Chr | Mutation (hg38) | CAid | Gene | Transcript | Linkouts |
---|---|---|---|---|---|
3 | g.190408419G>A | CA117865 | CLDN16 | c.488G>A (p.Gly163Asp) c.115-1484G>A (n.115-1484G>A) c.698G>A (p.Gly233Asp) c.325-1484G>A (n.325-1484G>A) | ClinVar dbSNP |
3 | g.190408419G= | CA1428762794 | CLDN16 | c.488G= (p.Gly163=) c.115-1484G= (n.115-1484G=) c.698G= (p.Gly233=) c.325-1484G= (n.325-1484G=) | dbSNP |