Product Details

SNP ID
rs13124141
Assay Type
Functionally tested
NCBI dbSNP Submissions
NA
Location
Chr.4:9771613 on Build GRCh38
Set Membership
Context Sequence [VIC/FAM]
CATCCCAGTCAGGCTGACTCCAAGA[A/G]GCTAAGATGACTTCACCTTGAGTGG
Phenotype
MIM: 606142
Polymorphism
A/G, Transition substitution
Allele Nomenclature
Literature Links
SLC2A9 PubMed Links

Gene Details

Gene
SLC2A9
Gene Name
solute carrier family 2 member 9
Transcript Accession SNP Location SNP Type Codon Change Amino Acid Change 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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