ClinVar Miner

List of variants in gene PKP2 reported as benign

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Gene type:
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Total variants: 73
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HGVS dbSNP
NM_004572.3(PKP2):c.-264G>A
NM_004572.3(PKP2):c.1012A>G (p.Thr338Ala) rs139851304
NM_004572.3(PKP2):c.1097T>C (p.Leu366Pro) rs1046116
NM_004572.3(PKP2):c.1114G>C (p.Ala372Pro) rs200586695
NM_004572.3(PKP2):c.1116T>C (p.Ala372=) rs142742483
NM_004572.3(PKP2):c.1171-10T>C rs200122872
NM_004572.3(PKP2):c.1171-11T>C rs183414126
NM_004572.3(PKP2):c.1171-146A>G
NM_004572.3(PKP2):c.1171-17A>G rs372942306
NM_004572.3(PKP2):c.1230C>T (p.Asp410=) rs148364390
NM_004572.3(PKP2):c.1323G>T (p.Arg441=) rs3748278
NM_004572.3(PKP2):c.1372A>G (p.Ile458Val) rs199571473
NM_004572.3(PKP2):c.1378+177T>A
NM_004572.3(PKP2):c.1419C>T (p.Gly473=) rs377424658
NM_004572.3(PKP2):c.1510+78A>G
NM_004572.3(PKP2):c.1511-18A>G rs113698150
NM_004572.3(PKP2):c.1550A>G (p.Asn517Ser) rs144536197
NM_004572.3(PKP2):c.156G>A (p.Lys52=) rs201210997
NM_004572.3(PKP2):c.1577C>T (p.Thr526Met) rs146882581
NM_004572.3(PKP2):c.1592T>G (p.Ile531Ser) rs147240502
NM_004572.3(PKP2):c.1641T>C (p.Asn547=) rs143782040
NM_004572.3(PKP2):c.1671C>T (p.Asn557=) rs535581825
NM_004572.3(PKP2):c.1688+140T>C
NM_004572.3(PKP2):c.1688+9A>G rs397517004
NM_004572.3(PKP2):c.1689-13dup rs200009796
NM_004572.3(PKP2):c.174G>T (p.Glu58Asp) rs146708884
NM_004572.3(PKP2):c.1759G>A (p.Val587Ile) rs146102241
NM_004572.3(PKP2):c.1806+331G>A
NM_004572.3(PKP2):c.1807-195T>C
NM_004572.3(PKP2):c.195C>T (p.Ala65=) rs397517014
NM_004572.3(PKP2):c.1971+235T>C
NM_004572.3(PKP2):c.1972-148A>G
NM_004572.3(PKP2):c.1995G>A (p.Pro665=) rs146144731
NM_004572.3(PKP2):c.209G>T (p.Ser70Ile) rs75909145
NM_004572.3(PKP2):c.2133C>T (p.Ala711=) rs529442984
NM_004572.3(PKP2):c.2145+45G>A rs10772008
NM_004572.3(PKP2):c.2146-152C>T
NM_004572.3(PKP2):c.2146-157G>T
NM_004572.3(PKP2):c.2146-185G>C
NM_004572.3(PKP2):c.2169A>G (p.Thr723=) rs377504106
NM_004572.3(PKP2):c.2202C>G (p.Thr734=) rs587781109
NM_004572.3(PKP2):c.223+286G>A
NM_004572.3(PKP2):c.2299+183C>G
NM_004572.3(PKP2):c.2299+7C>T rs74072938
NM_004572.3(PKP2):c.2300-11_2300-10insT rs746936605
NM_004572.3(PKP2):c.2300-11delT rs746936605
NM_004572.3(PKP2):c.2300-195A>G
NM_004572.3(PKP2):c.2300-21_2300-20delGT rs200266270
NM_004572.3(PKP2):c.2300-21delG rs57690055
NM_004572.3(PKP2):c.2300-6T>C rs368531764
NM_004572.3(PKP2):c.2392A>G (p.Thr798Ala) rs112592855
NM_004572.3(PKP2):c.2431C>A (p.Arg811Ser) rs139734328
NM_004572.3(PKP2):c.2485G>A (p.Asp829Asn) rs151264959
NM_004572.3(PKP2):c.2489+13_2489+14insC rs149968852
NM_004572.3(PKP2):c.2489+72G>A
NM_004572.3(PKP2):c.2489+73delT
NM_004572.3(PKP2):c.2490-104C>G
NM_004572.3(PKP2):c.2490-170C>T
NM_004572.3(PKP2):c.2490-56C>A
NM_004572.3(PKP2):c.2578-60C>A
NM_004572.3(PKP2):c.2578-69G>A
NM_004572.3(PKP2):c.2615C>T (p.Thr872Ile) rs370599966
NM_004572.3(PKP2):c.306C>A (p.Ser102=) rs376613662
NM_004572.3(PKP2):c.387G>A (p.Gln129=) rs768974835
NM_004572.3(PKP2):c.406G>A (p.Val136Met) rs567795321
NM_004572.3(PKP2):c.706G>T (p.Ala236Ser) rs62001015
NM_004572.3(PKP2):c.76G>A (p.Asp26Asn) rs143004808
NM_004572.3(PKP2):c.791C>T (p.Ala264Val) rs62001016
NM_004572.3(PKP2):c.819G>A (p.Pro273=) rs3748279
NM_004572.3(PKP2):c.927C>T (p.Ala309=) rs200152448
NM_004572.3(PKP2):c.939C>T (p.Ser313=) rs61729381
NM_004572.3(PKP2):c.951G>A (p.Ala317=) rs61729382
NM_004572.3(PKP2):c.972G>A (p.Ala324=) rs142636176

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