Product Details

SNP ID
rs200999586
Assay Type
Functionally tested
NCBI dbSNP Submissions
9
Location
Chr.1:231163932 on Build GRCh38
Set Membership
Context Sequence [VIC/FAM]
TGTACTGCGTGAGCTGTCGAACCCC[A/G]GTGTGTTATCTGTGCCTGGAGGAGG
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_001004342.3 819 Silent Mutation CCA,CCG P321P NP_001004342.3
NM_001300889.1 819 Silent Mutation CCA,CCG P259P NP_001287818.1
XM_011544192.2 819 Silent Mutation CCA,CCG P321P XP_011542494.1
XM_017001323.1 819 Silent Mutation CCA,CCG P321P XP_016856812.1

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