DMD c.691T>A ;(p.Y231N)

Variant ID: X-32717369-A-T

NM_004006.2(DMD):c.691T>A;(p.Y231N)

This variant was identified in 8 publications

View GRCh38 version.




Publications:


Refinement of evolutionary medicine predictions based on clinical evidence for the manifestations of Mendelian diseases.

Scientific Reports
Šimčíková, Daniela D; Heneberg, Petr P
Publication Date: 2019-12-09

Variant appearance in text: DMD: Y231N
PubMed Link: 31819097
Variant Present in the following documents:
  • 41598_2019_54976_MOESM2_ESM.xlsx, sheet 8
View BVdb publication page



Clinical and genetic characteristics of female dystrophinopathy carriers.

Molecular Medicine Reports
Zhong, Jingzi J; Xie, Yanshu Y; Bhandari, Vidata V; Chen, Gang G; Dang, Yiwu Y; Liao, Haixia H; Zhang, Jiapeng J; Lan, Dan D
Publication Date: 2019-04

Variant appearance in text: DMD: 691T>A; Tyr231Asn
PubMed Link: 30816495
Variant Present in the following documents:
  • mmr-19-04-3035.pdf
View BVdb publication page



Structural Interface Forms and Their Involvement in Stabilization of Multidomain Proteins or Protein Complexes.

International Journal Of Molecular Sciences
Dygut, Jacek J; Kalinowska, Barbara B; Banach, Mateusz M; Piwowar, Monika M; Konieczny, Leszek L; Roterman, Irena I
Publication Date: 2016-10-18

Variant appearance in text: DMD: Y231N
PubMed Link: 27763556
Variant Present in the following documents:
  • Main text
  • ijms-17-01741.pdf
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Deletion of Dystrophin In-Frame Exon 5 Leads to a Severe Phenotype: Guidance for Exon Skipping Strategies.

Plos One
Toh, Zhi Yon Charles ZY; Thandar Aung-Htut, May M; Pinniger, Gavin G; Adams, Abbie M AM; Krishnaswarmy, Sudarsan S; Wong, Brenda L BL; Fletcher, Sue S; Wilton, Steve D SD
Publication Date: 2016

Variant appearance in text: DMD: Y231N
PubMed Link: 26745801
Variant Present in the following documents:
  • Main text
  • pone.0145620.pdf
View BVdb publication page



The Dystrophin Complex: Structure, Function, and Implications for Therapy.

Comprehensive Physiology
Gao, Quan Q QQ; McNally, Elizabeth M EM
Publication Date: 2015-07-01

Variant appearance in text: DMD: Y231N
PubMed Link: 26140716
Variant Present in the following documents:
  • Main text
View BVdb publication page



Thermodynamic stability, unfolding kinetics, and aggregation of the N-terminal actin-binding domains of utrophin and dystrophin.

Proteins
Singh, Surinder M SM; Molas, Justine F JF; Kongari, Narsimulu N; Bandi, Swati S; Armstrong, Geoffrey S GS; Winder, Steve J SJ; Mallela, Krishna M G KM
Publication Date: 2012-05

Variant appearance in text: DMD: Y231N
PubMed Link: 22275054
Variant Present in the following documents:
  • Main text
View BVdb publication page



Missense mutations in dystrophin that trigger muscular dystrophy decrease protein stability and lead to cross-beta aggregates.

Proceedings Of The National Academy Of Sciences Of The United States Of America
Singh, Surinder M SM; Kongari, Narsimulu N; Cabello-Villegas, Javier J; Mallela, Krishna M G KM
Publication Date: 2010-08-24

Variant appearance in text: DMD: Y231N
PubMed Link: 20696926
Variant Present in the following documents:
  • Main text
View BVdb publication page



Disease-causing missense mutations in actin binding domain 1 of dystrophin induce thermodynamic instability and protein aggregation.

Proceedings Of The National Academy Of Sciences Of The United States Of America
Henderson, Davin M DM; Lee, Ann A; Ervasti, James M JM
Publication Date: 2010-05-25

Variant appearance in text: DMD: Y231N
PubMed Link: 20457930
Variant Present in the following documents:
  • Main text
View BVdb publication page