Product Details

SNP ID
rs12622238
Assay Type
Functionally Tested
NCBI dbSNP Submissions
NA
Location
Chr.2:9212519 on Build GRCh38
Set Membership
HapMap
Context Sequence [VIC/FAM]
TGATCTACTCCTGAGGTGGTGGCCA[A/G]CTCGGCGTCTGCGGTAGGATTTTCA
Phenotype
MIM: 603817
Polymorphism
A/G, Transition Substitution
Allele Nomenclature
Literature Links
ASAP2 PubMed Links
Additional Information
For this assay, SNP(s) [rs142424565] 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
ASAP2
Gene Name
ArfGAP with SH3 domain, ankyrin repeat and PH domain 2
Transcript Accession SNP Location SNP Type Codon Change Amino Acid Change Protein ID
NM_001135191.1 Intron NP_001128663.1
NM_003887.2 Intron NP_003878.1
XM_006711898.1 Intron XP_006711961.1
XM_006711901.3 Intron XP_006711964.1
XM_006711902.1 Intron XP_006711965.1
XM_011510403.2 Intron XP_011508705.1
XM_011510404.2 Intron XP_011508706.1
XM_011510405.2 Intron XP_011508707.1
XM_011510406.2 Intron XP_011508708.1
XM_011510407.2 Intron XP_011508709.1
XM_011510408.2 Intron XP_011508710.1
XM_011510409.1 Intron XP_011508711.1

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