SNP - dbSNP |
dbSNP | Type | Alleles | Het | Se(het) | Fxn-class | Gene Name | Assembly | Chr-pos | Sequence | Entrez Gene |
rs6399939 | snp | C/T | 0.32 | 0.24 | intron-variant | Klhl28 | Mm_Celera | 12:64959911 | CATAGATGATACATA[C/T]TACACAGATCTAGAT | 66689 |
rs6400527 | snp | A/C | 0.5 | 0 | intron-variant | Klhl28 | Mm_Celera | 12:64960043 | CATCTTAAAATCTCA[A/C]GTTTTCTCATGTGCT | 66689 |
rs13474010 | snp | A/G | 0.401235 | 0.199068 | synonymous-codon | Klhl28 | Mm_Celera | 12:64957447 | CGCCTATACGGGCAC[A/G]GTTTTCATTTCTCAG | 66689 |
rs29122999 | snp | A/G | 0.359862 | 0.224567 | intron-variant | Klhl28 | Mm_Celera | 12:64944405 | CCTAAAATGCAACTC[A/G]TTTTTGACTGAACAA | 66689 |
rs29124882 | snp | A/G | 0.444444 | 0.157135 | intron-variant | Klhl28 | Mm_Celera | 12:64955295 | CTAAATCCCTTAAAT[A/G]GTATACATAACCCCT | 66689 |
rs29130277 | snp | C/T | 0.465374 | 0.126941 | upstream-variant-2KB, synonymous-codon | Klhl28, Fam179b | Mm_Celera | 12:64966420 | GCTTGTGGAAGGCGG[C/T]AGTGAGGAGAAGAGG | 66689 |
rs29132782 | snp | A/G | 0.497041 | 0.0383476 | upstream-variant-2KB | Klhl28, Fam179b | Mm_Celera | 12:64965656 | TTACATGGACTACAT[A/G]ACCCAGCATCCACCG | 66689 |
rs29137110 | snp | G/T | 0.5 | 0 | intron-variant | Klhl28 | Mm_Celera | 12:64945425 | AATGGATGACTGTGA[G/T]CATCCACTTCTGTAT | 66689 |
rs29139087 | snp | A/G | 0.444444 | 0.157135 | intron-variant | Klhl28 | Mm_Celera | 12:64944316 | TGCCTTTTAAGTAAC[A/G]TCATTTGAGTTTAGG | 66689 |
rs29139318 | snp | C/T | 0.456747 | 0.140554 | intron-variant | Klhl28 | Mm_Celera | 12:64956430 | TCATTCAAACCAACT[C/T]CTATCCTCAGTCTGC | 66689 |
rs29143465 | snp | C/T | 0.432133 | 0.171253 | intron-variant | Klhl28 | Mm_Celera | 12:64945201 | GGCTTCCAGAGACAA[C/T]GCTGGCTTGACTCAG | 66689 |
rs29144773 | snp | A/G | 0.375 | 0.216506 | intron-variant | Klhl28 | Mm_Celera | 12:64944620 | GTGGAAGGGCGGGGG[A/G]GGGAAACAGTGAGCA | 66689 |
rs29145782 | snp | C/T | 0.5 | 0 | intron-variant | Klhl28 | Mm_Celera | 12:64954970 | TAGCCATTCAGAGGC[C/T]AGTCTTTGCTCTTTT | 66689 |
rs29146388 | snp | A/C | 0.5 | 0 | intron-variant | Klhl28 | Mm_Celera | 12:64951980 | GAAAATAACTATTGG[A/C]AATAGTGTTGTGCAA | 66689 |
rs29147038 | snp | A/C | 0.444444 | 0.157135 | intron-variant, downstream-variant-500B | Klhl28 | Mm_Celera | 12:64945898 | TTAAAAAGAAGAAGA[A/C]GAAAAAGAGTTTTGA | 66689 |
rs29147530 | snp | G/T | 0.487535 | 0.077957 | utr-variant-3-prime | Klhl28 | Mm_Celera | 12:64943085 | ATACACTCCAGAGTC[G/T]GAACTTCTCTCATCC | 66689 |
rs29155438 | snp | C/T | 0.48 | 0.0979796 | intron-variant | Klhl28 | Mm_Celera | 12:64960370 | AGGGAGCCAGACGGC[C/T]TGCTTTCAGCTCGCC | 66689 |
rs29159432 | snp | A/G | 0.493827 | 0.0552116 | utr-variant-3-prime | Klhl28 | Mm_Celera | 12:64943118 | GTAAATCAAATACAG[A/G]TCAAGAAAGAAGAGC | 66689 |
rs29166387 | snp | C/G | 0.444444 | 0.157135 | intron-variant, utr-variant-3-prime | Klhl28 | Mm_Celera | 12:64949193 | AAACAAACAAACAAA[C/G]TAGGCTAGATAGTTA | 66689 |
rs29168906 | snp | C/T | 0.493827 | 0.0552116 | intron-variant, upstream-variant-2KB | Klhl28, LOC105244909 | Mm_Celera | 12:64961568 | AGAAAAGAAGATCTG[C/T]GTAAAAAAATCCAAT | 66689 |
rs29171317 | snp | C/T | 0.493827 | 0.0552116 | synonymous-codon | Klhl28 | Mm_Celera | 12:64957117 | TTCTTGTACATCGTA[C/T]TTGATCCAAGATTCT | 66689 |
rs29175613 | snp | C/T | 0.375 | 0.216506 | intron-variant | Klhl28 | Mm_Celera | 12:64954411 | GCTGGTAAAAAAAGC[C/T]CATCAAAGATTTCAT | 66689 |
rs29180024 | snp | A/G | 0.5 | 0 | intron-variant, utr-variant-3-prime | Klhl28 | Mm_Celera | 12:64947221 | TCTCTAGTCAAAAAC[A/G]GGGAAGACGACAAGA | 66689 |
rs29181860 | snp | A/G | 0.415225 | 0.187619 | intron-variant, downstream-variant-500B | Klhl28 | Mm_Celera | 12:64946063 | TGGGGCTCAGATGAA[A/G]ATAGCCCTTTGTAGT | 66689 |
rs29184050 | snp | C/T | 0.497041 | 0.0383476 | intron-variant, utr-variant-3-prime | Klhl28 | Mm_Celera | 12:64947703 | TCCCAATGAAGACCA[C/T]ACACTCCCACTGTGA | 66689 |
rs29188756 | snp | C/G | 0.497778 | 0.0332592 | utr-variant-3-prime | Klhl28 | Mm_Celera | 12:64942870 | AATATGATACGAAAA[C/G]CACTGTTTTGCAACC | 66689 |
rs29189746 | snp | A/C | 0.444444 | 0.157135 | intron-variant | Klhl28 | Mm_Celera | 12:64958867 | AGTGTATTTTTATGT[A/C]TAATTAGAGATTTTT | 66689 |
rs29191521 | snp | C/G | 0.497778 | 0.0332592 | utr-variant-3-prime | Klhl28 | Mm_Celera | 12:64942930 | AGCAGAAAGAGCACT[C/G]TGATGATTGGCTTGT | 66689 |
rs29192867 | snp | G/T | 0.5 | 0 | intron-variant | Klhl28 | Mm_Celera | 12:64952255 | CAGTTGCCCCATGAC[G/T]AAGATGCATTCTTAG | 66689 |
rs29193725 | snp | G/T | 0.444444 | 0.157135 | intron-variant | Klhl28 | Mm_Celera | 12:64945831 | GGGGATTTTTGAAGG[G/T]AAAACTAGGAAAGGG | 66689 |
rs29199531 | snp | A/G | 0.492188 | 0.0620098 | utr-variant-3-prime | Klhl28 | Mm_Celera | 12:64942940 | GCACTCTGATGATTG[A/G]CTTGTTATTTACAAT | 66689 |
rs29203741 | snp | A/G | 0.444444 | 0.157135 | intron-variant, upstream-variant-2KB, nc-transcript-variant | Klhl28, Fam179b, LOC105244909 | Mm_Celera | 12:64964052 | AAAATAAAAAATTAA[A/G]AACATTTTAATTATG | 66689 |
rs29204048 | snp | C/T | 0.401235 | 0.199068 | intron-variant, utr-variant-3-prime | Klhl28 | Mm_Celera | 12:64947145 | AACTGAGGTCATTTC[C/T]ACTAAAAGCAGGAAA | 66689 |
rs29207369 | snp | A/G | 0.444444 | 0.157135 | intron-variant | Klhl28 | GRCm38.p3 | 12:64955869 | AATGATGTAATATCA[A/G]ATTTTCTATTGGAGA | 66689 |
rs29208509 | snp | C/G | 0.5 | 0 | intron-variant, upstream-variant-2KB | Klhl28, LOC105244909 | Mm_Celera | 12:64962945 | TTAAATAAGATTTAT[C/G]TATAAGATCATCTTA | 66689 |
rs29208668 | snp | C/T | 0.459184 | 0.136902 | intron-variant, upstream-variant-2KB | Klhl28, LOC105244909 | Mm_Celera | 12:64962972 | CTTAAAAGGTACTAA[C/T]AAAGGTGACAGTGTA | 66689 |
rs29210192 | snp | A/G | 0.444444 | 0.157135 | intron-variant | Klhl28 | GRCm38.p3 | 12:64945804 | GGGGAGGGGGGGGGG[A/G]GAGAGGATATAGGGG | 66689 |
rs29212088 | snp | A/G | 0.46875 | 0.121031 | intron-variant, upstream-variant-2KB | Klhl28, LOC105244909 | Mm_Celera | 12:64961483 | AAGCTACAAAGAGGT[A/G]GTGCTGAAATCAGCT | 66689 |
rs29218243 | snp | A/G | 0.444444 | 0.157135 | intron-variant, upstream-variant-2KB, nc-transcript-variant | Klhl28, Fam179b, LOC105244909 | Mm_Celera | 12:64964177 | TCAAGATTTCAAAAA[A/G]TAATATAGCTGGGTA | 66689 |
rs29221678 | snp | A/T | 0.401235 | 0.199068 | intron-variant, utr-variant-3-prime | Klhl28 | Mm_Celera | 12:64946952 | ACAGGGATAAGGACA[A/T]GATCTATGAAAGGGC | 66689 |
rs29222633 | snp | A/C | 0.432133 | 0.171253 | intron-variant | Klhl28 | Mm_Celera | 12:64944668 | CACTCAGCAAATAGC[A/C]AAGCAAGAGGAGCAC | 66689 |
rs29490759 | snp | C/T | 0.456747 | 0.140554 | intron-variant | Klhl28 | Mm_Celera | 12:64954686 | TCTCTCCAAACACTT[C/T]TTAAACTACTCCATT | 66689 |
rs33846378 | snp | C/T | 0.487535 | 0.077957 | missense | Klhl28 | Mm_Celera | 12:64950146 | CTAGCATGACTCCGA[C/T]GCCAAAGTGAATCCT | 66689 |
rs33847517 | snp | A/G | 0.489796 | 0.070696 | intron-variant, upstream-variant-2KB | Klhl28, Fam179b | Mm_Celera | 12:64965206 | AGGTTCTCCTGTACT[A/G]CTAAGCAGGCTGCAG | 66689 |
rs45660144 | snp | C/T | 0.124444 | 0.216185 | upstream-variant-2KB, utr-variant-5-prime | Klhl28, Fam179b | Mm_Celera | 12:64965597 | TCATTCTGGCTACGT[C/T]CAGACTTCCTCTTCC | 66689 |
rs45781467 | snp | G/T | 0.231111 | 0.249285 | intron-variant | Klhl28 | Mm_Celera | 12:64953049 | GAACAACCGCCTGAC[G/T]ACATTGAGGTGGGAG | 66689 |
rs45925237 | snp | A/G | 0.132653 | 0.220748 | intron-variant | Klhl28 | Mm_Celera | 12:64944057 | CACTATGTAACTTAT[A/G]TCTTAAAAATCCTTA | 66689 |
rs45957016 | snp | A/G | 0.244898 | 0.249948 | intron-variant | Klhl28 | Mm_Celera | 12:64960675 | ACAAAGTGTGAACTA[A/G]AGCCAGAGAAGTCTG | 66689 |
rs45991098 | snp | C/T | 0.132653 | 0.220748 | intron-variant, utr-variant-3-prime | Klhl28 | Mm_Celera | 12:64946869 | GAAACAGATGAGAAA[C/T]ACTGGACAGGCAAGA | 66689 |
rs46058291 | snp | C/T | 0.132653 | 0.220748 | intron-variant | Klhl28 | Mm_Celera | 12:64955208 | TGTCTCTGACACATT[C/T]TCTTCTTTGCTTGAC | 66689 |
rs46111776 | snp | C/T | 0.124444 | 0.216185 | missense | Klhl28 | Mm_Celera | 12:64956995 | AGATGTTTACAGGTG[C/T]GATCATCACGGATAA | 66689 |
rs46265514 | snp | A/T | 0.124444 | 0.216185 | intron-variant, downstream-variant-500B | Klhl28 | Mm_Celera | 12:64946015 | CAGCACATCCACATT[A/T]GCAGGCTTACATACA | 66689 |
rs46267693 | snp | A/C | 0.231111 | 0.249285 | intron-variant | Klhl28 | Mm_Celera | 12:64958592 | ATACTAAGATCATTA[A/C]AAAGACCTAGAAGTG | 66689 |
rs46381813 | snp | C/T | 0.231111 | 0.249285 | intron-variant | Klhl28 | Mm_Celera | 12:64955161 | CCAAACAGCCTTTAG[C/T]TTTGTGTGTGACCTA | 66689 |
rs46442365 | snp | A/G | 0.32 | 0.24 | synonymous-codon | Klhl28 | GRCm38.p3 | 12:64950180 | ATCAGCCATGGGCGC[A/G]ACCATCTCCCAGGAG | 66689 |
rs46448158 | snp | A/G | 0.244898 | 0.249948 | intron-variant | Klhl28 | Mm_Celera | 12:64953956 | TCAAACCTTCCTGAC[A/G]CATCTGTTGCTCTCT | 66689 |
rs46792639 | snp | A/G | 0.124444 | 0.216185 | synonymous-codon | Klhl28 | Mm_Celera | 12:64943573 | CCCTGAGTGACCACC[A/G]ACTACATACAGGTAG | 66689 |
rs46891905 | snp | A/G | 0.124444 | 0.216185 | intron-variant, utr-variant-3-prime | Klhl28 | Mm_Celera | 12:64946773 | GCAAACAAACATGAG[A/G]TGAGGTAAGAACATC | 66689 |
rs46953452 | snp | C/T | 0.231111 | 0.249285 | intron-variant | Klhl28 | Mm_Celera | 12:64950489 | GATGTTACAATCCTT[C/T]ATACAAAATAGTGGT | 66689 |
rs46957741 | snp | G/T | 0.124444 | 0.216185 | intron-variant | Klhl28 | Mm_Celera | 12:64950498 | ATCCTTCATACAAAA[G/T]AGTGGTGCAGTACAT | 66689 |
rs46958350 | snp | A/G | 0.124444 | 0.216185 | intron-variant | Klhl28 | Mm_Celera | 12:64958995 | TGGAGGGATGATTCT[A/G]GTGGTGTATTGTAGG | 66689 |
rs47092929 | snp | A/G | 0.142012 | 0.225474 | intron-variant | Klhl28 | Mm_Celera | 12:64958691 | AACAGTCTGAGAAGA[A/G]TCACCTTAGCTCCAG | 66689 |
rs47387174 | snp | A/C/G | 0.489796 | 0.070696 | intron-variant | Klhl28 | GRCm38.p3 | 12:64944742 | CCAGGAGACAGACAC[A/C/G]CTGGAAAAATGAAGT | 66689 |
rs47415549 | snp | A/G | 0.124444 | 0.216185 | synonymous-codon | Klhl28 | Mm_Celera | 12:64957462 | TGTGCCCGTATAGGC[A/G]TACTCCACAATGGCC | 66689 |
rs47496700 | snp | A/G | 0.124444 | 0.216185 | synonymous-codon | Klhl28 | Mm_Celera | 12:64957495 | CAGCGCAGCTTCATC[A/G]ATGCACTGAAACTCA | 66689 |
rs47579682 | snp | A/C | | | intron-variant | Klhl28 | Mm_Celera | 12:64955997 | TATGAAAGAAAAGAC[A/C]AAAAAAAACCCTCAA | 66689 |
rs47602137 | snp | C/T | 0.124444 | 0.216185 | downstream-variant-500B | Klhl28 | Mm_Celera | 12:64942151 | TAAGCCGTCAGCTGC[C/T]GTAACAGTTTTGTTT | 66689 |
rs47672219 | snp | A/G | 0.231111 | 0.249285 | intron-variant | Klhl28 | Mm_Celera | 12:64958132 | GCTTTGTAAAGGTTC[A/G]CTGTTGTTAAACTGC | 66689 |
rs47674467 | snp | C/G | | | intron-variant, utr-variant-3-prime | Klhl28 | Mm_Celera | 12:64948263 | AGGCATAGAAAGTAT[C/G]TTCAGTAAAATAAAC | 66689 |
rs47747693 | snp | A/G | | | intron-variant, utr-variant-3-prime | Klhl28 | Mm_Celera | 12:64948389 | CCTCCATGACATATT[A/G]CAAATGATACTAGGG | 66689 |
rs47820933 | snp | A/G | 0.124444 | 0.216185 | intron-variant | Klhl28 | Mm_Celera | 12:64950407 | CTTTGTGAACAGGAC[A/G]CAATAGCTGAAAGTT | 66689 |
rs48030100 | snp | A/C | 0.408163 | 0.193609 | intron-variant, upstream-variant-2KB | Klhl28, LOC105244909 | Mm_Celera | 12:64962294 | TGTACTTATTAATGA[A/C]GACTTCTTAAATTGT | 66689 |
rs48057929 | snp | C/T | 0.231111 | 0.249285 | intron-variant | Klhl28 | Mm_Celera | 12:64955129 | AGCTATGGTTCATAT[C/T]GGCATCTGCCTCACT | 66689 |
rs48068443 | snp | A/G | 0.32 | 0.24 | intron-variant | Klhl28 | Mm_Celera | 12:64951055 | ACTTTATTCCATTAA[A/G]CAACATGAGAAAAGA | 66689 |
rs48209024 | snp | A/G | 0.231111 | 0.249285 | intron-variant | Klhl28 | Mm_Celera | 12:64950453 | TAGATATCCATGAGG[A/G]ACTGCAGGGTCAATT | 66689 |
rs48550908 | snp | A/C | 0.124444 | 0.216185 | downstream-variant-500B | Klhl28 | Mm_Celera | 12:64942134 | TAACTATTTCTTTTA[A/C]ATAAGCCGTCAGCTG | 66689 |
rs48596014 | snp | A/G | 0.124444 | 0.216185 | intron-variant | Klhl28 | Mm_Celera | 12:64953060 | TGACGACATTGAGGT[A/G]GGAGAAGTGATCGGA | 66689 |
rs48629851 | snp | G/T | 0.124444 | 0.216185 | intron-variant, utr-variant-3-prime | Klhl28 | Mm_Celera | 12:64947636 | AGGCCTCACAGCCTA[G/T]CGGCATCTACCTCAC | 66689 |
rs48658978 | snp | C/T | 0.132653 | 0.220748 | intron-variant | Klhl28 | Mm_Celera | 12:64952798 | TGACGGGTGAGAAAG[C/T]ACATCTCTGAAGAAA | 66689 |
rs48723879 | snp | C/T | 0.124444 | 0.216185 | synonymous-codon | Klhl28 | Mm_Celera | 12:64957078 | CCGTACACTGTTCAG[C/T]AGCTGGGCTAAGTAC | 66689 |
rs48889347 | snp | C/T | 0.132653 | 0.220748 | utr-variant-3-prime | Klhl28 | GRCm38.p3 | 12:64942490 | AAGTAACAATGAAAA[C/T]GCTAATCAAAGTGTA | 66689 |
rs48914307 | snp | A/G | 0.32 | 0.24 | downstream-variant-500B, utr-variant-3-prime | Klhl28 | Mm_Celera | 12:64942402 | AGTCACCATTCAAAA[A/G]CCATGGGAAGTATAA | 66689 |
rs48926536 | snp | C/G | 0.124444 | 0.216185 | intron-variant | Klhl28 | Mm_Celera | 12:64944713 | GGAAGGATCTGAGGG[C/G]CTCCACATGCCCACC | 66689 |
rs48929857 | snp | A/G | 0.231111 | 0.249285 | synonymous-codon | Klhl28 | GRCm38.p3 | 12:64957291 | CAAATAAAGGTCATG[A/G]CAACCGTAAGTCTCC | 66689 |
rs49060861 | snp | C/T | 0.124444 | 0.216185 | intron-variant | Klhl28 | Mm_Celera | 12:64952667 | TTTGTTCACTCTGGA[C/T]ATGGGTAAAATTTTA | 66689 |
rs49071699 | snp | A/G | 0.231111 | 0.249285 | synonymous-codon | Klhl28 | GRCm38.p3 | 12:64951705 | CACGCTAGTTTCAAT[A/G]CCACCTATAACAAAG | 66689 |
rs49086559 | snp | C/T | 0.124444 | 0.216185 | synonymous-codon | Klhl28 | Mm_Celera | 12:64950204 | CCAGGAGTCCTTACT[C/T]GGATCGTAACGCTCC | 66689 |
rs49188321 | snp | C/T | 0.32 | 0.24 | intron-variant | Klhl28 | Mm_Celera | 12:64955190 | TACACTGCATCGTGC[C/T]ACTGTCTCTGACACA | 66689 |
rs49189031 | snp | C/T | 0.32 | 0.24 | intron-variant | Klhl28 | Mm_Celera | 12:64952751 | AATGAAGTCCTTCCT[C/T]ATGCAGTGTCAGATA | 66689 |
rs49204466 | snp | C/T | 0.132653 | 0.220748 | utr-variant-3-prime | Klhl28 | Mm_Celera | 12:64943071 | TGTCCAGTCATACGA[C/T]ACACTCCAGAGTCTG | 66689 |
rs49219049 | snp | C/T | 0.32 | 0.24 | intron-variant | Klhl28 | Mm_Celera | 12:64956039 | AGTGTTGAAAGGCGA[C/T]TTGCATACAGAACTA | 66689 |
rs49272063 | snp | C/T | 0.124444 | 0.216185 | intron-variant, utr-variant-3-prime | Klhl28 | Mm_Celera | 12:64946912 | AGCATCAGTGACAGC[C/T]CATGTTATACAGAAG | 66689 |
rs49353874 | snp | C/T | 0.32 | 0.24 | intron-variant | Klhl28 | Mm_Celera | 12:64953491 | TCTAAGGGCAAACGG[C/T]AATCAATTTTATTAA | 66689 |
rs49355039 | snp | A/G | 0.32 | 0.24 | intron-variant | Klhl28 | Mm_Celera | 12:64955523 | TTAAATTTTGCTATG[A/G]TAGACTCAGTGAGGA | 66689 |
rs49507903 | snp | A/G | 0.124444 | 0.216185 | synonymous-codon | Klhl28 | Mm_Celera | 12:64957339 | AATACAATTACCAGG[A/G]TCAAGTTGGCTTTCA | 66689 |
rs49590738 | snp | C/T | 0.124444 | 0.216185 | synonymous-codon | Klhl28 | Mm_Celera | 12:64950093 | AATGCTTGACAAATG[C/T]GAGACACCGTTATGC | 66689 |
rs49644056 | snp | A/G | 0.32 | 0.24 | synonymous-codon | Klhl28 | GRCm38.p3 | 12:64957315 | AGTCTCCGCAAAACG[A/G]GAAATTCCAATACAA | 66689 |
rs49710431 | snp | A/C | 0.142012 | 0.225474 | intron-variant | Klhl28 | Mm_Celera | 12:64954464 | TTCCAAATTTTGAGA[A/C]AAGAGCATAGATATA | 66689 |
rs49774195 | snp | C/T | 0.231111 | 0.249285 | intron-variant | Klhl28 | Mm_Celera | 12:64953795 | TCTGACTTATCAATC[C/T]CATTTCTGCTACTGT | 66689 |
rs49835568 | snp | A/T | 0.260355 | 0.249785 | intron-variant | Klhl28 | Mm_Celera | 12:64950724 | TCATTCTTATTCTAA[A/T]AGTATGGTGACATGT | 66689 |