NM_000465.4(BARD1):c.368T>G (p.Leu123Trp) AND not provided

Germline classification:: Uncertain significance (1 submission)
Last evaluated:: Jun 26, 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:: RCV000236510.4

Allele description [Variation Report for NM_000465.4(BARD1):c.368T>G (p.Leu123Trp)]

NM_000465.4(BARD1):c.368T>G (p.Leu123Trp)

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.368T>G (p.Leu123Trp)

HGVS:

NC_000002.12:g.214781506A>C
NG_012047.3:g.33206T>G
NM_000465.4:c.368T>GMANE SELECT
NM_001282543.2:c.311T>G
NM_001282545.2:c.215+15555T>G
NM_001282548.2:c.158+27906T>G
NM_001282549.2:c.364+10791T>G
NP_000456.2:p.Leu123Trp
NP_001269472.1:p.Leu104Trp
LRG_297t1:c.368T>G
LRG_297:g.33206T>G
LRG_297p1:p.Leu123Trp
NC_000002.11:g.215646230A>C
NG_012047.2:g.33199T>G
NM_000465.2:c.368T>G
NM_000465.3:c.368T>G
NR_104212.2:n.333T>G
NR_104215.2:n.276T>G

Protein change:

L104W

Links:

dbSNP: rs879253930

NCBI 1000 Genomes Browser:

rs879253930

Molecular consequence:

NM_001282545.2:c.215+15555T>G - intron variant - [Sequence Ontology: SO:0001627]
NM_001282548.2:c.158+27906T>G - intron variant - [Sequence Ontology: SO:0001627]
NM_001282549.2:c.364+10791T>G - intron variant - [Sequence Ontology: SO:0001627]
NM_000465.4:c.368T>G - missense variant - [Sequence Ontology: SO:0001583]
NM_001282543.2:c.311T>G - missense variant - [Sequence Ontology: SO:0001583]
NR_104212.2:n.333T>G - non-coding transcript variant - [Sequence Ontology: SO:0001619]
NR_104215.2:n.276T>G - non-coding transcript variant - [Sequence Ontology: SO:0001619]

Condition(s)

Synonyms:: none provided
Identifiers:: MedGen: C3661900

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Submission Accession	Submitter	Review Status (Assertion method)	Clinical Significance (Last evaluated)	Origin	Method	Citations
SCV000292842	GeneDx	criteria provided, single submitter (GeneDx Variant Classification Process June 2021)	Uncertain significance (Jun 26, 2019)	germline	clinical testing	Citation Link

Submission Accession

Submitter

Review Status
(Assertion method)

Clinical Significance
(Last evaluated)

Origin

Method

Citations

SCV000292842

GeneDx

criteria provided, single submitter

(GeneDx Variant Classification Process June 2021)

Uncertain significance
(Jun 26, 2019)

germline

clinical testing

Citation Link

Help

Summary from all submissions

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

Details of each submission

From GeneDx, SCV000292842.13

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

Description

Not observed in large population cohorts (Lek et al., 2016); In silico analysis, which includes protein predictors and evolutionary conservation, supports that this variant does not alter protein structure/function; Has not been previously published as pathogenic or benign to our knowledge

#	Sample				Method		Observation
#	Origin	Affected	Number tested	Tissue	Purpose	Method	Individuals	Allele frequency	Families	Co-occurrences
1	germline	yes	not provided	not provided	not provided		not provided	not provided	not provided	not provided

Last Updated: Sep 29, 2024

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