Variant #0000817942 (NC_000016.9:g.57996913G>A, NM_001297.4:c.346C>T (CNGB1))
| Chromosome |
16 |
| Allele |
Unknown |
| Affects function (as reported) |
Affects function |
| Affects function (by curator) |
Not classified |
| Classification method |
ACMG |
| Clinical classification |
pathogenic (recessive) |
| DNA change (genomic) (Relative to hg19 / GRCh37) |
g.57996913G>A |
| DNA change (hg38) |
g.57963009G>A |
| Published as |
- |
| ISCN |
- |
| DB-ID |
CNGB1_000286 See all 4 reported entries |
| Variant remarks |
ACMG PVS1, PM2, PP3 |
| Reference |
- |
| ClinVar ID |
- |
| dbSNP ID |
- |
| Origin |
SUMMARY record |
| Segregation |
- |
| Frequency |
- |
| Re-site |
- |
| VIP |
- |
| Methylation |
- |
| Average frequency (gnomAD v.2.1.1) |
0 View details |
| Owner |
Johan den Dunnen |
| Database submission license |
Creative Commons Attribution-NonCommercial-ShareAlike 4.0 International |
| Created by |
Johan den Dunnen |
| Date created |
2021-10-31 14:57:51 +01:00 (CET) |
| Date last edited |
N/A |

Variant on transcripts
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