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NM_000431.4(MVK):c.447C>G (p.Tyr149Ter) AND Hyperimmunoglobulin D with periodic fever

Germline classification:
not provided (1 submission)
Review status:
no classification provided
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:
RCV000083845.1

Allele description [Variation Report for NM_000431.4(MVK):c.447C>G (p.Tyr149Ter)]

NM_000431.4(MVK):c.447C>G (p.Tyr149Ter)

Gene:
MVK:mevalonate kinase [Gene - OMIM - HGNC]
Variant type:
single nucleotide variant
Cytogenetic location:
12q24.11
Genomic location:
Preferred name:
NM_000431.4(MVK):c.447C>G (p.Tyr149Ter)
HGVS:
  • NC_000012.12:g.109581470C>G
  • NG_007702.1:g.12776C>G
  • NM_000431.4:c.447C>GMANE SELECT
  • NM_001114185.3:c.447C>G
  • NM_001301182.2:c.371+1524C>G
  • NP_000422.1:p.Tyr149Ter
  • NP_001107657.1:p.Tyr149Ter
  • LRG_156:g.12776C>G
  • NC_000012.11:g.110019275C>G
  • NM_000431.1:c.447C>G
Protein change:
Y149*
Links:
dbSNP: rs104895299
NCBI 1000 Genomes Browser:
rs104895299
Molecular consequence:
  • NM_001301182.2:c.371+1524C>G - intron variant - [Sequence Ontology: SO:0001627]
  • NM_000431.4:c.447C>G - nonsense - [Sequence Ontology: SO:0001587]
  • NM_001114185.3:c.447C>G - nonsense - [Sequence Ontology: SO:0001587]

Condition(s)

Name:
Hyperimmunoglobulin D with periodic fever (HIDS)
Synonyms:
Hyperimmunoglobulinemia D and periodic fever syndrome; Periodic fever Dutch type; Hyperimmunoglobulinemia D; See all synonyms [MedGen]
Identifiers:
MONDO: MONDO:0009849; MedGen: C0398691; Orphanet: 343; OMIM: 260920

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Assertion and evidence details

Help
Submission AccessionSubmitterReview Status
(Assertion method)		Clinical Significance
(Last evaluated)		OriginMethodCitations
SCV000115947Unité médicale des maladies autoinflammatoires, CHRU Montpellier
no classification provided
not providednot providednot provided

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

Description

also involved in OMIM 25117

SCV000115947

Help

Summary from all submissions

EthnicityOriginAffectedIndividualsFamiliesChromosomes testedNumber TestedFamily historyMethod
not providednot providednot providednot providednot providednot provided1not providedliterature only

Citations

PubMed

Organization of the mevalonate kinase (MVK) gene and identification of novel mutations causing mevalonic aciduria and hyperimmunoglobulinaemia D and periodic fever syndrome.

Houten SM, Koster J, Romeijn GJ, Frenkel J, Di Rocco M, Caruso U, Landrieu P, Kelley RI, Kuis W, Poll-The BT, Gibson KM, Wanders RJ, Waterham HR.

Eur J Hum Genet. 2001 Apr;9(4):253-9. Erratum in: Eur J Hum Genet 2001 Aug;9(8):651.

PubMed [citation]
PMID:
11313768

Details of each submission

From Unité médicale des maladies autoinflammatoires, CHRU Montpellier, SCV000115947.1

#EthnicityIndividualsChromosomes TestedFamily HistoryMethodCitations
1not providednot providednot providednot providednot provided PubMed (1)
#SampleMethodObservation
OriginAffectedNumber testedTissuePurposeMethodIndividualsAllele frequencyFamiliesCo-occurrences
1not providednot provided1not providednot providednot providednot providednot providednot provided

Last Updated: Apr 23, 2022