Num | GeneID | Chromosome | Position | Ref.allele | Alt.allele | Mutant type | Impacts | Amino acid change | SampleID |
---|---|---|---|---|---|---|---|---|---|
1 | BAA01g14900 | A01 | 7060134 | C | T | missense_variant | MODERATE | c.352G>A|p.Ala118Thr |
S19 |
2 | BAA01g14900 | A01 | 7064905 | G | A | upstream_gene_variant | MODIFIER | c.-4225C>T| |
S34 |
3 | BAA01g14900 | A01 | 7065167 | G | A | upstream_gene_variant | MODIFIER | c.-4487C>T| |
S234 |