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.

5 entries on 1 page. Showing entries 1 - 5.
Legend   How to query  

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     
+/+ 2 c.359T>A r.(?) p.(Met120Lys) Transmembrane 2 (101-121) Parent #2 - pathogenic g.150659443A>T g.150941656A>T - - CLRN1_000004 heterozygous PubMed: Joensuu 2001; USMA-USMA missense analysis USMA-missense variant in MSV3d - rs121908141 Germline - 0/302 controls - - - DNA SEQ - - USH3 - PubMed: Joensuu 2001 Proband M - Finland - - - - - 1 Anne-Françoise Roux
+/+ 2 c.359T>A r.(?) p.(Met120Lys) Transmembrane 2 (101-121) Parent #2 - pathogenic g.150659443A>T g.150941656A>T - - CLRN1_000004 heterozygous PubMed: Joensuu 2001; USMA-USMA missense analysis USMA-missense variant in MSV3d - rs121908141 Germline - 0/302 controls - - - DNA SEQ - - USH3 - PubMed: Joensuu 2001 Relative M - Finland - - - - - 1 Anne-Françoise Roux
+/+ 2 c.359T>A r.(?) p.(Met120Lys) Transmembrane 2 (101-121) Parent #1 - pathogenic g.150659443A>T g.150941656A>T - - CLRN1_000004 heterozygous PubMed: Joensuu 2001; USMA-USMA missense analysis USMA-missense variant in MSV3d - rs121908141 Germline - 0/302 controls - - - DNA SEQ - - USH3 - PubMed: Joensuu 2001 Proband - - Finland - - - - - 1 Anne-Françoise Roux
+/+ 2 c.359T>A r.(?) p.(Met120Lys) Transmembrane 2 (101-121) Parent #1 - pathogenic g.150659443A>T g.150941656A>T - - CLRN1_000004 heterozygous PubMed: Joensuu 2001; USMA-USMA missense analysis USMA-missense variant in MSV3d - rs121908141 Germline - 0/302 controls - - - DNA SEQ - - USH3 - PubMed: Joensuu 2001 Relative - - Finland - - - - - 1 Anne-Françoise Roux
+?/. - c.359T>A r.(?) p.(Met120Lys) - Parent #1 - likely pathogenic g.150659443A>T g.150941656A>T CLRN1 c.359T>A , p.(Met120Lys) - CLRN1_000004 heterozygous PubMed: Avela 2019 - - Germline yes - - - - DNA SEQ-NG, SEQ - targeted gene analysis or a next-generation sequencing-based gene panel retinal disease 21 PubMed: Avela 2019 - ? - Finland - - - - - 1 LOVD
Legend   How to query  


Screenscraping/webscraping (downloading large amounts of data using scripts) is strictly prohibited.
Use our APIs to retrieve data.