Chr Mutation (hg38) CAid Gene Transcript Linkouts
4g.6301180A>GCA215002WFS1c.1421A>G (p.Glu474Gly)
c.1362A>G
c.1385A>G (p.Glu462Gly)
c.1136A>G (p.Glu379Gly)
c.1044A>G (p.Arg348=)
n.1570A>G
c.1394A>G (p.Glu465Gly)
ClinVar dbSNP
4g.6301180A>CCA356174795WFS1c.1421A>C (p.Glu474Ala)
c.1362A>C
c.1385A>C (p.Glu462Ala)
c.1136A>C (p.Glu379Ala)
c.1044A>C (p.Arg348=)
n.1570A>C
c.1394A>C (p.Glu465Ala)
ClinVar dbSNP

Number of alleles fetched