NM_004333.6(BRAF):c.2128-10T>C AND not specified

Germline classification:: Likely benign (1 submission)
Last evaluated:: May 9, 2012
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:: RCV000037941.5

Allele description [Variation Report for NM_004333.6(BRAF):c.2128-10T>C]

NM_004333.6(BRAF):c.2128-10T>C

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.2128-10T>C

HGVS:

NC_000007.14:g.140734780A>G
NG_007873.3:g.194985T>C
NM_001354609.2:c.2128-10T>C
NM_001374244.1:c.2248-10T>C
NM_001374258.1:c.2248-10T>C
NM_001378467.1:c.2137-10T>C
NM_001378468.1:c.2127+5032T>C
NM_001378469.1:c.2062-10T>C
NM_001378470.1:c.2026-10T>C
NM_001378471.1:c.2017-10T>C
NM_001378472.1:c.1972-10T>C
NM_001378473.1:c.1972-10T>C
NM_001378474.1:c.2127+5032T>C
NM_001378475.1:c.1864-10T>C
NM_004333.6:c.2128-10T>CMANE SELECT
LRG_299t1:c.2128-10T>C
LRG_299:g.194985T>C
NC_000007.13:g.140434580A>G
NM_004333.4:c.2128-10T>C
c.2128-10T>C

Links:

dbSNP: rs397516898

NCBI 1000 Genomes Browser:

rs397516898

Molecular consequence:

NM_001354609.2:c.2128-10T>C - intron variant - [Sequence Ontology: SO:0001627]
NM_001374244.1:c.2248-10T>C - intron variant - [Sequence Ontology: SO:0001627]
NM_001374258.1:c.2248-10T>C - intron variant - [Sequence Ontology: SO:0001627]
NM_001378467.1:c.2137-10T>C - intron variant - [Sequence Ontology: SO:0001627]
NM_001378468.1:c.2127+5032T>C - intron variant - [Sequence Ontology: SO:0001627]
NM_001378469.1:c.2062-10T>C - intron variant - [Sequence Ontology: SO:0001627]
NM_001378470.1:c.2026-10T>C - intron variant - [Sequence Ontology: SO:0001627]
NM_001378471.1:c.2017-10T>C - intron variant - [Sequence Ontology: SO:0001627]
NM_001378472.1:c.1972-10T>C - intron variant - [Sequence Ontology: SO:0001627]
NM_001378473.1:c.1972-10T>C - intron variant - [Sequence Ontology: SO:0001627]
NM_001378474.1:c.2127+5032T>C - intron variant - [Sequence Ontology: SO:0001627]
NM_001378475.1:c.1864-10T>C - intron variant - [Sequence Ontology: SO:0001627]
NM_004333.6:c.2128-10T>C - intron variant - [Sequence Ontology: SO:0001627]

Observations:

Condition(s)

Synonyms:: AllHighlyPenetrant
Identifiers:: MedGen: CN169374

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Submission Accession	Submitter	Review Status (Assertion method)	Clinical Significance (Last evaluated)	Origin	Method	Citations
SCV000061606	Laboratory for Molecular Medicine, Mass General Brigham Personalized Medicine	criteria provided, single submitter (LMM Criteria)	Likely benign (May 9, 2012)	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

SCV000061606

Laboratory for Molecular Medicine, Mass General Brigham Personalized Medicine

criteria provided, single submitter

(LMM Criteria)

Likely benign
(May 9, 2012)

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	not provided	1	1	not provided	not provided	not provided	clinical testing

Citations

PubMed

A systematic approach to assessing the clinical significance of genetic variants.

Duzkale H, Shen J, McLaughlin H, Alfares A, Kelly MA, Pugh TJ, Funke BH, Rehm HL, Lebo MS.

Clin Genet. 2013 Nov;84(5):453-63. doi: 10.1111/cge.12257.

PubMed [citation]

PMID:: 24033266
PMCID:: PMC3995020

Details of each submission

From Laboratory for Molecular Medicine, Mass General Brigham Personalized Medicine, SCV000061606.5

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

Description

2128-10T>C in intron 17 of BRAF: This variant is located in the 3' splice region but does not affect the invariant -1 and -2 positions. Although positions -3 an d -5 to -12 are part of the splicing consensus sequence and variants involving t hese positions sometimes affect splicing, pathogenic splicing variants have not been reported in Noonan spectrum disorders. Therefore, this variant is likely to be benign.

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

Last Updated: Sep 29, 2024

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