Variant #0000016597 (NC_000011.9:g.125769895A>G, NM_145014.2:c.632A>G (HYLS1))

Chromosome 11
Allele Unknown
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.125769895A>G
DNA change (hg38) g.125900000A>G
Published as D211G
ISCN -
DB-ID HYLS1_000001
Variant remarks Finnish HLS1 Founder mutation: More than 64 Finnish cases (hom) with HLS1
Reference PubMed: Mee et al. 2005, PubMed: Paetau et al. 2008
ClinVar ID -
dbSNP ID rs104894232
Origin SUMMARY record
Segregation yes
Frequency -
Re-site -
VIP -
Methylation -
Average frequency (gnomAD v.2.1.1) 0.00114 View details
Owner Anne Polvi
Database submission license Creative Commons Attribution-NonCommercial-ShareAlike 4.0 InternationalCreative Commons License
Created by Anne Polvi
Date created 2012-12-04 15:57:46 +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     
HYLS1 NM_145014.2 +/+ 05 c.632A>G r.632a>g p.Asp211Gly


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