ClinVar Miner

List of variants in gene combination HCN4, LOC105370890, LOC126862173 reported as uncertain significance for heart conduction disease

Included ClinVar conditions (98):
Minimum submission review status: Collection method:
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Gene type:
ClinVar version:
Total variants: 52
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HGVS dbSNP gnomAD frequency
NM_005477.3(HCN4):c.1087A>G (p.Ile363Val) rs144168042 0.00008
NM_005477.3(HCN4):c.995G>A (p.Arg332Gln) rs368164073 0.00006
NM_005477.3(HCN4):c.1005G>A (p.Met335Ile) rs758797709 0.00003
NM_005477.3(HCN4):c.1094C>T (p.Ser365Leu) rs745346676 0.00002
NM_005477.3(HCN4):c.1073T>C (p.Ile358Thr) rs774060688 0.00001
NM_005477.3(HCN4):c.1115G>A (p.Arg372Gln) rs748658688 0.00001
NM_005477.3(HCN4):c.1132C>T (p.Arg378Cys) rs758468167 0.00001
NM_005477.3(HCN4):c.915C>A (p.Phe305Leu) rs1272107414 0.00001
NM_005477.3(HCN4):c.943C>T (p.Arg315Cys) rs1340301658 0.00001
NM_005477.3(HCN4):c.975G>T (p.Glu325Asp) rs778657724 0.00001
NM_005477.3(HCN4):c.988C>A (p.Pro330Thr) rs1555477316 0.00001
NM_005477.3(HCN4):c.989C>T (p.Pro330Leu) rs370442588 0.00001
NM_005477.3(HCN4):c.994C>T (p.Arg332Trp) rs141185786 0.00001
NM_005477.3(HCN4):c.1000A>G (p.Lys334Glu) rs1316189390
NM_005477.3(HCN4):c.1004T>G (p.Met335Arg)
NM_005477.3(HCN4):c.1009T>C (p.Tyr337His)
NM_005477.3(HCN4):c.1018A>G (p.Ser340Gly)
NM_005477.3(HCN4):c.1023G>C (p.Trp341Cys) rs1555477308
NM_005477.3(HCN4):c.1026C>G (p.Phe342Leu) rs2043017188
NM_005477.3(HCN4):c.1027A>T (p.Met343Leu)
NM_005477.3(HCN4):c.1053del (p.Val352fs)
NM_005477.3(HCN4):c.1054G>A (p.Val352Met) rs1170518463
NM_005477.3(HCN4):c.1063A>G (p.Ile355Val)
NM_005477.3(HCN4):c.1070T>A (p.Leu357His) rs2043016942
NM_005477.3(HCN4):c.1074T>A (p.Ile358=) rs1444977026
NM_005477.3(HCN4):c.1084C>T (p.Arg362Cys)
NM_005477.3(HCN4):c.1085G>A (p.Arg362His)
NM_005477.3(HCN4):c.1090G>C (p.Asp364His) rs151004999
NM_005477.3(HCN4):c.1090G>T (p.Asp364Tyr) rs151004999
NM_005477.3(HCN4):c.1103A>G (p.Tyr368Cys) rs2043016672
NM_005477.3(HCN4):c.1124G>A (p.Arg375His) rs1238684043
NM_005477.3(HCN4):c.1126A>G (p.Ile376Val)
NM_005477.3(HCN4):c.1133G>A (p.Arg378His) rs1347790774
NM_005477.3(HCN4):c.1139C>T (p.Thr380Met)
NM_005477.3(HCN4):c.1158dup (p.Arg387fs) rs2151221157
NM_005477.3(HCN4):c.1159C>G (p.Arg387Gly) rs1420807618
NM_005477.3(HCN4):c.1159C>T (p.Arg387Cys) rs1420807618
NM_005477.3(HCN4):c.1167dup (p.Arg390fs) rs2043016217
NM_005477.3(HCN4):c.1168C>T (p.Arg390Cys) rs918783630
NM_005477.3(HCN4):c.829C>G (p.Leu277Val)
NM_005477.3(HCN4):c.839T>C (p.Ile280Thr) rs2043018365
NM_005477.3(HCN4):c.881C>G (p.Pro294Arg) rs1216261955
NM_005477.3(HCN4):c.886A>G (p.Ile296Val)
NM_005477.3(HCN4):c.896A>G (p.Asn299Ser) rs1057518303
NM_005477.3(HCN4):c.925G>A (p.Asp309Asn)
NM_005477.3(HCN4):c.944G>A (p.Arg315His)
NM_005477.3(HCN4):c.946A>T (p.Thr316Ser) rs2043017887
NM_005477.3(HCN4):c.955G>A (p.Val319Met) rs773269320
NM_005477.3(HCN4):c.978C>G (p.Ile326Met)
NM_005477.3(HCN4):c.987C>A (p.Asp329Glu) rs1472247877
NM_005477.3(HCN4):c.988C>T (p.Pro330Ser) rs1555477316
NM_005477.3(HCN4):c.991C>A (p.Gln331Lys)

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