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
91151 BAA10g01110 A10 562086 G A upstream_gene_variant MODIFIER c.-4503C>T| S32
91152 BAA10g01110 A10 562243 G A upstream_gene_variant MODIFIER c.-4660C>T| S33
91153 BAA10g01140 A10 564577 G A synonymous_variant LOW c.561C>T|p.Asp187Asp S48
91154 BAA10g01130 A10 565476 C T upstream_gene_variant MODIFIER c.-4007G>A| S8
91155 BAA10g01140 A10 566603 G A upstream_gene_variant MODIFIER c.-526C>T| S256
91156 BAA10g01140 A10 569855 C T upstream_gene_variant MODIFIER c.-3778G>A| S165
S274
91157 BAA10g01140 A10 570063 C T upstream_gene_variant MODIFIER c.-3986G>A| S88
91158 BAA10g01140 A10 570790 G A upstream_gene_variant MODIFIER c.-4713C>T| S215
91159 BAA10g01140-BAA10g01150 A10 571511 C T intergenic_region MODIFIER n.571511C>T| S123
91160 BAA10g01140-BAA10g01150 A10 573452 C T intergenic_region MODIFIER n.573452C>T| S247
91161 BAA10g01140-BAA10g01150 A10 575086 C T intergenic_region MODIFIER n.575086C>T| S272
91162 BAA10g01140-BAA10g01150 A10 576882 G A intergenic_region MODIFIER n.576882G>A| S267
91163 BAA10g01150 A10 578603 C T downstream_gene_variant MODIFIER c.*3973G>A| S142
91164 BAA10g01150 A10 579350 G A downstream_gene_variant MODIFIER c.*3226C>T| S161
91165 BAA10g01150 A10 579872 C T downstream_gene_variant MODIFIER c.*2704G>A| S149
91166 BAA10g01150 A10 580988 G A downstream_gene_variant MODIFIER c.*1588C>T| S168
91167 BAA10g01150 A10 581504 C T downstream_gene_variant MODIFIER c.*1072G>A| S169
91168 BAA10g01150 A10 581680 C T downstream_gene_variant MODIFIER c.*896G>A| S244
91169 BAA10g01150 A10 581691 G A downstream_gene_variant MODIFIER c.*885C>T| S161
91170 BAA10g01150 A10 582428 G A downstream_gene_variant MODIFIER c.*148C>T| S158
91171 BAA10g01160 A10 582816 G A downstream_gene_variant MODIFIER c.*1329C>T| S111
91172 BAA10g01150 A10 583908 G A upstream_gene_variant MODIFIER c.-59C>T| S100
91173 BAA10g01160 A10 584270 C T missense_variant MODERATE c.532G>A|p.Val178Ile S269
91174 BAA10g01150 A10 586005 C T upstream_gene_variant MODIFIER c.-2156G>A| S206
S26
91175 BAA10g01170 A10 586323 G T missense_variant MODERATE c.611C>A|p.Ala204Glu S157
S163