Product Details

SNP ID

rs531425

Assay Type

Functionally Tested

NCBI dbSNP Submissions

NA

Location

Chr.12:9991647 on Build GRCh38

Set Membership

HapMap

Context Sequence [VIC/FAM]

CTCCAAATCTGCTTAATTATTGATA[A/G]GCTAGAAAAAAGATAAAGATTCAAG

Phenotype

MIM: 612088 MIM: 606783

Polymorphism

A/G, Transition Substitution

Allele Nomenclature

Literature Links

CLEC12A PubMed Links

Additional Information

For this assay, SNP(s) [rs115518238] are located under a probe 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

CLEC12A

Gene Name

C-type lectin domain family 12 member A

Transcript Accession	SNP Location	SNP Type	Codon Change	Amino Acid Change	Protein ID
NM_001207010.1	2667	Intron			NP_001193939.1
NM_001300730.1	2667	Intron			NP_001287659.1
NM_138337.5	2667	Intron			NP_612210.4
NM_201623.3	2667	Intron			NP_963917.2
XM_005253324.2	2667	Intron			XP_005253381.1
XM_006719033.3	2667	Intron			XP_006719096.1
XM_006719035.3	2667	Intron			XP_006719098.1
XM_006719036.3	2667	Intron			XP_006719099.1
XM_011520570.1	2667	Intron			XP_011518872.1
XM_011520571.2	2667	Intron			XP_011518873.2
XM_011520573.2	2667	Intron			XP_011518875.1

Gene

CLEC1B

Gene Name

C-type lectin domain family 1 member B

Transcript Accession	SNP Location	SNP Type	Codon Change	Amino Acid Change	Protein ID
NM_001099431.1	2667	Intron			NP_001092901.1
NM_016509.3	2667	Intron			NP_057593.3
XM_005253382.4	2667	Intron			XP_005253439.1
XM_011520685.2	2667	UTR 3			XP_011518987.1
XM_011520686.2	2667	Intron			XP_011518988.1
XM_017019395.1	2667	Intron			XP_016874884.1
XM_017019396.1	2667	Intron			XP_016874885.1

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