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
172751 BAA02g16470 A02 8039314 G A upstream_gene_variant MODIFIER c.-1812C>T| S276
172752 BAA02g16470 A02 8039409 G A upstream_gene_variant MODIFIER c.-1907C>T| S96
172753 BAA02g16470 A02 8040347 G A upstream_gene_variant MODIFIER c.-2845C>T| S87
172754 BAA02g16480 A02 8040469 C T missense_variant MODERATE c.3283G>A|p.Gly1095Arg S233
172755 BAA02g16480 A02 8040773 C T synonymous_variant LOW c.2979G>A|p.Arg993Arg S120
172756 BAA02g16480 A02 8040878 C T synonymous_variant LOW c.2874G>A|p.Lys958Lys S58
172757 BAA02g16480 A02 8040928 C T missense_variant MODERATE c.2824G>A|p.Glu942Lys S6
172758 BAA02g16470 A02 8041304 C T upstream_gene_variant MODIFIER c.-3802G>A| S139
172759 BAA02g16470 A02 8041417 A C upstream_gene_variant MODIFIER c.-3915T>G| S155
172760 BAA02g16470 A02 8041844 C T upstream_gene_variant MODIFIER c.-4342G>A| S244
172761 BAA02g16470 A02 8042068 G A upstream_gene_variant MODIFIER c.-4566C>T| S80
172762 BAA02g16470 A02 8042169 T A upstream_gene_variant MODIFIER c.-4667A>T| S241
172763 BAA02g16480 A02 8042583 C T intron_variant MODIFIER c.2542+664G>A| S245
172764 BAA02g16480 A02 8043749 C T synonymous_variant LOW c.2040G>A|p.Arg680Arg S50
172765 BAA02g16480 A02 8043750 C T missense_variant MODERATE c.2039G>A|p.Arg680Gln S187
172766 BAA02g16480 A02 8044601 C T missense_variant MODERATE c.1352G>A|p.Arg451Lys S78
S83
172767 BAA02g16480 A02 8045018 G A missense_variant MODERATE c.935C>T|p.Ser312Leu S74
172768 BAA02g16480 A02 8045184 C T missense_variant MODERATE c.769G>A|p.Glu257Lys S255
172769 BAA02g16480 A02 8045265 C T missense_variant MODERATE c.688G>A|p.Val230Ile S112
172770 BAA02g16480 A02 8045589 G A missense_variant MODERATE c.364C>T|p.Pro122Ser S10
172771 BAA02g16480 A02 8046627 G A upstream_gene_variant MODIFIER c.-675C>T| S190
172772 BAA02g16480 A02 8047037 C T upstream_gene_variant MODIFIER c.-1085G>A| S44
172773 BAA02g16480 A02 8048361 C T upstream_gene_variant MODIFIER c.-2409G>A| S42
172774 BAA02g16480 A02 8050754 C T upstream_gene_variant MODIFIER c.-4802G>A| S78
172775 BAA02g16490 A02 8051003 C T upstream_gene_variant MODIFIER c.-4407C>T| S139