Variant #0000002630 (NC_000011.9:g.6640040G>A, TPP1(NM_000391.3):c.196C>T)
Individual ID |
00002630 |
Chromosome |
11 |
Allele |
Unknown |
Affects function (as reported) |
Not classified |
Affects function (by curator) |
Not classified |
DNA change (genomic) (Relative to hg19 / GRCh37) |
g.6640040G>A |
Reference |
Sleat et al. 1999 Am J Hum Genet 64:1511-1523;Noher de HAc et al. 2005. Neuronal ceroid lipofuscinoses (Batten disease) in Latin America –an update, pp: 103-16.;A. Burkina pers comm |
DB-ID |
TPP1_000004 |
Frequency |
- |
Average frequency (gnomAD v.2.1.1) |
1.0E-5 View details |
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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