Variant #0000002352 (NC_000023.10:g.77287051G>T, ATP7A(NM_000052.6):c.1089G>T)
| Individual ID |
00002352 |
| Chromosome |
X |
| Allele |
Unknown |
| Affects function (as reported) |
Not classified |
| Affects function (by curator) |
Not classified |
| DNA change (genomic) (Relative to hg19 / GRCh37) |
g.77287051G>T |
| Reference |
Wang Q1, Ding Y, Wang JM, Huang QH, Zhao CF, Liu YP, Li XY, Wu TF, Song JQ, Wang YJ, Yang YL.(2014) |
| DB-ID |
ATP7A_000120 |
| 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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