Product Details

SNP ID

rs185070039

Assay Type

Functionally tested

NCBI dbSNP Submissions

2

Location

Chr.1:231163127 on Build GRCh38

Set Membership

Context Sequence [VIC/FAM]

CTGCCCCAGCCGCTCCTGCTTTCCC[A/G]GGGATCGGGGCTGCAGGCGGGCGCC

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	200	Missense Mutation	CAG,CGG	Q53R	NP_001004342.3
NM_001300889.1	200	Intron			NP_001287818.1
XM_011544192.2	200	Missense Mutation	CAG,CGG	Q53R	XP_011542494.1
XM_017001323.1	200	Missense Mutation	CAG,CGG	Q53R	XP_016856812.1

View Full Product Details