Num | GeneID | Chromosome | Position | Ref.allele | Alt.allele | Mutant type | Impacts | Amino acid change | SampleID |
---|---|---|---|---|---|---|---|---|---|
1 | BAA02g00680 | A02 | 351649 | C | T | missense_variant | MODERATE | c.1046C>T|p.Ser349Phe |
S142 |
2 | BAA02g00680 | A02 | 351744 | G | A | missense_variant | MODERATE | c.1141G>A|p.Val381Ile |
S163 |
3 | BAA02g00680 | A02 | 352618 | C | T | missense_variant | MODERATE | c.1709C>T|p.Ser570Phe |
S257 |
4 | BAA02g00680 | A02 | 353977 | C | T | synonymous_variant | LOW | c.2724C>T|p.Thr908Thr |
S186 |
5 | BAA02g00680 | A02 | 354178 | C | T | synonymous_variant | LOW | c.2925C>T|p.Leu975Leu |
S234 |
6 | BAA02g00680 | A02 | 354378 | G | A | missense_variant | MODERATE | c.3125G>A|p.Cys1042Tyr |
S9 |
7 | BAA02g00680 | A02 | 355213 | G | A | synonymous_variant | LOW | c.3876G>A|p.Thr1292Thr |
S209 |
8 | BAA02g00680 | A02 | 356122 | G | A | synonymous_variant | LOW | c.4335G>A|p.Val1445Val |
S126 |
9 | BAA02g00680 | A02 | 357480 | G | A | downstream_gene_variant | MODIFIER | c.*1132G>A| |
S45 |