NRAS c.246T>A ;(p.F82L)

Variant ID: 1-115256465-A-T

NM_002524.4(NRAS):c.246T>A;(p.F82L)

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:

Automated Facial Recognition for Noonan Syndrome Using Novel Deep Convolutional Neural Network With Additive Angular Margin Loss.

Frontiers In Genetics
Yang, Hang H; Hu, Xin-Rong XR; Sun, Ling L; Hong, Dian D; Zheng, Ying-Yi YY; Xin, Ying Y; Liu, Hui H; Lin, Min-Yin MY; Wen, Long L; Liang, Dong-Po DP; Wang, Shu-Shui SS
Publication Date: 2021

Variant appearance in text: NRAS: 246T>A; F82L
PubMed Link: 34163525
Variant Present in the following documents:
  • fgene-12-669841.pdf
View BVdb publication page