Product Details

SNP ID
rs62066592
Assay Type
Functionally tested
NCBI dbSNP Submissions
NA
Location
Chr.17:40555038 on Build GRCh38
Set Membership
Context Sequence [VIC/FAM]
GCCACCGTCTGGGCCAGGACCACCC[A/C]ATTGTAGGGCAGCTGGAAGACTATG
Phenotype
MIM: 600242
Polymorphism
A/C, Transversion 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_001301714.1 922 Missense Mutation GGG,TGG G218W NP_001288643.1
NM_001301716.1 922 Missense Mutation GGG,TGG G275W NP_001288645.1
NM_001301717.1 922 Missense Mutation GGG,TGG G275W NP_001288646.1
NM_001301718.1 922 Missense Mutation GGG,TGG G275W NP_001288647.1
NM_001838.3 922 Missense Mutation GGG,TGG G281W NP_001829.1

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