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See other NOS3 GT Assays ›
SNP ID:
rs2070744
Gene
NOS3
Gene Name
Set Membership:
-
Chromosome Location:
Chr.7: 150992991 - 150992991 on Build GRCh38
Polymorphism:
C/T, Transition substitution
Context Sequence [VIC/FAM]:

CCAGGGCATCAAGCTCTTCCCTGGC[C/T]GGCTGACCCTGCCTCAGCCCTAGTC

Assay ID C__15903863_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: 163729

Literature Links:

 NOS3 PubMed Links

Allele Nomenclature:

Minor Allele Frequency:
1000Genome Applied Biosystems® HapMap
Global
C (0.23)
(0.77)
Caucasian - Not Available CEPH (CEU) - Not Available
EAS
C (0.12)
(0.88)
African American - Not Available YRI (Yoruba) - Not Available
SAS
C (0.26)
(0.74)
Chinese - Not Available CHB (Han Chinese) - Not Available
AFR
C (0.14)
(0.86)
Japanese - Not Available JPT (Japanese) - Not Available
EUR
C (0.44)
(0.56)
AMR
C (0.26)
(0.74)
NOS3 - nitric oxide synthase 3
Transcript Accession SNP Location SNP Type Observed Codons Observed Amino Acid Protein ID
NM_000603.4 Intron NP_000594.2
NM_001160109.1 Intron NP_001153581.1
NM_001160110.1 Intron NP_001153582.1
NM_001160111.1 Intron NP_001153583.1
XM_006716002.3 Intron XP_006716065.1
XM_017012232.1 Intron XP_016867721.1
XM_017012233.1 Intron XP_016867722.1
XM_017012234.1 Intron XP_016867723.1

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More Information


Panther Classification:

Gene Ontology Categories:

Function(s) Process(es)


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