ZNF354C Y524C - 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.

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Curation:
Currentness:

ZNF354C Y524C

(ZNF354C Tyr524Cys)


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 @ chr5:178507004: 1.4% (148/10756) in EVS
  • G @ chr5:178439609: 1.6% (2/128) in GET-Evidence
  • Frequency shown in summary reports: 1.4% (148/10756)

Publications
 

Genomes
 

huAE6220 - CGI sample GS00253-DNA_H01_200_37
het G @ chr5:178507004

 

GS20502 - var-GS20502-1100-36-ASM
het G @ chr5:178439610

 

Other external references
 

    PolyPhen-2
  • Score: 0.979 (probably damaging)

Other in silico analyses
 

  • NBLOSUM100 score = 6
  • GET-Evidence autoscore = 2

Edit history
 

Gene search

"GENE" or "GENE A123C":

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