Variant #0000052822 (NC_000020.10:g.57484420C>G)
| Individual ID |
00029399 |
| 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.57484420C>G |
| DNA change (hg38) |
g.58909365C>G |
| Published as |
601C>G |
| ISCN |
- |
| DB-ID |
GNAS_000025 |
| Variant remarks |
gain of function |
| Reference |
Riminucci et al., 1999 |
| ClinVar ID |
- |
| dbSNP ID |
- |
| Origin |
Germline |
| Segregation |
- |
| Frequency |
- |
| Re-site |
- |
| VIP |
- |
| Methylation |
- |
| Average frequency (gnomAD v.2.1.1) |
0 View details |
| 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 14:34:57 +02:00 (CEST) |
| Date last edited |
2011-01-07 15:11:16 +01:00 (CET) |

Variant on transcripts
Screenings
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