Product Details

SNP ID

rs11557271

Assay Type

Functionally Tested

NCBI dbSNP Submissions

NA

Location

Chr.19:1555585 on Build GRCh38

Set Membership

Context Sequence [VIC/FAM]

GCTCTAGGAAAAGATATGAATGGCC[C/T]GGGTGGCCGGCGTGCGGCAGGCGGG

Phenotype

MIM: 611009

Polymorphism

C/T, Transition Substitution

Allele Nomenclature

Literature Links

MEX3D PubMed Links

Additional Information

For this assay, SNP(s) [rs114451952] 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

MEX3D

Gene Name

mex-3 RNA binding family member D

Transcript Accession	SNP Location	SNP Type	Codon Change	Amino Acid Change	Protein ID
NM_001174118.1	1934	Missense Mutation	CAG,CGG	Q645R	NP_001167589.1
NM_203304.3	1934	Missense Mutation	CAG,CGG	Q645R	NP_976049.3
XM_017026811.1	1934	Missense Mutation	CAG,CGG	Q411R	XP_016882300.1

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