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)
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Variant on transcripts


Gene     

AscendingTranscript     

Affects function     

Exon     

DNA change (cDNA)     

RNA change     

Protein     
GSN NM_000177.4 +/+ 4 c.640G>T r.(640g>u) p.(Asp214Tyr)


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