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
74751 BAA01g39370-BAA01g39380 A01 26166847 G A intergenic_region MODIFIER n.26166847G>A| S189
74752 BAA01g39370-BAA01g39380 A01 26167115 C T intergenic_region MODIFIER n.26167115C>T| S28
74753 BAA01g39380 A01 26167556 C T upstream_gene_variant MODIFIER c.-4701C>T| S150
74754 BAA01g39380 A01 26168864 G A upstream_gene_variant MODIFIER c.-3393G>A| S283
74755 BAA01g39380 A01 26169250 G A upstream_gene_variant MODIFIER c.-3007G>A| S197
74756 BAA01g39380 A01 26170340 G A upstream_gene_variant MODIFIER c.-1917G>A| S80
74757 BAA01g39380 A01 26172197 C T upstream_gene_variant MODIFIER c.-60C>T| S302
74758 BAA01g39380 A01 26172316 G A synonymous_variant LOW c.60G>A|p.Leu20Leu S108
74759 BAA01g39380 A01 26172777 G A downstream_gene_variant MODIFIER c.*213G>A| S296
74760 BAA01g39390 A01 26173357 C T missense_variant MODERATE c.866G>A|p.Arg289Gln S73
S91
74761 BAA01g39390 A01 26174185 G A synonymous_variant LOW c.474C>T|p.Thr158Thr S173
74762 BAA01g39390 A01 26174238 C T missense_variant MODERATE c.421G>A|p.Val141Met S192
74763 BAA01g39400 A01 26175949 C T missense_variant MODERATE c.949G>A|p.Ala317Thr S107
74764 BAA01g39390 A01 26176178 G A upstream_gene_variant MODIFIER c.-1125C>T| S25
74765 BAA01g39400 A01 26177066 C T splice_region_variant&intron_variant LOW c.388-8G>A| S277
74766 BAA01g39400 A01 26177180 G A synonymous_variant LOW c.354C>T|p.Ser118Ser S276
74767 BAA01g39400 A01 26177568 G A missense_variant MODERATE c.215C>T|p.Pro72Leu S33
74768 BAA01g39390 A01 26179061 C T upstream_gene_variant MODIFIER c.-4008G>A| S205
74769 BAA01g39410 A01 26179902 G A missense_variant MODERATE c.587G>A|p.Gly196Glu S20
74770 BAA01g39400 A01 26181182 C T upstream_gene_variant MODIFIER c.-3297G>A| S15
S2
S4
S6
74771 BAA01g39400 A01 26182620 G A upstream_gene_variant MODIFIER c.-4735C>T| S271
74772 BAA01g39400 A01 26182700 C T upstream_gene_variant MODIFIER c.-4815G>A| S198
74773 BAA01g39430 A01 26183545 G A missense_variant MODERATE c.955C>T|p.Leu319Phe S224
74774 BAA01g39430 A01 26183650 C T missense_variant MODERATE c.850G>A|p.Val284Ile S153
74775 BAA01g39420 A01 26187059 G A upstream_gene_variant MODIFIER c.-4826C>T| S5