Num | GeneID | Chromosome | Position | Ref.allele | Alt.allele | Mutant type | Impacts | Amino acid change | SampleID |
---|---|---|---|---|---|---|---|---|---|
1 | BAA02g16300 | A02 | 7945430 | C | T | missense_variant | MODERATE | c.434G>A|p.Ser145Asn |
S262 |
2 | BAA02g16300 | A02 | 7945695 | C | T | missense_variant | MODERATE | c.169G>A|p.Ala57Thr |
S135 |
3 | BAA02g16300 | A02 | 7947173 | C | T | upstream_gene_variant | MODIFIER | c.-1310G>A| |
S165 |
4 | BAA02g16300 | A02 | 7949780 | T | C | upstream_gene_variant | MODIFIER | c.-3917A>G| |
S98 |