Num | GeneID | Chromosome | Position | Ref.allele | Alt.allele | Mutant type | Impacts | Amino acid change | SampleID |
---|---|---|---|---|---|---|---|---|---|
1 | BAA10g19950 | A10 | 18136016 | C | T | missense_variant | MODERATE | c.164C>T|p.Pro55Leu |
S56 |
2 | BAA10g19950 | A10 | 18138200 | G | A | intron_variant | MODIFIER | c.1686-32G>A| |
S64 |
3 | BAA10g19950 | A10 | 18138369 | G | A | missense_variant | MODERATE | c.1823G>A|p.Gly608Glu |
S245 |
4 | BAA10g19950 | A10 | 18139261 | C | T | downstream_gene_variant | MODIFIER | c.*129C>T| |
S255 |