Num | GeneID | Chromosome | Position | Ref.allele | Alt.allele | Mutant type | Impacts | Amino acid change | SampleID |
---|---|---|---|---|---|---|---|---|---|
1 | BAA10g29130 | A10 | 22038639 | C | T | missense_variant | MODERATE | c.152C>T|p.Ser51Leu |
S2 |
2 | BAA10g29130 | A10 | 22039234 | C | T | synonymous_variant | LOW | c.747C>T|p.Val249Val |
S262 |
3 | BAA10g29130 | A10 | 22045571 | G | A | downstream_gene_variant | MODIFIER | c.*4994G>A| |
S256 |