| Num | GeneID | Chromosome | Position | Ref.allele | Alt.allele | Mutant type | Impacts | Amino acid change | SampleID |
|---|---|---|---|---|---|---|---|---|---|
| 1 | BAA10g20770 | A10 | 18526165 | C | T | missense_variant | MODERATE | c.7C>T|p.Pro3Ser |
S201 |
| 2 | BAA10g20770 | A10 | 18526585 | C | T | synonymous_variant | LOW | c.213C>T|p.Asn71Asn |
S54 |
| 3 | BAA10g20770 | A10 | 18526908 | C | T | synonymous_variant | LOW | c.448C>T|p.Leu150Leu |
S169 |
| 4 | BAA10g20770 | A10 | 18526935 | G | A | missense_variant | MODERATE | c.475G>A|p.Asp159Asn |
S286 |
| 5 | BAA10g20770 | A10 | 18527106 | G | A | synonymous_variant | LOW | c.522G>A|p.Gln174Gln |
S74 |
| 6 | BAA10g20770 | A10 | 18528008 | G | A | missense_variant | MODERATE | c.832G>A|p.Gly278Arg |
S278 |
| 7 | BAA10g20770 | A10 | 18528588 | G | A | downstream_gene_variant | MODIFIER | c.*68G>A| |
S293 |
| 8 | BAA10g20770 | A10 | 18528898 | T | C | downstream_gene_variant | MODIFIER | c.*378T>C| |
S119 |