Chr | Mutation (hg38) | CAid | Gene | Transcript | Linkouts |
---|---|---|---|---|---|
20 | g.53567166C>A | CA2369989181 | ZNF217,ZNF217-AS1 | c.*2122G>T (n.*2122G>T) n.556-3106C>A c.*1950G>T (n.*1950G>T) | dbSNP |
20 | g.53567166C>T | CA15961708 | ZNF217,ZNF217-AS1 | c.*2122G>A (n.*2122G>A) n.556-3106C>T c.*1950G>A (n.*1950G>A) | dbSNP gnomAD v2 gnomAD v3 gnomAD v4 |