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SNP ID

rs145871604

Assay Type

Functionally tested

NCBI dbSNP Submissions

NA

Location

Chr.12:7925916 on Build GRCh38

Set Membership

Context Sequence [VIC/FAM]

CATAGATGGGCTCTTGAACACCTGC[A/G]TCCTTGAAGATTCCTGTTGAGTAAT

Phenotype

MIM: 138170

Polymorphism

A/G, Transition substitution

Allele Nomenclature

Literature Links

SLC2A3 PubMed Links

Gene Details

Gene

SLC2A3

Gene Name

solute carrier family 2 member 3

Transcript Accession	SNP Location	SNP Type	Codon Change	Amino Acid Change	Protein ID
NM_006931.2		Intron			NP_008862.1

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