Variant #0000001637 (NC_000009.11:g.6592870C>T, NM_000170.2:c.1382G>A (GLDC))
| Chromosome |
9 |
| Allele |
Unknown |
| 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.6592870C>T |
| DNA change (hg38) |
g.6592870C>T |
| Published as |
- |
| ISCN |
- |
| DB-ID |
GLDC_000053 See all 12 reported entries |
| Variant remarks |
GCE mutation |
| Reference |
PubMed: Conter et al. 2006, Published originally: Van Hove JLK, Mathieu V, Schollen E, et al (2003) Prognosis of nonketotic hyperglycinemia. J Inherit Metab Dis 26(Supplement 2): A141-O |
| ClinVar ID |
- |
| dbSNP ID |
- |
| Origin |
SUMMARY record |
| Segregation |
yes |
| Frequency |
- |
| Re-site |
- |
| VIP |
- |
| Methylation |
- |
| Average frequency (gnomAD v.2.1.1) |
1.0E-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 13:28:30 +02:00 (CEST) |
| Date last edited |
2017-05-05 19:04:32 +02:00 (CEST) |

Variant on transcripts
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