| Num | GeneID | Chromosome | Position | Ref.allele | Alt.allele | Mutant type | Impacts | Amino acid change | SampleID |
|---|---|---|---|---|---|---|---|---|---|
| 1 | BAA01g46500 | A01 | 30997970 | C | T | missense_variant | MODERATE | c.86C>T|p.Ser29Phe |
S89 |
| 2 | BAA01g46500 | A01 | 30998025 | C | T | synonymous_variant | LOW | c.141C>T|p.Phe47Phe |
S159 S188 S298 |
| 3 | BAA01g46500 | A01 | 30998190 | C | T | synonymous_variant | LOW | c.306C>T|p.His102His |
S197 |
| 4 | BAA01g46500 | A01 | 30998660 | G | A | missense_variant | MODERATE | c.776G>A|p.Arg259Lys |
S127 |
| 5 | BAA01g46500 | A01 | 30998906 | C | T | missense_variant | MODERATE | c.1022C>T|p.Ser341Phe |
S181 |
| 6 | BAA01g46500 | A01 | 30999106 | G | A | missense_variant | MODERATE | c.1222G>A|p.Glu408Lys |
S166 |
| 7 | BAA01g46500 | A01 | 30999133 | G | A | missense_variant | MODERATE | c.1249G>A|p.Glu417Lys |
S274 |
| 8 | BAA01g46500 | A01 | 30999318 | G | A | synonymous_variant | LOW | c.1434G>A|p.Gly478Gly |
S249 |