Variant #0000971709 (NC_000002.11:g.99006150T>G, NM_001298.2:c.479T>G (CNGA3))
| Chromosome |
2 |
| Allele |
Unknown |
| Affects function (as reported) |
Probably affects function |
| Affects function (by curator) |
Not classified |
| Classification method |
- |
| Clinical classification |
likely pathogenic (recessive) |
| DNA change (genomic) (Relative to hg19 / GRCh37) |
g.99006150T>G |
| DNA change (hg38) |
g.98389687T>G |
| Published as |
- |
| ISCN |
- |
| DB-ID |
CNGA3_000207 See all 5 reported entries |
| Variant remarks |
ACMG PM2_mod, PM1_sup, PP3_sup, PS3_strong |
| Reference |
PubMed: Solaki 2023 |
| ClinVar ID |
- |
| dbSNP ID |
- |
| Origin |
SUMMARY record |
| 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 |
2024-03-13 10:27:56 +01:00 (CET) |
| Date last edited |
N/A |

Variant on transcripts
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