Num | GeneID | Chromosome | Position | Ref.allele | Alt.allele | Mutant type | Impacts | Amino acid change | SampleID |
---|---|---|---|---|---|---|---|---|---|
1 | BAA02g44680 | A02 | 36741906 | C | T | splice_region_variant&intron_variant | LOW | c.759+5G>A| |
S259 |
2 | BAA02g44680 | A02 | 36742697 | C | T | synonymous_variant | LOW | c.273G>A|p.Lys91Lys |
S124 |
3 | BAA02g44680 | A02 | 36742833 | G | A | missense_variant | MODERATE | c.137C>T|p.Thr46Ile |
S166 |