Num | GeneID | Chromosome | Position | Ref.allele | Alt.allele | Mutant type | Impacts | Amino acid change | SampleID |
---|---|---|---|---|---|---|---|---|---|
1 | BAA04g01770 | A04 | 1037743 | G | A | missense_variant | MODERATE | c.274C>T|p.Leu92Phe |
S177 |
2 | BAA04g01770 | A04 | 1037826 | G | A | missense_variant | MODERATE | c.191C>T|p.Pro64Leu |
S274 |
3 | BAA04g01770 | A04 | 1042103 | C | T | upstream_gene_variant | MODIFIER | c.-4087G>A| |
S1 S90 |
4 | BAA04g01770 | A04 | 1042653 | G | T | upstream_gene_variant | MODIFIER | c.-4637C>A| |
S47 |