NM_000059.3(BRCA2):c.5704G>A (p.Asp1902Asn) AND none provided

delete

Germline classification:: Benign (1 submission)
Last evaluated:: Jul 30, 2021
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:: RCV001283468.3

Allele description

NM_000059.3(BRCA2):c.5704G>A (p.Asp1902Asn)

Gene:

BRCA2:BRCA2 DNA repair associated [Gene - OMIM - HGNC]

Variant type:

single nucleotide variant

Cytogenetic location:

13q13.1

Genomic location:

Preferred name:

NM_000059.3(BRCA2):c.5704G>A (p.Asp1902Asn)

Other names:

D1902N; 5932 G>A; NP_000050.3:p.Asp1902Asn

HGVS:

NC_000013.11:g.32340059G>A
NG_012772.3:g.29580G>A
NP_000050.2:p.Asp1902Asn
LRG_293t1:c.5704G>A
LRG_293:g.29580G>A
LRG_293p1:p.Asp1902Asn
NC_000013.10:g.32914196G>A
NM_000059.3:c.5704G>A
NM_000059.4:c.5704G>AMANE SELECT
U43746.1:n.5932G>A
p.D1902N

Links:

dbSNP: rs4987048

NCBI 1000 Genomes Browser:

rs4987048

Condition(s)

Name:: none provided
Identifiers:: MedGen: CN235283

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Submission Accession	Submitter	Review Status (Assertion method)	Clinical Significance (Last evaluated)	Origin	Method	Citations
SCV000602746	ARUP Laboratories, Molecular Genetics and Genomics, ARUP Laboratories	criteria provided, single submitter (ARUP Molecular Germline Variant Investigation Process 2021)	Benign (Jul 30, 2021)	germline	clinical testing	Citation Link

Submission Accession

Submitter

Review Status
(Assertion method)

Clinical Significance
(Last evaluated)

Origin

Method

Citations

SCV000602746

ARUP Laboratories, Molecular Genetics and Genomics, ARUP Laboratories

criteria provided, single submitter

(ARUP Molecular Germline Variant Investigation Process 2021)

Benign
(Jul 30, 2021)

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

Details of each submission

From ARUP Laboratories, Molecular Genetics and Genomics, ARUP Laboratories, SCV000602746.5

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

Last Updated: Jan 15, 2022

ClinVar

Relating variation to medicine