NF1 c.3951T>G ;(p.V1317=)

Variant ID: 17-29563016-T-G

NM_001042492.2(NF1):c.3951T>G;(p.V1317=)

This variant was identified in 1 publication

View GRCh38 version.




Publications:


Targeted-capture massively-parallel sequencing enables robust detection of clinically informative mutations from formalin-fixed tumours.

Scientific Reports
Wong, Stephen Q SQ; Li, Jason J; Salemi, Renato R; Sheppard, Karen E KE; Do, Hongdo H; Tothill, Richard W RW; McArthur, Grant A GA; Dobrovic, Alexander A
Publication Date: 2013-12-13

Variant appearance in text: NF1: 3951T>G
PubMed Link: 24336498
Variant Present in the following documents:
  • Main text
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