Chr Mutation (hg38) CAid Gene Transcript Linkouts
1g.215782087A>CCA344836352USH2Ac.10695T>G (p.Tyr3565Ter)
1g.215782087A>GCA423313221USH2Ac.10695T>C (p.Tyr3565=)
1g.215782087A>TCA344836354USH2Ac.10695T>A (p.Tyr3565Ter)
1g.215782088T>ACA344836358USH2Ac.10694A>T (p.Tyr3565Phe)
1g.215782088T>CCA344836365USH2Ac.10694A>G (p.Tyr3565Cys)
gnomAD v4
1g.215782088T>GCA344836361USH2Ac.10694A>C (p.Tyr3565Ser)
1g.215782089A=CA1220416691USH2Ac.10693T= (p.Tyr3565=)
1g.215782089A>CCA344836369USH2Ac.10693T>G (p.Tyr3565Asp)
1g.215782089A>GCA344836370USH2Ac.10693T>C (p.Tyr3565His)
ClinVar dbSNP
1g.215782089A>TCA344836372USH2Ac.10693T>A (p.Tyr3565Asn)
1g.215782091_215782094dupCA2573131578USH2Ac.10690_10693dup (p.Tyr3565PhefsTer16)
ClinVar dbSNP
1g.215782090T>ACA423313225USH2Ac.10692A>T (p.Ser3564=)
ClinVar dbSNP gnomAD v3 gnomAD v4
1g.215782090T>CCA423313226USH2Ac.10692A>G (p.Ser3564=)
ClinVar dbSNP gnomAD v4
1g.215782090T>GCA423313227USH2Ac.10692A>C (p.Ser3564=)
1g.215782090T=CA1220416695USH2Ac.10692A= (p.Ser3564=)
1g.215782091G>ACA344836376USH2Ac.10691C>T (p.Ser3564Leu)
1g.215782091G>CCA344836380USH2Ac.10691C>G (p.Ser3564Ter)
ClinVar
1g.215782091G>TCA344836387USH2Ac.10691C>A (p.Ser3564Ter)
1g.215782092A>CCA344836391USH2Ac.10690T>G (p.Ser3564Ala)
1g.215782092A>GCA344836394USH2Ac.10690T>C (p.Ser3564Pro)
gnomAD v4
1g.215782092A>TCA344836397USH2Ac.10690T>A (p.Ser3564Thr)
1g.215782093A>CCA344836400USH2Ac.10689T>G (p.Tyr3563Ter)
1g.215782093A>GCA423313229USH2Ac.10689T>C (p.Tyr3563=)
ClinVar
1g.215782093A>TCA344836404USH2Ac.10689T>A (p.Tyr3563Ter)
ClinVar
1g.215782094T>ACA344836409USH2Ac.10688A>T (p.Tyr3563Phe)
1g.215782094T>CCA344836415USH2Ac.10688A>G (p.Tyr3563Cys)
1g.215782094T>GCA344836412USH2Ac.10688A>C (p.Tyr3563Ser)
1g.215782095A=CA1220416698USH2Ac.10687T= (p.Tyr3563=)
1g.215782095A>CCA344836420USH2Ac.10687T>G (p.Tyr3563Asp)
1g.215782095A>GCA1393956USH2Ac.10687T>C (p.Tyr3563His)
dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4
1g.215782095A>TCA344836425USH2Ac.10687T>A (p.Tyr3563Asn)
1g.215782096T>ACA344836432USH2Ac.10686A>T (p.Glu3562Asp)
1g.215782096T>CCA1393957USH2Ac.10686A>G (p.Glu3562=)
ClinVar dbSNP ExAC gnomAD v2 gnomAD v4
1g.215782096T>GCA344836444USH2Ac.10686A>C (p.Glu3562Asp)
1g.215782096T=CA1220416701USH2Ac.10686A= (p.Glu3562=)
1g.215782097T>ACA344836451USH2Ac.10685A>T (p.Glu3562Val)
1g.215782097T>CCA344836454USH2Ac.10685A>G (p.Glu3562Gly)
1g.215782097T>GCA344836460USH2Ac.10685A>C (p.Glu3562Ala)
1g.215782098C>ACA1393958USH2Ac.10684G>T (p.Glu3562Ter)
ClinVar dbSNP ExAC gnomAD v2 gnomAD v4
1g.215782098C=CA1149138083USH2Ac.10684G= (p.Glu3562=)
1g.215782098C>GCA344836467USH2Ac.10684G>C (p.Glu3562Gln)
1g.215782098C>TCA344836470USH2Ac.10684G>A (p.Glu3562Lys)
1g.215782099C>ACA344836478USH2Ac.10683G>T (p.Gln3561His)
1g.215782099C=CA1220416708USH2Ac.10683G= (p.Gln3561=)
1g.215782099C>GCA1393959USH2Ac.10683G>C (p.Gln3561His)
dbSNP ExAC gnomAD v2 gnomAD v4
1g.215782099C>TCA1393960USH2Ac.10683G>A (p.Gln3561=)
ClinVar dbSNP ExAC gnomAD v2 gnomAD v4
1g.215782100T>ACA344836483USH2Ac.10682A>T (p.Gln3561Leu)
1g.215782100T>CCA37437375USH2Ac.10682A>G (p.Gln3561Arg)
ClinVar dbSNP gnomAD v4
1g.215782100T>GCA344836489USH2Ac.10682A>C (p.Gln3561Pro)
1g.215782100T=CA1220416717USH2Ac.10682A= (p.Gln3561=)

Number of alleles fetched