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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