Product Details

SNP ID
rs149807260
Assay Type
Functionally tested
NCBI dbSNP Submissions
NA
Location
Chr.6:30137123 on Build GRCh38
Set Membership
Context Sequence [VIC/FAM]
TGAAGGAGGCCGTGAGCACCAACTG[C/T]GGACATCTCTTCTGTCGAGTGTGCC
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_001286633.1 904 Silent Mutation TGC,TGT C29C NP_001273562.1
NM_138700.4 904 Silent Mutation TGC,TGT C29C NP_619645.1
XM_011514305.1 904 Silent Mutation TGC,TGT C29C XP_011512607.1
XM_011514306.1 904 Silent Mutation TGC,TGT C29C XP_011512608.1
XM_011514308.1 904 Silent Mutation TGC,TGT C29C XP_011512610.1
XM_011514309.1 904 Silent Mutation TGC,TGT C29C XP_011512611.1

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