Variant #0000001579 (NC_000009.11:g.(?_6645245)_(6645307_?)del, NC_000009.11(NM_000170.2):c.(?_-1)_(255+1_256-1)del (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.(?_6645245)_(6645307_?)del |
DNA change (hg38) |
- |
Published as |
del Exon 1 |
ISCN |
- |
DB-ID |
GLDC_000006 See all 6 reported entries |
Variant remarks |
9 GCE families |
Reference |
PubMed: Kure et al. 2002, PubMed: Kure et al. 2006, PubMed: Contel et al. 2006, PubMed: Kanno et al. 2007 |
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 |
No license selected |
Created by |
Anne Polvi |
Date created |
2012-08-31 12:34:33 +02:00 (CEST) |
Date last edited |
2017-05-05 18:33:04 +02:00 (CEST) |

Variant on transcripts
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