Product Details

SNP ID

rs17041292

Assay Type

Functionally Tested

NCBI dbSNP Submissions

NA

Location

Chr.4:110053318 on Build GRCh38

Set Membership

HapMap

Context Sequence [VIC/FAM]

TTATTCCTACCTTATCCCTCATGTA[C/G]TTCACAGATGGCCTAAAACGCTTGC

Phenotype

MIM: 611546

Polymorphism

C/G, Transversion Substitution

Allele Nomenclature

Literature Links

ELOVL6 PubMed Links

Additional Information

For this assay, SNP(s) [rs75843541] 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

ELOVL6

Gene Name

ELOVL fatty acid elongase 6

Transcript Accession	SNP Location	SNP Type	Codon Change	Amino Acid Change	Protein ID
NM_001130721.1		Intron			NP_001124193.1
NM_024090.2		Intron			NP_076995.1
XM_011532233.2		Intron			XP_011530535.1
XM_011532234.2		Intron			XP_011530536.1
XM_011532235.2		Intron			XP_011530537.1

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