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
214501 BAA02g32090-BAA02g32100 A02 26484685 G A intergenic_region MODIFIER n.26484685G>A| S69
214502 BAA02g32090-BAA02g32100 A02 26484827 C T intergenic_region MODIFIER n.26484827C>T| S246
214503 BAA02g32090-BAA02g32100 A02 26485288 G A intergenic_region MODIFIER n.26485288G>A| S74
214504 BAA02g32090-BAA02g32100 A02 26485416 C T intergenic_region MODIFIER n.26485416C>T| S87
214505 BAA02g32090-BAA02g32100 A02 26485915 C A intergenic_region MODIFIER n.26485915C>A| S163
214506 BAA02g32090-BAA02g32100 A02 26486484 G A intergenic_region MODIFIER n.26486484G>A| S168
214507 BAA02g32090-BAA02g32100 A02 26486552 T A intergenic_region MODIFIER n.26486552T>A| S305
214508 BAA02g32090-BAA02g32100 A02 26486730 G A intergenic_region MODIFIER n.26486730G>A| S8
214509 BAA02g32100 A02 26497691 C T upstream_gene_variant MODIFIER c.-2134C>T| S261
214510 BAA02g32100 A02 26498786 G A upstream_gene_variant MODIFIER c.-1039G>A| S200
214511 BAA02g32100 A02 26504439 C T downstream_gene_variant MODIFIER c.*3476C>T| S182
214512 BAA02g32100 A02 26504514 C T downstream_gene_variant MODIFIER c.*3551C>T| S220
214513 BAA02g32100 A02 26504544 C T downstream_gene_variant MODIFIER c.*3581C>T| S206
214514 BAA02g32110 A02 26509048 C T upstream_gene_variant MODIFIER c.-647C>T| S167
214515 BAA02g32110 A02 26509339 C T upstream_gene_variant MODIFIER c.-356C>T| S206
214516 BAA02g32110 A02 26509363 G A upstream_gene_variant MODIFIER c.-332G>A| S256
214517 BAA02g32110 A02 26509553 G A upstream_gene_variant MODIFIER c.-142G>A| S142
214518 BAA02g32110 A02 26509871 C T synonymous_variant LOW c.177C>T|p.Ile59Ile S94
214519 BAA02g32110 A02 26510048 G A intron_variant MODIFIER c.247+107G>A| S35
214520 BAA02g32110 A02 26510306 G A splice_acceptor_variant&intron_variant HIGH c.248-1G>A| S187
214521 BAA02g32110 A02 26510307 C T missense_variant&splice_region_variant MODERATE c.248C>T|p.Ala83Val S289
S290
214522 BAA02g32110 A02 26512156 G A intron_variant MODIFIER c.374+1723G>A| S276
214523 BAA02g32110 A02 26513169 C T intron_variant MODIFIER c.375-1794C>T| S116
214524 BAA02g32110 A02 26519988 G A intron_variant MODIFIER c.626-968G>A| S56
214525 BAA02g32110 A02 26520098 G A intron_variant MODIFIER c.626-858G>A| S45