SNP - dbSNP |
dbSNP | Type | Alleles | Het | Se(het) | Fxn-class | Gene Name | Assembly | Chr-pos | Sequence | Entrez Gene |
rs4191664 | snp | A/C/T | 0.408163 | 0.193609 | intron-variant | Klhl4 | GRCm38.p3 | X:114510906 | ATGGAGAAAAGAAAG[A/C/T]ATTCCACAACAGAAC | 237010 |
rs6203341 | snp | A/T | 0.5 | 0 | intron-variant | Klhl4 | Mm_Celera | X:114476176 | ATTCACAGAAAAAAA[A/T]NTTTATGTGAAAACT | 237010 |
rs6203358 | snp | A/T | 0.5 | 0 | intron-variant | Klhl4 | Mm_Celera | X:114476175 | TTCACAGAAAAAAAN[A/T]TTTATGTGAAAACTC | 237010 |
rs6203377 | snp | G/T | 0.5 | 0 | intron-variant | Klhl4 | GRCm38.p3 | X:114476158 | TTATGTGAAAACTCC[G/T]ACNCCATGTTATTAT | 237010 |
rs6203773 | snp | C/T | 0.5 | 0 | intron-variant | Klhl4 | GRCm38.p3 | X:114476155 | TGTGAAAACTCCNAC[C/T]CCATGTTATTATGAA | 237010 |
rs6231649 | snp | A/G | 0.415225 | 0.187619 | downstream-variant-500B | Klhl4 | GRCm38.p3 | X:114561407 | GTGGTAAACAATGGC[A/G]CATTTACCTGTAACT | 237010 |
rs6363004 | snp | C/T | 0.5 | 0 | intron-variant | Klhl4 | GRCm38.p3 | X:114494270 | tctttttatttagtc[C/T]aagacccaagtccac | 237010 |
rs6363041 | snp | G/T | 0.5 | 0 | intron-variant | Klhl4 | GRCm38.p3 | X:114494253 | agacccaagtccact[G/T]aagagtgtgaccctc | 237010 |
rs6363111 | snp | A/G | 0.5 | 0 | intron-variant | Klhl4 | GRCm38.p3 | X:114494209 | gttAAATGTACATGT[A/G]ATGTTCTAATTTGTC | 237010 |
rs6363678 | snp | A/T | 0.5 | 0 | intron-variant | Klhl4 | Mm_Celera | X:114494087 | ggggggacactctgc[A/T]gtcttctcccctaac | 237010 |
rs29095454 | snp | C/G | 0.165289 | 0.235211 | intron-variant | Klhl4 | Mm_Celera | X:114546333 | AAATGAGCAAAATAG[C/G]AAATTTTTACAAGGG | 237010 |
rs29095455 | snp | G/T | 0.152778 | 0.230321 | intron-variant | Klhl4 | Mm_Celera | X:114545524 | TAGAAAGACAGAAGC[G/T]TTTTTTCCCTCTAAG | 237010 |
rs29095456 | snp | A/G | 0.165289 | 0.235211 | intron-variant | Klhl4 | Mm_Celera | X:114545368 | ATAAAAAGTGTGAAG[A/G]CTTTTTCCTACTTGT | 237010 |
rs29095457 | snp | A/G | 0.46281 | 0.131194 | intron-variant | Klhl4 | Mm_Celera | X:114543730 | GAAATGAAAGGAGCA[A/G]ATTCTGAAGGCAGTT | 237010 |
rs29095458 | snp | A/C | 0.46281 | 0.131194 | intron-variant | Klhl4 | Mm_Celera | X:114542621 | ATCAGTTATTTAGGA[A/C]TATATCAAGCACTTT | 237010 |
rs29095459 | snp | C/T | 0.359862 | 0.224567 | intron-variant | Klhl4 | GRCm38.p3 | X:114541330 | TCTTTGTAAATTTAG[C/T]CCTTTTATTTGATTA | 237010 |
rs29095460 | snp | C/T | 0.142012 | 0.225474 | intron-variant | Klhl4 | Mm_Celera | X:114541283 | TGTATTTAAACTTCC[C/T]CTGTTGTAATGTTTC | 237010 |
rs29095461 | snp | A/C | 0.444444 | 0.157135 | intron-variant | Klhl4 | GRCm38.p3 | X:114541254 | GCATTTGAAAATATT[A/C]TCTAATGAATCTCTG | 237010 |
rs29095462 | snp | C/T | 0.336735 | 0.234472 | intron-variant | Klhl4 | GRCm38.p3 | X:114539874 | ATATGAACTTCAATA[C/T]CATAATTTAAGCAAA | 237010 |
rs29095463 | snp | C/T | 0.391111 | 0.206368 | intron-variant | Klhl4 | Mm_Celera | X:114532564 | AACAAAAGTTATGCT[C/T]TAGGAGAGTAGTTTA | 237010 |
rs29095654 | snp | A/T | 0.456747 | 0.140554 | intron-variant | Klhl4 | Mm_Celera | X:114481054 | ACATTTTAAACAAAA[A/T]CCACTACATATTTGT | 237010 |
rs29095655 | snp | C/T | 0.432133 | 0.171253 | intron-variant | Klhl4 | Mm_Celera | X:114480574 | ACATGGAATATGCTT[C/T]TCCAGATGAAATTAA | 237010 |
rs29095656 | snp | C/T | 0.465374 | 0.126941 | intron-variant | Klhl4 | Mm_Celera | X:114480411 | AGTGAGTACTTGCTG[C/T]TTCTTAATTTGTATT | 237010 |
rs29095657 | snp | A/G | 0.124444 | 0.216185 | intron-variant | Klhl4 | Mm_Celera | X:114480401 | AATTATGAAAAGTGA[A/G]TACTTGCTGCTTCTT | 237010 |
rs29095658 | snp | A/T | 0.124444 | 0.216185 | intron-variant | Klhl4 | Mm_Celera | X:114479943 | CTTATTCACATGGAC[A/T]ACTAATATTTCTCTG | 237010 |
rs29095659 | snp | C/T | 0.432133 | 0.171253 | intron-variant | Klhl4 | Mm_Celera | X:114479437 | GCACAGCCACAAATG[C/T]CTCATTGTTTTGTTT | 237010 |
rs29095660 | snp | C/T | 0.444444 | 0.157135 | intron-variant | Klhl4 | Mm_Celera | X:114479344 | GTATCTGGGATAATA[C/T]GCATGGTGCATGTTT | 237010 |
rs29095661 | snp | A/G | 0.124444 | 0.216185 | intron-variant | Klhl4 | Mm_Celera | X:114479157 | ACCATTTCTCATTTT[A/G]CAATGCATATTATCA | 237010 |
rs29095662 | snp | C/T | 0.432133 | 0.171253 | intron-variant | Klhl4 | Mm_Celera | X:114478941 | AAGGTCCATAAGATG[C/T]TTGGTAATTATATGT | 237010 |
rs29095663 | snp | A/C | 0.415225 | 0.187619 | intron-variant | Klhl4 | Mm_Celera | X:114478835 | TTTTAATATCTCATG[A/C]GTATAAAAGCGCCTT | 237010 |
rs29095904 | snp | G/T | 0.345679 | 0.230967 | intron-variant | Klhl4 | Mm_Celera | X:114532329 | TTATTTTACATAATC[G/T]TCAATTAATGTTGCT | 237010 |
rs29095905 | snp | A/T | 0.260355 | 0.249785 | intron-variant | Klhl4 | Mm_Celera | X:114531356 | AGGAACACACAAACA[A/T]AAAAACACATGTATA | 237010 |
rs29095906 | snp | A/C | 0.359862 | 0.224567 | intron-variant | Klhl4 | Mm_Celera | X:114531352 | TAGAAGGAACACACA[A/C]ACATAAAAACACATG | 237010 |
rs29095907 | snp | A/C/T | 0.415225 | 0.187619 | intron-variant | Klhl4 | Mm_Celera | X:114531111 | CCAAACAATAGGATA[A/C/T]ATTTGCTTTCTAAAG | 237010 |
rs29095908 | snp | A/G | 0.444444 | 0.157135 | intron-variant | Klhl4 | GRCm38.p3 | X:114530903 | TATATTTATTGAATC[A/G]GCTAAAATACTCAAA | 237010 |
rs29095909 | snp | A/G | 0.432133 | 0.171253 | intron-variant | Klhl4 | Mm_Celera | X:114530766 | TTCAGGATGATTCAA[A/G]ATTGGCTCATTAGTT | 237010 |
rs29095910 | snp | G/T | 0.401235 | 0.199068 | intron-variant | Klhl4 | Mm_Celera | X:114530718 | AAATACTGAACTAAA[G/T]GTATAAGTCTATTAT | 237010 |
rs29095911 | snp | A/G | 0.432133 | 0.171253 | intron-variant | Klhl4 | Mm_Celera | X:114530672 | GCTACCGTGCTTTCA[A/G]TTGCACTCATTATAA | 237010 |
rs29095912 | snp | C/T | 0.432133 | 0.171253 | intron-variant | Klhl4 | Mm_Celera | X:114530517 | AGAAAATGACTAGGG[C/T]TCCTTTTCTATTTCT | 237010 |
rs29095913 | snp | C/T | 0.429688 | 0.173817 | intron-variant | Klhl4 | Mm_Celera | X:114529960 | AAAATATAGTAATTT[C/T]GTATTCTTGTTTTAC | 237010 |
rs29096194 | snp | C/T | 0.336735 | 0.234472 | intron-variant | Klhl4 | Mm_Celera | X:114478496 | TGCCTAAATTGAAAA[C/T]GATGAAATTTATTCT | 237010 |
rs29096195 | snp | A/G | 0.391111 | 0.206368 | intron-variant | Klhl4 | Mm_Celera | X:114478201 | TTCATTTTCCTGTTT[A/G]TTGTAGTGATTTTAT | 237010 |
rs29096196 | snp | A/G | 0.124444 | 0.216185 | intron-variant | Klhl4 | Mm_Celera | X:114477719 | ATAGAACAGGAAAGG[A/G]GAACTGTATTAATGA | 237010 |
rs29096197 | snp | C/T | 0.432133 | 0.171253 | intron-variant | Klhl4 | Mm_Celera | X:114477533 | TGCTGCTGTCCTGTC[C/T]ATTGGACTTGTAAGG | 237010 |
rs29096198 | snp | C/T | 0.124444 | 0.216185 | intron-variant | Klhl4 | Mm_Celera | X:114477448 | TATGGTACCTGCATA[C/T]ATCTTAAGCTAAAGA | 237010 |
rs29096199 | snp | C/G | 0.415225 | 0.187619 | intron-variant | Klhl4 | Mm_Celera | X:114477386 | GTGTTAAAAGAATTC[C/G]CACTATAATAAACAT | 237010 |
rs29096200 | snp | C/T | 0.444444 | 0.157135 | intron-variant | Klhl4 | Mm_Celera | X:114477200 | AGAAAAGATTTTCTC[C/T]TCTTTGTTTCAAGCC | 237010 |
rs29096201 | snp | C/T | 0.391111 | 0.206368 | intron-variant | Klhl4 | Mm_Celera | X:114477140 | TTGATTTTATGATAG[C/T]CATATGCCAACTGCA | 237010 |
rs29096202 | snp | A/G | 0.152778 | 0.230321 | intron-variant | Klhl4 | Mm_Celera | X:114477127 | ATTCTTCTGTCATTC[A/G]ATTTTATGATAGCCA | 237010 |
rs29096203 | snp | A/C | 0.444444 | 0.157135 | intron-variant | Klhl4 | Mm_Celera | X:114477018 | TAAACTTCCAAGCTT[A/C]ATTCACAAGTATGTA | 237010 |
rs29096354 | snp | A/T | 0.152778 | 0.230321 | intron-variant | Klhl4 | Mm_Celera | X:114529000 | TGTTTACACTAATGT[A/T]TATTGCTCATCAGTT | 237010 |
rs29096355 | snp | A/G | 0.492188 | 0.0620098 | intron-variant | Klhl4 | Mm_Celera | X:114525443 | TAATCTTCTTTGATG[A/G]TTTTTCCTTCATTTG | 237010 |
rs29096356 | snp | G/T | 0.165289 | 0.235211 | intron-variant | Klhl4 | Mm_Celera | X:114525249 | CTTAGCTCACAATGT[G/T]AGGTTTCCCAGCTTC | 237010 |
rs29096357 | snp | C/T | 0.391111 | 0.206368 | intron-variant | Klhl4 | Mm_Celera | X:114522240 | ATTGAAAGCTCTGCA[C/T]GATTATTTGTGATGC | 237010 |
rs29096358 | snp | A/G | 0.375 | 0.216506 | missense | Klhl4 | Mm_Celera | X:114521655 | ATGACCACCAGTTCT[A/G]ATGATCACTACCGTT | 237010 |
rs29096359 | snp | C/T | 0.18 | 0.24 | intron-variant | Klhl4 | GRCm38.p3 | X:114520885 | AGTGTCACACCAGGG[C/T]AAGCTCCATGTCCAG | 237010 |
rs29096360 | snp | A/G | 0.304688 | 0.243945 | intron-variant | Klhl4 | Mm_Celera | X:114517848 | ATAGAGATGAAGTTT[A/G]TAGGCTGTCAAGGGC | 237010 |
rs29096361 | snp | G/T | 0.244898 | 0.249948 | intron-variant | Klhl4 | Mm_Celera | X:114517819 | TCAGGTATACAGGGA[G/T]GCATCCAGAGTGTAT | 237010 |
rs29096362 | snp | A/C | 0.142012 | 0.225474 | intron-variant | Klhl4 | Mm_Celera | X:114515314 | ATATGCTGTCAAAAT[A/C]GACACCAATATACAA | 237010 |
rs29096363 | snp | A/G | 0.415225 | 0.187619 | intron-variant | Klhl4 | Mm_Celera | X:114515178 | CTGTTACTGCACTTT[A/G]GCATCTGGACTAGCT | 237010 |
rs29096684 | snp | C/T | 0.35503 | 0.226867 | intron-variant | Klhl4 | Mm_Celera | X:114476733 | CCATTGTGCCACATC[C/T]TTGATACAATTCCTT | 237010 |
rs29096685 | snp | C/T | 0.408163 | 0.193609 | intron-variant | Klhl4 | Mm_Celera | X:114476468 | ATTTCATAGGAAAGT[C/T]AGCATTTTCTTAAAA | 237010 |
rs29096686 | snp | A/G | 0.444444 | 0.157135 | intron-variant | Klhl4 | Mm_Celera | X:114476369 | TAGAATAAAATGATG[A/G]CAAACGTCTAGTCTA | 237010 |
rs29096687 | snp | C/T | 0.444444 | 0.157135 | intron-variant | Klhl4 | Mm_Celera | X:114476322 | GGCACTAAAACTGAA[C/T]AGAATAGAAAAGAGT | 237010 |
rs29096688 | snp | A/G | 0.345679 | 0.230967 | intron-variant | Klhl4 | Mm_Celera | X:114475927 | ATAAGAAACAACAAA[A/G]CAAAACAACAGCTTT | 237010 |
rs29096689 | snp | A/C | 0.124444 | 0.216185 | intron-variant | Klhl4 | Mm_Celera | X:114475782 | AATCTAGATACTTCA[A/C]AATGTGTTCCTGTTA | 237010 |
rs29096690 | snp | G/T | 0.391111 | 0.206368 | intron-variant | Klhl4 | Mm_Celera | X:114475565 | TTGAATTTGAGGTAG[G/T]ATTCTTAAGACGTGA | 237010 |
rs29096691 | snp | G/T | 0.124444 | 0.216185 | intron-variant | Klhl4 | Mm_Celera | X:114475247 | GTGAACAGGATTAAC[G/T]TTGACAAAAATAGAA | 237010 |
rs29096692 | snp | C/T | 0.124444 | 0.216185 | intron-variant | Klhl4 | Mm_Celera | X:114475100 | CATTTAGAATTCTTT[C/T]GGGTTTTAAGAGAAG | 237010 |
rs29096693 | snp | A/G | 0.124444 | 0.216185 | intron-variant | Klhl4 | Mm_Celera | X:114474950 | GAATAATCTGAGTTT[A/G]TGTGTAGCCAATCAG | 237010 |
rs29096774 | snp | A/C | 0.391111 | 0.206368 | intron-variant | Klhl4 | GRCm38.p3 | X:114512784 | ATCCTATTTTGTGTA[A/C]TGATTCTTCTAAATG | 237010 |
rs29096775 | snp | A/T | 0.391111 | 0.206368 | intron-variant | Klhl4 | GRCm38.p3 | X:114512708 | GGTGACCCAAGAACC[A/T]TTTTCTATAGCTTTA | 237010 |
rs29096776 | snp | A/C | 0.132653 | 0.220748 | intron-variant | Klhl4 | GRCm38.p3 | X:114512702 | GCCCAAGGTGACCCA[A/C]GAACCATTTTCTATA | 237010 |
rs29096777 | snp | C/T | 0.32 | 0.24 | intron-variant | Klhl4 | GRCm38.p3 | X:114506196 | AATACTATGAATAAA[C/T]ACATTTCATATGCTT | 237010 |
rs29096778 | snp | C/T | 0.408163 | 0.193609 | intron-variant | Klhl4 | GRCm38.p3 | X:114506007 | AAAACAGTGAACATA[C/T]AGTGTTTAAAAGTAC | 237010 |
rs29096779 | snp | G/T | 0.391111 | 0.206368 | intron-variant | Klhl4 | GRCm38.p3 | X:114505946 | TAGAGCCAAACACTA[G/T]CCTTTATATTATATT | 237010 |
rs29096780 | snp | C/T | 0.124444 | 0.216185 | intron-variant | Klhl4 | Mm_Celera | X:114505770 | GTGAAATTGAAGAAG[C/T]CCTTCAAGCACACTG | 237010 |
rs29096781 | snp | A/G/T | 0.391111 | 0.206368 | intron-variant | Klhl4 | GRCm38.p3 | X:114505585 | GGATTAAAGGGCTAT[A/G/T]CTTGTAGAGCAAAGA | 237010 |
rs29096782 | snp | A/C | 0.408163 | 0.193609 | intron-variant | Klhl4 | Mm_Celera | X:114505529 | TTATAAACCACCCTG[A/C]GTTTCCAATTATTTT | 237010 |
rs29096783 | snp | A/G | 0.32 | 0.24 | intron-variant | Klhl4 | Mm_Celera | X:114505516 | CTAAGACTTGATATT[A/G]TAAACCACCCTGAGT | 237010 |
rs29097174 | snp | C/T | 0.391111 | 0.206368 | intron-variant | Klhl4 | Mm_Celera | X:114505338 | GCTCTTTCATACATA[C/T]TTTCAAATAACAGAC | 237010 |
rs29097175 | snp | A/G | 0.391111 | 0.206368 | intron-variant | Klhl4 | Mm_Celera | X:114505208 | TCGTTTATGACAAGT[A/G]AAAGTTCACTTATTT | 237010 |
rs29097176 | snp | A/G | 0.408163 | 0.193609 | intron-variant | Klhl4 | GRCm38.p3 | X:114505155 | AATGAACCTGTATGC[A/G]TTTGCTTTTTTTATG | 237010 |
rs29097177 | snp | C/T | 0.375 | 0.216506 | intron-variant | Klhl4 | GRCm38.p3 | X:114505044 | TGAAAATCTTAATTA[C/T]ATATTTCAATCTAGG | 237010 |
rs29097178 | snp | C/T | 0.345679 | 0.230967 | intron-variant | Klhl4 | Mm_Celera | X:114504960 | TAATTGAAACAATTA[C/T]TTTTATTTAATTTAT | 237010 |
rs29097179 | snp | C/T | 0.391111 | 0.206368 | intron-variant | Klhl4 | Mm_Celera | X:114504898 | ATAATTCTGTCTCTA[C/T]AATATTCCATCATCA | 237010 |
rs29097180 | snp | A/G | 0.35503 | 0.226867 | intron-variant | Klhl4 | Mm_Celera | X:114504709 | TCTGCTGTCACCTGA[A/G]TGGATACTATACTTA | 237010 |
rs29097181 | snp | A/T | 0.456747 | 0.140554 | intron-variant | Klhl4 | GRCm38.p3 | X:114496005 | ATAGCTTTAGATTTC[A/T]TGGTTTGTAATTAGT | 237010 |
rs29097182 | snp | C/G | 0.429688 | 0.173817 | intron-variant | Klhl4 | Mm_Celera | X:114495943 | AATAACCATTAGTAT[C/G]GTTAACAATTACATT | 237010 |
rs29097183 | snp | C/T | 0.391111 | 0.206368 | intron-variant | Klhl4 | Mm_Celera | X:114494626 | TTTATTCAAGCCACT[C/T]AAATATTGTAGTATT | 237010 |
rs29097204 | snp | A/T | 0.401235 | 0.199068 | synonymous-codon | Klhl4 | Mm_Celera | X:114474843 | AGAAGATATGAGAGC[A/T]GGGTAAGAGTTTTTG | 237010 |
rs29097205 | snp | A/G | 0.444444 | 0.157135 | upstream-variant-2KB | Klhl4 | Mm_Celera | X:114473531 | GAGGACATCTCTTTC[A/G]ATATAACTTAGAAAA | 237010 |
rs29097206 | snp | C/T | 0.444444 | 0.157135 | upstream-variant-2KB | Klhl4 | Mm_Celera | X:114473477 | AGAGGCCAGAATGAT[C/T]GGAATGATGTGCTCA | 237010 |
rs29097207 | snp | C/G | 0.401235 | 0.199068 | upstream-variant-2KB | Klhl4 | Mm_Celera | X:114473458 | AGAGGTGTTTATATA[C/G]GCAAGAGGCCAGAAT | 237010 |
rs29097208 | snp | A/T | 0.391111 | 0.206368 | upstream-variant-2KB | Klhl4 | Mm_Celera | X:114473338 | TATTTTGAATACTAC[A/T]AGCAATGTGGTGATT | 237010 |
rs29097209 | snp | A/C | 0.277778 | 0.248452 | upstream-variant-2KB | Klhl4 | Mm_Celera | X:114472532 | ATGTATGTTAGTCTG[A/C]ATTAGAAATATTTGC | 237010 |
rs29097210 | snp | A/C | 0.35503 | 0.226867 | upstream-variant-2KB | Klhl4 | Mm_Celera | X:114472526 | CTATTGATGTATGTT[A/C]GTCTGAATTAGAAAT | 237010 |
rs29097211 | snp | C/T | 0.35503 | 0.226867 | upstream-variant-2KB | Klhl4 | Mm_Celera | X:114472504 | ATGCAATAATGTTGG[C/T]ATTGCACTATTGATG | 237010 |
rs29097212 | snp | A/C | 0.391111 | 0.206368 | upstream-variant-2KB | Klhl4 | Mm_Celera | X:114472459 | TATGAGTGTAAGACA[A/C]AAGATCTGGGCATAT | 237010 |
rs29097213 | snp | A/G | 0.35503 | 0.226867 | upstream-variant-2KB | Klhl4 | Mm_Celera | X:114472414 | AACATTGATTTTAAG[A/G]ATATGCTAAGAACAT | 237010 |