MYBPC3 c.1223+1G>T

Variant ID: 11-47365042-C-A

NM_000256.3(MYBPC3):c.1223+1G>T

This variant was identified in 1 publication

View GRCh38 version.



Variant-Specific Resource Links:
gnomAD v2.1.1
Mutalizer Name Checker
Google
UCSC Genome Browser
ClinVar
dbSNP

Publications:

Array-based resequencing assay for mutations causing hypertrophic cardiomyopathy.

Clinical Chemistry
Waldmüller, Stephan S; Müller, Melanie M; Rackebrandt, Kirsten K; Binner, Priska P; Poths, Sven S; Bonin, Michael M; Scheffold, Thomas T
Publication Date: 2008-04

Variant appearance in text: MYBPC3: 1223+1G>T
PubMed Link: 18258667
Variant Present in the following documents:
  • Main text
View BVdb publication page