Num | GeneID | Chromosome | Position | Ref.allele | Alt.allele | Mutant type | Impacts | Amino acid change | SampleID |
---|---|---|---|---|---|---|---|---|---|
1 | BAA10g22100 | A10 | 19177429 | G | A | missense_variant | MODERATE | c.238C>T|p.Pro80Ser |
S50 |
2 | BAA10g22100 | A10 | 19179522 | C | T | upstream_gene_variant | MODIFIER | c.-1054G>A| |
S235 |
3 | BAA10g22100 | A10 | 19182157 | G | A | upstream_gene_variant | MODIFIER | c.-3689C>T| |
S172 |