Variant #0000920377 (NC_000002.11:g.98986540G>A, NC_000002.11(NM_001298.2):c.101+1G>A (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.98986540G>A |
DNA change (hg38) |
g.98370077G>A |
Published as |
- |
ISCN |
- |
DB-ID |
CNGA3_000080 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) |
0.00027 View details |
Owner |
Johan den Dunnen |
Database submission license |
Creative Commons Attribution-NonCommercial-ShareAlike 4.0 International |
Created by |
Johan den Dunnen |
Date created |
2023-02-28 16:40:00 +01:00 (CET) |
Date last edited |
2023-03-02 14:07:53 +01:00 (CET) |

Variant on transcripts
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