Full data view for gene DSG2

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

12 entries on 1 page. Showing entries 1 - 12.
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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     
?/. 3 c.166G>A r.(?) p.(Val56Met) - Unknown - VUS g.29099850G>A g.31519887G>A NM_001943:c.G166A - DSG2_000008 - PubMed: Lopes 2013, Journal: Lopes 2013 - - Germline - 1/223 cases HCM - - - DNA SEQ - - CMH - PubMed: Lopes 2013, Journal: Lopes 2013 analysis of 223 cases - - United Kingdom (Great Britain) - - - - - 1 Johan den Dunnen
?/. 3 c.166G>A r.(?) p.(Val56Met) - Parent #1 - VUS g.29099850G>A g.31519887G>A NM_001943:c.G166A - DSG2_000008 - PubMed: Lopes 2013, Journal: Lopes 2013 - - Germline - 2/223 cases HCM - - - DNA SEQ - - CMH - PubMed: Lopes 2013, Journal: Lopes 2013 analysis of 223 cases - - United Kingdom (Great Britain) - - - - - 2 Johan den Dunnen
?/? 3 c.166G>A r.(?) p.(Val56Met) Cadherin 1 Unknown - VUS g.29099850G>A g.31519887G>A - - DSG2_000008 - PubMed: Syrris, ARVD/C database 7540 - - Germline - - - - - DNA SEQ - - ARVD/C - PubMed: Syrris - - - - - - - - - 1 Paul van der Zwaag
?/? 3 c.166G>A r.(?) p.(Val56Met) Cadherin 1 Unknown - VUS g.29099850G>A g.31519887G>A - - DSG2_000008 - PubMed: Posch, ARVD/C database 7540 - - Germline - - - - - DNA SEQ - - CMD - PubMed: Posch Susceptibility variation? - - - - - - - - 1 Paul van der Zwaag
?/? 3 c.166G>A r.(?) p.(Val56Met) Cadherin 1 Unknown - VUS g.29099850G>A g.31519887G>A - - DSG2_000008 - PubMed: Bhuiyan, ARVD/C database 7540 - - Germline - - - - - DNA SEQ - - ARVD/C - PubMed: Bhuiyan 1 major OR 2 minor TFC - - - - - - - - 1 Paul van der Zwaag
?/? 3 c.166G>A r.(?) p.(Val56Met) Cadherin 1 Parent #1 - VUS g.29099850G>A g.31519887G>A - - DSG2_000008 Share conclusion that p.Val56Met likely plays a contributory role PubMed: Dalal 2009, PubMed: den Haan, PubMed: Xu 2010, ARVD/C database 7540 - - Germline - - - - - DNA SEQ - - ARVD/C 20152563-Pat14 PubMed: Dalal 2009, PubMed: den Haan, PubMed: Xu 2010 Offspring has different combinations of two of these mutations. Controls were done voor DSG2 mutation only. M - United States - - - - - 4 Paul van der Zwaag
-/. - c.166G>A r.(?) p.(Val56Met) - Unknown - benign g.29099850G>A g.31519887G>A DSG2(NM_001943.3):c.166G>A (p.V56M), DSG2(NM_001943.5):c.166G>A (p.V56M) - DSG2_000008 VKGL data sharing initiative Nederland - - - CLASSIFICATION record - - - - - - - - - - - - - - - - - - - - - - -
-?/. - c.166G>A r.(?) p.(Val56Met) - Unknown - likely benign g.29099850G>A g.31519887G>A DSG2(NM_001943.3):c.166G>A (p.V56M), DSG2(NM_001943.5):c.166G>A (p.V56M) - DSG2_000008 VKGL data sharing initiative Nederland - - - CLASSIFICATION record - - - - - - - - - - - - - - - - - - - - - - -
-?/. - c.166G>A r.(?) p.(Val56Met) - Unknown - likely benign g.29099850G>A g.31519887G>A DSG2(NM_001943.3):c.166G>A (p.V56M), DSG2(NM_001943.5):c.166G>A (p.V56M) - DSG2_000008 VKGL data sharing initiative Nederland - - - CLASSIFICATION record - - - - - - - - - - - - - - - - - - - - - - -
-?/. - c.166G>A r.(?) p.(Val56Met) - Unknown - likely benign g.29099850G>A g.31519887G>A DSG2(NM_001943.3):c.166G>A (p.V56M), DSG2(NM_001943.5):c.166G>A (p.V56M) - DSG2_000008 VKGL data sharing initiative Nederland - - - CLASSIFICATION record - - - - - - - - - - - - - - - - - - - - - - -
-?/. - c.166G>A r.(?) p.(Val56Met) - Unknown - likely benign g.29099850G>A g.31519887G>A DSG2(NM_001943.3):c.166G>A (p.V56M), DSG2(NM_001943.5):c.166G>A (p.V56M) - DSG2_000008 VKGL data sharing initiative Nederland - - - CLASSIFICATION record - - - - - - - - - - - - - - - - - - - - - - -
?/. - c.166G>A r.(?) p.(Val56Met) - Parent #1 - VUS g.29099850G>A g.31519887G>A - - DSG2_000008 conflicting interpretations of pathogenicity; 2 heterozygous, no homozygous; Clinindb (India) PubMed: Narang 2020, Journal: Narang 2020 - rs121913013 Germline - 2/2795 individuals - - - DNA arraySNP - Infinium Global Screening Array v1.0 ? - PubMed: Narang 2020, Journal: Narang 2020 analysis 2794 individuals (India) - - India - - - - - 2 Mohammed Faruq
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