List of variants reported as pathogenic for Congenital prothrombin deficiency by OMIM

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: 11

Download table as spreadsheet

HGVS	dbSNP	gnomAD frequency
NM_000506.3(F2):c.1054G>A (p.Glu352Lys)	rs121918484	0.00001
NM_000506.3(F2):c.1381C>T (p.Arg461Trp)	rs121918478	0.00001
NM_000506.5(F2):c.260A>G (p.Tyr87Cys)	rs1227147475	0.00001
NM_000506.3(F2):c.1027G>A (p.Glu343Lys)	rs121918483
NM_000506.3(F2):c.1139T>C (p.Met380Thr)	rs121918481
NM_000506.3(F2):c.1273C>T (p.Arg425Cys)	rs121918479
NM_000506.3(F2):c.1785C>G (p.Asp595Glu)	rs121918486
NM_000506.3(F2):c.1802G>T (p.Gly601Val)	rs121918480
NM_000506.3(F2):c.940C>T (p.Arg314Cys)	rs121918477
NM_000506.5(F2):c.1274G>A (p.Arg425His)	rs121918485
NM_000506.5(F2):c.462_463insT (p.Asn155Ter)	rs387906522

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.