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NM_006005.3(WFS1):c.1210C>G (p.Pro404Ala) AND not specified

Germline classification:
Uncertain significance (1 submission)
Last evaluated:
Jul 25, 2017
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:
RCV000614845.6

Allele description [Variation Report for NM_006005.3(WFS1):c.1210C>G (p.Pro404Ala)]

NM_006005.3(WFS1):c.1210C>G (p.Pro404Ala)

Gene:
WFS1:wolframin ER transmembrane glycoprotein [Gene - OMIM - HGNC]
Variant type:
single nucleotide variant
Cytogenetic location:
4p16.1
Genomic location:
Preferred name:
NM_006005.3(WFS1):c.1210C>G (p.Pro404Ala)
HGVS:
  • NC_000004.12:g.6301005C>G
  • NG_011700.1:g.36156C>G
  • NM_001145853.1:c.1210C>G
  • NM_006005.3:c.1210C>GMANE SELECT
  • NP_001139325.1:p.Pro404Ala
  • NP_005996.2:p.Pro404Ala
  • LRG_1417t1:c.1210C>G
  • LRG_1417:g.36156C>G
  • LRG_1417p1:p.Pro404Ala
  • NC_000004.11:g.6302732C>G
Protein change:
P404A
Links:
dbSNP: rs756869880
NCBI 1000 Genomes Browser:
rs756869880
Molecular consequence:
  • NM_001145853.1:c.1210C>G - missense variant - [Sequence Ontology: SO:0001583]
  • NM_006005.3:c.1210C>G - missense variant - [Sequence Ontology: SO:0001583]
Observations:
1

Condition(s)

Synonyms:
AllHighlyPenetrant
Identifiers:
MedGen: CN169374

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Assertion and evidence details

Help
Submission AccessionSubmitterReview Status
(Assertion method)		Clinical Significance
(Last evaluated)		OriginMethodCitations
SCV000731806Laboratory for Molecular Medicine, Mass General Brigham Personalized Medicine
criteria provided, single submitter

(LMM Criteria)		Uncertain significance
(Jul 25, 2017) 		germlineclinical testing

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

Help

Summary from all submissions

EthnicityOriginAffectedIndividualsFamiliesChromosomes testedNumber TestedFamily historyMethod
not providedgermlinenot provided11not providednot providednot providedclinical testing

Citations

PubMed

A systematic approach to assessing the clinical significance of genetic variants.

Duzkale H, Shen J, McLaughlin H, Alfares A, Kelly MA, Pugh TJ, Funke BH, Rehm HL, Lebo MS.

Clin Genet. 2013 Nov;84(5):453-63. doi: 10.1111/cge.12257.

PubMed [citation]
PMID:
24033266
PMCID:
PMC3995020

Details of each submission

From Laboratory for Molecular Medicine, Mass General Brigham Personalized Medicine, SCV000731806.2

#EthnicityIndividualsChromosomes TestedFamily HistoryMethodCitations
1not provided1not providednot providedclinical testing PubMed (1)

Description

The p.Pro404Ala variant in WFS1 has not been previously reported in individuals with hearing loss or WFS1-related syndromes. It has been identified in 1/111718 European chromosomes by the Genome Aggregation Database (gnomAD, http://gnomad. broadinstitute.org; dbSNP rs756869880). Although this variant has been seen in t he general population, its frequency is not high enough to rule out a pathogenic role. Computational prediction tools and conservation analyses suggest that thi s variant may impact the protein, though this information is not predictive enou gh to determine pathogenicity. In summary, the clinical significance of this var iant is uncertain.

#SampleMethodObservation
OriginAffectedNumber testedTissuePurposeMethodIndividualsAllele frequencyFamiliesCo-occurrences
1germlinenot providednot providednot providednot provided1not provided1not provided

Last Updated: May 16, 2025