Variant #0000953296 (NC_000001.10:g.215956104A>G, NM_206933.2:c.10561T>C (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.215956104A>G |
| DNA change (hg38) |
g.215782762A>G |
| Published as |
- |
| ISCN |
- |
| DB-ID |
USH2A_000429 See all 40 reported entries |
| Variant remarks |
ACMG GN005 criteria: PS4_S PM2_P PM3_VS |
| Reference |
PubMed: Reurink, J. et al., 2021; PubMed: Bonnet, C. et al., 2016; PubMed: Le Quesne Stabej, P. et al., 2012; PubMed: Glockle, N. et al., 2014; PubMed: Weisschuh, N. et al., 2020; PubMed: Sloan-Heggen, C. M. et al., 2016; PubMed: Neuhaus, C. et al., 2017 |
| ClinVar ID |
- |
| dbSNP ID |
rs111033264 |
| 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 17:01:23 +01:00 (CET) |
| Date last edited |
2023-12-13 17:38:50 +01:00 (CET) |

Variant on transcripts
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