List of variants in gene MYBPC3 reported by Center of Genomic medicine, Geneva, University Hospital of Geneva

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: 16

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HGVS	dbSNP	gnomAD frequency
NM_000256.3(MYBPC3):c.1624G>C (p.Glu542Gln)	rs121909374	0.00006
NM_000256.3(MYBPC3):c.1484G>A (p.Arg495Gln)	rs200411226	0.00004
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.1505G>A (p.Arg502Gln)	rs397515907	0.00003
NM_000256.3(MYBPC3):c.2864_2865del (p.Pro955fs)	rs397515990	0.00001
NM_000256.3(MYBPC3):c.3697C>T (p.Gln1233Ter)	rs397516037	0.00001
NM_000256.3(MYBPC3):c.1800del (p.Lys600fs)	rs397515926
NM_000256.3(MYBPC3):c.1928-2A>G	rs397515937
NM_000256.3(MYBPC3):c.2149-2del	rs1555121488
NM_000256.3(MYBPC3):c.2766del (p.Gly922_Leu923insTer)	rs1565624196
NM_000256.3(MYBPC3):c.2905C>T (p.Gln969Ter)	rs397515992
NM_000256.3(MYBPC3):c.3324_3325del (p.Lys1108fs)	rs1060499673
NM_000256.3(MYBPC3):c.3460delinsCT (p.Thr1154fs)
NM_000256.3(MYBPC3):c.3559del (p.Leu1187fs)	rs1555120300
NM_000256.3(MYBPC3):c.3732C>A (p.Cys1244Ter)	rs730880600

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