Num | GeneID | Chromosome | Position | Ref.allele | Alt.allele | Mutant type | Impacts | Amino acid change | SampleID |
---|---|---|---|---|---|---|---|---|---|
1 | BAA02g46680 | A02 | 37876144 | C | T | synonymous_variant | LOW | c.1068G>A|p.Arg356Arg |
S33 |
2 | BAA02g46680 | A02 | 37876377 | G | A | missense_variant | MODERATE | c.835C>T|p.His279Tyr |
S8 |
3 | BAA02g46680 | A02 | 37876499 | C | T | missense_variant | MODERATE | c.713G>A|p.Arg238His |
S123 |
4 | BAA02g46680 | A02 | 37877597 | G | A | missense_variant | MODERATE | c.191C>T|p.Ser64Phe |
S72 S78 |
5 | BAA02g46680 | A02 | 37878255 | G | A | upstream_gene_variant | MODIFIER | c.-468C>T| |
S142 |
6 | BAA02g46680 | A02 | 37878337 | C | T | upstream_gene_variant | MODIFIER | c.-550G>A| |
S260 |
7 | BAA02g46680 | A02 | 37879098 | G | A | upstream_gene_variant | MODIFIER | c.-1311C>T| |
S296 |