| Num | GeneID | Chromosome | Position | Ref.allele | Alt.allele | Mutant type | Impacts | Amino acid change | SampleID |
|---|---|---|---|---|---|---|---|---|---|
| 1 | BAA03g04200 | A03 | 1780307 | C | T | missense_variant&splice_region_variant | MODERATE | c.560C>T|p.Pro187Leu |
S136 |
| 2 | BAA03g04200 | A03 | 1780397 | G | A | missense_variant | MODERATE | c.650G>A|p.Arg217Lys |
S246 |
| 3 | BAA03g04200 | A03 | 1780598 | G | A | synonymous_variant | LOW | c.777G>A|p.Lys259Lys |
S183 S198 |
| 4 | BAA03g04200 | A03 | 1780682 | C | T | synonymous_variant | LOW | c.861C>T|p.His287His |
S28 |
| 5 | BAA03g04200 | A03 | 1781009 | G | A | synonymous_variant | LOW | c.1188G>A|p.Ala396Ala |
S286 |
| 6 | BAA03g04200 | A03 | 1781293 | C | T | missense_variant | MODERATE | c.1394C>T|p.Ala465Val |
S240 |
| 7 | BAA03g04200 | A03 | 1782960 | C | T | synonymous_variant | LOW | c.2328C>T|p.Ile776Ile |
S223 |
| 8 | BAA03g04200 | A03 | 1782993 | G | A | stop_gained | HIGH | c.2361G>A|p.Trp787* |
S89 |
| 9 | BAA03g04200 | A03 | 1783136 | G | A | missense_variant | MODERATE | c.2504G>A|p.Gly835Asp |
S13 S168 S219 S278 S72 |
| 10 | BAA03g04200 | A03 | 1783269 | C | T | synonymous_variant | LOW | c.2637C>T|p.Val879Val |
S233 |