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
98701 BAA10g06120 A10 3155074 G A missense_variant MODERATE c.194C>T|p.Ser65Phe S50
98702 BAA10g06100 A10 3155860 G A upstream_gene_variant MODIFIER c.-3194C>T| S16
98703 BAA10g06120-BAA10g06130 A10 3164547 G A intergenic_region MODIFIER n.3164547G>A| S295
98704 BAA10g06120-BAA10g06130 A10 3164902 G A intergenic_region MODIFIER n.3164902G>A| S75
S81
98705 BAA10g06120-BAA10g06130 A10 3165437 G A intergenic_region MODIFIER n.3165437G>A| S187
98706 BAA10g06120-BAA10g06130 A10 3167036 G A intergenic_region MODIFIER n.3167036G>A| S15
98707 BAA10g06130 A10 3167833 G A upstream_gene_variant MODIFIER c.-4978G>A| S274
98708 BAA10g06130 A10 3169408 G A upstream_gene_variant MODIFIER c.-3403G>A| S223
98709 BAA10g06130 A10 3170943 G A upstream_gene_variant MODIFIER c.-1868G>A| S138
98710 BAA10g06130 A10 3171184 C T upstream_gene_variant MODIFIER c.-1627C>T| S244
98711 BAA10g06130 A10 3171902 C T upstream_gene_variant MODIFIER c.-909C>T| S53
S81
S92
98712 BAA10g06130 A10 3172501 C T upstream_gene_variant MODIFIER c.-310C>T| S193
98713 BAA10g06130 A10 3173014 C T synonymous_variant LOW c.204C>T|p.Leu68Leu S208
S93
98714 BAA10g06130 A10 3173587 C T synonymous_variant LOW c.777C>T|p.Ala259Ala S297
98715 BAA10g06140 A10 3174252 C T downstream_gene_variant MODIFIER c.*3757G>A| S119
98716 BAA10g06140 A10 3174762 C T downstream_gene_variant MODIFIER c.*3247G>A| S170
98717 BAA10g06130 A10 3175362 G A missense_variant MODERATE c.1519G>A|p.Ala507Thr S221
98718 BAA10g06130 A10 3175755 C T downstream_gene_variant MODIFIER c.*367C>T| S287
98719 BAA10g06130 A10 3177565 G A downstream_gene_variant MODIFIER c.*2177G>A| S203
98720 BAA10g06140 A10 3178319 C T missense_variant MODERATE c.1066G>A|p.Val356Met S41
98721 BAA10g06140 A10 3179596 C T splice_acceptor_variant&intron_variant HIGH c.421-1G>A| S277
98722 BAA10g06140 A10 3179777 G A missense_variant MODERATE c.326C>T|p.Ala109Val S308
98723 BAA10g06140 A10 3180012 G A synonymous_variant LOW c.201C>T|p.Ser67Ser S125
98724 BAA10g06140 A10 3180526 G A synonymous_variant LOW c.45C>T|p.Ile15Ile S202
98725 BAA10g06140 A10 3180964 C T upstream_gene_variant MODIFIER c.-394G>A| S202