MYH7 c.4499G>T ;(p.R1500L)

Variant ID: 14-23886382-C-A

NM_000257.2(MYH7):c.4499G>T;(p.R1500L)

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:

Population-based variation in cardiomyopathy genes.

Circulation. Cardiovascular Genetics
Golbus, Jessica R JR; Puckelwartz, Megan J MJ; Fahrenbach, John P JP; Dellefave-Castillo, Lisa M LM; Wolfgeher, Don D; McNally, Elizabeth M EM
Publication Date: 2012-08-01

Variant appearance in text: MYH7: R1500L
PubMed Link: 22763267
Variant Present in the following documents:
  • Main text
View BVdb publication page