List of variants reported as benign for Familial multiple trichoepitheliomata

Minimum submission review status:		Collection method:
Minimum conflict level: Report conflict between different conditions
Show significances as they were submitted (without aggregation into standard terms)
		ClinVar version:

Total variants: 39

Download table as spreadsheet

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.*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.*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

The information on this website is not intended for direct diagnostic use or medical decision-making without review by a genetics professional. Individuals should not change their health behavior solely on the basis of information contained on this website. Neither the University of Utah nor the National Institutes of Health independently verfies the submitted information. If you have questions about the information contained on this website, please see a health care professional.