Variant #0000852099 (NC_000009.11:g.126135899_126135914dup, NM_173689.5:c.3089_3104dup (CRB2))
| Chromosome |
9 |
| Allele |
Unknown |
| Affects function (as reported) |
Affects function |
| Affects function (by curator) |
Not classified |
| Classification method |
- |
| Clinical classification |
pathogenic |
| DNA change (genomic) (Relative to hg19 / GRCh37) |
g.126135899_126135914dup |
| DNA change (hg38) |
- |
| Published as |
CRB2(NM_173689.5):c.3089_3104dup (p.(Gly1036Alafs*43)), CRB2(NM_173689.7):c.3089_3104dupGGCCCGGCGCGGCCCC (p.G1036Afs*43) |
| ISCN |
- |
| DB-ID |
CRB2_000003 See all 4 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) |
Retrieve |
| Owner |
VKGL-NL_Utrecht |
| Database submission license |
Creative Commons Attribution-NonCommercial-ShareAlike 4.0 International |
| Created by |
VKGL-NL_Utrecht |
| Date created |
2022-05-09 15:40:45 +02:00 (CEST) |
| Date last edited |
2023-04-16 21:50:28 +02:00 (CEST) |

Variant on transcripts
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