Variant #0000016822 (NC_000009.11:g.124073097G>T, NM_000177.4:c.640G>T (GSN))
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.124073097G>T |
DNA change (hg38) |
g.121310819G>T |
Published as |
654G>T, D187Y |
ISCN |
- |
DB-ID |
GSN_000002 See all 5 reported entries |
Variant remarks |
1 Danish, 1 Czech, 1 Brazilian and 1 French FAF family (all hom) |
Reference |
PubMed: de la Chapelle et al. 1992, PubMed: Solari et al. 2011, PubMed: Chastan et al. 2006 |
ClinVar ID |
- |
dbSNP ID |
rs121909715 |
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 |
2012-12-10 17:24:38 +01:00 (CET) |
Date last edited |
2017-05-05 19:04:32 +02:00 (CEST) |

Variant on transcripts
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