FLT4 c.3331+1G>T

Variant ID: 5-180041067-C-A

NM_182925.4(FLT4):c.3331+1G>T

This variant was identified in 2 publications

View GRCh38 version.




Publications:


Evaluating High-Confidence Genes in Conotruncal Cardiac Defects by Gene Burden Analyses.

Journal Of The American Heart Association
Chui, Martin M C MMC; Mak, Christopher C Y CCY; Yu, Mullin H C MHC; Wong, Sandra Y Y SYY; Lun, Kin-Shing KS; Yung, Tak-Cheung TC; Kwong, Anna K Y AKY; Chow, Pak-Cheong PC; Chung, Brian H Y BHY
Publication Date: 2023-02-15

Variant appearance in text: FLT4: 3331+1G>T
PubMed Link: 36789878
Variant Present in the following documents:
  • JAH3-12-e028226.pdf
View BVdb publication page



Haploinsufficiency of vascular endothelial growth factor related signaling genes is associated with tetralogy of Fallot.

Genetics In Medicine : Official Journal Of The American College Of Medical Genetics
Reuter, Miriam S MS; Jobling, Rebekah R; Chaturvedi, Rajiv R RR; Manshaei, Roozbeh R; Costain, Gregory G; Heung, Tracy T; Curtis, Meredith M; Hosseini, S Mohsen SM; Liston, Eriskay E; Lowther, Chelsea C; Oechslin, Erwin E; Sticht, Heinrich H; Thiruvahindrapuram, Bhooma B; Mil, Spencer van SV; Wald, Rachel M RM; Walker, Susan S; Marshall, Christian R CR; Silversides, Candice K CK; Scherer, Stephen W SW; Kim, Raymond H RH; Bassett, Anne S AS
Publication Date: 2019-04

Variant appearance in text: FLT4: 3331+1G>T
PubMed Link: 30232381
Variant Present in the following documents:
  • Main text
  • 41436_2018_Article_260.pdf
View BVdb publication page