| Num | GeneID | Chromosome | Position | Ref.allele | Alt.allele | Mutant type | Impacts | Amino acid change | SampleID |
|---|---|---|---|---|---|---|---|---|---|
| 1 | BAA08g15770 | A08 | 13245895 | C | T | missense_variant | MODERATE | c.1661G>A|p.Ser554Asn |
S23 |
| 2 | BAA08g15770 | A08 | 13247392 | C | T | splice_acceptor_variant&intron_variant | HIGH | c.711-1G>A| |
S34 |
| 3 | BAA08g15770 | A08 | 13248107 | C | T | splice_region_variant&synonymous_variant | LOW | c.390G>A|p.Gln130Gln |
S183 S198 |
| 4 | BAA08g15770 | A08 | 13248452 | C | T | synonymous_variant | LOW | c.123G>A|p.Lys41Lys |
S159 |
| 5 | BAA08g15770 | A08 | 13249643 | C | T | upstream_gene_variant | MODIFIER | c.-1069G>A| |
S207 |