| Num | GeneID | Chromosome | Position | Ref.allele | Alt.allele | Mutant type | Impacts | Amino acid change | SampleID |
|---|---|---|---|---|---|---|---|---|---|
| 1 | BAA02g36060 | A02 | 31011569 | G | A | missense_variant | MODERATE | c.1466C>T|p.Ser489Phe |
S50 |
| 2 | BAA02g36060 | A02 | 31011678 | G | A | missense_variant | MODERATE | c.1357C>T|p.Pro453Ser |
S255 |
| 3 | BAA02g36060 | A02 | 31011961 | C | T | missense_variant | MODERATE | c.1074G>A|p.Met358Ile |
S262 |
| 4 | BAA02g36060 | A02 | 31012172 | C | T | missense_variant | MODERATE | c.863G>A|p.Gly288Glu |
S263 |
| 5 | BAA02g36060 | A02 | 31015616 | G | A | upstream_gene_variant | MODIFIER | c.-1613C>T| |
S240 |
| 6 | BAA02g36060 | A02 | 31016102 | C | T | upstream_gene_variant | MODIFIER | c.-2099G>A| |
S59 |
| 7 | BAA02g36060 | A02 | 31017126 | G | A | upstream_gene_variant | MODIFIER | c.-3123C>T| |
S61 |
| 8 | BAA02g36060 | A02 | 31017149 | G | A | upstream_gene_variant | MODIFIER | c.-3146C>T| |
S146 |
| 9 | BAA02g36060 | A02 | 31018345 | C | T | upstream_gene_variant | MODIFIER | c.-4342G>A| |
S202 |