ClinVar Miner

List of variants in gene HCN4 reported as uncertain significance by GeneDx

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Gene type:
ClinVar version:
Total variants: 121
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HGVS dbSNP gnomAD frequency
NM_005477.3(HCN4):c.2420G>A (p.Arg807His) rs200395062 0.00036
NM_005477.3(HCN4):c.302C>T (p.Ala101Val) rs781730381 0.00018
NM_005477.3(HCN4):c.2730C>A (p.Phe910Leu) rs200814534 0.00013
NM_005477.3(HCN4):c.2701G>A (p.Ala901Thr) rs201742383 0.00012
NM_005477.3(HCN4):c.2978C>T (p.Thr993Met) rs199798661 0.00011
NM_005477.3(HCN4):c.3195C>A (p.Val1065=) rs4493011 0.00010
NM_005477.3(HCN4):c.418G>A (p.Gly140Ser) rs773857091 0.00009
NM_005477.3(HCN4):c.724C>T (p.Arg242Cys) rs745880598 0.00008
NM_005477.3(HCN4):c.2669C>T (p.Pro890Leu) rs758929649 0.00007
NM_005477.3(HCN4):c.2695G>A (p.Val899Ile) rs370669201 0.00007
NM_005477.3(HCN4):c.3397G>C (p.Gly1133Arg) rs532186403 0.00007
NM_005477.3(HCN4):c.520C>T (p.Pro174Ser) rs542532555 0.00007
NM_005477.3(HCN4):c.2605G>A (p.Ala869Thr) rs775134377 0.00006
NM_005477.3(HCN4):c.2846G>A (p.Arg949Gln) rs752139441 0.00006
NM_005477.3(HCN4):c.2917G>A (p.Gly973Arg) rs200495478 0.00006
NM_005477.3(HCN4):c.3293C>T (p.Ala1098Val) rs1064797200 0.00006
NM_005477.3(HCN4):c.3461G>A (p.Arg1154Gln) rs145862018 0.00006
NM_005477.3(HCN4):c.1924G>A (p.Val642Met) rs779402752 0.00005
NM_005477.3(HCN4):c.2458G>A (p.Gly820Arg) rs761337460 0.00005
NM_005477.3(HCN4):c.2995C>T (p.Arg999Trp) rs538668505 0.00005
NM_005477.3(HCN4):c.3460C>T (p.Arg1154Trp) rs200896834 0.00005
NM_005477.3(HCN4):c.1636G>A (p.Asp546Asn) rs370884239 0.00004
NM_005477.3(HCN4):c.1722C>T (p.Ser574=) rs750941501 0.00004
NM_005477.3(HCN4):c.2197G>A (p.Val733Ile) rs376631391 0.00004
NM_005477.3(HCN4):c.2383C>T (p.Leu795Phe) rs1435000428 0.00004
NM_005477.3(HCN4):c.2903C>T (p.Pro968Leu) rs548194804 0.00004
NM_005477.3(HCN4):c.3409C>T (p.Pro1137Ser) rs773914774 0.00004
NM_005477.3(HCN4):c.3414del (p.Arg1140fs) rs746402732 0.00004
NM_005477.3(HCN4):c.3596T>A (p.Leu1199Gln) rs146751122 0.00004
NM_005477.3(HCN4):c.394A>C (p.Ile132Leu) rs772764704 0.00004
NM_005477.3(HCN4):c.1713C>T (p.Gly571=) rs754495351 0.00003
NM_005477.3(HCN4):c.1835G>A (p.Arg612His) rs528148663 0.00003
NM_005477.3(HCN4):c.2069A>G (p.Asn690Ser) rs776033369 0.00003
NM_005477.3(HCN4):c.2266G>A (p.Ala756Thr) rs143339036 0.00003
NM_005477.3(HCN4):c.2801G>A (p.Arg934His) rs369485237 0.00003
NM_005477.3(HCN4):c.2839G>A (p.Gly947Arg) rs753524680 0.00003
NM_005477.3(HCN4):c.2990C>A (p.Pro997His) rs375788137 0.00003
NM_005477.3(HCN4):c.3209G>A (p.Gly1070Asp) rs772839442 0.00003
NM_005477.3(HCN4):c.3232C>T (p.Arg1078Cys) rs781376523 0.00003
NM_005477.3(HCN4):c.3379G>A (p.Gly1127Arg) rs748279911 0.00003
NM_005477.3(HCN4):c.3582A>G (p.Pro1194=) rs375637572 0.00003
NM_005477.3(HCN4):c.1732C>T (p.Arg578Trp) rs752953709 0.00002
NM_005477.3(HCN4):c.2063A>G (p.Asn688Ser) rs778801845 0.00002
NM_005477.3(HCN4):c.2194G>A (p.Gly732Ser) rs199530458 0.00002
NM_005477.3(HCN4):c.2797G>A (p.Ala933Thr) rs762464413 0.00002
NM_005477.3(HCN4):c.2875C>G (p.Leu959Val) rs1057524285 0.00002
NM_005477.3(HCN4):c.3218C>T (p.Pro1073Leu) rs982016034 0.00002
NM_005477.3(HCN4):c.334G>A (p.Gly112Ser) rs765099391 0.00002
NM_005477.3(HCN4):c.556A>G (p.Thr186Ala) rs1085307696 0.00002
NM_005477.3(HCN4):c.725G>A (p.Arg242His) rs1253627105 0.00002
NM_005477.3(HCN4):c.1342G>A (p.Asp448Asn) rs1229232018 0.00001
NM_005477.3(HCN4):c.1402G>A (p.Ala468Thr) rs372632530 0.00001
NM_005477.3(HCN4):c.1661A>G (p.Tyr554Cys) rs767926374 0.00001
NM_005477.3(HCN4):c.1748A>G (p.Asn583Ser) rs1204195890 0.00001
NM_005477.3(HCN4):c.1896G>A (p.Met632Ile) rs200737571 0.00001
NM_005477.3(HCN4):c.1996C>T (p.Arg666Trp) rs199943122 0.00001
NM_005477.3(HCN4):c.2003G>A (p.Arg668Gln) rs757268783 0.00001
NM_005477.3(HCN4):c.2053A>C (p.Ser685Arg) rs1161776375 0.00001
NM_005477.3(HCN4):c.2182G>A (p.Asp728Asn) rs200468312 0.00001
NM_005477.3(HCN4):c.2273G>A (p.Arg758His) rs373284500 0.00001
NM_005477.3(HCN4):c.2399G>A (p.Arg800His) rs375180021 0.00001
NM_005477.3(HCN4):c.2453G>A (p.Gly818Asp) rs1224948931 0.00001
NM_005477.3(HCN4):c.2527G>A (p.Ala843Thr) rs777023781 0.00001
NM_005477.3(HCN4):c.2587G>A (p.Ala863Thr) rs767354516 0.00001
NM_005477.3(HCN4):c.2716G>A (p.Gly906Arg) rs373572497 0.00001
NM_005477.3(HCN4):c.2738C>T (p.Ala913Val) rs777560053 0.00001
NM_005477.3(HCN4):c.2902C>T (p.Pro968Ser) rs759692338 0.00001
NM_005477.3(HCN4):c.3028G>T (p.Ala1010Ser) rs748634893 0.00001
NM_005477.3(HCN4):c.3031T>C (p.Ser1011Pro) rs890395300 0.00001
NM_005477.3(HCN4):c.3172T>G (p.Ser1058Ala) rs1064796786 0.00001
NM_005477.3(HCN4):c.3382G>A (p.Gly1128Ser) rs779132775 0.00001
NM_005477.3(HCN4):c.3439G>A (p.Gly1147Ser) rs747427482 0.00001
NM_005477.3(HCN4):c.3448G>A (p.Val1150Ile) rs772491303 0.00001
NM_005477.3(HCN4):c.3487C>A (p.Pro1163Thr) rs779811451 0.00001
NM_005477.3(HCN4):c.3512G>T (p.Arg1171Ile) rs751152874 0.00001
NM_005477.3(HCN4):c.3581C>T (p.Pro1194Leu) rs147982868 0.00001
NM_005477.3(HCN4):c.594C>G (p.Asp198Glu) rs894325793 0.00001
NM_005477.3(HCN4):c.673G>A (p.Gly225Arg) rs767982466 0.00001
NM_005477.3(HCN4):c.743A>G (p.Lys248Arg) rs191744064 0.00001
NM_005477.3(HCN4):c.91G>A (p.Asp31Asn) rs757500423 0.00001
NM_005477.3(HCN4):c.-4C>A
NM_005477.3(HCN4):c.1346G>C (p.Cys449Ser) rs786205805
NM_005477.3(HCN4):c.1381T>C (p.Trp461Arg) rs1555475992
NM_005477.3(HCN4):c.1418T>C (p.Met473Thr) rs1226036490
NM_005477.3(HCN4):c.144C>G (p.Ile48Met) rs776352142
NM_005477.3(HCN4):c.1489C>G (p.Leu497Val)
NM_005477.3(HCN4):c.1494C>G (p.Ser498Arg) rs1567774949
NM_005477.3(HCN4):c.1805A>G (p.Asn602Ser) rs2549069983
NM_005477.3(HCN4):c.196G>A (p.Glu66Lys) rs786205803
NM_005477.3(HCN4):c.2116G>A (p.Val706Met) rs1359396157
NM_005477.3(HCN4):c.2143+5G>A rs547362030
NM_005477.3(HCN4):c.2207A>G (p.Tyr736Cys)
NM_005477.3(HCN4):c.236G>C (p.Gly79Ala) rs1555479039
NM_005477.3(HCN4):c.2377A>G (p.Ile793Val) rs1302650781
NM_005477.3(HCN4):c.2551A>G (p.Thr851Ala) rs1555475302
NM_005477.3(HCN4):c.2774T>G (p.Leu925Arg) rs375712962
NM_005477.3(HCN4):c.2804C>A (p.Ser935Tyr) rs775803239
NM_005477.3(HCN4):c.2878CCACCC[1] (p.Pro962_Pro963del) rs750207209
NM_005477.3(HCN4):c.2969C>G (p.Pro990Arg) rs755329686
NM_005477.3(HCN4):c.3100C>T (p.Pro1034Ser) rs1158677290
NM_005477.3(HCN4):c.3119G>A (p.Ser1040Asn)
NM_005477.3(HCN4):c.322G>C (p.Gly108Arg) rs1057524788
NM_005477.3(HCN4):c.3251A>T (p.Lys1084Met) rs751716200
NM_005477.3(HCN4):c.326G>A (p.Gly109Asp) rs2151228597
NM_005477.3(HCN4):c.3378C>G (p.Ser1126Arg) rs758673317
NM_005477.3(HCN4):c.3433A>G (p.Ile1145Val) rs2042867733
NM_005477.3(HCN4):c.343A>G (p.Ser115Gly) rs2549080472
NM_005477.3(HCN4):c.3488C>A (p.Pro1163His) rs756052150
NM_005477.3(HCN4):c.3497_3500del (p.Ser1166fs) rs774674047
NM_005477.3(HCN4):c.3502_3505del (p.Phe1168fs) rs786205259
NM_005477.3(HCN4):c.3536dup (p.Leu1180fs) rs1416588482
NM_005477.3(HCN4):c.403G>A (p.Gly135Ser) rs2151228560
NM_005477.3(HCN4):c.483_500dup (p.Ala162_Pro167dup) rs957058060
NM_005477.3(HCN4):c.491C>T (p.Ser164Leu) rs1214785817
NM_005477.3(HCN4):c.527C>T (p.Ser176Phe)
NM_005477.3(HCN4):c.580G>A (p.Ala194Thr)
NM_005477.3(HCN4):c.644A>G (p.Gln215Arg) rs2151228399
NM_005477.3(HCN4):c.752G>A (p.Gly251Glu)
NM_005477.3(HCN4):c.761T>C (p.Ile254Thr) rs2151228367
NM_005477.3(HCN4):c.767A>G (p.His256Arg) rs2549080079
NM_005477.3(HCN4):c.88G>C (p.Glu30Gln) rs786205802

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