Num | GeneID | Chromosome | Position | Ref.allele | Alt.allele | Mutant type | Impacts | Amino acid change | SampleID |
---|---|---|---|---|---|---|---|---|---|
1 | BAA02g11260 | A02 | 5078754 | G | A | missense_variant&splice_region_variant | MODERATE | c.20G>A|p.Arg7Lys |
S81 S85 |
2 | BAA02g11260 | A02 | 5079062 | C | T | stop_gained | HIGH | c.31C>T|p.Gln11* |
S200 |
3 | BAA02g11260 | A02 | 5079130 | C | T | synonymous_variant | LOW | c.99C>T|p.Asp33Asp |
S292 |
4 | BAA02g11260 | A02 | 5079840 | C | T | synonymous_variant | LOW | c.588C>T|p.Val196Val |
S9 |
5 | BAA02g11260 | A02 | 5079997 | G | A | missense_variant | MODERATE | c.745G>A|p.Ala249Thr |
S177 |
6 | BAA02g11260 | A02 | 5082346 | G | A | downstream_gene_variant | MODIFIER | c.*1492G>A| |
S197 |