| Num | GeneID | Chromosome | Position | Ref.allele | Alt.allele | Mutant type | Impacts | Amino acid change | SampleID |
|---|---|---|---|---|---|---|---|---|---|
| 1 | BAA10g19660 | A10 | 17964517 | C | T | downstream_gene_variant | MODIFIER | c.*4689G>A| |
S54 |
| 2 | BAA10g19660 | A10 | 17964876 | C | T | downstream_gene_variant | MODIFIER | c.*4330G>A| |
S157 S163 |
| 3 | BAA10g19660 | A10 | 17965422 | G | A | downstream_gene_variant | MODIFIER | c.*3784C>T| |
S1 S90 |
| 4 | BAA10g19660 | A10 | 17965550 | G | A | downstream_gene_variant | MODIFIER | c.*3656C>T| |
S118 |
| 5 | BAA10g19660 | A10 | 17969413 | C | T | synonymous_variant | LOW | c.1518G>A|p.Leu506Leu |
S183 |
| 6 | BAA10g19660 | A10 | 17969544 | C | T | missense_variant | MODERATE | c.1387G>A|p.Glu463Lys |
S169 |
| 7 | BAA10g19660 | A10 | 17969893 | G | A | synonymous_variant | LOW | c.1038C>T|p.Asn346Asn |
S88 |
| 8 | BAA10g19660 | A10 | 17972688 | C | T | stop_gained | HIGH | c.18G>A|p.Trp6* |
S119 |