Variant #0000012302 (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 It cannot be determined

whether R13 or R14 is deleted because the codon for each is identical. The deletion of either R13 or R14 is expected

to partially disrupt the stability of the pentamer structure of

this 52 amino acid protein.
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.39_42delAAGAinsG - p.Arg14del