Product Details

SNP ID

rs8523

Assay Type

Functionally Tested

NCBI dbSNP Submissions

NA

Location

Chr.6:10980820 on Build GRCh38

Set Membership

HapMap

Context Sequence [VIC/FAM]

AGATAATGCTTTTTATCTACAAAGA[G/A]AAATGGCTTCTGCAGCCTCCCTGTC

Phenotype

MIM: 611814 MIM: 616799

Polymorphism

G/A, Transition Substitution

Allele Nomenclature

Literature Links

ELOVL2 PubMed Links

Additional Information

For this assay, SNP(s) [rs41507245] 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

ELOVL2

Gene Name

ELOVL fatty acid elongase 2

Transcript Accession	SNP Location	SNP Type	Codon Change	Amino Acid Change	Protein ID
NM_017770.3	4013	UTR 3			NP_060240.3
XM_011514716.2	4013	UTR 3			XP_011513018.1
XM_011514717.2	4013	Intron			XP_011513019.1
XM_017010985.1	4013	Intron			XP_016866474.1

Gene

SYCP2L

Gene Name

synaptonemal complex protein 2 like

There are no transcripts associated with this gene.

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