Full data view for gene TCF4

Information The variants shown are described using the NM_001083962.1 transcript reference sequence.

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

Exon     

AscendingDNA change (cDNA)     

Haplotype     

ClassClinical     

RNA change     

Protein     

Allele     

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/Death     

VIP     

Data_av     

Treatment     

Panel size     

Owner     
+/. 8 c.514_517del - - r.(?) p.(Lys172Phefs*61) Parent #1 g.53017622_53017625del g.55350391_55350394del - - TCF4_000047 - - - - De novo - - - 0 - DNA SEQ - - PTHS - - - F - - - - 0 - - 1 Irina Giurgea
+?/+? 8 c.514_517del - - r.(?) p.(Lys172Phefs*61) Parent #1 g.53017622_53017625del g.55350391_55350394del - - TCF4_000047 ClinVar-ClinVar ID (RCV000079461.4) PubMed: Redin 2014 - - De novo - - - 0 - DNA SEQ - - ID - PubMed: Redin 2014 - - - - - - 0 - - 1 Irina Giurgea
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