GRM6 Q59P - 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!


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(GRM6 Gln59Pro)

You are viewing an old version of this page that was saved on December 27, 2009 at 3:56pm by Genome Importing Robot.

Added in this revision:

Short summary


Variant evidence
Computational -
Functional -
Case/Control -
Familial -
Clinical importance
Severity -
Treatability -
Penetrance -


Insufficiently evaluated not reviewed

(The "insufficiently evaluated" qualifier is assigned automatically based on the above evidence and importance scores.)

Inheritance pattern


Summary of published research, and additional commentary


Allele frequency

  • G @ chr5:178421770: 61.6% (3865/6274) in EVS
  • Frequency shown in summary reports: 61.6% (3865/6274)



Other external references

  • Score: 0 (benign)
    Web search results (1 hit -- see all)
  • BMC Evolutionary Biology
    GRM6. Q59P. CAG-CCG. A. C. C. C. C. C. C. C. Human. NOT. rs2645329. 63. GRM6. P141T ... G. Chimpanzee. 70. GRM6. A877D. GCC-GAC. C. A. A. A. A. A. A. A. Human. Fixed. 71. GRM7. A520P ...

Other in silico analyses

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

Edit history

Gene search

"GENE" or "GENE A123C":

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