| Num | GeneID | Chromosome | Position | Ref.allele | Alt.allele | Mutant type | Impacts | Amino acid change | SampleID |
|---|---|---|---|---|---|---|---|---|---|
| 1 | BAA10g26990 | A10 | 21178560 | C | T | splice_region_variant&synonymous_variant | LOW | c.783G>A|p.Pro261Pro |
S211 S227 |
| 2 | BAA10g26990 | A10 | 21178896 | C | T | synonymous_variant | LOW | c.522G>A|p.Arg174Arg |
S210 |
| 3 | BAA10g26990 | A10 | 21179518 | G | A | synonymous_variant | LOW | c.366C>T|p.Val122Val |
S85 |
| 4 | BAA10g26990 | A10 | 21180597 | G | A | upstream_gene_variant | MODIFIER | c.-537C>T| |
S150 |
| 5 | BAA10g26990 | A10 | 21180780 | G | A | upstream_gene_variant | MODIFIER | c.-720C>T| |
S271 |
| 6 | BAA10g26990 | A10 | 21181439 | C | T | upstream_gene_variant | MODIFIER | c.-1379G>A| |
S251 |
| 7 | BAA10g26990 | A10 | 21181461 | C | T | upstream_gene_variant | MODIFIER | c.-1401G>A| |
S68 |
| 8 | BAA10g26990 | A10 | 21183454 | G | A | upstream_gene_variant | MODIFIER | c.-3394C>T| |
S136 |