Variant #0000816586 (NC_000016.9:g.57994384A>G, NC_000016.9(NM_001297.4):c.583+2T>C (CNGB1))
| Chromosome |
16 |
| Allele |
Parent #1 |
| Affects function (as reported) |
Affects function |
| Affects function (by curator) |
Not classified |
| Classification method |
- |
| Clinical classification |
NA |
| DNA change (genomic) (Relative to hg19 / GRCh37) |
g.57994384A>G |
| DNA change (hg38) |
- |
| Published as |
- |
| ISCN |
- |
| DB-ID |
CNGB1_000246 See all 3 reported entries |
| Variant remarks |
in vitro splicing assay shows exon skipping |
| Reference |
PubMed: Mauro-Herrera 2021 |
| ClinVar ID |
- |
| dbSNP ID |
- |
| Origin |
In vitro (cloned) |
| Segregation |
- |
| Frequency |
- |
| Re-site |
- |
| VIP |
- |
| Methylation |
- |
| Average frequency (gnomAD v.2.1.1) |
1.0E-5 View details |
| Owner |
Johan den Dunnen |
| Database submission license |
Creative Commons Attribution-NonCommercial-ShareAlike 4.0 International |
| Created by |
Johan den Dunnen |
| Date created |
2021-10-26 19:48:03 +02:00 (CEST) |
| Date last edited |
N/A |

Variant on transcripts
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