Variant #0000504673 (NC_000001.10:g.197168819_197168823del, NM_201253.2:c.-68724_-68720del (CRB1))
| Chromosome |
1 |
| Allele |
Unknown |
| Affects function (as reported) |
Effect unknown |
| Affects function (by curator) |
Not classified |
| Classification method |
- |
| Clinical classification |
VUS |
| DNA change (genomic) (Relative to hg19 / GRCh37) |
g.197168819_197168823del |
| DNA change (hg38) |
g.197199689_197199693del |
| Published as |
ZBTB41(NM_194314.2):c.784_788del (p.(Lys262Ter)) |
| ISCN |
- |
| DB-ID |
CRB1_000296 |
| Variant remarks |
VKGL data sharing initiative Nederland |
| Reference |
- |
| ClinVar ID |
- |
| dbSNP ID |
- |
| Origin |
CLASSIFICATION record |
| Segregation |
- |
| Frequency |
- |
| Re-site |
- |
| VIP |
- |
| Methylation |
- |
| Average frequency (gnomAD v.2.1.1) |
Retrieve |
| Owner |
VKGL-NL_Leiden |
| Database submission license |
Creative Commons Attribution-NonCommercial-ShareAlike 4.0 International |
| Created by |
VKGL-NL_Leiden |
| Date created |
2019-07-18 18:22:55 +02:00 (CEST) |
| Date last edited |
2024-10-29 20:49:11 +01:00 (CET) |

Variant on transcripts
|