Variant #0000798991 (NC_000001.10:g.197398749G>A, NC_000001.10(NM_201253.2):c.2842+5G>A (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.197398749G>A |
| DNA change (hg38) |
- |
| Published as |
CRB1(NM_001257965.1):c.2770+5G>A, CRB1(NM_201253.2):c.2842+5G>A (p.?), CRB1(NM_201253.3):c.2842+5G>A |
| ISCN |
- |
| DB-ID |
CRB1_000034 See all 24 reported entries |
| 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) |
3.0E-5 View details |
| Owner |
VKGL-NL_Rotterdam |
| Database submission license |
Creative Commons Attribution-NonCommercial-ShareAlike 4.0 International |
| Created by |
VKGL-NL_Rotterdam |
| Date created |
2021-09-17 14:40:49 +02:00 (CEST) |
| Date last edited |
2025-07-08 13:22:38 +02:00 (CEST) |

Variant on transcripts
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