Num | GeneID | Chromosome | Position | Ref.allele | Alt.allele | Mutant type | Impacts | Amino acid change | SampleID |
---|---|---|---|---|---|---|---|---|---|
1 | BAA10g01200 | A10 | 604577 | G | A | upstream_gene_variant | MODIFIER | c.-3797G>A| |
S156 |
2 | BAA10g01200 | A10 | 609115 | G | A | missense_variant | MODERATE | c.742G>A|p.Val248Ile |
S208 S219 |
3 | BAA10g01200 | A10 | 609237 | C | T | synonymous_variant | LOW | c.864C>T|p.Asp288Asp |
S162 S299 |