Product Details

SNP ID

rs16829117

Assay Type

Functionally tested

NCBI dbSNP Submissions

NA

Location

Chr.2:148648860 on Build GRCh38

Set Membership

HapMap

Context Sequence [VIC/FAM]

ATCATGTCATCCTGTGTAGCCTCTT[A/C]TTTTGGACATCCAAACATCTTTTAC

Phenotype

MIM: 611000

Polymorphism

A/C, Transversion substitution

Allele Nomenclature

Literature Links

EPC2 PubMed Links

Gene Details

Gene

EPC2

Gene Name

enhancer of polycomb homolog 2

Transcript Accession	SNP Location	SNP Type	Codon Change	Amino Acid Change	Protein ID
NM_015630.3		Intron			NP_056445.3
XM_011510941.2		Intron			XP_011509243.1
XM_011510943.2		Intron			XP_011509245.1

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