Variant #0000050419 (NC_000020.10:g.57464773_57464823|bsrC)
| Individual ID |
00027198 |
| Chromosome |
20 |
| Allele |
Unknown |
| Affects function (as reported) |
Probably affects function |
| Affects function (by curator) |
Not classified |
| Classification method |
- |
| Clinical classification |
likely pathogenic |
| DNA change (genomic) (Relative to hg19 / GRCh37) |
g.57464773_57464823|bsrC |
| DNA change (hg38) |
- |
| Published as |
CG1-GNAS-DMR CG11 |
| ISCN |
- |
| DB-ID |
GNAS_000000 |
| Variant remarks |
normal methylation GNAS-DMR |
| Reference |
PubMed: Kagami 2014 |
| ClinVar ID |
- |
| dbSNP ID |
- |
| Origin |
Somatic |
| Segregation |
- |
| Frequency |
- |
| Re-site |
- |
| VIP |
- |
| Methylation |
normal levels |
| 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 |
2014-12-29 17:26:14 +01:00 (CET) |
| Date last edited |
2017-05-05 13:19:20 +02:00 (CEST) |

Variant on transcripts
Screenings
|