List of variants reported as benign for adenocarcinoma by Fulgent Genetics, Fulgent Genetics

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: 14

Download table as spreadsheet

HGVS	dbSNP	gnomAD frequency
NM_000545.8(HNF1A):c.1720A>G (p.Ser574Gly)	rs1169305	0.98610
NM_000546.6(TP53):c.215C>G (p.Pro72Arg)	rs1042522	0.62654
NM_000038.6(APC):c.4479G>A (p.Thr1493=)	rs41115	0.59177
NM_004655.4(AXIN2):c.1386C>T (p.Pro462=)	rs1133683	0.52439
NM_000038.6(APC):c.1458T>C (p.Tyr486=)	rs2229992	0.46792
NM_020975.6(RET):c.1264-5C>T	rs9282835	0.02749
NM_004360.5(CDH1):c.1849G>A (p.Ala617Thr)	rs33935154	0.01412
NM_004360.5(CDH1):c.-71C>G	rs34033771	0.00927
NM_000038.6(APC):c.4326T>A (p.Pro1442=)	rs67622085	0.00705
NM_024529.5(CDC73):c.308-16C>A	rs201766013	0.00252
NM_000546.6(TP53):c.139C>T (p.Pro47Ser)	rs1800371	0.00123
NM_144997.7(FLCN):c.1538+10A>C	rs12451312	0.00010
NM_020975.6(RET):c.2268C>T (p.Ala756=)	rs370791179	0.00001
NM_144997.7(FLCN):c.75G>A (p.Leu25=)	rs200350612

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.