List of variants in gene MYBPC3 reported by Human Genome Sequencing Center Clinical Lab, Baylor College of Medicine

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: 11

Download table as spreadsheet

HGVS	dbSNP	gnomAD frequency
NM_000256.3(MYBPC3):c.1504C>T (p.Arg502Trp)	rs375882485	0.00010
NM_000256.3(MYBPC3):c.1624G>C (p.Glu542Gln)	rs121909374	0.00006
NM_000256.3(MYBPC3):c.3330+2T>G	rs387906397	0.00004
NM_000256.3(MYBPC3):c.772G>A (p.Glu258Lys)	rs397516074	0.00004
NM_000256.3(MYBPC3):c.927-9G>A	rs397516083	0.00002
NM_000256.3(MYBPC3):c.3286G>T (p.Glu1096Ter)	rs121909377	0.00001
NM_000256.3(MYBPC3):c.3776del (p.Gln1259fs)	rs727503166	0.00001
NM_000256.3(MYBPC3):c.1168del (p.His390fs)	rs397515889
NM_000256.3(MYBPC3):c.177_187del (p.Glu60fs)	rs397515925
NM_000256.3(MYBPC3):c.655G>C (p.Val219Leu)	rs397516068
NM_000256.3(MYBPC3):c.905+1G>T	rs767698543

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.