Variant #0000920422 (NC_000002.11:g.98994259G>A, NM_001298.2:c.211G>A (CNGA3))
Chromosome |
2 |
Allele |
Unknown |
Affects function (as reported) |
Probably does not affect function |
Affects function (by curator) |
Not classified |
Classification method |
ACMG |
Clinical classification |
likely benign |
DNA change (genomic) (Relative to hg19 / GRCh37) |
g.98994259G>A |
DNA change (hg38) |
g.98377796G>A |
Published as |
- |
ISCN |
- |
DB-ID |
CNGA3_000301 See all 3 reported entries |
Variant remarks |
ACMG PM2_mod, BP4_sup, BS3_strong |
Reference |
PubMed: Solaki 2023 |
ClinVar ID |
VCV000858875 |
dbSNP ID |
- |
Origin |
SUMMARY record |
Segregation |
- |
Frequency |
- |
Re-site |
- |
VIP |
- |
Methylation |
- |
Average frequency (gnomAD v.2.1.1) |
0.00016 View details |
Owner |
Johan den Dunnen |
Database submission license |
Creative Commons Attribution-NonCommercial-ShareAlike 4.0 International |
Created by |
Johan den Dunnen |
Date created |
2023-03-02 14:15:45 +01:00 (CET) |
Date last edited |
2024-03-13 10:22:25 +01:00 (CET) |

Variant on transcripts
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