| Num | GeneID | Chromosome | Position | Ref.allele | Alt.allele | Mutant type | Impacts | Amino acid change | SampleID |
|---|---|---|---|---|---|---|---|---|---|
| 1 | BAA09g42940 | A09 | 49163261 | C | T | downstream_gene_variant | MODIFIER | c.*2814G>A| |
S256 |
| 2 | BAA09g42940 | A09 | 49163795 | C | T | downstream_gene_variant | MODIFIER | c.*2280G>A| |
S286 |
| 3 | BAA09g42940 | A09 | 49164379 | G | A | downstream_gene_variant | MODIFIER | c.*1696C>T| |
S268 |
| 4 | BAA09g42940 | A09 | 49165013 | C | T | downstream_gene_variant | MODIFIER | c.*1062G>A| |
S208 |
| 5 | BAA09g42940 | A09 | 49165096 | G | A | downstream_gene_variant | MODIFIER | c.*979C>T| |
S107 |
| 6 | BAA09g42940 | A09 | 49165761 | C | T | downstream_gene_variant | MODIFIER | c.*314G>A| |
S213 |
| 7 | BAA09g42940 | A09 | 49165838 | G | A | downstream_gene_variant | MODIFIER | c.*237C>T| |
S221 |
| 8 | BAA09g42940 | A09 | 49165923 | C | T | downstream_gene_variant | MODIFIER | c.*152G>A| |
S269 |
| 9 | BAA09g42940 | A09 | 49165965 | G | A | downstream_gene_variant | MODIFIER | c.*110C>T| |
S105 S106 |
| 10 | BAA09g42940 | A09 | 49166218 | G | A | missense_variant | MODERATE | c.832C>T|p.Leu278Phe |
S189 |
| 11 | BAA09g42940 | A09 | 49166833 | C | T | missense_variant | MODERATE | c.217G>A|p.Gly73Arg |
S280 |
| 12 | BAA09g42940 | A09 | 49167511 | C | T | upstream_gene_variant | MODIFIER | c.-462G>A| |
S43 |
| 13 | BAA09g42940 | A09 | 49168146 | C | T | upstream_gene_variant | MODIFIER | c.-1097G>A| |
S139 |
| 14 | BAA09g42940 | A09 | 49169363 | C | T | upstream_gene_variant | MODIFIER | c.-2314G>A| |
S117 |
| 15 | BAA09g42940 | A09 | 49171985 | C | T | upstream_gene_variant | MODIFIER | c.-4936G>A| |
S9 |