Product Details

SNP ID

rs78409055

Assay Type

Functionally Tested

NCBI dbSNP Submissions

NA

Location

Chr.19:7766741 on Build GRCh38

Set Membership

Context Sequence [VIC/FAM]

TGTCTAACTCCCAGCGGAACTGGCA[C/T]GACTCCGTCACCGCCTGCCAGGAAG

Phenotype

MIM: 605872

Polymorphism

C/T, Transition Substitution

Allele Nomenclature

Literature Links

CLEC4M PubMed Links

Additional Information

For this assay, SNP(s) [rs2277998] 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

CLEC4M

Gene Name

C-type lectin domain family 4 member M

Transcript Accession	SNP Location	SNP Type	Codon Change	Amino Acid Change	Protein ID
NM_001144904.1	919	Silent Mutation	CAC,CAT	H239H	NP_001138376.1
NM_001144905.1	919	Silent Mutation	CAC,CAT	H266H	NP_001138377.1
NM_001144906.1	919	Silent Mutation	CAC,CAT	H154H	NP_001138378.1
NM_001144907.1	919	Silent Mutation	CAC,CAT	H223H	NP_001138379.1
NM_001144908.1	919	Silent Mutation	CAC,CAT	H198H	NP_001138380.1
NM_001144909.1	919	Silent Mutation	CAC,CAT	H244H	NP_001138381.1
NM_001144910.1	919	Silent Mutation	CAC,CAT	H267H	NP_001138382.1
NM_001144911.1	919	Silent Mutation	CAC,CAT	H262H	NP_001138383.1
NM_014257.4	919	Silent Mutation	CAC,CAT	H290H	NP_055072.3
XM_006722611.2	919	Silent Mutation	CAC,CAT	H289H	XP_006722674.1
XM_006722612.3	919	Silent Mutation	CAC,CAT	H262H	XP_006722675.1
XM_006722613.3	919	Silent Mutation	CAC,CAT	H262H	XP_006722676.1
XM_006722614.3	919	Silent Mutation	CAC,CAT	H234H	XP_006722677.1
XM_006722615.2	919	Silent Mutation	CAC,CAT	H290H	XP_006722678.1

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