Variant #0000328580 (NC_000020.10:g.61444641_61444699del, NM_001853.3:c.-3776_-3718del (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.61444641_61444699del |
DNA change (hg38) |
g.62813289_62813347del |
Published as |
OGFR(NM_007346.2):c.1672_1730del (p.(Ser559IlefsTer15)) |
ISCN |
- |
DB-ID |
OGFR_000012 |
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 |
2018-01-15 20:58:59 +01:00 (CET) |
Date last edited |
2020-07-16 20:41:08 +02:00 (CEST) |

Variant on transcripts
|