Variant #0000920429 (NC_000002.11:g.98999840C>G, NC_000002.11(NM_001298.2):c.396-11C>G (CNGA3))
| Chromosome |
2 |
| 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.98999840C>G |
| DNA change (hg38) |
g.98383377C>G |
| Published as |
- |
| ISCN |
- |
| DB-ID |
CNGA3_000116 See all 10 reported entries |
| Variant remarks |
analysis variant in in vitro mini-gene splicing assay |
| Reference |
PubMed: Reuter 2021 |
| ClinVar ID |
- |
| dbSNP ID |
- |
| Origin |
In vitro (cloned) |
| 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 |
2023-03-02 14:48:51 +01:00 (CET) |
| Date last edited |
N/A |

Variant on transcripts
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