Variant #0000952755 (NC_000001.10:g.216462754T>C, NC_000001.10(NM_206933.2):c.1841-2A>G (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.216462754T>C |
| DNA change (hg38) |
g.216289412T>C |
| Published as |
- |
| ISCN |
- |
| DB-ID |
USH2A_000183 See all 43 reported entries |
| Variant remarks |
ACMG GN005 criteria: PVS1_VS PM2_P PM3_VS PP1_P |
| Reference |
PubMed: Falsini, B. et al., 2021; PubMed: Bonnet, C. et al., 2016; PubMed: Cabanillas, R. et al., 2018; PubMed: Le Quesne Stabej, P. et al., 2012; PubMed: Garcia-Garcia, G. et al., 2011; PubMed: Colombo, L. et al., 2022; PubMed: Mansard, L. et al., 2021; PubMed: Santana, E. E. et al., 2019; PubMed: Rodriguez-Munoz, A. et al., 2020; PubMed: Weisschuh, N. et al., 2020; PubMed: Colombo, L. et al., 2021 |
| ClinVar ID |
- |
| dbSNP ID |
rs397518003 |
| 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 16:51:01 +01:00 (CET) |
| Date last edited |
2023-12-13 17:38:50 +01:00 (CET) |

Variant on transcripts
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