All variants in the TCF4 gene

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     

RNA change     

Protein     

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     

Owner     
-?/. - c.944C>T - r.(?) p.(Ala315Val) - likely benign g.52928743G>A g.55261512G>A - - TCF4_000142 VKGL data sharing initiative Nederland - - - CLASSIFICATION record - - - 0 - VKGL-NL_Nijmegen
-?/. - c.944C>T - r.(?) p.(Ala315Val) - likely benign g.52928743G>A g.55261512G>A - - TCF4_000142 2 heterozygous, no homozygous; Clinindb (India) PubMed: Narang 2020, Journal: Narang 2020 - rs147445499 Germline - 2/2775 individuals - 0 - Mohammed Faruq
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