| Num | GeneID | Chromosome | Position | Ref.allele | Alt.allele | Mutant type | Impacts | Amino acid change | SampleID |
|---|---|---|---|---|---|---|---|---|---|
| 1 | BAA10g10010 | A10 | 11807004 | C | T | upstream_gene_variant | MODIFIER | c.-4669C>T| |
S124 |
| 2 | BAA10g10010 | A10 | 11807685 | G | A | upstream_gene_variant | MODIFIER | c.-3988G>A| |
S198 |
| 3 | BAA10g10010 | A10 | 11807839 | C | T | upstream_gene_variant | MODIFIER | c.-3834C>T| |
S244 |
| 4 | BAA10g10010 | A10 | 11807938 | C | T | upstream_gene_variant | MODIFIER | c.-3735C>T| |
S10 |
| 5 | BAA10g10010 | A10 | 11808037 | C | T | upstream_gene_variant | MODIFIER | c.-3636C>T| |
S11 |
| 6 | BAA10g10010 | A10 | 11808168 | G | A | upstream_gene_variant | MODIFIER | c.-3505G>A| |
S1 S90 |
| 7 | BAA10g10010 | A10 | 11808445 | C | T | upstream_gene_variant | MODIFIER | c.-3228C>T| |
S249 |
| 8 | BAA10g10010 | A10 | 11808655 | C | T | upstream_gene_variant | MODIFIER | c.-3018C>T| |
S298 |
| 9 | BAA10g10010 | A10 | 11808835 | C | T | upstream_gene_variant | MODIFIER | c.-2838C>T| |
S149 |
| 10 | BAA10g10010 | A10 | 11808904 | C | T | upstream_gene_variant | MODIFIER | c.-2769C>T| |
S37 |
| 11 | BAA10g10010 | A10 | 11808970 | C | T | upstream_gene_variant | MODIFIER | c.-2703C>T| |
S123 |
| 12 | BAA10g10010 | A10 | 11809085 | C | T | upstream_gene_variant | MODIFIER | c.-2588C>T| |
S238 |
| 13 | BAA10g10010 | A10 | 11809117 | C | T | upstream_gene_variant | MODIFIER | c.-2556C>T| |
S224 |
| 14 | BAA10g10010 | A10 | 11809508 | C | T | upstream_gene_variant | MODIFIER | c.-2165C>T| |
S54 |
| 15 | BAA10g10010 | A10 | 11809860 | C | A | upstream_gene_variant | MODIFIER | c.-1813C>A| |
S284 |
| 16 | BAA10g10010 | A10 | 11811513 | C | T | upstream_gene_variant | MODIFIER | c.-160C>T| |
S189 |
| 17 | BAA10g10010 | A10 | 11811882 | C | T | synonymous_variant | LOW | c.210C>T|p.Thr70Thr |
S259 |
| 18 | BAA10g10010 | A10 | 11811944 | C | T | missense_variant | MODERATE | c.272C>T|p.Thr91Ile |
S17 |
| 19 | BAA10g10010 | A10 | 11812883 | C | T | downstream_gene_variant | MODIFIER | c.*878C>T| |
S10 |
| 20 | BAA10g10010 | A10 | 11814554 | G | A | downstream_gene_variant | MODIFIER | c.*2549G>A| |
S295 |