Full data view for gene CERKL


This database is one of the ”Retinal and hearing impairment genetic variant databases”.
Information The variants shown are described using the transcript reference sequence.

2 entries on 1 page. Showing entries 1 - 2.
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Effect     

Exon     

AscendingDNA change (cDNA)     

RNA change     

Protein     

Allele     

Classification method     

Clinical classification     

DNA change (genomic) (hg19)     

DNA change (hg38)     

Published as     

ISCN     

DB-ID     

Variant remarks     

Reference     

ClinVar ID     

dbSNP ID     

Origin     

Segregation     

Frequency     

Re-site     

VIP     

Methylation     

Template     

Technique     

Tissue     

Remarks     

Disease     

ID_report     

Reference     

Remarks     

Gender     

Consanguinity     

Country     

Population     

Age at death     

VIP     

Data_av     

Treatment     

Panel size     

Owner     
+?/. 1 c.182T>A r.(?) p.(Val61Glu) Unknown - likely pathogenic g.182521552A>T g.181656825A>T CERKL Ex.1 c.182T>A p.(Val61Glu), Ex.6 c.847C>T p.(Arg283*) - CERKL_000104 compound heterozygous PubMed: Martin Merida 2019 - - Germline/De novo (untested) ? - - - - DNA SEQ-NG-I - - retinal disease RP-2225 PubMed: Martin Merida 2019 - ? - Spain - - - - - 1 LOVD
+?/. 1 c.182T>A r.(?) p.(Val61Glu) Unknown - likely pathogenic g.182521552A>T g.181656825A>T CERKL Ex.1 c.182T>A p.(Val61Glu), Ex.1 c.182T>A p.(Val61Glu), CRB1: Ex.7 c.2291G>A p.(Arg764His) - CERKL_000104 homozygous PubMed: Martin Merida 2019 - - Germline/De novo (untested) ? - - - - DNA SEQ-NG-I - - retinal disease RP-2730 PubMed: Martin Merida 2019 - ? - Spain - - - - - 1 LOVD
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