| Num | GeneID | Chromosome | Position | Ref.allele | Alt.allele | Mutant type | Impacts | Amino acid change | SampleID |
|---|---|---|---|---|---|---|---|---|---|
| 1 | BAA03g16400 | A03 | 7055053 | G | A | missense_variant | MODERATE | c.223G>A|p.Gly75Ser |
S68 |
| 2 | BAA03g16400 | A03 | 7055235 | G | A | missense_variant | MODERATE | c.405G>A|p.Met135Ile |
S231 |
| 3 | BAA03g16400 | A03 | 7056274 | G | A | missense_variant | MODERATE | c.1444G>A|p.Gly482Ser |
S135 |
| 4 | BAA03g16400 | A03 | 7056698 | G | A | missense_variant | MODERATE | c.1868G>A|p.Gly623Glu |
S16 |
| 5 | BAA03g16400 | A03 | 7056716 | G | A | missense_variant | MODERATE | c.1886G>A|p.Ser629Asn |
S169 |
| 6 | BAA03g16400 | A03 | 7056830 | C | T | missense_variant | MODERATE | c.2000C>T|p.Pro667Leu |
S81 S85 |
| 7 | BAA03g16400 | A03 | 7056915 | C | T | synonymous_variant | LOW | c.2085C>T|p.His695His |
S159 S243 |
| 8 | BAA03g16400 | A03 | 7060686 | C | T | downstream_gene_variant | MODIFIER | c.*3591C>T| |
S18 |