Num | GeneID | Chromosome | Position | Ref.allele | Alt.allele | Mutant type | Impacts | Amino acid change | SampleID |
---|---|---|---|---|---|---|---|---|---|
1 | BAA10g27150 | A10 | 21252636 | C | T | missense_variant | MODERATE | c.122G>A|p.Gly41Glu |
S5 |
2 | BAA10g27150 | A10 | 21257592 | C | T | upstream_gene_variant | MODIFIER | c.-4835G>A| |
S20 |
3 | BAA10g27150 | A10 | 21257602 | C | A | upstream_gene_variant | MODIFIER | c.-4845G>T| |
S298 |