Product Details

SNP ID

rs3020110

Assay Type

Functionally Tested

NCBI dbSNP Submissions

NA

Location

Chr.8:116954055 on Build GRCh38

Set Membership

HapMap

Context Sequence [VIC/FAM]

GAGGATGCAGAGAGTAGTCCTAACT[A/T]AGAAATAATTAGGAGAAGAATAATC

Phenotype

MIM: 611145

Polymorphism

A/T, Transversion Substitution

Allele Nomenclature

Literature Links

SLC30A8 PubMed Links

Additional Information

For this assay, SNP(s) [rs147955977] 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

SLC30A8

Gene Name

solute carrier family 30 member 8

Transcript Accession	SNP Location	SNP Type	Codon Change	Amino Acid Change	Protein ID
NM_001172811.1		Intron			NP_001166282.1
NM_001172813.1		Intron			NP_001166284.1
NM_001172814.1		Intron			NP_001166285.1
NM_001172815.2		Intron			NP_001166286.1
NM_173851.2		Intron			NP_776250.2

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