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NF1 c.1022_1023insGA ;(p.I342Tfs*35)
Variant ID: 17-29527573-T-TGA
NM_001042492.2(
NF1
):c.1022_1023insGA;(p.I342Tfs*35)
This variant was identified in 2 publications
View GRCh38 version.
Variant-Specific Resource Links:
gnomAD v2.1.1
Mutalizer Name Checker
Google
UCSC Genome Browser
ClinVar
dbSNP
Publications:
Risk of Optic Pathway Glioma in Neurofibromatosis Type 1: No Evidence of Genotype-Phenotype Correlations in A Large Independent Cohort.
Cancers
Melloni, Giulia G; Eoli, Marica M; Cesaretti, Claudia C; Bianchessi, Donatella D; Ibba, Maria Cristina MC; Esposito, Silvia S; Scuvera, Giulietta G; Morcaldi, Guido G; Micheli, Roberto R; Piozzi, Elena E; Avignone, Sabrina S; Chiapparini, Luisa L; Pantaleoni, Chiara C; Natacci, Federica F; Finocchiaro, Gaetano G; Saletti, Veronica V
Publication Date: 2019-11-21
Variant appearance in text: NF1: 1022_1023insGA; Ile342Thrfs*35
PubMed Link:
31766501
Variant Present in the following documents:
Main text
cancers-11-01838.pdf
View BVdb publication page