BDNF c.302C>A ;(p.P101H)

Variant ID: 11-27679810-G-T

NM_001709.4(BDNF):c.302C>A;(p.P101H)

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:

From Function to Phenotype: Impaired DNA Binding and Clustering Correlates with Clinical Severity in Males with Missense Mutations in MECP2.

Scientific Reports
Sheikh, Taimoor I TI; Ausió, Juan J; Faghfoury, Hannah H; Silver, Josh J; Lane, Jane B JB; Eubanks, James H JH; MacLeod, Patrick P; Percy, Alan K AK; Vincent, John B JB
Publication Date: 2016-12-08

Variant appearance in text: BDNF: P101H
PubMed Link: 27929079
Variant Present in the following documents:
  • Main text
  • srep38590.pdf
View BVdb publication page