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NM_000551.4(VHL):c.531_542delinsTC (p.Arg177fs) AND Von Hippel-Lindau syndrome

Germline classification:
Pathogenic (1 submission)
Last evaluated:
Nov 1, 2016
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:
RCV000660352.1

Allele description [Variation Report for NM_000551.4(VHL):c.531_542delinsTC (p.Arg177fs)]

NM_000551.4(VHL):c.531_542delinsTC (p.Arg177fs)

Genes:
LOC107303340:3p25 von Hippel-Lindau tumor suppressor, E3 ubiquitin protein ligase Alu-mediated recombination region [Gene]
VHL:von Hippel-Lindau tumor suppressor [Gene - OMIM - HGNC]
Variant type:
Indel
Cytogenetic location:
3p25.3
Genomic location:
Preferred name:
NM_000551.4(VHL):c.531_542delinsTC (p.Arg177fs)
HGVS:
  • NC_000003.12:g.10149854_10149865delinsTC
  • NG_008212.3:g.13220_13231delinsTC
  • NG_046756.1:g.7616_7627delinsTC
  • NM_000551.4:c.531_542delinsTCMANE SELECT
  • NM_001354723.2:c.*85_*96delinsTC
  • NM_198156.3:c.408_419delinsTC
  • NP_000542.1:p.Arg177fs
  • NP_937799.1:p.Arg136fs
  • LRG_322:g.13220_13231delinsTC
  • NC_000003.11:g.10191538_10191549delinsTC
  • NM_000551.3:c.531_542delACTGGACATCGTinsTC
Protein change:
R136fs
Links:
dbSNP: rs1553620331
NCBI 1000 Genomes Browser:
rs1553620331
Molecular consequence:
  • NM_001354723.2:c.*85_*96delinsTC - 3 prime UTR variant - [Sequence Ontology: SO:0001624]
  • NM_000551.4:c.531_542delinsTC - frameshift variant - [Sequence Ontology: SO:0001589]
  • NM_198156.3:c.408_419delinsTC - frameshift variant - [Sequence Ontology: SO:0001589]

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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Assertion and evidence details

Help
Submission AccessionSubmitterReview Status
(Assertion method)		Clinical Significance
(Last evaluated)		OriginMethodCitations
SCV000782420Center for Human Genetics, Inc, Center for Human Genetics, Inc
criteria provided, single submitter

(ACMG Guidelines, 2015)		Pathogenic
(Nov 1, 2016) 		germlineclinical testing

PubMed (1)
[See all records that cite this PMID]

Help

Summary from all submissions

EthnicityOriginAffectedIndividualsFamiliesChromosomes testedNumber TestedFamily historyMethod
not providedgermlineyesnot providednot providednot providednot providednot providedclinical testing

Citations

PubMed

Standards and guidelines for the interpretation of sequence variants: a joint consensus recommendation of the American College of Medical Genetics and Genomics and the Association for Molecular Pathology.

Richards S, Aziz N, Bale S, Bick D, Das S, Gastier-Foster J, Grody WW, Hegde M, Lyon E, Spector E, Voelkerding K, Rehm HL; ACMG Laboratory Quality Assurance Committee..

Genet Med. 2015 May;17(5):405-24. doi: 10.1038/gim.2015.30. Epub 2015 Mar 5.

PubMed [citation]
PMID:
25741868
PMCID:
PMC4544753

Details of each submission

From Center for Human Genetics, Inc, Center for Human Genetics, Inc, SCV000782420.1

#EthnicityIndividualsChromosomes TestedFamily HistoryMethodCitations
1not providednot providednot providednot providedclinical testing PubMed (1)
#SampleMethodObservation
OriginAffectedNumber testedTissuePurposeMethodIndividualsAllele frequencyFamiliesCo-occurrences
1germlineyesnot providednot providednot providednot providednot providednot providednot provided

Last Updated: Aug 5, 2023