SNP - dbSNP |
dbSNP | Type | Alleles | Het | Se(het) | Fxn-class | Gene Name | Assembly | Chr-pos | Sequence | Entrez Gene |
rs6175962 | snp | C/T | 0.359862 | 0.224567 | intron-variant | Klhl3, Gm33389 | Mm_Celera | 13:58081670 | ATATTTAAGCCTGAC[C/T]GAAAGACCACATCAC | 100503085 |
rs6176509 | snp | A/T | 0.5 | 0 | intron-variant | Klhl3, Gm33389 | Mm_Celera | 13:58081775 | TGCCATTTAAAGCCA[A/T]ATNTGATAAGCACAA | 100503085 |
rs6176513 | snp | A/C | 0.415225 | 0.187619 | intron-variant | Klhl3, Gm33389 | Mm_Celera | 13:58081778 | CATTTAAAGCCANAT[A/C]TGATAAGCACAAACA | 100503085 |
rs6177556 | snp | A/G | 0.5 | 0 | intron-variant | Klhl3, Gm33389 | Mm_Celera | 13:58081984 | CAAAAAGTAAAAACT[A/G]TACATATATGTACTT | 100503085 |
rs6245379 | snp | A/G | 0.5 | 0 | intron-variant | Klhl3 | GRCm38.p3 | 13:58065329 | TGCATCATGGAAAAC[A/G]GAATAGTTCTTGCTT | 100503085 |
rs6258752 | snp | C/T | 0.290657 | 0.246672 | intron-variant | Klhl3 | Mm_Celera | 13:58065565 | AAAAAGAAACTTGAG[C/T]GAAAACCACCCACTC | 100503085 |
rs6259207 | snp | A/G | 0.290657 | 0.246672 | intron-variant | Klhl3 | Mm_Celera | 13:58065598 | CACCAGCTCCTTGTA[A/G]TGATTCCCTGGTCCT | 100503085 |
rs6312498 | snp | C/T | 0.5 | 0 | intron-variant | Klhl3, Gm33389 | Mm_Celera | 13:58074888 | AAAGTAGCATATCTC[C/T]GTACCGTGTTGTGTT | 100503085 |
rs6312949 | snp | G/T | 0.5 | 0 | intron-variant | Klhl3, Gm33389 | Mm_Celera | 13:58074933 | TAGAAACTGCGGTCT[G/T]AAGANAAGGAAGCTG | 100503085 |
rs6312950 | snp | A/G | 0.5 | 0 | intron-variant | Klhl3, Gm33389 | Mm_Celera | 13:58074938 | ACTGCGGTCTNAAGA[A/G]AAGGAAGCTGCGGCA | 100503085 |
rs6313446 | snp | A/G | 0.290657 | 0.246672 | intron-variant | Klhl3, Gm33389 | Mm_Celera | 13:58075052 | TGAAGGTCAGTGAGC[A/G]GAAGCATTTGCCACA | 100503085 |
rs6332535 | snp | C/T | 0.304688 | 0.243945 | intron-variant | Klhl3 | Mm_Celera | 13:58043054 | TGACCCATGTCTAAA[C/T]GGGCAAGCAATCCCC | 100503085 |
rs13481828 | snp | A/G | 0.40238 | 0.198193 | intron-variant | Klhl3 | GRCm38.p3 | 13:58051262 | AGGAGGAGCTGGAGG[A/G]CAGAGGAGAAAAAGA | 100503085 |
rs29224146 | snp | A/G | 0.197531 | 0.244432 | intron-variant | Klhl3 | Mm_Celera | 13:58065380 | TTTCCTAAGAACCAG[A/G]GGAAACTGGCTTGAG | 100503085 |
rs29227305 | snp | A/C/T | 0.396694 | 0.202437 | intron-variant | Klhl3 | GRCm38.p3 | 13:58054121 | GTGAGGAGCAGAGTG[A/C/T]TTCTCTATTCCATCT | 100503085 |
rs29229565 | snp | A/T | 0.375 | 0.216506 | intron-variant | Klhl3 | Mm_Celera | 13:58041916 | CTCTCTCTCTCTCTC[A/T]TACACACACACACAC | 100503085 |
rs29230671 | snp | A/G | 0.5 | 0 | intron-variant, upstream-variant-2KB | Klhl3, Mir874 | Mm_Celera | 13:58023593 | AGATTTCCAACCTCC[A/G]TAGGCCTCACTTTCA | 100503085 |
rs29231491 | snp | C/G | 0.492188 | 0.0620098 | intron-variant | Klhl3 | Mm_Celera | 13:58018333 | AGTCTTGTTTCCACC[C/G]ACAGAACTGCGTAAC | 100503085 |
rs29231660 | snp | A/G | 0.5 | 0 | intron-variant | Klhl3 | Mm_Celera | 13:58014740 | CTACAGGATATCATG[A/G]CACCAGCCACAGACC | 100503085 |
rs29232224 | snp | A/G | 0.32 | 0.24 | intron-variant | Klhl3 | GRCm38.p3 | 13:58052369 | TTATGTATGGGGCTG[A/G]AGAGACAGCTCGGTG | 100503085 |
rs29233402 | snp | A/G | 0.487535 | 0.077957 | intron-variant | Klhl3 | Mm_Celera | 13:58009704 | CACAGGTCTCCCCGT[A/G]GGAACATTTCCTGAG | 100503085 |
rs29233574 | snp | C/T | 0.32 | 0.24 | intron-variant | Klhl3 | Mm_Celera | 13:58047817 | TTTTTTATTTATTTA[C/T]TTGCTTATTTATTTA | 100503085 |
rs29235437 | snp | A/C | 0.49827 | 0.0293608 | intron-variant | Klhl3 | GRCm38.p3 | 13:58041700 | CATGGCTGAGCCCCT[A/C]GGTAGCCTGACTTGA | 100503085 |
rs29237325 | snp | C/T | 0.444444 | 0.157135 | intron-variant | Klhl3 | Mm_Celera | 13:58036290 | AGGAGCAGAGAGCAG[C/T]CTTCCCTGGATTCAT | 100503085 |
rs29239550 | snp | A/G | 0.375 | 0.216506 | intron-variant | Klhl3 | GRCm38.p3 | 13:58042000 | GGGGGACAAGAGAGG[A/G]GGACAGAGAAGTGAG | 100503085 |
rs29240352 | snp | A/G | 0.444444 | 0.157135 | intron-variant | Klhl3 | Mm_Celera | 13:58035245 | GTGAGTCACTAGGTG[A/G]GTGGGACTCGAACCC | 100503085 |
rs29242183 | snp | C/T | 0.375 | 0.216506 | intron-variant | Klhl3 | GRCm38.p3 | 13:58046340 | TCTGTGCTGTCTACG[C/T]GTGTAACTGTGCCCA | 100503085 |
rs29242362 | snp | A/G | 0.444444 | 0.157135 | intron-variant | Klhl3 | GRCm38.p3 | 13:58037300 | AAAAGAGGATCAGGG[A/G]AGTGGGCACTGATGC | 100503085 |
rs29243227 | snp | C/T | 0.33241 | 0.236027 | downstream-variant-500B, utr-variant-3-prime | Klhl3 | Mm_Celera | 13:58004532 | TTCCAAATCTGGAAT[C/T]CATGACATCAGGTCA | 100503085 |
rs29243725 | snp | C/G | 0.49827 | 0.0293608 | intron-variant | Klhl3 | GRCm38.p3 | 13:58039876 | ATCCTTGACTCTTAT[C/G]AAACCGAACCCTTCC | 100503085 |
rs29245108 | snp | C/T | 0.387812 | 0.208586 | intron-variant | Klhl3 | GRCm38.p3 | 13:58040057 | GCTCCCTCTGGACAC[C/T]GGCTCTCAGTCTCTC | 100503085 |
rs29246001 | snp | G/T | 0.444444 | 0.157135 | intron-variant | Klhl3 | GRCm38.p3 | 13:58053368 | CATTCCTGCCCCATG[G/T]CAGGGTGTGTGACTT | 100503085 |
rs29249052 | snp | G/T | 0.375 | 0.216506 | intron-variant | Klhl3 | GRCm38.p3 | 13:58046878 | CACAGCCTGAAGGTT[G/T]TGCTGTCCTGGAATT | 100503085 |
rs29249886 | snp | C/T | 0.5 | 0 | intron-variant | Klhl3 | Mm_Celera | 13:58010938 | TCCCCCTCCCACTAA[C/T]GCAGAGCCTATGGGA | 100503085 |
rs29250826 | snp | C/T | 0.459184 | 0.136902 | intron-variant | Klhl3 | Mm_Celera | 13:58014409 | GCCATAAGGGAAGCG[C/T]TCTGTGTGCACCCAG | 100503085 |
rs29494689 | snp | A/G | 0.375 | 0.216506 | downstream-variant-500B | Klhl3 | Mm_Celera | 13:58004311 | ATCCCATTACAGATG[A/G]TTGTGAGCCACCATG | 100503085 |
rs29496099 | snp | A/C/G | 0.33241 | 0.236027 | intron-variant | Klhl3 | GRCm38.p3 | 13:58009850 | ATCCTATAGCTGCTC[A/C/G]TGGCTGTACCTCTAA | 100503085 |
rs29496108 | snp | C/G | 0.455 | 0.143091 | intron-variant | Klhl3 | Mm_Celera | 13:58030157 | CTACACTCCAGCATG[C/G]CCCGTTCCTCTGCCT | 100503085 |
rs29496274 | snp | A/G | 0.32 | 0.24 | intron-variant | Klhl3 | GRCm38.p3 | 13:58048042 | GCCTCCGCCCTGAAC[A/G]GAACCACTGAACAAG | 100503085 |
rs29496298 | snp | C/T | 0.375 | 0.216506 | intron-variant | Klhl3 | GRCm38.p3 | 13:58039892 | AAACCGAACCCTTCC[C/T]TCCACGCGTTTACAA | 100503085 |
rs29496464 | snp | A/G | 0.32 | 0.24 | intron-variant | Klhl3 | Mm_Celera | 13:58117346 | GGCCTTGCTGCTGAC[A/G]AGTCAGCAAGGGCCA | 100503085 |
rs29510186 | snp | G/T | 0.5 | 0 | intron-variant | Klhl3 | Mm_Celera | 13:58034231 | GAGAAATGAAAATAT[G/T]AAAAGTTAAAAAAAA | 100503085 |
rs29510415 | snp | A/G | 0.48 | 0.0979796 | intron-variant | Klhl3, Gm33389 | Mm_Celera | 13:58108903 | AAAAGTAGATCTTTT[A/G]GAAACCTTAAAAAAT | 100503085 |
rs29514101 | snp | G/T | 0.375 | 0.216506 | downstream-variant-500B | Klhl3 | Mm_Celera | 13:58004310 | GATCCCATTACAGAT[G/T]GTTGTGAGCCACCAT | 100503085 |
rs29516940 | snp | C/T | 0.32 | 0.24 | intron-variant | Klhl3 | Mm_Celera | 13:58047821 | TTATTTATTTATTTG[C/T]TTATTTATTTATTTA | 100503085 |
rs29517076 | snp | A/G | 0.444444 | 0.157135 | intron-variant | Klhl3 | Mm_Celera | 13:58031257 | GTAGCAGGGTGATAA[A/G]CAAGCTTTAGAAATA | 100503085 |
rs29517283 | snp | A/C | 0.426035 | 0.177515 | intron-variant | Klhl3 | GRCm38.p3 | 13:58049889 | ACAGATCCAGACAGC[A/C]TGGTGAGCAGGCTTA | 100503085 |
rs29538764 | snp | G/T | 0.375 | 0.216506 | intron-variant | Klhl3 | GRCm38.p3 | 13:58046339 | GTCTGTGCTGTCTAC[G/T]TGTGTAACTGTGCCC | 100503085 |
rs29550527 | snp | A/T | 0.375 | 0.216506 | upstream-variant-2KB | Klhl3 | Mm_Celera | 13:58125111 | CAACTAAGCTTGACG[A/T]CCTCTGCTGAGATTC | 100503085 |
rs29550914 | snp | A/T | 0.375 | 0.216506 | intron-variant | Klhl3 | GRCm38.p3 | 13:58046882 | GCCTGAAGGTTGTGC[A/T]GTCCTGGAATTGCCT | 100503085 |
rs29554456 | snp | G/T | 0.444444 | 0.157135 | intron-variant | Klhl3 | Mm_Celera | 13:58054235 | AGCAATGGCTTAGTG[G/T]TTAAGAGCACTGCCC | 100503085 |
rs29568014 | snp | C/T | 0.408163 | 0.193609 | intron-variant | Klhl3 | GRCm38.p3 | 13:58053104 | TCTTACAAACCAGCA[C/T]AGCCAGCCTCTGGCC | 100503085 |
rs29568467 | snp | A/G | 0.32 | 0.24 | intron-variant | Klhl3 | GRCm38.p3 | 13:58049498 | GAACCCAGCAGCCTC[A/G]GTCCAGACCAATCTA | 100503085 |
rs29570819 | snp | A/G | 0.492188 | 0.0620098 | intron-variant | Klhl3 | Mm_Celera | 13:58031276 | GCTTTAGAAATACAG[A/G]TTGTGCTGGTGCGAA | 100503085 |
rs29582860 | snp | C/T | 0.401235 | 0.199068 | intron-variant | Klhl3 | GRCm38.p3 | 13:58037356 | TCAAGAAGGAGGATT[C/T]AAGATCCATTGGCAA | 100503085 |
rs29583467 | snp | A/T | 0.375 | 0.216506 | intron-variant | Klhl3, Gm33389 | Mm_Celera | 13:58086264 | TGCTTGCAGCCGGGC[A/T]GTGGTGGTGCACGCC | 100503085 |
rs29586557 | snp | C/T | 0.5 | 0 | intron-variant | Klhl3 | Mm_Celera | 13:58014735 | CAGATCTACAGGATA[C/T]CATGACACCAGCCAC | 100503085 |
rs29588254 | snp | A/G | 0.375 | 0.216506 | intron-variant | Klhl3 | GRCm38.p3 | 13:58041127 | GTCAGAATGTCTGTC[A/G]CTAAGACTTACTTGT | 100503085 |
rs29630977 | snp | A/G | 0.444444 | 0.157135 | intron-variant | Klhl3 | GRCm38.p3 | 13:58054371 | GTATGCAAGTGGAGC[A/G]CAGATATACATGGAC | 100503085 |
rs29665404 | snp | C/T | 0.375 | 0.216506 | intron-variant | Klhl3 | Mm_Celera | 13:58046782 | GTGACTTTTTTTTTT[C/T]CACATATTTCTGCTC | 100503085 |
rs29666978 | snp | A/G | 0.49827 | 0.0293608 | intron-variant | Klhl3 | GRCm38.p3 | 13:58039900 | CCCTTCCTTCCACGC[A/G]TTTACAACAAGCCGT | 100503085 |
rs29683195 | snp | A/G | 0.429688 | 0.173817 | intron-variant | Klhl3 | GRCm38.p3 | 13:58051681 | TCCAGGTTAGTGTCC[A/G]CCCAGGTGATAACAG | 100503085 |
rs29710856 | snp | A/G | 0.375 | 0.216506 | intron-variant | Klhl3 | Mm_Celera | 13:58017505 | GTTTCTTATGTGTGT[A/G]AGTGTTTGGCCTGCA | 100503085 |
rs29720062 | snp | C/T | 0.32 | 0.24 | intron-variant | Klhl3 | GRCm38.p3 | 13:58046708 | CTTTGTCTAGTTGTT[C/T]TTCTTTTTCAATCTT | 100503085 |
rs29721742 | snp | C/T | 0.473373 | 0.11227 | intron-variant | Klhl3 | GRCm38.p3 | 13:58053227 | CAGTGAGAAAGAACA[C/T]GACTCTTCATGGCAA | 100503085 |
rs29729695 | snp | A/G | 0.444444 | 0.157135 | intron-variant | Klhl3 | GRCm38.p3 | 13:58053558 | GAACTTGGTGGGGGG[A/G]GAGGGTGAGAGAGAA | 100503085 |
rs29733473 | snp | C/T | 0.375 | 0.216506 | upstream-variant-2KB | Klhl3 | Mm_Celera | 13:58125112 | AACTAAGCTTGACGT[C/T]CTCTGCTGAGATTCT | 100503085 |
rs29761802 | snp | A/G | 0.444444 | 0.157135 | intron-variant | Klhl3 | Mm_Celera | 13:58031248 | GCTGTAGCTGTAGCA[A/G]GGTGATAAGCAAGCT | 100503085 |
rs29769777 | snp | A/G | 0.426035 | 0.177515 | intron-variant | Klhl3 | GRCm38.p3 | 13:58053781 | GCGAGAGCAGGACTT[A/G]TGCAGACAAAGCAAA | 100503085 |
rs29781657 | snp | A/G | 0.487535 | 0.077957 | intron-variant | Klhl3 | Mm_Celera | 13:58031477 | ATATATTGGGACGCC[A/G]TTTGTCAATGCCCTT | 100503085 |
rs29789603 | snp | A/G | 0.408163 | 0.193609 | intron-variant | Klhl3 | Mm_Celera | 13:58014540 | TGACCTCCCGTGGGA[A/G]AGCCATTTCCATCTG | 100503085 |
rs29806112 | snp | A/G | 0.32 | 0.24 | intron-variant | Klhl3 | Mm_Celera | 13:58052460 | GGCTCACAACCATCC[A/G]TAATGAGATCTGACG | 100503085 |
rs29811044 | snp | C/T | 0.207612 | 0.24638 | intron-variant | Klhl3 | GRCm38.p3 | 13:58055640 | GGCTACTATTTCTCA[C/T]CTCTTAATGGAATGT | 100503085 |
rs29817165 | snp | C/T | 0.444444 | 0.157135 | intron-variant | Klhl3 | Mm_Celera | 13:58035262 | TGGGACTCGAACCCA[C/T]GTCTTCTCCAAGAGT | 100503085 |
rs29823638 | snp | C/T | 0.444444 | 0.157135 | intron-variant | Klhl3 | GRCm38.p3 | 13:58054230 | TGTGCAGCAATGGCT[C/T]AGTGGTTAAGAGCAC | 100503085 |
rs29827430 | snp | C/T | 0.444444 | 0.157135 | intron-variant | Klhl3 | Mm_Celera | 13:58053309 | CAAACAACCCTGAAA[C/T]CCCAGAGATAATGAA | 100503085 |
rs29827923 | snp | C/T | 0.444444 | 0.157135 | intron-variant | Klhl3 | GRCm38.p3 | 13:58050333 | CCAAGGTGTGTTTCC[C/T]AGCACTGAGCAGCTC | 100503085 |
rs29850213 | snp | A/G | 0.375 | 0.216506 | intron-variant | Klhl3, Gm33389 | Mm_Celera | 13:58109782 | AAAGCACTTTACTAC[A/G]TCTGTCCCTCCAAAA | 100503085 |
rs29854127 | snp | A/C/G | 0.32 | 0.24 | intron-variant | Klhl3 | GRCm38.p3 | 13:58047820 | TTTATTTATTTATTT[A/C/G]CTTATTTATTTATTT | 100503085 |
rs29862058 | snp | C/G | 0.465374 | 0.126941 | downstream-variant-500B, utr-variant-3-prime | Klhl3 | Mm_Celera | 13:58004725 | TGGCTAGTTCTCTCT[C/G]GACCTCCAGAAGACA | 100503085 |
rs29870168 | snp | A/G | 0.489796 | 0.070696 | intron-variant | Klhl3 | GRCm38.p3 | 13:58053186 | GGTGTGGAGAAAAAA[A/G]GGAGGTAGAGACACA | 100503085 |
rs29879201 | snp | C/T | 0.475309 | 0.108333 | intron-variant | Klhl3 | Mm_Celera | 13:58033093 | GTGCTTTCACATTCC[C/T]TGTCTGTACTTCACT | 100503085 |
rs29886428 | snp | A/C | 0.336735 | 0.234472 | intron-variant | Klhl3 | GRCm38.p3 | 13:58050490 | AGTGCTGACTTCCCA[A/C]CAGGACCTCTACCAG | 100503085 |
rs29932267 | snp | A/C | 0.375 | 0.216506 | downstream-variant-500B | Klhl3 | Mm_Celera | 13:58004321 | AGATGGTTGTGAGCC[A/C]CCATGTGGCTGCTGG | 100503085 |
rs29932494 | snp | C/G | 0.444444 | 0.157135 | intron-variant | Klhl3 | GRCm38.p3 | 13:58054099 | TGGGAAGCAGACGAG[C/G]TTACAGGTGAGGAGC | 100503085 |
rs29958101 | snp | C/T | 0.32 | 0.24 | intron-variant | Klhl3 | GRCm38.p3 | 13:58046687 | CTGGCTGGAGTCATG[C/T]TATAACTTTGTCTAG | 100503085 |
rs29968968 | snp | A/G | 0.475309 | 0.108333 | intron-variant | Klhl3 | Mm_Celera | 13:58031058 | GATTGATGAAGGGAG[A/G]CCTTTGCCTCTGGAG | 100503085 |
rs29977877 | snp | A/G | 0.444444 | 0.157135 | intron-variant | Klhl3 | GRCm38.p3 | 13:58052105 | TCTCAGCAGCCCCTC[A/G]TCCCGCTGCCCCTTG | 100503085 |
rs29979965 | snp | C/T | 0.5 | 0 | intron-variant | Klhl3 | Mm_Celera | 13:58014681 | GAGAGTTCCTATCTG[C/T]GGGGACAGGGAAAGA | 100503085 |
rs29994062 | snp | G/T | 0.375 | 0.216506 | intron-variant | Klhl3 | GRCm38.p3 | 13:58055584 | TCTAATTCCATTGCA[G/T]TCAACAAACTTTCTA | 100503085 |
rs30004190 | snp | A/G | 0.391111 | 0.206368 | intron-variant | Klhl3 | GRCm38.p3 | 13:58051609 | TCAGAAGGCGGCATC[A/G]CTCTCTCTCGGGGCC | 100503085 |
rs30006781 | snp | C/T | 0.444444 | 0.157135 | intron-variant | Klhl3 | Mm_Celera | 13:58014344 | CTGGACATAGGCTCA[C/T]ACTGACAAGTGAAGA | 100503085 |
rs30012977 | snp | A/G | 0.375 | 0.216506 | intron-variant | Klhl3 | GRCm38.p3 | 13:58041520 | TGATGACGACAACTG[A/G]CTGTTGAATATTCAG | 100503085 |
rs30023813 | snp | A/C | 0.493827 | 0.0552116 | intron-variant | Klhl3, Gm33389 | GRCm38.p3 | 13:58072013 | CAAATTATCATAACA[A/C]CATGAAAAATTAGTA | 100503085 |
rs30040828 | snp | A/G | 0.265928 | 0.249492 | intron-variant | Klhl3 | Mm_Celera | 13:58026310 | AAAGCCTCAAGCTGC[A/G]TGTACATGTTGCTCC | 100503085 |
rs30055270 | snp | A/G | 0.375 | 0.216506 | intron-variant | Klhl3 | GRCm38.p3 | 13:58046546 | CTACTTTCCTGTGTG[A/G]TCTCCTTGTTTACGA | 100503085 |
rs30059445 | snp | A/C | 0.408163 | 0.193609 | intron-variant | Klhl3 | Mm_Celera | 13:58010854 | AAACAATCCAGACCA[A/C]GACCAGAGAGAAGGG | 100503085 |
rs30073194 | snp | C/T | 0.497041 | 0.0383476 | intron-variant | Klhl3 | GRCm38.p3 | 13:58053686 | TAATGGCTAGAAGCC[C/T]GTCACAGAGGCTGCT | 100503085 |
rs30076159 | snp | A/G | 0.375 | 0.216506 | intron-variant | Klhl3 | Mm_Celera | 13:58030618 | GGCCACAGTTCCCTG[A/G]GCTCTCCCCAGGCCG | 100503085 |
rs30078059 | snp | A/G | 0.375 | 0.216506 | intron-variant | Klhl3 | Mm_Celera | 13:58118225 | CTCAATTCTTTTCTT[A/G]ATCCAAAGAAAACCT | 100503085 |