Full data view for gene DSG2

Information The variants shown are described using the NM_001943.3 transcript reference sequence.

2 entries on 1 page. Showing entries 1 - 2.
Legend   How to query  

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     
?/. - c.3247G>A r.(?) p.(Gly1083Ser) - Unknown - VUS g.29126596G>A g.31546633G>A DSG2(NM_001943.5):c.3247G>A (p.G1083S) - DSG2_000060 VKGL data sharing initiative Nederland - - - CLASSIFICATION record - - - - - - - - - - - - - - - - - - - - - - -
?/? 15 c.3247G>A r.(?) p.(Gly1083Ser) C-terminus Parent #1 - VUS g.29126596G>A g.31546633G>A - - DSG2_000060 - PubMed: Bhuiyan, ARVD/C database 7582 - - Germline - - - - - DNA SEQ - - ARVD/C - PubMed: Bhuiyan Compound heteroygote: p.Pro205Leu and p.Gly1083Ser - - - - - - - - 1 Paul van der Zwaag
Legend   How to query  


Screenscraping/webscraping (downloading large amounts of data using scripts) is strictly prohibited.
Use our APIs to retrieve data.