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See other ABCC12 GT Assays ›
SNP ID:
rs9925287
Gene
ABCC12
Gene Name
Set Membership:
> HapMap > DME > Validated > Inventoried
Chromosome Location:
Chr.16: 48104348 - 48104348 on Build GRCh38
Polymorphism:
A/G, Transition substitution
Context Sequence [VIC/FAM]:

TGCCAGTGGGAGTCGTGTCAAAGAA[A/G]CTCATTGGGCTCTTTAAGATCTGTG

Assay ID C__25972550_20
Size 150 rxns
Availability Inventoried
Catalog # 4362691
Price
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Assay Details



Species:

 Human

dbSNP Submissions:

 NA

Phenotype:

 MIM: 607041

Literature Links:

 ABCC12 PubMed Links

Allele Nomenclature:

Minor Allele Frequency:
1000Genome Applied Biosystems® HapMap
Global
G (0.09)
(0.91)
Caucasian
G (0.00)
(1.00)
CEPH (CEU) - Not Available
EAS
G (0.00)
(1.00)
African American
G (0.21)
(0.79)
YRI (Yoruba)
G (0.29)
(0.71)
SAS
G (0.00)
(1.00)
Japanese
G (0.00)
(1.00)
CHB (Han Chinese) - Not Available
AFR
G (0.31)
(0.69)
Chinese
G (0.00)
(1.00)
JPT (Japanese) - Not Available
EUR
G (0.00)
(1.00)
AMR
G (0.03)
(0.97)
ABCC12 - ATP binding cassette subfamily C member 12
Transcript Accession SNP Location SNP Type Observed Codons Observed Amino Acid Protein ID
NM_033226.2 3040 Silent Mutation NP_150229.2

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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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