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NM_000059.4(BRCA2):c.2515dup (p.Tyr839fs) AND Familial cancer of breast

Germline classification:
Likely pathogenic (1 submission)
Last evaluated:
Sep 24, 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:
RCV003474436.1

Allele description [Variation Report for NM_000059.4(BRCA2):c.2515dup (p.Tyr839fs)]

NM_000059.4(BRCA2):c.2515dup (p.Tyr839fs)

Gene:
BRCA2:BRCA2 DNA repair associated [Gene - OMIM - HGNC]
Variant type:
Duplication
Cytogenetic location:
13q13.1
Genomic location:
Preferred name:
NM_000059.4(BRCA2):c.2515dup (p.Tyr839fs)
HGVS:
  • NC_000013.11:g.32336870dup
  • NG_012772.3:g.26391dup
  • NM_000059.4:c.2515dupMANE SELECT
  • NM_001406719.1:c.2515dup
  • NM_001406720.1:c.2515dup
  • NM_001406721.1:c.1909+3483dup
  • NM_001406722.1:c.424+5840dup
  • NP_000050.2:p.Tyr839Leufs
  • NP_000050.3:p.Tyr839fs
  • NP_001393648.1:p.Tyr839fs
  • NP_001393649.1:p.Tyr839fs
  • LRG_293t1:c.2515dup
  • LRG_293:g.26391dup
  • LRG_293p1:p.Tyr839Leufs
  • NC_000013.10:g.32911007dup
  • NM_000059.3:c.2515dup
  • NR_176251.1:n.2714dup
Protein change:
Y839fs
Molecular consequence:
  • NM_000059.4:c.2515dup - frameshift variant - [Sequence Ontology: SO:0001589]
  • NM_001406719.1:c.2515dup - frameshift variant - [Sequence Ontology: SO:0001589]
  • NM_001406720.1:c.2515dup - frameshift variant - [Sequence Ontology: SO:0001589]
  • NM_001406721.1:c.1909+3483dup - intron variant - [Sequence Ontology: SO:0001627]
  • NM_001406722.1:c.424+5840dup - intron variant - [Sequence Ontology: SO:0001627]
  • NR_176251.1:n.2714dup - non-coding transcript variant - [Sequence Ontology: SO:0001619]

Condition(s)

Name:
Familial cancer of breast
Synonyms:
Breast cancer, familial; Hereditary breast cancer
Identifiers:
MONDO: MONDO:0016419; MedGen: C0346153; OMIM: 114480

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Assertion and evidence details

Help
Submission AccessionSubmitterReview Status
(Assertion method)		Clinical Significance
(Last evaluated)		OriginMethodCitations
SCV004212903Baylor Genetics
criteria provided, single submitter

(ACMG Guidelines, 2015)		Likely pathogenic
(Sep 24, 2021) 		unknownclinical testing

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

Help

Summary from all submissions

EthnicityOriginAffectedIndividualsFamiliesChromosomes testedNumber TestedFamily historyMethod
not providedunknownunknownnot providednot providednot providednot providednot providedclinical testing

Citations

PubMed

Standards and guidelines for the interpretation of sequence variants: a joint consensus recommendation of the American College of Medical Genetics and Genomics and the Association for Molecular Pathology.

Richards S, Aziz N, Bale S, Bick D, Das S, Gastier-Foster J, Grody WW, Hegde M, Lyon E, Spector E, Voelkerding K, Rehm HL; ACMG Laboratory Quality Assurance Committee..

Genet Med. 2015 May;17(5):405-24. doi: 10.1038/gim.2015.30. Epub 2015 Mar 5.

PubMed [citation]
PMID:
25741868
PMCID:
PMC4544753

Details of each submission

From Baylor Genetics, SCV004212903.1

#EthnicityIndividualsChromosomes TestedFamily HistoryMethodCitations
1not providednot providednot providednot providedclinical testing PubMed (1)
#SampleMethodObservation
OriginAffectedNumber testedTissuePurposeMethodIndividualsAllele frequencyFamiliesCo-occurrences
1unknownunknownnot providednot providednot providednot providednot providednot providednot provided

Last Updated: Sep 8, 2024