Variant #0000263338 (NC_000023.10:g.77268502G>C, NM_000052.5:c.2299G>C (ATP7A))
| Chromosome |
X |
| Allele |
Unknown |
| Affects function (as reported) |
Does not affect function |
| Affects function (by curator) |
Not classified |
| Classification method |
- |
| Clinical classification |
benign |
| DNA change (genomic) (Relative to hg19 / GRCh37) |
g.77268502G>C |
| DNA change (hg38) |
g.78013005G>C |
| Published as |
ATP7A(NM_000052.6):c.2299G>C (p.V767L), ATP7A(NM_000052.7):c.2299G>C (p.V767L) |
| ISCN |
- |
| DB-ID |
ATP7A_000289 See all 7 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) |
0.2371 View details |
| Owner |
VKGL-NL_Rotterdam |
| Database submission license |
Creative Commons Attribution-NonCommercial-ShareAlike 4.0 International |
| Created by |
VKGL-NL_Rotterdam |
| Date created |
2018-01-15 20:58:59 +01:00 (CET) |
| Date last edited |
2021-09-17 14:40:49 +02:00 (CEST) |

Variant on transcripts
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