Full data view for gene DSC2

Information The variants shown are described using the NM_004949.3 transcript reference sequence.

8 entries on 1 page. Showing entries 1 - 8.
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.351A>G r.(?) p.(Thr117=) - Unknown - benign g.28672067T>C g.31092104T>C DSC2(NM_004949.3):c.351A>G (p.T117=), DSC2(NM_004949.5):c.351A>G (p.T117=), DSC2(NM_024422.4):c.351A>G (p.T117=), DSC2(NM_024422.6):c.351A>G (p....)) - DSC2_000004 VKGL data sharing initiative Nederland - - - CLASSIFICATION record - - - - - - - - - - - - - - - - - - - - - - -
-/. - c.351A>G r.(?) p.(Thr117=) - Unknown - benign g.28672067T>C g.31092104T>C DSC2(NM_004949.3):c.351A>G (p.T117=), DSC2(NM_004949.5):c.351A>G (p.T117=), DSC2(NM_024422.4):c.351A>G (p.T117=), DSC2(NM_024422.6):c.351A>G (p....)) - DSC2_000004 VKGL data sharing initiative Nederland - - - CLASSIFICATION record - - - - - - - - - - - - - - - - - - - - - - -
-?/. - c.351A>G r.(?) p.(Thr117=) - Unknown - likely benign g.28672067T>C g.31092104T>C DSC2(NM_004949.3):c.351A>G (p.T117=), DSC2(NM_004949.5):c.351A>G (p.T117=), DSC2(NM_024422.4):c.351A>G (p.T117=), DSC2(NM_024422.6):c.351A>G (p....)) - DSC2_000004 VKGL data sharing initiative Nederland - - - CLASSIFICATION record - - - - - - - - - - - - - - - - - - - - - - -
-/. - c.351A>G r.(?) p.(Thr117=) - Unknown - benign g.28672067T>C g.31092104T>C DSC2(NM_004949.3):c.351A>G (p.T117=), DSC2(NM_004949.5):c.351A>G (p.T117=), DSC2(NM_024422.4):c.351A>G (p.T117=), DSC2(NM_024422.6):c.351A>G (p....)) - DSC2_000004 VKGL data sharing initiative Nederland - - - CLASSIFICATION record - - - - - - - - - - - - - - - - - - - - - - -
-/- 3 c.351A>G r.(?) p.(=) propeptide Unknown - benign g.28672067T>C g.31092104T>C - - DSC2_000004 - PubMed: Posch, ARVD/C database 7605 - - Germline - - - - - DNA SEQ - - ? - PubMed: Posch - - - - - - - - - 1 Paul van der Zwaag
-/. - c.351A>G r.(?) p.(Thr117=) - Unknown - benign g.28672067T>C g.31092104T>C DSC2(NM_004949.3):c.351A>G (p.T117=), DSC2(NM_004949.5):c.351A>G (p.T117=), DSC2(NM_024422.4):c.351A>G (p.T117=), DSC2(NM_024422.6):c.351A>G (p....)) - DSC2_000004 VKGL data sharing initiative Nederland - - - CLASSIFICATION record - - - - - - - - - - - - - - - - - - - - - - -
?/. - c.351A>G r.(=) p.(=) - Parent #1 - VUS g.28672067T>C g.31092104T>C - - DSC2_000004 conflicting interpretations of pathogenicity; 12 heterozygous, no homozygous; Clinindb (India) PubMed: Narang 2020, Journal: Narang 2020 - rs117812913 Germline - 12/2795 individuals - - - DNA arraySNP - Infinium Global Screening Array v1.0 ? - PubMed: Narang 2020, Journal: Narang 2020 analysis 2794 individuals (India) - - India - - - - - 12 Mohammed Faruq
-/. - c.351A>G r.(?) p.(Thr117=) - Unknown - benign g.28672067T>C - DSC2(NM_004949.3):c.351A>G (p.T117=), DSC2(NM_004949.5):c.351A>G (p.T117=), DSC2(NM_024422.4):c.351A>G (p.T117=), DSC2(NM_024422.6):c.351A>G (p....)) - DSC2_000004 VKGL data sharing initiative Nederland - - - CLASSIFICATION record - - - - - - - - - - - - - - - - - - - - - - -
Legend   How to query  


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