All variants in the DHCR7 gene

Information The variants shown are described using the NM_001360.2 transcript reference sequence.

6 entries on 1 page. Showing entries 1 - 6.
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Effect     

Exon     

AscendingDNA change (cDNA)     

RNA change     

Protein     

Haplotype     

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     
+/+ 8 c.852C>A r.(?) p.(Phe284Leu) A - pathogenic g.71148969G>T g.71437923G>T - - DHCR7_000049 - PubMed: Yu et al. 2000 - - Unknown - - - 0 - Division of Human Genetics, Innsbruck
+/+ 8 c.852C>A r.(?) p.(Phe284Leu) - - pathogenic g.71148969G>T g.71437923G>T - - DHCR7_000049 - PubMed: Yu et al. 2000 - - Unknown - - - 0 - Division of Human Genetics, Innsbruck
+/+ 8 c.852C>A r.(?) p.(Phe284Leu) - - pathogenic g.71148969G>T g.71437923G>T - - DHCR7_000049 - PubMed: Yu et al. 2000 - - Unknown - - - 0 - Division of Human Genetics, Innsbruck
+/+ 8 c.852C>A r.(?) p.(Phe284Leu) - - pathogenic g.71148969G>T g.71437923G>T - - DHCR7_000049 - PubMed: Yu et al. 2000 - - Unknown - - - 0 - Division of Human Genetics, Innsbruck
+/+ 8 c.852C>A r.(?) p.(Phe284Leu) - - pathogenic g.71148969G>T g.71437923G>T - - DHCR7_000049 - PubMed: Yu et al. 2000 - - Unknown - - - 0 - Division of Human Genetics, Innsbruck
+/+ 8 c.852C>A r.(?) p.(Phe284Leu) - - pathogenic g.71148969G>T g.71437923G>T - - DHCR7_000049 - PubMed: Yu et al. 2000 - - Unknown - - - 0 - Division of Human Genetics, Innsbruck
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