CASP8AP2 T1567Shift - 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:

CASP8AP2 T1567Shift

(CASP8AP2 1567delTinsShift)


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

  • None available.

Publications
 

Genomes
 

 

hu0D879F - CGI sample GS00253-DNA_G01_200_37
het - @ chr6:90577707

 

 

hu43860C - CGI sample GS00253-DNA_A01_200_37
het - @ chr6:90577707

 

 

 

 

huAE6220 - CGI sample GS00253-DNA_H01_200_37
het - @ chr6:90577707

 

huBEDA0B - CGI sample GS00253-DNA_C01_200_37
het - @ chr6:90577707

 

 

 

huE80E3D - CGI sample GS00253-DNA_D01_200_37
het - @ chr6:90577707

 

Other in silico analyses
 

  • NBLOSUM100 score = 4
  • GET-Evidence autoscore = 2

Edit history
 

Gene search

"GENE" or "GENE A123C":

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