Variant #0000334737 (NC_000023.10:g.77224487C>T, NC_000023.10(NM_000052.5):c.-21-2631C>T (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.77224487C>T |
| DNA change (hg38) |
g.77968990C>T |
| Published as |
PGAM4(NM_001029891.2):c.649G>A (p.(Val217Ile)) |
| ISCN |
- |
| DB-ID |
ATP7A_000359 |
| 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) |
8.0E-5 View details |
| Owner |
VKGL-NL_Leiden |
| Database submission license |
Creative Commons Attribution-NonCommercial-ShareAlike 4.0 International |
| Created by |
VKGL-NL_Leiden |
| Date created |
2018-01-15 20:58:59 +01:00 (CET) |
| Date last edited |
2020-10-01 19:36:39 +02:00 (CEST) |

Variant on transcripts
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