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 International |
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) |

Variant on transcripts
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