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
52601 BAA01g28920 A01 18217689 C T upstream_gene_variant MODIFIER c.-1159C>T| S273
52602 BAA01g28920 A01 18220051 G A synonymous_variant LOW c.600G>A|p.Gln200Gln S161
S70
52603 BAA01g28920 A01 18221459 G A downstream_gene_variant MODIFIER c.*1327G>A| S100
52604 BAA01g28920 A01 18221877 C T downstream_gene_variant MODIFIER c.*1745C>T| S39
52605 BAA01g28920 A01 18222531 C T downstream_gene_variant MODIFIER c.*2399C>T| S177
52606 BAA01g28920 A01 18223080 C T downstream_gene_variant MODIFIER c.*2948C>T| S39
52607 BAA01g28920 A01 18223266 C T downstream_gene_variant MODIFIER c.*3134C>T| S256
52608 BAA01g28920 A01 18223467 G A downstream_gene_variant MODIFIER c.*3335G>A| S95
52609 BAA01g28920 A01 18223542 C T downstream_gene_variant MODIFIER c.*3410C>T| S133
52610 BAA01g28930 A01 18223941 C T missense_variant MODERATE c.1744G>A|p.Glu582Lys S157
52611 BAA01g28930 A01 18224082 C A stop_gained HIGH c.1603G>T|p.Glu535* S182
S252
S292
52612 BAA01g28930 A01 18224279 G A missense_variant MODERATE c.1406C>T|p.Ser469Leu S278
52613 BAA01g28930 A01 18225109 G A synonymous_variant LOW c.1017C>T|p.His339His S83
S88
52614 BAA01g28930 A01 18225740 C T intron_variant MODIFIER c.688-68G>A| S48
52615 BAA01g28940 A01 18227015 G A downstream_gene_variant MODIFIER c.*3949C>T| S288
52616 BAA01g28930 A01 18227185 C T missense_variant MODERATE c.245G>A|p.Ser82Asn S152
52617 BAA01g28930 A01 18227694 C T splice_acceptor_variant&intron_variant HIGH c.73-1G>A| S132
S137
S215
52618 BAA01g28930 A01 18228072 C T upstream_gene_variant MODIFIER c.-230G>A| S160
52619 BAA01g28930 A01 18228556 G A upstream_gene_variant MODIFIER c.-714C>T| S68
52620 BAA01g28930 A01 18229159 C T upstream_gene_variant MODIFIER c.-1317G>A| S88
52621 BAA01g28930 A01 18229223 G A upstream_gene_variant MODIFIER c.-1381C>T| S302
52622 BAA01g28930 A01 18229423 G A upstream_gene_variant MODIFIER c.-1581C>T| S238
52623 BAA01g28930 A01 18229769 G A upstream_gene_variant MODIFIER c.-1927C>T| S305
52624 BAA01g28930 A01 18229775 G A upstream_gene_variant MODIFIER c.-1933C>T| S265
52625 BAA01g28930 A01 18230203 C T upstream_gene_variant MODIFIER c.-2361G>A| S139