Num | GeneID | Chromosome | Position | Ref.allele | Alt.allele | Mutant type | Impacts | Amino acid change | SampleID |
---|---|---|---|---|---|---|---|---|---|
1 | BAA10g07120 | A10 | 3959690 | C | T | upstream_gene_variant | MODIFIER | c.-3717C>T| |
S277 |
2 | BAA10g07120 | A10 | 3961266 | G | A | upstream_gene_variant | MODIFIER | c.-2141G>A| |
S33 |
3 | BAA10g07120 | A10 | 3964101 | C | T | missense_variant | MODERATE | c.431C>T|p.Thr144Ile |
S139 |