NF1 c.3572C>G ;(p.T1191R)

Variant ID: 17-29560095-C-G

NM_001042492.2(NF1):c.3572C>G;(p.T1191R)

This variant was identified in 1 publication

View GRCh38 version.




Publications:


Increased rate of missense/in-frame mutations in individuals with NF1-related pulmonary stenosis: a novel genotype-phenotype correlation.

European Journal Of Human Genetics : Ejhg
Ben-Shachar, Shay S; Constantini, Shlomi S; Hallevi, Hen H; Sach, Emma K EK; Upadhyaya, Meena M; Evans, Gareth D GD; Huson, Susan M SM
Publication Date: 2013-05

Variant appearance in text: NF1: 3572C>G; T1191R
PubMed Link: 23047742
Variant Present in the following documents:
  • Main text
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