Variant #0000897860 (NC_000001.10:g.216256928C>T, NM_206933.2:c.5168G>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.216256928C>T |
DNA change (hg38) |
- |
Published as |
- |
ISCN |
- |
DB-ID |
USH2A_000718 See all 3 reported entries |
Variant remarks |
mini-gene splicing assay; changes ACMG to pathogenic |
Reference |
PubMed: Reurink 2022, Journal: Reurink 2022 |
ClinVar ID |
- |
dbSNP ID |
- |
Origin |
In vitro (cloned) |
Segregation |
- |
Frequency |
- |
Re-site |
- |
VIP |
- |
Methylation |
- |
Average frequency (gnomAD v.2.1.1) |
Retrieve |
Owner |
Janine Reurink |
Database submission license |
Creative Commons Attribution-NonCommercial-ShareAlike 4.0 International |
Created by |
Johan den Dunnen |
Date created |
2022-11-04 17:14:15 +01:00 (CET) |
Date last edited |
2022-11-15 15:12:42 +01:00 (CET) |

Variant on transcripts
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