NM_000551.4(VHL):c.179_182del (p.Arg60fs) AND Von Hippel-Lindau syndrome

Germline classification:: Pathogenic (1 submission)
Last evaluated:: Dec 21, 2023
Review status:: 1 star out of maximum of 4 stars
criteria provided, single submitter

Somatic classification of clinical impact:: None
Review status:: (0/4) 0 stars out of maximum of 4 stars
no assertion criteria provided

Somatic classification of oncogenicity:: None
Review status:: (0/4) 0 stars out of maximum of 4 stars
no assertion criteria provided

Record status:: current
Accession:: RCV004442550.1

Allele description [Variation Report for NM_000551.4(VHL):c.179_182del (p.Arg60fs)]

NM_000551.4(VHL):c.179_182del (p.Arg60fs)

Gene:

VHL:von Hippel-Lindau tumor suppressor [Gene - OMIM - HGNC]

Variant type:

Deletion

Cytogenetic location:

3p25.3

Genomic location:

Preferred name:

NM_000551.4(VHL):c.179_182del (p.Arg60fs)

HGVS:

NC_000003.12:g.10142026_10142029del
NG_008212.3:g.5392_5395del
NM_000551.4:c.179_182delMANE SELECT
NM_001354723.2:c.179_182del
NM_198156.3:c.179_182del
NP_000542.1:p.Arg60Profs
NP_000542.1:p.Arg60fs
NP_001341652.1:p.Arg60fs
NP_937799.1:p.Arg60fs
LRG_322t1:c.179_182del
LRG_322:g.5392_5395del
LRG_322p1:p.Arg60Profs
NC_000003.11:g.10183710_10183713del
NM_000551.3:c.179_182delGGCC
NR_176335.1:n.249_252del

Protein change:

R60fs

Molecular consequence:

NM_000551.4:c.179_182del - frameshift variant - [Sequence Ontology: SO:0001589]
NM_001354723.2:c.179_182del - frameshift variant - [Sequence Ontology: SO:0001589]
NM_198156.3:c.179_182del - frameshift variant - [Sequence Ontology: SO:0001589]
NR_176335.1:n.249_252del - non-coding transcript variant - [Sequence Ontology: SO:0001619]

Condition(s)

Name:: Von Hippel-Lindau syndrome (VHLS)
Synonyms:: VHL syndrome; Von Hippel-Lindau
Identifiers:: MONDO: MONDO:0008667; MedGen: C0019562; Orphanet: 892; OMIM: 193300

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Submission Accession	Submitter	Review Status (Assertion method)	Clinical Significance (Last evaluated)	Origin	Method	Citations
SCV004930835	Myriad Genetics, Inc.	criteria provided, single submitter (Myriad Autosomal Dominant, Autosomal Recessive and X-Linked Classification Criteria (2023))	Pathogenic (Dec 21, 2023)	unknown	clinical testing	Citation Link

Submission Accession

Submitter

Review Status
(Assertion method)

Clinical Significance
(Last evaluated)

Origin

Method

Citations

SCV004930835

Myriad Genetics, Inc.

criteria provided, single submitter

(Myriad Autosomal Dominant, Autosomal Recessive and X-Linked Classification Criteria (2023))

Pathogenic
(Dec 21, 2023)

unknown

clinical testing

Citation Link

Help

Summary from all submissions

Ethnicity	Origin	Affected	Individuals	Families	Chromosomes tested	Number Tested	Family history	Method
not provided	unknown	unknown	not provided	not provided	not provided	not provided	not provided	clinical testing

Details of each submission

From Myriad Genetics, Inc., SCV004930835.1

#	Ethnicity	Individuals	Chromosomes Tested	Family History	Method	Citations
1	not provided	not provided	not provided	not provided	clinical testing	not provided

Description

This variant is considered pathogenic. This variant creates a frameshift predicted to result in premature protein truncation.

#	Sample				Method		Observation
#	Origin	Affected	Number tested	Tissue	Purpose	Method	Individuals	Allele frequency	Families	Co-occurrences
1	unknown	unknown	not provided	not provided	not provided		not provided	not provided	not provided	not provided

Last Updated: May 7, 2024

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