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
42351 BAA01g26230 A01 14581502 C T upstream_gene_variant MODIFIER c.-3461G>A| S192
42352 BAA01g26250 A01 14582858 C T missense_variant MODERATE c.679G>A|p.Glu227Lys S184
42353 BAA01g26250 A01 14582976 C T synonymous_variant LOW c.561G>A|p.Gly187Gly S67
42354 BAA01g26260 A01 14583541 G A upstream_gene_variant MODIFIER c.-1055G>A| S278
42355 BAA01g26250 A01 14583718 G A missense_variant MODERATE c.71C>T|p.Ser24Phe S168
42356 BAA01g26250 A01 14583883 G A upstream_gene_variant MODIFIER c.-95C>T| S96
42357 BAA01g26250 A01 14584299 C T upstream_gene_variant MODIFIER c.-511G>A| S44
42358 BAA01g26250 A01 14584499 C T upstream_gene_variant MODIFIER c.-711G>A| S210
42359 BAA01g26250 A01 14584581 C T upstream_gene_variant MODIFIER c.-793G>A| S36
42360 BAA01g26250 A01 14584802 C T upstream_gene_variant MODIFIER c.-1014G>A| S19
42361 BAA01g26250 A01 14584827 G A upstream_gene_variant MODIFIER c.-1039C>T| S195
42362 BAA01g26260 A01 14585189 G A synonymous_variant LOW c.183G>A|p.Lys61Lys S123
42363 BAA01g26260 A01 14585685 C T missense_variant MODERATE c.305C>T|p.Ser102Phe S269
42364 BAA01g26260 A01 14585732 G A missense_variant MODERATE c.352G>A|p.Val118Ile S63
42365 BAA01g26260 A01 14585943 C T missense_variant MODERATE c.413C>T|p.Ser138Leu S113
S269
42366 BAA01g26250 A01 14588642 C A upstream_gene_variant MODIFIER c.-4854G>T| S15
S2
S3
S34
S4
S6
42367 BAA01g26270 A01 14588883 G A upstream_gene_variant MODIFIER c.-4017G>A| S195
42368 BAA01g26270 A01 14589566 C T upstream_gene_variant MODIFIER c.-3334C>T| S261
42369 BAA01g26270 A01 14589738 G A upstream_gene_variant MODIFIER c.-3162G>A| S187
42370 BAA01g26270 A01 14590555 G A upstream_gene_variant MODIFIER c.-2345G>A| S83
42371 BAA01g26270 A01 14591121 C T upstream_gene_variant MODIFIER c.-1779C>T| S112
42372 BAA01g26270 A01 14591725 G A upstream_gene_variant MODIFIER c.-1175G>A| S70
42373 BAA01g26270 A01 14594070 G A splice_region_variant&synonymous_variant LOW c.507G>A|p.Gly169Gly S284
42374 BAA01g26270 A01 14594587 C T intron_variant MODIFIER c.745-42C>T| S67
42375 BAA01g26270 A01 14594707 C T missense_variant MODERATE c.823C>T|p.Arg275Trp S225
S73