| Chr | Mutation (hg38) | CAid | Gene | Transcript | Linkouts |
|---|---|---|---|---|---|
| 3 | g.190388331T>G | CA117862 | CLDN16 | c.2T>G (p.Met1Arg) c.212T>G (p.Met71Arg) n.306+13728T>G | ClinVar dbSNP |
| 3 | g.190388331T>C | CA355762540 | CLDN16 | c.2T>C (p.Met1Thr) c.212T>C (p.Met71Thr) n.306+13728T>C | ClinVar dbSNP gnomAD v2 gnomAD v4 |
| 3 | g.190388331T= | CA1428775947 | CLDN16 | c.2T= (p.Met1=) c.212T= (p.Met71=) n.306+13728T= | dbSNP |