ClinVar Miner

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

Minimum submission review status: Collection method:
Minimum conflict level:
Gene type:
ClinVar version:
Total variants: 50
Download table as spreadsheet
HGVS dbSNP
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.11C>T (p.Pro4Leu) rs748689012
NM_000256.3(MYBPC3):c.1255C>T (p.Arg419Cys) rs368770848
NM_000256.3(MYBPC3):c.1316G>A (p.Gly439Asp) rs763045718
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.1471G>A (p.Val491Met) rs730880543
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.1822C>T (p.Pro608Ser) rs730880552
NM_000256.3(MYBPC3):c.1928-3C>T rs1415195455
NM_000256.3(MYBPC3):c.2005C>A (p.Leu669Met) rs1565626407
NM_000256.3(MYBPC3):c.2149-5C>G rs36211722
NM_000256.3(MYBPC3):c.2176C>T (p.Arg726Cys)
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.2398G>A (p.Gly800Arg) rs727504574
NM_000256.3(MYBPC3):c.2432_2434AGA[3] (p.Lys814del) rs727504288
NM_000256.3(MYBPC3):c.2447A>G (p.Tyr816Cys) rs1565625347
NM_000256.3(MYBPC3):c.2479C>A (p.Gln827Lys) rs375322174
NM_000256.3(MYBPC3):c.2562G>A (p.Met854Ile) rs730880572
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.2882C>T (p.Pro961Leu) rs373056282
NM_000256.3(MYBPC3):c.2909G>A (p.Arg970Gln) rs727504346
NM_000256.3(MYBPC3):c.3097C>T (p.Arg1033Trp) rs748909815
NM_000256.3(MYBPC3):c.3130C>G (p.Gln1044Glu) rs1565623421
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.315_320CCCTGC[4] (p.106_107PA[4])
NM_000256.3(MYBPC3):c.3433G>A (p.Val1145Ile) rs747606711
NM_000256.3(MYBPC3):c.3614G>A (p.Arg1205Gln) rs730880596
NM_000256.3(MYBPC3):c.3682C>T (p.Arg1228Cys) rs201312636
NM_000256.3(MYBPC3):c.446C>T (p.Ala149Val) rs779493486
NM_000256.3(MYBPC3):c.485A>T (p.Gln162Leu) rs1565631087
NM_000256.3(MYBPC3):c.505+6T>C rs397516055
NM_000256.3(MYBPC3):c.50G>A (p.Arg17Gln) rs374630007
NM_000256.3(MYBPC3):c.557C>T (p.Pro186Leu) rs727503216
NM_000256.3(MYBPC3):c.594C>A (p.Asp198Glu) rs1318614905
NM_000256.3(MYBPC3):c.676A>G (p.Ile226Val) rs1336201335
NM_000256.3(MYBPC3):c.684T>G (p.Asp228Glu) rs532498780
NM_000256.3(MYBPC3):c.713G>A (p.Arg238His) rs727504396
NM_000256.3(MYBPC3):c.73A>T (p.Ser25Cys) rs749970304
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.922C>T (p.Pro308Ser) rs1565629496
NM_000256.3(MYBPC3):c.923C>T (p.Pro308Leu) rs1330127507
NM_000256.3(MYBPC3):c.961G>A (p.Val321Met) rs200119454

The information on this website is not intended for direct diagnostic use or medical decision-making without review by a genetics professional. Individuals should not change their health behavior solely on the basis of information contained on this website. Neither the University of Utah nor the National Institutes of Health independently verfies the submitted information. If you have questions about the information contained on this website, please see a health care professional.