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USH2A c.13016del ;(p.G4339Efs*34)
Variant ID: 1-215848236-TC-T
NM_206933.2(
USH2A
):c.13016del;(p.G4339Efs*34)
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: USH2A: 13016delG
PubMed Link:
34599366
Variant Present in the following documents:
439_2021_2371_MOESM2_ESM.xlsx, sheet 1
View BVdb publication page