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TF c.80G>A ;(p.W27*)
Variant ID: 3-133467292-G-A
NM_001063.3(
TF
):c.80G>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