FBN1 c.4223G>T ;(p.C1408F)

Variant ID: 15-48764861-C-A

NM_000138.4(FBN1):c.4223G>T;(p.C1408F)

This variant was identified in 2 publications

View GRCh38 version.




Publications:


Next-generation sequencing for diagnosis of thoracic aortic aneurysms and dissections: diagnostic yield, novel mutations and genotype phenotype correlations.

Journal Of Translational Medicine
Poninska, J K JK; Bilinska, Z T ZT; Franaszczyk, M M; Michalak, E E; Rydzanicz, M M; Szpakowski, E E; Pollak, A A; Milanowska, B B; Truszkowska, G G; Chmielewski, P P; Sioma, A A; Janaszek-Sitkowska, H H; Klisiewicz, A A; Michalowska, I I; Makowiecka-Ciesla, M M; Kolsut, P P; Stawinski, P P; Foss-Nieradko, B B; Szperl, M M; Grzybowski, J J; Hoffman, P P; Januszewicz, A A; Kusmierczyk, M M; Ploski, R R
Publication Date: 2016-05-04

Variant appearance in text: FBN1: 4223G>T; C1408F
PubMed Link: 27146836
Variant Present in the following documents:
  • Main text
  • 12967_2016_Article_870.pdf
View BVdb publication page



The molecular genetics of Marfan syndrome and related disorders.

Journal Of Medical Genetics
Robinson, P N PN; Arteaga-Solis, E E; Baldock, C C; Collod-BĂ©roud, G G; Booms, P P; De Paepe, A A; Dietz, H C HC; Guo, G G; Handford, P A PA; Judge, D P DP; Kielty, C M CM; Loeys, B B; Milewicz, D M DM; Ney, A A; Ramirez, F F; Reinhardt, D P DP; Tiedemann, K K; Whiteman, P P; Godfrey, M M
Publication Date: 2006-10

Variant appearance in text: FBN1: C1408F
PubMed Link: 16571647
Variant Present in the following documents:
  • Main text
View BVdb publication page