| Num | GeneID | Chromosome | Position | Ref.allele | Alt.allele | Mutant type | Impacts | Amino acid change | SampleID | 
|---|---|---|---|---|---|---|---|---|---|
| 1 | BAA07g06690 | A07 | 16038645 | G | A | missense_variant | MODERATE | c.1865C>T|p.Thr622Ile | S262 | 
| 2 | BAA07g06690 | A07 | 16039050 | G | A | missense_variant | MODERATE | c.1460C>T|p.Ala487Val | S278 | 
| 3 | BAA07g06690 | A07 | 16039374 | T | C | missense_variant | MODERATE | c.1433A>G|p.Asp478Gly | S249 | 
| 4 | BAA07g06690 | A07 | 16039378 | C | T | missense_variant | MODERATE | c.1429G>A|p.Asp477Asn | S267 | 
| 5 | BAA07g06690 | A07 | 16039527 | G | A | missense_variant | MODERATE | c.1280C>T|p.Thr427Ile | S264 | 
| 6 | BAA07g06690 | A07 | 16039578 | G | A | missense_variant | MODERATE | c.1229C>T|p.Pro410Leu | S252 S292 | 
| 7 | BAA07g06690 | A07 | 16039613 | G | A | synonymous_variant | LOW | c.1194C>T|p.Val398Val | S12 | 
| 8 | BAA07g06690 | A07 | 16040070 | G | A | synonymous_variant | LOW | c.837C>T|p.Asp279Asp | S156 | 
| 9 | BAA07g06690 | A07 | 16040183 | C | T | missense_variant | MODERATE | c.724G>A|p.Glu242Lys | S261 | 
| 10 | BAA07g06690 | A07 | 16040644 | C | T | missense_variant | MODERATE | c.263G>A|p.Gly88Asp | S11 | 
| 11 | BAA07g06690 | A07 | 16045486 | G | A | upstream_gene_variant | MODIFIER | c.-4580C>T| | S264 | 
| 12 | BAA07g06690 | A07 | 16045814 | G | A | upstream_gene_variant | MODIFIER | c.-4908C>T| | S178 |