Full data view for gene DSP

Information The variants shown are described using the NM_004415.2 transcript reference sequence.

3 entries on 1 page. Showing entries 1 - 3.
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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     
+/. 24 c.6478C>T r.(?) p.(Arg2160*) - Unknown - pathogenic g.7583973C>T g.7583740C>T - - DSP_000301 not associated with ID phenotype PubMed: Gilissen 2014 - - De novo - - - - - DNA SEQ - - ID - PubMed: Gilissen 2014 - ? ? - - - - - - 1 Marianne Vos (LOVD-team)
+?/. - c.6478C>T r.(?) p.(Arg2160Ter) - Unknown - likely pathogenic g.7583973C>T g.7583740C>T DSP(NM_004415.4):c.6478C>T (p.R2160*) - DSP_000301 VKGL data sharing initiative Nederland - - - CLASSIFICATION record - - - - - - - - - - - - - - - - - - - - - - -
+?/. - c.6478C>T r.(?) p.(Arg2160Ter) - Unknown - likely pathogenic g.7583973C>T - DSP(NM_004415.4):c.6478C>T (p.R2160*) - DSP_000301 VKGL data sharing initiative Nederland - - - CLASSIFICATION record - - - - - - - - - - - - - - - - - - - - - - -
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