| Num | GeneID | Chromosome | Position | Ref.allele | Alt.allele | Mutant type | Impacts | Amino acid change | SampleID |
|---|---|---|---|---|---|---|---|---|---|
| 1 | BAA02g04780 | A02 | 2077969 | G | A | missense_variant | MODERATE | c.877G>A|p.Asp293Asn |
S81 S85 |
| 2 | BAA02g04780 | A02 | 2078196 | C | T | synonymous_variant | LOW | c.1104C>T|p.Phe368Phe |
S13 |
| 3 | BAA02g04780 | A02 | 2078293 | C | T | missense_variant | MODERATE | c.1201C>T|p.Pro401Ser |
S306 |
| 4 | BAA02g04780 | A02 | 2078495 | C | T | missense_variant | MODERATE | c.1403C>T|p.Ala468Val |
S82 S92 |
| 5 | BAA02g04780 | A02 | 2079018 | C | T | synonymous_variant | LOW | c.1926C>T|p.Phe642Phe |
S77 S82 |
| 6 | BAA02g04780 | A02 | 2079656 | G | A | missense_variant | MODERATE | c.2564G>A|p.Arg855Lys |
S237 |
| 7 | BAA02g04780 | A02 | 2080601 | G | A | synonymous_variant | LOW | c.3183G>A|p.Gln1061Gln |
S249 |