Num | GeneID | Chromosome | Position | Ref.allele | Alt.allele | Mutant type | Impacts | Amino acid change | SampleID |
---|---|---|---|---|---|---|---|---|---|
1 | BAA02g19010 | A02 | 9827830 | C | T | intron_variant | MODIFIER | c.352+48C>T| |
S308 |
2 | BAA02g19010 | A02 | 9828620 | C | T | missense_variant | MODERATE | c.725C>T|p.Thr242Ile |
S76 |
3 | BAA02g19010 | A02 | 9828782 | C | T | missense_variant | MODERATE | c.811C>T|p.Leu271Phe |
S40 S49 |