List of variants in gene MYBPC3 reported as likely benign by Illumina Laboratory Services, Illumina

Minimum submission review status:		Collection method:
Minimum conflict level: Report conflict between different conditions
Gene type: Distinguish antisense genes from sense genes
Show significances as they were submitted (without aggregation into standard terms)
		ClinVar version:

Total variants: 34

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HGVS	dbSNP	gnomAD frequency
NM_000256.3(MYBPC3):c.706A>G (p.Ser236Gly)	rs3729989	0.09621
NM_000256.3(MYBPC3):c.492C>T (p.Gly164=)	rs3218719	0.02170
NM_000256.3(MYBPC3):c.*236G>A	rs11570121	0.01781
NM_000256.3(MYBPC3):c.2601C>T (p.Ile867=)	rs11570097	0.01438
NM_000256.3(MYBPC3):c.1144C>T (p.Arg382Trp)	rs11570076	0.01409
NM_000256.3(MYBPC3):c.2498C>T (p.Ala833Val)	rs3729952	0.00756
NM_000256.3(MYBPC3):c.2686G>A (p.Val896Met)	rs35078470	0.00601
NM_000256.3(MYBPC3):c.530G>A (p.Arg177His)	rs201012766	0.00405
NM_000256.3(MYBPC3):c.977G>A (p.Arg326Gln)	rs34580776	0.00376
NM_000256.3(MYBPC3):c.2992C>G (p.Gln998Glu)	rs11570112	0.00247
NM_000256.3(MYBPC3):c.565G>A (p.Val189Ile)	rs11570052	0.00187
NM_000256.3(MYBPC3):c.646G>A (p.Ala216Thr)	rs201098973	0.00076
NM_000256.3(MYBPC3):c.478C>T (p.Arg160Trp)	rs193068692	0.00047
NM_000256.3(MYBPC3):c.*113G>T	rs117960173	0.00045
NM_000256.3(MYBPC3):c.3699G>A (p.Gln1233=)	rs200162906	0.00043
NM_000256.3(MYBPC3):c.1544A>G (p.Asn515Ser)	rs181834806	0.00039
NM_000256.3(MYBPC3):c.961G>A (p.Val321Met)	rs200119454	0.00025
NM_000256.3(MYBPC3):c.184A>C (p.Thr62Pro)	rs377225516	0.00024
NM_000256.3(MYBPC3):c.624G>C (p.Gln208His)	rs202139499	0.00017
NM_000256.3(MYBPC3):c.2210C>T (p.Thr737Met)	rs199893357	0.00016
NM_000256.3(MYBPC3):c.2149-5C>T	rs36211722	0.00014
NM_000256.3(MYBPC3):c.2460G>A (p.Arg820=)	rs532996422	0.00014
NM_000256.3(MYBPC3):c.501C>T (p.Thr167=)	rs397516054	0.00013
NM_000256.3(MYBPC3):c.2614G>A (p.Glu872Lys)	rs190765116	0.00012
NM_000256.3(MYBPC3):c.531C>T (p.Arg177=)	rs368035400	0.00012
NM_000256.3(MYBPC3):c.648C>T (p.Ala216=)	rs777418402	0.00009
NM_000256.3(MYBPC3):c.132C>T (p.Arg44=)	rs377579620	0.00006
NM_000256.3(MYBPC3):c.1790+7G>A	rs374852831	0.00003
NM_000256.3(MYBPC3):c.1003C>T (p.Arg335Cys)	rs730880630	0.00001
NM_000256.3(MYBPC3):c.2800C>T (p.Leu934=)	rs367980215	0.00001
NC_000011.10:g.47349937del	rs11570050
NM_000256.3(MYBPC3):c.*230del	rs376645369
NM_000256.3(MYBPC3):c.2854C>G (p.Pro952Ala)	rs554694434
NM_000256.3(MYBPC3):c.558G>T (p.Pro186=)	rs370962887

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