Variant #0000001423 (NC_000009.11:g.131303403T>C, NM_001003722.1:c.2051T>C (GLE1))
| Chromosome |
9 |
| Allele |
Unknown |
| Affects function (as reported) |
Affects function |
| Affects function (by curator) |
Affects function |
| Classification method |
- |
| Clinical classification |
pathogenic (recessive) |
| DNA change (genomic) (Relative to hg19 / GRCh37) |
g.131303403T>C |
| DNA change (hg38) |
g.128541124T>C |
| Published as |
- |
| ISCN |
- |
| DB-ID |
GLE1_000004 See all 7 reported entries |
| Variant remarks |
6 Finnish LAAHD patients (com-het) |
| Reference |
- |
| ClinVar ID |
- |
| dbSNP ID |
rs121434409 |
| Origin |
SUMMARY record |
| Segregation |
yes |
| Frequency |
- |
| Re-site |
- |
| VIP |
- |
| Methylation |
- |
| Average frequency (gnomAD v.2.1.1) |
4.0E-5 View details |
| Owner |
Anne Polvi |
| Database submission license |
Creative Commons Attribution-NonCommercial-ShareAlike 4.0 International |
| Created by |
Anne Polvi |
| Date created |
2012-08-01 09:53:10 +02:00 (CEST) |
| Date last edited |
2020-07-21 21:53:48 +02:00 (CEST) |

Variant on transcripts
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