Variant #0000535383 (NC_000008.10:g.87656009del, NM_019098.4:c.1148del (CNGB3))
| Chromosome |
8 |
| Allele |
Unknown |
| Affects function (as reported) |
Affects function |
| Affects function (by curator) |
Not classified |
| Classification method |
- |
| Clinical classification |
pathogenic |
| DNA change (genomic) (Relative to hg19 / GRCh37) |
g.87656009del |
| DNA change (hg38) |
g.86643781del |
| Published as |
CNGB3(NM_019098.4):c.1148delC (p.(Thr383Ilefs*13)), CNGB3(NM_019098.4):c.1148delC (p.T383Ifs*13), CNGB3(NM_019098.5):c.1148delC (p.T383Ifs*13) |
| ISCN |
- |
| DB-ID |
CNGB3_000001 See all 452 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) |
0.00174 View details |
| Owner |
VKGL-NL_AMC |
| Database submission license |
Creative Commons Attribution-NonCommercial-ShareAlike 4.0 International |
| Created by |
VKGL-NL_AMC |
| Date created |
2019-07-18 18:22:55 +02:00 (CEST) |
| Date last edited |
2023-01-11 15:44:22 +01:00 (CET) |

Variant on transcripts
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