Product Details

SNP ID

rs11631813

Assay Type

Functionally Tested

NCBI dbSNP Submissions

NA

Location

Chr.15:82262901 on Build GRCh38

Set Membership

HapMap

Context Sequence [VIC/FAM]

AAGCATGGGAGCCAAGAGTATGAGG[A/G]GCTGGTGTCTGTGTCAGATTTGTAG

Phenotype

Polymorphism

A/G, Transition Substitution

Allele Nomenclature

Literature Links

EFL1 PubMed Links

Additional Information

For this assay, SNP(s) [rs149892112] 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

EFL1

Gene Name

elongation factor like GTPase 1

Transcript Accession	SNP Location	SNP Type	Codon Change	Amino Acid Change	Protein ID
NM_001040610.2		Intron			NP_001035700.1
NM_001322844.1		Intron			NP_001309773.1
NM_001322845.1		Intron			NP_001309774.1
NM_024580.5		Intron			NP_078856.4
XM_011522000.1		Intron			XP_011520302.1

Gene

SAXO2

Gene Name

stabilizer of axonemal microtubules 2

Transcript Accession	SNP Location	SNP Type	Codon Change	Amino Acid Change	Protein ID
NM_001008226.1		Intron			NP_001008227.1

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