NM_000059.4(BRCA2):c.1097T>G (p.Leu366Ter) AND Hereditary breast ovarian cancer syndrome

This record was updated by the submitter. Please see the current version.

Germline classification:: Pathogenic (1 submission)
Last evaluated:: Dec 31, 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:: RCV001069551.7

Allele description

NM_000059.4(BRCA2):c.1097T>G (p.Leu366Ter)

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.1097T>G (p.Leu366Ter)

Other names:

1325T>G

HGVS:

NC_000013.11:g.32332575T>G
NG_012772.3:g.22096T>G
NM_000059.4:c.1097T>GMANE SELECT
NP_000050.2:p.Leu366Ter
NP_000050.3:p.Leu366Ter
LRG_293t1:c.1097T>G
LRG_293:g.22096T>G
LRG_293p1:p.Leu366Ter
NC_000013.10:g.32906712T>G
NM_000059.3:c.1097T>G
p.Leu366X

Protein change:

L366*

Links:

dbSNP: rs886040345

NCBI 1000 Genomes Browser:

rs886040345

Molecular consequence:

NM_000059.4:c.1097T>G - nonsense - [Sequence Ontology: SO:0001587]

Condition(s)

Name:: Hereditary breast ovarian cancer syndrome
Synonyms:: Hereditary breast and ovarian cancer syndrome; Hereditary breast and ovarian cancer; Hereditary breast and ovarian cancer syndrome (HBOC); See all synonyms [MedGen]
Identifiers:: MONDO: MONDO:0003582; MeSH: D061325; MedGen: C0677776; Orphanet: 145

Recent activity

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cytochrome c oxidase subunit 1, partial (mitochondrion) [Leiosoma concinnum]
cytochrome c oxidase subunit 1, partial (mitochondrion) [Leiosoma concinnum]
gi|1837664837|gb|QJP23800.1|

Protein
Rhaphiolepis umbellata voucher oOGA0072 trnH-psbA intergenic spacer, partial seq...
Rhaphiolepis umbellata voucher oOGA0072 trnH-psbA intergenic spacer, partial sequence; chloroplast
gi|2314652728|gnl|uoguelph|JWP3908- nH-psbA|gb|OK420242.1|

Nucleotide
Homo sapiens olfactory receptor family 1 subfamily L member 3 (OR1L3), mRNA
Homo sapiens olfactory receptor family 1 subfamily L member 3 (OR1L3), mRNA
gi|52546684|ref|NM_001005234.1|

Nucleotide

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Submission Accession	Submitter	Review Status (Assertion method)	Clinical Significance (Last evaluated)	Origin	Method	Citations
SCV001234727	Invitae	criteria provided, single submitter (Invitae Variant Classification Sherloc (09022015))	Pathogenic (Dec 31, 2019)	germline	clinical testing	PubMed (3) [See all records that cite these PMIDs] 20104584, 29446198, 28492532

Submission Accession

Submitter

Review Status
(Assertion method)

Clinical Significance
(Last evaluated)

Origin

Method

Citations

SCV001234727

Invitae

criteria provided, single submitter

(Invitae Variant Classification Sherloc (09022015))

Pathogenic
(Dec 31, 2019)

germline

clinical testing

PubMed (3)
[See all records that cite these PMIDs]

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

Citations

PubMed

Characterization of BRCA1 and BRCA2 deleterious mutations and variants of unknown clinical significance in unilateral and bilateral breast cancer: the WECARE study.

Borg A, Haile RW, Malone KE, Capanu M, Diep A, Törngren T, Teraoka S, Begg CB, Thomas DC, Concannon P, Mellemkjaer L, Bernstein L, Tellhed L, Xue S, Olson ER, Liang X, Dolle J, Børresen-Dale AL, Bernstein JL.

Hum Mutat. 2010 Mar;31(3):E1200-40. doi: 10.1002/humu.21202.

PubMed [citation]

PMID:: 20104584
PMCID:: PMC2928257

Mutational spectrum in a worldwide study of 29,700 families with BRCA1 or BRCA2 mutations.

Rebbeck TR, Friebel TM, Friedman E, Hamann U, Huo D, Kwong A, Olah E, Olopade OI, Solano AR, Teo SH, Thomassen M, Weitzel JN, Chan TL, Couch FJ, Goldgar DE, Kruse TA, Palmero EI, Park SK, Torres D, van Rensburg EJ, McGuffog L, Parsons MT, et al.

Hum Mutat. 2018 May;39(5):593-620. doi: 10.1002/humu.23406. Epub 2018 Mar 12.

PubMed [citation]

PMID:: 29446198
PMCID:: PMC5903938

See all PubMed Citations (3)

Details of each submission

From Invitae, SCV001234727.5

#	Ethnicity	Individuals	Chromosomes Tested	Family History	Method	Citations
1	not provided	not provided	not provided	not provided	clinical testing	PubMed (3)

Description

For these reasons, this variant has been classified as Pathogenic. Loss-of-function variants in BRCA2 are known to be pathogenic (PMID: 20104584). This variant has been observed in an individual with high risk of breast and/or ovarian cancer (PMID: 29446198). ClinVar contains an entry for this variant (Variation ID: 266609). This variant is not present in population databases (ExAC no frequency). This sequence change creates a premature translational stop signal (p.Leu366*) in the BRCA2 gene. It is expected to result in an absent or disrupted protein product.

#	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: Sep 1, 2024

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