Num | GeneID | Chromosome | Position | Ref.allele | Alt.allele | Mutant type | Impacts | Amino acid change | SampleID |
---|---|---|---|---|---|---|---|---|---|
1 | BAA02g09460 | A02 | 4168125 | C | T | missense_variant | MODERATE | c.184C>T|p.Arg62Cys |
S138 |
2 | BAA02g09460 | A02 | 4168209 | G | A | missense_variant | MODERATE | c.268G>A|p.Asp90Asn |
S225 S73 |
3 | BAA02g09460 | A02 | 4168368 | C | T | missense_variant | MODERATE | c.427C>T|p.Leu143Phe |
S116 |
4 | BAA02g09460 | A02 | 4168476 | C | T | stop_gained | HIGH | c.535C>T|p.Gln179* |
S256 |
5 | BAA02g09460 | A02 | 4170620 | C | T | downstream_gene_variant | MODIFIER | c.*1647C>T| |
S71 |
6 | BAA02g09460 | A02 | 4173185 | G | A | downstream_gene_variant | MODIFIER | c.*4212G>A| |
S174 |