ClinVar Miner

List of variants in gene HCN4 reported as benign for not provided

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Gene type:
ClinVar version:
Total variants: 41
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HGVS dbSNP gnomAD frequency
NM_005477.3(HCN4):c.1978+261T>C rs485294 0.97511
NM_005477.3(HCN4):c.3600A>G (p.Pro1200=) rs529004 0.88237
NM_005477.3(HCN4):c.1979-41A>G rs481579 0.80894
NM_005477.3(HCN4):c.1979-150G>A rs62015502 0.30009
NM_005477.3(HCN4):c.1210-216G>T rs76789737 0.28580
NM_005477.2(HCN4):c.-1076A>C rs7172796 0.22856
NM_005477.3(HCN4):c.1978+252C>T rs72741448 0.11507
NM_005477.3(HCN4):c.1737+20G>A rs115706632 0.01520
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.3033T>G (p.Ser1011=) rs186728422 0.00931
NM_005477.3(HCN4):c.2979G>A (p.Thr993=) rs75307879 0.00796
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.2673G>A (p.Ser891=) rs191092709 0.00666
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.2831C>T (p.Ala944Val) rs144450232 0.00416
NM_005477.3(HCN4):c.2601C>A (p.Ala867=) rs143188160 0.00352
NM_005477.3(HCN4):c.1371+8C>T rs199838832 0.00295
NM_005477.3(HCN4):c.2275G>A (p.Val759Ile) rs62641689 0.00258
NM_005477.3(HCN4):c.458A>G (p.Glu153Gly) rs560874115 0.00149
NM_005477.3(HCN4):c.546C>G (p.Pro182=) rs571671463 0.00122
NM_005477.3(HCN4):c.*2581C>T rs535089156 0.00083
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.1738-6C>T rs760763085 0.00014
NM_005477.3(HCN4):c.1459G>A (p.Val487Met) rs202037304 0.00001
GRCh37/hg19 15q24.1(chr15:73653485-73661123)x1
GRCh37/hg19 15q24.1(chr15:73660092-73660615)x1
GRCh37/hg19 15q24.1(chr15:73660092-73660714)x1
GRCh37/hg19 15q24.1(chr15:73660092-73661071)x1
GRCh37/hg19 15q24.1(chr15:73660092-73661123)x1
GRCh37/hg19 15q24.1(chr15:73660092-73661188)x1
GRCh37/hg19 15q24.1(chr15:73660092-73670196)x1
GRCh37/hg19 15q24.1(chr15:73660092-73670781)x1
GRCh37/hg19 15q24.1(chr15:73660092-73680301)x1
GRCh37/hg19 15q24.1(chr15:73660218-73680301)x1
GRCh37/hg19 15q24.1(chr15:73660269-73661123)x1
GRCh37/hg19 15q24.1(chr15:73660269-73669907)x3
NM_005477.3(HCN4):c.*112AC[3] rs35177144

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