Num | GeneID | Chromosome | Position | Ref.allele | Alt.allele | Mutant type | Impacts | Amino acid change | SampleID |
---|---|---|---|---|---|---|---|---|---|
1 | BAA10g26230 | A10 | 20886913 | G | A | upstream_gene_variant | MODIFIER | c.-482G>A| |
S143 |
2 | BAA10g26230 | A10 | 20887426 | C | T | missense_variant | MODERATE | c.32C>T|p.Ala11Val |
S28 |
3 | BAA10g26230 | A10 | 20887498 | C | T | missense_variant | MODERATE | c.104C>T|p.Ser35Leu |
S153 S213 |