Bibliome.ai browser hg19
Search
About
Stats
FAQ
NF1 c.1062+2T>G
Variant ID: 17-29527615-T-G
NM_001042492.2(
NF1
):c.1062+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:
Multilocus Inherited Neoplasia Allele Syndrome (MINAS): an update.
European Journal Of Human Genetics : Ejhg
McGuigan, Anthony A; Whitworth, James J; Andreou, Avgi A; Hearn, Timothy T; , ; Tischkowitz, Marc M; Maher, Eamonn R ER
Publication Date: 2022-03
Variant appearance in text: NF1: 1062+2T>G
PubMed Link:
34983940
Variant Present in the following documents:
41431_2021_1013_MOESM1_ESM.pdf
View BVdb publication page