Num | GeneID | Chromosome | Position | Ref.allele | Alt.allele | Mutant type | Impacts | Amino acid change | SampleID |
---|---|---|---|---|---|---|---|---|---|
1 | BAA04g00980 | A04 | 578045 | C | T | upstream_gene_variant | MODIFIER | c.-557C>T| |
S74 |
2 | BAA04g00980 | A04 | 578317 | C | T | upstream_gene_variant | MODIFIER | c.-285C>T| |
S41 |
3 | BAA04g00980 | A04 | 578756 | C | T | missense_variant | MODERATE | c.155C>T|p.Thr52Ile |
S294 |
4 | BAA04g00980 | A04 | 579256 | G | A | missense_variant | MODERATE | c.655G>A|p.Gly219Ser |
S205 |