Product Details

SNP ID

rs9861824

Assay Type

Functionally Tested

NCBI dbSNP Submissions

NA

Location

Chr.3:45029754 on Build GRCh38

Set Membership

Context Sequence [VIC/FAM]

CCTTTCCTGAAGCCCTGGTGTTTCA[A/G]AAAGACCAGGGTCCGCCCCAGGAGC

Phenotype

MIM: 187520

Polymorphism

A/G, Transition Substitution

Allele Nomenclature

Literature Links

CLEC3B PubMed Links

Additional Information

For this assay, SNP(s) [rs77356307] 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

CLEC3B

Gene Name

C-type lectin domain family 3 member B

Transcript Accession	SNP Location	SNP Type	Codon Change	Amino Acid Change	Protein ID
NM_001308394.1		Intron			NP_001295323.1
NM_003278.2		Intron			NP_003269.2
XM_017007116.1		Intron			XP_016862605.1
XM_017007117.1		Intron			XP_016862606.1

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