Full data view for gene DSC2

Information The variants shown are described using the NM_004949.3 transcript reference sequence.

4 entries on 1 page. Showing entries 1 - 4.
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Effect     

Exon     

AscendingDNA change (cDNA)     

RNA change     

Protein     

P-domain     

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     
+/+ 5i c.631-2A>G r.spl p.(Ile211Metfs*11) Cadherin 1 Unknown - pathogenic g.28667778T>C g.31087815T>C - - DSC2_000006 - PubMed: Heuser, ARVD/C database 7524 - - Germline - - - - - DNA SEQ - - ARVD/C - PubMed: Heuser - - - - - - - - - 1 Paul van der Zwaag
+/. - c.631-2A>G r.spl p.? - Parent #1 - pathogenic (dominant) g.28667778T>C - - - DSC2_000006 - PubMed: Roman 2020, Journal: Roman 2020 - - Germline - - - - - DNA SEQ, SEQ-NG - WES ARVC, HL HL021 PubMed: Roman 2020, Journal: Roman 2020 new-born screening - - United States - - - - - 1 Johan den Dunnen
+/. - c.631-2A>G r.spl? p.? - Unknown - pathogenic g.28667778T>C - DSC2(NM_024422.4):c.631-2A>G, DSC2(NM_024422.6):c.631-2A>G - DSC2_000006 VKGL data sharing initiative Nederland - - - CLASSIFICATION record - - - - - - - - - - - - - - - - - - - - - - -
+/. - c.631-2A>G r.spl? p.? - Unknown - pathogenic g.28667778T>C - DSC2(NM_024422.4):c.631-2A>G, DSC2(NM_024422.6):c.631-2A>G - DSC2_000006 VKGL data sharing initiative Nederland - - - CLASSIFICATION record - - - - - - - - - - - - - - - - - - - - - - -
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