ClinVar Miner

List of variants in gene HCN4 reported as likely benign for not provided

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Gene type:
ClinVar version:
Total variants: 86
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HGVS dbSNP gnomAD frequency
NM_005477.3(HCN4):c.107G>A (p.Gly36Glu) rs143090627 0.04452
NM_005477.3(HCN4):c.1591-237C>T rs145211410 0.01558
NM_005477.3(HCN4):c.1978+46G>A rs41277728 0.01318
NM_005477.3(HCN4):c.1978+260T>A rs140161480 0.01102
NM_005477.3(HCN4):c.2144-55A>G rs142989707 0.01062
NM_005477.3(HCN4):c.1683C>A (p.Gly561=) rs62641690 0.01030
NM_005477.3(HCN4):c.1210-103C>G rs73442004 0.00885
NM_005477.3(HCN4):c.-277_-268del rs577671006 0.00814
NM_005477.3(HCN4):c.2648C>G (p.Pro883Arg) rs148398509 0.00737
NM_005477.3(HCN4):c.2657C>T (p.Ala886Val) rs200575377 0.00352
NM_005477.3(HCN4):c.-189G>A rs548581131 0.00346
NM_005477.3(HCN4):c.2275G>A (p.Val759Ile) rs62641689 0.00258
NM_005477.3(HCN4):c.3587G>A (p.Arg1196His) rs147181577 0.00191
NM_005477.3(HCN4):c.3350C>T (p.Pro1117Leu) rs140402087 0.00185
NM_005477.3(HCN4):c.1978+3G>T rs113112855 0.00166
NM_005477.3(HCN4):c.1518C>T (p.Tyr506=) rs139590882 0.00163
NM_005477.3(HCN4):c.458A>G (p.Glu153Gly) rs560874115 0.00149
NM_005477.3(HCN4):c.1356C>T (p.Ser452=) rs148453034 0.00116
NM_005477.3(HCN4):c.3010C>T (p.Pro1004Ser) rs201418838 0.00084
NM_005477.3(HCN4):c.1653C>A (p.Ile551=) rs141966309 0.00083
NM_005477.3(HCN4):c.1703G>C (p.Ser568Thr) rs138714806 0.00076
NM_005477.3(HCN4):c.3577G>C (p.Glu1193Gln) rs200507617 0.00068
NM_005477.3(HCN4):c.2739G>A (p.Ala913=) rs373411041 0.00056
NM_005477.3(HCN4):c.3187C>A (p.Pro1063Thr) rs535227661 0.00049
NM_005477.3(HCN4):c.2694C>T (p.Gly898=) rs375169111 0.00046
NM_005477.3(HCN4):c.2800C>T (p.Arg934Cys) rs199638465 0.00045
NM_005477.3(HCN4):c.2210A>G (p.Gln737Arg) rs146732972 0.00043
NM_005477.3(HCN4):c.2181C>T (p.His727=) rs140354126 0.00036
NM_005477.3(HCN4):c.561T>C (p.Ala187=) rs375206856 0.00030
NM_005477.3(HCN4):c.1656C>T (p.His552=) rs148142070 0.00029
NM_005477.3(HCN4):c.1372-13C>T rs374981035 0.00028
NM_005477.3(HCN4):c.2668C>T (p.Pro890Ser) rs184801511 0.00026
NM_005477.3(HCN4):c.1536C>T (p.His512=) rs146306966 0.00024
NM_005477.3(HCN4):c.1635C>T (p.Pro545=) rs140015730 0.00024
NM_005477.3(HCN4):c.2109C>T (p.Phe703=) rs150378994 0.00021
NM_005477.3(HCN4):c.2465C>T (p.Thr822Met) rs201143364 0.00020
NM_005477.3(HCN4):c.1979-51T>A rs534315900 0.00018
NM_005477.3(HCN4):c.2313C>T (p.Pro771=) rs142298104 0.00016
NM_005477.3(HCN4):c.2904G>A (p.Pro968=) rs368145651 0.00016
NM_005477.3(HCN4):c.1738-6C>T rs760763085 0.00014
NM_005477.3(HCN4):c.3012G>A (p.Pro1004=) rs377602893 0.00014
NM_005477.3(HCN4):c.2025C>T (p.Ala675=) rs149033101 0.00013
NM_005477.3(HCN4):c.621C>G (p.Arg207=) rs727503958 0.00012
NM_005477.3(HCN4):c.2522C>T (p.Ser841Leu) rs200546024 0.00011
NM_005477.3(HCN4):c.2838C>T (p.Pro946=) rs552881314 0.00011
NM_005477.3(HCN4):c.3117G>A (p.Pro1039=) rs749785521 0.00011
NM_005477.3(HCN4):c.584C>T (p.Ala195Val) rs201375192 0.00011
NM_005477.3(HCN4):c.1437C>T (p.Ile479=) rs202001597 0.00009
NM_005477.3(HCN4):c.1815G>A (p.Thr605=) rs367753936 0.00009
NM_005477.3(HCN4):c.2604C>T (p.Pro868=) rs138773305 0.00009
NM_005477.3(HCN4):c.3531G>T (p.Gly1177=) rs375911378 0.00008
NM_005477.3(HCN4):c.3009G>A (p.Pro1003=) rs775401682 0.00007
NM_005477.3(HCN4):c.3351G>A (p.Pro1117=) rs375138488 0.00007
NM_005477.3(HCN4):c.1303C>T (p.Leu435=) rs746461789 0.00006
NM_005477.3(HCN4):c.258G>A (p.Lys86=) rs1019029244 0.00006
NM_005477.3(HCN4):c.1242C>T (p.Ala414=) rs376218786 0.00005
NM_005477.3(HCN4):c.1254C>T (p.Ile418=) rs373794941 0.00005
NM_005477.3(HCN4):c.1455G>A (p.Ala485=) rs148875639 0.00004
NM_005477.3(HCN4):c.2715C>T (p.Ala905=) rs745886315 0.00004
NM_005477.3(HCN4):c.2832G>A (p.Ala944=) rs747946171 0.00004
NM_005477.3(HCN4):c.2845C>T (p.Arg949Trp) rs755614529 0.00004
NM_005477.3(HCN4):c.3078C>T (p.Ser1026=) rs202188345 0.00004
NM_005477.3(HCN4):c.3396C>T (p.Ser1132=) rs369224427 0.00004
NM_005477.3(HCN4):c.2830G>A (p.Ala944Thr) rs777648103 0.00003
NM_005477.3(HCN4):c.3228C>T (p.Pro1076=) rs770161577 0.00003
NM_005477.3(HCN4):c.1818C>T (p.Ser606=) rs1247778865 0.00002
NM_005477.3(HCN4):c.3264G>A (p.Ala1088=) rs752705479 0.00002
NM_005477.3(HCN4):c.1459G>A (p.Val487Met) rs202037304 0.00001
NM_005477.3(HCN4):c.1473C>T (p.Asp491=) rs773250829 0.00001
NM_005477.3(HCN4):c.1560G>A (p.Leu520=) rs200033529 0.00001
NM_005477.3(HCN4):c.1692C>T (p.Phe564=) rs770857939 0.00001
NM_005477.3(HCN4):c.2055C>T (p.Ser685=) rs886042819 0.00001
NM_005477.3(HCN4):c.2268G>A (p.Ala756=) rs781114942 0.00001
NM_005477.3(HCN4):c.2526C>T (p.Pro842=) rs201499694 0.00001
NM_005477.3(HCN4):c.3126G>A (p.Pro1042=) rs1057521459 0.00001
NM_005477.3(HCN4):c.*2C>G rs2151213654
NM_005477.3(HCN4):c.1591-38_1591-15del rs768333616
NM_005477.3(HCN4):c.174C>T (p.Pro58=) rs920292438
NM_005477.3(HCN4):c.2274C>T (p.Arg758=) rs749766433
NM_005477.3(HCN4):c.2494C>T (p.Leu832=)
NM_005477.3(HCN4):c.2804C>T (p.Ser935Phe) rs775803239
NM_005477.3(HCN4):c.3105A>C (p.Pro1035=)
NM_005477.3(HCN4):c.3300T>C (p.Thr1100=) rs2151213924
NM_005477.3(HCN4):c.3378C>T (p.Ser1126=) rs758673317
NM_005477.3(HCN4):c.785+104dup rs145930956
NM_005477.3(HCN4):c.785+18T>A rs1412056222

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