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
166601 BAA02g12640 A02 5659296 C T missense_variant MODERATE c.2318G>A|p.Gly773Glu S299
166602 BAA02g12640 A02 5659949 G A synonymous_variant LOW c.1665C>T|p.Val555Val S17
166603 BAA02g12640 A02 5660127 G A missense_variant MODERATE c.1487C>T|p.Ser496Phe S98
166604 BAA02g12640 A02 5660458 G A missense_variant MODERATE c.1156C>T|p.Leu386Phe S156
166605 BAA02g12640 A02 5660947 G A intron_variant MODIFIER c.775-25C>T| S51
166606 BAA02g12640 A02 5662456 G A upstream_gene_variant MODIFIER c.-403C>T| S173
166607 BAA02g12640 A02 5662469 G A upstream_gene_variant MODIFIER c.-416C>T| S27
166608 BAA02g12640 A02 5662479 G A upstream_gene_variant MODIFIER c.-426C>T| S113
166609 BAA02g12640 A02 5662698 G A upstream_gene_variant MODIFIER c.-645C>T| S45
166610 BAA02g12640 A02 5663006 C T upstream_gene_variant MODIFIER c.-953G>A| S100
166611 BAA02g12640 A02 5663113 G A upstream_gene_variant MODIFIER c.-1060C>T| S202
166612 BAA02g12640 A02 5663774 G A upstream_gene_variant MODIFIER c.-1721C>T| S299
166613 BAA02g12640 A02 5664070 C T upstream_gene_variant MODIFIER c.-2017G>A| S167
166614 BAA02g12640 A02 5664229 C T upstream_gene_variant MODIFIER c.-2176G>A| S9
166615 BAA02g12640 A02 5664284 G A upstream_gene_variant MODIFIER c.-2231C>T| S198
166616 BAA02g12640 A02 5664302 G A upstream_gene_variant MODIFIER c.-2249C>T| S203
166617 BAA02g12640 A02 5664456 G A upstream_gene_variant MODIFIER c.-2403C>T| S295
166618 BAA02g12640 A02 5664941 G A upstream_gene_variant MODIFIER c.-2888C>T| S297
166619 BAA02g12640 A02 5665746 G A upstream_gene_variant MODIFIER c.-3693C>T| S303
166620 BAA02g12650 A02 5670656 C T downstream_gene_variant MODIFIER c.*337G>A| S267
166621 BAA02g12650 A02 5671127 G A missense_variant MODERATE c.1240C>T|p.Pro414Ser S67
166622 BAA02g12650 A02 5671348 G A missense_variant MODERATE c.1019C>T|p.Ser340Leu S37
166623 BAA02g12650 A02 5671353 G A synonymous_variant LOW c.1014C>T|p.Leu338Leu S67
166624 BAA02g12650 A02 5671443 C T missense_variant MODERATE c.1000G>A|p.Gly334Arg S175
166625 BAA02g12650 A02 5672671 G A intron_variant MODIFIER c.73+15C>T| S35