| Num | GeneID | Chromosome | Position | Ref.allele | Alt.allele | Mutant type | Impacts | Amino acid change | SampleID |
|---|---|---|---|---|---|---|---|---|---|
| 1 | BAA06g14990 | A06 | 7420810 | C | T | synonymous_variant | LOW | c.873C>T|p.Asn291Asn |
S281 |
| 2 | BAA06g14990 | A06 | 7421587 | C | T | missense_variant | MODERATE | c.1433C>T|p.Ser478Leu |
S263 |
| 3 | BAA06g14990 | A06 | 7421682 | C | T | missense_variant | MODERATE | c.1528C>T|p.Pro510Ser |
S183 S198 |
| 4 | BAA06g14990 | A06 | 7421883 | C | T | splice_region_variant&intron_variant | LOW | c.1724+5C>T| |
S267 |
| 5 | BAA06g14990 | A06 | 7422480 | G | A | synonymous_variant | LOW | c.1917G>A|p.Leu639Leu |
S240 |
| 6 | BAA06g14990 | A06 | 7422509 | C | T | missense_variant | MODERATE | c.1946C>T|p.Ser649Phe |
S115 |
| 7 | BAA06g14990 | A06 | 7422517 | G | A | missense_variant | MODERATE | c.1954G>A|p.Glu652Lys |
S177 |
| 8 | BAA06g14990 | A06 | 7424016 | C | T | synonymous_variant | LOW | c.2571C>T|p.Val857Val |
S63 |