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
175851 BAA02g18050-BAA02g18060 A02 9078360 G A intergenic_region MODIFIER n.9078360G>A| S256
175852 BAA02g18060 A02 9080165 G A upstream_gene_variant MODIFIER c.-4708G>A| S37
175853 BAA02g18060 A02 9080987 C T upstream_gene_variant MODIFIER c.-3886C>T| S38
175854 BAA02g18060 A02 9085783 G A missense_variant MODERATE c.911G>A|p.Ser304Asn S259
175855 BAA02g18080 A02 9086561 C T upstream_gene_variant MODIFIER c.-2679C>T| S240
175856 BAA02g18070 A02 9087144 G A missense_variant MODERATE c.1766C>T|p.Ser589Phe S133
175857 BAA02g18070 A02 9087771 G A missense_variant MODERATE c.1139C>T|p.Ala380Val S4
175858 BAA02g18070 A02 9088138 C T missense_variant MODERATE c.772G>A|p.Val258Ile S186
175859 BAA02g18070 A02 9088599 G A synonymous_variant LOW c.391C>T|p.Leu131Leu S70
175860 BAA02g18080 A02 9088703 G A upstream_gene_variant MODIFIER c.-537G>A| S260
175861 BAA02g18070 A02 9088976 C T synonymous_variant LOW c.213G>A|p.Lys71Lys S196
175862 BAA02g18070 A02 9089520 C T upstream_gene_variant MODIFIER c.-332G>A| S124
175863 BAA02g18070 A02 9089733 C T upstream_gene_variant MODIFIER c.-545G>A| S233
175864 BAA02g18070 A02 9091404 G A upstream_gene_variant MODIFIER c.-2216C>T| S168
175865 BAA02g18070 A02 9093277 C T upstream_gene_variant MODIFIER c.-4089G>A| S302
175866 BAA02g18070 A02 9093672 G A upstream_gene_variant MODIFIER c.-4484C>T| S116
175867 BAA02g18090 A02 9093892 C T missense_variant MODERATE c.128C>T|p.Ser43Phe S180
175868 BAA02g18080 A02 9095310 G A downstream_gene_variant MODIFIER c.*4213G>A| S217
175869 BAA02g18080 A02 9095755 G A downstream_gene_variant MODIFIER c.*4658G>A| S297
175870 BAA02g18100 A02 9096724 C T missense_variant MODERATE c.286G>A|p.Ala96Thr S5
175871 BAA02g18100 A02 9096964 C T missense_variant MODERATE c.46G>A|p.Glu16Lys S242
175872 BAA02g18100 A02 9097908 C T upstream_gene_variant MODIFIER c.-899G>A| S262
175873 BAA02g18100 A02 9098161 G A upstream_gene_variant MODIFIER c.-1152C>T| S272
175874 BAA02g18100 A02 9098206 G A upstream_gene_variant MODIFIER c.-1197C>T| S133
175875 BAA02g18100 A02 9098207 C T upstream_gene_variant MODIFIER c.-1198G>A| S283