Variant #0000011509 (NC_000012.11:-, MYL2(NM_000432.3):c.54C>A)

Chromosome 12
Allele Unknown
Affects function (as reported) Affects function
Affects function (by curator) Not classified
Type BL21 expression host cells; Sf9 cells
DNA change (genomic) (Relative to hg19 / GRCh37) -
Reference GenBank
DB-ID MYL2_00005 See all 2 reported entries
Frequency -
Variant remarks (The article doesn't mention if it's c.54C>A or c.54C>G.)

Associated with a typical form of hypertrophic cardiomyopathy, which causes increased left ventricular wall thickness and abnormal electrocardiograph find- ings with no mid-cavity obliteration; decreased the Ca2+ binding affinity ~3-fold compared with HCRLC-WT. No effect of phosphorylation on Ca2+ binding to F18L was observed.
ClassClinical -
Average frequency (gnomAD v.2.1.1) Retrieve
Owner Qi Ming
Database submission license No license selected
Created by Qi Ming
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Variant on transcripts


Gene     

AscendingTranscript     

Affects function     

Exon     

DNA change (cDNA)     

RNA change     

Protein     
MYL2 NM_000432.3 ./. 02 c.54C>A - p.Phe18Leu