NF1 c.6478A>G ;(p.K2160E)

Variant ID: 17-29664436-A-G

NM_001042492.2(NF1):c.6478A>G;(p.K2160E)

This variant was identified in 2 publications

View GRCh38 version.




Publications:


ABCA4 midigenes reveal the full splice spectrum of all reported noncanonical splice site variants in Stargardt disease.

Genome Research
Sangermano, Riccardo R; Khan, Mubeen M; Cornelis, Stéphanie S SS; Richelle, Valerie V; Albert, Silvia S; Garanto, Alejandro A; Elmelik, Duaa D; Qamar, Raheel R; Lugtenberg, Dorien D; van den Born, L Ingeborgh LI; Collin, Rob W J RWJ; Cremers, Frans P M FPM
Publication Date: 2018-01

Variant appearance in text: NF1: 6478A>G
PubMed Link: 29162642
Variant Present in the following documents:
  • 100.pdf
View BVdb publication page



Neurofibromatosis type 1-associated tumours: their somatic mutational spectrum and pathogenesis.

Human Genomics
Laycock-van Spyk, Sebastian S; Thomas, Nick N; Cooper, David N DN; Upadhyaya, Meena M
Publication Date: 2011-10

Variant appearance in text: NF1: 6478A>G
PubMed Link: 22155606
Variant Present in the following documents:
  • Main text
View BVdb publication page