NM_000256.3(MYBPC3):c.3329T>C (p.Met1110Thr) AND Cardiovascular phenotype

Germline classification:: Uncertain significance (1 submission)
Last evaluated:: Feb 2, 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:: RCV000622187.3

Allele description [Variation Report for NM_000256.3(MYBPC3):c.3329T>C (p.Met1110Thr)]

NM_000256.3(MYBPC3):c.3329T>C (p.Met1110Thr)

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.3329T>C (p.Met1110Thr)

HGVS:

NC_000011.10:g.47333195A>G
NG_007667.1:g.24508T>C
NM_000256.3:c.3329T>CMANE SELECT
NP_000247.2:p.Met1110Thr
LRG_386t1:c.3329T>C
LRG_386:g.24508T>C
LRG_386p1:p.Met1110Thr
NC_000011.9:g.47354746A>G

Protein change:

M1110T

Links:

dbSNP: rs1321563978

NCBI 1000 Genomes Browser:

rs1321563978

Molecular consequence:

NM_000256.3:c.3329T>C - missense variant - [Sequence Ontology: SO:0001583]

Condition(s)

Name:: Cardiovascular phenotype
Identifiers:: MedGen: CN230736

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Suillus spraguei
Suillus spraguei
Suillus spraguei Raw sequence reads

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root metagenome
root metagenome
Metatranscriptome of Pinus contorta CO500 inoculated with Suillus brevipes S120 and Suillus spraguei EM44 root tips from University of Florida, USA - S120(CO)xEM44xPcon_woFe_r3

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Submission Accession	Submitter	Review Status (Assertion method)	Clinical Significance (Last evaluated)	Origin	Method	Citations
SCV000736756	Ambry Genetics	criteria provided, single submitter (Ambry Variant Classification Scheme 2023)	Uncertain significance (Feb 2, 2017)	germline	clinical testing	Citation Link

Submission Accession

Submitter

Review Status
(Assertion method)

Clinical Significance
(Last evaluated)

Origin

Method

Citations

SCV000736756

Ambry Genetics

criteria provided, single submitter

(Ambry Variant Classification Scheme 2023)

Uncertain significance
(Feb 2, 2017)

germline

clinical testing

Citation Link

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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 Ambry Genetics, SCV000736756.5

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

Description

The p.M1110T variant (also known as c.3329T>C), located in coding exon 30 of the MYBPC3 gene, results from a T to C substitution at nucleotide position 3329. The methionine at codon 1110 is replaced by threonine, an amino acid with similar properties. This amino acid position is highly conserved in available vertebrate species. In addition, this alteration is predicted to be deleterious by in silico analysis. Since supporting evidence is limited at this time, the clinical significance of this alteration remains unclear.

#	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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