Product Details

SNP ID

rs4304840

Assay Type

Functionally tested

NCBI dbSNP Submissions

NA

Location

Chr.12:8515301 on Build GRCh38

Set Membership

HapMap

Context Sequence [VIC/FAM]

TGCTGTAGTTTTCATCTTACTTCTC[A/G]GTGTCTGTTTTATTGCAAGTTGTTT

Phenotype

MIM: 609964

Polymorphism

A/G, Transition substitution

Allele Nomenclature

Literature Links

CLEC4D PubMed Links

Gene Details

Gene

CLEC4D

Gene Name

C-type lectin domain family 4 member D

Transcript Accession	SNP Location	SNP Type	Codon Change	Amino Acid Change	Protein ID
NM_080387.4	287	Missense Mutation	AGT,GGT	S32G	NP_525126.2
XM_011520632.2	287	Missense Mutation	AGT,GGT	S32G	XP_011518934.1
XM_011520633.2	287	Missense Mutation	AGT,GGT	S32G	XP_011518935.1

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