Annotation Detail
Information
- Associated Genes
- SNCA
- Associated Variants
-
SNCA p.His50Gln (p.H50Q)
(
ENST00000336904.7,
ENST00000345009.8,
ENST00000394986.5,
ENST00000394989.6,
ENST00000394991.8,
ENST00000420646.6,
ENST00000502987.5,
ENST00000505199.5,
ENST00000506244.5,
ENST00000508895.5,
ENST00000611107.1,
ENST00000618500.4,
ENST00000673718.1,
ENST00000673902.1,
ENST00000674129.1 )
SNCA p.His50Gln (p.H50Q) ( ENST00000336904.7, ENST00000345009.8, ENST00000394986.5, ENST00000394989.6, ENST00000394991.8, ENST00000420646.6, ENST00000502987.5, ENST00000505199.5, ENST00000506244.5, ENST00000508895.5, ENST00000611107.1, ENST00000618500.4, ENST00000673718.1, ENST00000673902.1, ENST00000674129.1 ) - Associated Disease
- Presenile dementia
- Source Database
- DisGeNET
- Description
- Here, we describe a novel missense mutation in exon 4 of SNCA encoding a H50Q substitution in a patient with dopa-responsive Parkinson's disease with a family history of parkinsonism and dementia.
- Pubmed
- 23457019
- Original source reporting the Gene Disease association
- BeFree
- DisGENET score for the Gene Disease association
- 0.00352874433704394
- Year of publication
- 2013
Drugs