Product Details

SNP ID

rs150881

Assay Type

Functionally Tested

NCBI dbSNP Submissions

NA

Location

Chr.7:74175029 on Build GRCh38

Set Membership

HapMap

Context Sequence [VIC/FAM]

TGCGGGCGGGGGGAGACCAAGGAGA[C/T]AAATCCATCGTAGCTTCTTTGTATT

Phenotype

MIM: 603431

Polymorphism

C/T, Transition Substitution

Allele Nomenclature

Literature Links

EIF4H PubMed Links

Additional Information

For this assay, SNP(s) [rs77024906] 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

EIF4H

Gene Name

eukaryotic translation initiation factor 4H

Transcript Accession	SNP Location	SNP Type	Codon Change	Amino Acid Change	Protein ID
NM_022170.1		Intron			NP_071496.1
NM_031992.1		Intron			NP_114381.1
XM_011516556.1		Intron			XP_011514858.1
XM_011516557.1		Intron			XP_011514859.1

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