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
128701 BAA10g16790 A10 16444792 G A downstream_gene_variant MODIFIER c.*1498C>T| S234
128702 BAA10g16790 A10 16444904 C T downstream_gene_variant MODIFIER c.*1386G>A| S210
128703 BAA10g16790 A10 16445324 G A downstream_gene_variant MODIFIER c.*966C>T| S292
128704 BAA10g16790 A10 16445833 G A downstream_gene_variant MODIFIER c.*457C>T| S239
128705 BAA10g16790 A10 16446578 T C synonymous_variant LOW c.1593A>G|p.Arg531Arg S195
128706 BAA10g16790 A10 16446589 G A synonymous_variant LOW c.1582C>T|p.Leu528Leu S217
S248
128707 BAA10g16790 A10 16447368 G A missense_variant MODERATE c.1105C>T|p.Pro369Ser S132
S137
S89
128708 BAA10g16800 A10 16447811 G A upstream_gene_variant MODIFIER c.-4877G>A| S43
128709 BAA10g16790 A10 16448272 C T synonymous_variant LOW c.687G>A|p.Leu229Leu S210
S225
128710 BAA10g16800 A10 16449486 G A upstream_gene_variant MODIFIER c.-3202G>A| S144
128711 BAA10g16800 A10 16449492 C T upstream_gene_variant MODIFIER c.-3196C>T| S236
128712 BAA10g16790 A10 16450148 C T upstream_gene_variant MODIFIER c.-173G>A| S296
128713 BAA10g16810 A10 16455438 G A upstream_gene_variant MODIFIER c.-3888G>A| S130
128714 BAA10g16810 A10 16456471 G A upstream_gene_variant MODIFIER c.-2855G>A| S262
128715 BAA10g16810 A10 16457277 G A upstream_gene_variant MODIFIER c.-2049G>A| S138
128716 BAA10g16810 A10 16458101 G T upstream_gene_variant MODIFIER c.-1225G>T| S278
128717 BAA10g16810 A10 16458397 C T upstream_gene_variant MODIFIER c.-929C>T| S206
128718 BAA10g16810 A10 16458708 C T upstream_gene_variant MODIFIER c.-618C>T| S37
128719 BAA10g16810 A10 16459425 G A missense_variant MODERATE c.100G>A|p.Asp34Asn S280
128720 BAA10g16820 A10 16459807 G A downstream_gene_variant MODIFIER c.*1164C>T| S9
128721 BAA10g16820 A10 16460150 G A downstream_gene_variant MODIFIER c.*821C>T| S64
128722 BAA10g16810 A10 16460356 G A missense_variant MODERATE c.455G>A|p.Cys152Tyr S38
128723 BAA10g16820 A10 16461870 C T missense_variant MODERATE c.811G>A|p.Gly271Ser S133
128724 BAA10g16820 A10 16462171 G A missense_variant&splice_region_variant MODERATE c.665C>T|p.Thr222Ile S228
128725 BAA10g16820 A10 16462381 G A missense_variant MODERATE c.532C>T|p.Leu178Phe S239
S33