Variant #0000002767 (NC_000013.10:g.77574983A>G, CLN5(NM_006493.2):c.1103A>G)
Individual ID |
00002767 |
Chromosome |
13 |
Allele |
Unknown |
Affects function (as reported) |
Not classified |
Affects function (by curator) |
Not classified |
DNA change (genomic) (Relative to hg19 / GRCh37) |
g.77574983A>G |
Reference |
Savukoski et al. 1998 Nature Genetics 19:286-288;Xin et al 2010 Neurology 74:565-71 |
DB-ID |
CLN5_000027 |
Frequency |
- |
Average frequency (gnomAD v.2.1.1) |
0.14031 View details |
Owner |
Y Yang |
Database submission license |
Creative Commons Attribution-NonCommercial-ShareAlike 4.0 International |
Created by |
Y Yang |
Variant on transcripts
Screenings
|
|