Full data view for gene C1S

Ehlers Danlos Syndrome Variant Database


Information The variants shown are described using the NM_001734.3 transcript reference sequence.

2 entries on 1 page. Showing entries 1 - 2.
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Effect     

Exon     

AscendingDNA change (cDNA)     

RNA change     

Protein     

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     

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VIP     

Data_av     

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Panel size     

Owner     
+/. 12 c.1789G>T r.(?) p.(Glu597*) Paternal (confirmed) - pathogenic (recessive) g.7177677G>T g.7070373G>T - - C1S_000031 Compound heterozygosity c.[1789G>T];[1889G>A] identified in the female proband and her brother Journal: Abe 2009 - - Germline yes - - - - DNA SEQ blood - C1SD - Journal: Abe 2009 - F no Japan - - - - - 2 Christian Drouet
+/. 12 c.1789G>T r.(?) p.(Glu597*) Maternal (confirmed) - pathogenic (recessive) g.7177677G>T g.7070373G>T - - C1S_000031 Proband is a compound heterozygous carrier c.[1132-1135de]l;[1789G>T], with a complete C1s deficiency; his parents and heterozygous carriers of the family are presenting with one-half of the normal antigenic C1s PubMed: Endo 1999, Journal: Endo 1999 - - Germline yes - - - - DNA SEQ blood - C1SD patient PubMed: Endo 1999, Journal: Endo 1999 - M no Japan - - - - - 1 Christian Drouet
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