| Num | GeneID | Chromosome | Position | Ref.allele | Alt.allele | Mutant type | Impacts | Amino acid change | SampleID |
|---|---|---|---|---|---|---|---|---|---|
| 1 | BAA10g26590 | A10 | 21031913 | G | A | upstream_gene_variant | MODIFIER | c.-1614G>A| |
S13 |
| 2 | BAA10g26590 | A10 | 21035700 | C | T | synonymous_variant | LOW | c.1083C>T|p.Asp361Asp |
S281 |
| 3 | BAA10g26590 | A10 | 21036268 | G | A | missense_variant | MODERATE | c.1394G>A|p.Gly465Glu |
S130 |
| 4 | BAA10g26590 | A10 | 21037708 | G | A | synonymous_variant | LOW | c.2127G>A|p.Gln709Gln |
S255 |
| 5 | BAA10g26590 | A10 | 21038233 | C | T | synonymous_variant | LOW | c.2298C>T|p.Asp766Asp |
S291 |
| 6 | BAA10g26590 | A10 | 21039773 | C | T | downstream_gene_variant | MODIFIER | c.*871C>T| |
S157 S163 |
| 7 | BAA10g26590 | A10 | 21039954 | C | T | downstream_gene_variant | MODIFIER | c.*1052C>T| |
S48 |
| 8 | BAA10g26590 | A10 | 21040489 | C | T | downstream_gene_variant | MODIFIER | c.*1587C>T| |
S210 |