Variant #0000952608 (NC_000001.10:g.216595599G>T, NM_206933.2:c.80C>A (USH2A))
| Chromosome |
1 |
| Allele |
Unknown |
| Affects function (as reported) |
Affects function |
| Affects function (by curator) |
Not classified |
| Classification method |
ACMG |
| Clinical classification |
pathogenic |
| DNA change (genomic) (Relative to hg19 / GRCh37) |
g.216595599G>T |
| DNA change (hg38) |
g.216422257G>T |
| Published as |
- |
| ISCN |
- |
| DB-ID |
USH2A_002149 See all 3 reported entries |
| Variant remarks |
ACMG GN005 criteria: PVS1_VS PM2_P PM3_M |
| Reference |
PubMed: Meng, X. et al., 2021 |
| ClinVar ID |
- |
| dbSNP ID |
- |
| Origin |
SUMMARY record |
| Segregation |
- |
| Frequency |
- |
| Re-site |
- |
| VIP |
- |
| Methylation |
- |
| Average frequency (gnomAD v.2.1.1) |
Retrieve |
| Owner |
David Baux |
| Database submission license |
Creative Commons Attribution 4.0 International |
| Created by |
David Baux |
| Date created |
2023-12-12 16:49:59 +01:00 (CET) |
| Date last edited |
2023-12-13 17:38:50 +01:00 (CET) |

Variant on transcripts
|
Screenscraping/webscraping (downloading large amounts of data using scripts) is strictly prohibited.
Use our APIs to retrieve data.
|