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
100901 BAA10g07050 A10 3870043 G A upstream_gene_variant MODIFIER c.-2839C>T| S100
100902 BAA10g07050 A10 3870149 C T upstream_gene_variant MODIFIER c.-2945G>A| S150
100903 BAA10g07050 A10 3870353 G A upstream_gene_variant MODIFIER c.-3149C>T| S221
100904 BAA10g07050 A10 3871205 C T upstream_gene_variant MODIFIER c.-4001G>A| S41
100905 BAA10g07050 A10 3871770 G A upstream_gene_variant MODIFIER c.-4566C>T| S216
100906 BAA10g07050 A10 3872030 G A upstream_gene_variant MODIFIER c.-4826C>T| S219
S72
100907 BAA10g07050 A10 3872186 G A upstream_gene_variant MODIFIER c.-4982C>T| S303
100908 BAA10g07050-BAA10g07060 A10 3872308 G A intergenic_region MODIFIER n.3872308G>A| S164
100909 BAA10g07060 A10 3881640 C T upstream_gene_variant MODIFIER c.-815C>T| S123
100910 BAA10g07060 A10 3882525 G A missense_variant MODERATE c.71G>A|p.Gly24Glu S95
100911 BAA10g07060 A10 3882648 C T intron_variant MODIFIER c.168+26C>T| S270
100912 BAA10g07060 A10 3882854 C T missense_variant MODERATE c.310C>T|p.Pro104Ser S246
100913 BAA10g07060 A10 3883339 G A stop_gained HIGH c.722G>A|p.Trp241* S192
100914 BAA10g07060 A10 3884364 G A missense_variant MODERATE c.1660G>A|p.Glu554Lys S90
100915 BAA10g07060 A10 3884793 G A missense_variant MODERATE c.1977G>A|p.Met659Ile S237
100916 BAA10g07060 A10 3885231 C T intron_variant MODIFIER c.2191-50C>T| S88
100917 BAA10g07060 A10 3885757 C T missense_variant MODERATE c.2500C>T|p.Arg834Trp S191
100918 BAA10g07060 A10 3899634 G A missense_variant MODERATE c.11858G>A|p.Arg3953Gln S17
100919 BAA10g07060 A10 3899659 G A synonymous_variant LOW c.11883G>A|p.Lys3961Lys S267
100920 BAA10g07060 A10 3899692 C T synonymous_variant LOW c.11916C>T|p.Ser3972Ser S116
100921 BAA10g07070 A10 3900724 G A downstream_gene_variant MODIFIER c.*3187C>T| S12
100922 BAA10g07070 A10 3900792 C T downstream_gene_variant MODIFIER c.*3119G>A| S162
100923 BAA10g07070 A10 3900900 G T downstream_gene_variant MODIFIER c.*3011C>A| S85
100924 BAA10g07070 A10 3901365 G A downstream_gene_variant MODIFIER c.*2546C>T| S277
100925 BAA10g07070 A10 3901611 G A downstream_gene_variant MODIFIER c.*2300C>T| S103