NM_000059.4(BRCA2):c.517-12C>A AND Breast-ovarian cancer, familial, susceptibility to, 2

Germline classification:: Likely benign (2 submissions)
Last evaluated:: Oct 5, 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:: RCV000077745.5

Allele description [Variation Report for NM_000059.4(BRCA2):c.517-12C>A]

NM_000059.4(BRCA2):c.517-12C>A

Gene:

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

Variant type:

single nucleotide variant

Cytogenetic location:

13q13.1

Genomic location:

Preferred name:

NM_000059.4(BRCA2):c.517-12C>A

HGVS:

NC_000013.11:g.32326487C>A
NG_012772.3:g.16008C>A
NM_000059.4:c.517-12C>AMANE SELECT
LRG_293t1:c.517-12C>A
LRG_293:g.16008C>A
NC_000013.10:g.32900624C>A
NM_000059.3:c.517-12C>A

Nucleotide change:

IVS6-12C>A

Links:

dbSNP: rs398122795

NCBI 1000 Genomes Browser:

rs398122795

Molecular consequence:

NM_000059.4:c.517-12C>A - intron variant - [Sequence Ontology: SO:0001627]

Observations:

Condition(s)

Name:: Breast-ovarian cancer, familial, susceptibility to, 2 (BROVCA2)
Synonyms:: Breast-ovarian cancer, familial 2
Identifiers:: MONDO: MONDO:0012933; MedGen: C2675520; Orphanet: 145; OMIM: 612555

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Submission Accession	Submitter	Review Status (Assertion method)	Clinical Significance (Last evaluated)	Origin	Method	Citations
SCV000109548	Sharing Clinical Reports Project (SCRP)	no assertion criteria provided	Uncertain significance (Oct 28, 2008)	germline	clinical testing
SCV000489430	Counsyl	criteria provided, single submitter (Counsyl Autosomal Dominant Disease Classification criteria (2015))	Likely benign (Oct 5, 2016)	unknown	clinical testing	Counsyl Autosomal Dominant Disease Classification criteria (2015) Citation Link

Submission Accession

Submitter

Review Status
(Assertion method)

Clinical Significance
(Last evaluated)

Origin

Method

Citations

SCV000109548

Sharing Clinical Reports Project (SCRP)

no assertion criteria provided

Uncertain significance
(Oct 28, 2008)

germline

clinical testing

SCV000489430

Counsyl

criteria provided, single submitter

(Counsyl Autosomal Dominant Disease Classification criteria (2015))

Likely benign
(Oct 5, 2016)

unknown

clinical testing

Counsyl Autosomal Dominant Disease Classification criteria (2015)

Citation Link

Help

Summary from all submissions

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

Details of each submission

From Sharing Clinical Reports Project (SCRP), SCV000109548.2

#	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	not provided	1	not provided	not provided		not provided	not provided	not provided	not provided

From Counsyl, SCV000489430.2

#	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	unknown	unknown	not provided	not provided	not provided		not provided	not provided	not provided	not provided

Last Updated: Jun 2, 2024

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