ClinVar Miner

List of variants in gene CYLD reported as likely benign for Brooke-Spiegler syndrome

Included ClinVar conditions (4):
Minimum submission review status: Collection method:
Minimum conflict level:
Gene type:
ClinVar version:
Total variants: 37
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HGVS dbSNP
NM_015247.2(CYLD):c.*1102G>A rs141088048
NM_015247.2(CYLD):c.*1245T>C rs192470603
NM_015247.2(CYLD):c.*1341T>G rs140767609
NM_015247.2(CYLD):c.*1575G>A rs184344245
NM_015247.2(CYLD):c.*1590T>C rs528844666
NM_015247.2(CYLD):c.*1831G>A rs181246559
NM_015247.2(CYLD):c.*2150A>G rs563954578
NM_015247.2(CYLD):c.*2236C>T rs57638820
NM_015247.2(CYLD):c.*2305A>T rs559634329
NM_015247.2(CYLD):c.*2335T>C rs9646285
NM_015247.2(CYLD):c.*2369G>A rs16948829
NM_015247.2(CYLD):c.*2615A>G rs181056407
NM_015247.2(CYLD):c.*2646G>A rs563329143
NM_015247.2(CYLD):c.*2710C>T rs141928186
NM_015247.2(CYLD):c.*3070A>G rs144667145
NM_015247.2(CYLD):c.*3469T>C rs111951225
NM_015247.2(CYLD):c.*3614C>A rs372370285
NM_015247.2(CYLD):c.*3679T>C rs141888517
NM_015247.2(CYLD):c.*3731C>T rs551109634
NM_015247.2(CYLD):c.*3736G>A rs567662515
NM_015247.2(CYLD):c.*3739C>G rs16948836
NM_015247.2(CYLD):c.*382T>C rs142580891
NM_015247.2(CYLD):c.*4567C>T rs113748745
NM_015247.2(CYLD):c.*47G>A rs116979331
NM_015247.2(CYLD):c.*4885A>T rs184571054
NM_015247.2(CYLD):c.*4947G>A rs567438576
NM_015247.2(CYLD):c.*5086A>G rs572929759
NM_015247.2(CYLD):c.*5272C>T rs140875917
NM_015247.2(CYLD):c.*698T>G rs541975303
NM_015247.2(CYLD):c.*779G>A rs190787930
NM_015247.2(CYLD):c.*841G>A rs117537927
NM_015247.2(CYLD):c.1172T>C (p.Ile391Thr) rs138976689
NM_015247.2(CYLD):c.126G>A (p.Pro42=) rs202119806
NM_015247.2(CYLD):c.1292G>A (p.Gly431Glu) rs200494719
NM_015247.2(CYLD):c.1473C>T (p.Ile491=) rs75757530
NM_015247.2(CYLD):c.2319G>A (p.Leu773=) rs199912760
NM_015247.2(CYLD):c.922+9C>A rs528253971

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