| Chr | Mutation (hg38) | CAid | Gene | Transcript | Linkouts |
|---|---|---|---|---|---|
| 3 | g.190408416T>G | CA117864 | CLDN16 | c.485T>G (p.Phe162Cys) c.115-1487T>G (n.115-1487T>G) c.695T>G (p.Phe232Cys) c.325-1487T>G (n.325-1487T>G) | ClinVar dbSNP gnomAD v4 |
| 3 | g.190408416T= | CA1428762783 | CLDN16 | c.485T= (p.Phe162=) c.115-1487T= (n.115-1487T=) c.695T= (p.Phe232=) c.325-1487T= (n.325-1487T=) | dbSNP |