SNP - dbSNP |
dbSNP | Type | Alleles | Het | Se(het) | Fxn-class | Gene Name | Assembly | Chr-pos | Sequence | Entrez Gene |
rs13475184 | snp | A/G | | | utr-variant-5-prime, intron-variant, nc-transcript-variant | Rbck1 | Mm_Celera | 2:152332282 | CTTTGCAGACTTGGC[A/G]CGGGGCCTCCTTCGC | 24105 |
rs13475185 | snp | C/G | | | missense, nc-transcript-variant | Rbck1 | Mm_Celera | 2:152331090 | GCAGAGGAGATGGCC[C/G]TGAGCCTTGCCCGGG | 24105 |
rs13475186 | snp | C/T | | | synonymous-codon, nc-transcript-variant | Rbck1 | Mm_Celera | 2:152331004 | GCAGAGGGTGCCCCT[C/T]AGGGTGCAAGTAAAA | 24105 |
rs27369924 | snp | G/T | 0.32 | 0.24 | upstream-variant-2KB | Rbck1 | Mm_Celera | 2:152332704 | GGTATTGGATTGGCT[G/T]CTGTGCCCTCTGGTC | 24105 |
rs27369925 | snp | C/T | 0.444444 | 0.157135 | intron-variant | Rbck1 | Mm_Celera | 2:152330946 | CAGTCCCCTTTAATG[C/T]AAGGCACACTCACCT | 24105 |
rs27369926 | snp | C/T | 0.444444 | 0.157135 | intron-variant | Rbck1 | Mm_Celera | 2:152330901 | AGGGGGAAAAACAGA[C/T]AACCTGTGCACAGAC | 24105 |
rs27369927 | snp | C/T | 0.444444 | 0.157135 | intron-variant | Rbck1 | Mm_Celera | 2:152330707 | CTAACTCCGGAGGAT[C/T]TGCATGGCCCCTGCA | 24105 |
rs27369928 | snp | C/T | 0.444444 | 0.157135 | intron-variant | Rbck1 | Mm_Celera | 2:152330670 | GAGGAATAAACCCCA[C/T]GCTTGCTTCTAGCAG | 24105 |
rs27369929 | snp | A/G | 0.444444 | 0.157135 | intron-variant | Rbck1 | Mm_Celera | 2:152330375 | CCTTGTAGTAACAAA[A/G]CAAAATCTGTAAGTT | 24105 |
rs27369930 | snp | C/T | 0.444444 | 0.157135 | intron-variant | Rbck1 | Mm_Celera | 2:152330098 | GCAACTCCATAGTAA[C/T]AATACTAACGGGGGT | 24105 |
rs27369931 | snp | C/G | 0.444444 | 0.157135 | intron-variant | Rbck1 | Mm_Celera | 2:152329396 | CCACTGGACCCATGT[C/G]CAGCCTTCTGAGACC | 24105 |
rs27369932 | snp | C/T | 0.35503 | 0.226867 | intron-variant | Rbck1 | Mm_Celera | 2:152329111 | CCACCACCAAGGGCA[C/T]GCGTTCTTACTCTAG | 24105 |
rs27369933 | snp | C/T | 0.444444 | 0.157135 | intron-variant | Rbck1 | Mm_Celera | 2:152329079 | ATGAAGAGCCTCATA[C/T]GCACCAGGCAATCAC | 24105 |
rs27369934 | snp | A/G | 0.444444 | 0.157135 | intron-variant | Rbck1 | Mm_Celera | 2:152329016 | ACTTAAGTCCAAACT[A/G]CATCATTCCAAACCA | 24105 |
rs27369935 | snp | A/G | 0.444444 | 0.157135 | intron-variant | Rbck1 | Mm_Celera | 2:152329000 | AGTAACTGCCAGAGC[A/G]ACTTAAGTCCAAACT | 24105 |
rs27369936 | snp | C/T | 0.35503 | 0.226867 | intron-variant | Rbck1 | Mm_Celera | 2:152328937 | AGGCCAGGCCATAGC[C/T]TTTTCCAGATACACA | 24105 |
rs27369937 | snp | A/C | 0.277778 | 0.248452 | intron-variant | Rbck1 | Mm_Celera | 2:152328927 | AGCCTGAGACAGGCC[A/C]GGCCATAGCTTTTTC | 24105 |
rs27369938 | snp | G/T | 0.444444 | 0.157135 | intron-variant | Rbck1 | Mm_Celera | 2:152327064 | TCCTGACCCCTAGAT[G/T]GAGTTTCCCAAGCAC | 24105 |
rs27369939 | snp | C/G | 0.444444 | 0.157135 | synonymous-codon, nc-transcript-variant | Rbck1 | Mm_Celera | 2:152326313 | GGCACCGTCTCCATT[C/G]CGCCGAATGCCGTGT | 24105 |
rs27369940 | snp | C/T | 0.444444 | 0.157135 | synonymous-codon, nc-transcript-variant | Rbck1 | Mm_Celera | 2:152326256 | CCGCTGCAGCTCTTG[C/T]GGGTTGAGTGACGTG | 24105 |
rs27369941 | snp | A/G | 0.444444 | 0.157135 | intron-variant | Rbck1 | Mm_Celera | 2:152326208 | ATCGCTGACAGGGAA[A/G]ACTTCACCTTCCAAC | 24105 |
rs27369942 | snp | C/T | 0.124444 | 0.216185 | intron-variant | Rbck1 | Mm_Celera | 2:152325935 | CTCTGTACAACTCTC[C/T]GACTTTTCTACAGGT | 24105 |
rs27369943 | snp | A/T | 0.444444 | 0.157135 | intron-variant | Rbck1 | Mm_Celera | 2:152325113 | CAAATGAGACTGACT[A/T]TACTTGTGTCAATGT | 24105 |
rs27369944 | snp | C/T | 0.444444 | 0.157135 | intron-variant | Rbck1 | Mm_Celera | 2:152325102 | TGGCAAAAACCCAAA[C/T]GAGACTGACTTTACT | 24105 |
rs27369945 | snp | A/G | 0.408163 | 0.193609 | intron-variant | Rbck1 | Mm_Celera | 2:152325069 | ATCTTTTGCCACCAA[A/G]GACACTGGTTGGACA | 24105 |
rs27369946 | snp | C/T | 0.32 | 0.24 | intron-variant | Rbck1 | Mm_Celera | 2:152324684 | GTAACCACATGCTGA[C/T]AACCCACCTGGAGTC | 24105 |
rs27369947 | snp | C/T | 0.231111 | 0.249285 | intron-variant | Rbck1 | Mm_Celera | 2:152324128 | AGCTCTCAGTCAAGG[C/T]CAAGGTTATGGCTTA | 24105 |
rs27369948 | snp | A/T | 0.408163 | 0.193609 | intron-variant | Rbck1 | Mm_Celera | 2:152324079 | CACAACCAGAGAGTG[A/T]GCATCAGCCAGAGAA | 24105 |
rs27369949 | snp | A/G | 0.444444 | 0.157135 | intron-variant | Rbck1 | Mm_Celera | 2:152324036 | TCAAAGCGAGGACGC[A/G]GAGCAGGTGACGAGC | 24105 |
rs27369950 | snp | C/T | 0.444444 | 0.157135 | intron-variant | Rbck1 | Mm_Celera | 2:152323931 | TGAGGTTACAGGCCA[C/T]GGGGTGAGGATCTGA | 24105 |
rs27369951 | snp | C/T | 0.444444 | 0.157135 | intron-variant | Rbck1 | Mm_Celera | 2:152322400 | CCAAGGGCCCCACGC[C/T]TCTATTCACCCCACC | 24105 |
rs27369952 | snp | A/G | 0.32 | 0.24 | intron-variant | Rbck1 | Mm_Celera | 2:152322053 | CCCAATGAACTCTTG[A/G]GTGATGTCTGCTGGG | 24105 |
rs27369953 | snp | A/G | 0.231111 | 0.249285 | intron-variant | Rbck1 | Mm_Celera | 2:152321777 | GCAGATGCCATCTGT[A/G]GTTCTGATAGCGGAC | 24105 |
rs27369954 | snp | C/T | 0.444444 | 0.157135 | intron-variant | Rbck1 | GRCm38.p3 | 2:152321653 | TCCACCGAGTGGAAG[C/T]ACAGCCTCGCCCTTT | 24105 |
rs27369955 | snp | A/G | 0.444444 | 0.157135 | intron-variant | Rbck1 | Mm_Celera | 2:152321580 | GTGAAGGCCATCAGG[A/G]ACCAGCTCATACCAC | 24105 |
rs27369956 | snp | C/T | 0.444444 | 0.157135 | intron-variant | Rbck1 | Mm_Celera | 2:152321419 | CCTGAGCATGTAGTC[C/T]GTCCGCACTGATTAA | 24105 |
rs27369957 | snp | C/T | 0.244898 | 0.249948 | intron-variant | Rbck1 | Mm_Celera | 2:152321093 | GGAGACTTCAGAAGT[C/T]AGAGGAGACGGGAGT | 24105 |
rs27369958 | snp | A/G | 0.231111 | 0.249285 | intron-variant | Rbck1 | Mm_Celera | 2:152321062 | TTGGGCTAGAGAATC[A/G]TTTCATAATATTTTG | 24105 |
rs27369959 | snp | A/G | 0.444444 | 0.157135 | intron-variant | Rbck1 | Mm_Celera | 2:152320932 | CTCAGCAATGCCCAG[A/G]ACTGATCCACTCAGA | 24105 |
rs27369960 | snp | C/T | 0.444444 | 0.157135 | intron-variant | Rbck1 | Mm_Celera | 2:152320851 | TAAATATGGCCTTCT[C/T]AGGAAACCTCTGAGC | 24105 |
rs27369961 | snp | A/G | 0.444444 | 0.157135 | intron-variant | Rbck1 | Mm_Celera | 2:152320638 | GAAACAGGACAAAAT[A/G]CTACTAGAGGATGTC | 24105 |
rs27369962 | snp | C/T | 0.444444 | 0.157135 | intron-variant | Rbck1 | Mm_Celera | 2:152320199 | TTACATATTGCAAAA[C/T]TCACATACCTATACA | 24105 |
rs27369963 | snp | C/T | 0.444444 | 0.157135 | intron-variant | Rbck1 | Mm_Celera | 2:152319999 | ACCATCTTCTGGTGC[C/T]TCTACTCCACACAGA | 24105 |
rs27369964 | snp | A/G | 0.444444 | 0.157135 | intron-variant | Rbck1 | Mm_Celera | 2:152319576 | CACAGAGCCCCTTGA[A/G]CACTTAAAACCACCA | 24105 |
rs27369965 | snp | C/T | 0.444444 | 0.157135 | intron-variant | Rbck1 | Mm_Celera | 2:152319499 | TAACAACTGGAGGGT[C/T]TCTACTTCCCAAGGG | 24105 |
rs27369966 | snp | C/T | 0.444444 | 0.157135 | missense, nc-transcript-variant | Rbck1 | Mm_Celera | 2:152318798 | TCCCTGCAATTCATG[C/T]GCTCATGGATGGCCT | 24105 |
rs27369967 | snp | A/G | 0.444444 | 0.157135 | synonymous-codon, nc-transcript-variant | Rbck1 | Mm_Celera | 2:152318357 | CCAGCAGATCTCAGT[A/G]TGGCAGACTGTACAG | 24105 |
rs27369968 | snp | C/G | 0.408163 | 0.193609 | intron-variant | Rbck1 | Mm_Celera | 2:152317444 | TCCAGAACTATTTTC[C/G]TGTCTCTCTGCACTT | 24105 |
rs27369969 | snp | C/G/T | 0.444444 | 0.157135 | intron-variant | Rbck1 | GRCm38.p3 | 2:152317387 | AAGCCTGACAGACCT[C/G/T]AGCCCCCGCAAAGCA | 24105 |
rs27369970 | snp | A/G | 0.231111 | 0.249285 | intron-variant | Rbck1 | Mm_Celera | 2:152317367 | TTTGCTGCACAGCCA[A/G]GTCAAAGCCTGACAG | 24105 |
rs27369971 | snp | A/C | 0.132653 | 0.220748 | intron-variant | Rbck1 | Mm_Celera | 2:152317208 | ACAGCCGGTGACTCG[A/C]ATCCACAGAGCACTT | 24105 |
rs27369972 | snp | C/T | 0.408163 | 0.193609 | intron-variant | Rbck1 | Mm_Celera | 2:152317206 | TCACAGCCGGTGACT[C/T]GCATCCACAGAGCAC | 24105 |
rs27369973 | snp | C/G | 0.32 | 0.24 | intron-variant | Rbck1 | Mm_Celera | 2:152317197 | CCCAGGCACTCACAG[C/G]CGGTGACTCGCATCC | 24105 |
rs27369974 | snp | A/T | 0.35503 | 0.226867 | intron-variant | Rbck1 | Mm_Celera | 2:152317115 | GGATTCAGCTGTAGG[A/T]GGACCAGCACCCAGG | 24105 |
rs27369975 | snp | C/T | 0.444444 | 0.157135 | utr-variant-3-prime, nc-transcript-variant | Rbck1 | Mm_Celera | 2:152316565 | GCCTTAGGCCAAGGC[C/T]GTGTTTAATTAAGGC | 24105 |
rs27369976 | snp | A/C | 0.444444 | 0.157135 | utr-variant-3-prime, nc-transcript-variant | Rbck1 | Mm_Celera | 2:152316451 | ACATCAGCTTTAAGA[A/C]GTGCCCAGAAAGCCA | 24105 |
rs27369977 | snp | A/G | 0.444444 | 0.157135 | utr-variant-3-prime, nc-transcript-variant | Rbck1 | Mm_Celera | 2:152316419 | CTTACCAATCTACCT[A/G]GGCCCTGGATGGATT | 24105 |
rs27369978 | snp | C/T | 0.408163 | 0.193609 | utr-variant-3-prime, nc-transcript-variant | Rbck1 | GRCm38.p3 | 2:152316348 | CTTCTGGGAAAACCA[C/T]TTTAATTCACTTAAA | 24105 |
rs27369979 | snp | G/T | 0.444444 | 0.157135 | downstream-variant-500B | Rbck1 | Mm_Celera | 2:152316119 | TACATTTCCCCAGTC[G/T]GGGCTAATAATGCCC | 24105 |
rs27369980 | snp | A/C | 0.444444 | 0.157135 | downstream-variant-500B | Rbck1 | Mm_Celera | 2:152316106 | AAGCCCTTCTCGATA[A/C]ATTTCCCCAGTCTGG | 24105 |
rs29558397 | snp | A/G | 0.375 | 0.216506 | upstream-variant-2KB | Rbck1 | Mm_Celera | 2:152334474 | CAACCCAGGAGAGAG[A/G]TTGTTAACCCATACT | 24105 |
rs32867124 | snp | A/G | 0.375 | 0.216506 | intron-variant | Rbck1 | Mm_Celera | 2:152331853 | ATCGGAGTTCCCCCA[A/G]TTCTGAGTGAAAGGG | 24105 |
rs33028768 | snp | A/G | 0.375 | 0.216506 | upstream-variant-2KB | Rbck1 | Mm_Celera | 2:152334231 | ATCACACAGTGCAGG[A/G]TCAAATTTGAGATAC | 24105 |
rs33534918 | snp | A/C | 0.48 | 0.0979796 | intron-variant | Rbck1 | Mm_Celera | 2:152321184 | CCATCCTTTTTTAAG[A/C]CTACGGTAGAACTCA | 24105 |
rs46438028 | snp | C/T | | | intron-variant | Rbck1 | Mm_Celera | 2:152325504 | CCTCCTAAAGGCATG[C/T]GCCACTATGCCCAGC | 24105 |
rs46966910 | snp | A/T | | | intron-variant | Rbck1 | Mm_Celera | 2:152325837 | GGTCTATAGTGTGAG[A/T]TCCAGGATAGCCACA | 24105 |
rs48113754 | snp | A/T | | | intron-variant | Rbck1 | Mm_Celera | 2:152325545 | CAATTTTTTAAAATT[A/T]AAAAAAAAAAAAAGT | 24105 |
rs50098000 | snp | A/G | | | intron-variant | Rbck1 | Mm_Celera | 2:152325505 | CTCCTAAAGGCATGT[A/G]CCACTATGCCCAGCC | 24105 |
rs52403460 | snp | A/G | | | intron-variant | Rbck1 | Mm_Celera | 2:152325852 | TTCCAGGATAGCCAC[A/G]GACAGCTATACAGAG | 24105 |
rs212254597 | snp | C/T | | | downstream-variant-500B | Rbck1 | Mm_Celera | 2:152315985 | GCACTTTCAGAAACG[C/T]CTCTGCTCTTCTCCT | 24105 |
rs212380303 | snp | C/T | | | intron-variant | Rbck1 | Mm_Celera | 2:152325998 | ACCTTAGTTATCTCA[C/T]CAACATACAGATAGA | 24105 |
rs212442511 | snp | C/G | | | intron-variant | Rbck1 | Mm_Celera | 2:152325305 | ACACACACACACAGA[C/G]AGAGAGAGAAACAAG | 24105 |
rs212561706 | in-del | -/AAAC | | | intron-variant | Rbck1 | Mm_Celera | 2:152317862 | TGCATAAACAATAAA[-/AAAC]AAAGCCAGGCAACGG | 24105 |
rs212585364 | in-del | -/T | | | intron-variant | Rbck1 | Mm_Celera | 2:152326109 | TAAACGGCCCCTCCC[-/T]TCATGCCAGCCATGC | 24105 |
rs212645193 | snp | A/G | | | intron-variant | Rbck1 | Mm_Celera | 2:152321269 | AGCTATCTGATTCAA[A/G]CTGGCCTCAAGCTTT | 24105 |
rs212709367 | snp | A/G | | | intron-variant | Rbck1 | Mm_Celera | 2:152320477 | ATAAAAGAAACATAT[A/G]GGGGTGGGCAGTAGT | 24105 |
rs212770280 | snp | A/G | | | intron-variant | Rbck1 | Mm_Celera | 2:152329082 | AAGAGCCTCATATGC[A/G]CCAGGCAATCACTCC | 24105 |
rs212781783 | snp | A/C | | | upstream-variant-2KB | Rbck1 | Mm_Celera | 2:152333464 | TAAGGATCTGAGTTC[A/C]CAACTCAGTGGCCCC | 24105 |
rs212847629 | snp | A/G | | | intron-variant | Rbck1 | Mm_Celera | 2:152328405 | CAGACACACCAGGAG[A/G]AGGTATCAGATCCAA | 24105 |
rs212905287 | snp | A/G | | | intron-variant | Rbck1 | Mm_Celera | 2:152324157 | TAGCAGTGTGGTCAC[A/G]AGGTGAGTGGCAATG | 24105 |
rs212925554 | snp | A/T | | | intron-variant | Rbck1 | Mm_Celera | 2:152331839 | AGAACAGTGGCATTA[A/T]CGGAGTTCCCCCAGT | 24105 |
rs212967101 | snp | G/T | | | intron-variant | Rbck1 | Mm_Celera | 2:152322672 | TGACTTTTGAGGGGT[G/T]CCTTCCCTAGTTACT | 24105 |
rs213034644 | snp | A/G | | | intron-variant | Rbck1 | Mm_Celera | 2:152331150 | CATCAGTTTATGTGG[A/G]GAGGCTGGAGAGGTG | 24105 |
rs213549518 | snp | A/G | | | intron-variant | Rbck1 | Mm_Celera | 2:152321386 | GAATGGTTCATGTTG[A/G]CCCCTACAGGGAATC | 24105 |
rs213574992 | snp | A/C | | | missense, intron-variant, nc-transcript-variant | Rbck1 | Mm_Celera | 2:152322225 | CAATGAAGGGGCAAG[A/C]CACCTCCGCCTCCTG | 24105 |
rs213603291 | snp | C/T | | | intron-variant | Rbck1 | Mm_Celera | 2:152320795 | AGGCTTGAGTCAGGG[C/T]CTGAGGACATCTAGG | 24105 |
rs213991211 | snp | A/T | | | upstream-variant-2KB | Rbck1 | Mm_Celera | 2:152333062 | TCACAGATTAACAGA[A/T]ACACTGGGCACCCCC | 24105 |
rs214047979 | snp | C/T | | | intron-variant | Rbck1 | Mm_Celera | 2:152318552 | CGTTACAGAGGGCTC[C/T]CCAACCCAGACTCTT | 24105 |
rs214109966 | snp | A/G | | | intron-variant | Rbck1 | Mm_Celera | 2:152317342 | TCTCCCCTCGAGCAG[A/G]ACAGCAGGCTTTGCT | 24105 |
rs214155076 | snp | G/T | | | intron-variant | Rbck1 | Mm_Celera | 2:152331292 | CTCCTCTGTACCCTG[G/T]ACTCACGGAGTCCTC | 24105 |
rs214157512 | snp | A/G | | | intron-variant | Rbck1 | Mm_Celera | 2:152330148 | ACTAACTCTTTCACC[A/G]GAGTTGCCTAAGACC | 24105 |
rs214387122 | snp | C/G | | | missense, nc-transcript-variant | Rbck1 | Mm_Celera | 2:152324542 | GTGGTGACTCCGGTG[C/G]TGCATCTGGCTGTCC | 24105 |
rs214463818 | snp | G/T | | | intron-variant | Rbck1 | Mm_Celera | 2:152331888 | GGGGAGGGATGGATG[G/T]TCCCCTCTCGGTCCT | 24105 |
rs214487190 | snp | A/G | | | intron-variant | Rbck1 | Mm_Celera | 2:152327686 | ATAGTGAGCCACCAC[A/G]TGGGTGCTGAGAACC | 24105 |
rs214780593 | snp | G/T | | | intron-variant | Rbck1 | Mm_Celera | 2:152328296 | CTGGGGATGAGCCAG[G/T]GCCTTGCACTAGGGG | 24105 |
rs215384921 | snp | C/T | | | synonymous-codon, nc-transcript-variant | Rbck1 | Mm_Celera | 2:152318713 | AAGACTGTGCCTTAC[C/T]TTTAGCATCTCTGTC | 24105 |
rs215456818 | snp | A/C | | | intron-variant | Rbck1 | Mm_Celera | 2:152328328 | GTGTTCTACAGCTGA[A/C]CTGGGTCTCAGCCCC | 24105 |
rs215783648 | snp | G/T | | | intron-variant | Rbck1 | Mm_Celera | 2:152320047 | GCACCTCCCAGCAGG[G/T]AAAGCTAAGCTGAGA | 24105 |
rs215819866 | in-del | -/A | | | intron-variant | Rbck1 | Mm_Celera | 2:152318169 | GTAAATAAATCTTTT[-/A]AAAAAAAAAAAAATT | 24105 |
rs216388639 | snp | A/C | | | intron-variant | Rbck1 | Mm_Celera | 2:152326517 | ACTGTTTTCTGAGAC[A/C]GTGGAACTGTTGCTG | 24105 |