Num | GeneID | Chromosome | Position | Ref.allele | Alt.allele | Mutant type | Impacts | Amino acid change | SampleID |
---|---|---|---|---|---|---|---|---|---|
1 | BAA02g05350 | A02 | 2334078 | C | T | missense_variant | MODERATE | c.52C>T|p.His18Tyr |
S219 S72 |
2 | BAA02g05350 | A02 | 2334713 | C | T | missense_variant | MODERATE | c.530C>T|p.Thr177Ile |
S87 |
3 | BAA02g05350 | A02 | 2334926 | C | T | missense_variant | MODERATE | c.743C>T|p.Ser248Phe |
S263 |
4 | BAA02g05350 | A02 | 2336067 | C | T | missense_variant | MODERATE | c.1589C>T|p.Thr530Ile |
S183 S198 |
5 | BAA02g05350 | A02 | 2337318 | C | T | downstream_gene_variant | MODIFIER | c.*1157C>T| |
S274 |