Variant #0000659461 (NC_000023.10:g.77276563A>G, NM_000052.5:c.2903A>G (ATP7A))
| Chromosome |
X |
| Allele |
Unknown |
| Affects function (as reported) |
Probably does not affect function |
| Affects function (by curator) |
Not classified |
| Classification method |
- |
| Clinical classification |
likely benign |
| DNA change (genomic) (Relative to hg19 / GRCh37) |
g.77276563A>G |
| DNA change (hg38) |
g.78021066A>G |
| Published as |
ATP7A(NM_000052.6):c.2903A>G (p.E968G), ATP7A(NM_000052.7):c.2903A>G (p.E968G) |
| ISCN |
- |
| DB-ID |
ATP7A_000396 See all 4 reported entries |
| Variant remarks |
VKGL data sharing initiative Nederland |
| Reference |
- |
| ClinVar ID |
- |
| dbSNP ID |
- |
| Origin |
CLASSIFICATION record |
| Segregation |
- |
| Frequency |
- |
| Re-site |
- |
| VIP |
- |
| Methylation |
- |
| Average frequency (gnomAD v.2.1.1) |
0.00072 View details |
| Owner |
VKGL-NL_AMC |
| Database submission license |
Creative Commons Attribution-NonCommercial-ShareAlike 4.0 International |
| Created by |
VKGL-NL_AMC |
| Date created |
2020-03-23 16:13:27 +01:00 (CET) |
| Date last edited |
2022-11-01 13:01:21 +01:00 (CET) |

Variant on transcripts
|