Num | GeneID | Chromosome | Position | Ref.allele | Alt.allele | Mutant type | Impacts | Amino acid change | SampleID |
---|---|---|---|---|---|---|---|---|---|
1 | BAA01g40400 | A01 | 26786999 | C | T | missense_variant | MODERATE | c.313C>T|p.Pro105Ser |
S164 |
2 | BAA01g40400 | A01 | 26787093 | C | T | missense_variant | MODERATE | c.407C>T|p.Ala136Val |
S286 |
3 | BAA01g40400 | A01 | 26787475 | C | T | synonymous_variant | LOW | c.711C>T|p.Leu237Leu |
S168 |
4 | BAA01g40400 | A01 | 26788409 | C | T | missense_variant | MODERATE | c.1264C>T|p.Pro422Ser |
S164 |