Variant #0000002628 (NC_000011.9:g.6640423T>C, TPP1(NM_000391.3):c.89+4A>G)
| Individual ID |
00002628 |
| Chromosome |
11 |
| Allele |
Unknown |
| Affects function (as reported) |
Not classified |
| Affects function (by curator) |
Not classified |
| DNA change (genomic) (Relative to hg19 / GRCh37) |
g.6640423T>C |
| Reference |
Noher de HAc et al.2005. Neuronal ceroid lipofuscinoses (Batten disease) in LatinAmerica –an update, pp: 103-16. |
| DB-ID |
TPP1_000002 |
| 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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