NF1 c.1195_1196delinsTG ;(p.A399C)

Variant ID: 17-29528438-GC-TG

NM_001042492.2(NF1):c.1195_1196delinsTG;(p.A399C)

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:

Familial Myelodysplastic/Acute Leukemia Syndromes-Myeloid Neoplasms with Germline Predisposition.

Frontiers In Oncology
Baptista, Renata Lyrio Rafael RLR; Dos Santos, Anna Cláudia Evangelista ACE; Gutiyama, Luciana Mayumi LM; Solza, Cristiana C; Zalcberg, Ilana Renault IR
Publication Date: 2017

Variant appearance in text: NF1: A399C
PubMed Link: 28955657
Variant Present in the following documents:
  • Main text
  • fonc-07-00206.pdf
View BVdb publication page