Product Details

SNP ID
rs113286964
Assay Type
Functionally tested
NCBI dbSNP Submissions
NA
Location
Chr.6:30137212 on Build GRCh38
Set Membership
Context Sequence [VIC/FAM]
TTCTGCTGCCCCCTCTGCCGGAAGC[A/C]CTGTTCTGAGGAGGTGCTAGGGACA
Phenotype
MIM: 616976
Polymorphism
A/C, Transversion 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_001286633.1 993 Missense Mutation CAC,CCC H59P NP_001273562.1
NM_138700.4 993 Missense Mutation CAC,CCC H59P NP_619645.1
XM_011514305.1 993 Missense Mutation CAC,CCC H59P XP_011512607.1
XM_011514306.1 993 Missense Mutation CAC,CCC H59P XP_011512608.1
XM_011514308.1 993 Missense Mutation CAC,CCC H59P XP_011512610.1
XM_011514309.1 993 Missense Mutation CAC,CCC H59P XP_011512611.1

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