Chr | Mutation (hg38) | CAid | Gene | Transcript | Linkouts |
---|---|---|---|---|---|
15 | g.78513681T>C | CA16510567 | HYKK | c.337+256T>C (n.337+256T>C) n.432+256T>C | ClinVar dbSNP gnomAD v2 gnomAD v3 gnomAD v4 |
15 | g.78513681T= | CA2189557600 | HYKK | c.337+256T= (n.337+256T=) n.432+256T= | dbSNP |