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MYH7 c.1922G>A ;(p.G641D)
Variant ID: 14-23896483-C-T
NM_000257.2(
MYH7
):c.1922G>A;(p.G641D)
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:
Unequal allelic expression of wild-type and mutated β-myosin in familial hypertrophic cardiomyopathy.
Basic Research In Cardiology
Tripathi, Snigdha S; Schultz, Imke I; Becker, Edgar E; Montag, Judith J; Borchert, Bianca B; Francino, Antonio A; Navarro-Lopez, Francisco F; Perrot, Andreas A; Özcelik, Cemil C; Osterziel, Karl-Josef KJ; McKenna, William J WJ; Brenner, Bernhard B; Kraft, Theresia T
Publication Date: 2011-11
Variant appearance in text: MYH7: 1922G>A
PubMed Link:
21769673
Variant Present in the following documents:
Main text
View BVdb publication page