Variant #0000697178 (NC_000017.10:g.58235718C>A, NM_000717.3:c.655C>A (CA4))
| Chromosome |
17 |
| 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.58235718C>A |
| DNA change (hg38) |
- |
| Published as |
- |
| ISCN |
- |
| DB-ID |
CA4_000034 See all 2 reported entries |
| Variant remarks |
expression cloning shows drastically reduced enzyme activity, defective protein processing, impaired trafficking to cell surface resulting in abnormal intracellular retention |
| Reference |
PubMed: Datta 2009 |
| 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 |
2020-10-07 14:05:41 +02:00 (CEST) |
| Date last edited |
N/A |

Variant on transcripts
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