IDUA H33Q - 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:

IDUA H33Q

(IDUA His33Gln)


Short summary

 

Variant evidence
Computational -
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

  • G @ chr4:980971: 90.4% (3048/3370) in EVS
  • G @ chr4:970970: 75.0% (33/44) in GET-Evidence
  • Frequency shown in summary reports: 90.4% (3048/3370)

Publications
 

Genomes
 

 

 

 

 

 

 

 

 

 

 

 

 

 

 

 

 

 

 

 

 

 

 

 

 

 

 

 

 

GS10851 - var-GS10851-1100-36-ASM
hom G @ chr4:970971

 

GS18504 - var-GS18504-1100-36-ASM
hom G @ chr4:970971

 

GS18508 - var-GS18508-1100-36-ASM
hom G @ chr4:970971

 

GS18517 - var-GS18517-1100-36-ASM
hom G @ chr4:970971

 

GS18526 - var-GS18526-1100-36-ASM
het G @ chr4:970971

 

GS18537 - var-GS18537-1100-36-ASM
hom G @ chr4:970971

 

GS18555 - var-GS18555-1100-36-ASM
hom G @ chr4:970971

 

GS18558 - var-GS18558-1100-36-ASM
hom G @ chr4:970971

 

GS18942 - var-GS18942-1100-36-ASM
het G @ chr4:970971

 

GS18947 - var-GS18947-1100-36-ASM
het G @ chr4:970971

 

GS19649 - var-GS19649-1100-36-ASM
het G @ chr4:970971

 

GS19703 - var-GS19703-1100-36-ASM
hom G @ chr4:970971

 

GS19834 - var-GS19834-1100-36-ASM
het G @ chr4:970971

 

GS21767 - var-GS21767-1100-36-ASM
hom G @ chr4:970971

 

Other external references
 

    dbSNP
  • rs10794537
    www.ncbi.nlm.nih.gov/projects/SNP/snp_ref.cgi
    PolyPhen-2
  • Score: 0.008 (benign)

Other in silico analyses
 

  • NBLOSUM100 score = –1
  • GET-Evidence autoscore = 3

Edit history
 

Gene search

"GENE" or "GENE A123C":

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