Product Details

SNP ID

rs56204521

Assay Type

Functionally Tested

NCBI dbSNP Submissions

NA

Location

Chr.3:170996983 on Build GRCh38

Set Membership

Context Sequence [VIC/FAM]

AGTGATCAATCCTTTACTTCAAATT[G/T]TCTTACATTAGATTTGATCAAACTT

Phenotype

MIM: 138160

Polymorphism

G/T, Transversion Substitution

Allele Nomenclature

Literature Links

SLC2A2 PubMed Links

Additional Information

For this assay, SNP(s) [rs77733690] are located under a probe sequence. To help evaluate the possible impact of a given SNP on your experiment, please refer to the 1000 Genomes and NCBI dbSNP databases. A higher minor allele frequency in your study population represents a higher risk to assay performance.

Gene Details

Gene

SLC2A2

Gene Name

solute carrier family 2 member 2

Transcript Accession	SNP Location	SNP Type	Codon Change	Amino Acid Change	Protein ID
NM_000340.1	2804	UTR 3			NP_000331.1
NM_001278658.1	2804	UTR 3			NP_001265587.1
NM_001278659.1	2804	UTR 3			NP_001265588.1
XM_011513087.2	2804	UTR 3			XP_011511389.1
XM_011513089.2	2804	UTR 3			XP_011511391.1

View Full Product Details