Num | GeneID | Chromosome | Position | Ref.allele | Alt.allele | Mutant type | Impacts | Amino acid change | SampleID |
---|---|---|---|---|---|---|---|---|---|
1 | BAA10g18770 | A10 | 17462983 | G | A | upstream_gene_variant | MODIFIER | c.-4827G>A| |
S150 |
2 | BAA10g18770 | A10 | 17468627 | C | A | stop_gained&splice_region_variant | HIGH | c.726C>A|p.Tyr242* |
S133 |
3 | BAA10g18770 | A10 | 17470199 | G | A | missense_variant | MODERATE | c.1577G>A|p.Gly526Glu |
S62 |