ClinVar Miner

List of variants in gene MYBPC3 reported as likely benign by Invitae

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Gene type:
ClinVar version:
Total variants: 107
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HGVS dbSNP
NM_000256.3(MYBPC3):c.1008C>T (p.Ile336=) rs397515880
NM_000256.3(MYBPC3):c.1020C>T (p.Tyr340=) rs556616131
NM_000256.3(MYBPC3):c.1035G>A (p.Leu345=) rs779704622
NM_000256.3(MYBPC3):c.1038C>T (p.Arg346=) rs758016271
NM_000256.3(MYBPC3):c.108A>G (p.Ala36=) rs754870909
NM_000256.3(MYBPC3):c.1143C>A (p.Ile381=) rs1555122449
NM_000256.3(MYBPC3):c.1282T>C (p.Leu428=) rs758253767
NM_000256.3(MYBPC3):c.1286C>T (p.Ala429Val) rs370412052
NM_000256.3(MYBPC3):c.1293C>T (p.Asp431=) rs763808974
NM_000256.3(MYBPC3):c.12G>A (p.Pro4=) rs377292092
NM_000256.3(MYBPC3):c.1311G>C (p.Val437=) rs1060504240
NM_000256.3(MYBPC3):c.132C>T (p.Arg44=) rs377579620
NM_000256.3(MYBPC3):c.1370C>T (p.Thr457Met) rs370538243
NM_000256.3(MYBPC3):c.1392G>A (p.Leu464=) rs900306372
NM_000256.3(MYBPC3):c.1458-7C>T rs397515904
NM_000256.3(MYBPC3):c.1544A>G (p.Asn515Ser) rs181834806
NM_000256.3(MYBPC3):c.1566G>A (p.Ala522=) rs376041792
NM_000256.3(MYBPC3):c.1713G>A (p.Glu571=) rs1060504241
NM_000256.3(MYBPC3):c.1716T>C (p.Asn572=) rs1248057767
NM_000256.3(MYBPC3):c.1720C>A (p.Arg574=) rs61897383
NM_000256.3(MYBPC3):c.1758C>T (p.Pro586=) rs727505203
NM_000256.3(MYBPC3):c.1785C>T (p.Ile595=) rs572227730
NM_000256.3(MYBPC3):c.1813G>A (p.Asp605Asn) rs376736293
NM_000256.3(MYBPC3):c.1827C>G (p.Ala609=) rs535853707
NM_000256.3(MYBPC3):c.1869C>T (p.Cys623=) rs397515932
NM_000256.3(MYBPC3):c.1914C>T (p.Phe638=) rs377227442
NM_000256.3(MYBPC3):c.1944C>T (p.His648=) rs750861887
NM_000256.3(MYBPC3):c.1953C>T (p.Cys651=) rs936188645
NM_000256.3(MYBPC3):c.1986A>G (p.Val662=) rs961007973
NM_000256.3(MYBPC3):c.2064G>A (p.Thr688=) rs758224257
NM_000256.3(MYBPC3):c.207G>C (p.Arg69=) rs397515946
NM_000256.3(MYBPC3):c.2149-4C>G rs1324005699
NM_000256.3(MYBPC3):c.216C>A (p.Gly72=) rs760007714
NM_000256.3(MYBPC3):c.2190C>A (p.Thr730=) rs878853832
NM_000256.3(MYBPC3):c.2196C>T (p.Asp732=) rs397515955
NM_000256.3(MYBPC3):c.2211G>A (p.Thr737=) rs113265977
NM_000256.3(MYBPC3):c.2220G>C (p.Gly740=) rs1451991531
NM_000256.3(MYBPC3):c.2244C>T (p.Val748=) rs1555121454
NM_000256.3(MYBPC3):c.2250G>A (p.Thr750=) rs373338699
NM_000256.3(MYBPC3):c.2308+9G>A rs769533145
NM_000256.3(MYBPC3):c.237C>T (p.Tyr79=) rs730880698
NM_000256.3(MYBPC3):c.240A>G (p.Ala80=) rs770089112
NM_000256.3(MYBPC3):c.2466C>T (p.Asn822=) rs1555121239
NM_000256.3(MYBPC3):c.2469C>T (p.Phe823=) rs1555121238
NM_000256.3(MYBPC3):c.246T>C (p.Ile82=) rs372502369
NM_000256.3(MYBPC3):c.2487G>T (p.Leu829=) rs201040413
NM_000256.3(MYBPC3):c.2497G>A (p.Ala833Thr) rs199865688
NM_000256.3(MYBPC3):c.2603-10C>T rs765120057
NM_000256.3(MYBPC3):c.2712C>T (p.Tyr904=) rs1363489095
NM_000256.3(MYBPC3):c.2800C>T (p.Leu934=) rs367980215
NM_000256.3(MYBPC3):c.2805C>T (p.Pro935=) rs878853833
NM_000256.3(MYBPC3):c.2838A>G (p.Ala946=) rs376858768
NM_000256.3(MYBPC3):c.2870C>G (p.Thr957Ser) rs193922380
NM_000256.3(MYBPC3):c.2895G>A (p.Gln965=) rs1057524069
NM_000256.3(MYBPC3):c.2914C>T (p.Arg972Trp) rs193922382
NM_000256.3(MYBPC3):c.292+9C>T rs752388318
NM_000256.3(MYBPC3):c.2961C>T (p.Val987=) rs761700877
NM_000256.3(MYBPC3):c.2991C>T (p.Phe997=) rs1555120642
NM_000256.3(MYBPC3):c.2997C>T (p.Gly999=) rs377283955
NM_000256.3(MYBPC3):c.3137C>T (p.Thr1046Met) rs371061770
NM_000256.3(MYBPC3):c.3138G>A (p.Thr1046=) rs762154672
NM_000256.3(MYBPC3):c.3171G>A (p.Thr1057=) rs397516004
NM_000256.3(MYBPC3):c.3191-7C>T rs373012629
NM_000256.3(MYBPC3):c.3228C>T (p.Asp1076=) rs369999866
NM_000256.3(MYBPC3):c.3285G>A (p.Thr1095=) rs367927327
NM_000256.3(MYBPC3):c.3315C>T (p.Ala1105=) rs200372325
NM_000256.3(MYBPC3):c.3362G>A (p.Arg1121His) rs397516018
NM_000256.3(MYBPC3):c.3392T>C (p.Ile1131Thr) rs370890951
NM_000256.3(MYBPC3):c.3414C>T (p.Arg1138=) rs753671465
NM_000256.3(MYBPC3):c.3535G>A (p.Glu1179Lys) rs199669878
NM_000256.3(MYBPC3):c.3573G>A (p.Ser1191=) rs371488508
NM_000256.3(MYBPC3):c.363G>A (p.Pro121=) rs780768974
NM_000256.3(MYBPC3):c.3657G>T (p.Leu1219=) rs770157084
NM_000256.3(MYBPC3):c.3672C>T (p.Asp1224=) rs368221517
NM_000256.3(MYBPC3):c.3682C>T (p.Arg1228Cys) rs201312636
NM_000256.3(MYBPC3):c.372C>T (p.Ala124=) rs11570046
NM_000256.3(MYBPC3):c.3741C>T (p.Asp1247=) rs543376073
NM_000256.3(MYBPC3):c.3756C>G (p.Val1252=) rs374760003
NM_000256.3(MYBPC3):c.3777G>A (p.Gln1259=) rs746042492
NM_000256.3(MYBPC3):c.3815-10T>G rs397516043
NM_000256.3(MYBPC3):c.402C>T (p.Pro134=) rs397516046
NM_000256.3(MYBPC3):c.407-5C>T rs371312567
NM_000256.3(MYBPC3):c.465C>T (p.Gly155=) rs1381779840
NM_000256.3(MYBPC3):c.471C>T (p.Phe157=) rs150291001
NM_000256.3(MYBPC3):c.501C>T (p.Thr167=) rs397516054
NM_000256.3(MYBPC3):c.531C>T (p.Arg177=) rs368035400
NM_000256.3(MYBPC3):c.558G>A (p.Pro186=) rs370962887
NM_000256.3(MYBPC3):c.643C>T (p.Arg215Cys) rs397516063
NM_000256.3(MYBPC3):c.645C>T (p.Arg215=) rs397516064
NM_000256.3(MYBPC3):c.646G>A (p.Ala216Thr) rs201098973
NM_000256.3(MYBPC3):c.648C>T (p.Ala216=) rs777418402
NM_000256.3(MYBPC3):c.666C>T (p.Phe222=) rs371331114
NM_000256.3(MYBPC3):c.690G>A (p.Gln230=) rs1060504239
NM_000256.3(MYBPC3):c.765T>C (p.Thr255=) rs1555123092
NM_000256.3(MYBPC3):c.772+10C>T rs375525278
NM_000256.3(MYBPC3):c.772+9G>T rs566339669
NM_000256.3(MYBPC3):c.82G>A (p.Val28Met) rs776834755
NM_000256.3(MYBPC3):c.841C>A (p.Arg281=) rs371711564
NM_000256.3(MYBPC3):c.852-4A>C rs1235513938
NM_000256.3(MYBPC3):c.906-7G>T rs397516079
NM_000256.3(MYBPC3):c.906-9G>A rs758117772
NM_000256.3(MYBPC3):c.924G>A (p.Pro308=) rs771875597
NM_000256.3(MYBPC3):c.926+8C>G rs377595584
NM_000256.3(MYBPC3):c.926+8C>T rs377595584
NM_000256.3(MYBPC3):c.933G>A (p.Ser311=) rs374326087
NM_000256.3(MYBPC3):c.94G>A (p.Glu32Lys) rs730880575
NM_000256.3(MYBPC3):c.999C>T (p.Tyr333=) rs367947846

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