| Num | GeneID | Chromosome | Position | Ref.allele | Alt.allele | Mutant type | Impacts | Amino acid change | SampleID |
|---|---|---|---|---|---|---|---|---|---|
| 1 | BAA09g46880 | A09 | 51442280 | G | A | upstream_gene_variant | MODIFIER | c.-1778G>A| |
S53 |
| 2 | BAA09g46880 | A09 | 51443190 | G | A | upstream_gene_variant | MODIFIER | c.-868G>A| |
S271 |
| 3 | BAA09g46880 | A09 | 51443726 | C | T | upstream_gene_variant | MODIFIER | c.-332C>T| |
S35 |
| 4 | BAA09g46880 | A09 | 51445579 | G | A | synonymous_variant | LOW | c.645G>A|p.Glu215Glu |
S298 |
| 5 | BAA09g46880 | A09 | 51446027 | G | A | splice_acceptor_variant&intron_variant | HIGH | c.819-1G>A| |
S202 |
| 6 | BAA09g46880 | A09 | 51446380 | C | T | missense_variant | MODERATE | c.994C>T|p.Pro332Ser |
S25 |
| 7 | BAA09g46880 | A09 | 51446737 | C | T | synonymous_variant | LOW | c.1167C>T|p.Leu389Leu |
S9 |
| 8 | BAA09g46880 | A09 | 51448828 | G | A | missense_variant | MODERATE | c.2551G>A|p.Asp851Asn |
S107 |