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
159051 BAA02g06530 A02 2780985 C T synonymous_variant LOW c.126C>T|p.Thr42Thr S263
159052 BAA02g06530 A02 2781562 G A missense_variant MODERATE c.703G>A|p.Glu235Lys S283
159053 BAA02g06530 A02 2781640 C T missense_variant MODERATE c.781C>T|p.Arg261Cys S289
S290
159054 BAA02g06540 A02 2782540 C T synonymous_variant LOW c.2454G>A|p.Glu818Glu S183
S198
159055 BAA02g06540 A02 2783059 G A synonymous_variant LOW c.1935C>T|p.His645His S132
S137
S215
159056 BAA02g06540 A02 2783194 C T synonymous_variant LOW c.1800G>A|p.Gln600Gln S250
159057 BAA02g06540 A02 2784678 C T synonymous_variant LOW c.570G>A|p.Glu190Glu S183
S198
159058 BAA02g06540 A02 2785002 C T synonymous_variant LOW c.246G>A|p.Glu82Glu S46
159059 BAA02g06540 A02 2785712 G A upstream_gene_variant MODIFIER c.-157C>T| S136
159060 BAA02g06540 A02 2786886 G A upstream_gene_variant MODIFIER c.-1331C>T| S296
159061 BAA02g06540 A02 2789281 C T upstream_gene_variant MODIFIER c.-3726G>A| S270
159062 BAA02g06550 A02 2792638 C T upstream_gene_variant MODIFIER c.-680C>T| S277
159063 BAA02g06550 A02 2792756 G A upstream_gene_variant MODIFIER c.-562G>A| S189
159064 BAA02g06550 A02 2793442 G A missense_variant MODERATE c.125G>A|p.Gly42Glu S264
159065 BAA02g06550 A02 2793459 G A missense_variant MODERATE c.142G>A|p.Glu48Lys S269
159066 BAA02g06560 A02 2794105 C T upstream_gene_variant MODIFIER c.-746C>T| S124
159067 BAA02g06560 A02 2796735 G A missense_variant MODERATE c.1076G>A|p.Gly359Glu S207
159068 BAA02g06570 A02 2797923 G A upstream_gene_variant MODIFIER c.-3191G>A| S84
S93
159069 BAA02g06570 A02 2798548 A T upstream_gene_variant MODIFIER c.-2566A>T| S170
159070 BAA02g06570 A02 2798642 C T upstream_gene_variant MODIFIER c.-2472C>T| S257
159071 BAA02g06570 A02 2799117 C T upstream_gene_variant MODIFIER c.-1997C>T| S95
159072 BAA02g06570 A02 2800303 C T upstream_gene_variant MODIFIER c.-811C>T| S122
159073 BAA02g06570 A02 2800807 G A upstream_gene_variant MODIFIER c.-307G>A| S288
159074 BAA02g06570 A02 2801099 G A upstream_gene_variant MODIFIER c.-15G>A| S64
159075 BAA02g06570 A02 2802161 G A missense_variant MODERATE c.595G>A|p.Ala199Thr S170