Map1lc3b
SNP - dbSNP
dbSNPTypeAllelesHetSe(het)Fxn-classGene NameAssemblyChr-posSequenceEntrez Gene
rs8157767snpA/Gutr-variant-3-prime, intron-variantMap1lc3b, RGD1304884Rn_Celera19:53643364CAGCTGCACGGGAAG[A/G]CCAGCATTGCACACC64862
rs197020195snpA/G00intron-variantMap1lc3b, RGD1304884Rn_Celera19:53635937CGTCGGTCACCAGTG[A/G]GCTCGGCATTCCCTG64862
rs197177772snpC/T00intron-variant, downstream-variant-500BMap1lc3b, Zcchc14, RGD1304884Rn_Celera19:53644375ATCCAGGTCCGTCTC[C/T]AGCAGTGCTGTTAGC64862
rs197274873snpA/G00intron-variantMap1lc3b, RGD1304884Rn_Celera19:53639313GAACTCAGGACCTCC[A/G]GAAGAGCAGTCAGCG64862
rs197418859snpA/G00intron-variantMap1lc3b, RGD1304884Rn_Celera19:53641319GGTGGGATTGAAGGC[A/G]TGCACCACCATACCA64862
rs197477234snpC/T00intron-variantMap1lc3b, RGD1304884Rn_Celera19:53637491TTTAAGACAGGGTTT[C/T]TCCATGTAGCCCCGA64862
rs197666048snpC/T00intron-variant, downstream-variant-500BMap1lc3b, Zcchc14, RGD1304884Rn_Celera19:53644397GCTGTTAGCAGGCCC[C/T]GTCCTGGAAGGGCGG64862
rs197684899snpG/T00upstream-variant-2KB, intron-variantMap1lc3b, RGD1304884Rn_Celera19:53635377CTGGAACACCAGCTG[G/T]GCCATGCAAGGATTG64862
rs197829212snpA/G00utr-variant-3-prime, intron-variantMap1lc3b, RGD1304884Rn_Celera19:53643420GCACTCGCCTTGTAC[A/G]TGGTTCACACCTACT64862
rs197918670snpA/G00upstream-variant-2KB, intron-variantMap1lc3b, RGD1304884Rn_Celera19:53634735GCTGATGGAGTCGGG[A/G]GGCCTGCAGGAGTCA64862
rs197966825snpA/G00intron-variantMap1lc3b, RGD1304884Rn_Celera19:53638753TTGGTACAGTGTTGA[A/G]AATGAAGATTAGACT64862
rs198002331snpA/G00intron-variantMap1lc3b, RGD1304884Rn_Celera19:53636224TGGGAAAAATAAGGC[A/G]TGCACATTAGCTAGG64862
rs198327350snpC/T00intron-variantMap1lc3b, RGD1304884Rn_Celera19:53636760CAGGAGGCGTGTGGG[C/T]TTGCAGATTCTTAGT64862
rs198418869snpC/T00utr-variant-3-prime, intron-variantMap1lc3b, RGD1304884Rn_Celera19:53643775CTGTCCCTGCTAACC[C/T]CCAATGTTATGTTAC64862
rs198451495snpA/G00utr-variant-5-prime, intron-variantMap1lc3b, RGD1304884Rn_Celera19:53635676GTGATCGTCGCGGGA[A/G]CCAGATCGTCTGACC64862
rs198528137snpC/T00utr-variant-3-prime, intron-variantMap1lc3b, RGD1304884Rn_Celera19:53642991GAGCAGTGTCAGGGG[C/T]GGCCTCTTCCTGGGA64862
rs198584368snpA/G00intron-variantMap1lc3b, RGD1304884Rn_Celera19:53639419CCTTGGTTTACCAGG[A/G]CTGAAAAATTAACAA64862
rs198691378snpA/C00intron-variantMap1lc3b, RGD1304884Rn_Celera19:53638968GAGCTGGGGACTGAA[A/C]CCAGGGCCTTGCGCT64862
rs198788729snpA/G00intron-variantMap1lc3b, RGD1304884Rn_Celera19:53642321AGTTGCACAGGGGGC[A/G]TTCATAAGGTCTCAG64862
rs198886368snpC/T00utr-variant-3-prime, intron-variantMap1lc3b, RGD1304884Rn_Celera19:53643109GGCTCTGGCTTTGCC[C/T]GAAACAGGTCAGGTG64862
rs198923821snpG/T00upstream-variant-2KB, intron-variantMap1lc3b, RGD1304884Rn_Celera19:53635152CTTGCTTCTCTTAGG[G/T]ATACATACTCGTGAT64862
rs199016946snpA/G00upstream-variant-2KB, intron-variantMap1lc3b, RGD1304884Rn_Celera19:53635079GGAGAGTGACAGGCT[A/G]GACACTTAAGTAGGA64862
rs199171639snpA/G00intron-variantMap1lc3b, RGD1304884Rn_Celera19:53636948GGGCTCTTGTGGGAC[A/G]AGGAGATGCTGAAGC64862
rs199321136snpC/G00intron-variantMap1lc3b, RGD1304884Rn_Celera19:53642448TCAGTGTGCTTTTTC[C/G]GGGCCTAAGTTGTGG64862
rs199324382snpC/T00upstream-variant-2KB, intron-variantMap1lc3b, RGD1304884Rn_Celera19:53633906AGGGTGTCAGATCCC[C/T]GGGAGCTAGAGTTCC64862
rs199385698snpA/G00intron-variantMap1lc3b, RGD1304884Rn_Celera19:53639994ACTAAGGAAGCAGTC[A/G]CACTCAGGGTGGCAT64862
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