Variant #0000011503 (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 Blood
DNA change (genomic) (Relative to hg19 / GRCh37) -
Reference GenBank
DB-ID MYL2_00001 See all 2 reported entries
Frequency -
Variant remarks The Phe18Leu mutation was found in all clinically affected patients, in four unaffected, and in none of the three individuals with
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