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.

10 entries on 1 page. Showing entries 1 - 10.
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Effect     

Exon     

AscendingDNA change (cDNA)     

RNA change     

Protein     

P-domain     

Allele     

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Clinical classification     

DNA change (genomic) (hg19)     

DNA change (hg38)     

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ISCN     

DB-ID     

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Reference     

ClinVar ID     

dbSNP ID     

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Disease     

ID_report     

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Owner     
+/+ 2 c.368C>A r.(?) p.(Ala123Asp) - Paternal (inferred) - pathogenic g.150659434G>T g.150941647G>T - - CLRN1_000001 homozygous USMA-USMA missense analysis USMA-missense variant in MSV3d - - Germline - - - - - DNA SEQ - - USH3 - - Proband - - Canada - - - - - 1 Anne-Françoise Roux
+/+ 2 c.368C>A r.(?) p.(Ala123Asp) - Maternal (inferred) - pathogenic g.150659434G>T g.150941647G>T - - CLRN1_000001 homozygous USMA-USMA missense analysis USMA-missense variant in MSV3d - - Germline - - - - - DNA SEQ - - USH3 - - Proband - - Canada - - - - - 1 Anne-Françoise Roux
+/+ 2 c.368C>A r.(?) p.(Ala123Asp) - Paternal (inferred) - pathogenic g.150659434G>T g.150941647G>T - - CLRN1_000001 homozygous PubMed: Ebermann 2007; USMA-USMA missense analysis USMA-missense variant in MSV3d - - Germline - 0/386 controls - - - DNA SEQ - - USH1 - PubMed: Ebermann 2007 Proband - - Canada - - - - - 1 Anne-Françoise Roux
+/+ 2 c.368C>A r.(?) p.(Ala123Asp) - Maternal (inferred) - pathogenic g.150659434G>T g.150941647G>T - - CLRN1_000001 homozygous PubMed: Ebermann 2007; USMA-USMA missense analysis USMA-missense variant in MSV3d - - Germline - 0/386 controls - - - DNA SEQ - - USH1 - PubMed: Ebermann 2007 Proband - - Canada - - - - - 1 Anne-Françoise Roux
+/+ 2 c.368C>A r.(?) p.(Ala123Asp) - Paternal (inferred) - pathogenic g.150659434G>T g.150941647G>T - - CLRN1_000001 homozygous PubMed: Isosomppi 2009; USMA-USMA missense analysis USMA-missense variant in MSV3d - - Germline - 0/90 controls - - - DNA SEQ - - USH3 - PubMed: Isosomppi 2009 Proband - - Finland - - - - - 1 Anne-Françoise Roux
+/+ 2 c.368C>A r.(?) p.(Ala123Asp) - Maternal (inferred) - pathogenic g.150659434G>T g.150941647G>T - - CLRN1_000001 homozygous PubMed: Isosomppi 2009; USMA-USMA missense analysis USMA-missense variant in MSV3d - - Germline - 0/90 controls - - - DNA SEQ - - USH3 - PubMed: Isosomppi 2009 Proband - - Finland - - - - - 1 Anne-Françoise Roux
+/+ 2 c.368C>A r.(?) p.(Ala123Asp) - Paternal (inferred) - pathogenic g.150659434G>T g.150941647G>T - - CLRN1_000001 homozygous; mutation PubMed: Bonnet 2016; USMA-USMA missense analysis USMA-missense variant in MSV3d - - Germline - - - - - DNA SEQ, SEQ-NG-S - - USH2 - PubMed: Bonnet 2016 Proband - - France - - - - - 1 Crystel Bonnet
+/+ 2 c.368C>A r.(?) p.(Ala123Asp) - Paternal (inferred) - pathogenic g.150659434G>T g.150941647G>T - - CLRN1_000001 homozygous; mutation PubMed: Bonnet 2016; USMA-USMA missense analysis USMA-missense variant in MSV3d - - Germline - - - - - DNA SEQ, SEQ-NG-S - - USH2 - PubMed: Bonnet 2016 Proband - - France - - - - - 1 Crystel Bonnet
+/+ 2 c.368C>A r.(?) p.(Ala123Asp) - Maternal (inferred) - pathogenic g.150659434G>T g.150941647G>T - - CLRN1_000001 homozygous; mutation PubMed: Bonnet 2016; USMA-USMA missense analysis USMA-missense variant in MSV3d - - Germline - - - - - DNA SEQ, SEQ-NG-S - - USH2 - PubMed: Bonnet 2016 Proband - - France - - - - - 1 Crystel Bonnet
+/+ 2 c.368C>A r.(?) p.(Ala123Asp) - Maternal (inferred) - pathogenic g.150659434G>T g.150941647G>T - - CLRN1_000001 homozygous; mutation PubMed: Bonnet 2016; USMA-USMA missense analysis USMA-missense variant in MSV3d - - Germline - - - - - DNA SEQ, SEQ-NG-S - - USH2 - PubMed: Bonnet 2016 Proband - - France - - - - - 1 Crystel Bonnet
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