Variant #0000052872 (NC_000020.10:g.57485849C>T)
| Individual ID |
00029449 |
| Chromosome |
20 |
| Allele |
Maternal (confirmed) |
| Affects function (as reported) |
Affects function |
| Affects function (by curator) |
Probably affects function |
| Classification method |
- |
| Clinical classification |
pathogenic |
| DNA change (genomic) (Relative to hg19 / GRCh37) |
g.57485849C>T |
| DNA change (hg38) |
g.58910794C>T |
| Published as |
- |
| ISCN |
- |
| DB-ID |
GNAS_000064 |
| Variant remarks |
loss of function |
| Reference |
PubMed: Garavelli 2005 |
| ClinVar ID |
- |
| dbSNP ID |
- |
| Origin |
Germline |
| Segregation |
yes |
| Frequency |
- |
| Re-site |
- |
| VIP |
- |
| Methylation |
- |
| Average frequency (gnomAD v.2.1.1) |
Retrieve |
| Owner |
Francesca Marta Elli |
| Database submission license |
No license selected |
| Created by |
Francesca Marta Elli |
| Date created |
2012-05-21 13:39:16 +02:00 (CEST) |
| Date last edited |
2012-06-27 16:03:02 +02:00 (CEST) |

Variant on transcripts
Screenings
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