Num | GeneID | Chromosome | Position | Ref.allele | Alt.allele | Mutant type | Impacts | Amino acid change | SampleID |
---|---|---|---|---|---|---|---|---|---|
1 | BAA04g10880 | A04 | 16938560 | C | T | missense_variant | MODERATE | c.118G>A|p.Val40Met |
S143 |
2 | BAA04g10880 | A04 | 16938935 | G | A | upstream_gene_variant | MODIFIER | c.-258C>T| |
S261 |
3 | BAA04g10880 | A04 | 16939016 | C | T | upstream_gene_variant | MODIFIER | c.-339G>A| |
S8 |
4 | BAA04g10880 | A04 | 16939048 | C | T | upstream_gene_variant | MODIFIER | c.-371G>A| |
S293 |
5 | BAA04g10880 | A04 | 16940566 | C | T | upstream_gene_variant | MODIFIER | c.-1889G>A| |
S115 |
6 | BAA04g10880 | A04 | 16940994 | G | A | upstream_gene_variant | MODIFIER | c.-2317C>T| |
S269 |
7 | BAA04g10880 | A04 | 16942619 | G | A | upstream_gene_variant | MODIFIER | c.-3942C>T| |
S225 S73 |
8 | BAA04g10880 | A04 | 16942807 | C | T | upstream_gene_variant | MODIFIER | c.-4130G>A| |
S65 |
9 | BAA04g10880 | A04 | 16943586 | G | A | upstream_gene_variant | MODIFIER | c.-4909C>T| |
S144 |