Product Details

SNP ID

rs13151432

Assay Type

Functionally Tested

NCBI dbSNP Submissions

NA

Location

Chr.4:36007845 on Build GRCh38

Set Membership

Context Sequence [VIC/FAM]

GTTAGAGTAAAGTGGCAGATCAAAG[G/T]TCCTGGATGCAAAATCAGTGTACAA

Phenotype

MIM: 606645

Polymorphism

G/T, Transversion Substitution

Allele Nomenclature

Literature Links

ARAP2 PubMed Links

Additional Information

For this assay, SNP(s) [rs76345442] 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

ARAP2

Gene Name

ArfGAP with RhoGAP domain, ankyrin repeat and PH domain 2

Transcript Accession	SNP Location	SNP Type	Codon Change	Amino Acid Change	Protein ID
NM_015230.3		Intron			NP_056045.2
XM_017007698.1		Intron			XP_016863187.1
XM_017007699.1		Intron			XP_016863188.1
XM_017007700.1		Intron			XP_016863189.1
XM_017007701.1		Intron			XP_016863190.1
XM_017007702.1		Intron			XP_016863191.1

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