Variant #0000994408 (NC_000004.11:g.660377G>A, NM_000283.3:c.2326G>A (PDE6B))
| Chromosome |
4 |
| Allele |
Unknown |
| Affects function (as reported) |
Effect unknown |
| Affects function (by curator) |
Not classified |
| Classification method |
- |
| Clinical classification |
VUS |
| DNA change (genomic) (Relative to hg19 / GRCh37) |
g.660377G>A |
| DNA change (hg38) |
- |
| Published as |
PDE6B(NM_000283.3):c.2326G>A (p.D776N, p.(Asp776Asn)), PDE6B(NM_000283.4):c.2326G>A (p.D776N) |
| ISCN |
- |
| DB-ID |
PDE6B_000008 See all 13 reported entries |
| 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) |
5.0E-5 View details |
| Owner |
VKGL-NL_Leiden |
| Database submission license |
Creative Commons Attribution-NonCommercial-ShareAlike 4.0 International |
| Created by |
VKGL-NL_Leiden |
| Date created |
2024-08-28 13:16:32 +02:00 (CEST) |
| Date last edited |
N/A |

Variant on transcripts
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