NM_000465.4(BARD1):c.2212A>G (p.Ile738Val) AND Hereditary cancer-predisposing syndrome

Germline classification:: Benign (4 submissions)
Last evaluated:: May 11, 2021
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:: RCV000128965.10

Allele description [Variation Report for NM_000465.4(BARD1):c.2212A>G (p.Ile738Val)]

NM_000465.4(BARD1):c.2212A>G (p.Ile738Val)

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.2212A>G (p.Ile738Val)

Other names:

p.I738V:ATC>GTC; NP_000456.2:p.Ile738Val

HGVS:

NC_000002.12:g.214728798T>C
NG_012047.3:g.85914A>G
NM_000465.4:c.2212A>GMANE SELECT
NM_001282543.2:c.2155A>G
NM_001282545.2:c.859A>G
NM_001282548.2:c.802A>G
NM_001282549.2:c.673A>G
NP_000456.2:p.Ile738Val
NP_001269472.1:p.Ile719Val
NP_001269474.1:p.Ile287Val
NP_001269477.1:p.Ile268Val
NP_001269478.1:p.Ile225Val
LRG_297t1:c.2212A>G
LRG_297:g.85914A>G
LRG_297p1:p.Ile738Val
NC_000002.11:g.215593522T>C
NG_012047.2:g.85907A>G
NM_000465.2:c.2212A>G
NM_000465.3:c.2212A>G
NR_104212.2:n.2177A>G
NR_104215.2:n.2120A>G
NR_104216.2:n.1376A>G
p.I738V

Protein change:

I225V

Links:

dbSNP: rs61754118

NCBI 1000 Genomes Browser:

rs61754118

Molecular consequence:

NM_000465.4:c.2212A>G - missense variant - [Sequence Ontology: SO:0001583]
NM_001282543.2:c.2155A>G - missense variant - [Sequence Ontology: SO:0001583]
NM_001282545.2:c.859A>G - missense variant - [Sequence Ontology: SO:0001583]
NM_001282548.2:c.802A>G - missense variant - [Sequence Ontology: SO:0001583]
NM_001282549.2:c.673A>G - missense variant - [Sequence Ontology: SO:0001583]
NR_104212.2:n.2177A>G - non-coding transcript variant - [Sequence Ontology: SO:0001619]
NR_104215.2:n.2120A>G - non-coding transcript variant - [Sequence Ontology: SO:0001619]
NR_104216.2:n.1376A>G - non-coding transcript variant - [Sequence Ontology: SO:0001619]

Condition(s)

Name:: Hereditary cancer-predisposing syndrome
Synonyms:: Neoplastic Syndromes, Hereditary; Tumor predisposition; Cancer predisposition; See all synonyms [MedGen]
Identifiers:: MONDO: MONDO:0015356; MeSH: D009386; MedGen: C0027672

Recent activity

Clear Turn Off Turn On

Your browsing activity is empty.

Activity recording is turned off.

Turn recording back on

Help

Submission Accession	Submitter	Review Status (Assertion method)	Clinical Significance (Last evaluated)	Origin	Method	Citations
SCV000172847	Ambry Genetics	criteria provided, single submitter (Ambry Variant Classification Scheme 2023)	Benign (Jun 17, 2014)	germline	clinical testing	Citation Link,
SCV000267000	Vantari Genetics	criteria provided, single submitter (ACMG Guidelines, 2015)	Benign (Dec 18, 2015)	germline	clinical testing	PubMed (1) [See all records that cite this PMID]
SCV000292113	Color Diagnostics, LLC DBA Color Health	criteria provided, single submitter (ACMG Guidelines, 2015)	Benign (Nov 19, 2014)	germline	clinical testing	PubMed (1) [See all records that cite this PMID]
SCV002529589	Sema4, Sema4	criteria provided, single submitter (Sema4 Curation Guidelines)	Benign (May 11, 2021)	germline	curation	Citation Link

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, curation

Citations

PubMed

Standards and guidelines for the interpretation of sequence variants: a joint consensus recommendation of the American College of Medical Genetics and Genomics and the Association for Molecular Pathology.

Richards S, Aziz N, Bale S, Bick D, Das S, Gastier-Foster J, Grody WW, Hegde M, Lyon E, Spector E, Voelkerding K, Rehm HL; ACMG Laboratory Quality Assurance Committee..

Genet Med. 2015 May;17(5):405-24. doi: 10.1038/gim.2015.30. Epub 2015 Mar 5.

PubMed [citation]

PMID:: 25741868
PMCID:: PMC4544753

Details of each submission

From Ambry Genetics, SCV000172847.8

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

Description

This alteration is classified as benign based on a combination of the following: seen in unaffected individuals, population frequency, intact protein function, lack of segregation with disease, co-occurrence, RNA analysis, in silico models, amino acid conservation, lack of disease association in case-control studies, and/or the mechanism of disease or impacted region is inconsistent with a known cause of pathogenicity.

#	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

From Vantari Genetics, SCV000267000.1

#	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	germline	unknown	not provided	not provided	not provided		not provided	not provided	not provided	not provided

From Color Diagnostics, LLC DBA Color Health, SCV000292113.1

#	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	germline	unknown	not provided	not provided	not provided		not provided	not provided	not provided	not provided

From Sema4, Sema4, SCV002529589.1

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

#	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: Oct 20, 2024

ClinVar

Relating variation to medicine