Variant #0000328578 (NC_000020.10:g.61444635_61444645del, NM_001853.3:c.-3782_-3772del (COL9A3))
| Chromosome |
20 |
| 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.61444635_61444645del |
| DNA change (hg38) |
g.62813283_62813293del |
| Published as |
OGFR(NM_007346.2):c.1668_1678del (p.(Ser557AspfsTer33)) |
| ISCN |
- |
| DB-ID |
OGFR_000010 |
| 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) |
8.0E-5 View details |
| Owner |
VKGL-NL_Leiden |
| Database submission license |
Creative Commons Attribution-NonCommercial-ShareAlike 4.0 International |
| Created by |
VKGL-NL_Leiden |
| Date created |
2018-01-15 20:58:59 +01:00 (CET) |
| Date last edited |
2020-07-16 20:40:43 +02:00 (CEST) |

Variant on transcripts
|