NF1 c.34_36delinsTGG ;(p.A12W)

Variant ID: 17-29422361-GCC-TGG

NM_001042492.2(NF1):c.34_36delinsTGG;(p.A12W)

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:

Genetic mutation and biological pathway prediction based on whole slide images in breast carcinoma using deep learning.

Npj Precision Oncology
Qu, Hui H; Zhou, Mu M; Yan, Zhennan Z; Wang, He H; Rustgi, Vinod K VK; Zhang, Shaoting S; Gevaert, Olivier O; Metaxas, Dimitris N DN
Publication Date: 2021-09-23

Variant appearance in text: NF1: A12W
PubMed Link: 34556802
Variant Present in the following documents:
  • 41698_2021_225_MOESM1_ESM.pdf
View BVdb publication page