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
155701 BAA02g03790 A02 1668866 G A upstream_gene_variant MODIFIER c.-758G>A| S266
155702 BAA02g03780 A02 1670338 G A downstream_gene_variant MODIFIER c.*1975G>A| S235
155703 BAA02g03780 A02 1670685 C T downstream_gene_variant MODIFIER c.*2322C>T| S212
155704 BAA02g03780 A02 1670715 G A downstream_gene_variant MODIFIER c.*2352G>A| S158
155705 BAA02g03780 A02 1670970 G A downstream_gene_variant MODIFIER c.*2607G>A| S162
155706 BAA02g03780 A02 1671033 G A downstream_gene_variant MODIFIER c.*2670G>A| S263
155707 BAA02g03790 A02 1671267 G A synonymous_variant LOW c.549G>A|p.Lys183Lys S139
155708 BAA02g03800 A02 1674198 C T missense_variant MODERATE c.901G>A|p.Asp301Asn S19
155709 BAA02g03800 A02 1675075 G A missense_variant MODERATE c.518C>T|p.Ser173Phe S177
155710 BAA02g03800 A02 1676780 G A upstream_gene_variant MODIFIER c.-1188C>T| S125
155711 BAA02g03810 A02 1677326 G A synonymous_variant LOW c.9G>A|p.Thr3Thr S132
S137
S215
155712 BAA02g03820 A02 1678599 C T synonymous_variant LOW c.1689G>A|p.Arg563Arg S267
155713 BAA02g03820 A02 1678940 G T missense_variant MODERATE c.1455C>A|p.Asp485Glu S26
155714 BAA02g03800 A02 1679095 C T upstream_gene_variant MODIFIER c.-3503G>A| S179
155715 BAA02g03820 A02 1679230 G A missense_variant MODERATE c.1267C>T|p.Arg423Cys S282
155716 BAA02g03820 A02 1679343 G A missense_variant MODERATE c.1244C>T|p.Thr415Ile S53
155717 BAA02g03820 A02 1679532 C T missense_variant MODERATE c.1174G>A|p.Gly392Ser S188
155718 BAA02g03800 A02 1679997 C T upstream_gene_variant MODIFIER c.-4405G>A| S178
155719 BAA02g03820 A02 1680282 C T missense_variant MODERATE c.698G>A|p.Cys233Tyr S268
155720 BAA02g03810 A02 1680626 G A downstream_gene_variant MODIFIER c.*2280G>A| S261
155721 BAA02g03820 A02 1680730 C T synonymous_variant LOW c.540G>A|p.Gln180Gln S6
155722 BAA02g03820 A02 1680794 C T splice_region_variant&intron_variant LOW c.482-6G>A| S272
155723 BAA02g03820 A02 1681540 G A upstream_gene_variant MODIFIER c.-66C>T| S42
155724 BAA02g03820 A02 1681934 T C upstream_gene_variant MODIFIER c.-460A>G| S290
155725 BAA02g03820 A02 1685483 C T upstream_gene_variant MODIFIER c.-4009G>A| S111