ClinVar Miner

List of variants in gene CYLD reported as uncertain significance for Brooke-Spiegler syndrome

Included ClinVar conditions (7):
Minimum submission review status: Collection method:
Minimum conflict level:
Gene type:
ClinVar version:
Total variants: 78
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HGVS dbSNP gnomAD frequency
NM_001378743.1(CYLD):c.*3148T>C rs555603514 0.00118
NM_001378743.1(CYLD):c.*4388C>T rs781004605 0.00071
NM_001378743.1(CYLD):c.*1810A>T rs886052058 0.00030
NM_001378743.1(CYLD):c.*4947G>A rs567438576 0.00026
NM_001378743.1(CYLD):c.*2856T>C rs778856255 0.00024
NM_001378743.1(CYLD):c.*4885A>T rs184571054 0.00022
NM_001378743.1(CYLD):c.*4494G>A rs546313281 0.00019
NM_001378743.1(CYLD):c.*2556A>G rs747682326 0.00016
NM_001378743.1(CYLD):c.*59T>C rs950448066 0.00011
NM_001378743.1(CYLD):c.*1746C>T rs886052057 0.00010
NM_001378743.1(CYLD):c.2145T>C (p.Tyr715=) rs200905032 0.00008
NM_001378743.1(CYLD):c.665C>A (p.Thr222Lys) rs587778225 0.00007
NM_001378743.1(CYLD):c.*3151T>G rs759858517 0.00006
NM_001378743.1(CYLD):c.*2305A>T rs559634329 0.00005
NM_001378743.1(CYLD):c.*5060G>T rs888172609 0.00005
NM_001378743.1(CYLD):c.*1102G>A rs141088048 0.00004
NM_001378743.1(CYLD):c.*3384G>A rs886052066 0.00004
NM_001378743.1(CYLD):c.*3731C>T rs551109634 0.00004
NM_001378743.1(CYLD):c.*3851T>C rs930910588 0.00004
NM_001378743.1(CYLD):c.*1667G>T rs750022206 0.00003
NM_001378743.1(CYLD):c.*3229C>T rs752862278 0.00003
NM_001378743.1(CYLD):c.*3305A>G rs886052065 0.00003
NM_001378743.1(CYLD):c.*403T>C rs886052052 0.00003
NM_001378743.1(CYLD):c.*5384A>G rs886052072 0.00003
NM_001378743.1(CYLD):c.543C>T (p.Tyr181=) rs752294416 0.00003
NM_001378743.1(CYLD):c.*1245T>C rs192470603 0.00002
NM_001378743.1(CYLD):c.*3000C>G rs886052063 0.00002
NM_001378743.1(CYLD):c.*468A>C rs886052053 0.00002
NM_001378743.1(CYLD):c.1503C>T (p.Leu501=) rs752471076 0.00002
NM_001378743.1(CYLD):c.2589T>C (p.Ala863=) rs201868355 0.00002
NM_001378743.1(CYLD):c.*1308A>G rs886052054 0.00001
NM_001378743.1(CYLD):c.*1651G>A rs1206094648 0.00001
NM_001378743.1(CYLD):c.*206A>C rs1406870242 0.00001
NM_001378743.1(CYLD):c.*2113A>G rs1972238592 0.00001
NM_001378743.1(CYLD):c.*2424C>T rs1972268579 0.00001
NM_001378743.1(CYLD):c.*2975C>T rs886052062 0.00001
NM_001378743.1(CYLD):c.*3865C>T rs1281354923 0.00001
NM_001378743.1(CYLD):c.*4470C>A rs755710819 0.00001
NM_001378743.1(CYLD):c.*4691A>G rs886052069 0.00001
NM_001378743.1(CYLD):c.*4702C>T rs886052070 0.00001
NM_001378743.1(CYLD):c.-23A>C rs771486432 0.00001
NM_001378743.1(CYLD):c.1271C>A (p.Thr424Asn) rs759998669 0.00001
NM_001378743.1(CYLD):c.1294A>C (p.Ser432Arg) rs1248488179 0.00001
NM_001378743.1(CYLD):c.170A>G (p.His57Arg) rs767537235 0.00001
NM_001378743.1(CYLD):c.*1033T>A rs1972150827
NM_001378743.1(CYLD):c.*1034C>A rs1972151007
NM_001378743.1(CYLD):c.*1191C>G rs146935881
NM_001378743.1(CYLD):c.*1191C>T rs146935881
NM_001378743.1(CYLD):c.*1587dup rs886052055
NM_001378743.1(CYLD):c.*1727T>C rs886052056
NM_001378743.1(CYLD):c.*1983T>C rs867027657
NM_001378743.1(CYLD):c.*2026G>A rs1972229289
NM_001378743.1(CYLD):c.*2121_*2122del rs74757288
NM_001378743.1(CYLD):c.*2147T>G rs1323064285
NM_001378743.1(CYLD):c.*2438G>A rs886052061
NM_001378743.1(CYLD):c.*2521G>A rs937833973
NM_001378743.1(CYLD):c.*280A>G rs1972088853
NM_001378743.1(CYLD):c.*2848A>G rs1972303099
NM_001378743.1(CYLD):c.*29T>C rs1972065736
NM_001378743.1(CYLD):c.*3119del rs149875014
NM_001378743.1(CYLD):c.*3462A>G rs1972340927
NM_001378743.1(CYLD):c.*3589C>T rs1972351190
NM_001378743.1(CYLD):c.*3722T>G rs886052067
NM_001378743.1(CYLD):c.*4485G>C rs886052068
NM_001378743.1(CYLD):c.*4514C>G rs1303376683
NM_001378743.1(CYLD):c.*4530G>T rs748716852
NM_001378743.1(CYLD):c.*4841G>A rs886052071
NM_001378743.1(CYLD):c.*5327C>A rs1972483152
NM_001378743.1(CYLD):c.*779G>A rs190787930
NM_001378743.1(CYLD):c.-124+1988A>G rs886052051
NM_001378743.1(CYLD):c.1166C>G (p.Thr389Arg) rs200759332
NM_001378743.1(CYLD):c.1684+3A>C rs886040878
NM_001378743.1(CYLD):c.1684G>C (p.Ala562Pro) rs886040877
NM_001378743.1(CYLD):c.1778G>A (p.Gly593Asp) rs886040880
NM_001378743.1(CYLD):c.1950-5_1950-2del rs886040881
NM_001378743.1(CYLD):c.2041G>C (p.Asp681His) rs886040883
NM_001378743.1(CYLD):c.2342T>C (p.Leu781Pro) rs886040889
NM_001378743.1(CYLD):c.2465C>T (p.Thr822Ile) rs775394735

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