ClinVar Miner

List of variants in gene HCN4 reported as uncertain significance by Fulgent Genetics, Fulgent Genetics

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Total variants: 60
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HGVS dbSNP gnomAD frequency
NM_005477.3(HCN4):c.-529G>A rs879470594 0.00136
NM_005477.3(HCN4):c.*1598A>G rs749289571 0.00031
NM_005477.3(HCN4):c.418G>A (p.Gly140Ser) rs773857091 0.00009
NM_005477.3(HCN4):c.466G>A (p.Gly156Ser) rs924203370 0.00008
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.2917G>A (p.Gly973Arg) rs200495478 0.00006
NM_005477.3(HCN4):c.3305G>A (p.Arg1102His) rs548130184 0.00005
NM_005477.3(HCN4):c.3460C>T (p.Arg1154Trp) rs200896834 0.00005
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.2398C>T (p.Arg800Cys) rs181894662 0.00004
NM_005477.3(HCN4):c.2995C>T (p.Arg999Trp) rs538668505 0.00004
NM_005477.3(HCN4):c.3202C>T (p.Arg1068Cys) rs759356193 0.00004
NM_005477.3(HCN4):c.1713C>T (p.Gly571=) rs754495351 0.00003
NM_005477.3(HCN4):c.3293C>T (p.Ala1098Val) rs1064797200 0.00003
NM_005477.3(HCN4):c.3379G>A (p.Gly1127Arg) rs748279911 0.00003
NM_005477.3(HCN4):c.1871G>A (p.Arg624Gln) rs763842368 0.00002
NM_005477.3(HCN4):c.2555C>T (p.Pro852Leu) rs779241036 0.00002
NM_005477.3(HCN4):c.2807C>T (p.Pro936Leu) rs769959023 0.00002
NM_005477.3(HCN4):c.2833C>T (p.Pro945Ser) rs778739758 0.00002
NM_005477.3(HCN4):c.3148G>A (p.Gly1050Arg) rs1443227484 0.00002
NM_005477.3(HCN4):c.334G>A (p.Gly112Ser) rs765099391 0.00002
NM_005477.3(HCN4):c.1297G>A (p.Gly433Ser) rs573588965 0.00001
NM_005477.3(HCN4):c.134G>T (p.Arg45Leu) rs1416460262 0.00001
NM_005477.3(HCN4):c.1447C>T (p.Arg483Trp) rs1304145729 0.00001
NM_005477.3(HCN4):c.1465A>G (p.Met489Val) rs1157049194 0.00001
NM_005477.3(HCN4):c.1796C>T (p.Ala599Val) rs775019344 0.00001
NM_005477.3(HCN4):c.1987C>A (p.Leu663Met) rs1265876338 0.00001
NM_005477.3(HCN4):c.2309C>T (p.Thr770Met) rs763021264 0.00001
NM_005477.3(HCN4):c.2326C>A (p.Pro776Thr) rs148714049 0.00001
NM_005477.3(HCN4):c.2422C>T (p.Pro808Ser) rs2042879557 0.00001
NM_005477.3(HCN4):c.2495T>C (p.Leu832Pro) rs1404692878 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.2939G>C (p.Gly980Ala) rs367719274 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.3064C>T (p.Arg1022Ter) rs762950777 0.00001
NM_005477.3(HCN4):c.3172T>G (p.Ser1058Ala) rs1064796786 0.00001
NM_005477.3(HCN4):c.3203G>A (p.Arg1068His) rs776270218 0.00001
NM_005477.3(HCN4):c.3206G>A (p.Arg1069Gln) rs760242560 0.00001
NM_005477.3(HCN4):c.3289G>A (p.Gly1097Arg) rs753734843 0.00001
NM_005477.3(HCN4):c.493C>T (p.Pro165Ser) rs1489387068 0.00001
NM_005477.3(HCN4):c.2846G>C (p.Arg949Pro) rs752139441
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.3014C>G (p.Ser1005Cys) rs780624939
NM_005477.3(HCN4):c.3100C>T (p.Pro1034Ser) rs1158677290
NM_005477.3(HCN4):c.3242A>G (p.Gln1081Arg) rs1419820366
NM_005477.3(HCN4):c.3378C>G (p.Ser1126Arg) rs758673317
NM_005477.3(HCN4):c.3394_3402dup (p.Ser1132_Gly1134dup) rs1290501532
NM_005477.3(HCN4):c.3495_3498del (p.Ser1166fs) rs2151213747
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.3531del (p.Pro1179fs) rs749503920
NM_005477.3(HCN4):c.3536dup (p.Leu1180fs) rs1416588482
NM_005477.3(HCN4):c.358G>A (p.Gly120Arg) rs766202352
NM_005477.3(HCN4):c.483_500dup (p.Ala162_Pro167dup) rs957058060

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