Variant #0000952913 (NC_000001.10:g.216270538G>A, NM_206933.2:c.4645C>T (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.216270538G>A |
DNA change (hg38) |
g.216097196G>A |
Published as |
- |
ISCN |
- |
DB-ID |
USH2A_000103 See all 27 reported entries |
Variant remarks |
ACMG GN005 criteria: PVS1_VS PM2_P PM3_VS |
Reference |
PubMed: Gao, F. J. et al., 2021; PubMed: Molina-Ramirez, L. P. et al., 2020; PubMed: Reurink, J. et al., 2021; PubMed: Bonnet, C. et al., 2016; PubMed: Huang, L. et al., 2018; PubMed: Le Quesne Stabej, P. et al., 2012; PubMed: Garcia-Garcia, G. et al., 2011; PubMed: Sloan-Heggen, C. M. et al., 2016; PubMed: Bravo-Gil, N. et al., 2017 |
ClinVar ID |
- |
dbSNP ID |
rs199679165 |
Origin |
SUMMARY record |
Segregation |
- |
Frequency |
- |
Re-site |
- |
VIP |
- |
Methylation |
- |
Average frequency (gnomAD v.2.1.1) |
2.0E-5 View details |
Owner |
David Baux |
Database submission license |
Creative Commons Attribution 4.0 International |
Created by |
David Baux |
Date created |
2023-12-12 16:53:57 +01:00 (CET) |
Date last edited |
2023-12-13 17:38:50 +01:00 (CET) |

Variant on transcripts
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