Variant #0000011517 (NC_000012.11:-, MYL2(NM_000432.3):c.173G>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_00002 See all 5 reported entries
Frequency -
Variant remarks The Arg58Gln mutation was not observed in 210 control alleles subjected to SSCP analysis or in 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 ./. 04 c.173G>A - p.Arg58Gln