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 |

Variant on transcripts
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