Num | GeneID | Chromosome | Position | Ref.allele | Alt.allele | Mutant type | Impacts | Amino acid change | SampleID |
---|---|---|---|---|---|---|---|---|---|
1 | BAA02g19950 | A02 | 10470689 | G | A | upstream_gene_variant | MODIFIER | c.-2499G>A| |
S59 |
2 | BAA02g19950 | A02 | 10470841 | G | A | upstream_gene_variant | MODIFIER | c.-2347G>A| |
S188 |
3 | BAA02g19950 | A02 | 10471750 | C | T | upstream_gene_variant | MODIFIER | c.-1438C>T| |
S13 S140 S168 S279 S64 |
4 | BAA02g19950 | A02 | 10473060 | C | T | upstream_gene_variant | MODIFIER | c.-128C>T| |
S63 |
5 | BAA02g19950 | A02 | 10473590 | G | A | missense_variant | MODERATE | c.403G>A|p.Asp135Asn |
S303 |
6 | BAA02g19950 | A02 | 10473850 | G | A | synonymous_variant | LOW | c.663G>A|p.Glu221Glu |
S190 |
7 | BAA02g19950 | A02 | 10475340 | G | A | missense_variant | MODERATE | c.2153G>A|p.Gly718Glu |
S286 |
8 | BAA02g19950 | A02 | 10475703 | C | T | missense_variant | MODERATE | c.2516C>T|p.Ser839Phe |
S40 S49 |
9 | BAA02g19950 | A02 | 10475845 | G | A | synonymous_variant | LOW | c.2658G>A|p.Arg886Arg |
S247 |
10 | BAA02g19950 | A02 | 10477458 | G | A | downstream_gene_variant | MODIFIER | c.*56G>A| |
S206 S26 |