Variant #0000001690 (NC_000009.11:g.6540109G>T, NM_000170.2:c.2607C>A (GLDC))
| Chromosome |
9 |
| Allele |
Both (homozygous) |
| 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.6540109G>T |
| DNA change (hg38) |
g.6540109G>T |
| Published as |
3 cDNA splice variants: exon 22 del, exon 22-23 del and 87-bp ins |
| ISCN |
- |
| DB-ID |
GLDC_000105 See all 2 reported entries |
| Variant remarks |
9 homozygous consanguineous Israeli Bedouin kindred with GCE |
| Reference |
PubMed: Flusser et al. 2005 |
| ClinVar ID |
- |
| dbSNP ID |
- |
| Origin |
SUMMARY record |
| Segregation |
yes |
| Frequency |
- |
| Re-site |
- |
| VIP |
- |
| Methylation |
- |
| Average frequency (gnomAD v.2.1.1) |
9.0E-5 View details |
| Owner |
Anne Polvi |
| Database submission license |
Creative Commons Attribution-NonCommercial-ShareAlike 4.0 International |
| Created by |
Anne Polvi |
| Date created |
2012-09-05 10:24:55 +02:00 (CEST) |
| Date last edited |
2017-05-05 19:04:32 +02:00 (CEST) |

Variant on transcripts
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