Variant #0000971886 (NC_000002.11:g.99012429G>A, NM_001298.2:c.796G>A (CNGA3))
Chromosome |
2 |
Allele |
Unknown |
Affects function (as reported) |
Does not affect function |
Affects function (by curator) |
Not classified |
Classification method |
- |
Clinical classification |
NA |
DNA change (genomic) (Relative to hg19 / GRCh37) |
g.99012429G>A |
DNA change (hg38) |
g.98395966G>A |
Published as |
- |
ISCN |
- |
DB-ID |
CNGA3_000152 See all 3 reported entries |
Variant remarks |
in vitro functional analysis normalized overall luminescence signal (AUC) 0.88±0.11, normalized peak latency 0.94±0.02 |
Reference |
PubMed: Solaki 2023 |
ClinVar ID |
- |
dbSNP ID |
- |
Origin |
In vitro (cloned) |
Segregation |
- |
Frequency |
- |
Re-site |
- |
VIP |
- |
Methylation |
- |
Average frequency (gnomAD v.2.1.1) |
0.00024 View details |
Owner |
Johan den Dunnen |
Database submission license |
Creative Commons Attribution-NonCommercial-ShareAlike 4.0 International |
Created by |
Johan den Dunnen |
Date created |
2024-03-13 10:38:27 +01:00 (CET) |
Date last edited |
N/A |

Variant on transcripts
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