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NM_000059.4(BRCA2):c.2671G>C (p.Val891Leu) AND not provided

Germline classification:
Uncertain significance (1 submission)
Last evaluated:
Dec 23, 2019
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:
RCV001567191.4

Allele description [Variation Report for NM_000059.4(BRCA2):c.2671G>C (p.Val891Leu)]

NM_000059.4(BRCA2):c.2671G>C (p.Val891Leu)

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.2671G>C (p.Val891Leu)
HGVS:
  • NC_000013.11:g.32337026G>C
  • NG_012772.3:g.26547G>C
  • NM_000059.4:c.2671G>CMANE SELECT
  • NP_000050.2:p.Val891Leu
  • NP_000050.3:p.Val891Leu
  • LRG_293t1:c.2671G>C
  • LRG_293:g.26547G>C
  • LRG_293p1:p.Val891Leu
  • NC_000013.10:g.32911163G>C
  • NM_000059.3:c.2671G>C
Protein change:
V891L
Links:
dbSNP: rs756951335
NCBI 1000 Genomes Browser:
rs756951335
Molecular consequence:
  • NM_000059.4:c.2671G>C - missense variant - [Sequence Ontology: SO:0001583]

Condition(s)

Synonyms:
none provided
Identifiers:
MedGen: C3661900

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Assertion and evidence details

Submission AccessionSubmitterReview Status
(Assertion method)
Clinical Significance
(Last evaluated)
OriginMethodCitations
SCV001790834GeneDx
criteria provided, single submitter

(GeneDx Variant Classification Process June 2021)
Uncertain significance
(Dec 23, 2019)
germlineclinical testing

Citation Link

Summary from all submissions

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

Details of each submission

From GeneDx, SCV001790834.1

#EthnicityIndividualsChromosomes TestedFamily HistoryMethodCitations
1not providednot providednot providednot providedclinical testingnot provided

Description

Observed in individuals with multiple primary cancers (Chan 2018); In silico analysis, which includes protein predictors and evolutionary conservation, supports that this variant does not alter protein structure/function; Also known as 2899G>C; This variant is associated with the following publications: (PMID: 30093976)

#SampleMethodObservation
OriginAffectedNumber testedTissuePurposeMethodIndividualsAllele frequencyFamiliesCo-occurrences
1germlineyesnot providednot providednot providednot providednot providednot providednot provided

Last Updated: Sep 29, 2024