Variant #0000012298 (NC_000006.11:-, PLN(NM_002667.3):c.116T>G)

Chromosome 6
Allele Unknown
Affects function (as reported) Affects function
Affects function (by curator) Not classified
Type Substitution
DNA change (genomic) (Relative to hg19 / GRCh37) -
Reference GenBank
DB-ID PLN_00003 See all 5 reported entries
Frequency -
Variant remarks Mutations in PLN, such as the L39X, are rare among

patients with HCM. However, despite the low yield of

PLN-associated HCM genetic testing, the small size of

PLN and the paucity of genetic variation in PLN

among healthy subjects warrant consideration for its

inclusion in clinically available HCM gene test panels.
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.116T>G - p.Leu39X