Chr Mutation (hg38) CAid Gene Transcript Linkouts
13g.20189310A>CCA387461499GJB2c.272T>G (p.Val91Gly)
gnomAD v4
13g.20189310A>GCA387461500GJB2c.272T>C (p.Val91Ala)
13g.20189310A>TCA387461501GJB2c.272T>A (p.Val91Glu)
13g.20189311C>ACA387461504GJB2c.271G>T (p.Val91Leu)
13g.20189311C=CA2077139686GJB2c.271G= (p.Val91=)
13g.20189311C>GCA387461503GJB2c.271G>C (p.Val91Leu)
gnomAD v4
13g.20189311C>TCA387461502GJB2c.271G>A (p.Val91Met)
dbSNP gnomAD v3 gnomAD v4
13g.20189312T>ACA483153763GJB2c.270A>T (p.Leu90=)
13g.20189312T>CCA483153764GJB2c.270A>G (p.Leu90=)
dbSNP gnomAD v4
13g.20189312T>GCA483153765GJB2c.270A>C (p.Leu90=)
13g.20189312T=CA2077139689GJB2c.270A= (p.Leu90=)
13g.20189313delCA2695217711GJB2c.269del (p.Leu90GlnfsTer22)
13g.20189313A=CA2077139698GJB2c.269T= (p.Leu90=)
13g.20189313A>CCA387461505GJB2c.269T>G (p.Leu90Arg)
13g.20189313A>GCA172219GJB2c.269T>C (p.Leu90Pro)
ClinVar dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4
13g.20189313A>TCA387461506GJB2c.269T>A (p.Leu90Gln)
13g.20189313dupCA273448GJB2c.269dup (p.Val91SerfsTer11)
ClinVar dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4
13g.20189315_20189336delCA2622252297GJB2c.248_269del (p.Phe83Ter)
gnomAD v4
13g.20189314G>ACA483153766GJB2c.268C>T (p.Leu90=)
ClinVar dbSNP gnomAD v4 COSMIC
13g.20189314G>CCA387461507GJB2c.268C>G (p.Leu90Val)
13g.20189314G=CA2077139706GJB2c.268C= (p.Leu90=)
13g.20189314G>TCA387461508GJB2c.268C>A (p.Leu90Ile)
13g.20189315delCA2499221953GJB2c.268del (p.Leu90Ter)
ClinVar dbSNP
13g.20189315G>ACA483153767GJB2c.267C>T (p.Leu89=)
dbSNP gnomAD v4
13g.20189315G>CCA176160GJB2c.267C>G (p.Leu89=)
ClinVar dbSNP gnomAD v2 gnomAD v3 gnomAD v4
13g.20189315G=CA2077139709GJB2c.267C= (p.Leu89=)
13g.20189315G>TCA483153768GJB2c.267C>A (p.Leu89=)
ClinVar
13g.20189316A=CA2077139714GJB2c.266T= (p.Leu89=)
13g.20189316A>CCA387461509GJB2c.266T>G (p.Leu89Arg)
13g.20189316A>GCA387461510GJB2c.266T>C (p.Leu89Pro)
ClinVar dbSNP
13g.20189316A>TCA387461511GJB2c.266T>A (p.Leu89His)
dbSNP gnomAD v4
13g.20189317G>ACA6904293GJB2c.265C>T (p.Leu89Phe)
ClinVar dbSNP ExAC gnomAD v2 gnomAD v4
13g.20189317G>CCA387461512GJB2c.265C>G (p.Leu89Val)
13g.20189317G=CA2077139717GJB2c.265C= (p.Leu89=)
13g.20189317G>TCA387461513GJB2c.265C>A (p.Leu89Ile)
13g.20189318C>ACA483153769GJB2c.264G>T (p.Ala88=)
13g.20189318C=CA2077139720GJB2c.264G= (p.Ala88=)
13g.20189318C>GCA6904295GJB2c.264G>C (p.Ala88=)
ClinVar dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4
13g.20189318C>TCA6904294GJB2c.264G>A (p.Ala88=)
ClinVar dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4 COSMIC
13g.20189319G>ACA387461514GJB2c.263C>T (p.Ala88Val)
ClinVar dbSNP
13g.20189319G>CCA387461516GJB2c.263C>G (p.Ala88Gly)
ClinVar dbSNP
13g.20189319G=CA2077139726GJB2c.263C= (p.Ala88=)
13g.20189319G>TCA387461515GJB2c.263C>A (p.Ala88Glu)
ClinVar dbSNP
13g.20189320C>ACA387461517GJB2c.262G>T (p.Ala88Ser)
gnomAD v4
13g.20189320C=CA2077139729GJB2c.262G= (p.Ala88=)
13g.20189320C>GCA387461518GJB2c.262G>C (p.Ala88Pro)
13g.20189320C>TCA387461519GJB2c.262G>A (p.Ala88Thr)
dbSNP gnomAD v3 gnomAD v4
13g.20189321T>ACA483153770GJB2c.261A>T (p.Pro87=)
13g.20189321T>CCA483153771GJB2c.261A>G (p.Pro87=)
13g.20189321T>GCA483153772GJB2c.261A>C (p.Pro87=)

Number of alleles fetched