Product Details

SNP ID
rs200089970
Assay Type
Functionally tested
NCBI dbSNP Submissions
3
Location
Chr.1:231163008 on Build GRCh38
Set Membership
Context Sequence [VIC/FAM]
TGAAGTGTCCCGTGTGCGGCTCTCT[G/T]TTTCGGGAGCCTATCATCCTGCCCT
Phenotype
MIM: 610584
Polymorphism
G/T, 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 81 Silent Mutation CTG,CTT L13L NP_001004342.3
NM_001300889.1 81 Silent Mutation CTG,CTT L13L NP_001287818.1
XM_011544192.2 81 Silent Mutation CTG,CTT L13L XP_011542494.1
XM_017001323.1 81 Silent Mutation CTG,CTT L13L XP_016856812.1

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