SNP - dbSNP |
dbSNP | Type | Alleles | Het | Se(het) | Fxn-class | Gene Name | Assembly | Chr-pos | Sequence | Entrez Gene |
rs6170619 | snp | C/T | 0.456747 | 0.140554 | intron-variant | Kcmf1 | Mm_Celera | 6:72862287 | TATAGGTTCACAGTC[C/T]ATATGGCTCAAAATG | 74287 |
rs6305187 | snp | A/G | 0.5 | 0 | intron-variant | Kcmf1 | Mm_Celera | 6:72888287 | taaatctttttaaaa[A/G]GTACAATAAATCATG | 74287 |
rs6305257 | snp | A/T | 0.415225 | 0.187619 | intron-variant | Kcmf1 | Mm_Celera | 6:72888330 | CCCAACAGATTGAAG[A/T]CGTCATTAAGGGTGG | 74287 |
rs6306270 | snp | A/G | 0.5 | 0 | intron-variant | Kcmf1 | Mm_Celera | 6:72888514 | gggcaggaggattag[A/G]agttcaagtcatctg | 74287 |
rs13470006 | snp | A/T | 0.49827 | 0.0293608 | utr-variant-3-prime | Kcmf1 | Mm_Celera | 6:72841728 | TAGAGCTGCCTTGGT[A/T]GTTAGGGTGTGGAGG | 74287 |
rs29860228 | snp | C/G | 0.375 | 0.216506 | intron-variant | Kcmf1 | Mm_Celera | 6:72875460 | TTTCCTGAGTGTATC[C/G]TAATCCATTCAAGTT | 74287 |
rs29869102 | snp | C/T | 0.375 | 0.216506 | intron-variant | Kcmf1 | GRCm38.p3 | 6:72890890 | ACAACGCATAAAAAG[C/T]GGTTTTCTAAATGAA | 74287 |
rs29869958 | snp | A/C | 0.444444 | 0.157135 | intron-variant | Kcmf1 | GRCm38.p3 | 6:72895670 | AGAAGTACAACTAGG[A/C]TGGCAGTGAATTCCT | 74287 |
rs29876802 | snp | C/T | 0.42 | 0.183303 | intron-variant | Kcmf1 | Mm_Celera | 6:72871140 | CAATCAAGCTCAAAG[C/T]ATCATTGACAAAAGA | 74287 |
rs29885308 | snp | C/T | 0.375 | 0.216506 | intron-variant | Kcmf1 | GRCm38.p3 | 6:72893903 | CCTGTCTCAGAAAAC[C/T]ACAGTTGAGGACCAG | 74287 |
rs29918040 | snp | C/T | 0.32 | 0.24 | intron-variant | Kcmf1 | Mm_Celera | 6:72893423 | CCAGTTATGTACACA[C/T]AGCAAACAAACAAAC | 74287 |
rs29920881 | snp | A/C | 0.444444 | 0.157135 | intron-variant | Kcmf1 | Mm_Celera | 6:72867399 | CTTGAACCCCCCCAC[A/C]CACACACACACATGT | 74287 |
rs29923597 | snp | A/C | 0.444444 | 0.157135 | intron-variant | Kcmf1 | Mm_Celera | 6:72881896 | TCATGCCCCCCCCCA[A/C]CCCCCAGTCCTTTGA | 74287 |
rs29963588 | snp | C/T | 0.32 | 0.24 | intron-variant | Kcmf1 | GRCm38.p3 | 6:72898507 | AACACCTATACAGGA[C/T]TTGGAAAATCTTAGG | 74287 |
rs29975320 | snp | A/G | 0.444444 | 0.157135 | intron-variant | Kcmf1 | GRCm38.p3 | 6:72895656 | CTGTCTTTTGACAGA[A/G]AAGTACAACTAGGAT | 74287 |
rs30013116 | snp | G/T | 0.444444 | 0.157135 | intron-variant | Kcmf1 | Mm_Celera | 6:72859631 | ACTTTTTTTTTTTTT[G/T]GGGGGGGGGGGTTGG | 74287 |
rs30063907 | snp | C/T | 0.32 | 0.24 | intron-variant | Kcmf1 | Mm_Celera | 6:72843533 | AAGGACCTTTCTCTT[C/T]CCCGCTGTACTCTTC | 74287 |
rs30066180 | snp | A/C | 0.375 | 0.216506 | intron-variant | Kcmf1 | GRCm38.p3 | 6:72896472 | CCAGCTGCAGGACCC[A/C]CAGCTCTACAGCTCC | 74287 |
rs30068137 | snp | C/T | 0.375 | 0.216506 | intron-variant | Kcmf1 | GRCm38.p3 | 6:72894766 | GAACAAAGAAAGACA[C/T]GAACTATCTTTTTAA | 74287 |
rs30119561 | snp | A/T | 0.375 | 0.216506 | utr-variant-3-prime | Kcmf1 | GRCm38.p3 | 6:72841978 | GAGGTGGTGAGATTT[A/T]AAAAAACAAGACAAC | 74287 |
rs30165316 | snp | C/T | 0.375 | 0.216506 | downstream-variant-500B | Kcmf1 | Mm_Celera | 6:72840818 | GGTTAACTTCATTTT[C/T]TAAATTAAACTGCCC | 74287 |
rs30169017 | snp | G/T | 0.444444 | 0.157135 | intron-variant | Kcmf1 | GRCm38.p3 | 6:72860447 | ATTATAGAAAAAAGT[G/T]AAAGTCCTAAAATAA | 74287 |
rs30173360 | snp | G/T | 0.375 | 0.216506 | intron-variant | Kcmf1 | Mm_Celera | 6:72863761 | CTGGGTAGAGTTCCA[G/T]TTTGGGATGATGAGA | 74287 |
rs30177103 | snp | A/G | 0.456747 | 0.140554 | intron-variant | Kcmf1 | Mm_Celera | 6:72846404 | ACATAGACTGGCCTC[A/G]AACTCTGGCTTCATC | 74287 |
rs30217196 | snp | C/T | 0.375 | 0.216506 | intron-variant | Kcmf1 | GRCm38.p3 | 6:72849259 | TCTTACCCCGAATGC[C/T]TTTGAGAAACGCAGT | 74287 |
rs30226062 | snp | A/G | 0.375 | 0.216506 | intron-variant | Kcmf1 | Mm_Celera | 6:72867984 | CCTGACCCCAGCCCT[A/G]GGATTATCTTTTACA | 74287 |
rs30268045 | snp | A/G | 0.375 | 0.216506 | intron-variant | Kcmf1 | GRCm38.p3 | 6:72894583 | CAGTGCAGAGTACAC[A/G]AGACCCTGCCTCAGA | 74287 |
rs30270647 | snp | C/T | 0.495 | 0.0497494 | intron-variant | Kcmf1 | GRCm38.p3 | 6:72896395 | GTCAGTCAGTCCCTG[C/T]ACTTGCTCAGGACCC | 74287 |
rs30327596 | snp | A/G | 0.32 | 0.24 | intron-variant | Kcmf1 | Mm_Celera | 6:72858281 | AGTTTTCAAGTTTAG[A/G]CTTCATATTTTATTC | 74287 |
rs30329586 | snp | A/G | 0.444444 | 0.157135 | intron-variant | Kcmf1 | Mm_Celera | 6:72853837 | GTTGTGAGCCACCAT[A/G]TGGTTGCTGGGAATT | 74287 |
rs30365329 | snp | A/T | 0.444444 | 0.157135 | intron-variant | Kcmf1 | GRCm38.p3 | 6:72860448 | TTATAGAAAAAAGTG[A/T]AAGTCCTAAAATAAA | 74287 |
rs30371281 | snp | A/G | 0.32 | 0.24 | intron-variant | Kcmf1 | Mm_Celera | 6:72895920 | CAGACATGGTGCTAC[A/G]TGCCTGTTAGCTGGG | 74287 |
rs30374437 | snp | C/T | 0.290657 | 0.246672 | intron-variant | Kcmf1 | GRCm38.p3 | 6:72870455 | TGTGGTGGTGTCCGC[C/T]TCACAAGATCCCAGC | 74287 |
rs30412719 | snp | A/G | 0.375 | 0.216506 | intron-variant | Kcmf1 | GRCm38.p3 | 6:72895833 | TACTGCAAGGCCAGG[A/G]ATGCAGCTTGGCTGT | 74287 |
rs30453856 | snp | A/G | 0.48 | 0.0979796 | intron-variant | Kcmf1 | Mm_Celera | 6:72873783 | AGTATTGAAGCTCAT[A/G]GCTAGGAAGATGTTC | 74287 |
rs30459161 | snp | A/G | 0.444444 | 0.157135 | intron-variant | Kcmf1 | Mm_Celera | 6:72867734 | TCTTTTTAAAGAAAG[A/G]TTTATTTATTTTATT | 74287 |
rs30465530 | snp | A/T | 0.32 | 0.24 | intron-variant | Kcmf1 | Mm_Celera | 6:72896081 | AGCCAGAGACAGTTT[A/T]AAAAAAAAACCTAGA | 74287 |
rs30509431 | snp | A/G/T | 0.444444 | 0.157135 | intron-variant | Kcmf1 | GRCm38.p3 | 6:72867793 | ACACAAGAAGGCATC[A/G/T]GATCCCATTACAGAT | 74287 |
rs30514414 | snp | A/G | 0.375 | 0.216506 | intron-variant | Kcmf1 | GRCm38.p3 | 6:72893253 | CAAACTGAACTTTAT[A/G]TGAAGAATCTAGAAA | 74287 |
rs30611485 | snp | C/T | 0.487535 | 0.077957 | intron-variant | Kcmf1 | Mm_Celera | 6:72891124 | CAGTGAAAATTACAA[C/T]GATCCATCTACAGTT | 74287 |
rs30654976 | snp | A/T | 0.375 | 0.216506 | intron-variant | Kcmf1 | GRCm38.p3 | 6:72898462 | TTCCCTCGGCGATAA[A/T]CTGCCTCCTCAAACT | 74287 |
rs30705614 | snp | A/G | 0.484429 | 0.0868505 | intron-variant | Kcmf1 | Mm_Celera | 6:72868262 | CACTACACCACAAAC[A/G]ACACAAGAGCACAAT | 74287 |
rs30710164 | snp | A/C | 0.375 | 0.216506 | intron-variant | Kcmf1 | Mm_Celera | 6:72858444 | ACACACAGTCCAGGA[A/C]TGCTTAGTACACAAG | 74287 |
rs30711487 | snp | C/T | 0.375 | 0.216506 | intron-variant | Kcmf1 | Mm_Celera | 6:72884558 | TCTTCCTGCCTCAAC[C/T]TCCCTCAGCTGCTGG | 74287 |
rs30714385 | snp | C/T | 0.375 | 0.216506 | upstream-variant-2KB | Kcmf1 | Mm_Celera | 6:72901442 | TTCCCTGAACTTGAG[C/T]TGTGAAAGTCAGGCT | 74287 |
rs30732941 | snp | A/G | 0.5 | 0 | upstream-variant-2KB | Kcmf1 | Mm_Celera | 6:72900614 | CTGGAGTTAAGACGT[A/G]TTCAGCCCTGGGATT | 74287 |
rs30823726 | snp | G/T | 0.444444 | 0.157135 | intron-variant | Kcmf1 | Mm_Celera | 6:72894249 | GGCCTGCCTGAGACA[G/T]TGTAAGTTCACAGAG | 74287 |
rs30830532 | snp | G/T | 0.444444 | 0.157135 | upstream-variant-2KB | Kcmf1 | Mm_Celera | 6:72901124 | CTCAGATAGCCCGAG[G/T]CAGTCCTTGAATTGC | 74287 |
rs30851840 | snp | C/T | 0.444444 | 0.157135 | intron-variant | Kcmf1 | Mm_Celera | 6:72845427 | CCACATGGTGGCTCA[C/T]CTGTAATGGGATCTG | 74287 |
rs30877227 | snp | A/G | 0.375 | 0.216506 | upstream-variant-2KB | Kcmf1 | Mm_Celera | 6:72900959 | CAAAGGAAGGACCCT[A/G]TTTGTTACAATATTT | 74287 |
rs30905099 | snp | C/T | 0.444444 | 0.157135 | intron-variant | Kcmf1 | GRCm38.p3 | 6:72852769 | GAACTGTGAGCTCTT[C/T]CCTAGAAACGCAGGC | 74287 |
rs30916868 | snp | A/T | 0.375 | 0.216506 | upstream-variant-2KB | Kcmf1 | Mm_Celera | 6:72901278 | GGAATTCCGCACACT[A/T]CAGACCGGCCTGAGG | 74287 |
rs30936207 | snp | C/G | 0.475309 | 0.108333 | intron-variant | Kcmf1 | Mm_Celera | 6:72868361 | GGCACACTGCCTCAT[C/G]TCAGCCTGGAGGAAT | 74287 |
rs30962660 | snp | A/G | 0.444444 | 0.157135 | intron-variant | Kcmf1 | Mm_Celera | 6:72875444 | TGTCACATGAAAAAT[A/G]TTTCCTGAGTGTATC | 74287 |
rs30965253 | snp | A/G | 0.359862 | 0.224567 | intron-variant | Kcmf1 | Mm_Celera | 6:72859478 | TCCCCTTCGCTGTCT[A/G]TTGTCTACCTCTCAA | 74287 |
rs30996218 | snp | A/T | 0.33241 | 0.236027 | intron-variant | Kcmf1 | GRCm38.p3 | 6:72895050 | GTCACACAACCCTGG[A/T]GAACACAGTACAAAA | 74287 |
rs31013641 | snp | A/G | 0.375 | 0.216506 | upstream-variant-2KB | Kcmf1 | Mm_Celera | 6:72901285 | CGCACACTACAGACC[A/G]GCCTGAGGAAGACTA | 74287 |
rs36244966 | snp | A/C | 0.142012 | 0.225474 | intron-variant | Kcmf1 | Mm_Celera | 6:72848188 | AACACAAACACCAAC[A/C]TTTACTTTACCCGAA | 74287 |
rs36245494 | snp | A/C | 0.124444 | 0.216185 | downstream-variant-500B | Kcmf1 | Mm_Celera | 6:72840905 | TCCCAGAATTTGTGC[A/C]GAAGAGGGAAAGTAC | 74287 |
rs36246543 | snp | C/T | 0.124444 | 0.216185 | intron-variant | Kcmf1 | GRCm38.p3 | 6:72868193 | CAGCAAAGGGGCTAA[C/T]CTGAGTGAGTGGAAG | 74287 |
rs36249356 | snp | A/C | 0.124444 | 0.216185 | intron-variant | Kcmf1 | Mm_Celera | 6:72864000 | AGGACCTGAGTTCAG[A/C]TCCTATCAGCAAGTG | 74287 |
rs36257259 | snp | C/G | 0.444444 | 0.157135 | intron-variant | Kcmf1 | Mm_Celera | 6:72859403 | CTTAAAGAGACAAGG[C/G]CAGGTTAAAGAGATG | 74287 |
rs36275195 | snp | A/G | 0.124444 | 0.216185 | intron-variant | Kcmf1 | Mm_Celera | 6:72843299 | GAGTTCAGTGGATTC[A/G]GTGAGGCTGAAAACA | 74287 |
rs36283420 | snp | C/T | 0.124444 | 0.216185 | intron-variant | Kcmf1 | Mm_Celera | 6:72882185 | TCAAGCTAGAAATCC[C/T]AACTTTCAGCTCCTT | 74287 |
rs36302927 | snp | C/T | 0.375 | 0.216506 | intron-variant | Kcmf1 | Mm_Celera | 6:72852505 | ACTGTGATTTGGTAA[C/T]GAGTCTCTAATGCCC | 74287 |
rs36314518 | snp | A/C | 0.444444 | 0.157135 | intron-variant | Kcmf1 | GRCm38.p3 | 6:72843943 | GACAGTCACTGGCTG[A/C]CCATGGAACATGGAC | 74287 |
rs36360904 | snp | A/T | 0.142012 | 0.225474 | utr-variant-3-prime | Kcmf1 | Mm_Celera | 6:72841588 | GTCTCATAGAAATTG[A/T]TCAGAAGCTGCGCAT | 74287 |
rs36367656 | snp | C/T | 0.375 | 0.216506 | intron-variant | Kcmf1 | Mm_Celera | 6:72848866 | TTTCTGCTCATTTCA[C/T]CAGAGGAGTTAGCAG | 74287 |
rs36368055 | snp | C/G | 0.21875 | 0.248039 | intron-variant | Kcmf1 | Mm_Celera | 6:72871024 | CCCCAACCAGGGAAA[C/G]CAATGAAAGAGGTGT | 74287 |
rs36397113 | snp | A/G | 0.18 | 0.24 | intron-variant | Kcmf1 | Mm_Celera | 6:72874364 | CTGAAATTTGTTTTC[A/G]TCTATAAAAAGATGG | 74287 |
rs36413932 | snp | A/T | 0.345679 | 0.230967 | intron-variant | Kcmf1 | Mm_Celera | 6:72874300 | TTACTGAAGAGAGAA[A/T]GCCATTCAAATACTT | 74287 |
rs36418429 | snp | C/T | 0.124444 | 0.216185 | intron-variant | Kcmf1 | Mm_Celera | 6:72889260 | TCAGTAGGATCTGAA[C/T]ATGTAGGCTTCTTAT | 74287 |
rs36433977 | snp | A/G | 0.124444 | 0.216185 | intron-variant | Kcmf1 | Mm_Celera | 6:72883645 | ACAAACAAACCTTCA[A/G]CTTTCTAATCTATGA | 74287 |
rs36442768 | snp | C/T | 0.48 | 0.0979796 | intron-variant | Kcmf1 | Mm_Celera | 6:72880668 | ATGGAGAGAAGCCAT[C/T]CCCAAAAGTTGTCCT | 74287 |
rs36470507 | snp | C/T | 0.32 | 0.24 | intron-variant | Kcmf1 | GRCm38.p3 | 6:72891615 | TTCCTAGGTAAAATC[C/T]AAGCCTCTGGCTATC | 74287 |
rs36473761 | snp | C/T | 0.124444 | 0.216185 | intron-variant | Kcmf1 | Mm_Celera | 6:72891497 | CAAGCTTCATGCCCA[C/T]TGCCTCTCCTATGCC | 74287 |
rs36475685 | snp | A/C | 0.124444 | 0.216185 | intron-variant | Kcmf1 | Mm_Celera | 6:72883582 | ATTTGATGCAAAATT[A/C]TAGCTTAGTTTTTTT | 74287 |
rs36576972 | snp | C/T | 0.48 | 0.0979796 | intron-variant | Kcmf1 | Mm_Celera | 6:72884968 | CTTATCCACTTCCCT[C/T]CTACTTACACACAGA | 74287 |
rs36606148 | snp | A/C | 0.231111 | 0.249285 | intron-variant | Kcmf1 | Mm_Celera | 6:72890940 | AGGGTACAAGTCATG[A/C]CACTGGTGCTCAACA | 74287 |
rs36607319 | snp | A/G | 0.48 | 0.0979796 | intron-variant | Kcmf1 | Mm_Celera | 6:72882395 | ACCCAGTCTCAGGGG[A/G]CCAGAGCTCCACACA | 74287 |
rs36614299 | snp | G/T | 0.408163 | 0.193609 | intron-variant | Kcmf1 | Mm_Celera | 6:72869025 | TACAAGCAGGCCACA[G/T]AAAACACACTGTTCA | 74287 |
rs36615860 | snp | A/G | 0.132653 | 0.220748 | intron-variant | Kcmf1 | Mm_Celera | 6:72885831 | AGGAAAAAAAACCAC[A/G]AATTTTTCCAAGTGT | 74287 |
rs36616802 | snp | A/G | 0.124444 | 0.216185 | intron-variant | Kcmf1 | Mm_Celera | 6:72880999 | CCAGCCCCACATCTT[A/G]TCAATTTAAAACAAT | 74287 |
rs36620880 | snp | A/C | 0.391111 | 0.206368 | intron-variant | Kcmf1 | Mm_Celera | 6:72885869 | TGCTACTTTGCAAAA[A/C]TTGTTTGGTACACCA | 74287 |
rs36625611 | snp | A/G | 0.124444 | 0.216185 | intron-variant | Kcmf1 | Mm_Celera | 6:72845754 | AGAGAGTGTGAGACA[A/G]CACATTATGCTCTGG | 74287 |
rs36632850 | snp | A/G | 0.35503 | 0.226867 | intron-variant | Kcmf1 | Mm_Celera | 6:72859420 | AGGTTAAAGAGATGA[A/G]GCCACTGGGAATGTG | 74287 |
rs36637786 | snp | C/T | 0.391111 | 0.206368 | intron-variant | Kcmf1 | Mm_Celera | 6:72887148 | AGTCCTGAGGGTGTA[C/T]TTTTAGGCGACACAC | 74287 |
rs36640374 | snp | A/G | 0.124444 | 0.216185 | intron-variant | Kcmf1 | Mm_Celera | 6:72883224 | TTATATGACTGAGGA[A/G]CTTTGAAAAGAATAC | 74287 |
rs36645718 | snp | A/G | 0.124444 | 0.216185 | intron-variant | Kcmf1 | Mm_Celera | 6:72889194 | TCTATCTATAACTAT[A/G]GCCACACAAACATCA | 74287 |
rs36648751 | snp | C/G | 0.231111 | 0.249285 | intron-variant | Kcmf1 | Mm_Celera | 6:72881349 | ACTGTGGCAGCCTGA[C/G]CTCAGTGTATCTATG | 74287 |
rs36653031 | snp | A/C | 0.124444 | 0.216185 | intron-variant | Kcmf1 | Mm_Celera | 6:72888695 | TCTAGCCCCTGAAAT[A/C]AGGTCCTAAAACAAA | 74287 |
rs36681460 | snp | A/G | 0.32 | 0.24 | intron-variant | Kcmf1 | Mm_Celera | 6:72882213 | CTTCCATAATCCTAC[A/G]CCTAATCAATTACCA | 74287 |
rs36685412 | snp | A/C | 0.124444 | 0.216185 | intron-variant | Kcmf1 | Mm_Celera | 6:72887708 | ACTGTGCTCCATCCT[A/C]AAGGCCTGAATTTTA | 74287 |
rs36690074 | snp | A/G | 0.124444 | 0.216185 | intron-variant | Kcmf1 | Mm_Celera | 6:72885031 | TTCAATGTATCTCCC[A/G]TTTTTGTAGTTCTGT | 74287 |
rs36722011 | snp | A/G | 0.124444 | 0.216185 | intron-variant | Kcmf1 | Mm_Celera | 6:72886086 | ACGCATTAGGGCTGA[A/G]TAATACCAAAATAAA | 74287 |
rs36722078 | snp | C/T | 0.124444 | 0.216185 | intron-variant | Kcmf1 | Mm_Celera | 6:72887464 | TAGCTGCATGTCATT[C/T]CAGTGATCTGATGGG | 74287 |
rs36723173 | snp | C/T | 0.48 | 0.0979796 | intron-variant | Kcmf1 | Mm_Celera | 6:72880643 | GCCTGCTGACTTAAG[C/T]TTCCAGCGAATGGAG | 74287 |
rs36732852 | snp | A/G | 0.444444 | 0.157135 | intron-variant | Kcmf1 | GRCm38.p3 | 6:72866059 | AAGGAATTACAAAGG[A/G]AATAAAAACGGTCTT | 74287 |
rs36759099 | snp | G/T | 0.124444 | 0.216185 | intron-variant | Kcmf1 | Mm_Celera | 6:72869602 | AGAATCTCTCCACAC[G/T]GAAAGGTGGGCCGAG | 74287 |
rs36769346 | snp | C/T | 0.375 | 0.216506 | utr-variant-3-prime | Kcmf1 | GRCm38.p3 | 6:72841257 | TTGACCTCTGGTGTA[C/T]CAGGAGCCCAGCGAG | 74287 |