| Num | GeneID | Chromosome | Position | Ref.allele | Alt.allele | Mutant type | Impacts | Amino acid change | SampleID |
|---|---|---|---|---|---|---|---|---|---|
| 1 | BAA02g12200 | A02 | 5495801 | G | A | missense_variant | MODERATE | c.1894C>T|p.Pro632Ser |
S235 |
| 2 | BAA02g12200 | A02 | 5497053 | C | T | missense_variant | MODERATE | c.1000G>A|p.Val334Ile |
S262 |
| 3 | BAA02g12200 | A02 | 5497388 | C | T | missense_variant | MODERATE | c.665G>A|p.Gly222Asp |
S257 |
| 4 | BAA02g12200 | A02 | 5497606 | G | A | missense_variant | MODERATE | c.533C>T|p.Thr178Ile |
S173 |
| 5 | BAA02g12200 | A02 | 5498943 | C | T | splice_region_variant&intron_variant | LOW | c.102+8G>A| |
S1 S90 |
| 6 | BAA02g12200 | A02 | 5499005 | G | A | synonymous_variant | LOW | c.48C>T|p.Leu16Leu |
S80 |
| 7 | BAA02g12200 | A02 | 5502363 | C | T | upstream_gene_variant | MODIFIER | c.-3311G>A| |
S6 |