Num | GeneID | Chromosome | Position | Ref.allele | Alt.allele | Mutant type | Impacts | Amino acid change | SampleID |
---|---|---|---|---|---|---|---|---|---|
1 | BAA10g00940 | A10 | 448580 | C | T | missense_variant | MODERATE | c.695C>T|p.Ser232Phe |
S52 |
2 | BAA10g00940 | A10 | 450443 | G | A | downstream_gene_variant | MODIFIER | c.*1826G>A| |
S19 |
3 | BAA10g00940 | A10 | 450609 | C | T | downstream_gene_variant | MODIFIER | c.*1992C>T| |
S244 |
4 | BAA10g00940 | A10 | 450672 | C | T | downstream_gene_variant | MODIFIER | c.*2055C>T| |
S294 |