SNP - dbSNP |
dbSNP | Type | Alleles | Het | Se(het) | Fxn-class | Gene Name | Assembly | Chr-pos | Sequence | Entrez Gene |
rs4227917 | snp | A/C | 0.226843 | 0.248925 | intron-variant | Klhl18 | GRCm38.p3 | 9:110469220 | TGGGTGGAAGTGATG[A/C]TTTTACGCTCTCTGT | 270201 |
rs4227918 | snp | C/T | 0.21875 | 0.248039 | intron-variant | Klhl18 | GRCm38.p3 | 9:110469186 | CTGACTCTCCTGCGC[C/T]GGGGCAGATGGCATG | 270201 |
rs4227919 | snp | C/T | 0.21875 | 0.248039 | intron-variant | Klhl18 | GRCm38.p3 | 9:110469131 | AAACCACCTTAGAGT[C/T]ACTTCTGAGCCTGGA | 270201 |
rs4227920 | snp | C/T | 0.375 | 0.216506 | intron-variant | Klhl18 | GRCm38.p3 | 9:110469028 | GCTGACTTCTAGATG[C/T]AAATTAATTAATTAA | 270201 |
rs4227922 | snp | G/T | 0.244898 | 0.249948 | intron-variant | Klhl18 | GRCm38.p3 | 9:110468975 | ATTTTTTGGTAGGGG[G/T]TGGGGGTGGA | 270201 |
rs6165799 | snp | A/G | 0.5 | 0 | intron-variant | Klhl18 | GRCm38.p3 | 9:110436869 | AACAAGCAGAAGGTC[A/G]CTAGCTACCTTTCCT | 270201 |
rs6167511 | snp | C/T | 0.5 | 0 | intron-variant | Klhl18 | GRCm38.p3 | 9:110437207 | TAATAAGCCCTACTC[C/T]AGGGCTACTCTCTGG | 270201 |
rs6171953 | snp | C/T | 0.5 | 0 | intron-variant | Klhl18 | GRCm38.p3 | 9:110431402 | AGACTGGCTTTAGAA[C/T]GTGCTGATGAGTTGG | 270201 |
rs6173075 | snp | A/G | 0.5 | 0 | intron-variant | Klhl18 | GRCm38.p3 | 9:110431579 | ACGGGATTCCTCACC[A/G]CCAGATTTTCTAGAA | 270201 |
rs6173623 | snp | C/G | 0.5 | 0 | intron-variant | Klhl18 | GRCm38.p3 | 9:110431680 | TTCTCTGACCCCACA[C/G]TCCTTCACANCAGGC | 270201 |
rs6173643 | snp | C/G | 0.5 | 0 | intron-variant | Klhl18 | GRCm38.p3 | 9:110431690 | CCACANTCCTTCACA[C/G]CAGGCCTCACTGCTG | 270201 |
rs6390748 | snp | A/G | 0.5 | 0 | intron-variant | Klhl18 | GRCm38.p3 | 9:110468689 | GCTTTGCTCCTCAAG[A/G]AGTGTATTCTTCCCC | 270201 |
rs6391190 | snp | A/G | 0.290657 | 0.246672 | intron-variant | Klhl18 | GRCm38.p3 | 9:110468720 | TGTGACTACTTTAGA[A/G]ACCAGGGACTCTAAA | 270201 |
rs6391340 | snp | C/T | 0.5 | 0 | intron-variant | Klhl18 | GRCm38.p3 | 9:110468789 | GAATAAACTAGTCAA[C/T]GAGTGTTCGGAAGTT | 270201 |
rs6392377 | snp | A/G | 0.5 | 0 | intron-variant | Klhl18 | GRCm38.p3 | 9:110468943 | cctcaactacagatc[A/G]agactctgtatcaaa | 270201 |
rs13474314 | snp | A/G | | | utr-variant-3-prime | Klhl18 | GRCm38.p3 | 9:110428326 | AACACCTGCTGCAGC[A/G]CTGGCCCAGCTCCCC | 270201 |
rs30181085 | snp | C/T | 0.375 | 0.216506 | intron-variant | Klhl18 | Mm_Celera | 9:110463827 | GGAGGCAGAGGCAGG[C/T]GAATTTCTGAGTTCG | 270201 |
rs30191915 | snp | C/G/T | 0.444444 | 0.157135 | intron-variant | Klhl18 | GRCm38.p3 | 9:110450180 | CAGAGGAGAGGGAGC[C/G/T]GGGGAGCACAGAGGA | 270201 |
rs33284565 | snp | G/T | 0.231111 | 0.249285 | intron-variant | Klhl18 | Mm_Celera | 9:110468063 | GTCAACGAGTTGAAA[G/T]TAGGAAGGTGAGGGC | 270201 |
rs33284566 | snp | A/G | 0.32 | 0.24 | intron-variant | Klhl18 | GRCm38.p3 | 9:110468067 | ACGAGTTGAAAGTAG[A/G]AAGGTGAGGGCCACG | 270201 |
rs33284568 | snp | C/G | 0.244898 | 0.249948 | intron-variant | Klhl18 | Mm_Celera | 9:110468123 | CATGCTCTAGGAAAA[C/G]TGTGGTTTCATTTTG | 270201 |
rs33284570 | snp | C/T | 0.124444 | 0.216185 | intron-variant | Klhl18 | Mm_Celera | 9:110468189 | AACAGAGGAGCCTCA[C/T]GCACACAACAACAAA | 270201 |
rs33284572 | snp | C/T | 0.124444 | 0.216185 | intron-variant | Klhl18 | Mm_Celera | 9:110468252 | ACAGGCTTCTGACGG[C/T]CATTCACCCCGCCAA | 270201 |
rs33285534 | snp | C/T | 0.244898 | 0.249948 | intron-variant | Klhl18 | GRCm38.p3 | 9:110468327 | AACAGGGTTGCAGAC[C/T]GCTGAGCCTCCAGCT | 270201 |
rs33285536 | snp | C/T | 0.32 | 0.24 | intron-variant | Klhl18 | Mm_Celera | 9:110468369 | CTGTCAGGCAGCATT[C/T]CGTGCACAGTCTCTC | 270201 |
rs33285538 | snp | C/T | 0.124444 | 0.216185 | intron-variant | Klhl18 | Mm_Celera | 9:110468398 | TCACAGCCGCCCAGT[C/T]GGCATCCAAACGTTA | 270201 |
rs33285540 | snp | A/T | 0.124444 | 0.216185 | intron-variant | Klhl18 | Mm_Celera | 9:110468512 | TGAAGCAGGCTCACC[A/T]TGTAGCCAAGACTAG | 270201 |
rs33286564 | snp | A/G | 0.124444 | 0.216185 | intron-variant | Klhl18 | Mm_Celera | 9:110469498 | TTGCAGACAGGGAAC[A/G]ACTTCAGACTCACAT | 270201 |
rs33286566 | snp | C/T | 0.231111 | 0.249285 | intron-variant | Klhl18 | GRCm38.p3 | 9:110469520 | GACTCACATGTGCAG[C/T]GCTCCAAGCCAGCTT | 270201 |
rs33286568 | snp | C/T | 0.497778 | 0.0332592 | intron-variant | Klhl18 | GRCm38.p3 | 9:110470008 | TCAGGAGAAAGGATG[C/T]GACCTGGATCTGGGA | 270201 |
rs33286570 | snp | C/T | 0.124444 | 0.216185 | intron-variant | Klhl18 | Mm_Celera | 9:110470056 | GAACCTGATGCTCAC[C/T]TTGGAACTCTGTCAG | 270201 |
rs33286572 | snp | A/G | 0.124444 | 0.216185 | intron-variant | Klhl18 | Mm_Celera | 9:110470697 | CTAGGTTCACTCGTC[A/G]GCCGTGGACTTTGAG | 270201 |
rs33287344 | snp | C/T | 0.124444 | 0.216185 | intron-variant | Klhl18 | Mm_Celera | 9:110470709 | GTCAGCCGTGGACTT[C/T]GAGGTGTGAGAAGAC | 270201 |
rs33287345 | snp | C/G | 0.132653 | 0.220748 | intron-variant | Klhl18 | Mm_Celera | 9:110471507 | ACTATTGAAGTAGAG[C/G]AGTAGACTGCAAACT | 270201 |
rs33287347 | snp | G/T | 0.336735 | 0.234472 | intron-variant | Klhl18 | GRCm38.p3 | 9:110472001 | CAATTATCATCAAGG[G/T]CGGAAGCATGGCAGC | 270201 |
rs33287348 | snp | C/T | 0.497778 | 0.0332592 | intron-variant | Klhl18 | GRCm38.p3 | 9:110472095 | AAAAGACTGGCATCT[C/T]AGGCAGCTAAAGGGA | 270201 |
rs33287349 | snp | C/T | 0.260355 | 0.249785 | intron-variant | Klhl18 | GRCm38.p3 | 9:110473142 | TTGAATCCTTAGCAG[C/T]CAGGTGGGTAATGAT | 270201 |
rs33287351 | snp | G/T | 0.124444 | 0.216185 | intron-variant | Klhl18 | Mm_Celera | 9:110473575 | ACCTTCTCAACAGGT[G/T]GAGCTCCCTGACTCC | 270201 |
rs33287353 | snp | A/G | 0.231111 | 0.249285 | intron-variant | Klhl18 | GRCm38.p3 | 9:110473777 | AATCCCAGGGTGAGC[A/G]ATACGAACAAGGCCA | 270201 |
rs33288444 | snp | G/T | 0.124444 | 0.216185 | intron-variant | Klhl18 | Mm_Celera | 9:110473888 | TAAACCGCTAACCAA[G/T]TCTTTAGAATCTGCT | 270201 |
rs33288446 | snp | A/C | 0.32 | 0.24 | intron-variant | Klhl18 | Mm_Celera | 9:110474184 | ACTGAGACTTGCACT[A/C]TCAGTCGGAAAGACG | 270201 |
rs33288448 | snp | A/G | 0.32 | 0.24 | intron-variant | Klhl18 | Mm_Celera | 9:110474228 | ATTGTTCCTTTGCCT[A/G]AATGGAAAAGATTTT | 270201 |
rs33288450 | snp | C/T | 0.165289 | 0.235211 | intron-variant | Klhl18 | Mm_Celera | 9:110474368 | TGACCACACTCCATC[C/T]ATCTACCACACAGCT | 270201 |
rs33288452 | snp | A/C | 0.244898 | 0.249948 | intron-variant | Klhl18 | GRCm38.p3 | 9:110474526 | GAGAGAGAGAGAGAG[A/C]GCGTGCAGGTGCCAC | 270201 |
rs33289183 | snp | C/T | 0.336735 | 0.234472 | intron-variant | Klhl18 | Mm_Celera | 9:110457103 | CTTTCTGAACACTAA[C/T]CCTGAGCGAGCAGCT | 270201 |
rs33289364 | snp | A/C | 0.48 | 0.0979796 | intron-variant | Klhl18 | GRCm38.p3 | 9:110474693 | GCCTAAATCCTAGCG[A/C]AAAACTTCTTTCTTA | 270201 |
rs33289366 | snp | C/G | 0.32 | 0.24 | upstream-variant-2KB, intron-variant | Kif9, Klhl18 | GRCm38.p3 | 9:110475957 | TTTTCCAGCATGGAA[C/G]AGAGTAGCCCACATC | 270201 |
rs33289368 | snp | C/G | 0.132653 | 0.220748 | utr-variant-5-prime, upstream-variant-2KB, missense | Kif9, Klhl18 | Mm_Celera | 9:110476998 | TGTACACAGCCAGTC[C/G]GCTAGCTGTCCTGGT | 270201 |
rs33289370 | snp | A/T | 0.124444 | 0.216185 | utr-variant-5-prime, upstream-variant-2KB, missense | Kif9, Klhl18 | Mm_Celera | 9:110477018 | GCTGTCCTGGTTGCG[A/T]ACAGAGCTCCCTCAA | 270201 |
rs33289372 | snp | A/G | 0.124444 | 0.216185 | intron-variant, upstream-variant-2KB | Kif9, Klhl18 | Mm_Celera | 9:110477384 | CGGTGTCATCACTTA[A/G]AGCCTTCTAACTACC | 270201 |
rs33289955 | snp | A/G | 0.297521 | 0.245442 | intron-variant | Klhl18 | GRCm38.p3 | 9:110457202 | GCTGATTTCTCTTAC[A/G]CATTCTCTGCCTTAT | 270201 |
rs33289957 | snp | C/T | 0.165289 | 0.235211 | intron-variant | Klhl18 | Mm_Celera | 9:110457359 | GTTGACACTGGATGT[C/T]TTCATAGATTGTGCT | 270201 |
rs33289959 | snp | C/T | 0.260355 | 0.249785 | intron-variant | Klhl18 | GRCm38.p3 | 9:110457393 | CCTGCTTTTGTGAGC[C/T]TGAATCTGAAACTTG | 270201 |
rs33289961 | snp | A/G | 0.244898 | 0.249948 | intron-variant | Klhl18 | Mm_Celera | 9:110458095 | GGCAGGGCTTCACTC[A/G]GGCAGAGGTGCTGTG | 270201 |
rs33289963 | snp | C/T | 0.197531 | 0.244432 | intron-variant | Klhl18 | GRCm38.p3 | 9:110458228 | TAAGAGGATCAAGCT[C/T]TCAGAATCATTATGT | 270201 |
rs33290004 | snp | A/G | 0.124444 | 0.216185 | intron-variant, upstream-variant-2KB | Kif9, Klhl18 | Mm_Celera | 9:110477445 | AATGGGACCAAGGCA[A/G]TCTGTCACACACATT | 270201 |
rs33290006 | snp | A/T | 0.231111 | 0.249285 | intron-variant, upstream-variant-2KB, utr-variant-5-prime | Kif9, Klhl18 | GRCm38.p3 | 9:110478022 | GATGGTGGACCCACC[A/T]ATGGAGATTCAGTCA | 270201 |
rs33290008 | snp | A/T | 0.124444 | 0.216185 | intron-variant, upstream-variant-2KB, utr-variant-5-prime | Kif9, Klhl18 | Mm_Celera | 9:110478156 | TAAACGGCACGACCC[A/T]TATCCTCAAGCAGCT | 270201 |
rs33290010 | snp | A/G | 0.124444 | 0.216185 | intron-variant, upstream-variant-2KB | Kif9, Klhl18 | Mm_Celera | 9:110478284 | TCCGCGGCACTGTTG[A/G]CTAGTGGGCTCCCGA | 270201 |
rs33290012 | snp | C/G | 0.124444 | 0.216185 | intron-variant, upstream-variant-2KB | Kif9, Klhl18 | Mm_Celera | 9:110478337 | GGCTTGTTGCCAACT[C/G]CGCATGACTCCAGGG | 270201 |
rs33290784 | snp | C/T | 0.124444 | 0.216185 | intron-variant, upstream-variant-2KB | Kif9, Klhl18 | Mm_Celera | 9:110478586 | ATAAGACTCTTGGGG[C/T]TTGTGTTCAGAAAGG | 270201 |
rs33290786 | snp | A/G | 0.124444 | 0.216185 | intron-variant, upstream-variant-2KB | Kif9, Klhl18 | Mm_Celera | 9:110478632 | GAAACTGAGTATTGA[A/G]TAAAAGAAGCACAGC | 270201 |
rs33290895 | snp | A/G | 0.32 | 0.24 | intron-variant | Klhl18 | GRCm38.p3 | 9:110458905 | GGCCCCTGTGCTAAA[A/G]GTCTGGTCCTGAGCT | 270201 |
rs33290897 | snp | C/T | 0.46281 | 0.131194 | intron-variant | Klhl18 | GRCm38.p3 | 9:110459212 | TTGAACCTGTGGCCT[C/T]GTACACACTGCTCAG | 270201 |
rs33290899 | snp | C/T | 0.497041 | 0.0383476 | intron-variant | Klhl18 | Mm_Celera | 9:110460184 | ACAGAGGAACCTTGA[C/T]CAGCTTGTTAGAAGC | 270201 |
rs33290901 | snp | C/T | 0.165289 | 0.235211 | intron-variant | Klhl18 | GRCm38.p3 | 9:110461202 | TCACATACCATTCTT[C/T]CCCGTGAAACAGGCA | 270201 |
rs33290903 | snp | A/G | 0.426035 | 0.177515 | intron-variant | Klhl18 | GRCm38.p3 | 9:110461816 | GATCCAGTTCAGGAC[A/G]GCTGATGTGGGCCCT | 270201 |
rs33291775 | snp | C/T | 0.18 | 0.24 | intron-variant | Klhl18 | Mm_Celera | 9:110461861 | AAACAAGCTCCCAAG[C/T]AGTGCTGATGCTCTG | 270201 |
rs33291777 | snp | A/T | 0.132653 | 0.220748 | intron-variant | Klhl18 | Mm_Celera | 9:110462026 | CAGAAGAAAGAAAAC[A/T]CGGGTCATTTCCAAA | 270201 |
rs33291779 | snp | C/T | 0.132653 | 0.220748 | intron-variant | Klhl18 | GRCm38.p3 | 9:110462125 | CAGTGTTCTAGGACC[C/T]CAGTGGCTGCACACA | 270201 |
rs33291781 | snp | C/T | 0.277778 | 0.248452 | intron-variant | Klhl18 | Mm_Celera | 9:110462709 | GCGGTACCTTGAAGA[C/T]GCTGGTTGCTGCACA | 270201 |
rs33291783 | snp | A/G | 0.497778 | 0.0332592 | intron-variant | Klhl18 | GRCm38.p3 | 9:110464030 | TGGGGTTGACGTGAG[A/G]ACCTGAGGCTTGCTG | 270201 |
rs33292655 | snp | A/G | 0.18 | 0.24 | intron-variant | Klhl18 | Mm_Celera | 9:110464951 | TCAGCAAAGTGTGCC[A/G]TGTTACCACATCTTA | 270201 |
rs33292657 | snp | C/T | 0.489796 | 0.070696 | intron-variant | Klhl18 | GRCm38.p3 | 9:110466303 | ATCCCTGCTAAATTA[C/T]AGACAATACAACAAA | 270201 |
rs33292658 | snp | A/G | 0.142012 | 0.225474 | intron-variant | Klhl18 | Mm_Celera | 9:110467925 | TTCATTTTGTCCTCA[A/G]CTGGAAGAAATGATG | 270201 |
rs45972673 | snp | A/C | 0.459184 | 0.136902 | intron-variant | Klhl18 | Mm_Celera | 9:110455087 | GGCTACGCCTTTTCG[A/C]TGACTGAGGTGCTCA | 270201 |
rs46345798 | snp | A/G | 0.124444 | 0.216185 | intron-variant | Klhl18 | Mm_Celera | 9:110446987 | AATTTTGTTCCCAGC[A/G]TTGTTAGAAACTCCC | 270201 |
rs46367507 | snp | A/C | 0.124444 | 0.216185 | intron-variant | Klhl18 | GRCm38.p3 | 9:110438062 | CCTGCCCATCACCAT[A/C]CACGGCTCACACCCT | 270201 |
rs46543003 | snp | A/G | 0.124444 | 0.216185 | intron-variant | Klhl18 | Mm_Celera | 9:110438362 | CCACTGCTTACTCCC[A/G]GAACCTGCTGATCCC | 270201 |
rs46655162 | snp | A/G | 0.152778 | 0.230321 | intron-variant | Klhl18 | GRCm38.p3 | 9:110448379 | CCAACCGCACACACC[A/G]GGAGCTGAATGGAGC | 270201 |
rs46664052 | snp | A/T | 0.231111 | 0.249285 | intron-variant | Klhl18 | GRCm38.p3 | 9:110456066 | AATAACCCTGCCAGA[A/T]TCTTCCAAGAATGGC | 270201 |
rs46720281 | snp | C/T | 0.124444 | 0.216185 | intron-variant | Klhl18 | Mm_Celera | 9:110452621 | CTCTTCTATCCTGGC[C/T]GACCTCACTGTATCC | 270201 |
rs46969345 | snp | A/G | 0.124444 | 0.216185 | intron-variant | Klhl18 | Mm_Celera | 9:110452054 | TTATTGCCATTATAA[A/G]TTACTGGCATTATAG | 270201 |
rs47096491 | snp | A/G | 0.244898 | 0.249948 | intron-variant | Klhl18 | Mm_Celera | 9:110449652 | AATCTCTGGTGATTA[A/G]ATGGCCTTTAGCTTA | 270201 |
rs47223157 | snp | A/T | 0.124444 | 0.216185 | intron-variant | Klhl18 | Mm_Celera | 9:110440295 | TGTTCTCTTGCCACA[A/T]TGTCTGACTTAGCTT | 270201 |
rs47281269 | snp | A/G | 0.32 | 0.24 | intron-variant | Klhl18 | GRCm38.p3 | 9:110455800 | CTTTATCGGAACTCC[A/G]AGTTTATTAAAAGGC | 270201 |
rs47320965 | snp | A/G | 0.32 | 0.24 | intron-variant | Klhl18 | GRCm38.p3 | 9:110455781 | AACACACACTGCTTC[A/G]GCACTTTATCGGAAC | 270201 |
rs47396328 | snp | C/T | 0.32 | 0.24 | intron-variant | Klhl18 | GRCm38.p3 | 9:110453262 | AGTGAGGCACTTGAG[C/T]ACCTGGGTCATTTAC | 270201 |
rs47634605 | snp | C/G | 0.132653 | 0.220748 | intron-variant | Klhl18 | GRCm38.p3 | 9:110438805 | TGTGTGAGTTAACTG[C/G]CTGCTCCAAATCCTT | 270201 |
rs47697300 | snp | C/T | 0.231111 | 0.249285 | intron-variant | Klhl18 | GRCm38.p3 | 9:110449876 | AAAAAGGGACTCATG[C/T]GGGTTAAGGATCTAA | 270201 |
rs47761475 | snp | A/G | 0.124444 | 0.216185 | intron-variant | Klhl18 | Mm_Celera | 9:110456037 | CAAGCAGCTCACATG[A/G]TGTCACAGGAGAAAA | 270201 |
rs47788297 | snp | A/G | 0.497778 | 0.0332592 | intron-variant | Klhl18 | Mm_Celera | 9:110441021 | AGTGGATCAAAGGCA[A/G]TAGTGATGACCCCAG | 270201 |
rs47803192 | snp | C/T | 0.124444 | 0.216185 | intron-variant | Klhl18 | Mm_Celera | 9:110439161 | AGGCAGGTCCTCAGG[C/T]GATCCAGCTTTCCTC | 270201 |
rs48044886 | snp | A/C | 0.336735 | 0.234472 | intron-variant | Klhl18 | Mm_Celera | 9:110438627 | GCAGAGGGCAGGGAG[A/C]CTCCGGGAAGCCCCA | 270201 |
rs48100306 | snp | A/C | 0.244898 | 0.249948 | intron-variant | Klhl18 | GRCm38.p3 | 9:110452563 | CATAGAGAATGAAAT[A/C]GAAATCCCAGCCGTG | 270201 |
rs48267004 | snp | C/T | | | intron-variant | Klhl18 | Mm_Celera | 9:110466187 | AAATAATTATATTTT[C/T]AATAATGATCAAATG | 270201 |
rs48399329 | snp | C/T | 0.32 | 0.24 | intron-variant | Klhl18 | GRCm38.p3 | 9:110451333 | TAGCAAGGAGAGTCC[C/T]ACAAATGCCTGCAGT | 270201 |
rs48496815 | snp | C/T | 0.152778 | 0.230321 | intron-variant | Klhl18 | Mm_Celera | 9:110441397 | CCAATAGTGCCACCA[C/T]ACAAAATGGTTGTTA | 270201 |
rs48555909 | snp | A/G | 0.391111 | 0.206368 | intron-variant | Klhl18 | GRCm38.p3 | 9:110449078 | GAAAGTGTAAAGAAT[A/G]GCAACTGGCAGCACC | 270201 |
rs48619389 | snp | A/G | 0.124444 | 0.216185 | intron-variant | Klhl18 | Mm_Celera | 9:110440271 | GGCAGCTGTGTCTGA[A/G]GTATCCTGTGTTCTC | 270201 |