| Num | GeneID | Chromosome | Position | Ref.allele | Alt.allele | Mutant type | Impacts | Amino acid change | SampleID |
|---|---|---|---|---|---|---|---|---|---|
| 1 | BAA10g25060 | A10 | 20406397 | C | T | synonymous_variant | LOW | c.849G>A|p.Glu283Glu |
S142 |
| 2 | BAA10g25060 | A10 | 20406500 | C | T | missense_variant&splice_region_variant | MODERATE | c.746G>A|p.Gly249Glu |
S13 S168 S219 |
| 3 | BAA10g25060 | A10 | 20407885 | C | T | upstream_gene_variant | MODIFIER | c.-109G>A| |
S235 |
| 4 | BAA10g25060 | A10 | 20409688 | G | A | upstream_gene_variant | MODIFIER | c.-1912C>T| |
S279 |
| 5 | BAA10g25060 | A10 | 20409696 | C | T | upstream_gene_variant | MODIFIER | c.-1920G>A| |
S18 |
| 6 | BAA10g25060 | A10 | 20410662 | G | A | upstream_gene_variant | MODIFIER | c.-2886C>T| |
S136 |
| 7 | BAA10g25060 | A10 | 20410781 | C | T | upstream_gene_variant | MODIFIER | c.-3005G>A| |
S116 |
| 8 | BAA10g25060 | A10 | 20410798 | C | T | upstream_gene_variant | MODIFIER | c.-3022G>A| |
S140 |
| 9 | BAA10g25060 | A10 | 20411637 | C | T | upstream_gene_variant | MODIFIER | c.-3861G>A| |
S238 |
| 10 | BAA10g25060 | A10 | 20412029 | C | T | upstream_gene_variant | MODIFIER | c.-4253G>A| |
S199 |
| 11 | BAA10g25060 | A10 | 20412250 | C | T | upstream_gene_variant | MODIFIER | c.-4474G>A| |
S215 |