ClinVar Miner

List of variants studied for papillary adenocarcinoma by Baylor Genetics

Included ClinVar conditions (8):

Familial cancer of breast; Classic Hodgkin lymphoma; Ovarian neoplasm; Thyroid cancer, nonmedullary, 1
Hereditary papillary renal cell carcinoma
Osteofibrous dysplasia; Papillary renal cell carcinoma type 1; Hepatocellular carcinoma; Autosomal recessive nonsyndromic hearing loss 97
Ovarian serous surface papillary adenocarcinoma
Papillary renal cell carcinoma type 1
Papillary thyroid carcinoma
Thyroid cancer, nonmedullary, 1
Von Hippel-Lindau syndrome; Cerebellar hemangioblastoma; Papillary renal cell carcinoma type 1; Skin adenoma

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

Total variants: 3

Download table as spreadsheet

HGVS	dbSNP	gnomAD frequency
NM_000245.4(MET):c.1099A>G (p.Ile367Val)	rs774146015	0.00001
NM_000245.4(MET):c.1450C>T (p.His484Tyr)	rs771272439	0.00001
NM_000245.4(MET):c.2828C>T (p.Thr943Ile)	rs2116992551

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.