TF c.81G>A ;(p.W27*)

Variant ID: 3-133467293-G-A

NM_001063.3(TF):c.81G>A;(p.W27*)

This variant was identified in 1 publication

View GRCh38 version.



Variant-Specific Resource Links:
gnomAD v2.1.1
Mutalizer Name Checker
Google
UCSC Genome Browser
ClinVar
dbSNP

Publications:

The genetic etiology of hearing loss in Japan revealed by the social health insurance-based genetic testing of 10K patients.

Human Genetics
Usami, Shin-Ichi SI; Nishio, Shin-Ya SY
Publication Date: 2022-04

Variant appearance in text: TF: Trp27Ter
PubMed Link: 34599366
Variant Present in the following documents:
  • 439_2021_Article_2371.pdf
View BVdb publication page