| Num | GeneID | Chromosome | Position | Ref.allele | Alt.allele | Mutant type | Impacts | Amino acid change | SampleID |
|---|---|---|---|---|---|---|---|---|---|
| 1 | BAA01g01680 | A01 | 742534 | G | A | missense_variant | MODERATE | c.1280C>T|p.Thr427Met |
S138 |
| 2 | BAA01g01680 | A01 | 742710 | C | T | synonymous_variant | LOW | c.1104G>A|p.Thr368Thr |
S53 |
| 3 | BAA01g01680 | A01 | 742776 | G | A | synonymous_variant | LOW | c.1038C>T|p.Leu346Leu |
S276 |
| 4 | BAA01g01680 | A01 | 743620 | C | T | missense_variant | MODERATE | c.442G>A|p.Glu148Lys |
S139 |
| 5 | BAA01g01680 | A01 | 743687 | G | A | synonymous_variant | LOW | c.375C>T|p.Leu125Leu |
S308 |
| 6 | BAA01g01680 | A01 | 744049 | C | T | missense_variant | MODERATE | c.13G>A|p.Val5Met |
S277 |
| 7 | BAA01g01680 | A01 | 747343 | C | T | upstream_gene_variant | MODIFIER | c.-3282G>A| |
S155 S211 |
| 8 | BAA01g01680 | A01 | 748187 | C | T | upstream_gene_variant | MODIFIER | c.-4126G>A| |
S164 |