Product Details

SNP ID
hCV26374361
Assay Type
Functionally tested
NCBI dbSNP Submissions
NA
Location
Chr.4:9771576 on Build GRCh38
Set Membership
Context Sequence [VIC/FAM]
ATGATATGTTCATCTATGCAACACA[G/T]ATCAATGGGTTCATCCCAGTCAGGC
Phenotype
MIM: 606142
Polymorphism
G/T, Transversion 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

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