Product Details

SNP ID

rs4938347

Assay Type

Functionally Tested

NCBI dbSNP Submissions

NA

Location

Chr.11:117151043 on Build GRCh38

Set Membership

HapMap

Context Sequence [VIC/FAM]

TTCTATAAACCGCAAAACCCCAGAT[A/T]TTTTTCCTTTTCATAGTCCTTTGCA

Phenotype

MIM: 602508

Polymorphism

A/T, Transversion Substitution

Allele Nomenclature

Literature Links

PAFAH1B2 PubMed Links

Additional Information

For this assay, SNP(s) [rs373735449] 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

PAFAH1B2

Gene Name

platelet activating factor acetylhydrolase 1b catalytic subunit 2

Transcript Accession	SNP Location	SNP Type	Codon Change	Amino Acid Change	Protein ID
NM_001184746.1		Intron			NP_001171675.1
NM_001184747.1		Intron			NP_001171676.1
NM_001184748.1		Intron			NP_001171677.1
NM_001309431.1		Intron			NP_001296360.1
NM_002572.3		Intron			NP_002563.1
XM_017017840.1		Intron			XP_016873329.1

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