List of variants studied for adenocarcinoma by CZECANCA consortium

Minimum submission review status:		Collection method:
Minimum conflict level: Report conflict between different conditions
		ClinVar version:

Total variants: 7

Download table as spreadsheet

HGVS	dbSNP	gnomAD frequency
NM_000143.4(FH):c.1127A>C (p.Gln376Pro)	rs200796606	0.00005
NM_000535.7(PMS2):c.1144+250_2175-1948del
NM_002485.5(NBN):c.657_661del (p.Lys219fs)	rs587776650
NM_005732.4(RAD50):c.1875C>G (p.Tyr625Ter)	rs149201802
NM_005732.4(RAD50):c.2046del (p.Val683fs)
NM_005732.4(RAD50):c.2524+1_2524+9del
NM_020975.6(RET):c.2304G>C (p.Glu768Asp)	rs78014899

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.