Product Details

SNP ID

rs12443828

Assay Type

Functionally Tested

NCBI dbSNP Submissions

NA

Location

Chr.16:81450595 on Build GRCh38

Set Membership

HapMap

Context Sequence [VIC/FAM]

ATGACTTTCTGCACAAATGGAAGGG[A/T]TTATTGTTACCTAAAAATGGGTGGC

Phenotype

MIM: 610112

Polymorphism

A/T, Transversion Substitution

Allele Nomenclature

Literature Links

CMIP PubMed Links

Additional Information

For this assay, SNP(s) [rs80327237] 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

CMIP

Gene Name

c-Maf inducing protein

Transcript Accession	SNP Location	SNP Type	Codon Change	Amino Acid Change	Protein ID
NM_030629.2		Intron			NP_085132.1
NM_198390.2		Intron			NP_938204.2
XM_005256179.4		Intron			XP_005256236.4
XM_005256181.2		Intron			XP_005256238.1
XM_005256182.1		Intron			XP_005256239.1
XM_011523352.1		Intron			XP_011521654.1
XM_011523353.1		Intron			XP_011521655.1
XM_017023733.1		Intron			XP_016879222.1

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