FLNB c.2251G>C ;(p.G751R)

Variant ID: 3-58095354-G-C

NM_001457.3(FLNB):c.2251G>C;(p.G751R)

This variant was identified in 3 publications

View GRCh38 version.




Publications:


Phenotype and genotype in patients with Larsen syndrome: clinical homogeneity and allelic heterogeneity in seven patients.

Bmc Medical Genetics
Girisha, Katta Mohan KM; Bidchol, Abdul Mueed AM; Graul-Neumann, Luitgard L; Gupta, Ashish A; Hehr, Ute U; Lessel, Davor D; Nader, Sean S; Shah, Hitesh H; Wickert, Julia J; Kutsche, Kerstin K
Publication Date: 2016-04-06

Variant appearance in text: FLNB: Gly751Arg
PubMed Link: 27048506
Variant Present in the following documents:
  • Main text
  • 12881_2016_Article_290.pdf
View BVdb publication page



Reproducible Analysis of Post-Translational Modifications in Proteomes--Application to Human Mutations.

Plos One
Holehouse, Alex S AS; Naegle, Kristen M KM
Publication Date: 2015

Variant appearance in text: rs28937587
PubMed Link: 26659599
Variant Present in the following documents:
  • pone.0144692.s002.xlsx, sheet 1
View BVdb publication page



GESPA: classifying nsSNPs to predict disease association.

Bmc Bioinformatics
Khurana, Jay K JK; Reeder, Jay E JE; Shrimpton, Antony E AE; Thakar, Juilee J
Publication Date: 2015-07-25

Variant appearance in text: FLNB: G751R
PubMed Link: 26206375
Variant Present in the following documents:
  • 12859_2015_673_MOESM1_ESM.xls, sheet 4
View BVdb publication page