Variant #0000696676 (NC_000006.11:g.(161990449_162206805)_(162394450_162475122)del, PARK2(NM_004562.2):c.(618+1_619-1)_(871+1_872-1)del)

Individual ID 00313596
Chromosome 6
Allele Unknown
Affects function (as reported) Affects function
Affects function (by curator) Affects function
Classification method -
Clinical classification pathogenic
DNA change (genomic) (Relative to hg19 / GRCh37) g.(161990449_162206805)_(162394450_162475122)del
DNA change (hg38) g.(161569417_161785773)_(161973418_162054090)del
Published as c.619-?_871+?del
ISCN -
DB-ID PARK2_000097 See all 2 reported entries
Variant remarks -
Reference PubMed: Lucking 2000
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 The Parkinson's Institute - Birgitt Schuele
Database submission license No license selected
Created by The Parkinson's Institute - Birgitt Schuele
Options




Variant on transcripts


Gene     

AscendingTranscript     

Affects function     

Exon     

DNA change (cDNA)     

RNA change     

Protein     
PARK2 NM_004562.2 +/+ 5i_7i c.(618+1_619-1)_(871+1_872-1)del r.? p.?



Screenings


AscendingScreening ID     

Template     

Technique     

Tissue     

Remarks     

Genes screened     

Variants found     

Owner     
0000314768 DNA PCRq - - PARK2 1 The Parkinson's Institute - Birgitt Schuele