Variant #0000016821 (NC_000009.11:g.124073097G>A, NM_000177.4:c.640G>A (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>A |
| DNA change (hg38) |
g.121310819G>A |
| Published as |
654G>A, D187N |
| ISCN |
- |
| DB-ID |
GSN_000001 See all 23 reported entries |
| Variant remarks |
Finnish major mutation: >28 Finnish FAF families and FAF patients (all homo). Also 2 American FAF families, 1 Dutch FAF family and 5 Japanese FAF families (all hom), and 1 Mexican patient with FAF (het). |
| Reference |
PubMed: Levy 1990, PubMed: Maury 1990, PubMed: Hiltunen 1991, PubMed: Paunio 1992, PubMed: de la Chapelle 1992a, PubMed: 1992b, PubMed: Taira 2012, PubMed: Gonzalez-Rodriguez 2014 |
| ClinVar ID |
- |
| dbSNP ID |
rs121909715 |
| Origin |
SUMMARY record |
| Segregation |
yes |
| Frequency |
- |
| Re-site |
- |
| VIP |
- |
| Methylation |
- |
| Average frequency (gnomAD v.2.1.1) |
0 View details |
| Owner |
Anne Polvi |
| Database submission license |
Creative Commons Attribution-NonCommercial-ShareAlike 4.0 International |
| 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
|
Screenscraping/webscraping (downloading large amounts of data using scripts) is strictly prohibited.
Use our APIs to retrieve data.
|