| Num | GeneID | Chromosome | Position | Ref.allele | Alt.allele | Mutant type | Impacts | Amino acid change | SampleID |
|---|---|---|---|---|---|---|---|---|---|
| 1 | BAA03g55620 | A03 | 27449664 | C | T | upstream_gene_variant | MODIFIER | c.-3901C>T| |
S180 |
| 2 | BAA03g55620 | A03 | 27450278 | G | A | upstream_gene_variant | MODIFIER | c.-3287G>A| |
S291 |
| 3 | BAA03g55620 | A03 | 27451059 | C | A | upstream_gene_variant | MODIFIER | c.-2506C>A| |
S246 |
| 4 | BAA03g55620 | A03 | 27451526 | G | A | upstream_gene_variant | MODIFIER | c.-2039G>A| |
S196 |
| 5 | BAA03g55620 | A03 | 27451727 | G | A | upstream_gene_variant | MODIFIER | c.-1838G>A| |
S17 |
| 6 | BAA03g55620 | A03 | 27453217 | C | T | upstream_gene_variant | MODIFIER | c.-348C>T| |
S183 S198 |
| 7 | BAA03g55620 | A03 | 27453787 | C | T | missense_variant | MODERATE | c.223C>T|p.Pro75Ser |
S273 |
| 8 | BAA03g55620 | A03 | 27454146 | C | T | missense_variant | MODERATE | c.436C>T|p.Pro146Ser |
S132 S137 S215 S237 |
| 9 | BAA03g55620 | A03 | 27454266 | G | A | missense_variant | MODERATE | c.556G>A|p.Glu186Lys |
S291 |
| 10 | BAA03g55620 | A03 | 27455337 | G | A | missense_variant | MODERATE | c.1298G>A|p.Gly433Glu |
S69 |
| 11 | BAA03g55620 | A03 | 27455927 | G | A | downstream_gene_variant | MODIFIER | c.*49G>A| |
S34 |
| 12 | BAA03g55620 | A03 | 27456558 | C | T | downstream_gene_variant | MODIFIER | c.*680C>T| |
S8 |
| 13 | BAA03g55620 | A03 | 27456977 | C | T | downstream_gene_variant | MODIFIER | c.*1099C>T| |
S107 |
| 14 | BAA03g55620 | A03 | 27457532 | G | A | downstream_gene_variant | MODIFIER | c.*1654G>A| |
S28 |
| 15 | BAA03g55620 | A03 | 27457547 | C | T | downstream_gene_variant | MODIFIER | c.*1669C>T| |
S126 |
| 16 | BAA03g55620 | A03 | 27457938 | C | T | downstream_gene_variant | MODIFIER | c.*2060C>T| |
S34 |
| 17 | BAA03g55620 | A03 | 27458648 | G | A | downstream_gene_variant | MODIFIER | c.*2770G>A| |
S268 |