Num | GeneID | Chromosome | Position | Ref.allele | Alt.allele | Mutant type | Impacts | Amino acid change | SampleID |
---|---|---|---|---|---|---|---|---|---|
1 | BAA02g01690 | A02 | 748090 | G | A | upstream_gene_variant | MODIFIER | c.-4760G>A| |
S291 |
2 | BAA02g01690 | A02 | 749520 | G | A | upstream_gene_variant | MODIFIER | c.-3330G>A| |
S215 |
3 | BAA02g01690 | A02 | 751195 | G | A | upstream_gene_variant | MODIFIER | c.-1655G>A| |
S209 |
4 | BAA02g01690 | A02 | 752471 | G | A | upstream_gene_variant | MODIFIER | c.-379G>A| |
S33 |
5 | BAA02g01690 | A02 | 752868 | G | A | missense_variant | MODERATE | c.19G>A|p.Gly7Arg |
S271 |
6 | BAA02g01690 | A02 | 753160 | G | A | synonymous_variant | LOW | c.210G>A|p.Pro70Pro |
S126 |
7 | BAA02g01690 | A02 | 753357 | C | T | missense_variant | MODERATE | c.407C>T|p.Ala136Val |
S298 |