List of variants in gene APC studied for Neoplasm of the large intestine

Minimum submission review status:		Collection method:
Minimum conflict level: Report conflict between different conditions
Gene type: Distinguish antisense genes from sense genes
		ClinVar version:

Total variants: 9

Download table as spreadsheet

HGVS	dbSNP	gnomAD frequency
NM_000038.6(APC):c.2626C>T (p.Arg876Ter)	rs121913333
NM_000038.6(APC):c.3340C>T (p.Arg1114Ter)	rs121913331
NM_000038.6(APC):c.3916G>T (p.Glu1306Ter)	rs121913462
NM_000038.6(APC):c.4012C>T (p.Gln1338Ter)	rs121913327
NM_000038.6(APC):c.4099C>T (p.Gln1367Ter)	rs121913328
NM_000038.6(APC):c.4132C>T (p.Gln1378Ter)	rs121913329
NM_000038.6(APC):c.4135G>T (p.Glu1379Ter)	rs121913326
NM_000038.6(APC):c.4285C>T (p.Gln1429Ter)	rs74535574
NM_000038.6(APC):c.4348C>T (p.Arg1450Ter)	rs121913332

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.