Variant #0001060437 (NC_000013.10:g.113514610_113514612delinsAAG, NM_015205.2:c.2737_2739delinsAAG (ATP11A))
| Chromosome |
13 |
| Allele |
Unknown |
| Affects function (as reported) |
Affects function |
| Affects function (by curator) |
Not classified |
| Classification method |
- |
| Clinical classification |
NA |
| DNA change (genomic) (Relative to hg19 / GRCh37) |
g.113514610_113514612delinsAAG |
| DNA change (hg38) |
g.112860296_112860298delinsAAG |
| Published as |
- |
| ISCN |
- |
| DB-ID |
ATP11A_000026 |
| Variant remarks |
in vitro expression shows incorrect subcellular protein localisation and reduced PS internalization in plasma membrane |
| Reference |
PubMed: Sun 2020 |
| ClinVar ID |
- |
| dbSNP ID |
- |
| Origin |
In vitro (cloned) |
| Segregation |
- |
| Frequency |
- |
| Re-site |
- |
| VIP |
- |
| Methylation |
- |
| Average frequency (gnomAD v.2.1.1) |
Retrieve |
| Owner |
Johan den Dunnen |
| Database submission license |
Creative Commons Attribution-NonCommercial-ShareAlike 4.0 International |
| Created by |
Johan den Dunnen |
| Date created |
2025-12-02 13:39:59 +01:00 (CET) |
| Date last edited |
N/A |

Variant on transcripts
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