Product Details

SNP ID

rs11465393

Assay Type

Functionally tested

NCBI dbSNP Submissions

NA

Location

Chr.19:7743110 on Build GRCh38

Set Membership

HapMap

Context Sequence [VIC/FAM]

TGTTCTTCATCCCTGGAGCAGGAGG[C/A]TGCGGACTTTTTGCAGATCCAGAAT

Phenotype

MIM: 604672

Polymorphism

C/A, Transversion substitution

Allele Nomenclature

Literature Links

CD209 PubMed Links

Gene Details

Gene

CD209

Gene Name

CD209 molecule

Transcript Accession	SNP Location	SNP Type	Codon Change	Amino Acid Change	Protein ID
NM_001144893.1	828	Missense Mutation	GCC,TCC	A246S	NP_001138365.1
NM_001144894.1	828	Missense Mutation	GCC,TCC	A338S	NP_001138366.1
NM_001144895.1	828	Missense Mutation	GCC,TCC	A290S	NP_001138367.1
NM_001144896.1	828	Missense Mutation	GCC,TCC	A358S	NP_001138368.1
NM_001144897.1	828	Missense Mutation	GCC,TCC	A376S	NP_001138369.1
NM_001144899.1	828	Missense Mutation	GCC,TCC	A221S	NP_001138371.1
NM_021155.3	828	Missense Mutation	GCC,TCC	A382S	NP_066978.1
XM_005272472.4	828	Missense Mutation	GCC,TCC	A244S	XP_005272529.1

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