ClinVar Miner

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

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Gene type:
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Total variants: 38
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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.3337A>G (p.Met1113Val) rs142735148 0.00983
NM_005477.3(HCN4):c.2648C>G (p.Pro883Arg) rs148398509 0.00737
NM_005477.3(HCN4):c.2275G>A (p.Val759Ile) rs62641689 0.00258
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.1371+9G>A rs200303699 0.00048
NM_005477.3(HCN4):c.1536C>T (p.His512=) rs146306966 0.00024
NM_005477.3(HCN4):c.1797G>A (p.Ala599=) rs371484779 0.00014
NM_005477.3(HCN4):c.3531G>T (p.Gly1177=) rs375911378 0.00008
NM_005477.3(HCN4):c.1729C>T (p.Leu577=) rs1057523463 0.00006
NM_005477.3(HCN4):c.2652C>T (p.Pro884=) rs373814254 0.00006
NM_005477.3(HCN4):c.1722C>T (p.Ser574=) rs750941501 0.00004
NM_005477.3(HCN4):c.1632G>A (p.Pro544=) rs544585089 0.00003
NM_005477.3(HCN4):c.249C>T (p.Gly83=) rs1183278712 0.00003
NM_005477.3(HCN4):c.102G>A (p.Glu34=) rs764116333 0.00002
NM_005477.3(HCN4):c.1338T>G (p.Pro446=) rs780604251 0.00002
NM_005477.3(HCN4):c.1401C>T (p.Tyr467=) rs753580737 0.00002
NM_005477.3(HCN4):c.3264G>A (p.Ala1088=) rs752705479 0.00002
NM_005477.3(HCN4):c.785+13A>C rs573865102 0.00002
NM_005477.3(HCN4):c.1978+8A>G rs1057522491 0.00001
NM_005477.3(HCN4):c.2121G>A (p.Ala707=) rs1354885005 0.00001
NM_005477.3(HCN4):c.2508G>A (p.Ala836=) rs766293595 0.00001
NM_005477.3(HCN4):c.3276C>T (p.Ala1092=) rs1370521798 0.00001
NM_005477.3(HCN4):c.3468A>G (p.Thr1156=) rs947950341 0.00001
NM_005477.3(HCN4):c.785+8_785+10dup rs759445840 0.00001
NM_005477.3(HCN4):c.-31C>T rs1555479101
NM_005477.3(HCN4):c.1599G>A (p.Gln533=) rs1555475630
NM_005477.3(HCN4):c.1812G>A (p.Val604=) rs1057523478
NM_005477.3(HCN4):c.2199C>G (p.Val733=) rs1555475400
NM_005477.3(HCN4):c.2637C>T (p.Ser879=) rs769042435
NM_005477.3(HCN4):c.2745T>A (p.Gly915=) rs1297073936
NM_005477.3(HCN4):c.2946G>A (p.Leu982=) rs1057522333
NM_005477.3(HCN4):c.3171A>C (p.Ala1057=) rs1057522384
NM_005477.3(HCN4):c.3327A>G (p.Ser1109=) rs1057521832
NM_005477.3(HCN4):c.338C>T (p.Thr113Met) rs786205801
NM_005477.3(HCN4):c.450C>T (p.Ala150=)
NM_005477.3(HCN4):c.555C>T (p.Asp185=) rs998732998

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