Chr Mutation (hg38) CAid Gene Transcript Linkouts
Xg.71223993G>ACA413501776GJB1c.286G>A (p.Ala96Thr)
Xg.71223993G>CCA413501778GJB1c.286G>C (p.Ala96Pro)
ClinVar dbSNP
Xg.71223993G=CA2436388281GJB1c.286G= (p.Ala96=)
Xg.71223993G>TCA413501779GJB1c.286G>T (p.Ala96Ser)
Xg.71223994C>ACA413501781GJB1c.287C>A (p.Ala96Asp)
Xg.71223994C=CA2436388282GJB1c.287C= (p.Ala96=)
Xg.71223994C>GCA330997722GJB1c.287C>G (p.Ala96Gly)
ClinVar dbSNP
Xg.71223994C>TCA413501782GJB1c.287C>T (p.Ala96Val)
ClinVar dbSNP
Xg.71223995T>ACA516821369GJB1c.288T>A (p.Ala96=)
Xg.71223995T>CCA516821370GJB1c.288T>C (p.Ala96=)
Xg.71223995T>GCA516821368GJB1c.288T>G (p.Ala96=)
Xg.71223996C>ACA413501784GJB1c.289C>A (p.His97Asn)
Xg.71223996C>GCA413501786GJB1c.289C>G (p.His97Asp)
Xg.71223996C>TCA413501788GJB1c.289C>T (p.His97Tyr)
Xg.71223997A>CCA413501790GJB1c.290A>C (p.His97Pro)
Xg.71223997A>GCA413501793GJB1c.290A>G (p.His97Arg)
ClinVar dbSNP
Xg.71223997A>TCA413501791GJB1c.290A>T (p.His97Leu)
Xg.71223998C>ACA413501794GJB1c.291C>A (p.His97Gln)
Xg.71223998C>GCA413501796GJB1c.291C>G (p.His97Gln)
Xg.71223998C>TCA516821371GJB1c.291C>T (p.His97=)
Xg.71223999C>ACA413501798GJB1c.292C>A (p.Gln98Lys)
Xg.71223999C=CA2436388283GJB1c.292C= (p.Gln98=)
Xg.71223999C>GCA413501799GJB1c.292C>G (p.Gln98Glu)
Xg.71223999C>TCA413501801GJB1c.292C>T (p.Gln98Ter)
ClinVar dbSNP
Xg.71224000A>CCA413501803GJB1c.293A>C (p.Gln98Pro)
Xg.71224000A>GCA413501804GJB1c.293A>G (p.Gln98Arg)
Xg.71224000A>TCA413501806GJB1c.293A>T (p.Gln98Leu)
Xg.71224001G>ACA516821372GJB1c.294G>A (p.Gln98=)
ClinVar dbSNP
Xg.71224001G>CCA413501807GJB1c.294G>C (p.Gln98His)
gnomAD v4
Xg.71224001G=CA2436388284GJB1c.294G= (p.Gln98=)
Xg.71224001G>TCA413501809GJB1c.294G>T (p.Gln98His)
gnomAD v4
Xg.71224002C>ACA413501810GJB1c.295C>A (p.Gln99Lys)
Xg.71224002C=CA2436388285GJB1c.295C= (p.Gln99=)
Xg.71224002C>GCA413501812GJB1c.295C>G (p.Gln99Glu)
Xg.71224002C>TCA413501814GJB1c.295C>T (p.Gln99Ter)
ClinVar dbSNP
Xg.71224004_71224006dupCA891844219GJB1c.297_299dup (p.Gln99_His100insGln)
ClinVar dbSNP
Xg.71224003A>CCA413501815GJB1c.296A>C (p.Gln99Pro)
Xg.71224003A>GCA413501818GJB1c.296A>G (p.Gln99Arg)
Xg.71224003A>TCA413501816GJB1c.296A>T (p.Gln99Leu)
Xg.71224004A=CA2436388286GJB1c.297A= (p.Gln99=)
Xg.71224004A>CCA413501820GJB1c.297A>C (p.Gln99His)
Xg.71224004A>GCA516821373GJB1c.297A>G (p.Gln99=)
ClinVar dbSNP gnomAD v2 gnomAD v3 gnomAD v4
Xg.71224004A>TCA413501821GJB1c.297A>T (p.Gln99His)
Xg.71224007_71224008delCA2579640066GJB1c.300_301del (p.Ile101ArgfsTer8)
Xg.71224005C>ACA413501823GJB1c.298C>A (p.His100Asn)
Xg.71224005C=CA2436388287GJB1c.298C= (p.His100=)
Xg.71224005C>GCA413501825GJB1c.298C>G (p.His100Asp)
Xg.71224005C>TCA413501826GJB1c.298C>T (p.His100Tyr)
ClinVar dbSNP
Xg.71224006A=CA2436388288GJB1c.299A= (p.His100=)
Xg.71224006A>CCA413501828GJB1c.299A>C (p.His100Pro)
COSMIC

Number of alleles fetched