Num | GeneID | Chromosome | Position | Ref.allele | Alt.allele | Mutant type | Impacts | Amino acid change | SampleID |
---|---|---|---|---|---|---|---|---|---|
1 | BAA02g43970 | A02 | 36295835 | C | T | synonymous_variant | LOW | c.243C>T|p.Tyr81Tyr |
S105 S106 |
2 | BAA02g43970 | A02 | 36296331 | G | A | missense_variant | MODERATE | c.739G>A|p.Glu247Lys |
S34 |
3 | BAA02g43970 | A02 | 36298543 | C | T | missense_variant | MODERATE | c.1393C>T|p.Leu465Phe |
S228 |
4 | BAA02g43970 | A02 | 36298734 | G | A | missense_variant | MODERATE | c.1477G>A|p.Glu493Lys |
S67 |
5 | BAA02g43970 | A02 | 36298907 | C | T | missense_variant | MODERATE | c.1558C>T|p.Pro520Ser |
S284 S83 |
6 | BAA02g43970 | A02 | 36299513 | G | A | synonymous_variant | LOW | c.1884G>A|p.Gln628Gln |
S188 |
7 | BAA02g43970 | A02 | 36300540 | C | T | splice_region_variant&intron_variant | LOW | c.2386-8C>T| |
S135 |
8 | BAA02g43970 | A02 | 36300873 | C | T | missense_variant | MODERATE | c.2711C>T|p.Thr904Ile |
S63 |
9 | BAA02g43970 | A02 | 36302910 | G | A | downstream_gene_variant | MODIFIER | c.*1467G>A| |
S266 |
10 | BAA02g43970 | A02 | 36304089 | C | T | downstream_gene_variant | MODIFIER | c.*2646C>T| |
S123 |