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NM_004333.6(BRAF):c.957C>T (p.Ser319=) AND Cardiovascular phenotype

Germline classification:
Likely benign (1 submission)
Last evaluated:
May 23, 2024
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:
RCV004601317.1

Allele description [Variation Report for NM_004333.6(BRAF):c.957C>T (p.Ser319=)]

NM_004333.6(BRAF):c.957C>T (p.Ser319=)

Gene:
BRAF:B-Raf proto-oncogene, serine/threonine kinase [Gene - OMIM - HGNC]
Variant type:
single nucleotide variant
Cytogenetic location:
7q34
Genomic location:
Preferred name:
NM_004333.6(BRAF):c.957C>T (p.Ser319=)
HGVS:
  • NC_000007.14:g.140800385G>A
  • NG_007873.3:g.129380C>T
  • NM_001354609.2:c.957C>T
  • NM_001374244.1:c.957C>T
  • NM_001374258.1:c.957C>T
  • NM_004333.6:c.957C>TMANE SELECT
  • NP_001341538.1:p.Ser319=
  • NP_001361173.1:p.Ser319=
  • NP_001361187.1:p.Ser319=
  • NP_004324.2:p.Ser319=
  • LRG_299t1:c.957C>T
  • LRG_299:g.129380C>T
  • NC_000007.13:g.140500185G>A
  • NC_000007.13:g.140500185G>A
  • NM_004333.4:c.957C>T
Links:
dbSNP: rs754029526
NCBI 1000 Genomes Browser:
rs754029526
Molecular consequence:
  • NM_001354609.2:c.957C>T - synonymous variant - [Sequence Ontology: SO:0001819]
  • NM_001374244.1:c.957C>T - synonymous variant - [Sequence Ontology: SO:0001819]
  • NM_001374258.1:c.957C>T - synonymous variant - [Sequence Ontology: SO:0001819]
  • NM_004333.6:c.957C>T - synonymous variant - [Sequence Ontology: SO:0001819]

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
SCV005100895Ambry Genetics
criteria provided, single submitter

(Ambry Variant Classification Scheme 2023)		Likely benign
(May 23, 2024) 		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, SCV005100895.1

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

Description

This alteration is classified as likely 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.

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

Last Updated: Feb 25, 2025