Num | GeneID | Chromosome | Position | Ref.allele | Alt.allele | Mutant type | Impacts | Amino acid change | SampleID |
---|---|---|---|---|---|---|---|---|---|
1 | BAA09g59130 | A09 | 57424668 | C | T | missense_variant | MODERATE | c.167C>T|p.Ala56Val |
S135 |
2 | BAA09g59130 | A09 | 57426865 | G | A | missense_variant | MODERATE | c.1169G>A|p.Gly390Glu |
S202 |
3 | BAA09g59130 | A09 | 57427715 | G | A | downstream_gene_variant | MODIFIER | c.*388G>A| |
S241 |