Chr Mutation (hg38) CAid Gene Transcript Linkouts
13g.20189132_20189151delCA2695217664GJB2c.431_450del (p.Val144AspfsTer?)
13g.20189133_20189151delCA2695217665GJB2c.431_449del (p.Val144AlafsTer18)
13g.20189146A>CCA387461151GJB2c.436T>G (p.Phe146Val)
13g.20189146A>GCA387461152GJB2c.436T>C (p.Phe146Leu)
13g.20189146A>TCA387461153GJB2c.436T>A (p.Phe146Ile)
13g.20189147_20189148delCA2695217667GJB2c.435_436del (p.Phe146ArgfsTer?)
13g.20189146_20189149delinsAGATCA2077139221GJB2c.433_436delinsATCT (p.Ile145=)
13g.20189147G>ACA483153958GJB2c.435C>T (p.Ile145=)
ClinVar dbSNP gnomAD v2 gnomAD v4
13g.20189147G>CCA387461154GJB2c.435C>G (p.Ile145Met)
13g.20189147G=CA2077139228GJB2c.435C= (p.Ile145=)
13g.20189147G>TCA483153959GJB2c.435C>A (p.Ile145=)
13g.20189149_20189151delCA246460156GJB2c.433_435del (p.Ile145del)
ClinVar dbSNP gnomAD v2 gnomAD v3 gnomAD v4
13g.20189148A>CCA387461155GJB2c.434T>G (p.Ile145Ser)
13g.20189148A>GCA387461156GJB2c.434T>C (p.Ile145Thr)
13g.20189148A>TCA387461157GJB2c.434T>A (p.Ile145Asn)
13g.20189149T>ACA387461158GJB2c.433A>T (p.Ile145Phe)
13g.20189149T>CCA387461159GJB2c.433A>G (p.Ile145Val)
13g.20189149T>GCA387461160GJB2c.433A>C (p.Ile145Leu)
13g.20189150G>ACA483153960GJB2c.432C>T (p.Val144=)
ClinVar
13g.20189150G>CCA483153961GJB2c.432C>G (p.Val144=)
13g.20189150G>TCA483153962GJB2c.432C>A (p.Val144=)
ClinVar gnomAD v4
13g.20189151A>CCA387461163GJB2c.431T>G (p.Val144Gly)
13g.20189151A>GCA387461162GJB2c.431T>C (p.Val144Ala)
13g.20189151A>TCA387461161GJB2c.431T>A (p.Val144Asp)
13g.20189152C>ACA387461164GJB2c.430G>T (p.Val144Phe)
13g.20189152C=CA2077139234GJB2c.430G= (p.Val144=)
13g.20189152C>GCA387461165GJB2c.430G>C (p.Val144Leu)
gnomAD v4
13g.20189152C>TCA387461166GJB2c.430G>A (p.Val144Ile)
dbSNP
13g.20189153C>ACA483153963GJB2c.429G>T (p.Arg143=)
ClinVar dbSNP gnomAD v4
13g.20189153C>GCA483153964GJB2c.429G>C (p.Arg143=)
13g.20189153C>TCA483153965GJB2c.429G>A (p.Arg143=)
gnomAD v4
13g.20189154C>ACA387461167GJB2c.428G>T (p.Arg143Leu)
gnomAD v4
13g.20189154C=CA2077139238GJB2c.428G= (p.Arg143=)
13g.20189154C>GCA387461168GJB2c.428G>C (p.Arg143Pro)
13g.20189154C>TCA257677GJB2c.428G>A (p.Arg143Gln)
ClinVar dbSNP gnomAD v3 gnomAD v4 COSMIC
13g.20189155G>ACA172234GJB2c.427C>T (p.Arg143Trp)
ClinVar dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4
13g.20189155G>CCA387461169GJB2c.427C>G (p.Arg143Gly)
13g.20189155G=CA2077139242GJB2c.427C= (p.Arg143=)
13g.20189155G>TCA483153966GJB2c.427C>A (p.Arg143=)
13g.20189156G>ACA483153967GJB2c.426C>T (p.Phe142=)
gnomAD v4
13g.20189156G>CCA387461170GJB2c.426C>G (p.Phe142Leu)
13g.20189156G=CA2077139248GJB2c.426C= (p.Phe142=)
13g.20189156G>TCA261647GJB2c.426C>A (p.Phe142Leu)
ClinVar dbSNP
13g.20189161_20189163delCA2580614612GJB2c.424_426del (p.Phe142del)
ClinVar
13g.20189157A=CA2077139253GJB2c.425T= (p.Phe142=)
13g.20189157A>CCA387461171GJB2c.425T>G (p.Phe142Cys)
gnomAD v4
13g.20189157A>GCA6904271GJB2c.425T>C (p.Phe142Ser)
ClinVar dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4
13g.20189157A>TCA387461172GJB2c.425T>A (p.Phe142Tyr)
13g.20189158A>CCA387461174GJB2c.424T>G (p.Phe142Val)
13g.20189158A>GCA387461175GJB2c.424T>C (p.Phe142Leu)

Number of alleles fetched