MYH7 c.4036C>T ;(p.Q1346*)

Variant ID: 14-23887552-G-A

NM_000257.2(MYH7):c.4036C>T;(p.Q1346*)

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:

Pediatric cardiomyopathy: importance of genetic and metabolic evaluation.

Journal Of Cardiac Failure
Kindel, Steven J SJ; Miller, Erin M EM; Gupta, Resmi R; Cripe, Linda H LH; Hinton, Robert B RB; Spicer, Robert L RL; Towbin, Jeffrey A JA; Ware, Stephanie M SM
Publication Date: 2012-05

Variant appearance in text: MYH7: Q1346X
PubMed Link: 22555271
Variant Present in the following documents:
  • Main text
View BVdb publication page