Chr Mutation (hg38) CAid Gene Transcript Linkouts
5g.112841156delCA16618090APCc.5616del (p.Cys1873ValfsTer8)
c.*5568del (n.*5568del)
c.5508del (p.Cys1837ValfsTer8)
c.5562del (p.Cys1855ValfsTer8)
c.*4884del (n.*4884del)
c.230+12184del
c.5592del (p.Cys1865ValfsTer8)
c.5487del (p.Cys1830ValfsTer8)
c.5478del (p.Cys1827ValfsTer8)
c.5439del (p.Cys1814ValfsTer8)
c.5385del (p.Cys1796ValfsTer8)
c.5289del (p.Cys1764ValfsTer8)
c.5259del (p.Cys1754ValfsTer8)
c.5184del (p.Cys1729ValfsTer8)
c.5082del (p.Cys1695ValfsTer8)
c.4713del (p.Cys1572ValfsTer8)
ClinVar dbSNP
5g.112841156C=CA3124061241APCc.5616C= (p.Tyr1872=)
c.*5568C= (n.*5568C=)
c.5508C= (p.Tyr1836=)
c.5562C= (p.Tyr1854=)
c.*4884C= (n.*4884C=)
c.230+12184C=
c.5592C= (p.Tyr1864=)
c.5487C= (p.Tyr1829=)
c.5478C= (p.Tyr1826=)
c.5439C= (p.Tyr1813=)
c.5385C= (p.Tyr1795=)
c.5289C= (p.Tyr1763=)
c.5259C= (p.Tyr1753=)
c.5184C= (p.Tyr1728=)
c.5082C= (p.Tyr1694=)
c.4713C= (p.Tyr1571=)
dbSNP dbSNP

Number of alleles fetched