| Chr | Mutation (hg38) | CAid | Gene | Transcript | Linkouts |
|---|---|---|---|---|---|
| 3 | g.190404834T>C | CA117863 | CLDN16 | c.290T>C (p.Leu97Pro) c.115-5069T>C (n.115-5069T>C) c.500T>C (p.Leu167Pro) c.325-5069T>C (n.325-5069T>C) n.482T>C | ClinVar dbSNP gnomAD v4 |
| 3 | g.190404834T= | CA1428759429 | CLDN16 | c.290T= (p.Leu97=) c.115-5069T= (n.115-5069T=) c.500T= (p.Leu167=) c.325-5069T= (n.325-5069T=) n.482T= | dbSNP |