Variant #0000129755 (NC_000017.10:g.66526546C>T)
| Individual ID |
00080696 |
| 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.66526546C>T |
| DNA change (hg38) |
g.68530405C>T |
| Published as |
- |
| ISCN |
- |
| DB-ID |
PRKAR1A_000010 See all 21 reported entries |
| Variant remarks |
- |
| Reference |
PubMed: Linglart et al.2012 |
| ClinVar ID |
- |
| dbSNP ID |
- |
| Origin |
Not applicable |
| 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 |
2016-09-05 10:30:13 +02:00 (CEST) |
| Date last edited |
N/A |

Variant on transcripts
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