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See other CYP2R1 GT Assays ›
SNP ID:
rs10741657
Gene
CYP2R1 LOC107984314
Gene Name
Set Membership:
> HapMap
Chromosome Location:
Chr.11: 14893332 - 14893332 on Build GRCh38
Polymorphism:
A/G, Transition substitution
Context Sequence [VIC/FAM]:

TGGTTGGGGAGATACTTTAGCAGGC[A/G]AGGGCTGTCAAGGAAAGTCTTATTA

Assay ID C___2958430_10
Size
Availability Made To Order
Catalog # 4351379
Price
Your Price
Online offer:
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Assay Details



Species:

 Human

dbSNP Submissions:

 NA

Phenotype:

 MIM: 608713

Literature Links:

 CYP2R1 PubMed Links

Allele Nomenclature:

Minor Allele Frequency:
1000Genome Applied Biosystems® HapMap
Global
A (0.31)
(0.69)
Caucasian - Not Available CEPH (CEU)
A (0.37)
(0.63)
EAS
A (0.32)
(0.68)
African American - Not Available YRI (Yoruba)
A (0.22)
(0.78)
SAS
A (0.36)
(0.64)
Chinese - Not Available JPT (Japanese)
A (0.40)
(0.60)
AFR
A (0.22)
(0.78)
Japanese - Not Available CHB (Han Chinese)
A (0.36)
(0.64)
EUR
A (0.38)
(0.62)
AMR
A (0.28)
(0.72)
CYP2R1 - cytochrome P450 family 2 subfamily R member 1
Transcript Accession SNP Location SNP Type Observed Codons Observed Amino Acid Protein ID
NM_024514.4 5582 Intron NP_078790.2
XM_005252788.1 5582 Intron XP_005252845.1
XM_005252789.2 5582 Intron XP_005252846.1
XM_011519895.1 5582 Intron XP_011518197.1
XM_011519898.2 5582 UTR 5 XP_011518200.1
XM_017017190.1 5582 Intron XP_016872679.1
XM_017017191.1 5582 Intron XP_016872680.1
XM_017017192.1 5582 Intron XP_016872681.1
XM_017017193.1 5582 Intron XP_016872682.1
XM_017017194.1 5582 Intron XP_016872683.1
XM_017017195.1 5582 Intron XP_016872684.1
LOC107984314 - uncharacterized LOC107984314
There are no transcripts associated with this gene.

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