rs48600412 | snp | C/T | 0.124444 | 0.216185 | intron-variant | Cblb | Mm_Celera | 16:52186642 | TCACATGACATCACT[C/T]TAACAGATGAACTAA | 208650 |
rs48605793 | snp | C/T | 0.32 | 0.24 | upstream-variant-2KB | Cblb | GRCm38.p3 | 16:52030580 | GTTACCAGACTGTTT[C/T]CTTTTACACGGCTAT | 208650 |
rs48613314 | snp | C/T | | | intron-variant | Cblb | GRCm38.p3 | 16:52115156 | AGGCTACTGCCAGAA[C/T]GTATACAGAAATGTA | 208650 |
rs48615753 | snp | C/G/T | 0.124444 | 0.216185 | intron-variant | Cblb | Mm_Celera | 16:52182694 | GATCGGCTTCTAATT[C/G/T]TGGACACGTTTCGTT | 208650 |
rs48627582 | snp | A/G | 0.152778 | 0.230321 | intron-variant | Cblb | Mm_Celera | 16:52076106 | CATACTTTATAGCCG[A/G]CTAAAGATTCTGAAA | 208650 |
rs48636285 | snp | A/G | 0.375 | 0.216506 | intron-variant | Cblb | GRCm38.p3 | 16:52092475 | AATTCTGCCACATTC[A/G]GTTTCTCTGTGCTGT | 208650 |
rs48639930 | snp | A/G | 0.165289 | 0.235211 | intron-variant | Cblb | Mm_Celera | 16:52140712 | AGAAAGTATATAACA[A/G]TCTGCAAGTAGAGCT | 208650 |
rs48652198 | snp | C/T | 0.391111 | 0.206368 | intron-variant | Cblb | Mm_Celera | 16:52171281 | TTTCAGAAACAATCA[C/T]ATTAGATTCACAGAA | 208650 |
rs48653020 | snp | A/G | 0.32 | 0.24 | intron-variant | Cblb | GRCm38.p3 | 16:52199908 | ATTTTCCTGTGTGTT[A/G]GCATAAGTTCATAGG | 208650 |
rs48653357 | snp | A/G | 0.375 | 0.216506 | intron-variant | Cblb | GRCm38.p3 | 16:52094660 | CTCTGCCAGTCGGAG[A/G]GAAGCTAGACATTTC | 208650 |
rs48655881 | snp | C/T | 0.375 | 0.216506 | intron-variant | Cblb | GRCm38.p3 | 16:52090012 | CATGGACACAGGCTA[C/T]GATGAACAATTATTT | 208650 |
rs48656477 | snp | G/T | 0.32 | 0.24 | intron-variant | Cblb | GRCm38.p3 | 16:52202991 | TTAGATTCTTATGCA[G/T]TTGGGATTAGTGAGT | 208650 |
rs48660835 | snp | C/G | 0.497778 | 0.0332592 | intron-variant | Cblb | GRCm38.p3 | 16:52172719 | TTGATACCATGAACT[C/G]TTATTTCCATATCAT | 208650 |
rs48665267 | snp | A/C | 0.32 | 0.24 | intron-variant | Cblb | Mm_Celera | 16:52184289 | TGACTGACAGATAGG[A/C]GACTGCAAGGCCATC | 208650 |
rs48669839 | snp | A/G | 0.244898 | 0.249948 | intron-variant | Cblb | GRCm38.p3 | 16:52164501 | GTCAGCGCCTCCCTC[A/G]GGAACACAGCAGGCA | 208650 |
rs48677644 | snp | C/T | 0.444444 | 0.157135 | intron-variant, utr-variant-5-prime | Cblb | GRCm38.p3 | 16:52047689 | CAGAAAGACTGCCCA[C/T]GGTAGTTCCTGCTGC | 208650 |
rs48693053 | snp | A/G | 0.124444 | 0.216185 | intron-variant | Cblb | GRCm38.p3 | 16:52072066 | TTGAATTCAAGCACA[A/G]CCTTTTAATTTCAGC | 208650 |
rs48693132 | snp | C/G | 0.124444 | 0.216185 | intron-variant | Cblb | Mm_Celera | 16:52078559 | GTGACCTGGACATTG[C/G]TGAGTCTCCTCTGTG | 208650 |
rs48693831 | snp | A/G | 0.231111 | 0.249285 | intron-variant | Cblb | GRCm38.p3 | 16:52193349 | TCTATTCAGACAAGA[A/G]TACACACTAAGGCTT | 208650 |
rs48702802 | snp | C/T | 0.152778 | 0.230321 | intron-variant | Cblb | Mm_Celera | 16:52144644 | ATGTTTGATCTAGTG[C/T]TGTGCTTACTATTGG | 208650 |
rs48709041 | snp | G/T | 0.260355 | 0.249785 | intron-variant | Cblb | GRCm38.p3 | 16:52143654 | TAAAACTAGGAGTAT[G/T]TTGCTGTAATTTGGC | 208650 |
rs48710321 | snp | A/G | 0.124444 | 0.216185 | intron-variant | Cblb | GRCm38.p3 | 16:52185862 | GGTGTAACTAAAATC[A/G]TACTCAAATGTGTTT | 208650 |
rs48722421 | snp | A/C | 0.132653 | 0.220748 | intron-variant | Cblb | Mm_Celera | 16:52146984 | CATCCAACAGGGAAC[A/C]CTGAACCTGGACTAC | 208650 |
rs48724769 | snp | A/C | 0.32 | 0.24 | intron-variant | Cblb | GRCm38.p3 | 16:52150744 | TACCCAAAATGGAAG[A/C]ATTCAATCTTGTTTC | 208650 |
rs48749114 | snp | C/T | 0.260355 | 0.249785 | intron-variant | Cblb | Mm_Celera | 16:52147359 | GAAGCTGAGTTTCTC[C/T]GGGTGCGGCTTCTCT | 208650 |
rs48752267 | snp | A/G | 0.124444 | 0.216185 | intron-variant | Cblb | GRCm38.p3 | 16:52136354 | TGCCCTTGTCAGTTT[A/G]GCATGACCCACTTCT | 208650 |
rs48752977 | snp | C/T | 0.124444 | 0.216185 | intron-variant | Cblb | Mm_Celera | 16:52194325 | CCTGTGTTTTTACAG[C/T]GCCTTTTCTCTGTAG | 208650 |
rs48757600 | snp | A/G | 0.132653 | 0.220748 | intron-variant | Cblb | GRCm38.p3 | 16:52160295 | CTGTAACTGTGCTCC[A/G]TGTATAAGTTTATCG | 208650 |
rs48758024 | snp | A/T | 0.497778 | 0.0332592 | intron-variant | Cblb | GRCm38.p3 | 16:52177829 | GTTAGGAAGATATGA[A/T]TTTTCGGCATTTGAT | 208650 |
rs48763155 | snp | A/G | 0.165289 | 0.235211 | intron-variant | Cblb | GRCm38.p3 | 16:52130555 | CACTAGTCCTCAAAA[A/G]TTCTGAAGCATGTCA | 208650 |
rs48778029 | snp | G/T | 0.231111 | 0.249285 | intron-variant | Cblb | Mm_Celera | 16:52103315 | TCATAGGGCAGCTGT[G/T]GTTGATACTTCAGGG | 208650 |
rs48797710 | snp | G/T | 0.42 | 0.183303 | intron-variant | Cblb | GRCm38.p3 | 16:52091062 | AAGGAGCACTAAAGC[G/T]GAGAAAGGGTCAGTT | 208650 |
rs48798198 | snp | A/T | 0.48 | 0.0979796 | intron-variant | Cblb | Mm_Celera | 16:52182540 | TCAATTTTATTTTAT[A/T]TATTTTCCCAAATGA | 208650 |
rs48806905 | snp | G/T | 0.231111 | 0.249285 | intron-variant | Cblb | GRCm38.p3 | 16:52148277 | TATTTGTGCCCAGTC[G/T]AGCAGGCCTCAGATT | 208650 |
rs48806978 | snp | A/G | 0.124444 | 0.216185 | intron-variant | Cblb | Mm_Celera | 16:52104883 | CGCTGAGCCTTCGCT[A/G]CTCCACGTTCACTAT | 208650 |
rs48833246 | snp | A/G | 0.260355 | 0.249785 | intron-variant | Cblb | GRCm38.p3 | 16:52186965 | GAGGCTTTCAAGTGC[A/G]GTTCTGGAGCTTTAA | 208650 |
rs48843532 | snp | C/T | 0.5 | 0 | intron-variant | Cblb | GRCm38.p3 | 16:52095377 | CCCTTCTTTCTCCCT[C/T]GGTGTACAATGGTTT | 208650 |
rs48847279 | snp | A/G | 0.32 | 0.24 | intron-variant | Cblb | GRCm38.p3 | 16:52188875 | ATTCTGTAAGTCAGG[A/G]AAGTGCTGAATCCAC | 208650 |
rs48855939 | snp | A/G | 0.152778 | 0.230321 | intron-variant | Cblb | Mm_Celera | 16:52141637 | GACTTCAGAAGACAA[A/G]CACCTTCCTGGCATG | 208650 |
rs48857542 | snp | A/G | 0.244898 | 0.249948 | intron-variant | Cblb | Mm_Celera | 16:52132196 | GTTTTAAACTTCAAT[A/G]TGATCTATTCTGCTT | 208650 |
rs48857799 | snp | C/T | 0.142012 | 0.225474 | intron-variant | Cblb | Mm_Celera | 16:52142225 | GCAGTACCTGAAACC[C/T]CATGGTGAGCGAACG | 208650 |
rs48859053 | snp | C/G | 0.165289 | 0.235211 | intron-variant | Cblb | GRCm38.p3 | 16:52132954 | TCGCTGGGGTGTGAA[C/G]AGGAAAGTGAAAGCA | 208650 |
rs48880251 | snp | C/T | 0.231111 | 0.249285 | intron-variant | Cblb | GRCm38.p3 | 16:52183197 | CAGATTGGATTTTCT[C/T]TTCCCTCTTGGTAGG | 208650 |
rs48888737 | snp | G/T | 0.244898 | 0.249948 | intron-variant | Cblb | GRCm38.p3 | 16:52063384 | ACCTTGAGCTGCCCT[G/T]TATCTGTTCTAGTTA | 208650 |
rs48889118 | snp | G/T | 0.152778 | 0.230321 | intron-variant | Cblb | Mm_Celera | 16:52142043 | TAGAACATTACAAAG[G/T]TTTAGTAATCACACG | 208650 |
rs48889656 | snp | C/G | 0.244898 | 0.249948 | intron-variant | Cblb | Mm_Celera | 16:52158679 | AAAGCAATTGATGAG[C/G]TCAACTTGTAAGTGA | 208650 |
rs48893311 | snp | A/T | 0.32 | 0.24 | intron-variant | Cblb | GRCm38.p3 | 16:52154394 | CATTATCCTATTTAC[A/T]TGAAAAATCTTACAT | 208650 |
rs48897172 | snp | C/T | 0.32 | 0.24 | intron-variant | Cblb | GRCm38.p3 | 16:52073038 | CTTTATGTGTTGTTC[C/T]GGGACTATCATGAGG | 208650 |
rs48904915 | snp | C/T | 0.345679 | 0.230967 | intron-variant | Cblb | GRCm38.p3 | 16:52093687 | CAGAGCTCTGCTGGA[C/T]ACTTGGGAACCCACC | 208650 |
rs48906809 | snp | C/T | 0.231111 | 0.249285 | intron-variant | Cblb | Mm_Celera | 16:52100933 | GAACGGTTTACACCC[C/T]GTGATGAGAAGAGTG | 208650 |
rs48912673 | snp | C/T | 0.32 | 0.24 | intron-variant | Cblb | Mm_Celera | 16:52116809 | CTTCAATCACAGCTT[C/T]TGAGATCAGTGCAAC | 208650 |
rs48915070 | snp | C/T | 0.244898 | 0.249948 | intron-variant | Cblb | GRCm38.p3 | 16:52199823 | CTGGCTGTGGGCTCC[C/T]GGTGAGGGACTTCAT | 208650 |
rs48921556 | snp | C/T | 0.124444 | 0.216185 | intron-variant | Cblb | Mm_Celera | 16:52151812 | GTTCACCTCGTGTCA[C/T]CTAGAAATTGGCGAG | 208650 |
rs48923212 | snp | A/G | 0.231111 | 0.249285 | intron-variant | Cblb | Mm_Celera | 16:52133556 | GAACCCTGGGCCATT[A/G]GGAGATAGTGTGTGT | 208650 |
rs48927753 | snp | G/T | 0.197531 | 0.244432 | intron-variant | Cblb | Mm_Celera | 16:52141244 | AATAAATTTTATGAT[G/T]TCTTTTAGATACATT | 208650 |
rs48932812 | snp | G/T | 0.124444 | 0.216185 | intron-variant | Cblb | Mm_Celera | 16:52156076 | ATCATGACTTTTGTA[G/T]TATTTCACCAACCTT | 208650 |
rs48939205 | snp | A/C | | | intron-variant | Cblb | Mm_Celera | 16:52082278 | CTTTCTACCACTCAG[A/C]CGTAACTCCCTGCCT | 208650 |
rs48942142 | snp | A/G | 0.231111 | 0.249285 | intron-variant | Cblb | Mm_Celera | 16:52189556 | ATTTAATGACCAAAC[A/G]TCACAAAGATGGCAG | 208650 |
rs48952469 | snp | G/T | 0.142012 | 0.225474 | intron-variant | Cblb | Mm_Celera | 16:52140742 | TTGATTTAAACAGTT[G/T]TAGGATAGGCTATAA | 208650 |
rs48956894 | snp | G/T | 0.391111 | 0.206368 | intron-variant | Cblb | Mm_Celera | 16:52171580 | CTCTCAACATTCATG[G/T]AAGCCCTATTGCACA | 208650 |
rs48957784 | snp | C/T | 0.32 | 0.24 | intron-variant | Cblb | GRCm38.p3 | 16:52086105 | GGATATCTTTCAGCA[C/T]CCGAAATTTGTACAT | 208650 |
rs48961697 | snp | C/T | 0.32 | 0.24 | intron-variant | Cblb | GRCm38.p3 | 16:52085785 | CAACGCTGGCTGTCC[C/T]TCTGGTGTGCTTGGC | 208650 |
rs48963376 | snp | C/T | 0.244898 | 0.249948 | intron-variant | Cblb | GRCm38.p3 | 16:52075969 | TTTTGGTTTTGCCAG[C/T]GGTCTTGTTTATTGA | 208650 |
rs48976113 | snp | G/T | 0.124444 | 0.216185 | intron-variant | Cblb | Mm_Celera | 16:52088049 | AATGCTTTGAAAAGT[G/T]GTTCTCTGTGTATAT | 208650 |
rs48980961 | snp | A/G | 0.32 | 0.24 | intron-variant | Cblb | GRCm38.p3 | 16:52072568 | TGAGTGTGCTTCAGT[A/G]GGTATCAGCCTCCCA | 208650 |
rs48984474 | snp | G/T | 0.124444 | 0.216185 | intron-variant | Cblb | Mm_Celera | 16:52154162 | GAGCTTTCCAACAAA[G/T]CCTTAAGGAGAGCCC | 208650 |
rs48989148 | snp | A/G | 0.375 | 0.216506 | intron-variant, upstream-variant-2KB | Cblb | Mm_Celera | 16:52046140 | TGTGCTGACATGATA[A/G]AAGCTCCTGCCGGTG | 208650 |
rs48991488 | snp | G/T | | | intron-variant | Cblb | GRCm38.p3 | 16:52114828 | AAAACTACGTTTTGT[G/T]ATAAAGTGCTTTGTT | 208650 |
rs48994458 | snp | C/T | 0.244898 | 0.249948 | intron-variant | Cblb | GRCm38.p3 | 16:52117789 | CTAGTTCTGTTTTCA[C/T]TGTCTTCTGTAAAAT | 208650 |
rs48995432 | snp | C/T | | | intron-variant | Cblb | GRCm38.p3 | 16:52115027 | CACTTAACCTACAGG[C/T]CAAGTACTCCCCCTA | 208650 |
rs48996730 | snp | A/G | 0.231111 | 0.249285 | intron-variant | Cblb | Mm_Celera | 16:52069251 | GGATTTGATATTACA[A/G]AAGATGTGTGGAACC | 208650 |
rs48999944 | snp | A/G | 0.32 | 0.24 | intron-variant | Cblb | Mm_Celera | 16:52169585 | CTCTTTAAGGTCTGT[A/G]CTCCATTGTGTGTAT | 208650 |
rs49011066 | snp | C/T | 0.124444 | 0.216185 | intron-variant | Cblb | Mm_Celera | 16:52194100 | CCAGAATTCTTTCTT[C/T]AGCCAACCAGCTGGG | 208650 |
rs49028818 | snp | C/T | 0.132653 | 0.220748 | intron-variant | Cblb | GRCm38.p3 | 16:52055667 | ACCTTTTTCTCGGGT[C/T]GTCAGTCATTTGCTG | 208650 |
rs49039161 | snp | A/T | 0.124444 | 0.216185 | intron-variant | Cblb | Mm_Celera | 16:52069704 | TTTATGCCCTAACTC[A/T]CTCAAAGACAGGATT | 208650 |
rs49040112 | snp | A/C | 0.124444 | 0.216185 | intron-variant | Cblb | Mm_Celera | 16:52088336 | CTCTTCACCACTGAC[A/C]GAGCCAACATTCCCA | 208650 |
rs49044738 | snp | C/T | 0.152778 | 0.230321 | intron-variant | Cblb | Mm_Celera | 16:52120354 | AAGTGATACATTATA[C/T]TATAACATTTTAAAA | 208650 |
rs49048361 | snp | A/G | 0.124444 | 0.216185 | intron-variant | Cblb | GRCm38.p3 | 16:52156399 | ATTTTAATTTTAAAA[A/G]GAAAAAGTTCAGTAG | 208650 |
rs49069869 | snp | A/C | 0.132653 | 0.220748 | intron-variant | Cblb | Mm_Celera | 16:52130910 | AAACACAGAATAATC[A/C]AGTGACCATATTCCG | 208650 |
rs49071974 | snp | A/G | 0.124444 | 0.216185 | intron-variant | Cblb | Mm_Celera | 16:52135061 | AGCAACCTGATGACC[A/G]TGTATGTGATGCTGC | 208650 |
rs49073280 | snp | C/T | 0.345679 | 0.230967 | intron-variant | Cblb | Mm_Celera | 16:52117309 | ATTTGAAGACAGGGA[C/T]TGTCTCATTTAGCTT | 208650 |
rs49076965 | snp | A/G | 0.124444 | 0.216185 | intron-variant | Cblb | Mm_Celera | 16:52181666 | CCTGTGTTCTGGGCT[A/G]TGTAGAGACCCCTCT | 208650 |
rs49084789 | snp | A/G | 0.391111 | 0.206368 | intron-variant | Cblb | GRCm38.p3 | 16:52148520 | ACGGATTCTCACAGC[A/G]CCACAGTGTATTTGA | 208650 |
rs49093613 | snp | A/G | 0.124444 | 0.216185 | intron-variant | Cblb | Mm_Celera | 16:52198388 | GTGGTGCTGTGGATC[A/G]CACGAGCGTGACATA | 208650 |
rs49096128 | snp | C/T | 0.231111 | 0.249285 | intron-variant | Cblb | GRCm38.p3 | 16:52197362 | GATCTGAAACAGTCT[C/T]GAGTTCTGCATTCTG | 208650 |
rs49103643 | snp | C/T | 0.132653 | 0.220748 | intron-variant | Cblb | Mm_Celera | 16:52064719 | TTACCGGCAAACATA[C/T]CAGAGTCTGTTTCTC | 208650 |
rs49127464 | snp | C/T | 0.444444 | 0.157135 | intron-variant | Cblb | GRCm38.p3 | 16:52167923 | TGCCATAAATGTAAA[C/T]ACAAAGCTGGCCTTC | 208650 |
rs49137552 | snp | A/G | | | intron-variant | Cblb | GRCm38.p3 | 16:52203266 | TGTTGTGCTTTTTGT[A/G]CAGCTTGAAGGGACT | 208650 |
rs49143617 | snp | C/T | 0.244898 | 0.249948 | intron-variant | Cblb | GRCm38.p3 | 16:52157026 | AAGTAATTTGTTCTG[C/T]GTGCTGTGAGCCCCA | 208650 |
rs49145345 | snp | C/T | 0.408163 | 0.193609 | intron-variant | Cblb | Mm_Celera | 16:52162050 | CTGCCGTCTGTATGG[C/T]GGTCACTAACATTGT | 208650 |
rs49159843 | snp | A/G | 0.231111 | 0.249285 | intron-variant | Cblb | GRCm38.p3 | 16:52088059 | AAAGTGGTTCTCTGT[A/G]TATATGGACAAAAGT | 208650 |
rs49162918 | snp | A/G | 0.142012 | 0.225474 | intron-variant | Cblb | GRCm38.p3 | 16:52060999 | TTTCAATGTGTAAAC[A/G]GCCTTTTAAAGAAAT | 208650 |
rs49163780 | snp | A/G | 0.231111 | 0.249285 | intron-variant | Cblb | Mm_Celera | 16:52127903 | ATAGGTGACAGCCTA[A/G]ATGACGAAGCCATCT | 208650 |
rs49183920 | snp | C/T | 0.132653 | 0.220748 | intron-variant | Cblb | Mm_Celera | 16:52065161 | ATCACTGCACATATT[C/T]TCTTCTCTCCATGCG | 208650 |
rs49203612 | snp | C/T | 0.32 | 0.24 | intron-variant | Cblb | GRCm38.p3 | 16:52155152 | GCCAGTCTGGCCATG[C/T]CTCATGTCCTGCGTG | 208650 |
rs49212909 | snp | C/T | 0.231111 | 0.249285 | intron-variant | Cblb | Mm_Celera | 16:52121958 | CCTTTGTACTGTTCT[C/T]CCTCTGTCCTGGATG | 208650 |
rs49224446 | snp | A/T | 0.124444 | 0.216185 | intron-variant | Cblb | Mm_Celera | 16:52133320 | TCTGCAGGGAACTGA[A/T]GCAGGTGCTGTGAAG | 208650 |
rs49226411 | snp | A/G | 0.124444 | 0.216185 | intron-variant | Cblb | Mm_Celera | 16:52149674 | TACACTGCAGTCAGT[A/G]TGAGCCACTTGTCAA | 208650 |
rs49230034 | snp | A/G | 0.32 | 0.24 | intron-variant | Cblb | GRCm38.p3 | 16:52073285 | TATTTAAGAATGAAA[A/G]GAAGAAATTGAGAAT | 208650 |
rs49231179 | snp | A/G | 0.32 | 0.24 | intron-variant | Cblb | GRCm38.p3 | 16:52176388 | ACAGTCAGGGTTTTA[A/G]GAAACAAATTACTGA | 208650 |
rs49232128 | snp | C/T | 0.124444 | 0.216185 | intron-variant | Cblb | Mm_Celera | 16:52194973 | TAGTGTGGCCCTATG[C/T]CTTGCTCTTGTGTTT | 208650 |
rs49234182 | snp | A/G | 0.124444 | 0.216185 | intron-variant | Cblb | Mm_Celera | 16:52154676 | CTCAAAGAGAATTAC[A/G]ATTTGAGCGTCCAGA | 208650 |
rs49238257 | snp | A/G | 0.244898 | 0.249948 | intron-variant | Cblb | Mm_Celera | 16:52065495 | CTATTATAAACTCAG[A/G]TACTCTAGACTAAAC | 208650 |
rs49244349 | snp | A/G | 0.32 | 0.24 | intron-variant | Cblb | GRCm38.p3 | 16:52179552 | TTGCAATTGTAGACA[A/G]AAACAGTAAAATAAC | 208650 |
rs49246240 | snp | C/G | 0.473373 | 0.11227 | intron-variant | Cblb | GRCm38.p3 | 16:52166648 | GCTGAGAGCCTCCCC[C/G]ATGCATAACTCGGTG | 208650 |
rs49252992 | snp | A/G | 0.124444 | 0.216185 | intron-variant | Cblb | Mm_Celera | 16:52138351 | TATTTTCCTGTTTCT[A/G]ATTAATAGTATTAGT | 208650 |
rs49256006 | snp | C/T | 0.32 | 0.24 | intron-variant | Cblb | GRCm38.p3 | 16:52072654 | GATAACCAAGTTACA[C/T]TCCTTCCAAATAGCT | 208650 |
rs49262181 | snp | A/G | 0.165289 | 0.235211 | intron-variant | Cblb | Mm_Celera | 16:52128427 | ACAGAAATTAAATAT[A/G]TGTTATAAAAATGAA | 208650 |
rs49267113 | snp | C/T | 0.132653 | 0.220748 | intron-variant | Cblb | Mm_Celera | 16:52135472 | ATCCAACCTGAAGGC[C/T]AGTTGGTCAATCTTT | 208650 |
rs49279600 | snp | A/T | 0.277778 | 0.248452 | intron-variant | Cblb | Mm_Celera | 16:52165697 | ATTGCCATGATAATA[A/T]AATTAATATATAATT | 208650 |
rs49283944 | snp | C/T | 0.231111 | 0.249285 | intron-variant | Cblb | GRCm38.p3 | 16:52186488 | TCCATTAGGTTGAAA[C/T]GTTAAAAGCAGTTTA | 208650 |
rs49291238 | snp | G/T | 0.124444 | 0.216185 | intron-variant | Cblb | Mm_Celera | 16:52178912 | AGAGAGCCCAGCTGT[G/T]CGTGAAAAGCCTGAC | 208650 |
rs49294674 | snp | A/G | 0.32 | 0.24 | intron-variant | Cblb | GRCm38.p3 | 16:52203103 | TGCCAGGTAAGGTGG[A/G]ATGGGCAGCAGACAG | 208650 |
rs49304995 | snp | C/T | 0.444444 | 0.157135 | intron-variant | Cblb | GRCm38.p3 | 16:52092903 | TAATAGGCTAGCTCA[C/T]AAGAAAGCATTTTCC | 208650 |
rs49307037 | snp | A/G | 0.231111 | 0.249285 | intron-variant | Cblb | Mm_Celera | 16:52136054 | TGTCAAAAGTCAGGA[A/G]CTTAATAAGTTTAAA | 208650 |
rs49308281 | snp | A/G | | | intron-variant | Cblb | GRCm38.p3 | 16:52114782 | AAAATGTATAGAACA[A/G]GTTGTTCACAGAAAT | 208650 |
rs49312174 | snp | G/T | 0.124444 | 0.216185 | intron-variant | Cblb | Mm_Celera | 16:52086634 | TCAGCATTTAGGTCT[G/T]GTCTTTCCTTTGGCC | 208650 |
rs49312703 | snp | C/G | 0.124444 | 0.216185 | intron-variant | Cblb | Mm_Celera | 16:52185591 | TTCCCTAAGGTGTCA[C/G]AGGGCCAGCGTTTAT | 208650 |
rs49319012 | snp | A/G | 0.32 | 0.24 | intron-variant | Cblb | GRCm38.p3 | 16:52068746 | GACTCAGCCCTCCAT[A/G]CATCCATTGTGTTAC | 208650 |
rs49321671 | snp | A/G | 0.231111 | 0.249285 | utr-variant-3-prime | Cblb | GRCm38.p3 | 16:52206843 | ACCCACAGCATATTC[A/G]CCTCCACTCTCAGAA | 208650 |
rs49321957 | snp | A/T | 0.489796 | 0.070696 | intron-variant | Cblb | GRCm38.p3 | 16:52167556 | AATTCTTTAAGGTTA[A/T]TTCACTACAGTGTGA | 208650 |
rs49343434 | snp | A/G | 0.165289 | 0.235211 | intron-variant | Cblb | Mm_Celera | 16:52141493 | CATGGAAGGCTTTTC[A/G]TAGATGACTGCCATT | 208650 |
rs49346401 | snp | A/C | 0.231111 | 0.249285 | intron-variant | Cblb | GRCm38.p3 | 16:52087133 | TAAGGTAGTTCAGCT[A/C]TTTTTTGATGACTTT | 208650 |
rs49347988 | snp | A/C | 0.32 | 0.24 | intron-variant | Cblb | GRCm38.p3 | 16:52067440 | GCATTGTCACATGAA[A/C]TATTAAGCTTTAGTA | 208650 |
rs49358705 | snp | A/C | 0.244898 | 0.249948 | intron-variant | Cblb | GRCm38.p3 | 16:52204404 | TATCTCACTGTTTCA[A/C]TGGTATCTGTCTTTG | 208650 |
rs49366321 | snp | C/G | 0.244898 | 0.249948 | intron-variant | Cblb | GRCm38.p3 | 16:52177001 | CACACTCTCCTTGTC[C/G]TTTGATATTGTCACA | 208650 |
rs49370276 | snp | A/G | 0.32 | 0.24 | intron-variant | Cblb | GRCm38.p3 | 16:52107150 | TAGAAATGGTTCTTA[A/G]CTGGATGTGAGTTTC | 208650 |
rs49381593 | snp | A/G | 0.124444 | 0.216185 | intron-variant | Cblb | Mm_Celera | 16:52133065 | CTCACCAAGTCTGAC[A/G]AGTCCTCGGATTTCA | 208650 |
rs49381709 | snp | A/G | 0.231111 | 0.249285 | intron-variant | Cblb | Mm_Celera | 16:52075080 | TCATTTCTAGTTTGC[A/G]TGTACTTGAACTTCA | 208650 |
rs49383265 | snp | C/G | | | intron-variant | Cblb | GRCm38.p3 | 16:52107969 | GAGTCTTGGTTAGCA[C/G]AATTTTTTTTTTTTT | 208650 |
rs49385449 | snp | C/T | 0.142012 | 0.225474 | intron-variant | Cblb | Mm_Celera | 16:52187077 | ATGAGAAAGGATATA[C/T]TTCATCCTAGAAAAC | 208650 |
rs49396989 | snp | C/G | 0.244898 | 0.249948 | intron-variant | Cblb | GRCm38.p3 | 16:52160220 | AGTACTGTAAAGTAG[C/G]CCTTCTGGCAATTTT | 208650 |
rs49406405 | snp | A/C | 0.124444 | 0.216185 | intron-variant | Cblb | GRCm38.p3 | 16:52088783 | TGAGGCTCAGGCAAA[A/C]GGGGGCTAGGTTGGG | 208650 |
rs49408364 | snp | A/G | 0.32 | 0.24 | intron-variant | Cblb | GRCm38.p3 | 16:52191602 | CTCATGAGTCCAGCC[A/G]GCTAGCAGAAGGACA | 208650 |
rs49413142 | snp | C/T | 0.124444 | 0.216185 | intron-variant | Cblb | Mm_Celera | 16:52070909 | CATAAGCAAAAGAGG[C/T]ACTTGGTATTTGAAT | 208650 |
rs49442180 | snp | C/T | 0.244898 | 0.249948 | intron-variant | Cblb | GRCm38.p3 | 16:52159525 | AAAATGCAAAGCTGT[C/T]AAGATGTCAGGTAAA | 208650 |
rs49442904 | snp | C/G | 0.231111 | 0.249285 | intron-variant | Cblb | Mm_Celera | 16:52187539 | CCTCCTACCTCTTCT[C/G]TTGGGCCTTCCTCCA | 208650 |
rs49451586 | snp | C/T | 0.5 | 0 | intron-variant, utr-variant-5-prime | Cblb | Mm_Celera | 16:52048165 | TAGCAGTATCAGTTC[C/T]GGGATGGATATGTCA | 208650 |
rs49453859 | snp | A/T | 0.124444 | 0.216185 | intron-variant | Cblb | Mm_Celera | 16:52117389 | TATTCACAATCTGCA[A/T]GCATAGTTGGATGGA | 208650 |
rs49462138 | snp | G/T | 0.124444 | 0.216185 | intron-variant | Cblb | Mm_Celera | 16:52200134 | CATTAGGCTTAAGTT[G/T]GTTCCTGGTTTTCTA | 208650 |
rs49463512 | snp | A/G | 0.124444 | 0.216185 | intron-variant | Cblb | Mm_Celera | 16:52171230 | TGAACGTGGAATTCA[A/G]AATCACATGTTAGAT | 208650 |
rs49475177 | snp | A/G | 0.32 | 0.24 | intron-variant | Cblb | Mm_Celera | 16:52179418 | CTCTCCTTTTTTATC[A/G]GCATGGTGATTTTCC | 208650 |
rs49479586 | snp | C/T | 0.244898 | 0.249948 | intron-variant | Cblb | Mm_Celera | 16:52162992 | CACTTCTAAATTTGG[C/T]TTCGTATTGATCACT | 208650 |
rs49484401 | snp | C/T | 0.132653 | 0.220748 | intron-variant | Cblb | Mm_Celera | 16:52165202 | ACTTGGCTTCTATCC[C/T]ATGACTCCTGGCTAG | 208650 |
rs49484748 | snp | G/T | 0.124444 | 0.216185 | intron-variant | Cblb | GRCm38.p3 | 16:52073327 | TGTTGTTGTTTACAC[G/T]TCAGTATTTGGAGTC | 208650 |
rs49501352 | snp | C/T | 0.132653 | 0.220748 | intron-variant | Cblb | Mm_Celera | 16:52200013 | TCCCAATTAACCTGT[C/T]TGGAAGCTTATCCTG | 208650 |
rs49507852 | snp | A/G | 0.32 | 0.24 | intron-variant | Cblb | Mm_Celera | 16:52127501 | TAGGCTATTACATGT[A/G]GCAGTGCTATGAAGA | 208650 |
rs49517177 | snp | C/T | 0.132653 | 0.220748 | intron-variant | Cblb | GRCm38.p3 | 16:52165901 | GGCTAAAATGGAAAT[C/T]GAGTAATCTGTGTCT | 208650 |
rs49517193 | snp | C/T | 0.124444 | 0.216185 | intron-variant | Cblb | GRCm38.p3 | 16:52139185 | TGATTTATGTCACAG[C/T]TCTATCACAGCAGCC | 208650 |
rs49520980 | snp | G/T | 0.124444 | 0.216185 | intron-variant | Cblb | Mm_Celera | 16:52197393 | TGTATTCTAAGCACA[G/T]TTATGTGAAGATTTT | 208650 |
rs49527555 | snp | G/T | 0.32 | 0.24 | intron-variant | Cblb | GRCm38.p3 | 16:52184572 | ATCTCTTGTTAATCG[G/T]GCTGATGAGTGCTCC | 208650 |
rs49542124 | snp | A/G | 0.142012 | 0.225474 | intron-variant | Cblb | GRCm38.p3 | 16:52162403 | TTCTCCCCAGTGTGA[A/G]TGGTTTGAATGTTAT | 208650 |
rs49545908 | snp | A/G | 0.32 | 0.24 | intron-variant | Cblb | GRCm38.p3 | 16:52176195 | CAGTGCCTGAAATTA[A/G]ACCAGAGTGCAATTT | 208650 |
rs49555568 | snp | A/G | 0.32 | 0.24 | intron-variant | Cblb | Mm_Celera | 16:52186554 | CGAATTAAGAGTTCA[A/G]TATAATGCAGACTCT | 208650 |
rs49560297 | snp | A/G | 0.277778 | 0.248452 | intron-variant | Cblb | Mm_Celera | 16:52119921 | TAACTAAGAAATGAA[A/G]TAAGCTCAAAAATAA | 208650 |
rs49563355 | snp | A/T | 0.152778 | 0.230321 | intron-variant | Cblb | Mm_Celera | 16:52076130 | TCTGAAATCATTGGA[A/T]GAGTTTAAGTAGCTG | 208650 |
rs49565114 | snp | C/T | 0.231111 | 0.249285 | intron-variant | Cblb | Mm_Celera | 16:52191790 | AGCTCCATGATTTCC[C/T]GTCCACAAACCCAAG | 208650 |
rs49575067 | snp | A/G | 0.124444 | 0.216185 | intron-variant | Cblb | Mm_Celera | 16:52131028 | GCTCTGCCGTCGATG[A/G]CCCTGATTCCCTGAC | 208650 |
rs49590331 | snp | C/T | 0.124444 | 0.216185 | intron-variant | Cblb | Mm_Celera | 16:52076941 | ATGTCCTAGTGCTGA[C/T]TCCACATGCACTGCA | 208650 |
rs49591270 | snp | C/T | 0.426035 | 0.177515 | intron-variant | Cblb | Mm_Celera | 16:52163973 | CTTTCCATATGGAAG[C/T]TTAAGGAAAAAATAT | 208650 |
rs49591296 | snp | G/T | 0.489796 | 0.070696 | intron-variant | Cblb | Mm_Celera | 16:52091786 | AATTAGAATAAGCAG[G/T]AGTTGGCATGGGCTA | 208650 |
rs49591480 | snp | A/T | 0.124444 | 0.216185 | intron-variant | Cblb | Mm_Celera | 16:52184065 | TCTCTAAGCAAAATC[A/T]TGGCTTTGCATGCAT | 208650 |
rs49593829 | snp | C/T | 0.231111 | 0.249285 | intron-variant | Cblb | GRCm38.p3 | 16:52073191 | AGGATCTTGGAAGTG[C/T]GCTAATCTTGTTCTT | 208650 |
rs49600251 | snp | A/T | 0.231111 | 0.249285 | intron-variant | Cblb | GRCm38.p3 | 16:52102655 | TGTGCTTTTTATTTT[A/T]AGAGTATGGATGTGA | 208650 |
rs49603409 | snp | G/T | 0.231111 | 0.249285 | intron-variant | Cblb | GRCm38.p3 | 16:52076028 | AAACAAAAACAAGCA[G/T]TTGACTAGCACAGGA | 208650 |
rs49605575 | snp | A/G | 0.124444 | 0.216185 | intron-variant | Cblb | Mm_Celera | 16:52193728 | ATTCATTTAAAAATC[A/G]CAAGCTTCAGGTCTG | 208650 |
rs49606301 | snp | C/T | 0.32 | 0.24 | intron-variant | Cblb | GRCm38.p3 | 16:52179897 | CTTTGAAAGGTGGCC[C/T]CAGAAAGTATCACCG | 208650 |
rs49608323 | snp | A/G | 0.132653 | 0.220748 | intron-variant | Cblb | Mm_Celera | 16:52162651 | CTGCGTTCTGGGATC[A/G]TATTTAATGGTGGTT | 208650 |
rs49613625 | snp | C/T | 0.408163 | 0.193609 | intron-variant | Cblb | GRCm38.p3 | 16:52129411 | GTTAGGACTTTAGTT[C/T]TCTGTGTCTGCTAAG | 208650 |
rs49614586 | snp | A/G | 0.244898 | 0.249948 | intron-variant | Cblb | GRCm38.p3 | 16:52162942 | GGTTTCTGACTTTTA[A/G]ACTCTGCCTTAGAAA | 208650 |
rs49615152 | snp | C/T | 0.459184 | 0.136902 | intron-variant | Cblb | GRCm38.p3 | 16:52195192 | AAGTATTCCTGTATC[C/T]CAGTTCTCCTTCTGG | 208650 |
rs49619391 | snp | A/G | 0.124444 | 0.216185 | intron-variant | Cblb | Mm_Celera | 16:52186917 | TCTGTGTCAAGACCC[A/G]AGAGTGTTGCTCGCT | 208650 |
rs49630138 | snp | C/T | 0.231111 | 0.249285 | downstream-variant-500B | Cblb | GRCm38.p3 | 16:52208304 | TGTGAAAAGGCTGCT[C/T]TGGAGAAGATTACAC | 208650 |
rs49630640 | snp | A/G | 0.124444 | 0.216185 | intron-variant | Cblb | Mm_Celera | 16:52077804 | CAAACTGGCCATTTA[A/G]GTGGTGATTAAGTTG | 208650 |
rs49638026 | snp | A/G | 0.124444 | 0.216185 | intron-variant | Cblb | Mm_Celera | 16:52102670 | AAGAGTATGGATGTG[A/G]GAACCCTTCTTTGGT | 208650 |
rs49653800 | snp | C/T | 0.152778 | 0.230321 | intron-variant | Cblb | Mm_Celera | 16:52145794 | TGTAGACATTGTACC[C/T]TGTTATTTACCTCTG | 208650 |
rs49666407 | snp | G/T | 0.32 | 0.24 | intron-variant | Cblb | GRCm38.p3 | 16:52189004 | ATAGTGCTCCTTCTT[G/T]AAATGCAGGTGAGGA | 208650 |
rs49668187 | snp | A/G | 0.124444 | 0.216185 | intron-variant | Cblb | Mm_Celera | 16:52155059 | TTGCATCCTGTCCAT[A/G]TAAAAGGAGCTACAC | 208650 |
rs49668778 | snp | A/G | 0.231111 | 0.249285 | intron-variant | Cblb | Mm_Celera | 16:52134768 | GTAGCTTCAGCCTTG[A/G]AAGTATTGCAGTATG | 208650 |
rs49675300 | snp | A/G | 0.32 | 0.24 | intron-variant | Cblb | Mm_Celera | 16:52186686 | AGCTGGGAAATTTTA[A/G]GCGATTTTCATAGCA | 208650 |
rs49681354 | snp | A/G | 0.124444 | 0.216185 | intron-variant | Cblb | Mm_Celera | 16:52078861 | GATGTCGATGACCAA[A/G]AGAACACATTCTCTA | 208650 |
rs49693840 | snp | C/G | 0.391111 | 0.206368 | intron-variant | Cblb | Mm_Celera | 16:52170948 | AAGTAGAGATAGCAC[C/G]AGACTAACGTGACCA | 208650 |
rs49696150 | snp | A/G | 0.244898 | 0.249948 | intron-variant | Cblb | GRCm38.p3 | 16:52195023 | AACTAACCAAGCAAC[A/G]AGCCACAGCAATGCC | 208650 |
rs49709554 | snp | A/T | 0.42 | 0.183303 | intron-variant | Cblb | Mm_Celera | 16:52178416 | AGGAATAATTTCTTT[A/T]TGCTTTGCTGTTTAC | 208650 |
rs49713200 | snp | G/T | | | intron-variant | Cblb | Mm_Celera | 16:52134506 | AATTATTCTTTCTTG[G/T]TATTCTTATTGTAAG | 208650 |
rs49713231 | snp | C/T | 0.142012 | 0.225474 | intron-variant | Cblb | Mm_Celera | 16:52146347 | TCTGTAATATATTGT[C/T]AAACCTTGAATCTAA | 208650 |
rs49714694 | snp | A/C | 0.32 | 0.24 | intron-variant | Cblb | GRCm38.p3 | 16:52100289 | AACCCTGAATGCAGA[A/C]AATCTGAAGAATTAT | 208650 |
rs49724610 | snp | A/G | 0.32 | 0.24 | utr-variant-3-prime | Cblb | GRCm38.p3 | 16:52207562 | GCTACAACCTTCAGA[A/G]GTCTGTTTGCTAACT | 208650 |
rs49742057 | snp | A/G | 0.124444 | 0.216185 | upstream-variant-2KB | Cblb | Mm_Celera | 16:52030220 | CTCAGGAGCCTTCAC[A/G]GTAATAATTGTAGCA | 208650 |
rs49746055 | snp | C/G | 0.32 | 0.24 | intron-variant | Cblb | GRCm38.p3 | 16:52181750 | ATCTCTTAACAAACA[C/G]AGCTTTAAAAATCAA | 208650 |
rs49748890 | snp | C/G | 0.345679 | 0.230967 | intron-variant | Cblb | GRCm38.p3 | 16:52096886 | AGAACTGACATTTTT[C/G]TAAGGTAAGATTTTA | 208650 |
rs49749255 | snp | C/G | 0.132653 | 0.220748 | intron-variant | Cblb | GRCm38.p3 | 16:52054116 | GCAAGTTCTTCATTG[C/G]TGTCCCTTTTTCAAA | 208650 |
rs49751763 | snp | C/T | 0.124444 | 0.216185 | intron-variant | Cblb | Mm_Celera | 16:52185186 | TATGAAGACTCAATA[C/T]GTAACTGTTCTTAAA | 208650 |
rs49756254 | snp | A/G | 0.152778 | 0.230321 | intron-variant | Cblb | Mm_Celera | 16:52145752 | TGTGCCTGAAAACTT[A/G]TAGCCACAGGTACAT | 208650 |
rs49757240 | snp | C/T | 0.152778 | 0.230321 | intron-variant | Cblb | Mm_Celera | 16:52130642 | TAGGAAGAGAATAAA[C/T]CAAATCCTATAAGAT | 208650 |
rs49757559 | snp | C/T | 0.391111 | 0.206368 | intron-variant | Cblb | Mm_Celera | 16:52178530 | AACGGTCCTCTGTCG[C/T]GGGAGGTGGTGACGT | 208650 |
rs49763238 | snp | A/G | 0.124444 | 0.216185 | upstream-variant-2KB | Cblb | Mm_Celera | 16:52030603 | ACGGCTATCAAGGAC[A/G]GAGCCCAGAAAGAGA | 208650 |
rs49765589 | snp | C/T | 0.142012 | 0.225474 | intron-variant | Cblb | Mm_Celera | 16:52132080 | CAAGCACTTACAAAA[C/T]AAAATCATCCTTATA | 208650 |
rs49768994 | snp | A/C | 0.124444 | 0.216185 | intron-variant | Cblb | Mm_Celera | 16:52129545 | ATCAATAACTGCCTA[A/C]GATTGCTAAATACTT | 208650 |
rs49773466 | snp | G/T | 0.124444 | 0.216185 | intron-variant | Cblb | Mm_Celera | 16:52173243 | AGTCACTCGCTTCTA[G/T]AGTGAAATTTCAATG | 208650 |
rs49780125 | snp | C/G | 0.244898 | 0.249948 | intron-variant | Cblb | GRCm38.p3 | 16:52190355 | CTTTGGTAAAGCAGT[C/G]TAGGTAGACGTGGAG | 208650 |
rs49783906 | snp | A/G | 0.244898 | 0.249948 | intron-variant | Cblb | GRCm38.p3 | 16:52198341 | AGCATCTCAGTCTTG[A/G]TTCAGGAGCAGCTCG | 208650 |
rs49786014 | snp | A/T | 0.124444 | 0.216185 | downstream-variant-500B | Cblb | Mm_Celera | 16:52208462 | TAAGAGTAGGTAAAA[A/T]TTCTTAATGAGTAAA | 208650 |
rs49787759 | snp | C/T | 0.124444 | 0.216185 | intron-variant | Cblb | Mm_Celera | 16:52200106 | AATCCTTGTTGTTTC[C/T]TTCCATAGACTACAT | 208650 |
rs49788715 | snp | C/G | | | intron-variant | Cblb | GRCm38.p3 | 16:52115073 | CACCGCTTGCTGAGT[C/G]TACAGACTGAGGAAG | 208650 |
rs49793690 | snp | C/T | 0.231111 | 0.249285 | intron-variant | Cblb | GRCm38.p3 | 16:52082174 | CCGTGGAGAATTTGG[C/T]TTCGTTGTGCTCAGG | 208650 |
rs49800978 | snp | C/T | 0.32 | 0.24 | intron-variant | Cblb | GRCm38.p3 | 16:52082091 | GTTCATTAAACTATG[C/T]GAAGTGACAAATTAT | 208650 |
rs49811938 | snp | A/G | 0.32 | 0.24 | utr-variant-3-prime | Cblb | GRCm38.p3 | 16:52204745 | TATTCCAGGAGTATG[A/G]GACAGAAGGACTGAG | 208650 |
rs49822616 | snp | C/T | 0.124444 | 0.216185 | utr-variant-3-prime | Cblb | Mm_Celera | 16:52205464 | ATCCACCCAGGAGTG[C/T]CATAATGCTGTAAAA | 208650 |
rs49831503 | snp | C/T | 0.231111 | 0.249285 | intron-variant | Cblb | GRCm38.p3 | 16:52182860 | GTTTCCAGTTGATTT[C/T]AGTGTATCCTTATCA | 208650 |
rs49841476 | snp | A/G | 0.336735 | 0.234472 | intron-variant | Cblb | Mm_Celera | 16:52170829 | AGGGAAGGAATTGCA[A/G]TGCATATAAGGATAA | 208650 |
rs49863879 | snp | C/T | 0.21875 | 0.248039 | intron-variant | Cblb | GRCm38.p3 | 16:52093261 | TAATTAATGTGGCAC[C/T]CTGTTAAAATAATGA | 208650 |
rs49865398 | snp | C/T | 0.231111 | 0.249285 | intron-variant | Cblb | Mm_Celera | 16:52151083 | TTTAGTCTGTTGATC[C/T]GAGAGAAGTTAAAGG | 208650 |
rs49879028 | snp | G/T | 0.132653 | 0.220748 | intron-variant | Cblb | GRCm38.p3 | 16:52058584 | AACTGACTTGCTGGA[G/T]AAGGAAGATCAATGT | 208650 |
rs49885345 | snp | A/G | 0.124444 | 0.216185 | intron-variant | Cblb | Mm_Celera | 16:52068313 | GCCAAATTCTGCTAC[A/G]TCTTGGATGCAGAGC | 208650 |
rs49896451 | snp | C/T | 0.124444 | 0.216185 | intron-variant | Cblb | Mm_Celera | 16:52179199 | CTGAATTGGAGATGT[C/T]TTCTGTTCAGGTAAG | 208650 |
rs49903132 | snp | A/G | 0.124444 | 0.216185 | intron-variant | Cblb | GRCm38.p3 | 16:52156060 | CTAGTCAGTTAAGCA[A/G]ATCATGACTTTTGTA | 208650 |
rs49904829 | snp | C/G | 0.5 | 0 | intron-variant | Cblb | GRCm38.p3 | 16:52096482 | CCTGCTGTATCCTCA[C/G]CCTCATCTACTCCTG | 208650 |
rs49922154 | snp | G/T | 0.132653 | 0.220748 | intron-variant | Cblb | Mm_Celera | 16:52136873 | TTTAATATGACATAT[G/T]TAAAGAAGCTAGTGG | 208650 |
rs49925071 | snp | G/T | 0.32 | 0.24 | intron-variant | Cblb | GRCm38.p3 | 16:52187451 | TTCTGGTCTAGTTGA[G/T]TTTTTTTTCTTGTCC | 208650 |
rs49931684 | snp | A/C | 0.165289 | 0.235211 | intron-variant | Cblb | Mm_Celera | 16:52144315 | GACATTTCAGATGAA[A/C]CTGTACAAAGTGCGG | 208650 |
rs49931946 | snp | A/G | | | intron-variant | Cblb | GRCm38.p3 | 16:52197325 | AGTTTAAAACCTCGG[A/G]GCTGGAGTCTTTTTT | 208650 |
rs49939014 | snp | C/T | 0.132653 | 0.220748 | intron-variant | Cblb | Mm_Celera | 16:52163550 | GAGAATGCACAGCAT[C/T]TGCCTTTTAGTATCT | 208650 |
rs49940631 | snp | C/T | 0.42 | 0.183303 | intron-variant | Cblb | GRCm38.p3 | 16:52142362 | AATGTAACATCCAGA[C/T]GACACTTACTCAGTT | 208650 |
rs49945063 | snp | C/T | 0.32 | 0.24 | intron-variant | Cblb | GRCm38.p3 | 16:52155809 | CTTCCTGGGACCCTG[C/T]GAGGTGTCTATTTGG | 208650 |
rs49948462 | snp | A/G | 0.231111 | 0.249285 | intron-variant | Cblb | GRCm38.p3 | 16:52129875 | CCCATTTGGATCATC[A/G]AGGGATATCTCTGTA | 208650 |
rs49952396 | snp | A/G | 0.124444 | 0.216185 | intron-variant | Cblb | GRCm38.p3 | 16:52074105 | GTATTGGGTGTTATG[A/G]TATCTTGTGATAACT | 208650 |
rs49960588 | snp | A/T | 0.124444 | 0.216185 | intron-variant | Cblb | Mm_Celera | 16:52153868 | CTTATGAACTGAAAG[A/T]AACTGCTCCAGCCCA | 208650 |
rs49974937 | snp | G/T | 0.231111 | 0.249285 | intron-variant | Cblb | Mm_Celera | 16:52134994 | GGGGTCTGGAGCCTG[G/T]TACCTCAGAAGGAGC | 208650 |
rs49976063 | snp | A/C | 0.244898 | 0.249948 | intron-variant | Cblb | Mm_Celera | 16:52095638 | ATAGGAGACACAAAA[A/C]TCTTAGTGAAACACT | 208650 |
rs49982449 | snp | C/G | 0.444444 | 0.157135 | intron-variant | Cblb | GRCm38.p3 | 16:52129607 | AACCTTAATCAGAGT[C/G]TGACGTGTGTTTCTC | 208650 |
rs49995158 | snp | C/T | 0.408163 | 0.193609 | intron-variant | Cblb | Mm_Celera | 16:52165408 | AGACTGGCAGGTGTT[C/T]TTCTTTTCATTTTAA | 208650 |
rs49995282 | snp | A/G | 0.444444 | 0.157135 | intron-variant | Cblb | GRCm38.p3 | 16:52090580 | GCAATGGACTTTGTC[A/G]CAGCAGAGAAGGAGA | 208650 |
rs50002481 | snp | C/T | 0.244898 | 0.249948 | intron-variant | Cblb | GRCm38.p3 | 16:52057368 | GACTACCAACTTTTA[C/T]GTTCATCCGCTTCAT | 208650 |
rs50010930 | snp | C/T | 0.473373 | 0.11227 | intron-variant | Cblb | GRCm38.p3 | 16:52192962 | ATGTCCAGATTTTAA[C/T]ATTCTACGTTTTCAG | 208650 |
rs50022056 | snp | A/G/T | 0.244898 | 0.249948 | intron-variant | Cblb | Mm_Celera | 16:52194543 | TTTCTTTTGATTTCC[A/G/T]TTTCTTATCCAGATA | 208650 |
rs50032613 | snp | C/G | 0.497778 | 0.0332592 | intron-variant | Cblb | GRCm38.p3 | 16:52170759 | ACCGGACCTCCATGG[C/G]AATAACAGAAAGGGA | 208650 |
rs50033023 | snp | C/G | 0.35503 | 0.226867 | intron-variant | Cblb | GRCm38.p3 | 16:52094313 | TGATTGACATTTTCC[C/G]AGGACATTTGTTGGA | 208650 |
rs50045019 | snp | A/G | 0.391111 | 0.206368 | intron-variant | Cblb | Mm_Celera | 16:52175513 | TCAAATACTGCCAGG[A/G]AAAATTATTTTAAGG | 208650 |
rs50065535 | snp | C/T | 0.32 | 0.24 | intron-variant | Cblb | GRCm38.p3 | 16:52156312 | TTATCTAAAATAAAC[C/T]AATCAATGCATGTGC | 208650 |
rs50068009 | snp | A/G | 0.124444 | 0.216185 | intron-variant | Cblb | Mm_Celera | 16:52152089 | AAATATTTACCCACA[A/G]TTGGTAAGCACAAGA | 208650 |
rs50075278 | snp | A/C/T | 0.32 | 0.24 | intron-variant | Cblb | GRCm38.p3 | 16:52156566 | TTCCCAACTCAGGAG[A/C/T]GATGTGCATCACTGA | 208650 |
rs50078862 | snp | C/T | 0.489796 | 0.070696 | intron-variant | Cblb | GRCm38.p3 | 16:52202183 | TCGGTTATTCCAAAA[C/T]GTCAGTTTGGGCTTT | 208650 |
rs50079075 | snp | A/G | 0.391111 | 0.206368 | intron-variant | Cblb | GRCm38.p3 | 16:52134608 | GAGCGAACTTGCCTC[A/G]CGTAATCAAGACCGG | 208650 |
rs50081174 | snp | C/T | | | intron-variant | Cblb | Mm_Celera | 16:52082160 | ATAGAAGTACCTTTC[C/T]GTGGAGAATTTGGTT | 208650 |
rs50084203 | snp | C/T | 0.152778 | 0.230321 | intron-variant | Cblb | GRCm38.p3 | 16:52141902 | TATTTGGTAATAATT[C/T]TTTTCCACTTTCTTT | 208650 |
rs50110820 | snp | A/G/T | 0.444444 | 0.157135 | intron-variant | Cblb | GRCm38.p3 | 16:52042527 | CAGCTTTCATTGTAG[A/G/T]GTGCAGCTCAGATAG | 208650 |
rs50119627 | snp | A/G | 0.32 | 0.24 | intron-variant | Cblb | GRCm38.p3 | 16:52072759 | GAGAAGGGAATCGTC[A/G]TCATAGAACAGTTAC | 208650 |
rs50124423 | snp | A/G | 0.132653 | 0.220748 | intron-variant | Cblb | GRCm38.p3 | 16:52162868 | GTCCAGGGAAACATT[A/G]TCAGTTACAAAGAAT | 208650 |
rs50138152 | snp | C/T | 0.231111 | 0.249285 | intron-variant | Cblb | GRCm38.p3 | 16:52199887 | CCCAGATTCTGTGTC[C/T]TCTGGATTTTCCTGT | 208650 |
rs50142923 | snp | A/G | 0.32 | 0.24 | intron-variant | Cblb | GRCm38.p3 | 16:52179350 | AGCAAGTAAAATGGC[A/G]TATTATTTAAAATGC | 208650 |
rs50143918 | snp | A/T | 0.124444 | 0.216185 | intron-variant | Cblb | Mm_Celera | 16:52190571 | GTAACTCATTGAAAG[A/T]CTGTGGAGCTGTTAA | 208650 |
rs50145436 | snp | G/T | 0.21875 | 0.248039 | intron-variant | Cblb | Mm_Celera | 16:52139996 | TTTTTTCCTTCCTAA[G/T]TCAAAGAAACTCTTT | 208650 |
rs50146654 | snp | A/T | 0.231111 | 0.249285 | intron-variant | Cblb | Mm_Celera | 16:52136007 | ACTGAGAGGGTGCAT[A/T]TTAATTGAGCCCTTA | 208650 |
rs50147449 | snp | A/T | 0.32 | 0.24 | intron-variant | Cblb | Mm_Celera | 16:52168882 | TCCTGTATTTTGCAA[A/T]TTGTTTCTTATATGT | 208650 |
rs50148510 | snp | G/T | 0.124444 | 0.216185 | intron-variant | Cblb | Mm_Celera | 16:52193602 | TTTTTCGCAGTTGAA[G/T]TAACTATTCAGTGAG | 208650 |
rs50162702 | snp | A/T | 0.132653 | 0.220748 | intron-variant | Cblb | Mm_Celera | 16:52126139 | CATGTGATGTGTTTC[A/T]TTTTAATGATATTGG | 208650 |
rs50170544 | snp | A/T | 0.132653 | 0.220748 | intron-variant | Cblb | Mm_Celera | 16:52158945 | CAGATTTGAGCTTCC[A/T]GAGGGGCAAGTCTGT | 208650 |
rs50174619 | snp | A/T | 0.32 | 0.24 | intron-variant | Cblb | GRCm38.p3 | 16:52073440 | CACTTCTGAACTGTG[A/T]TGACCTTTGCTGCAC | 208650 |
rs50181036 | snp | G/T | 0.124444 | 0.216185 | intron-variant | Cblb | Mm_Celera | 16:52134977 | TAGCATAAAGCAAGT[G/T]TGGGGTCTGGAGCCT | 208650 |
rs50184939 | snp | C/T | 0.32 | 0.24 | intron-variant | Cblb | GRCm38.p3 | 16:52195696 | CATCATGAGTCGAGT[C/T]ATCACTAATCACTGT | 208650 |
rs50193673 | snp | A/G | 0.124444 | 0.216185 | intron-variant | Cblb | GRCm38.p3 | 16:52087439 | AGAAAAGTGATGATG[A/G]CAGGTTAGCTGAGGA | 208650 |
rs50198952 | snp | A/C | 0.375 | 0.216506 | intron-variant | Cblb | GRCm38.p3 | 16:52096022 | GGGCTGAACGTCTTC[A/C]AGGCAGAACACCTGC | 208650 |
rs50201841 | snp | A/C | 0.124444 | 0.216185 | intron-variant | Cblb | Mm_Celera | 16:52107946 | TGAATTATAGTTATA[A/C]GATTGTTGAGTCTTG | 208650 |
rs50203258 | snp | A/C | 0.231111 | 0.249285 | intron-variant | Cblb | GRCm38.p3 | 16:52132458 | GATGTGGAAGACGAA[A/C]TTAAATACTGGGCAG | 208650 |
rs50228076 | snp | G/T | 0.32 | 0.24 | intron-variant | Cblb | GRCm38.p3 | 16:52197222 | ATTAACACTCGGTTC[G/T]GATTCCAGGATGGGA | 208650 |
rs50229760 | snp | A/G | 0.32 | 0.24 | intron-variant | Cblb | GRCm38.p3 | 16:52100040 | TAACCATAGGTTCAC[A/G]GGTGCTTAGGAATGC | 208650 |
rs50237589 | snp | A/T | 0.444444 | 0.157135 | intron-variant | Cblb | Mm_Celera | 16:52160302 | TGTGCTCCGTGTATA[A/T]GTTTATCGCCTGCTC | 208650 |
rs50237656 | snp | A/G | 0.231111 | 0.249285 | intron-variant | Cblb | GRCm38.p3 | 16:52071145 | GAAACACACCCCTGG[A/G]CTTCAGGCTGAGACT | 208650 |
rs50241833 | snp | C/T | 0.132653 | 0.220748 | intron-variant | Cblb | GRCm38.p3 | 16:52163340 | CAGTATGTAGCTCTC[C/T]GCTTTACTAAGTCCT | 208650 |
rs50250425 | snp | C/G | 0.260355 | 0.249785 | intron-variant | Cblb | Mm_Celera | 16:52184241 | AGCTCTGTTCAGACA[C/G]TGTTAGTGGCTGAGC | 208650 |
rs50258796 | snp | A/C | 0.32 | 0.24 | utr-variant-3-prime | Cblb | Mm_Celera | 16:52205398 | ACTATAAAAGAGCTT[A/C]TCTTGTTAGTTTAAG | 208650 |
rs50259635 | snp | A/G | 0.132653 | 0.220748 | intron-variant | Cblb | Mm_Celera | 16:52160115 | CTAGAGGCCCTGCAA[A/G]GAGAGTCAGTGTCAC | 208650 |
rs50263494 | snp | A/T | 0.152778 | 0.230321 | intron-variant | Cblb | Mm_Celera | 16:52078079 | TGAAGTATGTCTCTC[A/T]GCCAGCTCTGTTTGT | 208650 |
rs50263793 | snp | A/C/G | 0.244898 | 0.249948 | intron-variant | Cblb | GRCm38.p3 | 16:52119281 | GTCTAAAGTGTGTGC[A/C/G]TGTGAGACGGTGATA | 208650 |
rs50268839 | snp | C/T | 0.231111 | 0.249285 | intron-variant | Cblb | Mm_Celera | 16:52134076 | TTGTATTTTGATCTG[C/T]TAATTGGTTCTCTTT | 208650 |
rs50270580 | snp | G/T | 0.277778 | 0.248452 | intron-variant | Cblb | GRCm38.p3 | 16:52194516 | TCACAGTCTTTATTT[G/T]GGGATGCATTCTTTC | 208650 |
rs50274427 | snp | A/G | 0.32 | 0.24 | intron-variant | Cblb | GRCm38.p3 | 16:52156020 | TCATGATTTAATTAA[A/G]TGGCTCTTATGTCTA | 208650 |
rs50302647 | snp | C/G | 0.32 | 0.24 | intron-variant | Cblb | GRCm38.p3 | 16:52154860 | TCCTCTTGCAAAGCA[C/G]GACAGCAACAGCCAT | 208650 |
rs50305144 | snp | C/T | 0.489796 | 0.070696 | intron-variant | Cblb | GRCm38.p3 | 16:52163143 | GTGATGGTGAAATTG[C/T]ACATAAGCAGTGGGA | 208650 |
rs50317936 | snp | C/T | 0.231111 | 0.249285 | intron-variant | Cblb | GRCm38.p3 | 16:52159495 | AAAACATGGTTCATG[C/T]TTTAAACCACACAGA | 208650 |
rs50320097 | snp | A/G | 0.32 | 0.24 | intron-variant | Cblb | Mm_Celera | 16:52103776 | TATTATTTTAATTTT[A/G]CTAGAACAATTTTTG | 208650 |
rs50322109 | snp | G/T | 0.444444 | 0.157135 | intron-variant | Cblb | GRCm38.p3 | 16:52095670 | CAATACTCAGCTACA[G/T]TCTGTTTTTTAAAGA | 208650 |
rs50324633 | snp | A/G | 0.132653 | 0.220748 | intron-variant | Cblb | Mm_Celera | 16:52161863 | GGATCTCATTAAAGC[A/G]TCTTCTAAAGTCGTT | 208650 |
rs50337943 | snp | A/G | 0.5 | 0 | intron-variant | Cblb | GRCm38.p3 | 16:52050995 | CACATAAGACTGGCC[A/G]TAAATTGCATCTGTG | 208650 |
rs50349360 | snp | A/C | 0.231111 | 0.249285 | intron-variant | Cblb | Mm_Celera | 16:52184318 | TCAGTCATCCACGCC[A/C]TCTTTACTCAGTGTG | 208650 |
rs50357946 | snp | A/C | 0.124444 | 0.216185 | intron-variant | Cblb | Mm_Celera | 16:52069889 | AAATCAAGAGCAGAT[A/C]AAAATGTCCACTAAT | 208650 |
rs50359869 | snp | C/G | 0.124444 | 0.216185 | intron-variant | Cblb | Mm_Celera | 16:52135726 | CGGCGTGTGTTCTCT[C/G]GGTAATTGCTTTCCA | 208650 |
rs50378462 | snp | C/T | 0.152778 | 0.230321 | intron-variant | Cblb | Mm_Celera | 16:52186940 | TGCTCGCTCCCTTGG[C/T]CTCTGTCCAGAGGCT | 208650 |
rs50389821 | snp | C/T | 0.124444 | 0.216185 | utr-variant-3-prime | Cblb | Mm_Celera | 16:52207493 | CATGGTCCCACAATT[C/T]CAGTAGATAGCCCTT | 208650 |
rs50401376 | snp | C/T | 0.231111 | 0.249285 | intron-variant | Cblb | GRCm38.p3 | 16:52154647 | TCTAAATAATGAATA[C/T]AGAAGAAAGAAGTCT | 208650 |
rs50402494 | snp | A/G | 0.244898 | 0.249948 | intron-variant | Cblb | GRCm38.p3 | 16:52124590 | ATCAATGGCCGCCCG[A/G]TAACAATCTATTTTC | 208650 |
rs50413640 | snp | G/T | 0.132653 | 0.220748 | intron-variant | Cblb | GRCm38.p3 | 16:52158821 | TGTGTCATTATAGGT[G/T]ACTGGCAAACACAAC | 208650 |
rs50416855 | snp | A/G | | | intron-variant | Cblb | GRCm38.p3 | 16:52142611 | TTTAGACCAAATTGT[A/G]AATATCAATTTAAAA | 208650 |
rs50419977 | snp | A/T | 0.444444 | 0.157135 | intron-variant | Cblb | GRCm38.p3 | 16:52090504 | CCTCAGAAGGATGTC[A/T]GGAGCTTCCCTCCAC | 208650 |
rs50428118 | snp | C/T | 0.231111 | 0.249285 | intron-variant | Cblb | GRCm38.p3 | 16:52106225 | TAAATGACTACCCCA[C/T]ATATTTGAATGTGAA | 208650 |
rs50432350 | snp | A/C | 0.489796 | 0.070696 | intron-variant | Cblb | GRCm38.p3 | 16:52095988 | TATCTCAGGCTCTTT[A/C]AGATGGTGATAACAC | 208650 |
rs50447862 | snp | A/G | 0.336735 | 0.234472 | intron-variant | Cblb | Mm_Celera | 16:52126115 | TTGACGTCATTAAGA[A/G]TTAAACAGCATGTGA | 208650 |
rs50451315 | snp | C/G | 0.486111 | 0.0821678 | intron-variant | Cblb | GRCm38.p3 | 16:52142252 | AACGCTGCGCTCGCA[C/G]TCGTGGACTACAGTA | 208650 |
rs50464026 | snp | C/T | 0.124444 | 0.216185 | intron-variant | Cblb | Mm_Celera | 16:52135925 | GGAGAAAACGCCCTG[C/T]TGTTCCCAGCTCTGA | 208650 |
rs50471510 | snp | C/T | 0.444444 | 0.157135 | intron-variant | Cblb | GRCm38.p3 | 16:52050376 | CTTGAGGGCAGTGAA[C/T]GTCCTGGCTGCCTTT | 208650 |
rs50477296 | snp | A/G | 0.32 | 0.24 | intron-variant | Cblb | GRCm38.p3 | 16:52103851 | ATAAAATTTATTGGT[A/G]TGTGTCTGTTTGACT | 208650 |
rs50479804 | snp | C/T | 0.124444 | 0.216185 | intron-variant | Cblb | GRCm38.p3 | 16:52154023 | TGGAGAAGTTGAATG[C/T]TGTGGACCTCAGAAG | 208650 |
rs50481027 | snp | C/T | 0.132653 | 0.220748 | intron-variant | Cblb | Mm_Celera | 16:52160190 | TGGGTTAGAGCTGCA[C/T]GTGACACACTCTGTA | 208650 |
rs50481684 | snp | C/T | 0.277778 | 0.248452 | intron-variant | Cblb | GRCm38.p3 | 16:52059135 | TTTAGTTTAAGGAAA[C/T]AGAAGATTTACCTGA | 208650 |
rs50487424 | snp | G/T | 0.124444 | 0.216185 | intron-variant | Cblb | Mm_Celera | 16:52104890 | CCTTCGCTACTCCAC[G/T]TTCACTATTCTATTT | 208650 |
rs50505333 | snp | A/G | 0.124444 | 0.216185 | intron-variant | Cblb | Mm_Celera | 16:52079891 | ATCTCCCAATGTGCC[A/G]TTCAAATGTTGTGTC | 208650 |
rs50518093 | snp | A/G | 0.124444 | 0.216185 | intron-variant | Cblb | Mm_Celera | 16:52126329 | TGCAAAGTATTCAAA[A/G]GCCCTCATCTTTAGC | 208650 |
rs50523513 | snp | A/G | 0.231111 | 0.249285 | intron-variant | Cblb | GRCm38.p3 | 16:52154261 | ATACAGTTGGGAAAG[A/G]GTAGGTGCAGAGTCC | 208650 |
rs50523708 | snp | C/G | 0.244898 | 0.249948 | intron-variant | Cblb | GRCm38.p3 | 16:52064610 | CAGGTGACTTTAGCT[C/G]TCAGTACCACAGGGG | 208650 |
rs50527769 | snp | C/T | | | intron-variant, utr-variant-5-prime | Cblb | GRCm38.p3 | 16:52048208 | AGAATGGAGCTTCAC[C/T]GCTGGGCCATCTTTG | 208650 |
rs50538953 | snp | A/G | 0.124444 | 0.216185 | intron-variant | Cblb | Mm_Celera | 16:52178452 | GACAATTGTAGTTTT[A/G]GCATATTAATCACAA | 208650 |
rs50548966 | snp | G/T | 0.391111 | 0.206368 | intron-variant | Cblb | Mm_Celera | 16:52168118 | TTACTGAGAGGTGGA[G/T]TTTCATCCTATTTCT | 208650 |
rs50550278 | snp | C/G | 0.444444 | 0.157135 | intron-variant | Cblb | Mm_Celera | 16:52052014 | GCACTGAGAATGGCA[C/G]GGTAATGGTTTCTGA | 208650 |
rs50552866 | snp | C/T | 0.48 | 0.0979796 | intron-variant | Cblb | GRCm38.p3 | 16:52099576 | TCATCTCACTAAAAT[C/T]GTCTCCCTGGGATAG | 208650 |
rs50559599 | snp | A/G | 0.124444 | 0.216185 | intron-variant | Cblb | Mm_Celera | 16:52104515 | GTTTTGTTATGTCAT[A/G]AAGCAAACTATGTAT | 208650 |
rs50569075 | snp | C/T | 0.124444 | 0.216185 | intron-variant | Cblb | GRCm38.p3 | 16:52087255 | AACCTTTTCTATGCT[C/T]AGGCTCCAGGCGATT | 208650 |
rs50574167 | snp | C/G | 0.142012 | 0.225474 | intron-variant | Cblb | GRCm38.p3 | 16:52146849 | CTGCTTCTCCTGCAG[C/G]TTTAATTAGGGACAT | 208650 |
rs50576319 | snp | A/T | 0.391111 | 0.206368 | intron-variant | Cblb | Mm_Celera | 16:52202940 | TGATATATACAGCGC[A/T]GGTTTTGCATCTAGC | 208650 |
rs50581565 | snp | C/T | 0.124444 | 0.216185 | intron-variant | Cblb | Mm_Celera | 16:52193838 | TTCTTCAAGTTTTTT[C/T]CCCTCATCAGCTTTC | 208650 |
rs50581654 | snp | A/C | 0.489796 | 0.070696 | intron-variant | Cblb | GRCm38.p3 | 16:52156898 | TGTGACTGTAAAATG[A/C]TGAGTTGTTGCCTTT | 208650 |
rs50584720 | snp | C/T | 0.32 | 0.24 | intron-variant | Cblb | Mm_Celera | 16:52087519 | CTGGTCCCTGTACCA[C/T]ACAGAAAGCAGCACA | 208650 |
rs50585838 | snp | C/G | 0.132653 | 0.220748 | intron-variant | Cblb | Mm_Celera | 16:52132658 | ACCTAAAGCTCCTGA[C/G]TTAAAGATTTCTGAT | 208650 |
rs50586078 | snp | A/G | 0.489796 | 0.070696 | intron-variant | Cblb | GRCm38.p3 | 16:52091998 | ATTAAAAATTGACAT[A/G]CATTACAAGGTCAAA | 208650 |
rs50586523 | snp | A/G | 0.124444 | 0.216185 | intron-variant | Cblb | Mm_Celera | 16:52196998 | TTTCTGAATATACTG[A/G]CAAATTAAGGAGGTG | 208650 |
rs50588805 | snp | A/C | 0.444444 | 0.157135 | intron-variant | Cblb | GRCm38.p3 | 16:52142127 | GTGCCAAACATTCTA[A/C]ACTCGACTCAGCCAG | 208650 |
rs50592591 | snp | A/T | 0.244898 | 0.249948 | intron-variant | Cblb | GRCm38.p3 | 16:52062488 | CGTCTTACACCTTTG[A/T]TGTCCTACTTTGTTG | 208650 |
rs50625047 | snp | A/G | 0.124444 | 0.216185 | intron-variant | Cblb | Mm_Celera | 16:52151825 | CACCTAGAAATTGGC[A/G]AGAAAGATTGGAAAG | 208650 |
rs50630482 | snp | C/T | 0.231111 | 0.249285 | intron-variant | Cblb | GRCm38.p3 | 16:52100690 | GGTTCAGCTGGAAGA[C/T]CCACTGGGAAGTTAT | 208650 |
rs50635385 | snp | C/T | 0.124444 | 0.216185 | intron-variant | Cblb | Mm_Celera | 16:52148188 | AGGAGGGCGGGTTGA[C/T]GGTGAGGTGTAAATC | 208650 |
rs50636996 | snp | G/T | 0.132653 | 0.220748 | intron-variant | Cblb | Mm_Celera | 16:52197106 | ACAGATTGTTATATG[G/T]GTAATGGGTTTGGAA | 208650 |
rs50649045 | snp | G/T | 0.244898 | 0.249948 | intron-variant | Cblb | GRCm38.p3 | 16:52176726 | TTGCATGTTACATAT[G/T]AGCCATAGCTGTAAG | 208650 |
rs50657005 | snp | A/G | 0.124444 | 0.216185 | intron-variant | Cblb | Mm_Celera | 16:52152258 | TTTCAGTATTTGAGG[A/G]CTGTAAATCCTTGCT | 208650 |
rs50666587 | snp | A/G/T | 0.132653 | 0.220748 | intron-variant | Cblb | Mm_Celera | 16:52174567 | AGTAAAGACAGAAGC[A/G/T]GTGGAATTGGGTTTA | 208650 |
rs50682426 | snp | C/G | 0.244898 | 0.249948 | intron-variant | Cblb | GRCm38.p3 | 16:52122940 | GACTCAGATGTCTAA[C/G]AGGCTTCACTCACTC | 208650 |
rs50685015 | snp | C/G | 0.260355 | 0.249785 | intron-variant | Cblb | Mm_Celera | 16:52190339 | TACCCTCCTGGACTA[C/G]CTTTGGTAAAGCAGT | 208650 |
rs50686036 | snp | A/C | 0.132653 | 0.220748 | synonymous-codon | Cblb | Mm_Celera | 16:52164442 | CATTCAGAAAGGCAT[A/C]GTGCGCTCTCCGTGT | 208650 |
rs50688910 | snp | A/G | 0.124444 | 0.216185 | intron-variant | Cblb | Mm_Celera | 16:52103692 | CAATGAGAAAGCATG[A/G]GACAACCTCCGAACT | 208650 |
rs50689548 | snp | A/G | 0.124444 | 0.216185 | intron-variant | Cblb | Mm_Celera | 16:52104953 | TGTTTTTTGATACAT[A/G]TTACCCAGGTCATGC | 208650 |
rs50694651 | snp | C/T | 0.124444 | 0.216185 | synonymous-codon | Cblb | Mm_Celera | 16:52152579 | GCCCATCATTGTGGA[C/T]CCCTTCGACCCCAGA | 208650 |
rs50703179 | snp | A/G | 0.375 | 0.216506 | intron-variant | Cblb | GRCm38.p3 | 16:52114847 | AAGTGCTTTGTTAGC[A/G]GGTTCTTAAGAAACG | 208650 |
rs50708915 | snp | C/T | 0.32 | 0.24 | intron-variant | Cblb | GRCm38.p3 | 16:52153768 | AGAAACGACATCCTG[C/T]TGCTCTATCTATAAG | 208650 |
rs50711347 | snp | C/G | 0.124444 | 0.216185 | intron-variant | Cblb | Mm_Celera | 16:52154347 | ACTCTTGGAATTTCT[C/G]TCCGGGAGTTCCACA | 208650 |
rs50719803 | snp | A/T | 0.142012 | 0.225474 | intron-variant | Cblb | GRCm38.p3 | 16:52162467 | TAGTTAATTTCTCAG[A/T]AAGTCTGTCTGTCAC | 208650 |
rs50723028 | snp | A/G | 0.132653 | 0.220748 | intron-variant | Cblb | GRCm38.p3 | 16:52165853 | GTAAAAGAAACATAA[A/G]AGGTTATTAGAAATG | 208650 |
rs50735975 | snp | A/G | 0.231111 | 0.249285 | intron-variant | Cblb | GRCm38.p3 | 16:52196814 | TTGATGCCACTTTCC[A/G]CCTAATGTATATTGT | 208650 |
rs50739219 | snp | A/G | 0.132653 | 0.220748 | intron-variant | Cblb | Mm_Celera | 16:52167572 | TTCACTACAGTGTGA[A/G]TGTAAGGAGAATGCA | 208650 |
rs50751337 | snp | A/G | 0.32 | 0.24 | intron-variant | Cblb | GRCm38.p3 | 16:52081874 | ATTAATTTTCAGTTC[A/G]GAATTAACCAAACTG | 208650 |
rs50757151 | snp | A/G | 0.408163 | 0.193609 | intron-variant | Cblb | GRCm38.p3 | 16:52127801 | TCCTTTGGTTTTTCT[A/G]TACTGATGTCATAAC | 208650 |
rs50758488 | snp | C/T | 0.231111 | 0.249285 | intron-variant | Cblb | GRCm38.p3 | 16:52130502 | CTGGGAATGGCTGAG[C/T]TCTAAAAGGGAGAGA | 208650 |
rs50759337 | snp | A/G | 0.132653 | 0.220748 | intron-variant | Cblb | Mm_Celera | 16:52162288 | ACCAGAGCTGAAAGG[A/G]AAAGATCGGGTTCTG | 208650 |
rs50761827 | snp | A/G | 0.124444 | 0.216185 | intron-variant | Cblb | GRCm38.p3 | 16:52069920 | GTCAAGTCACCAAGC[A/G]CTTTGGACTTTTCAC | 208650 |
rs50765407 | snp | A/C | 0.489796 | 0.070696 | intron-variant | Cblb | GRCm38.p3 | 16:52096263 | TGAAACAATGGATGG[A/C]AGTAATTTCTGCAAG | 208650 |
rs50765707 | snp | C/G | 0.124444 | 0.216185 | intron-variant | Cblb | Mm_Celera | 16:52148151 | TGCAATGGAGCAGGC[C/G]TGAGGAGTACCCAGG | 208650 |
rs50768827 | snp | A/G | 0.124444 | 0.216185 | intron-variant | Cblb | Mm_Celera | 16:52120162 | AAGTTCTCATTTGAC[A/G]TTAGGAAGTGCCTAC | 208650 |
rs50770133 | snp | A/G | 0.21875 | 0.248039 | intron-variant | Cblb | Mm_Celera | 16:52094512 | CTAAGGTTAGGAACA[A/G]CCATACTGGGTGGAT | 208650 |
rs50770531 | snp | C/T | 0.489796 | 0.070696 | intron-variant | Cblb | GRCm38.p3 | 16:52163897 | CTTCTGCAGCACATG[C/T]CCGGGCCCTCTGAGA | 208650 |
rs50780763 | snp | G/T | 0.231111 | 0.249285 | intron-variant | Cblb | Mm_Celera | 16:52151496 | TGAATTTGGAAGGCT[G/T]AACCAAACCTAATGA | 208650 |
rs50784776 | snp | C/G | 0.375 | 0.216506 | intron-variant | Cblb | Mm_Celera | 16:52114522 | TACCATTTTATTCCA[C/G]TAGTATGAACATTCT | 208650 |
rs50790137 | snp | C/T | 0.231111 | 0.249285 | intron-variant | Cblb | GRCm38.p3 | 16:52078399 | GTTGTGGAATAGGTA[C/T]GCTTAGTGAGTCCAA | 208650 |
rs50798148 | snp | C/T | 0.244898 | 0.249948 | intron-variant | Cblb | Mm_Celera | 16:52147299 | CCACGGAAGAGTTTG[C/T]CCAGAATACCAAGTA | 208650 |
rs50800361 | snp | G/T | 0.124444 | 0.216185 | utr-variant-3-prime | Cblb | Mm_Celera | 16:52206512 | TTTGTTTGGATGGTC[G/T]TATGTTGCTTCTGCT | 208650 |
rs50803859 | snp | A/G | 0.231111 | 0.249285 | intron-variant | Cblb | Mm_Celera | 16:52197192 | TTATTGGTAGTCAGT[A/G]ATGGGTAGTTTGCCA | 208650 |
rs50806791 | snp | A/T | 0.231111 | 0.249285 | intron-variant | Cblb | GRCm38.p3 | 16:52187779 | CGAACAGGTTTTCAC[A/T]CCCCTTGATAGTATT | 208650 |
rs50821634 | snp | A/C | 0.231111 | 0.249285 | intron-variant | Cblb | Mm_Celera | 16:52128723 | ACTTTGTAAAGTAGA[A/C]CCAAGGTGCAAGAGT | 208650 |
rs50829917 | snp | A/T | 0.165289 | 0.235211 | intron-variant | Cblb | Mm_Celera | 16:52140843 | ATAGTGGATTAGTTT[A/T]TATTATACTTTTCCT | 208650 |
rs50839001 | snp | A/G | 0.497778 | 0.0332592 | intron-variant | Cblb | GRCm38.p3 | 16:52134106 | TAAACTTTCGGATTA[A/G]AAACAATACATAATT | 208650 |
rs50857735 | snp | A/G | 0.32 | 0.24 | intron-variant | Cblb | GRCm38.p3 | 16:52102631 | CTTAAGTGTCTCTCC[A/G]TTATACTTTGTGCTT | 208650 |
rs50865429 | snp | C/G | 0.132653 | 0.220748 | intron-variant | Cblb | Mm_Celera | 16:52162000 | TCTTCGGCTTGTTCC[C/G]TGAAGATTTTCTGTT | 208650 |
rs50879971 | snp | A/C | 0.142012 | 0.225474 | intron-variant | Cblb | Mm_Celera | 16:52145655 | TCGATGGAAAACCTC[A/C]TGGAGTGCTTGTTTT | 208650 |
rs50885998 | snp | C/T | 0.444444 | 0.157135 | intron-variant | Cblb | GRCm38.p3 | 16:52150528 | CCTTTTTTGAATGAC[C/T]CGATATAATGTAGAT | 208650 |
rs50889554 | snp | A/G | 0.124444 | 0.216185 | intron-variant | Cblb | Mm_Celera | 16:52087926 | GCTTCCTTTTAAGCC[A/G]TTTTACCAAGTGCCG | 208650 |
rs50899249 | snp | A/T | | | intron-variant, utr-variant-5-prime | Cblb | GRCm38.p3 | 16:52048805 | CTTCGAATCTCTTAG[A/T]GAAGTAGCCGGGAGT | 208650 |
rs50902345 | snp | A/G | 0.124444 | 0.216185 | intron-variant | Cblb | Mm_Celera | 16:52130239 | TTTTCGCTCATTTCT[A/G]CTCAGTTTCTCCAGA | 208650 |
rs50904195 | snp | A/C | 0.142012 | 0.225474 | intron-variant | Cblb | GRCm38.p3 | 16:52062463 | AGCTGATAGTTTAGA[A/C]GTTGAACTCCGTCTT | 208650 |
rs50908909 | snp | G/T | 0.124444 | 0.216185 | intron-variant | Cblb | GRCm38.p3 | 16:52170293 | TTCCTAAAATATCAC[G/T]CTAACCTTAGACAAT | 208650 |
rs50911621 | snp | G/T | 0.124444 | 0.216185 | intron-variant | Cblb | Mm_Celera | 16:52197271 | TCTACCAGTTCAGCC[G/T]GTAGTTGATGCCACT | 208650 |
rs50922764 | snp | C/T | | | intron-variant, utr-variant-5-prime | Cblb | GRCm38.p3 | 16:52048456 | GTTCAGACTGGTTTC[C/T]TGCTGGTCTTTTTAT | 208650 |
rs50927286 | snp | C/T | 0.5 | 0 | intron-variant, upstream-variant-2KB | Cblb | Mm_Celera | 16:52046669 | ATGTTTCATAGGTCA[C/T]GTGTTTCTAGGCCTA | 208650 |
rs50936369 | snp | A/G | 0.231111 | 0.249285 | intron-variant | Cblb | GRCm38.p3 | 16:52134841 | CTCTCGTCTCTTGCC[A/G]TGGTACCTGGAGAGA | 208650 |
rs50939298 | snp | C/T | 0.244898 | 0.249948 | intron-variant | Cblb | GRCm38.p3 | 16:52060228 | CTGAGATTTGGCAGC[C/T]GGGGCCAGTTCCGGG | 208650 |
rs50941034 | snp | C/T | 0.231111 | 0.249285 | intron-variant | Cblb | GRCm38.p3 | 16:52189474 | TTTCCTGAGTCTCTG[C/T]CACATTAGCAGAAAG | 208650 |
rs50941155 | snp | C/G | 0.132653 | 0.220748 | intron-variant | Cblb | Mm_Celera | 16:52130916 | AGAATAATCAAGTGA[C/G]CATATTCCGTGGAGC | 208650 |
rs50943097 | snp | C/G | 0.231111 | 0.249285 | intron-variant | Cblb | GRCm38.p3 | 16:52106850 | GTAAATCGTTGCTGA[C/G]CTCTTCCACTTCTTT | 208650 |
rs50943704 | snp | C/G | 0.132653 | 0.220748 | intron-variant | Cblb | GRCm38.p3 | 16:52057515 | AGAGCAGGACCTAAG[C/G]TGTATCTTGCAGGAT | 208650 |
rs50945320 | snp | C/G | 0.231111 | 0.249285 | intron-variant | Cblb | GRCm38.p3 | 16:52070421 | AGGTGAAGTTACCCT[C/G]TCAGTATCTAGACTG | 208650 |
rs50946086 | snp | C/T | 0.231111 | 0.249285 | intron-variant | Cblb | Mm_Celera | 16:52139054 | AACATTAAACAAGTC[C/T]ATGACCAAATTTTAA | 208650 |
rs50950252 | snp | A/G | 0.231111 | 0.249285 | intron-variant | Cblb | GRCm38.p3 | 16:52071838 | TGGCATTAGGCCAGG[A/G]GACTGACTATTTTAG | 208650 |
rs50965774 | snp | A/G | 0.489796 | 0.070696 | intron-variant | Cblb | GRCm38.p3 | 16:52166498 | CGTGCTCTTTAACTA[A/G]CTCCATGTTCTGGAC | 208650 |
rs50968972 | snp | A/G | 0.132653 | 0.220748 | intron-variant | Cblb | Mm_Celera | 16:52184159 | AGCTTTATTTTCTGA[A/G]CTTATTTTCTGGCCT | 208650 |
rs50972837 | snp | G/T | 0.32 | 0.24 | intron-variant | Cblb | GRCm38.p3 | 16:52103475 | AGACAGCAGGCTACC[G/T]AAGGGAAAAACTTCC | 208650 |
rs50977592 | snp | A/G | 0.32 | 0.24 | intron-variant | Cblb | GRCm38.p3 | 16:52189867 | GCGATGCCTTCAGAT[A/G]ACAGCAGAGTTCCTG | 208650 |
rs50979164 | snp | C/T | 0.124444 | 0.216185 | intron-variant | Cblb | Mm_Celera | 16:52132851 | ACTACTTGACTACTT[C/T]AAGGTGCATACATTA | 208650 |
rs50984177 | snp | C/T | 0.132653 | 0.220748 | intron-variant | Cblb | Mm_Celera | 16:52158918 | GCCCCACCTTGTGTC[C/T]ACCTCAACTGGCAGA | 208650 |
rs51007301 | snp | C/G | 0.444444 | 0.157135 | intron-variant | Cblb | Mm_Celera | 16:52052385 | GTGAGTTTACTGGTA[C/G]TTTCTTCAGTCGTTT | 208650 |
rs51010194 | snp | C/T | 0.444444 | 0.157135 | intron-variant | Cblb | GRCm38.p3 | 16:52156263 | TAAAACCAGGCCACG[C/T]CTAATGTTTTTGTCA | 208650 |
rs51014456 | snp | A/C | 0.124444 | 0.216185 | intron-variant | Cblb | Mm_Celera | 16:52134938 | AGCTTCCTTTCAAAC[A/C]TTTCCCAGGTCCATT | 208650 |
rs51017751 | snp | G/T | 0.124444 | 0.216185 | intron-variant | Cblb | Mm_Celera | 16:52119110 | GTGCAGGGCCTCTTA[G/T]TCCACACACAATAGA | 208650 |
rs51027419 | snp | C/T | 0.408163 | 0.193609 | intron-variant | Cblb | Mm_Celera | 16:52163814 | AATGTCATTCACCAT[C/T]CCCTAAGTGTAGCTT | 208650 |
rs51030079 | snp | G/T | 0.142012 | 0.225474 | intron-variant | Cblb | Mm_Celera | 16:52076154 | GTAGCTGAATACTTT[G/T]GTCACTCAACACCTC | 208650 |
rs51030367 | snp | A/T | 0.132653 | 0.220748 | intron-variant | Cblb | Mm_Celera | 16:52063291 | AGACCGGGGCTTTGG[A/T]TCAGGCTTTCCTTGT | 208650 |
rs51032351 | snp | A/G | 0.32 | 0.24 | intron-variant | Cblb | GRCm38.p3 | 16:52195236 | AAATTGATGGGGACC[A/G]AAAGAAGAGGTGCTA | 208650 |
rs51036406 | snp | A/G | 0.231111 | 0.249285 | intron-variant | Cblb | Mm_Celera | 16:52151643 | AAGTCAAGACTGCAG[A/G]CTCGGCAGTAGTCAG | 208650 |
rs51064982 | snp | A/T | 0.124444 | 0.216185 | downstream-variant-500B | Cblb | Mm_Celera | 16:52208176 | CATATCCACCTTACA[A/T]AAGGGCTTAGTCACC | 208650 |
rs51077156 | snp | A/C/T | 0.142012 | 0.225474 | synonymous-codon | Cblb | GRCm38.p3 | 16:52166252 | AAAGCCTGGCGTCAC[A/C/T]GCAAACTCCAGCTTA | 208650 |
rs51080421 | snp | C/T | 0.231111 | 0.249285 | synonymous-codon | Cblb | GRCm38.p3 | 16:52166159 | GGACCAGCCCATGCC[C/T]CTCGAAGCCTGGTGC | 208650 |
rs51088923 | snp | A/G | 0.132653 | 0.220748 | intron-variant | Cblb | Mm_Celera | 16:52163543 | TCACATAGAGAATGC[A/G]CAGCATCTGCCTTTT | 208650 |
rs51112025 | snp | C/T | 0.396694 | 0.202437 | intron-variant | Cblb | Mm_Celera | 16:52203633 | CTGATGCTTTTTTTT[C/T]CCTCTGTTTGCATTT | 208650 |
rs51118569 | snp | C/G | 0.124444 | 0.216185 | intron-variant | Cblb | Mm_Celera | 16:52129964 | ATTGCCAGGTGATAG[C/G]TATGGCCCATCAGTG | 208650 |
rs51137464 | snp | C/T | 0.32 | 0.24 | intron-variant | Cblb | GRCm38.p3 | 16:52177327 | CCTGAATGCTCTCTA[C/T]TATAGCTGGTTGACC | 208650 |
rs51139210 | snp | A/C | 0.48 | 0.0979796 | intron-variant | Cblb | GRCm38.p3 | 16:52094691 | CCAGTCCTTTCTCTG[A/C]CATCCCACAATGGTA | 208650 |
rs51140988 | snp | C/T | 0.124444 | 0.216185 | intron-variant | Cblb | Mm_Celera | 16:52129246 | TGACTTTATACTTTA[C/T]ACACACAAAAGAGTG | 208650 |
rs51144238 | snp | C/T | 0.124444 | 0.216185 | intron-variant | Cblb | Mm_Celera | 16:52150637 | CGTATTAAATTGGTC[C/T]TGTAACTTTAAGGTT | 208650 |
rs51163344 | snp | C/T | 0.124444 | 0.216185 | intron-variant | Cblb | Mm_Celera | 16:52185212 | TTAAATGAACCATAT[C/T]GTGCCCGTTAAAAAG | 208650 |
rs51163795 | snp | A/G | 0.124444 | 0.216185 | intron-variant | Cblb | Mm_Celera | 16:52135033 | TAAAGCAAGCCTGCC[A/G]AGGTGCAACCATAGC | 208650 |
rs51165301 | snp | A/G | 0.142012 | 0.225474 | intron-variant | Cblb | Mm_Celera | 16:52144329 | AACTGTACAAAGTGC[A/G]GTTGACCTTTCACCT | 208650 |
rs51165738 | snp | C/T | 0.35503 | 0.226867 | intron-variant | Cblb | GRCm38.p3 | 16:52129817 | CACTCTGTAATCACT[C/T]GGGTTTGTGTTGGGC | 208650 |
rs51186450 | snp | A/G | 0.231111 | 0.249285 | intron-variant | Cblb | Mm_Celera | 16:52195453 | TGTCTGCCTGATCAC[A/G]TGGAGCCACTCAGGG | 208650 |
rs51191563 | snp | A/T | 0.197531 | 0.244432 | intron-variant | Cblb | Mm_Celera | 16:52087151 | TTTTGATGACTTTGC[A/T]TTGTTGACTTCTTGC | 208650 |
rs51194078 | snp | C/T | 0.124444 | 0.216185 | intron-variant | Cblb | Mm_Celera | 16:52167780 | TGAAACAAGCTCTCA[C/T]GTGAAGAGACATTTA | 208650 |
rs51197154 | snp | A/G | 0.497778 | 0.0332592 | intron-variant | Cblb | Mm_Celera | 16:52155584 | TCAGAGTTCTACAAG[A/G]AGATTGGGGTGTGGC | 208650 |
rs51200343 | snp | A/G | | | intron-variant | Cblb | GRCm38.p3 | 16:52055552 | TCCTTGGCATGTGGA[A/G]GCAGAACTTCAGAAT | 208650 |
rs51201224 | snp | A/C | 0.231111 | 0.249285 | intron-variant | Cblb | Mm_Celera | 16:52126350 | CATCTTTAGCAGGCT[A/C]CCCAATGGTTCCTGG | 208650 |
rs51206394 | snp | C/T | 0.408163 | 0.193609 | intron-variant | Cblb | Mm_Celera | 16:52167052 | AGAATTTCACCTCTT[C/T]AGCTCAGATTCAGTT | 208650 |
rs51210517 | snp | C/T | 0.124444 | 0.216185 | intron-variant | Cblb | Mm_Celera | 16:52184269 | AGCTGCCTGGGGCCT[C/T]CTGATGACTGACAGA | 208650 |
rs51215291 | snp | C/T | 0.124444 | 0.216185 | intron-variant | Cblb | Mm_Celera | 16:52137653 | GAATCGAGCAGAATG[C/T]TGAGAGAAATAAATC | 208650 |
rs51215589 | snp | A/G | 0.231111 | 0.249285 | upstream-variant-2KB | Cblb | GRCm38.p3 | 16:52030803 | TGTGGAGTTTTTACT[A/G]TCCTGGGACGATTTA | 208650 |
rs51216879 | snp | A/G | 0.152778 | 0.230321 | intron-variant | Cblb | Mm_Celera | 16:52139786 | AGTGGTGCCTTCAGT[A/G]TGTTGCTCATGCCTA | 208650 |
rs51227576 | snp | A/C | 0.124444 | 0.216185 | intron-variant | Cblb | GRCm38.p3 | 16:52076739 | AGCCCACAGGACTGT[A/C]GAACGATTTGCAGGA | 208650 |
rs51228755 | snp | G/T | 0.231111 | 0.249285 | intron-variant | Cblb | Mm_Celera | 16:52180897 | TTACATCAGATGCTC[G/T]CTGACTAACAAAAGA | 208650 |
rs51261308 | snp | G/T | | | intron-variant, utr-variant-5-prime | Cblb | GRCm38.p3 | 16:52048581 | TTGATGGCTTCAAAC[G/T]TTTGGCAACTGTGTT | 208650 |
rs51269754 | snp | A/G | | | intron-variant | Cblb | GRCm38.p3 | 16:52114989 | AGGGCCTGTTATTGT[A/G]TAGAACTGTTATGTC | 208650 |
rs51278073 | snp | A/T | 0.444444 | 0.157135 | intron-variant | Cblb | GRCm38.p3 | 16:52114579 | ACATTTCTATATCCA[A/T]TTAAAGTGAAGGATT | 208650 |
rs51283136 | snp | C/T | 0.444444 | 0.157135 | intron-variant | Cblb | Mm_Celera | 16:52053226 | AGCCTCCTTCCTTTA[C/T]GTACACTATGCCTTC | 208650 |
rs51283969 | snp | C/T | 0.48 | 0.0979796 | intron-variant | Cblb | GRCm38.p3 | 16:52089816 | TATTTCTGTCTATAT[C/T]TCATTACTCATTAAA | 208650 |
rs51301353 | snp | A/T | 0.231111 | 0.249285 | intron-variant | Cblb | GRCm38.p3 | 16:52159363 | ACTCTTGCCTTTTTA[A/T]GGTGAAATTATATTG | 208650 |
rs51302999 | snp | C/T | 0.489796 | 0.070696 | intron-variant | Cblb | GRCm38.p3 | 16:52163876 | TGACGCAGCATAGAA[C/T]CTTGACTTCTGCAGC | 208650 |
rs51307901 | snp | A/T | 0.244898 | 0.249948 | intron-variant | Cblb | Mm_Celera | 16:52075049 | TAAAAAATTTTGTTC[A/T]ATACTCCTAGATTTT | 208650 |
rs51309038 | snp | C/T | 0.32 | 0.24 | intron-variant | Cblb | GRCm38.p3 | 16:52176178 | GGCACAATTAGATAC[C/T]GCAGTGCCTGAAATT | 208650 |
rs51309874 | snp | C/G | 0.231111 | 0.249285 | intron-variant | Cblb | Mm_Celera | 16:52133527 | TTTCTTTTCACATTT[C/G]CCTTATTGCAGGAGA | 208650 |
rs51324207 | snp | A/C | 0.5 | 0 | intron-variant | Cblb | Mm_Celera | 16:52094954 | ACACTGTAGAACAAC[A/C]GTGTTACCGCCCACG | 208650 |
rs51331999 | snp | A/G | 0.124444 | 0.216185 | intron-variant | Cblb | Mm_Celera | 16:52132492 | ATGTGTTTATTTTAC[A/G]TTTCTAGTGGCTTAA | 208650 |
rs51336894 | snp | C/T | 0.32 | 0.24 | intron-variant | Cblb | GRCm38.p3 | 16:52075866 | GCCTGGGAGTGTTAG[C/T]GTAAATGCTGATCCA | 208650 |
rs51337850 | snp | A/G | 0.124444 | 0.216185 | intron-variant | Cblb | GRCm38.p3 | 16:52193652 | TTAGCATATTTTGGG[A/G]TGTCTAATATAGTAC | 208650 |
rs51342835 | snp | C/G | 0.142012 | 0.225474 | intron-variant | Cblb | Mm_Celera | 16:52147657 | TCACATAAAAAAGGC[C/G]ATCACTGTCAATGCC | 208650 |
rs51350809 | snp | C/G | 0.124444 | 0.216185 | intron-variant | Cblb | Mm_Celera | 16:52070878 | TGCTCGGATGGCAGA[C/G]TACCATTTTCTCATG | 208650 |
rs51353352 | snp | A/G | 0.132653 | 0.220748 | intron-variant | Cblb | GRCm38.p3 | 16:52164817 | TTTCATAATGTCATA[A/G]CAAGAAAAATGCCAG | 208650 |
rs51364284 | snp | A/T | 0.277778 | 0.248452 | intron-variant | Cblb | Mm_Celera | 16:52125992 | ACAGATATCAATACA[A/T]TCTGAATAAAGTATC | 208650 |
rs51376355 | snp | A/T | 0.32 | 0.24 | intron-variant | Cblb | GRCm38.p3 | 16:52190325 | GTGCCTTGCAAGGCT[A/T]CCCTCCTGGACTAGC | 208650 |
rs51382229 | snp | A/G | 0.132653 | 0.220748 | intron-variant | Cblb | Mm_Celera | 16:52159912 | TATTTCTAGAAACTT[A/G]AACTTTGCAACAGGA | 208650 |
rs51387536 | snp | A/G | 0.231111 | 0.249285 | synonymous-codon | Cblb | Mm_Celera | 16:52135872 | GAAATACAGCACCAA[A/G]CCTGGAAGGTAAGCA | 208650 |
rs51396740 | snp | C/G | 0.231111 | 0.249285 | intron-variant | Cblb | GRCm38.p3 | 16:52106459 | TGCTTACTATGGTCT[C/G]TGCTTTGGGCTACAA | 208650 |
rs51397508 | snp | A/C/G | 0.244898 | 0.249948 | intron-variant | Cblb | Mm_Celera | 16:52184346 | GTGCTGCTTCCACTT[A/C/G]AGGCCAGCTCAGTCG | 208650 |
rs51400433 | snp | C/T | 0.231111 | 0.249285 | synonymous-codon | Cblb | GRCm38.p3 | 16:52152657 | CATGCTTGACTTGGA[C/T]GATGACGATGATCGA | 208650 |
rs51406776 | snp | C/T | 0.124444 | 0.216185 | intron-variant | Cblb | Mm_Celera | 16:52165463 | CAGCAACTGCTCTGC[C/T]ATTTAGATCTTCACT | 208650 |
rs51427076 | snp | A/G | 0.124444 | 0.216185 | intron-variant | Cblb | Mm_Celera | 16:52143890 | AGCTTAAAAGGTGGT[A/G]TTGAGGAGACAGTGA | 208650 |
rs51430214 | snp | C/G | 0.152778 | 0.230321 | intron-variant | Cblb | Mm_Celera | 16:52140594 | TGTTGGGAAAGGACA[C/G]CATGGGAGAGCTTCA | 208650 |
rs51436442 | snp | C/T | 0.497778 | 0.0332592 | intron-variant | Cblb | GRCm38.p3 | 16:52089155 | TCCAGACTGACACAA[C/T]ACAGACTGTAATCTT | 208650 |
rs51439397 | snp | A/G | 0.32 | 0.24 | intron-variant | Cblb | GRCm38.p3 | 16:52182114 | AAATAATCTGAAAAA[A/G]TGTTTTAGTCCCAAG | 208650 |
rs51445641 | snp | C/T | 0.231111 | 0.249285 | intron-variant | Cblb | Mm_Celera | 16:52149252 | GTTTTCACTGGTAAC[C/T]TCTCTCACCTTAAAT | 208650 |
rs51450265 | snp | A/C | 0.231111 | 0.249285 | intron-variant | Cblb | Mm_Celera | 16:52135887 | GCCTGGAAGGTAAGC[A/C]CTAATCTGGACGATC | 208650 |
rs51452177 | snp | A/G | 0.165289 | 0.235211 | intron-variant | Cblb | Mm_Celera | 16:52144256 | AAACTGACTTGCGAT[A/G]AATTTTGATTTGCTG | 208650 |
rs51454859 | snp | C/T | 0.32 | 0.24 | intron-variant | Cblb | GRCm38.p3 | 16:52087595 | AGAAAATGAAAATGG[C/T]AGACTTTCAAACCTG | 208650 |
rs51479273 | snp | A/G | 0.32 | 0.24 | intron-variant | Cblb | GRCm38.p3 | 16:52190831 | TTGAGGTTTTCAACA[A/G]CAGTTGTCTTGTCTA | 208650 |
rs51479781 | snp | G/T | 0.132653 | 0.220748 | intron-variant | Cblb | Mm_Celera | 16:52185415 | GCCAGCCGTTACTAA[G/T]CTAGGAGCTTAAGGG | 208650 |
rs51487795 | snp | G/T | 0.124444 | 0.216185 | intron-variant | Cblb | Mm_Celera | 16:52135550 | CCTTTTGCCCTCTCT[G/T]TTGTACTCCAAAGAA | 208650 |
rs51494544 | snp | A/T | 0.231111 | 0.249285 | utr-variant-3-prime | Cblb | Mm_Celera | 16:52206743 | ATCAGCATAGCCTAA[A/T]ACCTAGAGTTGCCCC | 208650 |
rs51496505 | snp | A/G | 0.142012 | 0.225474 | intron-variant | Cblb | Mm_Celera | 16:52193347 | CTTCTATTCAGACAA[A/G]AGTACACACTAAGGC | 208650 |
rs51517833 | snp | A/G | 0.396694 | 0.202437 | intron-variant | Cblb | GRCm38.p3 | 16:52093890 | GCTCACGTGTTTGAT[A/G]GAGAAATAAACAGGA | 208650 |
rs51519183 | snp | C/T | 0.231111 | 0.249285 | intron-variant | Cblb | GRCm38.p3 | 16:52081622 | TCATCTGTGATGAAA[C/T]GTTTCTCTCTTGACC | 208650 |
rs51532013 | snp | C/T | 0.260355 | 0.249785 | intron-variant | Cblb | Mm_Celera | 16:52170335 | CACAGGAAAAGATTC[C/T]GAACATACGTGTTAA | 208650 |
rs51543943 | snp | A/G | 0.297521 | 0.245442 | intron-variant | Cblb | Mm_Celera | 16:52146759 | AAAGGAAGTTCAGAC[A/G]TAGTTTCTACTTTAA | 208650 |
rs51545549 | snp | G/T | 0.231111 | 0.249285 | utr-variant-3-prime | Cblb | GRCm38.p3 | 16:52207866 | ACAGCAATAGAAAGT[G/T]TTCTTCTCAGTTCCT | 208650 |
rs51566766 | snp | A/G | 0.124444 | 0.216185 | intron-variant | Cblb | Mm_Celera | 16:52195866 | CAGAGAAACACCCAT[A/G]TAACGGGACTAAACT | 208650 |
rs51578891 | snp | C/T | 0.165289 | 0.235211 | intron-variant | Cblb | Mm_Celera | 16:52055195 | AATACAAACAGCAGC[C/T]CACACAGTTGGGTGA | 208650 |