Users can query the SNP information according to the gene ID.


Gene ID

Results: 1 - 13 of 13 records


Num GeneID Chromosome Position Ref.allele Alt.allele Mutant type Impacts Amino acid change SampleID
1 BAA03g02940 A03 1282858 C T upstream_gene_variant MODIFIER c.-4777C>T| S263
2 BAA03g02940 A03 1283142 C T upstream_gene_variant MODIFIER c.-4493C>T| S179
3 BAA03g02940 A03 1283163 C T upstream_gene_variant MODIFIER c.-4472C>T| S265
4 BAA03g02940 A03 1287783 G A stop_gained HIGH c.149G>A|p.Trp50* S41
5 BAA03g02940 A03 1287853 C T synonymous_variant LOW c.219C>T|p.Val73Val S74
6 BAA03g02940 A03 1288151 C T missense_variant MODERATE c.517C>T|p.Leu173Phe S83
S88
7 BAA03g02940 A03 1288565 G A missense_variant MODERATE c.577G>A|p.Gly193Arg S17
8 BAA03g02940 A03 1288844 G A missense_variant MODERATE c.856G>A|p.Glu286Lys S39
9 BAA03g02940 A03 1288918 G A synonymous_variant LOW c.930G>A|p.Gln310Gln S115
10 BAA03g02940 A03 1292929 C T downstream_gene_variant MODIFIER c.*3897C>T| S252
11 BAA03g02940 A03 1292980 G A downstream_gene_variant MODIFIER c.*3948G>A| S54
12 BAA03g02940 A03 1293379 G A downstream_gene_variant MODIFIER c.*4347G>A| S119
13 BAA03g02940 A03 1293974 C T downstream_gene_variant MODIFIER c.*4942C>T| S33