| Num | GeneID | Chromosome | Position | Ref.allele | Alt.allele | Mutant type | Impacts | Amino acid change | SampleID |
|---|---|---|---|---|---|---|---|---|---|
| 1 | BAA02g18600 | A02 | 9531273 | C | T | missense_variant | MODERATE | c.406G>A|p.Gly136Ser |
S135 |
| 2 | BAA02g18600 | A02 | 9531301 | G | A | synonymous_variant | LOW | c.378C>T|p.Leu126Leu |
S191 |
| 3 | BAA02g18600 | A02 | 9531478 | G | A | synonymous_variant | LOW | c.201C>T|p.Leu67Leu |
S166 |
| 4 | BAA02g18600 | A02 | 9531584 | C | T | missense_variant | MODERATE | c.95G>A|p.Gly32Glu |
S277 |
| 5 | BAA02g18600 | A02 | 9531655 | C | T | splice_region_variant&intron_variant | LOW | c.27-3G>A| |
S124 |
| 6 | BAA02g18600 | A02 | 9532028 | C | T | missense_variant&splice_region_variant | MODERATE | c.26G>A|p.Ser9Asn |
S165 |
| 7 | BAA02g18600 | A02 | 9535799 | C | T | upstream_gene_variant | MODIFIER | c.-3746G>A| |
S255 |
| 8 | BAA02g18600 | A02 | 9536827 | C | T | upstream_gene_variant | MODIFIER | c.-4774G>A| |
S55 |