Product Details

SNP ID

rs4652319

Assay Type

Functionally Tested

NCBI dbSNP Submissions

65

Location

Chr.1:178740831 on Build GRCh38

Set Membership

HapMap

Context Sequence [VIC/FAM]

GTAGGCTTTGGTGTCAGACATTTGA[C/T]ATTAGAATTCTGGCTTTTTTACCAG

Phenotype

Polymorphism

C/T, Transition Substitution

Allele Nomenclature

Literature Links

RALGPS2 PubMed Links

Additional Information

For this assay, SNP(s) [rs75215226] 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

RALGPS2

Gene Name

Ral GEF with PH domain and SH3 binding motif 2

Transcript Accession	SNP Location	SNP Type	Codon Change	Amino Acid Change	Protein ID
NM_001286247.1		Intron			NP_001273176.1
NM_152663.4		Intron			NP_689876.2
XM_006711410.3		Intron			XP_006711473.1
XM_006711411.3		Intron			XP_006711474.1
XM_011509688.1		Intron			XP_011507990.1
XM_017001591.1		Intron			XP_016857080.1

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