All variants in the CLCN5 gene

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

2 entries on 1 page. Showing entries 1 - 2.
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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     
+/. 9 c.1399C>T r.(?) p.(Arg467*) - pathogenic g.49853406C>T g.50088749C>T - - CLCN5_000041 - PubMed: Mansour-Hendili et al. 2015 - - Unknown - - - 0 - Rosa Vargas-Poussou
+/. - c.1399C>T r.(?) p.(Arg467Ter) - pathogenic g.49853406C>T g.50088749C>T - - CLCN5_000041 VKGL data sharing initiative Nederland - - - CLASSIFICATION record - - - 0 - VKGL-NL_Nijmegen
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