| Num | GeneID | Chromosome | Position | Ref.allele | Alt.allele | Mutant type | Impacts | Amino acid change | SampleID |
|---|---|---|---|---|---|---|---|---|---|
| 1 | BAA10g00900 | A10 | 416762 | C | T | upstream_gene_variant | MODIFIER | c.-3166C>T| |
S37 |
| 2 | BAA10g00900 | A10 | 418900 | C | T | upstream_gene_variant | MODIFIER | c.-1028C>T| |
S286 |
| 3 | BAA10g00900 | A10 | 419619 | C | T | upstream_gene_variant | MODIFIER | c.-309C>T| |
S165 |
| 4 | BAA10g00900 | A10 | 420027 | C | T | missense_variant | MODERATE | c.100C>T|p.His34Tyr |
S12 |