Num | GeneID | Chromosome | Position | Ref.allele | Alt.allele | Mutant type | Impacts | Amino acid change | SampleID |
---|---|---|---|---|---|---|---|---|---|
1 | BAA05g14600 | A05 | 7700406 | G | A | missense_variant | MODERATE | c.278G>A|p.Gly93Glu |
S38 |
2 | BAA05g14600 | A05 | 7702130 | C | T | downstream_gene_variant | MODIFIER | c.*1045C>T| |
S233 |
3 | BAA05g14600 | A05 | 7702822 | C | T | downstream_gene_variant | MODIFIER | c.*1737C>T| |
S273 |