| Num | GeneID | Chromosome | Position | Ref.allele | Alt.allele | Mutant type | Impacts | Amino acid change | SampleID |
|---|---|---|---|---|---|---|---|---|---|
| 1 | BAA03g34700 | A03 | 16085511 | G | A | upstream_gene_variant | MODIFIER | c.-2942G>A| |
S269 |
| 2 | BAA03g34700 | A03 | 16086447 | G | A | upstream_gene_variant | MODIFIER | c.-2006G>A| |
S249 |
| 3 | BAA03g34700 | A03 | 16088780 | G | A | missense_variant | MODERATE | c.328G>A|p.Val110Ile |
S305 |
| 4 | BAA03g34700 | A03 | 16089427 | C | T | missense_variant | MODERATE | c.898C>T|p.His300Tyr |
S241 |
| 5 | BAA03g34700 | A03 | 16089607 | G | A | missense_variant | MODERATE | c.1078G>A|p.Gly360Ser |
S302 |
| 6 | BAA03g34700 | A03 | 16089935 | C | T | missense_variant | MODERATE | c.1406C>T|p.Thr469Ile |
S139 |
| 7 | BAA03g34700 | A03 | 16090074 | G | A | synonymous_variant | LOW | c.1545G>A|p.Val515Val |
S257 |
| 8 | BAA03g34700 | A03 | 16090419 | C | T | synonymous_variant | LOW | c.1734C>T|p.Ile578Ile |
S273 |
| 9 | BAA03g34700 | A03 | 16090453 | G | A | missense_variant | MODERATE | c.1768G>A|p.Asp590Asn |
S291 |
| 10 | BAA03g34700 | A03 | 16091141 | G | A | missense_variant | MODERATE | c.2200G>A|p.Ala734Thr |
S162 |
| 11 | BAA03g34700 | A03 | 16092679 | C | T | downstream_gene_variant | MODIFIER | c.*564C>T| |
S270 |
| 12 | BAA03g34700 | A03 | 16094428 | C | T | downstream_gene_variant | MODIFIER | c.*2313C>T| |
S57 |