Chr | Mutation (hg38) | CAid | Gene | Transcript | Linkouts |
---|---|---|---|---|---|
12 | g.108250412T>C | CA13631809 | WSCD2 | c.*2069T>C (n.*2069T>C) | dbSNP gnomAD v2 gnomAD v3 gnomAD v4 |
12 | g.108250412T>G | CA243281246 | WSCD2 | c.*2069T>G (n.*2069T>G) | dbSNP |
12 | g.108250412T= | CA2061868559 | WSCD2 | c.*2069T= (n.*2069T=) | dbSNP |