Variant #0000002735 (NC_000016.9:g.28493426C>G, CLN3(NM_000086.2):c.1056G>C)
Individual ID |
00002735 |
Chromosome |
16 |
Allele |
Unknown |
Affects function (as reported) |
Not classified |
Affects function (by curator) |
Not classified |
DNA change (genomic) (Relative to hg19 / GRCh37) |
g.28493426C>G |
Reference |
Leman et al. Hum Genet 116:236 2005 |
DB-ID |
CLN3_000040 |
Frequency |
- |
Average frequency (gnomAD v.2.1.1) |
Retrieve |
Owner |
Y Yang |
Database submission license |
Creative Commons Attribution-NonCommercial-ShareAlike 4.0 International |
Created by |
Y Yang |
Variant on transcripts
Screenings
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