Full data view for gene TCAP

This database is one of the gene variant databases from the Leiden Muscular Dystrophy pages
Information The variants shown are described using the NM_003673.3 transcript reference sequence.

3 entries on 1 page. Showing entries 1 - 3.
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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     

Consanguinity     

Country     

Population     

Age at death     

VIP     

Data_av     

Treatment     

Panel size     

Owner     
-?/. - c.*76G>T r.(=) p.(=) Unknown - likely benign g.37822438G>T g.39666185G>T TCAP(NM_003673.3):c.*76G>T - TCAP_000027 VKGL data sharing initiative Nederland - - - CLASSIFICATION record - - - 0 - - - - - - - - - - - - - - - - - - -
-?/. 2 c.*76G>T r.(?) p.(=) Parent #1 - likely benign g.37822438G>T g.39666185G>T g.826G>T - TCAP_000027 not in 200 control chromosomes PubMed: Andersen 2009 - - Germline - - - 0 - DNA SEQ - - CMH 19035361-PatM PubMed: Andersen 2009 only in index patients - - Denmark - - 0 - - 2 Johan den Dunnen
-?/. - c.*76G>T r.(=) p.(=) Unknown - likely benign g.37822438G>T g.39666185G>T TCAP(NM_003673.3):c.*76G>T - TCAP_000027 VKGL data sharing initiative Nederland - - - CLASSIFICATION record - - - - - - - - - - - - - - - - - - - - - - -
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