Product Details

SNP ID
rs146694134
Assay Type
Functionally tested
NCBI dbSNP Submissions
NA
Location
Chr.17:40554879 on Build GRCh38
Set Membership
Context Sequence [VIC/FAM]
TTGAAGAGCTTGAAGAGATCGTTGC[A/G]GAACTTGACGCCGATGAAGGCGTAC
Phenotype
MIM: 600242
Polymorphism
A/G, Transition substitution
Allele Nomenclature
Literature Links
CCR7 PubMed Links

Gene Details

Gene
CCR7
Gene Name
C-C motif chemokine receptor 7
Transcript Accession SNP Location SNP Type Codon Change Amino Acid Change Protein ID
NM_001301714.1 1081 Missense Mutation CGC,TGC R271C NP_001288643.1
NM_001301716.1 1081 Missense Mutation CGC,TGC R328C NP_001288645.1
NM_001301717.1 1081 Missense Mutation CGC,TGC R328C NP_001288646.1
NM_001301718.1 1081 Missense Mutation CGC,TGC R328C NP_001288647.1
NM_001838.3 1081 Missense Mutation CGC,TGC R334C NP_001829.1

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