Num | GeneID | Chromosome | Position | Ref.allele | Alt.allele | Mutant type | Impacts | Amino acid change | SampleID |
---|---|---|---|---|---|---|---|---|---|
1 | BAA10g30050 | A10 | 22391248 | C | T | missense_variant | MODERATE | c.1697C>T|p.Pro566Leu |
S112 |
2 | BAA10g30050 | A10 | 22394224 | C | T | downstream_gene_variant | MODIFIER | c.*2927C>T| |
S97 |
3 | BAA10g30050 | A10 | 22394929 | C | T | downstream_gene_variant | MODIFIER | c.*3632C>T| |
S34 |