SNP - dbSNP |
dbSNP | Type | Alleles | Het | Se(het) | Fxn-class | Gene Name | Assembly | Chr-pos | Sequence | Entrez Gene |
rs3669288 | snp | A/G | 0.5 | 0 | intron-variant | Klhl32 | Mm_Celera | 4:24794382 | CCTTATCAGCAAGGG[A/G]GAACGCTAGGATAGC | 212390 |
rs3674837 | snp | G/T | 0.5 | 0 | intron-variant | Klhl32 | Mm_Celera | 4:24707024 | TCTGACATCTTGGAA[G/T]CTTTCTCGATGGTTC | 212390 |
rs3678775 | snp | A/G | 0.444444 | 0.157135 | intron-variant | Klhl32 | GRCm38.p3 | 4:24687798 | AGCATGGTAGCTTCC[A/G]GTGTCCAATGGCTTC | 212390 |
rs3678869 | snp | C/T | 0.5 | 0 | intron-variant | Klhl32 | GRCm38.p3 | 4:24798828 | GCCAGGTCCCATGGC[C/T]AGCAGCAATAGCTGG | 212390 |
rs3680190 | snp | A/C | 0.429688 | 0.173817 | intron-variant | Klhl32 | GRCm38.p3 | 4:24799036 | CTGGCTGGAAGAAAA[A/C]GTTCTCTGGAGAAAA | 212390 |
rs3702624 | snp | C/T | 0.5 | 0 | intron-variant | Klhl32 | Mm_Celera | 4:24682782 | AATAGAATGTGATGG[C/T]TATTGTTGCTGGCCA | 212390 |
rs3702824 | snp | A/G | 0.48 | 0.0979796 | intron-variant | Klhl32 | GRCm38.p3 | 4:24712101 | TGCATTTTCCCAAAG[A/G]ATTTATGCTTGGGCA | 212390 |
rs3703856 | snp | G/T | 0.5 | 0 | intron-variant | Klhl32 | Mm_Celera | 4:24682998 | AGAGCCTACTCTTTG[G/T]GATTCTGTTATTTAC | 212390 |
rs3704373 | snp | A/G | 0.5 | 0 | intron-variant | Klhl32 | Mm_Celera | 4:24683029 | TGAAGACCAGTTGAC[A/G]CACCCAGCCTTGTGG | 212390 |
rs3704436 | snp | A/G | 0.5 | 0 | intron-variant | Klhl32 | Mm_Celera | 4:24683059 | GACTGAACAACTATT[A/G]GAATCTTGGACTTTC | 212390 |
rs3704940 | snp | C/G | 0.5 | 0 | intron-variant | Klhl32 | Mm_Celera | 4:24683118 | ACTACAAACTGTAAG[C/G]CATTCTAATAAATCT | 212390 |
rs3718877 | snp | A/C | 0.489796 | 0.070696 | intron-variant | Klhl32 | GRCm38.p3 | 4:24712364 | ATCTAGTCTGGCATT[A/C]TAGCAGACTGGATGT | 212390 |
rs4136505 | snp | C/T | 0.475309 | 0.108333 | intron-variant | Klhl32 | GRCm38.p3 | 4:24712425 | AAGTCCCCTGAAAGC[C/T]GAGAGCACACTGTTA | 212390 |
rs4180146 | snp | G/T | 0.444444 | 0.157135 | intron-variant | Klhl32 | Mm_Celera | 4:24821968 | TTGTCAAGCTGCTAG[G/T]GTGTGCTCTCTCTAG | 212390 |
rs4191414 | snp | A/T | 0.32 | 0.24 | intron-variant | Klhl32 | Mm_Celera | 4:24821775 | AAGCCAACATTCACG[A/T]GGAAACTGAACAACA | 212390 |
rs4205853 | snp | A/G | 0.444444 | 0.157135 | intron-variant | Klhl32 | Mm_Celera | 4:24821810 | TCTCAATGATACCTT[A/G]GTCAAGGAAAGAATA | 212390 |
rs4205854 | snp | C/T | 0.444444 | 0.157135 | intron-variant | Klhl32 | Mm_Celera | 4:24822023 | AGGAAGCAAATTCAC[C/T]CAAGAGGCATAGAAG | 212390 |
rs4205855 | snp | A/G | 0.493827 | 0.228978 | intron-variant | Klhl32 | Mm_Celera | 4:24822032 | ATTCACCCAAGAGGA[A/G]TATAGGGTAGGAAAT | 212390 |
rs4215966 | snp | A/C | 0.5 | 0 | intron-variant | Klhl32 | Mm_Celera | 4:24821795 | CTGAACAACACTCTT[A/C]CACAATGATACCTTG | 212390 |
rs6199124 | snp | G/T | 0.5 | 0 | intron-variant | Klhl32 | Mm_Celera | 4:24822209 | atgtctcccttttca[G/T]ttctgattttgttan | 212390 |
rs6199149 | snp | A/G | 0.5 | 0 | intron-variant | Klhl32 | Mm_Celera | 4:24822194 | nttctgattttgtta[A/G]ttagggtgcttttcc | 212390 |
rs6200088 | snp | C/T | 0.5 | 0 | intron-variant | Klhl32 | Mm_Celera | 4:24813450 | tattttctttattta[C/T]atttcctagncccgc | 212390 |
rs6200103 | snp | A/T | 0.5 | 0 | intron-variant | Klhl32 | Mm_Celera | 4:24813460 | atttanatttcctag[A/T]cccgccttcccctcc | 212390 |
rs6200630 | snp | A/G | 0.5 | 0 | intron-variant | Klhl32 | Mm_Celera | 4:24813548 | gcatagaaccttcac[A/G]ggacctagCTACAAT | 212390 |
rs6201518 | snp | A/G | 0.5 | 0 | intron-variant | Klhl32 | Mm_Celera | 4:24813691 | GAGAAAATATATGGC[A/G]TAGAAATCCCAAACT | 212390 |
rs6210261 | snp | A/C | 0.5 | 0 | intron-variant | Klhl32 | Mm_Celera | 4:24702978 | acactcattattggc[A/C]aaaatgaaggctgtt | 212390 |
rs6210306 | snp | A/C/T | 0.5 | 0 | intron-variant | Klhl32 | Mm_Celera | 4:24703009 | ctaacaagctttgta[A/C/T]tacctacctacataa | 212390 |
rs6210809 | snp | A/T | 0.5 | 0 | intron-variant | Klhl32 | Mm_Celera | 4:24703078 | acctgcaatctctag[A/T]acaacaacaaataaa | 212390 |
rs6224208 | snp | C/T | 0.5 | 0 | intron-variant | Klhl32 | Mm_Celera | 4:24703261 | TTATTCAATAATAAA[C/T]AATGTCCATTATTTT | 212390 |
rs6250126 | snp | C/T | 0.5 | 0 | intron-variant | Klhl32 | Mm_Celera | 4:24822005 | aaatttgcttccttt[C/T]gttctagtgctttaa | 212390 |
rs6259664 | snp | G/T | 0.46281 | 0.131194 | intron-variant | Klhl32 | GRCm38.p3 | 4:24711806 | ACACGTCCAATGGGC[G/T]CACGGCNAGAAACCC | 212390 |
rs6259672 | snp | A/G | 0.415225 | 0.187619 | intron-variant | Klhl32 | GRCm38.p3 | 4:24711813 | CAATGGGCNCACGGC[A/G]AGAAACCCTCATAGC | 212390 |
rs6261242 | snp | G/T | 0.5 | 0 | intron-variant | Klhl32 | Mm_Celera | 4:24712132 | GGAATAAGCGAAGGC[G/T]CAACTCCTTGTGTTT | 212390 |
rs6275404 | snp | C/G | 0.5 | 0 | intron-variant | Klhl32 | Mm_Celera | 4:24712416 | AAGGGAGGCAAGTCC[C/G]CTGAAAGCTGAGAGC | 212390 |
rs6288125 | snp | A/G | 0.5 | 0 | intron-variant | Klhl32 | Mm_Celera | 4:24822247 | atctgatggtgtttt[A/G]gntttcttcaggatc | 212390 |
rs6288126 | snp | A/C | 0.64 | 0.08 | intron-variant | Klhl32 | Mm_Celera | 4:24822245 | CTGATGGTGTTTTGG[A/C]TTTCTTCAGGATCTG | 212390 |
rs6304258 | snp | G/T | 0.231111 | 0.249285 | intron-variant | Klhl32 | Mm_Celera | 4:24687521 | CAGCCATGGCAACCG[G/T]AAAATGTCCACATGA | 212390 |
rs6304972 | snp | A/G | 0.5 | 0 | intron-variant | Klhl32 | Mm_Celera | 4:24822117 | tttctcaaagaacca[A/G]ctccatatttgtttg | 212390 |
rs6305393 | snp | C/T | 0.21875 | 0.248039 | intron-variant | Klhl32 | Mm_Celera | 4:24687771 | CTCAGCTCTGCTTAA[C/T]TGTATGTAATAAGCA | 212390 |
rs6305439 | snp | A/G | 0.5 | 0 | intron-variant | Klhl32 | Mm_Celera | 4:24687801 | ATGGTAGCTTCCGGT[A/G]TCCNATGGCTTCTCC | 212390 |
rs6305443 | snp | A/T | 0.5 | 0 | intron-variant | Klhl32 | Mm_Celera | 4:24687805 | TAGCTTCCGGTNTCC[A/T]ATGGCTTCTCCATCA | 212390 |
rs6310371 | snp | C/T | 0.5 | 0 | intron-variant | Klhl32 | GRCm38.p3 | 4:24822297 | catttcatccnggtt[C/T]tccagtttggttgag | 212390 |
rs6310785 | snp | C/G | 0.5 | 0 | intron-variant | Klhl32 | Mm_Celera | 4:24822276 | tttggttgagtatag[C/G]cttttntagaaggnt | 212390 |
rs6310788 | snp | A/G | 0.611111 | 0.124226 | intron-variant | Klhl32 | Mm_Celera | 4:24822270 | TGAGTATAGCCTTTT[A/G]TAAAAGGATCTGATG | 212390 |
rs6310807 | snp | A/G | 0.5 | 0 | intron-variant | Klhl32 | Mm_Celera | 4:24822262 | gncttttntagaagg[A/G]tctgatggtnttttg | 212390 |
rs6310827 | snp | G/T | 0.5 | 0 | intron-variant | Klhl32 | Mm_Celera | 4:24822252 | gaaggntctgatggt[G/T]ttttggatttcttca | 212390 |
rs6327462 | snp | A/G | 0.5 | 0 | intron-variant | Klhl32 | Mm_Celera | 4:24721733 | tgggggaaaagtcta[A/G]ctaactggtgagctt | 212390 |
rs6327967 | snp | C/T | 0.5 | 0 | intron-variant | Klhl32 | Mm_Celera | 4:24721824 | ATATGTTCAGGCACA[C/T]ATACATCCACCACAC | 212390 |
rs6328450 | snp | A/C | 0.5 | 0 | intron-variant | Klhl32 | Mm_Celera | 4:24721879 | AAATACAATGATGTA[A/C]CCTTAGATGNTGAAA | 212390 |
rs6328474 | snp | C/G | 0.5 | 0 | intron-variant | Klhl32 | Mm_Celera | 4:24721889 | ATGTANCCTTAGATG[C/G]TGAAAACACTAAAGA | 212390 |
rs6328517 | snp | C/T | 0.5 | 0 | intron-variant | Klhl32 | Mm_Celera | 4:24721920 | TAATTCTAATTCCTA[C/T]AGACCCAGAGATCTA | 212390 |
rs6329014 | snp | C/T | 0.5 | 0 | intron-variant | Klhl32 | Mm_Celera | 4:24721957 | GTTTTCCTACAGATA[C/T]TAAGATGTAGAATAT | 212390 |
rs6329118 | snp | A/G | 0.5 | 0 | intron-variant | Klhl32 | Mm_Celera | 4:24722017 | GAAGGAAGAAGTAAA[A/G]CACAAAAAGAAAAGA | 212390 |
rs6329585 | snp | A/T | 0.5 | 0 | intron-variant | Klhl32 | Mm_Celera | 4:24722068 | AGCATTGCTTTCTGA[A/T]TTTTACGGCAGATTT | 212390 |
rs6342555 | snp | C/T | 0.207612 | 0.24638 | intron-variant | Klhl32 | Mm_Celera | 4:24722192 | CATCCAGAAAGGAGG[C/T]CAGCTGTCAGGCAAT | 212390 |
rs6342604 | snp | A/G | 0.5 | 0 | intron-variant | Klhl32 | Mm_Celera | 4:24722226 | AAGAGCAGTCATCAA[A/G]GAGTTCCCTACAGCT | 212390 |
rs6343271 | snp | C/T | 0.444444 | 0.157135 | intron-variant | Klhl32 | Mm_Celera | 4:24822172 | GATGCTGTCCCTGTC[C/T]TCTAGTGAGTCTGGC | 212390 |
rs6344323 | snp | A/C | 0.5 | 0 | intron-variant | Klhl32 | Mm_Celera | 4:24822009 | gggtaaatttgcttc[A/C]ttttattctagagct | 212390 |
rs6344962 | snp | A/G | 0.56 | 0.195959 | intron-variant | Klhl32 | Mm_Celera | 4:24821897 | AGAAATGCTTTCATT[A/G]TGTCCCACAATTTTG | 212390 |
rs6353472 | snp | C/T | 0.5 | 0 | intron-variant | Klhl32 | Mm_Celera | 4:24821773 | GAAAGCCAACATTCA[C/T]GTGGAAACTGAATAA | 212390 |
rs6370687 | snp | C/T | 0.5 | 0 | intron-variant | Klhl32 | Mm_Celera | 4:24822240 | ggtgttttggatttc[C/T]tcangatctgttgtt | 212390 |
rs6370700 | snp | C/G/T | 0.666667 | 0.1283 | intron-variant | Klhl32 | Mm_Celera | 4:24822236 | TTTTGGATTTCTTCA[C/G/T]GATCTGTTGTTATGT | 212390 |
rs6399200 | snp | A/C/G/T | 0.697531 | 0.0647413 | intron-variant | Klhl32 | Mm_Celera | 4:24821955 | AGTGTGTGCTCTTTC[A/C/G/T]AATTTTTTTTTTTTT | 212390 |
rs6399213 | snp | A/C/G | 0.591716 | 0.14899 | intron-variant | Klhl32 | Mm_Celera | 4:24821953 | TGTGTGCTTTCTCTA[A/C/G]TTTCTTTTTGGAGGC | 212390 |
rs6401185 | snp | C/T | 0.72 | 0.0979796 | intron-variant | Klhl32 | Mm_Celera | 4:24821846 | AAGAAATTAGGGACT[C/T]TTTAGAGTTCAATGA | 212390 |
rs6402882 | snp | C/T | 0.5 | 0 | intron-variant | Klhl32 | Mm_Celera | 4:24821886 | cacaacatacccaaa[C/T]ttctgggacacaatg | 212390 |
rs13474166 | snp | C/G | | | intron-variant | Klhl32 | Mm_Celera | 4:24643710 | CTGGCCTTCCCACCA[C/G]GTGGGTTAAAACAGA | 212390 |
rs13477612 | snp | C/T | 0.496219 | 0.0433136 | intron-variant | Klhl32 | Mm_Celera | 4:24712720 | AAGCCATCAAGAGTG[C/T]GTATAGGCGGAGCCA | 212390 |
rs27718968 | snp | A/G | 0.124444 | 0.216185 | intron-variant | Klhl32 | GRCm38.p3 | 4:24718835 | CACGAGAGTTTTGGA[A/G]TTTTCATTATGGAGA | 212390 |
rs27718969 | snp | A/G | 0.124444 | 0.216185 | intron-variant | Klhl32 | GRCm38.p3 | 4:24718824 | CTGACCTCTTTCACG[A/G]GAGTTTTGGAGTTTT | 212390 |
rs27718970 | snp | A/G | 0.124444 | 0.216185 | intron-variant | Klhl32 | GRCm38.p3 | 4:24718782 | GCTTCTTTCTGGACA[A/G]TAGCTACTCCCTGAA | 212390 |
rs27718971 | snp | A/G | 0.132653 | 0.220748 | intron-variant | Klhl32 | GRCm38.p3 | 4:24718360 | AATGTCTCCTATATT[A/G]TGAACAGGTCCTAGA | 212390 |
rs27718972 | snp | C/T | 0.35503 | 0.226867 | intron-variant | Klhl32 | GRCm38.p3 | 4:24716639 | ACAACCCCCAGACCA[C/T]ATCTTTCCAATCACA | 212390 |
rs27718973 | snp | A/G | 0.46875 | 0.121031 | intron-variant | Klhl32 | GRCm38.p3 | 4:24716590 | CCATATAAACAACCA[A/G]GAGACAAAACCACAT | 212390 |
rs27718974 | snp | C/T | 0.375 | 0.216506 | intron-variant | Klhl32 | GRCm38.p3 | 4:24716435 | CGCTACCCAAGCATA[C/T]ACCCTTGTTACCATG | 212390 |
rs27718975 | snp | C/T | 0.459184 | 0.136902 | intron-variant | Klhl32 | GRCm38.p3 | 4:24716419 | CTGTAAAGATAACCA[C/T]CGCTACCCAAGCATA | 212390 |
rs27718976 | snp | A/C | 0.277778 | 0.248452 | intron-variant | Klhl32 | Mm_Celera | 4:24716361 | ACACCTATTCAACAG[A/C]AAGTCTTTTCTAATC | 212390 |
rs27718977 | snp | C/T | 0.444444 | 0.157135 | intron-variant | Klhl32 | Mm_Celera | 4:24716339 | TGGATGCTGAAGGCA[C/T]GGGAGCACACCTATT | 212390 |
rs27718978 | snp | A/G | 0.42 | 0.183303 | intron-variant | Klhl32 | Mm_Celera | 4:24716072 | GAACTTATTTTCATA[A/G]AGTTTGTGGATGGGG | 212390 |
rs27718979 | snp | C/T | 0.459184 | 0.136902 | intron-variant | Klhl32 | Mm_Celera | 4:24716018 | GTTTGCCACTGACAT[C/T]TTCCTACCTAGCAAC | 212390 |
rs27718980 | snp | G/T | 0.277778 | 0.248452 | intron-variant | Klhl32 | Mm_Celera | 4:24716012 | TTTAGAGTTTGCCAC[G/T]GACATTTTCCTACCT | 212390 |
rs27718981 | snp | C/T | 0.260355 | 0.249785 | intron-variant | Klhl32 | Mm_Celera | 4:24716005 | ACACATCTTTAGAGT[C/T]TGCCACTGACATTTT | 212390 |
rs27718982 | snp | A/C | 0.336735 | 0.234472 | intron-variant | Klhl32 | GRCm38.p3 | 4:24715927 | CAAAGGGATCATCAA[A/C]ACACAATCCTATGCT | 212390 |
rs27718983 | snp | A/G | 0.231111 | 0.249285 | intron-variant | Klhl32 | Mm_Celera | 4:24715800 | ATGGAGCTGAATGCA[A/G]TTATTAAGTCCGTGG | 212390 |
rs27718984 | snp | A/G | 0.415225 | 0.187619 | intron-variant | Klhl32 | GRCm38.p3 | 4:24715508 | AGTAGGGTTGATGCC[A/G]ATTCCCTTTATTTTG | 212390 |
rs27718985 | snp | A/G | 0.493827 | 0.0552116 | intron-variant | Klhl32 | GRCm38.p3 | 4:24715421 | ATTCTCCAGAACATG[A/G]GAGCGAAACCAAAGA | 212390 |
rs27718986 | snp | A/C/G | 0.132653 | 0.220748 | intron-variant | Klhl32 | GRCm38.p3 | 4:24715395 | GGGCCAGCTTCATAA[A/C/G]ACAGGGGCAGATTCT | 212390 |
rs27718987 | snp | A/G | 0.336735 | 0.234472 | intron-variant | Klhl32 | GRCm38.p3 | 4:24714767 | AGAATGGAGCTCAGT[A/G]TTTTAAGAAAAGCAC | 212390 |
rs27718988 | snp | A/C | 0.459184 | 0.136902 | intron-variant | Klhl32 | GRCm38.p3 | 4:24714755 | TGAATAGCGTACAGA[A/C]TGGAGCTCAGTATTT | 212390 |
rs27718989 | snp | C/T | 0.493827 | 0.0552116 | intron-variant | Klhl32 | GRCm38.p3 | 4:24714340 | CAACACAAATCTGAA[C/T]GTATAAGGCATTAGG | 212390 |
rs27718990 | snp | A/G | 0.124444 | 0.216185 | intron-variant | Klhl32 | Mm_Celera | 4:24714320 | CGTATAGTCTAGAAA[A/G]CTGTCAACACAAATC | 212390 |
rs27718991 | snp | C/T | 0.124444 | 0.216185 | intron-variant | Klhl32 | Mm_Celera | 4:24714040 | CTGAGTTGGTGCCTT[C/T]GAAAAATTGTAACTT | 212390 |
rs27718992 | snp | A/G | 0.142012 | 0.225474 | intron-variant | Klhl32 | Mm_Celera | 4:24713771 | AAGAGGAGGAGGATG[A/G]AACTTGTTATAATTC | 212390 |
rs27718993 | snp | A/G | 0.260355 | 0.249785 | intron-variant | Klhl32 | GRCm38.p3 | 4:24713659 | GTACAGGATTGATCT[A/G]AACCATCTGTGAGGA | 212390 |
rs27718994 | snp | A/G | 0.401235 | 0.199068 | intron-variant | Klhl32 | GRCm38.p3 | 4:24713200 | CTTCCTCTAGTCTGA[A/G]TGGGAATGTCGCTAG | 212390 |
rs27718995 | snp | A/G | 0.132653 | 0.220748 | intron-variant | Klhl32 | Mm_Celera | 4:24713127 | GACCCCAGTGCTTCA[A/G]CACCACAGGAGTGGC | 212390 |
rs27718996 | snp | C/T | 0.387812 | 0.208586 | intron-variant | Klhl32 | GRCm38.p3 | 4:24713099 | TTACTAATGTGGGCA[C/T]GGCCTTGTTAAGGAC | 212390 |
rs27718997 | snp | A/G | 0.487535 | 0.077957 | intron-variant | Klhl32 | GRCm38.p3 | 4:24713057 | GTAAGTGTGGGAAGA[A/G]TTGATAAAGTCCTGA | 212390 |
rs27718998 | snp | A/T | 0.32 | 0.24 | intron-variant | Klhl32 | GRCm38.p3 | 4:24712991 | GATAAGACTTACTCA[A/T]TGACTGTGAGCACAG | 212390 |
rs27718999 | snp | A/G | 0.32 | 0.24 | intron-variant | Klhl32 | Mm_Celera | 4:24712820 | GAGAAACTACATTTG[A/G]CTGTGAGGAACGAGA | 212390 |