Product Details

SNP ID

rs28528780

Assay Type

Functionally Tested

NCBI dbSNP Submissions

NA

Location

Chr.5:50441293 on Build GRCh38

Set Membership

Context Sequence [VIC/FAM]

GGGTAGGACGCTGAAGAAAAGGCGG[A/C]ATGGGAGGGGCCCGGCCGCCTTGCC

Phenotype

MIM: 615669

Polymorphism

A/C, Transversion Substitution

Allele Nomenclature

Literature Links

EMB PubMed Links

Additional Information

For this assay, SNP(s) [rs115322616] are located under a primer 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

EMB

Gene Name

embigin

Transcript Accession	SNP Location	SNP Type	Codon Change	Amino Acid Change	Protein ID
NM_198449.2		Intron			NP_940851.1
XM_011543146.2		Intron			XP_011541448.1

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