Num | GeneID | Chromosome | Position | Ref.allele | Alt.allele | Mutant type | Impacts | Amino acid change | SampleID |
---|---|---|---|---|---|---|---|---|---|
1 | BAA10g33840 | A10 | 23977359 | C | T | missense_variant | MODERATE | c.203C>T|p.Ala68Val |
S262 |
2 | BAA10g33840 | A10 | 23977460 | C | T | missense_variant | MODERATE | c.304C>T|p.Arg102Cys |
S150 |
3 | BAA10g33840 | A10 | 23979701 | G | A | downstream_gene_variant | MODIFIER | c.*2221G>A| |
S43 |