ClinVar Miner

List of variants in gene MYBPC3 reported as likely benign by PreventionGenetics, part of Exact Sciences

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Total variants: 51
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HGVS dbSNP gnomAD frequency
NM_000256.3(MYBPC3):c.1144C>T (p.Arg382Trp) rs11570076 0.01409
NM_000256.3(MYBPC3):c.2686G>A (p.Val896Met) rs35078470 0.00601
NM_000256.3(MYBPC3):c.1519G>A (p.Gly507Arg) rs35736435 0.00177
NM_000256.3(MYBPC3):c.1608T>A (p.Ala536=) rs200224422 0.00176
NM_000256.3(MYBPC3):c.1564G>A (p.Ala522Thr) rs11570082 0.00120
NM_000256.3(MYBPC3):c.2997C>T (p.Gly999=) rs377283955 0.00071
NM_000256.3(MYBPC3):c.3102C>T (p.Ala1034=) rs200663253 0.00058
NM_000256.3(MYBPC3):c.3672C>T (p.Asp1224=) rs368221517 0.00055
NM_000256.3(MYBPC3):c.3699G>A (p.Gln1233=) rs200162906 0.00043
NM_000256.3(MYBPC3):c.906-7G>T rs397516079 0.00036
NM_000256.3(MYBPC3):c.3279C>T (p.Gly1093=) rs36212064 0.00029
NM_000256.3(MYBPC3):c.2873C>T (p.Thr958Ile) rs376504548 0.00025
NM_000256.3(MYBPC3):c.1813G>A (p.Asp605Asn) rs376736293 0.00020
NM_000256.3(MYBPC3):c.3276C>T (p.Val1092=) rs376344765 0.00019
NM_000256.3(MYBPC3):c.246T>C (p.Ile82=) rs372502369 0.00016
NM_000256.3(MYBPC3):c.501C>T (p.Thr167=) rs397516054 0.00013
NM_000256.3(MYBPC3):c.12G>A (p.Pro4=) rs377292092 0.00012
NM_000256.3(MYBPC3):c.2614G>A (p.Glu872Lys) rs190765116 0.00012
NM_000256.3(MYBPC3):c.1467C>T (p.Asp489=) rs35690719 0.00011
NM_000256.3(MYBPC3):c.1989T>A (p.Ala663=) rs375467797 0.00010
NM_000256.3(MYBPC3):c.93C>T (p.Ala31=) rs397516085 0.00008
NM_000256.3(MYBPC3):c.2196C>T (p.Asp732=) rs397515955 0.00007
NM_000256.3(MYBPC3):c.132C>T (p.Arg44=) rs377579620 0.00006
NM_000256.3(MYBPC3):c.1335G>A (p.Thr445=) rs727503205 0.00006
NM_000256.3(MYBPC3):c.237C>T (p.Tyr79=) rs730880698 0.00006
NM_000256.3(MYBPC3):c.1227-10C>T rs374673836 0.00005
NM_000256.3(MYBPC3):c.150C>T (p.Ser50=) rs368918487 0.00004
NM_000256.3(MYBPC3):c.2149-8C>G rs397515950 0.00004
NM_000256.3(MYBPC3):c.2517C>T (p.Gly839=) rs370561202 0.00004
NM_000256.3(MYBPC3):c.2640C>T (p.Asp880=) rs397515980 0.00004
NM_000256.3(MYBPC3):c.2808G>A (p.Thr936=) rs370530334 0.00004
NM_000256.3(MYBPC3):c.3297G>A (p.Gly1099=) rs371301665 0.00004
NM_000256.3(MYBPC3):c.2064G>A (p.Thr688=) rs758224257 0.00003
NM_000256.3(MYBPC3):c.3315C>A (p.Ala1105=) rs200372325 0.00003
NM_000256.3(MYBPC3):c.667G>A (p.Glu223Lys) rs397516069 0.00003
NM_000256.3(MYBPC3):c.1290C>T (p.Asp430=) rs200664621 0.00002
NM_000256.3(MYBPC3):c.147C>T (p.Ile49=) rs774273586 0.00002
NM_000256.3(MYBPC3):c.1352-16C>T rs886038274 0.00001
NM_000256.3(MYBPC3):c.1352-5G>A rs770888201 0.00001
NM_000256.3(MYBPC3):c.3579C>T (p.Ile1193=) rs541204647 0.00001
NM_000256.3(MYBPC3):c.821+8G>A rs1362987965 0.00001
NM_000256.3(MYBPC3):c.1224-61_1224-53dup rs1565628380
NM_000256.3(MYBPC3):c.1927+590G>C
NM_000256.3(MYBPC3):c.2149-73C>G
NM_000256.3(MYBPC3):c.25+10G>A rs368489793
NM_000256.3(MYBPC3):c.2544G>T (p.Ala848=)
NM_000256.3(MYBPC3):c.3490+3G>A rs763653429
NM_000256.3(MYBPC3):c.558G>T (p.Pro186=) rs370962887
NM_000256.3(MYBPC3):c.772+9G>A rs566339669
NM_000256.3(MYBPC3):c.906-37C>T
NM_000256.3(MYBPC3):c.909C>T (p.Asp303=) rs200713257

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