| Num | GeneID | Chromosome | Position | Ref.allele | Alt.allele | Mutant type | Impacts | Amino acid change | SampleID |
|---|---|---|---|---|---|---|---|---|---|
| 1 | BAA10g21050 | A10 | 18651730 | C | T | upstream_gene_variant | MODIFIER | c.-1754C>T| |
S67 |
| 2 | BAA10g21050 | A10 | 18653688 | C | T | synonymous_variant | LOW | c.129C>T|p.Leu43Leu |
S146 |
| 3 | BAA10g21050 | A10 | 18653833 | G | A | missense_variant | MODERATE | c.274G>A|p.Glu92Lys |
S71 |
| 4 | BAA10g21050 | A10 | 18653966 | C | T | missense_variant | MODERATE | c.407C>T|p.Pro136Leu |
S38 |
| 5 | BAA10g21050 | A10 | 18654171 | C | T | synonymous_variant | LOW | c.612C>T|p.Asn204Asn |
S107 |
| 6 | BAA10g21050 | A10 | 18654570 | C | T | missense_variant | MODERATE | c.935C>T|p.Ser312Leu |
S95 |
| 7 | BAA10g21050 | A10 | 18654708 | C | T | missense_variant | MODERATE | c.1073C>T|p.Pro358Leu |
S168 |
| 8 | BAA10g21050 | A10 | 18654891 | C | T | missense_variant | MODERATE | c.1256C>T|p.Ala419Val |
S305 |
| 9 | BAA10g21050 | A10 | 18656628 | C | T | missense_variant | MODERATE | c.2525C>T|p.Ser842Leu |
S189 |
| 10 | BAA10g21050 | A10 | 18657311 | G | A | synonymous_variant | LOW | c.3120G>A|p.Leu1040Leu |
S63 |
| 11 | BAA10g21050 | A10 | 18657859 | C | T | downstream_gene_variant | MODIFIER | c.*461C>T| |
S45 |
| 12 | BAA10g21050 | A10 | 18657898 | C | T | downstream_gene_variant | MODIFIER | c.*500C>T| |
S199 |