| Num | GeneID | Chromosome | Position | Ref.allele | Alt.allele | Mutant type | Impacts | Amino acid change | SampleID |
|---|---|---|---|---|---|---|---|---|---|
| 1 | BAA05g27980 | A05 | 32049604 | G | A | upstream_gene_variant | MODIFIER | c.-2328G>A| |
S249 |
| 2 | BAA05g27980 | A05 | 32051449 | G | A | upstream_gene_variant | MODIFIER | c.-483G>A| |
S16 |
| 3 | BAA05g27980 | A05 | 32053061 | C | T | synonymous_variant | LOW | c.477C>T|p.Ser159Ser |
S8 |
| 4 | BAA05g27980 | A05 | 32054332 | G | A | intron_variant | MODIFIER | c.711+228G>A| |
S161 |
| 5 | BAA05g27980 | A05 | 32054694 | C | T | missense_variant | MODERATE | c.722C>T|p.Ala241Val |
S164 |
| 6 | BAA05g27980 | A05 | 32054906 | C | T | splice_region_variant&intron_variant | LOW | c.822+5C>T| |
S140 |
| 7 | BAA05g27980 | A05 | 32055576 | C | T | splice_region_variant&intron_variant | LOW | c.1231-6C>T| |
S16 |
| 8 | BAA05g27980 | A05 | 32056498 | C | T | synonymous_variant | LOW | c.1644C>T|p.Asp548Asp |
S105 S106 |
| 9 | BAA05g27980 | A05 | 32057611 | C | T | missense_variant | MODERATE | c.2083C>T|p.Pro695Ser |
S117 |
| 10 | BAA05g27980 | A05 | 32059358 | C | T | splice_region_variant&intron_variant | LOW | c.2853+6C>T| |
S295 |