Variant #0000953239 (NC_000001.10:g.215987141G>A, NM_206933.2:c.9676C>T (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.215987141G>A |
| DNA change (hg38) |
g.215813799G>A |
| Published as |
- |
| ISCN |
- |
| DB-ID |
USH2A_001600 See all 11 reported entries |
| Variant remarks |
ACMG GN005 criteria: PVS1_VS PM2_P PM3_M PP1_M |
| Reference |
PubMed: Gao, F. J. et al., 2021; PubMed: Meng, X. et al., 2021; PubMed: Colombo, L. et al., 2022; PubMed: Jauregui, R. et al., 2020; PubMed: Neuhaus, C. et al., 2017 |
| ClinVar ID |
- |
| dbSNP ID |
rs760858249 |
| 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 17:00:45 +01:00 (CET) |
| Date last edited |
2023-12-13 17:38:50 +01:00 (CET) |

Variant on transcripts
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