ClinVar Miner

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

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Gene type:
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Total variants: 54
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HGVS dbSNP
NM_000256.3(MYBPC3):c.1173C>T (p.Asp391=) rs377328238
NM_000256.3(MYBPC3):c.1286C>T (p.Ala429Val) rs370412052
NM_000256.3(MYBPC3):c.1347G>T (p.Val449=) rs539453748
NM_000256.3(MYBPC3):c.1351+4G>A rs777487971
NM_000256.3(MYBPC3):c.1371G>A (p.Thr457=) rs538072263
NM_000256.3(MYBPC3):c.1458-7C>T rs397515904
NM_000256.3(MYBPC3):c.148A>G (p.Ser50Gly) rs373164247
NM_000256.3(MYBPC3):c.1494C>G (p.Thr498=) rs397515906
NM_000256.3(MYBPC3):c.1506G>T (p.Arg502=) rs1481158714
NM_000256.3(MYBPC3):c.1519G>A (p.Gly507Arg) rs35736435
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.1578A>T (p.Ala526=) rs766721220
NM_000256.3(MYBPC3):c.1608T>A (p.Ala536=) rs200224422
NM_000256.3(MYBPC3):c.1720C>A (p.Arg574=) rs61897383
NM_000256.3(MYBPC3):c.1813G>A (p.Asp605Asn) rs376736293
NM_000256.3(MYBPC3):c.2010C>T (p.Asp670=) rs558051480
NM_000256.3(MYBPC3):c.2013C>T (p.Val671=) rs1168755518
NM_000256.3(MYBPC3):c.207G>C (p.Arg69=) rs397515946
NM_000256.3(MYBPC3):c.2136G>A (p.Val712=) rs876657511
NM_000256.3(MYBPC3):c.2178C>T (p.Arg726=) rs370676057
NM_000256.3(MYBPC3):c.237C>T (p.Tyr79=) rs730880698
NM_000256.3(MYBPC3):c.2382G>A (p.Pro794=) rs1565625459
NM_000256.3(MYBPC3):c.2391C>T (p.Tyr797=) rs727504864
NM_000256.3(MYBPC3):c.246T>C (p.Ile82=) rs372502369
NM_000256.3(MYBPC3):c.2497G>A (p.Ala833Thr) rs199865688
NM_000256.3(MYBPC3):c.284T>C (p.Ile95Thr) rs727504945
NM_000256.3(MYBPC3):c.2870C>G (p.Thr957Ser) rs193922380
NM_000256.3(MYBPC3):c.2876C>A (p.Thr959Lys) rs730880697
NM_000256.3(MYBPC3):c.2904G>C (p.Leu968=) rs747974933
NM_000256.3(MYBPC3):c.3106C>T (p.Arg1036Cys) rs61729664
NM_000256.3(MYBPC3):c.3191-4G>A rs764672273
NM_000256.3(MYBPC3):c.3285G>A (p.Thr1095=) rs367927327
NM_000256.3(MYBPC3):c.3326C>T (p.Thr1109Ile) rs397516016
NM_000256.3(MYBPC3):c.3392T>C (p.Ile1131Thr) rs370890951
NM_000256.3(MYBPC3):c.3606T>C (p.Cys1202=) rs1032233055
NM_000256.3(MYBPC3):c.362C>T (p.Pro121Leu) rs551888783
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.3723A>G (p.Arg1241=) rs1565622343
NM_000256.3(MYBPC3):c.3741C>T (p.Asp1247=) rs543376073
NM_000256.3(MYBPC3):c.3765C>G (p.Ala1255=) rs1354801986
NM_000256.3(MYBPC3):c.3815-16delG rs1565621965
NM_000256.3(MYBPC3):c.405A>G (p.Lys135=) rs727504318
NM_000256.3(MYBPC3):c.450C>T (p.Pro150=) rs377520770
NM_000256.3(MYBPC3):c.471C>T (p.Phe157=) rs150291001
NM_000256.3(MYBPC3):c.478C>T (p.Arg160Trp) rs193068692
NM_000256.3(MYBPC3):c.501C>T (p.Thr167=) rs397516054
NM_000256.3(MYBPC3):c.565G>A (p.Val189Ile) rs11570052
NM_000256.3(MYBPC3):c.624G>C (p.Gln208His) rs202139499
NM_000256.3(MYBPC3):c.648C>T (p.Ala216=) rs777418402
NM_000256.3(MYBPC3):c.87C>T (p.Phe29=) rs764557472
NM_000256.3(MYBPC3):c.909C>T (p.Asp303=) rs200713257
NM_000256.3(MYBPC3):c.933G>C (p.Ser311=) rs374326087

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