Num | GeneID | Chromosome | Position | Ref.allele | Alt.allele | Mutant type | Impacts | Amino acid change | SampleID |
---|---|---|---|---|---|---|---|---|---|
1 | BAA02g00670 | A02 | 347445 | C | T | missense_variant | MODERATE | c.716G>A|p.Gly239Asp |
S157 |
2 | BAA02g00670 | A02 | 348271 | G | A | synonymous_variant | LOW | c.183C>T|p.Thr61Thr |
S286 |
3 | BAA02g00670 | A02 | 348392 | C | T | missense_variant | MODERATE | c.62G>A|p.Gly21Glu |
S1 S90 |
4 | BAA02g00670 | A02 | 352336 | G | A | upstream_gene_variant | MODIFIER | c.-3883C>T| |
S242 |