Num | GeneID | Chromosome | Position | Ref.allele | Alt.allele | Mutant type | Impacts | Amino acid change | SampleID |
---|---|---|---|---|---|---|---|---|---|
1 | BAA10g19630 | A10 | 17950211 | G | A | missense_variant | MODERATE | c.713C>T|p.Pro238Leu |
S130 |
2 | BAA10g19630 | A10 | 17950498 | C | T | synonymous_variant | LOW | c.426G>A|p.Arg142Arg |
S18 |
3 | BAA10g19630 | A10 | 17950573 | G | A | synonymous_variant | LOW | c.351C>T|p.Phe117Phe |
S71 |
4 | BAA10g19630 | A10 | 17952038 | C | T | upstream_gene_variant | MODIFIER | c.-1115G>A| |
S189 |