Variant #0000443256 (NC_000017.10:g.15142880del, PMP22(NM_000304.3):c.227del)

Individual ID 00210579
Chromosome 17
Allele Unknown
Affects function (as reported) Affects function
Affects function (by curator) Not classified
Classification method -
Clinical classification pathogenic
DNA change (genomic) (Relative to hg19 / GRCh37) g.15142880del
DNA change (hg38) g.15239563del
Published as 227delG
ISCN -
DB-ID PMP22_000017
Variant remarks -
Reference PubMed: Luigetti 2008
ClinVar ID -
dbSNP ID -
Origin Germline
Segregation -
Frequency -
Re-site -
VIP 0
Methylation -
Average frequency (gnomAD v.2.1.1) Variant not found in online data sets
Owner Johan den Dunnen
Database submission license Creative Commons Attribution-NonCommercial-ShareAlike 4.0 InternationalCreative Commons License
Created by Johan den Dunnen
Options




Variant on transcripts


Gene     

AscendingTranscript     

Affects function     

Exon     

DNA change (cDNA)     

RNA change     

Protein     
PMP22 NM_000304.3 +/. 4 c.227del r.(?) p.(Ser76Thrfs*35)



Screenings


AscendingScreening ID     

Template     

Technique     

Tissue     

Remarks     

Genes screened     

Variants found     

Owner     
0000211655 DNA SEQ - - PMP22 1 Johan den Dunnen