Product Details

SNP ID

rs28550346

Assay Type

Functionally Tested

NCBI dbSNP Submissions

NA

Location

Chr.17:19243132 on Build GRCh38

Set Membership

Context Sequence [VIC/FAM]

CCTTGTTTCTCAAACTCCTGTGTGC[A/G]GCAGAAGCACCCAGAGGGCTTGCTG

Phenotype

MIM: 607263

Polymorphism

A/G, Transition Substitution

Allele Nomenclature

Literature Links

EPN2 PubMed Links

Additional Information

For this assay, SNP(s) [rs117339802] 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

EPN2

Gene Name

epsin 2

Transcript Accession	SNP Location	SNP Type	Codon Change	Amino Acid Change	Protein ID
NM_001102664.1		Intron			NP_001096134.1
NM_014964.4		Intron			NP_055779.2
NM_148921.3		Intron			NP_683723.2

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