Num | GeneID | Chromosome | Position | Ref.allele | Alt.allele | Mutant type | Impacts | Amino acid change | SampleID |
---|---|---|---|---|---|---|---|---|---|
1 | BAA10g06050 | A10 | 3113577 | C | T | synonymous_variant | LOW | c.1539G>A|p.Thr513Thr |
S247 |
2 | BAA10g06050 | A10 | 3113753 | G | A | stop_gained | HIGH | c.1363C>T|p.Gln455* |
S216 |
3 | BAA10g06050 | A10 | 3115182 | C | T | missense_variant | MODERATE | c.308G>A|p.Arg103Gln |
S176 |