Num | GeneID | Chromosome | Position | Ref.allele | Alt.allele | Mutant type | Impacts | Amino acid change | SampleID |
---|---|---|---|---|---|---|---|---|---|
1 | BAA09g58660 | A09 | 57239447 | C | T | missense_variant | MODERATE | c.296C>T|p.Ser99Phe |
S119 |
2 | BAA09g58660 | A09 | 57239549 | C | T | missense_variant | MODERATE | c.398C>T|p.Ala133Val |
S203 |
3 | BAA09g58660 | A09 | 57239550 | C | T | synonymous_variant | LOW | c.399C>T|p.Ala133Ala |
S205 |
4 | BAA09g58660 | A09 | 57244169 | C | T | downstream_gene_variant | MODIFIER | c.*3486C>T| |
S279 |