Num | GeneID | Chromosome | Position | Ref.allele | Alt.allele | Mutant type | Impacts | Amino acid change | SampleID |
---|---|---|---|---|---|---|---|---|---|
1 | BAA02g41850 | A02 | 34976026 | C | T | intron_variant | MODIFIER | c.342-1054C>T| |
S100 |
2 | BAA02g41850 | A02 | 34977256 | G | A | synonymous_variant | LOW | c.447G>A|p.Glu149Glu |
S282 |
3 | BAA02g41850 | A02 | 34977491 | G | A | synonymous_variant | LOW | c.609G>A|p.Lys203Lys |
S56 |
4 | BAA02g41850 | A02 | 34977529 | G | A | missense_variant | MODERATE | c.647G>A|p.Cys216Tyr |
S36 |
5 | BAA02g41850 | A02 | 34977692 | G | A | stop_gained | HIGH | c.810G>A|p.Trp270* |
S286 |
6 | BAA02g41850 | A02 | 34978086 | G | A | intron_variant | MODIFIER | c.826+378G>A| |
S209 |
7 | BAA02g41850 | A02 | 34978223 | G | A | intron_variant | MODIFIER | c.826+515G>A| |
S136 |
8 | BAA02g41850 | A02 | 34979195 | G | A | intron_variant | MODIFIER | c.924+200G>A| |
S44 |
9 | BAA02g41850 | A02 | 34979513 | C | T | synonymous_variant | LOW | c.1008C>T|p.Leu336Leu |
S193 |