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See other PPARG GT Assays ›
SNP ID:
rs1801282
Gene
PPARG
Gene Name
Set Membership:
> HapMap > DME > Validated > Inventoried
Chromosome Location:
Chr.3: 12351626 - 12351626 on Build GRCh38
Polymorphism:
C/G, Transversion substitution
Context Sequence [VIC/FAM]:

AACTCTGGGAGATTCTCCTATTGAC[C/G]CAGAAAGCGATTCCTTCACTGATAC

Assay ID C___1129864_10
Size VIC-FAM | 150 rxns
Availability Inventoried
Catalog # 4362691
Price
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Assay Details



Species:

 Human

dbSNP Submissions:

 NA

Phenotype:

 MIM: 601487

Literature Links:

 PPARG PubMed Links

Allele Nomenclature:

Minor Allele Frequency:
1000Genome Applied Biosystems® HapMap
Global
G (0.07)
(0.93)
Caucasian
G (0.18)
(0.82)
CEPH (CEU)
G (0.10)
(0.90)
EAS
G (0.03)
(0.97)
African American
G (0.02)
(0.98)
YRI (Yoruba) - Not Available
SAS
G (0.12)
(0.88)
Japanese
G (0.03)
(0.97)
JPT (Japanese)
G (0.04)
(0.96)
AFR
G (0.01)
(0.99)
Chinese
G (0.01)
(0.99)
CHB (Han Chinese)
G (0.02)
(0.98)
EUR
G (0.12)
(0.88)
AMR
G (0.12)
(0.88)
PPARG - peroxisome proliferator activated receptor gamma
Transcript Accession SNP Location SNP Type Observed Codons Observed Amino Acid Protein ID
NM_005037.5 2153 Intron NP_005028.4
NM_015869.4 2153 Missense Mutation CCA,GCA P,A 12 NP_056953.2
NM_138711.3 2153 Intron NP_619725.2
NM_138712.3 2153 Intron NP_619726.2
XM_011533841.2 2153 Intron XP_011532143.1
XM_011533842.2 2153 Missense Mutation CCA,GCA P,A 12 XP_011532144.1
XM_011533843.2 2153 Missense Mutation CCA,GCA P,A 12 XP_011532145.1
XM_011533844.1 2153 Intron XP_011532146.1

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More Information


Set Membership:

 HapMap DME Validated Inventoried

Panther Classification:

Gene Ontology Categories:

Function(s) Process(es)


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