Num | GeneID | Chromosome | Position | Ref.allele | Alt.allele | Mutant type | Impacts | Amino acid change | SampleID |
---|---|---|---|---|---|---|---|---|---|
1 | BAA02g09160 | A02 | 4052611 | C | T | synonymous_variant | LOW | c.975G>A|p.Glu325Glu |
S183 S198 |
2 | BAA02g09160 | A02 | 4052698 | C | T | synonymous_variant | LOW | c.888G>A|p.Thr296Thr |
S273 |
3 | BAA02g09160 | A02 | 4053355 | C | T | stop_gained | HIGH | c.231G>A|p.Trp77* |
S202 |
4 | BAA02g09160 | A02 | 4053456 | G | A | missense_variant | MODERATE | c.130C>T|p.Pro44Ser |
S5 |
5 | BAA02g09160 | A02 | 4053510 | G | A | stop_gained | HIGH | c.76C>T|p.Gln26* |
S168 |
6 | BAA02g09160 | A02 | 4053538 | C | T | missense_variant | MODERATE | c.48G>A|p.Met16Ile |
S277 |
7 | BAA02g09160 | A02 | 4056436 | C | T | upstream_gene_variant | MODIFIER | c.-2851G>A| |
S205 S240 |
8 | BAA02g09160 | A02 | 4058020 | T | C | upstream_gene_variant | MODIFIER | c.-4435A>G| |
S18 |
9 | BAA02g09160 | A02 | 4058068 | G | T | upstream_gene_variant | MODIFIER | c.-4483C>A| |
S40 S49 |
10 | BAA02g09160 | A02 | 4058107 | C | T | upstream_gene_variant | MODIFIER | c.-4522G>A| |
S138 |