Num | GeneID | Chromosome | Position | Ref.allele | Alt.allele | Mutant type | Impacts | Amino acid change | SampleID |
---|---|---|---|---|---|---|---|---|---|
1 | BAA02g38900 | A02 | 33091984 | C | T | upstream_gene_variant | MODIFIER | c.-2242C>T| |
S260 |
2 | BAA02g38900 | A02 | 33095547 | G | A | missense_variant | MODERATE | c.406G>A|p.Gly136Ser |
S281 |
3 | BAA02g38900 | A02 | 33100464 | G | A | downstream_gene_variant | MODIFIER | c.*4582G>A| |
S223 |
4 | BAA02g38900 | A02 | 33100473 | G | A | downstream_gene_variant | MODIFIER | c.*4591G>A| |
S280 |
5 | BAA02g38900 | A02 | 33100576 | G | A | downstream_gene_variant | MODIFIER | c.*4694G>A| |
S11 |
6 | BAA02g38900 | A02 | 33100578 | C | T | downstream_gene_variant | MODIFIER | c.*4696C>T| |
S283 |