Variant #0000011514 (NC_000012.11:-, MYL2(NM_000432.3):c.141C>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_00011 See all 2 reported entries
Frequency -
Variant remarks No other mutations were identified in this patient in the additional seven FHC genes screened. There was no family history of sudden death.
ClassClinical -
Average frequency (gnomAD v.2.1.1) Retrieve
Owner Qi Ming
Database submission license No license selected
Created by Qi Ming
Options




Variant on transcripts


Gene     

AscendingTranscript     

Affects function     

Exon     

DNA change (cDNA)     

RNA change     

Protein     
MYL2 NM_000432.3 ./. 03 c.141C>A - p.Asn47Lys