ClinVar Miner

List of variants in gene PKP2 reported as likely benign by Color

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Gene type:
ClinVar version:
Total variants: 157
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HGVS dbSNP
NM_001005242.3(PKP2):c.-10C>T
NM_001005242.3(PKP2):c.1035G>A (p.Gly345=)
NM_001005242.3(PKP2):c.1044C>T (p.Asp348=)
NM_001005242.3(PKP2):c.1080C>T (p.Leu360=) rs397516984
NM_001005242.3(PKP2):c.1086A>G (p.Ala362=)
NM_001005242.3(PKP2):c.1093A>G (p.Met365Val) rs143900944
NM_001005242.3(PKP2):c.1104C>T (p.Ser368=)
NM_001005242.3(PKP2):c.1114G>C (p.Ala372Pro) rs200586695
NM_001005242.3(PKP2):c.1137C>T (p.His379=)
NM_001005242.3(PKP2):c.1171-10T>C rs200122872
NM_001005242.3(PKP2):c.1171-11T>C rs183414126
NM_001005242.3(PKP2):c.1171-13G>A
NM_001005242.3(PKP2):c.1212A>G (p.Leu404=) rs1592750669
NM_001005242.3(PKP2):c.1236G>A (p.Gln412=)
NM_001005242.3(PKP2):c.123G>T (p.Ala41=)
NM_001005242.3(PKP2):c.12C>T (p.Pro4=) rs397516991
NM_001005242.3(PKP2):c.1372A>G (p.Ile458Val) rs199571473
NM_001005242.3(PKP2):c.1379-2005A>G rs397516995
NM_001005242.3(PKP2):c.1379-2019C>T rs149930872
NM_001005242.3(PKP2):c.1379-2054C>T rs144620127
NM_001005242.3(PKP2):c.1379-2056C>T
NM_001005242.3(PKP2):c.1379-2065G>A
NM_001005242.3(PKP2):c.1379-2067G>A rs138538072
NM_001005242.3(PKP2):c.1379-2071G>A rs776244945
NM_001005242.3(PKP2):c.1379-2103A>G
NM_001005242.3(PKP2):c.1379-2109G>A rs139159464
NM_001005242.3(PKP2):c.1379-2111C>T
NM_001005242.3(PKP2):c.1379-2119C>A
NM_001005242.3(PKP2):c.1445C>T (p.Thr482Met) rs146882581
NM_001005242.3(PKP2):c.1446G>A (p.Thr482=)
NM_001005242.3(PKP2):c.1504G>A (p.Ala502Thr) rs368740836
NM_001005242.3(PKP2):c.1515G>A (p.Leu505=)
NM_001005242.3(PKP2):c.1593G>A (p.Ala531=) rs760093803
NM_001005242.3(PKP2):c.1593G>T (p.Ala531=) rs760093803
NM_001005242.3(PKP2):c.1608C>T (p.Asp536=) rs397517006
NM_001005242.3(PKP2):c.1614C>T (p.Leu538=)
NM_001005242.3(PKP2):c.1620C>T (p.Asp540=)
NM_001005242.3(PKP2):c.1627G>A (p.Val543Ile) rs146102241
NM_001005242.3(PKP2):c.1675-3C>T
NM_001005242.3(PKP2):c.1737A>G (p.Pro579=)
NM_001005242.3(PKP2):c.1839+6T>C
NM_001005242.3(PKP2):c.1840-13T>C
NM_001005242.3(PKP2):c.1840-7T>C
NM_001005242.3(PKP2):c.1848G>A (p.Gln616=) rs759353036
NM_001005242.3(PKP2):c.1851C>T (p.Asp617=)
NM_001005242.3(PKP2):c.1852G>A (p.Val618Met)
NM_001005242.3(PKP2):c.1863G>A (p.Pro621=) rs146144731
NM_001005242.3(PKP2):c.1872G>A (p.Lys624=)
NM_001005242.3(PKP2):c.1878C>T (p.Asn626=)
NM_001005242.3(PKP2):c.1932C>T (p.Ser644=)
NM_001005242.3(PKP2):c.1955A>G (p.Asn652Ser) rs140852019
NM_001005242.3(PKP2):c.195C>T (p.Ala65=) rs397517014
NM_001005242.3(PKP2):c.1965A>G (p.Gln655=) rs727505293
NM_001005242.3(PKP2):c.1998G>C (p.Thr666=)
NM_001005242.3(PKP2):c.2013A>G (p.Pro671=)
NM_001005242.3(PKP2):c.2018C>T (p.Pro673Leu) rs144018320
NM_001005242.3(PKP2):c.2061G>A (p.Leu687=)
NM_001005242.3(PKP2):c.2072G>A (p.Arg691Gln)
NM_001005242.3(PKP2):c.2121G>A (p.Ser707=) rs139098675
NM_001005242.3(PKP2):c.2168-5T>C
NM_001005242.3(PKP2):c.2200A>G (p.Ile734Val)
NM_001005242.3(PKP2):c.2233A>G (p.Ile745Val) rs551045165
NM_001005242.3(PKP2):c.224-7A>G
NM_001005242.3(PKP2):c.224-9T>C
NM_001005242.3(PKP2):c.2299C>A (p.Arg767Ser) rs139734328
NM_001005242.3(PKP2):c.2338G>A (p.Ala780Thr)
NM_001005242.3(PKP2):c.2353G>A (p.Asp785Asn) rs151264959
NM_001005242.3(PKP2):c.2355T>C (p.Asp785=) rs142362933
NM_001005242.3(PKP2):c.2388T>C (p.Ala796=)
NM_001005242.3(PKP2):c.2391C>T (p.Ser797=)
NM_001005242.3(PKP2):c.2446-11dup rs397517024
NM_001005242.3(PKP2):c.2499C>A (p.His833Gln) rs202094467
NM_001005242.3(PKP2):c.293T>C (p.Val98Ala)
NM_001005242.3(PKP2):c.29A>G (p.Tyr10Cys)
NM_001005242.3(PKP2):c.302G>A (p.Arg101His) rs149542398
NM_001005242.3(PKP2):c.306C>A (p.Ser102=) rs376613662
NM_001005242.3(PKP2):c.337-4G>A
NM_001005242.3(PKP2):c.360A>G (p.Glu120=)
NM_001005242.3(PKP2):c.390C>T (p.Tyr130=)
NM_001005242.3(PKP2):c.405C>T (p.Ser135=)
NM_001005242.3(PKP2):c.411A>G (p.Glu137=) rs1591829029
NM_001005242.3(PKP2):c.419C>T (p.Ser140Phe) rs150821281
NM_001005242.3(PKP2):c.420C>T (p.Ser140=)
NM_001005242.3(PKP2):c.468G>A (p.Pro156=) rs756166702
NM_001005242.3(PKP2):c.498C>T (p.Tyr166=)
NM_001005242.3(PKP2):c.505A>G (p.Ser169Gly) rs139139859
NM_001005242.3(PKP2):c.558C>T (p.Ala186=) rs184522105
NM_001005242.3(PKP2):c.582T>C (p.Tyr194=) rs532048791
NM_001005242.3(PKP2):c.591C>T (p.Ser197=)
NM_001005242.3(PKP2):c.611G>A (p.Arg204His) rs755215178
NM_001005242.3(PKP2):c.714G>A (p.Pro238=) rs727503372
NM_001005242.3(PKP2):c.749G>A (p.Arg250His)
NM_001005242.3(PKP2):c.795G>T (p.Gly265=) rs375268778
NM_001005242.3(PKP2):c.819G>T (p.Pro273=)
NM_001005242.3(PKP2):c.81C>T (p.Ser27=)
NM_001005242.3(PKP2):c.826C>T (p.Pro276Ser) rs201944276
NM_001005242.3(PKP2):c.888C>T (p.His296=) rs397517029
NM_001005242.3(PKP2):c.899C>A (p.Thr300Lys)
NM_001005242.3(PKP2):c.918C>T (p.Pro306=) rs368656084
NM_001005242.3(PKP2):c.921T>C (p.Ser307=)
NM_001005242.3(PKP2):c.934T>G (p.Ser312Ala)
NM_001005242.3(PKP2):c.93G>A (p.Ala31=)
NM_004572.3(PKP2):c.*5A>G rs1398323423
NM_004572.3(PKP2):c.1035-9T>C rs1057522716
NM_004572.3(PKP2):c.1101A>G (p.Pro367=) rs776927054
NM_004572.3(PKP2):c.1231G>A (p.Val411Ile) rs192041220
NM_004572.3(PKP2):c.1251G>T (p.Gly417=) rs567854722
NM_004572.3(PKP2):c.1308A>G (p.Leu436=) rs1439169005
NM_004572.3(PKP2):c.1326G>A (p.Leu442=) rs377076035
NM_004572.3(PKP2):c.1415C>T (p.Pro472Leu) rs758950276
NM_004572.3(PKP2):c.1421C>T (p.Ala474Val) rs373399921
NM_004572.3(PKP2):c.1449T>C (p.Thr483=) rs781397552
NM_004572.3(PKP2):c.1464C>T (p.Gly488=)
NM_004572.3(PKP2):c.1476G>A (p.Thr492=) rs140301552
NM_004572.3(PKP2):c.1511-5T>C rs189036647
NM_004572.3(PKP2):c.1584G>A (p.Thr528=) rs727504098
NM_004572.3(PKP2):c.1596C>T (p.Ile532=) rs145387575
NM_004572.3(PKP2):c.165G>T (p.Arg55=) rs1472609900
NM_004572.3(PKP2):c.1707C>T (p.Gly569=) rs780049494
NM_004572.3(PKP2):c.1812G>A (p.Thr604=) rs773662874
NM_004572.3(PKP2):c.184C>A (p.Gln62Lys) rs199601548
NM_004572.3(PKP2):c.1974A>G (p.Gln658=) rs138901574
NM_004572.3(PKP2):c.212C>T (p.Ser71Phe) rs796597346
NM_004572.3(PKP2):c.2130G>A (p.Thr710=) rs371089832
NM_004572.3(PKP2):c.2130G>T (p.Thr710=) rs371089832
NM_004572.3(PKP2):c.213C>T (p.Ser71=) rs1173618581
NM_004572.3(PKP2):c.2146-7A>G rs1555141645
NM_004572.3(PKP2):c.2151G>A (p.Pro717=) rs147995773
NM_004572.3(PKP2):c.2202C>G (p.Thr734=) rs587781109
NM_004572.3(PKP2):c.2300-4G>C rs376231586
NM_004572.3(PKP2):c.2303A>C (p.Lys768Thr) rs201487421
NM_004572.3(PKP2):c.2322G>A (p.Leu774=) rs886049320
NM_004572.3(PKP2):c.2349G>A (p.Pro783=) rs753226330
NM_004572.3(PKP2):c.2397G>A (p.Leu799=)
NM_004572.3(PKP2):c.2433C>T (p.Arg811=) rs369166666
NM_004572.3(PKP2):c.2499C>T (p.Ser833=) rs1330430218
NM_004572.3(PKP2):c.2553G>A (p.Thr851=) rs199900632
NM_004572.3(PKP2):c.2578-9A>T rs1057524088
NM_004572.3(PKP2):c.2589G>A (p.Lys863=) rs777477467
NM_004572.3(PKP2):c.2619C>T (p.Ala873=) rs747191995
NM_004572.3(PKP2):c.387G>A (p.Gln129=) rs768974835
NM_004572.3(PKP2):c.45C>T (p.Thr15=) rs759214983
NM_004572.3(PKP2):c.486G>A (p.Thr162=) rs189040311
NM_004572.3(PKP2):c.576G>A (p.Pro192=) rs373380483
NM_004572.3(PKP2):c.600G>A (p.Val200=) rs781305034
NM_004572.3(PKP2):c.720G>A (p.Leu240=) rs777567315
NM_004572.3(PKP2):c.741G>C (p.Gly247=) rs762366326
NM_004572.3(PKP2):c.804C>T (p.Val268=)
NM_004572.3(PKP2):c.837C>T (p.Pro279=) rs572938229
NM_004572.3(PKP2):c.900G>A (p.Thr300=) rs140235564
NM_004572.3(PKP2):c.901C>T (p.Leu301=) rs1565599048
NM_004572.3(PKP2):c.925G>A (p.Ala309Thr) rs761677945
NM_004572.3(PKP2):c.927C>T (p.Ala309=) rs200152448
NM_004572.3(PKP2):c.953A>C (p.His318Pro) rs181098323
NM_004572.3(PKP2):c.963C>T (p.Val321=) rs202207343
NM_004572.3(PKP2):c.964G>T (p.Gly322Cys) rs200069860
NM_004572.3(PKP2):c.996G>A (p.Leu332=) rs144574595

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