Product Details

SNP ID

hCV27849710

Assay Type

Functionally Tested

NCBI dbSNP Submissions

NA

Location

Chr.19:14582948 on Build GRCh38

Set Membership

Context Sequence [VIC/FAM]

TTCTGTGCGTGAATCCAAACTGGGG[A/G]GAAAGGCTCTGTGTGTATGTGTGTG

Phenotype

MIM: 616838

Polymorphism

A/G, Transition Substitution

Allele Nomenclature

Literature Links

CLEC17A PubMed Links

Additional Information

For this assay, SNP(s) [rs116924878] 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

CLEC17A

Gene Name

C-type lectin domain family 17 member A

Transcript Accession	SNP Location	SNP Type	Codon Change	Amino Acid Change	Protein ID
NM_001204118.1		Intron			NP_001191047.1
NM_207390.3		Intron			NP_997273.3

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