NM_004333.6(BRAF):c.61G>A (p.Gly21Arg) AND not specified

Germline classification:: not provided (1 submission)
Last evaluated:: Sep 19, 2013
Review status:: no classification provided

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:: RCV000120255.1

Allele description [Variation Report for NM_004333.6(BRAF):c.61G>A (p.Gly21Arg)]

NM_004333.6(BRAF):c.61G>A (p.Gly21Arg)

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.61G>A (p.Gly21Arg)

HGVS:

NC_000007.14:g.140924643C>T
NG_007873.3:g.5122G>A
NM_001354609.2:c.61G>A
NM_001374244.1:c.61G>A
NM_001374258.1:c.61G>A
NM_001378467.1:c.61G>A
NM_001378468.1:c.61G>A
NM_001378469.1:c.61G>A
NM_001378470.1:c.61G>A
NM_001378471.1:c.61G>A
NM_001378474.1:c.61G>A
NM_001378475.1:c.61G>A
NM_004333.6:c.61G>AMANE SELECT
NP_001341538.1:p.Gly21Arg
NP_001361173.1:p.Gly21Arg
NP_001361187.1:p.Gly21Arg
NP_001365396.1:p.Gly21Arg
NP_001365397.1:p.Gly21Arg
NP_001365398.1:p.Gly21Arg
NP_001365399.1:p.Gly21Arg
NP_001365400.1:p.Gly21Arg
NP_001365403.1:p.Gly21Arg
NP_001365404.1:p.Gly21Arg
NP_004324.2:p.Gly21Arg
LRG_299:g.5122G>A
NC_000007.13:g.140624443C>T

Protein change:

G21R

Links:

dbSNP: rs587778113

NCBI 1000 Genomes Browser:

rs587778113

Molecular consequence:

NM_001354609.2:c.61G>A - missense variant - [Sequence Ontology: SO:0001583]
NM_001374244.1:c.61G>A - missense variant - [Sequence Ontology: SO:0001583]
NM_001374258.1:c.61G>A - missense variant - [Sequence Ontology: SO:0001583]
NM_001378467.1:c.61G>A - missense variant - [Sequence Ontology: SO:0001583]
NM_001378468.1:c.61G>A - missense variant - [Sequence Ontology: SO:0001583]
NM_001378469.1:c.61G>A - missense variant - [Sequence Ontology: SO:0001583]
NM_001378470.1:c.61G>A - missense variant - [Sequence Ontology: SO:0001583]
NM_001378471.1:c.61G>A - missense variant - [Sequence Ontology: SO:0001583]
NM_001378474.1:c.61G>A - missense variant - [Sequence Ontology: SO:0001583]
NM_001378475.1:c.61G>A - missense variant - [Sequence Ontology: SO:0001583]
NM_004333.6:c.61G>A - missense variant - [Sequence Ontology: SO:0001583]

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
SCV000084405	ITMI	no classification provided	not provided	germline	reference population	PubMed (1) [See all records that cite this PMID]

Submission Accession

Submitter

Review Status
(Assertion method)

Clinical Significance
(Last evaluated)

Origin

Method

Citations

SCV000084405

ITMI

no classification provided

not provided

germline

reference population

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

Description

Please see associated publication for description of ethnicities: SCV000084405

Help

Summary from all submissions

Ethnicity	Origin	Affected	Individuals	Families	Chromosomes tested	Number Tested	Family history	Method
African	germline	unknown	not provided	not provided	not provided	43	not provided	reference population
African_European	germline	unknown	not provided	not provided	not provided	46	not provided	reference population
Central_Asian	germline	unknown	not provided	not provided	not provided	50	not provided	reference population
East_Asian	germline	unknown	not provided	not provided	not provided	62	not provided	reference population
European	germline	unknown	not provided	not provided	not provided	331	not provided	reference population
Hispanic	germline	unknown	not provided	not provided	not provided	118	not provided	reference population
Whole_cohort	germline	unknown	not provided	not provided	not provided	681	not provided	reference population

Citations

PubMed

Germline variation in cancer-susceptibility genes in a healthy, ancestrally diverse cohort: implications for individual genome sequencing.

Bodian DL, McCutcheon JN, Kothiyal P, Huddleston KC, Iyer RK, Vockley JG, Niederhuber JE.

PLoS One. 2014;9(4):e94554. doi: 10.1371/journal.pone.0094554.

PubMed [citation]

PMID:: 24728327
PMCID:: PMC3984285

Details of each submission

From ITMI, SCV000084405.1

#	Ethnicity	Individuals	Chromosomes Tested	Family History	Method	Citations
1	African	not provided	not provided	not provided	reference population	PubMed (1)
2	African_European	not provided	not provided	not provided	reference population	PubMed (1)
3	Central_Asian	not provided	not provided	not provided	reference population	PubMed (1)
4	East_Asian	not provided	not provided	not provided	reference population	PubMed (1)
5	European	not provided	not provided	not provided	reference population	PubMed (1)
6	Hispanic	not provided	not provided	not provided	reference population	PubMed (1)
7	Whole_cohort	not provided	not provided	not provided	reference population	PubMed (1)

#	Sample				Method		Observation
#	Origin	Affected	Number tested	Tissue	Purpose	Method	Individuals	Allele frequency	Families	Co-occurrences
1	germline	unknown	43	not provided	discovery		not provided	0	not provided	not provided
2	germline	unknown	46	not provided	discovery		not provided	0	not provided	not provided
3	germline	unknown	50	not provided	discovery		not provided	0	not provided	not provided
4	germline	unknown	62	not provided	discovery		not provided	0	not provided	not provided
5	germline	unknown	331	not provided	discovery		not provided	0.0015	not provided	not provided
6	germline	unknown	118	not provided	discovery		not provided	0	not provided	not provided
7	germline	unknown	681	not provided	discovery		not provided	0.0007	not provided	not provided

Last Updated: Sep 17, 2022

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