Chr Mutation (hg38) CAid Gene Transcript Linkouts
1g.215647502_215648786delCA3260665404USH2Ac.14344-20_14791+20del
1g.215648674_215648702delCA3054205787USH2Ac.14409_14437del (p.Ile4803MetfsTer9)
ClinVar
1g.215648681_215648705delCA2697554898USH2Ac.14407_14431del (p.Ile4803SerfsTer12)
ClinVar dbSNP
1g.215648689_215648702delinsGGCCTCTACTCCAACA1220363204USH2Ac.14408_14421delinsTTGGAGTAGAGGCC (p.Ile4803=)
1g.215648690_215648702delCA1012188225USH2Ac.14408_14420del (p.Ile4803ThrfsTer16)
ClinVar dbSNP gnomAD v3 gnomAD v4
1g.215648690_215648703delinsTGACA2580617945USH2Ac.14407_14420delinsTCA (p.Ile4803SerfsTer15)
ClinVar dbSNP
1g.215648702A=CA1220363207USH2Ac.14408T= (p.Ile4803=)
dbSNP
1g.215648702A>CCA344833946USH2Ac.14408T>G (p.Ile4803Ser)
1g.215648702A>GCA37390402USH2Ac.14408T>C (p.Ile4803Thr)
ClinVar dbSNP gnomAD v4
1g.215648702A>TCA344833951USH2Ac.14408T>A (p.Ile4803Asn)
1g.215648703T>ACA344833953USH2Ac.14407A>T (p.Ile4803Phe)
1g.215648703T>CCA1393023USH2Ac.14407A>G (p.Ile4803Val)
ClinVar dbSNP ExAC gnomAD v2 gnomAD v4
1g.215648703T>GCA344833956USH2Ac.14407A>C (p.Ile4803Leu)
1g.215648703T=CA1220363208USH2Ac.14407A= (p.Ile4803=)
dbSNP
1g.215648703_215648704insGACA1012188254USH2Ac.14406_14407insTC (p.Ile4803SerfsTer4)
ClinVar dbSNP gnomAD v3 gnomAD v4
1g.215648704A=CA3077339299USH2Ac.14406T= (p.Ser4802=)
dbSNP
1g.215648704A>CCA423425689USH2Ac.14406T>G (p.Ser4802=)
1g.215648704A>GCA423425690USH2Ac.14406T>C (p.Ser4802=)
dbSNP gnomAD v4
1g.215648704A>TCA423425693USH2Ac.14406T>A (p.Ser4802=)
1g.215648705G>ACA1393024USH2Ac.14405C>T (p.Ser4802Phe)
ClinVar dbSNP ExAC gnomAD v2 gnomAD v4
1g.215648705G>CCA344833957USH2Ac.14405C>G (p.Ser4802Cys)
1g.215648705G=CA1220363209USH2Ac.14405C= (p.Ser4802=)
dbSNP
1g.215648705G>TCA344833961USH2Ac.14405C>A (p.Ser4802Tyr)
dbSNP
1g.215648706A=CA1143413562USH2Ac.14404T= (p.Ser4802=)
dbSNP
1g.215648706A>CCA37390431USH2Ac.14404T>G (p.Ser4802Ala)
ClinVar dbSNP gnomAD v2 gnomAD v3 gnomAD v4
1g.215648706A>GCA344833967USH2Ac.14404T>C (p.Ser4802Pro)
ClinVar dbSNP
1g.215648706A>TCA344833970USH2Ac.14404T>A (p.Ser4802Thr)
1g.215648706_215648708delinsAGTCA1220363210USH2Ac.14402_14404delinsACT (p.Tyr4801=)
1g.215648709_215648711delCA913072743USH2Ac.14402_14404del (p.Tyr4801del)
1g.215648707G>ACA423425695USH2Ac.14403C>T (p.Tyr4801=)
ClinVar dbSNP gnomAD v4
1g.215648707G>CCA344833972USH2Ac.14403C>G (p.Tyr4801Ter)
1g.215648707G=CA3075692454USH2Ac.14403C= (p.Tyr4801=)
dbSNP
1g.215648707G>TCA344833975USH2Ac.14403C>A (p.Tyr4801Ter)
1g.215648707_215648708delCA529002037USH2Ac.14402_14403del (p.Tyr4801PhefsTer20)
ClinVar dbSNP gnomAD v2 gnomAD v4
1g.215648708T>ACA344833977USH2Ac.14402A>T (p.Tyr4801Phe)
1g.215648708T>CCA344833982USH2Ac.14402A>G (p.Tyr4801Cys)
1g.215648708T>GCA344833980USH2Ac.14402A>C (p.Tyr4801Ser)
1g.215648712_215648715delCA423425697USH2Ac.14399_14402del (p.Asn4800ThrfsTer5)
1g.215648709A>CCA344833986USH2Ac.14401T>G (p.Tyr4801Asp)
1g.215648709A>GCA344833989USH2Ac.14401T>C (p.Tyr4801His)
1g.215648709A>TCA344833991USH2Ac.14401T>A (p.Tyr4801Asn)
1g.215648710G>ACA423425699USH2Ac.14400C>T (p.Asn4800=)
1g.215648710G>CCA344833993USH2Ac.14400C>G (p.Asn4800Lys)
1g.215648710G>TCA344833995USH2Ac.14400C>A (p.Asn4800Lys)
1g.215648711T>ACA344833999USH2Ac.14399A>T (p.Asn4800Ile)
1g.215648711T>CCA344834001USH2Ac.14399A>G (p.Asn4800Ser)
1g.215648711T>GCA344834004USH2Ac.14399A>C (p.Asn4800Thr)
1g.215648712T>ACA344834007USH2Ac.14398A>T (p.Asn4800Tyr)
1g.215648712T>CCA1393025USH2Ac.14398A>G (p.Asn4800Asp)
ClinVar dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4
1g.215648712T>GCA344834010USH2Ac.14398A>C (p.Asn4800His)

Number of alleles fetched