Num | GeneID | Chromosome | Position | Ref.allele | Alt.allele | Mutant type | Impacts | Amino acid change | SampleID |
---|---|---|---|---|---|---|---|---|---|
1 | BAA02g46730 | A02 | 37895012 | G | A | missense_variant | MODERATE | c.17C>T|p.Ser6Phe |
S291 |
2 | BAA02g46730 | A02 | 37898850 | C | T | upstream_gene_variant | MODIFIER | c.-3822G>A| |
S65 |
3 | BAA02g46730 | A02 | 37898862 | G | A | upstream_gene_variant | MODIFIER | c.-3834C>T| |
S56 |
4 | BAA02g46730 | A02 | 37899802 | G | A | upstream_gene_variant | MODIFIER | c.-4774C>T| |
S245 |