All variants in the CLCN5 gene

Information The variants shown are described using the NM_000084.4 transcript reference sequence.

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Effect     

Exon     

AscendingDNA change (cDNA)     

RNA change     

Protein     

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     

Owner     
+/. 8i c.1347+1G>T r.1058_1347del p.Gly353fs - pathogenic g.49851528G>T g.50086871G>T IVS8+1G>T - CLCN5_000093 - PubMed: Tosetto 2009, OMIM:var0014 - - Unknown - - - 0 - Johan den Dunnen
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