| Num | GeneID | Chromosome | Position | Ref.allele | Alt.allele | Mutant type | Impacts | Amino acid change | SampleID |
|---|---|---|---|---|---|---|---|---|---|
| 43751 | BAA01g26740 | A01 | 15028988 | C | T | downstream_gene_variant | MODIFIER | c.*1517C>T| |
S206 S26 |
| 43752 | BAA01g26740 | A01 | 15029044 | G | A | downstream_gene_variant | MODIFIER | c.*1573G>A| |
S68 |
| 43753 | BAA01g26740 | A01 | 15029403 | C | T | downstream_gene_variant | MODIFIER | c.*1932C>T| |
S302 |
| 43754 | BAA01g26740 | A01 | 15029598 | G | A | downstream_gene_variant | MODIFIER | c.*2127G>A| |
S100 S219 |
| 43755 | BAA01g26740 | A01 | 15030440 | C | T | downstream_gene_variant | MODIFIER | c.*2969C>T| |
S184 |
| 43756 | BAA01g26740 | A01 | 15030684 | G | A | downstream_gene_variant | MODIFIER | c.*3213G>A| |
S97 |
| 43757 | BAA01g26740 | A01 | 15031365 | C | T | downstream_gene_variant | MODIFIER | c.*3894C>T| |
S146 |
| 43758 | BAA01g26740 | A01 | 15031667 | C | T | downstream_gene_variant | MODIFIER | c.*4196C>T| |
S148 S30 S31 |
| 43759 | BAA01g26740 | A01 | 15031805 | C | T | downstream_gene_variant | MODIFIER | c.*4334C>T| |
S61 |
| 43760 | BAA01g26740 | A01 | 15032059 | C | T | downstream_gene_variant | MODIFIER | c.*4588C>T| |
S232 |
| 43761 | BAA01g26740 | A01 | 15032369 | A | T | downstream_gene_variant | MODIFIER | c.*4898A>T| |
S8 |
| 43762 | BAA01g26750 | A01 | 15032787 | C | T | downstream_gene_variant | MODIFIER | c.*686G>A| |
S36 |
| 43763 | BAA01g26750 | A01 | 15032932 | G | A | downstream_gene_variant | MODIFIER | c.*541C>T| |
S60 |
| 43764 | BAA01g26750 | A01 | 15033407 | G | A | downstream_gene_variant | MODIFIER | c.*66C>T| |
S74 |
| 43765 | BAA01g26750 | A01 | 15033412 | C | T | downstream_gene_variant | MODIFIER | c.*61G>A| |
S155 S211 |
| 43766 | BAA01g26750 | A01 | 15033672 | C | T | missense_variant | MODERATE | c.1049G>A|p.Cys350Tyr |
S174 S241 S27 S39 |
| 43767 | BAA01g26750 | A01 | 15034572 | C | T | missense_variant | MODERATE | c.499G>A|p.Val167Ile |
S125 |
| 43768 | BAA01g26750 | A01 | 15035665 | G | A | upstream_gene_variant | MODIFIER | c.-595C>T| |
S291 |
| 43769 | BAA01g26760 | A01 | 15036661 | C | T | missense_variant | MODERATE | c.952G>A|p.Glu318Lys |
S256 |
| 43770 | BAA01g26760 | A01 | 15037093 | G | A | missense_variant | MODERATE | c.520C>T|p.Pro174Ser |
S74 |
| 43771 | BAA01g26750 | A01 | 15037181 | G | A | upstream_gene_variant | MODIFIER | c.-2111C>T| |
S15 S2 S3 S34 S4 S6 |
| 43772 | BAA01g26750 | A01 | 15037290 | G | A | upstream_gene_variant | MODIFIER | c.-2220C>T| |
S228 |
| 43773 | BAA01g26750 | A01 | 15037315 | G | A | upstream_gene_variant | MODIFIER | c.-2245C>T| |
S187 |
| 43774 | BAA01g26750 | A01 | 15037430 | G | A | upstream_gene_variant | MODIFIER | c.-2360C>T| |
S178 |
| 43775 | BAA01g26760 | A01 | 15037561 | C | T | missense_variant | MODERATE | c.363G>A|p.Met121Ile |
S267 |