Num | GeneID | Chromosome | Position | Ref.allele | Alt.allele | Mutant type | Impacts | Amino acid change | SampleID |
---|---|---|---|---|---|---|---|---|---|
1 | BAA09g22920 | A09 | 14462408 | C | T | missense_variant | MODERATE | c.508G>A|p.Gly170Ser |
S8 |
2 | BAA09g22920 | A09 | 14462744 | G | A | synonymous_variant | LOW | c.288C>T|p.Leu96Leu |
S4 |
3 | BAA09g22920 | A09 | 14462786 | G | A | synonymous_variant | LOW | c.246C>T|p.Leu82Leu |
S167 |
4 | BAA09g22920 | A09 | 14466980 | G | A | upstream_gene_variant | MODIFIER | c.-3949C>T| |
S167 |