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
33451 BAA01g22790 A01 11533258 T A downstream_gene_variant MODIFIER c.*2056A>T| S135
33452 BAA01g22790 A01 11533302 T A downstream_gene_variant MODIFIER c.*2012A>T| S195
33453 BAA01g22790 A01 11533983 G A downstream_gene_variant MODIFIER c.*1331C>T| S28
33454 BAA01g22790 A01 11535352 G A missense_variant MODERATE c.427C>T|p.Pro143Ser S287
33455 BAA01g22790 A01 11536580 G A upstream_gene_variant MODIFIER c.-802C>T| S274
33456 BAA01g22790 A01 11537055 G A upstream_gene_variant MODIFIER c.-1277C>T| S105
S106
33457 BAA01g22790 A01 11537383 C T upstream_gene_variant MODIFIER c.-1605G>A| S247
33458 BAA01g22790 A01 11537729 C T upstream_gene_variant MODIFIER c.-1951G>A| S297
33459 BAA01g22790 A01 11538745 C T upstream_gene_variant MODIFIER c.-2967G>A| S43
33460 BAA01g22790 A01 11538992 C T upstream_gene_variant MODIFIER c.-3214G>A| S261
33461 BAA01g22790 A01 11539241 C T upstream_gene_variant MODIFIER c.-3463G>A| S159
S243
33462 BAA01g22790 A01 11539829 G A upstream_gene_variant MODIFIER c.-4051C>T| S94
33463 BAA01g22790 A01 11540021 C T upstream_gene_variant MODIFIER c.-4243G>A| S184
33464 BAA01g22800 A01 11540689 C T missense_variant MODERATE c.919G>A|p.Asp307Asn S169
S173
33465 BAA01g22800 A01 11540998 C T missense_variant MODERATE c.610G>A|p.Asp204Asn S8
33466 BAA01g22800 A01 11543026 G A upstream_gene_variant MODIFIER c.-1419C>T| S244
33467 BAA01g22800 A01 11543065 G A upstream_gene_variant MODIFIER c.-1458C>T| S163
33468 BAA01g22800-BAA01g22810 A01 11546902 C T intergenic_region MODIFIER n.11546902C>T| S47
33469 BAA01g22810 A01 11547742 C T downstream_gene_variant MODIFIER c.*4201G>A| S44
33470 BAA01g22810 A01 11551476 G A downstream_gene_variant MODIFIER c.*467C>T| S14
33471 BAA01g22810 A01 11552240 G A missense_variant MODERATE c.1244C>T|p.Pro415Leu S281
33472 BAA01g22810 A01 11552534 C T synonymous_variant LOW c.1032G>A|p.Glu344Glu S11
33473 BAA01g22810 A01 11553254 G A intron_variant MODIFIER c.526-12C>T| S209
33474 BAA01g22810 A01 11555302 C T intron_variant MODIFIER c.525+333G>A| S182
33475 BAA01g22810 A01 11555496 G A intron_variant MODIFIER c.525+139C>T| S262