Product Details

SNP ID
rs202034220
Assay Type
Functionally tested
NCBI dbSNP Submissions
NA
Location
Chr.6:30137206 on Build GRCh38
Set Membership
Context Sequence [VIC/FAM]
GGGGTCTTCTGCTGCCCCCTCTGCC[A/G]GAAGCCCTGTTCTGAGGAGGTGCTA
Phenotype
MIM: 616976
Polymorphism
A/G, 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_001286633.1 987 Missense Mutation CAG,CGG Q57R NP_001273562.1
NM_138700.4 987 Missense Mutation CAG,CGG Q57R NP_619645.1
XM_011514305.1 987 Missense Mutation CAG,CGG Q57R XP_011512607.1
XM_011514306.1 987 Missense Mutation CAG,CGG Q57R XP_011512608.1
XM_011514308.1 987 Missense Mutation CAG,CGG Q57R XP_011512610.1
XM_011514309.1 987 Missense Mutation CAG,CGG Q57R XP_011512611.1

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