Num | GeneID | Chromosome | Position | Ref.allele | Alt.allele | Mutant type | Impacts | Amino acid change | SampleID |
---|---|---|---|---|---|---|---|---|---|
1 | BAA02g39720 | A02 | 33693252 | G | A | missense_variant | MODERATE | c.292C>T|p.His98Tyr |
S255 |
2 | BAA02g39720 | A02 | 33693420 | G | A | missense_variant | MODERATE | c.208C>T|p.Pro70Ser |
S132 S137 S215 S89 |
3 | BAA02g39720 | A02 | 33693524 | G | A | missense_variant | MODERATE | c.104C>T|p.Ser35Phe |
S136 S286 |
4 | BAA02g39720 | A02 | 33693637 | G | A | missense_variant | MODERATE | c.76C>T|p.Leu26Phe |
S265 |
5 | BAA02g39720 | A02 | 33694175 | C | T | upstream_gene_variant | MODIFIER | c.-463G>A| |
S38 |
6 | BAA02g39720 | A02 | 33695633 | C | T | upstream_gene_variant | MODIFIER | c.-1921G>A| |
S122 |
7 | BAA02g39720 | A02 | 33695778 | C | T | upstream_gene_variant | MODIFIER | c.-2066G>A| |
S212 |
8 | BAA02g39720 | A02 | 33697142 | C | T | upstream_gene_variant | MODIFIER | c.-3430G>A| |
S65 |