ClinVar Miner

List of variants in gene HCN4 reported as uncertain significance by Eurofins NTD LLC (GA)

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Total variants: 39
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HGVS dbSNP gnomAD frequency
NM_005477.3(HCN4):c.458A>G (p.Glu153Gly) rs560874115 0.00149
NM_005477.3(HCN4):c.1356C>T (p.Ser452=) rs148453034 0.00116
NM_005477.3(HCN4):c.3010C>T (p.Pro1004Ser) rs201418838 0.00084
NM_005477.3(HCN4):c.2739G>A (p.Ala913=) rs373411041 0.00056
NM_005477.3(HCN4):c.1371+9G>A rs200303699 0.00048
NM_005477.3(HCN4):c.2800C>T (p.Arg934Cys) rs199638465 0.00045
NM_005477.3(HCN4):c.2181C>T (p.His727=) rs140354126 0.00036
NM_005477.3(HCN4):c.2025C>T (p.Ala675=) rs149033101 0.00013
NM_005477.3(HCN4):c.621C>G (p.Arg207=) rs727503958 0.00012
NM_005477.3(HCN4):c.3117G>A (p.Pro1039=) rs749785521 0.00011
NM_005477.3(HCN4):c.1815G>A (p.Thr605=) rs367753936 0.00009
NM_005477.3(HCN4):c.2864C>T (p.Pro955Leu) rs371562763 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.3596T>A (p.Leu1199Gln) rs146751122 0.00004
NM_005477.3(HCN4):c.394A>C (p.Ile132Leu) rs772764704 0.00004
NM_005477.3(HCN4):c.*8C>T rs767027074 0.00003
NM_005477.3(HCN4):c.1915G>A (p.Val639Met) rs563194186 0.00003
NM_005477.3(HCN4):c.2801G>A (p.Arg934His) rs369485237 0.00003
NM_005477.3(HCN4):c.2370T>C (p.Ser790=) rs747648596 0.00002
NM_005477.3(HCN4):c.2555C>T (p.Pro852Leu) rs779241036 0.00002
NM_005477.3(HCN4):c.3131G>A (p.Arg1044Gln) rs750637152 0.00002
NM_005477.3(HCN4):c.3197C>A (p.Pro1066His) rs765155640 0.00002
NM_005477.3(HCN4):c.3383G>T (p.Gly1128Val) rs727503957 0.00002
NM_005477.3(HCN4):c.1459G>A (p.Val487Met) rs202037304 0.00001
NM_005477.3(HCN4):c.2055C>T (p.Ser685=) rs886042819 0.00001
NM_005477.3(HCN4):c.2273G>A (p.Arg758His) rs373284500 0.00001
NM_005477.3(HCN4):c.2523G>A (p.Ser841=) rs768157473 0.00001
NM_005477.3(HCN4):c.2527G>A (p.Ala843Thr) rs777023781 0.00001
NM_005477.3(HCN4):c.3304C>T (p.Arg1102Cys) rs760392343 0.00001
NM_005477.3(HCN4):c.3363G>C (p.Arg1121Ser) rs794727919 0.00001
NM_005477.3(HCN4):c.433C>G (p.Pro145Ala) rs886043525 0.00001
NM_005477.3(HCN4):c.743A>G (p.Lys248Arg) rs191744064 0.00001
NM_005477.3(HCN4):c.1462G>A (p.Gly488Ser) rs886042821
NM_005477.3(HCN4):c.1641C>T (p.Thr547=) rs1567771524
NM_005477.3(HCN4):c.2553A>G (p.Thr851=) rs748390169
NM_005477.3(HCN4):c.2804C>T (p.Ser935Phe) rs775803239
NM_005477.3(HCN4):c.3116C>G (p.Pro1039Arg) rs572132730
NM_005477.3(HCN4):c.321C>T (p.Gly107=) rs1555479019

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