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     

Population     

Age at death     

VIP     

Data_av     

Treatment     

Panel size     

Owner     
+/. - c.433+1G>A r.spl p.? - Both (homozygous) - pathogenic g.150659368C>T g.150941581C>T - - CLRN1_000233 - Sharon, submitted - - Germline - - - - - DNA SEQ - - USH3A - Sharon, submitted - M yes Israel Beduin - - - - 1 Dror Sharon
+/. - c.433+1G>A r.spl? p.? - Both (homozygous) ACMG pathogenic (recessive) g.150659368C>T g.150941581C>T c.433+1G>A, NA - CLRN1_000233 - PubMed: Abu-Ameerh 2020 - rs201205811 Germline yes - - - - DNA SEQ-NG blood Whole-exome sequencing retinal disease F1-B_IV-16 PubMed: Abu-Ameerh 2020 Family 1B M yes Jordan - - - - - 1 LOVD
+/. - c.433+1G>A r.spl? p.? - Both (homozygous) ACMG pathogenic (recessive) g.150659368C>T g.150941581C>T c.433+1G>A, NA - CLRN1_000233 - PubMed: Abu-Ameerh 2020 - rs201205811 Germline yes - - - - DNA SEQ-NG blood Whole-exome sequencing retinal disease F1-B_IV-17 PubMed: Abu-Ameerh 2020 Family 1B M yes Jordan - - - - - 1 LOVD
+/. - c.433+1G>A r.spl? p.? - Both (homozygous) ACMG pathogenic (recessive) g.150659368C>T g.150941581C>T c.433+1G>A, NA - CLRN1_000233 - PubMed: Abu-Ameerh 2020 - rs201205811 Germline yes - - - - DNA SEQ-NG blood Whole-exome sequencing retinal disease F1-B_IV-18 PubMed: Abu-Ameerh 2020 Family 1B M yes Jordan - - - - - 1 LOVD
+/. - c.433+1G>A r.spl? p.? - Both (homozygous) ACMG pathogenic (recessive) g.150659368C>T g.150941581C>T c.433+1G>A, NA - CLRN1_000233 - PubMed: Abu-Ameerh 2020 - rs201205811 Germline yes - - - - DNA SEQ-NG blood Whole-exome sequencing retinal disease F1-B_IV-19 PubMed: Abu-Ameerh 2020 Family 1B F yes Jordan - - - - - 1 LOVD
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