List of variants in gene APC reported as benign by ARUP Laboratories, Molecular Genetics and Genomics, ARUP Laboratories

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: 44

Download table as spreadsheet

HGVS	dbSNP	gnomAD frequency
NM_000038.6(APC):c.5465T>A (p.Val1822Asp)	rs459552	0.82099
NM_000038.6(APC):c.1408+743G>A	rs2545162	0.60798
NM_000038.6(APC):c.5034G>A (p.Gly1678=)	rs42427	0.59504
NM_000038.6(APC):c.5880G>A (p.Pro1960=)	rs465899	0.59308
NM_000038.6(APC):c.5268T>G (p.Ser1756=)	rs866006	0.59230
NM_000038.6(APC):c.4479G>A (p.Thr1493=)	rs41115	0.59177
NM_000038.6(APC):c.1635G>A (p.Ala545=)	rs351771	0.59150
NM_000038.6(APC):c.-19+734C>T	rs2020383	0.51721
NM_000038.6(APC):c.1458T>C (p.Tyr486=)	rs2229992	0.46792
NM_000038.6(APC):c.-19+647A>G	rs2019720	0.38718
NM_001127511.3(APC):c.-31T>G	rs78429131	0.09154
NM_000038.6(APC):c.645+32C>T	rs2909961	0.06662
NM_001354897.2(APC):c.-245A>C	rs75580617	0.04642
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.1312+27G>A	rs74975092	0.00973
NM_001127511.3(APC):c.78C>A (p.Ser26Arg)	rs113782655	0.00928
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.3949G>C (p.Glu1317Gln)	rs1801166	0.00570
NM_000038.6(APC):c.1958+8T>C	rs62626346	0.00510
NM_000038.6(APC):c.532-32T>C	rs112108777	0.00505
NM_000038.6(APC):c.5250C>G (p.Val1750=)	rs2229997	0.00497
NM_000038.6(APC):c.933+30A>G	rs145211300	0.00412
NM_000038.6(APC):c.7862C>G (p.Ser2621Cys)	rs72541816	0.00358
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.3264G>A (p.Lys1088=)	rs114774495	0.00255
NM_000038.6(APC):c.3386T>C (p.Leu1129Ser)	rs143638171	0.00250
NM_000038.6(APC):c.705A>G (p.Leu235=)	rs147036141	0.00213
NM_000038.6(APC):c.6921G>A (p.Ser2307=)	rs2229993	0.00143
NM_000038.6(APC):c.5790A>G (p.Gln1930=)	rs141152252	0.00097
NM_000038.6(APC):c.8043G>C (p.Pro2681=)	rs149347068	0.00092
NM_000038.6(APC):c.2805C>T (p.Tyr935=)	rs137854575	0.00040
NM_000038.6(APC):c.-18-13T>G	rs1554067089
NM_000038.6(APC):c.1512T>C (p.Ala504=)	rs1561554267
NM_000038.6(APC):c.3462AGA[2] (p.Glu1157del)	rs386833391
NM_000038.6(APC):c.5265_5268delinsATCG (p.Ala1755_Ser1756=)	rs1554086584
NM_001127511.3(APC):c.-126dup	rs565045828

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.