Product Details

SNP ID
rs10821163
Assay Type
Functionally Tested
NCBI dbSNP Submissions
NA
Location
Chr.9:93580778 on Build GRCh38
Set Membership
HapMap
Context Sequence [VIC/FAM]
TATTTGTTGGGCTTGTATTCTGTAC[C/G]GAGTTCAGAGCTGGCTGTGAGGGCC
Phenotype
MIM: 604351
Polymorphism
C/G, Transversion Substitution
Allele Nomenclature
Literature Links
PHF2 PubMed Links
Additional Information
For this assay, SNP(s) [rs7038444] 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
PHF2
Gene Name
PHD finger protein 2
Transcript Accession SNP Location SNP Type Codon Change Amino Acid Change Protein ID
NM_005392.3 Intron NP_005383.3
XM_005252051.2 Intron XP_005252108.1
XM_006717143.2 Intron XP_006717206.1

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