Product Details

SNP ID
rs138694095
Assay Type
Functionally tested
NCBI dbSNP Submissions
NA
Location
Chr.19:7743094 on Build GRCh38
Set Membership
Context Sequence [VIC/FAM]
GGCTGGAGAAAGAAACTGTTCTTCA[C/T]CCCTGGAGCAGGAGGCTGCGGACTT
Phenotype
MIM: 604672
Polymorphism
C/T, Transition 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_001144893.1 844 Missense Mutation GAT,GGT D251G NP_001138365.1
NM_001144894.1 844 Missense Mutation GAT,GGT D343G NP_001138366.1
NM_001144895.1 844 Missense Mutation GAT,GGT D295G NP_001138367.1
NM_001144896.1 844 Missense Mutation GAT,GGT D363G NP_001138368.1
NM_001144897.1 844 Missense Mutation GAT,GGT D381G NP_001138369.1
NM_001144899.1 844 Missense Mutation GAT,GGT D226G NP_001138371.1
NM_021155.3 844 Missense Mutation GAT,GGT D387G NP_066978.1
XM_005272472.4 844 Missense Mutation GAT,GGT D249G XP_005272529.1

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