Variant #0000897863 (NC_000001.10:g.215972249C>A, NM_206933.2:c.9958G>T (USH2A))
| Chromosome |
1 |
| Allele |
Unknown |
| Affects function (as reported) |
Probably affects function |
| Affects function (by curator) |
Not classified |
| Classification method |
ACMG |
| Clinical classification |
likely pathogenic |
| DNA change (genomic) (Relative to hg19 / GRCh37) |
g.215972249C>A |
| DNA change (hg38) |
- |
| Published as |
- |
| ISCN |
- |
| DB-ID |
USH2A_000877 See all 41 reported entries |
| Variant remarks |
mini-gene splicing assay; changes ACMG to likely pathogenic |
| Reference |
PubMed: Reurink 2022, Journal: Reurink 2022 |
| ClinVar ID |
- |
| dbSNP ID |
- |
| Origin |
In vitro (cloned) |
| Segregation |
- |
| Frequency |
- |
| Re-site |
- |
| VIP |
- |
| Methylation |
- |
| Average frequency (gnomAD v.2.1.1) |
Retrieve |
| Owner |
Janine Reurink |
| Database submission license |
Creative Commons Attribution-NonCommercial-ShareAlike 4.0 International |
| Created by |
Johan den Dunnen |
| Date created |
2022-11-04 17:14:15 +01:00 (CET) |
| Date last edited |
2022-11-15 15:16:07 +01:00 (CET) |

Variant on transcripts
|