Num | GeneID | Chromosome | Position | Ref.allele | Alt.allele | Mutant type | Impacts | Amino acid change | SampleID |
---|---|---|---|---|---|---|---|---|---|
1 | BAA02g27860 | A02 | 15692384 | C | T | missense_variant | MODERATE | c.985G>A|p.Gly329Arg |
S139 |
2 | BAA02g27860 | A02 | 15693510 | G | A | missense_variant | MODERATE | c.392C>T|p.Ala131Val |
S293 |
3 | BAA02g27860 | A02 | 15698554 | C | T | upstream_gene_variant | MODIFIER | c.-4451G>A| |
S301 S304 |