Num | GeneID | Chromosome | Position | Ref.allele | Alt.allele | Mutant type | Impacts | Amino acid change | SampleID |
---|---|---|---|---|---|---|---|---|---|
1 | BAA09g10000 | A09 | 5524749 | C | T | missense_variant | MODERATE | c.569G>A|p.Gly190Asp |
S269 |
2 | BAA09g10000 | A09 | 5525865 | C | T | upstream_gene_variant | MODIFIER | c.-548G>A| |
S153 |
3 | BAA09g10000 | A09 | 5526925 | G | A | upstream_gene_variant | MODIFIER | c.-1608C>T| |
S81 S85 |
4 | BAA09g10000 | A09 | 5527293 | G | A | upstream_gene_variant | MODIFIER | c.-1976C>T| |
S15 S3 |
5 | BAA09g10000 | A09 | 5527842 | C | T | upstream_gene_variant | MODIFIER | c.-2525G>A| |
S85 |