Variant #0000344812 (NC_000001.10:g.215901565_215901566del, NM_206933.2:c.11875_11876del (USH2A))
Chromosome |
1 |
Allele |
Unknown |
Affects function (as reported) |
Affects function |
Affects function (by curator) |
Not classified |
Classification method |
- |
Clinical classification |
pathogenic |
DNA change (genomic) (Relative to hg19 / GRCh37) |
g.215901565_215901566del |
DNA change (hg38) |
g.215728223_215728224del |
Published as |
USH2A(NM_206933.4):c.11875_11876delCA (p.Q3959Nfs*53) |
ISCN |
- |
DB-ID |
USH2A_000276 See all 20 reported entries |
Variant remarks |
VKGL data sharing initiative Nederland |
Reference |
- |
ClinVar ID |
- |
dbSNP ID |
- |
Origin |
CLASSIFICATION record |
Segregation |
- |
Frequency |
- |
Re-site |
- |
VIP |
- |
Methylation |
- |
Average frequency (gnomAD v.2.1.1) |
Retrieve |
Owner |
VKGL-NL_Nijmegen |
Database submission license |
Creative Commons Attribution-NonCommercial-ShareAlike 4.0 International |
Created by |
VKGL-NL_Nijmegen |
Date created |
2018-01-15 20:58:59 +01:00 (CET) |
Date last edited |
2025-07-08 13:22:38 +02:00 (CEST) |

Variant on transcripts
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