Chr Mutation (hg38) CAid Gene Transcript Linkouts
Xg.71223657_71223971delCA2739273574GJB1c.-16-35_264del
ClinVar
Xg.71223836G>ACA516821187GJB1c.129G>A (p.Val43=)
ClinVar dbSNP
Xg.71223836G>CCA516821188GJB1c.129G>C (p.Val43=)
Xg.71223836G>TCA516821190GJB1c.129G>T (p.Val43=)
Xg.71223837T>ACA413501040GJB1c.130T>A (p.Trp44Arg)
Xg.71223837T>CCA413501042GJB1c.130T>C (p.Trp44Arg)
Xg.71223837T>GCA413501044GJB1c.130T>G (p.Trp44Gly)
Xg.71223838G>ACA10581119GJB1c.131G>A (p.Trp44Ter)
ClinVar dbSNP
Xg.71223838G>CCA413501049GJB1c.131G>C (p.Trp44Ser)
Xg.71223838G=CA2436388172GJB1c.131G= (p.Trp44=)
Xg.71223838G>TCA413501047GJB1c.131G>T (p.Trp44Leu)
ClinVar dbSNP
Xg.71223841dupCA2697553165GJB1c.134dup (p.Asp46Ter)
ClinVar
Xg.71223841delCA2695234560GJB1c.134del (p.Gly45ValfsTer?)
Xg.71223839G>ACA413501057GJB1c.132G>A (p.Trp44Ter)
ClinVar dbSNP COSMIC
Xg.71223839G>CCA10584635GJB1c.132G>C (p.Trp44Cys)
ClinVar dbSNP
Xg.71223839G=CA2436388173GJB1c.132G= (p.Trp44=)
Xg.71223839G>TCA413501055GJB1c.132G>T (p.Trp44Cys)
COSMIC
Xg.71223840G>ACA413501060GJB1c.133G>A (p.Gly45Ser)
gnomAD v4
Xg.71223840G>CCA413501062GJB1c.133G>C (p.Gly45Arg)
ClinVar
Xg.71223840G>TCA413501064GJB1c.133G>T (p.Gly45Cys)
Xg.71223841G>ACA413501066GJB1c.134G>A (p.Gly45Asp)
gnomAD v4
Xg.71223841G>CCA413501067GJB1c.134G>C (p.Gly45Ala)
Xg.71223841G>TCA413501069GJB1c.134G>T (p.Gly45Val)
Xg.71223842T>ACA516821195GJB1c.135T>A (p.Gly45=)
Xg.71223842T>CCA516821197GJB1c.135T>C (p.Gly45=)
dbSNP gnomAD v3
Xg.71223842T>GCA516821199GJB1c.135T>G (p.Gly45=)
ClinVar dbSNP
Xg.71223842T=CA2436388174GJB1c.135T= (p.Gly45=)
Xg.71223843G>ACA413501073GJB1c.136G>A (p.Asp46Asn)
ClinVar
Xg.71223843G>CCA413501075GJB1c.136G>C (p.Asp46His)
Xg.71223843G>TCA413501077GJB1c.136G>T (p.Asp46Tyr)
Xg.71223844A=CA2436388175GJB1c.137A= (p.Asp46=)
Xg.71223844A>CCA413501084GJB1c.137A>C (p.Asp46Ala)
Xg.71223844A>GCA413501083GJB1c.137A>G (p.Asp46Gly)
ClinVar dbSNP
Xg.71223844A>TCA413501081GJB1c.137A>T (p.Asp46Val)
ClinVar dbSNP
Xg.71223845T>ACA413501085GJB1c.138T>A (p.Asp46Glu)
Xg.71223845T>CCA516821202GJB1c.138T>C (p.Asp46=)
dbSNP gnomAD v2 gnomAD v4
Xg.71223845T>GCA413501086GJB1c.138T>G (p.Asp46Glu)
ClinVar dbSNP gnomAD v4
Xg.71223845T=CA2436388176GJB1c.138T= (p.Asp46=)
Xg.71223846G>ACA413501088GJB1c.139G>A (p.Glu47Lys)
ClinVar dbSNP
Xg.71223846G>CCA413501092GJB1c.139G>C (p.Glu47Gln)
Xg.71223846G=CA2436388177GJB1c.139G= (p.Glu47=)
Xg.71223846G>TCA413501093GJB1c.139G>T (p.Glu47Ter)
Xg.71223847A=CA2436388178GJB1c.140A= (p.Glu47=)
Xg.71223847A>CCA413501095GJB1c.140A>C (p.Glu47Ala)
Xg.71223847A>GCA413501096GJB1c.140A>G (p.Glu47Gly)
ClinVar dbSNP
Xg.71223847A>TCA413501098GJB1c.140A>T (p.Glu47Val)
ClinVar dbSNP
Xg.71223848_71223850dupCA915951181GJB1c.141_143dup (p.Lys48_Ser49insLys)
ClinVar dbSNP
Xg.71223848G>ACA516821206GJB1c.141G>A (p.Glu47=)
gnomAD v4
Xg.71223848G>CCA413501100GJB1c.141G>C (p.Glu47Asp)
Xg.71223848G>TCA413501103GJB1c.141G>T (p.Glu47Asp)

Number of alleles fetched