Product Details

SNP ID

rs4602287

Assay Type

Functionally Tested

NCBI dbSNP Submissions

NA

Location

Chr.20:35780106 on Build GRCh38

Set Membership

HapMap

Context Sequence [VIC/FAM]

CCAGTGCTCTTACATCCCTCTCTCT[C/G]TAGCTAACGTGCTTTTTCCCCTAGA

Phenotype

MIM: 610335

Polymorphism

C/G, Transversion Substitution

Allele Nomenclature

Literature Links

PHF20 PubMed Links

Additional Information

For this assay, SNP(s) [rs77189140] 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

PHF20

Gene Name

PHD finger protein 20

Transcript Accession	SNP Location	SNP Type	Codon Change	Amino Acid Change	Protein ID
NM_016436.4		Intron			NP_057520.2
XM_005260421.2		Intron			XP_005260478.1
XM_011528843.1		Intron			XP_011527145.1
XM_011528844.1		Intron			XP_011527146.1
XM_017027864.1		Intron			XP_016883353.1
XM_017027865.1		Intron			XP_016883354.1
XM_017027866.1		Intron			XP_016883355.1
XM_017027867.1		Intron			XP_016883356.1
XM_017027868.1		Intron			XP_016883357.1
XM_017027869.1		Intron			XP_016883358.1
XM_017027870.1		Intron			XP_016883359.1
XM_017027871.1		Intron			XP_016883360.1

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