Variant #0000003567 (NC_000006.11:g.162206892T>C, PARK2(NM_004562.2):c.783A>G)
Individual ID |
00003567 |
Chromosome |
6 |
Allele |
Unknown |
Affects function (as reported) |
Not classified |
Affects function (by curator) |
Not classified |
DNA change (genomic) (Relative to hg19 / GRCh37) |
g.162206892T>C |
Reference |
Hedrich K, 2002;Clark LN, 2006;Okubadejo N, 2008;Brüggemann N, 2009 |
DB-ID |
PARK2_000119 |
Frequency |
- |
Average frequency (gnomAD v.2.1.1) |
Genomic location of variant could not be determined |
Owner |
Y Yang |
Database submission license |
Creative Commons Attribution-NonCommercial-ShareAlike 4.0 International |
Created by |
Y Yang |
Variant on transcripts
Screenings
|
|