Num | GeneID | Chromosome | Position | Ref.allele | Alt.allele | Mutant type | Impacts | Amino acid change | SampleID |
---|---|---|---|---|---|---|---|---|---|
1 | BAA02g08780 | A02 | 3886247 | G | A | missense_variant | MODERATE | c.1291G>A|p.Glu431Lys |
S163 |
2 | BAA02g08780 | A02 | 3886346 | G | A | missense_variant | MODERATE | c.1390G>A|p.Gly464Arg |
S282 |
3 | BAA02g08780 | A02 | 3886749 | C | T | missense_variant | MODERATE | c.1793C>T|p.Pro598Leu |
S23 |
4 | BAA02g08780 | A02 | 3886770 | C | T | missense_variant | MODERATE | c.1814C>T|p.Ser605Phe |
S192 |
5 | BAA02g08780 | A02 | 3887008 | G | A | synonymous_variant | LOW | c.2052G>A|p.Arg684Arg |
S192 |
6 | BAA02g08780 | A02 | 3887706 | G | A | missense_variant | MODERATE | c.2750G>A|p.Gly917Glu |
S10 |
7 | BAA02g08780 | A02 | 3888116 | C | T | downstream_gene_variant | MODIFIER | c.*49C>T| |
S104 |
8 | BAA02g08780 | A02 | 3888328 | C | T | downstream_gene_variant | MODIFIER | c.*261C>T| |
S183 S198 |
9 | BAA02g08780 | A02 | 3888665 | C | T | downstream_gene_variant | MODIFIER | c.*598C>T| |
S179 |
10 | BAA02g08780 | A02 | 3890936 | G | A | downstream_gene_variant | MODIFIER | c.*2869G>A| |
S17 |
11 | BAA02g08780 | A02 | 3892825 | C | T | downstream_gene_variant | MODIFIER | c.*4758C>T| |
S295 |