Users can query the SNP information according to the gene ID.


Gene ID

Results: 1 - 489298 of 489298 records


Num GeneID Chromosome Position Ref.allele Alt.allele Mutant type Impacts Amino acid change SampleID
175051 BAA02g17680 A02 8807403 G A synonymous_variant LOW c.1729C>T|p.Leu577Leu S237
175052 BAA02g17680 A02 8807911 C T synonymous_variant LOW c.1221G>A|p.Arg407Arg S212
175053 BAA02g17680 A02 8808419 C T missense_variant MODERATE c.713G>A|p.Arg238Gln S179
175054 BAA02g17680 A02 8808489 C T missense_variant MODERATE c.643G>A|p.Gly215Arg S255
175055 BAA02g17680 A02 8809905 G A upstream_gene_variant MODIFIER c.-774C>T| S256
175056 BAA02g17680 A02 8809906 C T upstream_gene_variant MODIFIER c.-775G>A| S182
175057 BAA02g17680 A02 8811714 C T upstream_gene_variant MODIFIER c.-2583G>A| S271
175058 BAA02g17680 A02 8812696 C T upstream_gene_variant MODIFIER c.-3565G>A| S32
175059 BAA02g17690 A02 8814169 G A missense_variant MODERATE c.422G>A|p.Ser141Asn S293
175060 BAA02g17690 A02 8815017 C T missense_variant MODERATE c.1078C>T|p.Pro360Ser S25
175061 BAA02g17690 A02 8815214 G A missense_variant MODERATE c.1192G>A|p.Glu398Lys S98
175062 BAA02g17700 A02 8815344 G A upstream_gene_variant MODIFIER c.-274G>A| S184
175063 BAA02g17710 A02 8815822 C T upstream_gene_variant MODIFIER c.-2096C>T| S233
175064 BAA02g17710 A02 8815859 G A upstream_gene_variant MODIFIER c.-2059G>A| S45
175065 BAA02g17710 A02 8815929 C T upstream_gene_variant MODIFIER c.-1989C>T| S105
S106
175066 BAA02g17700 A02 8816314 C T stop_gained HIGH c.259C>T|p.Gln87* S230
175067 BAA02g17700 A02 8816942 C T stop_gained HIGH c.619C>T|p.Gln207* S128
175068 BAA02g17710 A02 8817426 C T upstream_gene_variant MODIFIER c.-492C>T| S277
175069 BAA02g17710 A02 8818048 C T splice_region_variant&intron_variant LOW c.124+7C>T| S216
175070 BAA02g17720 A02 8818242 C A upstream_gene_variant MODIFIER c.-4567C>A| S95
175071 BAA02g17720 A02 8818414 G A upstream_gene_variant MODIFIER c.-4395G>A| S12
175072 BAA02g17710 A02 8818723 C T missense_variant MODERATE c.401C>T|p.Ser134Phe S186
175073 BAA02g17710 A02 8818829 G A missense_variant MODERATE c.430G>A|p.Ala144Thr S207
175074 BAA02g17710 A02 8818841 G A missense_variant MODERATE c.442G>A|p.Gly148Arg S260
175075 BAA02g17710 A02 8820962 C T missense_variant MODERATE c.875C>T|p.Pro292Leu S233