Variant #0000953376 (NC_000001.10:g.215901658T>C, NM_206933.2:c.11780A>G (USH2A))
| Chromosome |
1 |
| Allele |
Unknown |
| Affects function (as reported) |
Effect unknown |
| Affects function (by curator) |
Not classified |
| Classification method |
ACMG |
| Clinical classification |
VUS |
| DNA change (genomic) (Relative to hg19 / GRCh37) |
g.215901658T>C |
| DNA change (hg38) |
g.215728316T>C |
| Published as |
- |
| ISCN |
- |
| DB-ID |
USH2A_002523 See all 4 reported entries |
| Variant remarks |
ACMG GN005 criteria: PM2_P PM3_M |
| Reference |
PubMed: He, C. et al., 2020; PubMed: Meng, X. et al., 2021 |
| 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 17:02:17 +01:00 (CET) |
| Date last edited |
2023-12-13 17:38:50 +01:00 (CET) |

Variant on transcripts
|