Variant #0000935776 (NC_000016.9:g.56226265G>T, NM_020988.2:c.118G>T (GNAO1))
| Chromosome |
16 |
| Allele |
Unknown |
| Affects function (as reported) |
Affects function |
| Affects function (by curator) |
Not classified |
| Classification method |
- |
| Clinical classification |
pathogenic |
| DNA change (genomic) (Relative to hg19 / GRCh37) |
g.56226265G>T |
| DNA change (hg38) |
g.56192353G>T |
| Published as |
- |
| ISCN |
- |
| DB-ID |
GNAO1_000067 See all 3 reported entries |
| Variant remarks |
- |
| Reference |
Journal: Saez Gonzalez 2023 |
| ClinVar ID |
- |
| dbSNP ID |
rs886041715 |
| Origin |
SUMMARY record |
| Segregation |
- |
| Frequency |
- |
| Re-site |
- |
| VIP |
- |
| Methylation |
- |
| Average frequency (gnomAD v.2.1.1) |
Retrieve |
| Owner |
Harald Mikkers |
| Database submission license |
Creative Commons Attribution-NonCommercial-ShareAlike 4.0 International |
| Created by |
Johan den Dunnen |
| Date created |
2023-08-14 14:11:00 +02:00 (CEST) |
| Date last edited |
2023-10-20 16:04:56 +02:00 (CEST) |

Variant on transcripts
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