Variant #0000817952 (NC_000016.9:g.57984428_57984449dup, NC_000016.9(NM_001297.4):c.875-5_891dup (CNGB1))
| Chromosome |
16 |
| Allele |
Unknown |
| Affects function (as reported) |
Probably affects function |
| Affects function (by curator) |
Not classified |
| Classification method |
ACMG |
| Clinical classification |
VUS |
| DNA change (genomic) (Relative to hg19 / GRCh37) |
g.57984428_57984449dup |
| DNA change (hg38) |
g.57950524_57950545dup |
| Published as |
- |
| ISCN |
- |
| DB-ID |
CNGB1_000192 See all 3 reported entries |
| Variant remarks |
- |
| Reference |
- |
| ClinVar ID |
- |
| dbSNP ID |
- |
| Origin |
SUMMARY record |
| Segregation |
- |
| Frequency |
- |
| Re-site |
- |
| VIP |
- |
| Methylation |
- |
| Average frequency (gnomAD v.2.1.1) |
Retrieve |
| 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 |
2021-11-03 08:58:41 +01:00 (CET) |

Variant on transcripts
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