Product Details

SNP ID

rs10036800

Assay Type

Functionally Tested

NCBI dbSNP Submissions

NA

Location

Chr.5:175482708 on Build GRCh38

Set Membership

HapMap

Context Sequence [VIC/FAM]

CTGATCCTACCAACTCTATGAGCCA[A/C]CTCTTACCTGTGTTTTATAGATGAC

Phenotype

MIM: 615569

Polymorphism

A/C, Transversion Substitution

Allele Nomenclature

Literature Links

SFXN1 PubMed Links

Additional Information

For this assay, SNP(s) [rs115003842] 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

SFXN1

Gene Name

sideroflexin 1

Transcript Accession	SNP Location	SNP Type	Codon Change	Amino Acid Change	Protein ID
NM_001322977.1		Intron			NP_001309906.1
NM_001322978.1		Intron			NP_001309907.1
NM_001322980.1		Intron			NP_001309909.1
NM_001322981.1		Intron			NP_001309910.1
NM_001322982.1		Intron			NP_001309911.1
NM_001322983.1		Intron			NP_001309912.1
NM_022754.6		Intron			NP_073591.2

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