Num | GeneID | Chromosome | Position | Ref.allele | Alt.allele | Mutant type | Impacts | Amino acid change | SampleID |
---|---|---|---|---|---|---|---|---|---|
1 | BAA09g45990 | A09 | 50956562 | G | A | missense_variant | MODERATE | c.206C>T|p.Thr69Ile |
S72 S78 |
2 | BAA09g45990 | A09 | 50956756 | G | A | synonymous_variant | LOW | c.12C>T|p.Thr4Thr |
S177 |
3 | BAA09g45990 | A09 | 50957958 | G | A | upstream_gene_variant | MODIFIER | c.-1191C>T| |
S98 |
4 | BAA09g45990 | A09 | 50958464 | C | T | upstream_gene_variant | MODIFIER | c.-1697G>A| |
S295 |
5 | BAA09g45990 | A09 | 50961430 | C | T | upstream_gene_variant | MODIFIER | c.-4663G>A| |
S295 |