Variant #0000174909 (NC_000003.11:g.8775642G>A, NM_033337.2:c.80G>A (CAV3))
| Chromosome |
3 |
| 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.8775642G>A |
| DNA change (hg38) |
g.8733956G>A |
| Published as |
R26Q |
| ISCN |
- |
| DB-ID |
CAV3_000007 See all 34 reported entries |
| Variant remarks |
expression cloning C2C12 cells, CAV3-GFP retention in Golgi influencing MG53/DYSF localisation, defective membrane repair |
| Reference |
PubMed: Cai 20029 |
| 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 |
2012-04-15 15:58:24 +02:00 (CEST) |
| Date last edited |
2020-07-14 21:50:58 +02:00 (CEST) |

Variant on transcripts
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