FBN1 c.3964G>A ;(p.D1322N)

Variant ID: 15-48773852-C-T

NM_000138.4(FBN1):c.3964G>A;(p.D1322N)

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: 3964G>A; Asp1322Asn
PubMed Link: 33735269
Variant Present in the following documents:
  • pone.0248532.s001.xlsx, sheet 1
View BVdb publication page



The clinical spectrum of missense mutations of the first aspartic acid of cbEGF-like domains in fibrillin-1 including a recessive family.

Human Mutation
Hilhorst-Hofstee, Yvonne Y; Rijlaarsdam, Marry E B ME; Scholte, Arthur J H A AJ; Swart-van den Berg, Marietta M; Versteegh, Michel I M MI; van der Schoot-van Velzen, Iris I; Schäbitz, Hans-Joachim HJ; Bijlsma, Emilia K EK; Baars, Marieke J MJ; Kerstjens-Frederikse, Wilhelmina S WS; Giltay, Jacques C JC; Hamel, Ben C BC; Breuning, Martijn H MH; Pals, Gerard G
Publication Date: 2010-12

Variant appearance in text: FBN1: 3964G>A; Asp1322Asn
PubMed Link: 20886638
Variant Present in the following documents:
  • Main text
  • humu0031-E1915.pdf
View BVdb publication page