Variant #0000012299 (NC_000006.11:-, PLN(NM_002667.3):c.39_42delAAGAinsG)

Chromosome 6
Allele Unknown
Affects function (as reported) Affects function
Affects function (by curator) Not classified
Type Insertion/Deletion
DNA change (genomic) (Relative to hg19 / GRCh37) -
Reference GenBank
DB-ID PLN_00011 See all 2 reported entries
Frequency -
Variant remarks chronic suppression of either

basal SERCA2a activity (PLN-R14Del mutant) or the stimulatory

effect of the -adrenergic signaling pathway (PLN-R9C mutant)

(11) result in human cardiomyopathy and heart failure;absence of PLN inhibition by the PLN-L39stop mutant,

associated with the lack of regulatory inhibition of SERCA2a and

increased cardiac work, may also result in heart failure.
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     
PLN NM_002667.3 ./. 02 c.39_42delAAGAinsG - p.Arg14del