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 |