Variant #0000952774 (NC_000001.10:g.216424275C>G, NM_206933.2:c.2137G>C (USH2A))
Chromosome |
1 |
Allele |
Unknown |
Affects function (as reported) |
Does not affect function |
Affects function (by curator) |
Not classified |
Classification method |
ACMG |
Clinical classification |
benign |
DNA change (genomic) (Relative to hg19 / GRCh37) |
g.216424275C>G |
DNA change (hg38) |
g.216250933C>G |
Published as |
- |
ISCN |
- |
DB-ID |
USH2A_000021 See all 22 reported entries |
Variant remarks |
ACMG GN005 criteria: PP3_P BA1 BS2_S |
Reference |
PubMed: Aller, E. et al., 2006 |
ClinVar ID |
- |
dbSNP ID |
rs696723 |
Origin |
SUMMARY record |
Segregation |
- |
Frequency |
- |
Re-site |
- |
VIP |
- |
Methylation |
- |
Average frequency (gnomAD v.2.1.1) |
0.02297 View details |
Owner |
David Baux |
Database submission license |
Creative Commons Attribution 4.0 International |
Created by |
David Baux |
Date created |
2023-12-12 16:51:47 +01:00 (CET) |
Date last edited |
2023-12-13 17:38:50 +01:00 (CET) |

Variant on transcripts
|