| Num | GeneID | Chromosome | Position | Ref.allele | Alt.allele | Mutant type | Impacts | Amino acid change | SampleID |
|---|---|---|---|---|---|---|---|---|---|
| 1 | BAA10g00180 | A10 | 78791 | C | T | downstream_gene_variant | MODIFIER | c.*4920G>A| |
S152 |
| 2 | BAA10g00180 | A10 | 83829 | C | T | missense_variant | MODERATE | c.2156G>A|p.Ser719Asn |
S135 |
| 3 | BAA10g00180 | A10 | 83999 | C | T | synonymous_variant | LOW | c.1986G>A|p.Val662Val |
S23 |
| 4 | BAA10g00180 | A10 | 84159 | C | T | missense_variant | MODERATE | c.1826G>A|p.Arg609Lys |
S162 |
| 5 | BAA10g00180 | A10 | 86085 | G | A | synonymous_variant | LOW | c.156C>T|p.Ile52Ile |
S99 |
| 6 | BAA10g00180 | A10 | 88114 | G | A | upstream_gene_variant | MODIFIER | c.-1874C>T| |
S198 |