Num | GeneID | Chromosome | Position | Ref.allele | Alt.allele | Mutant type | Impacts | Amino acid change | SampleID |
---|---|---|---|---|---|---|---|---|---|
1 | BAA01g04900 | A01 | 2175142 | G | A | stop_gained | HIGH | c.1429C>T|p.Gln477* |
S204 |
2 | BAA01g04900 | A01 | 2175306 | G | A | missense_variant | MODERATE | c.1265C>T|p.Ala422Val |
S61 |
3 | BAA01g04900 | A01 | 2175406 | G | A | synonymous_variant | LOW | c.1239C>T|p.Phe413Phe |
S295 |
4 | BAA01g04900 | A01 | 2176302 | C | T | synonymous_variant | LOW | c.639G>A|p.Leu213Leu |
S221 |
5 | BAA01g04900 | A01 | 2177737 | G | A | synonymous_variant | LOW | c.76C>T|p.Leu26Leu |
S161 |
6 | BAA01g04900 | A01 | 2179783 | G | A | upstream_gene_variant | MODIFIER | c.-1971C>T| |
S129 |