Num | GeneID | Chromosome | Position | Ref.allele | Alt.allele | Mutant type | Impacts | Amino acid change | SampleID |
---|---|---|---|---|---|---|---|---|---|
1 | BAA09g38120 | A09 | 46137655 | C | T | missense_variant | MODERATE | c.179G>A|p.Ser60Asn |
S92 |
2 | BAA09g38120 | A09 | 46140271 | C | T | upstream_gene_variant | MODIFIER | c.-2359G>A| |
S108 |
3 | BAA09g38120 | A09 | 46142064 | G | A | upstream_gene_variant | MODIFIER | c.-4152C>T| |
S188 |