Variant #0000011512 (NC_000012.11:-, MYL2(NM_000432.3):c.283C>G)

Chromosome 12
Allele Unknown
Affects function (as reported) Affects function
Affects function (by curator) Not classified
Type BL21 expression host cells; Sf9 cells
DNA change (genomic) (Relative to hg19 / GRCh37) -
Reference GenBank
DB-ID MYL2_00007 See all 2 reported entries
Frequency -
Variant remarks Associated with a particular subtype of cardiac hypertrophy defined by mid-left ventricular obstruction; decreased the Ca2+ binding affinity 3-fold compared with HCRLC-WT. P95A mutant also had an increase in alpha-helical content upon Ca2+ binding.
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 ./. 05 c.283C>G - p.Pro95Ala