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
39551 BAA01g25310 A01 13650871 C T synonymous_variant LOW c.630C>T|p.Ile210Ile S200
39552 BAA01g25300 A01 13651342 C T upstream_gene_variant MODIFIER c.-3045G>A| S303
39553 BAA01g25300 A01 13651475 G A upstream_gene_variant MODIFIER c.-3178C>T| S175
39554 BAA01g25320 A01 13661746 C T upstream_gene_variant MODIFIER c.-2982C>T| S150
39555 BAA01g25320 A01 13663716 C T upstream_gene_variant MODIFIER c.-1012C>T| S10
39556 BAA01g25330 A01 13664794 C T downstream_gene_variant MODIFIER c.*4597G>A| S142
39557 BAA01g25320 A01 13665085 G A missense_variant MODERATE c.106G>A|p.Ala36Thr S70
39558 BAA01g25320 A01 13665273 C T synonymous_variant LOW c.294C>T|p.Pro98Pro S210
39559 BAA01g25320 A01 13665898 G A splice_donor_variant&intron_variant HIGH c.918+1G>A| S292
39560 BAA01g25320 A01 13666525 G A missense_variant MODERATE c.1438G>A|p.Glu480Lys S144
39561 BAA01g25320 A01 13666684 C T missense_variant MODERATE c.1511C>T|p.Ser504Phe S104
S52
39562 BAA01g25320 A01 13667672 G A splice_donor_variant&intron_variant HIGH c.2342+1G>A| S144
39563 BAA01g25320 A01 13668327 C T missense_variant MODERATE c.2789C>T|p.Pro930Leu S167
39564 BAA01g25320 A01 13669059 C T downstream_gene_variant MODIFIER c.*455C>T| S38
39565 BAA01g25320 A01 13669227 C T downstream_gene_variant MODIFIER c.*623C>T| S182
39566 BAA01g25320 A01 13669235 C T downstream_gene_variant MODIFIER c.*631C>T| S69
39567 BAA01g25330 A01 13669632 G A missense_variant MODERATE c.2048C>T|p.Pro683Leu S172
S217
39568 BAA01g25330 A01 13669736 C T synonymous_variant LOW c.1944G>A|p.Lys648Lys S150
39569 BAA01g25330 A01 13669773 C T missense_variant MODERATE c.1907G>A|p.Gly636Glu S202
S69
39570 BAA01g25330 A01 13670892 C T missense_variant MODERATE c.1244G>A|p.Gly415Glu S20
39571 BAA01g25330 A01 13670921 G A synonymous_variant LOW c.1215C>T|p.Tyr405Tyr S94
39572 BAA01g25330 A01 13671636 C T missense_variant MODERATE c.688G>A|p.Glu230Lys S153
39573 BAA01g25330 A01 13671900 C T missense_variant MODERATE c.424G>A|p.Glu142Lys S183
39574 BAA01g25330 A01 13671926 C T missense_variant MODERATE c.398G>A|p.Arg133Lys S198
39575 BAA01g25330 A01 13672051 C T stop_gained HIGH c.273G>A|p.Trp91* S160