Num | GeneID | Chromosome | Position | Ref.allele | Alt.allele | Mutant type | Impacts | Amino acid change | SampleID |
---|---|---|---|---|---|---|---|---|---|
1 | BAA09g38980 | A09 | 46680356 | C | T | missense_variant | MODERATE | c.626G>A|p.Arg209His |
S240 |
2 | BAA09g38980 | A09 | 46680416 | C | T | missense_variant | MODERATE | c.566G>A|p.Cys189Tyr |
S294 |
3 | BAA09g38980 | A09 | 46680960 | C | T | missense_variant | MODERATE | c.22G>A|p.Val8Ile |
S208 S219 |
4 | BAA09g38980 | A09 | 46684667 | C | T | upstream_gene_variant | MODIFIER | c.-3686G>A| |
S223 |
5 | BAA09g38980 | A09 | 46684848 | G | A | upstream_gene_variant | MODIFIER | c.-3867C>T| |
S107 |
6 | BAA09g38980 | A09 | 46685704 | C | T | upstream_gene_variant | MODIFIER | c.-4723G>A| |
S153 |
7 | BAA09g38980 | A09 | 46685866 | G | A | upstream_gene_variant | MODIFIER | c.-4885C>T| |
S70 |