| Num | GeneID | Chromosome | Position | Ref.allele | Alt.allele | Mutant type | Impacts | Amino acid change | SampleID |
|---|---|---|---|---|---|---|---|---|---|
| 1 | BAA02g07890 | A02 | 3396378 | C | T | missense_variant | MODERATE | c.2588G>A|p.Arg863His |
S212 |
| 2 | BAA02g07890 | A02 | 3396467 | G | A | synonymous_variant | LOW | c.2499C>T|p.Phe833Phe |
S282 |
| 3 | BAA02g07890 | A02 | 3399434 | C | T | splice_donor_variant&intron_variant | HIGH | c.1437+1G>A| |
S42 |
| 4 | BAA02g07890 | A02 | 3400328 | C | T | missense_variant | MODERATE | c.544G>A|p.Asp182Asn |
S6 |
| 5 | BAA02g07890 | A02 | 3401714 | G | A | missense_variant | MODERATE | c.377C>T|p.Ala126Val |
S271 |
| 6 | BAA02g07890 | A02 | 3405683 | C | T | upstream_gene_variant | MODIFIER | c.-3593G>A| |
S299 |