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See other OR6Q1 GT Assays ›
SNP ID:
rs2513726
Gene
OR6Q1 OR9Q1 VN2R9P
Gene Name
Set Membership:
> HapMap > Validated
Chromosome Location:
Chr.11: 58031470 - 58031470 on Build GRCh38
Polymorphism:
A/G, Transition substitution
Context Sequence [VIC/FAM]:

TACCTCTTGTCTCAGCTAACATTTT[A/G]TGGCCCAAATGTCATTGACCATTTC

Assay ID C__11666543_10
Size
Availability Made To Order
Catalog # 4351379
Price
Your Price
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Assay Details



Species:

 Human

dbSNP Submissions:

 NA

Phenotype:

Literature Links:

 OR6Q1 PubMed Links

Allele Nomenclature:

Minor Allele Frequency:
1000Genome Applied Biosystems® HapMap
Global
G (0.41)
(0.59)
Caucasian
G (0.24)
(0.76)
CEPH (CEU)
G (0.25)
(0.75)
EAS
A (0.32)
(0.68)
African American
G (0.44)
(0.56)
YRI (Yoruba)
G (0.33)
(0.67)
SAS
G (0.46)
(0.54)
Japanese
A (0.49)
(0.51)
JPT (Japanese)
A (0.40)
(0.60)
AFR
G (0.32)
(0.68)
Chinese
A (0.21)
(0.79)
CHB (Han Chinese)
A (0.31)
(0.69)
EUR
G (0.29)
(0.71)
AMR
G (0.27)
(0.73)
OR6Q1 - olfactory receptor family 6 subfamily Q member 1 (gene/pseudogene)
Transcript Accession SNP Location SNP Type Observed Codons Observed Amino Acid Protein ID
NM_001005186.2 518 Missense Mutation TAT,TGT Y,C 173 NP_001005186.2
OR9Q1 - olfactory receptor family 9 subfamily Q member 1
Transcript Accession SNP Location SNP Type Observed Codons Observed Amino Acid Protein ID
NM_001005212.3 518 Intron NP_001005212.1
VN2R9P - vomeronasal 2 receptor 9 pseudogene
There are no transcripts associated with this gene.

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