Full data view for gene DSG2

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

8 entries on 1 page. Showing entries 1 - 8.
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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     

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VIP     

Data_av     

Treatment     

Panel size     

Owner     
-/. - c.2137G>A r.(?) p.(Glu713Lys) - Unknown - benign g.29122618G>A g.31542655G>A DSG2(NM_001943.3):c.2137G>A (p.E713K), DSG2(NM_001943.5):c.2137G>A (p.E713K), DSG2-AS1(NR_045216.1):n.1811-334C>T - DSG2_000045 VKGL data sharing initiative Nederland - - - CLASSIFICATION record - - - - - - - - - - - - - - - - - - - - - - -
-/. - c.2137G>A r.(?) p.(Glu713Lys) - Unknown - benign g.29122618G>A g.31542655G>A DSG2(NM_001943.3):c.2137G>A (p.E713K), DSG2(NM_001943.5):c.2137G>A (p.E713K), DSG2-AS1(NR_045216.1):n.1811-334C>T - DSG2_000045 VKGL data sharing initiative Nederland - - - CLASSIFICATION record - - - - - - - - - - - - - - - - - - - - - - -
-/. - c.2137G>A r.(?) p.(Glu713Lys) - Unknown - benign g.29122618G>A g.31542655G>A DSG2(NM_001943.3):c.2137G>A (p.E713K), DSG2(NM_001943.5):c.2137G>A (p.E713K), DSG2-AS1(NR_045216.1):n.1811-334C>T - DSG2_000045 VKGL data sharing initiative Nederland - - - CLASSIFICATION record - - - - - - - - - - - - - - - - - - - - - - -
-/. - c.2137G>A r.(?) p.(Glu713Lys) - Unknown - benign g.29122618G>A g.31542655G>A DSG2(NM_001943.3):c.2137G>A (p.E713K), DSG2(NM_001943.5):c.2137G>A (p.E713K), DSG2-AS1(NR_045216.1):n.1811-334C>T - DSG2_000045 VKGL data sharing initiative Nederland - - - CLASSIFICATION record - - - - - - - - - - - - - - - - - - - - - - -
-/- 14 c.2137G>A r.(?) p.(Glu713Lys) Intracellular cadherin segment Unknown - benign g.29122618G>A g.31542655G>A - - DSG2_000045 - PubMed: Posch, ARVD/C database 7569 - - Germline - - - - - DNA SEQ - - ? - PubMed: Posch - - - - - - - - - 1 Paul van der Zwaag
+/- 14 c.2137G>A r.(?) p.(Glu713Lys) Intracellular cadherin segment Unknown - pathogenic g.29122618G>A g.31542655G>A - - DSG2_000045 - PubMed: Basso, ARVD/C database 7569 - - Germline - - - - - DNA SEQ - - ARVD/C - PubMed: Basso - - - - - - - - - 1 Paul van der Zwaag
+?/- 14 c.2137G>A r.(?) p.(Glu713Lys) Intracellular cadherin segment Unknown - likely pathogenic g.29122618G>A g.31542655G>A - - DSG2_000045 - PubMed: Yu, ARVD/C database 7569 - - Germline - - - - - DNA SEQ - - ARVD/C - PubMed: Yu - - - - - - - - - 1 Paul van der Zwaag
-/- 14 c.2137G>A r.(?) p.(Glu713Lys) Intracellular cadherin segment Unknown - benign g.29122618G>A g.31542655G>A - - DSG2_000045 - PubMed: Milting, ARVD/C database 7569 - - Germline - - - - - DNA SEQ - - ? - PubMed: Milting - - - - - - - - - 1 Paul van der Zwaag
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