Num | GeneID | Chromosome | Position | Ref.allele | Alt.allele | Mutant type | Impacts | Amino acid change | SampleID |
---|---|---|---|---|---|---|---|---|---|
1 | BAA02g00640 | A02 | 335762 | C | T | upstream_gene_variant | MODIFIER | c.-2355C>T| |
S257 |
2 | BAA02g00640 | A02 | 339237 | C | T | missense_variant | MODERATE | c.386C>T|p.Thr129Ile |
S47 |
3 | BAA02g00640 | A02 | 342523 | C | T | downstream_gene_variant | MODIFIER | c.*2096C>T| |
S47 |
4 | BAA02g00640 | A02 | 342650 | G | A | downstream_gene_variant | MODIFIER | c.*2223G>A| |
S265 |
5 | BAA02g00640 | A02 | 342856 | G | A | downstream_gene_variant | MODIFIER | c.*2429G>A| |
S25 |