NM_004333.6(BRAF):c.78G>T (p.Glu26Asp) AND Cardiofaciocutaneous syndrome 1

Germline classification:: Benign (1 submission)
Last evaluated:: Nov 1, 2016
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:: RCV000659284.9

Allele description [Variation Report for NM_004333.6(BRAF):c.78G>T (p.Glu26Asp)]

NM_004333.6(BRAF):c.78G>T (p.Glu26Asp)

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.78G>T (p.Glu26Asp)

Other names:

p.E26D:GAG>GAT

HGVS:

NC_000007.14:g.140924626C>A
NG_007873.3:g.5139G>T
NM_001354609.2:c.78G>T
NM_001374244.1:c.78G>T
NM_001374258.1:c.78G>T
NM_001378467.1:c.78G>T
NM_001378468.1:c.78G>T
NM_001378469.1:c.78G>T
NM_001378470.1:c.78G>T
NM_001378471.1:c.78G>T
NM_001378474.1:c.78G>T
NM_001378475.1:c.78G>T
NM_004333.6:c.78G>TMANE SELECT
NP_001341538.1:p.Glu26Asp
NP_001361173.1:p.Glu26Asp
NP_001361187.1:p.Glu26Asp
NP_001365396.1:p.Glu26Asp
NP_001365397.1:p.Glu26Asp
NP_001365398.1:p.Glu26Asp
NP_001365399.1:p.Glu26Asp
NP_001365400.1:p.Glu26Asp
NP_001365403.1:p.Glu26Asp
NP_001365404.1:p.Glu26Asp
NP_004324.2:p.Glu26Asp
NP_004324.2:p.Glu26Asp
LRG_299t1:c.78G>T
LRG_299:g.5139G>T
LRG_299p1:p.Glu26Asp
NC_000007.13:g.140624426C>A
NM_004333.4:c.78G>T
c.78G>T

Protein change:

E26D

Links:

dbSNP: rs371877084

Molecular consequence:

NM_001354609.2:c.78G>T - missense variant - [Sequence Ontology: SO:0001583]
NM_001374244.1:c.78G>T - missense variant - [Sequence Ontology: SO:0001583]
NM_001374258.1:c.78G>T - missense variant - [Sequence Ontology: SO:0001583]
NM_001378467.1:c.78G>T - missense variant - [Sequence Ontology: SO:0001583]
NM_001378468.1:c.78G>T - missense variant - [Sequence Ontology: SO:0001583]
NM_001378469.1:c.78G>T - missense variant - [Sequence Ontology: SO:0001583]
NM_001378470.1:c.78G>T - missense variant - [Sequence Ontology: SO:0001583]
NM_001378471.1:c.78G>T - missense variant - [Sequence Ontology: SO:0001583]
NM_001378474.1:c.78G>T - missense variant - [Sequence Ontology: SO:0001583]
NM_001378475.1:c.78G>T - missense variant - [Sequence Ontology: SO:0001583]
NM_004333.6:c.78G>T - missense variant - [Sequence Ontology: SO:0001583]

Condition(s)

Name:: Cardiofaciocutaneous syndrome 1 (CFC1)
Synonyms:: BRAF-Related Cardiofaciocutaneous Syndrome
Identifiers:: MONDO: MONDO:0007265; MedGen: CN029449; Orphanet: 1340; OMIM: 115150

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Submission Accession	Submitter	Review Status (Assertion method)	Clinical Significance (Last evaluated)	Origin	Method	Citations
SCV000781084	Center for Human Genetics, Inc, Center for Human Genetics, Inc	criteria provided, single submitter (ACMG Guidelines, 2015)	Benign (Nov 1, 2016)	germline	clinical testing	PubMed (1) [See all records that cite this PMID]

Submission Accession

Submitter

Review Status
(Assertion method)

Clinical Significance
(Last evaluated)

Origin

Method

Citations

SCV000781084

Center for Human Genetics, Inc, Center for Human Genetics, Inc

criteria provided, single submitter

(ACMG Guidelines, 2015)

Benign
(Nov 1, 2016)

germline

clinical testing

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

Help

Summary from all submissions

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

Citations

PubMed

Standards and guidelines for the interpretation of sequence variants: a joint consensus recommendation of the American College of Medical Genetics and Genomics and the Association for Molecular Pathology.

Richards S, Aziz N, Bale S, Bick D, Das S, Gastier-Foster J, Grody WW, Hegde M, Lyon E, Spector E, Voelkerding K, Rehm HL; ACMG Laboratory Quality Assurance Committee.

Genet Med. 2015 May;17(5):405-24. doi: 10.1038/gim.2015.30. Epub 2015 Mar 5.

PubMed [citation]

PMID:: 25741868
PMCID:: PMC4544753

Details of each submission

From Center for Human Genetics, Inc, Center for Human Genetics, Inc, SCV000781084.1

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

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

Last Updated: Jul 27, 2026

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