Num | GeneID | Chromosome | Position | Ref.allele | Alt.allele | Mutant type | Impacts | Amino acid change | SampleID |
---|---|---|---|---|---|---|---|---|---|
1 | BAA09g39090 | A09 | 46798443 | G | A | missense_variant | MODERATE | c.227G>A|p.Gly76Glu |
S69 |
2 | BAA09g39090 | A09 | 46800107 | C | T | missense_variant | MODERATE | c.448C>T|p.Leu150Phe |
S242 |
3 | BAA09g39090 | A09 | 46801310 | C | T | downstream_gene_variant | MODIFIER | c.*649C>T| |
S219 S72 |