GLIS3 S424P - 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:

GLIS3 S424P

(GLIS3 Ser424Pro)


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 @ chr9:4118208: 99.9% (8183/8194) in EVS
  • G @ chr9:4108207: 100.0% (88/88) in GET-Evidence
  • Frequency shown in summary reports: 99.9% (8183/8194)

Publications
 

Genomes
 

 

 

 

 

 

 

 

 

 

 

 

 

 

 

 

 

 

 

 

 

 

 

 

 

 

huAE6220 - CGI sample GS00253-DNA_H01_200_37
hom G @ chr9:4118208

 

 

 

 

 

 

huE80E3D - CGI sample GS00253-DNA_D01_200_37
hom G @ chr9:4118208

 

 

 

GS06985 - var-GS06985-1100-36-ASM
hom G @ chr9:4108208

 

GS07357 - var-GS07357-1100-36-ASM
hom G @ chr9:4108208

 

GS10851 - var-GS10851-1100-36-ASM
hom G @ chr9:4108208

 

GS12004 - var-GS12004-1100-36-ASM
hom G @ chr9:4108208

 

GS18501 - var-GS18501-1100-36-ASM
hom G @ chr9:4108208

 

GS18502 - var-GS18502-1100-36-ASM
hom G @ chr9:4108208

 

GS18504 - var-GS18504-1100-36-ASM
hom G @ chr9:4108208

 

GS18505 - var-GS18505-1100-36-ASM
hom G @ chr9:4108208

 

GS18508 - var-GS18508-1100-36-ASM
hom G @ chr9:4108208

 

GS18517 - var-GS18517-1100-36-ASM
hom G @ chr9:4108208

 

GS18526 - var-GS18526-1100-36-ASM
hom G @ chr9:4108208

 

GS18537 - var-GS18537-1100-36-ASM
hom G @ chr9:4108208

 

GS18555 - var-GS18555-1100-36-ASM
hom G @ chr9:4108208

 

GS18558 - var-GS18558-1100-36-ASM
hom G @ chr9:4108208

 

GS18940 - var-GS18940-1100-36-ASM
hom G @ chr9:4108208

 

GS18942 - var-GS18942-1100-36-ASM
hom G @ chr9:4108208

 

GS18947 - var-GS18947-1100-36-ASM
hom G @ chr9:4108208

 

GS18956 - var-GS18956-1100-36-ASM
hom G @ chr9:4108208

 

GS19017 - var-GS19017-1100-36-ASM
hom G @ chr9:4108208

 

GS19020 - var-GS19020-1100-36-ASM
hom G @ chr9:4108208

 

GS19025 - var-GS19025-1100-36-ASM
hom G @ chr9:4108208

 

GS19026 - var-GS19026-1100-36-ASM
hom G @ chr9:4108208

 

GS19129 - var-GS19129-1100-36-ASM
hom G @ chr9:4108208

 

GS19648 - var-GS19648-1100-36-ASM
hom G @ chr9:4108208

 

GS19649 - var-GS19649-1100-36-ASM
hom G @ chr9:4108208

 

GS19669 - var-GS19669-1100-36-ASM
hom G @ chr9:4108208

 

GS19700 - var-GS19700-1100-36-ASM
hom G @ chr9:4108208

 

GS19703 - var-GS19703-1100-36-ASM
hom G @ chr9:4108208

 

GS19704 - var-GS19704-1100-36-ASM
hom G @ chr9:4108208

 

GS19735 - var-GS19735-1100-36-ASM
hom G @ chr9:4108208

 

GS19834 - var-GS19834-1100-36-ASM
hom G @ chr9:4108208

 

GS20509 - var-GS20509-1100-36-ASM
hom G @ chr9:4108208

 

GS21767 - var-GS21767-1100-36-ASM
hom G @ chr9:4108208

 

Other external references
 

    dbSNP
  • rs806052
    www.ncbi.nlm.nih.gov/projects/SNP/snp_ref.cgi
    Web search results (0 hits -- see all)

Other in silico analyses
 

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

Edit history
 

Gene search

"GENE" or "GENE A123C":

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