NM_000465.4(BARD1):c.394T>G (p.Leu132Val) AND Familial cancer of breast

Germline classification:: Uncertain significance (1 submission)
Last evaluated:: Nov 23, 2022
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:: RCV003607457.2

Allele description [Variation Report for NM_000465.4(BARD1):c.394T>G (p.Leu132Val)]

NM_000465.4(BARD1):c.394T>G (p.Leu132Val)

Gene:

BARD1:BRCA1 associated RING domain 1 [Gene - OMIM - HGNC]

Variant type:

single nucleotide variant

Cytogenetic location:

2q35

Genomic location:

Preferred name:

NM_000465.4(BARD1):c.394T>G (p.Leu132Val)

HGVS:

NC_000002.12:g.214781480A>C
NG_012047.3:g.33232T>G
NM_000465.4:c.394T>GMANE SELECT
NM_001282543.2:c.337T>G
NM_001282545.2:c.215+15581T>G
NM_001282548.2:c.158+27932T>G
NM_001282549.2:c.364+10817T>G
NP_000456.2:p.Leu132Val
NP_001269472.1:p.Leu113Val
LRG_297t1:c.394T>G
LRG_297:g.33232T>G
LRG_297p1:p.Leu132Val
NC_000002.11:g.215646204A>C
NM_000465.2:c.394T>G
NR_104212.2:n.359T>G
NR_104215.2:n.302T>G

Protein change:

L113V

Molecular consequence:

NM_001282545.2:c.215+15581T>G - intron variant - [Sequence Ontology: SO:0001627]
NM_001282548.2:c.158+27932T>G - intron variant - [Sequence Ontology: SO:0001627]
NM_001282549.2:c.364+10817T>G - intron variant - [Sequence Ontology: SO:0001627]
NM_000465.4:c.394T>G - missense variant - [Sequence Ontology: SO:0001583]
NM_001282543.2:c.337T>G - missense variant - [Sequence Ontology: SO:0001583]
NR_104212.2:n.359T>G - non-coding transcript variant - [Sequence Ontology: SO:0001619]
NR_104215.2:n.302T>G - 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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Submission Accession	Submitter	Review Status (Assertion method)	Clinical Significance (Last evaluated)	Origin	Method	Citations
SCV004411283	Labcorp Genetics (formerly Invitae), Labcorp	criteria provided, single submitter (Invitae Variant Classification Sherloc (09022015))	Uncertain significance (Nov 23, 2022)	germline	clinical testing	PubMed (1) [See all records that cite this PMID]

Submission Accession

Submitter

Review Status
(Assertion method)

Clinical Significance
(Last evaluated)

Origin

Method

Citations

SCV004411283

Labcorp Genetics (formerly Invitae), Labcorp

criteria provided, single submitter

(Invitae Variant Classification Sherloc (09022015))

Uncertain significance
(Nov 23, 2022)

germline

clinical testing

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

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

Sherloc: a comprehensive refinement of the ACMG-AMP variant classification criteria.

Nykamp K, Anderson M, Powers M, Garcia J, Herrera B, Ho YY, Kobayashi Y, Patil N, Thusberg J, Westbrook M; Invitae Clinical Genomics Group., Topper S.

Genet Med. 2017 Oct;19(10):1105-1117. doi: 10.1038/gim.2017.37. Epub 2017 May 11. Erratum in: Genet Med. 2020 Jan;22(1):240. doi: 10.1038/s41436-019-0624-9.

PubMed [citation]

PMID:: 28492532
PMCID:: PMC5632818

Details of each submission

From Labcorp Genetics (formerly Invitae), Labcorp, SCV004411283.1

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

Description

In summary, the available evidence is currently insufficient to determine the role of this variant in disease. Therefore, it has been classified as a Variant of Uncertain Significance. Algorithms developed to predict the effect of missense changes on protein structure and function (SIFT, PolyPhen-2, Align-GVGD) all suggest that this variant is likely to be tolerated. This variant has not been reported in the literature in individuals affected with BARD1-related conditions. This variant is not present in population databases (gnomAD no frequency). This sequence change replaces leucine, which is neutral and non-polar, with valine, which is neutral and non-polar, at codon 132 of the BARD1 protein (p.Leu132Val).

#	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 29, 2024

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