List of variants in gene APC reported as benign by Genome Diagnostics Laboratory, Amsterdam University Medical Center

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

Total variants: 15

Download table as spreadsheet

HGVS	dbSNP	gnomAD frequency
NM_000038.6(APC):c.7704A>G (p.Gly2568=)	rs35043160	0.02992
NM_000038.6(APC):c.7504G>A (p.Gly2502Ser)	rs2229995	0.01693
NM_000038.6(APC):c.3732A>G (p.Gln1244=)	rs74380081	0.01174
NM_000038.6(APC):c.1695A>G (p.Glu565=)	rs77921116	0.01170
NM_000038.6(APC):c.7201C>T (p.Leu2401=)	rs2229994	0.01134
NM_000038.6(APC):c.2608C>T (p.Pro870Ser)	rs33974176	0.00917
NM_000038.6(APC):c.4326T>A (p.Pro1442=)	rs67622085	0.00705
NM_000038.6(APC):c.5265G>A (p.Ala1755=)	rs34506289	0.00675
NM_000038.6(APC):c.1959G>A (p.Arg653=)	rs72541809	0.00583
NM_000038.6(APC):c.1958+8T>C	rs62626346	0.00510
NM_000038.6(APC):c.3471G>A (p.Glu1157=)	rs143927847	0.00308
NM_000038.6(APC):c.3165A>T (p.Ile1055=)	rs61734287	0.00286
NM_000038.6(APC):c.6921G>A (p.Ser2307=)	rs2229993	0.00143
NM_000038.6(APC):c.3462AGA[2] (p.Glu1157del)	rs386833391
NM_000038.6(APC):c.423-4dup	rs730881230

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.