Num | GeneID | Chromosome | Position | Ref.allele | Alt.allele | Mutant type | Impacts | Amino acid change | SampleID |
---|---|---|---|---|---|---|---|---|---|
1 | BAA02g11700 | A02 | 5303441 | C | T | missense_variant | MODERATE | c.1735G>A|p.Val579Met |
S255 |
2 | BAA02g11700 | A02 | 5303614 | C | T | missense_variant | MODERATE | c.1562G>A|p.Arg521Lys |
S165 |
3 | BAA02g11700 | A02 | 5303738 | G | A | missense_variant | MODERATE | c.1438C>T|p.Pro480Ser |
S298 |
4 | BAA02g11700 | A02 | 5303759 | G | A | synonymous_variant | LOW | c.1417C>T|p.Leu473Leu |
S158 |
5 | BAA02g11700 | A02 | 5307438 | G | A | missense_variant | MODERATE | c.413C>T|p.Thr138Ile |
S303 |
6 | BAA02g11700 | A02 | 5308958 | C | T | upstream_gene_variant | MODIFIER | c.-726G>A| |
S263 |
7 | BAA02g11700 | A02 | 5309057 | G | A | upstream_gene_variant | MODIFIER | c.-825C>T| |
S161 |
8 | BAA02g11700 | A02 | 5312377 | G | A | upstream_gene_variant | MODIFIER | c.-4145C>T| |
S82 S92 |