Product Details

SNP ID

rs3809852

Assay Type

Functionally Tested

NCBI dbSNP Submissions

NA

Location

Chr.17:4439855 on Build GRCh38

Set Membership

HapMap

Context Sequence [VIC/FAM]

GGCACAGAGGGTGGGTGGGGTATGG[A/G]CCTGAGGGACAGTCTAGGCAGGAGC

Phenotype

MIM: 611701

Polymorphism

A/G, Transition Substitution

Allele Nomenclature

Literature Links

SPNS3 PubMed Links

Additional Information

For this assay, SNP(s) [rs78337983] 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

SPNS3

Gene Name

sphingolipid transporter 3 (putative)

Transcript Accession	SNP Location	SNP Type	Codon Change	Amino Acid Change	Protein ID
NM_001320449.1		Intron			NP_001307378.1
NM_182538.4		Intron			NP_872344.3
XM_011523723.1		Intron			XP_011522025.1
XM_011523724.1		Intron			XP_011522026.1
XM_011523725.1		Intron			XP_011522027.1
XM_011523726.2		Intron			XP_011522028.1
XM_011523728.2		Intron			XP_011522030.1
XM_017024345.1		Intron			XP_016879834.1

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