| Num | GeneID | Chromosome | Position | Ref.allele | Alt.allele | Mutant type | Impacts | Amino acid change | SampleID |
|---|---|---|---|---|---|---|---|---|---|
| 1 | BAA02g29250 | A02 | 16717013 | C | T | missense_variant | MODERATE | c.631C>T|p.Leu211Phe |
S65 |
| 2 | BAA02g29250 | A02 | 16717087 | G | A | stop_gained | HIGH | c.705G>A|p.Trp235* |
S210 |
| 3 | BAA02g29250 | A02 | 16717606 | G | A | splice_region_variant&intron_variant | LOW | c.1128+5G>A| |
S302 |
| 4 | BAA02g29250 | A02 | 16718192 | C | T | synonymous_variant | LOW | c.1539C>T|p.Asn513Asn |
S122 |
| 5 | BAA02g29250 | A02 | 16719169 | G | A | missense_variant | MODERATE | c.2212G>A|p.Glu738Lys |
S291 |
| 6 | BAA02g29250 | A02 | 16720324 | C | T | downstream_gene_variant | MODIFIER | c.*615C>T| |
S135 S266 |