NM_000256.3(MYBPC3):c.3232T>C (p.Trp1078Arg) AND not provided

Germline classification:: Uncertain significance (1 submission)
Last evaluated:: Nov 18, 2017
Review status:: 1 star out of maximum of 4 stars
criteria provided, single submitter

Somatic classification of clinical impact:: None
Review status:: (0/4) 0 stars out of maximum of 4 stars
no assertion criteria provided

Somatic classification of oncogenicity:: None
Review status:: (0/4) 0 stars out of maximum of 4 stars
no assertion criteria provided

Record status:: current
Accession:: RCV000788384.2

Allele description [Variation Report for NM_000256.3(MYBPC3):c.3232T>C (p.Trp1078Arg)]

NM_000256.3(MYBPC3):c.3232T>C (p.Trp1078Arg)

Gene:

MYBPC3:myosin binding protein C3 [Gene - OMIM - HGNC]

Variant type:

single nucleotide variant

Cytogenetic location:

11p11.2

Genomic location:

Preferred name:

NM_000256.3(MYBPC3):c.3232T>C (p.Trp1078Arg)

HGVS:

NC_000011.10:g.47333292A>G
NG_007667.1:g.24411T>C
NM_000256.3:c.3232T>CMANE SELECT
NP_000247.2:p.Trp1078Arg
LRG_386t1:c.3232T>C
LRG_386:g.24411T>C
LRG_386p1:p.Trp1078Arg
NC_000011.9:g.47354843A>G

Protein change:

W1078R

Links:

dbSNP: rs773543130

NCBI 1000 Genomes Browser:

rs773543130

Molecular consequence:

NM_000256.3:c.3232T>C - missense variant - [Sequence Ontology: SO:0001583]

Condition(s)

Synonyms:: none provided
Identifiers:: MedGen: C3661900

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Submission Accession	Submitter	Review Status (Assertion method)	Clinical Significance (Last evaluated)	Origin	Method	Citations
SCV000927471	Blueprint Genetics	criteria provided, single submitter (Blueprint Genetics Variant Classification Scheme)	Uncertain significance (Nov 18, 2017)	germline	clinical testing	Citation Link

Submission Accession

Submitter

Review Status
(Assertion method)

Clinical Significance
(Last evaluated)

Origin

Method

Citations

SCV000927471

Blueprint Genetics

criteria provided, single submitter

(Blueprint Genetics Variant Classification Scheme)

Uncertain significance
(Nov 18, 2017)

germline

clinical testing

Citation Link

Help

Summary from all submissions

Ethnicity	Origin	Affected	Individuals	Families	Chromosomes tested	Number Tested	Family history	Method
not provided	germline	unknown	not provided	not provided	not provided	not provided	not provided	clinical testing

Details of each submission

From Blueprint Genetics, SCV000927471.1

#	Ethnicity	Individuals	Chromosomes Tested	Family History	Method	Citations
1	not provided	not provided	not provided	not provided	clinical testing	not provided

#	Sample				Method		Observation
#	Origin	Affected	Number tested	Tissue	Purpose	Method	Individuals	Allele frequency	Families	Co-occurrences
1	germline	unknown	not provided	not provided	not provided		not provided	not provided	not provided	not provided

Last Updated: May 7, 2024

ClinVar

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