Full data view for gene CAPN3

This database is one of the gene variant databases from the Leiden Muscular Dystrophy pages
Information The variants shown are described using the NM_000070.2 transcript reference sequence.

2 entries on 1 page. Showing entries 1 - 2.
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Effect     

Exon     

AscendingDNA change (cDNA)     

RNA change     

Protein     

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     
+/. 1 c.8C>A r.(?) p.(Thr3Asn) Parent #1 - pathogenic g.42652011C>A g.42359813C>A - - CAPN3_000332 - - - - Germline - - - 0 - DNA SSCA - - LGMD - - - - - Finland - - 0 - - 1 Amets Sáenz
+/. 1 c.8C>A r.(?) p.(Thr3Asn) Parent #2 - pathogenic g.42652011C>A g.42359813C>A - - CAPN3_000332 - - - - Germline - - - 0 - DNA SSCA - - LGMD - - - - - Finland - - 0 - - 1 Amets Sáenz
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