Variant #0000880275 (NC_000001.10:g.215848408A>G, NM_206933.2:c.12845T>C (USH2A))
| Chromosome |
1 |
| Allele |
Unknown |
| Affects function (as reported) |
Probably affects function |
| Affects function (by curator) |
Probably affects function |
| Classification method |
ACMG |
| Clinical classification |
likely pathogenic |
| DNA change (genomic) (Relative to hg19 / GRCh37) |
g.215848408A>G |
| DNA change (hg38) |
g.215675066A>G |
| Published as |
- |
| ISCN |
- |
| DB-ID |
USH2A_000315 See all 10 reported entries |
| Variant remarks |
PM2_Sup PM3_St PP1_Sup following GN005 |
| Reference |
- |
| ClinVar ID |
- |
| dbSNP ID |
- |
| 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 |
2022-10-05 10:18:01 +02:00 (CEST) |
| Date last edited |
2022-10-05 10:28:03 +02:00 (CEST) |

Variant on transcripts
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