NM_000551.4(VHL):c.304_305dup (p.Pro103fs) AND Von Hippel-Lindau syndrome

Germline classification:: Pathogenic (1 submission)
Last evaluated:: Aug 1, 2018
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:: RCV000767255.1

Allele description [Variation Report for NM_000551.4(VHL):c.304_305dup (p.Pro103fs)]

NM_000551.4(VHL):c.304_305dup (p.Pro103fs)

Gene:

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

Variant type:

Duplication

Cytogenetic location:

3p25.3

Genomic location:

Preferred name:

NM_000551.4(VHL):c.304_305dup (p.Pro103fs)

HGVS:

NC_000003.12:g.10142151_10142152dup
NG_008212.3:g.5517_5518dup
NM_000551.4:c.304_305dupMANE SELECT
NM_001354723.2:c.304_305dup
NM_198156.3:c.304_305dup
NP_000542.1:p.Pro103fs
NP_001341652.1:p.Pro103fs
NP_937799.1:p.Pro103fs
LRG_322:g.5517_5518dup
NC_000003.11:g.10183835_10183836dup
NM_000551.3:c.304_305dupCC

Protein change:

P103fs

Links:

dbSNP: rs1559426145

NCBI 1000 Genomes Browser:

rs1559426145

Molecular consequence:

NM_000551.4:c.304_305dup - frameshift variant - [Sequence Ontology: SO:0001589]
NM_001354723.2:c.304_305dup - frameshift variant - [Sequence Ontology: SO:0001589]
NM_198156.3:c.304_305dup - frameshift variant - [Sequence Ontology: SO:0001589]

Observations:

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
SCV000897802	Genomic Diagnostic Laboratory, Division of Genomic Diagnostics, Children's Hospital of Philadelphia	criteria provided, single submitter (DGD Variant Analysis Guidelines)	Pathogenic (Aug 1, 2018)	germline	clinical testing	Citation Link

Submission Accession

Submitter

Review Status
(Assertion method)

Clinical Significance
(Last evaluated)

Origin

Method

Citations

SCV000897802

Genomic Diagnostic Laboratory, Division of Genomic Diagnostics, Children's Hospital of Philadelphia

criteria provided, single submitter

(DGD Variant Analysis Guidelines)

Pathogenic
(Aug 1, 2018)

germline

clinical testing

Citation Link

Help

Summary from all submissions

Ethnicity	Origin	Affected	Individuals	Families	Chromosomes tested	Number Tested	Family history	Method
not provided	germline	yes	1	not provided	not provided	not provided	not provided	clinical testing

Details of each submission

From Genomic Diagnostic Laboratory, Division of Genomic Diagnostics, Children's Hospital of Philadelphia, SCV000897802.1

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

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

Last Updated: Aug 11, 2024

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