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
101751 BAA10g07300 A10 4149827 C T downstream_gene_variant MODIFIER c.*2593C>T| S60
101752 BAA10g07300 A10 4150285 C T downstream_gene_variant MODIFIER c.*3051C>T| S282
101753 BAA10g07300 A10 4150342 C T downstream_gene_variant MODIFIER c.*3108C>T| S84
S93
101754 BAA10g07300 A10 4150987 C T downstream_gene_variant MODIFIER c.*3753C>T| S206
S26
101755 BAA10g07300 A10 4151186 C T downstream_gene_variant MODIFIER c.*3952C>T| S235
101756 BAA10g07300 A10 4151380 G A downstream_gene_variant MODIFIER c.*4146G>A| S186
101757 BAA10g07300 A10 4151781 G A downstream_gene_variant MODIFIER c.*4547G>A| S302
101758 BAA10g07300-BAA10g07310 A10 4152645 G A intergenic_region MODIFIER n.4152645G>A| S207
101759 BAA10g07310 A10 4159787 G A synonymous_variant LOW c.384C>T|p.His128His S85
101760 BAA10g07310 A10 4159797 C T missense_variant MODERATE c.374G>A|p.Gly125Glu S88
101761 BAA10g07310 A10 4160324 C T upstream_gene_variant MODIFIER c.-80G>A| S225
S73
101762 BAA10g07310 A10 4160381 G A upstream_gene_variant MODIFIER c.-137C>T| S43
101763 BAA10g07310 A10 4160491 G A upstream_gene_variant MODIFIER c.-247C>T| S165
101764 BAA10g07310 A10 4160769 C T upstream_gene_variant MODIFIER c.-525G>A| S139
101765 BAA10g07310 A10 4161230 C T upstream_gene_variant MODIFIER c.-986G>A| S242
101766 BAA10g07310 A10 4161902 G A upstream_gene_variant MODIFIER c.-1658C>T| S45
101767 BAA10g07320 A10 4167163 G A downstream_gene_variant MODIFIER c.*1827C>T| S283
101768 BAA10g07320 A10 4167848 G A downstream_gene_variant MODIFIER c.*1142C>T| S267
S32
101769 BAA10g07320 A10 4168595 C T downstream_gene_variant MODIFIER c.*395G>A| S155
S211
101770 BAA10g07320 A10 4168881 C T downstream_gene_variant MODIFIER c.*109G>A| S84
S93
101771 BAA10g07320 A10 4169026 G A synonymous_variant LOW c.1518C>T|p.Leu506Leu S43
101772 BAA10g07320 A10 4169061 G A synonymous_variant LOW c.1483C>T|p.Leu495Leu S103
101773 BAA10g07320 A10 4169681 C T synonymous_variant LOW c.1164G>A|p.Gln388Gln S122
101774 BAA10g07320 A10 4169691 G A missense_variant MODERATE c.1154C>T|p.Pro385Leu S17
101775 BAA10g07320 A10 4169816 C T synonymous_variant LOW c.1029G>A|p.Leu343Leu S238