Variant #0000952803 (NC_000001.10:g.216420126G>T, NM_206933.2:c.2610C>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.216420126G>T |
DNA change (hg38) |
g.216246784G>T |
Published as |
- |
ISCN |
- |
DB-ID |
USH2A_000594 See all 33 reported entries |
Variant remarks |
ACMG GN005 criteria: PVS1_VS PM2_P PM3_VS |
Reference |
PubMed: Fakin, A. et al., 2019; PubMed: Bonnet, C. et al., 2016; PubMed: Le Quesne Stabej, P. et al., 2012; PubMed: Weisschuh, N. et al., 2020; PubMed: Neuhaus, C. et al., 2017 |
ClinVar ID |
- |
dbSNP ID |
rs767078782 |
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 |
2023-12-12 16:52:01 +01:00 (CET) |
Date last edited |
2023-12-13 17:38:50 +01:00 (CET) |

Variant on transcripts
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