Num | GeneID | Chromosome | Position | Ref.allele | Alt.allele | Mutant type | Impacts | Amino acid change | SampleID |
---|---|---|---|---|---|---|---|---|---|
1 | BAA05g00160 | A05 | 105916 | G | A | missense_variant | MODERATE | c.671C>T|p.Thr224Ile |
S23 |
2 | BAA05g00160 | A05 | 106026 | G | A | synonymous_variant | LOW | c.561C>T|p.Leu187Leu |
S46 |
3 | BAA05g00160 | A05 | 106256 | C | T | missense_variant | MODERATE | c.403G>A|p.Glu135Lys |
S88 |
4 | BAA05g00160 | A05 | 110654 | G | A | upstream_gene_variant | MODIFIER | c.-3996C>T| |
S155 |