Num | GeneID | Chromosome | Position | Ref.allele | Alt.allele | Mutant type | Impacts | Amino acid change | SampleID |
---|---|---|---|---|---|---|---|---|---|
1 | BAA06g01770 | A06 | 1107619 | C | T | upstream_gene_variant | MODIFIER | c.-3878C>T| |
S142 |
2 | BAA06g01770 | A06 | 1108046 | T | C | upstream_gene_variant | MODIFIER | c.-3451T>C| |
S292 |
3 | BAA06g01770 | A06 | 1111572 | C | T | missense_variant | MODERATE | c.76C>T|p.Leu26Phe |
S95 |