| Num | GeneID | Chromosome | Position | Ref.allele | Alt.allele | Mutant type | Impacts | Amino acid change | SampleID |
|---|---|---|---|---|---|---|---|---|---|
| 1 | BAA09g08770 | A09 | 4903056 | C | T | missense_variant | MODERATE | c.206C>T|p.Ser69Phe |
S193 |
| 2 | BAA09g08770 | A09 | 4903277 | G | A | splice_region_variant&intron_variant | LOW | c.343-8G>A| |
S205 |
| 3 | BAA09g08770 | A09 | 4903327 | G | A | missense_variant | MODERATE | c.385G>A|p.Asp129Asn |
S167 |
| 4 | BAA09g08770 | A09 | 4904951 | G | A | missense_variant | MODERATE | c.952G>A|p.Gly318Arg |
S125 |
| 5 | BAA09g08770 | A09 | 4905247 | G | A | missense_variant | MODERATE | c.1178G>A|p.Gly393Glu |
S146 |
| 6 | BAA09g08770 | A09 | 4908844 | C | T | downstream_gene_variant | MODIFIER | c.*3218C>T| |
S107 |
| 7 | BAA09g08770 | A09 | 4910610 | C | T | downstream_gene_variant | MODIFIER | c.*4984C>T| |
S70 |