FLT4 c.2300G>C ;(p.G767A)

Variant ID: 5-180047715-C-G

NM_182925.4(FLT4):c.2300G>C;(p.G767A)

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:

Variant filtering, digenic variants, and other challenges in clinical sequencing: a lesson from fibrillinopathies.

Clinical Genetics
Najafi, Arash A; Caspar, Sylvan M SM; Meienberg, Janine J; Rohrbach, Marianne M; Steinmann, Beat B; Matyas, Gabor G
Publication Date: 2020-02

Variant appearance in text: FLT4: 2300G>C; Gly767Ala
PubMed Link: 31506931
Variant Present in the following documents:
  • CGE-97-235-s002.xlsx, sheet 1
View BVdb publication page