VCV001726834.3 - ClinVar

NM_153676.4(USH1C):c.546G>A (p.Trp182Ter)

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.

(2)

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/Likely pathogenic

criteria provided, multiple submitters, no conflicts

Somatic

No data submitted for somatic clinical impact

Somatic

No data submitted for oncogenicity

Variant Details

Identifiers

NM_153676.4(USH1C):c.546G>A (p.Trp182Ter)

Variation ID: 1726834 Accession: VCV001726834.3

Type and length

single nucleotide variant, 1 bp

Location

Cytogenetic: 11p15.1 11: 17526786 (GRCh38) [ NCBI UCSC ] 11: 17548333 (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	Nov 19, 2022	Feb 14, 2024	Jul 25, 2023

HGVS

Nucleotide	Protein	Molecular consequence
NM_153676.4:c.546G>A MANE Select Help Transcripts from the Matched Annotation from the NCBI and EMBL-EBI (MANE) collaboration.	NP_710142.1:p.Trp182Ter	nonsense
NM_005709.4:c.546G>A MANE Plus Clinical Help Transcripts from the Matched Annotation from the NCBI and EMBL-EBI (MANE) collaboration.	NP_005700.2:p.Trp182Ter	nonsense
NM_001297764.2:c.546G>A	NP_001284693.1:p.Trp182Ter	nonsense
NR_123738.2:n.655G>A		non-coding transcript variant
NC_000011.10:g.17526786C>T
NC_000011.9:g.17548333C>T
NG_011883.2:g.22631G>A

... more HGVS ... less HGVS

Protein change

W182*

Other names

Canonical SPDI

NC_000011.10:17526785:C: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

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.
USH1C		-	-	GRCh38 GRCh37	1378	1402

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.
Usher syndrome type 1C	Likely pathogenic (1)	criteria provided, single submitter	Jan 2, 2022	RCV002310518.2
not provided	Pathogenic (1)	criteria provided, single submitter	Jul 25, 2023	RCV003565518.2

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.
Likely pathogenic (Jan 02, 2022)	criteria provided, single submitter (Myriad Women's Health Autosomal Recessive and X-Linked Classification Criteria (2021)) Method: clinical testing	Usher syndrome type 1C Affected status: unknown Allele origin: unknown	Myriad Genetics, Inc. Accession: SCV002603238.2 First in ClinVar: Nov 19, 2022 Last updated: Dec 24, 2022	Comment: NM_005709.3(USH1C):c.546G>A(W182) is expected to be pathogenic in the context of USH1C-related disorders. This variant is predicted to lead to an abnormal or absent protein product … (more) NM_005709.3(USH1C):c.546G>A(W182) is expected to be pathogenic in the context of USH1C-related disorders. This variant is predicted to lead to an abnormal or absent protein product due to the creation of a premature termination codon in USH1C, a gene where loss-of-function variants are known to be pathogenic. Please note: this variant was assessed in the context of healthy population screening. (less)
Pathogenic (Jul 25, 2023)	criteria provided, single submitter (Invitae Variant Classification Sherloc (09022015)) Method: clinical testing	not provided Affected status: unknown Allele origin: germline	Labcorp Genetics (formerly Invitae), Labcorp Accession: SCV004308639.1 First in ClinVar: Feb 14, 2024 Last updated: Feb 14, 2024	Publications: PubMed (4) PubMed: 10973247‚ 17407589‚ 20301442‚ 21203349 Comment: This variant is not present in population databases (gnomAD no frequency). This variant has not been reported in the literature in individuals affected with USH1C-related … (more) This variant is not present in population databases (gnomAD no frequency). This variant has not been reported in the literature in individuals affected with USH1C-related conditions. ClinVar contains an entry for this variant (Variation ID: 1726834). For these reasons, this variant has been classified as Pathogenic. This sequence change creates a premature translational stop signal (p.Trp182*) in the USH1C gene. It is expected to result in an absent or disrupted protein product. Loss-of-function variants in USH1C are known to be pathogenic (PMID: 10973247, 17407589, 20301442, 21203349). (less)

Comment:

NM_005709.3(USH1C):c.546G>A(W182*) is expected to be pathogenic in the context of USH1C-related disorders. This variant is predicted to lead to an abnormal or absent protein product due to the creation of a premature termination codon in USH1C, a gene where loss-of-function variants are known to be pathogenic. Please note: this variant was assessed in the context of healthy population screening.

Comment:

This variant is not present in population databases (gnomAD no frequency). This variant has not been reported in the literature in individuals affected with USH1C-related conditions. ClinVar contains an entry for this variant (Variation ID: 1726834). For these reasons, this variant has been classified as Pathogenic. This sequence change creates a premature translational stop signal (p.Trp182*) in the USH1C gene. It is expected to result in an absent or disrupted protein product. Loss-of-function variants in USH1C are known to be pathogenic (PMID: 10973247, 17407589, 20301442, 21203349).

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
Usher Syndrome Type I.	Adam MP	-	2020	PMID: 20301442
Novel mutations in the USH1C gene in Usher syndrome patients.	Aparisi MJ	Molecular vision	2010	PMID: 21203349
Deafblindness in French Canadians from Quebec: a predominant founder mutation in the USH1C gene provides the first genetic link with the Acadian population.	Ebermann I	Genome biology	2007	PMID: 17407589
A defect in harmonin, a PDZ domain-containing protein expressed in the inner ear sensory hair cells, underlies Usher syndrome type 1C.	Verpy E	Nature genetics	2000	PMID: 10973247

Text-mined citations for this variant ...

Record last updated Sep 29, 2024

ClinVar Genomic variation as it relates to human health

NM_153676.4(USH1C):c.546G>A (p.Trp182Ter)

Variant Details

Genes

Conditions - Germline

Submissions - Germline

Germline Functional Evidence

Citations for germline classification of this variant

Text-mined citations for this variant ...