Variant #0000011506 (NC_000012.11:-, MYL2(NM_000432.3):c.52T>C)

Chromosome 12
Allele Unknown
Affects function (as reported) Affects function
Affects function (by curator) Not classified
Type Human cosmid
DNA change (genomic) (Relative to hg19 / GRCh37) -
Reference GenBank
DB-ID MYL2_00001 See all 2 reported entries
Frequency -
Variant remarks Detected from the mutations in the regulatory light chain.

The amino acids that are mutated, as well as he flanking sequence, show strong evolutionary conservation. The cardiac morphology in three patients from two unrelated families with the Glu22Lys mutation was strikingly similar to that seen in patients with ELC mutation.
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.52T>C - p.Phe18Leu