Chr | Mutation (hg38) | CAid | Gene | Transcript | Linkouts |
---|---|---|---|---|---|
8 | g.86666870G>A | CA12815844 | CNGB3 | c.852+55C>T (n.852+55C>T) c.438+55C>T (n.438+55C>T) | ClinVar dbSNP gnomAD v2 gnomAD v3 gnomAD v4 |
8 | g.86666870G= | CA1799825025 | CNGB3 | c.852+55C= (n.852+55C=) c.438+55C= (n.438+55C=) | dbSNP |