Variant #0000003984 (NC_000023.10:g.153297718C>T, MECP2(NM_004992.3):c.317G>A)
| Individual ID |
00003984 |
| Chromosome |
X |
| Allele |
Unknown |
| Affects function (as reported) |
Not classified |
| Affects function (by curator) |
Not classified |
| DNA change (genomic) (Relative to hg19 / GRCh37) |
g.153297718C>T |
| Reference |
Bienvenu T1, CarriƩ A, de Roux N, Vinet MC, Jonveaux P, Couvert P, Villard L, Arzimanoglou A, Beldjord C, Fontes M, Tardieu M, Chelly J.(2000) |
| DB-ID |
MECP2_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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