FLT4 c.2577G>T ;(p.V859=)

Variant ID: 5-180046735-C-A

NM_182925.4(FLT4):c.2577G>T;(p.V859=)

This variant was identified in 1 publication

View GRCh38 version.




Publications:


Case Report: The novel hemizygous mutation in the SSR4 gene caused congenital disorder of glycosylation type iy: A case study and literature review.

Frontiers In Genetics
Wang, Jun J; Gou, Xingqing X; Wang, Xiyi X; Zhang, Jing J; Zhao, Nan N; Wang, Xiaohong X
Publication Date: 2022

Variant appearance in text: FLT4: V859V; rs1349433335
PubMed Link: 36386804
Variant Present in the following documents:
  • Table1.xls, sheet 1
View BVdb publication page