Product Details

SNP ID
rs138944432
Assay Type
Functionally Tested
NCBI dbSNP Submissions
NA
Location
Chr.17:62633141 on Build GRCh38
Set Membership
Context Sequence [VIC/FAM]
AATGAGATCATGAACGTATGAGATA[C/T]GTCCCTGGTACACTACTGGGCACAG
Phenotype
MIM: 612264
Polymorphism
C/T, Transition Substitution
Allele Nomenclature
Literature Links
MRC2 PubMed Links

Gene Details

Gene
MRC2
Gene Name
mannose receptor C type 2
Transcript Accession SNP Location SNP Type Codon Change Amino Acid Change Protein ID
NM_006039.4 Intron NP_006030.2
XM_011525543.2 Intron XP_011523845.1

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