Variant #0001010391 (NC_000001.10:g.197297979_197297987del, NM_201253.2:c.498_506del (CRB1))
Chromosome |
1 |
Allele |
Unknown |
Affects function (as reported) |
Affects function |
Affects function (by curator) |
Not classified |
Classification method |
ACMG |
Clinical classification |
pathogenic (recessive) |
DNA change (genomic) (Relative to hg19 / GRCh37) |
g.197297979_197297987del |
DNA change (hg38) |
g.197328849_197328857del |
Published as |
- |
ISCN |
- |
DB-ID |
CRB1_000211 See all 71 reported entries |
Variant remarks |
ACMG PS4, PM2, PM3, PM4 |
Reference |
- |
ClinVar ID |
- |
dbSNP ID |
rs748136623 |
Origin |
SUMMARY record |
Segregation |
- |
Frequency |
- |
Re-site |
- |
VIP |
- |
Methylation |
- |
Average frequency (gnomAD v.2.1.1) |
Retrieve |
Owner |
Marta Corton |
Database submission license |
Creative Commons Attribution-NonCommercial-ShareAlike 4.0 International |
Created by |
Johan den Dunnen |
Date created |
2024-09-30 17:29:59 +02:00 (CEST) |
Date last edited |
N/A |

Variant on transcripts
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