List of variants in gene TCAP reported as uncertain significance by Laboratory for Molecular Medicine, Mass General Brigham Personalized Medicine

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: 11

Download table as spreadsheet

HGVS	dbSNP	gnomAD frequency
NM_003673.4(TCAP):c.313G>C (p.Glu105Gln)	rs146906267	0.00051
NM_003673.4(TCAP):c.458G>A (p.Arg153His)	rs149585781	0.00021
NM_003673.4(TCAP):c.337C>T (p.Leu113Phe)	rs372312912	0.00014
NM_003673.4(TCAP):c.388C>T (p.Arg130Cys)	rs374886575	0.00009
NM_003673.4(TCAP):c.269C>T (p.Pro90Leu)	rs727504427	0.00003
NM_003673.4(TCAP):c.16C>A (p.Leu6Met)	rs201664428	0.00002
NM_003673.4(TCAP):c.301G>A (p.Ala101Thr)	rs727503455	0.00002
NM_003673.4(TCAP):c.473G>A (p.Arg158His)	rs397516864	0.00001
NM_003673.4(TCAP):c.388C>A (p.Arg130Ser)	rs374886575
NM_003673.4(TCAP):c.472C>A (p.Arg158Ser)	rs397516863
NM_003673.4(TCAP):c.493C>G (p.Gln165Glu)	rs397516865

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.