| Num | GeneID | Chromosome | Position | Ref.allele | Alt.allele | Mutant type | Impacts | Amino acid change | SampleID |
|---|---|---|---|---|---|---|---|---|---|
| 1 | BAA10g26190 | A10 | 20872511 | C | T | splice_acceptor_variant&intron_variant | HIGH | c.2221-1G>A| |
S302 |
| 2 | BAA10g26190 | A10 | 20876230 | G | A | missense_variant | MODERATE | c.118C>T|p.Leu40Phe |
S284 |
| 3 | BAA10g26190 | A10 | 20878656 | G | A | upstream_gene_variant | MODIFIER | c.-2309C>T| |
S57 |