ClinVar Miner

List of variants in gene MYBPC3 reported as uncertain significance for Cardiomyopathy

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Total variants: 103
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HGVS dbSNP
NM_000256.3(MYBPC3):c.-11C>T
NM_000256.3(MYBPC3):c.1000G>A (p.Glu334Lys) rs573916965
NM_000256.3(MYBPC3):c.1037G>A (p.Arg346His) rs397515883
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.1104G>A (p.Lys368=)
NM_000256.3(MYBPC3):c.11C>T (p.Pro4Leu)
NM_000256.3(MYBPC3):c.1222A>G (p.Ser408Gly)
NM_000256.3(MYBPC3):c.1255C>T (p.Arg419Cys) rs368770848
NM_000256.3(MYBPC3):c.1316G>A (p.Gly439Asp)
NM_000256.3(MYBPC3):c.1373G>A (p.Arg458His) rs374255707
NM_000256.3(MYBPC3):c.13G>C (p.Gly5Arg) rs201278114
NM_000256.3(MYBPC3):c.1409G>A (p.Arg470Gln) rs776734314
NM_000256.3(MYBPC3):c.1433C>T (p.Ser478Leu) rs730880540
NM_000256.3(MYBPC3):c.1458-6G>A rs375347534
NM_000256.3(MYBPC3):c.145A>T (p.Ile49Phe)
NM_000256.3(MYBPC3):c.1461G>A (p.Leu487=)
NM_000256.3(MYBPC3):c.1468G>A (p.Gly490Arg) rs200625851
NM_000256.3(MYBPC3):c.1471G>A (p.Val491Met) rs730880543
NM_000256.3(MYBPC3):c.148A>G (p.Ser50Gly) rs373164247
NM_000256.3(MYBPC3):c.1513_1515delAAG (p.Lys505del) rs727504287
NM_000256.3(MYBPC3):c.1786G>A (p.Gly596Arg) rs199728019
NM_000256.3(MYBPC3):c.1814A>G (p.Asp605Gly) rs372371774
NM_000256.3(MYBPC3):c.1816G>A (p.Val606Ile) rs368482358
NM_000256.3(MYBPC3):c.1822C>T (p.Pro608Ser) rs730880552
NM_000256.3(MYBPC3):c.1827C>G (p.Ala609=) rs535853707
NM_000256.3(MYBPC3):c.1831G>A (p.Glu611Lys) rs730880555
NM_000256.3(MYBPC3):c.1841A>G (p.Tyr614Cys) rs727503194
NM_000256.3(MYBPC3):c.1850T>C (p.Val617Ala)
NM_000256.3(MYBPC3):c.1919C>T (p.Pro640Leu)
NM_000256.3(MYBPC3):c.1928-3C>T
NM_000256.3(MYBPC3):c.1961G>A (p.Arg654His) rs1800565
NM_000256.3(MYBPC3):c.2005C>A (p.Leu669Met)
NM_000256.3(MYBPC3):c.202G>A (p.Val68Met)
NM_000256.3(MYBPC3):c.2034T>C (p.Ala678=)
NM_000256.3(MYBPC3):c.2149-5C>G
NM_000256.3(MYBPC3):c.2171G>A (p.Arg724Gln)
NM_000256.3(MYBPC3):c.2176C>T (p.Arg726Cys)
NM_000256.3(MYBPC3):c.2198G>A (p.Arg733His) rs534345197
NM_000256.3(MYBPC3):c.2269G>A (p.Val757Met) rs369790992
NM_000256.3(MYBPC3):c.2320G>A (p.Ala774Thr) rs368104687
NM_000256.3(MYBPC3):c.2381C>T (p.Pro794Leu) rs730880565
NM_000256.3(MYBPC3):c.2398G>A (p.Gly800Arg) rs727504574
NM_000256.3(MYBPC3):c.2441_2443delAGA (p.Lys814del) rs727504288
NM_000256.3(MYBPC3):c.2447A>G (p.Tyr816Cys)
NM_000256.3(MYBPC3):c.2479C>A (p.Gln827Lys) rs375322174
NM_000256.3(MYBPC3):c.2534G>A (p.Arg845His) rs730880568
NM_000256.3(MYBPC3):c.2562G>A (p.Met854Ile) rs730880572
NM_000256.3(MYBPC3):c.2599A>G (p.Ile867Val) rs768339148
NM_000256.3(MYBPC3):c.2618C>T (p.Pro873Leu) rs371401403
NM_000256.3(MYBPC3):c.2672G>A (p.Arg891Gln) rs727504378
NM_000256.3(MYBPC3):c.2728C>A (p.Pro910Thr) rs397515985
NM_000256.3(MYBPC3):c.2737+9C>T
NM_000256.3(MYBPC3):c.2815C>T (p.Arg939Trp) rs534366414
NM_000256.3(MYBPC3):c.2877G>A (p.Thr959=) rs727503181
NM_000256.3(MYBPC3):c.2882C>T (p.Pro961Leu) rs373056282
NM_000256.3(MYBPC3):c.2905+5G>T rs193922381
NM_000256.3(MYBPC3):c.2909G>A (p.Arg970Gln) rs727504346
NM_000256.3(MYBPC3):c.2938C>G (p.Arg980Gly) rs397515994
NM_000256.3(MYBPC3):c.305C>T (p.Pro102Leu) rs730880610
NM_000256.3(MYBPC3):c.3064C>T (p.Arg1022Cys) rs397515999
NM_000256.3(MYBPC3):c.3097C>T (p.Arg1033Trp) rs748909815
NM_000256.3(MYBPC3):c.3107G>A (p.Arg1036His) rs374255381
NM_000256.3(MYBPC3):c.3130C>G (p.Gln1044Glu)
NM_000256.3(MYBPC3):c.3137C>T (p.Thr1046Met) rs371061770
NM_000256.3(MYBPC3):c.3148G>A (p.Glu1050Lys) rs780449220
NM_000256.3(MYBPC3):c.3224C>G (p.Thr1075Ser) rs150786409
NM_000256.3(MYBPC3):c.3229G>T (p.Ala1077Ser) rs397516009
NM_000256.3(MYBPC3):c.3335_3337dupGGT (p.Trp1112_Phe1113insTrp) rs730880673
NM_000256.3(MYBPC3):c.3407_3409delACT (p.Tyr1136del) rs730880674
NM_000256.3(MYBPC3):c.3433G>A (p.Val1145Ile)
NM_000256.3(MYBPC3):c.3614G>A (p.Arg1205Gln) rs730880596
NM_000256.3(MYBPC3):c.3628-6T>C rs1057520329
NM_000256.3(MYBPC3):c.3668A>G (p.Glu1223Gly)
NM_000256.3(MYBPC3):c.3682C>T (p.Arg1228Cys) rs201312636
NM_000256.3(MYBPC3):c.3744_3758del (p.Gly1249_Cys1253del) rs730880676
NM_000256.3(MYBPC3):c.446C>T (p.Ala149Val) rs779493486
NM_000256.3(MYBPC3):c.485A>T (p.Gln162Leu)
NM_000256.3(MYBPC3):c.505+6T>C
NM_000256.3(MYBPC3):c.50G>A (p.Arg17Gln) rs374630007
NM_000256.3(MYBPC3):c.534G>T (p.Val178=)
NM_000256.3(MYBPC3):c.557C>T (p.Pro186Leu) rs727503216
NM_000256.3(MYBPC3):c.566T>A (p.Val189Asp) rs397516060
NM_000256.3(MYBPC3):c.568A>G (p.Lys190Glu)
NM_000256.3(MYBPC3):c.594C>A (p.Asp198Glu)
NM_000256.3(MYBPC3):c.602G>A (p.Ser201Asn)
NM_000256.3(MYBPC3):c.624G>C (p.Gln208His) rs202139499
NM_000256.3(MYBPC3):c.654+2_654+4dupTGG rs730880682
NM_000256.3(MYBPC3):c.676A>G (p.Ile226Val)
NM_000256.3(MYBPC3):c.684T>G (p.Asp228Glu)
NM_000256.3(MYBPC3):c.713G>A (p.Arg238His) rs727504396
NM_000256.3(MYBPC3):c.73A>T (p.Ser25Cys)
NM_000256.3(MYBPC3):c.754T>C (p.Phe252Leu)
NM_000256.3(MYBPC3):c.776C>G (p.Ala259Gly)
NM_000256.3(MYBPC3):c.787G>A (p.Gly263Arg) rs373730381
NM_000256.3(MYBPC3):c.818G>A (p.Arg273His) rs376461745
NM_000256.3(MYBPC3):c.82G>A (p.Val28Met) rs776834755
NM_000256.3(MYBPC3):c.841C>T (p.Arg281Trp) rs371711564
NM_000256.3(MYBPC3):c.906-7G>T rs397516079
NM_000256.3(MYBPC3):c.922C>T (p.Pro308Ser)
NM_000256.3(MYBPC3):c.923C>T (p.Pro308Leu)
NM_000256.3(MYBPC3):c.961G>A (p.Val321Met) rs200119454
NM_000256.3:c.327_332dup

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