| Num | GeneID | Chromosome | Position | Ref.allele | Alt.allele | Mutant type | Impacts | Amino acid change | SampleID |
|---|---|---|---|---|---|---|---|---|---|
| 1 | BAA02g00590 | A02 | 321663 | G | A | splice_region_variant&intron_variant | LOW | c.706-8C>T| |
S9 |
| 2 | BAA02g00590 | A02 | 321907 | C | T | missense_variant | MODERATE | c.532G>A|p.Asp178Asn |
S281 |
| 3 | BAA02g00590 | A02 | 322901 | C | T | upstream_gene_variant | MODIFIER | c.-463G>A| |
S278 |
| 4 | BAA02g00590 | A02 | 323085 | C | T | upstream_gene_variant | MODIFIER | c.-647G>A| |
S18 |
| 5 | BAA02g00590 | A02 | 324833 | C | T | upstream_gene_variant | MODIFIER | c.-2395G>A| |
S38 |
| 6 | BAA02g00590 | A02 | 326130 | G | A | upstream_gene_variant | MODIFIER | c.-3692C>T| |
S20 |
| 7 | BAA02g00590 | A02 | 326341 | C | T | upstream_gene_variant | MODIFIER | c.-3903G>A| |
S243 S299 |