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.

4 entries on 1 page. Showing entries 1 - 4.
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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.401C>T r.(?) p.(Pro134Leu) - Unknown - VUS g.150659401G>A - CLRN1(NM_001195794.1):c.401C>T (p.P134L) - CLRN1_000251 VKGL data sharing initiative Nederland - - - CLASSIFICATION record - - - - - - - - - - - - - - - - - - - - - - -
?/. - c.401C>T r.(?) p.(Pro134Leu) - Unknown ACMG VUS g.150659401G>A g.150941614G>A CLRN1:NM_174878 c.C401T, p.P134L - CLRN1_000251 heterozygous, individual solved, variant non-causal PubMed: Rodriguez-Munoz 2020 - - Germline ? - - - - DNA SEQ-NG-I blood - retinal disease RPN-296 PubMed: Rodriguez-Munoz 2020 family fRPN-139, proband M - Spain - - - - - 1 LOVD
?/. - c.401C>T r.(?) p.(Pro134Leu) - Unknown ACMG VUS g.150659401G>A - - - CLRN1_000251 - Mansard 2021, submitted - rs768357756 Germline - - - - - DNA SEQ-NG, SEQ - - USH2A - PubMed: Mansard et al, 2021 - F - - - - - - - 1 Anne-Françoise Roux
?/. - c.401C>T r.(?) p.(Pro134Leu) - Unknown ACMG VUS g.150659401G>A - - - CLRN1_000251 - Mansard 2021, submitted - rs768357756 Germline - - - - - DNA SEQ-NG, SEQ - - USH2A - PubMed: Mansard et al, 2021 - M - - - - - - - 1 Anne-Françoise Roux
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