| Num | GeneID | Chromosome | Position | Ref.allele | Alt.allele | Mutant type | Impacts | Amino acid change | SampleID |
|---|---|---|---|---|---|---|---|---|---|
| 1 | BAA06g01060 | A06 | 748895 | G | A | missense_variant | MODERATE | c.704C>T|p.Ala235Val |
S255 |
| 2 | BAA06g01060 | A06 | 749238 | G | A | synonymous_variant | LOW | c.525C>T|p.Thr175Thr |
S221 |
| 3 | BAA06g01060 | A06 | 749442 | G | A | splice_region_variant&intron_variant | LOW | c.408-4C>T| |
S184 |
| 4 | BAA06g01060 | A06 | 749688 | G | A | missense_variant | MODERATE | c.355C>T|p.Pro119Ser |
S111 |
| 5 | BAA06g01060 | A06 | 754094 | C | T | upstream_gene_variant | MODIFIER | c.-3771G>A| |
S139 |