Product Details

SNP ID
rs142879289
Assay Type
Functionally tested
NCBI dbSNP Submissions
6
Location
Chr.1:231163827 on Build GRCh38
Set Membership
Context Sequence [VIC/FAM]
GCGGCGGCTGCAAGAGCCCGGGAGG[A/C]GCGGGGGCGGGGGCGACTGGGGGCA
Phenotype
MIM: 610584
Polymorphism
A/C, Transversion 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_001004342.3 714 Silent Mutation GGA,GGC G286G NP_001004342.3
NM_001300889.1 714 Silent Mutation GGA,GGC G224G NP_001287818.1
XM_011544192.2 714 Silent Mutation GGA,GGC G286G XP_011542494.1
XM_017001323.1 714 Silent Mutation GGA,GGC G286G XP_016856812.1

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