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.
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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     
+/. 2i c.238+2T>G r.[110_238del, 238_239ins238+1_238+36, ..] p.[Lys37_Gly80del, Gly80Ser_Ile81ins(12)] Parent #1 - pathogenic g.153640553T>G g.154412216T>G - - TAZ_000053 RNA 0.52/0.15 and some other; CL6/MLCL5 PubMed: Kirwin 2014 - - Unknown - - - - - DNA, RNA RT-PCR, SEQ - - BTHS;MGCA2 - PubMed: Kirwin 2014 BTHS M - - - - - Barth Syndrome Foundation - 1 Johan den Dunnen
+/. 2i c.238+2T>G r.[110_238del] p.Lys37_Gly80del Parent #1 - pathogenic g.153640553T>G g.154412216T>G - - TAZ_000053 CL6/MLCL5 PubMed: Johnston 1997, PubMed: Schlame 2003, PubMed: Gonzalez 2005, - - Unknown - - - - - DNA, RNA RT-PCR, SEQ - - BTHS;MGCA2 - PubMed: Johnston 1997, PubMed: Schlame 2003, PubMed: Gonzalez 2005, - M - - - - - Barth Syndrome Foundation - 1 Johan den Dunnen
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