Product Details

SNP ID
rs199723848
Assay Type
Functionally tested
NCBI dbSNP Submissions
NA
Location
Chr.6:30137310 on Build GRCh38
Set Membership
Context Sequence [VIC/FAM]
GGAGAGCAGACTTCTTCTATGTGTG[A/G]AATGCCTGGTGTCCCCTGAACACAT
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 1091 Missense Mutation AAA,GAA K92E NP_001273562.1
NM_138700.4 1091 Missense Mutation AAA,GAA K92E NP_619645.1
XM_011514305.1 1091 Missense Mutation AAA,GAA K92E XP_011512607.1
XM_011514306.1 1091 Missense Mutation AAA,GAA K92E XP_011512608.1
XM_011514308.1 1091 Missense Mutation AAA,GAA K92E XP_011512610.1
XM_011514309.1 1091 Missense Mutation AAA,GAA K92E XP_011512611.1

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