ClinVar Miner

List of variants in gene CYLD reported as benign by Illumina Laboratory Services, Illumina

Minimum submission review status: Collection method:
Minimum conflict level:
Gene type:
ClinVar version:
Total variants: 41
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HGVS dbSNP gnomAD frequency
NM_001378743.1(CYLD):c.*4561G>A rs17314948 0.05808
NM_001378743.1(CYLD):c.2412C>T (p.Asp804=) rs2066852 0.05803
NM_001378743.1(CYLD):c.*837A>G rs3743781 0.05586
NM_001378743.1(CYLD):c.2109-10G>A rs11865799 0.05482
NM_001378743.1(CYLD):c.*4888_*4889del rs143814807 0.05387
NM_001378743.1(CYLD):c.*841G>A rs117537927 0.02289
NM_001378743.1(CYLD):c.*2369G>A rs16948829 0.01401
NM_001378743.1(CYLD):c.*3739C>G rs16948836 0.01185
NM_001378743.1(CYLD):c.*2236C>T rs57638820 0.00896
NM_001378743.1(CYLD):c.1473C>T (p.Ile491=) rs75757530 0.00802
NM_001378743.1(CYLD):c.*2335T>C rs9646285 0.00710
NM_001378743.1(CYLD):c.*139G>A rs148107725 0.00707
NM_001378743.1(CYLD):c.*1831G>A rs181246559 0.00599
NM_001378743.1(CYLD):c.*3469T>C rs111951225 0.00586
NM_001378743.1(CYLD):c.*1575G>A rs184344245 0.00532
NM_001378743.1(CYLD):c.*1341T>G rs140767609 0.00470
NM_001378743.1(CYLD):c.*3070A>G rs144667145 0.00435
NM_001378743.1(CYLD):c.*4567C>T rs113748745 0.00336
NM_001378743.1(CYLD):c.*2710C>T rs141928186 0.00225
NM_001378743.1(CYLD):c.*1590T>C rs528844666 0.00218
NM_001378743.1(CYLD):c.*47G>A rs116979331 0.00210
NM_001378743.1(CYLD):c.*698T>G rs541975303 0.00179
NM_001378743.1(CYLD):c.*3736G>A rs567662515 0.00058
NM_001378743.1(CYLD):c.*2615A>G rs181056407 0.00042
NM_001378743.1(CYLD):c.126G>A (p.Pro42=) rs202119806 0.00037
NM_001378743.1(CYLD):c.*382T>C rs142580891 0.00017
NM_001378743.1(CYLD):c.913+5G>T rs200435608 0.00014
NM_001378743.1(CYLD):c.*5086A>G rs572929759 0.00010
NM_001378743.1(CYLD):c.2469+10C>T rs374473837 0.00010
NM_001378743.1(CYLD):c.*3614C>A rs372370285 0.00008
NM_001378743.1(CYLD):c.*3679T>C rs141888517 0.00004
NM_001378743.1(CYLD):c.59T>G (p.Ile20Ser) rs764097337 0.00004
NM_001378743.1(CYLD):c.1172T>C (p.Ile391Thr) rs138976689 0.00001
NM_001378743.1(CYLD):c.2319G>A (p.Leu773=) rs199912760 0.00001
NM_001378743.1(CYLD):c.*2122del rs74757288
NM_001378743.1(CYLD):c.*2150A>G rs563954578
NM_001378743.1(CYLD):c.*2646G>A rs563329143
NM_001378743.1(CYLD):c.*5272C>T rs140875917
NM_001378743.1(CYLD):c.*831C>T rs144877731
NM_001378743.1(CYLD):c.1292G>A (p.Gly431Glu) rs200494719
NM_001378743.1(CYLD):c.922+9C>A rs528253971

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