Product Details

SNP ID
rs708184
Assay Type
Functionally Tested
NCBI dbSNP Submissions
NA
Location
Chr.12:27535338 on Build GRCh38
Set Membership
HapMap
Context Sequence [VIC/FAM]
AATTTAAAAATTAAAAAACTAAGCA[G/T]TGAAGTTTTTAGCATGAATTTACTC
Phenotype
MIM: 603141
Polymorphism
G/T, Transversion Substitution
Allele Nomenclature
Literature Links
PPFIBP1 PubMed Links
Additional Information
For this assay, SNP(s) [rs142453813] 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
PPFIBP1
Gene Name
PPFIA binding protein 1
Transcript Accession SNP Location SNP Type Codon Change Amino Acid Change Protein ID
NM_001198915.1 Intron NP_001185844.1
NM_001198916.1 Intron NP_001185845.1
NM_003622.3 Intron NP_003613.3
NM_177444.2 Intron NP_803193.2
XM_005253505.1 Intron XP_005253562.1
XM_005253507.1 Intron XP_005253564.1
XM_005253508.1 Intron XP_005253565.1
XM_005253509.1 Intron XP_005253566.1
XM_006719159.3 Intron XP_006719222.1
XM_017020056.1 Intron XP_016875545.1
XM_017020057.1 Intron XP_016875546.1
XM_017020058.1 Intron XP_016875547.1
XM_017020059.1 Intron XP_016875548.1
XM_017020060.1 Intron XP_016875549.1
XM_017020061.1 Intron XP_016875550.1
XM_017020062.1 Intron XP_016875551.1
XM_017020063.1 Intron XP_016875552.1
XM_017020064.1 Intron XP_016875553.1
XM_017020065.1 Intron XP_016875554.1
XM_017020066.1 Intron XP_016875555.1
XM_017020067.1 Intron XP_016875556.1
XM_017020068.1 Intron XP_016875557.1
XM_017020069.1 Intron XP_016875558.1
XM_017020070.1 Intron XP_016875559.1
XM_017020071.1 Intron XP_016875560.1
XM_017020072.1 Intron XP_016875561.1
XM_017020073.1 Intron XP_016875562.1
XM_017020074.1 Intron XP_016875563.1
XM_017020075.1 Intron XP_016875564.1
XM_017020076.1 Intron XP_016875565.1
XM_017020077.1 Intron XP_016875566.1
XM_017020078.1 Intron XP_016875567.1

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