Variant #0000953256 (NC_000001.10:g.215972295dup, NM_206933.2:c.9912dup (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.215972295dup |
| DNA change (hg38) |
g.215798953dup |
| Published as |
9912dupA |
| ISCN |
- |
| DB-ID |
USH2A_000618 See all 3 reported entries |
| Variant remarks |
ACMG GN005 criteria: PVS1_VS PM2_P PM3_M |
| Reference |
PubMed: Lenassi, E. et al., 2015; PubMed: Le Quesne Stabej, P. et al., 2012 |
| ClinVar ID |
- |
| dbSNP ID |
rs759255743 |
| 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 17:00:45 +01:00 (CET) |
| Date last edited |
2023-12-13 17:38:50 +01:00 (CET) |

Variant on transcripts
|