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
76751 BAA01g40560 A01 26863314 G A downstream_gene_variant MODIFIER c.*185C>T| S208
S219
76752 BAA01g40570 A01 26863577 G A downstream_gene_variant MODIFIER c.*2659C>T| S189
76753 BAA01g40560 A01 26865087 C T upstream_gene_variant MODIFIER c.-466G>A| S305
76754 BAA01g40560 A01 26865809 C T upstream_gene_variant MODIFIER c.-1188G>A| S159
S243
76755 BAA01g40560 A01 26866187 G A upstream_gene_variant MODIFIER c.-1566C>T| S207
76756 BAA01g40570 A01 26866355 C T missense_variant MODERATE c.955G>A|p.Val319Met S17
76757 BAA01g40560 A01 26867559 C T upstream_gene_variant MODIFIER c.-2938G>A| S130
76758 BAA01g40560 A01 26869009 G A upstream_gene_variant MODIFIER c.-4388C>T| S185
76759 BAA01g40570 A01 26871203 G A upstream_gene_variant MODIFIER c.-2365C>T| S280
76760 BAA01g40570 A01 26871718 C T upstream_gene_variant MODIFIER c.-2880G>A| S203
76761 BAA01g40570 A01 26871982 C T upstream_gene_variant MODIFIER c.-3144G>A| S289
S290
76762 BAA01g40570 A01 26872445 C T upstream_gene_variant MODIFIER c.-3607G>A| S115
76763 BAA01g40570-BAA01g40580 A01 26875375 C T intergenic_region MODIFIER n.26875375C>T| S192
76764 BAA01g40580 A01 26875836 T C downstream_gene_variant MODIFIER c.*4985A>G| S19
S305
76765 BAA01g40580 A01 26875837 C T downstream_gene_variant MODIFIER c.*4984G>A| S94
76766 BAA01g40580 A01 26875871 G A downstream_gene_variant MODIFIER c.*4950C>T| S58
76767 BAA01g40580 A01 26876186 C T downstream_gene_variant MODIFIER c.*4635G>A| S12
76768 BAA01g40580 A01 26876802 C T downstream_gene_variant MODIFIER c.*4019G>A| S251
76769 BAA01g40580 A01 26877113 G A downstream_gene_variant MODIFIER c.*3708C>T| S241
76770 BAA01g40580 A01 26877199 C T downstream_gene_variant MODIFIER c.*3622G>A| S118
76771 BAA01g40580 A01 26877775 C T downstream_gene_variant MODIFIER c.*3046G>A| S267
76772 BAA01g40580 A01 26878031 C T downstream_gene_variant MODIFIER c.*2790G>A| S292
76773 BAA01g40580 A01 26878617 T A downstream_gene_variant MODIFIER c.*2204A>T| S206
S26
76774 BAA01g40580 A01 26878678 C T downstream_gene_variant MODIFIER c.*2143G>A| S20
76775 BAA01g40580 A01 26879155 C T downstream_gene_variant MODIFIER c.*1666G>A| S32