NM_004333.6(BRAF):c.918C>G (p.Ser306=) AND not provided

Germline classification:: Uncertain significance (1 submission)
Last evaluated:: Jun 2, 2015
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:: RCV000724862.6

Allele description [Variation Report for NM_004333.6(BRAF):c.918C>G (p.Ser306=)]

NM_004333.6(BRAF):c.918C>G (p.Ser306=)

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.918C>G (p.Ser306=)

HGVS:

NC_000007.14:g.140800424G>C
NG_007873.3:g.129341C>G
NM_001354609.2:c.918C>G
NM_001374244.1:c.918C>G
NM_001374258.1:c.918C>G
NM_001378467.1:c.927C>G
NM_001378468.1:c.918C>G
NM_001378469.1:c.918C>G
NM_001378470.1:c.816C>G
NM_001378471.1:c.918C>G
NM_001378472.1:c.762C>G
NM_001378473.1:c.762C>G
NM_001378474.1:c.918C>G
NM_001378475.1:c.654C>G
NM_004333.6:c.918C>GMANE SELECT
NP_001341538.1:p.Ser306=
NP_001361173.1:p.Ser306=
NP_001361187.1:p.Ser306=
NP_001365396.1:p.Ser309=
NP_001365397.1:p.Ser306=
NP_001365398.1:p.Ser306=
NP_001365399.1:p.Ser272=
NP_001365400.1:p.Ser306=
NP_001365401.1:p.Ser254=
NP_001365402.1:p.Ser254=
NP_001365403.1:p.Ser306=
NP_001365404.1:p.Ser218=
NP_004324.2:p.Ser306=
LRG_299t1:c.918C>G
LRG_299:g.129341C>G
NC_000007.13:g.140500224G>C
NM_004333.4:c.918C>G

Links:

dbSNP: rs794727865

NCBI 1000 Genomes Browser:

rs794727865

Molecular consequence:

NM_001354609.2:c.918C>G - synonymous variant - [Sequence Ontology: SO:0001819]
NM_001374244.1:c.918C>G - synonymous variant - [Sequence Ontology: SO:0001819]
NM_001374258.1:c.918C>G - synonymous variant - [Sequence Ontology: SO:0001819]
NM_001378467.1:c.927C>G - synonymous variant - [Sequence Ontology: SO:0001819]
NM_001378468.1:c.918C>G - synonymous variant - [Sequence Ontology: SO:0001819]
NM_001378469.1:c.918C>G - synonymous variant - [Sequence Ontology: SO:0001819]
NM_001378470.1:c.816C>G - synonymous variant - [Sequence Ontology: SO:0001819]
NM_001378471.1:c.918C>G - synonymous variant - [Sequence Ontology: SO:0001819]
NM_001378472.1:c.762C>G - synonymous variant - [Sequence Ontology: SO:0001819]
NM_001378473.1:c.762C>G - synonymous variant - [Sequence Ontology: SO:0001819]
NM_001378474.1:c.918C>G - synonymous variant - [Sequence Ontology: SO:0001819]
NM_001378475.1:c.654C>G - synonymous variant - [Sequence Ontology: SO:0001819]
NM_004333.6:c.918C>G - synonymous variant - [Sequence Ontology: SO:0001819]

Observations:

Condition(s)

Synonyms:: none provided; RECLASSIFIED - ADRA2C POLYMORPHISM; RECLASSIFIED - ADRB1 POLYMORPHISM
Identifiers:: MedGen: C3661900

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Submission Accession	Submitter	Review Status (Assertion method)	Clinical Significance (Last evaluated)	Origin	Method	Citations
SCV000232196	Eurofins Ntd Llc (ga)	criteria provided, single submitter (EGL Classification Definitions 2015)	Uncertain significance (Jun 2, 2015)	germline	clinical testing	Citation Link

Submission Accession

Submitter

Review Status
(Assertion method)

Clinical Significance
(Last evaluated)

Origin

Method

Citations

SCV000232196

Eurofins Ntd Llc (ga)

criteria provided, single submitter

(EGL Classification Definitions 2015)

Uncertain significance
(Jun 2, 2015)

germline

clinical testing

Citation Link

Help

Summary from all submissions

Ethnicity	Origin	Affected	Individuals	Families	Chromosomes tested	Number Tested	Family history	Method
not provided	germline	unknown	1	not provided	not provided	not provided	not provided	clinical testing

Details of each submission

From Eurofins Ntd Llc (ga), SCV000232196.5

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

#	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		1	not provided	not provided	not provided

Last Updated: Feb 16, 2025

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