Variant #0000921504 (NC_000001.10:g.216251475G>A, NM_206933.2:c.5528C>T (USH2A))
| Chromosome |
1 |
| Allele |
Unknown |
| Affects function (as reported) |
Probably affects function |
| Affects function (by curator) |
Probably affects function |
| Classification method |
ACMG |
| Clinical classification |
likely pathogenic |
| DNA change (genomic) (Relative to hg19 / GRCh37) |
g.216251475G>A |
| DNA change (hg38) |
g.216078133G>A |
| Published as |
- |
| ISCN |
- |
| DB-ID |
USH2A_000717 See all 7 reported entries |
| Variant remarks |
PM2_P, PM3_S, PP1_P following ClinGen GN005 |
| Reference |
- |
| ClinVar ID |
- |
| dbSNP ID |
rs200209833 |
| 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 |
2023-03-17 17:45:01 +01:00 (CET) |
| Date last edited |
2023-03-17 17:46:28 +01:00 (CET) |

Variant on transcripts
|