Variant #0000467908 (NC_000001.10:g.147246903T>G, NM_005266.6:c.-1581A>C (GJA5))
| Chromosome |
1 |
| Allele |
Unknown |
| Affects function (as reported) |
Effect unknown |
| Affects function (by curator) |
Not classified |
| Classification method |
- |
| Clinical classification |
VUS |
| DNA change (genomic) (Relative to hg19 / GRCh37) |
g.147246903T>G |
| DNA change (hg38) |
g.147774791T>G |
| Published as |
c.-162-1419A>C |
| ISCN |
- |
| DB-ID |
GJA5_000014 |
| Variant remarks |
in perfect LD with -175G>A and -61A>G |
| Reference |
- |
| ClinVar ID |
- |
| dbSNP ID |
rs12408178 |
| Origin |
Germline |
| 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 |
2012-11-25 14:45:27 +01:00 (CET) |
| Date last edited |
2012-11-25 14:48:04 +01:00 (CET) |

Variant on transcripts
|
Screenscraping/webscraping (downloading large amounts of data using scripts) is strictly prohibited.
Use our APIs to retrieve data.
|