ClinVar Miner

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

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Gene type:
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Total variants: 58
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HGVS dbSNP gnomAD frequency
NM_001620.3(AHNAK):c.16224G>A (p.Leu5408=) rs61625484 0.04911
NM_001620.3(AHNAK):c.6740A>C (p.Lys2247Thr) rs61524789 0.02870
NM_001620.3(AHNAK):c.9540C>T (p.Asp3180=) rs147436257 0.01120
NM_001620.3(AHNAK):c.15223G>A (p.Val5075Met) rs114515655 0.01079
NM_001620.3(AHNAK):c.7377T>C (p.Asp2459=) rs75858820 0.01068
NM_001620.3(AHNAK):c.2145T>C (p.Tyr715=) rs114557263 0.01066
NM_001620.3(AHNAK):c.12911A>G (p.Asp4304Gly) rs11828907 0.00996
NM_001620.3(AHNAK):c.11187G>A (p.Lys3729=) rs73500265 0.00983
NM_001620.3(AHNAK):c.4479T>C (p.Asp1493=) rs114233286 0.00943
NM_001620.3(AHNAK):c.7973G>T (p.Gly2658Val) rs145624418 0.00931
NM_001620.3(AHNAK):c.4569T>C (p.Phe1523=) rs114078400 0.00924
NM_001620.3(AHNAK):c.8909T>G (p.Leu2970Trp) rs148663483 0.00913
NM_001620.3(AHNAK):c.10760A>G (p.Asn3587Ser) rs115937732 0.00909
NM_001620.3(AHNAK):c.12381G>A (p.Pro4127=) rs141008505 0.00901
NM_001620.3(AHNAK):c.3188G>A (p.Arg1063Lys) rs115660558 0.00900
NM_001620.3(AHNAK):c.8417G>A (p.Cys2806Tyr) rs76672664 0.00879
NM_001620.3(AHNAK):c.1176G>A (p.Gln392=) rs114187073 0.00877
NM_001620.3(AHNAK):c.1178G>A (p.Gly393Glu) rs116379346 0.00877
NM_001620.3(AHNAK):c.5832G>T (p.Val1944=) rs141172382 0.00853
NM_001620.3(AHNAK):c.4891G>A (p.Gly1631Ser) rs115000832 0.00694
NM_001620.3(AHNAK):c.8409T>C (p.Asp2803=) rs77433327 0.00678
NM_001620.3(AHNAK):c.12493A>G (p.Ile4165Val) rs79785607 0.00653
NM_001620.3(AHNAK):c.12480C>T (p.Gly4160=) rs151066838 0.00587
NM_001620.3(AHNAK):c.6618T>G (p.Val2206=) rs149402141 0.00565
NM_001620.3(AHNAK):c.14211C>T (p.Gly4737=) rs114273507 0.00561
NM_001620.3(AHNAK):c.17420C>T (p.Ser5807Phe) rs116528762 0.00558
NM_001620.3(AHNAK):c.921C>T (p.Pro307=) rs115603331 0.00552
NM_001620.3(AHNAK):c.4490C>G (p.Pro1497Arg) rs116499851 0.00531
NM_001620.3(AHNAK):c.16318G>A (p.Val5440Met) rs112663036 0.00419
NM_001620.3(AHNAK):c.17097G>A (p.Glu5699=) rs111551528 0.00362
NM_001620.3(AHNAK):c.13875C>T (p.Pro4625=) rs12793602 0.00346
NM_001620.3(AHNAK):c.4644T>G (p.Ile1548Met) rs78951730 0.00337
NM_001620.3(AHNAK):c.8937C>T (p.Gly2979=) rs150176979 0.00329
NM_001620.3(AHNAK):c.5866G>T (p.Val1956Leu) rs142705171 0.00300
NM_001620.3(AHNAK):c.3057T>C (p.Asp1019=) rs114307125 0.00294
NM_001620.3(AHNAK):c.4714A>G (p.Met1572Val) rs115693058 0.00178
NM_001620.3(AHNAK):c.4997A>G (p.Lys1666Arg) rs115036524 0.00167
NM_001620.3(AHNAK):c.10764C>T (p.Ala3588=) rs140469618 0.00135
NM_001620.3(AHNAK):c.10133T>C (p.Ile3378Thr) rs141698114 0.00125
NM_001620.3(AHNAK):c.6898T>C (p.Phe2300Leu) rs138917652 0.00116
NM_001620.3(AHNAK):c.7301G>A (p.Gly2434Asp) rs114407546 0.00086
NM_001620.3(AHNAK):c.16487G>A (p.Gly5496Glu) rs141151380 0.00083
NM_001620.3(AHNAK):c.17584C>G (p.Leu5862Val) rs142839608 0.00068
NM_001620.3(AHNAK):c.258G>A (p.Leu86=) rs79854453 0.00064
NM_001620.3(AHNAK):c.7562C>G (p.Pro2521Arg) rs143391519 0.00039
NM_001620.3(AHNAK):c.1235G>T (p.Ser412Ile) rs202011056 0.00006
NM_001620.3(AHNAK):c.12113A>G (p.Lys4038Arg)
NM_001620.3(AHNAK):c.12497A>G (p.Lys4166Arg)
NM_001620.3(AHNAK):c.1298A>G (p.Lys433Arg)
NM_001620.3(AHNAK):c.13907T>C (p.Ile4636Thr)
NM_001620.3(AHNAK):c.15724G>C (p.Gly5242Arg) rs116243978
NM_001620.3(AHNAK):c.17387C>T (p.Thr5796Met)
NM_001620.3(AHNAK):c.252G>A (p.Leu84=)
NM_001620.3(AHNAK):c.3815G>C (p.Arg1272Pro) rs115325511
NM_001620.3(AHNAK):c.4097_4099del (p.Ile1366del)
NM_001620.3(AHNAK):c.5297G>T (p.Gly1766Val) rs76414066
NM_001620.3(AHNAK):c.9425A>G (p.Gln3142Arg)
NM_001620.3(AHNAK):c.9886C>T (p.Pro3296Ser)

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