| Num | GeneID | Chromosome | Position | Ref.allele | Alt.allele | Mutant type | Impacts | Amino acid change | SampleID |
|---|---|---|---|---|---|---|---|---|---|
| 1 | BAA02g29740 | A02 | 17060213 | C | A | stop_gained | HIGH | c.1240G>T|p.Glu414* |
S14 |
| 2 | BAA02g29740 | A02 | 17060265 | C | T | splice_acceptor_variant&intron_variant | HIGH | c.1189-1G>A| |
S76 |
| 3 | BAA02g29740 | A02 | 17060982 | C | T | missense_variant | MODERATE | c.622G>A|p.Asp208Asn |
S92 |
| 4 | BAA02g29740 | A02 | 17061071 | G | A | missense_variant | MODERATE | c.533C>T|p.Ser178Phe |
S17 S95 |
| 5 | BAA02g29740 | A02 | 17062511 | G | A | upstream_gene_variant | MODIFIER | c.-908C>T| |
S259 |
| 6 | BAA02g29740 | A02 | 17062886 | C | T | upstream_gene_variant | MODIFIER | c.-1283G>A| |
S131 |
| 7 | BAA02g29740 | A02 | 17064821 | G | A | upstream_gene_variant | MODIFIER | c.-3218C>T| |
S149 |
| 8 | BAA02g29740 | A02 | 17065528 | G | A | upstream_gene_variant | MODIFIER | c.-3925C>T| |
S36 |
| 9 | BAA02g29740 | A02 | 17065597 | G | A | upstream_gene_variant | MODIFIER | c.-3994C>T| |
S260 |
| 10 | BAA02g29740 | A02 | 17066368 | G | A | upstream_gene_variant | MODIFIER | c.-4765C>T| |
S150 |
| 11 | BAA02g29740 | A02 | 17066435 | C | T | upstream_gene_variant | MODIFIER | c.-4832G>A| |
S2 |