Num | GeneID | Chromosome | Position | Ref.allele | Alt.allele | Mutant type | Impacts | Amino acid change | SampleID |
---|---|---|---|---|---|---|---|---|---|
1 | BAA09g64760 | A09 | 59966561 | C | T | missense_variant | MODERATE | c.544G>A|p.Asp182Asn |
S52 |
2 | BAA09g64760 | A09 | 59967670 | G | A | upstream_gene_variant | MODIFIER | c.-566C>T| |
S38 |
3 | BAA09g64760 | A09 | 59968143 | G | A | upstream_gene_variant | MODIFIER | c.-1039C>T| |
S10 |
4 | BAA09g64760 | A09 | 59968280 | C | T | upstream_gene_variant | MODIFIER | c.-1176G>A| |
S61 |
5 | BAA09g64760 | A09 | 59968379 | C | T | upstream_gene_variant | MODIFIER | c.-1275G>A| |
S104 |
6 | BAA09g64760 | A09 | 59969636 | T | A | upstream_gene_variant | MODIFIER | c.-2532A>T| |
S158 |
7 | BAA09g64760 | A09 | 59969829 | G | A | upstream_gene_variant | MODIFIER | c.-2725C>T| |
S178 |
8 | BAA09g64760 | A09 | 59970383 | C | T | upstream_gene_variant | MODIFIER | c.-3279G>A| |
S245 |
9 | BAA09g64760 | A09 | 59970669 | C | T | upstream_gene_variant | MODIFIER | c.-3565G>A| |
S230 S73 |