Variant #0000001633 (NC_000009.11:g.6602147G>A, NM_000170.2:c.1117C>T (GLDC))
Chromosome |
9 |
Allele |
Maternal (confirmed) |
Affects function (as reported) |
Probably affects function |
Affects function (by curator) |
Probably affects function |
Classification method |
- |
Clinical classification |
likely pathogenic |
DNA change (genomic) (Relative to hg19 / GRCh37) |
g.6602147G>A |
DNA change (hg38) |
g.6602147G>A |
Published as |
- |
ISCN |
- |
DB-ID |
GLDC_000049 See all 8 reported entries |
Variant remarks |
1 French GCE patient (Patient 25; com-het) |
Reference |
PubMed: Conter et al. 2006 |
ClinVar ID |
- |
dbSNP ID |
rs150171524 |
Origin |
SUMMARY record |
Segregation |
yes |
Frequency |
- |
Re-site |
- |
VIP |
- |
Methylation |
- |
Average frequency (gnomAD v.2.1.1) |
2.0E-5 View details |
Owner |
Anne Polvi |
Database submission license |
Creative Commons Attribution-NonCommercial-ShareAlike 4.0 International |
Created by |
Anne Polvi |
Date created |
2012-09-04 13:01:23 +02:00 (CEST) |
Date last edited |
2017-05-05 19:04:32 +02:00 (CEST) |

Variant on transcripts
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