| Num | GeneID | Chromosome | Position | Ref.allele | Alt.allele | Mutant type | Impacts | Amino acid change | SampleID |
|---|---|---|---|---|---|---|---|---|---|
| 1 | BAA01g41140 | A01 | 27366885 | C | T | missense_variant | MODERATE | c.724G>A|p.Gly242Arg |
S251 |
| 2 | BAA01g41140 | A01 | 27367392 | C | T | missense_variant | MODERATE | c.283G>A|p.Asp95Asn |
S92 |
| 3 | BAA01g41140 | A01 | 27367650 | C | T | splice_acceptor_variant&intron_variant | HIGH | c.26-1G>A| |
S233 |
| 4 | BAA01g41140 | A01 | 27371233 | G | A | upstream_gene_variant | MODIFIER | c.-3179C>T| |
S245 |
| 5 | BAA01g41140 | A01 | 27371468 | G | A | upstream_gene_variant | MODIFIER | c.-3414C>T| |
S209 |
| 6 | BAA01g41140 | A01 | 27371635 | G | A | upstream_gene_variant | MODIFIER | c.-3581C>T| |
S268 |
| 7 | BAA01g41140 | A01 | 27372274 | G | A | upstream_gene_variant | MODIFIER | c.-4220C>T| |
S218 |
| 8 | BAA01g41140 | A01 | 27372459 | C | T | upstream_gene_variant | MODIFIER | c.-4405G>A| |
S269 |
| 9 | BAA01g41140 | A01 | 27373027 | C | T | upstream_gene_variant | MODIFIER | c.-4973G>A| |
S78 |