Variant #0000953176 (NC_000001.10:g.216040513C>A, NC_000001.10(NM_206933.2):c.8682-1G>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.216040513C>A |
| DNA change (hg38) |
g.215867171C>A |
| Published as |
- |
| ISCN |
- |
| DB-ID |
USH2A_002544 See all 2 reported entries |
| Variant remarks |
ACMG GN005 criteria: PVS1_VS PS1_S PM2_P |
| Reference |
PubMed: Qu, L. H. et al., 2020 |
| ClinVar ID |
- |
| dbSNP ID |
- |
| 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 16:59:43 +01:00 (CET) |
| Date last edited |
2023-12-13 17:38:50 +01:00 (CET) |

Variant on transcripts
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