List of variants in gene MYBPC3 reported as uncertain significance by Mendelics

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: 29

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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.3787C>T (p.Arg1263Trp)	rs370338674	0.00038
NM_000256.3(MYBPC3):c.961G>A (p.Val321Met)	rs200119454	0.00025
NM_000256.3(MYBPC3):c.2728C>A (p.Pro910Thr)	rs397515985	0.00021
NM_000256.3(MYBPC3):c.2684G>A (p.Arg895His)	rs372628478	0.00019
NM_000256.3(MYBPC3):c.461T>C (p.Ile154Thr)	rs373946195	0.00019
NM_000256.3(MYBPC3):c.624G>C (p.Gln208His)	rs202139499	0.00017
NM_000256.3(MYBPC3):c.1321G>A (p.Glu441Lys)	rs193922377	0.00016
NM_000256.3(MYBPC3):c.1000G>A (p.Glu334Lys)	rs573916965	0.00006
NM_000256.3(MYBPC3):c.2197C>T (p.Arg733Cys)	rs397515956	0.00006
NM_000256.3(MYBPC3):c.104G>A (p.Arg35Gln)	rs397515885	0.00004
NM_000256.3(MYBPC3):c.2311G>A (p.Val771Met)	rs371488302	0.00004
NM_000256.3(MYBPC3):c.3065G>C (p.Arg1022Pro)	rs397516000	0.00004
NM_000256.3(MYBPC3):c.787G>A (p.Gly263Arg)	rs373730381	0.00004
NM_000256.3(MYBPC3):c.2198G>A (p.Arg733His)	rs534345197	0.00003
NM_000256.3(MYBPC3):c.223G>A (p.Asp75Asn)	rs375471260	0.00003
NM_000256.3(MYBPC3):c.305C>T (p.Pro102Leu)	rs730880610	0.00003
NM_000256.3(MYBPC3):c.3343G>A (p.Val1115Ile)	rs531189495	0.00003
NM_000256.3(MYBPC3):c.994G>A (p.Glu332Lys)	rs397516086	0.00003
NM_000256.3(MYBPC3):c.2504G>T (p.Arg835Leu)	rs527305885	0.00002
NM_000256.3(MYBPC3):c.251G>A (p.Gly84Asp)	rs569824900	0.00002
NM_000256.3(MYBPC3):c.643C>T (p.Arg215Cys)	rs397516063	0.00002
NM_000256.3(MYBPC3):c.682G>A (p.Asp228Asn)	rs369300885	0.00002
NM_000256.3(MYBPC3):c.1147C>G (p.Leu383Val)	rs11570077	0.00001
NM_000256.3(MYBPC3):c.1363C>T (p.Leu455Phe)	rs747686377	0.00001
NM_000256.3(MYBPC3):c.3763G>A (p.Ala1255Thr)	rs727503167	0.00001
NM_000256.3(MYBPC3):c.817C>T (p.Arg273Cys)	rs551119259	0.00001
NM_000256.3(MYBPC3):c.1084A>G (p.Ser362Gly)	rs730880633
NM_000256.3(MYBPC3):c.2618C>T (p.Pro873Leu)	rs371401403

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