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
31751 BAA01g21970 A01 10954998 G A upstream_gene_variant MODIFIER c.-1117C>T| S59
31752 BAA01g21970 A01 10956265 C T upstream_gene_variant MODIFIER c.-2384G>A| S111
31753 BAA01g21970 A01 10956801 G A upstream_gene_variant MODIFIER c.-2920C>T| S123
31754 BAA01g21970 A01 10958309 C T upstream_gene_variant MODIFIER c.-4428G>A| S167
31755 BAA01g21980 A01 10958483 G A splice_region_variant&stop_retained_variant LOW c.345G>A|p.Ter115Ter S34
31756 BAA01g21970 A01 10958591 G A upstream_gene_variant MODIFIER c.-4710C>T| S9
31757 BAA01g21990 A01 10962756 C T synonymous_variant LOW c.225C>T|p.Val75Val S286
31758 BAA01g21990 A01 10962804 C T synonymous_variant LOW c.273C>T|p.Ser91Ser S91
31759 BAA01g21990 A01 10962807 A C synonymous_variant LOW c.276A>C|p.Ser92Ser S91
31760 BAA01g21990 A01 10962816 G A synonymous_variant LOW c.285G>A|p.Ala95Ala S91
31761 BAA01g21990 A01 10962832 G A missense_variant MODERATE c.301G>A|p.Val101Ile S126
31762 BAA01g21990 A01 10962834 T C synonymous_variant LOW c.303T>C|p.Val101Val S91
31763 BAA01g21990 A01 10962837 T C synonymous_variant LOW c.306T>C|p.Leu102Leu S91
31764 BAA01g21990 A01 10962841 C T missense_variant MODERATE c.310C>T|p.His104Tyr S91
31765 BAA01g21990 A01 10962846 T C synonymous_variant LOW c.315T>C|p.Tyr105Tyr S91
31766 BAA01g21990 A01 10962857 A G missense_variant MODERATE c.326A>G|p.Asn109Ser S91
31767 BAA01g21990 A01 10962876 C A synonymous_variant LOW c.345C>A|p.Val115Val S91
31768 BAA01g21990 A01 10962888 T A synonymous_variant LOW c.357T>A|p.Val119Val S91
31769 BAA01g21990 A01 10962889 G T missense_variant MODERATE c.358G>T|p.Val120Phe S91
31770 BAA01g21990 A01 10962890 T C missense_variant MODERATE c.359T>C|p.Val120Ala S91
31771 BAA01g21990 A01 10962897 C G synonymous_variant LOW c.366C>G|p.Ser122Ser S91
31772 BAA01g21990 A01 10962905 G A missense_variant MODERATE c.374G>A|p.Gly125Asp S32
31773 BAA01g21990 A01 10962908 G A missense_variant MODERATE c.377G>A|p.Gly126Asp S91
31774 BAA01g21990 A01 10962909 C T synonymous_variant LOW c.378C>T|p.Gly126Gly S91
31775 BAA01g21990 A01 10962911 A T missense_variant MODERATE c.380A>T|p.Asp127Val S91