ClinVar Miner

List of variants in gene CYLD reported as uncertain significance for Cylindromatosis, familial

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Total variants: 43
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HGVS dbSNP
NM_015247.2(CYLD):c.*1308A>G rs886052054
NM_015247.2(CYLD):c.*1587dup rs886052055
NM_015247.2(CYLD):c.*1667G>T rs750022206
NM_015247.2(CYLD):c.*1727T>C rs886052056
NM_015247.2(CYLD):c.*1746C>T rs886052057
NM_015247.2(CYLD):c.*1810A>T rs886052058
NM_015247.2(CYLD):c.*1983T>C rs867027657
NM_015247.2(CYLD):c.*2121_*2122del rs74757288
NM_015247.2(CYLD):c.*2438G>A rs886052061
NM_015247.2(CYLD):c.*2556A>G rs747682326
NM_015247.2(CYLD):c.*2856T>C rs778856255
NM_015247.2(CYLD):c.*2975C>T rs886052062
NM_015247.2(CYLD):c.*3000C>G rs886052063
NM_015247.2(CYLD):c.*3119del rs149875014
NM_015247.2(CYLD):c.*3148T>C rs555603514
NM_015247.2(CYLD):c.*3229C>T rs752862278
NM_015247.2(CYLD):c.*3305A>G rs886052065
NM_015247.2(CYLD):c.*3384G>A rs886052066
NM_015247.2(CYLD):c.*3722T>G rs886052067
NM_015247.2(CYLD):c.*403T>C rs886052052
NM_015247.2(CYLD):c.*4388C>T rs781004605
NM_015247.2(CYLD):c.*4470C>A rs755710819
NM_015247.2(CYLD):c.*4485G>C rs886052068
NM_015247.2(CYLD):c.*4494G>A rs546313281
NM_015247.2(CYLD):c.*468A>C rs886052053
NM_015247.2(CYLD):c.*4691A>G rs886052069
NM_015247.2(CYLD):c.*4702C>T rs886052070
NM_015247.2(CYLD):c.*4841G>A rs886052071
NM_015247.2(CYLD):c.*5384A>G rs886052072
NM_015247.2(CYLD):c.*831C>T rs144877731
NM_015247.2(CYLD):c.-161A>G rs886052051
NM_015247.2(CYLD):c.-23A>C rs771486432
NM_015247.2(CYLD):c.-366G>C rs886052050
NM_015247.2(CYLD):c.1166C>G (p.Thr389Arg) rs200759332
NM_015247.2(CYLD):c.1503C>T (p.Leu501=) rs752471076
NM_015247.2(CYLD):c.1684+3A>C rs886040878
NM_015247.2(CYLD):c.1684G>C (p.Ala562Pro) rs886040877
NM_015247.2(CYLD):c.1778G>A (p.Gly593Asp) rs886040880
NM_015247.2(CYLD):c.2041G>C (p.Asp681His) rs886040883
NM_015247.2(CYLD):c.2145T>C (p.Tyr715=) rs200905032
NM_015247.2(CYLD):c.2465C>T (p.Thr822Ile) rs775394735
NM_015247.2(CYLD):c.543C>T (p.Tyr181=) rs752294416
NM_015247.2(CYLD):c.59T>G (p.Ile20Ser) rs764097337

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