| Num | GeneID | Chromosome | Position | Ref.allele | Alt.allele | Mutant type | Impacts | Amino acid change | SampleID |
|---|---|---|---|---|---|---|---|---|---|
| 1 | BAA02g00450 | A02 | 246650 | G | A | upstream_gene_variant | MODIFIER | c.-2103G>A| |
S5 |
| 2 | BAA02g00450 | A02 | 246869 | C | T | upstream_gene_variant | MODIFIER | c.-1884C>T| |
S6 |
| 3 | BAA02g00450 | A02 | 247520 | G | A | upstream_gene_variant | MODIFIER | c.-1233G>A| |
S249 |
| 4 | BAA02g00450 | A02 | 247543 | C | T | upstream_gene_variant | MODIFIER | c.-1210C>T| |
S186 |
| 5 | BAA02g00450 | A02 | 247787 | G | A | upstream_gene_variant | MODIFIER | c.-966G>A| |
S206 S26 |
| 6 | BAA02g00450 | A02 | 247891 | G | A | upstream_gene_variant | MODIFIER | c.-862G>A| |
S151 S153 S257 S262 S263 |
| 7 | BAA02g00450 | A02 | 248919 | C | T | missense_variant | MODERATE | c.85C>T|p.Leu29Phe |
S185 |
| 8 | BAA02g00450 | A02 | 249300 | G | A | missense_variant | MODERATE | c.275G>A|p.Gly92Asp |
S33 |
| 9 | BAA02g00450 | A02 | 251623 | G | A | downstream_gene_variant | MODIFIER | c.*1479G>A| |
S25 |