Num | GeneID | Chromosome | Position | Ref.allele | Alt.allele | Mutant type | Impacts | Amino acid change | SampleID |
---|---|---|---|---|---|---|---|---|---|
1 | BAA05g04500 | A05 | 2167600 | C | T | missense_variant | MODERATE | c.413G>A|p.Gly138Asp |
S277 |
2 | BAA05g04500 | A05 | 2171567 | G | A | upstream_gene_variant | MODIFIER | c.-2873C>T| |
S163 |
3 | BAA05g04500 | A05 | 2171775 | C | T | upstream_gene_variant | MODIFIER | c.-3081G>A| |
S202 |