Num | GeneID | Chromosome | Position | Ref.allele | Alt.allele | Mutant type | Impacts | Amino acid change | SampleID |
---|---|---|---|---|---|---|---|---|---|
1 | BAA09g39600 | A09 | 47119623 | G | A | upstream_gene_variant | MODIFIER | c.-261G>A| |
S291 |
2 | BAA09g39600 | A09 | 47119662 | G | A | upstream_gene_variant | MODIFIER | c.-222G>A| |
S177 |
3 | BAA09g39600 | A09 | 47120223 | C | T | missense_variant | MODERATE | c.340C>T|p.Pro114Ser |
S278 |