Variant #0000001645 (NC_000009.11:g.6554673C>T, NM_000170.2:c.2311G>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.6554673C>T |
| DNA change (hg38) |
g.6554673C>T |
| Published as |
- |
| ISCN |
- |
| DB-ID |
GLDC_000061 See all 12 reported entries |
| Variant remarks |
4 or more GCE families. |
| Reference |
PubMed: Kure et al. 2004, PubMed: Conter et al. 2006, Originally published: Kure S, et al (2003) A comprehensive mutation analysis of GLDC, AMT and GCSH in glycine encephalopathy. J Inherit Metab Dis 26(Supplement 2): 132-O. |
| 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 |
2012-09-04 14:13:03 +02:00 (CEST) |
| Date last edited |
2017-05-05 18:33:04 +02:00 (CEST) |

Variant on transcripts
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