Product Details

SNP ID
rs143531930
Assay Type
Functionally tested
NCBI dbSNP Submissions
NA
Location
Chr.19:7743060 on Build GRCh38
Set Membership
Context Sequence [VIC/FAM]
TCTGCTACGCAGGAGGGGGGTTTGG[G/T]GTGGCAGGGGCTGGAGAAAGAAACT
Phenotype
MIM: 604672
Polymorphism
G/T, 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_001144893.1 878 Silent Mutation ACA,ACC T262T NP_001138365.1
NM_001144894.1 878 Silent Mutation ACA,ACC T354T NP_001138366.1
NM_001144895.1 878 Silent Mutation ACA,ACC T306T NP_001138367.1
NM_001144896.1 878 Silent Mutation ACA,ACC T374T NP_001138368.1
NM_001144897.1 878 Silent Mutation ACA,ACC T392T NP_001138369.1
NM_001144899.1 878 Silent Mutation ACA,ACC T237T NP_001138371.1
NM_021155.3 878 Silent Mutation ACA,ACC T398T NP_066978.1
XM_005272472.4 878 Silent Mutation ACA,ACC T260T XP_005272529.1

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