MYBPC3 c.505+6T>G

Variant ID: 11-47371559-A-C

NM_000256.3(MYBPC3):c.505+6T>G

This variant was identified in 1 publication

View GRCh38 version.




Publications:


Identification of an elusive spliceogenic MYBPC3 variant in an otherwise genotype-negative hypertrophic cardiomyopathy pedigree.

Scientific Reports
Torrado, Mario M; Maneiro, Emilia E; Lamounier Junior, Arsonval A; Fernández-Burriel, Miguel M; Sánchez Giralt, Sara S; Martínez-Carapeto, Ana A; Cazón, Laura L; Santiago, Elisa E; Ochoa, Juan Pablo JP; McKenna, William J WJ; Santomé, Luis L; Monserrat, Lorenzo L
Publication Date: 2022-05-04

Variant appearance in text: MYBPC3: 505+6T>G
PubMed Link: 35508642
Variant Present in the following documents:
  • Main text
  • 41598_2022_11159_MOESM1_ESM.pdf
  • 41598_2022_Article_11159.pdf
View BVdb publication page