Variant #0001010365 (NC_000001.10:g.197297642G>T, NM_201253.2:c.161G>T (CRB1))
| Chromosome |
1 |
| Allele |
Unknown |
| Affects function (as reported) |
Effect unknown |
| Affects function (by curator) |
Not classified |
| Classification method |
ACMG |
| Clinical classification |
VUS |
| DNA change (genomic) (Relative to hg19 / GRCh37) |
g.197297642G>T |
| DNA change (hg38) |
g.197328512G>T |
| Published as |
- |
| ISCN |
- |
| DB-ID |
CRB1_000411 See all 4 reported entries |
| Variant remarks |
ACMG PM2, PP3, PP2, BP6 |
| Reference |
- |
| ClinVar ID |
- |
| dbSNP ID |
rs140428156 |
| Origin |
SUMMARY record |
| Segregation |
- |
| Frequency |
- |
| Re-site |
- |
| VIP |
- |
| Methylation |
- |
| Average frequency (gnomAD v.2.1.1) |
0.0004 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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