Product Details

SNP ID

rs12077118

Assay Type

Functionally Tested

NCBI dbSNP Submissions

26

Location

Chr.1:167734713 on Build GRCh38

Set Membership

HapMap

Context Sequence [VIC/FAM]

AAAGAGAGGCGTTGGGGGTAGGTCC[C/T]GAGGAGAATCAGCAGTGTCTTGCAA

Phenotype

MIM: 604376

Polymorphism

C/T, Transition Substitution

Allele Nomenclature

Literature Links

MPZL1 PubMed Links

Additional Information

For this assay, SNP(s) [rs79468622] 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

MPZL1

Gene Name

myelin protein zero like 1

Transcript Accession	SNP Location	SNP Type	Codon Change	Amino Acid Change	Protein ID
NM_001146191.1		Intron			NP_001139663.1
NM_003953.5		Intron			NP_003944.1
NM_024569.4		Intron			NP_078845.3

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