Variant #0000953307 (NC_000001.10:g.215955412G>A, NM_206933.2:c.10712C>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.215955412G>A |
| DNA change (hg38) |
g.215782070G>A |
| Published as |
- |
| ISCN |
- |
| DB-ID |
USH2A_000115 See all 70 reported entries |
| Variant remarks |
ACMG GN005 criteria: PM2_P PM3_VS |
| Reference |
PubMed: Gao, F. J. et al., 2021; PubMed: Falsini, B. et al., 2021; PubMed: Reurink, J. et al., 2021; PubMed: Meng, X. et al., 2021; PubMed: Bonnet, C. et al., 2016; PubMed: Aller, E. et al., 2006; PubMed: Colombo, L. et al., 2022; PubMed: Wafa, T. T. et al., 2021; PubMed: Mansard, L. et al., 2021; PubMed: Karali, M. et al., 2019; PubMed: Weisschuh, N. et al., 2020; PubMed: Colombo, L. et al., 2021; PubMed: Jauregui, R. et al., 2020; PubMed: Inaba, A. et al., 2020; PubMed: Bravo-Gil, N. et al., 2016; PubMed: Bravo-Gil, N. et al., 2017 |
| ClinVar ID |
- |
| dbSNP ID |
rs202175091 |
| Origin |
SUMMARY record |
| Segregation |
- |
| Frequency |
- |
| Re-site |
- |
| VIP |
- |
| Methylation |
- |
| Average frequency (gnomAD v.2.1.1) |
1.0E-5 View details |
| Owner |
David Baux |
| Database submission license |
Creative Commons Attribution 4.0 International |
| Created by |
David Baux |
| Date created |
2023-12-12 17:01:40 +01:00 (CET) |
| Date last edited |
2023-12-13 17:38:50 +01:00 (CET) |

Variant on transcripts
|