Variant #0000880276 (NC_000001.10:g.215955412G>A, NM_206933.2:c.10712C>T (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.215955412G>A |
| DNA change (hg38) |
g.215782070G>A |
| Published as |
- |
| ISCN |
- |
| DB-ID |
USH2A_000115 See all 70 reported entries |
| Variant remarks |
PM2_Sup PM3_St PP1_M PP4_Sup following GN005 |
| Reference |
- |
| ClinVar ID |
ClinVar-48355 |
| dbSNP ID |
rs202175091 |
| Origin |
SUMMARY record |
| Segregation |
- |
| Frequency |
- |
| Re-site |
- |
| VIP |
- |
| Methylation |
- |
| Average frequency (gnomAD v.2.1.1) |
1.0E-5 View details |
| Owner |
David Baux |
| Database submission license |
Creative Commons Attribution 4.0 International |
| Created by |
David Baux |
| Date created |
2022-10-05 10:34:01 +02:00 (CEST) |
| Date last edited |
2022-10-05 10:36:14 +02:00 (CEST) |

Variant on transcripts
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