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
14701 BAA01g11420 A01 5287287 G A missense_variant&splice_region_variant MODERATE c.850C>T|p.Pro284Ser S37
S76
14702 BAA01g11410 A01 5287616 G A downstream_gene_variant MODIFIER c.*2496G>A| S159
S243
14703 BAA01g11420 A01 5287940 C T synonymous_variant LOW c.681G>A|p.Lys227Lys S231
14704 BAA01g11410 A01 5287988 C T downstream_gene_variant MODIFIER c.*2868C>T| S176
14705 BAA01g11420 A01 5289186 C T missense_variant MODERATE c.4G>A|p.Ala2Thr S210
14706 BAA01g11420 A01 5289274 G A upstream_gene_variant MODIFIER c.-85C>T| S226
14707 BAA01g11420 A01 5289448 A T upstream_gene_variant MODIFIER c.-259T>A| S180
14708 BAA01g11420 A01 5290812 G A upstream_gene_variant MODIFIER c.-1623C>T| S69
14709 BAA01g11420 A01 5292251 G A upstream_gene_variant MODIFIER c.-3062C>T| S8
14710 BAA01g11420 A01 5293169 C T upstream_gene_variant MODIFIER c.-3980G>A| S48
14711 BAA01g11440 A01 5295905 C T missense_variant MODERATE c.859G>A|p.Gly287Arg S61
14712 BAA01g11440 A01 5296065 G A missense_variant MODERATE c.784C>T|p.Leu262Phe S116
14713 BAA01g11440 A01 5296082 C T missense_variant MODERATE c.767G>A|p.Gly256Glu S170
14714 BAA01g11430 A01 5296900 C T downstream_gene_variant MODIFIER c.*3097C>T| S18
14715 BAA01g11430 A01 5297313 G A downstream_gene_variant MODIFIER c.*3510G>A| S205
14716 BAA01g11440 A01 5297958 C T synonymous_variant LOW c.462G>A|p.Lys154Lys S54
14717 BAA01g11430 A01 5298563 C T downstream_gene_variant MODIFIER c.*4760C>T| S19
14718 BAA01g11440 A01 5299432 G A upstream_gene_variant MODIFIER c.-509C>T| S239
14719 BAA01g11440 A01 5299793 G A upstream_gene_variant MODIFIER c.-870C>T| S149
14720 BAA01g11440 A01 5299955 C T upstream_gene_variant MODIFIER c.-1032G>A| S155
S211
14721 BAA01g11450 A01 5300897 G A missense_variant MODERATE c.1069C>T|p.Leu357Phe S138
14722 BAA01g11450 A01 5301662 G A stop_gained HIGH c.304C>T|p.Arg102* S139
14723 BAA01g11450 A01 5301687 G A synonymous_variant LOW c.279C>T|p.Ala93Ala S9
14724 BAA01g11440 A01 5303736 C T upstream_gene_variant MODIFIER c.-4813G>A| S151
14725 BAA01g11440 A01 5303781 G A upstream_gene_variant MODIFIER c.-4858C>T| S241