Num | GeneID | Chromosome | Position | Ref.allele | Alt.allele | Mutant type | Impacts | Amino acid change | SampleID |
---|---|---|---|---|---|---|---|---|---|
1 | BAA02g38950 | A02 | 33197635 | G | A | upstream_gene_variant | MODIFIER | c.-1106G>A| |
S280 |
2 | BAA02g38950 | A02 | 33199536 | G | A | synonymous_variant | LOW | c.510G>A|p.Gly170Gly |
S176 |
3 | BAA02g38950 | A02 | 33200548 | C | T | missense_variant | MODERATE | c.1309C>T|p.Pro437Ser |
S260 |