MYH7 c.1493del ;(p.Q498Rfs*49)

Variant ID: 14-23897794-CT-C

NM_000257.2(MYH7):c.1493del;(p.Q498Rfs*49)

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:

Retrospective analysis of clinical phenotype and prognosis of hypertrophic cardiomyopathy complicated with hypertension.

Scientific Reports
Luo, Qin Q; Chen, Jin J; Zhang, Tianhua T; Tang, Xiaoyu X; Yu, Bilian B
Publication Date: 2020-01-15

Variant appearance in text: MYH7: 1493delA
PubMed Link: 31941943
Variant Present in the following documents:
  • Main text
  • 41598_2019_Article_57230.pdf
View BVdb publication page