APOBEC3F A78V - 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:

APOBEC3F A78V

(APOBEC3F Ala78Val)


You are viewing an old version of this page that was saved on June 23, 2011 at 12:04am by Genome Importing Robot.

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
 

hu04FD18

 

hu728FFF - PGP11 (hu728FFF) build 36, substitution variants
het T @ chr22:37770095

 

hu9385BA

 

huAE6220

 

huBEDA0B

 

huE80E3D

 

NA12878

 

NA18507

 

NA18517

 

NA18555

 

NA18956

 

snp-18

 

Deleted in this revision:

snp-18

 

Other external references
 

    dbSNP
  • rs5750728
    www.ncbi.nlm.nih.gov/projects/SNP/snp_ref.cgi

Other in silico analyses
 

  • NBLOSUM100 score = 2
  • GET-Evidence autoscore = 1

Edit history
 

Gene search

"GENE" or "GENE A123C":

Log in