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 |
rs27719000 | snp | A/G | 0.375 | 0.216506 | intron-variant | Klhl32 | Mm_Celera | 4:24712729 | AGAGTGTGTATAGGC[A/G]GAGCCAAATGTCATA | 212390 |
rs27719001 | snp | A/G | 0.32 | 0.24 | intron-variant | Klhl32 | Mm_Celera | 4:24712654 | CAGTGATGTTCAGCT[A/G]TTCTGGATGGGACAG | 212390 |
rs27719002 | snp | C/T | 0.32 | 0.24 | intron-variant | Klhl32 | Mm_Celera | 4:24712609 | AGGGAAAAAATATCC[C/T]AAAGACGCCAACATG | 212390 |
rs27719003 | snp | A/G | 0.5 | 0 | intron-variant | Klhl32 | GRCm38.p3 | 4:24712495 | GCTTAGTAGTCTAGA[A/G]GAGTTTGGCTCAGAT | 212390 |
rs27719004 | snp | A/G | 0.497778 | 0.0332592 | intron-variant | Klhl32 | GRCm38.p3 | 4:24712488 | CCACAGTGCTTAGTA[A/G]TCTAGAGGAGTTTGG | 212390 |
rs27719005 | snp | A/T | 0.277778 | 0.248452 | intron-variant | Klhl32 | Mm_Celera | 4:24712366 | CTAGTCTGGCATTCT[A/T]GCAGACTGGATGTTC | 212390 |
rs27719006 | snp | C/G | 0.495868 | 0.0452663 | intron-variant | Klhl32 | GRCm38.p3 | 4:24711716 | GGCATCCAGGATAAC[C/G]TCCAAAGTGTGGAAA | 212390 |
rs27719007 | snp | C/T | 0.497041 | 0.0383476 | intron-variant | Klhl32 | GRCm38.p3 | 4:24711706 | TCACACAACTGGCAT[C/T]CAGGATAACGTCCAA | 212390 |
rs27719008 | snp | C/T | 0.260355 | 0.249785 | intron-variant | Klhl32 | GRCm38.p3 | 4:24711589 | GAGGAGCAAGAAGAG[C/T]GAACAGACTTGCAGA | 212390 |
rs27719009 | snp | C/T | 0.444444 | 0.157135 | intron-variant | Klhl32 | GRCm38.p3 | 4:24711524 | ATTTCTGCAAATCCT[C/T]AAGGAAGAGGCTTTG | 212390 |
rs27719010 | snp | A/G | 0.5 | 0 | intron-variant | Klhl32 | Mm_Celera | 4:24711456 | TGAAAACACTCATCT[A/G]ATTCTGGACATTAAT | 212390 |
rs27719011 | snp | C/T | 0.444444 | 0.157135 | intron-variant | Klhl32 | GRCm38.p3 | 4:24710534 | TCCTTGGGACATCAG[C/T]TGGCTTACCAAAGTT | 212390 |
rs27719012 | snp | C/T | 0.277778 | 0.248452 | intron-variant | Klhl32 | Mm_Celera | 4:24710272 | TGGCAGAGTCAAAGC[C/T]TTCACCAGATAAGGC | 212390 |
rs27719013 | snp | C/T | 0.244898 | 0.249948 | intron-variant | Klhl32 | Mm_Celera | 4:24710247 | ATGGGCAGGGCATGT[C/T]TCAGATCCATGGCAG | 212390 |
rs27719014 | snp | A/G | 0.48 | 0.0979796 | intron-variant | Klhl32 | GRCm38.p3 | 4:24710160 | ATGCTTATGACACTC[A/G]GCTCTCTCTAAATAC | 212390 |
rs27719015 | snp | C/T | 0.277778 | 0.248452 | intron-variant | Klhl32 | Mm_Celera | 4:24710004 | CCATATCTTGGCTCT[C/T]GGTCAATATTCTTTC | 212390 |
rs27719016 | snp | C/T | 0.277778 | 0.248452 | intron-variant | Klhl32 | Mm_Celera | 4:24709973 | GTAAGTGCACTCTTT[C/T]TCCAAATGGGGCCAT | 212390 |
rs27719017 | snp | A/C | 0.277778 | 0.248452 | intron-variant | Klhl32 | GRCm38.p3 | 4:24709932 | GGTAATTCACTCCCA[A/C]ATCCATATGGAAATT | 212390 |
rs27719018 | snp | A/G | 0.32 | 0.24 | intron-variant | Klhl32 | Mm_Celera | 4:24709667 | AAACACAGCTATCAC[A/G]GTCATGAAACCATAA | 212390 |
rs27719019 | snp | C/T | 0.277778 | 0.248452 | intron-variant | Klhl32 | Mm_Celera | 4:24709605 | CCTGTAATGACACAC[C/T]TTCATTGTCTTCATG | 212390 |
rs27719020 | snp | C/T | 0.48 | 0.0979796 | intron-variant | Klhl32 | Mm_Celera | 4:24709594 | AACTTACAAGCCCTG[C/T]AATGACACACTTTCA | 212390 |
rs27719021 | snp | C/T | 0.444444 | 0.157135 | intron-variant | Klhl32 | Mm_Celera | 4:24709496 | TCTCCTCTGGCCACA[C/T]GGATTGGGTGGGTAC | 212390 |
rs27719022 | snp | C/T | 0.277778 | 0.248452 | intron-variant | Klhl32 | Mm_Celera | 4:24709285 | CCAACAGTTTTCCTA[C/T]ATCCCAAACTCTGTT | 212390 |
rs27719023 | snp | C/T | 0.277778 | 0.248452 | intron-variant | Klhl32 | Mm_Celera | 4:24709222 | GTATCCTAATTATTG[C/T]AAGACAGGCCCCTCT | 212390 |
rs27719024 | snp | C/T | 0.244898 | 0.249948 | intron-variant | Klhl32 | Mm_Celera | 4:24709080 | TCAATAAAGAGAAAG[C/T]GATCAGCTACATGAA | 212390 |
rs27719025 | snp | C/T | 0.444444 | 0.157135 | intron-variant | Klhl32 | Mm_Celera | 4:24708895 | GTGTAGTTTTTCTAT[C/T]AGTTGGTAGGGGACA | 212390 |
rs27719026 | snp | A/G | 0.277778 | 0.248452 | intron-variant | Klhl32 | Mm_Celera | 4:24708784 | TCAAGAACCTGCTAG[A/G]TTGTAGAAACACACA | 212390 |
rs27719027 | snp | A/T | 0.32 | 0.24 | intron-variant | Klhl32 | Mm_Celera | 4:24708764 | GGATCCTCTTCTCTG[A/T]GTCCTCAAGAACCTG | 212390 |
rs27719028 | snp | A/G | 0.345679 | 0.230967 | intron-variant | Klhl32 | Mm_Celera | 4:24708637 | CTGTACATGGATGCC[A/G]AATCAGTCTGCTGCC | 212390 |
rs27719029 | snp | C/T | 0.277778 | 0.248452 | intron-variant | Klhl32 | Mm_Celera | 4:24708557 | TTAAGCCAGGATCTT[C/T]TCTAGTATTCCCCAG | 212390 |
rs27719030 | snp | A/T | 0.444444 | 0.157135 | intron-variant | Klhl32 | Mm_Celera | 4:24708397 | GGGTGCACAGCTCAC[A/T]TATCCATTTCCCCAT | 212390 |
rs27719031 | snp | C/T | 0.48 | 0.0979796 | intron-variant | Klhl32 | Mm_Celera | 4:24708315 | AAATACACAACAGCA[C/T]AGTGTTCATGAATTT | 212390 |
rs27719032 | snp | A/G | 0.32 | 0.24 | intron-variant | Klhl32 | Mm_Celera | 4:24708261 | TTGACAAACGAAACA[A/G]CATAAATTTGTTGTG | 212390 |
rs27719033 | snp | A/G | 0.48 | 0.0979796 | intron-variant | Klhl32 | Mm_Celera | 4:24708094 | AGCTGGGTACACTGT[A/G]AACTTCTGACTTTTT | 212390 |
rs27719034 | snp | C/T | 0.277778 | 0.248452 | intron-variant | Klhl32 | Mm_Celera | 4:24707589 | CAAGGGCCAGTGAGA[C/T]CATGGGACAAATGGC | 212390 |
rs27719035 | snp | A/G | 0.408163 | 0.193609 | intron-variant | Klhl32 | Mm_Celera | 4:24707435 | AAATGATTCTAAACA[A/G]AAACAAAGTAATTGG | 212390 |
rs27719036 | snp | C/T | 0.32 | 0.24 | intron-variant | Klhl32 | Mm_Celera | 4:24707394 | GACCTATTCACAGCA[C/T]ATTTAGACAAATTTT | 212390 |
rs27719037 | snp | A/G | 0.277778 | 0.248452 | intron-variant | Klhl32 | Mm_Celera | 4:24707362 | GATGGGTAGGGTAGC[A/G]AGAGTGGATGATAAA | 212390 |
rs27719038 | snp | C/T | 0.444444 | 0.157135 | intron-variant | Klhl32 | Mm_Celera | 4:24707139 | TAAAAAATAGTTAAA[C/T]AGTACTGTCAAGTTG | 212390 |
rs27719039 | snp | C/T | 0.244898 | 0.249948 | intron-variant | Klhl32 | Mm_Celera | 4:24707051 | GTTCATGTTGACAAT[C/T]AGCAAAAAGAAATTA | 212390 |
rs27719040 | snp | C/T | 0.444444 | 0.157135 | intron-variant | Klhl32 | Mm_Celera | 4:24706884 | TTCCTGTCTATGTAT[C/T]ACTGAGTATTGTCTG | 212390 |
rs27719041 | snp | G/T | 0.244898 | 0.249948 | intron-variant | Klhl32 | Mm_Celera | 4:24706816 | ACTATACACAAATAG[G/T]CATGATGGTATGTCT | 212390 |
rs27719042 | snp | A/G | 0.244898 | 0.249948 | intron-variant | Klhl32 | Mm_Celera | 4:24706757 | GACGTGAGCATGGTC[A/G]TCCAGTCTCCATCTG | 212390 |
rs27719043 | snp | A/G | 0.277778 | 0.248452 | intron-variant | Klhl32 | Mm_Celera | 4:24706662 | AAACTGCACTTTGAC[A/G]GAAGTAAAACACATG | 212390 |
rs27719044 | snp | A/G | 0.277778 | 0.248452 | intron-variant | Klhl32 | Mm_Celera | 4:24706566 | CCCACAACAGAAGCG[A/G]AGGACATTTGTGAAA | 212390 |
rs27719045 | snp | A/T | 0.444444 | 0.157135 | intron-variant | Klhl32 | Mm_Celera | 4:24706384 | CATTAGAATAACATA[A/T]TCTAAAAGCAGGTTG | 212390 |
rs27719046 | snp | A/T | 0.277778 | 0.248452 | intron-variant | Klhl32 | Mm_Celera | 4:24706357 | CCAAAAGAGTAAAGA[A/T]ATGTAAGGCTGCATT | 212390 |
rs27719047 | snp | A/T | 0.489796 | 0.070696 | intron-variant | Klhl32 | Mm_Celera | 4:24706065 | CTCCTAGAGGAGGCA[A/T]CTATCCAAAGAAACA | 212390 |
rs27719048 | snp | A/C | 0.277778 | 0.248452 | intron-variant | Klhl32 | GRCm38.p3 | 4:24705918 | GGGAAAGAGCCCACA[A/C]TATGATCTGGAAGTT | 212390 |
rs27719049 | snp | A/T | 0.277778 | 0.248452 | intron-variant | Klhl32 | Mm_Celera | 4:24705822 | AGACTATTAAAGGAA[A/T]ACAGTGGACTAGGGA | 212390 |
rs27719050 | snp | G/T | 0.32 | 0.24 | intron-variant | Klhl32 | Mm_Celera | 4:24705671 | GGAAGAAAGCTCCAG[G/T]GGTTTCCTCATCCAT | 212390 |
rs27719051 | snp | A/T | 0.46875 | 0.121031 | intron-variant | Klhl32 | GRCm38.p3 | 4:24705643 | CCAGTAGGGCTGGTC[A/T]CTCAGGAAGAGAGGA | 212390 |
rs27719052 | snp | C/T | 0.32 | 0.24 | intron-variant | Klhl32 | Mm_Celera | 4:24705600 | AAGAGCTCTGGACAG[C/T]AGTGGGCATGCTGGA | 212390 |
rs27719053 | snp | C/T | 0.408163 | 0.193609 | intron-variant | Klhl32 | Mm_Celera | 4:24705521 | AAGCTCAGGACACCC[C/T]GTTTCAAAAACAAAA | 212390 |
rs27719054 | snp | A/G | 0.277778 | 0.248452 | intron-variant | Klhl32 | Mm_Celera | 4:24705469 | GATACTGCCTGATGC[A/G]CTCTAGGCTGAGCAG | 212390 |
rs27719055 | snp | A/C | 0.408163 | 0.193609 | intron-variant | Klhl32 | Mm_Celera | 4:24705453 | GAAGGCTGAGTGTGA[A/C]GATACTGCCTGATGC | 212390 |
rs27719056 | snp | C/T | 0.277778 | 0.248452 | intron-variant | Klhl32 | Mm_Celera | 4:24705431 | GTGGCTAATATGAAA[C/T]TGCTGGGAAGGCTGA | 212390 |
rs27719057 | snp | C/T | 0.444444 | 0.157135 | intron-variant | Klhl32 | Mm_Celera | 4:24705414 | GGAGTTGGAACAGTA[C/T]GGTGGCTAATATGAA | 212390 |
rs27719058 | snp | C/T | 0.132653 | 0.220748 | intron-variant | Klhl32 | Mm_Celera | 4:24699850 | CAACATATCAATTTA[C/T]AGATAACAGAACAAA | 212390 |
rs27719059 | snp | A/G | 0.124444 | 0.216185 | intron-variant | Klhl32 | Mm_Celera | 4:24699811 | GACATTTGTGAAGCT[A/G]ACTCTAAAGCTGGAC | 212390 |
rs27719060 | snp | A/C | 0.21875 | 0.248039 | intron-variant | Klhl32 | Mm_Celera | 4:24699787 | GTGACACATGTGAAG[A/C]CATATGAAGACATTT | 212390 |
rs27719061 | snp | A/G | 0.124444 | 0.216185 | intron-variant | Klhl32 | Mm_Celera | 4:24699770 | GACAGATAAAAAACC[A/G]CGTGACACATGTGAA | 212390 |
rs27719062 | snp | A/G | 0.124444 | 0.216185 | intron-variant | Klhl32 | Mm_Celera | 4:24699669 | ATGTGGCTTGCCATG[A/G]ACAGAGGCTAGAAAC | 212390 |
rs27719063 | snp | A/G | 0.124444 | 0.216185 | intron-variant | Klhl32 | Mm_Celera | 4:24699656 | GATACTCAAGGGAAT[A/G]TGGCTTGCCATGGAC | 212390 |
rs27719064 | snp | C/G | 0.48 | 0.0979796 | intron-variant | Klhl32 | GRCm38.p3 | 4:24699235 | TGTGTTTCTCCACAC[C/G]GACCAAGAGGGCACA | 212390 |
rs27719065 | snp | G/T | 0.493827 | 0.0552116 | intron-variant | Klhl32 | GRCm38.p3 | 4:24699194 | ATAGAATTCTCAGTA[G/T]AGGCATGTGTATGTT | 212390 |
rs27719066 | snp | A/G | 0.42 | 0.183303 | intron-variant | Klhl32 | GRCm38.p3 | 4:24699181 | GCATCCCTGATTTAT[A/G]GAATTCTCAGTAGAG | 212390 |
rs27719067 | snp | A/T | 0.297521 | 0.245442 | intron-variant | Klhl32 | GRCm38.p3 | 4:24699104 | AGTTTCTCCCTTCAA[A/T]AGACGGCAACCTTGG | 212390 |
rs27719068 | snp | A/G | 0.142012 | 0.225474 | intron-variant | Klhl32 | GRCm38.p3 | 4:24699026 | ACCTGGTGAAACAAA[A/G]GACACTACTATTAAT | 212390 |
rs27719069 | snp | C/T | 0.124444 | 0.216185 | intron-variant | Klhl32 | Mm_Celera | 4:24698906 | CCTACGAGCAGATAC[C/T]GGCAGCCTGTTTCTG | 212390 |
rs27719070 | snp | C/T | 0.486111 | 0.0821678 | intron-variant | Klhl32 | Mm_Celera | 4:24698834 | TTTCCATTTTCCCCC[C/T]GGTTTTTGCTTTAAA | 212390 |
rs27719071 | snp | A/T | 0.231111 | 0.249285 | intron-variant | Klhl32 | Mm_Celera | 4:24698380 | TCTTTCACATAAAAG[A/T]GCTAAACTAATGCCG | 212390 |
rs27719072 | snp | A/G | 0.493827 | 0.0552116 | intron-variant | Klhl32 | GRCm38.p3 | 4:24698248 | AACAGAAGAAAACAA[A/G]GCAAAACGAGAAACA | 212390 |
rs27719073 | snp | C/T | 0.231111 | 0.249285 | intron-variant | Klhl32 | Mm_Celera | 4:24698206 | AGAACACCTTCAGTC[C/T]GAGGAAGCGACCAGT | 212390 |
rs27719074 | snp | A/G | 0.260355 | 0.249785 | intron-variant | Klhl32 | Mm_Celera | 4:24698141 | GCTACTCAAAGATGA[A/G]TAGCAAGCATCTAGG | 212390 |
rs27719075 | snp | G/T | 0.231111 | 0.249285 | intron-variant | Klhl32 | Mm_Celera | 4:24698106 | ATCCGCCCTAGAGAT[G/T]CTCCTCAGGTTAGTT | 212390 |
rs27719076 | snp | G/T | 0.444444 | 0.157135 | intron-variant | Klhl32 | GRCm38.p3 | 4:24698046 | TGTAGGATGACGAAT[G/T]AGCATGGTCAGGGGT | 212390 |
rs27719077 | snp | C/T | 0.231111 | 0.249285 | intron-variant | Klhl32 | Mm_Celera | 4:24697871 | GAAAAAAAAAGGAAA[C/T]CGTTAAGACTGGTAT | 212390 |
rs27719078 | snp | A/G | 0.260355 | 0.249785 | intron-variant | Klhl32 | Mm_Celera | 4:24697594 | ACATACTCAGTTCAC[A/G]TAATGTGGAGAATAG | 212390 |
rs27719079 | snp | A/T | 0.260355 | 0.249785 | intron-variant | Klhl32 | Mm_Celera | 4:24697442 | TCACTGTAGGAAGTA[A/T]TTCCAATGGAACAGA | 212390 |
rs27719080 | snp | C/T | 0.124444 | 0.216185 | intron-variant | Klhl32 | Mm_Celera | 4:24697339 | AGAAGAAAGAGCCTC[C/T]AATAAGTCACTGCTG | 212390 |
rs27719081 | snp | A/G | 0.260355 | 0.249785 | intron-variant | Klhl32 | Mm_Celera | 4:24697253 | AGGATAAATTGTTTT[A/G]TACAGAATATCCACC | 212390 |
rs27719082 | snp | C/T | 0.231111 | 0.249285 | intron-variant | Klhl32 | Mm_Celera | 4:24697002 | CCTTATCGTTTTCAC[C/T]GAGAAAGAATTGAAA | 212390 |
rs27719083 | snp | A/T | 0.231111 | 0.249285 | intron-variant | Klhl32 | Mm_Celera | 4:24696958 | CAACTAGCTGGTGGC[A/T]GACTTTGAGTTGATA | 212390 |
rs27719084 | snp | C/T | 0.231111 | 0.249285 | intron-variant | Klhl32 | Mm_Celera | 4:24696897 | TGGCAAACCTGACAT[C/T]CTGGCTTACCCGTGC | 212390 |
rs27719085 | snp | A/G | 0.231111 | 0.249285 | intron-variant | Klhl32 | Mm_Celera | 4:24696873 | CTGGAGCCAACCATG[A/G]ATGATGTTTGGCAAA | 212390 |
rs27719086 | snp | C/T | 0.124444 | 0.216185 | intron-variant | Klhl32 | Mm_Celera | 4:24696707 | TAACAAATTAGAATG[C/T]TGAAATCACTTGCTC | 212390 |
rs27719087 | snp | C/T | 0.124444 | 0.216185 | intron-variant | Klhl32 | Mm_Celera | 4:24696654 | TCCTTTCTTTAAAAA[C/T]TCACAAAGAAGATAC | 212390 |
rs27719088 | snp | A/G | 0.231111 | 0.249285 | intron-variant | Klhl32 | Mm_Celera | 4:24696471 | TTGATTCTGAACTCC[A/G]GCATCCACAAGATAC | 212390 |
rs27719089 | snp | C/G | 0.231111 | 0.249285 | intron-variant | Klhl32 | Mm_Celera | 4:24696298 | TTGAGCTTCAGAGAC[C/G]AGGGCACATATCTCA | 212390 |
rs27719090 | snp | A/G | 0.387812 | 0.208586 | intron-variant | Klhl32 | GRCm38.p3 | 4:24695896 | GACAGAGGACTGGAG[A/G]TAACAAGGTGTGCTA | 212390 |
rs27719091 | snp | A/C | 0.231111 | 0.249285 | intron-variant | Klhl32 | Mm_Celera | 4:24695813 | GGAGATTCTAGAGTG[A/C]CTACTGGCTTTTGGC | 212390 |
rs27719092 | snp | A/T | 0.396694 | 0.202437 | intron-variant | Klhl32 | Mm_Celera | 4:24695560 | GTTTGTTATTTGGTT[A/T]AAAAAAAAAAAGCTA | 212390 |
rs27719093 | snp | A/C | 0.231111 | 0.249285 | intron-variant | Klhl32 | Mm_Celera | 4:24695323 | ATGTCACAGGAGATA[A/C]ATCAATACAGAAAAT | 212390 |
rs27719094 | snp | G/T | 0.465374 | 0.126941 | intron-variant | Klhl32 | GRCm38.p3 | 4:24695282 | GTTATGTCACTTAAG[G/T]TCAGGTGAATTTGGG | 212390 |
rs27719095 | snp | A/T | 0.231111 | 0.249285 | intron-variant | Klhl32 | Mm_Celera | 4:24695236 | AAGGATGCTGTATCT[A/T]CTTTGAGGACTAGGA | 212390 |
rs27719096 | snp | C/T | 0.231111 | 0.249285 | intron-variant | Klhl32 | Mm_Celera | 4:24694923 | ACAGGAGCAATGTGC[C/T]ACCACGCTGGCTCTT | 212390 |
rs27719097 | snp | C/T | 0.455 | 0.143091 | intron-variant | Klhl32 | GRCm38.p3 | 4:24694850 | ATTGCTGGCCTCAGT[C/T]ACCATGAGCTTCAAA | 212390 |
rs27719098 | snp | C/T | 0.408163 | 0.193609 | intron-variant | Klhl32 | GRCm38.p3 | 4:24693920 | AAAAAATATTTACTT[C/T]ATTCTGTTGGGTATA | 212390 |
rs27719099 | snp | A/G | 0.124444 | 0.216185 | intron-variant | Klhl32 | Mm_Celera | 4:24693600 | TGGCCTTTCCTCTGG[A/G]TTTTCATTCAAGTTC | 212390 |
rs27719100 | snp | C/T | 0.132653 | 0.220748 | intron-variant | Klhl32 | Mm_Celera | 4:24693488 | TCTACATACAGATCT[C/T]CAGCAGGGTACCTGC | 212390 |
rs27719101 | snp | C/T | 0.124444 | 0.216185 | intron-variant | Klhl32 | Mm_Celera | 4:24693429 | GGTTGCCCTGACCCT[C/T]TAGGCTTTCTTGCTG | 212390 |
rs27719102 | snp | C/G | 0.124444 | 0.216185 | intron-variant | Klhl32 | Mm_Celera | 4:24693300 | AAATGCTTCGCCAGT[C/G]CTTGCACATAAGGCT | 212390 |
rs27719103 | snp | A/T | 0.124444 | 0.216185 | intron-variant | Klhl32 | Mm_Celera | 4:24693255 | TAAGTATCCTCAAAA[A/T]TCACCGCTGCCATGT | 212390 |
rs27719104 | snp | C/G | 0.124444 | 0.216185 | intron-variant | Klhl32 | Mm_Celera | 4:24693231 | GTCCAACAAAACTTG[C/G]TTTGCCTGTAAGTAT | 212390 |
rs27719105 | snp | C/T | 0.231111 | 0.249285 | intron-variant | Klhl32 | Mm_Celera | 4:24693219 | GAAATGGTGAATGTC[C/T]AACAAAACTTGGTTT | 212390 |
rs27719106 | snp | A/G | 0.124444 | 0.216185 | intron-variant | Klhl32 | Mm_Celera | 4:24693124 | TAACATACAGCAGCT[A/G]TGGTAACTGTTGTTT | 212390 |
rs27719107 | snp | A/C | 0.124444 | 0.216185 | intron-variant | Klhl32 | Mm_Celera | 4:24693078 | AAGAGCGTTCTGAAA[A/C]CGTGTCCAGTGCTAG | 212390 |
rs27719108 | snp | A/G | 0.231111 | 0.249285 | intron-variant | Klhl32 | Mm_Celera | 4:24693052 | TTCATATCTAAATAC[A/G]AGGAAACATGAAGAG | 212390 |
rs27719109 | snp | C/T | 0.231111 | 0.249285 | intron-variant | Klhl32 | Mm_Celera | 4:24693026 | CCGTGGACAATATCT[C/T]GAGTCAAATTTTCAT | 212390 |
rs27719110 | snp | A/G | 0.124444 | 0.216185 | intron-variant | Klhl32 | Mm_Celera | 4:24692971 | GTCATCTTTAGTTTC[A/G]AATCGTAGCAGAAGA | 212390 |
rs27719111 | snp | C/T | 0.124444 | 0.216185 | intron-variant | Klhl32 | Mm_Celera | 4:24692970 | TGTCATCTTTAGTTT[C/T]GAATCGTAGCAGAAG | 212390 |
rs27719112 | snp | C/T | 0.21875 | 0.248039 | intron-variant | Klhl32 | GRCm38.p3 | 4:24692744 | GTTTTCTTCACTGGG[C/T]CATAAAGGCATCAGT | 212390 |
rs27719113 | snp | A/G | 0.231111 | 0.249285 | intron-variant | Klhl32 | Mm_Celera | 4:24692703 | TTATTATGGACACGT[A/G]TTTGGGTCATACATT | 212390 |
rs27719114 | snp | C/G | 0.124444 | 0.216185 | intron-variant | Klhl32 | Mm_Celera | 4:24692626 | AGAAGGCCCACCTGT[C/G]ATCAACAAAGGCGGC | 212390 |
rs27719115 | snp | G/T | 0.124444 | 0.216185 | intron-variant | Klhl32 | Mm_Celera | 4:24692417 | TGAAATTAAAAAAAT[G/T]TGTTGCATTGTGAAT | 212390 |
rs27719116 | snp | C/G | 0.231111 | 0.249285 | intron-variant | Klhl32 | Mm_Celera | 4:24692340 | CATTTGAAGCAGAGA[C/G]TAACTCTTCCCGTTT | 212390 |
rs27719117 | snp | A/G | 0.124444 | 0.216185 | intron-variant | Klhl32 | Mm_Celera | 4:24692001 | TAGTAGGTAGCTAAG[A/G]CACTTTGTTACTGAC | 212390 |
rs27719118 | snp | C/T | 0.124444 | 0.216185 | intron-variant | Klhl32 | Mm_Celera | 4:24691736 | TAAACAGAAGTATCA[C/T]TTTTGATTTCCAGAA | 212390 |
rs27719119 | snp | G/T | 0.124444 | 0.216185 | intron-variant | Klhl32 | Mm_Celera | 4:24691617 | TTTATTTCTAAGAAT[G/T]TCACTGACTTGTGAA | 212390 |
rs27719120 | snp | A/T | 0.124444 | 0.216185 | intron-variant | Klhl32 | Mm_Celera | 4:24691475 | CTTTCCCAAAACATG[A/T]TACCTCAAGTCCAGG | 212390 |
rs27719121 | snp | C/T | 0.231111 | 0.249285 | intron-variant | Klhl32 | Mm_Celera | 4:24691459 | AGTTTTATACCAATG[C/T]CTTTCCCAAAACATG | 212390 |
rs27719122 | snp | A/G | 0.124444 | 0.216185 | intron-variant | Klhl32 | Mm_Celera | 4:24691444 | TGATGACATCTACTG[A/G]GTTTTATACCAATGT | 212390 |
rs27719123 | snp | C/G | 0.124444 | 0.216185 | intron-variant | Klhl32 | Mm_Celera | 4:24691377 | TTGCTCTTTATCCAC[C/G]CAGCACTGCAGTTTA | 212390 |
rs27719124 | snp | A/G | 0.124444 | 0.216185 | intron-variant | Klhl32 | Mm_Celera | 4:24691361 | CTCCCTGGCCTGTCA[A/G]TTGCTCTTTATCCAC | 212390 |
rs27719125 | snp | A/G | 0.124444 | 0.216185 | intron-variant | Klhl32 | Mm_Celera | 4:24691345 | TTGGCTACTCTGACG[A/G]CTCCCTGGCCTGTCA | 212390 |
rs27719126 | snp | A/C | 0.124444 | 0.216185 | intron-variant | Klhl32 | Mm_Celera | 4:24691204 | TATCTAGAGTCTGAT[A/C]TGCACTGCCCAGGAG | 212390 |
rs27719127 | snp | C/T | 0.124444 | 0.216185 | intron-variant | Klhl32 | Mm_Celera | 4:24691161 | ACATCCCACTGAACT[C/T]CTTGGATGGTAAAAA | 212390 |
rs27719128 | snp | C/T | 0.132653 | 0.220748 | intron-variant | Klhl32 | Mm_Celera | 4:24691077 | ATAATGACATCTATA[C/T]AACAACTTTGCTCTA | 212390 |
rs27719129 | snp | A/C | 0.142012 | 0.225474 | intron-variant | Klhl32 | Mm_Celera | 4:24691047 | AATGCTTTCCTCAAT[A/C]TTGTAGTTAAGCTGA | 212390 |
rs27719130 | snp | C/T | 0.124444 | 0.216185 | intron-variant | Klhl32 | Mm_Celera | 4:24690899 | AGGAAGCAAGAGGGC[C/T]TGAGATGTTTGATTG | 212390 |
rs27719131 | snp | A/G | 0.142012 | 0.225474 | intron-variant | Klhl32 | Mm_Celera | 4:24690826 | ACTGCCTTACTTTGA[A/G]TTATAGTCAAAGTAA | 212390 |
rs27719132 | snp | C/T | 0.124444 | 0.216185 | intron-variant | Klhl32 | Mm_Celera | 4:24690805 | AATCCACATAAAATG[C/T]TGAATACTGCCTTAC | 212390 |
rs27719133 | snp | A/G | 0.132653 | 0.220748 | intron-variant | Klhl32 | Mm_Celera | 4:24690245 | TAACGGACTACTTGA[A/G]CCAAAATATTTTGAC | 212390 |
rs27719134 | snp | A/G | 0.132653 | 0.220748 | intron-variant | Klhl32 | Mm_Celera | 4:24690234 | GATTTCTCCATTAAC[A/G]GACTACTTGAACCAA | 212390 |
rs27719135 | snp | A/G | 0.132653 | 0.220748 | intron-variant | Klhl32 | Mm_Celera | 4:24690142 | AAGTACACACAATGG[A/G]CATTATAACACAAGC | 212390 |
rs27719136 | snp | C/G | 0.142012 | 0.225474 | intron-variant | Klhl32 | Mm_Celera | 4:24690085 | CCAAGTGGAGAACCT[C/G]GTAATAATAATTCAA | 212390 |
rs27719137 | snp | C/T | 0.124444 | 0.216185 | intron-variant | Klhl32 | Mm_Celera | 4:24689491 | TTAGTTACAGTGAGG[C/T]CAACAAGTATGGAGT | 212390 |
rs27719138 | snp | A/C | 0.21875 | 0.248039 | intron-variant | Klhl32 | Mm_Celera | 4:24688923 | ACCAAACACAAATAT[A/C]TATCTTTTAGGCTTA | 212390 |
rs27719139 | snp | A/G | 0.132653 | 0.220748 | intron-variant | Klhl32 | Mm_Celera | 4:24688881 | ACAAATAATTAGGTC[A/G]ATGTAAGTAGAACTA | 212390 |
rs27719140 | snp | C/T | 0.231111 | 0.249285 | intron-variant | Klhl32 | Mm_Celera | 4:24688659 | TCGATCTGACCAGAC[C/T]ATAAACTGTTTAGAA | 212390 |
rs27719141 | snp | A/C | 0.124444 | 0.216185 | intron-variant | Klhl32 | Mm_Celera | 4:24688593 | TTCTGTAACTGTCAG[A/C]AATGACCATTCCTAC | 212390 |
rs27719142 | snp | C/T | 0.132653 | 0.220748 | intron-variant | Klhl32 | Mm_Celera | 4:24688510 | CTTAGATCTAGTCAA[C/T]TGCCTGCTCCTATCC | 212390 |
rs27719143 | snp | A/G | 0.375 | 0.216506 | intron-variant | Klhl32 | GRCm38.p3 | 4:24688462 | TTACATCTAGATTTC[A/G]GTATCATGAGTCCCC | 212390 |
rs27719144 | snp | A/G | 0.142012 | 0.225474 | intron-variant | Klhl32 | Mm_Celera | 4:24688090 | AATTCATAACTTAAT[A/G]GGTCTTTAACCTACA | 212390 |
rs27719145 | snp | A/G | 0.132653 | 0.220748 | intron-variant | Klhl32 | Mm_Celera | 4:24687965 | TGATGCAAGGTCAAA[A/G]TGAAGAATGTGGCCT | 212390 |
rs27719146 | snp | G/T | 0.132653 | 0.220748 | intron-variant | Klhl32 | Mm_Celera | 4:24687845 | GGGTAGTGTAGCTGA[G/T]CCCAGATTTTCTATT | 212390 |
rs27719147 | snp | C/T | 0.132653 | 0.220748 | intron-variant | Klhl32 | Mm_Celera | 4:24687679 | AGCTCAACCTGTCTC[C/T]TTGATCCCACTATAT | 212390 |
rs27719148 | snp | A/G | 0.132653 | 0.220748 | intron-variant | Klhl32 | Mm_Celera | 4:24687566 | CCAGGCATTCCTCTG[A/G]GCCATGTGCTGATGC | 212390 |
rs27719149 | snp | C/T | 0.142012 | 0.225474 | intron-variant | Klhl32 | Mm_Celera | 4:24686641 | AAATCTGCAGTGCTT[C/T]CTGTCCATGTCAGGA | 212390 |
rs27719150 | snp | A/C | 0.132653 | 0.220748 | intron-variant | Klhl32 | Mm_Celera | 4:24686617 | GCTCCTTAAAAACAC[A/C]ATGCCCACAAATCTG | 212390 |
rs27719151 | snp | A/G | 0.132653 | 0.220748 | intron-variant | Klhl32 | Mm_Celera | 4:24686586 | AGAATGATGCTCTGA[A/G]TTCTACCTTTTCATT | 212390 |
rs27719152 | snp | C/T | 0.132653 | 0.220748 | intron-variant | Klhl32 | Mm_Celera | 4:24686475 | CTATATTAATAGAGC[C/T]AAGAATGCTAAGTAG | 212390 |
rs27719153 | snp | A/G | 0.132653 | 0.220748 | intron-variant | Klhl32 | Mm_Celera | 4:24686092 | GTGTGCGATATGTAT[A/G]TGATTATGTGGGTAC | 212390 |
rs27719154 | snp | A/G | 0.444444 | 0.157135 | intron-variant | Klhl32 | Mm_Celera | 4:24685504 | CTTAAAGAACCAAAA[A/G]CAATGTTCTCCTTGA | 212390 |
rs27719155 | snp | A/G | 0.459184 | 0.136902 | intron-variant | Klhl32 | Mm_Celera | 4:24685290 | GTTACTTGAAAGCCC[A/G]CAACTTGAAAAGTCC | 212390 |
rs27719156 | snp | G/T | 0.396694 | 0.202437 | intron-variant | Klhl32 | GRCm38.p3 | 4:24685119 | GCATCATGGCACAAA[G/T]AGGGGAGTGGGCAAG | 212390 |
rs27719157 | snp | C/T | 0.473373 | 0.11227 | intron-variant | Klhl32 | GRCm38.p3 | 4:24684839 | AAGGAATACAGAAGT[C/T]ACTGAACCAGATTTT | 212390 |
rs27719158 | snp | C/T | 0.408163 | 0.193609 | intron-variant | Klhl32 | Mm_Celera | 4:24684785 | GATCCAGTCACACTT[C/T]CACTGAAATAACCCT | 212390 |
rs27719159 | snp | A/G | 0.48 | 0.0979796 | intron-variant | Klhl32 | Mm_Celera | 4:24684769 | TATGCAAGTTGATGG[A/G]GATCCAGTCACACTT | 212390 |
rs27719160 | snp | A/G | 0.473373 | 0.11227 | intron-variant | Klhl32 | Mm_Celera | 4:24684742 | AAAAAGATGACCCCT[A/G]AAGTCTACTACTATG | 212390 |
rs27719161 | snp | C/T | 0.473373 | 0.11227 | intron-variant | Klhl32 | Mm_Celera | 4:24683917 | GTCTAGAGGATGCTA[C/T]GAGACAAGCTATAGG | 212390 |
rs27719162 | snp | A/C | 0.42 | 0.183303 | intron-variant | Klhl32 | Mm_Celera | 4:24683848 | TATCTTTAGATGCTC[A/C]CCATTCTCACTTTAT | 212390 |
rs27719163 | snp | C/T | 0.493827 | 0.0552116 | intron-variant | Klhl32 | Mm_Celera | 4:24683821 | GCCTATTAAGTATAA[C/T]AAGAATGACAGTATC | 212390 |
rs27719164 | snp | A/C | 0.459184 | 0.136902 | intron-variant | Klhl32 | GRCm38.p3 | 4:24683696 | GCATCACACACAGCC[A/C]GGACTCTGGGAACCC | 212390 |
rs27719165 | snp | A/G | 0.46875 | 0.121031 | intron-variant | Klhl32 | Mm_Celera | 4:24683608 | TTATATGCCAAACCC[A/G]ACTAAACATGGAGCT | 212390 |
rs27719166 | snp | A/G | 0.426035 | 0.177515 | intron-variant | Klhl32 | Mm_Celera | 4:24683574 | TTAATCTCACAGAAA[A/G]GACTTGTGTCTTGAA | 212390 |
rs27719167 | snp | A/T | 0.46281 | 0.131194 | intron-variant | Klhl32 | Mm_Celera | 4:24683518 | ATCCTACTTTAATGG[A/T]ACCGAAAGATGAAAT | 212390 |
rs27719168 | snp | C/T | 0.46281 | 0.131194 | intron-variant | Klhl32 | Mm_Celera | 4:24683419 | AGTGAGGATTAAGGA[C/T]GAAATACAAAACAAA | 212390 |
rs27719169 | snp | A/G | 0.46875 | 0.121031 | intron-variant | Klhl32 | Mm_Celera | 4:24683358 | TCTACCCTTCCTGTA[A/G]TTTAGTTTAGCTTTT | 212390 |
rs27719170 | snp | C/T | 0.132653 | 0.220748 | synonymous-codon | Klhl32 | Mm_Celera | 4:24682166 | GCTCTTCAGGAGCTC[C/T]GAGAGATGCTTCACT | 212390 |
rs27719171 | snp | A/G | 0.132653 | 0.220748 | intron-variant | Klhl32 | Mm_Celera | 4:24682040 | CCTTCCTGAGGTCAG[A/G]CACCATGTCCTTACC | 212390 |
rs27719172 | snp | C/T | 0.459184 | 0.136902 | intron-variant | Klhl32 | GRCm38.p3 | 4:24682001 | TTGTTGCTCCAGAGT[C/T]CTTCCCTTTCTAATC | 212390 |
rs27719173 | snp | C/T | 0.35503 | 0.226867 | intron-variant | Klhl32 | GRCm38.p3 | 4:24681930 | CCTTCAGTGACTTGC[C/T]TAACTAGGGAGCAGG | 212390 |
rs27719174 | snp | C/T | 0.132653 | 0.220748 | intron-variant | Klhl32 | Mm_Celera | 4:24681907 | AAGTTGGGCTGCAGA[C/T]CTGGTAGCCTTCAGT | 212390 |
rs27719175 | snp | A/G | 0.375 | 0.216506 | intron-variant | Klhl32 | Mm_Celera | 4:24681882 | GAAGCCACAGTAGTG[A/G]CCTCATCCCAAGTTG | 212390 |
rs27719176 | snp | A/G | 0.5 | 0 | intron-variant | Klhl32 | GRCm38.p3 | 4:24681825 | ATATTTTTTGTCTTC[A/G]AGAGAAAATTCTTTT | 212390 |
rs27719177 | snp | A/G | 0.244898 | 0.249948 | intron-variant | Klhl32 | Mm_Celera | 4:24681734 | ATTCCTTTAGATTCA[A/G]TGGCTTAAGTATGTA | 212390 |
rs27719178 | snp | A/G | 0.473373 | 0.11227 | intron-variant | Klhl32 | Mm_Celera | 4:24681553 | ACCCAAACTTAAATC[A/G]TCAAAATTAGCCAAC | 212390 |
rs27719179 | snp | C/T | 0.46875 | 0.121031 | intron-variant | Klhl32 | Mm_Celera | 4:24680711 | TGTTATAAGGAATCA[C/T]GCTATTAACTATCTG | 212390 |
rs27719180 | snp | G/T | 0.473373 | 0.11227 | intron-variant | Klhl32 | Mm_Celera | 4:24680697 | ATGTCTGAAAACGCT[G/T]TTATAAGGAATCATG | 212390 |
rs27719181 | snp | C/T | 0.426035 | 0.177515 | intron-variant | Klhl32 | GRCm38.p3 | 4:24680540 | GATAGAGCAATAGAT[C/T]AGAGTACACGGAATC | 212390 |
rs27719182 | snp | C/T | 0.459184 | 0.136902 | intron-variant | Klhl32 | GRCm38.p3 | 4:24680364 | CATAATGAACCATGG[C/T]AGGAAGATTTGTTTT | 212390 |
rs27719183 | snp | A/T | 0.426035 | 0.177515 | intron-variant | Klhl32 | GRCm38.p3 | 4:24680236 | GGATTTAAATTGAAT[A/T]ATCAACTCTCCAACA | 212390 |
rs27719184 | snp | A/G | 0.473373 | 0.11227 | intron-variant | Klhl32 | GRCm38.p3 | 4:24680140 | AGCTAGGCAGCGAAG[A/G]GAGAAGGGATAAAAT | 212390 |
rs27719185 | snp | A/G | 0.46281 | 0.131194 | intron-variant | Klhl32 | GRCm38.p3 | 4:24680058 | TAGCAGATAGCAACT[A/G]TTCATATCATCCTGC | 212390 |
rs27719186 | snp | C/T | 0.48 | 0.0979796 | intron-variant | Klhl32 | Mm_Celera | 4:24680026 | TCTGCCCATAGAACC[C/T]TGAACTTCTCCTAGT | 212390 |
rs27719187 | snp | A/G | 0.486111 | 0.0821678 | intron-variant | Klhl32 | Mm_Celera | 4:24679985 | TCCTGAACATTTTTG[A/G]TAAGATAAGTGCTTA | 212390 |
rs27719188 | snp | C/T | 0.132653 | 0.220748 | intron-variant | Klhl32 | Mm_Celera | 4:24679944 | TCAGGTGTTAGATGA[C/T]ACATTTTGACCAGTG | 212390 |
rs27719189 | snp | G/T | 0.35503 | 0.226867 | intron-variant | Klhl32 | GRCm38.p3 | 4:24679705 | TGGATTGGAAGGGTG[G/T]CTCTGCTCTGTAAAC | 212390 |
rs27719190 | snp | A/C | 0.489796 | 0.070696 | intron-variant | Klhl32 | Mm_Celera | 4:24679593 | TGCAACCATGGCAAA[A/C]CTTCCTAGAAATGCC | 212390 |
rs27719191 | snp | A/G | 0.48 | 0.0979796 | intron-variant | Klhl32 | Mm_Celera | 4:24679573 | ACCGCATCCTCAACA[A/G]CTCTTGCAACCATGG | 212390 |
rs27719192 | snp | A/G | 0.459184 | 0.136902 | intron-variant | Klhl32 | GRCm38.p3 | 4:24679491 | TTCATACTCTGAGCT[A/G]GCCATAGTAAATTCT | 212390 |
rs27719193 | snp | A/C | 0.486111 | 0.0821678 | intron-variant | Klhl32 | GRCm38.p3 | 4:24679446 | GAATCCATTGTGTTT[A/C]TTTTTCCCTTAATGA | 212390 |
rs27719194 | snp | C/T | 0.375 | 0.216506 | intron-variant | Klhl32 | GRCm38.p3 | 4:24679422 | GTGTTAGTAAAAAAC[C/T]GACATACAGAATCCA | 212390 |
rs27719195 | snp | C/G | 0.132653 | 0.220748 | intron-variant | Klhl32 | Mm_Celera | 4:24679385 | CAGATGTCACAAGAA[C/G]AGGTGACTTCAAATC | 212390 |
rs27719196 | snp | A/C | 0.132653 | 0.220748 | intron-variant | Klhl32 | Mm_Celera | 4:24679349 | CTAAGGCAGTGCCTA[A/C]AACTATGGGAAAATA | 212390 |
rs27719197 | snp | A/T | 0.132653 | 0.220748 | intron-variant | Klhl32 | Mm_Celera | 4:24679288 | TTCTATACAGACAGA[A/T]TGGAATTTTCCTGAT | 212390 |
rs27719198 | snp | A/G | 0.132653 | 0.220748 | intron-variant | Klhl32 | Mm_Celera | 4:24678781 | TTTAAGACATGGGAT[A/G]GGGATTTGTCAAAGT | 212390 |
rs27719199 | snp | A/T | 0.484429 | 0.0868505 | intron-variant | Klhl32 | Mm_Celera | 4:24678399 | TAGTTGGCTCATGGG[A/T]CCACAAAATGGTCAT | 212390 |
rs27719200 | snp | C/T | 0.132653 | 0.220748 | intron-variant | Klhl32 | Mm_Celera | 4:24677988 | AAACGAAGGAAAACC[C/T]GTCTGGATAAGACTA | 212390 |
rs27719201 | snp | C/G | 0.465374 | 0.126941 | intron-variant | Klhl32 | GRCm38.p3 | 4:24677811 | AGAAATCATTGTCCT[C/G]AAGACATAAACCAAG | 212390 |
rs27719202 | snp | A/C | 0.475309 | 0.108333 | intron-variant | Klhl32 | Mm_Celera | 4:24677778 | GATAATAATTTGGTG[A/C]CTTTCCTTTGGAACT | 212390 |
rs27719203 | snp | C/T | 0.132653 | 0.220748 | intron-variant | Klhl32 | Mm_Celera | 4:24677751 | GCTGGTTGTGTTTCT[C/T]CTTTCTTTGAAGATA | 212390 |
rs27719204 | snp | C/G | 0.459184 | 0.136902 | intron-variant | Klhl32 | GRCm38.p3 | 4:24677677 | CTGGTAGAAATTTGC[C/G]AGACAACACAGTGAG | 212390 |
rs27719205 | snp | C/T | 0.486111 | 0.0821678 | intron-variant | Klhl32 | Mm_Celera | 4:24677185 | TTGAATTATTTCATT[C/T]TGAGCTGTTTTTCTT | 212390 |
rs27719206 | snp | C/T | 0.46875 | 0.121031 | intron-variant | Klhl32 | GRCm38.p3 | 4:24677071 | GAGATTCACCTCCCA[C/T]TCTAGAGAAATCTAG | 212390 |
rs27719207 | snp | G/T | 0.124444 | 0.216185 | intron-variant | Klhl32 | Mm_Celera | 4:24676926 | CAACTGTGCTCTGTT[G/T]TCCACCTCAAGAGAC | 212390 |
rs27719208 | snp | C/G | 0.46281 | 0.131194 | intron-variant | Klhl32 | GRCm38.p3 | 4:24676901 | GTCTTGGGGAAGAAA[C/G]AGAGTTATCCAACTG | 212390 |
rs27719209 | snp | A/C | 0.444444 | 0.157135 | intron-variant | Klhl32 | GRCm38.p3 | 4:24676356 | AAGCATTGTTAGAGA[A/C]TATATAGGAAGTGTT | 212390 |
rs27719210 | snp | A/C | 0.48 | 0.0979796 | intron-variant | Klhl32 | GRCm38.p3 | 4:24676317 | GAAGAAAGTGTCTAC[A/C]AGCCAAGGACAACAA | 212390 |
rs27719211 | snp | C/T | 0.277778 | 0.248452 | intron-variant | Klhl32 | Mm_Celera | 4:24676295 | AGCATGGACATCTTA[C/T]GAATAGGAAGAAAGT | 212390 |
rs27719212 | snp | A/G | 0.42 | 0.183303 | intron-variant | Klhl32 | GRCm38.p3 | 4:24676271 | GGATTATACCAGCTC[A/G]AAAGAGATAGCATGG | 212390 |
rs27719213 | snp | C/T | 0.444444 | 0.157135 | intron-variant | Klhl32 | GRCm38.p3 | 4:24676040 | TTTTAAAAGGCCAAA[C/T]GCATTGTCTATACCG | 212390 |
rs27719214 | snp | A/C | 0.132653 | 0.220748 | intron-variant | Klhl32 | Mm_Celera | 4:24675958 | AAGAGGCTGTTGACT[A/C]CCCTCTCCAGTCTGT | 212390 |
rs27719215 | snp | C/G | 0.336735 | 0.234472 | intron-variant | Klhl32 | Mm_Celera | 4:24675937 | AACAAAAAATCATCA[C/G]CACAGAAGAGGCTGT | 212390 |
rs27719216 | snp | C/G | 0.132653 | 0.220748 | intron-variant | Klhl32 | Mm_Celera | 4:24675858 | GAAAATGAGTAAGTT[C/G]AAACACCATGCATGG | 212390 |
rs27719217 | snp | C/G | 0.142012 | 0.225474 | intron-variant | Klhl32 | GRCm38.p3 | 4:24675789 | AGTCACTCAGGGCCT[C/G]CACCTTCTGACTATG | 212390 |
rs27719218 | snp | C/T | 0.473373 | 0.11227 | intron-variant | Klhl32 | GRCm38.p3 | 4:24675730 | GATCAGAAGTATATT[C/T]GGGTCAGGTTATCAT | 212390 |
rs27719219 | snp | C/T | 0.197531 | 0.244432 | intron-variant | Klhl32 | Mm_Celera | 4:24675681 | ACAGGGATGCATTGG[C/T]TCACCAGTTGCAGTG | 212390 |
rs27719220 | snp | C/T | 0.493827 | 0.0552116 | intron-variant | Klhl32 | GRCm38.p3 | 4:24675675 | AGAAGCACAGGGATG[C/T]ATTGGTTCACCAGTT | 212390 |
rs27719221 | snp | A/G | 0.32 | 0.24 | intron-variant | Klhl32 | Mm_Celera | 4:24675668 | GTAAATCAGAAGCAC[A/G]GGGATGCATTGGTTC | 212390 |
rs27719222 | snp | A/G | 0.489796 | 0.070696 | intron-variant | Klhl32 | GRCm38.p3 | 4:24675666 | GTGTAAATCAGAAGC[A/G]CAGGGATGCATTGGT | 212390 |
rs27719223 | snp | A/G | 0.456747 | 0.140554 | intron-variant | Klhl32 | GRCm38.p3 | 4:24675549 | ATAGGTACAAAGTTA[A/G]GGGACAGGAATTTGC | 212390 |
rs27719224 | snp | A/G | 0.290657 | 0.246672 | intron-variant | Klhl32 | GRCm38.p3 | 4:24675444 | CACTGAGATATACCC[A/G]GCCTTTCCTAATTTT | 212390 |
rs27719225 | snp | C/T | 0.142012 | 0.225474 | intron-variant | Klhl32 | Mm_Celera | 4:24675363 | TAAAATGTCTTCTTA[C/T]GTCTCCATTTCTTTA | 212390 |
rs27719226 | snp | G/T | 0.231111 | 0.249285 | intron-variant | Klhl32 | Mm_Celera | 4:24675343 | CACAGAGAACCGCAA[G/T]AGCTTAAAATGTCTT | 212390 |
rs27719227 | snp | A/C | 0.132653 | 0.220748 | intron-variant | Klhl32 | Mm_Celera | 4:24675244 | GAAGCACGGCCATAG[A/C]ACACAGAAGAATAAG | 212390 |
rs27719228 | snp | G/T | 0.132653 | 0.220748 | intron-variant | Klhl32 | Mm_Celera | 4:24675224 | GTTATCATGAATGAA[G/T]GACTGAAGCACGGCC | 212390 |
rs27719229 | snp | A/G | 0.375 | 0.216506 | intron-variant | Klhl32 | GRCm38.p3 | 4:24675196 | GGCTGCCACAGCAGG[A/G]CCTCAGTACCTAGTT | 212390 |
rs27719230 | snp | C/G | 0.426035 | 0.177515 | intron-variant | Klhl32 | GRCm38.p3 | 4:24675175 | CAAGAGTGCTCAGTA[C/G]CATCTGGCTGCCACA | 212390 |
rs27719231 | snp | C/T | 0.142012 | 0.225474 | intron-variant | Klhl32 | Mm_Celera | 4:24675160 | ACTTACCGCAGGCAG[C/T]AAGAGTGCTCAGTAC | 212390 |
rs27719232 | snp | C/T | 0.432133 | 0.171253 | intron-variant | Klhl32 | GRCm38.p3 | 4:24674998 | AGGAACCCTGGATGC[C/T]GAGGGAATGTCCAAG | 212390 |
rs27719233 | snp | A/G | 0.49827 | 0.0293608 | intron-variant | Klhl32 | Mm_Celera | 4:24674738 | ACAACTTATGCACAA[A/G]AATAGACAAGGATAA | 212390 |
rs27719234 | snp | C/G | 0.304688 | 0.243945 | intron-variant, downstream-variant-500B | Klhl32, Gm31436 | Mm_Celera | 4:24674552 | ATTTAATAGAATGTA[C/G]AAGACTGTATCCGCT | 212390 |
rs27719235 | snp | A/G | 0.359862 | 0.224567 | intron-variant, downstream-variant-500B | Klhl32, Gm31436 | GRCm38.p3 | 4:24674484 | AAAAGAAGCATCCTC[A/G]GGACTGCACCATTTG | 212390 |
rs27719236 | snp | A/G | 0.260355 | 0.249785 | intron-variant, downstream-variant-500B | Klhl32, Gm31436 | Mm_Celera | 4:24674431 | AAGTACCAAGCCCAG[A/G]CAGAACAGCATCTCT | 212390 |
rs27719237 | snp | C/G | 0.132653 | 0.220748 | intron-variant, downstream-variant-500B | Klhl32, Gm31436 | Mm_Celera | 4:24674412 | AATACACAGTAGCAT[C/G]TTCAAGTACCAAGCC | 212390 |
rs27719238 | snp | A/C | 0.231111 | 0.249285 | intron-variant, downstream-variant-500B | Klhl32, Gm31436 | Mm_Celera | 4:24674353 | GCTACCGGGGAAGCG[A/C]CCGCACGGAGAATTA | 212390 |
rs27719239 | snp | C/T | 0.48 | 0.0979796 | intron-variant, nc-transcript-variant | Klhl32, Gm31436 | Mm_Celera | 4:24674066 | TCATATCTCATAAAT[C/T]ACCTTCTTGTTCTGT | 212390 |
rs27719240 | snp | A/C | 0.32 | 0.24 | intron-variant, nc-transcript-variant | Klhl32, Gm31436 | Mm_Celera | 4:24673716 | GATAAAACTTGCCTC[A/C]TACACTATAATAAGT | 212390 |
rs27719241 | snp | C/T | 0.35503 | 0.226867 | intron-variant, nc-transcript-variant | Klhl32, Gm31436 | Mm_Celera | 4:24673598 | GATGCTTGGTGTATT[C/T]TGAGAGAATAAAGTA | 212390 |
rs27719242 | snp | A/T | 0.277778 | 0.248452 | intron-variant, nc-transcript-variant | Klhl32, Gm31436 | Mm_Celera | 4:24673451 | TTTTTGCTGTTTCCC[A/T]CAGAGTTGTACAAGA | 212390 |
rs27719243 | snp | A/C | 0.35503 | 0.226867 | intron-variant, nc-transcript-variant | Klhl32, Gm31436 | GRCm38.p3 | 4:24673301 | CATTCTGACGAACAT[A/C]AGGTACTTCACTGAG | 212390 |
rs27719244 | snp | A/G | 0.142012 | 0.225474 | intron-variant, nc-transcript-variant | Klhl32, Gm31436 | Mm_Celera | 4:24673295 | CCTTGGCATTCTGAC[A/G]AACATAAGGTACTTC | 212390 |
rs27719245 | snp | A/G | 0.297521 | 0.245442 | intron-variant, nc-transcript-variant | Klhl32, Gm31436 | GRCm38.p3 | 4:24673249 | AAGTCGCCTCACAGG[A/G]TCTGCAAGTGACTCC | 212390 |
rs27719246 | snp | A/G | 0.124444 | 0.216185 | intron-variant, nc-transcript-variant | Klhl32, Gm31436 | Mm_Celera | 4:24673164 | TAGAAACCATAGCCT[A/G]CGGATTTGCCCAGTC | 212390 |
rs27719247 | snp | A/G | 0.277778 | 0.248452 | intron-variant | Klhl32, Gm31436 | GRCm38.p3 | 4:24673023 | TATCTCTTAAACTCC[A/G]TATCTAGGCTGTTAT | 212390 |
rs27719248 | snp | C/T | 0.152778 | 0.230321 | intron-variant | Klhl32, Gm31436 | Mm_Celera | 4:24672972 | GACACTAATACCAAA[C/T]CAATACATACCGATT | 212390 |
rs27719249 | snp | G/T | 0.336735 | 0.234472 | intron-variant | Klhl32, Gm31436 | GRCm38.p3 | 4:24672945 | AGTGACCTGGTACTG[G/T]ACAACATGGAAGACA | 212390 |
rs27719250 | snp | C/T | 0.473373 | 0.11227 | intron-variant | Klhl32, Gm31436 | GRCm38.p3 | 4:24672829 | CTTTGAGTTCTTGGG[C/T]CACTCTACATAGATG | 212390 |
rs27719251 | snp | C/T | 0.46281 | 0.131194 | intron-variant, nc-transcript-variant | Klhl32, Gm31436 | Mm_Celera | 4:24672653 | ACAGGGCTCATGCAC[C/T]CCAGGTAAGTACCCA | 212390 |
rs27719252 | snp | C/T | 0.277778 | 0.248452 | intron-variant, nc-transcript-variant | Klhl32, Gm31436 | Mm_Celera | 4:24672639 | GGTAGAGATGGACTA[C/T]AGGGCTCATGCACTC | 212390 |
rs27719253 | snp | C/T | 0.152778 | 0.230321 | intron-variant, nc-transcript-variant | Klhl32, Gm31436 | Mm_Celera | 4:24672579 | GTGGCCTTGGAATCA[C/T]TTGTTTCCAGATATT | 212390 |
rs27719254 | snp | A/G | 0.444444 | 0.157135 | intron-variant, nc-transcript-variant | Klhl32, Gm31436 | Mm_Celera | 4:24672564 | GTTCTCATGCAGACC[A/G]TGGCCTTGGAATCAC | 212390 |
rs27719255 | snp | C/T | 0.48 | 0.0979796 | intron-variant, nc-transcript-variant | Klhl32, Gm31436 | GRCm38.p3 | 4:24672532 | AAAGAGAACCTAAGA[C/T]TCATCTCTTTCTATG | 212390 |
rs27719256 | snp | C/T | 0.48 | 0.0979796 | intron-variant, nc-transcript-variant | Klhl32, Gm31436 | GRCm38.p3 | 4:24672468 | GAGGTGCTAGAACCA[C/T]GATGGAGAACGTCAT | 212390 |
rs27719257 | snp | C/T | 0.165289 | 0.235211 | intron-variant | Klhl32, Gm31436 | GRCm38.p3 | 4:24672355 | ACATCAAGGTCCTTT[C/T]AACTCTCCCTAAAAT | 212390 |
rs27719258 | snp | A/G | 0.375 | 0.216506 | intron-variant | Klhl32, Gm31436 | Mm_Celera | 4:24672348 | TTGGAAAACATCAAG[A/G]TCCTTTCAACTCTCC | 212390 |
rs27719259 | snp | C/T | 0.46281 | 0.131194 | intron-variant | Klhl32, Gm31436 | Mm_Celera | 4:24672255 | AACAAAATATGAGTG[C/T]CTCTTACCAATACTG | 212390 |
rs27719260 | snp | C/G | 0.444444 | 0.157135 | intron-variant | Klhl32, Gm31436 | Mm_Celera | 4:24672252 | TTGAACAAAATATGA[C/G]TGCCTCTTACCAATA | 212390 |
rs27719261 | snp | A/G | 0.124444 | 0.216185 | intron-variant | Klhl32, Gm31436 | Mm_Celera | 4:24672218 | AATCTCAAGTGTGAT[A/G]GGCTCTTTTGACTTG | 212390 |
rs27719262 | snp | A/C | 0.495868 | 0.0452663 | intron-variant | Klhl32, Gm31436 | GRCm38.p3 | 4:24672188 | AGAGCACACACTAGG[A/C]AGACAGAAGTTTTCA | 212390 |
rs27719263 | snp | C/G | 0.260355 | 0.249785 | intron-variant | Klhl32, Gm31436 | Mm_Celera | 4:24671912 | GTTTTCCTTTCAGCT[C/G]TGAGTAATTTCCCAT | 212390 |
rs27719264 | snp | A/G | 0.408163 | 0.193609 | intron-variant | Klhl32, Gm31436 | GRCm38.p3 | 4:24671832 | TGCCAGTCTCACACC[A/G]GAAGAGAAGGATGCT | 212390 |
rs27719265 | snp | A/G | 0.231111 | 0.249285 | intron-variant | Klhl32, Gm31436 | Mm_Celera | 4:24671707 | TCAGCATTGGTGAAC[A/G]CCTTTATTTACCACA | 212390 |
rs27719266 | snp | C/T | 0.277778 | 0.248452 | intron-variant | Klhl32, Gm31436 | GRCm38.p3 | 4:24671678 | AGAGCAAAGCCCGCT[C/T]TTCAGGAATCCTGTC | 212390 |
rs27719267 | snp | C/T | 0.444444 | 0.157135 | intron-variant | Klhl32, Gm31436 | GRCm38.p3 | 4:24671635 | CACGTAGCCCCTTTA[C/T]AGCATCCGAATCTTA | 212390 |
rs27735044 | snp | C/T | 0.124444 | 0.216185 | upstream-variant-2KB, intron-variant | Klhl32, Gm31379 | Mm_Celera | 4:24851789 | AGGTTTGTGTTCTTC[C/T]ATACACTGGAGCTAG | 212390 |
rs27735045 | snp | A/G | 0.142012 | 0.225474 | upstream-variant-2KB, nc-transcript-variant | Klhl32, Gm31379 | Mm_Celera | 4:24851691 | AGTGGTAGACTTGAA[A/G]TTGGAGAGAAATACT | 212390 |
rs27735046 | snp | C/T | 0.132653 | 0.220748 | upstream-variant-2KB, nc-transcript-variant | Klhl32, Gm31379 | Mm_Celera | 4:24851455 | TTTAAGAAACCATAG[C/T]CTGCATAGGTAGACT | 212390 |
rs27735047 | snp | G/T | 0.124444 | 0.216185 | upstream-variant-2KB | Klhl32, Gm31379 | Mm_Celera | 4:24851191 | CGAGCCGCTTGTCGC[G/T]GGTCACGCGCACAGC | 212390 |
rs27735048 | snp | G/T | 0.484429 | 0.0868505 | upstream-variant-2KB | Klhl32, Gm31379 | GRCm38.p3 | 4:24851177 | CGCGCTCCCGCACCC[G/T]AGCCGCTTGTCGCGG | 212390 |
rs27735049 | snp | A/G | 0.459184 | 0.136902 | utr-variant-5-prime, upstream-variant-2KB | Klhl32, Gm31379 | GRCm38.p3 | 4:24850907 | CGCGCTCTGGCGTGT[A/G]TGTGGATGCGAGTCG | 212390 |
rs27735050 | snp | A/G | 0.124444 | 0.216185 | intron-variant, upstream-variant-2KB | Klhl32, Gm31379 | Mm_Celera | 4:24850725 | CCTGTCACAAGGAGA[A/G]AGACTGGCTTACCCG | 212390 |
rs27735051 | snp | C/T | 0.260355 | 0.249785 | intron-variant, upstream-variant-2KB | Klhl32, Gm31379 | Mm_Celera | 4:24850712 | CACTAATTCCGAACC[C/T]GTCACAAGGAGAGAG | 212390 |
rs27735052 | snp | C/T | 0.124444 | 0.216185 | intron-variant, upstream-variant-2KB | Klhl32, Gm31379 | Mm_Celera | 4:24850399 | AAGTTGCCACAAGGT[C/T]CTCAATGCACATACT | 212390 |
rs27735053 | snp | C/T | 0.124444 | 0.216185 | intron-variant, upstream-variant-2KB | Klhl32, Gm31379 | Mm_Celera | 4:24850069 | TGTTGCCTTAGAAAT[C/T]CACAGGCGCTGTTCC | 212390 |
rs27735054 | snp | C/G | 0.124444 | 0.216185 | intron-variant, upstream-variant-2KB | Klhl32, Gm31379 | Mm_Celera | 4:24850033 | GAAACGCTGTATGTC[C/G]TGAGTGAATGTCATC | 212390 |
rs27735055 | snp | C/T | 0.231111 | 0.249285 | intron-variant, upstream-variant-2KB | Klhl32, Gm31379 | Mm_Celera | 4:24849946 | ATAGAAACGAAGCTT[C/T]AACTTCTAATCAACC | 212390 |
rs27735056 | snp | A/G | 0.375 | 0.216506 | intron-variant, upstream-variant-2KB | Klhl32, Gm31379 | GRCm38.p3 | 4:24849782 | GTCCAGGTACGAGGG[A/G]CTCCTGTGAGGTCAG | 212390 |
rs27735057 | snp | A/T | 0.231111 | 0.249285 | intron-variant, upstream-variant-2KB | Klhl32, Gm31379 | Mm_Celera | 4:24849735 | TTCACTCACTAAACA[A/T]CTGAGAGGAAAAGAA | 212390 |
rs27735058 | snp | A/G | 0.231111 | 0.249285 | intron-variant, upstream-variant-2KB | Klhl32, Gm31379 | Mm_Celera | 4:24849541 | TTTGACAGAACTCAA[A/G]ATCTAAATTAAAGAA | 212390 |
rs27735059 | snp | C/G | 0.124444 | 0.216185 | intron-variant, upstream-variant-2KB | Klhl32, Gm31379 | Mm_Celera | 4:24849325 | AGCTATGCTCTGAGA[C/G]TGAGTGATGGTTTGG | 212390 |
rs27735060 | snp | A/G | 0.124444 | 0.216185 | intron-variant | Klhl32 | Mm_Celera | 4:24849240 | TCAACTTAATGAAAA[A/G]AGCTTGGATCCGAAC | 212390 |
rs27735061 | snp | A/G | 0.142012 | 0.225474 | intron-variant | Klhl32 | Mm_Celera | 4:24849238 | AATCAACTTAATGAA[A/G]AGAGCTTGGATCCGA | 212390 |
rs27735062 | snp | C/G | 0.124444 | 0.216185 | intron-variant | Klhl32 | Mm_Celera | 4:24849012 | AGCCTCAGTACTGAA[C/G]GACCATGTACCAGGA | 212390 |
rs27735063 | snp | C/T | 0.244898 | 0.249948 | intron-variant | Klhl32 | Mm_Celera | 4:24848971 | ACAAATGTAGTAATT[C/T]GAATCCCAGAACCGG | 212390 |
rs27735064 | snp | A/G | 0.124444 | 0.216185 | intron-variant | Klhl32 | Mm_Celera | 4:24848697 | TTTGTTTCAACATAT[A/G]CAAAATTCTCACCAA | 212390 |
rs27735065 | snp | C/G | 0.493827 | 0.0552116 | intron-variant | Klhl32 | Mm_Celera | 4:24848264 | AACCTACAATTAAAG[C/G]AAGATTCTATTCTAT | 212390 |
rs27735066 | snp | G/T | 0.132653 | 0.220748 | intron-variant | Klhl32 | Mm_Celera | 4:24848188 | AGGACTCAGGACTGT[G/T]GCATCTTGCAGTATC | 212390 |
rs27735067 | snp | G/T | 0.124444 | 0.216185 | intron-variant | Klhl32 | Mm_Celera | 4:24848186 | AGAGGACTCAGGACT[G/T]TGGCATCTTGCAGTA | 212390 |
rs27735068 | snp | A/G | 0.124444 | 0.216185 | intron-variant | Klhl32 | Mm_Celera | 4:24848129 | GCCTCTGGAAGCAAC[A/G]GGATGTGTGTTCTGA | 212390 |
rs27735069 | snp | C/T | 0.124444 | 0.216185 | intron-variant | Klhl32 | Mm_Celera | 4:24848062 | AGGACACTGTACATC[C/T]AGCAGGAGACTGATG | 212390 |
rs27735070 | snp | A/G | 0.197531 | 0.244432 | intron-variant | Klhl32 | Mm_Celera | 4:24848007 | TTGTTCTAGTTTCAT[A/G]TTCTTCATCTATAAC | 212390 |
rs27735071 | snp | A/G | 0.231111 | 0.249285 | intron-variant | Klhl32 | Mm_Celera | 4:24847950 | AAGGACAAAGGGAAC[A/G]CAAAGAGCAAAGGAA | 212390 |
rs27735072 | snp | A/G | 0.124444 | 0.216185 | intron-variant | Klhl32 | Mm_Celera | 4:24847923 | ATATTCTATAACCTC[A/G]ACTAGGTAACTAAGG | 212390 |
rs27735073 | snp | A/G | 0.231111 | 0.249285 | intron-variant | Klhl32 | Mm_Celera | 4:24847802 | CCTAGGGCTTTAACC[A/G]TGCTACACATTCTAT | 212390 |
rs27735074 | snp | A/G | 0.132653 | 0.220748 | intron-variant | Klhl32 | Mm_Celera | 4:24847609 | TTCACCTTTTAATGG[A/G]TCAAAAGGTCTGCAT | 212390 |
rs27735075 | snp | A/C | 0.408163 | 0.193609 | intron-variant | Klhl32 | Mm_Celera | 4:24847563 | GCTATCCTCTAGTTC[A/C]TATTTCCAACTTGAA | 212390 |
rs27735076 | snp | A/T | 0.35503 | 0.226867 | intron-variant | Klhl32 | Mm_Celera | 4:24847541 | CAGCACTTTGGCTCT[A/T]ACTAGGGCTATCCTC | 212390 |
rs27735077 | snp | C/T | 0.124444 | 0.216185 | intron-variant | Klhl32 | Mm_Celera | 4:24847534 | ATGAGCTCAGCACTT[C/T]GGCTCTAACTAGGGC | 212390 |
rs27735078 | snp | C/T | 0.124444 | 0.216185 | intron-variant | Klhl32 | Mm_Celera | 4:24847403 | ACATGGATTGTCCTC[C/T]AAGTCTACAATGCCT | 212390 |
rs27735079 | snp | C/T | 0.124444 | 0.216185 | intron-variant | Klhl32 | Mm_Celera | 4:24847361 | CTAGTCCCCTGCCGT[C/T]GGAGCTTTTACAGAA | 212390 |
rs27735080 | snp | A/G | 0.124444 | 0.216185 | intron-variant | Klhl32 | Mm_Celera | 4:24846907 | CTTTTATCTGCAAAA[A/G]TACCGAAATCCGTGA | 212390 |
rs27735081 | snp | A/C | 0.260355 | 0.249785 | intron-variant | Klhl32 | GRCm38.p3 | 4:24846814 | GTGAGGAATGACAGA[A/C]GAACACTTCTAACCA | 212390 |
rs27735082 | snp | C/T | 0.124444 | 0.216185 | intron-variant | Klhl32 | Mm_Celera | 4:24846439 | GGTCACTAAAGGTTT[C/T]CTTCTAGATTTGAAC | 212390 |
rs27735083 | snp | A/T | 0.444444 | 0.157135 | intron-variant | Klhl32 | GRCm38.p3 | 4:24846342 | ACTTTAATCCATGTG[A/T]AACTTCCACAGACTA | 212390 |
rs27735084 | snp | C/T | 0.444444 | 0.157135 | intron-variant | Klhl32 | GRCm38.p3 | 4:24846334 | GATGCAGTACTTTAA[C/T]CCATGTGAAACTTCC | 212390 |
rs27735085 | snp | C/T | 0.124444 | 0.216185 | intron-variant | Klhl32 | Mm_Celera | 4:24846305 | ATCGTTGGCAGCTCT[C/T]GTAGCCAGTCACTGA | 212390 |
rs27735086 | snp | A/G | 0.35503 | 0.226867 | intron-variant | Klhl32 | GRCm38.p3 | 4:24846290 | CTATTTTACTTCGCC[A/G]TCGTTGGCAGCTCTC | 212390 |
rs27735087 | snp | A/T | 0.426035 | 0.177515 | intron-variant | Klhl32 | GRCm38.p3 | 4:24846190 | AGCATGGCAAGAGAA[A/T]GCTCAAGCTATCTCC | 212390 |
rs27735088 | snp | A/G | 0.231111 | 0.249285 | intron-variant | Klhl32 | GRCm38.p3 | 4:24846167 | ACTGGAAGAAATGTT[A/G]AGCCAAGAGCATGGC | 212390 |
rs27735089 | snp | G/T | 0.493827 | 0.0552116 | intron-variant | Klhl32 | Mm_Celera | 4:24846118 | CCCAATAAGGAGAAG[G/T]AAAATGTTCTGGGGT | 212390 |
rs27735090 | snp | C/T | 0.124444 | 0.216185 | intron-variant | Klhl32 | Mm_Celera | 4:24846057 | ACCCAGTTAGAAATG[C/T]CAAGACCAGGAAGAA | 212390 |
rs27735091 | snp | C/T | 0.231111 | 0.249285 | intron-variant | Klhl32 | Mm_Celera | 4:24846015 | CTTAGGTCAACCACT[C/T]TTGCAAGGCAGGTCT | 212390 |
rs27735092 | snp | A/G | 0.132653 | 0.220748 | intron-variant | Klhl32 | Mm_Celera | 4:24845991 | AGTGCTTCCTCCTGC[A/G]CACCAAATCTTAGGT | 212390 |
rs27735093 | snp | G/T | 0.124444 | 0.216185 | intron-variant | Klhl32 | Mm_Celera | 4:24845781 | GCTTCCAAGCTGAGT[G/T]TGTAAGACTGTTACT | 212390 |
rs27735094 | snp | C/T | 0.444444 | 0.157135 | intron-variant | Klhl32 | GRCm38.p3 | 4:24845743 | TACATTTCCTGATGC[C/T]GTCCCATATGTGGAG | 212390 |
rs27735095 | snp | C/T | 0.142012 | 0.225474 | intron-variant | Klhl32 | Mm_Celera | 4:24845651 | AGAATCCATAAGATT[C/T]TCTTTCTTCATTTAA | 212390 |
rs27735096 | snp | A/G | 0.124444 | 0.216185 | intron-variant | Klhl32 | Mm_Celera | 4:24845613 | ATGTATCCTGCCTCA[A/G]ATAAATGTGTAGGGG | 212390 |
rs27735097 | snp | A/T | 0.336735 | 0.234472 | intron-variant | Klhl32 | GRCm38.p3 | 4:24845586 | CCTGGCTCATCTGAG[A/T]TGGAAAGCAGAATGT | 212390 |
rs27735098 | snp | A/G/T | 0.124444 | 0.216185 | intron-variant | Klhl32 | GRCm38.p3 | 4:24845516 | CCTGCACGCCAAGTC[A/G/T]GTTGTTCTGTCGGGG | 212390 |
rs27735099 | snp | A/G | 0.401235 | 0.199068 | intron-variant | Klhl32 | GRCm38.p3 | 4:24845480 | AATCAGCTGGGATGG[A/G]ACTGCTTATTCCATC | 212390 |
rs27735100 | snp | G/T | 0.493827 | 0.0552116 | intron-variant | Klhl32 | GRCm38.p3 | 4:24845214 | CTGAGGTGCTGGAGA[G/T]ATGTCACTTGGTTGT | 212390 |
rs27735101 | snp | C/T | 0.297521 | 0.245442 | intron-variant | Klhl32 | Mm_Celera | 4:24844079 | CACAGCATGTGATGA[C/T]GTCTGTCATGACAGG | 212390 |
rs27735102 | snp | C/T | 0.444444 | 0.157135 | intron-variant | Klhl32 | GRCm38.p3 | 4:24843907 | AGGGCAGCCCTGCCA[C/T]ATGCTTCCAGTTAGG | 212390 |
rs27735103 | snp | C/T | 0.391111 | 0.206368 | intron-variant | Klhl32 | GRCm38.p3 | 4:24843729 | CCTGGTGATGGGTTT[C/T]CTCTCCAAGATGGCA | 212390 |
rs27735104 | snp | A/C | 0.401235 | 0.199068 | intron-variant | Klhl32 | GRCm38.p3 | 4:24843708 | GAGAGCTCACTCAAG[A/C]AGCACCCTGGTGATG | 212390 |
rs27735105 | snp | A/C | 0.456747 | 0.140554 | intron-variant | Klhl32 | GRCm38.p3 | 4:24843450 | CAGATGGGGGCCCAT[A/C]GAGAGCTCTTGCAGT | 212390 |
rs27735106 | snp | G/T | 0.231111 | 0.249285 | intron-variant | Klhl32 | Mm_Celera | 4:24843408 | GAAAGGCCAGATCTA[G/T]CCCTGCCAGGTATTG | 212390 |
rs27735107 | snp | C/T | 0.375 | 0.216506 | intron-variant | Klhl32 | GRCm38.p3 | 4:24843348 | ATCATGAAAGGAAAT[C/T]GCTAGTTGTCTAGAA | 212390 |
rs27735108 | snp | A/C/T | 0.495868 | 0.0452663 | intron-variant | Klhl32 | GRCm38.p3 | 4:24843273 | TTGACAGAAAGCCTG[A/C/T]GGACTTCTTTTCTTT | 212390 |
rs27735109 | snp | C/T | 0.124444 | 0.216185 | intron-variant | Klhl32 | Mm_Celera | 4:24843171 | TTCCTAGCTGAAGGT[C/T]TGGGAACAAAAAGGA | 212390 |
rs27735110 | snp | C/T | 0.124444 | 0.216185 | intron-variant | Klhl32 | Mm_Celera | 4:24842200 | CAACAAAATCTATAT[C/T]TGCAAAGAACCCATA | 212390 |
rs27735111 | snp | A/G | 0.277778 | 0.248452 | intron-variant | Klhl32 | Mm_Celera | 4:24841896 | ACATTTTATAAGTCT[A/G]GTAGTGTGTGTATTT | 212390 |
rs27735112 | snp | A/C | 0.35503 | 0.226867 | intron-variant | Klhl32 | Mm_Celera | 4:24841697 | AGCAGCATTTTCATA[A/C]AGTACCAAACACCAT | 212390 |
rs27735113 | snp | C/G | 0.497041 | 0.0383476 | intron-variant | Klhl32 | Mm_Celera | 4:24841660 | CTAAAGGGTTTGCAT[C/G]CATATCACAGCCTGC | 212390 |
rs27735114 | snp | C/T | 0.21875 | 0.248039 | intron-variant | Klhl32 | Mm_Celera | 4:24841589 | AGAAACAATCGGGCA[C/T]GTCAGTTCAAGGACA | 212390 |
rs27735115 | snp | C/G | 0.277778 | 0.248452 | intron-variant | Klhl32 | GRCm38.p3 | 4:24841579 | AGAAGAGAAGAGAAA[C/G]AATCGGGCATGTCAG | 212390 |
rs27735116 | snp | C/T | 0.124444 | 0.216185 | intron-variant | Klhl32 | Mm_Celera | 4:24841385 | AAAGCCAATAAGCCA[C/T]GCCCAAATAAAACCA | 212390 |
rs27735117 | snp | C/T | 0.426035 | 0.177515 | intron-variant | Klhl32 | Mm_Celera | 4:24841345 | AATACCCTCCAGAAA[C/T]GAGAAAGTGCTCTCA | 212390 |
rs27735118 | snp | A/T | 0.459184 | 0.136902 | intron-variant | Klhl32 | GRCm38.p3 | 4:24841253 | TAAATGCTGTATTTT[A/T]AAAAGGCTCACGCTG | 212390 |
rs27735119 | snp | A/G | 0.444444 | 0.157135 | intron-variant | Klhl32 | GRCm38.p3 | 4:24841170 | TGAGGGCAGACAAAG[A/G]GAATTTGTCATAAAG | 212390 |
rs27735120 | snp | C/T | 0.444444 | 0.157135 | intron-variant | Klhl32 | Mm_Celera | 4:24841033 | TCATTAACTGTGGTC[C/T]TGCCCTCTGGAAACC | 212390 |
rs27735121 | snp | A/G | 0.124444 | 0.216185 | intron-variant | Klhl32 | Mm_Celera | 4:24841013 | AAAGCCTTAAGGTAA[A/G]TGCCTCATTAACTGT | 212390 |
rs27735122 | snp | A/T | 0.124444 | 0.216185 | intron-variant | Klhl32 | Mm_Celera | 4:24840981 | TCTGCCCAGGAACCC[A/T]AGCAATCATAGATGG | 212390 |
rs27735123 | snp | C/G | 0.48 | 0.0979796 | intron-variant | Klhl32 | Mm_Celera | 4:24840974 | TGTGGACTCTGCCCA[C/G]GAACCCAAGCAATCA | 212390 |
rs27735124 | snp | A/T | 0.444444 | 0.157135 | intron-variant | Klhl32 | Mm_Celera | 4:24840875 | GAGGGTTATTCCAAC[A/T]AGGCCCACCCCAGGC | 212390 |
rs27735125 | snp | C/T | 0.35503 | 0.226867 | intron-variant | Klhl32 | Mm_Celera | 4:24840788 | CGTAAAGGGTATATA[C/T]AAGTTGATCCCTACA | 212390 |
rs27735126 | snp | C/T | 0.391111 | 0.206368 | intron-variant | Klhl32 | Mm_Celera | 4:24840655 | GCTTGATCTTAAACG[C/T]CACACTGGATCTCTC | 212390 |
rs27735127 | snp | C/T | 0.473373 | 0.11227 | intron-variant | Klhl32 | Mm_Celera | 4:24840630 | CAGCTCTGACTCACT[C/T]TGAAGGTCAGCTTGA | 212390 |
rs27735128 | snp | A/G | 0.5 | 0 | intron-variant | Klhl32 | Mm_Celera | 4:24840597 | ATATAGAGAAGATCC[A/G]GGGACCTTGATTTAA | 212390 |
rs27735129 | snp | C/T | 0.493827 | 0.0552116 | intron-variant | Klhl32 | Mm_Celera | 4:24840559 | CAGATTCTAATATAG[C/T]ATCCATAGAGTATTT | 212390 |
rs27735130 | snp | C/T | 0.132653 | 0.220748 | intron-variant | Klhl32 | Mm_Celera | 4:24840522 | GAACTGTTTTGAATA[C/T]ACAAACAATTCTATA | 212390 |
rs27735131 | snp | C/G | 0.231111 | 0.249285 | intron-variant | Klhl32 | Mm_Celera | 4:24840488 | GGCTCCCAAGTTATA[C/G]CTCCTTGTAGAACCA | 212390 |
rs27735132 | snp | C/T | 0.124444 | 0.216185 | intron-variant | Klhl32 | Mm_Celera | 4:24840477 | TGTCCAACCCTGGCT[C/T]CCAAGTTATACCTCC | 212390 |
rs27735133 | snp | C/T | 0.391111 | 0.206368 | intron-variant | Klhl32 | Mm_Celera | 4:24840464 | GCGCAAGTTGCCATG[C/T]CCAACCCTGGCTCCC | 212390 |
rs27735134 | snp | A/G | 0.489796 | 0.070696 | intron-variant | Klhl32 | Mm_Celera | 4:24840442 | TAGAAAACAGAAGCT[A/G]ACTGTGGCGCAAGTT | 212390 |
rs27735135 | snp | A/G | 0.489796 | 0.070696 | intron-variant | Klhl32 | GRCm38.p3 | 4:24840057 | GGGAGTAAGAAAAAA[A/G]ATTGGTACACAATCC | 212390 |
rs27735136 | snp | A/G | 0.426035 | 0.177515 | intron-variant | Klhl32 | GRCm38.p3 | 4:24839957 | CTGAGTATCCAGAGC[A/G]CTAGCTTAGCCCGTG | 212390 |
rs27735137 | snp | C/T | 0.132653 | 0.220748 | intron-variant | Klhl32 | Mm_Celera | 4:24839956 | CCTGAGTATCCAGAG[C/T]GCTAGCTTAGCCCGT | 212390 |
rs27735138 | snp | C/G | 0.231111 | 0.249285 | intron-variant | Klhl32 | Mm_Celera | 4:24839642 | GCTGCATCCACTGCA[C/G]AGATAACACTCTCCA | 212390 |
rs27735139 | snp | A/G | 0.484429 | 0.0868505 | intron-variant | Klhl32 | GRCm38.p3 | 4:24839534 | CAAAAAGCAAACTAC[A/G]ATCTGAAAACTGGAA | 212390 |
rs27735140 | snp | C/T | 0.493827 | 0.0552116 | intron-variant | Klhl32 | GRCm38.p3 | 4:24839500 | TGTTCAGAACATGTG[C/T]TTTGAGGCTTCGACA | 212390 |
rs27735141 | snp | A/G | 0.487535 | 0.077957 | intron-variant | Klhl32 | GRCm38.p3 | 4:24839458 | GTCTCGGTGCTTAAC[A/G]GTTCCGTACCTCCTA | 212390 |
rs27735142 | snp | G/T | 0.142012 | 0.225474 | intron-variant | Klhl32 | Mm_Celera | 4:24839407 | CTTTCATGGCTGGTC[G/T]AATGGCAAAGATTCC | 212390 |
rs27735143 | snp | C/T | 0.444444 | 0.157135 | intron-variant | Klhl32 | GRCm38.p3 | 4:24839390 | TCTCTGAAGTGCATT[C/T]CCTTTCATGGCTGGT | 212390 |
rs27735144 | snp | A/G | 0.132653 | 0.220748 | intron-variant | Klhl32 | Mm_Celera | 4:24839242 | GACAGAGACACATGT[A/G]ACATCCACTTGCCCC | 212390 |
rs27735145 | snp | C/T | 0.33241 | 0.236027 | intron-variant | Klhl32 | GRCm38.p3 | 4:24839220 | GAATAGTGTTTCAGT[C/T]CCCAGGGACAGAGAC | 212390 |
rs27735146 | snp | A/G | 0.46875 | 0.121031 | intron-variant | Klhl32 | GRCm38.p3 | 4:24839187 | TACGTAACACAATGA[A/G]AGTCACCATAACAGT | 212390 |
rs27735147 | snp | G/T | 0.359862 | 0.224567 | intron-variant | Klhl32 | GRCm38.p3 | 4:24839150 | TATTAAAACGTTCTG[G/T]TAAGACTAGTTAACT | 212390 |
rs27735148 | snp | C/T | 0.48 | 0.0979796 | intron-variant | Klhl32 | GRCm38.p3 | 4:24838948 | CTTTTATTTCTCCTT[C/T]GGCTGTCCTTGCCAC | 212390 |
rs27735149 | snp | C/T | 0.124444 | 0.216185 | intron-variant | Klhl32 | Mm_Celera | 4:24838700 | TCTCTCTCATTTTTT[C/T]ATTGCATGTGGCCAC | 212390 |
rs27735150 | snp | A/G | 0.35503 | 0.226867 | intron-variant | Klhl32 | GRCm38.p3 | 4:24838540 | GTTAATCTGTGTTGT[A/G]CTCTGCACCTCAGGA | 212390 |
rs27735151 | snp | A/G | 0.359862 | 0.224567 | intron-variant | Klhl32 | Mm_Celera | 4:24838460 | GCTGAGAAAGGGCTC[A/G]CTGACGGGTGGAAGA | 212390 |
rs27735152 | snp | A/G | 0.124444 | 0.216185 | intron-variant | Klhl32 | Mm_Celera | 4:24837850 | AAGATTATTCTAGGT[A/G]TGGGGCCTAACTCCC | 212390 |
rs27735153 | snp | A/T | 0.124444 | 0.216185 | intron-variant | Klhl32 | Mm_Celera | 4:24837782 | TGCTCAAATTATAGG[A/T]TGCAGGATGAAAATC | 212390 |
rs27735154 | snp | A/G | 0.231111 | 0.249285 | intron-variant | Klhl32 | Mm_Celera | 4:24837077 | GGACAGATTCCATGT[A/G]CATGCTGAGGGAAGT | 212390 |
rs27735155 | snp | G/T | 0.132653 | 0.220748 | intron-variant | Klhl32 | Mm_Celera | 4:24837022 | AGTGATGATGTTCAC[G/T]AAGGGAAAGGAATGC | 212390 |
rs27735156 | snp | A/G | 0.231111 | 0.249285 | intron-variant | Klhl32 | Mm_Celera | 4:24836511 | GTAGATAACACACTG[A/G]ATCCTGGTAACAGCT | 212390 |
rs27735157 | snp | A/T | 0.231111 | 0.249285 | intron-variant | Klhl32 | Mm_Celera | 4:24836488 | GTCTATTTGCTGTAT[A/T]AGAAGCTGTAGATAA | 212390 |
rs27735158 | snp | C/T | 0.124444 | 0.216185 | intron-variant | Klhl32 | Mm_Celera | 4:24836463 | AGGATGAAAGCTATA[C/T]ACAGGTCAAGTCTAT | 212390 |
rs27735159 | snp | C/G | 0.124444 | 0.216185 | intron-variant | Klhl32 | Mm_Celera | 4:24836441 | CCAGTGAGGCACAGT[C/G]CTAGAAAGGATGAAA | 212390 |
rs27735160 | snp | C/T | 0.124444 | 0.216185 | intron-variant | Klhl32 | Mm_Celera | 4:24836393 | GGTTGGAACAACCAA[C/T]CTCTGTGCATTACCA | 212390 |
rs27735161 | snp | A/G | 0.46281 | 0.131194 | intron-variant | Klhl32 | GRCm38.p3 | 4:24836272 | ACCAGACACCAAACA[A/G]TGAAATTTATATAAT | 212390 |
rs27735162 | snp | C/T | 0.132653 | 0.220748 | intron-variant | Klhl32 | Mm_Celera | 4:24836177 | CAAGATGAATCATTA[C/T]CACCTTGGACCCATC | 212390 |
rs27735163 | snp | A/G | 0.231111 | 0.249285 | intron-variant | Klhl32 | Mm_Celera | 4:24836164 | ATCAAGTCTCTCCCA[A/G]GATGAATCATTACCA | 212390 |
rs27735164 | snp | G/T | 0.132653 | 0.220748 | intron-variant | Klhl32 | Mm_Celera | 4:24836131 | CATCACCCATAAATG[G/T]ATAATCACAGTAGAA | 212390 |
rs27735165 | snp | C/T | 0.132653 | 0.220748 | intron-variant | Klhl32 | Mm_Celera | 4:24836115 | AGCTTGCCTCTGTTC[C/T]CATCACCCATAAATG | 212390 |
rs27735166 | snp | A/G | 0.260355 | 0.249785 | intron-variant | Klhl32 | Mm_Celera | 4:24836077 | CATTATTTATTATTG[A/G]AAACTCTAGAGGGAG | 212390 |
rs27735167 | snp | A/G | 0.132653 | 0.220748 | intron-variant | Klhl32 | Mm_Celera | 4:24836047 | TTGGACTTTTAAATC[A/G]TAGGTGTCATTAAGC | 212390 |
rs27736068 | snp | C/T | 0.244898 | 0.249948 | intron-variant | Klhl32, Gm31436 | Mm_Celera | 4:24671604 | CCCAGAACCCAAGGG[C/T]CACGGAATGGTCCAT | 212390 |
rs27736069 | snp | A/G | 0.124444 | 0.216185 | intron-variant | Klhl32, Gm31436 | Mm_Celera | 4:24671587 | TAGGTCCACTTCTAA[A/G]GCCCAGAACCCAAGG | 212390 |
rs27736070 | snp | C/G | 0.124444 | 0.216185 | intron-variant | Klhl32, Gm31436 | Mm_Celera | 4:24671488 | AAACTGGATGACGTG[C/G]TGACACTGATGGCTC | 212390 |
rs27736071 | snp | C/T | 0.124444 | 0.216185 | intron-variant | Klhl32, Gm31436 | Mm_Celera | 4:24671338 | ACTCAGCTGCTATGG[C/T]ACATCCCATCCATTG | 212390 |
rs27736072 | snp | C/T | 0.124444 | 0.216185 | intron-variant | Klhl32, Gm31436 | Mm_Celera | 4:24671316 | ACACTCTTGCACTTT[C/T]TCAGGGACTCAGCTG | 212390 |
rs27736073 | snp | A/G | 0.231111 | 0.249285 | intron-variant | Klhl32, Gm31436 | GRCm38.p3 | 4:24671187 | GCATAGACTTCAAGA[A/G]TAAAATCCCAAGCTG | 212390 |
rs27736074 | snp | C/T | 0.375 | 0.216506 | intron-variant | Klhl32, Gm31436 | GRCm38.p3 | 4:24671112 | TCTAGAGAGAATTCA[C/T]TGTAAGGCCTGCTGC | 212390 |
rs27736075 | snp | C/T | 0.124444 | 0.216185 | intron-variant | Klhl32, Gm31436 | Mm_Celera | 4:24671057 | TAGCAGGCTTTCCCA[C/T]TTTCCATGTAGTAAT | 212390 |
rs27736076 | snp | A/G | 0.124444 | 0.216185 | intron-variant | Klhl32, Gm31436 | Mm_Celera | 4:24670980 | TTTCTTGGCCAAACT[A/G]TACAGTGCAATGGCA | 212390 |
rs27736077 | snp | C/T | 0.375 | 0.216506 | intron-variant | Klhl32, Gm31436 | GRCm38.p3 | 4:24670924 | CAGGTTAGCTTTTAA[C/T]ATCTTAACTAAGTAG | 212390 |
rs27736078 | snp | G/T | 0.493827 | 0.0552116 | intron-variant, nc-transcript-variant | Klhl32, Gm31436 | GRCm38.p3 | 4:24670906 | ATCCGCTGGCTCAGC[G/T]TTCAGGTTAGCTTTT | 212390 |
rs27736079 | snp | A/G | 0.401235 | 0.199068 | intron-variant, nc-transcript-variant | Klhl32, Gm31436 | GRCm38.p3 | 4:24670857 | GAGTGCACTGCTTTG[A/G]ATTGTGCTCAGCACT | 212390 |
rs27736080 | snp | C/G | 0.132653 | 0.220748 | intron-variant, nc-transcript-variant | Klhl32, Gm31436 | Mm_Celera | 4:24670837 | TTCAGGATTCTACCT[C/G]TCTGGAGTGCACTGC | 212390 |
rs27736081 | snp | A/G | 0.396694 | 0.202437 | intron-variant, nc-transcript-variant | Klhl32, Gm31436 | GRCm38.p3 | 4:24670408 | AGTGGCAGAGAACGG[A/G]GCAGAACCACCAATC | 212390 |
rs27736082 | snp | A/G | 0.124444 | 0.216185 | intron-variant, nc-transcript-variant | Klhl32, Gm31436 | Mm_Celera | 4:24670390 | CTCCCCTGCTGTACC[A/G]CAAGTGGCAGAGAAC | 212390 |
rs27736083 | snp | A/G | 0.165289 | 0.235211 | intron-variant, nc-transcript-variant | Klhl32, Gm31436 | GRCm38.p3 | 4:24670312 | GACATGAAGAGCTGA[A/G]AAAGACTTCATTCAT | 212390 |
rs27736084 | snp | A/C | 0.124444 | 0.216185 | intron-variant, nc-transcript-variant | Klhl32, Gm31436 | Mm_Celera | 4:24669588 | ATTGACAGCCAAACT[A/C]TATCCGTGCAATATC | 212390 |
rs27736085 | snp | C/G | 0.18 | 0.24 | intron-variant, nc-transcript-variant | Klhl32, Gm31436 | GRCm38.p3 | 4:24669142 | CAAAGCATCCCGAGA[C/G]AGACAGTTGAGGGGA | 212390 |
rs27736086 | snp | A/T | 0.132653 | 0.220748 | intron-variant, nc-transcript-variant | Klhl32, Gm31436 | Mm_Celera | 4:24668703 | GAGCTTCAACCAGGT[A/T]CAAGATCTACACAAA | 212390 |
rs27736087 | snp | A/G | 0.124444 | 0.216185 | intron-variant, nc-transcript-variant | Klhl32, Gm31436 | Mm_Celera | 4:24668688 | ATAGACTTCTACACT[A/G]AGCTTCAACCAGGTA | 212390 |
rs27736088 | snp | C/T | 0.132653 | 0.220748 | intron-variant, nc-transcript-variant | Klhl32, Gm31436 | Mm_Celera | 4:24668603 | ATCATGTGTTTTTCT[C/T]TGTAATAGGTTTGAA | 212390 |
rs27736089 | snp | C/T | 0.197531 | 0.244432 | intron-variant, nc-transcript-variant | Klhl32, Gm31436 | Mm_Celera | 4:24668506 | TGTACAGGCTGGAAA[C/T]AGAAGTAAGGGGTTC | 212390 |
rs27736090 | snp | C/T | 0.444444 | 0.157135 | intron-variant, nc-transcript-variant | Klhl32, Gm31436 | Mm_Celera | 4:24668495 | CCAGACCGCCATGTA[C/T]AGGCTGGAAATAGAA | 212390 |
rs27736091 | snp | C/T | 0.132653 | 0.220748 | intron-variant, upstream-variant-2KB | Klhl32, Gm31436 | Mm_Celera | 4:24666913 | CCATAGACATAATTG[C/T]TTTATCACTGTCACA | 212390 |
rs27736092 | snp | A/C | 0.132653 | 0.220748 | intron-variant, upstream-variant-2KB | Klhl32, Gm31436 | Mm_Celera | 4:24666860 | ATGAAAACACCTGAA[A/C]TGAAGTTACAACTGT | 212390 |
rs27736093 | snp | C/G | 0.132653 | 0.220748 | intron-variant, upstream-variant-2KB | Klhl32, Gm31436 | GRCm38.p3 | 4:24666637 | TGAATTATTACCCAA[C/G]GACCTTTTTTACCAC | 212390 |
rs27736094 | snp | C/T | 0.231111 | 0.249285 | intron-variant, upstream-variant-2KB | Klhl32, Gm31436 | Mm_Celera | 4:24666575 | AGGGCTGGATTAACA[C/T]CATAATGGGATTCAA | 212390 |
rs27736095 | snp | C/G | 0.124444 | 0.216185 | intron-variant, upstream-variant-2KB | Klhl32, Gm31436 | Mm_Celera | 4:24666544 | ACACATTCTAAATAG[C/G]ACCACTGCTTAAGTA | 212390 |
rs27736096 | snp | C/T | 0.132653 | 0.220748 | intron-variant | Klhl32 | Mm_Celera | 4:24665816 | TTCTACTTCTTGTAA[C/T]AGGAATTGGTTATGG | 212390 |
rs27736097 | snp | A/G | 0.444444 | 0.157135 | intron-variant | Klhl32 | GRCm38.p3 | 4:24665544 | GTCCCAAAAGGAGAG[A/G]AACGGTCAGTCCAAG | 212390 |
rs27736098 | snp | A/G | 0.124444 | 0.216185 | intron-variant | Klhl32 | Mm_Celera | 4:24665380 | GTGTTGAAACCCACA[A/G]GTGTTTGCTGAGTGG | 212390 |
rs27736099 | snp | A/C | 0.124444 | 0.216185 | intron-variant | Klhl32 | Mm_Celera | 4:24665363 | ACTGTACTTAGCTTC[A/C]GGTGTTGAAACCCAC | 212390 |
rs27736100 | snp | A/C | 0.132653 | 0.220748 | intron-variant | Klhl32 | Mm_Celera | 4:24665243 | GGAACCACGAGCTTG[A/C]TACTTTCTGGAGCTG | 212390 |
rs27736101 | snp | C/T | 0.345679 | 0.230967 | intron-variant | Klhl32 | GRCm38.p3 | 4:24664730 | GAAGAGGCACAGGGC[C/T]TAAGCTGCCAATGCA | 212390 |
rs27736102 | snp | G/T | 0.345679 | 0.230967 | intron-variant | Klhl32 | GRCm38.p3 | 4:24664671 | CATTCATTCTGAAGA[G/T]GGTTGGTCATAGAGC | 212390 |
rs27736103 | snp | A/G | 0.132653 | 0.220748 | intron-variant | Klhl32 | Mm_Celera | 4:24664592 | AGGTAGTAATGCTAC[A/G]GTCAATTGGTGCACA | 212390 |
rs27736104 | snp | C/T | 0.132653 | 0.220748 | intron-variant | Klhl32 | Mm_Celera | 4:24664476 | AGCAGATATATTGTG[C/T]ACTCATACTCCCCAA | 212390 |
rs27736105 | snp | C/T | 0.142012 | 0.225474 | intron-variant | Klhl32 | Mm_Celera | 4:24664280 | ACAGAGATGTGGTTG[C/T]AGCCATGGACTGTCT | 212390 |
rs27736106 | snp | G/T | 0.345679 | 0.230967 | intron-variant | Klhl32 | GRCm38.p3 | 4:24664259 | TGGCAGGTACAGTGC[G/T]TGGAGACAGAGATGT | 212390 |
rs27736107 | snp | A/G | 0.132653 | 0.220748 | intron-variant | Klhl32 | Mm_Celera | 4:24663940 | CTAAATTAAGAATCA[A/G]TTGCTTGAGCTGACT | 212390 |
rs27736108 | snp | A/G | 0.132653 | 0.220748 | intron-variant | Klhl32 | Mm_Celera | 4:24663778 | AGTCTAGGTCTTTCC[A/G]AAGAATATTTGTTTT | 212390 |
rs27736109 | snp | G/T | 0.244898 | 0.249948 | intron-variant | Klhl32 | Mm_Celera | 4:24663699 | TAAGTTGTGTGGCTT[G/T]GTTTGTTTGGCCATA | 212390 |
rs27736110 | snp | A/C | 0.132653 | 0.220748 | intron-variant | Klhl32 | Mm_Celera | 4:24663654 | TGGTCCTGTCTTTAC[A/C]AATGACCTAGGAATT | 212390 |
rs27736111 | snp | A/G | 0.142012 | 0.225474 | intron-variant | Klhl32 | Mm_Celera | 4:24663569 | AAGAAACACAGTATT[A/G]AATGTTTCCCATATT | 212390 |
rs27736112 | snp | C/T | 0.165289 | 0.235211 | intron-variant | Klhl32 | Mm_Celera | 4:24663308 | GTAAATTTTATCATT[C/T]AAACAATATGTAGAG | 212390 |
rs27736113 | snp | C/T | 0.244898 | 0.249948 | intron-variant | Klhl32 | Mm_Celera | 4:24663165 | GCACTCACAACTATT[C/T]CTGTAACGATGTATC | 212390 |
rs27736114 | snp | C/T | 0.132653 | 0.220748 | intron-variant | Klhl32 | Mm_Celera | 4:24663149 | CACACACTCAGCCCA[C/T]GCACTCACAACTATT | 212390 |
rs27736115 | snp | C/T | 0.142012 | 0.225474 | intron-variant | Klhl32 | Mm_Celera | 4:24663129 | ATTAGAGTCTTAGCG[C/T]CCACCACACACTCAG | 212390 |
rs27736116 | snp | C/T | 0.345679 | 0.230967 | intron-variant | Klhl32 | GRCm38.p3 | 4:24663121 | GTGTGAGGATTAGAG[C/T]CTTAGCGCCCACCAC | 212390 |
rs27736117 | snp | A/G | 0.456747 | 0.140554 | intron-variant | Klhl32 | GRCm38.p3 | 4:24663017 | CTGTGAGGGAAATGC[A/G]GCAAGGTAGAAAGGA | 212390 |
rs27736118 | snp | A/C | 0.132653 | 0.220748 | intron-variant | Klhl32 | Mm_Celera | 4:24662997 | ATGACGATTTGGCAC[A/C]TACCCTGTGAGGGAA | 212390 |
rs27736119 | snp | A/G | 0.142012 | 0.225474 | intron-variant | Klhl32 | Mm_Celera | 4:24662578 | ATTTGACCAAAACAA[A/G]TGCATAAATATAGAA | 212390 |
rs27736120 | snp | A/T | 0.32 | 0.24 | intron-variant | Klhl32 | Mm_Celera | 4:24662277 | CATAAACAATCCATC[A/T]TATATATTAATAGCT | 212390 |
rs27736121 | snp | C/T | 0.142012 | 0.225474 | intron-variant | Klhl32 | Mm_Celera | 4:24661386 | CCACGCCACGGGTTT[C/T]CATAGAATGAATAGT | 212390 |
rs27736122 | snp | A/G | 0.132653 | 0.220748 | intron-variant | Klhl32 | Mm_Celera | 4:24661380 | TGGTATCCACGCCAC[A/G]GGTTTCCATAGAATG | 212390 |
rs27736123 | snp | A/G | 0.244898 | 0.249948 | intron-variant | Klhl32 | Mm_Celera | 4:24660750 | TGTCGCTGACACTGG[A/G]CCAACCACTTCTCCT | 212390 |
rs27736124 | snp | A/G | 0.132653 | 0.220748 | intron-variant | Klhl32 | GRCm38.p3 | 4:24660512 | GAGAAATGCCACATG[A/G]AAAGCTCTAAGCTGA | 212390 |
rs27736125 | snp | C/T | 0.132653 | 0.220748 | intron-variant | Klhl32 | GRCm38.p3 | 4:24660409 | TCAGTCTGATCTGGC[C/T]GACCTTTGCATCACT | 212390 |
rs27736126 | snp | C/T | 0.132653 | 0.220748 | intron-variant | Klhl32 | GRCm38.p3 | 4:24660398 | CTGCTTTTAATTCAG[C/T]CTGATCTGGCTGACC | 212390 |
rs27736127 | snp | C/T | 0.408163 | 0.193609 | intron-variant | Klhl32 | GRCm38.p3 | 4:24659731 | CCCCTTTGCATGAAA[C/T]GTGTGCTCTAATAAA | 212390 |
rs27736128 | snp | C/T | 0.345679 | 0.230967 | intron-variant | Klhl32 | Mm_Celera | 4:24659517 | CATATGACGCATAGG[C/T]GATTTTTCCTCCGAG | 212390 |
rs27736129 | snp | A/G | 0.142012 | 0.225474 | intron-variant | Klhl32 | Mm_Celera | 4:24659095 | GGAAGTTTCTGCAAT[A/G]CAAGTAAGCAGGCAT | 212390 |
rs27736130 | snp | A/G | 0.244898 | 0.249948 | intron-variant | Klhl32 | Mm_Celera | 4:24658720 | CAGATCAGCACATTT[A/G]AACATAATGAGCAGC | 212390 |
rs27736131 | snp | C/T | 0.152778 | 0.230321 | intron-variant | Klhl32 | Mm_Celera | 4:24658684 | ATGTTAAAGGGTAGA[C/T]GTGGGCAGTGAGCAG | 212390 |
rs27736132 | snp | A/T | 0.260355 | 0.249785 | intron-variant | Klhl32 | Mm_Celera | 4:24658627 | AAGAACACAATAACT[A/T]ATCAACCAGCTGACA | 212390 |
rs27736133 | snp | A/G | 0.260355 | 0.249785 | intron-variant | Klhl32 | Mm_Celera | 4:24658572 | CAGAGCCTGAACAGC[A/G]TCATAAACCACCTCT | 212390 |
rs27736134 | snp | C/T | 0.132653 | 0.220748 | intron-variant | Klhl32 | Mm_Celera | 4:24658514 | TAAAGGTTCGTGTGA[C/T]GATATGTCCTTCCCA | 212390 |
rs27736135 | snp | A/G | 0.132653 | 0.220748 | intron-variant | Klhl32 | Mm_Celera | 4:24658366 | TAAGCAGTGACTGTT[A/G]CTTTGGTGTTCAGCT | 212390 |
rs27736136 | snp | A/C | 0.345679 | 0.230967 | intron-variant | Klhl32 | GRCm38.p3 | 4:24658307 | GTCCTGATGACACAT[A/C]CTCTTTTCATTGGGA | 212390 |
rs27736137 | snp | A/C | 0.244898 | 0.249948 | intron-variant | Klhl32 | Mm_Celera | 4:24658211 | AAGCAGGTTGTCATG[A/C]GATGAGTGATCAAGT | 212390 |
rs27736138 | snp | A/G | 0.152778 | 0.230321 | intron-variant | Klhl32 | Mm_Celera | 4:24658193 | GTTATTTAAGACATG[A/G]AAAAGCAGGTTGTCA | 212390 |
rs27736139 | snp | G/T | 0.297521 | 0.245442 | intron-variant | Klhl32 | Mm_Celera | 4:24658120 | GAAGAGAGATAAGGG[G/T]AATATAATCAGAATA | 212390 |
rs27736140 | snp | C/T | 0.277778 | 0.248452 | intron-variant | Klhl32 | GRCm38.p3 | 4:24654746 | ATGTAATTCAAATGA[C/T]TGTAAACTCTCCAGA | 212390 |
rs27736141 | snp | C/T | 0.35503 | 0.226867 | intron-variant | Klhl32 | Mm_Celera | 4:24654690 | GTCATTATTTTCTCA[C/T]CAATAACTGTAAAGT | 212390 |
rs27736142 | snp | C/T | 0.244898 | 0.249948 | intron-variant | Klhl32 | GRCm38.p3 | 4:24654596 | GTTTAATGCAAGCCA[C/T]CTAAATACTTAGCAT | 212390 |
rs27736143 | snp | A/G | 0.132653 | 0.220748 | intron-variant | Klhl32 | Mm_Celera | 4:24654522 | TAAACTTTAAAATCC[A/G]TCTGGTTTCAGTGTC | 212390 |
rs27736144 | snp | A/G | 0.132653 | 0.220748 | intron-variant | Klhl32 | Mm_Celera | 4:24654391 | TGGATGTATAAAGCC[A/G]TGTTATTCCCCTTGC | 212390 |
rs27736145 | snp | C/T | 0.244898 | 0.249948 | intron-variant | Klhl32 | Mm_Celera | 4:24654209 | CTTAGTCTGTTTCTT[C/T]TAGTTTTCTTAAGCA | 212390 |
rs27736146 | snp | A/T | 0.375 | 0.216506 | intron-variant | Klhl32 | GRCm38.p3 | 4:24654071 | CTGTCCCTTCCCAAG[A/T]CTCAAGAAGCTAAGT | 212390 |
rs27736147 | snp | C/T | 0.375 | 0.216506 | intron-variant | Klhl32 | GRCm38.p3 | 4:24653703 | CACTACTCTTATTCA[C/T]TGTATCCTGCCAACA | 212390 |
rs27736148 | snp | A/G | 0.35503 | 0.226867 | intron-variant | Klhl32 | GRCm38.p3 | 4:24653628 | GAAAGGTTATCCTGG[A/G]AACTGATGGCTTTCC | 212390 |
rs27736149 | snp | A/G | 0.359862 | 0.224567 | intron-variant | Klhl32 | GRCm38.p3 | 4:24652427 | TGCTGTCAACTTGAA[A/G]CCTCAGTTGCATATG | 212390 |
rs27736150 | snp | A/G | 0.32 | 0.24 | intron-variant | Klhl32 | GRCm38.p3 | 4:24652335 | CTTTTACAATTTATG[A/G]CATTTTCAGAACATA | 212390 |
rs27736151 | snp | C/T | 0.473373 | 0.11227 | intron-variant | Klhl32 | GRCm38.p3 | 4:24652225 | GTCTTTGCATGGTTT[C/T]CCCCAATACTACATG | 212390 |
rs27736152 | snp | A/G | 0.375 | 0.216506 | intron-variant | Klhl32 | GRCm38.p3 | 4:24651770 | CTCACAAAGCCTTCT[A/G]AAGTTCTCAGAAATA | 212390 |
rs27736153 | snp | A/T | 0.42 | 0.183303 | intron-variant | Klhl32 | GRCm38.p3 | 4:24651566 | AACACATAAGCCAAG[A/T]GCAGTGAACACACCT | 212390 |
rs27736154 | snp | A/G | 0.444444 | 0.157135 | intron-variant | Klhl32 | GRCm38.p3 | 4:24651558 | ATTTTGCTAACACAT[A/G]AGCCAAGTGCAGTGA | 212390 |
rs27736155 | snp | C/T | 0.5 | 0 | intron-variant | Klhl32 | Mm_Celera | 4:24651484 | TTAAATTAAATGAAC[C/T]CTACGAGGTACCAGC | 212390 |
rs27736156 | snp | C/T | 0.444444 | 0.157135 | intron-variant | Klhl32 | GRCm38.p3 | 4:24651375 | TCCAGATGCCCAAGG[C/T]TTCTGCATCCACCTG | 212390 |
rs27736157 | snp | G/T | 0.444444 | 0.157135 | intron-variant | Klhl32 | GRCm38.p3 | 4:24651293 | AGACCATTGCTGCAT[G/T]GTGAAATAAGCTGAT | 212390 |
rs27736158 | snp | A/G | 0.46875 | 0.121031 | intron-variant | Klhl32 | GRCm38.p3 | 4:24651252 | GTTTAATCTCTAGGA[A/G]GACAAAGGAGGAGGT | 212390 |
rs27736159 | snp | A/G | 0.18 | 0.24 | intron-variant | Klhl32 | GRCm38.p3 | 4:24651161 | ATAATGGATTTGAAT[A/G]CTGGATGTAACTAAC | 212390 |
rs27736160 | snp | A/G | 0.444444 | 0.157135 | intron-variant | Klhl32 | GRCm38.p3 | 4:24650980 | AACTTCCCAATTAAT[A/G]TGACTTGATATTTGA | 212390 |
rs27736161 | snp | A/G | 0.375 | 0.216506 | intron-variant | Klhl32 | GRCm38.p3 | 4:24650599 | AGCCCATGGTGGGTA[A/G]TGCCATCATAGCTCA | 212390 |
rs27736162 | snp | C/T | 0.426035 | 0.177515 | intron-variant | Klhl32 | GRCm38.p3 | 4:24650345 | AGATAGCAACAACAT[C/T]TCTCCTGTATAGCGC | 212390 |
rs27736163 | snp | A/G | 0.429688 | 0.173817 | synonymous-codon | Klhl32 | GRCm38.p3 | 4:24650102 | TTGGTGGTATTCCAG[A/G]GCCTCGTTGACAAGG | 212390 |
rs27736164 | snp | C/T | 0.197531 | 0.244432 | synonymous-codon | Klhl32 | GRCm38.p3 | 4:24649850 | TCCTCCTGCTACAAA[C/T]AGGAAGTCCCCCATG | 212390 |
rs27736165 | snp | A/G | 0.32 | 0.24 | missense | Klhl32 | GRCm38.p3 | 4:24649666 | TAGGTAGAACTTGGC[A/G]CAGTTCATTTCTGCC | 212390 |
rs27736166 | snp | A/G | 0.297521 | 0.245442 | intron-variant | Klhl32 | Mm_Celera | 4:24649473 | GCCACTCTCCAGAAG[A/G]TGACTTTTAAATTTA | 212390 |
rs27736167 | snp | A/G | 0.46875 | 0.121031 | intron-variant | Klhl32 | GRCm38.p3 | 4:24649391 | CTCTCTATAGAGTAG[A/G]TGCTCAATAAATGAT | 212390 |
rs27736168 | snp | C/T | 0.32 | 0.24 | intron-variant | Klhl32 | GRCm38.p3 | 4:24649223 | AGTGGTCGTGGATGT[C/T]CCCCCACAGTTCATC | 212390 |
rs27736169 | snp | A/G | 0.375 | 0.216506 | intron-variant | Klhl32 | GRCm38.p3 | 4:24649080 | ATAGACAGCACAGCT[A/G]AGCCCTGGAAGAGAG | 212390 |
rs27736170 | snp | C/T | 0.345679 | 0.230967 | intron-variant | Klhl32 | GRCm38.p3 | 4:24648846 | GAGAAAGATGAGCAA[C/T]GCCTGCTTGAAGCTA | 212390 |
rs27736171 | snp | A/T | 0.46875 | 0.121031 | intron-variant | Klhl32 | GRCm38.p3 | 4:24648785 | TGCCTCATAGACTTC[A/T]GTACAACAACATGGC | 212390 |
rs27736172 | snp | C/T | 0.444444 | 0.157135 | intron-variant | Klhl32 | GRCm38.p3 | 4:24648766 | TTGTGAGACTGATGG[C/T]GCATGCCTCATAGAC | 212390 |
rs27736173 | snp | C/T | 0.396694 | 0.202437 | intron-variant | Klhl32 | GRCm38.p3 | 4:24648640 | GAGGGATCTTTGTGT[C/T]ATCTATGTGTTCCTG | 212390 |
rs27736174 | snp | C/G | 0.444444 | 0.157135 | intron-variant | Klhl32 | Mm_Celera | 4:24648564 | TCCCAGAGGCCTTCA[C/G]TTCCTAATGTGGTTA | 212390 |
rs27736175 | snp | A/G | 0.375 | 0.216506 | intron-variant | Klhl32 | Mm_Celera | 4:24648126 | GACCTCCTGTTATTA[A/G]TGAAGTCTCAGTCAC | 212390 |
rs27736176 | snp | A/G | 0.46875 | 0.121031 | intron-variant | Klhl32 | GRCm38.p3 | 4:24647692 | TTGGAAAGAGGAAAC[A/G]ATGACCCTTATTGAA | 212390 |
rs27736177 | snp | C/T | 0.359862 | 0.224567 | intron-variant | Klhl32 | GRCm38.p3 | 4:24647356 | AGCCTGCTCCACTCA[C/T]GGCTACATTCGCAAT | 212390 |
rs27736178 | snp | A/G | 0.32 | 0.24 | intron-variant | Klhl32 | GRCm38.p3 | 4:24647020 | ATGGGGCACAAAGCA[A/G]GAATGAGCACAGTAC | 212390 |
rs27736179 | snp | C/T | 0.304688 | 0.243945 | intron-variant | Klhl32 | GRCm38.p3 | 4:24646915 | GCTAACAGGCATAGC[C/T]ATCCAACTTAGCTTT | 212390 |
rs27736180 | snp | A/G | 0.375 | 0.216506 | intron-variant | Klhl32 | Mm_Celera | 4:24645309 | CAGCCACCAGAGGAA[A/G]GGGATTAGTGATAGC | 212390 |
rs27736181 | snp | C/T | 0.375 | 0.216506 | intron-variant | Klhl32 | Mm_Celera | 4:24645222 | ATCTGAGGACTGATG[C/T]TGTCCGTGTGCACAT | 212390 |
rs27736184 | snp | C/T | 0.142012 | 0.225474 | intron-variant | Klhl32 | Mm_Celera | 4:24641627 | TTTCCTGCATCTCTC[C/T]TTACAAGTTACTCAA | 212390 |
rs27736185 | snp | A/G | 0.415225 | 0.187619 | intron-variant | Klhl32 | Mm_Celera | 4:24641501 | TTTCTTCACAGTCTC[A/G]TCCCTCCTACCTGTT | 212390 |
rs27736186 | snp | C/T | 0.391111 | 0.206368 | intron-variant | Klhl32 | Mm_Celera | 4:24641087 | CTGGGCTATTTCTAA[C/T]GTAGAAACCTTTTAT | 212390 |
rs27736187 | snp | A/T | 0.297521 | 0.245442 | intron-variant | Klhl32 | GRCm38.p3 | 4:24640724 | CGTGGCTTCCCTCTC[A/T]GCTCAGTAGCAAAGT | 212390 |
rs27736188 | snp | C/G | 0.35503 | 0.226867 | intron-variant | Klhl32 | GRCm38.p3 | 4:24640431 | CTACAACAAAAACTA[C/G]TGGCTGTATGGTTTA | 212390 |
rs27736189 | snp | A/G | 0.444444 | 0.157135 | intron-variant | Klhl32 | GRCm38.p3 | 4:24640340 | GAGAGTTATGTCATG[A/G]ATACGTTCTAGTCAC | 212390 |
rs27736190 | snp | C/T | 0.297521 | 0.245442 | intron-variant | Klhl32 | GRCm38.p3 | 4:24640163 | GATGTTGTTTATGTT[C/T]TCAAAAGTGAATGAC | 212390 |
rs27736191 | snp | C/G | 0.359862 | 0.224567 | intron-variant | Klhl32 | Mm_Celera | 4:24640084 | CAAGTCTCTTACCCA[C/G]GCTACCGTATTTTGC | 212390 |
rs27736192 | snp | A/C | 0.345679 | 0.230967 | intron-variant | Klhl32 | Mm_Celera | 4:24639993 | GGAGAAAAAGTCTGG[A/C]GTTTTCAACTTACAA | 212390 |
rs27736193 | snp | C/T | 0.32 | 0.24 | intron-variant | Klhl32 | GRCm38.p3 | 4:24639782 | GTCCCAGCCTCTGTG[C/T]AGCAATCTCCAGTGC | 212390 |
rs27736194 | snp | A/C | 0.142012 | 0.225474 | intron-variant | Klhl32 | Mm_Celera | 4:24639711 | GTCAGAATCCTGCCT[A/C]CAAAACCTCTGCTCA | 212390 |
rs27736195 | snp | C/T | 0.142012 | 0.225474 | intron-variant | Klhl32 | Mm_Celera | 4:24639066 | ATCCTCTGAGACAAG[C/T]GGCACAATGAGAATA | 212390 |
rs27736196 | snp | C/T | 0.260355 | 0.249785 | intron-variant | Klhl32 | Mm_Celera | 4:24637097 | GTCCTACGCTTTCAT[C/T]CTAGAAGGAGAGGCC | 212390 |
rs27736197 | snp | C/T | 0.142012 | 0.225474 | intron-variant | Klhl32 | Mm_Celera | 4:24636597 | CAAGGCAAAAGCATT[C/T]TTCTTAAGCTTCCCT | 212390 |
rs27736198 | snp | C/T | 0.124444 | 0.216185 | intron-variant | Klhl32 | Mm_Celera | 4:24636506 | CCAATGTCAAATAAG[C/T]CTTTAAAAACTGCCA | 212390 |
rs27736199 | snp | A/G | 0.42 | 0.183303 | intron-variant | Klhl32 | GRCm38.p3 | 4:24636480 | CTGCAGGTCCTCCGC[A/G]CTCCCCCTGCCCAAT | 212390 |
rs27736200 | snp | C/T | 0.124444 | 0.216185 | intron-variant | Klhl32 | Mm_Celera | 4:24636474 | GATATACTGCAGGTC[C/T]TCCGCACTCCCCCTG | 212390 |
rs27736201 | snp | A/G | 0.244898 | 0.249948 | intron-variant | Klhl32 | Mm_Celera | 4:24636449 | TTTTACTTTTGAACT[A/G]CACCTTAAAGATATA | 212390 |
rs27736202 | snp | A/G | 0.124444 | 0.216185 | intron-variant | Klhl32 | Mm_Celera | 4:24635502 | ATACAACTGATCACC[A/G]TGCTCTTCAGAATTA | 212390 |
rs27736203 | snp | C/T | 0.124444 | 0.216185 | intron-variant | Klhl32 | Mm_Celera | 4:24635424 | ATATTTATTGCACTG[C/T]GTACTAAATATACAG | 212390 |
rs27736204 | snp | A/G | 0.444444 | 0.157135 | intron-variant | Klhl32 | Mm_Celera | 4:24635263 | CATAATCACCAGATT[A/G]ATGTCCAGGTCACCT | 212390 |
rs27736205 | snp | C/G | 0.487535 | 0.077957 | intron-variant | Klhl32 | Mm_Celera | 4:24635129 | ACTTGCTTCCTGTCT[C/G]ATTAAAAACAGAAGG | 212390 |
rs27736206 | snp | C/T | 0.48 | 0.0979796 | intron-variant | Klhl32 | Mm_Celera | 4:24635028 | GAAAAGGAAAAGAAA[C/T]CACATTTAAGAAACC | 212390 |
rs27736207 | snp | C/T | 0.5 | 0 | intron-variant | Klhl32 | Mm_Celera | 4:24634978 | TTTTTAAAGAAAGCA[C/T]TCTTTGGATGTATTG | 212390 |
rs27736208 | snp | A/G | 0.444444 | 0.157135 | intron-variant | Klhl32 | GRCm38.p3 | 4:24634779 | CCTAAACTCTGGTAA[A/G]GAGACTGAATCCGCC | 212390 |
rs27736209 | snp | C/T | 0.401235 | 0.199068 | intron-variant | Klhl32 | GRCm38.p3 | 4:24634741 | ACATAAAGAGATGGG[C/T]ACGTGTCCAGGCCAA | 212390 |
rs27736210 | snp | C/T | 0.359862 | 0.224567 | intron-variant | Klhl32 | GRCm38.p3 | 4:24634680 | AAGATGAATATGTAA[C/T]TTTAAGCTAACTTAG | 212390 |
rs27736211 | snp | C/T | 0.475309 | 0.108333 | intron-variant | Klhl32 | GRCm38.p3 | 4:24634552 | ATTTTCCATCTCTGT[C/T]TTCCTTGACTGTCTT | 212390 |
rs27736212 | snp | C/T | 0.124444 | 0.216185 | intron-variant | Klhl32 | Mm_Celera | 4:24634518 | AACCTCATGTTTCCA[C/T]AGAGTTGATTACAAA | 212390 |
rs27736213 | snp | C/T | 0.124444 | 0.216185 | intron-variant | Klhl32 | Mm_Celera | 4:24634496 | TCCTCGCTCTGGTGC[C/T]GAAGAAAACCTCATG | 212390 |
rs27736214 | snp | C/T | 0.231111 | 0.249285 | intron-variant | Klhl32 | Mm_Celera | 4:24634482 | CTCCAAAGTTCTTTT[C/T]CTCGCTCTGGTGCCG | 212390 |
rs27736215 | snp | A/G | 0.48 | 0.0979796 | intron-variant | Klhl32 | Mm_Celera | 4:24633872 | TTTCATGTTTGTGAT[A/G]TACACTAAGCTCTGT | 212390 |
rs27736216 | snp | A/G | 0.48 | 0.0979796 | intron-variant | Klhl32 | Mm_Celera | 4:24633861 | GACATGCTTCTTTTC[A/G]TGTTTGTGATATACA | 212390 |
rs27736217 | snp | C/T | 0.142012 | 0.225474 | intron-variant | Klhl32 | Mm_Celera | 4:24633497 | TTCAGACTTTCTATT[C/T]AAGTAGAAACCACAA | 212390 |
rs27736218 | snp | A/T | 0.475309 | 0.108333 | intron-variant | Klhl32 | GRCm38.p3 | 4:24633471 | TTTTACAGGGCTAAT[A/T]CCTAAGAGACTTCAG | 212390 |
rs27736219 | snp | C/T | 0.487535 | 0.077957 | intron-variant | Klhl32 | GRCm38.p3 | 4:24633384 | CGAACCTGAAGACTG[C/T]CGGTTACCAAATGGG | 212390 |
rs27736220 | snp | A/G | 0.124444 | 0.216185 | intron-variant | Klhl32 | Mm_Celera | 4:24633283 | TAAAATTTGCTGAGC[A/G]TTTCATTTCCTAAAA | 212390 |
rs27736221 | snp | A/T | 0.132653 | 0.220748 | intron-variant | Klhl32 | Mm_Celera | 4:24633144 | GGGGTAAATGGTATC[A/T]AGGAGAGAATAACAA | 212390 |
rs27736222 | snp | A/T | 0.124444 | 0.216185 | intron-variant | Klhl32 | Mm_Celera | 4:24633095 | ATTTCTTTGGAAAAA[A/T]ACATACAGCAAAAGT | 212390 |
rs27736223 | snp | G/T | 0.124444 | 0.216185 | intron-variant | Klhl32 | Mm_Celera | 4:24633068 | TGTGCATTAGCAAGG[G/T]GACAGTTTGCTATTT | 212390 |
rs27736224 | snp | A/T | 0.124444 | 0.216185 | intron-variant | Klhl32 | Mm_Celera | 4:24633061 | TAAGCTCTGTGCATT[A/T]GCAAGGTGACAGTTT | 212390 |
rs27736225 | snp | C/T | 0.124444 | 0.216185 | intron-variant | Klhl32 | Mm_Celera | 4:24632962 | GGTGTTCTGCATGGC[C/T]GGATAAAGGATAGGC | 212390 |
rs27736226 | snp | C/T | 0.142012 | 0.225474 | intron-variant | Klhl32 | Mm_Celera | 4:24632907 | CTTGGGAGTAAGCAA[C/T]GGGTATACTGAGGGT | 212390 |
rs27736227 | snp | A/G | 0.231111 | 0.249285 | synonymous-codon | Klhl32 | Mm_Celera | 4:24632655 | TACCTGGTTAGGTTC[A/G]TATACCATCAGTCTG | 212390 |
rs27736228 | snp | A/G | 0.231111 | 0.249285 | intron-variant | Klhl32 | Mm_Celera | 4:24632579 | GGCACTCTGATGAAC[A/G]GTTCCTGTGGAGATC | 212390 |
rs27736229 | snp | C/T | 0.142012 | 0.225474 | intron-variant | Klhl32 | Mm_Celera | 4:24632506 | ATACCAATGAGGAAC[C/T]GAAGGCTTTCCCCGC | 212390 |
rs27736230 | snp | C/T | 0.231111 | 0.249285 | intron-variant | Klhl32 | Mm_Celera | 4:24632412 | AGAAGGACATCGCTA[C/T]AATCAAAATCCTCTC | 212390 |
rs27736231 | snp | A/T | 0.487535 | 0.077957 | intron-variant | Klhl32 | GRCm38.p3 | 4:24632403 | ATCCCTTACAGAAGG[A/T]CATCGCTACAATCAA | 212390 |
rs27736232 | snp | G/T | 0.124444 | 0.216185 | intron-variant | Klhl32 | Mm_Celera | 4:24632341 | CAAATGGCATTATTT[G/T]ATTTGAGACTAACAA | 212390 |
rs27736233 | snp | A/G | 0.124444 | 0.216185 | intron-variant | Klhl32 | Mm_Celera | 4:24632242 | AGAAAGGACCCAGCT[A/G]TTAGAGGCACACCAT | 212390 |
rs27736234 | snp | A/G | 0.124444 | 0.216185 | intron-variant | Klhl32 | Mm_Celera | 4:24632008 | TCCTAATATTGCACT[A/G]ATGGACAGTAAACCT | 212390 |
rs27736235 | snp | A/G | 0.231111 | 0.249285 | intron-variant | Klhl32 | Mm_Celera | 4:24631953 | TACTTGTGGTACCCA[A/G]CCCAGATGCAACCTG | 212390 |
rs27736236 | snp | A/G | 0.231111 | 0.249285 | intron-variant | Klhl32 | Mm_Celera | 4:24631780 | GACCCATGAACATCC[A/G]ATCTCTGCAATCTAT | 212390 |
rs27736237 | snp | A/G | 0.124444 | 0.216185 | intron-variant | Klhl32 | Mm_Celera | 4:24631723 | AACCATGTGTGCACC[A/G]AACTCAGGCTTCTGC | 212390 |
rs27736238 | snp | C/T | 0.124444 | 0.216185 | intron-variant | Klhl32 | Mm_Celera | 4:24631546 | AATAAGCATCAGGGC[C/T]GAATGATAGAGTTAT | 212390 |
rs27736239 | snp | A/G | 0.124444 | 0.216185 | intron-variant | Klhl32 | Mm_Celera | 4:24631523 | TCTCCACAAAGGCCT[A/G]GAAGAGAAATAAGCA | 212390 |
rs27736240 | snp | C/T | 0.124444 | 0.216185 | intron-variant | Klhl32 | Mm_Celera | 4:24631010 | GCTCATTTCTAATTT[C/T]TCAGAGTAAACTGCA | 212390 |
rs27736241 | snp | C/T | 0.124444 | 0.216185 | intron-variant | Klhl32 | Mm_Celera | 4:24630912 | CGTGTGCCATTTATT[C/T]TCTATTGGCACATAT | 212390 |
rs27736242 | snp | A/G | 0.124444 | 0.216185 | intron-variant | Klhl32 | Mm_Celera | 4:24630887 | CACTTAAGCACTTTT[A/G]CACTATAGACGTGTG | 212390 |
rs27736243 | snp | C/T | 0.124444 | 0.216185 | intron-variant | Klhl32 | Mm_Celera | 4:24630652 | GGCTATGAGCACAGA[C/T]ATGCTTGTATAAACA | 212390 |
rs27736244 | snp | A/G | 0.124444 | 0.216185 | intron-variant | Klhl32 | Mm_Celera | 4:24630508 | ACTTCCTTTCTCATA[A/G]ACACTCAGCATATAG | 212390 |
rs27736245 | snp | C/T | 0.124444 | 0.216185 | intron-variant | Klhl32 | Mm_Celera | 4:24630421 | AAGTCAACCATGGCT[C/T]GAAATTTAAATCCCA | 212390 |
rs27736246 | snp | C/G | 0.142012 | 0.225474 | intron-variant | Klhl32 | Mm_Celera | 4:24630389 | TAAAATGCCATGCAA[C/G]TTTTAAAATTATATG | 212390 |
rs27736247 | snp | C/T | 0.124444 | 0.216185 | intron-variant | Klhl32 | Mm_Celera | 4:24630207 | TATTTACAATTATGC[C/T]TTTTGCCAAATAAGG | 212390 |
rs27736248 | snp | A/G | 0.132653 | 0.220748 | intron-variant | Klhl32 | Mm_Celera | 4:24630183 | TCTGAATCCTCTCAT[A/G]TCTTAACATATTTAC | 212390 |
rs27736249 | snp | A/G | 0.124444 | 0.216185 | intron-variant | Klhl32 | Mm_Celera | 4:24630080 | GGAGTTAAGGTGAAG[A/G]CTACACCCCCATTCT | 212390 |
rs27736250 | snp | A/G | 0.124444 | 0.216185 | intron-variant | Klhl32 | Mm_Celera | 4:24630036 | GATTTGGGGGGAGGC[A/G]TATAAACATCAAGTA | 212390 |
rs27736251 | snp | C/T | 0.142012 | 0.225474 | intron-variant | Klhl32 | Mm_Celera | 4:24629873 | TGCATGGCCTCTGTC[C/T]TAAAAATACAGGAAT | 212390 |
rs27736252 | snp | C/T | 0.244898 | 0.249948 | intron-variant | Klhl32 | Mm_Celera | 4:24629816 | ACTTACATGAGAGCC[C/T]GTCCTGACTTAGAAA | 212390 |
rs27736253 | snp | A/G | 0.489796 | 0.070696 | intron-variant | Klhl32 | GRCm38.p3 | 4:24629792 | TGGCTTTACAATTGA[A/G]ATAATAAAACTTACA | 212390 |
rs27736254 | snp | C/T | 0.32 | 0.24 | intron-variant | Klhl32 | Mm_Celera | 4:24629645 | TTGAGATGACTTAGG[C/T]TTAAGCACATGGTCA | 212390 |
rs27736255 | snp | C/T | 0.124444 | 0.216185 | synonymous-codon | Klhl32 | Mm_Celera | 4:24629284 | AAGCACATAAAGCTT[C/T]CTTTGGACAGCAGCC | 212390 |
rs27736256 | snp | C/T | 0.444444 | 0.157135 | intron-variant | Klhl32 | GRCm38.p3 | 4:24628805 | ATTTAGGGTTGTACT[C/T]TGGCTGTCCATGAAA | 212390 |
rs27736257 | snp | A/G | 0.432133 | 0.171253 | intron-variant | Klhl32 | GRCm38.p3 | 4:24628763 | AGGGTAAAGAAAACA[A/G]TTTGTGCTATGCATT | 212390 |
rs27736258 | snp | A/G | 0.444444 | 0.157135 | intron-variant | Klhl32 | GRCm38.p3 | 4:24628737 | TTAGCTAAAAATCAC[A/G]CATGTCTTCCAGGGT | 212390 |
rs27736259 | snp | G/T | 0.124444 | 0.216185 | intron-variant | Klhl32 | Mm_Celera | 4:24628659 | GCTTCTCTTGGTCCT[G/T]TGAGAACCTACACAG | 212390 |
rs27736260 | snp | C/T | 0.48 | 0.0979796 | intron-variant | Klhl32 | GRCm38.p3 | 4:24628620 | TCTCGTTTGAGTATC[C/T]ACTAAGGGAAAGTGA | 212390 |
rs27736261 | snp | A/G | 0.484429 | 0.0868505 | intron-variant | Klhl32 | GRCm38.p3 | 4:24628615 | AAAGTTCTCGTTTGA[A/G]TATCCACTAAGGGAA | 212390 |
rs27736262 | snp | C/T | 0.401235 | 0.199068 | intron-variant | Klhl32 | GRCm38.p3 | 4:24628558 | TTAAAACAGAAAATA[C/T]ACCATTAGCTCGTTA | 212390 |
rs27736263 | snp | C/T | 0.455 | 0.143091 | intron-variant | Klhl32 | Mm_Celera | 4:24628198 | ATGAGTGGCCAGAAA[C/T]GCAGCTCTTATGCAC | 212390 |
rs27736264 | snp | A/G | 0.142012 | 0.225474 | intron-variant | Klhl32 | Mm_Celera | 4:24628032 | GATCCTACCATTGGT[A/G]GATGTTAGCCATAGG | 212390 |
rs27736265 | snp | A/C | 0.432133 | 0.171253 | intron-variant | Klhl32 | GRCm38.p3 | 4:24628013 | TTAAAACAGCCTGGC[A/C]AGGGATCCTACCATT | 212390 |
rs27736266 | snp | C/T | 0.124444 | 0.216185 | intron-variant | Klhl32 | Mm_Celera | 4:24627804 | CCTGAAAGTTCAGTA[C/T]GTACAGTAGGCCGAA | 212390 |
rs27736267 | snp | A/G | 0.132653 | 0.220748 | intron-variant | Klhl32 | Mm_Celera | 4:24627759 | CAGAATCACAGCTCC[A/G]GGGATCTAGGATCTG | 212390 |
rs27736268 | snp | A/C | 0.408163 | 0.193609 | intron-variant | Klhl32 | Mm_Celera | 4:24627554 | ATTATATTAAAGTTC[A/C]CAAGCTGAGACTAGT | 212390 |
rs27736269 | snp | C/G | 0.152778 | 0.230321 | intron-variant | Klhl32 | Mm_Celera | 4:24627477 | CTCTTCAAATGAAGA[C/G]AAATAGCAGACAAAA | 212390 |
rs27736270 | snp | A/G | 0.473373 | 0.11227 | intron-variant | Klhl32 | GRCm38.p3 | 4:24627390 | TATAGACAAGTGCTT[A/G]CCTTCATAAAGCAAC | 212390 |
rs27736271 | snp | A/C | 0.359862 | 0.224567 | intron-variant | Klhl32 | Mm_Celera | 4:24627371 | TAATATTTGGGCCCA[A/C]AAATATAGACAAGTG | 212390 |
rs27736272 | snp | A/G | 0.231111 | 0.249285 | intron-variant | Klhl32 | Mm_Celera | 4:24627186 | GTGAATCTATGTTTC[A/G]TTAGGACCAGGGCGA | 212390 |
rs27736273 | snp | A/T | 0.473373 | 0.11227 | intron-variant | Klhl32 | GRCm38.p3 | 4:24626863 | CCTCGCTGAACCATC[A/T]GCAGAAACTTCAAAA | 212390 |
rs27736274 | snp | G/T | 0.415225 | 0.187619 | intron-variant | Klhl32 | GRCm38.p3 | 4:24626837 | TTCTGCAGCTGAATT[G/T]CGAAACATAACCTCG | 212390 |
rs27736275 | snp | C/G | 0.444444 | 0.157135 | intron-variant | Klhl32 | Mm_Celera | 4:24626492 | TGCTGGGATCCTCTG[C/G]CAAAAAGGAAGCACA | 212390 |
rs27736276 | snp | A/G | 0.231111 | 0.249285 | intron-variant | Klhl32 | Mm_Celera | 4:24626474 | CCACCCAGAAACCAC[A/G]AATGCTGGGATCCTC | 212390 |
rs27736277 | snp | C/T | 0.42 | 0.183303 | intron-variant | Klhl32 | GRCm38.p3 | 4:24625875 | AAGTAGACCCTTGAA[C/T]GCCGTCTTGAAAGCA | 212390 |
rs27736278 | snp | G/T | 0.18 | 0.24 | intron-variant | Klhl32 | Mm_Celera | 4:24625791 | TTGCGGTGAGAGAAA[G/T]CGAGAGGAGAAAGGA | 212390 |
rs27736279 | snp | A/G | 0.489796 | 0.070696 | intron-variant | Klhl32 | GRCm38.p3 | 4:24625715 | CCAAAAGGGGCAATC[A/G]AGTTTTCATATCTGT | 212390 |
rs27736280 | snp | A/G | 0.493827 | 0.0552116 | intron-variant | Klhl32 | GRCm38.p3 | 4:24625706 | TCTATTCAGCCAAAA[A/G]GGGCAATCAAGTTTT | 212390 |
rs27736281 | snp | C/T | 0.32 | 0.24 | intron-variant | Klhl32 | Mm_Celera | 4:24624316 | ACCAGGAATTATTAA[C/T]ACTGAATCAGTGGGC | 212390 |
rs27736282 | snp | C/T | 0.5 | 0 | intron-variant | Klhl32 | Mm_Celera | 4:24624067 | GGAATAGATGGAATT[C/T]CCAGGAGGCTAAGGA | 212390 |
rs27736283 | snp | C/T | 0.32 | 0.24 | intron-variant | Klhl32 | Mm_Celera | 4:24624043 | CTTTGTAGGAGTGTG[C/T]TAGTCACAGGAATAG | 212390 |
rs27736284 | snp | C/T | 0.408163 | 0.193609 | intron-variant | Klhl32 | GRCm38.p3 | 4:24623918 | AGAGTCAACTCTGCA[C/T]GTAGTCATATGACTT | 212390 |
rs27736285 | snp | G/T | 0.5 | 0 | intron-variant | Klhl32 | GRCm38.p3 | 4:24623860 | TAGTGGTACAAGTGC[G/T]TGTGCTACCAGGCCA | 212390 |
rs27736286 | snp | G/T | 0.21875 | 0.248039 | intron-variant | Klhl32 | GRCm38.p3 | 4:24622511 | TGACTAGATCTGAAG[G/T]CAGCAACAGAGTAGA | 212390 |
rs27736287 | snp | A/G | 0.444444 | 0.157135 | intron-variant | Klhl32 | GRCm38.p3 | 4:24622290 | ATACTTTAAGTGTGC[A/G]TCTGATTCTCACGAC | 212390 |
rs27736288 | snp | A/G | 0.375 | 0.216506 | intron-variant | Klhl32 | Mm_Celera | 4:24622181 | GAGACGCTCTGAACT[A/G]CTTAACTATACTCTT | 212390 |
rs27736289 | snp | A/G | 0.5 | 0 | intron-variant | Klhl32 | GRCm38.p3 | 4:24622107 | GGAGCAGTCTGCTAA[A/G]ATAAGAGTATTGGCT | 212390 |
rs27736290 | snp | C/T | 0.165289 | 0.235211 | intron-variant | Klhl32 | GRCm38.p3 | 4:24622030 | ATGGCTTCTTATGCG[C/T]GTCACTCCAGGTGGC | 212390 |
rs27736291 | snp | G/T | 0.495868 | 0.0452663 | intron-variant | Klhl32 | GRCm38.p3 | 4:24621805 | CACATCAGATTAGAG[G/T]CAGGCTACATGCCAG | 212390 |
rs27736292 | snp | G/T | 0.244898 | 0.249948 | intron-variant | Klhl32 | Mm_Celera | 4:24620892 | GTTACAAGAGCAACA[G/T]CTATGCCTCTATTGC | 212390 |
rs27736293 | snp | C/T | 0.297521 | 0.245442 | utr-variant-3-prime | Klhl32 | GRCm38.p3 | 4:24617308 | ACCTGTAAGACACGA[C/T]AGGGAAGCACTGAGA | 212390 |
rs27736294 | snp | G/T | 0.48 | 0.0979796 | downstream-variant-500B, utr-variant-3-prime | Klhl32 | Mm_Celera | 4:24617054 | CCTGCTGTGTAAGGT[G/T]CCTTACTGACAGTGT | 212390 |
rs27736295 | snp | C/G/T | 0.132653 | 0.220748 | downstream-variant-500B, utr-variant-3-prime | Klhl32 | GRCm38.p3 | 4:24616999 | CTGATGCTTGAGTAA[C/G/T]GAAAAGGCCTAAGTA | 212390 |
rs27736296 | snp | G/T | 0.277778 | 0.248452 | downstream-variant-500B, utr-variant-3-prime | Klhl32 | Mm_Celera | 4:24616944 | TCCCGCTGAACTTCT[G/T]CTGAGGAATGCTGCA | 212390 |
rs27736297 | snp | C/T | 0.260355 | 0.249785 | downstream-variant-500B, utr-variant-3-prime | Klhl32 | Mm_Celera | 4:24616932 | TATCTGATGTCATCC[C/T]GCTGAACTTCTGCTG | 212390 |
rs27736298 | snp | C/T | 0.231111 | 0.249285 | utr-variant-3-prime | Klhl32 | Mm_Celera | 4:24616397 | TATCAACTTGGAAAA[C/T]GTCTATTAGAACTGC | 212390 |
rs27736299 | snp | C/T | 0.260355 | 0.249785 | utr-variant-3-prime | Klhl32 | Mm_Celera | 4:24616198 | AGAAATGACCTCCAG[C/T]CGTGGCAAGATTAGA | 212390 |
rs27736300 | snp | A/G | 0.244898 | 0.249948 | utr-variant-3-prime | Klhl32 | Mm_Celera | 4:24616075 | GAAAACTAGTTTTTC[A/G]TTGGCTTATGATGAT | 212390 |
rs27736301 | snp | A/G | 0.124444 | 0.216185 | utr-variant-3-prime | Klhl32 | Mm_Celera | 4:24615934 | TAGAACAGTGCTTTC[A/G]GTATCATACAGCAAT | 212390 |
rs27736302 | snp | C/T | 0.231111 | 0.249285 | utr-variant-3-prime | Klhl32 | Mm_Celera | 4:24615772 | TGAAGGCTCATGGGC[C/T]GCTTTTAAACCGTTC | 212390 |
rs27736303 | snp | A/C | 0.277778 | 0.248452 | utr-variant-3-prime | Klhl32 | Mm_Celera | 4:24615640 | CTGCTAGAGAGAAAA[A/C]CCCATGTATCAAGTA | 212390 |
rs27736304 | snp | A/C | 0.444444 | 0.157135 | utr-variant-3-prime | Klhl32 | Mm_Celera | 4:24615423 | TGTCCAAACTGCAAA[A/C]AGTACCCCATGAAGA | 212390 |
rs27736305 | snp | A/G | 0.444444 | 0.157135 | utr-variant-3-prime | Klhl32 | Mm_Celera | 4:24615332 | GAAAGCGATCCAATC[A/G]TACAACCTTTCCTTC | 212390 |
rs27736306 | snp | A/G | 0.375 | 0.216506 | utr-variant-3-prime | Klhl32 | Mm_Celera | 4:24615288 | ACCAAATACGATTCC[A/G]CAGACTTTTTCACTG | 212390 |
rs27736307 | snp | C/T | 0.5 | 0 | utr-variant-3-prime | Klhl32 | Mm_Celera | 4:24615270 | TAGGACTTGCTTATA[C/T]ACACCAAATACGATT | 212390 |
rs27736308 | snp | C/T | 0.444444 | 0.157135 | utr-variant-3-prime | Klhl32 | Mm_Celera | 4:24615032 | TACTGCACCTTGCAT[C/T]GTGGGTAGAAGCTGT | 212390 |
rs27736309 | snp | G/T | 0.444444 | 0.157135 | utr-variant-3-prime | Klhl32 | GRCm38.p3 | 4:24615013 | TTTTAGAGATATGGG[G/T]TTTTACTGCACCTTG | 212390 |
rs27736310 | snp | C/T | 0.444444 | 0.157135 | utr-variant-3-prime | Klhl32 | GRCm38.p3 | 4:24614981 | GTGCCACAGTTGTAA[C/T]TTACTTGGCATTTTA | 212390 |
rs27736311 | snp | C/T | 0.444444 | 0.157135 | utr-variant-3-prime | Klhl32 | GRCm38.p3 | 4:24614958 | AAAACAAGAGGAAGG[C/T]ACAGGAAGTGCCACA | 212390 |
rs27736312 | snp | C/T | 0.5 | 0 | utr-variant-3-prime | Klhl32 | GRCm38.p3 | 4:24614927 | GGGACACTACTTATG[C/T]ACATTAGGTATGAGG | 212390 |
rs27736313 | snp | C/G | 0.444444 | 0.157135 | utr-variant-3-prime | Klhl32 | GRCm38.p3 | 4:24614906 | TCAACTTTTGCAATA[C/G]CTGAAGGGACACTAC | 212390 |
rs27736314 | snp | C/T | 0.444444 | 0.157135 | utr-variant-3-prime | Klhl32 | Mm_Celera | 4:24614500 | TTTTCAGGTTGGCTT[C/T]TTTGAACTCTCTTGG | 212390 |
rs27736315 | snp | A/G | 0.375 | 0.216506 | downstream-variant-500B | Klhl32 | Mm_Celera | 4:24614257 | ATATATTACCTGGTC[A/G]AGCAAGAGTGTAAAA | 212390 |
rs27736316 | snp | A/G | 0.5 | 0 | downstream-variant-500B | Klhl32 | Mm_Celera | 4:24614253 | TTAAATATATTACCT[A/G]GTCGAGCAAGAGTGT | 212390 |
rs27751668 | snp | G/T | 0.165289 | 0.235211 | intron-variant | Klhl32 | Mm_Celera | 4:24835965 | ATGATGGCAACAGCA[G/T]CCCAGAAATGCTTTG | 212390 |
rs27751669 | snp | A/G | 0.124444 | 0.216185 | intron-variant | Klhl32 | Mm_Celera | 4:24835914 | TTGACAGAAGCGAAC[A/G]TTTCTGATGAGAAAG | 212390 |
rs27751670 | snp | A/G | 0.132653 | 0.220748 | intron-variant | Klhl32 | Mm_Celera | 4:24835910 | ATTCTTGACAGAAGC[A/G]AACGTTTCTGATGAG | 212390 |
rs27751671 | snp | C/T | 0.124444 | 0.216185 | intron-variant | Klhl32 | Mm_Celera | 4:24835742 | TGTCACTGTCATTCA[C/T]CCTCCTGTGTGAGCT | 212390 |
rs27751672 | snp | C/T | 0.35503 | 0.226867 | intron-variant | Klhl32 | GRCm38.p3 | 4:24835598 | TTGTCAGAGCCTGAG[C/T]TCCACTCCCTAACAA | 212390 |
rs27751673 | snp | C/G | 0.231111 | 0.249285 | intron-variant | Klhl32 | GRCm38.p3 | 4:24835591 | CAGAGCCTTGTCAGA[C/G]CCTGAGCTCCACTCC | 212390 |
rs27751674 | snp | C/T | 0.231111 | 0.249285 | intron-variant | Klhl32 | GRCm38.p3 | 4:24835557 | CTCTCCCTTTCTCCT[C/T]TTGAATTCTCACATC | 212390 |
rs27751675 | snp | C/T | 0.231111 | 0.249285 | intron-variant | Klhl32 | GRCm38.p3 | 4:24835491 | CAGAAGCTGTGACTA[C/T]TGTTTCCTCAGTGAG | 212390 |
rs27751676 | snp | A/G | 0.142012 | 0.225474 | intron-variant | Klhl32 | GRCm38.p3 | 4:24835473 | CCTGGGTTCTCCCAC[A/G]GCCAGAAGCTGTGAC | 212390 |
rs27751677 | snp | A/T | 0.231111 | 0.249285 | intron-variant | Klhl32 | GRCm38.p3 | 4:24835460 | TGAGCGGTGGCCTCC[A/T]GGGTTCTCCCACGGC | 212390 |
rs27751678 | snp | C/G/T | 0.132653 | 0.220748 | intron-variant | Klhl32 | Mm_Celera | 4:24835439 | CCAGTCTCTCTGATA[C/G/T]GAACCTGAGCGGTGG | 212390 |
rs27751679 | snp | C/T | 0.124444 | 0.216185 | intron-variant | Klhl32 | Mm_Celera | 4:24835329 | ACCTCACTATTCAAC[C/T]GAGTGCCAAACCCTA | 212390 |
rs27751680 | snp | A/C | 0.124444 | 0.216185 | intron-variant | Klhl32 | Mm_Celera | 4:24835309 | TCTCAAGATCTCTCT[A/C]CTTTACCTCACTATT | 212390 |
rs27751681 | snp | C/T | 0.132653 | 0.220748 | intron-variant | Klhl32 | Mm_Celera | 4:24835181 | ACGTTTTAAAGACCC[C/T]TCAAATTTAGTACTG | 212390 |
rs27751682 | snp | A/G | 0.124444 | 0.216185 | intron-variant | Klhl32 | Mm_Celera | 4:24835114 | TGTACCATAGATTCG[A/G]AGTCTGTGTGCTATA | 212390 |
rs27751683 | snp | C/G | 0.124444 | 0.216185 | intron-variant | Klhl32 | Mm_Celera | 4:24835103 | CAGTCAAACAGTGTA[C/G]CATAGATTCGGAGTC | 212390 |
rs27751684 | snp | C/T | 0.132653 | 0.220748 | intron-variant | Klhl32 | Mm_Celera | 4:24834943 | AATTAATGAAACATA[C/T]AAGGGATTACCAGTC | 212390 |
rs27751685 | snp | C/T | 0.260355 | 0.249785 | intron-variant | Klhl32 | Mm_Celera | 4:24834914 | ATACAACATTGGCTA[C/T]CAATACACTTTCAAA | 212390 |
rs27751686 | snp | A/G | 0.244898 | 0.249948 | intron-variant | Klhl32 | Mm_Celera | 4:24834887 | GTCCTTTCCAGCTCT[A/G]AAGTTTAGCATATAC | 212390 |
rs27751687 | snp | C/T | 0.231111 | 0.249285 | intron-variant | Klhl32 | Mm_Celera | 4:24834789 | TGCAAAACAGATGCA[C/T]AGAAAGACAGACCAC | 212390 |
rs27751688 | snp | C/T | 0.124444 | 0.216185 | intron-variant | Klhl32 | Mm_Celera | 4:24834713 | ATTTATTAATCACTT[C/T]AGGCTTTCTTCCCCA | 212390 |
rs27751689 | snp | A/G | 0.124444 | 0.216185 | intron-variant | Klhl32 | Mm_Celera | 4:24834675 | TCTAACATGTTGCCT[A/G]TACAAGGTCATCTCC | 212390 |
rs27751690 | snp | A/G | 0.231111 | 0.249285 | intron-variant | Klhl32 | Mm_Celera | 4:24834611 | CTCTAAGTCTCTAGT[A/G]CTGACAGACTCCTTA | 212390 |
rs27751691 | snp | C/T | 0.142012 | 0.225474 | intron-variant | Klhl32 | Mm_Celera | 4:24834558 | TTACAAATGTCCTCT[C/T]TCACTTCTTTGTTTT | 212390 |
rs27751692 | snp | C/T | 0.304688 | 0.243945 | intron-variant | Klhl32 | GRCm38.p3 | 4:24834390 | GGCCATAACAATCAT[C/T]TACTCCAAAATAAGC | 212390 |
rs27751693 | snp | G/T | 0.277778 | 0.248452 | intron-variant | Klhl32 | Mm_Celera | 4:24834319 | CTCAACCTTGTAAGA[G/T]CCAATTCTAGAAGAA | 212390 |
rs27751694 | snp | A/G | 0.231111 | 0.249285 | intron-variant | Klhl32 | Mm_Celera | 4:24834280 | ACGTAAAAGCACATT[A/G]CCCATGTAAATGATA | 212390 |
rs27751695 | snp | A/G | 0.21875 | 0.248039 | intron-variant | Klhl32 | Mm_Celera | 4:24834209 | ATTGTCAGCTTCTGT[A/G]TGCATGGGAGATCTC | 212390 |
rs27751696 | snp | A/G | 0.46875 | 0.121031 | intron-variant | Klhl32 | GRCm38.p3 | 4:24834172 | GAAATTATATTGATA[A/G]CCGATAAGAACAGGA | 212390 |
rs27751697 | snp | A/G | 0.231111 | 0.249285 | intron-variant | Klhl32 | Mm_Celera | 4:24834065 | CTTCCTGAATCAGCT[A/G]GTCTGTATCTTGGGC | 212390 |
rs27751698 | snp | C/G | 0.124444 | 0.216185 | intron-variant | Klhl32 | Mm_Celera | 4:24834053 | CACTGTAACTCACTT[C/G]CTGAATCAGCTGGTC | 212390 |
rs27751699 | snp | A/G | 0.132653 | 0.220748 | intron-variant | Klhl32 | Mm_Celera | 4:24833947 | GTAGACTTCTGAAAT[A/G]TATTTTTGTGAGGCA | 212390 |
rs27751700 | snp | A/G | 0.231111 | 0.249285 | intron-variant | Klhl32 | Mm_Celera | 4:24833892 | GTGGCCAGGGAGAAG[A/G]GAAAGAAGCACAAAG | 212390 |
rs27751701 | snp | A/C | 0.260355 | 0.249785 | intron-variant | Klhl32 | Mm_Celera | 4:24833852 | ACATCTCCCTCCTCT[A/C]GAAAACTAGAGTAAG | 212390 |
rs27751702 | snp | G/T | 0.124444 | 0.216185 | intron-variant | Klhl32 | Mm_Celera | 4:24833827 | TACCATTCATGTTCC[G/T]ACAGACATGACATCT | 212390 |
rs27751703 | snp | C/T | 0.444444 | 0.157135 | intron-variant | Klhl32 | GRCm38.p3 | 4:24833814 | TCACCACCACAGATA[C/T]CATTCATGTTCCTAC | 212390 |
rs27751704 | snp | C/T | 0.231111 | 0.249285 | intron-variant | Klhl32 | Mm_Celera | 4:24833294 | ACTTGAAGAAGCGAG[C/T]TAAAGAAACCATACT | 212390 |
rs27751705 | snp | C/T | 0.231111 | 0.249285 | intron-variant | Klhl32 | Mm_Celera | 4:24833257 | AATACTTTCTGCATA[C/T]AAGAATGGCTTTCGA | 212390 |
rs27751706 | snp | A/G | 0.290657 | 0.246672 | intron-variant | Klhl32 | Mm_Celera | 4:24833204 | ATAAGACCACAGTCT[A/G]AGAAAGAACTAAAGC | 212390 |
rs27751707 | snp | A/G | 0.124444 | 0.216185 | intron-variant | Klhl32 | Mm_Celera | 4:24833054 | ACTCCAGCTGCTCCC[A/G]TCTTTGATATAACCA | 212390 |
rs27751708 | snp | A/G | 0.231111 | 0.249285 | intron-variant | Klhl32 | Mm_Celera | 4:24833026 | GCATGATCAGTAATC[A/G]CTGTCTCATCTGACT | 212390 |
rs27751709 | snp | C/T | 0.124444 | 0.216185 | intron-variant | Klhl32 | Mm_Celera | 4:24832781 | TGGCATTCTTCAAGA[C/T]CTTATGCCATGAGTC | 212390 |
rs27751710 | snp | A/C | 0.124444 | 0.216185 | intron-variant | Klhl32 | Mm_Celera | 4:24832728 | TCAGGGCATTTCATA[A/C]TCAAGAACTCTGAGA | 212390 |
rs27751711 | snp | A/G | 0.48 | 0.0979796 | intron-variant | Klhl32 | GRCm38.p3 | 4:24832649 | AGCACAAGGTGCAGG[A/G]CAAGTACAGAGCATC | 212390 |
rs27751712 | snp | A/G | 0.124444 | 0.216185 | intron-variant | Klhl32 | Mm_Celera | 4:24832641 | CATTCTAAAGCACAA[A/G]GTGCAGGGCAAGTAC | 212390 |
rs27751713 | snp | A/C | 0.124444 | 0.216185 | intron-variant | Klhl32 | Mm_Celera | 4:24832580 | AAAACAACATTTTCC[A/C]AATTCTTCTATTGAA | 212390 |
rs27751714 | snp | C/T | 0.124444 | 0.216185 | intron-variant | Klhl32 | Mm_Celera | 4:24832525 | AACTTCTGCAAATCA[C/T]GTAGCCTTTATGGGC | 212390 |
rs27751715 | snp | A/G | 0.408163 | 0.193609 | intron-variant | Klhl32 | GRCm38.p3 | 4:24832300 | AAGAAAAGTCCCGTT[A/G]GGCCATTAAGGGATT | 212390 |
rs27751716 | snp | A/G | 0.231111 | 0.249285 | intron-variant | Klhl32 | GRCm38.p3 | 4:24832033 | TTTGAGAAAAGAAAG[A/G]CTCACAGGAGAAAAG | 212390 |
rs27751717 | snp | A/G | 0.415225 | 0.187619 | intron-variant | Klhl32 | Mm_Celera | 4:24831346 | CCAAGAAAGTTTAAC[A/G]CTATTGAGGCTATGA | 212390 |
rs27751718 | snp | C/T | 0.124444 | 0.216185 | intron-variant | Klhl32 | Mm_Celera | 4:24831143 | GATGATCCTTGATTC[C/T]TAAGCAATTAAAGAT | 212390 |
rs27751719 | snp | A/C | 0.142012 | 0.225474 | intron-variant | Klhl32 | Mm_Celera | 4:24830878 | AGCCCTTGGGCAGCT[A/C]TTTGCAAAAGAACAA | 212390 |
rs27751720 | snp | A/T | 0.231111 | 0.249285 | intron-variant | Klhl32 | Mm_Celera | 4:24830849 | GACATCTCAGAAGCC[A/T]GAGGCAGCTCAGTAG | 212390 |
rs27751721 | snp | C/G | 0.231111 | 0.249285 | intron-variant | Klhl32 | Mm_Celera | 4:24830820 | AGGAACTGCCCACAA[C/G]AGGTTGGGATGGAGA | 212390 |
rs27751722 | snp | C/G/T | 0.345679 | 0.230967 | intron-variant | Klhl32 | GRCm38.p3 | 4:24830615 | AAATAAAAATATGTC[C/G/T]AGTAGTTCATGATAA | 212390 |
rs27751723 | snp | A/C | 0.290657 | 0.246672 | intron-variant | Klhl32 | Mm_Celera | 4:24830410 | AATGGCTTCCCAGAT[A/C]TCTGGAGTTGTATAT | 212390 |
rs27751724 | snp | A/G | 0.132653 | 0.220748 | intron-variant | Klhl32 | Mm_Celera | 4:24830302 | TTTATTCTCTCCAAA[A/G]GTCTGTGCTGTCTGG | 212390 |
rs27751725 | snp | A/G | 0.132653 | 0.220748 | intron-variant | Klhl32 | Mm_Celera | 4:24830105 | CCATATGAGCAAATG[A/G]CTGCACCACAAATAA | 212390 |
rs27751726 | snp | A/C | 0.142012 | 0.225474 | intron-variant | Klhl32 | Mm_Celera | 4:24829818 | ACAGATGGGATAATG[A/C]TCGCAGAGGAGTGTG | 212390 |
rs27751727 | snp | A/G | 0.456747 | 0.140554 | intron-variant | Klhl32 | GRCm38.p3 | 4:24829812 | AGCTTCACAGATGGG[A/G]TAATGCTCGCAGAGG | 212390 |
rs27751728 | snp | A/G | 0.132653 | 0.220748 | intron-variant | Klhl32 | Mm_Celera | 4:24829740 | TTTACATGAGATAGA[A/G]GAGGAGGAGCAAGAG | 212390 |
rs27751729 | snp | C/T | 0.132653 | 0.220748 | intron-variant | Klhl32 | Mm_Celera | 4:24829674 | TAGAGACAAGAAAGT[C/T]TTCCACACAATGTCT | 212390 |
rs27751730 | snp | C/T | 0.132653 | 0.220748 | intron-variant | Klhl32 | Mm_Celera | 4:24829594 | AGTAGTCAGGGAGGG[C/T]GCTGAAGAAATAAAG | 212390 |
rs27751731 | snp | C/T | 0.132653 | 0.220748 | intron-variant | Klhl32 | Mm_Celera | 4:24829323 | GATGGAGACAGGACT[C/T]TTGGTGAAGTGAACT | 212390 |
rs27751732 | snp | C/G | 0.132653 | 0.220748 | intron-variant | Klhl32 | Mm_Celera | 4:24829301 | GAGGAGACTAATGAC[C/G]TAGAGTGATGGAGAC | 212390 |
rs27751733 | snp | C/T | 0.142012 | 0.225474 | intron-variant | Klhl32 | Mm_Celera | 4:24829254 | CAGGAAGAACAGGGA[C/T]AGAGGGCTATAAAGG | 212390 |
rs27751734 | snp | A/G | 0.132653 | 0.220748 | intron-variant | Klhl32 | Mm_Celera | 4:24829092 | CTCATGAAATTAAGT[A/G]AAAGATGCCATTAAC | 212390 |
rs27751735 | snp | A/G | 0.426035 | 0.177515 | intron-variant | Klhl32 | Mm_Celera | 4:24829035 | AGCTTCAATTACAAT[A/G]CCAAAGTCATTAGTC | 212390 |
rs27751736 | snp | A/C | 0.197531 | 0.244432 | intron-variant | Klhl32 | Mm_Celera | 4:24828305 | TACCAAAAGTATTTC[A/C]TTTCAGGAACAAATT | 212390 |
rs27751737 | snp | A/C | 0.456747 | 0.140554 | intron-variant | Klhl32 | GRCm38.p3 | 4:24827722 | CCGCTTAGTCTCCTG[A/C]ATGAGTTTGGTTCCT | 212390 |
rs27751738 | snp | A/C | 0.493827 | 0.0552116 | intron-variant | Klhl32 | Mm_Celera | 4:24827552 | TTTATTAACATGGCA[A/C]CTGATAAAAGGTGTC | 212390 |
rs27751739 | snp | C/T | 0.359862 | 0.224567 | intron-variant | Klhl32 | GRCm38.p3 | 4:24827487 | GTCATGAATGCATAT[C/T]GTGGAGTAAGATTTA | 212390 |
rs27751740 | snp | A/G | 0.444444 | 0.157135 | intron-variant | Klhl32 | GRCm38.p3 | 4:24827293 | CACCTCATGTCATAA[A/G]CAGGCTAATTCTACC | 212390 |
rs27751741 | snp | A/C | 0.132653 | 0.220748 | intron-variant | Klhl32 | Mm_Celera | 4:24827157 | TTGCAAAACCTTGAT[A/C]TAAGCCACACAAAAA | 212390 |
rs27751742 | snp | G/T | 0.132653 | 0.220748 | intron-variant | Klhl32 | Mm_Celera | 4:24826572 | TTAGTCATAAACATT[G/T]TACTCCTAAAACGGT | 212390 |
rs27751743 | snp | C/G/T | 0.132653 | 0.220748 | intron-variant | Klhl32 | GRCm38.p3 | 4:24825813 | CAGAGCCTGTCTACG[C/G/T]CTGACTCTGTCCCTT | 212390 |
rs27751744 | snp | A/C | 0.444444 | 0.157135 | intron-variant | Klhl32 | GRCm38.p3 | 4:24825593 | GAGAGCGAGGACTTG[A/C]CACAAAAACAACATA | 212390 |
rs27751745 | snp | A/C | 0.375 | 0.216506 | intron-variant | Klhl32 | GRCm38.p3 | 4:24825525 | AGGTCTCGGAAGGCA[A/C]TGGTGGAGAACTCAG | 212390 |
rs27751746 | snp | C/T | 0.244898 | 0.249948 | intron-variant | Klhl32 | Mm_Celera | 4:24825317 | ATACACAACTAAATG[C/T]GATAATCCAAAGAAC | 212390 |
rs27751747 | snp | A/G | 0.132653 | 0.220748 | intron-variant | Klhl32 | Mm_Celera | 4:24825151 | GAGACAGAACCAAGC[A/G]TAGCCATTTCCTACA | 212390 |
rs27751748 | snp | C/T | 0.484429 | 0.0868505 | intron-variant | Klhl32 | Mm_Celera | 4:24824998 | TGTGGGGTGTGCAAA[C/T]GTCTAATGGATTCAT | 212390 |
rs27751749 | snp | C/T | 0.444444 | 0.157135 | intron-variant | Klhl32 | Mm_Celera | 4:24808619 | AGATGAACTGAATGC[C/T]AGATAATAAAATAGC | 212390 |
rs27751750 | snp | A/G | 0.444444 | 0.157135 | intron-variant | Klhl32 | Mm_Celera | 4:24808373 | GAAGCAACACAGTTT[A/G]AGAGTGTAATTAGGA | 212390 |
rs27751751 | snp | C/T | 0.375 | 0.216506 | intron-variant | Klhl32 | Mm_Celera | 4:24808346 | GAAGATGGTGCCCAT[C/T]AAAGCATTGAAGAAG | 212390 |
rs27751752 | snp | A/C | 0.124444 | 0.216185 | intron-variant | Klhl32 | Mm_Celera | 4:24807178 | ATTCAAAACTGTGCT[A/C]TATGGATAAAACCTG | 212390 |
rs27751753 | snp | C/T | 0.124444 | 0.216185 | intron-variant | Klhl32 | Mm_Celera | 4:24807164 | TCCCACTTCAAAAAA[C/T]TCAAAACTGTGCTAT | 212390 |
rs27751754 | snp | A/G | 0.432133 | 0.171253 | intron-variant | Klhl32 | GRCm38.p3 | 4:24806733 | GAGTGCTTGCCTCCT[A/G]TTGTCGACGGCTACG | 212390 |
rs27751755 | snp | A/G | 0.124444 | 0.216185 | intron-variant | Klhl32 | Mm_Celera | 4:24806722 | CCAGGGTATGTGAGT[A/G]CTTGCCTCCTATTGT | 212390 |
rs27751756 | snp | A/T | 0.132653 | 0.220748 | intron-variant | Klhl32 | Mm_Celera | 4:24806618 | GGTCAGAAGCATCAG[A/T]CACATCTGCAGAAAT | 212390 |
rs27751757 | snp | C/T | 0.132653 | 0.220748 | intron-variant | Klhl32 | Mm_Celera | 4:24806614 | CAGTGGTCAGAAGCA[C/T]CAGACACATCTGCAG | 212390 |
rs27751758 | snp | A/G | 0.124444 | 0.216185 | intron-variant | Klhl32 | Mm_Celera | 4:24806559 | TCCATCCAGTTTAGG[A/G]TTTTTGGGCACCATC | 212390 |
rs27751759 | snp | C/T | 0.124444 | 0.216185 | intron-variant | Klhl32 | Mm_Celera | 4:24806549 | AAAAGTCATTTCCAT[C/T]CAGTTTAGGGTTTTT | 212390 |
rs27751760 | snp | G/T | 0.231111 | 0.249285 | intron-variant | Klhl32 | Mm_Celera | 4:24805006 | ACCGGTTCATCCAGC[G/T]AGATATATCTGAGTT | 212390 |
rs27751761 | snp | A/G | 0.124444 | 0.216185 | intron-variant | Klhl32 | Mm_Celera | 4:24804994 | ACTCCAATAAACACC[A/G]GTTCATCCAGCGAGA | 212390 |
rs27751762 | snp | C/T | 0.456747 | 0.140554 | intron-variant | Klhl32 | GRCm38.p3 | 4:24804938 | ACGAAGGCAGGCCTT[C/T]ATTAACTTAGCTGCA | 212390 |
rs27751763 | snp | A/T | 0.124444 | 0.216185 | intron-variant | Klhl32 | Mm_Celera | 4:24804889 | AGGAGGTGGAAGATT[A/T]CCTAAGTGAAGTAGT | 212390 |
rs27751764 | snp | G/T | 0.124444 | 0.216185 | intron-variant | Klhl32 | Mm_Celera | 4:24804761 | CCCGGCTTAACAACA[G/T]TCTCTTGTAGAGGTA | 212390 |
rs27751765 | snp | C/T | 0.444444 | 0.157135 | intron-variant | Klhl32 | GRCm38.p3 | 4:24804748 | GGGCCTCACAATACC[C/T]GGCTTAACAACATTC | 212390 |
rs27751766 | snp | C/G | 0.231111 | 0.249285 | intron-variant | Klhl32 | Mm_Celera | 4:24804708 | TACCTCAAAATCAAA[C/G]AAGTATAATTACCTG | 212390 |
rs27751767 | snp | A/T | 0.231111 | 0.249285 | intron-variant | Klhl32 | Mm_Celera | 4:24804655 | AGGATATGAACCTGC[A/T]CTAAGATTCTGACCT | 212390 |
rs27751768 | snp | C/T | 0.231111 | 0.249285 | intron-variant | Klhl32 | Mm_Celera | 4:24804564 | TAATAATGAAAAATG[C/T]TGTGTTCTCATCAGG | 212390 |
rs27751769 | snp | C/T | 0.142012 | 0.225474 | intron-variant | Klhl32 | Mm_Celera | 4:24804467 | CAATAATGTCAAATC[C/T]CAACTCTGCCGTATG | 212390 |
rs27751770 | snp | C/T | 0.124444 | 0.216185 | intron-variant | Klhl32 | Mm_Celera | 4:24804375 | TTAGGTTTCTACACA[C/T]GCACATGCTTGCTCC | 212390 |
rs27751771 | snp | C/T | 0.124444 | 0.216185 | intron-variant | Klhl32 | Mm_Celera | 4:24804330 | GCTAAAACATCCCAA[C/T]GTCCACAGAAATTCC | 212390 |
rs27751772 | snp | C/T | 0.124444 | 0.216185 | intron-variant | Klhl32 | Mm_Celera | 4:24804200 | TGGGTCATGGATGGC[C/T]GAGAAACTTCTGACA | 212390 |
rs27751773 | snp | A/T | 0.124444 | 0.216185 | intron-variant | Klhl32 | Mm_Celera | 4:24803187 | ACCAAAAATGGTGCA[A/T]ATTCCAGGACACAGT | 212390 |
rs27751774 | snp | A/G | 0.132653 | 0.220748 | intron-variant | Klhl32 | Mm_Celera | 4:24803100 | AGGACTAACTAAAAC[A/G]ATGCAAATTGAGCAT | 212390 |
rs27751775 | snp | A/G | 0.459184 | 0.136902 | intron-variant | Klhl32 | GRCm38.p3 | 4:24803062 | CTGAGGTTACTCCAT[A/G]GATGCTGGACCCATG | 212390 |
rs27751776 | snp | C/T | 0.304688 | 0.243945 | intron-variant | Klhl32 | Mm_Celera | 4:24802976 | TCAAAACTAAGAAAA[C/T]AGTTCTGCTGTTTTA | 212390 |
rs27751777 | snp | C/T | 0.142012 | 0.225474 | intron-variant | Klhl32 | Mm_Celera | 4:24802823 | GTTTTTCTTTTACAT[C/T]TTGCTAATGTACCTA | 212390 |
rs27751778 | snp | A/T | 0.231111 | 0.249285 | intron-variant | Klhl32 | Mm_Celera | 4:24802774 | TTTAATCCCTACAAA[A/T]ATGAGTTGTGCAGTG | 212390 |
rs27751779 | snp | C/G | 0.231111 | 0.249285 | intron-variant | Klhl32 | Mm_Celera | 4:24802647 | AACAATTGTTAAGAA[C/G]CAGCAGATGCAGAAT | 212390 |
rs27751780 | snp | G/T | 0.290657 | 0.246672 | intron-variant | Klhl32 | Mm_Celera | 4:24802638 | CACAGAGCTAACAAT[G/T]GTTAAGAAGCAGCAG | 212390 |
rs27751781 | snp | A/G | 0.375 | 0.216506 | intron-variant | Klhl32 | Mm_Celera | 4:24802519 | ATGAATTAAGAATGT[A/G]CCACCATAGAAAAGT | 212390 |
rs27751782 | snp | A/G | 0.142012 | 0.225474 | intron-variant | Klhl32 | Mm_Celera | 4:24802385 | CAGTTCCCTGCTAGC[A/G]GTGCTCATGGCAGGT | 212390 |
rs27751783 | snp | G/T | 0.35503 | 0.226867 | intron-variant | Klhl32 | Mm_Celera | 4:24802340 | GATACATTTCAAACA[G/T]TATGTGATAGAAAAA | 212390 |
rs27751784 | snp | G/T | 0.124444 | 0.216185 | intron-variant | Klhl32 | Mm_Celera | 4:24802304 | TAGAACAGTTCACCA[G/T]TAAGGTATTATATCT | 212390 |
rs27751785 | snp | C/T | 0.124444 | 0.216185 | intron-variant | Klhl32 | Mm_Celera | 4:24802267 | TACTAATCCAGCAAA[C/T]TGAGAAAAGAATCTT | 212390 |
rs27751786 | snp | C/T | 0.124444 | 0.216185 | intron-variant | Klhl32 | Mm_Celera | 4:24802096 | AGACTTGCTTAGCAA[C/T]CCATTATTGCTACAG | 212390 |
rs27751787 | snp | C/T | 0.244898 | 0.249948 | intron-variant | Klhl32 | GRCm38.p3 | 4:24802067 | ATTCAAGCCACATTG[C/T]TTAATTAGCTGAGAG | 212390 |
rs27751788 | snp | A/C | 0.336735 | 0.234472 | intron-variant | Klhl32 | Mm_Celera | 4:24801971 | CTTTCACTTATTTCT[A/C]GTGTAAGTTCTGACA | 212390 |
rs27751789 | snp | A/G | 0.391111 | 0.206368 | intron-variant | Klhl32 | Mm_Celera | 4:24801863 | TCTGGTTAGGTATTC[A/G]ATTATTACTGCATAT | 212390 |
rs27751790 | snp | A/G | 0.48 | 0.0979796 | intron-variant | Klhl32 | Mm_Celera | 4:24801722 | GCTTATTTACAAAAG[A/G]GATATATTACACTGT | 212390 |
rs27751791 | snp | G/T | 0.18 | 0.24 | intron-variant | Klhl32 | Mm_Celera | 4:24801710 | TAGGGTAAAAATGCT[G/T]ATTTACAAAAGGGAT | 212390 |
rs27751792 | snp | C/T | 0.408163 | 0.193609 | intron-variant | Klhl32 | GRCm38.p3 | 4:24801612 | ACATTTTGTAATACA[C/T]CCAATTGCCAAAATT | 212390 |
rs27751793 | snp | A/G | 0.396694 | 0.202437 | intron-variant | Klhl32 | Mm_Celera | 4:24801588 | AACTCTCCTTAGAGA[A/G]TCTAGCTCACATTTT | 212390 |
rs27751794 | snp | A/T | 0.375 | 0.216506 | intron-variant | Klhl32 | GRCm38.p3 | 4:24801508 | GCTTTTAATGAGTGA[A/T]GCAACTCTAAACAGA | 212390 |
rs27751795 | snp | C/T | 0.42 | 0.183303 | intron-variant | Klhl32 | GRCm38.p3 | 4:24801494 | CACCCTTTGCCTTGG[C/T]TTTTAATGAGTGAAG | 212390 |
rs27751796 | snp | C/T | 0.375 | 0.216506 | intron-variant | Klhl32 | GRCm38.p3 | 4:24801434 | GTGTGCTCGGCAGAA[C/T]TGAAGTTCCTGGCCT | 212390 |
rs27751797 | snp | A/G | 0.124444 | 0.216185 | intron-variant | Klhl32 | Mm_Celera | 4:24801334 | CAAGCACTCATTGAC[A/G]AAGCCACACACAGAG | 212390 |
rs27751798 | snp | A/G | 0.48 | 0.0979796 | intron-variant | Klhl32 | GRCm38.p3 | 4:24801202 | ACACCTGCAGTGATC[A/G]GAACCACAGACACTA | 212390 |
rs27751799 | snp | A/G | 0.152778 | 0.230321 | intron-variant | Klhl32 | GRCm38.p3 | 4:24801189 | GATCTTACGAACTAC[A/G]CCTGCAGTGATCGGA | 212390 |
rs27751800 | snp | A/C | 0.297521 | 0.245442 | intron-variant | Klhl32 | Mm_Celera | 4:24801146 | AGATAGAAAGAAAAA[A/C]CATCCAATAGTCACG | 212390 |
rs27751801 | snp | C/T | 0.260355 | 0.249785 | intron-variant | Klhl32 | Mm_Celera | 4:24800942 | GAAAAATGCAAAGAG[C/T]ATTCTAGAAGCTCAT | 212390 |
rs27751802 | snp | C/T | 0.497041 | 0.0383476 | intron-variant | Klhl32 | GRCm38.p3 | 4:24800894 | CAAGCATTCCAGCTG[C/T]ATTAAAGAGTATAAG | 212390 |
rs27751803 | snp | C/G | 0.32 | 0.24 | utr-variant-5-prime, intron-variant | Klhl32 | GRCm38.p3 | 4:24800843 | TCCTCAAGCTGGGTC[C/G]TCAGAGTCAGGCTTA | 212390 |
rs27751804 | snp | C/T | 0.336735 | 0.234472 | intron-variant | Klhl32 | Mm_Celera | 4:24800759 | GTACTGCGTTGTTCC[C/T]GGGTTCAGCTCGCCA | 212390 |
rs27751805 | snp | A/T | 0.5 | 0 | intron-variant | Klhl32 | Mm_Celera | 4:24800439 | AAAATCATGACTGTT[A/T]TGTTTATTCAGTCAA | 212390 |
rs27751806 | snp | A/G | 0.132653 | 0.220748 | intron-variant | Klhl32 | Mm_Celera | 4:24800382 | CTAAGTTTGATCAAG[A/G]GGTCTTAGTGGTTCA | 212390 |
rs27751807 | snp | G/T | 0.244898 | 0.249948 | intron-variant | Klhl32 | Mm_Celera | 4:24800271 | AGTGATTTGCCTTTT[G/T]CTCAAAGGGTTACCA | 212390 |
rs27751808 | snp | A/G | 0.5 | 0 | intron-variant | Klhl32 | Mm_Celera | 4:24800216 | GGTCAATATTCAGAG[A/G]CAGCATAGTTTTCTA | 212390 |
rs27751809 | snp | C/G | 0.48 | 0.0979796 | intron-variant | Klhl32 | Mm_Celera | 4:24800180 | ACTTCTGAATCCTCC[C/G]CAAAGGGATTGCATT | 212390 |
rs27751810 | snp | A/G | 0.231111 | 0.249285 | intron-variant | Klhl32 | Mm_Celera | 4:24800000 | ACGGTTTTCATCACG[A/G]CATTTGCATTGCTGG | 212390 |
rs27751811 | snp | C/T | 0.132653 | 0.220748 | intron-variant | Klhl32 | GRCm38.p3 | 4:24799915 | GCCTCGGTGCACCGC[C/T]CAGCTCAGCTCATCC | 212390 |
rs27751812 | snp | C/T | 0.124444 | 0.216185 | intron-variant | Klhl32 | Mm_Celera | 4:24799765 | CCTCAGTTCTATTAC[C/T]TCTCTTCTTATTTCT | 212390 |
rs27751813 | snp | C/T | 0.244898 | 0.249948 | intron-variant | Klhl32 | Mm_Celera | 4:24799740 | TAATTCCTCACACTC[C/T]ACAGCTATTCCTCAG | 212390 |
rs27751814 | snp | C/T | 0.408163 | 0.193609 | intron-variant | Klhl32 | Mm_Celera | 4:24799715 | GACAGCTCTATTTAA[C/T]AGAAATATCTAATTC | 212390 |
rs27751815 | snp | C/T | 0.48 | 0.0979796 | intron-variant | Klhl32 | GRCm38.p3 | 4:24799613 | ACTGCAACAAACTCA[C/T]AAGAGGCATAAAGCA | 212390 |
rs27751816 | snp | A/C | 0.124444 | 0.216185 | intron-variant | Klhl32 | Mm_Celera | 4:24799606 | ATTGCTGACTGCAAC[A/C]AACTCACAAGAGGCA | 212390 |
rs27751817 | snp | A/C | 0.124444 | 0.216185 | intron-variant | Klhl32 | Mm_Celera | 4:24799559 | GAAATACTGCTGGCC[A/C]TTGAACACCATTCCC | 212390 |
rs27751818 | snp | C/G | 0.231111 | 0.249285 | intron-variant | Klhl32 | Mm_Celera | 4:24799533 | TAAAATCAACCGATC[C/G]CTGATGATAAGAAAT | 212390 |
rs27751819 | snp | C/T | 0.336735 | 0.234472 | intron-variant | Klhl32 | Mm_Celera | 4:24799389 | ATCATTTTGGCAGGG[C/T]ACCAGATCTAGCATA | 212390 |
rs27751820 | snp | A/T | 0.132653 | 0.220748 | intron-variant | Klhl32 | Mm_Celera | 4:24799377 | TAGTCCACGTGTATC[A/T]TTTTGGCAGGGTACC | 212390 |
rs27751821 | snp | A/G | 0.124444 | 0.216185 | intron-variant | Klhl32 | Mm_Celera | 4:24799257 | GGCAGAAGGATGGGA[A/G]CTGATTACCATAAAT | 212390 |
rs27751822 | snp | A/G | 0.493827 | 0.0552116 | intron-variant | Klhl32 | GRCm38.p3 | 4:24799241 | CCACAGTGGAAGACA[A/G]GGCAGAAGGATGGGA | 212390 |
rs27751823 | snp | A/C | 0.336735 | 0.234472 | intron-variant | Klhl32 | Mm_Celera | 4:24799226 | GGGAAGGAGATGACT[A/C]CACAGTGGAAGACAG | 212390 |
rs27751824 | snp | A/G | 0.124444 | 0.216185 | intron-variant | Klhl32 | Mm_Celera | 4:24799027 | CTAATGTGGCTGGCT[A/G]GAAGAAAACGTTCTC | 212390 |
rs27751825 | snp | A/G | 0.124444 | 0.216185 | intron-variant | Klhl32 | Mm_Celera | 4:24798978 | GACATGAAGTGACTA[A/G]TGGGGATAACAAGAT | 212390 |
rs27751826 | snp | A/G | 0.465374 | 0.126941 | intron-variant | Klhl32 | Mm_Celera | 4:24798299 | AGTTTCAGAATTTAA[A/G]CCTGTTAAGAAGAGA | 212390 |
rs27751827 | snp | C/G | 0.336735 | 0.234472 | intron-variant | Klhl32 | Mm_Celera | 4:24798082 | GCAAGTCATGGCTTG[C/G]TTTGCTTCTTAAGGG | 212390 |
rs27751828 | snp | C/T | 0.391111 | 0.206368 | intron-variant | Klhl32 | Mm_Celera | 4:24797812 | AACTTGATGTCCCAA[C/T]AGTAGGGCAACTGGA | 212390 |
rs27751829 | snp | A/G | 0.32 | 0.24 | intron-variant | Klhl32 | Mm_Celera | 4:24797623 | CTTGGGACCACGGCA[A/G]TAGCTGAGGCCTCTC | 212390 |
rs27751830 | snp | A/T | 0.48 | 0.0979796 | intron-variant | Klhl32 | GRCm38.p3 | 4:24797523 | GTGTGGGCCAGGGCA[A/T]CCAAGAGCCATGGCA | 212390 |
rs27751831 | snp | A/C | 0.495868 | 0.0452663 | intron-variant | Klhl32 | GRCm38.p3 | 4:24797484 | ACTGAGTAACCGCAG[A/C]TGAGGTGATGACTCA | 212390 |
rs27751832 | snp | A/G | 0.473373 | 0.11227 | intron-variant | Klhl32 | GRCm38.p3 | 4:24797425 | CAGACAGACTGACAC[A/G]CTCTTCTACAGAAAT | 212390 |
rs27751833 | snp | G/T | 0.375 | 0.216506 | intron-variant | Klhl32 | Mm_Celera | 4:24797419 | GGAGCACAGACAGAC[G/T]GACACACTCTTCTAC | 212390 |
rs27751834 | snp | A/G | 0.336735 | 0.234472 | intron-variant | Klhl32 | GRCm38.p3 | 4:24797352 | CCCTGAGACAAAGAA[A/G]AGAAGATGTACGCAG | 212390 |
rs27751835 | snp | A/G | 0.142012 | 0.225474 | intron-variant | Klhl32 | Mm_Celera | 4:24797347 | TACCACCCTGAGACA[A/G]AGAAGAGAAGATGTA | 212390 |
rs27751836 | snp | C/T | 0.408163 | 0.193609 | intron-variant | Klhl32 | GRCm38.p3 | 4:24797275 | AGGACAGTGGCACAC[C/T]AAGTAAGTACTCTCA | 212390 |
rs27751837 | snp | A/G | 0.124444 | 0.216185 | intron-variant | Klhl32 | Mm_Celera | 4:24797260 | CATATTCAGTGTATC[A/G]GGACAGTGGCACACC | 212390 |
rs27751838 | snp | C/T | 0.231111 | 0.249285 | intron-variant | Klhl32 | Mm_Celera | 4:24796732 | GCATAGAGTTAACTC[C/T]TCAATCCCAGAAATC | 212390 |
rs27751839 | snp | A/G | 0.244898 | 0.249948 | intron-variant | Klhl32 | Mm_Celera | 4:24796698 | AATGTCTGCTTTAGC[A/G]CAAATGGCTACTTTG | 212390 |
rs27751840 | snp | A/T | 0.124444 | 0.216185 | intron-variant | Klhl32 | Mm_Celera | 4:24796660 | CAGAGCACGCTTCTG[A/T]CAGTGGCCTCCTGCT | 212390 |
rs27751841 | snp | A/C | 0.124444 | 0.216185 | intron-variant | Klhl32 | Mm_Celera | 4:24796654 | CAAATGCAGAGCACG[A/C]TTCTGACAGTGGCCT | 212390 |
rs27751842 | snp | C/G | 0.124444 | 0.216185 | intron-variant | Klhl32 | Mm_Celera | 4:24796595 | AATCATGACTTTGAG[C/G]CAGTAACTTTCATTC | 212390 |
rs27751843 | snp | A/C | 0.124444 | 0.216185 | intron-variant | Klhl32 | Mm_Celera | 4:24796414 | AGAGCACCATTTCTG[A/C]ATCTCACAGGACTGG | 212390 |
rs27751844 | snp | A/G | 0.124444 | 0.216185 | intron-variant | Klhl32 | Mm_Celera | 4:24796398 | AAGCTGCCACTGTCC[A/G]AGAGCACCATTTCTG | 212390 |
rs27751845 | snp | A/G | 0.231111 | 0.249285 | intron-variant | Klhl32 | Mm_Celera | 4:24796366 | GCTCACAGGCACCCT[A/G]CCAGGTTACTCCAGG | 212390 |
rs27751846 | snp | G/T | 0.124444 | 0.216185 | intron-variant | Klhl32 | Mm_Celera | 4:24795977 | CAGATTTGAGAAGAT[G/T]CTTAAAACTGGGAAA | 212390 |
rs27751847 | snp | A/C | 0.375 | 0.216506 | intron-variant | Klhl32 | Mm_Celera | 4:24795725 | TGATCGCAGACTGAG[A/C]ACAGAAACCGAAGGC | 212390 |
rs27751848 | snp | A/C | 0.489796 | 0.070696 | intron-variant | Klhl32 | GRCm38.p3 | 4:24795679 | GTGCACAGGACAGCG[A/C]GAAGAGGTGAGGCTC | 212390 |
rs27751849 | snp | C/T | 0.21875 | 0.248039 | intron-variant | Klhl32 | Mm_Celera | 4:24795619 | CTTACCTCTCAGCTA[C/T]AAAGCTGCAAAAGCC | 212390 |
rs27751850 | snp | A/G | 0.165289 | 0.235211 | intron-variant | Klhl32 | Mm_Celera | 4:24795584 | ACACATCATCCTTGT[A/G]TTCGCAAAGCAGTCT | 212390 |
rs27751851 | snp | C/G | 0.152778 | 0.230321 | intron-variant | Klhl32 | Mm_Celera | 4:24795579 | TCTCAACACATCATC[C/G]TTGTATTCGCAAAGC | 212390 |
rs27751852 | snp | C/G | 0.152778 | 0.230321 | intron-variant | Klhl32 | Mm_Celera | 4:24795552 | GAATTCAAAGGCCCA[C/G]TAATCAACAAGTCTC | 212390 |
rs27751853 | snp | C/T | 0.197531 | 0.244432 | intron-variant | Klhl32 | Mm_Celera | 4:24795541 | GCATTTGGCAAGAAT[C/T]CAAAGGCCCAGTAAT | 212390 |
rs27751854 | snp | A/G | 0.21875 | 0.248039 | intron-variant | Klhl32 | Mm_Celera | 4:24795464 | CAACACTTGGCAGAA[A/G]AGCCTAAATATTTTA | 212390 |
rs27751855 | snp | A/C | 0.18 | 0.24 | intron-variant | Klhl32 | Mm_Celera | 4:24795323 | AAAGAGCAACTGTGA[A/C]CTGCAGCTTGGCAAA | 212390 |
rs27751856 | snp | C/T | 0.152778 | 0.230321 | intron-variant | Klhl32 | Mm_Celera | 4:24795303 | GTGAGTAACTCCTGG[C/T]GGGAAAAGAGCAACT | 212390 |
rs27751857 | snp | A/G | 0.244898 | 0.249948 | intron-variant | Klhl32 | Mm_Celera | 4:24795233 | CCAAATCTAGTGCAT[A/G]ATCCACATCACTATT | 212390 |
rs27751858 | snp | A/G | 0.32 | 0.24 | intron-variant | Klhl32 | Mm_Celera | 4:24794818 | TAATCACAAAATTAT[A/G]CAATCATGCTTCAAA | 212390 |
rs27751859 | snp | G/T | 0.48 | 0.0979796 | intron-variant | Klhl32 | Mm_Celera | 4:24794719 | AGGTTCAAAAGCTCC[G/T]GTTGAGTTTATATTT | 212390 |
rs27751860 | snp | A/C | 0.21875 | 0.248039 | intron-variant | Klhl32 | Mm_Celera | 4:24794088 | TTTATCAAACATTTC[A/C]TGCTGGGAAGCACCA | 212390 |
rs27751861 | snp | A/G | 0.165289 | 0.235211 | intron-variant | Klhl32 | Mm_Celera | 4:24794049 | CCTAATTCTTCCTGG[A/G]AAAAGCCGGTGCACT | 212390 |
rs27751862 | snp | C/G | 0.48 | 0.0979796 | intron-variant | Klhl32 | Mm_Celera | 4:24793940 | GGAGACAAAGTCTTA[C/G]CCACACTGTTGCTTT | 212390 |
rs27751863 | snp | A/T | 0.21875 | 0.248039 | intron-variant | Klhl32 | Mm_Celera | 4:24793826 | AGTGAACTCCTTTGA[A/T]ATCTGAGTAAGAATA | 212390 |
rs27751864 | snp | A/T | 0.444444 | 0.157135 | intron-variant | Klhl32 | Mm_Celera | 4:24793690 | CAATTCTAGCTTAGA[A/T]CATCAAAAATCTCTC | 212390 |
rs27751865 | snp | A/G | 0.165289 | 0.235211 | intron-variant | Klhl32 | Mm_Celera | 4:24793183 | CACGTGTGGCATCAA[A/G]CACAGCATCAGTCAG | 212390 |
rs27751866 | snp | A/G | 0.408163 | 0.193609 | intron-variant | Klhl32 | Mm_Celera | 4:24793039 | TTTATTTTGGTTTTG[A/G]TTTTGCTAAGGTTTA | 212390 |
rs27751867 | snp | C/G | 0.32 | 0.24 | intron-variant | Klhl32 | Mm_Celera | 4:24793015 | TCTCTTGGTAGCTCC[C/G]TGGGGTTTTTTATTT | 212390 |
rs27751868 | snp | G/T | 0.21875 | 0.248039 | intron-variant | Klhl32 | Mm_Celera | 4:24792905 | CTAGTGCCCTGTGAG[G/T]CTGACCTTCCTGTTC | 212390 |
rs27751869 | snp | C/G | 0.297521 | 0.245442 | synonymous-codon | Klhl32 | Mm_Celera | 4:24792779 | GCACAGCCTCTGGCC[C/G]GTCAGCATTTCTTGA | 212390 |
rs27751870 | snp | A/G | 0.142012 | 0.225474 | synonymous-codon | Klhl32 | Mm_Celera | 4:24792692 | GGCGATCAGGGTCAC[A/G]TCGCAGAGAATGCCA | 212390 |
rs27751871 | snp | C/T | 0.444444 | 0.157135 | intron-variant | Klhl32 | Mm_Celera | 4:24792356 | CCATATCTTCATATG[C/T]CATGCATGTCACTGC | 212390 |
rs27751872 | snp | C/T | 0.489796 | 0.070696 | intron-variant | Klhl32 | Mm_Celera | 4:24792212 | TTAATAGCACATGCA[C/T]TCATTTGTACAAGGT | 212390 |
rs27751873 | snp | A/C | 0.444444 | 0.157135 | intron-variant | Klhl32 | Mm_Celera | 4:24792205 | GCAGCCTTTAATAGC[A/C]CATGCATTCATTTGT | 212390 |
rs27751874 | snp | A/C | 0.277778 | 0.248452 | intron-variant | Klhl32 | Mm_Celera | 4:24791968 | TTCCACTTTACTTTC[A/C]CTTTACTCCATCTGA | 212390 |
rs27751875 | snp | C/T | 0.48 | 0.0979796 | intron-variant | Klhl32 | Mm_Celera | 4:24791859 | AATGTTCTTATTCCA[C/T]CTCTGTGTGGGCTGT | 212390 |
rs27751876 | snp | C/T | 0.21875 | 0.248039 | intron-variant | Klhl32 | GRCm38.p3 | 4:24791111 | GCACTACTACAAAAA[C/T]AAACCTGCAAATCGG | 212390 |
rs27751877 | snp | A/G | 0.5 | 0 | intron-variant | Klhl32 | Mm_Celera | 4:24789568 | AAAAGAGAAAAGTCT[A/G]CAGAGCAGAAGAGAG | 212390 |
rs27751878 | snp | A/T | 0.444444 | 0.157135 | intron-variant | Klhl32 | GRCm38.p3 | 4:24789519 | ATACTAAGAGGGTGG[A/T]GAGTGTGGGAAGCAC | 212390 |
rs27751879 | snp | A/G | 0.165289 | 0.235211 | intron-variant | Klhl32 | Mm_Celera | 4:24789472 | GGTGTTATAATCTCT[A/G]GGGCTAAACTAGGCA | 212390 |
rs27751880 | snp | C/T | 0.5 | 0 | intron-variant | Klhl32 | Mm_Celera | 4:24788460 | AAGGATTTATTTTTA[C/T]ATCATACTGAAATGT | 212390 |
rs27751881 | snp | A/G | 0.277778 | 0.248452 | intron-variant | Klhl32 | Mm_Celera | 4:24787290 | TCTAGTTTGCCTTTT[A/G]TTGCTGTGAAGAAAA | 212390 |
rs27751882 | snp | A/G | 0.5 | 0 | intron-variant | Klhl32 | GRCm38.p3 | 4:24787037 | CTATGAAAATTAGGA[A/G]ACATTTCACTACTTT | 212390 |
rs27751883 | snp | C/T | 0.444444 | 0.157135 | intron-variant | Klhl32 | Mm_Celera | 4:24787011 | TTAAGAACTGAATTA[C/T]ACATGAATTACTATG | 212390 |
rs27751884 | snp | C/T | 0.244898 | 0.249948 | intron-variant | Klhl32 | Mm_Celera | 4:24786872 | ATGTGTCAAATACCA[C/T]ACTTTAAAGCATAAA | 212390 |
rs27751885 | snp | A/G | 0.345679 | 0.230967 | intron-variant | Klhl32 | Mm_Celera | 4:24786789 | AGTTTACACCAAAGC[A/G]TGAGCCTGTTGACTC | 212390 |
rs27751886 | snp | C/T | 0.21875 | 0.248039 | intron-variant | Klhl32 | Mm_Celera | 4:24786699 | CACAGGAAGTCAAAG[C/T]GCTTTGTGCTCAACT | 212390 |
rs27751887 | snp | C/T | 0.277778 | 0.248452 | intron-variant | Klhl32 | Mm_Celera | 4:24786561 | ATTTAGTTATATGTT[C/T]GACAAATGCCACACT | 212390 |
rs27751888 | snp | C/T | 0.5 | 0 | intron-variant | Klhl32 | Mm_Celera | 4:24786488 | CTCAGACAGGCTCCT[C/T]ACCTCACTCATCTCA | 212390 |
rs27751889 | snp | A/T | 0.244898 | 0.249948 | intron-variant | Klhl32 | Mm_Celera | 4:24786234 | GCATGGCCAGGCACC[A/T]CTAATCAATCCAAGA | 212390 |
rs27751890 | snp | G/T | 0.18 | 0.24 | intron-variant | Klhl32 | Mm_Celera | 4:24786216 | CACTAGCACCCAGGT[G/T]GAGCATGGCCAGGCA | 212390 |
rs27751891 | snp | A/G | 0.197531 | 0.244432 | intron-variant | Klhl32 | Mm_Celera | 4:24786130 | GAATAAAACCACGCT[A/G]TTCTGAACTATCAAA | 212390 |
rs27751892 | snp | A/G | 0.444444 | 0.157135 | intron-variant | Klhl32 | Mm_Celera | 4:24786005 | GCATTGCCTAGCCCT[A/G]CACAGAGGTTCAGGA | 212390 |
rs27751893 | snp | C/G | 0.32 | 0.24 | intron-variant | Klhl32 | Mm_Celera | 4:24785972 | TAAGAGTGTGTGAAG[C/G]CTGAGCCTAGCACCT | 212390 |
rs27751894 | snp | A/G | 0.21875 | 0.248039 | intron-variant | Klhl32 | GRCm38.p3 | 4:24785868 | ACCCATGAGATGAAA[A/G]AGATGGTGCTTAGTG | 212390 |
rs27751895 | snp | A/G | 0.277778 | 0.248452 | intron-variant | Klhl32 | GRCm38.p3 | 4:24785815 | CCTTGGTAGAACAGC[A/G]AACTGAGAGGCAAAG | 212390 |
rs27751896 | snp | C/T | 0.277778 | 0.248452 | intron-variant | Klhl32 | Mm_Celera | 4:24785758 | AGAGGAGAATCAGCA[C/T]AGAGGCTCATGAGAG | 212390 |
rs27751897 | snp | C/T | 0.277778 | 0.248452 | intron-variant | Klhl32 | Mm_Celera | 4:24785605 | AATACTGCTATGGAC[C/T]TTCCTACCTTGGCTA | 212390 |
rs27751898 | snp | C/T | 0.48 | 0.0979796 | intron-variant | Klhl32 | Mm_Celera | 4:24785584 | TCCAATTCAGTTTTA[C/T]TCAACAATACTGCTA | 212390 |
rs27751899 | snp | C/G | 0.277778 | 0.248452 | intron-variant | Klhl32 | GRCm38.p3 | 4:24785350 | TTGAAACAGCCTCTA[C/G]AACCATAAATGACCT | 212390 |
rs27751900 | snp | A/C | 0.244898 | 0.249948 | intron-variant | Klhl32 | Mm_Celera | 4:24785221 | GAAAATTACACAGCA[A/C]TATGCAGGCTCTAAG | 212390 |
rs27751901 | snp | A/C | 0.375 | 0.216506 | intron-variant | Klhl32 | Mm_Celera | 4:24785214 | CAAACCTGAAAATTA[A/C]ACAGCACTATGCAGG | 212390 |
rs27751902 | snp | A/C | 0.21875 | 0.248039 | intron-variant | Klhl32 | Mm_Celera | 4:24784704 | GCCACTTTTTAGAAT[A/C]CCAGTAGGCAGTATT | 212390 |
rs27751903 | snp | A/G | 0.444444 | 0.157135 | intron-variant | Klhl32 | Mm_Celera | 4:24784685 | CCCTTAGTCCAGGCT[A/G]TAAGCCACTTTTTAG | 212390 |
rs27751904 | snp | G/T | 0.345679 | 0.230967 | intron-variant | Klhl32 | Mm_Celera | 4:24784674 | CATCTGCTCTTCCCT[G/T]AGTCCAGGCTGTAAG | 212390 |
rs27751905 | snp | C/G | 0.18 | 0.24 | intron-variant | Klhl32 | Mm_Celera | 4:24784616 | ATACATCTATCAACT[C/G]CACATCCTAACCATG | 212390 |
rs27751906 | snp | C/T | 0.408163 | 0.193609 | intron-variant | Klhl32 | Mm_Celera | 4:24784590 | GAAGTTTTACCATTC[C/T]TTTCCTATCCATACA | 212390 |
rs27751907 | snp | C/T | 0.132653 | 0.220748 | intron-variant | Klhl32 | Mm_Celera | 4:24784450 | CTTCAATGGAACAGC[C/T]TCCTTTAAAATTCTT | 212390 |
rs27751908 | snp | A/C | 0.260355 | 0.249785 | intron-variant | Klhl32 | Mm_Celera | 4:24781106 | TATTAGGAAATAAGA[A/C]AAATGAATATATTAA | 212390 |
rs27751909 | snp | A/C | 0.132653 | 0.220748 | intron-variant | Klhl32 | Mm_Celera | 4:24781035 | GTATAAATGCTGCAA[A/C]GACCTGCCCCCCTTT | 212390 |
rs27751910 | snp | A/G | 0.429688 | 0.173817 | intron-variant | Klhl32 | Mm_Celera | 4:24780572 | ATGAAGATCTAAGAA[A/G]TAAGTTCCACTAAGT | 212390 |
rs27751911 | snp | C/G | 0.132653 | 0.220748 | intron-variant | Klhl32 | Mm_Celera | 4:24780371 | AGTAAAGCAATGAGT[C/G]ATGGAGCAGGCTGCT | 212390 |
rs27751912 | snp | A/G | 0.132653 | 0.220748 | intron-variant | Klhl32 | Mm_Celera | 4:24780249 | TGAACGACATGTGAT[A/G]TCAATTGTCAGAGAA | 212390 |
rs27751913 | snp | C/T | 0.142012 | 0.225474 | intron-variant | Klhl32 | Mm_Celera | 4:24780076 | ACCATGAACTTATAA[C/T]GTGTTTCTTAAAATG | 212390 |
rs27751914 | snp | C/G | 0.132653 | 0.220748 | intron-variant | Klhl32 | Mm_Celera | 4:24779921 | TGAAGAGAGTGTAAA[C/G]AAAAGCAATGCTGCA | 212390 |
rs27751915 | snp | A/C | 0.132653 | 0.220748 | intron-variant | Klhl32 | Mm_Celera | 4:24779511 | TGTAACAAGCTATTC[A/C]CTTGATGTTTACAAA | 212390 |
rs27751916 | snp | G/T | 0.132653 | 0.220748 | intron-variant | Klhl32 | Mm_Celera | 4:24777918 | TTTGTTTCTTTCTTC[G/T]TATACACAACATGAG | 212390 |
rs27751917 | snp | A/G | 0.132653 | 0.220748 | intron-variant | Klhl32 | Mm_Celera | 4:24777846 | AACATTTGAACCAAA[A/G]GACAATATCCAAACA | 212390 |
rs27751918 | snp | C/T | 0.197531 | 0.244432 | intron-variant | Klhl32 | Mm_Celera | 4:24777585 | CAAAGAAGGTGACAA[C/T]TGTATGTGGGCAGCT | 212390 |
rs27751919 | snp | C/G | 0.465374 | 0.126941 | intron-variant | Klhl32 | GRCm38.p3 | 4:24777580 | TTTATCAAAGAAGGT[C/G]ACAACTGTATGTGGG | 212390 |
rs27751920 | snp | A/G | 0.244898 | 0.249948 | intron-variant | Klhl32 | Mm_Celera | 4:24768108 | ACTTGACTTTGACTG[A/G]ACATGGCGGCTGATG | 212390 |
rs27751921 | snp | A/C | 0.32 | 0.24 | intron-variant | Klhl32 | Mm_Celera | 4:24768085 | CTAAGCTAGAGCTCT[A/C]ATTTTCTACTTGACT | 212390 |
rs27751922 | snp | C/G | 0.244898 | 0.249948 | intron-variant | Klhl32 | Mm_Celera | 4:24767636 | GTACCATCGGCCTCT[C/G]TGTACCATGGAATAC | 212390 |
rs27751923 | snp | A/C | 0.277778 | 0.248452 | intron-variant | Klhl32 | Mm_Celera | 4:24767265 | GATTTATATAGTGTG[A/C]GGAACAGCCTTTAAG | 212390 |
rs27751924 | snp | A/G | 0.5 | 0 | intron-variant | Klhl32 | Mm_Celera | 4:24765806 | CGTGGAAAGAAACTA[A/G]GAAAGGAGGTAGAGA | 212390 |
rs27751925 | snp | A/G | 0.124444 | 0.216185 | intron-variant | Klhl32 | Mm_Celera | 4:24765606 | ATTAACCTTCCCACG[A/G]CATTCCCACTGTATG | 212390 |
rs27751926 | snp | A/G | 0.124444 | 0.216185 | intron-variant | Klhl32 | Mm_Celera | 4:24765569 | ATAACACCCCTGGGA[A/G]TTCTAGCTGCTTCCA | 212390 |
rs27751927 | snp | A/T | 0.132653 | 0.220748 | intron-variant | Klhl32 | Mm_Celera | 4:24765290 | CAGGATAATGAATAC[A/T]GGGAGCCATAAGAAT | 212390 |
rs27751928 | snp | A/G | 0.124444 | 0.216185 | intron-variant | Klhl32 | Mm_Celera | 4:24765108 | TCGAATAAAATACAT[A/G]TAAAGGGCTGTACAC | 212390 |