SNP - dbSNP |
dbSNP | Type | Alleles | Het | Se(het) | Fxn-class | Gene Name | Assembly | Chr-pos | Sequence | Entrez Gene |
rs6203257 | snp | A/C | 0.5 | 0 | intron-variant | Polk | Mm_Celera | 13:96531628 | gactagtgatcaatc[A/C]ncttagcgcctgtac | 27015 |
rs6203258 | snp | G/T | 0.5 | 0 | intron-variant | Polk | Mm_Celera | 13:96531629 | actagtgatcaatcn[G/T]cttagcgcctgtacc | 27015 |
rs6204507 | snp | A/G | 0.290657 | 0.246672 | intron-variant | Polk | Mm_Celera | 13:96531889 | AAGTTCAGGAAATCT[A/G]TCTTCTTTAGTAGAG | 27015 |
rs6204987 | snp | A/G | 0.290657 | 0.246672 | intron-variant | Polk | Mm_Celera | 13:96531939 | CCCATTAAATAACGT[A/G]TCAGTTCAAAAGTAA | 27015 |
rs6205051 | snp | A/G | 0.5 | 0 | intron-variant | Polk | Mm_Celera | 13:96531972 | TCCCGAGTCCAGTTT[A/G]TGCTTTTCNNTTTTG | 27015 |
rs6205068 | snp | A/T | 0.35124 | 0.228584 | intron-variant | Polk | GRCm38.p3 | 13:96531981 | CAGTTTGTGCTTTTC[A/T]GTTTTGCTGATGAGC | 27015 |
rs6205069 | snp | A/G | 0.5 | 0 | intron-variant | Polk | GRCm38.p3 | 13:96531981 | AGTTTNTGCTTTTCN[A/G]TTTTGCTGATGAGCT | 27015 |
rs6205634 | snp | C/T | 0.5 | 0 | intron-variant | Polk | Mm_Celera | 13:96532074 | ACAGAGTCAGGAACA[C/T]ATAAAANTATGAAAA | 27015 |
rs6205647 | snp | C/T | 0.5 | 0 | intron-variant | Polk | Mm_Celera | 13:96532081 | CAGGAACANATAAAA[C/T]TATGAAAAGCTAAAT | 27015 |
rs6206126 | snp | A/G/T | 0.5 | 0 | intron-variant | Polk | GRCm38.p3 | 13:96532130 | GCCATGTGCTCGCTC[A/G/T]CTCGCTCGCCTGCAT | 27015 |
rs6259175 | snp | C/T | 0.498615 | 0.0262793 | intron-variant | Polk | GRCm38.p3 | 13:96501676 | TATCTCCTTAACCTT[C/T]GAAAAGAACAACAAA | 27015 |
rs6259710 | snp | A/G | 0.401235 | 0.199068 | intron-variant | Polk | GRCm38.p3 | 13:96501774 | TTACTTTGCAACTAT[A/G]TTAATGATCCTGCAA | 27015 |
rs6260303 | snp | C/T | 0.5 | 0 | intron-variant | Polk | Mm_Celera | 13:96501918 | TGAGGCAACCTGAAC[C/T]CAGCAAGCCAAATAA | 27015 |
rs6260840 | snp | A/G | 0.42 | 0.183303 | intron-variant | Polk | GRCm38.p3 | 13:96502029 | GCTCTCTCTCATTTC[A/G]TTTGTGAAGATGCTT | 27015 |
rs6261282 | snp | A/G | 0.5 | 0 | intron-variant | Polk | Mm_Celera | 13:96502094 | ATTTTAGAGAACAGT[A/G]CATTTCAGTTAATTA | 27015 |
rs13472433 | snp | G/T | 0.260355 | 0.249785 | missense, downstream-variant-500B | Polk | Mm_Celera | 13:96483801 | ATTGAAAGCAGCAAG[G/T]ATGGACACTCTAGAG | 27015 |
rs13481958 | snp | A/G | 0.464965 | 0.127632 | intron-variant | Polk | Mm_Celera | 13:96516579 | TTATGACTTGACAGT[A/G]CTGCACTTCTGTTAT | 27015 |
rs29224240 | snp | C/T | 0.5 | 0 | intron-variant | Polk | Mm_Celera | 13:96517362 | TTGCTTGGATATACA[C/T]TGTCATTCCTCTTAA | 27015 |
rs29225894 | snp | C/T | 0.5 | 0 | intron-variant | Polk | Mm_Celera | 13:96519597 | GATTTCCAGGAGAGC[C/T]AGGGTTACACAGAGA | 27015 |
rs29226131 | snp | A/C/T | 0.375 | 0.216506 | intron-variant | Polk | GRCm38.p3 | 13:96522277 | TGCTGCTTTGCCTAA[A/C/T]GGATGGTGTCCTTGG | 27015 |
rs29226296 | snp | A/G | 0.5 | 0 | intron-variant | Polk | Mm_Celera | 13:96520894 | CACAGGTGCCATCTC[A/G]TGGAGTGTACTTAAG | 27015 |
rs29226444 | snp | C/G | 0.484429 | 0.0868505 | missense, utr-variant-3-prime | Polk | Mm_Celera | 13:96484115 | ATGTTTCAAAACTCT[C/G]GCTCAGCTTCTTTAA | 27015 |
rs29226989 | snp | A/C | 0.375 | 0.216506 | intron-variant | Polk | Mm_Celera | 13:96498095 | CACTTCTGTATTTGC[A/C]AGGTACTGGCATAGC | 27015 |
rs29227322 | snp | A/G | 0.32 | 0.24 | intron-variant | Polk | GRCm38.p3 | 13:96482621 | TACATTAATTAAACT[A/G]GGGTGTGTGTGCATG | 27015 |
rs29228306 | snp | A/C | 0.197531 | 0.244432 | intron-variant | Polk | Mm_Celera | 13:96499308 | TGTCTCGCCCTGGCG[A/C]CCTCTACTCCCGGAA | 27015 |
rs29228924 | snp | A/G | 0.375 | 0.216506 | intron-variant | Polk | Mm_Celera | 13:96523766 | TCCATAAAAAGAATC[A/G]GGGAATGTTACTTCT | 27015 |
rs29231217 | snp | C/T | 0.444444 | 0.157135 | intron-variant | Polk | Mm_Celera | 13:96533129 | TTTCTTGTTCTTTCA[C/T]GACTCCGCCTTGCAG | 27015 |
rs29232188 | snp | A/C | 0.444444 | 0.157135 | intron-variant | Polk | GRCm38.p3 | 13:96486104 | GCTCTTTTTCATAGA[A/C]TTCATGCAGTGGTCT | 27015 |
rs29234018 | snp | A/T | 0.465374 | 0.126941 | intron-variant | Polk | Mm_Celera | 13:96535804 | TGACAGAGGCTACAA[A/T]GACCTATTAACCAGA | 27015 |
rs29234041 | snp | C/T | 0.375 | 0.216506 | intron-variant | Polk | GRCm38.p3 | 13:96524832 | CAATTTTCTTGTATC[C/T]GTTGAGACTTACTGC | 27015 |
rs29234068 | snp | A/C | 0.5 | 0 | intron-variant | Polk | Mm_Celera | 13:96540638 | GTCTTTAATAAAATG[A/C]CAGGTCCAAATGCCC | 27015 |
rs29235375 | snp | A/C | 0.375 | 0.216506 | intron-variant | Polk | GRCm38.p3 | 13:96511168 | AGGAATGAAGAGATG[A/C]TTGCACAACGTGTTC | 27015 |
rs29236047 | snp | A/G | 0.415225 | 0.187619 | intron-variant | Polk | Mm_Celera | 13:96499552 | TCTCCAACACAGCAC[A/G]ACACTTGCCAGCTAG | 27015 |
rs29236220 | snp | C/T | 0.493827 | 0.0552116 | intron-variant | Polk | GRCm38.p3 | 13:96489418 | AACCTAACACACAGT[C/T]AAGTAAAAATATCTA | 27015 |
rs29236530 | snp | C/T | 0.5 | 0 | intron-variant | Polk | Mm_Celera | 13:96491289 | GCACATCCTCCCACC[C/T]CAACATTCTCTTTAA | 27015 |
rs29238011 | snp | A/G | 0.375 | 0.216506 | intron-variant | Polk | GRCm38.p3 | 13:96513180 | TTGGGAAGCAAACAC[A/G]ATGTTCTCCAGTAGG | 27015 |
rs29238341 | snp | A/G | 0.32 | 0.24 | utr-variant-3-prime | Polk | Mm_Celera | 13:96481159 | TCTGTAGACCAGGTT[A/G]TCCTCAAATTCAGAG | 27015 |
rs29238615 | snp | A/G | 0.375 | 0.216506 | intron-variant | Polk | GRCm38.p3 | 13:96536108 | TGTATGGTAGAATAA[A/G]ATCAGGAAACACAAA | 27015 |
rs29240232 | snp | A/C | 0.48 | 0.0979796 | intron-variant | Polk | Mm_Celera | 13:96538094 | GTATAAACATACATC[A/C]ACTCATGTAGATATG | 27015 |
rs29240270 | snp | A/G | 0.5 | 0 | intron-variant | Polk | Mm_Celera | 13:96517746 | TCTCAATTAGTGATC[A/G]AGGGGGAAAGGCCCC | 27015 |
rs29240810 | snp | C/T | 0.444444 | 0.157135 | intron-variant | Polk | GRCm38.p3 | 13:96521260 | CGATTTAAATAGATG[C/T]AACCTATTCTGGGGA | 27015 |
rs29242532 | snp | C/T | 0.375 | 0.216506 | intron-variant | Polk | Mm_Celera | 13:96532609 | GCCCCCCCCCCCCCT[C/T]TTAAAGATAGATTCT | 27015 |
rs29242689 | snp | A/G | 0.375 | 0.216506 | intron-variant | Polk | GRCm38.p3 | 13:96511267 | TATGTCAGGTGTTAA[A/G]TTCTTCCCACAAAAA | 27015 |
rs29243101 | snp | C/G | 0.5 | 0 | intron-variant | Polk | Mm_Celera | 13:96534733 | AGTGACTGAGTAACC[C/G]TCATGTCTGCCTGTT | 27015 |
rs29243324 | snp | A/G | 0.48 | 0.0979796 | intron-variant | Polk | Mm_Celera | 13:96511351 | AGAAAATGAAAGTTT[A/G]CTAAGATTAAGAGAT | 27015 |
rs29243887 | snp | A/G | 0.444444 | 0.157135 | upstream-variant-2KB, intron-variant | Col4a3bp, Polk | Mm_Celera | 13:96540817 | AGCTGGACAGCGGCC[A/G]TTTTTATTATGAAAT | 27015 |
rs29243968 | snp | C/T | 0.401235 | 0.199068 | intron-variant | Polk | Mm_Celera | 13:96510583 | GTAATAATTACAATA[C/T]GCCTAAAATATGAAT | 27015 |
rs29244008 | snp | A/T | 0.197531 | 0.244432 | intron-variant | Polk | Mm_Celera | 13:96491624 | CGAGTACTTCCTCCG[A/T]AAGTCAGCGTGCTTC | 27015 |
rs29244276 | snp | C/T | 0.459184 | 0.136902 | intron-variant | Polk | GRCm38.p3 | 13:96536129 | GAAACACAAATTATC[C/T]TTTGTTTAAAATTCC | 27015 |
rs29244647 | snp | C/T | 0.375 | 0.216506 | intron-variant | Polk | Mm_Celera | 13:96531483 | TGCACACAAGCTCCC[C/T]GTTAAATGCTTTCTT | 27015 |
rs29246631 | snp | A/G | 0.444444 | 0.157135 | utr-variant-3-prime | Polk | GRCm38.p3 | 13:96481810 | AATGGTACCATGGTG[A/G]CTAAGCATGGAGGAG | 27015 |
rs29247402 | snp | A/G | 0.5 | 0 | intron-variant | Polk | Mm_Celera | 13:96517895 | CTTCTTGACCTGCTT[A/G]AGTTCCAGTTCTGAC | 27015 |
rs29249392 | snp | A/G | 0.5 | 0 | upstream-variant-2KB, utr-variant-5-prime | Col4a3bp, Polk | Mm_Celera | 13:96542536 | GGAGGCTGCGCGGCG[A/G]ACGGAGCGCCAGCCT | 27015 |
rs29249969 | snp | A/G | 0.35503 | 0.226867 | intron-variant | Polk | Mm_Celera | 13:96501279 | TGATATTAAGAAAAT[A/G]ACTGTTTGGCAAACA | 27015 |
rs29250342 | snp | C/G | 0.475309 | 0.108333 | intron-variant | Polk | Mm_Celera | 13:96500571 | GCTGTGAAGACGTTA[C/G]ACACATGAAATGTGG | 27015 |
rs29495290 | snp | A/G | 0.444444 | 0.157135 | intron-variant | Polk | Mm_Celera | 13:96498943 | GAGAGGGAGAGAGAA[A/G]AATGTTTACAGATAT | 27015 |
rs29496925 | snp | A/G | 0.359862 | 0.224567 | intron-variant | Polk | Mm_Celera | 13:96525363 | AGGTTCAGGCAGGAG[A/G]AACACTTGAGTCCGA | 27015 |
rs29497576 | snp | C/G | 0.48 | 0.0979796 | intron-variant | Polk | Mm_Celera | 13:96537924 | CCTACAACATAAAAA[C/G]AGGACATCAACAGGG | 27015 |
rs29507713 | snp | C/T | 0.375 | 0.216506 | intron-variant | Polk | Mm_Celera | 13:96497780 | TTTCAAATGCTATCC[C/T]CACAAGCCCCCTATA | 27015 |
rs29509759 | snp | C/T | 0.207612 | 0.24638 | intron-variant | Polk | Mm_Celera | 13:96493146 | GTGCGGAACTAAGTA[C/T]AGGACTTTTATTTAG | 27015 |
rs29511399 | snp | C/T | 0.444444 | 0.157135 | intron-variant | Polk | Mm_Celera | 13:96500861 | GCAAGCTTGAGGACC[C/T]GAGTTCAGATCTACA | 27015 |
rs29513948 | snp | A/G | 0.359862 | 0.224567 | intron-variant | Polk | GRCm38.p3 | 13:96502523 | CCCCAATCATGAACA[A/G]CTGAGGGGAATGTAG | 27015 |
rs29514034 | snp | A/G | 0.432133 | 0.171253 | intron-variant | Polk | Mm_Celera | 13:96535693 | GATTAATCCAGCTAC[A/G]TTTAGTACTCAAGAC | 27015 |
rs29514859 | snp | C/T | 0.265928 | 0.249492 | intron-variant | Polk | GRCm38.p3 | 13:96511774 | GTCTACTGAGTTGGT[C/T]CAAGTTAGCAAAGGC | 27015 |
rs29517745 | snp | A/T | 0.391111 | 0.206368 | intron-variant | Polk | Mm_Celera | 13:96532916 | CCTCTCCTATAGAAC[A/T]CTTTCTGATATTGTA | 27015 |
rs29527533 | snp | C/T | 0.5 | 0 | intron-variant | Polk | Mm_Celera | 13:96532608 | CGCCCCCCCCCCCCC[C/T]TTTAAAGATAGATTC | 27015 |
rs29529845 | snp | A/G | 0.387812 | 0.208586 | intron-variant | Polk | Mm_Celera | 13:96535780 | TTTTAACGGGCCTGC[A/G]AAGAGCACTGACAGA | 27015 |
rs29530488 | snp | C/T | 0.32 | 0.24 | intron-variant | Polk | GRCm38.p3 | 13:96511686 | AATTTCTTTTCAAAA[C/T]CTTCAATTTCTACTA | 27015 |
rs29531355 | snp | A/G | 0.188366 | 0.242283 | intron-variant | Polk | GRCm38.p3 | 13:96511260 | TATGGAGTATGTCAG[A/G]TGTTAAGTTCTTCCC | 27015 |
rs29532316 | snp | C/T | 0.277778 | 0.248452 | intron-variant | Polk | Mm_Celera | 13:96486504 | CTGAGTCTTGAACAT[C/T]GCACCTCATGGACTT | 27015 |
rs29532957 | snp | C/T | 0.277778 | 0.248452 | intron-variant | Polk | GRCm38.p3 | 13:96517041 | GTAATTCTTGTGAGA[C/T]GGTACTACATAGAAG | 27015 |
rs29533875 | snp | C/T | 0.48 | 0.0979796 | utr-variant-3-prime | Polk | GRCm38.p3 | 13:96481800 | CGGAAGCATCAATGG[C/T]ACCATGGTGGCTAAG | 27015 |
rs29545101 | snp | A/T | 0.375 | 0.216506 | intron-variant | Polk | Mm_Celera | 13:96531553 | ACAGTAACTATTAAG[A/T]TACTCTTATTTATTG | 27015 |
rs29546865 | snp | C/T | 0.401235 | 0.199068 | utr-variant-3-prime | Polk | GRCm38.p3 | 13:96481846 | GGTGAGGTTGCTCCA[C/T]GTGGCTCAGAGTCCT | 27015 |
rs29552705 | snp | A/G | 0.5 | 0 | intron-variant | Polk | GRCm38.p3 | 13:96512985 | ACAATGAGAATGTCG[A/G]AAGGTATGGTCATCT | 27015 |
rs29553248 | snp | A/C | 0.5 | 0 | intron-variant | Polk | Mm_Celera | 13:96519646 | ACACCCCACTCCCCA[A/C]CCCCACCCCTCAACT | 27015 |
rs29553961 | snp | C/T | 0.5 | 0 | intron-variant | Polk | Mm_Celera | 13:96537141 | CTCACAGATAAAAGA[C/T]ACCACTAGGCCCCAG | 27015 |
rs29556466 | snp | A/G | 0.444444 | 0.157135 | intron-variant | Polk | GRCm38.p3 | 13:96524770 | AACTCAGGACCTCTG[A/G]AAGAGCAGTCAGTGC | 27015 |
rs29556541 | snp | C/G | 0.5 | 0 | intron-variant | Polk | Mm_Celera | 13:96517639 | TATCTGTACTGGCTG[C/G]TGTTGTGTCAACTTG | 27015 |
rs29562760 | snp | A/G | 0.265928 | 0.249492 | intron-variant | Polk | GRCm38.p3 | 13:96516385 | GCAACGAAACTGTCT[A/G]TCCTTTGAAGCCAGG | 27015 |
rs29566613 | snp | C/T | 0.5 | 0 | intron-variant | Polk | GRCm38.p3 | 13:96508800 | ACCGGTCTCCCCACA[C/T]AGGGCTGGGGTTACA | 27015 |
rs29566800 | snp | A/G | 0.475309 | 0.108333 | utr-variant-3-prime | Polk | GRCm38.p3 | 13:96481735 | ATGGACATCATGGCC[A/G]ATTCTAACTGCATCT | 27015 |
rs29569954 | snp | A/T | 0.5 | 0 | intron-variant | Polk | Mm_Celera | 13:96534729 | GGTTAGTGACTGAGT[A/T]ACCCTCATGTCTGCC | 27015 |
rs29570298 | snp | A/T | 0.5 | 0 | intron-variant | Polk | GRCm38.p3 | 13:96507084 | AAAATAACAATTTTG[A/T]ACTTGAAGTTTTAAT | 27015 |
rs29583438 | snp | A/G | 0.444444 | 0.157135 | intron-variant | Polk | GRCm38.p3 | 13:96517302 | CTGAGCTATTTCTAC[A/G]TTTGGCTATCATGAA | 27015 |
rs29586082 | snp | C/G | 0.444444 | 0.157135 | intron-variant | Polk | Mm_Celera | 13:96534601 | TGAGAGGTTAGGGAC[C/G]CAGCTTTATGTTATG | 27015 |
rs29588085 | snp | G/T | 0.5 | 0 | intron-variant | Polk | Mm_Celera | 13:96500830 | GAGATGCCTTAGCGG[G/T]TAAAGCGCTTGCCAC | 27015 |
rs29625387 | snp | C/T | 0.444444 | 0.157135 | intron-variant | Polk | GRCm38.p3 | 13:96507335 | AGAGTAATTGTAGGA[C/T]GTAGGTTATAGCTAT | 27015 |
rs29632796 | snp | A/G | 0.375 | 0.216506 | intron-variant | Polk | Mm_Celera | 13:96491640 | AAGTCAGCGTGCTTC[A/G]TGCGGGGGCTGGCAC | 27015 |
rs29633246 | snp | A/C | 0.42 | 0.183303 | intron-variant | Polk | GRCm38.p3 | 13:96515116 | CACTTAACCTGTCTC[A/C]TAACAAACGCATCTC | 27015 |
rs29636538 | snp | C/T | 0.5 | 0 | intron-variant | Polk | Mm_Celera | 13:96491242 | CCTCTGAAACAATGG[C/T]CAGTGATTTTACCTG | 27015 |
rs29663440 | snp | C/T | 0.444444 | 0.157135 | intron-variant | Polk | Mm_Celera | 13:96500210 | GCTTTGATTTGGTGT[C/T]TGTATTAAACTTGTT | 27015 |
rs29672522 | snp | C/T | 0.5 | 0 | intron-variant | Polk | GRCm38.p3 | 13:96512728 | AAACTCAATAAAAAA[C/T]AAAAGAAAAGTCAAC | 27015 |
rs29678843 | snp | A/T | 0.375 | 0.216506 | intron-variant | Polk | Mm_Celera | 13:96499542 | AGCGTTCGAATCTCC[A/T]ACACAGCACGACACT | 27015 |
rs29679224 | snp | C/T | 0.207612 | 0.24638 | intron-variant | Polk | Mm_Celera | 13:96499001 | AGTTGCAATCTTTAA[C/T]TATGGTGTATGAGTT | 27015 |
rs29685280 | snp | A/G | 0.375 | 0.216506 | intron-variant | Polk | Mm_Celera | 13:96517650 | GCTGCTGTTGTGTCA[A/G]CTTGACACAGGCTGG | 27015 |
rs29686441 | snp | C/T | 0.492188 | 0.0620098 | intron-variant | Polk | Mm_Celera | 13:96484430 | ACCAAAACCAGTCAG[C/T]CTCAAATTGTACAGA | 27015 |
rs29686958 | snp | A/G | 0.5 | 0 | intron-variant | Polk | Mm_Celera | 13:96512596 | AAACACATTTTGTAT[A/G]TCTGCTCAGTGAAAA | 27015 |
rs29715177 | snp | C/T | 0.5 | 0 | intron-variant | Polk | Mm_Celera | 13:96519627 | AAACCCTGTCTTGAA[C/T]AACACACCCCACTCC | 27015 |
rs29724870 | snp | C/T | 0.5 | 0 | intron-variant | Polk | Mm_Celera | 13:96518081 | AATGCCTATTCATAT[C/T]ATTTGACCATTTTTT | 27015 |