Product Details

SNP ID
rs117065429
Assay Type
Functionally tested
NCBI dbSNP Submissions
5
Location
Chr.1:231163986 on Build GRCh38
Set Membership
Context Sequence [VIC/FAM]
GGCACGCCAAGCACGAGGTGAAGCC[A/G]CTGGGGGCCATGTGGAAGCAGCACA
Phenotype
MIM: 610584
Polymorphism
A/G, Transition substitution
Allele Nomenclature
Literature Links
TRIM67 PubMed Links

Gene Details

Gene
TRIM67
Gene Name
tripartite motif containing 67
Transcript Accession SNP Location SNP Type Codon Change Amino Acid Change Protein ID
NM_001004342.3 873 Silent Mutation CCA,CCG P339P NP_001004342.3
NM_001300889.1 873 Silent Mutation CCA,CCG P277P NP_001287818.1
XM_011544192.2 873 Silent Mutation CCA,CCG P339P XP_011542494.1
XM_017001323.1 873 Silent Mutation CCA,CCG P339P XP_016856812.1

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