Variant #0000012296 (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 This result indicated that PLN gene mutation may not be a common cause for DCM in the Chinese population in Chengdu.
ClassClinical -
Average frequency (gnomAD v.2.1.1) Retrieve
Owner Qi Ming
Database submission license No license selected
Created by Qi Ming
Options




Variant on transcripts


Gene     

AscendingTranscript     

Affects function     

Exon     

DNA change (cDNA)     

RNA change     

Protein     
PLN NM_002667.3 ./. 02 c.116T>G - p.Leu39X