| Num | GeneID | Chromosome | Position | Ref.allele | Alt.allele | Mutant type | Impacts | Amino acid change | SampleID |
|---|---|---|---|---|---|---|---|---|---|
| 1 | BAA09g57970 | A09 | 56957554 | C | T | splice_acceptor_variant&intron_variant | HIGH | c.214-1G>A| |
S183 S198 |
| 2 | BAA09g57970 | A09 | 56957790 | G | A | missense_variant | MODERATE | c.151C>T|p.Leu51Phe |
S184 |
| 3 | BAA09g57970 | A09 | 56958183 | C | T | missense_variant | MODERATE | c.62G>A|p.Gly21Glu |
S252 |
| 4 | BAA09g57970 | A09 | 56961283 | G | A | upstream_gene_variant | MODIFIER | c.-2951C>T| |
S4 |
| 5 | BAA09g57970 | A09 | 56961775 | G | A | upstream_gene_variant | MODIFIER | c.-3443C>T| |
S1 |
| 6 | BAA09g57970 | A09 | 56962256 | C | T | upstream_gene_variant | MODIFIER | c.-3924G>A| |
S120 |