| Num | GeneID | Chromosome | Position | Ref.allele | Alt.allele | Mutant type | Impacts | Amino acid change | SampleID |
|---|---|---|---|---|---|---|---|---|---|
| 1 | BAA05g05790 | A05 | 2801703 | G | A | synonymous_variant | LOW | c.126G>A|p.Leu42Leu |
S230 |
| 2 | BAA05g05790 | A05 | 2802175 | G | A | missense_variant | MODERATE | c.434G>A|p.Gly145Glu |
S112 |
| 3 | BAA05g05790 | A05 | 2802248 | C | T | splice_region_variant&synonymous_variant | LOW | c.507C>T|p.Ser169Ser |
S15 S3 |
| 4 | BAA05g05790 | A05 | 2802610 | C | T | synonymous_variant | LOW | c.715C>T|p.Leu239Leu |
S174 S27 |
| 5 | BAA05g05790 | A05 | 2802696 | G | A | synonymous_variant | LOW | c.801G>A|p.Ser267Ser |
S89 |
| 6 | BAA05g05790 | A05 | 2802781 | C | T | missense_variant&splice_region_variant | MODERATE | c.886C>T|p.Pro296Ser |
S284 |
| 7 | BAA05g05790 | A05 | 2802974 | G | A | synonymous_variant | LOW | c.996G>A|p.Glu332Glu |
S279 |
| 8 | BAA05g05790 | A05 | 2803818 | C | T | missense_variant | MODERATE | c.1757C>T|p.Ser586Phe |
S157 |
| 9 | BAA05g05790 | A05 | 2804415 | G | A | missense_variant | MODERATE | c.2275G>A|p.Ala759Thr |
S165 |