| Num | GeneID | Chromosome | Position | Ref.allele | Alt.allele | Mutant type | Impacts | Amino acid change | SampleID |
|---|---|---|---|---|---|---|---|---|---|
| 1 | BAA09g28950 | A09 | 19106199 | G | A | downstream_gene_variant | MODIFIER | c.*3528C>T| |
S232 |
| 2 | BAA09g28950 | A09 | 19106566 | C | T | downstream_gene_variant | MODIFIER | c.*3161G>A| |
S211 S227 |
| 3 | BAA09g28950 | A09 | 19109691 | C | T | downstream_gene_variant | MODIFIER | c.*36G>A| |
S30 S31 |
| 4 | BAA09g28950 | A09 | 19109722 | G | A | downstream_gene_variant | MODIFIER | c.*5C>T| |
S69 |
| 5 | BAA09g28950 | A09 | 19109855 | C | T | missense_variant | MODERATE | c.1249G>A|p.Gly417Ser |
S117 |
| 6 | BAA09g28950 | A09 | 19111166 | G | A | missense_variant | MODERATE | c.811C>T|p.His271Tyr |
S130 |
| 7 | BAA09g28950 | A09 | 19111479 | C | T | splice_region_variant&intron_variant | LOW | c.635-4G>A| |
S183 S198 |
| 8 | BAA09g28950 | A09 | 19114503 | G | A | upstream_gene_variant | MODIFIER | c.-1816C>T| |
S225 |
| 9 | BAA09g28950 | A09 | 19116278 | C | T | upstream_gene_variant | MODIFIER | c.-3591G>A| |
S28 |