TNRC18 P2393L - 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:

TNRC18 P2393L

(TNRC18 Pro2393Leu)


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 @ chr7:5353344: 9.1% (712/7782) in EVS
  • A @ chr7:5319869: 2.8% (3/106) in GET-Evidence
  • Frequency shown in summary reports: 9.1% (712/7782)

Publications
 

Genomes
 

 

 

 

 

GS10851 - var-GS10851-1100-36-ASM
het A @ chr7:5319870

 

GS19834 - var-GS19834-1100-36-ASM
het A @ chr7:5319870

 

Other external references
 

    dbSNP
  • rs12532973
    www.ncbi.nlm.nih.gov/projects/SNP/snp_ref.cgi

Other in silico analyses
 

  • NBLOSUM100 score = 7
  • GET-Evidence autoscore = 1

Edit history
 

Gene search

"GENE" or "GENE A123C":

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