MYH7 c.1777del ;(p.W593Gfs*63)

Variant ID: 14-23896905-CA-C

NM_000257.2(MYH7):c.1777del;(p.W593Gfs*63)

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:

Impact of QT variables on clinical outcome of genotyped hypertrophic cardiomyopathy.

Annals Of Noninvasive Electrocardiology : The Official Journal Of The International Society For Holter And Noninvasive Electrocardiology, Inc
Uchiyama, Katsuharu K; Hayashi, Kenshi K; Fujino, Noboru N; Konno, Tetsuo T; Sakamoto, Yuichiro Y; Sakata, Kenji K; Kawashiri, Masa-aki MA; Ino, Hidekazu H; Yamagishi, Masakazu M
Publication Date: 2009-01

Variant appearance in text: MYH7: 1777delT
PubMed Link: 19149795
Variant Present in the following documents:
  • Main text
View BVdb publication page