MYBPC3 c.2860G>A ;(p.A954T)

Variant ID: 11-47356638-C-T

NM_000256.3(MYBPC3):c.2860G>A;(p.A954T)

This variant was identified in 1 publication

View GRCh38 version.




Publications:


Quantitative approaches to variant classification increase the yield and precision of genetic testing in Mendelian diseases: the case of hypertrophic cardiomyopathy.

Genome Medicine
Walsh, Roddy R; Mazzarotto, Francesco F; Whiffin, Nicola N; Buchan, Rachel R; Midwinter, William W; Wilk, Alicja A; Li, Nicholas N; Felkin, Leanne L; Ingold, Nathan N; Govind, Risha R; Ahmad, Mian M; Mazaika, Erica E; Allouba, Mona M; Zhang, Xiaolei X; de Marvao, Antonio A; Day, Sharlene M SM; Ashley, Euan E; Colan, Steven D SD; Michels, Michelle M; Pereira, Alexandre C AC; Jacoby, Daniel D; Ho, Carolyn Y CY; Thomson, Kate L KL; Watkins, Hugh H; Barton, Paul J R PJR; Olivotto, Iacopo I; Cook, Stuart A SA; Ware, James S JS
Publication Date: 2019-01-29

Variant appearance in text: MYBPC3: 2860G>A; A954T
PubMed Link: 30696458
Variant Present in the following documents:
  • 13073_2019_616_MOESM1_ESM.xlsx, sheet 6
View BVdb publication page