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.
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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     

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Segregation     

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Re-site     

VIP     

Methylation     

Template     

Technique     

Tissue     

Remarks     

Disease     

ID_report     

Reference     

Remarks     

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VIP     

Data_av     

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Panel size     

Owner     
+/. - c.3340C>T r.(?) p.(Gln1114*) - Unknown - pathogenic g.29126689C>T g.31546726C>T - - DSG2_000190 - PubMed: Sahlin 2019, Journal: Sahlin 2019 - - Germline ? - - - - DNA SEQ-NG - HaloPlex gene panel (70 heart genes) ? 250 PubMed: Sahlin 2019, Journal: Sahlin 2019 stillbirth cohort (290 cases from Sweden) M - Sweden - - - - - 1 Ellika Sahlin
?/. - c.3340C>T r.(?) p.(Gln1114*) - Unknown ACMG VUS g.29126689C>T g.31546726C>T - - DSG2_000190 this variant was detected as an incidental finding, but not reported back to the individual. Reason: class 3 (PVS1-moderate, PM2) - - - Germline ? - - - - DNA SEQ-NG-I - - CPT II deficiency, infantile 162067 - - M ? Germany - - - - - 1 Andreas Laner
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