| Num | GeneID | Chromosome | Position | Ref.allele | Alt.allele | Mutant type | Impacts | Amino acid change | SampleID |
|---|---|---|---|---|---|---|---|---|---|
| 1 | BAA10g05690 | A10 | 2914167 | C | T | synonymous_variant | LOW | c.3192G>A|p.Gln1064Gln |
S260 |
| 2 | BAA10g05690 | A10 | 2915744 | G | A | missense_variant | MODERATE | c.2222C>T|p.Pro741Leu |
S233 |
| 3 | BAA10g05690 | A10 | 2915784 | G | A | missense_variant | MODERATE | c.2182C>T|p.Leu728Phe |
S20 |
| 4 | BAA10g05690 | A10 | 2916679 | G | A | splice_region_variant&intron_variant | LOW | c.1561+8C>T| |
S208 S219 |
| 5 | BAA10g05690 | A10 | 2916716 | G | A | missense_variant | MODERATE | c.1532C>T|p.Ala511Val |
S284 |
| 6 | BAA10g05690 | A10 | 2917886 | G | A | stop_gained | HIGH | c.853C>T|p.Gln285* |
S255 |
| 7 | BAA10g05690 | A10 | 2921322 | C | T | upstream_gene_variant | MODIFIER | c.-1709G>A| |
S177 |