Variant #0000129223 (NC_000017.10:g.66525095A>G)
| Individual ID |
00080174 |
| Chromosome |
17 |
| Allele |
Unknown |
| Affects function (as reported) |
Probably affects function |
| Affects function (by curator) |
Probably affects function |
| Classification method |
- |
| Clinical classification |
likely pathogenic |
| DNA change (genomic) (Relative to hg19 / GRCh37) |
g.66525095A>G |
| DNA change (hg38) |
- |
| Published as |
- |
| ISCN |
- |
| DB-ID |
PRKAR1A_000017 |
| Variant remarks |
- |
| Reference |
PubMed: Linglart et al. 2012 |
| ClinVar ID |
- |
| dbSNP ID |
- |
| Origin |
Germline |
| Segregation |
? |
| 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 |
2016-09-02 15:57:31 +02:00 (CEST) |
| Date last edited |
2016-09-04 12:42:18 +02:00 (CEST) |

Variant on transcripts
Screenings
|