Variant #0000952811 (NC_000001.10:g.216419926C>T, NC_000001.10(NM_206933.2):c.2809+1G>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.216419926C>T |
| DNA change (hg38) |
g.216246584C>T |
| Published as |
- |
| ISCN |
- |
| DB-ID |
USH2A_000361 See all 6 reported entries |
| Variant remarks |
ACMG GN005 criteria: PVS1_VS PM2_P PM3_P |
| Reference |
PubMed: Mansard, L. et al., 2021; PubMed: Sloan-Heggen, C. M. et al., 2016 |
| ClinVar ID |
- |
| dbSNP ID |
rs759433119 |
| Origin |
SUMMARY record |
| Segregation |
- |
| Frequency |
- |
| Re-site |
- |
| VIP |
- |
| Methylation |
- |
| Average frequency (gnomAD v.2.1.1) |
0 View details |
| Owner |
David Baux |
| Database submission license |
Creative Commons Attribution 4.0 International |
| Created by |
David Baux |
| Date created |
2023-12-12 16:52:39 +01:00 (CET) |
| Date last edited |
2023-12-13 17:38:50 +01:00 (CET) |

Variant on transcripts
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