Variant #0000952999 (NC_000001.10:g.216246438C>T, NC_000001.10(NM_206933.2):c.5776+1G>A (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.216246438C>T |
| DNA change (hg38) |
g.216073096C>T |
| Published as |
- |
| ISCN |
- |
| DB-ID |
USH2A_000175 See all 32 reported entries |
| Variant remarks |
ACMG GN005 criteria: PVS1_VS PM2_P PM3_VS PP1_M |
| Reference |
PubMed: Lenassi, E. et al., 2015; PubMed: Molina-Ramirez, L. P. et al., 2020; PubMed: Bonnet, C. et al., 2016; PubMed: Glockle, N. et al., 2014; PubMed: Colombo, L. et al., 2022; PubMed: Mansard, L. et al., 2021; PubMed: Karali, M. et al., 2019; PubMed: Khalaileh, A. et al., 2018; PubMed: Weisschuh, N. et al., 2020; PubMed: Colombo, L. et al., 2021; PubMed: Neuhaus, C. et al., 2017 |
| ClinVar ID |
- |
| dbSNP ID |
rs876657731 |
| 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 16:56:01 +01:00 (CET) |
| Date last edited |
2023-12-13 17:38:50 +01:00 (CET) |

Variant on transcripts
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