Variant #0000052958 (NC_000020.10:g.57485806_57485807del)
| Individual ID |
00029535 |
| Chromosome |
20 |
| Allele |
Paternal (inferred) |
| 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.57485806_57485807del |
| DNA change (hg38) |
g.58910751_58910752del |
| Published as |
1107-1108delTG |
| ISCN |
- |
| DB-ID |
GNAS_000044 See all 3 reported entries |
| Variant remarks |
loss of function |
| Reference |
PubMed: Schimmel 2010 |
| ClinVar ID |
- |
| dbSNP ID |
- |
| Origin |
De novo |
| 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 |
2012-08-31 13:45:19 +02:00 (CEST) |
| Date last edited |
2020-07-16 20:22:23 +02:00 (CEST) |

Variant on transcripts
Screenings
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