Variant #0000001332 (NC_000017.10:g.44051754T>C, MAPT(NM_005910.5):c.224T>C)
| Individual ID |
00001332 |
| Chromosome |
17 |
| Allele |
Unknown |
| Affects function (as reported) |
Not classified |
| Affects function (by curator) |
Not classified |
| DNA change (genomic) (Relative to hg19 / GRCh37) |
g.44051754T>C |
| Reference |
Gallo M1, Tomaino C, Puccio G, Frangipane F, Curcio SA, Bernardi L, Geracitano S, Anfossi M, Mirabelli M, Colao R, Vasso F, Smirne N, Maletta RG, Bruni AC.(2010) |
| DB-ID |
MAPT_000022 |
| Frequency |
- |
| Average frequency (gnomAD v.2.1.1) |
0 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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