NF1 c.3928_3930inv ;(p.T1310C)

Variant ID: 17-29562993-ACA-TGT

NM_001042492.2(NF1):c.3928_3930inv;(p.T1310C)

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:

A genome-wide analysis of colorectal cancer in a child with Noonan syndrome.

Pediatric Blood & Cancer
Prasad, Rahul M RM; Mody, Rajen J RJ; Myers, George G; Mullins, Melisa M; Naji, Zaher Z; Geiger, James D JD
Publication Date: 2018-11

Variant appearance in text: NF1: T1310C
PubMed Link: 30039904
Variant Present in the following documents:
  • Main text
View BVdb publication page