VCV000831557.2 - ClinVar

NC_000010.11:g.(?_87863161)_(88948936_?)del

Germline

Classification

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.

(1)

Stars represent the aggregate review status, or the level of review supporting the aggregate germline classification for this VCV record. This value is calculated by NCBI based on data from submitters. Read our rules for calculating the review status. The number of submissions which contribute to this review status is shown in parentheses.

Pathogenic

criteria provided, single submitter

Somatic

No data submitted for somatic clinical impact

Somatic

No data submitted for oncogenicity

Variant Details

Identifiers

NC_000010.11:g.(?_87863161)_(88948936_?)del

Variation ID: 831557 Accession: VCV000831557.2

Type and length

Deletion, 1,085,776 bp

Location

Cytogenetic: 10q23.31 10: 89622918-90708693 (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	Apr 15, 2020	Mar 26, 2023	Sep 7, 2022

HGVS

Nucleotide	Protein	Molecular consequence
NC_000010.10:g.(?_89622918)_(90708693_?)del

Protein change

Other names

Canonical SPDI

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

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.
PTEN		Sufficient evidence for dosage pathogenicity	No evidence available	GRCh38 GRCh38 GRCh37	3149	3666
ACTA2		Little evidence for dosage pathogenicity	No evidence available	GRCh38 GRCh37	352	657
ANKRD22	-	-	-	GRCh38 GRCh37	14	44
KLLN		-	-	GRCh38 GRCh38 GRCh37	24	371
LIPF		-	-	GRCh38 GRCh37	22	46
LIPJ		-	-	GRCh38 GRCh37	21	52
LIPK		-	-	GRCh38 GRCh37	30	55
LIPM		-	-	GRCh38 GRCh37	20	50
LIPN		-	-	GRCh38 GRCh37	98	125
RNLS		-	-	GRCh38 GRCh37	70	102

There is 1 more gene affected by this variant. See the full set of genes in Variation Viewer (GRCh37) and ClinGen Dosage Sensitivity Map.

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.
PTEN hamartoma tumor syndrome	Pathogenic (1)	criteria provided, single submitter	Sep 7, 2022	RCV001032107.3

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 (Sep 07, 2022)	criteria provided, single submitter (Invitae Variant Classification Sherloc (09022015)) Method: clinical testing	PTEN hamartoma tumor syndrome Affected status: unknown Allele origin: germline	Labcorp Genetics (formerly Invitae), Labcorp Accession: SCV001195414.2 First in ClinVar: Apr 15, 2020 Last updated: Mar 26, 2023	Publications: PubMed (7) PubMed: 9467011‚ 21194675‚ 18456716‚ 21926107‚ 22382802‚ 23132533‚ 23335809 Comment: A gross deletion of the genomic region encompassing the full coding sequence of the PTEN gene has been identified. Loss-of-function variants in PTEN are known … (more) A gross deletion of the genomic region encompassing the full coding sequence of the PTEN gene has been identified. Loss-of-function variants in PTEN are known to be pathogenic (PMID: 9467011, 21194675). The boundaries of this event are unknown as they extend beyond the assayed region for this gene and therefore may encompass additional genes. A similar copy number variant has been observed in individual(s) with PTEN hamartoma tumor syndrome (PMID: 18456716, 21926107, 22382802, 23132533, 23335809). For these reasons, this variant has been classified as Pathogenic. (less)

Comment:

A gross deletion of the genomic region encompassing the full coding sequence of the PTEN gene has been identified. Loss-of-function variants in PTEN are known to be pathogenic (PMID: 9467011, 21194675). The boundaries of this event are unknown as they extend beyond the assayed region for this gene and therefore may encompass additional genes. A similar copy number variant has been observed in individual(s) with PTEN hamartoma tumor syndrome (PMID: 18456716, 21926107, 22382802, 23132533, 23335809). For these reasons, this variant has been classified as Pathogenic.

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.

Comment:

Citations for germline classification of this variant

Title	Author	Journal	Year	Link
High cumulative risks of cancer in patients with PTEN hamartoma tumour syndrome.	Bubien V	Journal of medical genetics	2013	PMID: 23335809
The clinical consequences of hemizygosity across 2 MB of 10q23 are restricted to Cowden syndrome.	Lewis CM	Breast cancer research and treatment	2012	PMID: 23132533
Exon-level array CGH in a large clinical cohort demonstrates increased sensitivity of diagnostic testing for Mendelian disorders.	Aradhya S	Genetics in medicine : official journal of the American College of Medical Genetics	2012	PMID: 22382802
Two distinct thyroid tumours in a patient with Cowden syndrome carrying both a 10q23 and a mitochondrial DNA germline deletion.	Pradella LM	Journal of medical genetics	2011	PMID: 21926107
A clinical scoring system for selection of patients for PTEN mutation testing is proposed on the basis of a prospective study of 3042 probands.	Tan MH	American journal of human genetics	2011	PMID: 21194675
Contribution of PTEN large rearrangements in Cowden disease: a multiplex amplifiable probe hybridisation (MAPH) screening approach.	Chibon F	Journal of medical genetics	2008	PMID: 18456716
Mutation spectrum and genotype-phenotype analyses in Cowden disease and Bannayan-Zonana syndrome, two hamartoma syndromes with germline PTEN mutation.	Marsh DJ	Human molecular genetics	1998	PMID: 9467011

Text-mined citations for this variant ...

Record last updated Sep 29, 2024

ClinVar Genomic variation as it relates to human health

NC_000010.11:g.(?_87863161)_(88948936_?)del

Variant Details

Genes

Conditions - Germline

Submissions - Germline

Germline Functional Evidence

Citations for germline classification of this variant

Text-mined citations for this variant ...