Product Details

SNP ID

rs71526132

Assay Type

Functionally Tested

NCBI dbSNP Submissions

NA

Location

Chr.8:17498867 on Build GRCh38

Set Membership

Context Sequence [VIC/FAM]

ACTGGGCTTAGGAGCCTGGGAAGGC[A/G]AATAGAAGCTAGCTGGGGAGACAGG

Phenotype

MIM: 601872

Polymorphism

A/G, Transition Substitution

Allele Nomenclature

Literature Links

SLC7A2 PubMed Links

Additional Information

For this assay, SNP(s) [rs78313762] 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

SLC7A2

Gene Name

solute carrier family 7 member 2

Transcript Accession	SNP Location	SNP Type	Codon Change	Amino Acid Change	Protein ID
NM_001008539.3		Intron			NP_001008539.3
NM_001164771.1		Intron			NP_001158243.1
NM_003046.5		Intron			NP_003037.4
XM_005273610.4		Intron			XP_005273667.1
XM_005273611.4		Intron			XP_005273668.1
XM_005273612.4		Intron			XP_005273669.1
XM_017013746.1		Intron			XP_016869235.1
XM_017013747.1		Intron			XP_016869236.1

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