Variant #0000624177 (NC_000020.10:g.57429067C>A, NM_000516.4:c.-37715C>A (GNAS))
| Chromosome |
20 |
| 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.57429067C>A |
| DNA change (hg38) |
g.58854012C>A |
| Published as |
GNAS(NM_001077490.2):c.560C>A (p.S187*) |
| ISCN |
- |
| DB-ID |
GNAS_000461 |
| Variant remarks |
VKGL data sharing initiative Nederland |
| Reference |
- |
| ClinVar ID |
- |
| dbSNP ID |
- |
| Origin |
CLASSIFICATION record |
| Segregation |
- |
| Frequency |
- |
| Re-site |
- |
| VIP |
- |
| Methylation |
- |
| Average frequency (gnomAD v.2.1.1) |
0 View details |
| Owner |
VKGL-NL_Rotterdam |
| Database submission license |
Creative Commons Attribution-NonCommercial-ShareAlike 4.0 International |
| Created by |
VKGL-NL_Rotterdam |
| Date created |
2019-12-06 12:43:26 +01:00 (CET) |
| Date last edited |
2020-07-16 18:49:03 +02:00 (CEST) |

Variant on transcripts
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