RPGRIP1L D1264N - GET-Evidence

Note: This variant has not been sufficiently evaluated by a GET-Evidence editor.

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Curation:
Currentness:

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RPGRIP1L D1264N

(RPGRIP1L Asp1264Asn)


You are viewing an old version of this page that was saved on March 29, 2011 at 8:55pm 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

  • T @ chr16:53639438: 4.1% (445/10758) in EVS
  • T @ chr16:52196938: 8.6% (11/128) in GET-Evidence
  • Frequency shown in summary reports: 4.1% (445/10758)

Publications
 

Genomes
 

GS06985 - var-GS06985-1100-36-ASM
het T @ chr16:52196939

 

GS18526 - var-GS18526-1100-36-ASM
het T @ chr16:52196939

 

Added in this revision:

GS18537 - var-GS18537-1100-36-ASM
hom T @ chr16:52196939

 

NA07022

 

NA18555

 

snp-2

 

Other external references
 

    dbSNP
  • rs3213758
    www.ncbi.nlm.nih.gov/projects/SNP/snp_ref.cgi
    GeneTests
  • GeneTests records for the RPGRIP1L gene
    Joubert Syndrome
    Meckel Syndrome
    Nephronophthisis 8
    RPGRIP1L-Related Joubert Syndrome
    RPGRIP1L-Related Meckel Syndrome
    www.ncbi.nlm.nih.gov/sites/GeneTests/lab/gene/RPGRIP1L
    PolyPhen-2
  • Score: 0 (benign)
    Web search results (0 hits -- see all)

Other in silico analyses
 

  • NBLOSUM100 score = –1
  • GET-Evidence autoscore = 3

Edit history
 

Gene search

"GENE" or "GENE A123C":

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