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
88751 BAA01g47360 A01 31567344 G A upstream_gene_variant MODIFIER c.-2331G>A| S230
88752 BAA01g47350 A01 31567642 G A synonymous_variant LOW c.180C>T|p.Leu60Leu S133
88753 BAA01g47360 A01 31570185 G A missense_variant MODERATE c.382G>A|p.Asp128Asn S159
88754 BAA01g47360 A01 31570594 G A missense_variant MODERATE c.791G>A|p.Gly264Glu S54
88755 BAA01g47360 A01 31570728 C T missense_variant MODERATE c.925C>T|p.His309Tyr S103
88756 BAA01g47360 A01 31570995 G A missense_variant MODERATE c.1072G>A|p.Asp358Asn S126
88757 BAA01g47350 A01 31572216 G A upstream_gene_variant MODIFIER c.-4085C>T| S128
88758 BAA01g47350 A01 31572298 C T upstream_gene_variant MODIFIER c.-4167G>A| S190
88759 BAA01g47350 A01 31572398 C T upstream_gene_variant MODIFIER c.-4267G>A| S228
88760 BAA01g47350 A01 31572638 G A upstream_gene_variant MODIFIER c.-4507C>T| S79
S84
88761 BAA01g47370 A01 31579173 C T missense_variant MODERATE c.326C>T|p.Ser109Phe S20
88762 BAA01g47370 A01 31579635 G A missense_variant MODERATE c.673G>A|p.Gly225Arg S176
88763 BAA01g47370 A01 31579917 C T missense_variant MODERATE c.863C>T|p.Ala288Val S149
88764 BAA01g47370 A01 31580341 G A synonymous_variant LOW c.1287G>A|p.Lys429Lys S270
88765 BAA01g47370 A01 31580642 G A missense_variant MODERATE c.1588G>A|p.Glu530Lys S277
88766 BAA01g47390 A01 31582201 C T synonymous_variant LOW c.351C>T|p.Ile117Ile S283
88767 BAA01g47380 A01 31582671 G A upstream_gene_variant MODIFIER c.-1284C>T| S277
88768 BAA01g47380 A01 31583670 G A upstream_gene_variant MODIFIER c.-2283C>T| S271
88769 BAA01g47380 A01 31584437 C T upstream_gene_variant MODIFIER c.-3050G>A| S106
88770 BAA01g47380 A01 31584762 C T upstream_gene_variant MODIFIER c.-3375G>A| S74
88771 BAA01g47380 A01 31584972 G A upstream_gene_variant MODIFIER c.-3585C>T| S69
88772 BAA01g47380 A01 31585001 C T upstream_gene_variant MODIFIER c.-3614G>A| S152
88773 BAA01g47380 A01 31585963 G A upstream_gene_variant MODIFIER c.-4576C>T| S205
88774 BAA01g47400 A01 31586849 G A upstream_gene_variant MODIFIER c.-3399G>A| S52
88775 BAA01g47400 A01 31586852 G A upstream_gene_variant MODIFIER c.-3396G>A| S167
S270