ClinVar Miner

List of variants in gene HCN4 reported by Illumina Laboratory Services, Illumina

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Gene type:
ClinVar version:
Total variants: 81
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HGVS dbSNP gnomAD frequency
NM_005477.3(HCN4):c.3600A>G (p.Pro1200=) rs529004 0.88237
NM_005477.3(HCN4):c.*708A>G rs2623999 0.82454
NM_005477.3(HCN4):c.*1989G>A rs549377 0.80150
NM_005477.3(HCN4):c.*414C>A rs3743496 0.28353
NM_005477.3(HCN4):c.*2445C>T rs524457 0.10289
NM_005477.3(HCN4):c.1558C>T (p.Leu520=) rs12909882 0.07848
NM_005477.3(HCN4):c.2556G>A (p.Pro852=) rs117819825 0.04888
NM_005477.3(HCN4):c.*2393C>G rs74933243 0.04870
NM_005477.3(HCN4):c.107G>A (p.Gly36Glu) rs143090627 0.04452
NM_005477.3(HCN4):c.*1197T>C rs117071871 0.03038
NM_005477.3(HCN4):c.*1659A>G rs79656991 0.02574
NM_005477.3(HCN4):c.*2354A>G rs11631286 0.01331
NM_005477.3(HCN4):c.1839C>T (p.Phe613=) rs117731813 0.01108
NM_005477.3(HCN4):c.1683C>A (p.Gly561=) rs62641690 0.01030
NM_005477.3(HCN4):c.3337A>G (p.Met1113Val) rs142735148 0.00983
NM_005477.3(HCN4):c.*127A>G rs41277726 0.00747
NM_005477.3(HCN4):c.2648C>G (p.Pro883Arg) rs148398509 0.00737
NM_005477.3(HCN4):c.1591-19C>A rs41279186 0.00720
NM_005477.3(HCN4):c.*1140G>A rs74786613 0.00668
NM_005477.3(HCN4):c.36C>G (p.Leu12=) rs201193660 0.00635
NM_005477.3(HCN4):c.3288C>T (p.Asp1096=) rs116042117 0.00490
NM_005477.3(HCN4):c.-189G>A rs548581131 0.00346
NM_005477.3(HCN4):c.*634C>T rs138059941 0.00309
NM_005477.3(HCN4):c.1371+8C>T rs199838832 0.00295
NM_005477.3(HCN4):c.*1490A>C rs187377882 0.00291
NM_005477.3(HCN4):c.2275G>A (p.Val759Ile) rs62641689 0.00258
NM_005477.3(HCN4):c.*1482A>G rs191013007 0.00212
NM_005477.3(HCN4):c.3350C>T (p.Pro1117Leu) rs140402087 0.00185
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.-529G>A rs879470594 0.00136
NM_005477.3(HCN4):c.1356C>T (p.Ser452=) rs148453034 0.00116
NM_005477.3(HCN4):c.*2581C>T rs535089156 0.00083
NM_005477.3(HCN4):c.1703G>C (p.Ser568Thr) rs138714806 0.00076
NM_005477.3(HCN4):c.2739G>A (p.Ala913=) rs373411041 0.00056
NM_005477.3(HCN4):c.*1085A>C rs563333401 0.00036
NM_005477.3(HCN4):c.*1598A>G rs749289571 0.00031
NM_005477.3(HCN4):c.-132G>C rs952368455 0.00031
NM_005477.3(HCN4):c.*2010A>C rs550566467 0.00018
NM_005477.3(HCN4):c.-547G>C rs577325559 0.00016
NM_005477.3(HCN4):c.-364C>G rs1008967231 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.2701G>A (p.Ala901Thr) rs201742383 0.00012
NM_005477.3(HCN4):c.584C>T (p.Ala195Val) rs201375192 0.00011
NM_005477.3(HCN4):c.*980C>T rs767610327 0.00006
NM_005477.3(HCN4):c.2917G>A (p.Gly973Arg) rs200495478 0.00006
NM_005477.3(HCN4):c.*2585G>A rs770482289 0.00005
NM_005477.3(HCN4):c.*1172A>G rs561112458 0.00004
NM_005477.3(HCN4):c.*592G>A rs758508473 0.00004
NM_005477.3(HCN4):c.2845C>T (p.Arg949Trp) rs755614529 0.00004
NM_005477.3(HCN4):c.2938G>A (p.Gly980Arg) rs780719805 0.00004
NM_005477.3(HCN4):c.249C>T (p.Gly83=) rs1183278712 0.00003
NM_005477.3(HCN4):c.*844G>A rs185261766 0.00002
NM_005477.3(HCN4):c.*901C>T rs1464478840 0.00002
NM_005477.3(HCN4):c.3081C>T (p.Pro1027=) rs1226393084 0.00002
NM_005477.3(HCN4):c.3218C>T (p.Pro1073Leu) rs982016034 0.00002
NM_005477.3(HCN4):c.375C>T (p.Ser125=) rs1310424203 0.00002
NM_005477.3(HCN4):c.*104A>T rs1053318527 0.00001
NM_005477.3(HCN4):c.*2241T>C rs1441893786 0.00001
NM_005477.3(HCN4):c.1657G>A (p.Asp553Asn) rs104894485 0.00001
NM_005477.3(HCN4):c.3130C>T (p.Arg1044Trp) rs553950644 0.00001
NM_005477.3(HCN4):c.3205C>T (p.Arg1069Trp) rs770658894 0.00001
NM_005477.3(HCN4):c.577G>T (p.Gly193Cys) rs2043135036 0.00001
NM_005477.3(HCN4):c.*1205A>G rs572355448
NM_005477.3(HCN4):c.*168A>G rs2042863984
NM_005477.3(HCN4):c.*1834G>T rs1279314845
NM_005477.3(HCN4):c.*44C>T rs2042865036
NM_005477.3(HCN4):c.*767C>T rs571705929
NM_005477.3(HCN4):c.*847A>G rs2042858705
NM_005477.3(HCN4):c.-114G>A rs2043140776
NM_005477.3(HCN4):c.-188G>T rs2043141200
NM_005477.3(HCN4):c.-497G>A rs932616633
NM_005477.3(HCN4):c.-518A>G rs2043143421
NM_005477.3(HCN4):c.-585C>A rs140161530
NM_005477.3(HCN4):c.1844T>G (p.Val615Gly) rs2042890755
NM_005477.3(HCN4):c.2143+8G>A rs2042883869
NM_005477.3(HCN4):c.2175C>G (p.Val725=) rs2042882216
NM_005477.3(HCN4):c.2314G>A (p.Val772Ile) rs776635828
NM_005477.3(HCN4):c.319G>A (p.Gly107Ser) rs2043137058
NM_005477.3(HCN4):c.522G>A (p.Pro174=) rs1302048506

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