ClinVar Miner

List of variants in gene HCN4 reported by Athena Diagnostics Inc

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Total variants: 29
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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.1558C>T (p.Leu520=) rs12909882 0.07848
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.3033T>G (p.Ser1011=) rs186728422 0.00931
NM_005477.3(HCN4):c.2648C>G (p.Pro883Arg) rs148398509 0.00737
NM_005477.3(HCN4):c.2673G>A (p.Ser891=) rs191092709 0.00666
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.2657C>T (p.Ala886Val) rs200575377 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.1518C>T (p.Tyr506=) rs139590882 0.00163
NM_005477.3(HCN4):c.546C>G (p.Pro182=) rs571671463 0.00122
NM_005477.3(HCN4):c.1356C>T (p.Ser452=) rs148453034 0.00116
NM_005477.3(HCN4):c.2694C>T (p.Gly898=) rs375169111 0.00046
NM_005477.3(HCN4):c.2800C>T (p.Arg934Cys) rs199638465 0.00045
NM_005477.3(HCN4):c.2420G>A (p.Arg807His) rs200395062 0.00036
NM_005477.3(HCN4):c.1656C>T (p.His552=) rs148142070 0.00029
NM_005477.3(HCN4):c.1738-6C>T rs760763085 0.00014
NM_005477.3(HCN4):c.2730C>A (p.Phe910Leu) rs200814534 0.00014
NM_005477.3(HCN4):c.621C>G (p.Arg207=) rs727503958 0.00012
NM_005477.3(HCN4):c.2652C>T (p.Pro884=) rs373814254 0.00006
NM_005477.3(HCN4):c.2537C>T (p.Pro846Leu) rs747467877 0.00005
NM_005477.3(HCN4):c.3388G>A (p.Gly1130Arg) rs1326171404 0.00001
NM_005477.3(HCN4):c.3448G>A (p.Val1150Ile) rs772491303 0.00001
NM_005477.3(HCN4):c.529G>T (p.Ala177Ser) rs1567801731

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