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.
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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     

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VIP     

Data_av     

Treatment     

Panel size     

Owner     
+/+ 1 c.118T>G r.(?) p.(Cys40Gly) - Paternal (inferred) - pathogenic g.150690378A>C g.150972591A>C - - CLRN1_000011 homozygous PubMed: Aller 2004; USMA-USMA missense analysis USMA-missense variant in MSV3d - rs121908143 Germline - 0/192 controls - - - DNA SEQ - - USH3 - PubMed: Aller 2004 Proband - - Spain - - - - - 1 Anne-Françoise Roux
+/+ 1 c.118T>G r.(?) p.(Cys40Gly) - Maternal (inferred) - pathogenic g.150690378A>C g.150972591A>C - - CLRN1_000011 homozygous PubMed: Aller 2004; USMA-USMA missense analysis USMA-missense variant in MSV3d - rs121908143 Germline - 0/192 controls - - - DNA SEQ - - USH3 - PubMed: Aller 2004 Proband - - Spain - - - - - 1 Anne-Françoise Roux
+/. - c.118T>G r.(?) p.(Cys40Gly) - Unknown - pathogenic g.150690378A>C g.150972591A>C NM_174878.2:118T>G (Cys40Gly) - CLRN1_000011 - PubMed: Haer-Wigman 2017 - - Germline - - - - - DNA SEQ-NG - gene panel ? 1929 PubMed: Haer-Wigman 2017 patient - no Netherlands - - - - - 1 LOVD
+?/. - c.118T>G r.(?) p.(Cys40Gly) - Unknown - likely pathogenic g.150690378A>C g.150972591A>C CLRN1(USH3A);NM_001195794.1;c.[118T>G];[65T>A];p.[(Cys40Gly)];[(Leu22His)] - CLRN1_000011 compound heterozygous PubMed: Jiman 2020 - - Unknown ? - - - - DNA SEQ-NG-I - 176 genes panel retinal disease 12 PubMed: Jiman 2020 - F - (United Kingdom (Great Britain)) - - - - - 1 LOVD
+?/. - c.118T>G r.(?) p.(Cys40Gly) - Unknown ACMG likely pathogenic (recessive) g.150690378A>C g.150972591A>C - - CLRN1_000011 ACMG PM2, PM1_SUPPORTING, PP2, PP5_STRONG PubMed: Weisschuh 2024 4399 - Germline - - - - - DNA SEQ-NG - WGS ? USHII-364 PubMed: Weisschuh 2024 patient, no family history F - Germany - - - - - 1 Johan den Dunnen
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