| Num | GeneID | Chromosome | Position | Ref.allele | Alt.allele | Mutant type | Impacts | Amino acid change | SampleID |
|---|---|---|---|---|---|---|---|---|---|
| 1 | BAA02g44450 | A02 | 36608568 | T | G | synonymous_variant | LOW | c.951A>C|p.Gly317Gly |
S225 |
| 2 | BAA02g44450 | A02 | 36608658 | G | A | synonymous_variant | LOW | c.861C>T|p.Tyr287Tyr |
S168 |
| 3 | BAA02g44450 | A02 | 36609022 | C | T | missense_variant | MODERATE | c.710G>A|p.Ser237Asn |
S180 |
| 4 | BAA02g44450 | A02 | 36609176 | G | A | missense_variant | MODERATE | c.556C>T|p.Leu186Phe |
S53 |
| 5 | BAA02g44450 | A02 | 36609220 | A | C | missense_variant | MODERATE | c.512T>G|p.Val171Gly |
S143 S204 S297 S44 |
| 6 | BAA02g44450 | A02 | 36609885 | G | A | missense_variant | MODERATE | c.70C>T|p.Pro24Ser |
S146 |
| 7 | BAA02g44450 | A02 | 36610044 | G | A | upstream_gene_variant | MODIFIER | c.-90C>T| |
S8 |