SNP - dbSNP |
dbSNP | Type | Alleles | Het | Se(het) | Fxn-class | Gene Name | Assembly | Chr-pos | Sequence | Entrez Gene |
rs3672947 | snp | C/T | 0.5 | 0 | intron-variant | Kbtbd2 | Mm_Celera | 6:56790004 | TTGCAAAAGCAAGAT[C/T]TTTTAGTTAATTAAC | 210973 |
rs3673649 | snp | A/G | 0.5 | 0 | intron-variant | Kbtbd2 | Mm_Celera | 6:56790144 | AACTGGATTCAAAGG[A/G]TGCTATTTCTAAATT | 210973 |
rs3690413 | snp | A/T | 0.444444 | 0.157135 | intron-variant | Kbtbd2 | Mm_Celera | 6:56790544 | ACATAATCAAATGGG[A/T]CTTGAAATCAAGAAG | 210973 |
rs4138828 | snp | A/C/T | 0.48 | 0.0979796 | intron-variant | Kbtbd2 | Mm_Celera | 6:56790336 | TATCTCTCTGTAGTG[A/C/T]GTTCTCTCGTAGAAA | 210973 |
rs6163774 | snp | A/C/T | 0.418802 | 0.184407 | synonymous-codon | Kbtbd2 | GRCm38.p3 | 6:56779496 | TGCACTCCACTGCCA[A/C/T]GCACAAGGCAAAGGG | 210973 |
rs6163860 | snp | C/T | 0.471655 | 0.115624 | synonymous-codon | Kbtbd2 | GRCm38.p3 | 6:56779550 | CTCAGTGTCGTATCT[C/T]TCTACAGTCCTCCGG | 210973 |
rs6373567 | snp | C/T | 0.444444 | 0.157135 | downstream-variant-500B | Kbtbd2 | Mm_Celera | 6:56777056 | TCCTACATATGCCAT[C/T]TTCATGCCTTTACTA | 210973 |
rs6374000 | snp | A/G/T | 0.5 | 0 | downstream-variant-500B | Kbtbd2 | Mm_Celera | 6:56777104 | AATTACAAAGTAGGC[A/G/T]ATCAACAGTTATGAT | 210973 |
rs6374616 | snp | C/T | 0.5 | 0 | downstream-variant-500B | Kbtbd2 | Mm_Celera | 6:56777237 | TTAAAGGGACAATTG[C/T]ATCAATTTAAAGCCT | 210973 |
rs6375189 | snp | G/T | 0.5 | 0 | downstream-variant-500B | Kbtbd2 | Mm_Celera | 6:56777348 | CAGTGAAGAGGGctc[G/T]ctctctctctctctc | 210973 |
rs6375215 | snp | C/T | 0.5 | 0 | downstream-variant-500B | Kbtbd2 | Mm_Celera | 6:56777368 | ctctctctctctctc[C/T]ctctctctctctctc | 210973 |
rs6388241 | snp | C/T | 0.473373 | 0.11227 | downstream-variant-500B | Kbtbd2 | Mm_Celera | 6:56777446 | TACTTAAATCTGTTC[C/T]GGCAAAACCTCAAAT | 210973 |
rs13471831 | snp | A/G | 0.495 | 0.0497494 | utr-variant-3-prime | Kbtbd2 | Mm_Celera | 6:56778180 | GCAAGATCTGCTCTC[A/G]GTCTATGGTATTACA | 210973 |
rs13471832 | snp | C/T | 0.455 | 0.143091 | utr-variant-3-prime | Kbtbd2 | Mm_Celera | 6:56778255 | TTTTAGTATAATTCC[C/T]CTGCACTTAACACTA | 210973 |
rs13471833 | snp | A/C | 0.432133 | 0.171253 | utr-variant-3-prime | Kbtbd2 | Mm_Celera | 6:56778316 | CTGAGATTATCTTAG[A/C]ATATGTATTGGATTC | 210973 |
rs13471834 | snp | C/T | 0.432133 | 0.171253 | utr-variant-3-prime | Kbtbd2 | Mm_Celera | 6:56778339 | CAGTGTGGTATCTCA[C/T]AATTGTGCTGAGATT | 210973 |
rs29885873 | snp | A/T | 0.465374 | 0.126941 | intron-variant | Kbtbd2 | Mm_Celera | 6:56783828 | ATCTTGTACACAGGA[A/T]AGAAGACAATGCTTG | 210973 |
rs29917795 | snp | C/T | 0.432133 | 0.171253 | intron-variant | Kbtbd2 | Mm_Celera | 6:56784646 | CTTGCCCAAATGATA[C/T]CCTGGGCTTAATCTC | 210973 |
rs29920143 | snp | C/T | 0.375 | 0.216506 | intron-variant, upstream-variant-2KB, utr-variant-5-prime | Kbtbd2 | Mm_Celera | 6:56796860 | CTTTCAAGTTTACTA[C/T]CTTAATTCCTTGCTT | 210973 |
rs29929958 | snp | A/C/T | 0.48 | 0.0979796 | intron-variant | Kbtbd2 | Mm_Celera | 6:56784814 | GTCCTAAGAGCCAAA[A/C/T]GGCAGCTGTGCTGTG | 210973 |
rs29969840 | snp | C/T | 0.375 | 0.216506 | upstream-variant-2KB, utr-variant-5-prime | Kbtbd2 | Mm_Celera | 6:56798157 | GAAGTATTGGCACCA[C/T]CGAGATAACCCGCAG | 210973 |
rs30015623 | snp | C/T | 0.444444 | 0.157135 | intron-variant | Kbtbd2 | Mm_Celera | 6:56787867 | AGATAAGAAAATCCA[C/T]GTCTGAAACTGCATG | 210973 |
rs30075532 | snp | A/C | 0.465374 | 0.126941 | intron-variant | Kbtbd2 | Mm_Celera | 6:56787946 | GATGGACTCTGGCTC[A/C]CTGAGGACTGTACCA | 210973 |
rs30115552 | snp | C/T | 0.5 | 0 | intron-variant | Kbtbd2 | Mm_Celera | 6:56787916 | GAAACCAAGGCACTG[C/T]ACAGGGAACTGCACG | 210973 |
rs30122097 | snp | A/T | 0.432133 | 0.171253 | intron-variant | Kbtbd2 | Mm_Celera | 6:56784579 | CAAAGCCAGCTTAAA[A/T]TTTTAAACTTTCAAA | 210973 |
rs30175074 | snp | C/G | 0.5 | 0 | intron-variant | Kbtbd2 | Mm_Celera | 6:56783541 | GAGTTCGAGGCCAAC[C/G]TGATCTACAAAGTGA | 210973 |
rs30256749 | snp | C/T | 0.375 | 0.216506 | upstream-variant-2KB, utr-variant-5-prime | Kbtbd2 | Mm_Celera | 6:56798026 | GAGTGGGGGCCAGCA[C/T]TGCACCCCGGGAAGC | 210973 |
rs30276602 | snp | C/G | 0.244898 | 0.249948 | utr-variant-3-prime | Kbtbd2 | Mm_Celera | 6:56777898 | TTTTAAGATGGAGAA[C/G]TACATCAGCAGCAGG | 210973 |
rs30277738 | snp | C/T | 0.444444 | 0.157135 | synonymous-codon | Kbtbd2 | GRCm38.p3 | 6:56779010 | TTTCCCCACAGTGCA[C/T]CGAAAATCTCTCCCT | 210973 |
rs30277741 | snp | C/T | 0.124444 | 0.216185 | synonymous-codon | Kbtbd2 | Mm_Celera | 6:56779526 | GCTCACCATTGTCCA[C/T]TCATCCTTCTCAGTG | 210973 |
rs30278964 | snp | A/G | 0.475309 | 0.108333 | intron-variant | Kbtbd2 | Mm_Celera | 6:56780431 | AAAAAAAGATGACAC[A/G]TAGAAAAAAAAAGGT | 210973 |
rs30278966 | snp | A/T | 0.124444 | 0.216185 | intron-variant | Kbtbd2 | Mm_Celera | 6:56780504 | TCCATACTCCCAGCC[A/T]CCAGTTTACTTTTAT | 210973 |
rs30278968 | snp | C/T | 0.475309 | 0.108333 | intron-variant | Kbtbd2 | Mm_Celera | 6:56780778 | CTGATTGTTTTTGTA[C/T]ACAGGTTCTCGTTAC | 210973 |
rs30278970 | snp | C/G | 0.124444 | 0.216185 | intron-variant | Kbtbd2 | Mm_Celera | 6:56780793 | TACAGGTTCTCGTTA[C/G]AGTAGCTGAGGCTGA | 210973 |
rs30278972 | snp | C/T | 0.124444 | 0.216185 | intron-variant | Kbtbd2 | Mm_Celera | 6:56781234 | ACAAATAATAAATCT[C/T]CCAAAAGAATCTAAA | 210973 |
rs30279914 | snp | C/T | 0.124444 | 0.216185 | intron-variant | Kbtbd2 | Mm_Celera | 6:56781276 | TAAGTCTATTAAACA[C/T]GAATGAATTTAGGCT | 210973 |
rs30279916 | snp | A/G | 0.124444 | 0.216185 | intron-variant | Kbtbd2 | Mm_Celera | 6:56781543 | TACCCCTGGAAAATG[A/G]AGGAGGGAACCCAAA | 210973 |
rs30279918 | snp | C/T | 0.165289 | 0.235211 | intron-variant | Kbtbd2 | Mm_Celera | 6:56781689 | TTTTATATACAAAAT[C/T]TGACCCATATAAAAT | 210973 |
rs30279920 | snp | A/C/G | 0.165289 | 0.235211 | intron-variant | Kbtbd2 | Mm_Celera | 6:56781694 | TATACAAAATCTGAC[A/C/G]CATATAAAATCTGCA | 210973 |
rs30279922 | snp | A/G | 0.432133 | 0.171253 | synonymous-codon | Kbtbd2 | GRCm38.p3 | 6:56781903 | CTGCAAGGCGGCAGC[A/G]TCCACATTCCTCAGG | 210973 |
rs30280004 | snp | G/T | 0.124444 | 0.216185 | intron-variant | Kbtbd2 | Mm_Celera | 6:56785255 | CAAAACCCTCAAACT[G/T]AAAAAGGTCTGCAAA | 210973 |
rs30280006 | snp | A/G | 0.124444 | 0.216185 | intron-variant | Kbtbd2 | Mm_Celera | 6:56785330 | GAACAGTGGCATAAA[A/G]CAAGGATGGCAGTGA | 210973 |
rs30280007 | snp | C/T | 0.444444 | 0.157135 | intron-variant | Kbtbd2 | Mm_Celera | 6:56785362 | AATGGTTATCAAATA[C/T]TGTCACGAGAACACA | 210973 |
rs30280009 | snp | C/T | 0.124444 | 0.216185 | intron-variant | Kbtbd2 | Mm_Celera | 6:56785381 | CACGAGAACACACTA[C/T]TTCAGTCAAGTAACT | 210973 |
rs30280011 | snp | C/T | 0.48 | 0.0979796 | intron-variant | Kbtbd2 | Mm_Celera | 6:56785479 | TTATTGACCAACTGA[C/T]TGACTGATTGCATGT | 210973 |
rs30280013 | snp | A/G | 0.493827 | 0.0552116 | intron-variant | Kbtbd2 | Mm_Celera | 6:56786410 | CATGTACTATACTAT[A/G]TGGCCATATACTATA | 210973 |
rs30280954 | snp | A/T | 0.124444 | 0.216185 | intron-variant | Kbtbd2 | Mm_Celera | 6:56782079 | ACACTTTCAAAGGCA[A/T]TGAGAAAGTCATATA | 210973 |
rs30280956 | snp | C/T | 0.124444 | 0.216185 | intron-variant | Kbtbd2 | Mm_Celera | 6:56782098 | GAAAGTCATATATAA[C/T]CCAGGGCTGAAGACA | 210973 |
rs30280958 | snp | A/T | 0.497778 | 0.0332592 | intron-variant | Kbtbd2 | Mm_Celera | 6:56782570 | CTTATCTAGTTATCT[A/T]TGCACCAAGCTGCCT | 210973 |
rs30280960 | snp | A/G | 0.497778 | 0.0332592 | intron-variant | Kbtbd2 | Mm_Celera | 6:56782869 | TAAGAAAGCTGCCAA[A/G]AGCTGACTACACACT | 210973 |
rs30280962 | snp | A/G | 0.465374 | 0.126941 | intron-variant | Kbtbd2 | Mm_Celera | 6:56783869 | GATGAACTCTTCTCT[A/G]AGATGGACACTCTAT | 210973 |
rs30281125 | snp | C/T | 0.391111 | 0.206368 | intron-variant | Kbtbd2 | Mm_Celera | 6:56786494 | GGCTATAAAACTAGT[C/T]CAATCACAAGATCAT | 210973 |
rs30281127 | snp | A/G | 0.124444 | 0.216185 | intron-variant | Kbtbd2 | Mm_Celera | 6:56786508 | TCCAATCACAAGATC[A/G]TAACGATACGAAGCT | 210973 |
rs30281129 | snp | C/T | 0.408163 | 0.193609 | intron-variant | Kbtbd2 | Mm_Celera | 6:56786547 | ACACATGTACTGAAC[C/T]ATGTTCTCAATAAAT | 210973 |
rs30281131 | snp | C/T | 0.459184 | 0.136902 | intron-variant | Kbtbd2 | Mm_Celera | 6:56787054 | GAAAATACTGTTCCC[C/T]TTAAATTGCAATATT | 210973 |
rs30281133 | snp | A/G | 0.124444 | 0.216185 | intron-variant | Kbtbd2 | Mm_Celera | 6:56787084 | TAAACAGTACTAATA[A/G]AAGATAAAAGTTGCA | 210973 |
rs30281915 | snp | G/T | 0.497778 | 0.0332592 | intron-variant | Kbtbd2 | Mm_Celera | 6:56787101 | AGATAAAAGTTGCAC[G/T]GTCTTCAAAAATCTT | 210973 |
rs30281917 | snp | A/C | 0.444444 | 0.157135 | intron-variant | Kbtbd2 | Mm_Celera | 6:56787605 | GGCTTATGATTTACA[A/C]CTAAGTCATTAAGAA | 210973 |
rs30281919 | snp | A/C | 0.124444 | 0.216185 | intron-variant | Kbtbd2 | Mm_Celera | 6:56787626 | TCATTAAGAAGAGAG[A/C]GCTTATGAACTCAGG | 210973 |
rs30281923 | snp | A/G | 0.124444 | 0.216185 | intron-variant | Kbtbd2 | Mm_Celera | 6:56788497 | ACTGTCACTGACACT[A/G]CATGGAGCCTGGTAA | 210973 |
rs30282064 | snp | C/T | 0.455 | 0.143091 | intron-variant | Kbtbd2 | Mm_Celera | 6:56783897 | TATACACAAACAGAG[C/T]TCAAGAGCCCAATGT | 210973 |
rs30282066 | snp | C/T | 0.42 | 0.183303 | intron-variant | Kbtbd2 | Mm_Celera | 6:56783934 | CTAGAAAAGTGGCTA[C/T]GAAACCAGCGCAGGC | 210973 |
rs30282068 | snp | G/T | 0.444444 | 0.157135 | intron-variant | Kbtbd2 | Mm_Celera | 6:56784157 | GCTTATGTGAAGACC[G/T]GTTGAGTCAAAAGGA | 210973 |
rs30282070 | snp | C/G | 0.124444 | 0.216185 | intron-variant | Kbtbd2 | Mm_Celera | 6:56784161 | ATGTGAAGACCTGTT[C/G]AGTCAAAAGGAAATA | 210973 |
rs30282072 | snp | G/T | 0.444444 | 0.157135 | intron-variant | Kbtbd2 | Mm_Celera | 6:56784313 | GGAAACTGTACTTAA[G/T]AATTCCAGTTTAAAA | 210973 |
rs30282825 | snp | G/T | 0.124444 | 0.216185 | intron-variant | Kbtbd2 | Mm_Celera | 6:56788621 | GCAACAATTATCTCC[G/T]AAAAATTATTTCAGT | 210973 |
rs30282827 | snp | A/G | 0.391111 | 0.206368 | intron-variant | Kbtbd2 | Mm_Celera | 6:56788644 | ATTTCAGTCTGCTGT[A/G]TAACTCTTCAGTTTA | 210973 |
rs30282829 | snp | C/G | 0.444444 | 0.157135 | intron-variant | Kbtbd2 | Mm_Celera | 6:56788862 | TGCATAAAAACTTAA[C/G]TAAAACACAGAGATG | 210973 |
rs30282831 | snp | A/C | 0.459184 | 0.136902 | intron-variant | Kbtbd2 | Mm_Celera | 6:56789059 | CCCCAAAGCTTTAAC[A/C]CTGAAAGACTGTACT | 210973 |
rs30282832 | snp | C/T | 0.396694 | 0.202437 | intron-variant | Kbtbd2 | Mm_Celera | 6:56789073 | CACTGAAAGACTGTA[C/T]TGATGAAGCCTCACT | 210973 |
rs30282916 | snp | A/G | 0.124444 | 0.216185 | intron-variant | Kbtbd2 | Mm_Celera | 6:56785244 | TCATACTCACTCAAA[A/G]CCCTCAAACTGAAAA | 210973 |
rs30283424 | snp | C/T | 0.408163 | 0.193609 | intron-variant | Kbtbd2 | Mm_Celera | 6:56789123 | GCGCTGGTTCCACTG[C/T]TTGTTCTGGCATAGC | 210973 |
rs30283425 | snp | C/T | 0.48 | 0.0979796 | synonymous-codon, intron-variant | Kbtbd2 | GRCm38.p3 | 6:56789338 | TTTCAACTGTTCCAA[C/T]AAGGACACAGCATAT | 210973 |
rs30283426 | snp | C/T | 0.48 | 0.0979796 | upstream-variant-2KB, utr-variant-5-prime | Kbtbd2 | Mm_Celera | 6:56798087 | TTGCTATATGGGCTG[C/T]TTTCCTTAGTTCCAG | 210973 |
rs30283427 | snp | A/C | 0.497778 | 0.0332592 | upstream-variant-2KB, utr-variant-5-prime | Kbtbd2 | Mm_Celera | 6:56798120 | TCCATCGCTTTCAGA[A/C]GTTCCGCTTGCTAAG | 210973 |
rs30283428 | snp | A/C | 0.444444 | 0.157135 | upstream-variant-2KB, utr-variant-5-prime | Kbtbd2 | Mm_Celera | 6:56798223 | AAATGATGCCTCCAG[A/C]CAGTTTTTACTGCAA | 210973 |
rs30283430 | snp | C/T | 0.489796 | 0.070696 | upstream-variant-2KB | Kbtbd2 | Mm_Celera | 6:56798427 | TAGAACAAGTCCAGT[C/T]TTGAAAATAAGAATG | 210973 |
rs30283432 | snp | A/C | 0.444444 | 0.157135 | upstream-variant-2KB | Kbtbd2 | Mm_Celera | 6:56798589 | GAACGACACCAGACT[A/C]TTTAAAAGTGCTGGT | 210973 |
rs30284754 | snp | A/G | 0.459184 | 0.136902 | upstream-variant-2KB | Kbtbd2 | Mm_Celera | 6:56798885 | AGCACATAGCACAAG[A/G]AACTTCTTTGTAGTT | 210973 |
rs30284756 | snp | C/T | 0.48 | 0.0979796 | upstream-variant-2KB | Kbtbd2 | Mm_Celera | 6:56798924 | TGCTCTTCATCTTGA[C/T]TGCGTGAATATGGAA | 210973 |
rs30320587 | snp | G/T | 0.444444 | 0.157135 | intron-variant | Kbtbd2 | Mm_Celera | 6:56780462 | AAAAAGATGCTGAGA[G/T]TTTGAACTCAGGACC | 210973 |
rs30415750 | snp | C/T | 0.5 | 0 | intron-variant | Kbtbd2 | Mm_Celera | 6:56783558 | GATCTACAAAGTGAG[C/T]TCCAGGACAGCAAGG | 210973 |
rs30417659 | snp | A/C | 0.5 | 0 | intron-variant | Kbtbd2 | Mm_Celera | 6:56782387 | TGAGAAATGACTATA[A/C]ACACGAAAACAGGTA | 210973 |
rs30512095 | snp | A/G | 0.5 | 0 | intron-variant | Kbtbd2 | Mm_Celera | 6:56783544 | TTCGAGGCCAACGTG[A/G]TCTACAAAGTGAGTT | 210973 |
rs30700917 | snp | C/T | 0.5 | 0 | intron-variant | Kbtbd2 | Mm_Celera | 6:56782360 | AGCAGTTAACTAGAG[C/T]TATGGGAGGGATGAG | 210973 |
rs30761829 | snp | C/T | 0.444444 | 0.157135 | intron-variant | Kbtbd2 | Mm_Celera | 6:56782185 | TTCACAGTCACATAA[C/T]GGAATACTATCCAGC | 210973 |
rs30764283 | snp | A/C | 0.5 | 0 | intron-variant | Kbtbd2 | Mm_Celera | 6:56787923 | AGGCACTGTACAGGG[A/C]ACTGCACGATGGACT | 210973 |
rs30800525 | snp | C/T | 0.375 | 0.216506 | intron-variant | Kbtbd2 | Mm_Celera | 6:56793918 | GCATATGTGTGTGTG[C/T]GTGTGCATGTGTGTG | 210973 |
rs30800598 | snp | C/T | 0.48 | 0.0979796 | intron-variant | Kbtbd2 | Mm_Celera | 6:56796549 | TACAAATAAAAGCTT[C/T]ATCCACAGTCTGACT | 210973 |
rs30904291 | snp | A/T | 0.5 | 0 | intron-variant | Kbtbd2 | Mm_Celera | 6:56782743 | CATACCCACTCAACT[A/T]CAACACTATCCAGCC | 210973 |
rs45725058 | snp | A/T | | | intron-variant | Kbtbd2 | Mm_Celera | 6:56792238 | ACCACTTAAATTTAG[A/T]GCCTAACTGTGAAGG | 210973 |
rs45736014 | snp | C/T | | | intron-variant | Kbtbd2 | Mm_Celera | 6:56796551 | CAAATAAAAGCTTCA[C/T]CCACAGTCTGACTAG | 210973 |
rs45812547 | snp | C/T | | | intron-variant | Kbtbd2 | Mm_Celera | 6:56792183 | AAGACATCGTTAATA[C/T]TCTGAACCCATTCTG | 210973 |
rs45829244 | snp | C/T | | | intron-variant | Kbtbd2 | Mm_Celera | 6:56795000 | GCTCCTTTACCTCTC[C/T]GTCTTACTCAGGCTC | 210973 |
rs45890837 | snp | A/G | | | upstream-variant-2KB, utr-variant-5-prime | Kbtbd2 | Mm_Celera | 6:56797893 | CACCCATCCTCAGGG[A/G]TGGCCTAGAAAAATC | 210973 |
rs45955055 | snp | G/T | | | intron-variant | Kbtbd2 | Mm_Celera | 6:56794039 | GAACTCTTCCAAAGC[G/T]TTTTCAGGGTCATCC | 210973 |
rs45974803 | snp | C/T | | | intron-variant | Kbtbd2 | Mm_Celera | 6:56786041 | GACAGAATTTTGGTA[C/T]TGGGGAGAGAACTGG | 210973 |
rs45983907 | snp | C/T | | | intron-variant | Kbtbd2 | Mm_Celera | 6:56796083 | ACTTAAACATCTAAA[C/T]CACTCAAGGCATAGA | 210973 |
rs45987243 | snp | A/G | | | intron-variant | Kbtbd2 | Mm_Celera | 6:56795256 | GGGTAGAGCCCCTTA[A/G]CACTGACTGTGACTA | 210973 |
rs46056099 | snp | A/C | | | intron-variant | Kbtbd2 | Mm_Celera | 6:56792514 | AGTAAGTTTGTTAGA[A/C]TCTATTACACTGCAT | 210973 |