FBN1 c.4143G>C ;(p.K1381N)

Variant ID: 15-48766519-C-G

NM_000138.4(FBN1):c.4143G>C;(p.K1381N)

This variant was identified in 2 publications

View GRCh38 version.




Publications:


Assembly assay identifies a critical region of human fibrillin-1 required for 10-12 nm diameter microfibril biogenesis.

Plos One
Jensen, Sacha A SA; Atwa, Ondine O; Handford, Penny A PA
Publication Date: 2021

Variant appearance in text: FBN1: K1381N
PubMed Link: 33735269
Variant Present in the following documents:
  • Main text
  • pone.0248532.pdf
  • pone.0248532.s001.xlsx, sheet 1
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Identification of the minimal combination of clinical features in probands for efficient mutation detection in the FBN1 gene.

European Journal Of Human Genetics : Ejhg
Stheneur, Chantal C; Collod-Béroud, Gwenaëlle G; Faivre, Laurence L; Buyck, Jean François JF; Gouya, Laurent L; Le Parc, Jean-Marie JM; Moura, Bertrand B; Muti, Christine C; Grandchamp, Bernard B; Sultan, Gilles G; Claustres, Mireille M; Aegerter, Philippe P; Chevallier, Bertrand B; Jondeau, Guillaume G; Boileau, Catherine C
Publication Date: 2009-09

Variant appearance in text: FBN1: 4143G>C
PubMed Link: 19293843
Variant Present in the following documents:
  • Main text
View BVdb publication page