ClinVar Miner

List of variants in gene MYBPC3 reported as likely benign by Ambry Genetics

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Gene type:
ClinVar version:
Total variants: 53
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HGVS dbSNP
NM_000256.3(MYBPC3):c.1008C>T (p.Ile336=) rs397515880
NM_000256.3(MYBPC3):c.108A>G (p.Ala36=) rs754870909
NM_000256.3(MYBPC3):c.1173C>T (p.Asp391=) rs377328238
NM_000256.3(MYBPC3):c.132C>T (p.Arg44=) rs377579620
NM_000256.3(MYBPC3):c.1392G>A (p.Leu464=) rs900306372
NM_000256.3(MYBPC3):c.1519G>A (p.Gly507Arg) rs35736435
NM_000256.3(MYBPC3):c.1563C>T (p.Asp521=) rs367915627
NM_000256.3(MYBPC3):c.1564G>A (p.Ala522Thr) rs11570082
NM_000256.3(MYBPC3):c.1593G>A (p.Gly531=) rs727503199
NM_000256.3(MYBPC3):c.1602G>A (p.Ala534=) rs370945942
NM_000256.3(MYBPC3):c.1608T>A (p.Ala536=) rs200224422
NM_000256.3(MYBPC3):c.1776G>A (p.Val592=) rs727503196
NM_000256.3(MYBPC3):c.1812C>T (p.Asp604=) rs397515929
NM_000256.3(MYBPC3):c.1855G>A (p.Glu619Lys) rs200352299
NM_000256.3(MYBPC3):c.1863C>T (p.Phe621=) rs193922378
NM_000256.3(MYBPC3):c.1914C>T (p.Phe638=) rs377227442
NM_000256.3(MYBPC3):c.2010C>T (p.Asp670=) rs558051480
NM_000256.3(MYBPC3):c.2064G>A (p.Thr688=) rs758224257
NM_000256.3(MYBPC3):c.2149-5C>T rs36211722
NM_000256.3(MYBPC3):c.237C>T (p.Tyr79=) rs730880698
NM_000256.3(MYBPC3):c.2460G>A (p.Arg820=) rs532996422
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.2800C>T (p.Leu934=) rs367980215
NM_000256.3(MYBPC3):c.2856T>G (p.Pro952=) rs397515989
NM_000256.3(MYBPC3):c.2859A>G (p.Gly953=) rs886038777
NM_000256.3(MYBPC3):c.2870C>G (p.Thr957Ser) rs193922380
NM_000256.3(MYBPC3):c.2914C>T (p.Arg972Trp) rs193922382
NM_000256.3(MYBPC3):c.2961C>T (p.Val987=) rs761700877
NM_000256.3(MYBPC3):c.3004C>T (p.Arg1002Trp) rs3729799
NM_000256.3(MYBPC3):c.3090G>T (p.Leu1030=) rs770351760
NM_000256.3(MYBPC3):c.3102C>T (p.Ala1034=) rs200663253
NM_000256.3(MYBPC3):c.3106C>T (p.Arg1036Cys) rs61729664
NM_000256.3(MYBPC3):c.3228C>T (p.Asp1076=) rs369999866
NM_000256.3(MYBPC3):c.3276C>T (p.Val1092=) rs376344765
NM_000256.3(MYBPC3):c.3279C>T (p.Gly1093=) rs36212064
NM_000256.3(MYBPC3):c.3285G>A (p.Thr1095=) rs367927327
NM_000256.3(MYBPC3):c.3392T>C (p.Ile1131Thr) rs370890951
NM_000256.3(MYBPC3):c.3408C>T (p.Tyr1136=) rs193922383
NM_000256.3(MYBPC3):c.348C>A (p.Ala116=) rs886039198
NM_000256.3(MYBPC3):c.3492C>T (p.Gly1164=) rs779273875
NM_000256.3(MYBPC3):c.3654C>T (p.Gly1218=) rs374755212
NM_000256.3(MYBPC3):c.3657G>T (p.Leu1219=) rs770157084
NM_000256.3(MYBPC3):c.3699G>A (p.Gln1233=) rs200162906
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.531C>T (p.Arg177=) rs368035400
NM_000256.3(MYBPC3):c.565G>A (p.Val189Ile) rs11570052
NM_000256.3(MYBPC3):c.666C>T (p.Phe222=) rs371331114
NM_000256.3(MYBPC3):c.81C>T (p.Ala27=) rs761547225
NM_000256.3(MYBPC3):c.909C>T (p.Asp303=) rs200713257
NM_000256.3(MYBPC3):c.933G>C (p.Ser311=) rs374326087
NM_000256.3(MYBPC3):c.999C>T (p.Tyr333=) rs367947846

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