Product Details

SNP ID

rs11053592

Assay Type

Functionally Tested

NCBI dbSNP Submissions

NA

Location

Chr.12:10117575 on Build GRCh38

Set Membership

HapMap

Context Sequence [VIC/FAM]

AAGATTCTATTAGAGATATGGCAGA[C/T]GTACTCTCTGAGCTATTTAATTGAT

Phenotype

MIM: 606264

Polymorphism

C/T, Transition Substitution

Allele Nomenclature

Literature Links

CLEC7A PubMed Links

Additional Information

For this assay, SNP(s) [rs140187470] 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

CLEC7A

Gene Name

C-type lectin domain family 7 member A

Transcript Accession	SNP Location	SNP Type	Codon Change	Amino Acid Change	Protein ID
NM_022570.4	1577	UTR 3			NP_072092.2
NM_197947.2	1577	UTR 3			NP_922938.1
NM_197948.2	1577	UTR 3			NP_922939.1
NM_197949.2	1577	UTR 3			NP_922940.1
NM_197950.2	1577	UTR 3			NP_922941.1
NM_197954.2	1577	Intron			NP_922945.1
XM_006719135.3	1577	Intron			XP_006719198.1
XM_017019822.1	1577	UTR 3			XP_016875311.1
XM_017019823.1	1577	UTR 3			XP_016875312.1

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