| Num | GeneID | Chromosome | Position | Ref.allele | Alt.allele | Mutant type | Impacts | Amino acid change | SampleID |
|---|---|---|---|---|---|---|---|---|---|
| 1 | BAA01g10680 | A01 | 4905799 | G | A | upstream_gene_variant | MODIFIER | c.-4986G>A| |
S240 |
| 2 | BAA01g10680 | A01 | 4908078 | G | A | upstream_gene_variant | MODIFIER | c.-2707G>A| |
S239 |
| 3 | BAA01g10680 | A01 | 4909674 | C | T | upstream_gene_variant | MODIFIER | c.-1111C>T| |
S270 |
| 4 | BAA01g10680 | A01 | 4910724 | C | T | upstream_gene_variant | MODIFIER | c.-61C>T| |
S267 |
| 5 | BAA01g10680 | A01 | 4912193 | G | A | splice_acceptor_variant&intron_variant | HIGH | c.928-1G>A| |
S159 S243 |
| 6 | BAA01g10680 | A01 | 4912327 | G | A | missense_variant | MODERATE | c.1061G>A|p.Gly354Asp |
S33 |
| 7 | BAA01g10680 | A01 | 4912929 | C | T | synonymous_variant | LOW | c.1402C>T|p.Leu468Leu |
S53 |
| 8 | BAA01g10680 | A01 | 4916806 | G | A | downstream_gene_variant | MODIFIER | c.*3010G>A| |
S162 |
| 9 | BAA01g10680 | A01 | 4917417 | C | T | downstream_gene_variant | MODIFIER | c.*3621C>T| |
S42 |