Num | GeneID | Chromosome | Position | Ref.allele | Alt.allele | Mutant type | Impacts | Amino acid change | SampleID |
---|---|---|---|---|---|---|---|---|---|
1 | BAA09g26960 | A09 | 17516033 | G | A | missense_variant | MODERATE | c.919C>T|p.Pro307Ser |
S224 |
2 | BAA09g26960 | A09 | 17519141 | C | T | upstream_gene_variant | MODIFIER | c.-1892G>A| |
S131 |
3 | BAA09g26960 | A09 | 17522100 | G | A | upstream_gene_variant | MODIFIER | c.-4851C>T| |
S216 |