Num | GeneID | Chromosome | Position | Ref.allele | Alt.allele | Mutant type | Impacts | Amino acid change | SampleID |
---|---|---|---|---|---|---|---|---|---|
1 | BAA01g29960 | A01 | 19018498 | C | T | missense_variant | MODERATE | c.1217G>A|p.Ser406Asn |
S240 |
2 | BAA01g29960 | A01 | 19021749 | C | T | stop_gained | HIGH | c.815G>A|p.Trp272* |
S87 |
3 | BAA01g29960 | A01 | 19021756 | C | T | missense_variant | MODERATE | c.808G>A|p.Val270Met |
S264 |
4 | BAA01g29960 | A01 | 19023338 | C | T | stop_gained | HIGH | c.321G>A|p.Trp107* |
S125 |
5 | BAA01g29960 | A01 | 19023550 | C | T | missense_variant | MODERATE | c.209G>A|p.Gly70Glu |
S127 |
6 | BAA01g29960 | A01 | 19024470 | C | T | upstream_gene_variant | MODIFIER | c.-712G>A| |
S18 |
7 | BAA01g29960 | A01 | 19028132 | G | A | upstream_gene_variant | MODIFIER | c.-4374C>T| |
S241 |