NF1 c.888+2T>G

Variant ID: 17-29509685-T-G

NM_001042492.2(NF1):c.888+2T>G

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:

Analytical Performance of NGS-Based Molecular Genetic Tests Used in the Diagnostic Workflow of Pheochromocytoma/Paraganglioma.

Cancers
Sarkadi, Balazs B; Liko, Istvan I; Nyiro, Gabor G; Igaz, Peter P; Butz, Henriett H; Patocs, Attila A
Publication Date: 2021-08-22

Variant appearance in text: NF1: 888+2T>G
PubMed Link: 34439371
Variant Present in the following documents:
  • Main text
  • cancers-13-04219.pdf
View BVdb publication page