Variant #0000952796 (NC_000001.10:g.216420304_216420305del, NM_206933.2:c.2431_2432del (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.216420304_216420305del |
DNA change (hg38) |
g.216246962_216246963del |
Published as |
2431_2432delAA |
ISCN |
- |
DB-ID |
USH2A_000196 See all 10 reported entries |
Variant remarks |
ACMG GN005 criteria: PVS1_VS PM2_P PM3_S |
Reference |
PubMed: Perez-Carro, R. et al., 2018 |
ClinVar ID |
- |
dbSNP ID |
rs2102545818 |
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 16:52:01 +01:00 (CET) |
Date last edited |
2023-12-13 17:38:50 +01:00 (CET) |

Variant on transcripts
|