Variant #0000953513 (NC_000001.10:g.215847440A>C, NC_000001.10(NM_206933.2):c.13811+2T>G (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.215847440A>C |
| DNA change (hg38) |
g.215674098A>C |
| Published as |
- |
| ISCN |
- |
| DB-ID |
USH2A_000751 See all 8 reported entries |
| Variant remarks |
ACMG GN005 criteria: PVS1_VS PM2_P PM3_S |
| Reference |
PubMed: Bonnet, C. et al., 2016; PubMed: Perez-Carro, R. et al., 2018; PubMed: Garcia Bohorquez, B. et al., 2021; PubMed: Mansard, L. et al., 2021; PubMed: Aparisi, M. J. et al., 2014 |
| ClinVar ID |
- |
| dbSNP ID |
rs766515318 |
| Origin |
SUMMARY record |
| Segregation |
- |
| Frequency |
- |
| Re-site |
- |
| VIP |
- |
| Methylation |
- |
| Average frequency (gnomAD v.2.1.1) |
0 View details |
| Owner |
David Baux |
| Database submission license |
Creative Commons Attribution 4.0 International |
| Created by |
David Baux |
| Date created |
2023-12-12 17:04:04 +01:00 (CET) |
| Date last edited |
2023-12-13 17:38:50 +01:00 (CET) |

Variant on transcripts
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