| Num | GeneID | Chromosome | Position | Ref.allele | Alt.allele | Mutant type | Impacts | Amino acid change | SampleID |
|---|---|---|---|---|---|---|---|---|---|
| 1 | BAA10g01700 | A10 | 817619 | G | T | missense_variant | MODERATE | c.494G>T|p.Gly165Val |
S184 |
| 2 | BAA10g01700 | A10 | 818974 | C | T | missense_variant | MODERATE | c.1628C>T|p.Ser543Phe |
S110 |
| 3 | BAA10g01700 | A10 | 819300 | C | T | missense_variant | MODERATE | c.1879C>T|p.Leu627Phe |
S34 |
| 4 | BAA10g01700 | A10 | 819515 | G | A | missense_variant | MODERATE | c.2021G>A|p.Arg674Lys |
S217 S248 |
| 5 | BAA10g01700 | A10 | 824770 | C | T | downstream_gene_variant | MODIFIER | c.*4992C>T| |
S98 |