Product Details

SNP ID

rs11950448

Assay Type

Functionally Tested

NCBI dbSNP Submissions

NA

Location

Chr.5:43360163 on Build GRCh38

Set Membership

HapMap

Context Sequence [VIC/FAM]

TTGGGCAATTACACTACCGGGTAAT[C/G]CTGCACAAATGAAAACTCAAATGTC

Phenotype

MIM: 605240

Polymorphism

C/G, Transversion Substitution

Allele Nomenclature

Literature Links

CCL28 PubMed Links

Additional Information

For this assay, SNP(s) [rs77589834] 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

CCL28

Gene Name

C-C motif chemokine ligand 28

Transcript Accession	SNP Location	SNP Type	Codon Change	Amino Acid Change	Protein ID
NM_001301873.1		Intron			NP_001288802.1
NM_001301874.1		Intron			NP_001288803.1
NM_001301875.1		Intron			NP_001288804.1
NM_148672.3		Intron			NP_683513.1

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