NF1 c.688del ;(p.E230Nfs*51)

Variant ID: 17-29508761-TG-T

NM_001042492.2(NF1):c.688del;(p.E230Nfs*51)

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:

Effective identification of cancer predisposition syndromes in children with cancer employing a questionnaire.

Familial Cancer
Schwermer, Miriam M; Behnert, Astrid A; Dörgeloh, Beate B; Ripperger, Tim T; Kratz, Christian P CP
Publication Date: 2021-10

Variant appearance in text: NF1: 688del
PubMed Link: 33651299
Variant Present in the following documents:
  • Main text
View BVdb publication page


Effective identification of cancer predisposition syndromes in children with cancer employing a questionnaire.

Familial Cancer
Schwermer, Miriam M; Behnert, Astrid A; Dörgeloh, Beate B; Ripperger, Tim T; Kratz, Christian P CP
Publication Date: 2021-10

Variant appearance in text: NF1: 688del
PubMed Link: 33651299
Variant Present in the following documents:
  • Main text
View BVdb publication page