Num | GeneID | Chromosome | Position | Ref.allele | Alt.allele | Mutant type | Impacts | Amino acid change | SampleID |
---|---|---|---|---|---|---|---|---|---|
1 | BAA10g00800 | A10 | 375642 | G | A | upstream_gene_variant | MODIFIER | c.-4562G>A| |
S13 |
2 | BAA10g00800 | A10 | 380604 | C | T | missense_variant | MODERATE | c.214C>T|p.Pro72Ser |
S61 |
3 | BAA10g00800 | A10 | 385024 | C | T | downstream_gene_variant | MODIFIER | c.*4204C>T| |
S27 |