Chr Mutation (hg38) CAid Gene Transcript Linkouts
3g.190409949T>GCA117874CLDN16c.621T>G (p.Tyr207Ter)
c.*11T>G (n.*11T>G)
c.831T>G (p.Tyr277Ter)
c.371T>G (n.371T>G)
ClinVar dbSNP gnomAD v4
3g.190409949T>CCA437418654CLDN16c.621T>C (p.Tyr207=)
c.*11T>C (n.*11T>C)
c.831T>C (p.Tyr277=)
c.371T>C (n.371T>C)
dbSNP gnomAD v4
3g.190409949T=CA1428764527CLDN16c.621T= (p.Tyr207=)
c.*11T= (n.*11T=)
c.831T= (p.Tyr277=)
c.371T= (n.371T=)
dbSNP

Number of alleles fetched