Num | GeneID | Chromosome | Position | Ref.allele | Alt.allele | Mutant type | Impacts | Amino acid change | SampleID |
---|---|---|---|---|---|---|---|---|---|
1 | BAA01g18560 | A01 | 9095431 | C | T | stop_gained | HIGH | c.1869G>A|p.Trp623* |
S117 |
2 | BAA01g18560 | A01 | 9096483 | G | A | missense_variant | MODERATE | c.1051C>T|p.Arg351Trp |
S40 S49 |
3 | BAA01g18560 | A01 | 9096730 | C | T | synonymous_variant | LOW | c.804G>A|p.Gln268Gln |
S216 |
4 | BAA01g18560 | A01 | 9096854 | C | T | missense_variant | MODERATE | c.680G>A|p.Arg227Lys |
S302 |
5 | BAA01g18560 | A01 | 9097418 | C | T | synonymous_variant | LOW | c.330G>A|p.Arg110Arg |
S255 |
6 | BAA01g18560 | A01 | 9098655 | T | C | upstream_gene_variant | MODIFIER | c.-757A>G| |
S204 |
7 | BAA01g18560 | A01 | 9099067 | C | T | upstream_gene_variant | MODIFIER | c.-1169G>A| |
S230 |
8 | BAA01g18560 | A01 | 9100327 | C | T | upstream_gene_variant | MODIFIER | c.-2429G>A| |
S112 |
9 | BAA01g18560 | A01 | 9102548 | G | A | upstream_gene_variant | MODIFIER | c.-4650C>T| |
S162 |
10 | BAA01g18560 | A01 | 9102561 | C | T | upstream_gene_variant | MODIFIER | c.-4663G>A| |
S36 |