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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