Product Details

SNP ID

rs140291848

Assay Type

Functionally Tested

NCBI dbSNP Submissions

NA

Location

Chr.5:138510702 on Build GRCh38

Set Membership

Context Sequence [VIC/FAM]

AATCTGTGTAAGCTCCATAAGATGA[C/G]GTTAGATGAGAAAAGGGCTCAGGGA

Phenotype

MIM: 600285

Polymorphism

C/G, Transversion Substitution

Allele Nomenclature

Literature Links

ETF1 PubMed Links

Additional Information

For this assay, SNP(s) [rs146495877] are located under a probe and SNP(s) [rs146495877] 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

ETF1

Gene Name

eukaryotic translation termination factor 1

Transcript Accession	SNP Location	SNP Type	Codon Change	Amino Acid Change	Protein ID
NM_001256302.1		Intron			NP_001243231.1
NM_001282185.1		Intron			NP_001269114.1
NM_001291974.1		Intron			NP_001278903.1
NM_001291975.1		Intron			NP_001278904.1
NM_004730.3		Intron			NP_004721.1
XM_005271921.1		Intron			XP_005271978.1
XM_017009221.1		Intron			XP_016864710.1
XM_017009222.1		Intron			XP_016864711.1

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