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SNP ID:
rs201233519
Gene
OR4K13
Gene Name
olfactory receptor family 4 subfamily K member 13
Set Membership:
-
Chromosome Location:
Chr.14: 20034674 - 20034674 on Build GRCh38
Polymorphism:
A/G, Transition substitution
Context Sequence [VIC/FAM]:

CCCACGAAGACCACAGAGAATCCCA[A/G]GAAGAATAAAATCTGAAGATTTTGA

Assay ID C_190070541_10
Size
Availability Made To Order
Catalog # 4351379
Price
Your Price
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Genomic Map

Build 38.2 Human Chr.14: C_190070541_10
Created with Raphaël 2.1.2H?H?????H?????????????????????????HOR4K13OR4K1320,030,30020,030,40020,030,50020,030,60020,030,70020,030,80020,030,90020,031,00020,031,10020,031,20020,031,30020,031,40020,031,50020,031,60020,031,70020,031,80020,031,90020,032,00020,032,10020,032,20020,032,30020,032,40020,032,50020,032,60020,032,70020,032,80020,032,90020,033,00020,033,10020,033,20020,033,30020,033,40020,033,50020,033,60020,033,70020,033,80020,033,90020,034,00020,034,10020,034,20020,034,30020,034,40020,034,50020,034,60020,034,70020,034,80020,034,90020,035,00020,035,10020,035,20020,035,30020,035,40020,035,50020,035,60020,035,70020,035,80020,035,90020,036,00020,036,10020,036,20020,036,30020,036,40020,036,50020,036,60020,036,70020,036,80020,036,90020,037,00020,037,10020,037,20020,037,30020,037,40020,037,50020,037,60020,037,70020,037,80020,037,90020,038,00020,038,10020,038,20020,038,300
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Assay Details



Species:

 Human

dbSNP Submissions:

 NA

Phenotype:

Literature Links:

 OR4K13 PubMed Links

Allele Nomenclature:

Minor Allele Frequency:
1000Genome Applied Biosystems® HapMap
Global
G (0.00)
(1.00)
Caucasian - Not Available CEPH (CEU) - Not Available
EAS
G (0.00)
(1.00)
African American - Not Available YRI (Yoruba) - Not Available
SAS
G (0.00)
(1.00)
Chinese - Not Available CHB (Han Chinese) - Not Available
AFR
G (0.00)
(1.00)
Japanese - Not Available JPT (Japanese) - Not Available
EUR
G (0.00)
(1.00)
AMR
G (0.00)
(1.00)
OR4K13 - olfactory receptor family 4 subfamily K member 13
Transcript Accession SNP Location SNP Type Observed Codons Observed Amino Acid Protein ID
NM_001004714.1 85 Silent Mutation NP_001004714.1

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