Variant #0000001679 (NC_000009.11:g.6540050C>G, NC_000009.11(NM_000170.2):c.2665+1G>C (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.6540050C>G |
DNA change (hg38) |
g.6540050C>G |
Published as |
- |
ISCN |
- |
DB-ID |
GLDC_000094 See all 14 reported entries |
Variant remarks |
2 GCE families |
Reference |
PubMed: Kure et al. 2006 |
ClinVar ID |
- |
dbSNP ID |
rs149070244 |
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 |
No license selected |
Created by |
Anne Polvi |
Date created |
2012-09-05 09:27:55 +02:00 (CEST) |
Date last edited |
2020-06-25 12:32:58 +02:00 (CEST) |

Variant on transcripts
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