ARMC4 R787C - 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:

(See the latest version)

ARMC4 R787C

(ARMC4 Arg787Cys)


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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

  • A @ chr10:28224075: 1.5% (162/10758) in EVS
  • A @ chr10:28264080: 5.5% (7/128) in GET-Evidence
  • Frequency shown in summary reports: 1.5% (162/10758)

Publications
 

Genomes
 

GS18537 - var-GS18537-1100-36-ASM
het A @ chr10:28264081

 

GS18558 - var-GS18558-1100-36-ASM
het A @ chr10:28264081

 

GS18942 - var-GS18942-1100-36-ASM
het A @ chr10:28264081

 

Added in this revision:

GS19669 - var-GS19669-1100-36-ASM
het A @ chr10:28264081

 

Other external references
 

    dbSNP
  • rs35242712
    www.ncbi.nlm.nih.gov/projects/SNP/snp_ref.cgi
    PolyPhen-2
  • Score: 0.001 (benign)

Other in silico analyses
 

  • NBLOSUM100 score = 8
  • GET-Evidence autoscore = 0

Edit history
 

Gene search

"GENE" or "GENE A123C":

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