Product Details

SNP ID

rs148793965

Assay Type

Functionally Tested

NCBI dbSNP Submissions

NA

Location

Chr.16:15407831 on Build GRCh38

Set Membership

Context Sequence [VIC/FAM]

TTTTTTTCCCAATTCCAGAGTGGAC[C/T]GATGTACTGGCCCTTTGTACAGGTA

Phenotype

Polymorphism

C/T, Transition Substitution

Allele Nomenclature

Literature Links

MPV17L PubMed Links

Additional Information

For this assay, SNP(s) [rs542512244] 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

MPV17L

Gene Name

MPV17 mitochondrial inner membrane protein like

Transcript Accession	SNP Location	SNP Type	Codon Change	Amino Acid Change	Protein ID
NM_001128423.1	533	Missense Mutation	CCG,CTG	P130L	NP_001121895.1
NM_173803.3	533	Silent Mutation	ACC,ACT	T106T	NP_776164.2
XM_017023108.1	533	Intron			XP_016878597.1

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