Product Details

SNP ID

rs7717865

Assay Type

Functionally Tested

NCBI dbSNP Submissions

NA

Location

Chr.5:151414457 on Build GRCh38

Set Membership

HapMap

Context Sequence [VIC/FAM]

GCACCTAGGGTCTTGTGAGCCAGAT[G/T]AAGGTATTTGGAATATATCTTGTCC

Phenotype

MIM: 606561

Polymorphism

G/T, Transversion Substitution

Allele Nomenclature

Literature Links

SLC36A1 PubMed Links

Additional Information

For this assay, SNP(s) [rs76836253] 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

SLC36A1

Gene Name

solute carrier family 36 member 1

Transcript Accession	SNP Location	SNP Type	Codon Change	Amino Acid Change	Protein ID
NM_001308150.1		Intron			NP_001295079.1
NM_001308151.1		Intron			NP_001295080.1
NM_078483.3		Intron			NP_510968.2
XM_005268386.1		Intron			XP_005268443.1
XM_006714759.3		Intron			XP_006714822.1
XM_011537580.2		Intron			XP_011535882.1
XM_011537581.1		Intron			XP_011535883.1
XM_011537583.2		Intron			XP_011535885.1
XM_011537584.2		Intron			XP_011535886.1
XM_011537585.1		Intron			XP_011535887.1
XM_011537586.2		Intron			XP_011535888.1
XM_011537587.2		Intron			XP_011535889.1
XM_011537588.2		Intron			XP_011535890.1
XM_011537589.2		Intron			XP_011535891.1
XM_011537590.1		Intron			XP_011535892.1
XM_011537591.1		Intron			XP_011535893.1
XM_011537592.2		Intron			XP_011535894.1
XM_011537593.2		Intron			XP_011535895.1
XM_011537594.1		Intron			XP_011535896.1
XM_011537595.2		Intron			XP_011535897.2
XM_011537596.2		Intron			XP_011535898.2
XM_017009216.1		Intron			XP_016864705.1
XM_017009217.1		Intron			XP_016864706.1
XM_017009218.1		Intron			XP_016864707.1
XM_017009219.1		Intron			XP_016864708.1
XM_017009220.1		Intron			XP_016864709.1

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