All transcript variants in gene TCF4

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

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Effect     

Exon     

AscendingDNA change (cDNA)     

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     
+/. - c.1134del pathogenic r.(?) p.(Leu379Tyrfs*12) g.52924560del - TCF4(NM_001243236,NM_001243235,NM_001243234,NM_001243232,NM_001243233,NM_001243231,NM_001083962,NM_003199,NM_001243230,NM_001243228,NM_001243227,N...) - TCF4_000139 VKGL data sharing initiative Nederland - - - CLASSIFICATION record - - - 0 - VKGL-NL
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