Variant #0000921503 (NC_000001.10:g.215990476G>A, NM_206933.2:c.9433C>T (USH2A))
Chromosome |
1 |
Allele |
Unknown |
Affects function (as reported) |
Effect unknown |
Affects function (by curator) |
Effect unknown |
Classification method |
ACMG |
Clinical classification |
VUS |
DNA change (genomic) (Relative to hg19 / GRCh37) |
g.215990476G>A |
DNA change (hg38) |
g.215817134G>A |
Published as |
- |
ISCN |
- |
DB-ID |
USH2A_001187 See all 16 reported entries |
Variant remarks |
PM2_P, PM3_S following ClinGen GN005 |
Reference |
- |
ClinVar ID |
- |
dbSNP ID |
rs267598373 |
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 |
2023-03-17 17:42:01 +01:00 (CET) |
Date last edited |
2023-03-17 17:43:36 +01:00 (CET) |

Variant on transcripts
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