VCV000165297.5 - ClinVar

NM_153700.2(STRC):c.(?_3795)_(4993_?)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

NM_153700.2(STRC):c.(?_3795)_(4993_?)del

Variation ID: 165297 Accession: VCV000165297.5

Type and length

Deletion, 4,866 bp

Location

Cytogenetic: 15q15.3 15: 43600534-43605399 (GRCh38) [ NCBI UCSC ] 15: 43892732-43897597 (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	Jan 30, 2015	Aug 26, 2019	Jan 6, 2014

HGVS

Nucleotide	Protein	Molecular consequence
NM_153700.2:c.(?_3795)_(4993_?)del MANE Select Help Transcripts from the Matched Annotation from the NCBI and EMBL-EBI (MANE) collaboration.
NC_000015.10:g.(?_43600534)_(43605399_?)del
NC_000015.9:g.(?_43892732)_(43897597_?)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.
STRC		-	-	GRCh38 GRCh37	270	318

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.
Rare genetic deafness	Pathogenic (1)	criteria provided, single submitter	Jan 6, 2014	RCV000151936.5

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 (Jan 06, 2014)	criteria provided, single submitter (LMM Criteria) Method: clinical testing	Rare genetic deafness (Autosomal recessive inheritance) Affected status: not provided Allele origin: germline	Laboratory for Molecular Medicine, Mass General Brigham Personalized Medicine Accession: SCV000200469.5 First in ClinVar: Jan 30, 2015 Last updated: Aug 26, 2019	Publications: PubMed (1) PubMed: 22147502 Comment: The exon 19-26 deletion in STRC has been previously reported in one individual w ith hearing loss by our laboratory (LMM unpublished data). Multi-exon deletions … (more) The exon 19-26 deletion in STRC has been previously reported in one individual w ith hearing loss by our laboratory (LMM unpublished data). Multi-exon deletions in STRC, which overlap with exons 19-26, have been reported in several individu als with hearing loss (Francey 2011). This variant leads to a copy number loss o f exons 19 through 26 in the STRC gene and introduces a frameshift, which is pre dicted to lead to a truncated or absent protein. In summary, this variant meets our criteria to be classified as pathogenic (http://pcpgm.partners.org/LMM). It should be noted that exact breakpoints of the detected deletion could not be de termined due to limitations of the testing methodology. (less) Number of individuals with the variant: 2

Comment:

The exon 19-26 deletion in STRC has been previously reported in one individual w ith hearing loss by our laboratory (LMM unpublished data). Multi-exon deletions in STRC, which overlap with exons 19-26, have been reported in several individu als with hearing loss (Francey 2011). This variant leads to a copy number loss o f exons 19 through 26 in the STRC gene and introduces a frameshift, which is pre dicted to lead to a truncated or absent protein. In summary, this variant meets our criteria to be classified as pathogenic (http://pcpgm.partners.org/LMM). It should be noted that exact breakpoints of the detected deletion could not be de termined due to limitations of the testing methodology.

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
Genome-wide SNP genotyping identifies the Stereocilin (STRC) gene as a major contributor to pediatric bilateral sensorineural hearing impairment.	Francey LJ	American journal of medical genetics. Part A	2012	PMID: 22147502

Text-mined citations for this variant ...

Record last updated Dec 25, 2023

ClinVar Genomic variation as it relates to human health

NM_153700.2(STRC):c.(?_3795)_(4993_?)del

Variant Details

Genes

Conditions - Germline

Submissions - Germline

Germline Functional Evidence

Citations for germline classification of this variant

Text-mined citations for this variant ...