Num | GeneID | Chromosome | Position | Ref.allele | Alt.allele | Mutant type | Impacts | Amino acid change | SampleID |
---|---|---|---|---|---|---|---|---|---|
1 | BAA02g09090 | A02 | 4017842 | C | T | missense_variant | MODERATE | c.10G>A|p.Ala4Thr |
S115 |
2 | BAA02g09090 | A02 | 4020819 | C | T | upstream_gene_variant | MODIFIER | c.-2968G>A| |
S3 |
3 | BAA02g09090 | A02 | 4021937 | G | A | upstream_gene_variant | MODIFIER | c.-4086C>T| |
S188 |
4 | BAA02g09090 | A02 | 4021969 | G | A | upstream_gene_variant | MODIFIER | c.-4118C>T| |
S143 |