NF1 c.915_918del ;(p.K305Nfs*11)

Variant ID: 17-29527466-AAGCT-A

NM_001042492.2(NF1):c.915_918del;(p.K305Nfs*11)

This variant was identified in 1 publication

View GRCh38 version.




Publications:


Whole-exome sequencing identifies somatic ATRX mutations in pheochromocytomas and paragangliomas.

Nature Communications
Fishbein, Lauren L; Khare, Sanika S; Wubbenhorst, Bradley B; DeSloover, Daniel D; D'Andrea, Kurt K; Merrill, Shana S; Cho, Nam Woo NW; Greenberg, Roger A RA; Else, Tobias T; Montone, Kathleen K; LiVolsi, Virginia V; Fraker, Douglas D; Daber, Robert R; Cohen, Debbie L DL; Nathanson, Katherine L KL
Publication Date: 2015-01-21

Variant appearance in text: NF1: 915_918del
PubMed Link: 25608029
Variant Present in the following documents:
  • Main text
  • NIHMS650280-supplement-1.pdf
View BVdb publication page