VCV002839878.1 - ClinVar

NM_000304.4(PMP22):c.396del (p.Ser131_Tyr132insTer)

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

NM_000304.4(PMP22):c.396del (p.Ser131_Tyr132insTer)

Variation ID: 2839878 Accession: VCV002839878.1

Type and length

Deletion, 1 bp

Location

Cytogenetic: 17p12 17: 15231004 (GRCh38) [ NCBI UCSC ] 17: 15134321 (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	Feb 20, 2024	Feb 20, 2024	Feb 22, 2023

HGVS

Nucleotide	Protein	Molecular consequence
NM_000304.4:c.396del MANE Select Help Transcripts from the Matched Annotation from the NCBI and EMBL-EBI (MANE) collaboration.	NP_000295.1:p.Ser131_Tyr132insTer	nonsense
NM_001281455.2:c.396del	NP_001268384.1:p.Ser131_Tyr132insTer	nonsense
NM_001281456.2:c.396del	NP_001268385.1:p.Ser131_Tyr132insTer	nonsense
NM_153321.3:c.396del	NP_696996.1:p.Ser131_Tyr132insTer	nonsense
NM_153322.3:c.396del	NP_696997.1:p.Ser131_Tyr132insTer	nonsense
NR_104017.2:n.491del		non-coding transcript variant
NR_104018.2:n.391del		non-coding transcript variant
NC_000017.11:g.15231004del
NC_000017.10:g.15134321del
NG_007949.1:g.39324del
LRG_263:g.39324del
LRG_263t1:c.396del	LRG_263p1:p.Tyr132Terfs

... more HGVS ... less HGVS

Protein change

Other names

Canonical SPDI

NC_000017.11:15231003:G:

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.
PMP22		Sufficient evidence for dosage pathogenicity	No evidence available	GRCh38 GRCh37	407	525

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.
Charcot-Marie-Tooth disease, type I	Pathogenic (1)	criteria provided, single submitter	Feb 22, 2023	RCV003742041.2

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 (Feb 22, 2023)	criteria provided, single submitter (Invitae Variant Classification Sherloc (09022015)) Method: clinical testing	Charcot-Marie-Tooth disease, type I Affected status: unknown Allele origin: germline	Labcorp Genetics (formerly Invitae), Labcorp Accession: SCV004499527.1 First in ClinVar: Feb 20, 2024 Last updated: Feb 20, 2024	Publications: PubMed (3) PubMed: 21149811‚ 21252112‚ 23965407 Comment: This sequence change creates a premature translational stop signal (p.Tyr132) in the PMP22 gene. While this is not anticipated to result in nonsense mediated decay, … (more) This sequence change creates a premature translational stop signal (p.Tyr132) in the PMP22 gene. While this is not anticipated to result in nonsense mediated decay, it is expected to disrupt the last 29 amino acid(s) of the PMP22 protein. This variant is not present in population databases (gnomAD no frequency). This variant has not been reported in the literature in individuals affected with PMP22-related conditions. This variant disrupts a region of the PMP22 protein in which other variant(s) (p.Leu145Argfs*10) have been determined to be pathogenic (PMID: 21149811, 21252112, 23965407). This suggests that this is a clinically significant region of the protein, and that variants that disrupt it are likely to be disease-causing. For these reasons, this variant has been classified as Pathogenic. (less)

Comment:

This sequence change creates a premature translational stop signal (p.Tyr132*) in the PMP22 gene. While this is not anticipated to result in nonsense mediated decay, it is expected to disrupt the last 29 amino acid(s) of the PMP22 protein. This variant is not present in population databases (gnomAD no frequency). This variant has not been reported in the literature in individuals affected with PMP22-related conditions. This variant disrupts a region of the PMP22 protein in which other variant(s) (p.Leu145Argfs*10) have been determined to be pathogenic (PMID: 21149811, 21252112, 23965407). This suggests that this is a clinically significant region of the protein, and that variants that disrupt it are likely to be disease-causing. 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
Hereditary neuropathy with liability to pressure palsy: two cases of difficult diagnosis.	Beydoun SR	Journal of clinical neuromuscular disease	2013	PMID: 23965407
Inherited demyelinating neuropathies with micromutations of peripheral myelin protein 22 gene.	Taioli F	Brain : a journal of neurology	2011	PMID: 21252112
Analyzing histopathological features of rare charcot-marie-tooth neuropathies to unravel their pathogenesis.	Benedetti S	Archives of neurology	2010	PMID: 21149811

Text-mined citations for this variant ...

Record last updated Sep 30, 2024

ClinVar Genomic variation as it relates to human health

NM_000304.4(PMP22):c.396del (p.Ser131_Tyr132insTer)

Variant Details

Genes

Conditions - Germline

Submissions - Germline

Germline Functional Evidence

Citations for germline classification of this variant

Text-mined citations for this variant ...