Num | GeneID | Chromosome | Position | Ref.allele | Alt.allele | Mutant type | Impacts | Amino acid change | SampleID |
---|---|---|---|---|---|---|---|---|---|
1 | BAA02g44630 | A02 | 36726429 | C | T | synonymous_variant | LOW | c.120C>T|p.Ser40Ser |
S219 |
2 | BAA02g44630 | A02 | 36727176 | C | T | splice_region_variant&intron_variant | LOW | c.674-7C>T| |
S112 |
3 | BAA02g44630 | A02 | 36728150 | G | A | missense_variant | MODERATE | c.1406G>A|p.Arg469Lys |
S5 |