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
24501 BAA01g17770 A01 8627585 C T missense_variant MODERATE c.236C>T|p.Ser79Phe S146
24502 BAA01g17770 A01 8628316 G A missense_variant MODERATE c.967G>A|p.Gly323Arg S275
24503 BAA01g17770 A01 8628572 G C missense_variant MODERATE c.1223G>C|p.Ser408Thr S262
24504 BAA01g17760 A01 8629359 G A downstream_gene_variant MODIFIER c.*4544G>A| S217
24505 BAA01g17770 A01 8630623 G A intron_variant MODIFIER c.1293+1981G>A| S129
24506 BAA01g17770 A01 8630805 C T intron_variant MODIFIER c.1293+2163C>T| S247
24507 BAA01g17770 A01 8631462 A T intron_variant MODIFIER c.1293+2820A>T| S149
24508 BAA01g17770 A01 8631525 G A intron_variant MODIFIER c.1293+2883G>A| S212
24509 BAA01g17770 A01 8631709 C T intron_variant MODIFIER c.1293+3067C>T| S177
24510 BAA01g17770 A01 8633448 C T intron_variant MODIFIER c.1293+4806C>T| S113
24511 BAA01g17770 A01 8633924 C T intron_variant MODIFIER c.1293+5282C>T| S44
24512 BAA01g17770 A01 8634300 G A intron_variant MODIFIER c.1293+5658G>A| S40
S49
24513 BAA01g17770 A01 8634355 C T intron_variant MODIFIER c.1293+5713C>T| S160
24514 BAA01g17770 A01 8634441 C T intron_variant MODIFIER c.1293+5799C>T| S164
24515 BAA01g17770 A01 8634551 T C intron_variant MODIFIER c.1293+5909T>C| S43
24516 BAA01g17770 A01 8634699 C T intron_variant MODIFIER c.1293+6057C>T| S247
24517 BAA01g17770 A01 8637618 C T intron_variant MODIFIER c.1294-7680C>T| S158
24518 BAA01g17770 A01 8640034 C T intron_variant MODIFIER c.1294-5264C>T| S36
24519 BAA01g17770 A01 8640102 C T intron_variant MODIFIER c.1294-5196C>T| S62
24520 BAA01g17770 A01 8640106 C T intron_variant MODIFIER c.1294-5192C>T| S20
24521 BAA01g17780 A01 8641584 C T downstream_gene_variant MODIFIER c.*4227G>A| S99
24522 BAA01g17780 A01 8642483 C T downstream_gene_variant MODIFIER c.*3328G>A| S146
24523 BAA01g17780 A01 8643210 C T downstream_gene_variant MODIFIER c.*2601G>A| S70
24524 BAA01g17780 A01 8643561 C T downstream_gene_variant MODIFIER c.*2250G>A| S284
24525 BAA01g17780 A01 8644011 C T downstream_gene_variant MODIFIER c.*1800G>A| S47