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
10451 BAA01g08430 A01 3725633 C T splice_region_variant&intron_variant LOW c.2932+7C>T| S36
10452 BAA01g08430 A01 3726415 G A downstream_gene_variant MODIFIER c.*542G>A| S234
10453 BAA01g08440 A01 3727232 C T stop_gained HIGH c.2190G>A|p.Trp730* S213
10454 BAA01g08440 A01 3727513 C T missense_variant MODERATE c.1909G>A|p.Glu637Lys S198
10455 BAA01g08440 A01 3727519 C T missense_variant MODERATE c.1903G>A|p.Val635Ile S139
10456 BAA01g08440 A01 3727804 G A missense_variant MODERATE c.1618C>T|p.Arg540Trp S172
S217
10457 BAA01g08440 A01 3728704 C T missense_variant MODERATE c.718G>A|p.Gly240Arg S81
S85
10458 BAA01g08430 A01 3729309 G A downstream_gene_variant MODIFIER c.*3436G>A| S224
10459 BAA01g08440 A01 3730062 T G upstream_gene_variant MODIFIER c.-368A>C| S83
S9
10460 BAA01g08440 A01 3731476 G A upstream_gene_variant MODIFIER c.-1782C>T| S161
S244
10461 BAA01g08440 A01 3733021 G A upstream_gene_variant MODIFIER c.-3327C>T| S96
10462 BAA01g08440 A01 3733248 C T upstream_gene_variant MODIFIER c.-3554G>A| S68
10463 BAA01g08440 A01 3733391 C T upstream_gene_variant MODIFIER c.-3697G>A| S65
10464 BAA01g08440 A01 3733544 G A upstream_gene_variant MODIFIER c.-3850C>T| S224
10465 BAA01g08440 A01 3734318 G A upstream_gene_variant MODIFIER c.-4624C>T| S289
S290
10466 BAA01g08450 A01 3737951 G A synonymous_variant LOW c.210G>A|p.Glu70Glu S142
10467 BAA01g08450 A01 3738962 G A missense_variant&splice_region_variant MODERATE c.802G>A|p.Asp268Asn S34
10468 BAA01g08450 A01 3740133 G A missense_variant MODERATE c.1606G>A|p.Glu536Lys S301
S304
10469 BAA01g08450 A01 3741135 C T downstream_gene_variant MODIFIER c.*45C>T| S249
10470 BAA01g08450 A01 3741257 G A downstream_gene_variant MODIFIER c.*167G>A| S153
10471 BAA01g08450 A01 3742435 C T downstream_gene_variant MODIFIER c.*1345C>T| S48
10472 BAA01g08460 A01 3744202 C T missense_variant MODERATE c.593G>A|p.Cys198Tyr S264
10473 BAA01g08460 A01 3744486 C T missense_variant MODERATE c.388G>A|p.Asp130Asn S44
10474 BAA01g08460 A01 3744984 G A synonymous_variant LOW c.246C>T|p.Pro82Pro S202
10475 BAA01g08460 A01 3745008 G A synonymous_variant LOW c.222C>T|p.Leu74Leu S69