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NM_000257.4(MYH7):c.3499C>A (p.Arg1167Ser) AND Cardiovascular phenotype

Germline classification:
Uncertain significance (1 submission)
Last evaluated:
Jun 16, 2021
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:
RCV002459091.2

Allele description [Variation Report for NM_000257.4(MYH7):c.3499C>A (p.Arg1167Ser)]

NM_000257.4(MYH7):c.3499C>A (p.Arg1167Ser)

Gene:
MYH7:myosin heavy chain 7 [Gene - OMIM - HGNC]
Variant type:
single nucleotide variant
Cytogenetic location:
14q11.2
Genomic location:
Preferred name:
NM_000257.4(MYH7):c.3499C>A (p.Arg1167Ser)
HGVS:
  • NC_000014.9:g.23420072G>T
  • NG_007884.1:g.20590C>A
  • NM_000257.4:c.3499C>AMANE SELECT
  • NM_001407004.1:c.3499C>A
  • NP_000248.2:p.Arg1167Ser
  • NP_000248.2:p.Arg1167Ser
  • NP_001393933.1:p.Arg1167Ser
  • LRG_384t1:c.3499C>A
  • LRG_384:g.20590C>A
  • LRG_384p1:p.Arg1167Ser
  • NC_000014.8:g.23889281G>T
  • NM_000257.2:c.3499C>A
Protein change:
R1167S
Molecular consequence:
  • NM_000257.4:c.3499C>A - missense variant - [Sequence Ontology: SO:0001583]
  • NM_001407004.1:c.3499C>A - missense variant - [Sequence Ontology: SO:0001583]

Condition(s)

Name:
Cardiovascular phenotype
Identifiers:
MedGen: CN230736

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Assertion and evidence details

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Submission AccessionSubmitterReview Status
(Assertion method)		Clinical Significance
(Last evaluated)		OriginMethodCitations
SCV002615900Ambry Genetics
criteria provided, single submitter

(Ambry Variant Classification Scheme 2023)		Uncertain significance
(Jun 16, 2021) 		germlineclinical testing

Citation Link

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Summary from all submissions

EthnicityOriginAffectedIndividualsFamiliesChromosomes testedNumber TestedFamily historyMethod
not providedgermlineunknownnot providednot providednot providednot providednot providedclinical testing

Details of each submission

From Ambry Genetics, SCV002615900.2

#EthnicityIndividualsChromosomes TestedFamily HistoryMethodCitations
1not providednot providednot providednot providedclinical testingnot provided

Description

The p.R1167S variant (also known as c.3499C>A), located in coding exon 25 of the MYH7 gene, results from a C to A substitution at nucleotide position 3499. The arginine at codon 1167 is replaced by serine, an amino acid with dissimilar 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.

#SampleMethodObservation
OriginAffectedNumber testedTissuePurposeMethodIndividualsAllele frequencyFamiliesCo-occurrences
1germlineunknownnot providednot providednot providednot providednot providednot providednot provided

Last Updated: May 1, 2024