Chr | Mutation (hg38) | CAid | Gene | Transcript | Linkouts |
---|---|---|---|---|---|
3 | g.190410026C>T | CA355768843 | CLDN16 | c.698C>T (p.Thr233Ile) c.908C>T (p.Thr303Ile) | dbSNP gnomAD v3 gnomAD v4 |
3 | g.190410026C>G | CA117872 | CLDN16 | c.698C>G (p.Thr233Arg) c.908C>G (p.Thr303Arg) | ClinVar dbSNP |
3 | g.190410026C>A | CA355768841 | CLDN16 | c.698C>A (p.Thr233Lys) c.908C>A (p.Thr303Lys) | ClinVar dbSNP gnomAD v4 |