| Num | GeneID | Chromosome | Position | Ref.allele | Alt.allele | Mutant type | Impacts | Amino acid change | SampleID |
|---|---|---|---|---|---|---|---|---|---|
| 1 | BAA03g26900 | A03 | 12396397 | C | T | upstream_gene_variant | MODIFIER | c.-868C>T| |
S266 |
| 2 | BAA03g26900 | A03 | 12396843 | C | T | upstream_gene_variant | MODIFIER | c.-422C>T| |
S131 |
| 3 | BAA03g26900 | A03 | 12397507 | C | T | splice_region_variant&intron_variant | LOW | c.157+3C>T| |
S255 |
| 4 | BAA03g26900 | A03 | 12398137 | G | A | synonymous_variant | LOW | c.342G>A|p.Arg114Arg |
S167 |
| 5 | BAA03g26900 | A03 | 12398408 | G | A | missense_variant | MODERATE | c.530G>A|p.Arg177Lys |
S162 |
| 6 | BAA03g26900 | A03 | 12399629 | G | A | splice_acceptor_variant&intron_variant | HIGH | c.1487-1G>A| |
S103 |
| 7 | BAA03g26900 | A03 | 12399659 | G | A | missense_variant | MODERATE | c.1516G>A|p.Gly506Ser |
S119 |
| 8 | BAA03g26900 | A03 | 12401333 | C | T | synonymous_variant | LOW | c.2374C>T|p.Leu792Leu |
S97 |