Num | GeneID | Chromosome | Position | Ref.allele | Alt.allele | Mutant type | Impacts | Amino acid change | SampleID |
---|---|---|---|---|---|---|---|---|---|
1 | BAA10g17160 | A10 | 16660113 | C | T | upstream_gene_variant | MODIFIER | c.-761C>T| |
S246 |
2 | BAA10g17160 | A10 | 16660467 | G | A | upstream_gene_variant | MODIFIER | c.-407G>A| |
S303 |
3 | BAA10g17160 | A10 | 16662040 | C | T | missense_variant | MODERATE | c.652C>T|p.Leu218Phe |
S177 |