Num | GeneID | Chromosome | Position | Ref.allele | Alt.allele | Mutant type | Impacts | Amino acid change | SampleID |
---|---|---|---|---|---|---|---|---|---|
1 | BAA02g24170 | A02 | 13173973 | C | T | missense_variant | MODERATE | c.29C>T|p.Thr10Ile |
S296 |
2 | BAA02g24170 | A02 | 13174088 | C | T | synonymous_variant | LOW | c.144C>T|p.Pro48Pro |
S221 |
3 | BAA02g24170 | A02 | 13174091 | C | T | synonymous_variant | LOW | c.147C>T|p.Asn49Asn |
S80 |
4 | BAA02g24170 | A02 | 13175194 | C | T | synonymous_variant | LOW | c.904C>T|p.Leu302Leu |
S119 |