Product Details

SNP ID

rs7126383

Assay Type

Functionally Tested

NCBI dbSNP Submissions

NA

Location

Chr.11:7527397 on Build GRCh38

Set Membership

HapMap

Context Sequence [VIC/FAM]

GGTCAGAACTGGCCCATTGGATCTG[A/G]GGAAACCTACCCTTTAGCAGCAGAG

Phenotype

MIM: 603142

Polymorphism

A/G, Transition Substitution

Allele Nomenclature

Literature Links

PPFIBP2 PubMed Links

Additional Information

For this assay, SNP(s) [rs147881990] 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

PPFIBP2

Gene Name

PPFIA binding protein 2

Transcript Accession	SNP Location	SNP Type	Codon Change	Amino Acid Change	Protein ID
NM_001256568.1		Intron			NP_001243497.1
NM_001256569.1		Intron			NP_001243498.1
NM_003621.3		Intron			NP_003612.2
XM_005253177.2		Intron			XP_005253234.1
XM_006718349.2		Intron			XP_006718412.1
XM_006718350.2		Intron			XP_006718413.1
XM_006718351.2		Intron			XP_006718414.1
XM_006718352.2		Intron			XP_006718415.1
XM_006718353.2		Intron			XP_006718416.1
XM_011520413.2		Intron			XP_011518715.1
XM_011520414.2		Intron			XP_011518716.1
XM_011520415.2		Intron			XP_011518717.1
XM_011520416.2		Intron			XP_011518718.1
XM_011520417.2		Intron			XP_011518719.1
XM_011520418.2		Intron			XP_011518720.1
XM_011520419.2		Intron			XP_011518721.1
XM_011520420.2		Intron			XP_011518722.1
XM_017018443.1		Intron			XP_016873932.1
XM_017018444.1		Intron			XP_016873933.1
XM_017018445.1		Intron			XP_016873934.1
XM_017018446.1		Intron			XP_016873935.1
XM_017018447.1		Intron			XP_016873936.1

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