NF1 c.1501C>T ;(p.H501Y)

Variant ID: 17-29541577-C-T

NM_001042492.2(NF1):c.1501C>T;(p.H501Y)

This variant was identified in 2 publications

View GRCh38 version.




Publications:


Mutually exclusive genetic interactions and gene essentiality shape the genomic landscape of primary melanoma.

The Journal Of Pathology
BirkeƤlv, Sofia S; Harland, Mark M; Matsuyama, Larissa Satiko Alcantara Sekimoto LSAS; Rashid, Mamun M; Mehta, Ishan I; Laye, Jonathan P JP; Haase, Kerstin K; Mell, Tracey T; Iyer, Vivek V; Robles-Espinoza, Carla Daniela CD; McDermott, Ultan U; van Loo, Peter P; Kuijjer, Marieke L ML; Possik, Patricia A PA; Maria Engler, Silvya Stuchi SS; Bishop, D Timothy DT; Newton-Bishop, Julia J; Adams, David J DJ
Publication Date: 2022-10-11

Variant appearance in text: NF1: 1501C>T; H501Y
PubMed Link: 36219477
Variant Present in the following documents:
  • PATH-259-56-s004.xlsx, sheet 2
View BVdb publication page



Clinical impact of subclonal EGFR T790M mutations in advanced-stage EGFR-mutant non-small-cell lung cancers.

Nature Communications
Vaclova, Tereza T; Grazini, Ursula U; Ward, Lewis L; O'Neill, Daniel D; Markovets, Aleksandra A; Huang, Xiangning X; Chmielecki, Juliann J; Hartmaier, Ryan R; Thress, Kenneth S KS; Smith, Paul D PD; Barrett, J Carl JC; Downward, Julian J; de Bruin, Elza C EC
Publication Date: 2021-03-19

Variant appearance in text: NF1: 1501C>T; H501Y
PubMed Link: 33741979
Variant Present in the following documents:
  • 41467_2021_22057_MOESM1_ESM.pdf
View BVdb publication page