Variant #0000001583 (NC_000009.11:g.6645472del, NM_000170.2:c.28del (GLDC))
Chromosome |
9 |
Allele |
Unknown |
Affects function (as reported) |
Affects function |
Affects function (by curator) |
Affects function |
Classification method |
- |
Clinical classification |
pathogenic |
DNA change (genomic) (Relative to hg19 / GRCh37) |
g.6645472del |
DNA change (hg38) |
g.6645472del |
Published as |
- |
ISCN |
- |
DB-ID |
GLDC_000010 See all 2 reported entries |
Variant remarks |
1 GCE patient |
Reference |
PubMed: Conter et al. 2006 |
ClinVar ID |
- |
dbSNP ID |
- |
Origin |
SUMMARY record |
Segregation |
yes |
Frequency |
- |
Re-site |
- |
VIP |
- |
Methylation |
- |
Average frequency (gnomAD v.2.1.1) |
Retrieve |
Owner |
Anne Polvi |
Database submission license |
Creative Commons Attribution-NonCommercial-ShareAlike 4.0 International |
Created by |
Anne Polvi |
Date created |
2012-08-31 12:59:40 +02:00 (CEST) |
Date last edited |
2020-06-25 12:36:50 +02:00 (CEST) |

Variant on transcripts
|