Product Details

SNP ID

rs12412962

Assay Type

Functionally Tested

NCBI dbSNP Submissions

NA

Location

Chr.10:119149801 on Build GRCh38

Set Membership

HapMap

Context Sequence [VIC/FAM]

TCTCAGGGATATAAAGTAAAATTGC[A/T]TGACTTCCGGAAGGGAAAAATGGCT

Phenotype

MIM: 615564

Polymorphism

A/T, Transversion Substitution

Allele Nomenclature

Literature Links

SFXN4 PubMed Links

Additional Information

For this assay, SNP(s) [rs113691550] are located under a probe 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

SFXN4

Gene Name

sideroflexin 4

Transcript Accession	SNP Location	SNP Type	Codon Change	Amino Acid Change	Protein ID
NM_213649.1		Intron			NP_998814.1
XM_005269525.4		Intron			XP_005269582.1
XM_005269526.2		Intron			XP_005269583.1
XM_005269527.1		Intron			XP_005269584.1
XM_011539282.2		Intron			XP_011537584.1

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