| Num | GeneID | Chromosome | Position | Ref.allele | Alt.allele | Mutant type | Impacts | Amino acid change | SampleID |
|---|---|---|---|---|---|---|---|---|---|
| 1 | BAA10g00780 | A10 | 368083 | G | A | upstream_gene_variant | MODIFIER | c.-4953G>A| |
S192 |
| 2 | BAA10g00780 | A10 | 370068 | T | C | upstream_gene_variant | MODIFIER | c.-2968T>C| |
S189 |
| 3 | BAA10g00780 | A10 | 372139 | C | T | upstream_gene_variant | MODIFIER | c.-897C>T| |
S95 |
| 4 | BAA10g00780 | A10 | 372395 | G | A | upstream_gene_variant | MODIFIER | c.-641G>A| |
S148 S210 S30 |
| 5 | BAA10g00780 | A10 | 373102 | G | A | missense_variant | MODERATE | c.67G>A|p.Asp23Asn |
S69 |
| 6 | BAA10g00780 | A10 | 374133 | G | A | synonymous_variant | LOW | c.1098G>A|p.Glu366Glu |
S150 |
| 7 | BAA10g00780 | A10 | 374244 | G | A | synonymous_variant | LOW | c.1209G>A|p.Lys403Lys |
S276 |
| 8 | BAA10g00780 | A10 | 374433 | G | A | stop_gained | HIGH | c.1398G>A|p.Trp466* |
S20 |
| 9 | BAA10g00780 | A10 | 375077 | T | C | downstream_gene_variant | MODIFIER | c.*452T>C| |
S286 |
| 10 | BAA10g00780 | A10 | 375114 | C | T | downstream_gene_variant | MODIFIER | c.*489C>T| |
S171 |