Chr | Mutation (hg38) | CAid | Gene | Transcript | Linkouts |
---|---|---|---|---|---|
17 | g.61679808T>A | CA10649726 | BRIP1 | c.*3488A>T (n.*3488A>T) | ClinVar dbSNP gnomAD v2 gnomAD v3 gnomAD v4 |
17 | g.61679808T>C | CA773766852 | BRIP1 | c.*3488A>G (n.*3488A>G) | dbSNP gnomAD v3 gnomAD v4 |
17 | g.61679808T= | CA2269129105 | BRIP1 | c.*3488A= (n.*3488A=) | dbSNP |