NM_000256.3(MYBPC3):c.1370C>T (p.Thr457Met) AND Cardiovascular phenotype

Germline classification:: Benign (1 submission)
Last evaluated:: Sep 8, 2022
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:: RCV002381458.2

Allele description [Variation Report for NM_000256.3(MYBPC3):c.1370C>T (p.Thr457Met)]

NM_000256.3(MYBPC3):c.1370C>T (p.Thr457Met)

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.1370C>T (p.Thr457Met)

HGVS:

NC_000011.10:g.47342917G>A
NG_007667.1:g.14786C>T
NM_000256.3:c.1370C>TMANE SELECT
NP_000247.2:p.Thr457Met
LRG_386t1:c.1370C>T
LRG_386:g.14786C>T
LRG_386p1:p.Thr457Met
NC_000011.9:g.47364468G>A

Protein change:

T457M

Links:

dbSNP: rs370538243

NCBI 1000 Genomes Browser:

rs370538243

Molecular consequence:

NM_000256.3:c.1370C>T - missense variant - [Sequence Ontology: SO:0001583]

Condition(s)

Name:: Cardiovascular phenotype
Identifiers:: MedGen: CN230736

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Submission Accession	Submitter	Review Status (Assertion method)	Clinical Significance (Last evaluated)	Origin	Method	Citations
SCV002697200	Ambry Genetics	criteria provided, single submitter (Ambry Variant Classification Scheme 2023)	Benign (Sep 8, 2022)	germline	clinical testing	PubMed (1) [See all records that cite this PMID] Citation Link

Submission Accession

Submitter

Review Status
(Assertion method)

Clinical Significance
(Last evaluated)

Origin

Method

Citations

SCV002697200

Ambry Genetics

criteria provided, single submitter

(Ambry Variant Classification Scheme 2023)

Benign
(Sep 8, 2022)

germline

clinical testing

PubMed (1)
[See all records that cite this PMID]

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

Citations

PubMed

MYBPC3 gene variations in hypertrophic cardiomyopathy patients in India.

Tanjore RR, Rangaraju A, Kerkar PG, Calambur N, Nallari P.

Can J Cardiol. 2008 Feb;24(2):127-30.

PubMed [citation]

PMID:: 18273486
PMCID:: PMC2644567

Details of each submission

From Ambry Genetics, SCV002697200.2

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

Description

This alteration is classified as benign based on a combination of the following: seen in unaffected individuals, population frequency, intact protein function, lack of segregation with disease, co-occurrence, RNA analysis, in silico models, amino acid conservation, lack of disease association in case-control studies, and/or the mechanism of disease or impacted region is inconsistent with a known cause of pathogenicity.

#	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: Sep 29, 2024

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