Num | GeneID | Chromosome | Position | Ref.allele | Alt.allele | Mutant type | Impacts | Amino acid change | SampleID |
---|---|---|---|---|---|---|---|---|---|
1 | BAA06g06060 | A06 | 3369082 | G | A | missense_variant | MODERATE | c.1042G>A|p.Gly348Ser |
S292 |
2 | BAA06g06060 | A06 | 3370742 | C | T | missense_variant | MODERATE | c.1882C>T|p.Pro628Ser |
S28 |
3 | BAA06g06060 | A06 | 3371065 | C | T | splice_region_variant&intron_variant | LOW | c.2065-8C>T| |
S184 |