All variants in the TF gene

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

2 entries on 1 page. Showing entries 1 - 2.
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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     
+/. - c.2012G>A r.(?) p.(Gly671Glu) - pathogenic g.133496032G>A g.133777188G>A - - TF_000014 1 heterozygous, no homozygous; Clinindb (India) PubMed: Narang 2020, Journal: Narang 2020 - rs121918677 Germline - 1/2795 individuals - 0 - Mohammed Faruq
-?/. - c.2012G>A r.(?) p.(Gly671Glu) - likely benign g.133496032G>A - TF(NM_001354703.1):c.1880G>A (p.G627E) - TF_000014 VKGL data sharing initiative Nederland - - - CLASSIFICATION record - - - - - VKGL-NL_Rotterdam
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