ClinVar Miner

List of variants in gene HCN4 reported as uncertain significance for Sick sinus syndrome 2, autosomal dominant

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Total variants: 42
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HGVS dbSNP gnomAD frequency
NM_005477.3(HCN4):c.458A>G (p.Glu153Gly) rs560874115 0.00149
NM_005477.3(HCN4):c.-529G>A rs879470594 0.00136
NM_005477.3(HCN4):c.*1085A>C rs563333401 0.00036
NM_005477.3(HCN4):c.*1598A>G rs749289571 0.00031
NM_005477.3(HCN4):c.-132G>C rs952368455 0.00031
NM_005477.3(HCN4):c.*2010A>C rs550566467 0.00018
NM_005477.3(HCN4):c.-547G>C rs577325559 0.00016
NM_005477.3(HCN4):c.-364C>G rs1008967231 0.00014
NM_005477.3(HCN4):c.*980C>T rs767610327 0.00006
NM_005477.3(HCN4):c.2917G>A (p.Gly973Arg) rs200495478 0.00006
NM_005477.3(HCN4):c.*2585G>A rs770482289 0.00005
NM_005477.3(HCN4):c.*1172A>G rs561112458 0.00004
NM_005477.3(HCN4):c.*592G>A rs758508473 0.00004
NM_005477.3(HCN4):c.3209G>A (p.Gly1070Asp) rs772839442 0.00004
NM_005477.3(HCN4):c.249C>T (p.Gly83=) rs1183278712 0.00003
NM_005477.3(HCN4):c.3229G>A (p.Gly1077Ser) rs746291340 0.00003
NM_005477.3(HCN4):c.*901C>T rs1464478840 0.00002
NM_005477.3(HCN4):c.3081C>T (p.Pro1027=) rs1226393084 0.00002
NM_005477.3(HCN4):c.3218C>T (p.Pro1073Leu) rs982016034 0.00002
NM_005477.3(HCN4):c.375C>T (p.Ser125=) rs1310424203 0.00002
NM_005477.3(HCN4):c.*104A>T rs1053318527 0.00001
NM_005477.3(HCN4):c.*2241T>C rs1441893786 0.00001
NM_005477.3(HCN4):c.1657G>A (p.Asp553Asn) rs104894485 0.00001
NM_005477.3(HCN4):c.3130C>T (p.Arg1044Trp) rs553950644 0.00001
NM_005477.3(HCN4):c.3205C>T (p.Arg1069Trp) rs770658894 0.00001
NM_005477.3(HCN4):c.577G>T (p.Gly193Cys) rs2043135036 0.00001
NM_005477.3(HCN4):c.*1205A>G rs572355448
NM_005477.3(HCN4):c.*168A>G rs2042863984
NM_005477.3(HCN4):c.*1834G>T rs1279314845
NM_005477.3(HCN4):c.*44C>T rs2042865036
NM_005477.3(HCN4):c.*767C>T rs571705929
NM_005477.3(HCN4):c.*847A>G rs2042858705
NM_005477.3(HCN4):c.-114G>A rs2043140776
NM_005477.3(HCN4):c.-188G>T rs2043141200
NM_005477.3(HCN4):c.-497G>A rs932616633
NM_005477.3(HCN4):c.-518A>G rs2043143421
NM_005477.3(HCN4):c.1844T>G (p.Val615Gly) rs2042890755
NM_005477.3(HCN4):c.2143+8G>A rs2042883869
NM_005477.3(HCN4):c.2175C>G (p.Val725=) rs2042882216
NM_005477.3(HCN4):c.2314G>A (p.Val772Ile) rs776635828
NM_005477.3(HCN4):c.319G>A (p.Gly107Ser) rs2043137058
NM_005477.3(HCN4):c.522G>A (p.Pro174=) rs1302048506

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