Product Details

SNP ID
rs146546280
Assay Type
Functionally tested
NCBI dbSNP Submissions
NA
Location
Chr.12:9669744 on Build GRCh38
Set Membership
Context Sequence [VIC/FAM]
AGAAACTGGAGGCAAAATGCATGAC[A/C]GTAACAATGTGGAGAAAGACATTAC
Phenotype
MIM: 605659
Polymorphism
A/C, Transversion substitution
Allele Nomenclature
Literature Links
CLEC2D PubMed Links

Gene Details

Gene
CLEC2D
Gene Name
C-type lectin domain family 2 member D
Transcript Accession SNP Location SNP Type Codon Change Amino Acid Change Protein ID
NM_001004419.4 37 Missense Mutation AGT,CGT S4R NP_001004419.1
NM_001197317.2 37 Missense Mutation AGT,CGT S4R NP_001184246.1
NM_001197318.2 37 Missense Mutation AGT,CGT S4R NP_001184247.1
NM_001197319.2 37 Missense Mutation AGT,CGT S4R NP_001184248.1
NM_013269.5 37 Missense Mutation AGT,CGT S4R NP_037401.1

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