Full data view for gene TAZ

The variants collected by the Barth Syndrome Foundation were used to initiate this database
Information The variants shown are described using the NM_000116.3 transcript reference sequence.

2 entries on 1 page. Showing entries 1 - 2.
Legend   How to query  

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     
+/. 6 c.535C>G r.(?) p.(Pro179Ala) Parent #1 - pathogenic g.153647956C>G g.154419617C>G - - TAZ_000134 MYBPC3 Glu119Lys - VUS & two TTN VUS DB Barth Syndrome Foundation Harvard Partners (USA) - - Unknown - - - - - DNA SEQ - - BTHS;MGCA2 - DB Barth Syndrome Foundation Harvard Partners (USA) - M - United States - - - Barth Syndrome Foundation - 1 Johan den Dunnen
+?/. - c.535C>G r.(?) p.(Pro179Ala) Unknown - likely pathogenic g.153647956C>G g.154419617C>G - - TAZ_000134 variant assumed de novo PubMed: Hertz 2015, Journal: Hertz 2015 - - De novo - - - - - DNA SEQ-NG-I Blood - SIDS - PubMed: Hertz 2015, Journal: Hertz 2015 - F ? Denmark Denmark 00y00m - - - 1 Christin Hertz
Legend   How to query  


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