Full data view for gene DSG2

Information The variants shown are described using the NM_001943.3 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     
+?/? 5 c.437G>A r.(?) p.(Arg146His) Cadherin 1 Unknown - likely pathogenic g.29101120G>A g.31521157G>A - - DSG2_000077 - PubMed: van Tintelen, PubMed: Bhuiyan, ARVD/C database 7900 - - Germline - - - - - DNA SEQ - - ARVD/C - PubMed: van Tintelen, PubMed: Bhuiyan - - - - - - - - - 1 Paul van der Zwaag
?/. - c.437G>A r.(?) p.(Arg146His) - Unknown - VUS g.29101120G>A g.31521157G>A - - DSG2_000077 - PubMed: Xu 2010 - - Germline - - - - - DNA SEQ - - ARVD/C 20152563-Pat15 PubMed: Xu 2010 - M - Italy - - - - - 1 Johan den Dunnen
-?/. - c.437G>A r.(?) p.(Arg146His) - Unknown - likely benign g.29101120G>A g.31521157G>A DSG2(NM_001943.3):c.437G>A (p.R146H) - DSG2_000077 VKGL data sharing initiative Nederland - - - CLASSIFICATION record - - - - - - - - - - - - - - - - - - - - - - -
-?/. - c.437G>A r.(?) p.(Arg146His) - Unknown - likely benign g.29101120G>A - DSG2(NM_001943.3):c.437G>A (p.R146H) - DSG2_000077 VKGL data sharing initiative Nederland - - - CLASSIFICATION record - - - - - - - - - - - - - - - - - - - - - - -
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