VCV002583832.2 - ClinVar

NM_001903.5(CTNNA1):c.214_215del (p.Phe72fs)

Germline

Classification

criteria provided, single submitter. Learn more about how ClinVar calculates review status.

Pathogenic

This classification is based on the single submission received

The aggregate germline classification for this variant, typically for a monogenic or Mendelian disorder as in the ACMG/AMP guidelines, or for response to a drug. This value is calculated by NCBI based on data from submitters. Read our rules for calculating the aggregate classification.

Somatic

No data submitted for somatic clinical impact

Somatic

No data submitted for oncogenicity

Variant Details

Identifiers

NM_001903.5(CTNNA1):c.214_215del (p.Phe72fs)

Variation ID: 2583832 Accession: VCV002583832.2

Type and length

Deletion, 2 bp

Location

Cytogenetic: 5q31.2 5: 138783284-138783285 (GRCh38) [ NCBI UCSC ] 5: 138118973-138118974 (GRCh37) [ NCBI UCSC ]

Timeline in ClinVar

	First in ClinVar Help The date this variant first appeared in ClinVar with each type of classification.	Last submission Help The date of the most recent submission for each type of classification for this variant.	Last evaluated Help The most recent date that a submitter evaluated this variant for each type of classification.
Germline	Oct 21, 2023	Oct 28, 2023	May 25, 2023

HGVS

Nucleotide	Protein	Molecular consequence
NM_001903.5:c.214_215del MANE Select Help Transcripts from the Matched Annotation from the NCBI and EMBL-EBI (MANE) collaboration.	NP_001894.2:p.Phe72fs	frameshift
NM_001290307.3:c.214_215del	NP_001277236.1:p.Phe72fs	frameshift
NM_001290309.3:c.-9+1256_-9+1257del		intron variant
NM_001290310.3:c.-6+13_-6+14del		intron variant
NM_001323982.2:c.214_215del	NP_001310911.1:p.Phe72fs	frameshift
NM_001323983.1:c.214_215del	NP_001310912.1:p.Phe72fs	frameshift
NM_001323984.2:c.214_215del	NP_001310913.1:p.Phe72fs	frameshift
NM_001323985.2:c.214_215del	NP_001310914.1:p.Phe72fs	frameshift
NM_001323986.2:c.214_215del	NP_001310915.1:p.Phe72fs	frameshift
NC_000005.10:g.138783285_138783286del
NC_000005.9:g.138118974_138118975del
NG_047029.1:g.34890_34891del

... more HGVS ... less HGVS

Protein change

F72fs

Other names

Canonical SPDI

NC_000005.10:138783283:TTT:T

Functional consequence Help The effect of the variant on RNA or protein function, based on experimental evidence from submitters.

Global minor allele frequency (GMAF) Help The global minor allele frequency calculated by the 1000 Genomes Project. The minor allele at this location is indicated in parentheses and may be different from the allele represented by this VCV record.

Allele frequency Help The frequency of the allele represented by this VCV record.

Links

ClinGen: CA2582341647 VarSome

Genes

Gene	OMIM	ClinGen Gene Dosage Sensitivity Curation		Variation Viewer Help Links to Variation Viewer, a genome browser to view variation data from NCBI databases.	Related variants
Gene	OMIM	HI score Help The haploinsufficiency score for the gene, curated by ClinGen’s Dosage Sensitivity Curation task team.	TS score Help The triplosensitivity score for the gene, curated by ClinGen’s Dosage Sensitivity Curation task team.		Within gene Help The number of variants in ClinVar that are contained within this gene, with a link to view the list of variants.	All Help The number of variants in ClinVar for this gene, including smaller variants within the gene and larger CNVs that overlap or fully contain the gene.
CTNNA1		Sufficient evidence for dosage pathogenicity	No evidence available	GRCh38 GRCh37	3141	3205

Conditions - Germline

Condition Help The condition for this variant-condition (RCV) record in ClinVar.	Classification Help The aggregate germline classification for this variant-condition (RCV) record in ClinVar. The number of submissions that contribute to this aggregate classification is shown in parentheses. (# of submissions)	Review status Help The aggregate review status for this variant-condition (RCV) record in ClinVar. This value is calculated by NCBI based on data from submitters. Read our rules for calculating the review status.	Last evaluated Help The most recent date that a submitter evaluated this variant for the condition.	Variation/condition record Help The RCV accession number, with most recent version number, for the variant-condition record, with a link to the RCV web page.
Hereditary diffuse gastric adenocarcinoma	Pathogenic (1)	criteria provided, single submitter	May 25, 2023	RCV003334754.2

Submissions - Germline

Classification Help The submitted germline classification for each SCV record. (Last evaluated)	Review status Help Stars represent the review status, or the level of review supporting the submitted (SCV) record. This value is calculated by NCBI based on data from the submitter. Read our rules for calculating the review status. This column also includes a link to the submitter’s assertion criteria if provided, and the collection method. (Assertion criteria)	Condition Help The condition for the classification, provided by the submitter for this submitted (SCV) record. This column also includes the affected status and allele origin of individuals observed with this variant.	Submitter Help The submitting organization for this submitted (SCV) record. This column also includes the SCV accession and version number, the date this SCV first appeared in ClinVar, and the date that this SCV was last updated in ClinVar.	More information Help This column includes more information supporting the classification, including citations, the comment on classification, and detailed evidence provided as observations of the variant by the submitter.
Pathogenic (May 25, 2023) C Contributing to aggregate classification	criteria provided, single submitter (Myriad Autosomal Dominant, Autosomal Recessive and X-Linked Classification Criteria (2023)) Method: clinical testing	Hereditary diffuse gastric adenocarcinoma Affected status: unknown Allele origin: unknown	Myriad Genetics, Inc. Accession: SCV004043901.2 First in ClinVar: Oct 21, 2023 Last updated: Oct 28, 2023	Comment: This variant is considered pathogenic. This variant creates a frameshift predicted to result in premature protein truncation.

Germline Functional Evidence

There is no functional evidence in ClinVar for this variation. If you have generated functional data for this variation, please consider submitting that data to ClinVar.

Citations for germline classification of this variant

There are no citations for germline classification of this variant in ClinVar. If you know of citations for this variation, please consider submitting that information to ClinVar.

Text-mined citations for this variant ...

Record last updated Dec 22, 2024

ClinVar Genomic variation as it relates to human health

NM_001903.5(CTNNA1):c.214_215del (p.Phe72fs)

Variant Details

Genes

Conditions - Germline

Submissions - Germline

Germline Functional Evidence

Citations for germline classification of this variant

Text-mined citations for this variant ...