WFS1 V333I - GET-Evidence

Note: This variant has not been sufficiently evaluated by a GET-Evidence editor.

To be considered sufficiently evaluated a variant must have both "variant evidence" and "clinical importance" scores filled in.

Please help improve GET-Evidence by evaluating evidence for this variant!

Curation:
Currentness:

WFS1 V333I

(WFS1 Val333Ile)


Short summary

 

Variant evidence
Computational 2

Variant Effect Predictor (Ensembl ):
SIFT=tolerated(1);
PolyPhen=benign(0);
Condel=not_computable_was(-1)
Mutation Tasting Prediction: Polymorphism p value: 0.999998; protein features (might be) affected (Detail: aa 314-334 TRANSMEM Helical (potential) gets lost)
GVGD: GV 28.68; GD 0.00; Class C0
Multi-alignment of O76024.2 wolframin [Homo sapiens] with: XP_003278562.1 [Nomascus leucogenys] NP_001127593.1 [Pongo abelii] XP_002746054.1 [Callithrix jacchus] XP_001092811.1 [Macaca mulatta] XP_002924196.1 [Ailuropoda melanoleuca] XP_001499848.1 [Equus caballus] BAE26190.1 [Mus musculus] NP_035846.1 [Mus musculus] AAH46988.1 [Mus musculus] AAC64944.1 [Mus musculus]

Functional -
Case/Control -
Familial -
 
Clinical importance
Severity -
Treatability -
Penetrance -
 

Impact

Insufficiently evaluated not reviewed

(The "insufficiently evaluated" qualifier is assigned automatically based on the above evidence and importance scores.)

Inheritance pattern

unknown

Summary of published research, and additional commentary

 

Allele frequency

  • A @ chr4:6302519: 80.0% (8607/10758) in EVS
  • A @ chr4:6353419: 83.6% (107/128) in GET-Evidence
  • Frequency shown in summary reports: 80.0% (8607/10758)

Publications
 

Genomes
 

 

 

hu034DB1 - CGI sample GS00253-DNA_A02_200_37
hom A @ chr4:6302519

 

hu0D879F - CGI sample GS00253-DNA_G01_200_37
hom A @ chr4:6302519

 

 

 

 

 

 

 

 

 

 

 

 

 

hu43860C - CGI sample GS00253-DNA_A01_200_37
hom A @ chr4:6302519

 

 

 

hu604D39 - CGI sample GS00253-DNA_B02_200_37
hom A @ chr4:6302519

 

 

 

 

 

 

 

hu9385BA - CGI sample GS00253-DNA_E01_200_37
het A @ chr4:6302519

 

 

 

 

huAE6220 - CGI sample GS00253-DNA_H01_200_37
hom A @ chr4:6302519

 

 

 

huBEDA0B - CGI sample GS00253-DNA_C01_200_37
het A @ chr4:6302519

 

 

 

huE80E3D - CGI sample GS00253-DNA_D01_200_37
het A @ chr4:6302519

 

 

GS06985 - var-GS06985-1100-36-ASM
hom A @ chr4:6353420

 

GS06994 - var-GS06994-1100-36-ASM
het A @ chr4:6353420

 

GS07357 - var-GS07357-1100-36-ASM
hom A @ chr4:6353420

 

GS10851 - var-GS10851-1100-36-ASM
hom A @ chr4:6353420

 

GS12004 - var-GS12004-1100-36-ASM
het A @ chr4:6353420

 

GS18501 - var-GS18501-1100-36-ASM
hom A @ chr4:6353420

 

GS18502 - var-GS18502-1100-36-ASM
hom A @ chr4:6353420

 

GS18504 - var-GS18504-1100-36-ASM
hom A @ chr4:6353420

 

GS18505 - var-GS18505-1100-36-ASM
hom A @ chr4:6353420

 

GS18508 - var-GS18508-1100-36-ASM
hom A @ chr4:6353420

 

GS18517 - var-GS18517-1100-36-ASM
hom A @ chr4:6353420

 

GS18526 - var-GS18526-1100-36-ASM
hom A @ chr4:6353420

 

GS18537 - var-GS18537-1100-36-ASM
hom A @ chr4:6353420

 

GS18555 - var-GS18555-1100-36-ASM
hom A @ chr4:6353420

 

GS18558 - var-GS18558-1100-36-ASM
hom A @ chr4:6353420

 

GS18940 - var-GS18940-1100-36-ASM
hom A @ chr4:6353420

 

GS18942 - var-GS18942-1100-36-ASM
hom A @ chr4:6353420

 

GS18947 - var-GS18947-1100-36-ASM
hom A @ chr4:6353420

 

GS18956 - var-GS18956-1100-36-ASM
hom A @ chr4:6353420

 

GS19017 - var-GS19017-1100-36-ASM
hom A @ chr4:6353420

 

GS19020 - var-GS19020-1100-36-ASM
hom A @ chr4:6353420

 

GS19025 - var-GS19025-1100-36-ASM
hom A @ chr4:6353420

 

GS19026 - var-GS19026-1100-36-ASM
hom A @ chr4:6353420

 

GS19129 - var-GS19129-1100-36-ASM
hom A @ chr4:6353420

 

GS19238 - var-GS19238-1100-36-ASM
hom A @ chr4:6353420

 

GS19239 - var-GS19239-1100-36-ASM
hom A @ chr4:6353420

 

GS19240 - var-GS19240-1100-36-ASM
hom A @ chr4:6353420

 

GS19648 - var-GS19648-1100-36-ASM
hom A @ chr4:6353420

 

GS19649 - var-GS19649-1100-36-ASM
hom A @ chr4:6353420

 

GS19669 - var-GS19669-1100-36-ASM
het A @ chr4:6353420

 

GS19670 - var-GS19670-1100-36-ASM
hom A @ chr4:6353420

 

GS19700 - var-GS19700-1100-36-ASM
hom A @ chr4:6353420

 

GS19701 - var-GS19701-1100-36-ASM
hom A @ chr4:6353420

 

GS19703 - var-GS19703-1100-36-ASM
hom A @ chr4:6353420

 

GS19704 - var-GS19704-1100-36-ASM
hom A @ chr4:6353420

 

GS19735 - var-GS19735-1100-36-ASM
het A @ chr4:6353420

 

GS19834 - var-GS19834-1100-36-ASM
hom A @ chr4:6353420

 

GS20502 - var-GS20502-1100-36-ASM
het A @ chr4:6353420

 

GS21767 - var-GS21767-1100-36-ASM
hom A @ chr4:6353420

 

Other external references
 

    dbSNP
  • rs1801212
    www.ncbi.nlm.nih.gov/projects/SNP/snp_ref.cgi
    GeneTests
  • GeneTests records for the WFS1 gene
    Nonsyndromic Hearing Loss and Deafness, Autosomal Dominant
    DFNA 6/14/38 Nonsyndromic Hearing Loss and Deafness
    DFNA6/14/38 Nonsyndromic Low Frequency Sensorineural Hearing Los
    WFS1-Related Disorders
    Wolfram Syndrome
    Wolfram Syndrome-Like Disease
    www.ncbi.nlm.nih.gov/sites/GeneTests/lab/gene/WFS1
    Web search results (5 hits -- see all)
  • SNP link
    01 secretion machinery core component genes. 1 SNAP23. SNAP23. no cSNPs. on synaptic ... 18 Wfs1. WFS1. 1801212. V333I. AFD:.146 HAPMAP:..19. in crude vesicle ...
    www.cncr.vu.nl/presynaptic_SNPs.pdf
  • AceView: Gene:WFS1, a comprehensive annotation of human ...
    AceView offers a comprehensive annotation of human, mouse and nematode genes reconstructed by co-alignment and clustering of all publicly available mRNAs and ESTs on ...
    ncbi.nlm.nih.gov/IEB/Research/Acembly/...&a=clones&l=WFS1

Other in silico analyses
 

  • NBLOSUM100 score = –4
  • GET-Evidence autoscore = 3

Edit history
 

Gene search

"GENE" or "GENE A123C":

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