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NF1 c.1139T>G ;(p.L380R)
Variant ID: 17-29528131-T-G
NM_001042492.2(
NF1
):c.1139T>G;(p.L380R)
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:
Germline Predisposition to Hematolymphoid Neoplasia.
American Journal Of Clinical Pathology
Weinberg, Olga K OK; Kuo, Frank F; Calvo, Katherine R KR
Publication Date: 2019-08-01
Variant appearance in text: NF1: 1139T>G; Leu380Arg
PubMed Link:
31309983
Variant Present in the following documents:
Main text
View BVdb publication page