Product Details

SNP ID
rs111692925
Assay Type
Functionally tested
NCBI dbSNP Submissions
NA
Location
Chr.6:30137161 on Build GRCh38
Set Membership
Context Sequence [VIC/FAM]
TGTCGAGTGTGCCTGACACAGCATG[C/T]GGAGAAGGCCTCAGCCTCTGGGGTC
Phenotype
MIM: 616976
Polymorphism
C/T, Transition substitution
Allele Nomenclature
Literature Links
TRIM40 PubMed Links

Gene Details

Gene
TRIM40
Gene Name
tripartite motif containing 40
Transcript Accession SNP Location SNP Type Codon Change Amino Acid Change Protein ID
NM_001286633.1 942 Missense Mutation GCG,GTG A42V NP_001273562.1
NM_138700.4 942 Missense Mutation GCG,GTG A42V NP_619645.1
XM_011514305.1 942 Missense Mutation GCG,GTG A42V XP_011512607.1
XM_011514306.1 942 Missense Mutation GCG,GTG A42V XP_011512608.1
XM_011514308.1 942 Missense Mutation GCG,GTG A42V XP_011512610.1
XM_011514309.1 942 Missense Mutation GCG,GTG A42V XP_011512611.1

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