All variants in the CLCN5 gene

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

4 entries on 1 page. Showing entries 1 - 4.
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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     
+/. 6 c.635G>C r.(?) p.(Gly212Ala) - pathogenic g.49846416G>C g.50081759G>C - - CLCN5_000023 - PubMed: Mansour-Hendili et al. 2015 - - Germline - - - 0 - Rosa Vargas-Poussou
+/. 6 c.635G>C r.(?) p.(Gly212Ala) - pathogenic g.49846416G>C g.50081759G>C - - CLCN5_000023 - PubMed: Grand 2009 - - Unknown - - - 0 - Rosa Vargas-Poussou
+/. 6 c.635G>C r.(?) p.(Gly212Ala) - pathogenic g.49846416G>C g.50081759G>C - - CLCN5_000023 - PubMed: Grand 2009 - - Unknown - - - 0 - Rosa Vargas-Poussou
+/. 6 c.635G>C r.(?) p.(Gly212Ala) - pathogenic g.49846416G>C g.50081759G>C - - CLCN5_000023 - PubMed: Grand 2009 - - Unknown - - - 0 - Rosa Vargas-Poussou
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