| Num | GeneID | Chromosome | Position | Ref.allele | Alt.allele | Mutant type | Impacts | Amino acid change | SampleID |
|---|---|---|---|---|---|---|---|---|---|
| 1 | BAA10g00950 | A10 | 449240 | G | A | synonymous_variant | LOW | c.1398C>T|p.Phe466Phe |
S127 |
| 2 | BAA10g00950 | A10 | 449640 | A | C | missense_variant | MODERATE | c.1123T>G|p.Tyr375Asp |
S305 |
| 3 | BAA10g00950 | A10 | 454905 | G | A | upstream_gene_variant | MODIFIER | c.-3415C>T| |
S211 |
| 4 | BAA10g00950 | A10 | 455072 | C | T | upstream_gene_variant | MODIFIER | c.-3582G>A| |
S202 |