Num | GeneID | Chromosome | Position | Ref.allele | Alt.allele | Mutant type | Impacts | Amino acid change | SampleID |
---|---|---|---|---|---|---|---|---|---|
1 | BAA05g09080 | A05 | 4546213 | G | A | missense_variant | MODERATE | c.410C>T|p.Thr137Met |
S298 |
2 | BAA05g09080 | A05 | 4547433 | G | A | upstream_gene_variant | MODIFIER | c.-335C>T| |
S115 |
3 | BAA05g09080 | A05 | 4548540 | G | A | upstream_gene_variant | MODIFIER | c.-1442C>T| |
S246 S97 |
4 | BAA05g09080 | A05 | 4548822 | G | A | upstream_gene_variant | MODIFIER | c.-1724C>T| |
S152 |
5 | BAA05g09080 | A05 | 4551928 | C | T | upstream_gene_variant | MODIFIER | c.-4830G>A| |
S237 |
6 | BAA05g09080 | A05 | 4551991 | C | T | upstream_gene_variant | MODIFIER | c.-4893G>A| |
S195 |