Num | GeneID | Chromosome | Position | Ref.allele | Alt.allele | Mutant type | Impacts | Amino acid change | SampleID |
---|---|---|---|---|---|---|---|---|---|
1 | BAA02g38030 | A02 | 32474754 | C | T | missense_variant | MODERATE | c.376G>A|p.Val126Ile |
S63 |
2 | BAA02g38030 | A02 | 32474762 | G | A | missense_variant | MODERATE | c.368C>T|p.Ala123Val |
S286 |
3 | BAA02g38030 | A02 | 32474886 | G | A | synonymous_variant | LOW | c.244C>T|p.Leu82Leu |
S256 |
4 | BAA02g38030 | A02 | 32475420 | G | A | upstream_gene_variant | MODIFIER | c.-210C>T| |
S155 S211 |
5 | BAA02g38030 | A02 | 32478143 | C | T | upstream_gene_variant | MODIFIER | c.-2933G>A| |
S249 |
6 | BAA02g38030 | A02 | 32478166 | A | C | upstream_gene_variant | MODIFIER | c.-2956T>G| |
S136 S195 S203 S291 S85 |
7 | BAA02g38030 | A02 | 32478364 | C | T | upstream_gene_variant | MODIFIER | c.-3154G>A| |
S181 |