Num | GeneID | Chromosome | Position | Ref.allele | Alt.allele | Mutant type | Impacts | Amino acid change | SampleID |
---|---|---|---|---|---|---|---|---|---|
1 | BAA01g04000 | A01 | 1806568 | G | A | missense_variant | MODERATE | c.367C>T|p.Pro123Ser |
S67 |
2 | BAA01g04000 | A01 | 1807257 | G | A | upstream_gene_variant | MODIFIER | c.-323C>T| |
S219 |
3 | BAA01g04000 | A01 | 1807660 | C | T | upstream_gene_variant | MODIFIER | c.-726G>A| |
S58 |
4 | BAA01g04000 | A01 | 1808523 | C | T | upstream_gene_variant | MODIFIER | c.-1589G>A| |
S155 S211 |
5 | BAA01g04000 | A01 | 1810436 | C | T | upstream_gene_variant | MODIFIER | c.-3502G>A| |
S97 |
6 | BAA01g04000 | A01 | 1811926 | G | A | upstream_gene_variant | MODIFIER | c.-4992C>T| |
S129 |