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MYH7 c.1516A>T ;(p.I506F)
Variant ID: 14-23897771-T-A
NM_000257.2(
MYH7
):c.1516A>T;(p.I506F)
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:
Rare variants in genes encoding MuRF1 and MuRF2 are modifiers of hypertrophic cardiomyopathy.
International Journal Of Molecular Sciences
Su, Ming M; Wang, Jizheng J; Kang, Lianming L; Wang, Yilu Y; Zou, Yubao Y; Feng, Xinxing X; Wang, Dong D; Ahmad, Ferhaan F; Zhou, Xianliang X; Hui, Rutai R; Song, Lei L
Publication Date: 2014-05-26
Variant appearance in text: MYH7: 1516A>T
PubMed Link:
24865491
Variant Present in the following documents:
Main text
ijms-15-09302.pdf
View BVdb publication page