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BDNF c.235_236delinsGT ;(p.P79V)
Variant ID: 11-27679876-GG-AC
NM_001709.4(
BDNF
):c.235_236delinsGT;(p.P79V)
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:
Opportunities and challenges for the use of induced pluripotent stem cells in modelling neurodegenerative disease.
Open Biology
Wu, Yi-Ying YY; Chiu, Feng-Lan FL; Yeh, Chan-Shien CS; Kuo, Hung-Chih HC
Publication Date: 2019-01-31
Variant appearance in text: BDNF: P79V
PubMed Link:
30958120
Variant Present in the following documents:
Main text
rsob-9-180177.pdf
View BVdb publication page