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SNP ID:
rs53576
Gene
OXTR
Gene Name
Set Membership:
-
Chromosome Location:
Chr.3: 8762685 - 8762685 on Build GRCh38
Polymorphism:
A/G, Transition substitution
Context Sequence [VIC/FAM]:

AAAGGTGTACGGGACATGCCCGAGG[A/G]TCCTCAGTCCCACAGAAACAGGGAG

Assay ID C___3290335_10
Size
Availability Made To Order
Catalog # 4351379
Price
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Assay Details



Species:

 Human

dbSNP Submissions:

 NA

Phenotype:

 MIM: 167055

Literature Links:

 OXTR PubMed Links

Allele Nomenclature:

Minor Allele Frequency:
1000Genome Applied Biosystems® HapMap
Global
A (0.39)
(0.61)
Caucasian - Not Available CEPH (CEU) - Not Available
EAS
G (0.35)
(0.65)
African American - Not Available YRI (Yoruba) - Not Available
SAS
A (0.45)
(0.55)
Chinese - Not Available CHB (Han Chinese) - Not Available
AFR
A (0.19)
(0.81)
Japanese - Not Available JPT (Japanese) - Not Available
EUR
A (0.35)
(0.65)
AMR
A (0.36)
(0.64)
OXTR - oxytocin receptor
Transcript Accession SNP Location SNP Type Observed Codons Observed Amino Acid Protein ID
NM_000916.3 Intron NP_000907.2
XM_011533762.2 Intron XP_011532064.1

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More Information


Additional Information:

For this assay, SNP(s) [rs75943879] are located under a primer sequence. To help evaluate the possible impact of a given SNP on your experiment, please refer to the 1000 Genomes and NCBI dbSNP databases. A higher minor allele frequency in your study population represents a higher risk to assay performance.

Panther Classification:

Molecular Function -

G-protein coupled receptor

Gene Ontology Categories:

Function(s) Process(es)


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