NM_000465.4(BARD1):c.353A>G (p.Asn118Ser) AND not provided

Germline classification:: Uncertain significance (2 submissions)
Last evaluated:: Feb 12, 2024
Review status:: 2 stars out of maximum of 4 stars
criteria provided, multiple submitters, no conflicts

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:: RCV000656769.6

Allele description [Variation Report for NM_000465.4(BARD1):c.353A>G (p.Asn118Ser)]

NM_000465.4(BARD1):c.353A>G (p.Asn118Ser)

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.353A>G (p.Asn118Ser)

Other names:

p.N118S:AAT>AGT

HGVS:

NC_000002.12:g.214792308T>C
NG_012047.3:g.22404A>G
NM_000465.4:c.353A>GMANE SELECT
NM_001282543.2:c.296A>G
NM_001282545.2:c.215+4753A>G
NM_001282548.2:c.158+17104A>G
NM_001282549.2:c.353A>G
NP_000456.2:p.Asn118Ser
NP_001269472.1:p.Asn99Ser
NP_001269478.1:p.Asn118Ser
LRG_297t1:c.353A>G
LRG_297:g.22404A>G
LRG_297p1:p.Asn118Ser
NC_000002.11:g.215657032T>C
NG_012047.2:g.22397A>G
NM_000465.2:c.353A>G
NM_000465.3:c.353A>G
NR_104216.2:n.467A>G
p.N118S

Protein change:

N118S

Links:

dbSNP: rs142864491

NCBI 1000 Genomes Browser:

rs142864491

Molecular consequence:

NM_001282545.2:c.215+4753A>G - intron variant - [Sequence Ontology: SO:0001627]
NM_001282548.2:c.158+17104A>G - intron variant - [Sequence Ontology: SO:0001627]
NM_000465.4:c.353A>G - missense variant - [Sequence Ontology: SO:0001583]
NM_001282543.2:c.296A>G - missense variant - [Sequence Ontology: SO:0001583]
NM_001282549.2:c.353A>G - missense variant - [Sequence Ontology: SO:0001583]
NR_104216.2:n.467A>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
SCV000149543	GeneDx	criteria provided, single submitter (GeneDx Variant Classification Process June 2021)	Uncertain significance (Feb 12, 2024)	germline	clinical testing	Citation Link,
SCV000887593	Quest Diagnostics Nichols Institute San Juan Capistrano	criteria provided, single submitter (Quest Diagnostics criteria)	Uncertain significance (Feb 28, 2020)	unknown	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

SCV000149543

GeneDx

criteria provided, single submitter

(GeneDx Variant Classification Process June 2021)

Uncertain significance
(Feb 12, 2024)

germline

clinical testing

Citation Link,

SCV000887593

Quest Diagnostics Nichols Institute San Juan Capistrano

criteria provided, single submitter

(Quest Diagnostics criteria)

Uncertain significance
(Feb 28, 2020)

unknown

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	yes	not provided	not provided	not provided	not provided	not provided	clinical testing
not provided	unknown	unknown	not provided	not provided	not provided	not provided	not provided	clinical testing

Citations

PubMed

A Standardized DNA Variant Scoring System for Pathogenicity Assessments in Mendelian Disorders.

Karbassi I, Maston GA, Love A, DiVincenzo C, Braastad CD, Elzinga CD, Bright AR, Previte D, Zhang K, Rowland CM, McCarthy M, Lapierre JL, Dubois F, Medeiros KA, Batish SD, Jones J, Liaquat K, Hoffman CA, Jaremko M, Wang Z, Sun W, Buller-Burckle A, et al.

Hum Mutat. 2016 Jan;37(1):127-34. doi: 10.1002/humu.22918. Epub 2015 Oct 29.

PubMed [citation]

PMID:: 26467025
PMCID:: PMC4737317

Details of each submission

From GeneDx, SCV000149543.16

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

Description

Published functional studies demonstrate homology-directed repair similar to wild-type (PMID: 30925164); In silico analysis supports that this missense variant does not alter protein structure/function; This variant is associated with the following publications: (PMID: 33922147, 35264596, 28726808, 30925164, 18480049, 14647430, 25085752, 38136308)

#	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

From Quest Diagnostics Nichols Institute San Juan Capistrano, SCV000887593.3

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

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

Last Updated: Sep 29, 2024

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