ClinVar Miner

List of variants in gene MYBPC3 reported as uncertain significance by Stanford Center for Inherited Cardiovascular Disease,Stanford University

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Total variants: 58
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HGVS dbSNP
NM_000256.3(MYBPC3):c.1000G>A (p.Glu334Lys) rs573916965
NM_000256.3(MYBPC3):c.104G>A (p.Arg35Gln) rs397515885
NM_000256.3(MYBPC3):c.1219G>A (p.Gly407Ser) rs727505266
NM_000256.3(MYBPC3):c.1238A>G (p.Glu413Gly) rs730880532
NM_000256.3(MYBPC3):c.1321G>A (p.Glu441Lys) rs193922377
NM_000256.3(MYBPC3):c.13G>C (p.Gly5Arg) rs201278114
NM_000256.3(MYBPC3):c.1468G>A (p.Gly490Arg) rs200625851
NM_000256.3(MYBPC3):c.148A>G (p.Ser50Gly) rs373164247
NM_000256.3(MYBPC3):c.1775T>C (p.Val592Ala) rs876661364
NM_000256.3(MYBPC3):c.1786G>A (p.Gly596Arg) rs199728019
NM_000256.3(MYBPC3):c.184A>C (p.Thr62Pro) rs377225516
NM_000256.3(MYBPC3):c.1976T>C (p.Ile659Thr) rs397515941
NM_000256.3(MYBPC3):c.2011G>A (p.Val671Ile) rs876657869
NM_000256.3(MYBPC3):c.2197C>T (p.Arg733Cys) rs397515956
NM_000256.3(MYBPC3):c.2210C>T (p.Thr737Met) rs199893357
NM_000256.3(MYBPC3):c.2269G>A (p.Val757Met) rs369790992
NM_000256.3(MYBPC3):c.2381C>T (p.Pro794Leu) rs730880565
NM_000256.3(MYBPC3):c.2429G>A (p.Arg810His) rs375675796
NM_000256.3(MYBPC3):c.2435A>G (p.Lys812Arg) rs786204350
NM_000256.3(MYBPC3):c.2543C>A (p.Ala848Glu) rs730880569
NM_000256.3(MYBPC3):c.2573G>A (p.Ser858Asn) rs727503185
NM_000256.3(MYBPC3):c.2618C>A (p.Pro873His) rs371401403
NM_000256.3(MYBPC3):c.2870C>G (p.Thr957Ser) rs193922380
NM_000256.3(MYBPC3):c.2873C>T (p.Thr958Ile) rs376504548
NM_000256.3(MYBPC3):c.2882C>T (p.Pro961Leu) rs373056282
NM_000256.3(MYBPC3):c.2905+3G>C rs1060501483
NM_000256.3(MYBPC3):c.2909G>A (p.Arg970Gln) rs727504346
NM_000256.3(MYBPC3):c.2938C>T (p.Arg980Cys) rs397515994
NM_000256.3(MYBPC3):c.2942A>C (p.Gln981Pro) rs730880582
NM_000256.3(MYBPC3):c.3019T>C (p.Trp1007Arg) rs730880585
NM_000256.3(MYBPC3):c.3098G>A (p.Arg1033Gln) rs397516003
NM_000256.3(MYBPC3):c.3284C>T (p.Thr1095Met) rs755653624
NM_000256.3(MYBPC3):c.3362G>A (p.Arg1121His) rs397516018
NM_000256.3(MYBPC3):c.340A>G (p.Thr114Ala) rs730880612
NM_000256.3(MYBPC3):c.3569G>A (p.Arg1190His) rs117354682
NM_000256.3(MYBPC3):c.3581C>T (p.Ala1194Val) rs730880594
NM_000256.3(MYBPC3):c.3584G>T (p.Gly1195Val) rs730880595
NM_000256.3(MYBPC3):c.3676C>T (p.Arg1226Cys) rs397516033
NM_000256.3(MYBPC3):c.3682C>T (p.Arg1228Cys) rs201312636
NM_000256.3(MYBPC3):c.3751T>C (p.Tyr1251His) rs730880601
NM_000256.3(MYBPC3):c.3771C>A (p.Asn1257Lys) rs730880603
NM_000256.3(MYBPC3):c.3779G>A (p.Gly1260Asp) rs730880606
NM_000256.3(MYBPC3):c.461T>C (p.Ile154Thr) rs373946195
NM_000256.3(MYBPC3):c.464G>T (p.Gly155Val) rs1060501477
NM_000256.3(MYBPC3):c.497T>G (p.Val166Gly) rs876661366
NM_000256.3(MYBPC3):c.529C>T (p.Arg177Cys) rs193922385
NM_000256.3(MYBPC3):c.557C>T (p.Pro186Leu) rs727503216
NM_000256.3(MYBPC3):c.624G>C (p.Gln208His) rs202139499
NM_000256.3(MYBPC3):c.710A>C (p.Tyr237Ser) rs397516070
NM_000256.3(MYBPC3):c.713G>A (p.Arg238His) rs727504396
NM_000256.3(MYBPC3):c.756C>A (p.Phe252Leu) rs876661367
NM_000256.3(MYBPC3):c.836G>C (p.Gly279Ala) rs375774648
NM_000256.3(MYBPC3):c.845G>A (p.Arg282Gln) rs761520688
NM_000256.3(MYBPC3):c.884T>C (p.Phe295Ser) rs876661369
NM_000256.3(MYBPC3):c.94G>A (p.Glu32Lys) rs730880575
NM_000256.3(MYBPC3):c.961G>A (p.Val321Met) rs200119454
NM_000256.3(MYBPC3):c.964T>C (p.Trp322Arg) rs730880708
NM_000256.3(MYBPC3):c.994G>A (p.Glu332Lys) rs397516086

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