| Num | GeneID | Chromosome | Position | Ref.allele | Alt.allele | Mutant type | Impacts | Amino acid change | SampleID |
|---|---|---|---|---|---|---|---|---|---|
| 1 | BAA02g18440 | A02 | 9407770 | A | C | missense_variant | MODERATE | c.622T>G|p.Ser208Ala |
S5 |
| 2 | BAA02g18440 | A02 | 9407780 | G | A | synonymous_variant | LOW | c.612C>T|p.Cys204Cys |
S5 |
| 3 | BAA02g18440 | A02 | 9407789 | G | A | synonymous_variant | LOW | c.603C>T|p.Asp201Asp |
S5 |
| 4 | BAA02g18440 | A02 | 9407803 | C | T | missense_variant | MODERATE | c.589G>A|p.Val197Ile |
S5 |
| 5 | BAA02g18440 | A02 | 9407807 | A | T | missense_variant | MODERATE | c.585T>A|p.His195Gln |
S5 |
| 6 | BAA02g18440 | A02 | 9407887 | C | T | missense_variant | MODERATE | c.505G>A|p.Ala169Thr |
S163 |
| 7 | BAA02g18440 | A02 | 9408092 | G | A | synonymous_variant | LOW | c.300C>T|p.Asp100Asp |
S136 |
| 8 | BAA02g18440 | A02 | 9408268 | C | T | missense_variant | MODERATE | c.124G>A|p.Asp42Asn |
S242 |