Variant #0000002612 (NC_000001.10:g.40544331C>A, PPT1(NM_000310.3):c.628-1G>T)
| Individual ID |
00002612 |
| Chromosome |
1 |
| Allele |
Unknown |
| Affects function (as reported) |
Not classified |
| Affects function (by curator) |
Not classified |
| DNA change (genomic) (Relative to hg19 / GRCh37) |
g.40544331C>A |
| Reference |
Salonen et . Hum Mut (Online)15: 279 2000;Mole et al. Eur J Paed Neurol 5 (Suppl A):7-10 2001 |
| DB-ID |
PPT1_000038 |
| 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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