Num | GeneID | Chromosome | Position | Ref.allele | Alt.allele | Mutant type | Impacts | Amino acid change | SampleID |
---|---|---|---|---|---|---|---|---|---|
1 | BAA04g00080 | A04 | 27911 | C | T | synonymous_variant | LOW | c.879C>T|p.Ser293Ser |
S113 |
2 | BAA04g00080 | A04 | 29437 | G | A | missense_variant | MODERATE | c.1777G>A|p.Ala593Thr |
S289 |
3 | BAA04g00080 | A04 | 31055 | G | A | splice_region_variant&intron_variant | LOW | c.2608+5G>A| |
S251 |
4 | BAA04g00080 | A04 | 31392 | C | T | synonymous_variant | LOW | c.2709C>T|p.Asp903Asp |
S158 |