| Num | GeneID | Chromosome | Position | Ref.allele | Alt.allele | Mutant type | Impacts | Amino acid change | SampleID |
|---|---|---|---|---|---|---|---|---|---|
| 1 | BAA09g10460 | A09 | 5719291 | C | T | upstream_gene_variant | MODIFIER | c.-4523C>T| |
S298 |
| 2 | BAA09g10460 | A09 | 5720322 | G | A | upstream_gene_variant | MODIFIER | c.-3492G>A| |
S115 |
| 3 | BAA09g10460 | A09 | 5720660 | G | A | upstream_gene_variant | MODIFIER | c.-3154G>A| |
S46 |
| 4 | BAA09g10460 | A09 | 5721623 | G | A | upstream_gene_variant | MODIFIER | c.-2191G>A| |
S105 S106 |
| 5 | BAA09g10460 | A09 | 5723182 | C | T | upstream_gene_variant | MODIFIER | c.-632C>T| |
S206 S26 |
| 6 | BAA09g10460 | A09 | 5724292 | G | A | missense_variant | MODERATE | c.403G>A|p.Gly135Arg |
S73 S91 |
| 7 | BAA09g10460 | A09 | 5724769 | G | A | synonymous_variant | LOW | c.711G>A|p.Pro237Pro |
S190 |
| 8 | BAA09g10460 | A09 | 5724842 | G | A | missense_variant | MODERATE | c.784G>A|p.Val262Met |
S245 |
| 9 | BAA09g10460 | A09 | 5725239 | C | T | synonymous_variant | LOW | c.1020C>T|p.Leu340Leu |
S5 |