Num | GeneID | Chromosome | Position | Ref.allele | Alt.allele | Mutant type | Impacts | Amino acid change | SampleID |
---|---|---|---|---|---|---|---|---|---|
1 | BAA02g01950 | A02 | 864194 | C | T | downstream_gene_variant | MODIFIER | c.*3354G>A| |
S15 S3 |
2 | BAA02g01950 | A02 | 869446 | G | A | missense_variant | MODERATE | c.889C>T|p.Pro297Ser |
S146 |
3 | BAA02g01950 | A02 | 870650 | G | A | synonymous_variant | LOW | c.115C>T|p.Leu39Leu |
S41 |
4 | BAA02g01950 | A02 | 871228 | C | T | upstream_gene_variant | MODIFIER | c.-464G>A| |
S178 |
5 | BAA02g01950 | A02 | 871769 | C | T | upstream_gene_variant | MODIFIER | c.-1005G>A| |
S150 |
6 | BAA02g01950 | A02 | 874884 | G | A | upstream_gene_variant | MODIFIER | c.-4120C>T| |
S170 |