Num | GeneID | Chromosome | Position | Ref.allele | Alt.allele | Mutant type | Impacts | Amino acid change | SampleID |
---|---|---|---|---|---|---|---|---|---|
1 | BAA02g00830 | A02 | 398793 | C | T | missense_variant | MODERATE | c.191G>A|p.Arg64Lys |
S228 |
2 | BAA02g00830 | A02 | 399965 | G | A | upstream_gene_variant | MODIFIER | c.-607C>T| |
S199 |
3 | BAA02g00830 | A02 | 400019 | G | A | upstream_gene_variant | MODIFIER | c.-661C>T| |
S223 |
4 | BAA02g00830 | A02 | 400483 | C | T | upstream_gene_variant | MODIFIER | c.-1125G>A| |
S252 |
5 | BAA02g00830 | A02 | 401518 | C | T | upstream_gene_variant | MODIFIER | c.-2160G>A| |
S79 S84 |