Variant #0000174912 (NC_000003.11:g.8787313C>G, NM_033337.2:c.216C>G (CAV3))
Chromosome |
3 |
Allele |
Unknown |
Affects function (as reported) |
Probably affects function |
Affects function (by curator) |
Not classified |
Classification method |
- |
Clinical classification |
NA |
DNA change (genomic) (Relative to hg19 / GRCh37) |
g.8787313C>G |
DNA change (hg38) |
g.8745627C>G |
Published as |
C71W |
ISCN |
- |
DB-ID |
CAV3_000004 See all 17 reported entries |
Variant remarks |
expression cloning C2C12 cells, CAV3-GFP normal MG53 localisation, no effect 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) |
0.00138 View details |
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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