Full data view for gene CLRN1


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

8 entries on 1 page. Showing entries 1 - 8.
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Effect     

Exon     

AscendingDNA change (cDNA)     

RNA change     

Protein     

P-domain     

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     
+/+ 3 c.619C>T r.(?) p.(Arg207*) - Paternal (inferred) - pathogenic g.150645803G>A g.150928016G>A - - CLRN1_000015 homozygous PubMed: Licastro 2012 - - Germline - - - - - DNA SEQ, SEQ-NG-S - - USH3 - PubMed: Licastro 2012 Proband - - Italy - - - - - 1 Anne-Françoise Roux
+/+ 3 c.619C>T r.(?) p.(Arg207*) - Maternal (inferred) - pathogenic g.150645803G>A g.150928016G>A - - CLRN1_000015 homozygous PubMed: Licastro 2012 - - Germline - - - - - DNA SEQ, SEQ-NG-S - - USH3 - PubMed: Licastro 2012 Proband - - Italy - - - - - 1 Anne-Françoise Roux
+/+ 3 c.619C>T r.(?) p.(Arg207*) - Unknown - pathogenic g.150645803G>A g.150928016G>A - - CLRN1_000015 heterozygous PubMed: Garcia-Garcia 2012 - - Germline - 0/100 controls - - - DNA PE, SEQ - APEX USH3 - PubMed: Garcia-Garcia 2012 Proband M - Spain - - - - - 1 Anne-Françoise Roux
+/+ 3 c.619C>T r.(?) p.(Arg207*) - Unknown - pathogenic g.150645803G>A g.150928016G>A - - CLRN1_000015 heterozygous PubMed: Garcia-Garcia 2012 - - Germline - 0/100 controls - - - DNA PE, SEQ - APEX USH3 - PubMed: Garcia-Garcia 2012 Proband M - Spain - - - - - 1 Anne-Françoise Roux
+/+ 3 c.619C>T r.(?) p.(Arg207*) - Maternal (confirmed) - pathogenic g.150645803G>A g.150928016G>A - - CLRN1_000015 heterozygous PubMed: Garcia-Garcia 2012 - - Germline - 0/100 controls - - - DNA PE, SEQ - APEX USH3 - PubMed: Garcia-Garcia 2012 Proband M - Spain - - - - - 1 Anne-Françoise Roux
+/+ 3 c.619C>T r.(?) p.(Arg207*) - Parent #1 - pathogenic g.150645803G>A g.150928016G>A NM_001195794.1:C658T - p.R220X - CLRN1_000015 heterozygous; mutation PubMed: Jiang 2015 - - Germline - - - - - DNA SEQ, SEQ-NG-S - - USH1 - PubMed: Jiang 2015 Proband F - China - - - - - 1 Anne-Françoise Roux
+/. - c.619C>T r.(?) p.(Arg207*) - Both (homozygous) - pathogenic (recessive) g.150645803G>A - - - CLRN1_000015 - PubMed: Santana 2019 - - Germline - - - - - DNA SEQ, SEQ-NG - 14 gene panel USH FamUS-8 PubMed: Santana 2019 3-generation family, 4 affected (F, 3M), unaffected parents - yes Cuba white - - - - 4 Global Variome, with Curator vacancy
+/. - c.619C>T r.(?) p.(Arg207*) - Both (homozygous) - pathogenic (recessive) g.150645803G>A - - - CLRN1_000015 - PubMed: Santana 2019 - - Germline - - - - - DNA SEQ, SEQ-NG - 14 gene panel USH FamUS-12 PubMed: Santana 2019 2-generation family, 1 affected (M), unaffected parents M yes Cuba white - - - - 1 Global Variome, with Curator vacancy
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