Variant #0000953598 (NC_000001.10:g.215812574_215812575del, NM_206933.2:c.14977_14978del (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.215812574_215812575del |
DNA change (hg38) |
g.215639232_215639233del |
Published as |
14977_14978delTT |
ISCN |
- |
DB-ID |
USH2A_000272 See all 15 reported entries |
Variant remarks |
ACMG GN005 criteria: PVS1_VS PM2_P PM3_M |
Reference |
PubMed: Bonnet, C. et al., 2016; PubMed: Colombo, L. et al., 2022; PubMed: Colombo, L. et al., 2022; PubMed: Karali, M. et al., 2019; PubMed: Colombo, L. et al., 2021; PubMed: Eandi, C. M. et al., 2017 |
ClinVar ID |
- |
dbSNP ID |
rs747160949 |
Origin |
SUMMARY record |
Segregation |
- |
Frequency |
- |
Re-site |
- |
VIP |
- |
Methylation |
- |
Average frequency (gnomAD v.2.1.1) |
Retrieve |
Owner |
David Baux |
Database submission license |
Creative Commons Attribution 4.0 International |
Created by |
David Baux |
Date created |
2023-12-12 17:06:01 +01:00 (CET) |
Date last edited |
2023-12-13 17:38:50 +01:00 (CET) |

Variant on transcripts
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