Num | GeneID | Chromosome | Position | Ref.allele | Alt.allele | Mutant type | Impacts | Amino acid change | SampleID |
---|---|---|---|---|---|---|---|---|---|
1 | BAA09g62990 | A09 | 59130061 | G | A | missense_variant | MODERATE | c.1243C>T|p.Leu415Phe |
S23 |
2 | BAA09g62990 | A09 | 59135802 | C | T | upstream_gene_variant | MODIFIER | c.-4413G>A| |
S26 |
3 | BAA09g62990 | A09 | 59136383 | G | A | upstream_gene_variant | MODIFIER | c.-4994C>T| |
S187 |