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SNP ID:
rs938564
Gene
SLC2A9
Gene Name
Set Membership:
> HapMap
Chromosome Location:
Chr.4: 9920949 - 9920949 on Build GRCh38
Polymorphism:
G/T, Transversion substitution
Context Sequence [VIC/FAM]:

TCCAATGGCTGTTGTAATAATTGCA[G/T]GATATCATATACATTCAACCATGGC

Assay ID C___1216565_10
Size
Availability Made To Order
Catalog # 4351379
Price
Your Price
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Assay Details



Species:

 Human

dbSNP Submissions:

 NA

Phenotype:

 MIM: 606142

Literature Links:

 SLC2A9 PubMed Links

Allele Nomenclature:

Minor Allele Frequency:
1000Genome Applied Biosystems® HapMap
Global
G (0.29)
(0.71)
Caucasian - Not Available CEPH (CEU)
G (0.26)
(0.74)
EAS
G (0.01)
(0.99)
African American - Not Available YRI (Yoruba)
G (0.47)
(0.53)
SAS
G (0.20)
(0.80)
Chinese - Not Available JPT (Japanese)
G (0.01)
(0.99)
AFR
T (0.44)
(0.56)
Japanese - Not Available CHB (Han Chinese)
G (0.01)
(0.99)
EUR
G (0.22)
(0.78)
AMR
G (0.40)
(0.60)
SLC2A9 - solute carrier family 2 member 9
Transcript Accession SNP Location SNP Type Observed Codons Observed Amino Acid Protein ID
NM_001001290.1 Intron NP_001001290.1
NM_020041.2 Intron NP_064425.2
XM_006713968.3 Intron XP_006714031.1
XM_006713969.2 Intron XP_006714032.1
XM_011513856.2 Intron XP_011512158.1
XM_011513857.1 Intron XP_011512159.1
XM_011513858.1 Intron XP_011512160.1
XM_011513859.2 Intron XP_011512161.1
XM_011513860.2 Intron XP_011512162.1
XM_011513861.2 Intron XP_011512163.1
XM_011513862.2 Intron XP_011512164.1
XM_011513863.2 Intron XP_011512165.1
XM_011513864.2 Intron XP_011512166.1
XM_011513865.2 Intron XP_011512167.1
XM_011513866.2 Intron XP_011512168.1
XM_011513867.2 Intron XP_011512169.1
XM_011513868.2 Intron XP_011512170.1
XM_017008457.1 Intron XP_016863946.1
XM_017008458.1 Intron XP_016863947.1
XM_017008459.1 Intron XP_016863948.1
XM_017008460.1 Intron XP_016863949.1

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