| Num | GeneID | Chromosome | Position | Ref.allele | Alt.allele | Mutant type | Impacts | Amino acid change | SampleID |
|---|---|---|---|---|---|---|---|---|---|
| 1 | BAA06g26760 | A06 | 18377954 | C | T | upstream_gene_variant | MODIFIER | c.-4967C>T| |
S289 S290 |
| 2 | BAA06g26760 | A06 | 18378592 | G | A | upstream_gene_variant | MODIFIER | c.-4329G>A| |
S251 |
| 3 | BAA06g26760 | A06 | 18378989 | C | T | upstream_gene_variant | MODIFIER | c.-3932C>T| |
S278 |
| 4 | BAA06g26760 | A06 | 18379275 | G | A | upstream_gene_variant | MODIFIER | c.-3646G>A| |
S262 |
| 5 | BAA06g26760 | A06 | 18381395 | C | T | upstream_gene_variant | MODIFIER | c.-1526C>T| |
S232 |
| 6 | BAA06g26760 | A06 | 18381412 | C | T | upstream_gene_variant | MODIFIER | c.-1509C>T| |
S295 |
| 7 | BAA06g26760 | A06 | 18383106 | G | A | synonymous_variant | LOW | c.186G>A|p.Ala62Ala |
S233 |
| 8 | BAA06g26760 | A06 | 18383184 | G | A | synonymous_variant | LOW | c.264G>A|p.Gln88Gln |
S11 |
| 9 | BAA06g26760 | A06 | 18383297 | G | A | missense_variant | MODERATE | c.377G>A|p.Ser126Asn |
S219 |
| 10 | BAA06g26760 | A06 | 18384570 | G | A | missense_variant | MODERATE | c.883G>A|p.Ala295Thr |
S224 |
| 11 | BAA06g26760 | A06 | 18386701 | A | T | downstream_gene_variant | MODIFIER | c.*1880A>T| |
S277 |
| 12 | BAA06g26760 | A06 | 18387428 | C | T | downstream_gene_variant | MODIFIER | c.*2607C>T| |
S6 |
| 13 | BAA06g26760 | A06 | 18387751 | C | T | downstream_gene_variant | MODIFIER | c.*2930C>T| |
S189 |
| 14 | BAA06g26760 | A06 | 18387754 | C | T | downstream_gene_variant | MODIFIER | c.*2933C>T| |
S189 |