All variants in the TF gene

Information The variants shown are described using the NM_001063.3 transcript reference sequence.

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Effect     

Exon     

AscendingDNA change (cDNA)     

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     
+?/? 13i c.1623-63del r.spl? p.(?) - likely pathogenic g.133489289del g.133770445del 293-63del - TF_000012 in silico analysis indicate that this deletion is predicted to generate a higher score cryptic branch point leading to the production of an altered mRNA molecule - - - Germline - - - 0 - Yessine Amri
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