Num | GeneID | Chromosome | Position | Ref.allele | Alt.allele | Mutant type | Impacts | Amino acid change | SampleID |
---|---|---|---|---|---|---|---|---|---|
1 | BAA03g01770 | A03 | 808853 | C | T | missense_variant | MODERATE | c.827G>A|p.Gly276Asp |
S233 |
2 | BAA03g01770 | A03 | 808860 | C | T | missense_variant | MODERATE | c.820G>A|p.Ala274Thr |
S278 |
3 | BAA03g01770 | A03 | 809031 | C | T | missense_variant | MODERATE | c.649G>A|p.Gly217Arg |
S259 |
4 | BAA03g01770 | A03 | 809915 | C | T | upstream_gene_variant | MODIFIER | c.-6G>A| |
S268 |
5 | BAA03g01770 | A03 | 809998 | C | T | upstream_gene_variant | MODIFIER | c.-89G>A| |
S295 |
6 | BAA03g01770 | A03 | 810927 | C | T | upstream_gene_variant | MODIFIER | c.-1018G>A| |
S67 |