| Num | GeneID | Chromosome | Position | Ref.allele | Alt.allele | Mutant type | Impacts | Amino acid change | SampleID |
|---|---|---|---|---|---|---|---|---|---|
| 1 | BAA10g00300 | A10 | 134891 | G | A | splice_region_variant&intron_variant | LOW | c.778-7C>T| |
S245 |
| 2 | BAA10g00300 | A10 | 135612 | C | T | splice_region_variant&intron_variant | LOW | c.457+5G>A| |
S187 |
| 3 | BAA10g00300 | A10 | 136141 | C | T | missense_variant | MODERATE | c.94G>A|p.Ala32Thr |
S206 S26 |
| 4 | BAA10g00300 | A10 | 139096 | C | T | upstream_gene_variant | MODIFIER | c.-2627G>A| |
S282 |