SNP - dbSNP |
dbSNP | Type | Alleles | Het | Se(het) | Fxn-class | Gene Name | Assembly | Chr-pos | Sequence | Entrez Gene |
rs3659839 | snp | A/G | 0.5 | 0 | intron-variant | Map3k5 | Mm_Celera | 10:20106241 | TCGAGGAAGCATGTC[A/G]GTCCAGAAGTGGGAC | 26408 |
rs3659873 | snp | A/G | 0.48 | 0.0979796 | intron-variant | Map3k5 | Mm_Celera | 10:20106262 | GAAGTGGGACGGGCT[A/G]TGACCCTTCCAGTGC | 26408 |
rs3661063 | snp | C/T | 0.459184 | 0.136902 | intron-variant | Map3k5 | Mm_Celera | 10:20106416 | AACAAAGCCAGAGCC[C/T]GTATGTCCCACAAGG | 26408 |
rs3661128 | snp | G/T | 0.456747 | 0.140554 | intron-variant | Map3k5 | Mm_Celera | 10:20106453 | CTGCCTTGGAGCCCA[G/T]TGCCTTTCAGACCCT | 26408 |
rs3667453 | snp | C/T | 0.489796 | 0.070696 | intron-variant | Map3k5 | Mm_Celera | 10:20090123 | GGGAAGTGTGAGCAG[C/T]GGGCTCCAAGTGTAG | 26408 |
rs3684270 | snp | A/G/T | 0.5 | 0 | intron-variant | Map3k5 | GRCm38.p3 | 10:20074545 | TTCATTAGCCAGGAC[A/G/T]AGGCCACAACCTCAG | 26408 |
rs3686462 | snp | C/T | 0.48 | 0.0979796 | intron-variant | Map3k5 | Mm_Celera | 10:20084302 | TTGATGTGTCTGGCC[C/T]CGGTCTCTTGTGTAA | 26408 |
rs3686479 | snp | A/C/G | 0.5 | 0 | intron-variant | Map3k5 | GRCm38.p3 | 10:20084304 | GATGTGTCTGGCCCC[A/C/G]GTCTCTTGTGTAAGG | 26408 |
rs3688363 | snp | A/C/T | 0.5 | 0 | intron-variant | Map3k5 | GRCm38.p3 | 10:20084635 | ACCTTTGTGTTACAT[A/C/T]GGAATCATTTAAACT | 26408 |
rs6240498 | snp | C/T | 0.304688 | 0.243945 | intron-variant | Map3k5 | Mm_Celera | 10:20113535 | GGTGGTTAGCATGTG[C/T]GCAGAGGACAAAGCT | 26408 |
rs6240610 | snp | A/C | 0.32 | 0.24 | intron-variant | Map3k5 | Mm_Celera | 10:20113608 | AAATACTAAAGAATT[A/C]GCCAAGAGGGGCAGA | 26408 |
rs6241075 | snp | C/G | 0.5 | 0 | intron-variant | Map3k5 | Mm_Celera | 10:20113652 | ATTTGATCTGGAATG[C/G]TGNCAGCAACCAGCC | 26408 |
rs6241077 | snp | C/T | 0.5 | 0 | intron-variant | Map3k5 | Mm_Celera | 10:20113655 | TGATCTGGAATGNTG[C/T]CAGCAACCAGCCCTG | 26408 |
rs6241496 | snp | C/T | 0.444444 | 0.157135 | intron-variant | Map3k5 | Mm_Celera | 10:20113711 | ATGTCCTGTCTTCAC[C/T]ATCTAGGACGTCAGC | 26408 |
rs6242122 | snp | A/T | 0.5 | 0 | intron-variant | Map3k5 | Mm_Celera | 10:20113868 | CAGTCATCATTCTCA[A/T]TGCTGGATGGAGGNT | 26408 |
rs6242161 | snp | A/G | 0.304688 | 0.243945 | intron-variant | Map3k5 | Mm_Celera | 10:20113882 | ANTGCTGGATGGAGG[A/G]TAGCCTATTTATTTA | 26408 |
rs6242599 | snp | A/G | 0.32 | 0.24 | intron-variant | Map3k5 | Mm_Celera | 10:20113911 | TAATGCCATTGGTTC[A/G]ATGGTGCTATTCATT | 26408 |
rs6242628 | snp | G/T | 0.304688 | 0.243945 | intron-variant | Map3k5 | Mm_Celera | 10:20113932 | GCTATTCATTTAACA[G/T]AAGAGGAGTCAGTGG | 26408 |
rs6279742 | snp | C/T | 0.375 | 0.216506 | intron-variant | Map3k5 | Mm_Celera | 10:20049663 | TCTTGTGTGACACCT[C/T]GCTCTTATTNCTATG | 26408 |
rs6279755 | snp | C/G | 0.5 | 0 | intron-variant | Map3k5 | Mm_Celera | 10:20049673 | CACCTNGCTCTTATT[C/G]CTATGAGAGTCTCAA | 26408 |
rs6279778 | snp | A/G | 0.5 | 0 | intron-variant | Map3k5 | Mm_Celera | 10:20049694 | AGAGTCTCAAAGAAG[A/G]NCCCATAGGAANTAC | 26408 |
rs6279780 | snp | C/T | 0.5 | 0 | intron-variant | Map3k5 | Mm_Celera | 10:20049695 | GAGTCTCAAAGAAGN[C/T]CCCATAGGAANTACC | 26408 |
rs6280165 | snp | C/T | 0.5 | 0 | intron-variant | Map3k5 | Mm_Celera | 10:20049706 | AAGNNCCCATAGGAA[C/T]TACCTGATNCCTTCT | 26408 |
rs6280189 | snp | C/T | 0.5 | 0 | intron-variant | Map3k5 | Mm_Celera | 10:20049715 | TAGGAANTACCTGAT[C/T]CCTTCTAAAGACATG | 26408 |
rs6280220 | snp | C/T | 0.32 | 0.24 | intron-variant | Map3k5 | Mm_Celera | 10:20049737 | AAAGACATGAGGATA[C/T]TAACTCCCATGAGCT | 26408 |
rs6280307 | snp | G/T | 0.5 | 0 | intron-variant | Map3k5 | Mm_Celera | 10:20049785 | CTCTGCTTATTAAAG[G/T]TTCTGCTTTTATTAA | 26408 |
rs6296027 | snp | C/T | 0.5 | 0 | intron-variant | Map3k5 | Mm_Celera | 10:20050321 | gcaggaagccctggg[C/T]tcaatcnccagcacc | 26408 |
rs6296045 | snp | C/T | 0.5 | 0 | intron-variant | Map3k5 | Mm_Celera | 10:20050328 | gccctgggntcaatc[C/T]ccagcaccatagaag | 26408 |
rs6363257 | snp | C/T | 0.207612 | 0.24638 | synonymous-codon | Map3k5 | Mm_Celera | 10:20100125 | CGAACAGACGATTGG[C/T]TTCTATACGAAGCAG | 26408 |
rs6376269 | snp | A/G | 0.455 | 0.143091 | intron-variant | Map3k5 | Mm_Celera | 10:20100210 | AAGGTAGGGTGCCCC[A/G]TGCCTCAGCCTTCTG | 26408 |
rs6376287 | snp | C/T | 0.465374 | 0.126941 | intron-variant | Map3k5 | Mm_Celera | 10:20100222 | CCCGTGCCTCAGCCT[C/T]CTGCGGTTCTTTCTG | 26408 |
rs6376750 | snp | A/G | 0.5 | 0 | intron-variant | Map3k5 | Mm_Celera | 10:20100296 | CATTGTGAGTGGGGA[A/G]TAAGGAAATGGGAGC | 26408 |
rs6376800 | snp | C/T | 0.290657 | 0.246672 | intron-variant | Map3k5 | Mm_Celera | 10:20100327 | GGGTAACAGAGCTGC[C/T]AGTTCTTGTCCCCTG | 26408 |
rs6376891 | snp | C/T | 0.290657 | 0.246672 | intron-variant | Map3k5 | Mm_Celera | 10:20100365 | TTATGTTCATGCCAT[C/T]GTCTTCCGTATGGTA | 26408 |
rs6386111 | snp | A/G | 0.5 | 0 | intron-variant | Map3k5 | Mm_Celera | 10:20123970 | GGAGAAGGTGAGGGT[A/G]TGTTTTGAAATTTTT | 26408 |
rs6400883 | snp | C/T | 0.5 | 0 | intron-variant | Map3k5 | Mm_Celera | 10:20124392 | CAGGAGAGAGGTAGC[C/T]GGCTGGTACCCAGCT | 26408 |
rs13480529 | snp | C/T | 0.488166 | 0.0760073 | intron-variant | Map3k5 | Mm_Celera | 10:20103968 | AGAGAAGATTATAAA[C/T]AACTGATAACATAAA | 26408 |
rs29310917 | snp | A/C | 0.375 | 0.216506 | intron-variant | Map3k5 | Mm_Celera | 10:19971454 | CCAGGCAGAGCCAGG[A/C]GTGGTGGCGCACGCC | 26408 |
rs29314978 | snp | C/T | 0.375 | 0.216506 | intron-variant | Map3k5 | Mm_Celera | 10:19992308 | TAAACGCCTCTCCTG[C/T]ATGTGTTTGCTGTCA | 26408 |
rs29315298 | snp | C/T | 0.444444 | 0.157135 | intron-variant | Map3k5 | Mm_Celera | 10:19953984 | ATCAAATTTCAAATT[C/T]CTAGTTTCTATCAAT | 26408 |
rs29315629 | snp | C/G | 0.5 | 0 | intron-variant | Map3k5 | Mm_Celera | 10:19970772 | CTACTATAACAATAC[C/G]TTATAGGAAAGTTGC | 26408 |
rs29315920 | snp | A/C | 0.493827 | 0.0552116 | intron-variant | Map3k5 | Mm_Celera | 10:20128325 | CAAGTTTACACCGAT[A/C]ACACCGTTCACCATT | 26408 |
rs29316169 | snp | A/G | 0.444444 | 0.157135 | intron-variant | Map3k5 | Mm_Celera | 10:20102284 | TAGTTCTGTCCACCT[A/G]CCTGAAAAGTTCATG | 26408 |
rs29316197 | snp | A/G | 0.444444 | 0.157135 | intron-variant | Map3k5 | Mm_Celera | 10:19972026 | CGGGGAGATTGTGGC[A/G]ATGGCTAGCCAGCCA | 26408 |
rs29316802 | snp | A/G | 0.5 | 0 | intron-variant | Map3k5 | Mm_Celera | 10:19978542 | AAGCGGAACAGGAAA[A/G]ACAAGAAACAAATAA | 26408 |
rs29317144 | snp | G/T | 0.5 | 0 | intron-variant | Map3k5 | Mm_Celera | 10:20118629 | GATTTACATAGGATG[G/T]TGTTGTTGTTGTGTT | 26408 |
rs29317215 | snp | A/G | 0.5 | 0 | intron-variant | Map3k5 | Mm_Celera | 10:20105359 | CTGCGCCACCTCCTG[A/G]ACTCCACACAATGTA | 26408 |
rs29318542 | snp | A/G | 0.444444 | 0.157135 | intron-variant | Map3k5 | Mm_Celera | 10:19978422 | GCCAGTACTTTGGTG[A/G]GAAGTGGGTGGCCTT | 26408 |
rs29318550 | snp | A/C | 0.5 | 0 | intron-variant | Map3k5 | Mm_Celera | 10:20119616 | AACATTAGCAGGTGG[A/C]ACCCTAGCTTATGAG | 26408 |
rs29318681 | snp | C/T | 0.5 | 0 | intron-variant | Map3k5 | Mm_Celera | 10:20107022 | ATGCAGAATCTGACA[C/T]GTGACCCCTGCAAAA | 26408 |
rs29318836 | snp | A/G | 0.5 | 0 | intron-variant | Map3k5 | Mm_Celera | 10:20110674 | AGGAGGGGATGAGGG[A/G]AGAGAACATTAGGAG | 26408 |
rs29320251 | snp | G/T | 0.5 | 0 | intron-variant | Map3k5 | Mm_Celera | 10:19945997 | GGGGGATGGCTTAGC[G/T]GGTAAAGCACTTGCT | 26408 |
rs29320697 | snp | A/G | 0.444444 | 0.157135 | intron-variant | Map3k5 | Mm_Celera | 10:20112841 | AGGGATTTAAACTCT[A/G]CCCTAGCTTTATAGT | 26408 |
rs29321075 | snp | G/T | 0.456747 | 0.140554 | intron-variant | Map3k5 | Mm_Celera | 10:20112144 | GGCGGGAGTGTGAGC[G/T]CTTTAATGTCCATTG | 26408 |
rs29321318 | snp | A/G | 0.5 | 0 | intron-variant | Map3k5 | Mm_Celera | 10:20110652 | AGAAAGAAAAGGGGC[A/G]AGGTGCAGGAGGGGA | 26408 |
rs29323113 | snp | A/G | 0.197531 | 0.244432 | downstream-variant-500B | Map3k5 | Mm_Celera | 10:20143024 | ATTTTGAAGAAAGCC[A/G]GTCCCCTCTGCGTTA | 26408 |
rs29323118 | snp | A/G | 0.495868 | 0.0452663 | intron-variant | Map3k5 | Mm_Celera | 10:20127086 | CTCATCTGAGCAAAT[A/G]CAAGTGATTAACATT | 26408 |
rs29323841 | snp | A/G | 0.5 | 0 | intron-variant | Map3k5 | Mm_Celera | 10:20127090 | TCTGAGCAAATGCAA[A/G]TGATTAACATTGGAA | 26408 |
rs29323890 | snp | A/G | 0.49827 | 0.0293608 | intron-variant | Map3k5 | Mm_Celera | 10:20110579 | TGGAGAAACGGCTGC[A/G]TAGACAGCTTGTGTC | 26408 |
rs29323994 | snp | G/T | 0.444444 | 0.157135 | intron-variant | Map3k5 | Mm_Celera | 10:20107032 | TGACACGTGACCCCT[G/T]CAAAAGGGCTGGTCG | 26408 |
rs29324666 | snp | A/C | 0.444444 | 0.157135 | intron-variant | Map3k5 | Mm_Celera | 10:20117991 | GCCAGTAAGTGTAAT[A/C]TCTCTCTCTCTCTCT | 26408 |
rs29325346 | snp | C/T | 0.444444 | 0.157135 | intron-variant | Map3k5 | Mm_Celera | 10:20128075 | CAAGAGCTCTCATCT[C/T]AAATCACAAGCACGA | 26408 |
rs29325352 | snp | G/T | 0.359862 | 0.224567 | intron-variant | Map3k5 | Mm_Celera | 10:19987856 | TCTGTAGCTTCTCAA[G/T]TACACGCTCTGTTCC | 26408 |
rs29326256 | snp | A/G | 0.387812 | 0.208586 | intron-variant | Map3k5 | Mm_Celera | 10:20126270 | CACTCCTGGCCTGTC[A/G]AGTGCTCTTGTTGGG | 26408 |
rs29327336 | snp | C/T | 0.375 | 0.216506 | intron-variant | Map3k5 | Mm_Celera | 10:19997272 | ACCTACCCACTCCCC[C/T]CTCCTGGCCCTGGCG | 26408 |
rs29327699 | snp | A/G | 0.5 | 0 | intron-variant | Map3k5 | Mm_Celera | 10:20112472 | CAGTTCTGATCCCTC[A/G]GCCTATTTTATTTTT | 26408 |
rs29327742 | snp | C/G | 0.48 | 0.0979796 | intron-variant | Map3k5 | Mm_Celera | 10:20089724 | GTGACTGCCATTTTC[C/G]GTAGGAGTCAACTTC | 26408 |
rs29328046 | snp | A/G | 0.5 | 0 | intron-variant | Map3k5 | Mm_Celera | 10:20105311 | GGTGGGAAGGAGGAG[A/G]GAGAGACCCTTGTGC | 26408 |
rs29329216 | snp | A/G | 0.492188 | 0.0620098 | intron-variant | Map3k5 | Mm_Celera | 10:20107184 | TTATTTTTCATCATA[A/G]CTCGCAGAATCCCGA | 26408 |
rs29330025 | snp | A/T | 0.432133 | 0.171253 | intron-variant | Map3k5 | Mm_Celera | 10:20133330 | GTTCTTATTGAAAGT[A/T]TAACTTCACCTGCTT | 26408 |
rs29330029 | snp | C/T | 0.444444 | 0.157135 | intron-variant | Map3k5 | Mm_Celera | 10:20002942 | TAGACCAGGCTGGCC[C/T]CAAACTCAGAAATCC | 26408 |
rs29330830 | snp | G/T | 0.49827 | 0.0293608 | intron-variant | Map3k5 | Mm_Celera | 10:19947856 | ATTTTTTAAACATTC[G/T]TTTGAAGAGACAACT | 26408 |
rs29331360 | snp | A/G | 0.5 | 0 | intron-variant | Map3k5 | Mm_Celera | 10:20098721 | CGAACTCAGAAATCT[A/G]CCTGTCTCTGCCTCC | 26408 |
rs29331909 | snp | A/G | 0.444444 | 0.157135 | intron-variant | Map3k5 | Mm_Celera | 10:20093773 | CCTTGTGTTGACAGT[A/G]TCTGTTTTTTTTTTT | 26408 |
rs29334330 | snp | A/G | 0.497041 | 0.0383476 | intron-variant | Map3k5 | Mm_Celera | 10:20118923 | GTGTGCTTACAGCCT[A/G]GAGTTGTTCAGGAGC | 26408 |
rs29334493 | snp | A/G | 0.359862 | 0.224567 | intron-variant | Map3k5 | Mm_Celera | 10:20140093 | CTAAGGGAAGACAAT[A/G]TACCTAACCAAGTTC | 26408 |
rs29334801 | snp | A/G | 0.49827 | 0.0293608 | intron-variant | Map3k5 | Mm_Celera | 10:20099865 | ACTGAGTATCCTATT[A/G]CTGGCTGCCTTCAGA | 26408 |
rs29334854 | snp | C/T | 0.5 | 0 | intron-variant | Map3k5 | Mm_Celera | 10:20112791 | GTCAGCTGTGGCTCC[C/T]GTGTCCCCTCCCTCT | 26408 |
rs29335587 | snp | G/T | 0.391111 | 0.206368 | intron-variant | Map3k5 | Mm_Celera | 10:20112767 | TCAGGTTTCAGGTTA[G/T]CTCTGCGAGTCAGCT | 26408 |
rs29336298 | snp | A/G | 0.415225 | 0.187619 | intron-variant | Map3k5 | Mm_Celera | 10:20082380 | ACACCAGCTCTCGTC[A/G]TTGTAGGTTTTTTGA | 26408 |
rs29336321 | snp | A/G | 0.444444 | 0.157135 | intron-variant | Map3k5 | Mm_Celera | 10:20136562 | CCAAGAAGAGAAAAG[A/G]GAAATCAATCACAGT | 26408 |
rs29336908 | snp | A/G | 0.304688 | 0.243945 | intron-variant | Map3k5 | Mm_Celera | 10:20111121 | CAGCACGTAGAGAAT[A/G]GTTACTGTATCAGCC | 26408 |
rs29336942 | snp | A/G | 0.444444 | 0.157135 | intron-variant | Map3k5 | Mm_Celera | 10:20027684 | TCAACTTCACCAATA[A/G]ACATAGACTGTATAG | 26408 |
rs29337649 | snp | A/C | 0.5 | 0 | intron-variant | Map3k5 | Mm_Celera | 10:19966018 | GATCAGCTGGCCCTG[A/C]CAATGGCAGTGATGT | 26408 |
rs29338566 | snp | C/T | 0.475309 | 0.108333 | intron-variant | Map3k5 | Mm_Celera | 10:19955197 | AGCTTTCATCCTGTT[C/T]TGCCTCCACCTCATA | 26408 |
rs29338567 | snp | C/T | 0.475309 | 0.108333 | intron-variant | Map3k5 | Mm_Celera | 10:20118339 | TAAAGAGCTGGCTTG[C/T]TTGTGCCCAAAGGCA | 26408 |
rs29339371 | snp | A/C | 0.5 | 0 | intron-variant | Map3k5 | Mm_Celera | 10:20077231 | CACCACCACCACCCC[A/C]CCCCCACCACCCCCA | 26408 |
rs29340204 | snp | A/G | 0.444444 | 0.157135 | intron-variant | Map3k5 | Mm_Celera | 10:20107135 | AATTGTGTATATTGC[A/G]TATACAGAAACACAT | 26408 |
rs29341263 | snp | A/G | 0.375 | 0.216506 | intron-variant | Map3k5 | Mm_Celera | 10:20122719 | GGGTGTGTGTATCTC[A/G]TATGTGTGTGTTGTG | 26408 |
rs29341887 | snp | C/T | 0.444444 | 0.157135 | intron-variant | Map3k5 | Mm_Celera | 10:20077721 | GGTTCTGCTTTGTAA[C/T]TTCAAAGACTGTCAC | 26408 |
rs29342307 | snp | A/T | 0.444444 | 0.157135 | intron-variant | Map3k5 | Mm_Celera | 10:20102244 | CTTTCTGGGTTTGGG[A/T]CATCTCACTCAACAT | 26408 |
rs29342522 | snp | G/T | 0.5 | 0 | intron-variant | Map3k5 | Mm_Celera | 10:20112772 | TTTCAGGTTAGCTCT[G/T]CGAGTCAGCTGTGGC | 26408 |
rs29342907 | snp | C/T | 0.444444 | 0.157135 | intron-variant | Map3k5 | Mm_Celera | 10:20087885 | ATCCTAATCCCTGCC[C/T]ATGTCTCTTCTGCCC | 26408 |
rs29343131 | snp | A/G | 0.5 | 0 | intron-variant | Map3k5 | Mm_Celera | 10:20046865 | GTAGGCCCAGCACTT[A/G]GGGGGTGGCGCTAAG | 26408 |
rs29343421 | snp | A/G | 0.493827 | 0.0552116 | intron-variant | Map3k5 | Mm_Celera | 10:20082175 | TACGATCTGTGGACT[A/G]TTTGTTTCTTCATAA | 26408 |
rs29343976 | snp | G/T | 0.375 | 0.216506 | intron-variant | Map3k5 | Mm_Celera | 10:20102715 | GCTATTTCTTAGTTA[G/T]TTTTATTTCTTCTTT | 26408 |
rs29344113 | snp | A/G | 0.444444 | 0.157135 | intron-variant | Map3k5 | Mm_Celera | 10:20010851 | CTGCAGCCCATGGCC[A/G]AGTTGACGTCATGGG | 26408 |
rs29344313 | snp | C/T | 0.48 | 0.0979796 | intron-variant | Map3k5 | Mm_Celera | 10:20119166 | AAGCAATATGGTTCA[C/T]TCTTTTTCTTGCTGG | 26408 |
rs29344486 | snp | A/G | 0.48 | 0.0979796 | intron-variant | Map3k5 | Mm_Celera | 10:20121509 | GACTGCGAATGGAAA[A/G]GCAGGGGTGGAAGGC | 26408 |
rs29345916 | snp | C/T | 0.473373 | 0.11227 | intron-variant | Map3k5 | Mm_Celera | 10:20118906 | GCTACAGATTTTTAC[C/T]TGTGTGCTTACAGCC | 26408 |