ClinVar Miner

List of variants in gene PCDH19 reported as likely benign for not specified

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Gene type:
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Total variants: 45
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HGVS dbSNP gnomAD frequency
NM_001184880.2(PCDH19):c.6G>A (p.Glu2=) rs184883626 0.00997
NM_001184880.2(PCDH19):c.81C>T (p.Tyr27=) rs56307810 0.00942
NM_001184880.2(PCDH19):c.3319C>G (p.Arg1107Gly) rs191333060 0.00123
NM_001184880.2(PCDH19):c.2938C>T (p.Arg980Cys) rs3764758 0.00118
NM_001184880.2(PCDH19):c.3235C>G (p.Pro1079Ala) rs200854927 0.00074
NM_001184880.2(PCDH19):c.769G>C (p.Val257Leu) rs201713027 0.00065
NM_001184880.2(PCDH19):c.3439G>A (p.Val1147Ile) rs138771033 0.00040
NM_001184880.2(PCDH19):c.531G>A (p.Glu177=) rs192122222 0.00038
NM_001184880.2(PCDH19):c.1725C>T (p.Val575=) rs200471732 0.00021
NM_001184880.2(PCDH19):c.655C>T (p.Leu219=) rs377627937 0.00018
NM_001184880.2(PCDH19):c.513C>T (p.Asn171=) rs749602848 0.00016
NM_001184880.2(PCDH19):c.1700C>G (p.Pro567Arg) rs201989363 0.00013
NM_001184880.2(PCDH19):c.1107C>T (p.Ala369=) rs199879056 0.00011
NM_001184880.2(PCDH19):c.2965A>C (p.Asn989His) rs201611496 0.00011
NM_001184880.2(PCDH19):c.1877C>T (p.Thr626Ile) rs201764553 0.00007
NM_001184880.2(PCDH19):c.1656C>G (p.Ile552Met) rs779051005 0.00006
NM_001184880.2(PCDH19):c.540G>A (p.Thr180=) rs368094294 0.00006
NM_001184880.2(PCDH19):c.1644G>A (p.Thr548=) rs372952752 0.00005
NM_001184880.2(PCDH19):c.2939G>A (p.Arg980His) rs368872920 0.00005
NM_001184880.2(PCDH19):c.51G>A (p.Thr17=) rs756958731 0.00003
NM_001184880.2(PCDH19):c.-47C>T rs1057523140 0.00002
NM_001184880.2(PCDH19):c.117T>A (p.Ile39=) rs750597794 0.00002
NM_001184880.2(PCDH19):c.768C>T (p.Pro256=) rs761277974 0.00002
NM_001184880.2(PCDH19):c.798C>T (p.Asp266=) rs369638371 0.00002
NM_001184880.2(PCDH19):c.-38G>T rs760863131 0.00001
NM_001184880.2(PCDH19):c.1740C>G (p.Asn580Lys) rs763798306 0.00001
NM_001184880.2(PCDH19):c.2223G>A (p.Ser741=) rs907375983 0.00001
NM_001184880.2(PCDH19):c.2781T>C (p.Cys927=) rs1555977733 0.00001
NM_001184880.2(PCDH19):c.630G>A (p.Ala210=) rs781763211 0.00001
NM_001184880.2(PCDH19):c.741G>T (p.Val247=) rs1057521743 0.00001
NM_001184880.2(PCDH19):c.-38del rs1064795564
NM_001184880.2(PCDH19):c.-42del rs1555985910
NM_001184880.2(PCDH19):c.-9C>T rs773547239
NM_001184880.2(PCDH19):c.1815C>T (p.Tyr605=) rs1057521256
NM_001184880.2(PCDH19):c.2147+16C>T rs1057521156
NM_001184880.2(PCDH19):c.2767C>A (p.Arg923=) rs752763816
NM_001184880.2(PCDH19):c.3037C>T (p.Arg1013Trp) rs376406896
NM_001184880.2(PCDH19):c.3204C>A (p.Pro1068=) rs377415279
NM_001184880.2(PCDH19):c.3204C>T (p.Pro1068=) rs377415279
NM_001184880.2(PCDH19):c.3235C>A (p.Pro1079Thr) rs200854927
NM_001184880.2(PCDH19):c.3353G>A (p.Ser1118Asn) rs760088234
NM_001184880.2(PCDH19):c.3412C>T (p.Pro1138Ser) rs778782448
NM_001184880.2(PCDH19):c.3415G>A (p.Gly1139Ser) rs760947009
NM_001184880.2(PCDH19):c.438G>A (p.Thr146=) rs776584913
NM_001184880.2(PCDH19):c.648G>A (p.Pro216=) rs996601558

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