Chr | Mutation (hg38) | CAid | Gene | Transcript | Linkouts |
---|---|---|---|---|---|
17 | g.66806426C>G | CA2271451455 | PRKCA | c.*2389C>G (n.*2389C>G) | dbSNP |
17 | g.66806426C>T | CA14384742 | PRKCA | c.*2389C>T (n.*2389C>T) | dbSNP gnomAD v2 gnomAD v3 gnomAD v4 |
17 | g.66806426C= | CA2271451454 | PRKCA | c.*2389C= (n.*2389C=) | dbSNP |