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See other SNCA GT Assays ›
SNP ID:
rs9995651
Gene
SNCA
Gene Name
Set Membership:
> HapMap
Chromosome Location:
Chr.4: 89795026 - 89795026 on Build GRCh38
Polymorphism:
C/G, Transversion substitution
Context Sequence [VIC/FAM]:

AAGTGGTGAGAATTCAAATAGTTCT[C/G]GAACCCTATTTGTCATATCACTTCC

Assay ID C__29734260_10
Size
Availability Made To Order
Catalog # 4351379
Price
Your Price
Online offer:
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Assay Details



Species:

 Human

dbSNP Submissions:

 NA

Phenotype:

 MIM: 163890

Literature Links:

 SNCA PubMed Links

Allele Nomenclature:

Minor Allele Frequency:
1000Genome Applied Biosystems® HapMap
Global
G (0.06)
(0.94)
Caucasian - Not Available CEPH (CEU)
G (0.06)
(0.94)
EAS
G (0.00)
(1.00)
African American - Not Available YRI (Yoruba)
G (0.23)
(0.77)
SAS
G (0.03)
(0.97)
Chinese - Not Available CHB (Han Chinese) - Not Available
AFR
G (0.17)
(0.83)
Japanese - Not Available JPT (Japanese) - Not Available
EUR
G (0.04)
(0.96)
AMR
G (0.03)
(0.97)
SNCA - synuclein alpha
Transcript Accession SNP Location SNP Type Observed Codons Observed Amino Acid Protein ID
NM_000345.3 Intron NP_000336.1
NM_001146054.1 Intron NP_001139526.1
NM_001146055.1 Intron NP_001139527.1
NM_007308.2 Intron NP_009292.1
XM_011532203.1 Intron XP_011530505.1
XM_011532204.2 Intron XP_011530506.1
XM_011532205.2 Intron XP_011530507.1
XM_011532206.1 Intron XP_011530508.1
XM_011532207.1 Intron XP_011530509.1
XM_011532208.2 Intron XP_011530510.1
XM_017008562.1 Intron XP_016864051.1
XM_017008563.1 Intron XP_016864052.1

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More Information


Set Membership:

 HapMap

Panther Classification:

Gene Ontology Categories:

Function(s) Process(es)


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