| Num | GeneID | Chromosome | Position | Ref.allele | Alt.allele | Mutant type | Impacts | Amino acid change | SampleID |
|---|---|---|---|---|---|---|---|---|---|
| 1 | BAA09g13490 | A09 | 7733451 | G | A | stop_gained | HIGH | c.1174C>T|p.Gln392* |
S47 |
| 2 | BAA09g13490 | A09 | 7735573 | C | T | missense_variant | MODERATE | c.512G>A|p.Gly171Asp |
S6 |
| 3 | BAA09g13490 | A09 | 7735685 | G | A | synonymous_variant | LOW | c.483C>T|p.Leu161Leu |
S198 |
| 4 | BAA09g13490 | A09 | 7736986 | C | T | splice_acceptor_variant&intron_variant | HIGH | c.55-1G>A| |
S43 |
| 5 | BAA09g13490 | A09 | 7737526 | C | T | upstream_gene_variant | MODIFIER | c.-345G>A| |
S95 |
| 6 | BAA09g13490 | A09 | 7738447 | C | T | upstream_gene_variant | MODIFIER | c.-1266G>A| |
S140 |
| 7 | BAA09g13490 | A09 | 7738554 | C | T | upstream_gene_variant | MODIFIER | c.-1373G>A| |
S232 |
| 8 | BAA09g13490 | A09 | 7739180 | C | T | upstream_gene_variant | MODIFIER | c.-1999G>A| |
S279 |
| 9 | BAA09g13490 | A09 | 7741839 | C | T | upstream_gene_variant | MODIFIER | c.-4658G>A| |
S292 |