ClinVar Miner

List of variants in gene PCDH19 reported as likely benign

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Gene type:
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Total variants: 96
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HGVS dbSNP
NM_001184880.2(PCDH19):c.-119C>T
NM_001184880.2(PCDH19):c.-38G>T rs760863131
NM_001184880.2(PCDH19):c.-38del rs1064795564
NM_001184880.2(PCDH19):c.-42del rs1555985910
NM_001184880.2(PCDH19):c.-47C>T rs1057523140
NM_001184880.2(PCDH19):c.-9C>T rs773547239
NM_001184880.2(PCDH19):c.1092G>A (p.Pro364=) rs761099954
NM_001184880.2(PCDH19):c.1107C>T (p.Ala369=) rs199879056
NM_001184880.2(PCDH19):c.117T>A (p.Ile39=) rs750597794
NM_001184880.2(PCDH19):c.1294A>G (p.Met432Val) rs200728466
NM_001184880.2(PCDH19):c.1321G>C (p.Val441Leu) rs200126728
NM_001184880.2(PCDH19):c.1330A>G (p.Thr444Ala) rs201671718
NM_001184880.2(PCDH19):c.1353G>A (p.Pro451=) rs373795773
NM_001184880.2(PCDH19):c.1401G>T (p.Thr467=) rs794726896
NM_001184880.2(PCDH19):c.1407C>A (p.Gly469=) rs1060504502
NM_001184880.2(PCDH19):c.1434C>T (p.Arg478=) rs137962077
NM_001184880.2(PCDH19):c.1485G>A (p.Ser495=) rs184770215
NM_001184880.2(PCDH19):c.1569C>T (p.His523=) rs753119035
NM_001184880.2(PCDH19):c.1602G>A (p.Leu534=)
NM_001184880.2(PCDH19):c.1612G>A (p.Gly538Ser)
NM_001184880.2(PCDH19):c.1618C>T (p.Leu540Phe) rs374593325
NM_001184880.2(PCDH19):c.1656C>G (p.Ile552Met) rs779051005
NM_001184880.2(PCDH19):c.165C>G (p.Pro55=) rs1002430549
NM_001184880.2(PCDH19):c.1683G>A (p.Pro561=) rs192354176
NM_001184880.2(PCDH19):c.1700C>G (p.Pro567Arg) rs201989363
NM_001184880.2(PCDH19):c.1725C>T (p.Val575=) rs200471732
NM_001184880.2(PCDH19):c.1740C>G (p.Asn580Lys) rs763798306
NM_001184880.2(PCDH19):c.1815C>T (p.Tyr605=) rs1057521256
NM_001184880.2(PCDH19):c.1877C>T (p.Thr626Ile) rs201764553
NM_001184880.2(PCDH19):c.1968T>A (p.Ala656=) rs776150934
NM_001184880.2(PCDH19):c.1971C>G (p.Leu657=) rs770353924
NM_001184880.2(PCDH19):c.2024T>G (p.Val675Gly) rs780704524
NM_001184880.2(PCDH19):c.2037G>A (p.Leu679=) rs1060504503
NM_001184880.2(PCDH19):c.2052C>T (p.Ala684=) rs1555984966
NM_001184880.2(PCDH19):c.2147+16C>T rs1057521156
NM_001184880.2(PCDH19):c.2223G>A (p.Ser741=) rs907375983
NM_001184880.2(PCDH19):c.2288+9G>T rs753792839
NM_001184880.2(PCDH19):c.2301C>T (p.Tyr767=) rs1057524610
NM_001184880.2(PCDH19):c.2358C>T (p.Ile786=) rs768467022
NM_001184880.2(PCDH19):c.2419C>T (p.Leu807=) rs1555984464
NM_001184880.2(PCDH19):c.2430C>T (p.Ser810=) rs751223449
NM_001184880.2(PCDH19):c.2460G>A (p.Thr820=) rs766769854
NM_001184880.2(PCDH19):c.2496C>T (p.Phe832=) rs774555485
NM_001184880.2(PCDH19):c.2588T>G (p.Leu863Arg) rs796052792
NM_001184880.2(PCDH19):c.2598C>T (p.Asn866=) rs371444167
NM_001184880.2(PCDH19):c.2607T>C (p.Pro869=) rs766605694
NM_001184880.2(PCDH19):c.2616+13A>T rs903221490
NM_001184880.2(PCDH19):c.2616+19C>T rs1555984385
NM_001184880.2(PCDH19):c.2676-218C>T
NM_001184880.2(PCDH19):c.2767C>A (p.Arg923=) rs752763816
NM_001184880.2(PCDH19):c.2781T>C (p.Cys927=) rs1555977733
NM_001184880.2(PCDH19):c.2790T>C (p.Ala930=) rs375759744
NM_001184880.2(PCDH19):c.2796C>T (p.Asn932=) rs193148631
NM_001184880.2(PCDH19):c.2873G>A (p.Arg958Gln) rs748581653
NM_001184880.2(PCDH19):c.2938C>T (p.Arg980Cys) rs3764758
NM_001184880.2(PCDH19):c.2939G>A (p.Arg980His) rs368872920
NM_001184880.2(PCDH19):c.2965A>C (p.Asn989His) rs201611496
NM_001184880.2(PCDH19):c.2994T>C (p.Thr998=) rs745398684
NM_001184880.2(PCDH19):c.3012T>C (p.Ala1004=) rs181719144
NM_001184880.2(PCDH19):c.3037C>T (p.Arg1013Trp) rs376406896
NM_001184880.2(PCDH19):c.3078G>A (p.Pro1026=) rs1358480010
NM_001184880.2(PCDH19):c.309C>G (p.Leu103=) rs1057520954
NM_001184880.2(PCDH19):c.3120T>C (p.Asp1040=) rs199702403
NM_001184880.2(PCDH19):c.3127A>G (p.Ile1043Val) rs189342249
NM_001184880.2(PCDH19):c.3127A>T (p.Ile1043Phe) rs189342249
NM_001184880.2(PCDH19):c.315C>T (p.Val105=) rs1555985739
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.321C>T (p.Ser107=) rs767664406
NM_001184880.2(PCDH19):c.3235C>A (p.Pro1079Thr) rs200854927
NM_001184880.2(PCDH19):c.3235C>G (p.Pro1079Ala) rs200854927
NM_001184880.2(PCDH19):c.3280C>G (p.Leu1094Val) rs184545774
NM_001184880.2(PCDH19):c.3308A>G (p.Asn1103Ser)
NM_001184880.2(PCDH19):c.3319C>G (p.Arg1107Gly) rs191333060
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.3439G>A (p.Val1147Ile) rs138771033
NM_001184880.2(PCDH19):c.438G>A (p.Thr146=) rs776584913
NM_001184880.2(PCDH19):c.513C>T (p.Asn171=) rs749602848
NM_001184880.2(PCDH19):c.51G>A (p.Thr17=) rs756958731
NM_001184880.2(PCDH19):c.531G>A (p.Glu177=) rs192122222
NM_001184880.2(PCDH19):c.540G>A (p.Thr180=) rs368094294
NM_001184880.2(PCDH19):c.543C>A (p.Arg181=) rs780266148
NM_001184880.2(PCDH19):c.648G>A (p.Pro216=) rs996601558
NM_001184880.2(PCDH19):c.655C>T (p.Leu219=) rs377627937
NM_001184880.2(PCDH19):c.6G>A (p.Glu2=) rs184883626
NM_001184880.2(PCDH19):c.741G>T (p.Val247=) rs1057521743
NM_001184880.2(PCDH19):c.769G>C (p.Val257Leu) rs201713027
NM_001184880.2(PCDH19):c.789C>T (p.Ser263=) rs1338518342
NM_001184880.2(PCDH19):c.792T>C (p.Asp264=)
NM_001184880.2(PCDH19):c.798C>T (p.Asp266=) rs369638371
NM_001184880.2(PCDH19):c.81C>T (p.Tyr27=) rs56307810
NM_001184880.2(PCDH19):c.846C>T (p.Asn282=) rs750813033
NM_001184880.2(PCDH19):c.888C>T (p.Gly296=) rs368963363
NM_001184880.2(PCDH19):c.942G>A (p.Leu314=) rs773740606

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