Num | GeneID | Chromosome | Position | Ref.allele | Alt.allele | Mutant type | Impacts | Amino acid change | SampleID |
---|---|---|---|---|---|---|---|---|---|
1 | BAA10g26680 | A10 | 21070893 | G | A | missense_variant | MODERATE | c.29G>A|p.Gly10Asp |
S17 |
2 | BAA10g26680 | A10 | 21071733 | C | T | synonymous_variant | LOW | c.682C>T|p.Leu228Leu |
S79 S91 |
3 | BAA10g26680 | A10 | 21073251 | G | A | downstream_gene_variant | MODIFIER | c.*853G>A| |
S80 |