Num | GeneID | Chromosome | Position | Ref.allele | Alt.allele | Mutant type | Impacts | Amino acid change | SampleID |
---|---|---|---|---|---|---|---|---|---|
1 | BAA02g29100 | A02 | 16597443 | C | T | synonymous_variant | LOW | c.582G>A|p.Leu194Leu |
S77 |
2 | BAA02g29100 | A02 | 16597449 | C | T | synonymous_variant | LOW | c.576G>A|p.Val192Val |
S112 |
3 | BAA02g29100 | A02 | 16597742 | C | T | missense_variant | MODERATE | c.283G>A|p.Gly95Arg |
S119 |
4 | BAA02g29100 | A02 | 16597751 | C | T | missense_variant | MODERATE | c.274G>A|p.Val92Ile |
S301 S304 |
5 | BAA02g29100 | A02 | 16597766 | C | T | missense_variant | MODERATE | c.259G>A|p.Glu87Lys |
S140 |
6 | BAA02g29100 | A02 | 16598505 | G | A | upstream_gene_variant | MODIFIER | c.-481C>T| |
S187 |
7 | BAA02g29100 | A02 | 16599218 | C | T | upstream_gene_variant | MODIFIER | c.-1194G>A| |
S233 |
8 | BAA02g29100 | A02 | 16599717 | C | T | upstream_gene_variant | MODIFIER | c.-1693G>A| |
S112 |
9 | BAA02g29100 | A02 | 16601213 | G | A | upstream_gene_variant | MODIFIER | c.-3189C>T| |
S205 |
10 | BAA02g29100 | A02 | 16601227 | G | A | upstream_gene_variant | MODIFIER | c.-3203C>T| |
S122 |