Num | GeneID | Chromosome | Position | Ref.allele | Alt.allele | Mutant type | Impacts | Amino acid change | SampleID |
---|---|---|---|---|---|---|---|---|---|
1 | BAA10g15980 | A10 | 16070832 | G | A | missense_variant | MODERATE | c.295C>T|p.Pro99Ser |
S122 |
2 | BAA10g15980 | A10 | 16074496 | G | A | upstream_gene_variant | MODIFIER | c.-3370C>T| |
S61 |
3 | BAA10g15980 | A10 | 16074767 | C | T | upstream_gene_variant | MODIFIER | c.-3641G>A| |
S165 |
4 | BAA10g15980 | A10 | 16075905 | G | A | upstream_gene_variant | MODIFIER | c.-4779C>T| |
S69 |