Variant #0000052789 (NC_000020.10:g.57466782A>G)
| Individual ID |
00029366 |
| Chromosome |
20 |
| Allele |
Parent #1 |
| Affects function (as reported) |
Affects function |
| Affects function (by curator) |
Not classified |
| Classification method |
- |
| Clinical classification |
pathogenic |
| DNA change (genomic) (Relative to hg19 / GRCh37) |
g.57466782A>G |
| DNA change (hg38) |
g.58891727A>G |
| Published as |
- |
| ISCN |
- |
| DB-ID |
GNAS_000005 See all 4 reported entries |
| Variant remarks |
loss of function; suggested translation re-initiation (N-terminal antibody non-reactive, C-terminal reactive 77 kDa); GNAS activity 0.5 |
| Reference |
PubMed: Patten 1990, OMIM:var0001 |
| ClinVar ID |
- |
| dbSNP ID |
- |
| Origin |
Germline |
| Segregation |
yes |
| Frequency |
- |
| Re-site |
NcoI- |
| 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 |
2008-07-18 14:34:56 +02:00 (CEST) |
| Date last edited |
2012-05-18 09:46:56 +02:00 (CEST) |

Variant on transcripts
Screenings
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