Variant #0000011521 (NC_000012.11:-, MYL2(NM_000432.3):c.37G>A)

Chromosome 12
Allele Unknown
Affects function (as reported) Affects function
Affects function (by curator) Not classified
Type Blood
DNA change (genomic) (Relative to hg19 / GRCh37) -
Reference GenBank
DB-ID MYL2_00003 See all 4 reported entries
Frequency -
Variant remarks The present results suggest that either the MYL2 mutation or the MYH7 mutation alone may cause HCM respectively, but the presence of both MYL2 and the MYH7 mutation may result in a more severe disease than either mutation alone as seen in the case of the proband.
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.37G>A - p.Ala13Thr