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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