Num | GeneID | Chromosome | Position | Ref.allele | Alt.allele | Mutant type | Impacts | Amino acid change | SampleID |
---|---|---|---|---|---|---|---|---|---|
1 | BAA01g08990 | A01 | 3951704 | C | T | missense_variant | MODERATE | c.173G>A|p.Gly58Asp |
S88 |
2 | BAA01g08990 | A01 | 3953133 | G | A | upstream_gene_variant | MODIFIER | c.-895C>T| |
S23 |
3 | BAA01g08990 | A01 | 3953340 | G | A | upstream_gene_variant | MODIFIER | c.-1102C>T| |
S175 S177 |
4 | BAA01g08990 | A01 | 3956189 | C | T | upstream_gene_variant | MODIFIER | c.-3951G>A| |
S164 |
5 | BAA01g08990 | A01 | 3957142 | G | A | upstream_gene_variant | MODIFIER | c.-4904C>T| |
S157 S163 |