List of variants in gene MYBPC3 reported as uncertain significance by Women's Health and Genetics/Laboratory Corporation of America, LabCorp

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: 41

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HGVS	dbSNP	gnomAD frequency
NM_000256.3(MYBPC3):c.13G>C (p.Gly5Arg)	rs201278114	0.00055
NM_000256.3(MYBPC3):c.184A>C (p.Thr62Pro)	rs377225516	0.00024
NM_000256.3(MYBPC3):c.74G>A (p.Ser25Asn)	rs371140684	0.00021
NM_000256.3(MYBPC3):c.461T>C (p.Ile154Thr)	rs373946195	0.00019
NM_000256.3(MYBPC3):c.1321G>A (p.Glu441Lys)	rs193922377	0.00016
NM_000256.3(MYBPC3):c.2176C>T (p.Arg726Cys)	rs752200396	0.00011
NM_000256.3(MYBPC3):c.3742G>A (p.Gly1248Arg)	rs202147520	0.00007
NM_000256.3(MYBPC3):c.1000G>A (p.Glu334Lys)	rs573916965	0.00006
NM_000256.3(MYBPC3):c.1255C>T (p.Arg419Cys)	rs368770848	0.00006
NM_000256.3(MYBPC3):c.3190+4C>T	rs571457875	0.00005
NM_000256.3(MYBPC3):c.2783C>T (p.Ser928Leu)	rs773819168	0.00004
NM_000256.3(MYBPC3):c.3676C>T (p.Arg1226Cys)	rs397516033	0.00004
NM_000256.3(MYBPC3):c.1243A>C (p.Ile415Leu)	rs1269517446	0.00003
NM_000256.3(MYBPC3):c.2909G>A (p.Arg970Gln)	rs727504346	0.00003
NM_000256.3(MYBPC3):c.667G>A (p.Glu223Lys)	rs397516069	0.00003
NM_000256.3(MYBPC3):c.713G>A (p.Arg238His)	rs727504396	0.00002
NM_000256.3(MYBPC3):c.112G>A (p.Val38Met)	rs1299024877	0.00001
NM_000256.3(MYBPC3):c.1219G>A (p.Gly407Ser)	rs727505266	0.00001
NM_000256.3(MYBPC3):c.1766G>A (p.Arg589His)	rs397515923	0.00001
NM_000256.3(MYBPC3):c.1976T>C (p.Ile659Thr)	rs397515941	0.00001
NM_000256.3(MYBPC3):c.2915G>A (p.Arg972Gln)	rs761696555	0.00001
NM_000256.3(MYBPC3):c.3568C>T (p.Arg1190Cys)	rs755160084	0.00001
NM_000256.3(MYBPC3):c.3812G>A (p.Arg1271Gln)	rs762225417	0.00001
NM_000256.3(MYBPC3):c.1036C>T (p.Arg346Cys)	rs1236178301
NM_000256.3(MYBPC3):c.1072G>T (p.Asp358Tyr)	rs746267533
NM_000256.3(MYBPC3):c.1351+3G>T
NM_000256.3(MYBPC3):c.194C>T (p.Thr65Met)	rs753300898
NM_000256.3(MYBPC3):c.2432AGA[3] (p.Lys814del)	rs727504288
NM_000256.3(MYBPC3):c.2507T>C (p.Met836Thr)	rs1555121215
NM_000256.3(MYBPC3):c.2537T>A (p.Val846Asp)	rs193922379
NM_000256.3(MYBPC3):c.2557G>T (p.Gly853Cys)
NM_000256.3(MYBPC3):c.2602G>A (p.Gly868Ser)	rs775890771
NM_000256.3(MYBPC3):c.2618C>A (p.Pro873His)	rs371401403
NM_000256.3(MYBPC3):c.2618C>T (p.Pro873Leu)	rs371401403
NM_000256.3(MYBPC3):c.2737+20A>G	rs2095881689
NM_000256.3(MYBPC3):c.2905+5G>A	rs193922381
NM_000256.3(MYBPC3):c.293-19C>T
NM_000256.3(MYBPC3):c.3413G>C (p.Arg1138Pro)	rs187705120
NM_000256.3(MYBPC3):c.3797G>A (p.Cys1266Tyr)	rs397516041
NM_000256.3(MYBPC3):c.3815-1G>A	rs397516044
NM_000256.3(MYBPC3):c.909-8T>C	rs1260212325

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