Product Details

SNP ID

rs35776966

Assay Type

Functionally Tested

NCBI dbSNP Submissions

NA

Location

Chr.6:133987587 on Build GRCh38

Set Membership

HapMap

Context Sequence [VIC/FAM]

TTAAAATCTATGCAAGCTTAAGACT[C/T]TGGCTAAAGTGTGTTGGCTTCTTTT

Phenotype

MIM: 610372 MIM: 605521

Polymorphism

C/T, Transition Substitution

Allele Nomenclature

Literature Links

SLC2A12 PubMed Links

Additional Information

For this assay, SNP(s) [rs142078499] are located under a primer 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

SLC2A12

Gene Name

solute carrier family 2 member 12

Transcript Accession	SNP Location	SNP Type	Codon Change	Amino Acid Change	Protein ID
NM_145176.2	5593	UTR 3			NP_660159.1
XM_006715349.3	5593	Intron			XP_006715412.1
XM_017010311.1	5593	Intron			XP_016865800.1

Gene

TBPL1

Gene Name

TATA-box binding protein like 1

Transcript Accession	SNP Location	SNP Type	Codon Change	Amino Acid Change	Protein ID
NM_001253676.1	5593	Intron			NP_001240605.1
NM_004865.3	5593	Intron			NP_004856.1
XM_017011513.1	5593	Intron			XP_016867002.1

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