All transcript variants in gene TCF4

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

4 entries on 1 page. Showing entries 1 - 4.
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Effect     

Exon     

AscendingDNA change (cDNA)     

Haplotype     

ClassClinical     

RNA change     

Protein     

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     

Owner     
+/. 15 c.1153C>T - - r.(?) p.(Arg385*) g.52921925G>A g.55254694G>A - - TCF4_000003 - - - - Germline - - - 0 - Andreas Laner
+/. 15 c.1153C>T - - r.(?) p.(Arg385*) g.52921925G>A g.55254694G>A 1153C>T - TCF4_000003 not in 360 control chromosomes PubMed: Zweier 2007; PubMed: Peippo 2006 - - De novo - - - 0 - Johan den Dunnen
+?/+? 15 c.1153C>T - - r.(?) p.(Arg385*) g.52921925G>A g.55254694G>A - - TCF4_000003 ClinVar-ClinVar ID (RCV000007797.4) PubMed: Hamdan 2013 - - De novo - - - 0 - Irina Giurgea
+/. - c.1153C>T - pathogenic r.(?) p.(Arg385*) g.52921925G>A - TCF4(NM_001083962.1):c.1153C>T (p.Arg385*) - TCF4_000003 VKGL data sharing initiative Nederland - - - CLASSIFICATION record - - - 0 - VKGL-NL
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