Variant #0001030056 (NC_000008.10:g.87656917A>C, NC_000008.10(NM_019098.4):c.991-3T>G (CNGB3))
| Chromosome |
8 |
| Allele |
Unknown |
| 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.87656917A>C |
| DNA change (hg38) |
g.86644689A>C |
| Published as |
- |
| ISCN |
- |
| DB-ID |
CNGB3_000013 See all 18 reported entries |
| Variant remarks |
ACMG PM2_mod, PP3_mod, PM3_very strong, PVS1; consequence on splicing predicted from in vitro mini-gene splicing assay |
| Reference |
Rawnsley 2025, submitted |
| 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 |
Susanne Kohl |
| Database submission license |
Creative Commons Attribution-NonCommercial-ShareAlike 4.0 International |
| Created by |
Johan den Dunnen |
| Date created |
2025-03-26 11:06:12 +01:00 (CET) |
| Date last edited |
N/A |

Variant on transcripts
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