Variant #0001010611 (NC_000001.10:g.197396755T>C, NM_201253.2:c.2300T>C (CRB1))
| Chromosome |
1 |
| Allele |
Unknown |
| Affects function (as reported) |
Probably affects function |
| Affects function (by curator) |
Not classified |
| Classification method |
ACMG |
| Clinical classification |
likely pathogenic (recessive) |
| DNA change (genomic) (Relative to hg19 / GRCh37) |
g.197396755T>C |
| DNA change (hg38) |
g.197427625T>C |
| Published as |
- |
| ISCN |
- |
| DB-ID |
CRB1_000118 See all 5 reported entries |
| Variant remarks |
ACMG PM1, PM2, PP2, PP3, PP5 |
| Reference |
- |
| ClinVar ID |
- |
| dbSNP ID |
- |
| Origin |
SUMMARY record |
| Segregation |
- |
| Frequency |
- |
| Re-site |
- |
| VIP |
- |
| Methylation |
- |
| Average frequency (gnomAD v.2.1.1) |
1.0E-5 View details |
| 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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