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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