Product Details

SNP ID

rs6504116

Assay Type

Functionally tested

NCBI dbSNP Submissions

NA

Location

Chr.17:62639507 on Build GRCh38

Set Membership

HapMap

Context Sequence [VIC/FAM]

ACTGTAAATTGGTTCTGTTTTTCAG[A/G]ATTCAATCTTTCGGACAATATGTAA

Phenotype

MIM: 612264

Polymorphism

A/G, 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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